Variant report

Variant rs17054982
Chromosome Location chr13:37710044-37710045
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:37707200-37711400 Weak transcription Primary neutrophils fromperipheralblood blood
2 chr13:37707600-37710200 Enhancers Hela-S3 cervix
3 chr13:37707800-37710800 Enhancers NH-A brain
4 chr13:37708000-37710400 Enhancers Osteobl bone
5 chr13:37708200-37710800 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
6 chr13:37708200-37714200 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
7 chr13:37708400-37710200 Enhancers Adipose Nuclei Adipose
8 chr13:37708400-37714400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr13:37708800-37710600 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
10 chr13:37709000-37710400 Enhancers Placenta Amnion Placenta Amnion
11 chr13:37709200-37718200 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
12 chr13:37709400-37711400 Enhancers HUVEC blood vessel
13 chr13:37709400-37712200 Weak transcription NHLF lung
14 chr13:37709600-37712200 Weak transcription Fetal Intestine Large intestine
15 chr13:37709800-37710800 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
16 chr13:37710000-37714000 Enhancers NHDF-Ad bronchial

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