Tag | Content |
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EnhancerAtlas ID | HS101-15978 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr15:93467780-93470470 |
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 | chr15:93468877-93468895 | CTTTCCCTCCTTCCTTTC | - | 7.36 | Nr2f6(var.2) | MA0728.1 | chr15:93468249-93468264 | TGAACTTCTGACCTC | - | 6.38 | RARA | MA0729.1 | chr15:93468246-93468264 | TCTTGAACTTCTGACCTC | - | 6.88 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_27751 | chr15:93468143-93470213 | Fetal_Intestine |
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| Number: 1 | ID | Chromosome | Start | End |
GH15I092924 | chr15 | 93468221 | 93469825 |
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Enhancer Sequence | AGGTATCTAC TTTGCCCTGC AGTACAAATG TGCTGCTAGC CTAGGACAAG CTAGCAGACC 60 TTTGTTGTTC ATGAAAACTC ATTAGTATAT CTTGATGATG AAACCTACAG CCATTTTTTC 120 TAGTAATATA CAGTAGTATA TCTGAGGATA CAAATGAAGA CTTCTTTCTG CTCTATTAAG 180 GAAAATAAAT GACCTGAACC ATCCAATTAT AGGGAGGAAA GACAAATTTT TATACGCTTG 240 GTTTTTAACT TTATTTATTT ATTTTTGCAA CAGAGTCTTG CTCTGTTGCC CAGCCTGGAG 300 TGCGCAGTGG CACGATCTTG GCTCACTGCA ATCTCCGCCT CCCAGGTTCA AGTGATTCTC 360 CTGCCTCAGT CACCCAAGTA GTTGAGATTA CAGGTGTCTG CCACCACGCC CAGCTAATTT 420 TTGTATTTTT AGCGGAGACT GGGTTTCATC ATGTTGGCCA TTCTGGTCTT GAACTTCTGA 480 CCTCAGGTGA TCCACCTGCC TCGGCCTCCC AAAGTGCTGG GATTATAGAC CTGAGCCACC 540 ATGCCCAGCC TAAAATATAT TTTTAAGGTT AAAGTGAGCA GTTCCGGAAA GTTAATAATA 600 TGTAGTTATA GGTTGGATGG ACCTACAAGC CAGTCAGAAT GATTGCACTG TGCCTTTGAT 660 AATCATTATC CTAAAATGAG AACTTCTAAG GAAGGCTCTT GGTTTTCTAT GTACACCTCC 720 TTTTCACATG GTAGCTCTCT GTCCCCCTCC AAAAGCTTAT TACTCATGTA AGAGTACTCA 780 GTAGTGAGTA ACTCCACATA GTAGATTTTT CATGGAGGAG TTGACTTAGA TATCGGCTCT 840 CAAAAGGACA AATAAGAACA CAAGATAATT TTAGGATGTA AACATTATAA TATATGCTGT 900 AATAAAGTCA TAATAGTTGA GCTAGAATGC CTGGCTGGTA TCTTGAAGTG ATAAAACTAG 960 TTGATGTAGT AACACTGAAA TGATTTTGCC CTCCCAGTTA ATAAGGGCTC CATAAAAACC 1020 TGTGTTGAGT AAAAACTTTC ATAGCTCTAG CAGAGGGCCA GGTGTGGGCA TGGATAGACA 1080 GGCTAGAGTA AAGCGCACTT TCCCTCCTTC CTTTCTCTGC CAGGTTTTTT CAGAGTGTTT 1140 TATGTTTACT GCCTCTACCT ATATTTCCTA CCATTTGGTT ATTCCTAACT CCTTCTGTTT 1200 GGACCTTTTG TCCTTTAACT CCAAGGTGAT GCTAAGGCCG TTACAGAATC TGTGGACTTT 1260 GGGTTATGTG ATTACATTGG ATTCTAGTTG TAAAATGCCT ATTCTGGGCC ATCTTTTCTT 1320 TTGAAGCCTT GATTTTCTTC AGCTTACTTC ATCATTTTTA TGTTGTTGTT GTTGTTGTTA 1380 AAGTCATTGT TGATAATGTC CTTTCTTAGT GACATTGTTG GATCATTTTT CATAAAGATG 1440 AGACAGGGTC TTGCTCTGTC CCCCAGGCTG GAGTGCAGTG GTGCAATCAC AGCTCACTGC 1500 AGCCTTGATC TTCTGGGTTC AAGTGATCCT CCCACCTCAG CCTCCCAAGT AGCTGGGACT 1560 ACAGGCACGT ATTGACACAC CTGTCTAATT TTTAAATTTT GTTGTAGAGA CAGGATCTCC 1620 CTACGTAGCC CAGGCTGATC TTGAGCTCCT GAACTCAAGC CATTCTTCTG CCTGGACCTC 1680 CCAGGGTGGT GGGATTACAT GCCTGGCCCT ACACTTTTAA ATACAAACAT TTCACAAGTC 1740 TCAGCTAGTG GCTTCTTTTG TGCATGTTCT GAACCTTACT TTTCCAAATA TTCTCATGAC 1800 GTTAGCTGTC ACCTGTAATT TGATAACCCA TATTTCTCAT CTCAGCTTTT GCTACTTGCT 1860 TAATTTCTGT TACACCTTTT CATGTCAGTG TTCCACAATC CATTCAAATT CCTTTTGCTT 1920 ATGTGTGATT CTGTTAAAAG AATACAGAAT ATACTTAGTA GTAGTTATCT CTGGGGAAGA 1980 AAGTGAAAAT GATTTTTCTC CTCAACTAAT CTGTCTTTTA AACTTTTTAA ATCACTGGTG 2040 AGGATTGTTA CAGGTCTTAA AGGTTGTTAC AGGTCTACAA AAATCAGGTC TTAAAGGCAA 2100 AGGGCTAATT ACTGCTACAG AATAAAAAAT AGATGTGTTA GAGAAAGGGT GGCAGTGGTT 2160 CTCATTCTGA GAACTTCTAG CTAAGTGTTA GCAATGCCTC ATCTGCGTTT ATCTGGGATG 2220 TTACATGACC TGAGGAACTT AAAGAAAAAT ACAAATTCCT GATTCTTACT TAATTAGACT 2280 TAATGGGGGC TTTGCCGCTT GTATTTTCAG TTTCACAGGT GTGGGTTAGT GCAGTCAAGA 2340 CTGAAACTCA AAGCAGTAGG GAATTTAAAA TGTATCAGTA AATACTTTGT CTTTAGTGGA 2400 AGCAGCCGCT GTCTTACCTT TCTGTATTAT TCAGCTGTAT ATTTTAATGA TGGGTAAGCG 2460 GTGTACCATA TAGATTTATA GCTGTTAAGT AATGAAGACA TTGTTAAACT AATATTTCCT 2520 AGGATAATAT GCCTATTTTA AAAAAAATGG CGCTTTATTG TCTCATAAAT AGAACTAGCA 2580 AAACAACCCT TTTGATACTT GGTTACTTGA ATTCTCTTCA ATTGCAATAA ACGTTTGATA 2640 ATAATAATGG GGGTCAAGAA AAAAGATTAA TGCGTGGTCT CTTAATTTTA 2690
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