Variant report

Variant rs2615916
Chromosome Location chr11:33484729-33484730
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:33474600-33486000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr11:33475800-33485000 Weak transcription NH-A brain
3 chr11:33480600-33488800 Weak transcription Fetal Brain Female brain
4 chr11:33481000-33485800 Weak transcription Fetal Brain Male brain
5 chr11:33483200-33493000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr11:33483400-33486800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr11:33483600-33485400 Weak transcription A549 lung
8 chr11:33483600-33486000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
9 chr11:33483600-33486000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr11:33483800-33486000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr11:33484400-33485800 Enhancers HUVEC blood vessel
12 chr11:33484600-33484800 Enhancers IMR90 fetal lung fibroblasts Cell Line lung

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