Variant report

Variant rs12425589
Chromosome Location chr12:31371986-31371987
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:31368800-31373600 Weak transcription Brain Germinal Matrix brain
2 chr12:31369000-31372800 Weak transcription Gastric stomach
3 chr12:31369000-31373200 Weak transcription Fetal Heart heart
4 chr12:31369200-31373800 Weak transcription Adipose Nuclei Adipose
5 chr12:31370200-31372000 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
6 chr12:31370200-31372400 Enhancers H1 Cell Line embryonic stem cell
7 chr12:31370200-31372400 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
8 chr12:31370200-31372800 Enhancers ES-UCSF4 Cell Line embryonic stem cell
9 chr12:31370400-31372000 Enhancers H9 Cell Line embryonic stem cell
10 chr12:31370400-31375000 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
11 chr12:31370600-31372400 Weak transcription Pancreas Pancrea
12 chr12:31370800-31372000 Bivalent Enhancer iPS-20b Cell Line embryonic stem cell
13 chr12:31370800-31378400 Weak transcription Esophagus oesophagus
14 chr12:31371000-31372600 Bivalent Enhancer HUES6 Cell Line embryonic stem cell
15 chr12:31371400-31372200 Enhancers iPS-18 Cell Line embryonic stem cell
16 chr12:31371600-31372600 Bivalent Enhancer ES-I3 Cell Line embryonic stem cell
17 chr12:31371800-31372000 Flanking Bivalent TSS/Enh ES-WA7 Cell Line embryonic stem cell
18 chr12:31371800-31372200 Bivalent Enhancer iPS-15b Cell Line embryonic stem cell

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