Variant report

Variant rs10843912
Chromosome Location chr12:31373341-31373342
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:31368800-31373600 Weak transcription Brain Germinal Matrix brain
2 chr12:31369200-31373800 Weak transcription Adipose Nuclei Adipose
3 chr12:31370400-31375000 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
4 chr12:31370800-31378400 Weak transcription Esophagus oesophagus
5 chr12:31372000-31373800 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
6 chr12:31372200-31373600 Weak transcription iPS-18 Cell Line embryonic stem cell
7 chr12:31372800-31373800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
8 chr12:31372800-31375000 Enhancers Gastric stomach
9 chr12:31372800-31375400 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
10 chr12:31373000-31374200 Bivalent Enhancer Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
11 chr12:31373000-31374800 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
12 chr12:31373200-31373600 Enhancers Fetal Heart heart
13 chr12:31373200-31374200 Enhancers Brain Anterior Caudate brain
14 chr12:31373200-31378600 Enhancers Cortex derived primary cultured neurospheres brain
15 chr12:31373200-31379000 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
16 chr12:31373200-31380200 Weak transcription Pancreas Pancrea

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