Variant report

Variant rs11992534
Chromosome Location chr8:49762962-49762963
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:49758600-49766000 Enhancers Breast Myoepithelial Primary Cells Breast
2 chr8:49758800-49764600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr8:49758800-49765200 Weak transcription iPS-18 Cell Line embryonic stem cell
4 chr8:49761200-49764200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr8:49761200-49764400 Enhancers NHEK skin
6 chr8:49761600-49763800 Weak transcription Fetal Lung lung
7 chr8:49761600-49764000 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
8 chr8:49761800-49764000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr8:49762000-49763000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
10 chr8:49762400-49763000 Flanking Active TSS HMEC breast
11 chr8:49762400-49764000 Weak transcription Fetal Kidney kidney
12 chr8:49762800-49765600 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin

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