Tag | Content |
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EnhancerAtlas ID | HS053-14716 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr16:1882570-1883980 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HES2 | MA0616.2 | chr16:1883704-1883714 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr16:1883704-1883714 | GGCACGTGCC | - | 6.02 | ZNF263 | MA0528.1 | chr16:1882762-1882783 | CTCTCCTCTCCTTCCTTCCCT | - | 6.23 | ZNF263 | MA0528.1 | chr16:1882759-1882780 | CTTCTCTCCTCTCCTTCCTTC | - | 6.61 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_12522 | chr16:1883218-1883464 | CD34_adult |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 4 | Chromosome | Start | End |
chr16 | 1883240 | 1883546 | chr16 | 1882837 | 1883199 | chr16 | 1882695 | 1882750 | chr16 | 1882570 | 1882641 |
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| Number: 1 | ID | Chromosome | Start | End |
GH16I001832 | chr16 | 1882613 | 1884275 |
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Enhancer Sequence | GAGCCCAGGA ATTCAAGACC AGCCTGGGCA AAATGCCAAG ATCACTGTCT CTACAAAATG 60 TTTTAAAATT AACCGAGTAA GGTGGCTTCT CCTGAGCTCC TGGACACGGG GCTCAGTGGA 120 GGGGGCACCA TACCCACTCT TGCTGAACCA ACAGTGGGAG CCAAGCCAGC ACCAACCACG 180 ACACCCTCAC TTCTCTCCTC TCCTTCCTTC CCTGTCCACC CTCCCCATTC ACCTGGCTTC 240 ACAAACCCCC CAGTTCTCCC CAAGGGAGGA TGGAAGGCCT GTTCTGCACA ACTAGGTCAA 300 GTCGTTCATT ACCTTATCAC CACAATTTGG ACACTTAGGG GTGAACCTGC ATCCCTCCTC 360 TGTGGCTGCA CATGGTAAAA GCCAGATAAA ACATGACTGA CGATGGTTTA TCTCCCAACA 420 CCAGCCTTAG GAAACAGTTT CATATACTCA CTTTTTCCTT TTTTTTCAAT CCTGTGGTGG 480 AGGGCATGTA GCCTTCTAAA GTACCAGGTC AAACCTCCCA GGCCGTGGGT CAACACTGAC 540 CTTAGCGGTG GGTCTTCACA GCTGGAGTCT GCGCCCTGAA GCAAGTGACT CTCAATGGTG 600 TGCAGTTGAG CCGTTTACTT TGTGGCTGCT GCAAAGCAAA CAGATAAAGT GGCAGCTGTC 660 GTCCTCATGT CCTGAGTAGG TCCCCCTCAG AGTTCTGAGA CCCAGGCATG CTCATGAACC 720 TTTTGAAGTT GGTCTCCTCC CAGTTGATTC AGACTCAGTC ATGTCAGCCC TGAGCCAGCA 780 AGCCTCCACA AGCACTGGGC ACTCCAGTGT GTCACCAGAG AAGACCAGGG ACTAGAAGAG 840 CCCCAGGTGC TCAAAGCAGT CGCACAGGAT TGCCCACGAC TTTGGCTATT CCCACCCAGC 900 ACCAAGAGCC CCTTGCCCTC ATCCTGTCAG ATCTGTCAGA TGACGAGTCA CCACCCAGCT 960 CTCAGAAAGT AGTCTTTAGA GGTACTTTTT TTTTTTTTTT TTTTTTTTTT AAGACAGAGT 1020 CTCGCTCTGT CGCCCAGGCT GGAGTGCAGT GGCTGGATCT CAGCTCACTA CAACCTCCTC 1080 ATCCCAGGTT CAAGAGATTC TCCTGCCTCA GCCTCCCGAG TAGCTGGGAC AACAGGCACG 1140 TGCCACCACA CCCAGCTAAT TTTTTGTATT TTTAGTAGAG ATGGGGTTTC ACTGTGTTAG 1200 CCAGGATGGT CTCGATCTCC TGACTGCCTT GGCATCCCAA AGTGCTGGGA TTACAGGCAT 1260 GAGCCACCGT GCCCAGCCCT TGAGGTCCTA CTCTTTTTCC AGGGAACCAA GACAAATAAT 1320 AAACTGGCTT AAGAAAATAA ATCATTCACT CAGGATTAAG AAACTCACTC AAAGCCGTTC 1380 AACTACATGG AAAAGAAAAT AAATCATTCA 1410
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