Variant report

Variant rs7650273
Chromosome Location chr3:46376776-46376777
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:46375000-46376800 Enhancers Breast Myoepithelial Primary Cells Breast
2 chr3:46375600-46377600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr3:46375600-46377600 Enhancers HMEC breast
4 chr3:46375800-46377600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr3:46375800-46377600 Enhancers Hela-S3 cervix
6 chr3:46375800-46378200 Weak transcription Primary monocytes fromperipheralblood blood
7 chr3:46376000-46380000 Weak transcription Monocytes-CD14+_RO01746 blood
8 chr3:46376400-46376800 Enhancers Primary T helper 17 cells PMA-I stimulated --
9 chr3:46376400-46376800 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr3:46376400-46377000 Flanking Active TSS NHEK skin
11 chr3:46376400-46377400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
12 chr3:46376400-46377400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr3:46376400-46377600 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
14 chr3:46376600-46376800 Enhancers Fetal Intestine Small intestine
15 chr3:46376600-46376800 Bivalent Enhancer NHDF-Ad bronchial
16 chr3:46376600-46377400 Enhancers Fetal Kidney kidney
17 chr3:46376600-46377800 Enhancers Fetal Intestine Large intestine

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