Tag | Content |
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EnhancerAtlas ID | HS101-01809 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:68290300-68291670 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr1:68291657-68291669 | GAATGTTTGTTT | + | 7.22 | Foxq1 | MA0040.1 | chr1:68291556-68291567 | AATAAACAATG | - | 6.02 | POU4F2 | MA0683.1 | chr1:68290717-68290733 | CTCATCAAATATTTAT | - | 6 | STAT3 | MA0144.2 | chr1:68290351-68290362 | TTTCCCAGAAG | - | 6.62 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_27870 | chr1:68290075-68291524 | Fetal_Intestine | SE_28821 | chr1:68290031-68291919 | Fetal_Intestine_Large |
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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 |
GH01I067824 | chr1 | 68290102 | 68291361 |
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Enhancer Sequence | TGAGGATCAT ATATTATATA TTTTCAAAAA TATTGAAGTT GTATAAGCAA TTTTCCCAGA 60 AGTGTGAAGA ACAGGACAAG ATTGGCATGG AAGAGATAAA GCTAAGGTGG AGTTCAACAG 120 CTCAGGAGGA GGAGTCGAAG AAACCTGGGT TTAGGCAGGT AGGTTCTCAT GTGAAAGTCA 180 GTCAGAGAAA TCTCAGTCCA GAATTCAGGA GGTAAGCACA GTGAGTGTGG AGAGGGTAAT 240 TTCTGCCCTG TGTTATATTA CCTGCTGGAT GTGGGTGGCT CTGAGCCCCC GGATATTTAT 300 TACAGCCATA GGAAGTCAGA GAACTGTAGG TGAATGGGAG GCAAAGATAG GAACACTAGG 360 ATTACCTTCT AGGCAGCCTG CCAGGAGCAT TGATTTGCTC TTGGATAAAG CATGCTGCTC 420 ATCAAATATT TATGTTAAAA AAGAGGGCAA GGCATGTGCT GGAATATTCT GCTGAATTTG 480 ACAGAGATAT TCCTTGAAAA CTTGAGACTC CTGGAATTTT GTGTAATCAA ATCATACTAT 540 AAACACAACA GGTGAATTTG CTATTTAAAG AAATTCTGTA AGAAATTCTT AGGAATTGTC 600 ATCTTCTGCT CTTTCTGCTT TGGGAATCTG AGTATGTCTG AAGATAGCTG CATTTAACCA 660 GGTTAAATGT GAAAGGCATT CACGTTTCTG CATCTTTTAG TTTTTTTCAC AAGGTGTATT 720 GTCTCCAGAA AACAGCAGAT GGCCTAGGTC CGAAGTATGA ACCAGCACCT TGATCCTCAG 780 GACCACTGCC TTAGCAGTTA GATTCACTAA ACATGGCTGA TCCTACAGGC TGTGCAAATG 840 CCTCCCAGAA GAGGAGCCAG GAGAAGGAAG TTGATTCTGG CTACAGGCTT TCTAAAGGAT 900 CAACTTAAAA AAGCAAGAAA GTAGTACCAG TTGGTACTAA GGGGAACACA GACAAACTCT 960 CTGAGTTTGT GGTACCTTTG ATAACAAGAC TCCGCACCTT TTAACCTAAA CTAGAAGCCT 1020 TTTTCCAGAA GCAGCAGCTA CTCATAGGTA AGTTCCAAAG GCTCCTGCAA CCACTGTTAC 1080 TTGCATCCTG TCCCCAAGGA AAAAGGCCTA CGGCTGGTCA ATAAATAACA TGAATCCCTC 1140 TCCACGTTCC CAGGAGTTAC TACTACTCCA TTCCCTGCAC CAGGCCAACT ACACAACGGG 1200 TGCTGGTGAC CCTGGCAAGT ATTAGGCAAT ACTGAGCATG CTGGTGTTTA AGTAGCAATA 1260 AACAATGTCA ACAGCACCCA AAGTGCTGGT CTTTACCTAC CCCTCAGAAA TAATGAATTG 1320 AAGAGAAAGA AACTCATCAT AGGCAATGTG TACCACTGAA TGTTTGTTTC 1370
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