Variant report

Variant rs184042728
Chromosome Location chr10:1643162-1643163
allele A/C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:1634600-1648200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr10:1637600-1643800 Weak transcription Fetal Brain Male brain
3 chr10:1639800-1643600 Weak transcription Fetal Brain Female brain
4 chr10:1642200-1643200 Enhancers Breast Myoepithelial Primary Cells Breast
5 chr10:1642200-1643200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr10:1642400-1644000 Enhancers Dnd41 blood
7 chr10:1642600-1643200 Enhancers NHEK skin
8 chr10:1643000-1643200 Enhancers Esophagus oesophagus
9 chr10:1643000-1643400 Active TSS Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr10:1643000-1643400 Enhancers Brain Substantia Nigra brain
11 chr10:1643000-1643600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr10:1643000-1645000 Bivalent Enhancer Fetal Lung lung

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