Tag | Content |
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EnhancerAtlas ID | HS064-07597 | Organism | Homo sapiens | Tissue/cell | GM18507 | Coordinate | chr19:37017700-37019120 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
DUX4 | MA0468.1 | chr19:37018397-37018408 | TGATTAAATTA | - | 6.62 | RREB1 | MA0073.1 | chr19:37018895-37018915 | ACCCTCAACACCCCCTCACA | + | 6.08 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGAGGGCTGA CTGTTCATTC ACTGATTCAG CAAACATATA CATTTATGAT TATGTGTGCT 60 GAGAAACCTT GGTTTACAAT TTGTAATGGG ATATAACAAA TCAAAGGATC AAACTTACTT 120 AGAAGCCTTC TCTAAGATGT AAGTGCCTTA GAACCTGGCT AGACAGTGCT ATAAATTGCT 180 GAAACAGGTA CAGAGGGGAA ATAGATGGAG GCAGACTGCA GGAAGAAGGA GCCCTTTAGA 240 CATAAAGAGC TTGAAGTTCC CTGTAACTTC CAGGTGGACT GCACATTGGG CAATTAGATA 300 ATATGGATTA GGAGCTCAGG ACAAGCCTCC AGCAGAAACA GACATTTATT AGTCATCTGT 360 ATTAGATGAA GCCATGGATG GCAGTGTAAT GTTGTTGCTG ATAGGAGTAC TTAGATGATC 420 AAGGCCAGAA ACTTAGAAAC ACCAATAGTT AGGGGAAAAG CAGAAACTAA GTCCTGTCTT 480 CTTTGTATCT TTTACTTTTT CTGTATATTT CAAAACTATT AACCCTGTTA CTTTTTTATT 540 TTATTGAAAA ATATGTTAAG AATAAGTGTG ACAAGATACT TGAATATGTT GATATGTTAA 600 GAATAAGTGT GACAAGATAC TTGAAGATAG GATACTTCTA TCTTTGTATA CACAAGAAAA 660 GAATTTCCCC TATATTTACA AAAGGCTGGG GAAACCCTGA TTAAATTAGG AGTGAGATTG 720 CTGCCCTCAC TGACGAACTA GGGAGTTTCT TGACCTCTGC GCTAAAGGCA GGACAAGTAG 780 CTTCCAAATT CTGTGCCGTC TGCGCTATTG GAAACTACCT CTTAAAGATA TTCCTTAGTT 840 CAGGGTTTCT CCAAGCAACT GCACCAAAGT TTCTCCAAAG TATTAAGAAA AGTCAATGCC 900 TACTGGGTGT ACAGGCACCC AGTAACAAGT TTTTCCGAAA TCTTGCCTCT TTAAAAAAAT 960 AATGGAAAGG TAATGCTGAT TTTGTTTTCT ACTCCACAAT AGGTCTGCTT TTATATAAAA 1020 AATCACCTTT AAAATTACTT ATCCGCTCAA TTCCTTAGCC TTTTCCGTTT CCTATTTTCC 1080 AGAAAACGCA TCTTTATTAT TTTAGAAATG AGAAAAGTGA GGCTTAGAGG TTACTACCTC 1140 ACAAAGCCAT CCGTCCATCC TCACAAACTT GGAACCAGTT TCTCACTAAC TCTGCACCCT 1200 CAACACCCCC TCACACTCTC GGTCACCCAC CCGCGAACCC ACCCGAACTG TACCCCTGCC 1260 CCCAGCCACA CAAGCTCGGA TCACCGCACA TCATAGAAGG CGATTCCTCC CCTCCATACT 1320 CCCAGCCCCG TCGCAGGCAC TGCAAATCCT CCCCTCCAGC GTCCCTGGCC CGTTTCAGTG 1380 TCCAGAAACC CAAGTCCCAC AGGGCCGAAA CCCAACTCAC 1420
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