Variant report

Variant rs545426595
Chromosome Location chr1:186971264-186971265
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:186969000-186975400 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr1:186969800-186971400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
3 chr1:186969800-186971600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr1:186969800-186971600 Enhancers NHDF-Ad bronchial
5 chr1:186970000-186971600 Enhancers NH-A brain
6 chr1:186970000-186971800 Enhancers Hela-S3 cervix
7 chr1:186970200-186971400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
8 chr1:186970200-186971600 Enhancers HMEC breast
9 chr1:186970400-186971400 Enhancers NHLF lung
10 chr1:186970400-186971600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr1:186970800-186971600 Enhancers NHEK skin
12 chr1:186971200-186971600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived

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