Tag | Content |
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EnhancerAtlas ID | HS101-31006 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr3:151607950-151609560 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Mecom | MA0029.1 | chr3:151608834-151608848 | CCTTATCTTATCTA | - | 6.32 | PBX1 | MA0070.1 | chr3:151609548-151609560 | ACATCAATCATA | + | 6.11 |
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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 |
GH03I151889 | chr3 | 151607605 | 151608988 |
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Enhancer Sequence | TTTATAAACC ATAGAGGAGT ATCATTTTCT TTTCTTTTTT TTTTTTGAGA CAGCCTTGCT 60 CTGTCACCCA GGCTGGATGG AGTGCAGTGG CACCATCTCT GCTCACGGCA GCCTCTGCCT 120 CCAGGGTTCA AGGGATTCTC CTGTCTCAGC CTCCTGAGTA GCTGGGATTA CATGTGCTCG 180 CCACCACTCC CAGCTAATTT TTGTATTTTT AGTAGAGACG GGGTTTCACC ATGTTGATCA 240 GGCTAGTCTT GAACTCCTGG CCTCAAGTGA TCCTCCCACC TTGGCCTACC AAAGTGCTGA 300 GATTACAGGT GTGAGCCACT GTGCTTGACC TGGAGCATCA TTTTCAGTGG GAAAACACTG 360 ATATGGGGAG GAGAAATGTT TTTCCTTCTG AAAATGTTTT TTTTTCATTT AAGATTTAAC 420 TTTTTGACAA TATAGTTTAA AATTAATTTA ATGAATGCTA ATTTCCGAGC TTTCCATCCA 480 AAGTGTAGTA AGTCAAAATA TATAAAAGTG CATATTTTAA AAACCCTCAT TCAAGTTCGT 540 TTGTGGTAAA CTTCAAAATT ATTATCATAG GGTGAAAGAA TGAGAGGGCA GGTGTTGAAA 600 CAGATGATGT CTCAGCTTAC ATTGTACACA CTTCCTGTGG TTTTTTAACG TGTCAAAACT 660 AAGAAATAAA TATGGTGTGT TTGAAAATTG GCACATCCTA CCAGACTAAT ATGTGTACAC 720 AGTACACTAT TACCTCACCT TTAATATTCA TTGTGTCCAC AGCTGGGATA AATACTTGCG 780 TTGGGTGACC ATGGGGCAGA GCAGCCTGTG CTTTGTGTAT ATGAAGAGTT TTCTAGAAGG 840 TGAACTCATC CCAATAAAAA ACTGAGTCAA ACAGGCAAGT TCAGCCTTAT CTTATCTAAG 900 AATAAAGCCT CAGATAGAGG AGATGGGCAA TTCTGAGTGT AGCACAATGG AGCAAAGCGA 960 TTGTTCAAAA CGTTTATCTT TGGCAATCTC AGGAAAATGC CATGGAAAAT AACCTGGAGC 1020 AGAAGAGGGG AAGGAAGCAT GAGCATGTGA TTGTAAATGA GACACATCCC AGTGGCCTTA 1080 CATAAATATA CACCTGGGTA GAACTGTAGA CATGCTGAGG AGGTGGACTT GGAAAATTAT 1140 TGACATACAC AGAAAATTTT GCTGTTGTCT TTGTCCATGA TCTATTACAA CTGAACATCT 1200 GAGACAGGGT CAGTTAAAAA AATGAAGGCT TATTTAGTTC ATGATTTTGA AGGCCAAGAA 1260 GTCTAGAATC ATGGCACCAA CATCTGTTGA GGGCCTTTTT GCTCCATCAT AACCCGGCAG 1320 AAGGCATCAC AAAGCAAGAG AGCAAGAGCA TGTGTGTCAC GTATGTCAGC TCGGATCTCT 1380 CTTCCTTTTC TTATGAAGCT GCCAGTGCTA TCGTGGGGGT TCTGCCTTGA TGACTTTATC 1440 TAATGCTGAC TACTTCCCAA AGGTGCCACC TTCAATCAAG AATTTGGGGA TTAAGTCTCC 1500 AAAGCATGAT ATTTAGAAAA CATATTCAAA CCAGAGCATT ATGTATAGAC AGAAATATAC 1560 ACATATTTAG TACATTTTAA AAGAAAGTAA GGCTCACTAC ATCAATCATA 1610
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