The 2.0 version of rSNPBase

Variant report

Variant rs9547742
Chromosome Location chr13:37771688-37771689
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:37766400-37772000 Weak transcription Primary neutrophils fromperipheralblood blood
2 chr13:37768000-37771800 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
3 chr13:37768000-37772000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
4 chr13:37768600-37775400 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
5 chr13:37768600-37775400 Weak transcription NHLF lung
6 chr13:37769000-37772600 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
7 chr13:37769200-37772400 Weak transcription ES-WA7 Cell Line embryonic stem cell
8 chr13:37769400-37771800 Weak transcription Osteobl bone
9 chr13:37769400-37772800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
10 chr13:37769400-37775600 Weak transcription Muscle Satellite Cultured Cells --
11 chr13:37769600-37775400 Weak transcription NHDF-Ad bronchial
12 chr13:37769800-37773000 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
13 chr13:37770000-37772800 Weak transcription NH-A brain
14 chr13:37770800-37772800 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
15 chr13:37771200-37774200 Enhancers iPS-18 Cell Line embryonic stem cell

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Last update: Aug 31, 2015