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EnhancerAtlas ID | HS184-11949 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr16:1700750-1702490 | 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 | GCAGCAACTC TCCTACCTGA CGTGTGCAAC TGGGAGTTGG TGAATTCCTA AAATTGGTTA 60 AGGCAGAAAG CCGTAAAAAC AAGATACACA TGCCCTGAGC ATTTTGTAAA ACACAAGCCC 120 ATTGTCGTTC ACCAGCCAGT GGGCCGCTGC CCAGAGCCAT GTCTTGACTG GGGTCCACTC 180 CTTGGAATTC AAGTTGGTTT TTCTCTCAGA TCAGAAACTC CTCACAGGGA GGTCACATAG 240 AGGTGGACTG AGAAGTCACA GAGGTAGACT GAGCTCACAC AGAGGTCATG GAGAGGTGGA 300 TTGAGGTCAC ACAGAGGTCA CGGAGAAGTG GACTGAGAGG TCACAGAGAG GAGGACTCAG 360 AGGCCACAGG TCATGGAAAG GTAGATTGAG GTCACAGAGG TCACGAAAAG GTGGACTGAG 420 GTCACGGAGA GGTGGACTGA GGTCACACAG GTCACAAAAA GGTGGACTCA GAGGTCACAG 480 AGTTGGACAG GTTACACAGA GGTCACACGG TGGACTGAGA TCACGGAGAG CTGGACTGAG 540 GTCACACACA GGTTATGGAG AGGTCGACTG AGAGGTCACA CAGAGGTCAT CTAGGGGTGG 600 ATTTAGGTCA CGCACAGGTC ACGGAAAGGT GGACTGAGAG GTCACGGAGA GGTGGACTGA 660 GGTCACAGAG GTCACCTAGA GGTGAATTGT CACACAGAGG TCATGTTGAG GTGGACTGAG 720 GTCACACACA GGTCATCTAG AGGTGGATTG AGGTCACACA CAGGTCATCT AGAGGTGGAC 780 TGAGGTCACA CAGGTCATTT AGAGGTGGAT TGAGGTCACA CAGTTCACGG AGAGGTGGGC 840 TGAGGTCACA CAGAGGTCAT GGGGAGGTGG ACTGAGAGGT CACCTAGAGG TGGATTGAAG 900 TCACACAGAG GTAACCTAGA GGTGGACTGA GAGGTCACGG AGAGGTGGAC TGAGGTCACA 960 CAGAGGTCAC CTAGAGGTGG ATTGAGGTCA CACAGAGGTC ATAGAGAGGT GGACTGAGGT 1020 CACACAGGTC ACAGAGAGGT GGACTGAGAG GTCACACAGA GGTCACAGAA AGGTGGATTG 1080 AGGTCACACA GAGGTCACAG AAAGGTGGAC TGAGGTCACA CAGGTCATCT AGAGATGGAT 1140 TGAGGTCACA TGGAGGTCAC GGGGAGGTGA ACTGAGGTCA CAGAGAGGTC ACGTAGAAGT 1200 GGATTGAGGT CACACAGAGG TCATGGGGAG GTGGACTGAG GTCACAGGTC ATGTAGAGCT 1260 GGATTTAGGT CACACAGAGG TCACAGGGAG GTGGACTGAG AGGTCACGGA GAGGTAGACT 1320 GAGAGGTCAT GGGGAGGAGG ACTGAGAGCT TCTGCTCTGA GGGCCCAAAG TGGGAGGACT 1380 GCACAGAGCT GGGGCAGTGG AGAGAGGGGT GGCCATCTGA GGGGACCCCA GGATAGTGGC 1440 TTTTCCAGGG ATGGGACATC AGCTTGTGCC AGGCCAGTCA CCAAGGCAGG AGGGCACAGC 1500 ACATTTTCTG TAAACAGCAG GTGTCCCTTG GAGTGTGAGG TGTGGTCAGG AAAGTAGCAG 1560 GATGTGCAGA GTCACCACTT CTTGTTTGTC ACTGTGTCCT CCCACTGTCC TACGCGGGCT 1620 CGAGAGGCTG GGGTGGATGC TTGGCCAGGC CCCACCTGGC CTGGCTCAGC GCCTCTCCGT 1680 GTGCTGGCCC TTCCGTCCTT CTGTTCACTC ACAGGCCTCA GCGTTCCTTC AAAACTCTTT 1740
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