Tag | Content |
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EnhancerAtlas ID | HS113-14200 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr16:58467260-58468560 |
Target genes | Number: 10 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
DUX4 | MA0468.1 | chr16:58467260-58467271 | TAATCCAATCA | + | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_41220 | chr16:58467154-58468979 | Left_Ventricle |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr16 | 58467521 | 58467757 | chr16 | 58467871 | 58467940 |
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| Number: 1 | ID | Chromosome | Start | End |
GH16I058433 | chr16 | 58467155 | 58468979 |
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Enhancer Sequence | TAATCCAATC AAGTTGACAC TCAGTATTAA CTATCACGGA GCCATATGTG CAAAGCGATC 60 CCCAAATGCC AAAGGAGCCA AGAAACAAAG GAGGCAGACA AATCCTGTTT GTCAGTATTG 120 GATGATTTAT TGGGGGAACT CACAGACAGA AGCGTGGTCT TGGGTGGCCA TAATACAGGT 180 AGATCTCCCA CTGTTACTCC CAAGACCTCA GGCTTGTATA CCATAGAGAA AGGGTACATG 240 TGTTCCAGCA AGAAAATTAC AGGCACCCCT CCAGAACAGG CAAGAACACT GTGTGTGTCA 300 CAGCCCACAA TTTGTGCGAT AACATCAAGG TTGACGTGTT CTTACACTAG GGACAGGAAA 360 TAAAGTAGAA ACAAGGAGGC ATTCACAGGA CTAAGCTAAT CAGAAGTCAA ACCTAGGGAT 420 GCATCCAAAA TGGAGTTGCT CTTGTCTCTA CAGCTAGGAT TTAGAACCTG GACCTGGACG 480 CCTCACTGCT TCCTGCTTCC TTAGTGCCTT GTGGCCTGGA GTCAGAATAA TCTAGCTCAA 540 ACTTGGGAGT CAAATGCTCC AGGGTCTTGA ACTGGTCAGA GCTCTCAATG CCGTAAGTAC 600 CTACAACCCC CTTGGGATGT GCTGTGGGGG GACCATCAGG TGTCTCTGCA GCCCAGGAAA 660 GGCATTCACA GTGCCCTCAG GGAGAGTCTG CAAGGGCTGG CCAGAGCCGC TGCCCACAAG 720 GAAAGCTGGC CTAATGTGCT CTGGCTTCCC GCCTTTCTCC ATTTGGCCTA AGAACAGAGA 780 ACACCCTCAT CCCCCACCCT TACCCACACC CCCACTCCCA GGACTCCCCG GGCTGCAAGG 840 GTCACATGGC TGGGAGGAGG CGAGTCTGAG TGGGTCCCCT CCCAGCAGGC TGTCAGTGTG 900 AGATTACAAA TAACTGGCAG TTCCCATAAT TACTGTGCTG CCCAGAAGCC TGGGCTGTCT 960 ATTCTGAAGT AAGGGTGACT AAAGGTCAGG GCTCCACGAT CAGCCCCGGC TCAGGTTCTG 1020 GTTCTTCCAT GGTACTGGTC TCATGACCTC AGGCAAGTGA GCGAGGCAGG CAAGACTGGG 1080 GCTGGCACGC AGCTCACCCT CACTGCTGCA TTCAGTCCAT TCCAGCACCC ATCCATGAAT 1140 CAGCACCCAT TCTCCTGGCC AGCAGCCATC CCCTGACTGA TCAGCACCCA TCCCTCCTGA 1200 CCAGGACCCA TCCCCCCCAA TTATCACCCA CCCTCCTGAC CAGGACCCAT CCCCCTGACA 1260 AGCACACATC CCTCCTGACC AGCAGCCATC CCTCCTAACC 1300
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