Tag | Content |
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EnhancerAtlas ID | HS129-02351 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr1:159849160-159850340 |
Target genes | Number: 16 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr1:159850050-159850071 | CAATAGTTTCAGTTTTCTTTT | + | 6.75 | PRDM1 | MA0508.2 | chr1:159850040-159850050 | TCACTTTCAC | + | 6.02 | RUNX1 | MA0002.2 | chr1:159849469-159849480 | TTCTGTGGTTT | + | 6.32 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_09609 | chr1:159849306-159853172 | CD14 | SE_34829 | chr1:159848784-159853407 | HeLa | SE_53483 | chr1:159850002-159850755 | Spleen |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I159879 | chr1 | 159849771 | 159850572 |
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Enhancer Sequence | ACAGCATTAT CCTAGGTATT TTCAGCCTAG TCTGACTGGA CACATATTGA AGCATCCAGT 60 ATATTTTGAA TCATCAGTGA CCATTTCACA GGATTATTGT AAAGATTAAA AGAGATAACA 120 CGTGTAAAAC ACTTAGCACG GAGCCTATGC ACAGACTAGG TGCTCACTAA ATGATAGTTA 180 TGTGATTGTT ATTATGTAGG AATCATCTAT GTCCCCAAAC CTGCATTCTC ACTCTATTGC 240 TTGCATAGAG TGTCCCCAGC ATCCAATAAG AATACTAAAG CCAATAAGTG AGCTTCGCTG 300 AGCTTCATTT TCTGTGGTTT GTATTCAGAA CATATAGGTG TACCAAATAT GCCATTCAAA 360 TTATACTCAC ACCCTCCCCC TGGCCTTCTT TAAAAATCAC TACTATAGAG GAGCATAGAG 420 AAGTACAATG TGTTTCTGTC ATCATGGAAT TTCAAAACTA GCAGGGCAGA CAAGATCAAC 480 ACATGAAGAA TTTAATAACT TTCCTGCCAC CTTGAGTACT TCCTCCTCTT TTTACATAAA 540 TCCATGTTCA CTTTATCTAT ACCACTCTTA AAAGCCTTCT TCTACTCTCC AATCCCCGTA 600 GATCCCAATC ATTTTATTAC TCAATTTTGC CCCAGAATGA GCTGACACAT TCATGAGCTA 660 CATCCATCTG CAACTGTCTG CAGGTATGGC TCTCTCCTCC ACTGTGCATT TGCTCTGTCA 720 TATAGGTTCT TTGGTGGGAG ATGGGGGAAG ACTATTTTCT GAGTCTAGCA CCCAATACAG 780 GATGTCCAAT ATAGGCATTT GCACAAGAAA TTTATGTAAC CGCTGACTCA TGATTACCGG 840 GGGTATAATT ACGCAAGTCA TGACAAATCC ACAAAAAAAC TCACTTTCAC CAATAGTTTC 900 AGTTTTCTTT TCTGCCTGCA TATGGCCCTC ATCCCAACTT CTAATCAAAG GTGTTAATGA 960 GGTTAAAGCT AATTTGGTTG TCCTTTCTAG GCTGTCTCTG TTAACGAACA AGTGGACTGG 1020 CTAAGATGAA GAGACAAAGA AGCCAGGCCC TTGAACTAAG GATGTGCATC TTAGAATGAA 1080 GGTGCGGCTG CCTTCCACTG GAGTTCCCTT AGTTCTCAGG CCCTCCTCTC CCTGTGACAG 1140 ACATTCCATT CCTAACCAAA GGTCCCAGAA ACCAAGTCCC 1180
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