Tag | Content |
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EnhancerAtlas ID | HS101-17371 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr16:74633780-74636140 |
Target genes | Number: 11 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF4 | MA0039.3 | chr16:74635198-74635209 | GCAGGGTGTGG | - | 6.62 | PHOX2A | MA0713.1 | chr16:74635583-74635594 | TAATTAAATTA | - | 6.62 | PROP1 | MA0715.1 | chr16:74635583-74635594 | TAATTAAATTA | + | 6.32 | PROP1 | MA0715.1 | chr16:74635583-74635594 | TAATTAAATTA | - | 6.62 | Phox2b | MA0681.1 | chr16:74635583-74635594 | TAATTAAATTA | - | 6.62 |
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| Number: 1 | ID | Chromosome | Start | End |
GH16I074600 | chr16 | 74634121 | 74636150 |
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Enhancer Sequence | AATTAGCCAG GCATGGTGGC TGGTGCCTGT AATCCCTGCT ACTAGAGAGG TGGAGCCAGG 60 AGAATCGCTT GAATACAGGA GACAAAGGTT GCAGTGAGGT GAGATCGCGC CACTGCACTC 120 CAGCCTGGGT GACAGTGCGA GACTCCGTCT TAACCAAAAG CAAAACAAAA CAAAAAAACA 180 ACAGAGAAAG ATAATCCAGT GTTAGTGCTT TCTGAAGCAT GTGCTATTGG TAATATGCAA 240 GATGATTTCA GGTGGTATGT GTTGGTACTT ATATTTTATA GTCATATATT TAGTTTCATA 300 TATATTAGAG AAGTATACCT ACCACATCAA ATTCATGAGT TCACGTATAT TTCCGCTTAG 360 AACAAGGCTA AGTGGTGTTG TGTACCTATA GTCCCAGCTA CTCGGGAGGC TGAAGTGGGA 420 GGAGAGCTTG AGCCCAGGAG TTTGAGGTTG CAGTGAGCCA TGATCATGCC ACTGCACTCC 480 AGCCAGCCTG GGAGATAGAG TAAGACTTTC AAAGAAAAAA AAGAACAAGG ACAAAGCTAA 540 AGTAGACAGT CCTTGCTTAA GAAAAGAGGC CGGGTGCACT GGTTTACACC TGTAATCCTA 600 GCACTTTGGG AGGCCAAGAC AGGCAGATCA CTTGAGGTCA GAGGTTCAAG ACCAGCCTGG 660 CCAGTGTGGC GAAACCCCCG TTTTACTAAA AATACAAAAA TTAGCCGGGT GTGGTAGCGC 720 ATGTCTGCAG TCCCAGCTAC TCGGGAGGCT GAGGCAGAAA AATCACTTGA ACCCAGGAGG 780 CAGAGGTTGC AGTGAGCCAA GAATACGCCA TTGCACTCCA ATCTGGGCGA CTGAGAAAGA 840 TTCCACCTCA AAAAAAAAAA AAAAAAAAAA AACAAAAAAA AACAGTGACA GAAATTTCAA 900 GCTAAGAATA GCAGAGCTGT GTTCCACCCA AATCTAAATC CTAATTTTGT CTTATTACAC 960 TGCCCTAAAA TAATTTACTA TCTGTATGAC ATCAAGTGAT TAACACTCTT ATATAATCGC 1020 TTCTCGATCA CAACAATCTC ACTTATCAAA CCAACTGTAA GCAATGGTGG TGTCTTAAAG 1080 TACTAGTGTC CTTCCACAAT GATAGGTGTA TAATAGAAGA TCAATAATGA CTTGATTATG 1140 TGGTTAGATT GCTTCCAACC AGACAGACAG CATAGGAGGA AATTCCATAT TGGCTCAAAC 1200 AAAACAATCA TAATATATCC TAAAGCCAAA CAATGTTTGG ATTAATTGCT GTTTGAATTA 1260 TTCATTGTCA CTGATTCCCT CCATGAATGA ATATGGAATC AGGAACTGGT ACATATATAA 1320 TCCTAGAAAC TTTACAATAT ATACATACCC AGAGAATATA TACAGGAAAC GACTCATATA 1380 AGTTAGACAG CAGAGATCTT AGAAACCGTA CTGTAGGGGC AGGGTGTGGT GGCTCCGCCT 1440 GTAACCTCAG CATCCGGGAG GCAGAGGAGG GTGGGTCGGT TGAGCTCAGG AGTTAGAGAC 1500 CAACCTGGGC AACCCGGCAA GACCTTGTCT CTCTTAAAAT TAAAAAAAAA AAAAAGTATA 1560 CCCCAACTAC TCATTTAACA CATCAGGAAG CAGAGAGAGA AAATGCTTAC AGTCATTTGT 1620 TAGTTAATGG CACTGACAGC TCTAGTCTCA GTTCACTTTT TGTGATGTTC CATGGATTCA 1680 ATATAAATAT CAAGGAAATA CAACTAAATG CTTCCAGTGT TCTAGTACAA ATCCTGCTTA 1740 AGGTGAGTTG GGATTTGAAA CTCTTTTCAT AAAGCAGAAA TTCGGTTTAT GATGCACTCA 1800 GACTAATTAA ATTAGCGTTG GGTGATAACG CATTTGCCTG AGAAATCTAC AAATACTTCA 1860 ATGCACTGTT ACAACTCAGT TGTTCTTGTG TCCCATTTAG CATACATTTA TAAACCTATG 1920 GCATTCTCAA CAGTCACAGA CTAATGTCCT TAGCTACAAC CACCCATGGT ACATTAGAAA 1980 GAGTATGGTC TTTTAAGTCA AAAAGGACTT CCTGAACACC AGCTCTACCA CTTAGGATAT 2040 AACATCAGAC AACTTACTTT AGCTCTTTGA GCCTATTTCT CTGCTAAAAG AATAACACTA 2100 GCACTAGCAC TAGCACCTCA TTATCATTAT CATTGATAAT GATAGTCATT ATCAACAGTG 2160 AGACAATAGA GATGGTGTAG TCCACTATCT CAAGTATACA GTTAAGTGAA AGGTTAAAAG 2220 CAGAGTATAA AAATATTTAC CTATGAGTCT AAAAGGGGGT TTATGGTTTG CAACACTGAA 2280 ATGTTAATTC CTGTTCAATA CCTAAATTAG TTTATTTAAA TATTTACAAA GCATTCACTC 2340 TGTGCAAAGC TTAGAGCATG 2360
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