Variant report

Variant rs535210835
Chromosome Location chr7:111138784-111138785
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:111111400-111150600 Weak transcription Pancreas Pancrea
2 chr7:111123000-111159000 Weak transcription Aorta Aorta
3 chr7:111128800-111150600 Weak transcription Ovary ovary
4 chr7:111138000-111139200 Enhancers Pancreatic Islets Pancreatic Islet
5 chr7:111138200-111139800 Enhancers NHEK skin
6 chr7:111138400-111139800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr7:111138400-111139800 Enhancers Hela-S3 cervix
8 chr7:111138400-111139800 Enhancers HMEC breast
9 chr7:111138600-111138800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
10 chr7:111138600-111139000 Flanking Active TSS A549 lung
11 chr7:111138600-111139200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
12 chr7:111138600-111139600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr7:111138600-111139600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
14 chr7:111138600-111139600 Enhancers Stomach Mucosa stomach
15 chr7:111138600-111139800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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