Tag | Content |
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EnhancerAtlas ID | HS101-19349 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr17:66057310-66058490 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
PHOX2A | MA0713.1 | chr17:66058478-66058489 | TAATTAAATTA | - | 6.62 | PROP1 | MA0715.1 | chr17:66058478-66058489 | TAATTAAATTA | + | 6.32 | PROP1 | MA0715.1 | chr17:66058478-66058489 | TAATTAAATTA | - | 6.62 | Phox2b | MA0681.1 | chr17:66058478-66058489 | TAATTAAATTA | - | 6.62 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_38542 | chr17:66057215-66059044 | HUVEC | SE_44541 | chr17:66057329-66058622 | NHDF-Ad |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I068061 | chr17 | 66057615 | 66058263 |
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Enhancer Sequence | TGTCACCTAG GCTGGAGTGC AGTGGCACGA TCTTGACTCA CTGCAACCTC TGCCTCCCGA 60 GTTCAAGTGA TCCTCCTACC TCAGCCTCCC AAGTAGCTGG GGCTACAGGC TAACTTTAAA 120 TACCCAATAG ACGAGAGAAG GCTGGAGTCC AAATGACCGG TAGGAATGGT GGACGCTGAT 180 TGCGAGCTTT TTGGCACTGT GGCTGGGCCC GATACTCAGT AACTCTAGTA GGCCAACCAT 240 GACCCCTTAA GGAGGAACTG TTGTTTCCAT TTTATAGCAG GGGAAACTGA GGCTCATAGA 300 AGTTAAGAAA GTTGTTCCAG ATCCTACAGC AAGCCATTGT CTCTTCCCAG CCAAGGGAGA 360 CATTACACGA AGCACAAACA AGCCCTGTGG GTGGACATGG TGACATTTGG CACGTGTGCA 420 GTCTCAGTCT CGTTCAAGGG CCTGAAATGA GTCATCTACA AATCAAAGAA CCAGCCTCTC 480 CGGACACAGA ATGAGGCTGG TTTGTACATT AGGAGGAGCT GGACCCAGAT AATGTGGTTC 540 CAAGCAGAGA AGATAGCCTT ATTCCAATTG CGTCCCCTCT GCAAGCCCTT GGGAGCTGCC 600 CAGGCCCAGT GACCCATGGA AGAGAGGATG CTGTGCCCTA GTGTCCAAGC AGCACGGCTT 660 GGCTCAGTCC ACTGGGCTTC TTCCAGCTCA CGAACCTGTT TGTTTTTACC CTTCAATGTG 720 AACCAGATGT GGGCACCTTG CTCTCCAGGA GGTCCCTCAC CCGTACCCCC CCTACCAGGC 780 ATCATTGGCA GCCACAGCTG ATGGACCAGC CTCCTCCCTG CTCTCCGGCC TCTCTCACCC 840 CCATAGCCCC TCCCTCACTG CACCTCCTGC ACCTTCCCTT CCCCCAGCAC GATTTGAAAC 900 AGGAAATGAC ACTGGGCAGA TCTCAAAAGT CCATATGTCC TGGACACTCT CTCTAGGAAT 960 TTCCTGGGCC TCCAGCTTGC TCTGTGTCAT GTCCTTCCCA CTCACAGTAT CTGGGGGGAA 1020 AGAAGTGCTA AAGGAAAATG AGAGTGAGCA TCCCTCGTCC CCAGTGCTAT CTTATCCCAT 1080 TGTGATCTTG GGCAAGTGAT TTATCTATGT CTGCATGGAC TCATGAATGC AATAGGTTAT 1140 AATCCATGAC TCTCACTATT CACTGTAATA ATTAAATTAT 1180
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