Variant report

Variant rs2741068
Chromosome Location chr8:6760997-6760998
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:6757400-6761600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr8:6758000-6761200 Enhancers HepG2 liver
3 chr8:6758800-6761600 Enhancers HMEC breast
4 chr8:6759200-6767000 Weak transcription A549 lung
5 chr8:6760000-6761200 Enhancers Pancreas Pancrea
6 chr8:6760000-6761400 Enhancers Lung lung
7 chr8:6760000-6761600 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
8 chr8:6760000-6761600 Enhancers Esophagus oesophagus
9 chr8:6760000-6762200 Enhancers Fetal Intestine Large intestine
10 chr8:6760400-6761600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr8:6760400-6762000 Enhancers Fetal Lung lung
12 chr8:6760600-6761000 Flanking Active TSS Breast Myoepithelial Primary Cells Breast
13 chr8:6760600-6761000 Flanking Active TSS Fetal Kidney kidney
14 chr8:6760600-6761200 Flanking Active TSS NHEK skin
15 chr8:6760800-6761000 Enhancers Left Ventricle heart
16 chr8:6760800-6761200 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
17 chr8:6760800-6761200 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin02 Skin
18 chr8:6760800-6762600 Enhancers Fetal Intestine Small intestine

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