Tag | Content |
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EnhancerAtlas ID | HS116-14095 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr17:499390-500880 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP1 | MA0481.2 | chr17:500203-500215 | ATGTAAACAGAT | + | 6.62 | FOXP2 | MA0593.1 | chr17:500203-500214 | ATGTAAACAGA | + | 6.02 | Foxa2 | MA0047.2 | chr17:500200-500212 | CCAATGTAAACA | - | 6.62 | ZIC3 | MA0697.1 | chr17:500669-500684 | ACGCAGCAGGAGGTA | - | 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 |
GH17I000594 | chr17 | 497641 | 501338 |
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Enhancer Sequence | TCAGAAGATG TGGACCTGCA TGTGAAGAAG TTTTAGAAAT ATCTTTATTT ATTTTGCCTA 60 TAGTTTCCTT TTTATGTATG CACAAAAGTG ATATATGATT TGAAAGAAAC TATGTTGGAG 120 TAAGTGTGAA GAGCTCATCT CTTAGGTATA AAATACAGAT TCCAAGTGAG TAAAGAAAAT 180 GGCTACATAA TTCCAACGAA CTCATCTTGT TCAGTCTGCC ACAGGCCCTG CCCTTGATGA 240 CGTCCCACAG GTCCTGCCCT TGATGAGGCC CCACAGGACA CTCAGAAAGC TGCATGACCA 300 GGCAGTGCCA GGGTTCCACC TCTATCTGCA GATGACGCTG CCCTGCCCTG CCCTCCCCAC 360 CAACAGCACT CTTCTGCAGT GAGGAGGGAC CCTTGACCCT GCCACCACAG CACCCGGGTC 420 CTCTTGCAGC ACTTCTAGTG AGCTGAAGCA AGAGAGGAAT AATGGGAGAG ACTGCCTGAA 480 GTTTCCTTTT TTCTTACTTT TTTCCTGCAG GGCTGCCTCC TGCCTATGGC TACGTTATGA 540 ACGTGCTCAG TTTAGATAGT AGGTGCTGGA ATTTTGGCTA ACTGGCATTT CCCTTTGCAC 600 CAAGCAACTG CCCAAAGGGT TGATTCTCAG CTTAAACACT ACACTAAGTC ATTTAGCAGT 660 AATGTTTGGG CCGGGTTCTG AGTGTGTGAA TTCTGTCCAA AAGCTGAAGA TGTTTAAGCT 720 ATTTCCTCCT GGAGTTTGGT GGAATAATAA AAGGTTACTG TTGTCACAGT GAGGAGGTCT 780 GCAGCTGGTC CCACTTCCTT TCATTACTAC CCAATGTAAA CAGATTAAAT CGAACCGCTC 840 GGATCACCAG AAGGGACATT CCTTATTTCT GCTCCTTTCT GTTATGCTTT CAGTGTCCCT 900 CAGGCTCCTT TCAGATGTCA GTTTTTATCA TTGGGAATAT CTTGGCAACT GATTGCTCAG 960 GCCCTCTTGT AAACGAAATA CCTTCTTTCA GGTTCCCTCT CTCTTCTCAG CAGCGAGGCG 1020 TAAACTGCAG TAGTGAGCAG GGTGTGACCC TTACCTTGAG GGCCACATGG CTACTGACTG 1080 CAGCCATGAA ATGGGTTAGG TCACCCACAG AGCCGGCAGA GACCTTCCCT CCAACCACCT 1140 CTGGCTGATT TCACCACTAA CACCTGGTGG GGTCCCTCCC CCACCCCAAG AGGTCTGCTT 1200 TTGTTGTGCA CCCCACTCTG GGAAGAGGGA GATCCTGGGG CGCCCACCTA ATCAGCCACC 1260 AGCAAGGCCA GGGCTGGTGA CGCAGCAGGA GGTAAGGGAT GGCGTGGGTG GAGGCATTAG 1320 TCACTGGCAT GTAAGTGTTA TTACTAATCA GTAATAGCCC ATGAAATGGT GGGTGGATCA 1380 GCTAGATTAG GGGGTTTAGT TGTTTCTTTT GAGATGGAGT CTCACTCTGT CACCCAGGCT 1440 ATAGTGCAAT GGCGTGATCT CGGCTCACTG TAACCTCCGC CTCCCAAGTT 1490
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