Variant report

Variant rs1765628
Chromosome Location chr1:94839263-94839264
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:94834600-94849400 Weak transcription Primary T helper naive cells from peripheral blood blood
2 chr1:94836000-94841000 Weak transcription HepG2 liver
3 chr1:94838000-94839400 Enhancers Fetal Thymus thymus
4 chr1:94838600-94839400 Enhancers Primary neutrophils fromperipheralblood blood
5 chr1:94838800-94839600 Enhancers Primary hematopoietic stem cells short term culture blood
6 chr1:94839000-94839400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
7 chr1:94839000-94839400 Enhancers Monocytes-CD14+_RO01746 blood
8 chr1:94839000-94839600 Enhancers Primary monocytes fromperipheralblood blood
9 chr1:94839200-94844800 Weak transcription Stomach Mucosa stomach

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