Tag | Content |
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EnhancerAtlas ID | HS139-11937 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr12:24989970-24994340 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr12:24990020-24990038 | GGGAGGGAGAAAGGAAGG | + | 6.85 | EWSR1-FLI1 | MA0149.1 | chr12:24990049-24990067 | GGAAGGGAGGAAGGGGGG | + | 7.06 | EWSR1-FLI1 | MA0149.1 | chr12:24990057-24990075 | GGAAGGGGGGAGGGAAGG | + | 7.12 | EWSR1-FLI1 | MA0149.1 | chr12:24990028-24990046 | GAAAGGAAGGAAGAAAGA | + | 7.18 | EWSR1-FLI1 | MA0149.1 | chr12:24990061-24990079 | GGGGGGAGGGAAGGAAGG | + | 7.21 | EWSR1-FLI1 | MA0149.1 | chr12:24990024-24990042 | GGGAGAAAGGAAGGAAGA | + | 7.41 | EWSR1-FLI1 | MA0149.1 | chr12:24990045-24990063 | AGAAGGAAGGGAGGAAGG | + | 8.05 | EWSR1-FLI1 | MA0149.1 | chr12:24990065-24990083 | GGAGGGAAGGAAGGAAAG | + | 8.84 | ZNF263 | MA0528.1 | chr12:24990033-24990054 | GAAGGAAGAAAGAGAAGGAAG | + | 6.07 | ZNF263 | MA0528.1 | chr12:24990006-24990027 | GAGAGAGGGAGGGAGGGAGGG | + | 6.11 | ZNF263 | MA0528.1 | chr12:24990055-24990076 | GAGGAAGGGGGGAGGGAAGGA | + | 6.17 | ZNF263 | MA0528.1 | chr12:24990043-24990064 | AGAGAAGGAAGGGAGGAAGGG | + | 6.43 | ZNF263 | MA0528.1 | chr12:24990014-24990035 | GAGGGAGGGAGGGAGAAAGGA | + | 6.77 | ZNF263 | MA0528.1 | chr12:24990018-24990039 | GAGGGAGGGAGAAAGGAAGGA | + | 6.86 | ZNF263 | MA0528.1 | chr12:24990051-24990072 | AAGGGAGGAAGGGGGGAGGGA | + | 6.9 | ZNF263 | MA0528.1 | chr12:24990046-24990067 | GAAGGAAGGGAGGAAGGGGGG | + | 7.23 | ZNF263 | MA0528.1 | chr12:24990062-24990083 | GGGGGAGGGAAGGAAGGAAAG | + | 7.25 | ZNF263 | MA0528.1 | chr12:24990010-24990031 | GAGGGAGGGAGGGAGGGAGAA | + | 7.53 | ZNF263 | MA0528.1 | chr12:24990054-24990075 | GGAGGAAGGGGGGAGGGAAGG | + | 8 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_59142 | chr12:24965988-24994172 | Ly3 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 5 | Chromosome | Start | End |
chr12 | 24991472 | 24991796 | chr12 | 24992063 | 24992648 | chr12 | 24992180 | 24992695 | chr12 | 24993004 | 24993242 | chr12 | 24993406 | 24993693 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I024837 | chr12 | 24990687 | 24993837 |
