Variant report

Variant rs568135558
Chromosome Location chr7:17094264-17094265
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 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 chr7:17094200-17094400 Enhancers Primary monocytes fromperipheralblood blood
8 chr7:17094200-17095200 Weak transcription Dnd41 blood
9 chr7:17094200-17096600 Weak transcription Monocytes-CD14+_RO01746 blood

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