Tag | Content |
---|
EnhancerAtlas ID | HS030-00290 |
Organism | Homo sapiens |
Tissue/cell | CyT49 |
Coordinate | chr1:16492780-16495430 |
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: 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 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 2 | ID | Chromosome | Start | End |
GH01I016166 | chr1 | 16492707 | 16493355 | GH01I016167 | chr1 | 16493630 | 16496219 |
|
Enhancer Sequence | GCCCAGCCCC TCTCAGCCCC CTCTGCATCC CATCCATCAC TTCTCAGACA GGCCTCCCCA 60 GCCAGGTAGT CACCTCCTAG CGGCTCCATC TGTCTGTCTG TCTACCAACC CATCCATCCA 120 TCTGTCTGCC AGCCCATCCA TCATGCCACA GGCCACTTGT CCATTCTTGC CACCTTTCAC 180 ATGTTCCCTA GTTAGGCCCC TGTGGTATCC CCCAGCCAGC GCAGTGTAGG TGGGGGGCGT 240 GTGTTCATGT CAGTAGATAT GTCTGTGGCC GCCAGCATGC CTTGTGCTGA GCAGAGGGCA 300 AGGGACCTGG ATGAGGAGCT GGGGAGGGGT TGGGGACAGG AAGACTGGGA ACCTCTTGGT 360 GGGGGGCACA GCAGCTTCCC TGTGTATTCT CCCTGTGGTC TGTTGCACCA TAGGCATCAA 420 TGGCCTGCTC AAAAATAAAT ACACGACTGG AAAACTCTCC CACCTCCATT CTTTTTCCTT 480 TTTGGGGGGG TGGTGGGGAC AGAGTCTTGC TTTGTCCTCC AGGCTGGAGT GCAGTGGCAC 540 GATCTCAGCC CACTGCAACC TCCACCTCCT GAGTTCAAGC AGTTCTCCTG TCTCAGCCTC 600 CCAAGTTGCT GGGATTACAG GCCTGCGCCA CCACGCCTGG CTAATTTTTG TTTTTTGGTT 660 TTGTTTTTTC TTTTCCGGGA TGGAGTCTTG CTCTGTCACC CAGGCTGGAG TGCAATGGCC 720 GGATCTTGGC TCACTACAAC CTCCGCCTCC CGGATTCAAG TGATTCTCCT GCCTCAGCCT 780 CCCAAGTAGC TGGTATTACA GGCACGCGCC ACCACGCCTG GTTAATTTTT GTATTTTTAG 840 CAGAGATGGG GTTTCACCAT TTTGGCCAGG CTGGTCTCGA ACTCCTGACC TCAGGTGATC 900 CACCTGCCTC TGCCTCCCAA AATGCTGGGA TTACCGGCAT GAGCCACTGT GCCCGGCTTC 960 CGTTCTTCCT GATTACTTAA GAGGGGCCTG ACTAATGCCC AGCATGGTTG GGGACCCAGG 1020 CCCCTCAAGC CCTGGAAGTC CCTTGCCTGG GGTCATCCAG TCTCCTCCCT CAAAGGGCTC 1080 TCACTCCCCA CCGCCGCTCC CTCTCCTCTT CCTGCTGCTG AGAGACGAGA GACCAGCAGA 1140 AAGAGACTTG GAGAGACGGA GACACAGAGG CAGATGGAGA ATGCTGGGCG CCCGGGAAAG 1200 CCCAGGAAGG AGCCCGGGCC ACGTGGAGGA GAGGCAGGTG GGAGGAGGCA GGAGAGAGCA 1260 AGGCTGCCCA GGACAATGGA GCGGGACCGG AGGAGACGCG GGGAGGGACG CGGGCCAGGG 1320 GTGCGGTGGG GGGCACGGGG TGGAACTCCG GGTCCCGTAG GGCGGGGTGG GGGAGTGGGT 1380 GGGGGGATGG CCCACCTGCC GTGGGAGCGG GTCCGGAGGA AGCTAGGGTC TCGGGGTGGG 1440 AAGTGCTGTG TAGAAGCGAG CGCAAGAGGC GAGAGGAAGC GCGGCGGGGC GGCCCCTGTC 1500 CCAGCCTCAC CCCCATCCCC CCAAGTCTCG CACCCCGGTC CGCCCCAGCT TCCGGCTCCG 1560 CAGGTGCCGC CTTTGAGGGC CGCCGCTCGC AGTTTACCGC GGAGCCGGAG CCAGAGCCCC 1620 TTCCCCGCGG CGAGGAACTG CCTCTGCGTC TCGTAAAAGG GGTCTGGGCC TGGGGGGCGG 1680 CGGCCTCCGT CGCCATGGAA ACCGGGGCGG GGAGGCGGCG GCCCGGAGAG CCCCATGCAC 1740 TTTGCATACC ATTGCAGGTT CCTCCCCTTG GGCCCCGCCA GCCTCGCTGG GCCCGCCTCT 1800 CTCTCCGCCC CTCCTCCCCA AACCCATCAC CCTTGCCTTT ATTTGTCTTA AATTTATTTT 1860 AAAATGTATT TATTTATTTT TTTCAAACAG GATCTCGCTC TGTCACCCAG GCCAGAGTGC 1920 AGTGGTGCGA TCATGACTCT CTACAGCCTT CCATCTCCCC AGGCTCAGGT GATCCTCCCA 1980 CCCCAGTTTC CCAATAGCTG GGACCACCAC GCCTGGCTAA TTTTGTGTGT GTGTGTGGTG 2040 ATGTCGCCCT CTGTCACCCA GGCTGGAGTG CCGTGGCCAG ATCTTGGCCC ACTGCAACCT 2100 CCGCCTCCCA GGTTCAAGCA ATTCTCCTGC CTTAGCCTCC TGAGTAGCTG GGATTACAGG 2160 CGCGTGCCAT CACACCCGGC TAATTTTTTT GGTATTTTTA GTAGAGACGG GGTTTCACCA 2220 CGTTGACCAG GCTGATCTCA AACTCCTGAC CTCGTGATCT GCCTGCCTCA GCCTCCCAAA 2280 GTGCTGAGAT TACAGGCGTG AGCCACCGTG CCTGGCAATG CCCGGCAATT TTTGTATTAT 2340 AGAGACAGGG TCTTGCCATG TTGCCCAGGC TGGTGTTAAA CTCCTGGACT CAAACAACCT 2400 GCCCACCTCC GCCTCCCAAA GTGTTAGGAT TACAGGCATG AGCCACTGCA CTCGGCCACC 2460 CCTGCCTTTA AAAGTCACCT CCTCCAGGAA GCTTTCAGCC ACCACCACCA CGCCCGGTGG 2520 CACCACTGAC ACTTCATAAC AATAATAATT CATCATCACT GTGATCGTGG CTAGGCTTGG 2580 CTGAGCTTTG TCTCTGTGCT TCCTTCACCC CCATCTTCTT CTGTCCTCAT ACCAACCCTG 2640 TATGGAGAGG 2650
|