Tag | Content |
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EnhancerAtlas ID | HS043-02674 |
Organism | Homo sapiens |
Tissue/cell | Fetal_heart |
Coordinate | chr1:151445220-151446630 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:151445269-151445287 | CCTTTCTTCCATCATTCC | - | 6.52 | IRF1 | MA0050.2 | chr1:151446297-151446318 | TCCTACTTTCTTTTTCTCTCT | + | 6.59 | Myod1 | MA0499.1 | chr1:151445937-151445950 | GGGGACAGCTGGA | - | 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 |
GH01I151472 | chr1 | 151444981 | 151446490 |
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Enhancer Sequence | CTCGGCCTCC CAAAGTGCAG GGATTACAGC TTGGGCCACT GTGCCCAGCC CTTTCTTCCA 60 TCATTCCGTC CTCTCCTTCC TTCTTAATAC TGCTTGTCAA ACTGATTTTG CCACCCAGTT 120 TGAAAAAGAA GGTCTAGAGG ATTATCCCAA TCATTAACTA TTTCTGCAGG TTAGCTTACC 180 TTTCCAGAAT ACAGAATAGA ATTCAGCAAA CTGCCTCAAA GAGCAGTTTC TAGATTTGAC 240 TTCTTCCTCT AGGGTTTATG AAGTCATCAT ACTGAAGTGA CCTGGATTTC CCTATACGTG 300 AACCTCATGA CGTGGGAGCC CGGGGTAGGG AGGGACAGAT AACATGAGAA TCAATAGAAA 360 GAACTGCAAG GTCTGAAGAC AAGAACCATT TGTCTAGTGG AGTCTATTTT ATATCCATTT 420 TTTAAAAATC TCCATTTAAG ATATTTAGCT TCAACGTGCA CCTTGACCAA TTAATCCAAC 480 AAACAAAACT CTGGCTTGGG GGCCCAGTTA CTCACTTTCA TGGAAAGAGA CCTCTGTTTT 540 TAGAACCAGG GATCTTGTGA GTCCCTCCCA CGTCCCCAGC CCTTCTCTGG CCTCGGGTAA 600 CTTTTCCCTC CAGTTTGGTG GAAGGTTACA TTAGAAGAAA ATAGTCCCTA CCGTCTAGAA 660 AGTTTTCGGG GGGGGAAAAA AGGGCGTTGG ACGTGCGGGT GGGTGGGTAT ACCGGGAGGG 720 GACAGCTGGA GCCGCGAAGG CGCGGGGGCC CGCGGCGCGT GGGTGTGGAG GCCGCGGGGC 780 GGCAGGAGGC ACTGGGAAGC GGGGTGAAGA GCACCGAAGT CCAGAAAAGG GCAGTGTCCG 840 CCCTGCGCTC CTCTGCTGGC GCCCGCAACC CGGGAGGGAG CGGCGAGGCT CCGAAGGGTG 900 GGATTCGAGG TCTGAACCCT CGAGTGGGCT TGGGTTTTCA GGAGCCGCCT TTTCTTATTG 960 ATCATTTCTC TTTTGTCATC ATAATCTCTT GGCCTCAGAC TGAGTTAAGG GAGCCATAGT 1020 AGGAGTGCAG AAAATGAAGT GGAGGAAAAA AAAATGTGAT ATTTAAAATA TAGTTTTTCC 1080 TACTTTCTTT TTCTCTCTCA AATTAATTTA GATGTAAATA ACATTTTAAC AGGGCCCAAC 1140 ATCAGGCTCC TAGGCTCTGG CTGCTGGTCT CACTTGACAC CAGAATAAGA TTTTGGTGTG 1200 CTAGTAATTT TGCCAAATGG AGGCCTACTC CCCAAAACAT CACCGTGGTG CATGATGAAC 1260 ATTTCTGTAG GTGATGACGT GGAGTTTTTG TTTTACTTCA TTCTAATACA TGTCCCTGCT 1320 TCAAGTGGGT AAAATTATAC CTAGCTCAGC CCAGGTTTAA TTCAGATTAT TTAAAAAATT 1380 TCAGTGGCAA GTAATTTACG AGCTTCTCTT 1410
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