Tag | Content |
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EnhancerAtlas ID | HS103-00157 |
Organism | Homo sapiens |
Tissue/cell | HUES64 |
Coordinate | chr1:16492870-16496280 |
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: 17 | 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 | chr1:16492616-16493248 | Esophagus | 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 | chr1:16492706-16493355 | VACO_400 | 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 | chr1:16490206-16493455 | Pancreatic_islets | 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: 2 | ID | Chromosome | Start | End |
GH01I016166 | chr1 | 16492707 | 16493355 | GH01I016167 | chr1 | 16493630 | 16496219 |
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Enhancer Sequence | TGTCTGTCTG TCTACCAACC CATCCATCCA TCTGTCTGCC AGCCCATCCA TCATGCCACA 60 GGCCACTTGT CCATTCTTGC CACCTTTCAC ATGTTCCCTA GTTAGGCCCC TGTGGTATCC 120 CCCAGCCAGC GCAGTGTAGG TGGGGGGCGT GTGTTCATGT CAGTAGATAT GTCTGTGGCC 180 GCCAGCATGC CTTGTGCTGA GCAGAGGGCA AGGGACCTGG ATGAGGAGCT GGGGAGGGGT 240 TGGGGACAGG AAGACTGGGA ACCTCTTGGT GGGGGGCACA GCAGCTTCCC TGTGTATTCT 300 CCCTGTGGTC TGTTGCACCA TAGGCATCAA TGGCCTGCTC AAAAATAAAT ACACGACTGG 360 AAAACTCTCC CACCTCCATT CTTTTTCCTT TTTGGGGGGG TGGTGGGGAC AGAGTCTTGC 420 TTTGTCCTCC AGGCTGGAGT GCAGTGGCAC GATCTCAGCC CACTGCAACC TCCACCTCCT 480 GAGTTCAAGC AGTTCTCCTG TCTCAGCCTC CCAAGTTGCT GGGATTACAG GCCTGCGCCA 540 CCACGCCTGG CTAATTTTTG TTTTTTGGTT TTGTTTTTTC TTTTCCGGGA TGGAGTCTTG 600 CTCTGTCACC CAGGCTGGAG TGCAATGGCC GGATCTTGGC TCACTACAAC CTCCGCCTCC 660 CGGATTCAAG TGATTCTCCT GCCTCAGCCT CCCAAGTAGC TGGTATTACA GGCACGCGCC 720 ACCACGCCTG GTTAATTTTT GTATTTTTAG CAGAGATGGG GTTTCACCAT TTTGGCCAGG 780 CTGGTCTCGA ACTCCTGACC TCAGGTGATC CACCTGCCTC TGCCTCCCAA AATGCTGGGA 840 TTACCGGCAT GAGCCACTGT GCCCGGCTTC CGTTCTTCCT GATTACTTAA GAGGGGCCTG 900 ACTAATGCCC AGCATGGTTG GGGACCCAGG CCCCTCAAGC CCTGGAAGTC CCTTGCCTGG 960 GGTCATCCAG TCTCCTCCCT CAAAGGGCTC TCACTCCCCA CCGCCGCTCC CTCTCCTCTT 1020 CCTGCTGCTG AGAGACGAGA GACCAGCAGA AAGAGACTTG GAGAGACGGA GACACAGAGG 1080 CAGATGGAGA ATGCTGGGCG CCCGGGAAAG CCCAGGAAGG AGCCCGGGCC ACGTGGAGGA 1140 GAGGCAGGTG GGAGGAGGCA GGAGAGAGCA AGGCTGCCCA GGACAATGGA GCGGGACCGG 1200 AGGAGACGCG GGGAGGGACG CGGGCCAGGG GTGCGGTGGG GGGCACGGGG TGGAACTCCG 1260 GGTCCCGTAG GGCGGGGTGG GGGAGTGGGT GGGGGGATGG CCCACCTGCC GTGGGAGCGG 1320 GTCCGGAGGA AGCTAGGGTC TCGGGGTGGG AAGTGCTGTG TAGAAGCGAG CGCAAGAGGC 1380 GAGAGGAAGC GCGGCGGGGC