Variant report

Variant rs4374352
Chromosome Location chr2:37407178-37407179
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:37406200-37407800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr2:37406400-37407200 Enhancers Primary neutrophils fromperipheralblood blood
3 chr2:37406600-37408000 Enhancers Breast Myoepithelial Primary Cells Breast
4 chr2:37406800-37407800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr2:37406800-37407800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
6 chr2:37407000-37407200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr2:37407000-37407400 Active TSS Foreskin Fibroblast Primary Cells skin01 Skin
8 chr2:37407000-37407400 Bivalent Enhancer HepG2 liver
9 chr2:37407000-37407600 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
10 chr2:37407000-37407600 Enhancers HMEC breast
11 chr2:37407000-37407600 Enhancers NHEK skin
12 chr2:37407000-37407800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
13 chr2:37407000-37408000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
14 chr2:37407000-37408000 Enhancers Adipose Nuclei Adipose

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