Variant report

Variant rs59377546
Chromosome Location chr7:17098833-17098834
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:17095600-17108800 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr7:17095800-17099200 Enhancers Dnd41 blood
3 chr7:17096400-17100000 Enhancers Primary hematopoietic stem cells short term culture blood
4 chr7:17096600-17100000 Enhancers Primary hematopoietic stem cells blood
5 chr7:17096800-17100000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
6 chr7:17096800-17100400 Enhancers Primary monocytes fromperipheralblood blood
7 chr7:17097400-17099000 Enhancers Muscle Satellite Cultured Cells --
8 chr7:17097600-17099000 Enhancers HUVEC blood vessel
9 chr7:17097600-17099000 Enhancers NHDF-Ad bronchial
10 chr7:17097800-17099000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
11 chr7:17098000-17099000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
12 chr7:17098000-17099200 Flanking Active TSS Monocytes-CD14+_RO01746 blood
13 chr7:17098400-17099200 Enhancers Primary B cells from cord blood blood
14 chr7:17098800-17099400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
15 chr7:17098800-17101600 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
16 chr7:17098800-17102400 Weak transcription Osteobl bone
17 chr7:17098800-17107800 Weak transcription HMEC breast

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