Tag | Content |
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EnhancerAtlas ID | HS091-19359 | Organism | Homo sapiens | Tissue/cell | HepG2 | Coordinate | chr17:28924640-28925780 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ALX3 | MA0634.1 | chr17:28924808-28924818 | TTTAATTAGA | - | 6.02 | FOSL1 | MA0477.1 | chr17:28925121-28925132 | CATGAGTCACC | - | 6.62 | Foxd3 | MA0041.1 | chr17:28925173-28925185 | GAATATTTGTTT | + | 6.18 | JUND | MA0491.1 | chr17:28925121-28925132 | CATGAGTCACC | - | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CTTTTTGATG GGGTTGTTTG TTTTTTTCTT GTAAATTTGT TTGAGTTCAT TGTAGATTCT 60 GGATATTAGC CCTTTGTCAG ATGAGTAGGT TGCGAAAATT TTCTCCCATT TTGTAGGTTG 120 CCTATTCGCT CTGATGATAG TTTCTTTTGC TGTGCAGAAG CTCTTTAGTT TAATTAGATC 180 CCCAAAATGG AGTTTCTTAT GTCTTCCTCT TTCTACATAG ACACAGTAAC AGTCTGATCT 240 CTATTTCTTT CCCCCACAGA ATGCAGTAGC ATGATCATGG CTCACTGCAA CCTTGACCTC 300 TGTGGGCTCA GGTGATCCTC CTATCTCAGC CTTCCGAGTA GCTGGGCCTA TAGGTGCATG 360 CCACCACTCT CGGCTAATTT TTTGTAGATA TGAGGTTTCG CCATGTTGCC CACGTTGGTT 420 TCAAACTCCT GAGCTCAACT GATTCCTCTG CTTCAGCCTC CCAAAGTGCT AGGATTACAG 480 GCATGAGTCA CCATGCCCAG TCCTTGAATG GTTTTAAAGT GTTATTCTTA TCTGAATATT 540 TGTTTTAAAC AATAGTATTT AAACTTACAA GAAAGCCTAA ATACAAACCT CTGCATGTTA 600 ACCCTGTATA CATTTTTCTA TGCTGTCACT TACATTTTTG AATGTACTGC TTTAAACTTC 660 AAAACAAGCA GTCTCCCCCA GGTCTCCCAT CACCTTCTGA AATACTAACT TACATTAACT 720 AATATAAAGC TACAAATTAT GTTAGTTGGG TGGCTGGAAA CAAAGAATGT GCCATAAAAA 780 TAAGGCAAAT GTGAATGTGT ACATCAGTTT GCTAAGTTTT TTGCCACTGT TCAGCCTCTT 840 AAATTGTGGT AGCAGCTATT GTTCACATTG ATTTGTATAT ATCTGTAGTA CAAGGAAGCA 900 TTTCTAAAGG ACCTTGCTCA TTGTTCTGCA CAAAATAGCC ACTTAATATT TGTTGAATGA 960 ATTGCTGGCA CTATCTCTGG TATTTTTATT TTTATTTATT TATGTATTTA TTTTTGATAC 1020 GGAGCCTCAT TCTGTTGCCC AGGCTGAAGT GCAGTGGCGT GATCTTGGCT CACTGCCACC 1080 TCTCGGGATC AAGCGATTCT CGTGCCTTGG CCTCCCTAGT AGCTGGGACT ACAGGCATGC 1140
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