The 2.0 version of rSNPBase

Variant report

Variant rs1879582
Chromosome Location chr17:43570680-43570681
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr17:43568800-43575000 Weak transcription K562 blood
2 chr17:43569000-43571400 Weak transcription Primary hematopoietic stem cells short term culture blood
3 chr17:43569000-43571600 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
4 chr17:43569000-43572600 Weak transcription Primary B cells from cord blood blood
5 chr17:43569000-43577600 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
6 chr17:43569000-43583600 Weak transcription Right Atrium heart
7 chr17:43569000-43598000 Weak transcription Brain Germinal Matrix brain
8 chr17:43569200-43571000 Weak transcription Monocytes-CD14+_RO01746 blood
9 chr17:43569200-43571200 Weak transcription Fetal Muscle Leg muscle
10 chr17:43570000-43570800 Enhancers Fetal Intestine Large intestine
11 chr17:43570200-43571800 Enhancers Primary neutrophils fromperipheralblood blood
12 chr17:43570400-43573200 Enhancers Primary monocytes fromperipheralblood blood
13 chr17:43570600-43574600 Weak transcription HepG2 liver

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Last update: Aug 31, 2015