Tag | Content |
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EnhancerAtlas ID | HS092-15026 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr13:97776550-97778960 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF16 | MA0741.1 | chr13:97777875-97777886 | GACACGCCCCC | + | 6.32 | SP8 | MA0747.1 | chr13:97777875-97777887 | GACACGCCCCCT | + | 6.27 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_47388 | chr13:97772197-97779914 | Panc1 |
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| Number: 1 | ID | Chromosome | Start | End |
GH13I097124 | chr13 | 97776589 | 97781246 |
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Enhancer Sequence | CCAGCCATTG AGTTGATCTG GAGATGAGAC TCTGGGCAGA CACTGATGCA ATGCAGGTGA 60 GTGTGCCCCC AATAGCCCAG GCCTAGATGA CTCCTTCTGT CCCCACCAAC TCCTGCATGT 120 GGTGCTTGGC AGGCCACCCA CACGCCTTCA TCGAACCTTT TCCTTACAAG CTCCTGAGCT 180 CTGCCTGCCC ACCTTCTCTC AGCAAGTTGC TTTTTTGCAC AAATTACTCT TTTTTATAAG 240 CATAATTCCC AAAGAGAGAA TAAGAAGCTT TCTGGCGTAT CTATTAATCA TGAGGGAGAT 300 TGGAAGCTGG GAATAAGGAA AAGGGAGAAA GAGACCTATA AACTAAATAG AAAATGCCCA 360 TCTGAAACAA GCCTTCTCCG ACAGGCCCCC GGTAGGACCT GCACTCCTGT CCCTTACCTT 420 AGATGCCTCT TCCCTTTTCT TGCGTGTGTG TTGGGGCGGA GGACGGACGG GGTTAGGCAG 480 GGGAGCAAAG AGACTTTTCC CCTTTTATTT TCTTCCGTGA ATTATGACAA TGGTTTGAAG 540 TGCTCTTGCC TAGAAAACTG TGCTTGGAGG AGTGAAAATG AAAACATTTC AAGGTTGTAA 600 GGTGAATCTT CTTCTCTTAC AACCTTGGGT AGATCAACAC CAGGACACCC AAATTATTTC 660 GATTAAAGGA AGATATCTGA GTACAAGCTG CACTGTGCTG TTAATGAACA AAGAAAGAAA 720 ACAGTAATTG TTTTGCTAAG CTGTGTTTAT ATGAACAAAA GCCTCAGAAA GAGTTTAGCC 780 CTTGAAATTC TTCATGGGAC CTTGCGACAT CACCACTTAG GAGGGGGAAC TGATAATATG 840 TTTGCTGATT ATATGTGGGT GAGGACATTT TTGCAAGGGT TCCAGGGGCG ACTTCCAAAT 900 GGACATGAAT ATAGACTCAT GCAGAGGCTG CAGGAATTCA GGCCAATTGT GATACTCTGT 960 GATACTCACA AATTTGGGTC ACTCTCTCAA TTAGTTTAGC TCCTCATCTG TGTGAGTACA 1020 GAAACAAAAG CTACTTGGAG GCCTTGTGGG TTGGCAGAGC ATCTTAAAAT ACCCTCCTAA 1080 AGAGGCAGTG CTGCAAATTC AAAACAGACT TTCAAAATAA ACTCAGCAGG GCAGCACTCC 1140 GGGGGTGCTT CCAGAGCCAG CCCCCACCCC ACCCCCAGTT CTCAGTTCTA GGTGTTTGAA 1200 ACTGCAGTAC CCTTGGCTGT TACAATCCTC CCCTCCCCCA TGAGCCTGCT TCTCCCTGGA 1260 GGAATCAATC ATTCTGCAAT ACAGCTGAGA TTTCTACCAG TCCAGATGCA AGCTTTCACA 1320 AACCCGACAC GCCCCCTGTC TTCTGTTAGT CATTATCAAT CTTCCCGTTG TGGTGGAGGG 1380 AATTAGGTGT ACTTAGTGAG CTCTCAAATA AGTAAGTGGT CATGTGAAAA GCCAGGCATA 1440 TGATACATAC AGTCGGATCA GGACTTTAAT CTTGGAAGTC GTCTGGGACA TGGGGTGTTT 1500 TGCAGTAACA AGGACAATTC TCTCAGAACT AAATCCAAAT TCTGTCTGTC CTGTTTGTCT 1560 CAGGCATTTC TGCCACCAGA GCAAACTTTT TATGCTTTGG AGCATAAGTA CAGATCATCT 1620 GTTGTGCTTT AAAGTGGGTG TTTTTTTTTT TTTTTAAGGA GCTAATTCGG TTGTGCAATA 1680 CCATCAAGAG GCGCCACTTG TAAATTATAT TTAGGTGTGT GTGTGTTCCT CCCCTCGCGG 1740 GGCTGATGAA TCATATCCAT CTTCGTGTCA TTATGTAACT CTACACTTGC AAGAAGGGCT 1800 GCGAGCCCCT GCCATACACC AGAGGCTCCT GCCCATCTGC GCTCCACCCA GCAGGAGGGT 1860 CTCTGCTCTT CCAACACCAG CCTTGGCCTC TCTGCGGAAA AGCAAGTGTA GTGACTAACT 1920 CATCCTCTGT TCCCAGTTTT AACTGAAGGT CCTGTGTTCA AATGGGATCA GCTGGCCACA 1980 CTACCTGGTC TGGCTCTTTG CCCATTTCTG GCCTCAGGCG CTGAGGGTGT GGACATTAGC 2040 ACGGGTCCTA TGGGCTTGGG GTTCCATCCA GGCCTTCCTG TTCTAACAAG AAATCTGGAA 2100 GACTGCACAC CCTGGAGGCA GGAGGCAGGC CTGGGGTACA ACAAGATCTG CTGTGGTCGT 2160 GGAGAAGAGG ACAGCACTCC CTTTCCTCGT GGAAGTATGG ACAGGTGTGA AGGAGTTCCC 2220 TGTGCCGAAG CAGACAGGGG CCCTACAAGT GAGAGGTTGC TATTTCTATT ACATGGCAGT 2280 AAGAATGAAA CCAAGAGTCA TTGTGTATGT GGGGGAAGAA CACAAGGTTG GGAGCCAAAC 2340 TGGGTTTATA TATTAGTCAT GCCACTCATT TATTGTTTCT GGGATGAATT ATTTAGTCAC 2400 TGTCAGCCTC 2410
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