Variant report

Variant rs56686141
Chromosome Location chr13:49351357-49351358
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:49346600-49357200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
2 chr13:49346800-49352200 Weak transcription Left Ventricle heart
3 chr13:49347400-49352000 Enhancers Hela-S3 cervix
4 chr13:49347800-49352000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
5 chr13:49348400-49351400 Weak transcription Placenta Placenta
6 chr13:49349200-49351400 Enhancers NHLF lung
7 chr13:49349200-49356800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
8 chr13:49349600-49351400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr13:49350400-49351400 Enhancers NHDF-Ad bronchial
10 chr13:49350400-49356800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
11 chr13:49350600-49351400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
12 chr13:49351000-49351600 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
13 chr13:49351000-49352800 Weak transcription HMEC breast
14 chr13:49351200-49353000 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell

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