Tag | Content |
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EnhancerAtlas ID | HS094-16248 |
Organism | Homo sapiens |
Tissue/cell | hMADS-3 |
Coordinate | chr17:15088320-15089660 |
Target genes | Number: 10 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2C | MA0497.1 | chr17:15089163-15089178 | TGCTATTTTTATCTA | - | 6.32 |
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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 |
GH17I015184 | chr17 | 15088119 | 15089670 |
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Enhancer Sequence | AGCAGATAAG AAAAAAAAAA AAAACTTGCT GAAATGTTGA AACTCCTTGC TTATGAGATA 60 ACAAAACTGG CTGAAATTGG CCGGAACCAA TATGGCTGAC TGGAGTCTGT GCAGAACAAG 120 CTTGCTGACC TCACAGCCTA AGTTTCCACT GAATGTTTCA TATTAACGCC CCCTGAATTT 180 GCACATGTGA CCCATGAGGA GGCATGAAGG GATAACTGTG CGTACCTAAT GACATACCAG 240 ACCTCCCCTT TCCTTCCACC AATCACCTGC TAATCCCAGA ATCCACCCAT TAAACCTTGG 300 CTAATAAAAG TACTGCCATA AAGCCAGCAT AGGAAGACAG ATTTGAGCTG GACTGCTGTC 360 TCCTTGTTGG TCTACCTACA ATAAAATGCT TTTCTTGTCT CAAAACCCCA GTGTCATAGC 420 ACTGGCTTCT AGTGCATAGG GCAATGAGCT CTTTAGCTTG GTAACCACAT CGGTGACTCC 480 CTTGACCTGT GGCTTCTGGT TGGCTTTGAC CAATGAGAAA CTCAGGAAGA AAATTTCAGG 540 GTGGAAGGAG AATGAGACTG GAGCATTTAT TCTCCCATCC CCTTCTTTGC AAGGTCAACA 600 GAAGCTGTCT GAGTCCCAGG AACAAATATC GCAGCTGCTG TCGGGCCTTC CTTCCAGGTT 660 CTGAAGGAAA CTTTCCCCTA CCCCTTCAAG CCTTGGGTTG GTAATAGGAC TGCACTACCC 720 AGCTGGCATT TCCACACCCT TCCCATACCG TTATTGCCTA ATGTGAGTGT GACATCTGTT 780 GCCTGCTGGG AAGCTGACTG ACACACGTGG TTAAGCTGAC TTAACAAAAT GAGCTGGAAA 840 GCTTGCTATT TTTATCTATG CTCTGGAGCA CATTAACTAT TGCAAGAATT TTCTATTCCT 900 TGAAGGTCAA AGAACTGATC TCTAATTCCC TCTTAGCCTA GTATTTTAGG AATAAGATGG 960 TTCTCTGACA AATGTTTAAA ATTTTTCTCA TGGTGTTTTT TTTTAATTTA GGTTTCTTCT 1020 TCCTCAGTCA AGTTTAGTAA CTAATATTTC CTTTAAAAAT CACCCATTTC CTTAAAAGCT 1080 TTATATTTTT TAGCATGGAA CTATTTGCAG AATTCTCTTT TACTGTTTTC ATCCATTCAG 1140 AAGAACTTCC AGATTAATAA AAACTTTGCA TGACACTCAG AAACTTTGTA AGTAAATAAA 1200 AAGAAAAACT AGTTTTGTTC TTATGCAATT GATCCATGAA GCATAATATT TTTTTGTTAT 1260 ACTTGGCCAC CCAGAAACTA TGTACTACTC TCTTAAATTT GGGGACAACT GCATCATTTA 1320 ATCTGCATTC CCCTAGGTAG 1340
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