Variant report

Variant rs10150320
Chromosome Location chr14:67168568-67168569
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:67146000-67172000 Weak transcription Liver Liver
2 chr14:67148800-67169400 Weak transcription Primary T cells effector/memory enriched fromperipheralblood blood
3 chr14:67157600-67174800 Weak transcription HepG2 liver
4 chr14:67166600-67170600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
5 chr14:67168200-67168600 Active TSS H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
6 chr14:67168200-67168600 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
7 chr14:67168200-67168600 Enhancers NHEK skin
8 chr14:67168200-67168800 Strong transcription Breast Myoepithelial Primary Cells Breast
9 chr14:67168200-67168800 Genic enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr14:67168200-67168800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr14:67168200-67168800 ZNF genes & repeats Fetal Intestine Small intestine
12 chr14:67168200-67168800 ZNF genes & repeats Lung lung
13 chr14:67168200-67169000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr14:67168200-67169000 Enhancers HMEC breast
15 chr14:67168400-67168600 Enhancers Esophagus oesophagus
16 chr14:67168400-67168600 Enhancers Pancreas Pancrea
17 chr14:67168400-67168800 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived

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