Variant report

Variant rs12819069
Chromosome Location chr12:31390550-31390551
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:31388600-31391600 Weak transcription Liver Liver
2 chr12:31388800-31391600 Weak transcription Adipose Nuclei Adipose
3 chr12:31388800-31394600 Weak transcription Fetal Intestine Small intestine
4 chr12:31389000-31391600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
5 chr12:31389200-31391200 Weak transcription Fetal Intestine Large intestine
6 chr12:31389200-31391600 Weak transcription ES-I3 Cell Line embryonic stem cell
7 chr12:31389200-31391600 Weak transcription Breast Myoepithelial Primary Cells Breast
8 chr12:31389400-31391600 Enhancers GM12878-XiMat blood
9 chr12:31390200-31391400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
10 chr12:31390400-31390600 Enhancers Ganglion Eminence derived primary cultured neurospheres brain

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