Variant report

Variant rs11182359
Chromosome Location chr12:44363956-44363957
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:22 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:44342000-44367200 Weak transcription Sigmoid Colon Sigmoid Colon
2 chr12:44343600-44376800 Weak transcription Pancreas Pancrea
3 chr12:44354400-44367000 Weak transcription iPS-15b Cell Line embryonic stem cell
4 chr12:44356200-44368000 Weak transcription Breast Myoepithelial Primary Cells Breast
5 chr12:44358800-44367800 Weak transcription Esophagus oesophagus
6 chr12:44360000-44366200 Weak transcription Fetal Intestine Small intestine
7 chr12:44361400-44401400 Weak transcription Aorta Aorta
8 chr12:44363400-44364000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
9 chr12:44363400-44364000 Enhancers Hela-S3 cervix
10 chr12:44363400-44364000 Enhancers HSMMtube muscle
11 chr12:44363400-44364000 Enhancers HUVEC blood vessel
12 chr12:44363400-44364000 Enhancers NHDF-Ad bronchial
13 chr12:44363400-44364000 Enhancers NHEK skin
14 chr12:44363400-44364000 Enhancers Osteobl bone
15 chr12:44363400-44364600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
16 chr12:44363400-44364600 Enhancers HMEC breast
17 chr12:44363400-44365800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
18 chr12:44363600-44364000 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
19 chr12:44363600-44364000 Active TSS A549 lung
20 chr12:44363800-44364000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
21 chr12:44363800-44366000 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
22 chr12:44363800-44382400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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