Variant report

Variant rs73977622
Chromosome Location chr2:173508468-173508469
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:173494600-173510200 Weak transcription Primary T cells from cord blood blood
2 chr2:173499800-173513000 Weak transcription Pancreas Pancrea
3 chr2:173505000-173512000 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
4 chr2:173505200-173509000 Weak transcription Pancreatic Islets Pancreatic Islet
5 chr2:173505200-173511200 Weak transcription NHDF-Ad bronchial
6 chr2:173505400-173512000 Weak transcription HSMM muscle
7 chr2:173506600-173509600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
8 chr2:173507000-173508600 Enhancers NHLF lung
9 chr2:173507000-173510800 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
10 chr2:173507200-173509000 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
11 chr2:173507400-173508600 Enhancers HMEC breast
12 chr2:173507800-173508600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr2:173507800-173508600 Enhancers NH-A brain
14 chr2:173507800-173508800 Enhancers NHEK skin
15 chr2:173507800-173509400 Enhancers Fetal Stomach stomach
16 chr2:173508200-173509200 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
17 chr2:173508200-173510000 Enhancers HepG2 liver
18 chr2:173508200-173511800 Weak transcription Osteobl bone
19 chr2:173508400-173511600 Weak transcription Muscle Satellite Cultured Cells --

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