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Enhancer Sequence | AAAAAAGAAA AGAAAAGAAA GAGAGAAGGA AAGAAAGAGA GAGGGAGGGA GGGAGGGAGA 60 AAGGAAGGAA GAAAGAGAAG GAAGGGAGGA AGGGGGGAGG GAAGGAAGGA AAGTTATCTA 120 ATCATCTTCA GTTTACCCTT AACCAGTAAA ATAATGAGAT GGTTTTCCAC CAACAAACAG 180 TAAGAGTTAT TGCATGGTCT TAAGAGGAAT ATTCTGAAGT GAAAATTTAC CTTAGCAGAT 240 GAAAGGTGGT TACTAATTAG AATAATGTAG ATAGGGTCTT ACTCAGAAAA ACTGGTCATT 300 ACCAAACCTT CTAAGAATGC TATGGAGGAG GCTATCCCCA AGAAGTGTGC GTGCCTACTC 360 AGGCTGGTCA CTGCTTCCAC GCTGCCCTTG GAAAGTCTAA TTTTTTTTTT TTTTTTTTTT 420 TTTTAGGTTA CCCAGGCTGG AGTGCAGTGG CACCATCTCA GCTCACTGCA CCCTCTGCCT 480 CCCAGGGTCA AGTGATTCTC CTGCCTCAGC CTCCTGAGTA GCTGGGATTA CAGGTACGCG 540 CCACCACGCC TGGCTAATTT TTGTATTTTT AGTAGAGACG GGGTTTCACC ATGTTGGTCA 600 GGCTGGTCTC GAACTCCTGA GCTCAGATGA TCTGCCCACT TCGGCCTCCC AAAGTGCTGA 660 GATTACAGAT GTGAGCCACC GCACCCAGCC TAAGAGTCTA TCTTTAGTGA TTTTCAAACC 720 TGGTGGAGCA TCAGCAACAA GTATGGAGAT GCTGCCTTTG CTCTCTGAGA TTCAAATGTA 780 ATGGGCTTAT CAGAGTGAGC TCAAGCACGT GTACGGTTAA AAAAGAAGAC ATTCAAGAAA 840 CAAAACTCCA AAGCTGAGCT ACTGCTCTAC TGTGAGATGA CTGCAGACAT CCCTAACTAC 900 TGTGAGGTCT AGTAGGACAA TTGTTCACAG GCATCATGCA TGATCCATCA GCTGCACAAG 960 CTCTCCTTAC AGTACCCTCT GGCACTCAGC ATCTCCCTTT CCTCCCCACT TCTGACACCC 1020 AGGAGTCTGA ATCTAGTGAG TCCTGACACT GAGGCCACCA CCCTCTCCCT CAATACATGG 1080 TGGTTCTAGG CTCGCCCACT CCACTGGGGT TACATCAGAC ATGCCCAACA ATCAAGCTCT 1140 ATCTGGAATA CCAAACTCTA TCTTCATCCT TCTATCCTCA AAACTGGGCA TTGTGCCTAG 1200 CCCAGAGTGT ATATAATAAA TGTTTTTGAG TAAAAAATAA ACGAATAAGT TATCTTTGCT 1260 AGGATACAGC AGTATGGCTT TTTTGAATTT TGTTTCTGAA AATCATCTGC TGAAAATTGC 1320 TTTCTGGAAA GGAGAAAATT TGTTCTTGGC AATGTTCTTA GGGCTACTCT TTGTCATGTT 1380 TAGAAGTGTT GATGATCTCA AAATAAACAT GTGTTTTGCA ATAGCTAGCC AACTAGATAC 1440 ATAAATGTAT GGATCTATTT GTGTGTGTAT ATATATGTAC ACACACACAC ACACTTCCAG 1500 TGCCCCCAAA CCGGACCTTT CCTAAAGCTT GCTGAGCCCT GAGACTACAT GAAGTTAAAT 1560 GAAAACAGCA GCCCCGCATG TGCAAGTGCT GTTTTGTGAA ACATGTTTAA CACCCAGAAC 1620 TGTAACCACT AGCCTGAGGT CAAGGAACAG AACATCTGCT TCTCTGGTTG CCAGACAGAG 1680 ATGATGACAT GACAACATTT GGGTGAGAAA TATTCATTTT CCTCTGCAAC CACAAACATA 1740 CTTACAAGAG CCAGAAATCA CTCCAGATTG CCCAACATGA GGAAAACAGA ACCTACAAAT 1800 GCAGCTTGTT TTTGACAAAG AAGTCATTTT TAGGAGATGA GGAATTTAGA AGCAATAACA 1860 GCAGGATTCA TCTGTGACTT CCCAAAGTCA AACACTAATG GAAACCAGGA ATGTAGGTCT 1920 GCATAAGTGC CCTAAACACC ATCAGCACAA TTAGCCATTT ATTCTACAAA TACATATTGA 1980 GTGCTGTTTA CCGTTTTAAG CTCTATGAAT ACAGCAGTGA ACAAAACTGA CATATCTCCC 2040 TGCTTACTTT CTAATAGACA CAGGTAAACA TTTATTGTGT TGATAGTATG TTAGACTACA 2100 CAGGGGGAAA CAAAGAAGGA AAAGCAATGG AGAATGCTGG AATGCTGAGG AGAAATGGGA 2160 AATGGAGTTT ATGATTTTGA TTAAGAGCTC AAGGAAAGCC AGACTGAGAA TGGGATTTGT 2220 AAGCAAAGAT TTGGAGGATG TCAAAGAGCA AGCGGTACAG ACATCTGAGG AAGAGTGCTC 2280 CAAGTCGAGT CCGTATACAC GCCTGACGTG TCCGAGAAGA