Variant report

Variant rs56238033
Chromosome Location chr19:52264020-52264021
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:52259000-52269800 Weak transcription K562 blood
2 chr19:52263000-52264200 Enhancers Primary monocytes fromperipheralblood blood
3 chr19:52263200-52266400 Flanking Active TSS Primary neutrophils fromperipheralblood blood
4 chr19:52263800-52264400 Enhancers iPS-18 Cell Line embryonic stem cell
5 chr19:52263800-52264400 Enhancers Primary hematopoietic stem cells short term culture blood
6 chr19:52263800-52265000 Flanking Active TSS Primary hematopoietic stem cells blood
7 chr19:52263800-52265400 Flanking Active TSS Monocytes-CD14+_RO01746 blood
8 chr19:52264000-52264400 Enhancers H1 Cell Line embryonic stem cell
9 chr19:52264000-52264400 Enhancers ES-UCSF4 Cell Line embryonic stem cell
10 chr19:52264000-52264600 Enhancers H9 Cell Line embryonic stem cell
11 chr19:52264000-52264600 Enhancers HUES64 Cell Line embryonic stem cell
12 chr19:52264000-52264600 Enhancers iPS-20b Cell Line embryonic stem cell
13 chr19:52264000-52264800 Enhancers ES-I3 Cell Line embryonic stem cell
14 chr19:52264000-52264800 Enhancers iPS-15b Cell Line embryonic stem cell
15 chr19:52264000-52268400 Active TSS Primary B cells from cord blood blood

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