Tag | Content |
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EnhancerAtlas ID | HS112-05881 | Organism | Homo sapiens | Tissue/cell | KELLY | Coordinate | chr17:27297250-27298570 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EBF1 | MA0154.3 | chr17:27297481-27297495 | GTTCCCCTGGGAAT | - | 6.27 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CTTTTCAGAT ACACCAGCTG CTTCCTGTCC TGCCCCTCCC TGGGCTCTGT TTTCTCATCT 60 GTAAAGTAGG GATGGGGTAG GTGTATTGAA CCAGATGGTG TCCGAGGCCC TGGTCAGCAG 120 TATGAGGTCT TAAATATCAG ATCCATGTGC CCAGCTTCCC CTGGACATCC CTGTTGGATG 180 CTTCACACCC AGCCTGCCTC ATGCTAGGTG ACTGTCTTCC CCTAGCCAGC AGTTCCCCTG 240 GGAATGATCT TGCTATCTCC CTGGGTGTCC AAATCAGAAA CTGGCATCTT GCCTCCTCCC 300 TCATACCTGG TCAGTCATTC AGTCCTGTCA ACTGGATCTC AAATCTGTTC ATTACTCTTC 360 ATCCCCACTG CCATTCCCCA GCTTATCGCC GTTACTGTGC ACCTAGATCA CCGCAGCAGC 420 CTCCTGGCCA GCCTTCCTGC CTGTAGGGCT TAACCCACTC CTCCCTCTAC AGCAGTATTT 480 TCTGAACTAT AGCCAGCTAA CGGTCTTAGA TCTGTTGCTG ATCATGGTGC TTCCTTGTTT 540 AAGTCCTCCA GTGGCTCCCC ATTGAGTCTG TGAAGCCGAT AATATGTAGT TCAAACTCTT 600 TGCTTAGCCC TCAAGGCCCT GCCCAACTTG GCCCCTGCTG ACTGTCAGCT GGGCCTTACA 660 CCATGCCCCT CCGCATGTCA ATCGTGATTC TCTCTTTTTT CTGAGCCTCT TTCTCCGATC 720 CTTTCCCCTG GCTGTCACAG TCTCCTCTGC TATCATGCTG ATCTTCAGGC CCTCAGTCCC 780 TTGAGCATCT TTCTGGGCTC CATGCCTCCA TTCAGGCAAA CAAGGATTGG ACAACGACGG 840 ACTCTGCCCA GAGGGAAATT AGCAGCATGG CTTGATAGAA GGAACACTGG ATTGATTGGG 900 AGCCCAGAAA TCTGGGACCT CATCCTAACC ATGTGATCTT GGACAAATAT GCTGCTATTT 960 GAACTTCAGT TTCCTCATTT TATAAAACGA ACTAGTGGAG TTCTTTGCTA CTTAAAATGT 1020 GGTTCTTGGA CCAGCATCAG CAGCCTCACC TGGGAACTTG TAAGAAATGC AGAATCTTGG 1080 CTGGGCGCTG TGGCTCACGC CTGTAATCCC AGCACTTTGG GAGGCCAAGG CAGGTGGATC 1140 ACCTGAGGTC AGGATTTCAA GACCAGCCTG ACCAACATGG AGAAACCCCG TCTCTACTAA 1200 AAATACAAAG ATTAGCTGGG CGTGGTGGCA CATGCCTGTA ATCCCAGCTA CTCAAGCAGC 1260 TGAGGCAGGA GAATCGCTTG AACCTGGGAG GCGGAGGTTG CGGTGAGCCG AGATCGCGCC 1320
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