Variant report

Variant rs2702933
Chromosome Location chr8:6760142-6760143
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:6757200-6760600 Enhancers Breast Myoepithelial Primary Cells Breast
2 chr8:6757400-6761600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr8:6758000-6760600 Enhancers NHEK skin
4 chr8:6758000-6761200 Enhancers HepG2 liver
5 chr8:6758800-6761600 Enhancers HMEC breast
6 chr8:6759200-6767000 Weak transcription A549 lung
7 chr8:6759400-6760400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr8:6759800-6760800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr8:6760000-6760200 Enhancers Left Ventricle heart
10 chr8:6760000-6760400 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
11 chr8:6760000-6760600 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
12 chr8:6760000-6760600 Enhancers Fetal Kidney kidney
13 chr8:6760000-6760800 Enhancers Spleen Spleen
14 chr8:6760000-6761200 Enhancers Pancreas Pancrea
15 chr8:6760000-6761400 Enhancers Lung lung
16 chr8:6760000-6761600 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
17 chr8:6760000-6761600 Enhancers Esophagus oesophagus
18 chr8:6760000-6762200 Enhancers Fetal Intestine Large intestine

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