Variant report

Variant rs9969130
Chromosome Location chr7:17108932-17108933
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:17107000-17109400 Enhancers Primary T helper 17 cells PMA-I stimulated --
2 chr7:17107600-17109400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr7:17107800-17109200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr7:17107800-17109600 Enhancers HMEC breast
5 chr7:17108000-17110200 Weak transcription Lung lung
6 chr7:17108200-17109200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr7:17108400-17109000 Enhancers Fetal Lung lung
8 chr7:17108400-17109000 Enhancers HSMMtube muscle
9 chr7:17108400-17109000 Flanking Active TSS NHEK skin
10 chr7:17108400-17109200 Enhancers Monocytes-CD14+_RO01746 blood
11 chr7:17108400-17110800 Enhancers Primary monocytes fromperipheralblood blood
12 chr7:17108600-17109200 Enhancers Stomach Mucosa stomach
13 chr7:17108600-17109600 Flanking Active TSS GM12878-XiMat blood
14 chr7:17108600-17110400 Enhancers Breast Myoepithelial Primary Cells Breast
15 chr7:17108800-17109000 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
16 chr7:17108800-17109400 Enhancers Gastric stomach

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