The 2.0 version of rSNPBase

Variant report

Variant rs12495362
Chromosome Location chr3:17014806-17014807
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:16987400-17015600 Weak transcription Aorta Aorta
2 chr3:17005400-17015000 Weak transcription Primary T helper memory cells from peripheral blood 1 blood
3 chr3:17009200-17026600 Weak transcription Primary T killer memory cells from peripheral blood blood
4 chr3:17009800-17015000 Weak transcription Primary T helper memory cells from peripheral blood 2 blood
5 chr3:17010400-17015600 Weak transcription Right Ventricle heart
6 chr3:17011000-17015000 Weak transcription Primary T helper naive cells fromperipheralblood blood
7 chr3:17013400-17016200 Weak transcription Adipose Nuclei Adipose
8 chr3:17013800-17016200 Weak transcription Fetal Heart heart
9 chr3:17014400-17016000 ZNF genes & repeats Primary hematopoietic stem cells blood
10 chr3:17014600-17015400 Weak transcription Primary T cells fromperipheralblood blood
11 chr3:17014600-17015400 Weak transcription Primary T helper cells fromperipheralblood blood
12 chr3:17014600-17016600 Enhancers Primary T cells effector/memory enriched fromperipheralblood blood
13 chr3:17014800-17019600 Enhancers Primary T helper cells PMA-I stimulated --
14 chr3:17014800-17033600 Weak transcription Primary T cells from cord blood blood
15 chr3:17014800-17038800 Weak transcription Primary B cells from cord blood blood

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Last update: Aug 31, 2015