Tag | Content |
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EnhancerAtlas ID | HS003-00413 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr1:16493580-16496380 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
PLAG1 | MA0163.1 | chr1:16494542-16494556 | TCCCCTTGGGCCCC | - | 7.12 | RFX1 | MA0509.2 | chr1:16494467-16494483 | CGTCGCCATGGAAACC | + | 6.38 | RFX1 | MA0509.2 | chr1:16494467-16494483 | CGTCGCCATGGAAACC | - | 6.4 | RFX2 | MA0600.2 | chr1:16494467-16494483 | CGTCGCCATGGAAACC | + | 6.6 | RFX2 | MA0600.2 | chr1:16494467-16494483 | CGTCGCCATGGAAACC | - | 6.73 | RFX5 | MA0510.2 | chr1:16494467-16494483 | CGTCGCCATGGAAACC | - | 6.26 | RFX5 | MA0510.2 | chr1:16494467-16494483 | CGTCGCCATGGAAACC | + | 6.27 | RREB1 | MA0073.1 | chr1:16494145-16494165 | GGTGGGGGAGTGGGTGGGGG | - | 7.01 | ZNF263 | MA0528.1 | chr1:16494579-16494600 | TCTCTCCGCCCCTCCTCCCCA | - | 6.12 | ZNF263 | MA0528.1 | chr1:16494004-16494025 | GGAGGAGAGGCAGGTGGGAGG | + | 6.37 | ZNF263 | MA0528.1 | chr1:16494576-16494597 | CTCTCTCTCCGCCCCTCCTCC | - | 7.1 |
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| Number of super-enhancer constituents: 14 | ID | Coordinate | Tissue/cell |
SE_23091 | chr1:16493730-16494938 | Colon_Crypt_1 | SE_23091 | chr1:16495015-16496277 | Colon_Crypt_1 | SE_23751 | chr1:16493699-16494633 | Colon_Crypt_2 | SE_24743 | chr1:16493660-16494922 | Colon_Crypt_3 | SE_26540 | chr1:16493665-16496410 | Esophagus | SE_31527 | chr1:16493631-16494622 | Gastric | SE_34268 | chr1:16493420-16495012 | HCT-116 | SE_34628 | chr1:16493224-16496455 | HeLa | SE_47150 | chr1:16493248-16496088 | Panc1 | SE_56795 | chr1:16493661-16494984 | VACO_400 | SE_56795 | chr1:16495015-16496331 | VACO_400 | SE_57357 | chr1:16493697-16494611 | VACO_503 | SE_57939 | chr1:16493722-16494629 | VACO_9m | SE_65472 | chr1:16493525-16494995 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 16495240 | 16496278 | chr1 | 16493800 | 16494448 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I016167 | chr1 | 16493630 | 16496219 |
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Enhancer Sequence | GGCACGCGCC ACCACGCCTG GTTAATTTTT GTATTTTTAG CAGAGATGGG GTTTCACCAT 60 TTTGGCCAGG CTGGTCTCGA ACTCCTGACC TCAGGTGATC CACCTGCCTC TGCCTCCCAA 120 AATGCTGGGA TTACCGGCAT GAGCCACTGT GCCCGGCTTC CGTTCTTCCT GATTACTTAA 180 GAGGGGCCTG ACTAATGCCC AGCATGGTTG GGGACCCAGG CCCCTCAAGC CCTGGAAGTC 240 CCTTGCCTGG GGTCATCCAG TCTCCTCCCT CAAAGGGCTC TCACTCCCCA CCGCCGCTCC 300 CTCTCCTCTT CCTGCTGCTG AGAGACGAGA GACCAGCAGA AAGAGACTTG GAGAGACGGA 360 GACACAGAGG CAGATGGAGA ATGCTGGGCG CCCGGGAAAG CCCAGGAAGG AGCCCGGGCC 420 ACGTGGAGGA GAGGCAGGTG GGAGGAGGCA GGAGAGAGCA AGGCTGCCCA GGACAATGGA 480 GCGGGACCGG AGGAGACGCG GGGAGGGACG CGGGCCAGGG GTGCGGTGGG GGGCACGGGG 