Tag | Content |
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EnhancerAtlas ID | HS012-17965 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr3:16293480-16294400 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EBF1 | MA0154.3 | chr3:16294321-16294335 | AATCCCATGGGACT | - | 6.23 | EBF1 | MA0154.3 | chr3:16294321-16294335 | AATCCCATGGGACT | + | 6.62 | HNF4G | MA0484.1 | chr3:16293877-16293892 | AAGGTCCAAAGTTCA | + | 7.41 | Nr2f6(var.2) | MA0728.1 | chr3:16293877-16293892 | AAGGTCCAAAGTTCA | + | 6.49 | POU2F2 | MA0507.1 | chr3:16294299-16294312 | AAATGCAAATGTA | - | 6.03 | RARA | MA0729.1 | chr3:16293877-16293895 | AAGGTCCAAAGTTCAAGG | + | 7.27 |
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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 |
GH03I016251 | chr3 | 16292869 | 16295810 |
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Enhancer Sequence | GAGGACAAAG CTTCCAATCG TTTAACTGCC AAAACATACA TTGGGGTCAC TTATTGGTGA 60 GAAACATTTC TGTCCTGTCC TTACAGATTC TCTGTAACAT AATTCTAGTT TTTAAACCCT 120 CCCTTGCACA GAGATTAGGC CCCAGTTCTC ATAAATAAAA AATGCTTGGA GCATATTTAT 180 TGATTGCACG ACACCGTTTA TCCATTTTGA AGTGAGTAGT ACTAACCATC TTAACACTTT 240 TCCAAGCAGA AAGTTCTCCT TCATGGCTAA CTTCACTGAC TTTTTCCCCC TCTAACTCAG 300 CGTGGTATGG AGAGAGCTTA GCCAAGCCAG ATGGACAAGT CACTGATAGG CCACATTCTG 360 CTAGGAATAT GTAAGCTATA TATGGCAGAC TTTGTTTAAG GTCCAAAGTT CAAGGTTTCA 420 GCTATGGTCA CGCGGATCAT ATCAGACTTG AAGTGAGAGC TGCTGTCCTG ATTTGAAACA 480 GTCTGCATAA CAAACTGTTG GGCACCACTG AAATGTATCA GGGAACTCGC TGCAAAAAAA 540 AAAAAACACT CAAAATGAAT CATCCCAAAG TTCTAGCAAC CAGGAAACAG ACACAGTAAG 600 GTGAGTAGTC TACGTTCCCG TGGGCATTCT AGCTCATTTT TAATGACATC TTATGAGTAT 660 ATGGCTCCAT TTCTCTCCAT AATTAGAGTT AATAAATACC TTCAAGAGGA TGTTTATGGC 720 AGACTTTGGA ATATTAACTC GTTATTATCA GAGTTATGTT GCTGAAGGTG AAGCCTGGTT 780 TTGAATACAG AAACCACAGC CAATGCCTCA CTCACCTCAA AATGCAAATG TAGCAAAAAT 840 TAATCCCATG GGACTGTTGT CTCATGTCTG GCCAGAAAGA TGAGAATAAC TAATTTGTTT 900 GAAAGTTTCA ACTGCTTCCA 920
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