The 2.0 version of rSNPBase

Variant report

Variant rs62065448
Chromosome Location chr17:43569770-43569771
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr17:43568800-43575000 Weak transcription K562 blood
2 chr17:43569000-43570000 Weak transcription Fetal Intestine Large intestine
3 chr17:43569000-43570000 Enhancers HepG2 liver
4 chr17:43569000-43570200 Weak transcription Adipose Nuclei Adipose
5 chr17:43569000-43570400 Weak transcription Primary monocytes fromperipheralblood blood
6 chr17:43569000-43571400 Weak transcription Primary hematopoietic stem cells short term culture blood
7 chr17:43569000-43571600 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
8 chr17:43569000-43572600 Weak transcription Primary B cells from cord blood blood
9 chr17:43569000-43577600 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
10 chr17:43569000-43583600 Weak transcription Right Atrium heart
11 chr17:43569000-43598000 Weak transcription Brain Germinal Matrix brain
12 chr17:43569200-43571000 Weak transcription Monocytes-CD14+_RO01746 blood
13 chr17:43569200-43571200 Weak transcription Fetal Muscle Leg muscle
14 chr17:43569400-43569800 Enhancers Dnd41 blood
15 chr17:43569400-43570200 Weak transcription Primary neutrophils fromperipheralblood blood
16 chr17:43569600-43570600 Enhancers Fetal Intestine Small intestine

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Last update: Aug 31, 2015