Variant report

Variant rs3896361
Chromosome Location chr19:51713520-51713521
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:51704800-51715000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr19:51707600-51713600 Weak transcription Primary hematopoietic stem cells blood
3 chr19:51711400-51714000 Weak transcription GM12878-XiMat blood
4 chr19:51712000-51713600 Weak transcription Primary hematopoietic stem cells short term culture blood
5 chr19:51713200-51714000 Enhancers Fetal Brain Male brain
6 chr19:51713200-51714200 Enhancers Primary monocytes fromperipheralblood blood
7 chr19:51713400-51714000 Enhancers Primary neutrophils fromperipheralblood blood
8 chr19:51713400-51714200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
9 chr19:51713400-51715400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
10 chr19:51713400-51715800 Flanking Active TSS Monocytes-CD14+_RO01746 blood

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