Variant report

Variant rs495318
Chromosome Location chr7:17096540-17096541
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 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 chr7:17095200-17098200 Weak transcription Aorta Aorta
8 chr7:17095200-17098600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr7:17095600-17108800 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
10 chr7:17095800-17099200 Enhancers Dnd41 blood
11 chr7:17096000-17096800 Enhancers Osteobl bone
12 chr7:17096000-17097000 Enhancers Muscle Satellite Cultured Cells --
13 chr7:17096200-17096800 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
14 chr7:17096200-17096800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr7:17096400-17097200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
16 chr7:17096400-17100000 Enhancers Primary hematopoietic stem cells short term culture blood

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