Variant report

Variant rs13294926
Chromosome Location chr9:213091-213092
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:207800-213600 Enhancers Primary monocytes fromperipheralblood blood
2 chr9:208800-213200 Enhancers Primary neutrophils fromperipheralblood blood
3 chr9:209800-213400 Enhancers K562 blood
4 chr9:209800-213600 Weak transcription Primary hematopoietic stem cells short term culture blood
5 chr9:209800-214000 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
6 chr9:211000-214600 Flanking Active TSS Monocytes-CD14+_RO01746 blood
7 chr9:211400-213600 Weak transcription Pancreas Pancrea
8 chr9:211400-214000 Enhancers Primary B cells from cord blood blood
9 chr9:211400-214000 Weak transcription Spleen Spleen
10 chr9:212000-214400 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr9:212200-214000 Weak transcription Breast Myoepithelial Primary Cells Breast
12 chr9:212200-214000 Weak transcription Adipose Nuclei Adipose
13 chr9:212600-213600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
14 chr9:213000-214000 Weak transcription Primary hematopoietic stem cells blood
15 chr9:213000-215200 Active TSS Brain Substantia Nigra brain

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