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EnhancerAtlas ID | HS093-11096 | Organism | Homo sapiens | Tissue/cell | HL-60 | Coordinate | chr16:1700860-1702490 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxo1 | MA0480.1 | chr16:1702258-1702269 | TGTAAACAGCA | - | 6.14 | NR2F1 | MA0017.2 | chr16:1702024-1702037 | CAGAGGTCACAGG | + | 6.19 | NR2F1 | MA0017.2 | chr16:1701600-1701613 | CAGAGGTCATGGG | + | 6.22 | NR2F1 | MA0017.2 | chr16:1701964-1701977 | CAGAGGTCATGGG | + | 6.22 | Nr2f6 | MA0677.1 | chr16:1701987-1702001 | GAGGTCACAGGTCA | + | 6.51 | RARA(var.2) | MA0730.1 | chr16:1701021-1701038 | AGCTCACACAGAGGTCA | + | 6.27 | RARA(var.2) | MA0730.1 | chr16:1701238-1701255 | AGGTTACACAGAGGTCA | + | 6.51 | RARA(var.2) | MA0730.1 | chr16:1701418-1701435 | AGGTCACCTAGAGGTGA | + | 6.72 | RARA(var.2) | MA0730.1 | chr16:1701468-1701485 | AGGTCACACACAGGTCA | + | 7.12 | RARA(var.2) | MA0730.1 | chr16:1701500-1701517 | AGGTCACACACAGGTCA | + | 7.12 | RARA(var.2) | MA0730.1 | chr16:1701354-1701371 | AGGTCACGCACAGGTCA | + | 7.49 | RARA(var.2) | MA0730.1 | chr16:1701892-1701909 | AGGTCACATGGAGGTCA | + | 7.4 | RARA(var.2) | MA0730.1 | chr16:1701924-1701941 | AGGTCACAGAGAGGTCA | + | 7.56 | RARA(var.2) | MA0730.1 | chr16:1701053-1701070 | AGGTCACACAGAGGTCA | + | 8.18 | RARA(var.2) | MA0730.1 | chr16:1701322-1701339 | AGGTCACACAGAGGTCA | + | 8.18 | RARA(var.2) | MA0730.1 | chr16:1701592-1701609 | AGGTCACACAGAGGTCA | + | 8.18 | RARA(var.2) | MA0730.1 | chr16:1701702-1701719 | AGGTCACACAGAGGTCA | + | 8.18 | RARA(var.2) | MA0730.1 | chr16:1701734-1701751 | AGGTCACACAGAGGTCA | + | 8.18 | RARA(var.2) | MA0730.1 | chr16:1701798-1701815 | AGGTCACACAGAGGTCA | + | 8.18 | RARA(var.2) | MA0730.1 | chr16:1701830-1701847 | AGGTCACACAGAGGTCA | + | 8.18 | RARA(var.2) | MA0730.1 | chr16:1701956-1701973 | AGGTCACACAGAGGTCA | + | 8.18 | RARA(var.2) | MA0730.1 | chr16:1702016-1702033 | AGGTCACACAGAGGTCA | + | 8.18 | Rxra | MA0512.2 | chr16:1701987-1702001 | GAGGTCACAGGTCA | + | 6.26 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ACACAAGCCC ATTGTCGTTC ACCAGCCAGT GGGCCGCTGC CCAGAGCCAT GTCTTGACTG 60 GGGTCCACTC CTTGGAATTC AAGTTGGTTT TTCTCTCAGA TCAGAAACTC CTCACAGGGA 120 GGTCACATAG AGGTGGACTG AGAAGTCACA GAGGTAGACT GAGCTCACAC AGAGGTCATG 180 GAGAGGTGGA TTGAGGTCAC ACAGAGGTCA CGGAGAAGTG GACTGAGAGG TCACAGAGAG 240 GAGGACTCAG AGGCCACAGG TCATGGAAAG GTAGATTGAG GTCACAGAGG TCACGAAAAG 300 GTGGACTGAG GTCACGGAGA GGTGGACTGA GGTCACACAG GTCACAAAAA GGTGGACTCA 360 GAGGTCACAG AGTTGGACAG GTTACACAGA GGTCACACGG TGGACTGAGA TCACGGAGAG 420 CTGGACTGAG GTCACACACA GGTTATGGAG AGGTCGACTG AGAGGTCACA CAGAGGTCAT 480 CTAGGGGTGG ATTTAGGTCA CGCACAGGTC ACGGAAAGGT GGACTGAGAG GTCACGGAGA 540 GGTGGACTGA GGTCACAGAG GTCACCTAGA GGTGAATTGT CACACAGAGG TCATGTTGAG 600 GTGGACTGAG GTCACACACA GGTCATCTAG AGGTGGATTG AGGTCACACA CAGGTCATCT 660 AGAGGTGGAC TGAGGTCACA CAGGTCATTT AGAGGTGGAT TGAGGTCACA CAGTTCACGG 720 AGAGGTGGGC TGAGGTCACA CAGAGGTCAT GGGGAGGTGG ACTGAGAGGT CACCTAGAGG 780 TGGATTGAAG TCACACAGAG GTAACCTAGA GGTGGACTGA GAGGTCACGG AGAGGTGGAC 840 TGAGGTCACA CAGAGGTCAC CTAGAGGTGG ATTGAGGTCA CACAGAGGTC ATAGAGAGGT 900 GGACTGAGGT CACACAGGTC ACAGAGAGGT GGACTGAGAG GTCACACAGA GGTCACAGAA 960 AGGTGGATTG AGGTCACACA GAGGTCACAG AAAGGTGGAC TGAGGTCACA CAGGTCATCT 1020 AGAGATGGAT TGAGGTCACA TGGAGGTCAC GGGGAGGTGA ACTGAGGTCA CAGAGAGGTC 1080 ACGTAGAAGT GGATTGAGGT CACACAGAGG TCATGGGGAG GTGGACTGAG GTCACAGGTC 1140 ATGTAGAGCT GGATTTAGGT CACACAGAGG TCACAGGGAG GTGGACTGAG AGGTCACGGA 1200 GAGGTAGACT GAGAGGTCAT GGGGAGGAGG ACTGAGAGCT TCTGCTCTGA GGGCCCAAAG 1260 TGGGAGGACT GCACAGAGCT GGGGCAGTGG AGAGAGGGGT GGCCATCTGA GGGGACCCCA 1320 GGATAGTGGC TTTTCCAGGG ATGGGACATC AGCTTGTGCC AGGCCAGTCA CCAAGGCAGG 1380 AGGGCACAGC ACATTTTCTG TAAACAGCAG GTGTCCCTTG GAGTGTGAGG TGTGGTCAGG 1440 AAAGTAGCAG GATGTGCAGA GTCACCACTT CTTGTTTGTC ACTGTGTCCT CCCACTGTCC 1500 TACGCGGGCT CGAGAGGCTG GGGTGGATGC TTGGCCAGGC CCCACCTGGC CTGGCTCAGC 1560 GCCTCTCCGT GTGCTGGCCC TTCCGTCCTT CTGTTCACTC ACAGGCCTCA GCGTTCCTTC 1620 AAAACTCTTT 1630
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