Variant report

Variant rs79953582
Chromosome Location chr7:17094623-17094624
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:17089000-17098000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
2 chr7:17093800-17095600 Strong transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
3 chr7:17093800-17095800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr7:17093800-17097200 Enhancers HMEC breast
5 chr7:17093800-17097400 Enhancers NHEK skin
6 chr7:17093800-17097600 Enhancers Breast Myoepithelial Primary Cells Breast
7 chr7:17094200-17095200 Weak transcription Dnd41 blood
8 chr7:17094200-17096600 Weak transcription Monocytes-CD14+_RO01746 blood
9 chr7:17094400-17096800 Weak transcription Primary monocytes fromperipheralblood blood
10 chr7:17094600-17095200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr7:17094600-17096400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin

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