Variant report

Variant rs136231
Chromosome Location chr22:31213543-31213544
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr22:31199800-31218000 Weak transcription Gastric stomach
2 chr22:31201600-31217000 Weak transcription Brain Anterior Caudate brain
3 chr22:31203000-31217800 Weak transcription Brain Cingulate Gyrus brain
4 chr22:31203600-31217800 Weak transcription Brain Hippocampus Middle brain
5 chr22:31205600-31217000 Weak transcription Brain Angular Gyrus brain
6 chr22:31206400-31217000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
7 chr22:31206800-31218000 Weak transcription HSMM muscle
8 chr22:31207000-31218000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr22:31207200-31213600 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
10 chr22:31209000-31218000 Weak transcription A549 lung
11 chr22:31209600-31216000 Strong transcription NHEK skin
12 chr22:31211000-31217800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
13 chr22:31212600-31213600 Enhancers Left Ventricle heart
14 chr22:31213000-31213600 Enhancers Fetal Heart heart
15 chr22:31213200-31213600 Genic enhancers Hela-S3 cervix
16 chr22:31213200-31213800 Enhancers HSMMtube muscle
17 chr22:31213400-31213600 Bivalent Enhancer H1 Derived Mesenchymal Stem Cells ES cell derived
18 chr22:31213400-31213600 Active TSS iPS DF 19.11 Cell Line embryonic stem cell
19 chr22:31213400-31213800 Enhancers Brain Substantia Nigra brain

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