GGCCCCTGTC CCAGCCTCAC CCCCATCCCC CCAAGTCTCG 1440 CACCCCGGTC CGCCCCAGCT TCCGGCTCCG CAGGTGCCGC CTTTGAGGGC CGCCGCTCGC 1500 AGTTTACCGC GGAGCCGGAG CCAGAGCCCC TTCCCCGCGG CGAGGAACTG CCTCTGCGTC 1560 TCGTAAAAGG GGTCTGGGCC TGGGGGGCGG CGGCCTCCGT CGCCATGGAA ACCGGGGCGG 1620 GGAGGCGGCG GCCCGGAGAG CCCCATGCAC TTTGCATACC ATTGCAGGTT CCTCCCCTTG 1680 GGCCCCGCCA GCCTCGCTGG GCCCGCCTCT CTCTCCGCCC CTCCTCCCCA AACCCATCAC 1740 CCTTGCCTTT ATTTGTCTTA AATTTATTTT AAAATGTATT TATTTATTTT TTTCAAACAG 1800 GATCTCGCTC TGTCACCCAG GCCAGAGTGC AGTGGTGCGA TCATGACTCT CTACAGCCTT 1860 CCATCTCCCC AGGCTCAGGT GATCCTCCCA CCCCAGTTTC CCAATAGCTG GGACCACCAC 1920 GCCTGGCTAA TTTTGTGTGT GTGTGTGGTG ATGTCGCCCT CTGTCACCCA GGCTGGAGTG 1980 CCGTGGCCAG ATCTTGGCCC ACTGCAACCT CCGCCTCCCA GGTTCAAGCA ATTCTCCTGC 2040 CTTAGCCTCC TGAGTAGCTG GGATTACAGG CGCGTGCCAT CACACCCGGC TAATTTTTTT 2100 GGTATTTTTA GTAGAGACGG GGTTTCACCA CGTTGACCAG GCTGATCTCA AACTCCTGAC 2160 CTCGTGATCT GCCTGCCTCA GCCTCCCAAA GTGCTGAGAT TACAGGCGTG AGCCACCGTG 2220 CCTGGCAATG CCCGGCAATT TTTGTATTAT AGAGACAGGG TCTTGCCATG TTGCCCAGGC 2280 TGGTGTTAAA CTCCTGGACT CAAACAACCT GCCCACCTCC GCCTCCCAAA GTGTTAGGAT 2340 TACAGGCATG AGCCACTGCA CTCGGCCACC CCTGCCTTTA AAAGTCACCT CCTCCAGGAA 2400 GCTTTCAGCC ACCACCACCA CGCCCGGTGG CACCACTGAC ACTTCATAAC AATAATAATT 2460 CATCATCACT GTGATCGTGG CTAGGCTTGG CTGAGCTTTG TCTCTGTGCT TCCTTCACCC 2520 CCATCTTCTT CTGTCCTCAT ACCAACCCTG TATGGAGAGG CCACTTTTGT CGATATTTAC 2580 AAATGAGAAA ACTAAAGCTG GTAGGGGGTC TGCTCAAGGT CTCACACCTG GAAAATTCCC 2640 TCCTCATTCT AGTCTCAGTG TTCTCATTTG TAAAAAGGGA AGCTCGCACC AGGCGCTTGC 2700 CGAGTGACCA CGCAAGGGTG GGAATGAGAC CGCAGGTTTG TCTGAGCAGG GGCTGAGTGT 2760 GGCATTCTGA CTCTGAAGGC CTGTAGTCAG GGTATGCATG CTCTAGTTCA CCTCAGCCCG 2820 GCTGCGTCAC ACCCCCACTC TGTCCCCCAG TGCATCCCCA CCCTTGGGAC CCTAAGTGAA 2880 TCTCTCCAGA CCAAGCTCCT AGTGACTCAA GAGACATCTC TAAGGGGTCT TCCAGCTCTG 2940 CCATTCTGAA GTCTTAGCTT ATTGAGAGGG TGACTCCTTG TGCTGTCTCC CTCCTCTGAC 3000 TGGATGCTCC TGGGGGTGAG GGGCTGTGCC TCTCCTGTCA GACGGGACAC TGCTAAGGGT 3060 TAGGACACCT CTGTCACTCC CCTAGGTCTG TGGTCACTAG AAATGCCCAA ATCCAGGCTG 3120 AAGGCTGACC ATGTCTCTCC AAGCACAAGC ACACCCCAAG GTGCCCCAGT CCCTTGTCCT 3180 GATCCTGAGA TCTGAGGTCT ACAGGACTGG GTTCTTGGTG GGGAAACCTC CAGCTCTGCC 3240 ATAAAAAGAA AGCCTCATCC CAGACCTTCA GACCCGTTCC AGCACAGGCT CAGAAGAGGA 3300 GAAATGGGCC CAGAGACAAC TTCCAGGGCA GCAACACCAC AATCATCATC CCTTCTATTT 3360 AGTGATCTTG GCTATGTGCC CAAAACCTTT TTTTTTGAGA CAGAGTGTCA 3410
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