Variant report

Variant rs536383355
Chromosome Location chr13:51068453-51068454
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:51065600-51068600 Weak transcription HepG2 liver
2 chr13:51067600-51069400 Enhancers Fetal Thymus thymus
3 chr13:51067800-51069000 Enhancers Primary hematopoietic stem cells blood
4 chr13:51067800-51069200 Enhancers Primary monocytes fromperipheralblood blood
5 chr13:51067800-51069200 Enhancers Thymus Thymus
6 chr13:51068000-51068600 Enhancers Primary T helper memory cells from peripheral blood 2 blood
7 chr13:51068000-51068600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
8 chr13:51068000-51069200 Enhancers Primary hematopoietic stem cells short term culture blood
9 chr13:51068000-51069400 Enhancers Monocytes-CD14+_RO01746 blood
10 chr13:51068200-51068800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
11 chr13:51068200-51069200 Enhancers Primary neutrophils fromperipheralblood blood
12 chr13:51068200-51069200 Enhancers Primary T cells from cord blood blood
13 chr13:51068400-51068600 Flanking Active TSS Dnd41 blood
14 chr13:51068400-51068800 Enhancers Cortex derived primary cultured neurospheres brain

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