Tag | Content |
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EnhancerAtlas ID | HS101-16780 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr16:30015280-30016540 |
Target genes | Number: 42 | Name | Ensembl ID |
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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) |
RREB1 | MA0073.1 | chr16:30015304-30015324 | CCCCACACCACCCCAGCAGC | + | 6.22 | ZNF263 | MA0528.1 | chr16:30016147-30016168 | GGAGGAGTAGGGAGAGGAAGC | + | 7.02 | ZNF263 | MA0528.1 | chr16:30016144-30016165 | AGAGGAGGAGTAGGGAGAGGA | + | 7.74 |
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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 |
GH16I030004 | chr16 | 30015530 | 30016340 |
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Enhancer Sequence | CCCTGAGGCC TGACCCACCC TGGCCCCCAC ACCACCCCAG CAGCGGAGAT GAGGGTAAGT 60 GAGGGCTCCT TAGGAAGCAG AGAGGAGGCC ACAGGGCCAA ATGTGACACT CAGAAGGGCC 120 ACTGGAGACC ACGCATGGCG TTTCCTGCCA GCCCACTCAG CATCTAGCCC AGGGCCAGAC 180 TGGACACTGC CCCGCAGGAC CCAGCAGGCC TAAGCCTCAG GACCTCCATG TCCACACCAG 240 GTTCAGCCTC CTCTGCTGGC ACGTGACTTC TCCCCGTTTC CCGCCCCCCA GTGTCCTGAG 300 GCTGGGAGGG CATTAACAGA AACCACCTGA CACACAGCAG GTGCCCAGTT TGTGCCCACA 360 GACAAAGCAC GGGGACTGCA GAGGAGACCC ACAGAGCTCT CTAGGGAGGG TTTGTGAGGA 420 CCTGGCAGCG GGGGGGAGCT GAAGGGTTGA GCAGGGCAGA GGCCACTTCC CACCCTCAGA 480 GGACAAAGCA GGACTTCTGA CAAATAGAGC AGGATGCCCA GGGGGAGGGG CTGCCTGTCG 540 TCCCGCAGGC GGCACTCCCG CCCCGAGGCC CCGAGTGGCA CGGTGACGCG CTCAGGTCTG 600 TGTTTTAGAG CGCGCGCTCT GGCTGCCGTG CGGAGGAGCT GGATCTGGGA GAGGCTGCGG 660 GCAGGGAGTC CAGTTAGGAG GCTGGGACCG CAGCCCAGGT GAGCTAAGAG GAGGGCTGGG 720 CCTAGGCCAC AGCTGCCGGG ACCCCGAGGA GGGGCCCATC CAAGACATAA TACAAGCTTC 780 TTGGGGGCAG ATAAGCCGCT GGGGCTCCTG GCTCAGGCAG CCTGCAATAC CCTCCACCGA 840 ACCAGTGAGT GCCGCAGAAG AGGGAGAGGA GGAGTAGGGA GAGGAAGCTG GTGGCAGGTG 900 GCACCTCCGG GGCCGGCAGG CAGGCAAGCA CTCCAGGCCG ACTCCGCCTC TGGCTTAACC 960 CCTGTCTCAG GGCAGCCCAG GCGCCTCCCT GGAGAGGGCA GGTGCCCGGG CCTTTCCCTC 1020 CCGGTTTCCT GTGAGACACC CCCATCCCCT CATCTCACCT CTATCACCAC CCCCAGGCAC 1080 TTGCTGGTTT GAGGCTCTCG AGGGGCTGAG GGGGGCAGGC CCTGAGTGCA GCATGGGTTG 1140 GCCCAGCTGT GCCCAGGGCC TCTTCCCCCT CCCCAGAGCT GCCCTGGGGG GCAAAGCCTA 1200 GTCTCCTGAG GCCCCAGTGC CTCCCTGACT AGTCCCCCTG TGTTTCTTCC CCCTGCTGCA 1260
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