Variant report

Variant rs6911383
Chromosome Location chr6:32379682-32379683
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:32368400-32385600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr6:32378800-32381200 Enhancers Fetal Intestine Large intestine
3 chr6:32378800-32381200 Enhancers Fetal Intestine Small intestine
4 chr6:32379000-32379800 Flanking Active TSS Duodenum Mucosa Duodenum
5 chr6:32379400-32383400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
6 chr6:32379600-32379800 Flanking Bivalent TSS/Enh Rectal Mucosa Donor 29 rectum
7 chr6:32379600-32379800 Bivalent Enhancer Sigmoid Colon Sigmoid Colon
8 chr6:32379600-32380600 Bivalent Enhancer Rectal Mucosa Donor 31 rectum

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