Tag | Content |
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EnhancerAtlas ID | HS002-09367 |
Organism | Homo sapiens |
Tissue/cell | A375 |
Coordinate | chr8:29522270-29523480 |
Target genes | |
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 | CCCTGGTGTC TTGTGTCCAC AGATCCACGG CCATCATTTC CGCCAGAGAG TGGGGCAGAA 60 GTTTAAGGAT AAGTTATGTT GTCCAGGCGC AGTGGCTCAT GCTTGTAATC CTAGCACTTT 120 GGGAGGCCAA GGCAGGGGGA TCCCTTGAGC TCAGGAGTTT GAGACCAGCC TGGGTAACAT 180 GATGAAACCC TGTCTCTACA AAAAAAAATA CAAAAATTAC TGGGGTTTGG TGGAATGCAC 240 CTGTAGTCTC AGCTACTTGG AAGGCTGAGG TGTGAAGACC ACTTGAACCT GGGAGGTGGA 300 GTTTGCAGTG AGCTAAGATC ATGCCACTGC ACTCCAGCTC CAGCCTGGGT GATAGAATAA 360 GAGACGCTGT CTCCACAAAA ATAAAAAATA AGTTATGGAG GCAGCTCACA GTGCCAGGGT 420 GGAGGCAGCT CTGAATCCAG CCTCAACCCA ACCCTTGCCA AGAAAGGAAG CCCTCTGCCT 480 GTGCCCTTGC TTTCCTGAGT CCAGGGGAGA TTAACAAGGT TCCTTATGAC TCATTCTGTG 540 AGTCAGACAG GGGAAGAAAA ACAAGCACGT CAAAGTCTAA CTTTCGGATG TGTAAAGACT 600 TAGCAGTCTG ATCTGTGACC AAAACTGTTG ATTTGAAGAG CTGGGAAGGA AACCGTGAAG 660 TTCTCTCTCC TTTCATCGTC TGGGGCTGTG CCCTCTGTGG GCTTGCTAAG TAAAGGCTCA 720 GCTGGGAGGA AACAGAATCT GGAGAACGCC CAGCTGCTCC CACGGGAAGC ATCAGGGAAG 780 AAGGCAAGGT GTGAATTCTG CCTTCTGCTC TGCTGGGATC CCTTTCACAT CTCCTTTGTC 840 TCCAGGCAAT AACGGTCCCT GGCTGTTTCC AGGTGTGACT TCCGATCTTG AGTCCTGTCT 900 CCTTGTTTTG TGGTTCTAAA TCTTGGCCAC ACATTGGAAT CATCTGGGGA GATTTAAGAC 960 ATACTCATGC CTGGTTCTGC CTCCGGGGCC TAGGCTTCTA GATCTTTACA AGCTCCCTGG 1020 TGATTCTCAC ATGCAACCAA GCTTGTGATC ATAACTCCTC TGCAACACGT AAACTCTCCA 1080 TAGAAATTAT TTTTGTTATA GTTGCTTATC TCTCATTGTC TGATGACATG CTCTGTCCTA 1140 GATTAAAGAA TTACATGCTT TGGGAAGATA TTTCCATGGG TTGTGAAGCC TTTTTCTATA 1200 CCCCAAAGTC 1210
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