CTCATGATGT GGCCTGAGCA 2340 ATACCGAGAT TCACTGCTGT GGTTGTTTTC CCAAAGTGAC TGTGAACTCA ACCACAAGGC 2400 CTGGGTCTTA TTTTTCAGGG TATCTCCAGG GTCCAGGATA TGATACAATG CTTTGTTCAA 2460 ATGGTGAATA GCAAGCGTAT GGGTTAAATT ACTCATCAAC AGAGTGATGA TGTGTGATCT 2520 TGCCACCATG GGTGCTGTTA CTGAAATCAA AACTCCCATG AGTTACAAGC TGAGTGCCAC 2580 ACATAGTGAC TGTGCACAGC ACTGTGCTTT GAACACACAC TATCCACCAC CCCATCCACC 2640 TTCCTGCACC AGCCATCTCA ACCAACAGGA GCAGTGTGTG TGGGCGCTCA TGAAAAGACG 2700 GCAGGCTATT ACCGAAAGAA CTCTGTTTAT ACCTCCTATC GGTAACGTTT GTGAAAATCA 2760 GTATTGTGCT GATTTTCAAC TCGTTTGTTC ATTGTATTTT CTTAAAATCA TATGATATAA 2820 ATCAAAGTTA CTTCAGAATT GCATGTCTTT TTTTTTAGCC CAAAGGTTTT TCCTAACATT 2880 CTATTTACTT CAAATATATA TTCTATTTCC TTTCTCCTTA TTCTGAATTT TATTTGTTCT 2940 GTTAGATGAA CATCCCCAAA GTGAAGGAGT ATATTAAAAC TAAAGTTATC CCAGGCAACC 3000 ATAATCTGAA TAGTAACTAA CAGTCTTAAG GTCTTGTATA TTTTGCAAGA GGCAGAAGAC 3060 AAACTCACTC ATTTCTATTC TGACCTTTAA AAGCCATGGT GGAAATGTTT CATGATTATT 3120 GTTTGGATAA AGAACAATTT TCCACCAGGA CAGTTTCTGG TGTTTCTGGT TAAATCATGT 3180 AGCTCTGATT CAGAGTGTAC TTAAATTCTG ACATCTCCCA TCCATAAAAA TAATGATGGT 3240 ACCACCTCTG AATGATGTAA CTGTTTTTGT TTTGAGCTGT GTGGTTTTTT GGTGGAGTTT 3300 GGGGTGGGGG TAAGAGTGGG CAGATGGGAA GAAGGGTTGA ATCGGCCTAT TATCTTCTAA 3360 GTGCAGAGGT CAACACTGGC TACAATCTTC CAAGTGTAGC TTTTGTTATA TGTCACATAC 3420 AGTAACTCAA ATTTATAAAT CATAAATATT CCTGTATAAA TTTTATTTTC AAACAGTGCC 3480 AAGTACAAAC AGCAGGAATG GAAGGATGAG AATGATCTGT ATCTGGTTTT TCATATGCCA 3540 AGGACTACCA ATGGCCAAGC CCAGGACAAG GCTTACTCAC CATATCTTCT GTTTATTCTA 3600 CCTCTGACTG CAGTATAAGA CTCATCTTGT TAGTCTCTGC AACTAACACT AAAATTAGTA 3660 CTTAGCTCTG AATTCAGCCA CATCTAAATT ACCATTTTCC TCTTTTTGTA GCCAAATAAC 3720 ATTAGAGCAA GAGAGGCTAC TGTAGCTACT TTCAAATATA AACTGCATTT TAAAAAATTT 3780 AATTGAAACT ACTAACACTG AGACTTCATA AGTATTTGGA AACATCATTT ATATTTCTAG 3840 TCTCTATAAT TACTACTGTG AAATGAACAA CCTAAGAATG TAAACAAGTC TAAAAATACG 3900 CTTCTAAATT TGGTATGATT ATCAAAATTC TAATAGAAAT AAATGCCTGT TTTTCTCCCA 3960 CCGTTGGCCA TTTAATTCAA TATCATACAC GTTGCCAACA CTTCACTGAA CCCCTATGGT 4020 CTCTGCCAAC TAATAAAAAA AAACAGCAAA GAAAAGTAAT GAGTACTCAG GATATTAAAG 4080 ATAATAGAGA AATATTGATA TCTATAGTGG ATATATGAAA TTGTCTTGAA TGAACCAGGA 4140 TCTAGTTACA ATCCCAAGAT ACATTGATTT ATCTTTTAAA ATGGTGCTCT TTAATCAGAT 4200 TGAGTTCTAG AGTAAATTTG GAGAGATTGT GATACATTTT CAAAATATGT AGAAAAGGCA 4260 ACAATTGTTA AAACAATTAC AGCCAGAGAG TACACAAAAT CCTTCCAGTA GAATCAGTAC 4320 ACTGCATTTA TTACTCTAGC ATTTTATATA CGGTATATGG TGAATGACCA 4370
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