Tag | Content |
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EnhancerAtlas ID | HS139-10933 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr11:119438200-119439980 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFE2L1 | MA0089.2 | chr11:119439058-119439073 | GTATGACTCAGCATG | + | 6.73 | Nfe2l2 | MA0150.2 | chr11:119439056-119439071 | AAGTATGACTCAGCA | + | 7.48 | Nr2f6(var.2) | MA0728.1 | chr11:119438248-119438263 | TGAACTCCTGACCTC | - | 6.22 | RELA | MA0107.1 | chr11:119438566-119438576 | GGGAATTTCC | + | 6.02 | RREB1 | MA0073.1 | chr11:119438713-119438733 | GCATTGGGGGTGGGGGGTGG | - | 6.03 | TFAP2A | MA0003.3 | chr11:119438275-119438286 | CGCCTCAGGCT | + | 6.14 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I119567 | chr11 | 119438347 | 119439690 |
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Enhancer Sequence | TATTTTTCGT ATAGAGATGA GGTTTCACCA TATTGGCCAG GCTGGTCTTG AACTCCTGAC 60 CTCAGGTGAT CCACTCGCCT CAGGCTTCCA AAGTGTTGGG ATTATAGGTG TGAGCCACCG 120 CACTCGGCAT TTTTGAGAAT TTAGGAGATT AAGCACCTGT TCCCCACCCC TTGGGGTTTT 180 GAAAATTAGG TGGGAAGAAG CTGATTCTAG GTTTTGCAAG TAAAGGGGGA CCTAGTACTG 240 CTGGGGCCAG CTTGCACCCA GGAAGTGGCT GGTAGCTGAG CAGAATGAGC CACTGATGAC 300 AGCTTTGGCT CTTTGGCCTT AGGCCTAGTG GGTCCCCAGG GTTCTGCTGA TCTGAGCATT 360 TTGCTGGGGA ATTTCCCTTT TCTGAAAGGG CTCCACAATA AGGTGGTGGC ATCAGCTGGG 420 GCCTAGGCCA GGCACCTTCT GTCTATGGAC TCTGGCCTGA GTTTCAGGGA CATCTTGACT 480 CACAAGGGGA GCTTTTCCCT CCCACCAATC ATGGCATTGG GGGTGGGGGG TGGGCAGCCA 540 CCCTGGATAA CGTCACTCAG TGCATACCAC TGCTGGCCCC TGTGGCTGTT GCATGAAGAG 600 GAGACGGGGC TCCATTTTCC AGAAATCGTC TGTGCTAGGC ATCCCAGTGA GGGGGCTGAG 660 CCAACCTCTA AGTTTCCTCT AAGACACTAG GAAGCATTGG GGGAACCCTG GATGCACCCA 720 AGCAGGGACT GGATGGGGGA GGCTTGAGCA TTCGCTCTTT TCTCCCACAT GGGTTGGAGG 780 CCACTCTGCC TCATTATCGT CCTCTACATT TGCATGACTG CTGTCCTGTG AAAAATCTCC 840 GCTTGTGAGC CAGCACAAGT ATGACTCAGC ATGTCTCTTT AATTCCCTTC GGGCACGACC 900 ATCAGAGTCA GTTTACAATA ACCAGACGCC TGGCTTTACA ATCACTCCTC ATTGTTGACC 960 CAAAACAGCA TCCTGCAGCT TGATCATTGC CCATGTGCCA GACTTCTCTC AGAATGACTC 1020 TTATTTAAAA AAAAAAAAAA ATCACATCTG GTCCATTTAG TGGCCTAGAG CACATACCCT 1080 TGAGAATTCA TCAAGGCAGA AAGTATTTGT TATTCGAGGA TGGGTTTGAT TTTTGGCAAT 1140 GATGTTGAGG CTCTCTGAGT CAAGTCTGGA GGATTATGCA GCAGGGAGAG CTCTTTGCTT 1200 AGACCACTGC ATCAGACCAC CCTCCTCAAT CTCAGGGCTC AGCTACCACT TCCCTTCTAT 1260 AGCTCCCCCA GTCGCCATGG CAGATGTGGC CAGACACCTC ACTCTCTTGC CATCCGCCCA 1320 GGGTTTCTCT GACACCAAGG CCATGCCCGC CTCTTCCTTG TCTCAGGTGC ATTTTGCATG 1380 GTTCTTCAGA GGTTCCCTAG CAGGATGGAG CCTCAGTGAC CCACAGTGAT GACCAGCTCA 1440 GTTAAGAAAA CTTAGCTTGG CCTTTCTGCT TCCCTGTTTT ATGCTTCCCA ATCCCCCTTG 1500 GGATTCTAGG GAACCATTGC TTTTCCCTAG AATCTCTTTC CAAAATAAGC TACTTGAACC 1560 AAAGGCTCTT TATGTGGGGG AACCCAGGCA AGGACAGCTG CCCTGCTGAA TTTTTTGTAA 1620 GATTTCAACA GAGCTTGAGG ACGGAGTTGG GGGGAGTCTA TTGAGATACT AGGTCATAGG 1680 AATTCATAGT GTCCCGTGGC ATCATATATA TGGGCCATCT CTTTTGCTCT CTCTCCCCCT 1740 TTTTTAAAAA ACAGTTTTTT TTAGATATAA CTCACCTACC 1780
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