Variant report

Variant rs577132271
Chromosome Location chr7:17096057-17096058
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 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 chr7:17093800-17097200 Enhancers HMEC breast
3 chr7:17093800-17097400 Enhancers NHEK skin
4 chr7:17093800-17097600 Enhancers Breast Myoepithelial Primary Cells Breast
5 chr7:17094200-17096600 Weak transcription Monocytes-CD14+_RO01746 blood
6 chr7:17094400-17096800 Weak transcription Primary monocytes fromperipheralblood blood
7 chr7:17094600-17096400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
8 chr7:17095200-17098200 Weak transcription Aorta Aorta
9 chr7:17095200-17098600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr7:17095600-17108800 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
11 chr7:17095800-17096200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr7:17095800-17099200 Enhancers Dnd41 blood
13 chr7:17096000-17096800 Enhancers Osteobl bone
14 chr7:17096000-17097000 Enhancers Muscle Satellite Cultured Cells --

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