Variant report

Variant rs58810027
Chromosome Location chr11:10071345-10071346
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:10066600-10073600 Weak transcription NHLF lung
2 chr11:10066600-10073800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
3 chr11:10066600-10078600 Weak transcription Aorta Aorta
4 chr11:10066800-10072000 Weak transcription Osteobl bone
5 chr11:10066800-10073600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
6 chr11:10067000-10071400 Weak transcription A549 lung
7 chr11:10067000-10078400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
8 chr11:10067800-10071800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr11:10067800-10072200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr11:10067800-10078200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr11:10068200-10073600 Weak transcription Fetal Lung lung
12 chr11:10069000-10074400 Enhancers Hela-S3 cervix
13 chr11:10069800-10071800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
14 chr11:10070600-10071800 Enhancers Primary hematopoietic stem cells blood
15 chr11:10071200-10071400 Active TSS Primary hematopoietic stem cells G-CSF-mobilized Male --
16 chr11:10071200-10072000 Enhancers Primary hematopoietic stem cells short term culture blood
17 chr11:10071200-10073600 Weak transcription Ovary ovary

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