Tag | Content |
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EnhancerAtlas ID | HS086-03831 |
Organism | Homo sapiens |
Tissue/cell | HEK293 |
Coordinate | chr15:68851300-68852670 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CREB3 | MA0638.1 | chr15:68852418-68852432 | GGATGACGTGGCCG | - | 6.07 | CTCF | MA0139.1 | chr15:68852109-68852128 | TGCCCACCAGGGGGCGCGG | + | 6.98 | IRF1 | MA0050.2 | chr15:68852581-68852602 | TTTCTCTTTCTTTTTTCTTTT | + | 6.24 | IRF1 | MA0050.2 | chr15:68852575-68852596 | CCTTTCTTTCTCTTTCTTTTT | + | 7.41 | Pou2f3 | MA0627.1 | chr15:68851587-68851603 | GAGCATTTGCATAAGA | - | 6.03 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr15 | 68852038 | 68852173 | chr15 | 68852393 | 68852527 |
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| Number: 1 | ID | Chromosome | Start | End |
GH15I068557 | chr15 | 68849789 | 68852990 |
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Enhancer Sequence | GGCCACGCAG GAATGAGCGT GTCTGTCTTT CCCTACTTTA CCATCTTCAG TTTTAGTCAG 60 TAAATATGTT CGGAGATCCT ACCACGCGCT AGGCGCCGTT CTTCCTGCTT GGGAGGGGTA 120 AATACCTAGA AATGCGCGAA GTGTGGCTGG GCGTTGCCAG GAGAGCGGCC GGCACCCCAC 180 GGGGGCAGGG AGCAGACCTG ACTCAGTGGC GTCAGTGCTA CTTCAAAGCG GCAGCGCATT 240 TCATTAAAAA TCTGATGTAG AAATTACCCT GGGCTTTGTT TTGCAAAGAG CATTTGCATA 300 AGAAAAAATA ATCAGCCGGT TAATTCCCCC GTCCACTGGC AGGAAGAGAG ACAGCCTTCA 360 GAGAGTTTGG GACTCTCTCA TTCCCGGAGA ATTAAAAGCC TCCGAGACAT CCATTTTAGA 420 AGTTCTGGTC AATCGTTCTT AAAGTGCGGT CAGAAGACCC CTTGCGTCTG AATGGTTTGG 480 AGCACTCATA CAAGCAGAAT CCCTGCCCCA GTCTTGAGTC TGGGAACGGA GAAGGGAGCG 540 TCAGCGGGGT GGTGAGGGGG TAGCGGGGAG GGCGAAGTTG ACCGTGCCAA GCCGGCCCGC 600 TGGAAGAGCT GCAGGGACCA GACGGGGAGC AGACGGAACA AGCGTGCTGA TGGTAAGAGG 660 CCCCCAGACT TTTTCTTTCC CTAACCCTTT CCCTGTCTGG GCCTCCGTTT CCGGTTTTCC 720 GGTTGGTGCA GTGCTCTCTG GGGTTCTCCC AGGGGGACTG TCGGTGAGGC TGCGGCGCCC 780 GAGACCGCTC CACGTGCAGC TCCACGGCGT GCCCACCAGG GGGCGCGGCC CGCATCCTTC 840 CTCGGAGCTG CGGCGCTCCA GGACCAGCAG GTCTCCCGCA AACGCGCGCG CACGGAGAGC 900 ACAAGGCGTG TGGCTCTTGG CATGTGTGCC GGTTGGGGTC CTCTGGTAAG CAGACGCTGA 960 GATGGCGTTA GGAGTGCAAG AAGTTTGTTG GGGATTTAAA CCTGTGTAAG GACGACTGGC 1020 GGGGAGAGCC TCAGACGGCA ATGCAGATCT GACCAAGTCT CTGCCAGCCC AGCAGGGAGA 1080 TCCCGGTGGA GACTGCCGAT TTGAAGAGTC CCGCAATGGG ATGACGTGGC CGGGCACTTG 1140 CACCCGTGCA GTGCTCAGGC ATTGGCTGGG GGCTGCCTGG GAAGATCCGG ATATTGAATG 1200 TGAAAGACAG GAGGTGCTGG AGGCTGCTAA CTGTGCTCCC TACAGCTGGT CTGCAAGTTC 1260 ATTCATTGTT TTCTTCCTTT CTTTCTCTTT CTTTTTTCTT TTTCGTTCTT TTTTTTCTTT 1320 TTCTTTCTTT CTTTATTTTT TTTTTTCTTC TGAGACAGGT TCTCGCTCTG 1370
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