Tag | Content |
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EnhancerAtlas ID | HS112-15341 |
Organism | Homo sapiens |
Tissue/cell | KELLY |
Coordinate | chr9:110124890-110127080 |
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) |
ONECUT1 | MA0679.1 | chr9:110126589-110126603 | AAAAAATCAATAAA | + | 6.89 | ONECUT2 | MA0756.1 | chr9:110126589-110126603 | AAAAAATCAATAAA | + | 7.52 | ONECUT3 | MA0757.1 | chr9:110126589-110126603 | AAAAAATCAATAAA | + | 8.12 |
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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 |
GH09I107363 | chr9 | 110125860 | 110126233 |
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Enhancer Sequence | TTTACTGCTC ACTTTCAACC TAGCCCTTGT TGAGTGCGCT GTGCTCATGG TCTCATTTTT 60 CTCACTGGAT GTTGTGATCT CACAGGGACT TTATGAGTCA AATCTCATCA TCAGCTCCAC 120 TCTGTAGCCA GCCATACTTT AGAGATTCAG AACATGCCCA AAATTATAAA GCTGGCAAGT 180 ACCAAAGCCA GGCCTTGAAG CCAGCCTACT GATCTTCAAG CCCATGACTT TAACCTCTGT 240 ATAATCTTCA TCGGATGATG AAGGCATGAA AGCCCAGGTG ATCTTTCTCA ATTGAGCACT 300 GGAAGATTCT TAATGAGGGA CATCAGGAAA TGCTTCCTGG CAGAGGTGGC AAAAGAGATG 360 CAGGCCAGGA TGAGCACAAT GGCTCACGAC TGTAACCCCA ACACTTTGGG AGGCCAAGGC 420 AGAAGGATCA CTTGACCCCA GGAGATTGAG ACCAGCCTGG GCTAACATAG CGAGACCCCG 480 TCTCTACAAA ATAAAAATGA TAGGCCGAGC ACAGTGGCTC ACACCTGTAA TCCCAGCATT 540 TTGGGAGGCT GAGGCAGGCG GATCACTTGA GGTCAGGAGT TTGAGACCAG CCTGGCCAAC 600 ATGCTAAAAC CCTGTCTCTA CTACAAATAT AAAAATTAGC CAGGCATGGT GGTGGGTGCC 660 TGTAATCCCA GCTACGCAGG AGGCTGAGGC ATGAGAATCG CTTGAACCCA AGAGGCAAAA 720 GTTACAGTGA GCTGAGATCA TGCCACTGCA CTCCAGCCTG GGTGACGAAG TGAGACTCTG 780 TCTCAAAAAA ATAAATAAAA ATAAAATAAA ATAGCCAGGC ATGGAGGCAG CCCCCGTTGT 840 CCTTAGCTAC TTGAGAGGCT GAGGTGGGAG AATTGCTTGA GCCCAGTAGG TCTGCAGTGA 900 GCCATAATTG CACCACCGCT CTCCAGCCTG AGTGACAGAG TGAGATAGTG TCTCAAAAAA 960 AAAAAAAAAA AAAATACAGA GAGAGAAAGA AAGAGATGCA GAAACAGATG GCCTCTGTCT 1020 TATAGGCCCT GGGGGCAAGA CACTGGGCAG ACAGAGGGAA GCCACACAAA GAAGCCCAGC 1080 TGCACAGGCT CCAGGAGTGC TCCCAGATGC TGCAAGAATG CAGGCAGGGA GGGGACTGAA 1140 AAGTGGGATG GCCCTTGGCT TGGTCACTTC CTGCTGCTGA GGGAATCAGG TGTGTTCTAC 1200 GGTAAGATTT AAAAAATAAA ATGAGCCTAG GGAGAAAAAT CCAGGCTTGC TGAACTAATA 1260 AATCAGTGGG AGAGGTGAGC GCTTGCTCTA GTGAGGCATT TATGATTGGC TGCCTTTCAT 1320 TGAGCCACAC GGCGAGCTCA TTCGGTGAGC AGAAAGCCCG GCAGAGCAGG CCTGCGATCT 1380 GGCAGACTGC GGGGTCCAGT CCAGGCTGTG CTAATCTCTT CATCTTTCTG AGTCTCGGCT 1440 TCCTTATTTG TAATACAGGG GTGCTATATG TTCTACCTAC TTTACTGTGG TAGGAAGAGT 1500 CACTGAAATA AAGAAAACAA AAATTGCCTA TAATTCACAA AGTTCCTACA CAAGAAACCA 1560 GTAATAGTAT TCTTTTATAG GGAGGGGAAC GGGGTGGCTG GGAGATAGGA ATGGGAGGGA 1620 GACTTTATGG TGTGTATCTT TTTACATGTT TTGCTATTTT GAACCACAAG AATAAACTAT 1680 TCATTGAAAA AAACTTAGAA AAAAATCAAT AAAGGCAATA ATAAGGTCAG AACTAATAAT 1740 GCAAGCAATC GTCATTATCA TCATTATCAT GGTCAAAATC ACCAATGTCA TCATTATTTT 1800 ATTTATTTAT TTATTTTTTT GAGACGGAGT TTTGCTCTGT TGCCCAGGCT GGAGTGCAGT 1860 GGTGCGATCT CGGCTTAGTG CAACCTCCGC CTCCCAGGCT CAAGTGATTC TCCTCTTTCA 1920 ACCTCCCGAG TAGCTGGGAT TACAGGCATG CACCACCACG CCAGGGTAAC TTTTTGTATT 1980 TTTAGTACAT GTTGGCCAGG CTCGTCTCGA ACTCCTGACC TCAGGTGATC TGCCTGCCTT 2040 GGCCTCCCAA AGTGCTGGGA TTACAGGGTG AGCTGCTGTG CCTGGCCCAT TATTTAAAAG 2100 GTTATTTCCA CATAATCTTA CCAGTTTACT CTCAGTAAGT AAGTAAGTAG TAGTCAGTAA 2160 GTAAGAAATT GGTCATTGCC TCCAAAGTTC 2190
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