Variant report

Variant rs7743158
Chromosome Location chr6:12485863-12485864
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:12482600-12486200 Enhancers HMEC breast
2 chr6:12483600-12486600 Enhancers Placenta Amnion Placenta Amnion
3 chr6:12484000-12486400 Enhancers HepG2 liver
4 chr6:12484200-12486200 Enhancers Hela-S3 cervix
5 chr6:12484400-12486000 Flanking Active TSS NHEK skin
6 chr6:12484400-12487200 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
7 chr6:12484400-12487600 Weak transcription Aorta Aorta
8 chr6:12484400-12489600 Weak transcription NHDF-Ad bronchial
9 chr6:12484400-12490000 Weak transcription NHLF lung
10 chr6:12484400-12491400 Weak transcription Small Intestine intestine
11 chr6:12484600-12486000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr6:12484600-12486400 Flanking Active TSS A549 lung
13 chr6:12485000-12486800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
14 chr6:12485000-12489800 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
15 chr6:12485000-12490000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
16 chr6:12485200-12490000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
17 chr6:12485400-12486600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
18 chr6:12485400-12487000 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
19 chr6:12485800-12488600 Weak transcription HUVEC blood vessel

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