Variant report

Variant rs34279227
Chromosome Location chr3:98633285-98633286
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:98623600-98636400 Weak transcription Fetal Heart heart
2 chr3:98625400-98636600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
3 chr3:98625600-98637200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr3:98626400-98634400 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr3:98626600-98641600 Weak transcription NHLF lung
6 chr3:98632000-98634200 Enhancers Pancreatic Islets Pancreatic Islet
7 chr3:98632800-98633600 Enhancers HepG2 liver
8 chr3:98632800-98634600 Flanking Active TSS A549 lung
9 chr3:98632800-98635200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
10 chr3:98633000-98633400 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
11 chr3:98633000-98633600 Enhancers Liver Liver
12 chr3:98633000-98633800 Enhancers NH-A brain
13 chr3:98633000-98634800 Enhancers Osteobl bone
14 chr3:98633200-98633400 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
15 chr3:98633200-98633400 Enhancers HMEC breast
16 chr3:98633200-98633600 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
17 chr3:98633200-98633600 Bivalent Enhancer K562 blood
18 chr3:98633200-98635000 Enhancers Muscle Satellite Cultured Cells --

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