Variant report
Variant | rs17049705 |
---|---|
Chromosome Location | chr2:58947743-58947744 |
allele | A/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:58941200-58954600 | Weak transcription | Primary hematopoietic stem cells | blood |
2 | chr2:58943400-58948400 | Enhancers | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |
3 | chr2:58943800-58950200 | Enhancers | Primary hematopoietic stem cells G-CSF-mobilized Female | -- |
4 | chr2:58946600-58948600 | Enhancers | iPS-18 Cell Line | embryonic stem cell |
5 | chr2:58946600-58949200 | Enhancers | iPS-15b Cell Line | embryonic stem cell |
6 | chr2:58946800-58947800 | Enhancers | iPS-20b Cell Line | embryonic stem cell |
7 | chr2:58946800-58948200 | Enhancers | HUES64 Cell Line | embryonic stem cell |
8 | chr2:58947000-58948200 | Enhancers | ES-I3 Cell Line | embryonic stem cell |
9 | chr2:58947000-58948400 | Enhancers | HUES6 Cell Line | embryonic stem cell |
10 | chr2:58947400-58948000 | Enhancers | K562 | blood |
11 | chr2:58947600-58947800 | Flanking Active TSS | HUES48 Cell Line | embryonic stem cell |