Variant report

Variant rs1689511
Chromosome Location chr12:56467385-56467386
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:56437000-56472800 Weak transcription Right Atrium heart
2 chr12:56454400-56467800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
3 chr12:56466200-56472400 Weak transcription Placenta Amnion Placenta Amnion
4 chr12:56466400-56467400 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr12:56466400-56467400 Weak transcription NHEK skin
6 chr12:56466400-56471800 Weak transcription Hela-S3 cervix
7 chr12:56466400-56472600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
8 chr12:56466600-56472600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr12:56466600-56472800 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
10 chr12:56467000-56468000 Weak transcription HepG2 liver

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