Variant report

Variant rs34097781
Chromosome Location chr1:192669497-192669498
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:192667600-192673000 Enhancers Primary neutrophils fromperipheralblood blood
2 chr1:192668200-192669600 Enhancers A549 lung
3 chr1:192668400-192670800 Weak transcription Placenta Placenta
4 chr1:192669000-192669800 Enhancers NH-A brain
5 chr1:192669000-192671400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
6 chr1:192669000-192672000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
7 chr1:192669000-192672000 Enhancers Hela-S3 cervix
8 chr1:192669000-192673200 Enhancers NHLF lung
9 chr1:192669200-192672400 Enhancers Fetal Intestine Large intestine
10 chr1:192669200-192672400 Enhancers Osteobl bone
11 chr1:192669200-192672800 Enhancers Muscle Satellite Cultured Cells --
12 chr1:192669400-192669600 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
13 chr1:192669400-192670200 Flanking Active TSS HepG2 liver
14 chr1:192669400-192670600 Enhancers HSMM muscle
15 chr1:192669400-192671800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
16 chr1:192669400-192671800 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
17 chr1:192669400-192671800 Enhancers NHDF-Ad bronchial
18 chr1:192669400-192672200 Enhancers HUVEC blood vessel

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