Variant report

Variant rs182709559
Chromosome Location chr7:17097897-17097898
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 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 chr7:17095200-17098200 Weak transcription Aorta Aorta
3 chr7:17095200-17098600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr7:17095600-17108800 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
5 chr7:17095800-17099200 Enhancers Dnd41 blood
6 chr7:17096400-17100000 Enhancers Primary hematopoietic stem cells short term culture blood
7 chr7:17096600-17098000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
8 chr7:17096600-17098000 Enhancers Monocytes-CD14+_RO01746 blood
9 chr7:17096600-17100000 Enhancers Primary hematopoietic stem cells blood
10 chr7:17096800-17098000 Weak transcription HSMM muscle
11 chr7:17096800-17098000 Weak transcription Osteobl bone
12 chr7:17096800-17100000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
13 chr7:17096800-17100400 Enhancers Primary monocytes fromperipheralblood blood
14 chr7:17097200-17098200 Weak transcription HMEC breast
15 chr7:17097400-17098400 Weak transcription NHEK skin
16 chr7:17097400-17099000 Enhancers Muscle Satellite Cultured Cells --
17 chr7:17097600-17099000 Enhancers HUVEC blood vessel
18 chr7:17097600-17099000 Enhancers NHDF-Ad bronchial
19 chr7:17097800-17099000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell

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