Tag | Content |
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EnhancerAtlas ID | HS093-03126 |
Organism | Homo sapiens |
Tissue/cell | HL-60 |
Coordinate | chr1:231938740-231940230 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HOXA13 | MA0650.2 | chr1:231939911-231939922 | GTTTTATTGGT | - | 6.32 | YY1 | MA0095.2 | chr1:231938973-231938985 | CAACATGGCTGC | + | 6.14 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 231939533 | 231939668 | chr1 | 231939296 | 231939383 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I231803 | chr1 | 231938843 | 231939979 |
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Enhancer Sequence | TTCATTATCT ACTGCTGCCT AATAAAAAAT AAGTCACTTT AAGACGTAGT GACTTAAAAT 60 ATTACCAGTT ATTTATTTTG CCCATGGAAA TACAATTTGG GCAGGGCTTG GCAGGGACAG 120 CTAGGGTGGC TCAACTGGGG TGGGAGAATC CACACCCAAG ACGGTGCATA CATATGGTCT 180 GGCTGTTGAG TGCTCTCTAT GTGGGCCTCT CTATAGGCAG CTTGGCTTCC TTACAACATG 240 GCTGCTGGGT TCCAAGAGCA AGTGTCCCAA GAGAAAGGAA ATGGAAATTT CTTATTCTTA 300 AGGTCTGAAT TCAGACACTG GTATGCATCT CTATTAATGT GTAATAAGTG GCTCCTCAAA 360 CTTCATAGCT TGAAACAACA AACCTTTATC TCTCACAGTC TCTGAGAGAC AGGAGTCCAG 420 AGTGACTTAG CTGGGTGGCT CTGACTCAGG GTCTCATAAG GTCGCTGTTA AGACACACTT 480 TGGAGCTGCA GTCGTCTAAA GGCTTGGCTG GGGCTGAAAG ATCTGCTTCC AAACTCATGC 540 ATGTGTTGTT AACAGACGGC TTCAGTTCCT TGCCACAAGA GCTGTGCCCT AGGACCTCTT 600 GCAACATAGC AGCTGATTTC CTCAGAGCCA GTGATCTGAG GGAGAGAGAC CAAATAAGAC 660 AGAAGCCACA GATGCCAGGC GCGGTGGCTC ACGCCTATAA TCCCAGCACT TTGGGAGGCC 720 GAGGTGGGTG GATCACGAGG TCAGGAGATC AAGACCATCC TGGCTAACAT GGTGAAACCC 780 CGTCTCTACT AAAAATACAA AAAATTAGCT AGGCGTCATG GCGGGCGCCT GTAGTCCCAT 840 CTACTCGGGA GGCGGAGGCA GGAGAATGGC ATGAACCGGG AGGCGGAGCT TGCGGTGAGC 900 CCATATCGCG CCACTACACT CCAGCCTGGG TGACAGAGCA AGACTCCGTC TCAAAAAAAA 960 AAAAAAAAAA AAAAAAAAAA GCCACAGTGT CTTGTTAGGA CTTAGCCTTC AAAGTCACAC 1020 AGCATCACTT CTGCTTAGTG ACTAGAAGCA AGTCACTAAG TTCAGTTCAG CCCACAGGCA 1080 AGGGGAAGGA AACAGGTTTT ACCCCAAAGG AGGAGTATTA AAGAATTTGG TGGGCATATT 1140 TTTATAACCA CTGCAGTGTT ACTTCCATTG TGTTTTATTG GTCCAGCATT CCTGGTGTGC 1200 TGATTCAAGG GAAGGGCCAC TATAACAAGT CTCAATGAGA GGTGTGTCAA AGAGTTTCAG 1260 TGCCATGCTC TAAAAAGTGC CACAGTATTT ATTGAGACAG AAGGATTTTG AGAACTGAAG 1320 ACCTGGACAG AGAGCTTTTC AGTCAGAGGA AATGGCCTGT TCCATTTATT TACTGAAAAG 1380 AAAAATATCA TGGAGCATCT AGGAAGTGTC AGATCTGGTT CTAGGTACTG AGGATGCAGT 1440 AGAGAACAGG ACAAGATCCC CCTTCCTTTT TTTTTTTTTT TGAGGCAAGG 1490
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