The 2.0 version of rSNPBase

Variant report

Variant rs73444506
Chromosome Location chr7:137329551-137329552
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:137282800-137337400 Weak transcription HSMMtube muscle
2 chr7:137320200-137352600 Weak transcription Aorta Aorta
3 chr7:137321400-137337000 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr7:137325800-137337400 Weak transcription HSMM muscle
5 chr7:137327200-137337400 Weak transcription Osteobl bone
6 chr7:137327400-137337200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
7 chr7:137327400-137337200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
8 chr7:137328000-137337200 Weak transcription Brain Inferior Temporal Lobe brain
9 chr7:137328200-137340600 Weak transcription Adipose Nuclei Adipose
10 chr7:137328400-137330000 Strong transcription Ganglion Eminence derived primary cultured neurospheres brain
11 chr7:137328400-137330800 Strong transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
12 chr7:137328400-137331200 Strong transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
13 chr7:137328400-137332200 Weak transcription H9 Cell Line embryonic stem cell
14 chr7:137328400-137333000 Weak transcription Muscle Satellite Cultured Cells --
15 chr7:137328400-137348000 Weak transcription Fetal Brain Male brain
16 chr7:137329000-137330200 Strong transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived

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Last update: Aug 31, 2015