Variant report

Variant rs12749728
Chromosome Location chr1:66989380-66989381
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:66986200-66989400 Weak transcription HepG2 liver
2 chr1:66987000-66990400 Enhancers Hela-S3 cervix
3 chr1:66987200-66990200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
4 chr1:66987800-66992600 Weak transcription HUVEC blood vessel
5 chr1:66988000-66990800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr1:66988000-66993400 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
7 chr1:66988200-66989400 Weak transcription Muscle Satellite Cultured Cells --
8 chr1:66988200-66989400 Weak transcription NHLF lung
9 chr1:66988200-66993000 Weak transcription NHDF-Ad bronchial
10 chr1:66988400-66991600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr1:66988400-66998200 Weak transcription Osteobl bone
12 chr1:66989000-66989600 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
13 chr1:66989200-66989400 Enhancers NH-A brain
14 chr1:66989200-66989800 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
15 chr1:66989200-66990000 Enhancers Fetal Heart heart
16 chr1:66989200-66990800 Enhancers HSMMtube muscle
17 chr1:66989200-66991000 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived

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