Variant report

Variant rs61333674
Chromosome Location chr12:31370459-31370460
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:31367800-31370800 Enhancers Esophagus oesophagus
2 chr12:31368800-31373600 Weak transcription Brain Germinal Matrix brain
3 chr12:31369000-31372800 Weak transcription Gastric stomach
4 chr12:31369000-31373200 Weak transcription Fetal Heart heart
5 chr12:31369200-31373800 Weak transcription Adipose Nuclei Adipose
6 chr12:31370200-31370600 Enhancers Pancreas Pancrea
7 chr12:31370200-31371400 Enhancers HUES64 Cell Line embryonic stem cell
8 chr12:31370200-31372000 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
9 chr12:31370200-31372400 Enhancers H1 Cell Line embryonic stem cell
10 chr12:31370200-31372400 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
11 chr12:31370200-31372800 Enhancers ES-UCSF4 Cell Line embryonic stem cell
12 chr12:31370400-31370600 Flanking Bivalent TSS/Enh HUES6 Cell Line embryonic stem cell
13 chr12:31370400-31370600 Bivalent Enhancer iPS-18 Cell Line embryonic stem cell
14 chr12:31370400-31370800 Enhancers ES-I3 Cell Line embryonic stem cell
15 chr12:31370400-31371000 Enhancers HUES48 Cell Line embryonic stem cell
16 chr12:31370400-31371000 Bivalent Enhancer iPS-15b Cell Line embryonic stem cell
17 chr12:31370400-31371000 Enhancers Placenta Placenta
18 chr12:31370400-31372000 Enhancers H9 Cell Line embryonic stem cell
19 chr12:31370400-31375000 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived

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