Variant report

Variant rs6972606
Chromosome Location chr7:137498611-137498612
allele C/T
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 chr7:137490200-137501600 Weak transcription Osteobl bone
4 chr7:137490200-137504600 Weak transcription Brain Inferior Temporal Lobe brain
5 chr7:137490200-137505200 Weak transcription NH-A brain
6 chr7:137490400-137501000 Weak transcription Muscle Satellite Cultured Cells --
7 chr7:137490400-137505200 Weak transcription HSMM muscle
8 chr7:137494000-137505600 Weak transcription Aorta Aorta
9 chr7:137494400-137504400 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
10 chr7:137497800-137498800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr7:137497800-137499400 Enhancers Fetal Brain Male brain
12 chr7:137498000-137499000 Strong transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
13 chr7:137498000-137499200 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
14 chr7:137498200-137504400 Weak transcription Fetal Brain Female brain
15 chr7:137498600-137499200 Strong transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow

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