Variant report

Variant rs6916851
Chromosome Location chr6:12487767-12487768
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:12484400-12489600 Weak transcription NHDF-Ad bronchial
2 chr6:12484400-12490000 Weak transcription NHLF lung
3 chr6:12484400-12491400 Weak transcription Small Intestine intestine
4 chr6:12485000-12489800 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
5 chr6:12485000-12490000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
6 chr6:12485200-12490000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
7 chr6:12485800-12488600 Weak transcription HUVEC blood vessel
8 chr6:12486000-12490800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr6:12486200-12490200 Weak transcription Hela-S3 cervix
10 chr6:12486200-12490800 Weak transcription HMEC breast
11 chr6:12486600-12491400 Weak transcription Placenta Amnion Placenta Amnion
12 chr6:12487200-12487800 Genic enhancers A549 lung
13 chr6:12487200-12490600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
14 chr6:12487200-12490800 Weak transcription NHEK skin
15 chr6:12487400-12490000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
16 chr6:12487600-12488000 Enhancers Aorta Aorta
17 chr6:12487600-12489800 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung

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