Variant report

Variant rs546104482
Chromosome Location chr6:134268097-134268098
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:134266600-134272400 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
2 chr6:134266800-134272200 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
3 chr6:134267000-134272200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
4 chr6:134267800-134271600 Enhancers Liver Liver
5 chr6:134268000-134268200 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
6 chr6:134268000-134268200 Enhancers Gastric stomach
7 chr6:134268000-134268200 Enhancers Rectal Mucosa Donor 29 rectum
8 chr6:134268000-134268200 Enhancers Sigmoid Colon Sigmoid Colon
9 chr6:134268000-134268600 Enhancers Fetal Brain Female brain
10 chr6:134268000-134269000 Enhancers K562 blood
11 chr6:134268000-134270200 Enhancers Rectal Mucosa Donor 31 rectum
12 chr6:134268000-134270400 Enhancers Duodenum Mucosa Duodenum
13 chr6:134268000-134270400 Enhancers Pancreas Pancrea

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