540 TGGAACTCCG GGTCCCGTAG GGCGGGGTGG GGGAGTGGGT GGGGGGATGG CCCACCTGCC 600 GTGGGAGCGG GTCCGGAGGA AGCTAGGGTC TCGGGGTGGG AAGTGCTGTG TAGAAGCGAG 660 CGCAAGAGGC GAGAGGAAGC GCGGCGGGGC GGCCCCTGTC CCAGCCTCAC CCCCATCCCC 720 CCAAGTCTCG CACCCCGGTC CGCCCCAGCT TCCGGCTCCG CAGGTGCCGC CTTTGAGGGC 780 CGCCGCTCGC AGTTTACCGC GGAGCCGGAG CCAGAGCCCC TTCCCCGCGG CGAGGAACTG 840 CCTCTGCGTC TCGTAAAAGG GGTCTGGGCC TGGGGGGCGG CGGCCTCCGT CGCCATGGAA 900 ACCGGGGCGG GGAGGCGGCG GCCCGGAGAG CCCCATGCAC TTTGCATACC ATTGCAGGTT 960 CCTCCCCTTG GGCCCCGCCA GCCTCGCTGG GCCCGCCTCT CTCTCCGCCC CTCCTCCCCA 1020 AACCCATCAC CCTTGCCTTT ATTTGTCTTA AATTTATTTT AAAATGTATT TATTTATTTT 1080 TTTCAAACAG GATCTCGCTC TGTCACCCAG GCCAGAGTGC AGTGGTGCGA TCATGACTCT 1140 CTACAGCCTT CCATCTCCCC AGGCTCAGGT GATCCTCCCA CCCCAGTTTC CCAATAGCTG 1200 GGACCACCAC GCCTGGCTAA TTTTGTGTGT GTGTGTGGTG ATGTCGCCCT CTGTCACCCA 1260 GGCTGGAGTG CCGTGGCCAG ATCTTGGCCC ACTGCAACCT CCGCCTCCCA GGTTCAAGCA 1320 ATTCTCCTGC CTTAGCCTCC TGAGTAGCTG GGATTACAGG CGCGTGCCAT CACACCCGGC 1380 TAATTTTTTT GGTATTTTTA GTAGAGACGG GGTTTCACCA CGTTGACCAG GCTGATCTCA 1440 AACTCCTGAC CTCGTGATCT GCCTGCCTCA GCCTCCCAAA GTGCTGAGAT TACAGGCGTG 1500 AGCCACCGTG CCTGGCAATG CCCGGCAATT TTTGTATTAT AGAGACAGGG TCTTGCCATG 1560 TTGCCCAGGC TGGTGTTAAA CTCCTGGACT CAAACAACCT GCCCACCTCC GCCTCCCAAA 1620 GTGTTAGGAT TACAGGCATG AGCCACTGCA CTCGGCCACC CCTGCCTTTA AAAGTCACCT 1680 CCTCCAGGAA GCTTTCAGCC ACCACCACCA CGCCCGGTGG CACCACTGAC ACTTCATAAC 1740 AATAATAATT CATCATCACT GTGATCGTGG CTAGGCTTGG CTGAGCTTTG TCTCTGTGCT 1800 TCCTTCACCC CCATCTTCTT CTGTCCTCAT ACCAACCCTG TATGGAGAGG CCACTTTTGT 1860 CGATATTTAC AAATGAGAAA ACTAAAGCTG GTAGGGGGTC TGCTCAAGGT CTCACACCTG 1920 GAAAATTCCC TCCTCATTCT AGTCTCAGTG TTCTCATTTG TAAAAAGGGA AGCTCGCACC 1980 AGGCGCTTGC CGAGTGACCA CGCAAGGGTG GGAATGAGAC CGCAGGTTTG TCTGAGCAGG 2040 GGCTGAGTGT GGCATTCTGA CTCTGAAGGC CTGTAGTCAG GGTATGCATG CTCTAGTTCA 2100 CCTCAGCCCG GCTGCGTCAC ACCCCCACTC TGTCCCCCAG TGCATCCCCA CCCTTGGGAC 2160 CCTAAGTGAA TCTCTCCAGA CCAAGCTCCT AGTGACTCAA GAGACATCTC TAAGGGGTCT 2220 TCCAGCTCTG CCATTCTGAA GTCTTAGCTT ATTGAGAGGG TGACTCCTTG TGCTGTCTCC 2280 CTCCTCTGAC TGGATGCTCC TGGGGGTGAG GGGCTGTGCC TCTCCTGTCA GACGGGACAC 2340 TGCTAAGGGT TAGGACACCT CTGTCACTCC CCTAGGTCTG TGGTCACTAG AAATGCCCAA 2400 ATCCAGGCTG AAGGCTGACC ATGTCTCTCC AAGCACAAGC ACACCCCAAG GTGCCCCAGT 2460 CCCTTGTCCT GATCCTGAGA TCTGAGGTCT ACAGGACTGG GTTCTTGGTG GGGAAACCTC 2520 CAGCTCTGCC ATAAAAAGAA AGCCTCATCC CAGACCTTCA GACCCGTTCC AGCACAGGCT 2580 CAGAAGAGGA GAAATGGGCC CAGAGACAAC TTCCAGGGCA GCAACACCAC AATCATCATC 2640 CCTTCTATTT AGTGATCTTG GCTATGTGCC CAAAACCTTT TTTTTTGAGA CAGAGTGTCA 2700 CTCTGTCGCC CAGGCTAGCG TGCAGTGGCA TGATCTCAGC CCACTGCAAC CTTCATCTCC 2760 TGGGTTCAAG TGATTCTCCT GCCTCAGCCT CCTGAGTAGC 2800
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