Tag | Content |
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EnhancerAtlas ID | HS101-13000 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr13:101094820-101096620 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr13:101094903-101094922 | CTTCCAGCAGGGGGAAGTA | + | 6.27 | EWSR1-FLI1 | MA0149.1 | chr13:101096310-101096328 | CCTTCCTGGTTTCCTTTC | - | 6.28 | Nkx2-5(var.2) | MA0503.1 | chr13:101095446-101095457 | CTTGAGTGGTT | - | 6.32 | ONECUT1 | MA0679.1 | chr13:101095711-101095725 | AAAAAATCAATAAT | + | 7.64 | ONECUT2 | MA0756.1 | chr13:101095711-101095725 | AAAAAATCAATAAT | + | 7.95 | ONECUT3 | MA0757.1 | chr13:101095711-101095725 | AAAAAATCAATAAT | + | 8.42 |
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| Number: 1 | ID | Chromosome | Start | End |
GH13I100440 | chr13 | 101092621 | 101094896 |
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Enhancer Sequence | GTGTCTCCTA CATAGAAGGG AACGCCCAGT ATGGCCTAGG CAGTGTTCTA GACTCTGCAG 60 ATAGAACAAG GAACAAGACT TACCTTCCAG CAGGGGGAAG TAGATACTAA ACATGTAAAT 120 ACCTAAATAA GGTGATTTTA GTACTAAGAA GTTGGATGAA GACTATGAAA TTGATAGAAA 180 GTCACTAGAG AAGGCAGCTT TAGCAAGGAT GGCTAGGAAG TCCTCTCTGA ATAGCTAACA 240 CTGAGCTGAG ACCTACGAAG AGGAGGGGGC AAACGTGCAG AAGTCTGGGG GAAGGAAGTC 300 CCAGGTAGCA GAAGGGGCAA AGCAGAGGCT CTGAAACGGG ACAAGCTTGT TTTGTGTGAA 360 GGCCAGTTGG GGAGAGTGGA ACGAGGAAGA CAGAACCAGA TCATCTAGGG GCCAAAGAAC 420 TGTTTTGTTT TGTGTTGTTT CTTTCTATTC ATGTTGTGGA GCGTTTGGAG GGTTTGGGTA 480 GGAGAGTGAT GTGATGTGAT TTTTTAAATC ATTGCAGGCC TTGGGGTAGA GACAGAGAAA 540 TCATTGATTT GACCATTGCA GACCTCAGGT GAGAGGTACT GGTGGCTTAG ACCAGGAGGC 600 ACCGTCTGTT TCTATGGGGC TCACAACTTG AGTGGTTATT ACATTTTTAA ATAGTTGGGG 660 GAAAAAATTA AAGAAGAATG TTTCATCCAG CCTGGGCAAC ATAGTGAGAC CTTGTCTCTA 720 CAAATAATTT TTTTAAAAAT TGGCTGGGTA CAATGGTGCA TGCCTGTGGG TCCAGCTGCT 780 TGGGAGGTTG AGGTGGGAGA ATCGCTGGAG TCCAGGCAGT TGCTGTGGAG AGCTGTGACC 840 ATGCCACTGC ACTCCAGCCT GGGTGACAGC ATGAGACACT GTCAAAAAAA AAAAAAATCA 900 ATAATGTTTC ATGACCCATG AGAAGTATGA TGTCACATTC AGATCTTATT GATGATAAGC 960 AGTTAACTAG AACATAGCCA CATTCATTCA TTTTTGTCTG CCATGTATAG CTGCTTTTGC 1020 AGTTTTTGTC GTATGAAGCT GAATGCACAG ACTTTCTTGC CACGCAGCAG TTCAGTGGGT 1080 TATTGTGATT TTTTTTTTTT TAATCTCAGG ACCAAGATTA AAGTTTTTTG TGCAGAGTTG 1140 CAGGTAGCCA AATTACTTTT TGTATTCCTG TGCCTTAGAT TCCTCATCTG TAGAGCAAAA 1200 TTGAGATCGT CTTTCAGGTC TGTTTGCTCT CCACATCCTA AGGTCCTAGG TCTGAATCAG 1260 ACTTAGTTCT TCTGTTGTGG CTGCTTAGCA CATCAGGCTC CTAACTGAAT GATTGTAGTG 1320 GTGTTTTACT CGGTCTCCTA GCCTCGTCCT TCCCCATTCT ATGTATCTTC AGCATGACCT 1380 CAGACCACCG TCTTTCTAAA ACATGAGCAT GTCACACTCC AGTTCTTAAC TGTAAGAACT 1440 TTGTCAGGTA TGAGCTCTCT TTGTACAAGA TCTGACCTGG GTTTATAATT CCTTCCTGGT 1500 TTCCTTTCTT GCCACTTCCA CCTTCATCCA ACCCTATTTC TGGCCACGCT GAACTGCTTA 1560 ACATTCCCTA AACTTGCCAT GCCATCGTGC CATCCCTTAA TCTGAAATTT TTGTTAACTG 1620 TCTCATCAGC CCACAATTTT TTTTTTTTTT TTTGAGACGG TGTCTCGCTC TGTCTCCCAG 1680 GCTGAAGTGC AGTGGTGGTG CAATCTTGGC TCACTGCAAC CTCCACCTCC CAGGTTCAAG 1740 TGATTCTCCT GCCTCAGCCT CTTGAGTAGC TCGGATTACA GGTGCCACCA CCACGCCCGG 1800
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