Tag | Content |
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EnhancerAtlas ID | HS110-04725 |
Organism | Homo sapiens |
Tissue/cell | KATO3 |
Coordinate | chr8:29522230-29523640 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NKX2-3 | MA0672.1 | chr8:29522547-29522557 | ACCACTTGAA | + | 6.02 | TBX20 | MA0689.1 | chr8:29522536-29522547 | GAGGTGTGAAG | + | 6.02 | TBX21 | MA0690.1 | chr8:29523055-29523065 | AAGGTGTGAA | + | 6.02 | TBX2 | MA0688.1 | chr8:29523055-29523066 | AAGGTGTGAAT | + | 6.02 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_36200 | chr8:29521795-29524083 | HMEC | SE_56175 | chr8:29521146-29524085 | u87 | SE_64743 | chr8:29522155-29523799 | NHEK |
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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 |
GH08I029663 | chr8 | 29520941 | 29523835 |
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Enhancer Sequence | GATGCCAGAG AGAAATCAGT GGATACCCCC GGCCACAGAT CCCTGGTGTC TTGTGTCCAC 60 AGATCCACGG CCATCATTTC CGCCAGAGAG TGGGGCAGAA GTTTAAGGAT AAGTTATGTT 120 GTCCAGGCGC AGTGGCTCAT GCTTGTAATC CTAGCACTTT GGGAGGCCAA GGCAGGGGGA 180 TCCCTTGAGC TCAGGAGTTT GAGACCAGCC TGGGTAACAT GATGAAACCC TGTCTCTACA 240 AAAAAAAATA CAAAAATTAC TGGGGTTTGG TGGAATGCAC CTGTAGTCTC AGCTACTTGG 300 AAGGCTGAGG TGTGAAGACC ACTTGAACCT GGGAGGTGGA GTTTGCAGTG AGCTAAGATC 360 ATGCCACTGC ACTCCAGCTC CAGCCTGGGT GATAGAATAA GAGACGCTGT CTCCACAAAA 420 ATAAAAAATA AGTTATGGAG GCAGCTCACA GTGCCAGGGT GGAGGCAGCT CTGAATCCAG 480 CCTCAACCCA ACCCTTGCCA AGAAAGGAAG CCCTCTGCCT GTGCCCTTGC TTTCCTGAGT 540 CCAGGGGAGA TTAACAAGGT TCCTTATGAC TCATTCTGTG AGTCAGACAG GGGAAGAAAA 600 ACAAGCACGT CAAAGTCTAA CTTTCGGATG TGTAAAGACT TAGCAGTCTG ATCTGTGACC 660 AAAACTGTTG ATTTGAAGAG CTGGGAAGGA AACCGTGAAG TTCTCTCTCC TTTCATCGTC 720 TGGGGCTGTG CCCTCTGTGG GCTTGCTAAG TAAAGGCTCA GCTGGGAGGA AACAGAATCT 780 GGAGAACGCC CAGCTGCTCC CACGGGAAGC ATCAGGGAAG AAGGCAAGGT GTGAATTCTG 840 CCTTCTGCTC TGCTGGGATC CCTTTCACAT CTCCTTTGTC TCCAGGCAAT AACGGTCCCT 900 GGCTGTTTCC AGGTGTGACT TCCGATCTTG AGTCCTGTCT CCTTGTTTTG TGGTTCTAAA 960 TCTTGGCCAC ACATTGGAAT CATCTGGGGA GATTTAAGAC ATACTCATGC CTGGTTCTGC 1020 CTCCGGGGCC TAGGCTTCTA GATCTTTACA AGCTCCCTGG TGATTCTCAC ATGCAACCAA 1080 GCTTGTGATC ATAACTCCTC TGCAACACGT AAACTCTCCA TAGAAATTAT TTTTGTTATA 1140 GTTGCTTATC TCTCATTGTC TGATGACATG CTCTGTCCTA GATTAAAGAA TTACATGCTT 1200 TGGGAAGATA TTTCCATGGG TTGTGAAGCC TTTTTCTATA CCCCAAAGTC ATACTGCATC 1260 AGATATCAGT GCTAAAGATA AACCAGTGAT CGCCTATTTT GTCTATTTTA GGCCTGAAAA 1320 CAGAGTAAAG GGAAGACAAC AGCCTAATTT TATTCTAGCT TTTTTTCTCT TCAGTTTTCC 1380 CTTTCCATTC TTCTTCCCTA AGGCTCTCAA 1410
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