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Show only entries with motif concordance for any of the selected TFs:
Show only entries with known associations in:
5 results
Genome position
rs ID
Top 5 TFs
Top 3 cell types
chr6:125790654 G>A
 rs3734634
CTCF_HUMAN
K562 (myelogenous leukemia);  HepG2 (hepatoblastoma);  Peyer's patch...
chr6:125790720 T>C
 rs6932999
PHF8_HUMAN;  NRF1_HUMAN
K562 (myelogenous leukemia)
chr6:125790735 A>G
 rs3734633
NRF1_HUMAN;  MGAP_HUMAN
K562 (myelogenous leukemia)
chr6:125790760 C>T
 rs3734632
CTCF_HUMAN;  SPT5H_HUMAN
K562 (myelogenous leukemia)
chr6:125790762 C>G
 rs114145484
CTCF_HUMAN;  SPT5H_HUMAN
K562 (myelogenous leukemia)
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