Variant report

Variant rs543557531
Chromosome Location chr2:234942059-234942060
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:234934800-234942400 Enhancers Primary T helper memory cells from peripheral blood 2 blood
2 chr2:234937800-234942200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
3 chr2:234939000-234942200 Enhancers Primary T killer memory cells from peripheral blood blood
4 chr2:234939400-234942200 Enhancers Primary T helper naive cells from peripheral blood blood
5 chr2:234939400-234942400 Enhancers Primary T cells fromperipheralblood blood
6 chr2:234939400-234942400 Enhancers Primary Natural Killer cells fromperipheralblood blood
7 chr2:234939600-234942200 Enhancers Primary T cells effector/memory enriched fromperipheralblood blood
8 chr2:234939600-234942200 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
9 chr2:234939800-234942200 Enhancers Muscle Satellite Cultured Cells --
10 chr2:234939800-234942200 Enhancers HMEC breast
11 chr2:234940000-234942200 Enhancers NH-A brain
12 chr2:234940400-234942200 Enhancers HUVEC blood vessel
13 chr2:234941800-234952600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr2:234942000-234942200 Enhancers Osteobl bone
15 chr2:234942000-234943400 ZNF genes & repeats Primary T helper memory cells from peripheral blood 1 blood

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