Variant report

Variant rs60959469
Chromosome Location chr7:137491469-137491470
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:137486000-137501800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr7:137486600-137501800 Weak transcription HSMMtube muscle
3 chr7:137486800-137493800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
4 chr7:137489600-137491800 Enhancers iPS-15b Cell Line embryonic stem cell
5 chr7:137490000-137497800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr7:137490200-137492200 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
7 chr7:137490200-137501600 Weak transcription Osteobl bone
8 chr7:137490200-137504600 Weak transcription Brain Inferior Temporal Lobe brain
9 chr7:137490200-137505200 Weak transcription NH-A brain
10 chr7:137490400-137493600 Weak transcription Aorta Aorta
11 chr7:137490400-137498000 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
12 chr7:137490400-137501000 Weak transcription Muscle Satellite Cultured Cells --
13 chr7:137490400-137505200 Weak transcription HSMM muscle
14 chr7:137491000-137492400 Weak transcription Fetal Stomach stomach
15 chr7:137491000-137498000 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow

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