Variant report

Variant rs71557332
Chromosome Location chr6:26356853-26356854
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:26352600-26364200 Weak transcription NHEK skin
2 chr6:26352800-26364000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr6:26353000-26364200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr6:26355000-26361200 Weak transcription Duodenum Mucosa Duodenum
5 chr6:26355400-26364200 Weak transcription Fetal Intestine Small intestine
6 chr6:26355600-26358800 Weak transcription ES-WA7 Cell Line embryonic stem cell
7 chr6:26355800-26357400 Enhancers K562 blood
8 chr6:26356000-26358200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
9 chr6:26356200-26365400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
10 chr6:26356400-26358400 Weak transcription Thymus Thymus
11 chr6:26356400-26364400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
12 chr6:26356600-26359000 Weak transcription Fetal Thymus thymus
13 chr6:26356600-26360800 Weak transcription HepG2 liver

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