Variant report

Variant rs11698496
Chromosome Location chr20:22990350-22990351
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr20:22988400-22993400 Weak transcription Aorta Aorta
2 chr20:22988400-22995600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
3 chr20:22988800-22990400 Enhancers NHDF-Ad bronchial
4 chr20:22988800-22992000 Enhancers Breast Myoepithelial Primary Cells Breast
5 chr20:22989400-22991000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr20:22990200-22990800 Enhancers Primary hematopoietic stem cells blood
7 chr20:22990200-22990800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
8 chr20:22990200-22990800 Flanking Active TSS A549 lung
9 chr20:22990200-22990800 Enhancers HSMM muscle
10 chr20:22990200-22990800 Enhancers NHEK skin
11 chr20:22990200-22991000 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
12 chr20:22990200-22991000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
13 chr20:22990200-22991000 Enhancers Gastric stomach
14 chr20:22990200-22991000 Enhancers Right Ventricle heart
15 chr20:22990200-22991000 Enhancers Stomach Mucosa stomach
16 chr20:22990200-22991000 Enhancers HSMMtube muscle
17 chr20:22990200-22991200 Enhancers Primary hematopoietic stem cells short term culture blood
18 chr20:22990200-22991200 Enhancers Lung lung
19 chr20:22990200-22991200 Enhancers HMEC breast
20 chr20:22990200-22992400 Enhancers Placenta Amnion Placenta Amnion

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