Variant report

Variant rs12816652
Chromosome Location chr12:31390096-31390097
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:31386200-31390200 Bivalent Enhancer Fetal Muscle Trunk muscle
2 chr12:31388400-31390200 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
3 chr12:31388600-31391600 Weak transcription Liver Liver
4 chr12:31388800-31390200 Bivalent Enhancer Fetal Muscle Leg muscle
5 chr12:31388800-31391600 Weak transcription Adipose Nuclei Adipose
6 chr12:31388800-31394600 Weak transcription Fetal Intestine Small intestine
7 chr12:31389000-31391600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
8 chr12:31389200-31390400 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
9 chr12:31389200-31391200 Weak transcription Fetal Intestine Large intestine
10 chr12:31389200-31391600 Weak transcription ES-I3 Cell Line embryonic stem cell
11 chr12:31389200-31391600 Weak transcription Breast Myoepithelial Primary Cells Breast
12 chr12:31389400-31391600 Enhancers GM12878-XiMat blood

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