Variant report

Variant rs6967064
Chromosome Location chr7:111146186-111146187
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 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 chr7:111139800-111146600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
5 chr7:111139800-111148800 Weak transcription A549 lung
6 chr7:111139800-111149200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr7:111139800-111150800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr7:111140800-111148800 Weak transcription H1 Cell Line embryonic stem cell
9 chr7:111140800-111150600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr7:111146000-111146200 ZNF genes & repeats Fetal Intestine Small intestine

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