Tag | Content |
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EnhancerAtlas ID | HS059-12380 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr13:30145670-30148120 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr13:30145945-30145957 | AAATGTTTGTTT | + | 6.27 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_27414 | chr13:30145631-30147850 | Esophagus | SE_27414 | chr13:30147867-30148354 | Esophagus |
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| Number: 1 | ID | Chromosome | Start | End |
GH13I029572 | chr13 | 30146797 | 30148177 |
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Enhancer Sequence | GGGGGGTCCT CACTCATGGA TAGTCCCGCT CACCCAGAGG CCTTTCCATC TCAGTTTGGC 60 TTTTGGGCCA AATTTGGAAG CATTACACTT CATTAAGGAA ATGAAAGGCT TTTGCTTTAC 120 CTATTCCACC AGAGGGGCGG CTTCTCCAAT TTCTTCCACT CTGAACTCAG GCGGAAAAGG 180 ATTGCCCAGT CCAGAGCCGC TTTCCTCCTT CCAGGAGGTC TGGACACTCA CAAAGCCCAG 240 TTATTTGTTT TGCAAACTGT GTATACATTG AATGGAAATG TTTGTTTTCC ATATCCCGCT 300 TTACGTCTCT AAAGACAAAT GATTAAAGAA TCATTTCAAG GGCATTTTTT GTTTTGCTCA 360 TCCCCTCCAA CCTGCTTGTA TTAAGCAGCC TCACTTCCTG CCTTTTAACT TACATTTCTG 420 TCCACCTATC ATCCACTCTT CTTTGTTGAC CTTTGCGTGT ACAGTGTTGC TTCAAAAACC 480 TTCAAAGGAA AGGTCAAAGT GAAATGTCAC AAGGGAAGCA GGCCTGATGG CCAGTGGCCA 540 AGGAGGCACC AATGCCCAGG TCTGAGGCTG CCTGTGGCAT GCATGACACT GCCCCAAAAC 600 GCAGGTGGTG AGGGTGCAGC GGCCGCCTGT GGGTCCCAAG CACGACTCCA AGTGCGACAC 660 GCTGTCTAGG CCATCTGGTC CCACACCAAG TCACATCTGT GCCCAGAGAA GCCCAGTGGA 720 CCAGTGCGGG CCCCCCAGCC CTCAGGGCAG AGCCAGGACG CTTCACACAA GAGTCACTCA 780 TTGGATTTTC TACTCCACGC ACACGCTGTC AATAATGGCA GGCGCCACCT AAAGGGGCAG 840 GTGCCAGTGT AATTTAACAG GGGAGAAAAA GTACAGAGGC CACCCAGGAG GATGCTGGAA 900 AGACAGAGGG TGGGGAGTGG GAAGAAACAC TCAGGACCCG CGGCACCAGG GCGTGGGACT 960 AGAACGAAAA GCAAGAAGAC CATGTGAGGG GCAGGGGAGG AAGGACTGGC CGGATGCCAT 1020 CAGTTATCAT CAATATGAAG GGAATGAGCC CAAGGTAACT CTGAAATCCT AAACTTGGAT 1080 TTGGAAGCAC TGAATCTGAG CTGAGGGTGG CCCTCAGTAA GGCACTGTGG CCCTACCGCT 1140 CTGGTTCCCC CAGTCGTTCT CTGCCCTAGT TTGTAATCTA CAAAGTGATC AGAAGCTCAT 1200 AAAACATGGG CACGAGCACT ACAGTTGACC AGCACTGGGC GGGGAAGGTG ATCCTGGGAA 1260 ACCTGCATGG GACTGTGCAC ACCAACCACA CCAACCAGAA GCAGCCAACA CACACAACCG 1320 CAAGGGCCAA CTCAACATGG TAATCAACAT CTAAAGCTGC ACAATTTGAT GGAGGAAAAC 1380 TCCACTTGGA AGGGATAAGT GGTCCAGGAG AAACAGAGAC AGAAGCTCAA AGCTGTCAGA 1440 TCTGCCACAG ACAAGTGGCT GGTAAATACA AGAAACCTTT CTTGAAAATG CAGATAGCAA 1500 ATAATCTATC CTGGAGAGAA TAATGTCACG AAACATGAAA AATGTAAATG GTTTATTTGT 1560 GCTCTAAAAA CACAATGATT TAAACTGAAG GTCACTCAGG ACAATATTGT CATCAAAAAA 1620 TTCTTTGGTG ATGACATATA TCTGATAAAA TATTTATATT CCTAAATGAC AGTCAAAATA 1680 TCCTCGGATC AAAAAGCAGT CTTGCCACAT GTCCTGTGTC CAACAGAACA GATAGAACTA 1740 TCTGGCAAGC AGGTGGGGCT GTGAGAATCT GAAACGAGGA ACTTGGATGT GGAGCACACC 1800 CAGAGGCACG TGTTGCCGGG AGTGAGATCC CTGGGAGAAA AGAAGGCAGC TGTTACCAGA 1860 ATCGCGGGGA ACACCACACT CTGGCAGCTG AAGGAGGAAG TAGCACACAG ATGATGGGGA 1920 GGTGCAATTC TAGAGTCCAA AGGCAGACGG ACTTCTCTAA AGCCAGAGAG TGTCTGACTC 1980 TGTGTGTCTG CCTTAAGGCC CACATCGTCC CCTTTCAAAG TGCACCAGGA GCCACAAAAG 2040 ACAATGTGAC TGGATGGTAA CTTAGCAAAG AGCTGTCAGA TCAAATACAG GACTGCCCAG 2100 TTAAATCTAA ATTTCATGTG AATGACCAAT AATTGGTTAA TGTAAGTATG CCCCAAATAT 2160 ATCACAATGA TGTCCCAAAT ATTGCCAACA AATAATCTTT TAGTATAAAA AAGTTATACT 2220 AAAAAAAGTA TCCATTGCTT ATTTATAATT CAAATTTAAC TGGGCATCCA GTATTTTTAT 2280 TGCTAAACCT GGTAACCCTG GTTTGGTACT GACAGCTCAG GCCTCAGGCC TGAACACCTC 2340 CCCTTTGCCC AGCACCTTTC TAGCCGCAGA CCATGAACCC TGACTTCCAC AGGCATTTCT 2400 GCGTACCCAG CTACTAACAA GCAATGACTC CATTCTTTGA CAAGCTCTCT 2450
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