Variant report

Variant rs9296859
Chromosome Location chr6:56882494-56882495
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:56858600-56889400 Weak transcription Brain Hippocampus Middle brain
2 chr6:56864600-56890200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr6:56878600-56885800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr6:56878600-56905400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
5 chr6:56878800-56882600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
6 chr6:56879000-56891600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
7 chr6:56879200-56883800 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
8 chr6:56880800-56888400 Weak transcription Aorta Aorta
9 chr6:56881600-56884200 Enhancers K562 blood
10 chr6:56882000-56882600 Active TSS HUVEC blood vessel
11 chr6:56882400-56883400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived

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