Tag | Content |
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EnhancerAtlas ID | HS110-05136 |
Organism | Homo sapiens |
Tissue/cell | KATO3 |
Coordinate | chr9:139858390-139859430 |
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) |
GLI2 | MA0734.2 | chr9:139858430-139858445 | CGGGGTGGGTGGGCT | - | 6.12 | Klf1 | MA0493.1 | chr9:139858941-139858952 | GGCCACACCCA | + | 6.62 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_57277 | chr9:139858417-139859680 | VACO_400 |
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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 |
GH09I136963 | chr9 | 139858398 | 139859490 |
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Enhancer Sequence | GGGGAGAACA GACTCCACCG CTGGGCGGCA AGGCGAGGCA CGGGGTGGGT GGGCTGCAGG 60 GCTGGGGCTG GGGGTCAGCT CAGGGAGCAG CAAGCAGGCT CGGGGAACCC CTTCAGAGGC 120 ACCTGGGAGT TGGGGGAGGG GGCCCATCTC ATACCCACAC TGTCCTGTGA CCCTTCCAGG 180 GGGGACCATC CCAGGCCTGG CAGGGGAGAG GGAGCACCGT GCCCACCCTG GCCCTGGAGG 240 TGGTTCTGGG GCTTGGGGTA GTTTCTCTTC TGCTCTCCCC CTCCCCTCAG GCTGGACAGC 300 GCCGGGGTTC AGCCCCCTGT GACCGTGGGG CACCCTGGGC AGACGCTCGC TGACCAGGGG 360 CCCTGCAGGC CTGGCGCTGA CCTCAGACGG GCAGGGGGTC TGTGAACCCA ACGATTGCTG 420 CCTTGGGCAG CTGTAGGCGT GGCAGTGCCC CAGGGTTCAG CACCTGCCTG ACCACACGGC 480 ATCAAAGCCG CCTGTCCTCC CCAGCCCCCG CACAACCTGC CACTCCCTGC TCGGCAGAGG 540 AAGGAGACTC GGGCCACACC CAGGGAGGGA CCTCCTCTGG CTCGACATGG AAACCTAGGC 600 TGTAGCTCCC TGCTTCCCCG GCTGTGTTTG TGTGGCCTGG TGGCTGAATC TGCACAGAGA 660 GCAGGACGCC AGGTGCGCTC CCGGGAAGCT GTCCTAGAGA GGGGCCGGAC CGCACACCTG 720 GCGCTGGAAG CCTCCATGAC TGGATGTTTG CAAGAAACAG AAAGAAACTT CTGTCCAGTC 780 TCAGCCACAG GCACGCCAGG TCCTCTGCTG CCTTGCCGCA AGCTCGGGGG TTTCAGTGAG 840 ACCCTCTCCC ACTCCCACGG CCTCGAGTGG ACCAGGTAGC CCTGGTGTTG CTCCCTGGGT 900 GCTCTTGACC CCCCAAGGCG GCTACAGGAA GGAGAAAGGC CTATCTTGAA AGGACTGGAA 960 AACAGTGCGT CAGTATTTTA AAAATTAAGC TACACCATCA TAGGACCTGG CTATTGCCTT 1020 CCTGGGTATT TACCCAAAAG 1040
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