Variant report

Variant rs17024389
Chromosome Location chr1:215364192-215364193
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:215356000-215364800 Weak transcription NHLF lung
2 chr1:215356000-215368400 Weak transcription Fetal Brain Female brain
3 chr1:215356200-215364400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
4 chr1:215356200-215365200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
5 chr1:215362400-215364600 Weak transcription Osteobl bone
6 chr1:215362400-215365200 Weak transcription HSMM muscle
7 chr1:215362600-215364600 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
8 chr1:215363000-215364800 Weak transcription Muscle Satellite Cultured Cells --
9 chr1:215363600-215364200 Genic enhancers NHDF-Ad bronchial
10 chr1:215363600-215364600 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
11 chr1:215364000-215365400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
12 chr1:215364000-215366800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
13 chr1:215364000-215367400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived

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