Additional file 1: Table S1. of Genome-wide analysis of DNA methylation and gene expression defines molecular characteristics of Crohn’s disease-associated fibrosis Tammy Sadler Jeffrey Bhasin Yaomin Xu Jill Barnholz-Sloan Yanwen Chen Angela Ting Eleni Stylianou 10.6084/m9.figshare.c.3616010_D5.v1 https://springernature.figshare.com/articles/dataset/Additional_file_1_Table_S1_of_Genome-wide_analysis_of_DNA_methylation_and_gene_expression_defines_molecular_characteristics_of_Crohn_s_disease-associated_fibrosis/4378280 Differentially methylated regions (DMRs) between normal and fibrotic HIF. Each row represents one DMR. For each DMR, a unique ID, coordinates in the form of chr, start, end (hg19), and the DMR width are provided. Each DMR is categorized by a pattern code: “01” represents hypermethylation in fibrotic samples, and “10” represents hypomethylation in fibrotic samples. The “ratio” column represents the magnitude of the difference in sequencing signal as a log2 fold change, “p.value” is the unadjusted p value, and “q.value” is the Benjamini-Hochberg adjusted p value. “Genomic_context” specifies if the DMR falls within a portion of an annotated gene model. Multiple overlaps are resolved using the priority: promoter > exon > intron > 3′ end > intergenic. Overlap with CpG shores, islands, and shelves is provided, along with the distance to the nearest gene and the names of the nearest genes. (XLS 461 kb) 2016-03-12 05:00:00 DNA methylome Transcriptome Intestinal fibrosis Next generation sequencing RNA seq Omics Crohn’s disease Inflammatory bowel disease