| Tag | Content |
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EnhancerAtlas ID | HS060-12177 | Organism | Homo sapiens | Tissue/cell | GM12891 | Coordinate | chr16:1700790-1702490 | 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 | TGAATTCCTA AAATTGGTTA AGGCAGAAAG CCGTAAAAAC AAGATACACA TGCCCTGAGC 60
ATTTTGTAAA ACACAAGCCC ATTGTCGTTC ACCAGCCAGT GGGCCGCTGC CCAGAGCCAT 120
GTCTTGACTG GGGTCCACTC CTTGGAATTC AAGTTGGTTT TTCTCTCAGA TCAGAAACTC 180
CTCACAGGGA GGTCACATAG AGGTGGACTG AGAAGTCACA GAGGTAGACT GAGCTCACAC 240
AGAGGTCATG GAGAGGTGGA TTGAGGTCAC ACAGAGGTCA CGGAGAAGTG GACTGAGAGG 300
TCACAGAGAG GAGGACTCAG AGGCCACAGG TCATGGAAAG GTAGATTGAG GTCACAGAGG 360
TCACGAAAAG GTGGACTGAG GTCACGGAGA GGTGGACTGA GGTCACACAG GTCACAAAAA 420
GGTGGACTCA GAGGTCACAG AGTTGGACAG GTTACACAGA GGTCACACGG TGGACTGAGA 480
TCACGGAGAG CTGGACTGAG GTCACACACA GGTTATGGAG AGGTCGACTG AGAGGTCACA 540
CAGAGGTCAT CTAGGGGTGG ATTTAGGTCA CGCACAGGTC ACGGAAAGGT GGACTGAGAG 600
GTCACGGAGA GGTGGACTGA GGTCACAGAG GTCACCTAGA GGTGAATTGT CACACAGAGG 660
TCATGTTGAG GTGGACTGAG GTCACACACA GGTCATCTAG AGGTGGATTG AGGTCACACA 720
CAGGTCATCT AGAGGTGGAC TGAGGTCACA CAGGTCATTT AGAGGTGGAT TGAGGTCACA 780
CAGTTCACGG AGAGGTGGGC TGAGGTCACA CAGAGGTCAT GGGGAGGTGG ACTGAGAGGT 840
CACCTAGAGG TGGATTGAAG TCACACAGAG GTAACCTAGA GGTGGACTGA GAGGTCACGG 900
AGAGGTGGAC TGAGGTCACA CAGAGGTCAC CTAGAGGTGG ATTGAGGTCA CACAGAGGTC 960
ATAGAGAGGT GGACTGAGGT CACACAGGTC ACAGAGAGGT GGACTGAGAG GTCACACAGA 1020
GGTCACAGAA AGGTGGATTG AGGTCACACA GAGGTCACAG AAAGGTGGAC TGAGGTCACA 1080
CAGGTCATCT AGAGATGGAT TGAGGTCACA TGGAGGTCAC GGGGAGGTGA ACTGAGGTCA 1140
CAGAGAGGTC ACGTAGAAGT GGATTGAGGT CACACAGAGG TCATGGGGAG GTGGACTGAG 1200
GTCACAGGTC ATGTAGAGCT GGATTTAGGT CACACAGAGG TCACAGGGAG GTGGACTGAG 1260
AGGTCACGGA GAGGTAGACT GAGAGGTCAT GGGGAGGAGG ACTGAGAGCT TCTGCTCTGA 1320
GGGCCCAAAG TGGGAGGACT GCACAGAGCT GGGGCAGTGG AGAGAGGGGT GGCCATCTGA 1380
GGGGACCCCA GGATAGTGGC TTTTCCAGGG ATGGGACATC AGCTTGTGCC AGGCCAGTCA 1440
CCAAGGCAGG AGGGCACAGC ACATTTTCTG TAAACAGCAG GTGTCCCTTG GAGTGTGAGG 1500
TGTGGTCAGG AAAGTAGCAG GATGTGCAGA GTCACCACTT CTTGTTTGTC ACTGTGTCCT 1560
CCCACTGTCC TACGCGGGCT CGAGAGGCTG GGGTGGATGC TTGGCCAGGC CCCACCTGGC 1620
CTGGCTCAGC GCCTCTCCGT GTGCTGGCCC TTCCGTCCTT CTGTTCACTC ACAGGCCTCA 1680
GCGTTCCTTC AAAACTCTTT 1700
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