Tag | Content |
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EnhancerAtlas ID | HS101-28388 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr21:44706480-44708870 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr21:44706984-44707005 | TTTTTCTTTTACTTTTCCTTT | + | 6.81 | ZEB1 | MA0103.3 | chr21:44707404-44707415 | GGGCAGGTGGG | - | 6.14 |
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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 |
GH21I043286 | chr21 | 44706600 | 44709406 |
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Enhancer Sequence | GCAAAGAGTT CTCACTTTAT TGTTACTTTT TGTCTTTTCA CTACACGTAT GCAACATTTG 60 ATCTTATTTG CTATTTGTTT TTAAGAACTT TTCTTTTTTT AAAAAAGTTT ATTTATTTAA 120 TTTTTATTGA GATGAAGTCT CGCTATGTTA CCCAGGCTGG TCTTGAATGC CTGAGCTTAA 180 GTGATCCTCC TGCCTCAGTC TCCCAAAGTG CTGGGATTAC AGGTGTGAGC CACCGTACCC 240 AGCCTAAAAA CTTTCTTTTC ATTTGGAAAT AATTTTAGAA ACACAGAGAG TTACAACGAT 300 AGTCCAGAGA GCTCCTGTAG ATTCTATCCC TGCTTTCGCC TAATGTTCAC TCTTGATTAT 360 TTTTTAGTTT CAAATGTAAT CCATGTTGCT TGGAGAAAGC ATGGAAAATA TTGGAAATGA 420 AGTGGATTTT TAAAAAAAAA TCAGTTTAAT ATTAGCACTA AGACATAAAT CCAGTTACCT 480 TTAGGAATCT TTCTTTGCAG CATTTTTTTC TTTTACTTTT CCTTTGAAAT AATTATCAGA 540 TTACAGGAAG TGGCAAGGAG AGCAGACAGG GCTCTCATGG GCCCTTCACC CAGTTTCCCT 600 GCAACAGCTG CCGCTGATGT CACCATAGCG CTAACTGACA CCAGGAAATG GGTATTGTAC 660 GATGTGTGCA CAGTTCTCCA CCATTCGATC GCACGTGTAG ATTCATGAAG CCACCGCCCA 720 GTCCAGGGTG TCCCATCACC CAGCTATCTC TCTCGGGCTC CCCCTTGCTG GTCTCCTCCC 780 CCGAACCATC CTCAACCCCT AGCAACCACT CCTTTGTTCT CCAGTGCCAC ACTTGGTCAT 840 TTCGAGACAG TGGTATATAC AGAATCAGGC AGAACGTGAC CTTTTGGGAC TGGCCTTTTT 900 GCTTAGTGCA ATGCCCGTGA CATCGGGCAG GTGGGTGTGT GCAGTAGCTC ACCTCTTCCT 960 ACCGCTGTAT TCCAGACACC ACGGTGTGTT TAGCCGGTCA CCTGGTGAAG GACATCTGGG 1020 TTGGCTGTGT CCGGTTTGGG GCTGTTATAA ATAAAGATGC ATGAACACTC GTGTGCCCTT 1080 TTCGGTGTGA TCAGAAGTTT TTATTTCCTA GGGATAAATG CCCAAGAGTA CAATTGCTGG 1140 GTCATGGTAA TAGACTTAGT TTTTAAAGAA ACTGCCAAAG CCTGGCCTAC CATCCTTCCC 1200 TTCCCAGTGC ACCCACAGGA GGTGTCATTT TACATTCCCA GAAGCAGGAT ATGAGTCTGT 1260 TCTGTAATGC ACAGATACTA CTGATATTAT TTTGCTTGCG ATCAAATTGT ACCTGCTGTT 1320 TTATAATGGG CTTGTGTCCC TTGATATGAT CTTATGAGCA TTTCTCACAC GTATTTTCCT 1380 ACAGCTCCTT TAAAATTGCT GAATAAGGCA GCACGTGGGT AAACAGCCCC AGGGCCCAGT 1440 CCCACAGGGC TTACTTAAGC GCGTGTCCAC TCCATGGCCG CACCCGTGCA TCTGCTGCGG 1500 AACCTGGCGG GCACAATGCT AGGGGTGGGG CTGGAGTCAC CGAGACTTGG TCCTGCTCCA 1560 TGGGACTTAG AGCTGGTCCA CAGATGAACA CGTTGATCAC AGACCAGGAG TGCTGTGGGC 1620 GAGACTACAC AGAGTCCCGA GTATAAGCCG TGTTAGGTCA GGGAGAGTGC CCACCCATGT 1680 GATGTCTGGG CTGAGGTCTG GAGAAAATGC AAGCGTTCAA TAGGCTGGGG CAGGGGAGGG 1740 CTGGCTGTGC GCGCTCTATC TTCGTCAAAT CTATTTTATC TAATCATTTG CAAAAGCAAA 1800 TAACACGAGC TCTCTGTCCC GGGACAGGCA CACAGCTGTT GACTTTGTTC ACTGTTTTGT 1860 GCCCCTCACA AGCATGAACT GGGCATGACT CAGGCATTTG CAGAAAGAAT GTCAAATGTC 1920 ACCCAGAATA TCACTGTATA CAAGAGGTCT TTGCACACAG CTCCAATATT TTGCTTAGAG 1980 GTCAATCTCT GGAAGTTAAA TGGCTTGTTG CTGAATGCTG CATACATTTC CAAGGTCTAG 2040 ATACTGTTCT AAACCTTAGT GACTGCTCAT TTACACTCTG GACCCTAGAC TTCGGCGAGC 2100 ACCCTCTCTA GATGGCCACA CCATGAGTGT CTCACCAGGG CTCAGGGGCT GCCTATCCCC 2160 TTCCCTCCTG AGCTGGGCCC CCAAATCCTA AGGCTGGGTG TATATGGCCA AGTGCAGATG 2220 GAGGCAGGCT CTGTTTTCAG GAGCAGGACC TGATCCAAGT TTATTACCAA ATTAAATACT 2280 CCTCCCCCCT CCTCATCGTA GACCAAGGCA CAGGATTTGT TTGGAGCTTG GGGTGGGGAG 2340 GGAGGTGAAA TGATGGGAGG GTTTCCACAT GGGGTGGAGA GGGCAGGGTG 2390
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