Tag | Content |
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EnhancerAtlas ID | HS080-19228 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr2:100056250-100057430 |
Target genes | |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
PHOX2A | MA0713.1 | chr2:100056768-100056779 | TAATTCAATTA | + | 6.14 | Phox2b | MA0681.1 | chr2:100056768-100056779 | TAATTCAATTA | + | 6.14 | TEAD1 | MA0090.2 | chr2:100056983-100056993 | ATGGAATGTG | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 100056956 | 100057060 | chr2 | 100056540 | 100056696 |
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Enhancer Sequence | CAAATAACTT TCATAAAAAT GGATTTAAAA ACCTTACTTG AATTCTTATT CCTAGTTTTA 60 GTTTTTATGA AAGGTACTAT TCAACACATT AAATCTAATA CGAAACCAGA TGGTTTCAGT 120 AGGAAAAAAA CTGACTATAT TGATTAACCT ATTAATGAGC TAACTGTTGC ACAAATAGAC 180 AAAAAGTAAA GCCATGTCAA TGTGTGGGGG TAATTCAGTA AAATTTACAC CTAGAAAAAT 240 AAGGACGCTT GCCTTACTGA GAAGGGAAAT TGCACTTCAT TTCTAAGAAA TGCATATTTA 300 GATGCCAGGG TGGTACAAGG CAATCTGGAC CAAGTTTCCT GATGACAGCT TTATAAATGC 360 AGAACCCATG ACAAATGTTA TGCTAAAGTC ACATCCTGGC TCCTCTAGAC GTTTGTTTAG 420 AAATGCATTC ACGAGAATCA TCTAAGTAAC AAAAACAAAA ACCTGAATTA CAAAGCAGTA 480 ATTCATTCTA CTTAGGAATG TCCAAATGTC CATAGCATTA ATTCAATTAC AGCGCAGGCT 540 CCAGATGAAG GGCTGCCCTA CAGAGTAGTA AGCCACAGGT GAAATTACCA CAGTATTATC 600 AGGTTCCACC TAAAGCCCCT CACCCTAATA CCAACTTGGT TTATTAGTAA TGAGAGCCTG 660 ACTACACAGA AAAGTCCCAC AAGCTGGATG ATCACCCATT TCTGGGTTAG CTCAGGCTCT 720 GGCTAAACAT CATATGGAAT GTGACAGGCA ACTGTGAGTA GATGCCATGC TCACAGATGA 780 TCATGCCAGT GATGGGGAAA AAGACAAAGT AGATATGATT AAAAGAAGAA AAAAAGAAAA 840 CCTAATTTGT CACATGCAGA GAAAGTTCAG CCTCTTGAGA TAAACAGAAT GCAAGGGAGC 900 AAGAAGTCAC AGATGAGCAT TTCAAAGAAA TGTACAAAAT GTACTGAATA TACCCCCCAA 960 AAAAACCCCA GAAAACAACA AAAGTGATGT ACGTCAGAAA GTCTTACATC TAGTTTTGTG 1020 TCAAAAACAT TCAGACCCTT TACATGCATT ATAGCAACAC ATGCAACAGA AAGCCATATA 1080 TTGGCAGGAA AATACATTGT TAACATACAT TCTTGCTGTA CTATAGTTTC TCAGCCTAGA 1140 CAAATGGACA TTTGCAAAGT AGCTGTACTG GAAATATCAC 1180
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