The 2.0 version of rSNPBase

Variant report

Variant rs2053569
Chromosome Location chr14:32094721-32094722
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:32046200-32110600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr14:32069600-32102800 Weak transcription Primary T cells effector/memory enriched fromperipheralblood blood
3 chr14:32092000-32096000 Weak transcription Duodenum Smooth Muscle Duodenum
4 chr14:32092000-32096400 Weak transcription Fetal Lung lung
5 chr14:32092200-32099000 Weak transcription Aorta Aorta
6 chr14:32092200-32099600 Weak transcription Brain Hippocampus Middle brain
7 chr14:32092200-32100400 Weak transcription Rectal Smooth Muscle rectum
8 chr14:32092400-32094800 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
9 chr14:32092400-32100600 Weak transcription Left Ventricle heart
10 chr14:32092400-32103000 Weak transcription Primary T cells from cord blood blood
11 chr14:32092800-32096000 Weak transcription Fetal Intestine Small intestine
12 chr14:32092800-32096200 Weak transcription Lung lung
13 chr14:32093200-32102800 Weak transcription Primary B cells from peripheral blood blood
14 chr14:32094200-32095800 Enhancers HepG2 liver

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Last update: Aug 31, 2015