Variant report

Variant rs1432529
Chromosome Location chr2:182997280-182997281
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:182995600-182997800 Weak transcription HMEC breast
2 chr2:182996400-182999800 Enhancers Muscle Satellite Cultured Cells --
3 chr2:182996600-182999000 Enhancers NH-A brain
4 chr2:182996600-182999000 Enhancers NHLF lung
5 chr2:182996600-182999600 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
6 chr2:182996600-182999600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
7 chr2:182996600-183000000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
8 chr2:182996800-182999000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
9 chr2:182996800-182999000 Enhancers Hela-S3 cervix
10 chr2:182996800-183009800 Weak transcription Duodenum Smooth Muscle Duodenum
11 chr2:182997000-182998200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
12 chr2:182997000-182998600 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
13 chr2:182997000-182999200 Enhancers Osteobl bone
14 chr2:182997200-182998200 Enhancers HUVEC blood vessel
15 chr2:182997200-182998200 Weak transcription NHDF-Ad bronchial
16 chr2:182997200-182998600 Weak transcription Aorta Aorta
17 chr2:182997200-182998600 Weak transcription Gastric stomach
18 chr2:182997200-183002600 Weak transcription Fetal Kidney kidney

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