Tag | Content |
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EnhancerAtlas ID | HS101-14776 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr15:46211760-46214530 |
Target genes | |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr15:46213561-46213579 | AGAAGGTAGGAAGGAAAA | + | 6.18 | IRF1 | MA0050.2 | chr15:46214468-46214489 | TTTTTCTTTCTTTTTTTTTTT | + | 6.59 | JUN(var.2) | MA0489.1 | chr15:46212325-46212339 | GAAAAATGACTCAT | + | 6.68 |
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| Number: 2 | ID | Chromosome | Start | End |
GH15I045919 | chr15 | 46211948 | 46212830 | GH15I045921 | chr15 | 46213681 | 46213830 |
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Enhancer Sequence | GAAATAATTC AAGAAACTGG AGAAAATCTC CCTCTGTCTT TGCATGACTC GCGAGTCTTT 60 GGATCTGTGT TCCGCTCGTC CTTGTCTTCC ATAGCTTGTA TTGCTCTGGA TGATGGTGGA 120 GTGCCAGGAT TAGAGTATAA TGTGTATTCC CTTTTGTCTC TCTCTTGAGA CCTATGGTTA 180 ATTTTTTTTT TCACATGTAA GTAAAATAAG CAAATCTCTA AGAATACTAA TAGTAAAAAA 240 ATAGGGATGT TTCTCCTCCT CTCTCCGCTC TTGAAAAGCC CAGTACAGCC CGCTCCCATG 300 CATCAGCTGG GCTGGGCGGC CACACCTCTC CCTCCAAGGC TGATTCAGCA GTGAGTTTCG 360 TAAAGCTGTT CTGACGCTTG AGAAGTCCTC TTAACACTAA GCAGGTAGTG GATTATGGTT 420 GCTTACTTGC TTTATTTATT TATTTATTCA TCCTTTTGAT GTTTTCTTTC TAATAAGAGG 480 TATATGAGTC ATCTGTTGTG GACTTTATTT TGTGAAGGAA TGCTTGGCAT GATAAGAACT 540 CTGTAGAAGT TAACAAGTTG AAGAGGAAAA ATGACTCATC AACACCGACA TTTTATATCA 600 CTGTGTGGAA TGAAGAAAAA TACTACCACA AAATGGAGTT GTGGGTGATG GTTAGGAAAT 660 TAGACAAGAG CCATATAAAC AGAAAGGCAC TTCTTTTAGT TTTCTTTTTT TAAAAGTTTT 720 TTTTTACTTT TGTTTTTTAC AATAAAGAAC AGGACAAAAT GCATTTCTAT CCAATTGAAT 780 GATTTTAGTT AGTGAATATT TTAAAGAGAA AGTGAGTAGG GATGGTGGTA GAGGGTTGGA 840 GAAGACTCAC AGGGTAATAA ATCATAGCAA TTTAGAGAGT ACAGTTTGGG ACTATGCTAC 900 CATGGACTAG ATAAGGGTAT TAACTGGGAG CTAGACCTCT GGGTACTGAC ACCATGGGCT 960 AAATTAAGTG AAGAGCAGAT GAGGGTCACA CTCAAACCAT TCCCACCCCT GCTGTCTAGG 1020 TGTCATCTAC ATCTCAGCTA TAGCCAGAGA CCAACTTCTT AATGTTAGCT GGTTTGCTCT 1080 AGCTAAAACT GATTAACTTT ATTGAGGGCT AGTTTTTCTC TCTAAGAAGG TCCTTTTATT 1140 TACTTATTTA TTTTTGAGAC GGCATCTCGC TCTGTTGCCC AGGTGGGAGA GCAGTGGAGC 1200 AATCTCAGCC CACTGCAACC TTTGCCTCTG GGGTTCAAGC GATTCTTGTT CCTCAGCCTC 1260 CTGAGTAGCT GGGATTACAG GCATGCACCA CCATACCCAG CTAATTTTTT TCTTTTTTTT 1320 TTTTTGGTAG AGATGGGGTT TTACCATGTT GTCCTGGCTG GTCTCAAATT CCTGGCCTCA 1380 AGTGATCCGC CTGCCTCGGC CTCTTAAAGT GTTGGGATTA CAGGCATCGT GAGCCATGAC 1440 ACCTGGCCAG ATGGTCCTCT CTTTGCCCAA CTTTGTGCTA TCAGGAAGGA GGCCTGAGGA 1500 GCTATGAAGC ACGGACCAGC ATCTTTCTAA ATAACCAGAT CAACTGAATC AACTGTTATA 1560 GTCAAAGGAG TGACAGATAC TTCTTTAGAT CCTTCCTTCC TTGCATATTA ACAAAGTTAA 1620 CTTACATAGA ACAAAATACA CATCTTTTTA CAACATGCAA TTTTCATTGG TATATAGTGC 1680 AATGTTTTCC AACACAAAGT GCCTCTCAGT CTGACAAGAA TGATTCTTTA GAAAAGATCC 1740 CAGAGTTAAG ATAACCTGGA AAAGACAGCA GTAAAATAAA CCTTCTTCAA AAAATATTCT 1800 CAGAAGGTAG GAAGGAAAAG TGTGGTAGAC ACAGATATGT GCTGTCCTTC TGAGAAGGAC 1860 GTCTGCTTAG CTGTGGGGCT TTGGGGAGTG TGGTCAGCAA GATTGCTTCC AGCTGTCAGC 1920 TGCTTTGGGC TCTCTCAGCT AGAGACAGTC ACTTGGCCAG GTTTCTGCCT TTTCTAGGAT 1980 GGTCTGTCAT AACTGAGGGA GGTTTCAGCC CACCAGGCAG CTCAGATTGG CAATACACAT 2040 TTCTGAGCCT CCTGCCAGCT TCCTGAAGAC TTTATTAGGC CTGCGTTGCA GTTCAGCAAC 2100 TTCCTGATTC CTCAGTCCTG CTTCCACATG CTTTCTTTCA CAGGTGTTGA CTCTTAACAA 2160 ATAAGTGTCT TGCATCACAA ACGCCAATGA GATGTCTGCC GGGGAACCCA GCCTGTGACA 2220 ATTGGTGTCT GTTTCTGAAA AAGCAGGCAG TAAGATGCAG ATCTGTAAGG CAAAACTGTG 2280 AAGCAGACAG AATATAGTTC GAGAGCACCT CCCATTGCCC CATCTGCCCT GTTCCCACCC 2340 TACTGCCAAA TGTTCCCTTC CCAAATATCT AGGGTGGTCT TGCTCTTCTG GATCCCTCCA 2400 CTTCCCCATC CTATGGTTCC CTACACTCTA GGTCCTTTTG CTTTTGTCTC CTGGATATCA 2460 AAATTTATGT CTAATATATA GTACATGTAG GTATGAACAG AGGATGGTAT CTTAATGTTG 2520 CACTCAAAAA ATGTTTTCCC TTTACTGGGT ACAGTCAATT GGCATTCTTA AATATTGACT 2580 TTGTGCTATG AAATGTGGAA GGGATTGGTT TCTTGCCCAA GAGTTTCCTT GTTAGTTTCA 2640 CCTGCCTTCA GCCTTGTCCT TTGTACATGT GTTTGCCACA CTGTCCCTTA AACAGCCTTT 2700 CTTTCTTTTT TTTCTTTCTT TTTTTTTTTT TTTTTTGAGA TAGAGTCCTG CTCGGTTGCC 2760 CAGGCTGGAG 2770
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