Tag | Content |
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EnhancerAtlas ID | HS101-32980 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr4:89064150-89065930 |
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) |
EBF1 | MA0154.3 | chr4:89064366-89064380 | ATTCCCCAGGGATC | + | 6.2 | GLIS2 | MA0736.1 | chr4:89065349-89065363 | GACCCCCTGCAAAG | + | 6.27 | IRF1 | MA0050.2 | chr4:89065595-89065616 | TTTTACTTTTTTTTTTTTTTT | + | 6.16 | Pou2f3 | MA0627.1 | chr4:89064285-89064301 | TTATATGCAAATACTA | + | 6.09 | TBX20 | MA0689.1 | chr4:89064405-89064416 | CTTCACACCTT | - | 6.32 | TBX21 | MA0690.1 | chr4:89064406-89064416 | TTCACACCTT | - | 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 |
GH04I088142 | chr4 | 89064138 | 89070688 |
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Enhancer Sequence | CAACATATAC AGAATTTTTT CATCATTATT TCCTATACAA TATAGTATCA CAACTATTAC 60 CATAACATTT ACATTGTATT AGGTATTACA AGTAATCTAG AGATGATTTA AAGTATATGG 120 AACAATGCGT GTACATTATA TGCAAATACT ATGCCATGTT ATATCAGGAA CTTGAGCATA 180 TGTGGATTTG GGTGTCTGAG GGGAGTCTTG GAACCAATTC CCCAGGGATC TCTAGAGATA 240 ACTGTAATGT ATGGACTTCA CACCTTTACT TCAAAAAGGT TTTAAACCAT CTCCCCATGT 300 ATTCAGAAAC CAAAATACAC CAATTCCAAC ACTAGCAATC ACTTCTTCTA CTGCCATCCC 360 CATTTGATGT TCCTTCAGCC ACTGAGGAAA AGACTTCTTA AGAGTATCAA ATAACTTATT 420 GCTTGAATTT AAATAGCTCA CTGACTCAAG ACGGAAATTT TAAAGACACT TTTGTGAGGT 480 TTCCACAAAT AAAAGGCAAC AACTAGAGCT AAAGTACCCA AGAAAGAGTG ATCACCCATG 540 CCCATACAAG ACAGAGGGTA ACACTTATAA ATACAATCAC AATCTTAGAA GTGCCTGCAG 600 AGAAAGAGTT TGCCTTTCCT GTGATAGGAT TAAATGTGTA ATTCACATTA CTCAGGAGCT 660 GTTTCATTCC TGGCTAGGAT TCTAACAATC TTCCTCGGGA GATACAGGGC CTTAGTCATT 720 CATGAGTCAC AAACCAAGTG ATTAGACAGG TATAACCAAG GCACACCATC AAGCTGAAGC 780 ACGTTACATC AAAAAGAAAG GAAAAAAAAC AAACTTTAAT TCTAACACCA ATATGGAGCA 840 ATACACTTAC TCTAAGAAAA AAAACATAGT AAGGATTAAA TAAATAAAAT ATACCAACTC 900 AGCACCAGAC TCATCTCAAA GTGCCCGATC TCTAATGAAT ATAGTATTCT GGGTTTAGGG 960 AACTCTCTAA AAGTAACAAC TACCTTTAAG CAAACACCAG TCTTTCCCCA TGGTCAGAAG 1020 CTTTCTGGAC ATGTGTGCTG ATCTCATTGG ATTAGCATCA TCTTTTTATA TCAAGGAAAA 1080 TACCCATCAC ACAACGAGAT GTCCCTACAA CAAAAATCAA CCTCCCACCT GTTGCCGTTT 1140 CCTTATTTGC AGATTACCTG CTAAGGCTAA TCCATTTCTT TTTCTCTTTC TGTGTCCTAG 1200 ACCCCCTGCA AAGCCTTAAG TGAAAGGAAG CCTTCAAATG GCTTTACACT TTACCTGATC 1260 CCAGCCGATT CATGTTATTT GGCCTGATTA TGTATCTTAG CCAACTCAAA AAGCCCTTTC 1320 AAATAAGACA GAAGGGATTT GCATATGGAG ATTCTTTCCC CAGCTCTGCT GCCTCTTTCG 1380 TGCTGGTCTA CCTATGTCAT TCATACCTCG CCTTTCTTGT TGCTTCCTAA CTAGCAAGGC 1440 CACATTTTTA CTTTTTTTTT TTTTTTTTTT TTTTGAGATG GAGTTTCACT CTTGTTGCCC 1500 AGGCTGGAGT GCAATGGCAT GATCTAGGCT CACTGCAACC TCCGCCTCCC GGGTTCAAGT 1560 GATTCTCCTG CCTCAGTCTC CCTAGTAGCT GGGATTACAG GCCGATGCCA CAACGCCCAA 1620 CTAATTTTTG TATTTTTAGT AGAGACGAAG TTTCACCATG GTGGTCAAGG CTGGTTTCAA 1680 ACTCCTGACC TCAGGTGATC CGCCCACGTC GGCCTCCAAA AGTGCTGGGA TTATAGGTGT 1740 GAGCCACTGC GCCCAGCACA TTTTTACTTT TTTGAGAAGT 1780
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