Variant report

Variant rs72990126
Chromosome Location chr6:141171671-141171672
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:141165000-141188400 Weak transcription HepG2 liver
2 chr6:141166600-141172400 Enhancers NHDF-Ad bronchial
3 chr6:141166800-141172600 Enhancers HUVEC blood vessel
4 chr6:141166800-141173600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr6:141167600-141183000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
6 chr6:141167800-141172600 Enhancers Muscle Satellite Cultured Cells --
7 chr6:141169200-141176800 Weak transcription Hela-S3 cervix
8 chr6:141169400-141173600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
9 chr6:141170200-141172200 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
10 chr6:141170400-141172400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
11 chr6:141170400-141173400 Enhancers Osteobl bone
12 chr6:141170600-141172000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
13 chr6:141170600-141172200 Enhancers NHLF lung
14 chr6:141171200-141171800 Enhancers HSMM muscle
15 chr6:141171400-141172200 Enhancers NH-A brain
16 chr6:141171400-141172400 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
17 chr6:141171600-141171800 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
18 chr6:141171600-141171800 Enhancers Aorta Aorta

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