Variant report

Variant rs7957795
Chromosome Location chr12:118227358-118227359
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:118210000-118230800 Weak transcription Pancreas Pancrea
2 chr12:118224400-118227600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr12:118226000-118228400 Enhancers iPS-20b Cell Line embryonic stem cell
4 chr12:118226000-118229800 Enhancers ES-I3 Cell Line embryonic stem cell
5 chr12:118226200-118229600 Weak transcription Placenta Amnion Placenta Amnion
6 chr12:118226800-118227400 Enhancers iPS-15b Cell Line embryonic stem cell
7 chr12:118226800-118228400 Enhancers iPS-18 Cell Line embryonic stem cell
8 chr12:118226800-118228800 Enhancers H9 Cell Line embryonic stem cell
9 chr12:118226800-118228800 Enhancers HUES6 Cell Line embryonic stem cell
10 chr12:118226800-118228800 Enhancers HUES64 Cell Line embryonic stem cell
11 chr12:118226800-118228800 Enhancers ES-UCSF4 Cell Line embryonic stem cell
12 chr12:118226800-118229000 Enhancers HUES48 Cell Line embryonic stem cell
13 chr12:118227000-118228200 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
14 chr12:118227000-118228400 Enhancers H1 Cell Line embryonic stem cell
15 chr12:118227000-118229600 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
16 chr12:118227200-118227800 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived

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