Variant report

Variant rs61742012
Chromosome Location chr12:57351029-57351030
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:57346000-57354200 Weak transcription Skeletal Muscle Male skeletal muscle
2 chr12:57349000-57352000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr12:57349200-57351800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr12:57349200-57352000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr12:57349400-57351400 Active TSS Liver Liver
6 chr12:57349400-57352600 Enhancers Esophagus oesophagus
7 chr12:57350000-57351200 Bivalent/Poised TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
8 chr12:57350000-57351400 Weak transcription Spleen Spleen
9 chr12:57350200-57352000 Enhancers NHEK skin
10 chr12:57350400-57352000 ZNF genes & repeats Aorta Aorta
11 chr12:57350600-57351800 Enhancers A549 lung
12 chr12:57350600-57352000 Enhancers HMEC breast
13 chr12:57350800-57351400 Flanking Bivalent TSS/Enh HepG2 liver
14 chr12:57350800-57351600 Enhancers Duodenum Mucosa Duodenum
15 chr12:57350800-57352000 Enhancers Fetal Intestine Large intestine
16 chr12:57351000-57351400 Enhancers Fetal Intestine Small intestine
17 chr12:57351000-57351400 Enhancers Lung lung
18 chr12:57351000-57351800 Enhancers Breast Myoepithelial Primary Cells Breast
19 chr12:57351000-57351800 Enhancers Rectal Mucosa Donor 31 rectum

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