Variant report

Variant rs5762216
Chromosome Location chr22:27901918-27901919
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr22:27885000-27902800 Weak transcription Aorta Aorta
2 chr22:27897800-27902800 Weak transcription Pancreas Pancrea
3 chr22:27899800-27907800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr22:27900000-27905800 Enhancers Psoas Muscle Psoas
5 chr22:27900200-27903000 Enhancers Fetal Muscle Trunk muscle
6 chr22:27900400-27902400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr22:27901000-27902400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
8 chr22:27901200-27902600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
9 chr22:27901200-27902800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
10 chr22:27901400-27902800 Enhancers Breast Myoepithelial Primary Cells Breast
11 chr22:27901400-27906400 Weak transcription Adipose Nuclei Adipose
12 chr22:27901400-27906400 Enhancers Skeletal Muscle Male skeletal muscle
13 chr22:27901600-27902800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr22:27901600-27902800 Weak transcription Right Atrium heart
15 chr22:27901600-27902800 Enhancers NHEK skin
16 chr22:27901800-27902000 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin03 Skin
17 chr22:27901800-27906400 Enhancers Skeletal Muscle Female skeletal muscle

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