Variant report

Variant rs6583676
Chromosome Location chr10:91811625-91811626
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:91810400-91811800 Enhancers Fetal Heart heart
2 chr10:91810800-91812200 Enhancers Primary B cells from cord blood blood
3 chr10:91811000-91811800 Enhancers Primary B cells from peripheral blood blood
4 chr10:91811000-91812800 Flanking Active TSS NHEK skin
5 chr10:91811200-91811800 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr10:91811400-91811800 Flanking Active TSS GM12878-XiMat blood
7 chr10:91811400-91812800 Active TSS HMEC breast
8 chr10:91811600-91811800 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr10:91811600-91812400 Weak transcription Breast Myoepithelial Primary Cells Breast
10 chr10:91811600-91812800 Active TSS Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr10:91811600-91817600 Weak transcription Esophagus oesophagus

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