Variant report

Variant rs7323959
Chromosome Location chr13:50183179-50183180
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:50180800-50183200 Enhancers Primary B cells from peripheral blood blood
2 chr13:50181000-50185800 Enhancers Fetal Heart heart
3 chr13:50181200-50192000 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
4 chr13:50181400-50183200 Enhancers Primary monocytes fromperipheralblood blood
5 chr13:50181400-50183400 Enhancers Primary neutrophils fromperipheralblood blood
6 chr13:50181400-50183600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
7 chr13:50181400-50183600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
8 chr13:50181400-50183800 Enhancers Primary B cells from cord blood blood
9 chr13:50181400-50183800 Enhancers Primary hematopoietic stem cells blood
10 chr13:50181400-50185400 Weak transcription HepG2 liver
11 chr13:50181400-50194400 Weak transcription Right Ventricle heart
12 chr13:50182000-50184200 Weak transcription Fetal Muscle Leg muscle
13 chr13:50182200-50183800 Enhancers Primary hematopoietic stem cells short term culture blood
14 chr13:50182400-50183200 Enhancers Monocytes-CD14+_RO01746 blood
15 chr13:50183000-50183200 Enhancers Primary mononuclear cells fromperipheralblood Blood
16 chr13:50183000-50183200 Enhancers GM12878-XiMat blood

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