Variant report

Variant rs12135213
Chromosome Location chr1:66991390-66991391
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:66987800-66992600 Weak transcription HUVEC blood vessel
2 chr1:66988000-66993400 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
3 chr1:66988200-66993000 Weak transcription NHDF-Ad bronchial
4 chr1:66988400-66991600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
5 chr1:66988400-66998200 Weak transcription Osteobl bone
6 chr1:66989800-66991600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
7 chr1:66990000-66991600 Weak transcription Fetal Heart heart
8 chr1:66990600-66992000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
9 chr1:66990800-66991400 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
10 chr1:66990800-66994800 Enhancers NHLF lung
11 chr1:66991000-66992000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
12 chr1:66991200-66992000 Enhancers Muscle Satellite Cultured Cells --

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