Variant report

Variant rs2741070
Chromosome Location chr8:6761781-6761782
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:6759200-6767000 Weak transcription A549 lung
2 chr8:6760000-6762200 Enhancers Fetal Intestine Large intestine
3 chr8:6760400-6762000 Enhancers Fetal Lung lung
4 chr8:6760800-6762600 Enhancers Fetal Intestine Small intestine
5 chr8:6761000-6762000 Enhancers Breast Myoepithelial Primary Cells Breast
6 chr8:6761000-6762000 Enhancers Liver Liver
7 chr8:6761000-6762800 Enhancers Fetal Kidney kidney
8 chr8:6761200-6762000 Enhancers Duodenum Mucosa Duodenum
9 chr8:6761200-6762200 Weak transcription Pancreas Pancrea
10 chr8:6761400-6762200 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
11 chr8:6761400-6766200 Weak transcription NHEK skin
12 chr8:6761600-6762000 Enhancers HepG2 liver
13 chr8:6761600-6765800 Weak transcription Esophagus oesophagus
14 chr8:6761600-6766200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
15 chr8:6761600-6766400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
16 chr8:6761600-6766400 Weak transcription HMEC breast
17 chr8:6761600-6767800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived

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