Variant report

Variant rs2738141
Chromosome Location chr8:6760785-6760786
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 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 chr8:6759800-6760800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr8:6760000-6760800 Enhancers Spleen Spleen
7 chr8:6760000-6761200 Enhancers Pancreas Pancrea
8 chr8:6760000-6761400 Enhancers Lung lung
9 chr8:6760000-6761600 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
10 chr8:6760000-6761600 Enhancers Esophagus oesophagus
11 chr8:6760000-6762200 Enhancers Fetal Intestine Large intestine
12 chr8:6760400-6760800 Enhancers Fetal Heart heart
13 chr8:6760400-6761600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
14 chr8:6760400-6762000 Enhancers Fetal Lung lung
15 chr8:6760600-6760800 Genic enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
16 chr8:6760600-6760800 Enhancers Gastric stomach
17 chr8:6760600-6761000 Flanking Active TSS Breast Myoepithelial Primary Cells Breast
18 chr8:6760600-6761000 Flanking Active TSS Fetal Kidney kidney
19 chr8:6760600-6761200 Flanking Active TSS NHEK skin

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