Variant report

Variant rs7138914
Chromosome Location chr12:46962478-46962479
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:46956800-46963400 Weak transcription Aorta Aorta
2 chr12:46957000-46962800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
3 chr12:46957000-46963000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
4 chr12:46957000-46964800 Weak transcription NHDF-Ad bronchial
5 chr12:46958200-46962800 Weak transcription Hela-S3 cervix
6 chr12:46958400-46962800 Weak transcription Gastric stomach
7 chr12:46960400-46963800 ZNF genes & repeats Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr12:46961600-46963600 ZNF genes & repeats Primary Natural Killer cells fromperipheralblood blood
9 chr12:46961600-46970800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr12:46962000-46963400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell

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