Tag | Content |
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EnhancerAtlas ID | HS139-57897 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chrX:9895330-9897500 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chrX:9895671-9895692 | ACAAAAAAAGTGAAAGTGATT | - | 6.95 | Myod1 | MA0499.1 | chrX:9896301-9896314 | AGCAGCTGTCTCC | + | 6.21 | PRDM1 | MA0508.2 | chrX:9895680-9895690 | GTGAAAGTGA | - | 6.02 | SCRT1 | MA0743.1 | chrX:9895694-9895709 | AAGCAACAGGTGCAT | + | 6.41 | SCRT2 | MA0744.1 | chrX:9895694-9895707 | AAGCAACAGGTGC | + | 6.82 | SNAI2 | MA0745.2 | chrX:9895698-9895708 | AACAGGTGCA | + | 6.02 | SREBF1 | MA0595.1 | chrX:9895893-9895903 | GTGGGGTGAT | - | 6.02 |
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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 |
GH0XI009927 | chrX | 9895609 | 9896869 |
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Enhancer Sequence | AGTGACCCGT GATCACGCTG CTGCACTCCA GCCTGGGCAA AACAGCAAGA CCCTATCTCT 60 GTCTCCAAAA AAAAAAAAAA AAAAAAAAAA AAAAAAAAAG TAGGTGAGGA GGACCCTGTG 120 GTGTGTGTTC CTTAAGTCAT CTGCAAGATT CAGAAATTTT CCCATCCTCC TTGCTAAAGA 180 TAATTGTTAA CCCTATTCAG AAAACAGTGG TGGATTATTG ATTACAGAGC AGTTCAAAAC 240 TGTTTAGTTG TGTTGGGAAC ATTCACACAC AAGGTCCTTT CACGGAGAAC TTAACCATGG 300 TGTCTTGAAA AAATGCAGCT TCTCACCTTT TAAAATTCCG CACAAAAAAA GTGAAAGTGA 360 TTGAAAGCAA CAGGTGCATT TACATTGTGT TCAAGTGAGG GCATAACATG ATGCATGTAA 420 TAAATATTTG CTTGCAAGGC CCTGAAGGAA ATAGCCCAGA TCCCTGCCCT CTGTAGAGGT 480 GCTTTCAGCC CAGGGAGGAG CGTGGAGGCA GGTGAGCAAT GGGATGATTT GAGAGAGTCC 540 CCTTGCTGGG GCGTGACCTG GAGGTGGGGT GATGTCAGGG CAGGACTGGG GGAGCTGAGG 600 GCTGTGTGGA GGCAGGGGCA GTGCAAGGAG ACCTTGCATT CAGACATGGG GCTGGCTGTC 660 TCGTCGTGGA AGCAAAAATA GAGTAATGCC AGCAGGATCT CTAGAGTGTT TGTTTTTTTC 720 CTAACAGTGG TTTCGGTCCT GTCATAGCAT GCTGGGTGAC TGAGTACACT AATGGTGGCC 780 CTTCCTGCAG GTTTGTCCCC TTCATATAAG TTCTGTTTGG CTTTGAGGTG CTGTTTTAGA 840 GCTTCATGCT CTGTCTCCTT CAGTGGCGGC CAGCCCAGGG AGAATGGCAG GGCCGTGGGC 900 TCCATGTAGC AGATCTCTGA AGCCACTGCT GCTTGGAGCC TGCCGGCCCT CTCCCCTCTG 960 GGAACTGTGC AAGCAGCTGT CTCCTTGGGA ACGTGGCATT AGCATGTTTT GCATGAGAAT 1020 GAACACCAAC CAAGGCTGAA TATCAATTGG ATCCTAGAGT GCAGCTGCCT TTGAAATGTT 1080 CCTTTGTGTG GCCGAACTTC CTGCTGCAGT TGATTCCTGG AGCTTGTGCG AAGACACAAA 1140 GTCTTAAGTC ATCTTAGTGC CTTGCTTACT CTATCTCTGG ATCTTGCTGT CACCATTTAT 1200 TTTATCCTTA GAAGTATGGC AAAGAGAAAT GCATACATAT ATGCAGAGAC ACATGTCTAC 1260 ACACAGGCAC AACAGAGACA CACGTACCTA CACATGCACA CAACATATAC AACCCGGGCA 1320 CACACTCACA ACATGCATCT CCACACAGAC ACAACACAGG CACACATACC CACACACGCA 1380 TACAACGCAC AACACAGGCA CACACATACA ACACACATGG ACACAGAGAC ATGCATCTAC 1440 ACACATACAC AACCCAGGCG TACACATACA ACATACATCT ACACACAGAC ACATGTGTAC 1500 ATTCAGACAC AACCCAGACT CCTACATCTA CACATGCAAA CAACCAGACA TACACATACA 1560 ACGTACATCT ATGCAGAGAT ATACATCTAC ACACATACAC AGCGCAGGCA CACACACAGT 1620 GTACATATAG ACAGACAGAC ATTTATACAC ATACAACATG CATCTACACA CACAAAACAT 1680 AGACACAGAC AACATCTACA CATAGATCTG TACACATACA CACCAGATGC ATACAACATA 1740 TAGACATGCA CGTAACACAT AGACATGCAT CTGTGCGCAA GCACAACATG GACCACTCAC 1800 ACACACAACC TGCAGAGCTG CCTCTTGGAA CCAGTTAGAA ACAAAAGTTG GAATATGACC 1860 CCAGCAAGTC CCCAATCCCC ATTTTTGGTC CTTTTCTTCG TTTGTGTTGT TGACCCTGAT 1920 GGCCCAGATT CTTATCAACT GCGACAATAA AAACCAATTA GTGATTTTAT AGTTTGACTT 1980 TGCAAGGTGG GGGTGGGGGG CAAACTTGGT CCAGACATTG CTGTGCTGCT GCAGGTCTGA 2040 ATGAAGTGCA GTGTTGGGCT GGAGCGCGCC CCGTGCTGCA CTTCTGGCGT GGGAAGTGAC 2100 GATGCAGCAC ACACCACTCC CCTGAGAACA GAGCACCCAG CTCCTGTAGT TTGGCCCTCT 2160 AGGAAGATGG 2170
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