Variant report

Variant rs1359490
Chromosome Location chr1:92953855-92953856
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:92952200-92954000 Flanking Active TSS Primary T helper cells PMA-I stimulated --
2 chr1:92952600-92954200 Enhancers Primary T helper naive cells fromperipheralblood blood
3 chr1:92952800-92954200 Enhancers Fetal Thymus thymus
4 chr1:92952800-92955000 Enhancers Primary T helper cells fromperipheralblood blood
5 chr1:92952800-92991400 Weak transcription Pancreas Pancrea
6 chr1:92953000-92954000 Enhancers Primary T helper naive cells from peripheral blood blood
7 chr1:92953000-92954400 Enhancers Primary T cells from cord blood blood
8 chr1:92953200-92954000 Enhancers Primary neutrophils fromperipheralblood blood
9 chr1:92953200-92957600 Weak transcription HepG2 liver
10 chr1:92953200-92960400 Weak transcription Primary T helper 17 cells PMA-I stimulated --
11 chr1:92953400-92954000 Weak transcription Primary T killer naive cells fromperipheralblood blood
12 chr1:92953400-92954200 Enhancers Dnd41 blood
13 chr1:92953400-92954400 Enhancers Primary hematopoietic stem cells short term culture blood
14 chr1:92953400-92955800 Weak transcription Primary T helper memory cells from peripheral blood 1 blood
15 chr1:92953600-92954400 Enhancers Primary T killer memory cells from peripheral blood blood
16 chr1:92953800-92954400 Enhancers Primary T helper memory cells from peripheral blood 2 blood

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