Variant report

Variant rs534464652
Chromosome Location chr2:58958934-58958935
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:58948400-58960000 Weak transcription H1 Cell Line embryonic stem cell
2 chr2:58954600-58963200 Enhancers Primary hematopoietic stem cells blood
3 chr2:58955000-58964400 Enhancers Primary hematopoietic stem cells short term culture blood
4 chr2:58958000-58959000 Enhancers Monocytes-CD14+_RO01746 blood
5 chr2:58958000-58959200 Flanking Active TSS Primary hematopoietic stem cells G-CSF-mobilized Male --
6 chr2:58958600-58959000 Enhancers Primary monocytes fromperipheralblood blood
7 chr2:58958600-58959000 Enhancers HUVEC blood vessel
8 chr2:58958600-58959800 Weak transcription iPS-15b Cell Line embryonic stem cell
9 chr2:58958800-58959000 Enhancers HUES48 Cell Line embryonic stem cell
10 chr2:58958800-58959000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
11 chr2:58958800-58959000 Flanking Active TSS K562 blood
12 chr2:58958800-58959800 Weak transcription iPS-20b Cell Line embryonic stem cell
13 chr2:58958800-58960000 Weak transcription iPS-18 Cell Line embryonic stem cell
14 chr2:58958800-58961400 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived

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