Tag | Content |
---|
EnhancerAtlas ID | HS113-00370 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr1:16493540-16496350 |
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 |
|
| 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 |
|
| 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 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH01I016167 | chr1 | 16493630 | 16496219 |
|
Enhancer Sequence | TGATTCTCCT GCCTCAGCCT CCCAAGTAGC TGGTATTACA GGCACGCGCC ACCACGCCTG 60 GTTAATTTTT GTATTTTTAG CAGAGATGGG GTTTCACCAT TTTGGCCAGG CTGGTCTCGA 120 ACTCCTGACC TCAGGTGATC CACCTGCCTC TGCCTCCCAA AATGCTGGGA TTACCGGCAT 180 GAGCCACTGT GCCCGGCTTC CGTTCTTCCT GATTACTTAA GAGGGGCCTG ACTAATGCCC 240 AGCATGGTTG GGGACCCAGG CCCCTCAAGC CCTGGAAGTC CCTTGCCTGG GGTCATCCAG 300 TCTCCTCCCT CAAAGGGCTC TCACTCCCCA CCGCCGCTCC CTCTCCTCTT CCTGCTGCTG 360 AGAGACGAGA GACCAGCAGA AAGAGACTTG GAGAGACGGA GACACAGAGG CAGATGGAGA 420 ATGCTGGGCG CCCGGGAAAG CCCAGGAAGG AGCCCGGGCC ACGTGGAGGA GAGGCAGGTG 480 GGAGGAGGCA GGAGAGAGCA AGGCTGCCCA GGACAATGGA GCGGGACCGG AGGAGACGCG 540 GGGAGGGACG CGGGCCAGGG GTGCGGTGGG GGGCACGGGG TGGAACTCCG GGTCCCGTAG 600 GGCGGGGTGG GGGAGTGGGT GGGGGGATGG CCCACCTGCC GTGGGAGCGG GTCCGGAGGA 660 AGCTAGGGTC TCGGGGTGGG AAGTGCTGTG TAGAAGCGAG CGCAAGAGGC GAGAGGAAGC 720 GCGGCGGGGC GGCCCCTGTC CCAGCCTCAC CCCCATCCCC CCAAGTCTCG CACCCCGGTC 780 CGCCCCAGCT TCCGGCTCCG CAGGTGCCGC CTTTGAGGGC CGCCGCTCGC AGTTTACCGC 840 GGAGCCGGAG CCAGAGCCCC TTCCCCGCGG CGAGGAACTG CCTCTGCGTC TCGTAAAAGG 900 GGTCTGGGCC TGGGGGGCGG CGGCCTCCGT CGCCATGGAA ACCGGGGCGG GGAGGCGGCG 960 GCCCGGAGAG CCCCATGCAC TTTGCATACC ATTGCAGGTT CCTCCCCTTG GGCCCCGCCA 1020 GCCTCGCTGG GCCCGCCTCT CTCTCCGCCC CTCCTCCCCA AACCCATCAC CCTTGCCTTT 1080 ATTTGTCTTA AATTTATTTT AAAATGTATT TATTTATTTT TTTCAAACAG GATCTCGCTC 1140 TGTCACCCAG GCCAGAGTGC AGTGGTGCGA TCATGACTCT CTACAGCCTT CCATCTCCCC 1200 AGGCTCAGGT GATCCTCCCA CCCCAGTTTC CCAATAGCTG GGACCACCAC GCCTGGCTAA 1260 TTTTGTGTGT GTGTGTGGTG ATGTCGCCCT CTGTCACCCA GGCTGGAGTG CCGTGGCCAG 1320 ATCTTGGCCC ACTGCAACCT CCGCCTCCCA GGTTCAAGCA ATTCTCCTGC CTTAGCCTCC 1380 TGAGTAGCTG GGATTACAGG CGCGTGCCAT CACACCCGGC TAATTTTTTT GGTATTTTTA 1440 GTAGAGACGG GGTTTCACCA CGTTGACCAG GCTGATCTCA AACTCCTGAC CTCGTGATCT 1500 GCCTGCCTCA GCCTCCCAAA GTGCTGAGAT TACAGGCGTG AGCCACCGTG CCTGGCAATG 1560 CCCGGCAATT TTTGTATTAT AGAGACAGGG TCTTGCCATG TTGCCCAGGC TGGTGTTAAA 1620 CTCCTGGACT CAAACAACCT GCCCACCTCC GCCTCCCAAA GTGTTAGGAT TACAGGCATG 1680 AGCCACTGCA CTCGGCCACC CCTGCCTTTA AAAGTCACCT CCTCCAGGAA GCTTTCAGCC 1740 ACCACCACCA CGCCCGGTGG CACCACTGAC ACTTCATAAC AATAATAATT CATCATCACT 1800 GTGATCGTGG CTAGGCTTGG CTGAGCTTTG TCTCTGTGCT TCCTTCACCC CCATCTTCTT 1860 CTGTCCTCAT ACCAACCCTG TATGGAGAGG CCACTTTTGT CGATATTTAC AAATGAGAAA 1920 ACTAAAGCTG GTAGGGGGTC TGCTCAAGGT CTCACACCTG GAAAATTCCC TCCTCATTCT 1980 AGTCTCAGTG TTCTCATTTG TAAAAAGGGA AGCTCGCACC AGGCGCTTGC CGAGTGACCA 2040 CGCAAGGGTG GGAATGAGAC CGCAGGTTTG TCTGAGCAGG GGCTGAGTGT GGCATTCTGA 2100 CTCTGAAGGC CTGTAGTCAG GGTATGCATG CTCTAGTTCA CCTCAGCCCG GCTGCGTCAC 2160 ACCCCCACTC TGTCCCCCAG TGCATCCCCA CCCTTGGGAC CCTAAGTGAA TCTCTCCAGA 2220 CCAAGCTCCT AGTGACTCAA GAGACATCTC TAAGGGGTCT TCCAGCTCTG CCATTCTGAA 2280 GTCTTAGCTT ATTGAGAGGG TGACTCCTTG TGCTGTCTCC CTCCTCTGAC TGGATGCTCC 2340 TGGGGGTGAG GGGCTGTGCC TCTCCTGTCA GACGGGACAC TGCTAAGGGT TAGGACACCT 2400 CTGTCACTCC CCTAGGTCTG TGGTCACTAG AAATGCCCAA ATCCAGGCTG AAGGCTGACC 2460 ATGTCTCTCC AAGCACAAGC ACACCCCAAG GTGCCCCAGT CCCTTGTCCT GATCCTGAGA 2520 TCTGAGGTCT ACAGGACTGG GTTCTTGGTG GGGAAACCTC CAGCTCTGCC ATAAAAAGAA 2580 AGCCTCATCC CAGACCTTCA GACCCGTTCC AGCACAGGCT CAGAAGAGGA GAAATGGGCC 2640 CAGAGACAAC TTCCAGGGCA GCAACACCAC AATCATCATC CCTTCTATTT AGTGATCTTG 2700 GCTATGTGCC CAAAACCTTT TTTTTTGAGA CAGAGTGTCA CTCTGTCGCC CAGGCTAGCG 2760 TGCAGTGGCA TGATCTCAGC CCACTGCAAC CTTCATCTCC TGGGTTCAAG 2810
|