Tag | Content |
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EnhancerAtlas ID | HS197-04469 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr11:126454960-126457500 |
Target genes | Number: 10 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ONECUT3 | MA0757.1 | chr11:126456159-126456173 | CTAAAATCAATAAA | + | 6.3 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I126585 | chr11 | 126455285 | 126456615 |
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Enhancer Sequence | CCCGCCACCA CGCCCGGCTA ATTTTTTGTA TTTTTAGTAG GGACGGGGTT TCATCTTGTT 60 AGCCAGGATG GTCTCGATCT CCTGACCTCG CGATCCGTCA GCCTTGGCCT TCCAAAGTGC 120 TGGGATTACA GGCGTGAGCC ACCGCGCCCG GCCTCTTTTT TTTTTTTTTT TTTTTTTTTT 180 TTGAGATAGA GTCTCTGTTA GCCAGGCTGG GGTGCAATGG TGCAATGGCG AGATCTCGGC 240 TCACTGCAAC CTCTGCCTCC CTGATTCAAG TGATTCTTTT GCCACAGCCT CCCCAGTAGC 300 TGGGATTACT GGCACTCACC ACCACGCCCG GCTACATTTT GTATTTTCAG TAGAGATGGG 360 TTTTCAACCT GCGGGCCAGG CTGCTCTCGA ATTCCTGACC TCGTGTGATC CGCCCGCCTC 420 AGCCTCCCAA AGTGTTGGAA TCACAGGCAT GAGCCACCGC GCCCGGCCAG GAATTAACCT 480 TCACCAGGAT AGTTTGTGGA ATTTTATCAA GAGGCTTCGC TCCCATCTCC TGCTTTCTTA 540 ACAGAGTTTG GAAGCAGCGG ACCGGATAGG AAAACTGCTT AGGGTTCCAC CCTCATGCCA 600 AGTGGCAGAG GCCCCGGGGG AAGCCTCCTG CGGAACGTGG GAACAAAGGG ATGCGGGGCC 660 TAGCACTCTA CGCCGGTGTC TGTTCGTCTG TCCAGAAGGC TTGTCACACT CTGGGGGGGC 720 ATCTAGCTAA AAGGTACTCC ATCAATGTAA ACGACCGTCG CTCTCGTTAA GTTCCATCTG 780 TGTGTCTTAA AGCTCCCGCA CGGAACGTGA TTGGAGTTGG GCTTCAGCTT CCCTGTGCTG 840 CCTGAGACAG AGGAGGGAGA TGTTTTTCTT GGCAAATAAA TATGATATCA TAAGCCCTGG 900 CAGGATTCCA GCCTGAGTAA TGGCCGTCTG CCTTCCTAAT TCCCTCAGCA GCTTGGAACA 960 GGAACATTAC TCTTTACTTC CTCTCTTTAA AAACAAACTC TCTATTGGAG CGCATTACTC 1020 AGCCACAGGA TCCCTCCCCG GACGTGGCGG CATTCAGATG ATGGGAGGTG AGGAATGAGC 1080 TCAGATTACA GCGCACATTA GGGAAAACAC AGCAAGGCAT TTGGCCCAGA AAAGGCACCT 1140 GAGGACCTTG AATTAGAGCG GCCACTCCTC ATGTGTCCTT GTTCATGAGG AACATAGAGC 1200 TAAAATCAAT AAAAATCACA TTGTTTAGCG CTGCCGTTTC CCTGGTTTAA ATCATGAAGG 1260 AGTAAGTAGG TAATTAGGTA ATCCAGCTCG GACTGGATAG TTACCTTCAA GTACGAAGCG 1320 GTCTTGCTGA GACCCTCTCA CTGAACGCGA GCTGGGGGAA GGGTCTCGTG GCCTCTCTAC 1380 TCACAGGAGC ACTGCTGCCT CTAAGCACAT ACCCCGCCCT CTTTCTGCTT GTCATTAGTT 1440 CTTCCTAACA ACAGTTAGAG GCATCGGTGT TGTTACTTTC CATTTTATAA ACCCGAGGCT 1500 CAGTGAGACT AATTAGGTAA CTCGTTCAGG GCCATAAATT ATACATAGCA GAAGTCAGAG 1560 TTGAACTCGG GTCTTTTGGC TTCAGATTCA ATGTTTACAA CGCCACATCA AGCCTCATCA 1620 CTTTCTCTGG CCTGTGAGGA CTTGGGTGCT GCCACTTGTC CCTTTTGAAG TAGCGGATAC 1680 AAGGTGGCAC CGTGAAGGCA CTGGGTCAGG AGCTGGGACA CAGCTTTGCA TCACTTGGGC 1740 ACTGTTCTGC TGGGGCCTCC TTGGTAACCA ACCATCCAGG TGAGGATAAA AACTGACCCA 1800 GCTTGTAGAG AGATCTTGAG GCAGGCATGC AGCAAGGGCC CTAAAATTAC TGGGAGAAGG 1860 GCAAGTCACT GTTCGAAGGC TTGGGATGGT GAATTCAGCC AATAAACGTC CTTTGAACAC 1920 TTACTATGGC TAAGCATGGG GGCACAACTG TAAACCAGAG AGAGTCCCTG CCTCAGGGAG 1980 CTGGGAGTCA GTGGGAGAGA TGAATAAACA GGCAACGACG ATGCAGTGTG ATGGATGCTC 2040 CAGTGGAAGA GTCCAGAGCA CCGGGATGAT GTGTAGGGAG AGCCACTCAC CAGACATGGC 2100 AGTTCTTGGA AAATGTCCAC TGGGGACATG ACATCCAAGC TGAAACCCGA AGGACAAATA 2160 GGGGACAGGG AGATGAAGAC GGGGGCTGCA GAGCGTTCCA GGCTGTGGAG GCAGCGTGTG 2220 CAAAGGCTGG GAGGTCAGAA AGAACACACT CTGCTCCGGT GATGGCATGT TTGGTCTGGC 2280 CTGGAGCAGA GCTGCAGGGG AAGCTGTGAG GCATGAGGCA GAGAGGTAAG CCAGGAGTAG 2340 TTTGCAGACC CCTGGCTGGG CAGCTTTCCA ATCTGGAACA GTGGGTCATG GAGCCATCAC 2400 ATTCCCAAAC CCACAGCGCT TCCCTCTCAC CAACCCTGTA GCCTGCAGTC TTCACTGTGC 2460 TCTCGACTCC CCCAGCCTTT CATTGTATGT GGAAGAGGAG CCAGAAATGC ACCCAAACTG 2520 AAAGAGGAGC ACGCAGCACC 2540
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