Tag | Content |
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EnhancerAtlas ID | HS041-00109 |
Organism | Homo sapiens |
Tissue/cell | EWS502 |
Coordinate | chr1:3580320-3581810 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CDX2 | MA0465.1 | chr1:3580405-3580416 | TTTTATGGCCT | - | 6.02 | Zfx | MA0146.2 | chr1:3581312-3581326 | GAGGCCTCGGCTGG | - | 6 |
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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: 2 | ID | Chromosome | Start | End |
GH01I003663 | chr1 | 3580260 | 3580610 | GH01I003664 | chr1 | 3580740 | 3584717 |
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Enhancer Sequence | GGTCTGAAGG CTCTGATCTT CCTTTCTTCT GGGTCTAGGG CACATGAGGG TCTGTGACCT 60 AATTCAGAGG AAGGCCAGAG AACTCTTTTA TGGCCTGCCT CAGGGTGACA GGGAGCAGGA 120 GAGAGCATAC CTGCTTTCCC TGGCTTCTCA GATGCCACCG TGCCAGGTTT TGGGGTAGTG 180 GTATGTCTTG AGCCCAATCA GTACCCTGGG GGTCGTGGCC GGCCCCCCTC CCTCCATGCC 240 ACAGGCTCTC TGGAGAGGCC ACTGCTGTAT CCCCACTGTG AGCTCGATCT GAGCTGCCTA 300 TGGGACCACA CCTGAGAACC CCCAAGGGTG GCACTGGCAG ACTTGAGGTG CCCAAGTGAG 360 GCTGGTGCAG CCCCTCTGCC CTGCCAGTCT GGGCACGGGC CCCTGGGCAT CGCGACTCCT 420 ACCTTCCTAC CAGCCCAGAT GCAGGGCCTG AGCCGGCAGG GCTTCCACCC AGCCCAGGGT 480 GTGTCCCCCT ACCAGAGGCG CTGCATTGGA TAGGAAGGAC CCACCTGTTT CCCTGCCCAG 540 TACCAGCTGG CAGGCCCCCC GTGGCTCAGG GTGCCTGTGA GGAGGGGTGG GGGCTCTAAT 600 TGCTCACCTG CTGCTCTGAG GTGTCAGGCA GGGTTGGGGG TGGCACCTGG GGAAGGCTGG 660 GCTGAGGGGG CAGGCTGCCC CTCCTGCAGG AGAGGTGCAG TATTTCACTG GGTCCTTTGG 720 AAAGGGCAGG GAAGCTCCTG CTCGCCCGTA CTGCACCATT TCCTGTGATC TTAGCAATGA 780 CTTCCTGGCT CCATTTTCTC CACCAGTCCG AATACATGAG CCAGACCCGC AGCTTTCTCT 840 TCCACAGCCT CCTGGCCTCC GGGTCCACCT GGGTGGTGCC CACCCGCCAG ACTGGGGCCT 900 GGTGGTTGTA GGGGACGGGG AGCAGCCTTG CTTCAGTGTG GGTCATTCCT GACTGTGAGA 960 TGGTTGGGGG GCAGGGGTTG TAGAGTCTGT GGGAGGCCTC GGCTGGGCCT CAGAGAGGGG 1020 TATCTCTTCT GCAGAAAACC CAGCCACCCT TACCAGATGC GGTCAGGCTA CAAAGGGAAG 1080 ATGTGCTCCC TCTTTAGAGG CAGGTGATTC CTGTGAATCC GATGACCGAG ATAAGGTGCA 1140 CGATTCAGTG GGCAAGGCAA CTCACCATCC TCTCTTTATG GTCCTCGCAA TTTGCACCAT 1200 GCACAATGCA GGGTGAAGTC AGCCCCCAAA TTACAGAGGA AAGACTCTGC GGTCTTTGTC 1260 AGTTAAACAG GAGATGCAAA CTCCAAGCTA GTTAATGAGC TGTGATCGGC CACGCTCACG 1320 ATTCAGTGCA GGTCTCTCCT TCCTGCTATC ACAGTCTTTG CCGGCTGCAT CATGACTACC 1380 AACCAGTCCC CTCATAATTA CAAGAGTCTC CTGTCATGTT TTCTTCTGGA GCGAGGCATG 1440 CTCCAACTTG CTTCTGGGTT CTTAATTTTT GATCAGGGAC GGCTCCTTGA 1490
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