Variant report

Variant rs5749167
Chromosome Location chr22:31206672-31206673
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 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 chr22:31203000-31210000 Weak transcription NHDF-Ad bronchial
6 chr22:31203000-31217800 Weak transcription Brain Cingulate Gyrus brain
7 chr22:31203600-31217800 Weak transcription Brain Hippocampus Middle brain
8 chr22:31204000-31213400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
9 chr22:31204200-31207200 Strong transcription Hela-S3 cervix
10 chr22:31204800-31206800 Enhancers HSMM muscle
11 chr22:31205000-31206800 Enhancers HMEC breast
12 chr22:31205000-31207000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr22:31205000-31207200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr22:31205600-31212400 Weak transcription Right Atrium heart
15 chr22:31205600-31217000 Weak transcription Brain Angular Gyrus brain
16 chr22:31206200-31206800 Enhancers Right Ventricle heart
17 chr22:31206400-31217000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
18 chr22:31206600-31207000 Strong transcription Foreskin Keratinocyte Primary Cells skin03 Skin
19 chr22:31206600-31209600 Weak transcription NHEK skin

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