Tag | Content |
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EnhancerAtlas ID | HS059-06119 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr10:79252910-79255490 |
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) |
GFI1 | MA0038.2 | chr10:79255295-79255307 | TGCCGTGATTTC | - | 6.32 | NFYB | MA0502.1 | chr10:79255280-79255295 | ACATCGGCCAATGAG | + | 6.14 | SPI1 | MA0080.4 | chr10:79254718-79254732 | AAGTTCCCCTTTTT | - | 6.2 | SRF | MA0083.3 | chr10:79254811-79254827 | TTTCCAAATAAGGTCA | + | 6.01 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_47394 | chr10:79253866-79255202 | Panc1 | SE_65439 | chr10:79252812-79253539 | Pancreatic_islets | SE_65439 | chr10:79254027-79254618 | Pancreatic_islets | SE_65439 | chr10:79254824-79256429 | Pancreatic_islets |
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| Number: 2 | ID | Chromosome | Start | End |
GH10I077493 | chr10 | 79252813 | 79253539 | GH10I077494 | chr10 | 79253867 | 79256429 |
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Enhancer Sequence | GCTTCTGACA AGGCTTCCTA AATGCAGAGC CCTGGCTGCA GATCAGGAGA CCCTGGCCCC 60 TCCAAGGGCA CCCCGGCTAA TCAGCCTCTT CTTCTGACTT CTGACTCCAC CCCAGGACAG 120 GCATGGTGCT TCGAAAGCAG AAGTAAGGCA GCAGAACACT TGGAGAAGCC TCGCTGAGGG 180 CCAGGGCCTG GTGGTTCGGA TGGCAGCAAG CTGCCCCCAG GGACCCAAAA CCCAAAGGTC 240 AGGAATGTAG TACTGGCCAG CCAGGGCAGG CACTGCTGTG TGGTAGAAGA GAAGTCCAGA 300 ACTGTGAGGC GTCAAGCGTG AGTTGGAGGC AGGATGGCAG TGAGAATGCA CGCCCAACTG 360 AGCGAGTGCG TGTGAGTGAA TTATGTGTGT GGTTCAGTTT TAGGCACTGG GCAGATTTGC 420 AAAGCTCATC ACCCTCCTAG AGTTGCCTGC AAAAGGCCAC ATGTTTAACA CCACGTCAAT 480 CAATCAACGG AGGTGCACTG GGTGGGGAGT GTGTGGCCAA CCCAGCACGG GGAGCCGTGC 540 AGCTGCAGGG AAGAGAGCAT CTCTTTCCCC AGTGGCTCAT GGTCATAGCC GAGGACACAA 600 GACTGGCCCT TGTGGGAAAA TTGAGGGGAC CTGTTAAATG CTGACCTCTA ATGTGGTTCC 660 AGTTGAGTCA CCATATTTCT TGTGAACCTC CAAAGCACTG GAAGACTTCT GGGCCTCGCG 720 TGGCTGCAGG TGAAACATAC AGCCAATCAC TCCACCCTGG AGTCTTGGTT TCCTCCCCTG 780 CAGAATGAGA GTGACGCTGA TAAGACATCT CAGGCAGAGG CGAAGGAGGT GAGCCCTGTG 840 GGAATTTCGG CTGCCCCTGT GCCAGGCTGA ACAAGACAGG GCCTTTGCTT TCTGGGGGCT 900 GATGAGTCAT ATAAAGGGGA TAGAATCAAA CACTCAAAAG ACAATAACCG CAACACAGGG 960 CTGGGTGAAT AAATACACAA CTGGCTACTC AGAATGGGAT AACCATGGGA GAGGACTTTT 1020 AATGCCAAAG AAACTCACCA CGTTGCCTTT GACTTTGAAA AGTGATCTGT GCTTAATCTG 1080 GCATTTCGCC AATTGGACCA TGAGCAATGG GGTCCCAGTC CTCATTACCC AGTGCCTCCT 1140 TTGCTTCAGG CCAGGGCTGA ATAGGTACTT AGGACATTCC TAAGAAGGAC TGTGCAGGAG 1200 GAGGCTAGCC CAGCTGCCTG GCTAGCCTCA GCACACACAT TCCCTGGAAC AGCAGCCTCG 1260 CTTACTGCCA GACCCCACAG GGGTTTCTGC AGGGGCTGGA CAAACGGGCA CATGGGGATG 1320 AAAAGGGTAG AGTCCCCAGA GTCAGTCAAT GTCAGTGAAT TGGCAGCCGC TGCTCACAGA 1380 GCTGTCTGGA TTCTTTGCAG CCCAGAGAGC ACCTTTCACC ACCCAGATGG GGAGGCCTTG 1440 CCAACCCTGA GCCCCTCAGG GAGGTCATAC GTGTGATTCT CAGACACCAG AGGGAGCAGT 1500 TTTCCAGAGA GTGAAGAAAT GGGATCCGGG AAGCTTGGTG AATTCGTCTG CTGGGGCTGC 1560 CATCATAAAG TATCAAAAAC TGAGTTGGAT TAAATAATAG AAATGCATTG TCTCACAGGT 1620 CTGGAGGCCA GAAGTCTGAC ATGGAGATGT CGTTGGGGTC AGTTCCTTCT GAGGGCTGTG 1680 AGGGCACATG TGTTCCAGGC CTCTCTCCTA GTTTTCTTGT CCTTCCTTGG CTTACAGATT 1740 CATCACCGCA ATCTCTGCCT TCATCTTTAT AGGCATTCTC CCTGTGTGCA TGTCTGTCTC 1800 TGTGTCCAAA GTTCCCCTTT TTATAAATAT GACACCAGTT ATTTTGGGTT AGAGCCCACG 1860 CTAATGATCT CATCTTAACT TGATCATCTG CAAAGACCTT ATTTCCAAAT AAGGTCACAT 1920 TCACAGGTAC GGAGGGCTAG GACTTCATTA TCTGTTGGGG AGACACAATT CAACCAATAA 1980 TATTTGAGTT CCTCAAAGGA AAAACAGCTT TTTAAAAAGC CAAACTGAAA TTCCTAACAT 2040 TACTAATATA CTGGAACAGA GTCCCAAGAA GTAGGCTCAA TGTGTGAAGG AGCTTCCCGG 2100 TTCCAGCCCC CACGTTACCC CAGCCCAGGC CTTTGTGGCC TCCCGCCTGC ACTGCTCTGT 2160 GATGGGCCCC TTGCCGGCTG CCCTGACTTG GCCTGTCTCC CTTCTGCTAC CTCCGCATCA 2220 GGCTGCCACA CCTTGCATCT CACCACCAGG TCCACCTCGG TCACGACACC TTCCTGGTCT 2280 AAAGGCCCCA GTGGCAGTCA ACCACCCAGA GGGCTGACTG TGGCTCACTC CTTTTGACTT 2340 CAGCACCCTT GGTAATCTGC ACCAACAGAA ACATCGGCCA ATGAGTGCCG TGATTTCTCT 2400 GCCCGTTTTC TCATTCATGA AAGGGAGAAA AAACGAACTC TCCATGCATC TACTCCCAAC 2460 ACATTCCCCT GAGAAGCCTG CGGGGAAGCT CCCTGGGAGC CCATTGCCAA AGCTTCCACC 2520 TCATGGAGCT GGCGTGTACA CAGACAGGCA CAGCCTGCCG TGCTGGGCCA CCATACTGGT 2580
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