Variant report

Variant rs5007260
Chromosome Location chr6:32379047-32379048
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:7 , 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 chr6:32378800-32379400 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
3 chr6:32378800-32381200 Enhancers Fetal Intestine Large intestine
4 chr6:32378800-32381200 Enhancers Fetal Intestine Small intestine
5 chr6:32379000-32379200 Bivalent Enhancer HepG2 liver
6 chr6:32379000-32379600 Bivalent Enhancer Rectal Mucosa Donor 29 rectum
7 chr6:32379000-32379800 Flanking Active TSS Duodenum Mucosa Duodenum

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