Variant report

Variant rs2035671
Chromosome Location chr3:119875948-119875949
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:119872400-119877800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr3:119872400-119878800 Weak transcription Placenta Amnion Placenta Amnion
3 chr3:119872800-119877600 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
4 chr3:119875000-119877400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr3:119875200-119876000 Weak transcription Placenta Placenta
6 chr3:119875200-119876200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
7 chr3:119875200-119877200 Weak transcription Fetal Intestine Small intestine
8 chr3:119875200-119877800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr3:119875200-119896000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
10 chr3:119875400-119876200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
11 chr3:119875400-119876800 Enhancers IMR90 fetal lung fibroblasts Cell Line lung

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