Variant report

Variant rs139633716
Chromosome Location chr1:66987275-66987276
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:66985800-66988000 Enhancers A549 lung
2 chr1:66986200-66989400 Weak transcription HepG2 liver
3 chr1:66987000-66988000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr1:66987000-66988200 Enhancers Muscle Satellite Cultured Cells --
5 chr1:66987000-66988200 Enhancers NHLF lung
6 chr1:66987000-66988400 Enhancers Osteobl bone
7 chr1:66987000-66990400 Enhancers Hela-S3 cervix
8 chr1:66987200-66987600 Flanking Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
9 chr1:66987200-66987800 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
10 chr1:66987200-66987800 Flanking Active TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr1:66987200-66988000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
12 chr1:66987200-66988200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr1:66987200-66988200 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
14 chr1:66987200-66988200 Enhancers HMEC breast
15 chr1:66987200-66988200 Enhancers NHDF-Ad bronchial
16 chr1:66987200-66988200 Enhancers NHEK skin
17 chr1:66987200-66990200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin

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