Variant report

Variant rs2192442
Chromosome Location chr12:9963826-9963827
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:9962600-9964600 Enhancers Primary neutrophils fromperipheralblood blood
2 chr12:9962800-9964000 Flanking Active TSS Monocytes-CD14+_RO01746 blood
3 chr12:9962800-9965000 Enhancers Primary monocytes fromperipheralblood blood
4 chr12:9963000-9964000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr12:9963200-9964200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
6 chr12:9963200-9964600 Enhancers Primary B cells from cord blood blood
7 chr12:9963200-9964600 Enhancers Primary B cells from peripheral blood blood
8 chr12:9963200-9964600 Enhancers Primary T cells from cord blood blood
9 chr12:9963600-9966200 Weak transcription Thymus Thymus
10 chr12:9963800-9966000 Weak transcription Primary hematopoietic stem cells blood
11 chr12:9963800-9966200 Enhancers Primary hematopoietic stem cells short term culture blood
12 chr12:9963800-9966200 Weak transcription Primary T helper cells PMA-I stimulated --
13 chr12:9963800-9966200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
14 chr12:9963800-9966200 Weak transcription Fetal Thymus thymus
15 chr12:9963800-9966200 Weak transcription GM12878-XiMat blood

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