Variant report

Variant rs6583675
Chromosome Location chr10:91811398-91811399
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:91807800-91811400 ZNF genes & repeats GM12878-XiMat blood
2 chr10:91810400-91811600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr10:91810400-91811800 Enhancers Fetal Heart heart
4 chr10:91810800-91812200 Enhancers Primary B cells from cord blood blood
5 chr10:91811000-91811400 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr10:91811000-91811600 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
7 chr10:91811000-91811600 Enhancers Esophagus oesophagus
8 chr10:91811000-91811600 Enhancers Left Ventricle heart
9 chr10:91811000-91811800 Enhancers Primary B cells from peripheral blood blood
10 chr10:91811000-91812800 Flanking Active TSS NHEK skin
11 chr10:91811200-91811400 Weak transcription ES-I3 Cell Line embryonic stem cell
12 chr10:91811200-91811400 Flanking Active TSS HMEC breast
13 chr10:91811200-91811600 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
14 chr10:91811200-91811600 Enhancers Breast Myoepithelial Primary Cells Breast
15 chr10:91811200-91811600 Bivalent Enhancer Primary Natural Killer cells fromperipheralblood blood
16 chr10:91811200-91811600 Enhancers Lung lung
17 chr10:91811200-91811800 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin02 Skin

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