Variant report

Variant rs576210990
Chromosome Location chr22:31212872-31212873
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr22:31199400-31213000 Weak transcription Fetal Heart heart
2 chr22:31199800-31218000 Weak transcription Gastric stomach
3 chr22:31201600-31217000 Weak transcription Brain Anterior Caudate brain
4 chr22:31202800-31213200 Weak transcription HSMMtube muscle
5 chr22:31203000-31217800 Weak transcription Brain Cingulate Gyrus brain
6 chr22:31203600-31217800 Weak transcription Brain Hippocampus Middle brain
7 chr22:31204000-31213400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
8 chr22:31205600-31217000 Weak transcription Brain Angular Gyrus brain
9 chr22:31206400-31217000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
10 chr22:31206800-31218000 Weak transcription HSMM muscle
11 chr22:31207000-31218000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr22:31207200-31213600 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr22:31209000-31213200 Weak transcription Hela-S3 cervix
14 chr22:31209000-31218000 Weak transcription A549 lung
15 chr22:31209600-31216000 Strong transcription NHEK skin
16 chr22:31211000-31217800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
17 chr22:31212600-31213600 Enhancers Left Ventricle heart

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