Tag | Content |
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EnhancerAtlas ID | HS018-00210 |
Organism | Homo sapiens |
Tissue/cell | CD19+ |
Coordinate | chr1:16493710-16496430 |
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 | TTACCGGCAT GAGCCACTGT GCCCGGCTTC CGTTCTTCCT GATTACTTAA GAGGGGCCTG 60 ACTAATGCCC AGCATGGTTG GGGACCCAGG CCCCTCAAGC CCTGGAAGTC CCTTGCCTGG 120 GGTCATCCAG TCTCCTCCCT CAAAGGGCTC TCACTCCCCA CCGCCGCTCC CTCTCCTCTT 180 CCTGCTGCTG AGAGACGAGA GACCAGCAGA AAGAGACTTG GAGAGACGGA GACACAGAGG 240 CAGATGGAGA ATGCTGGGCG CCCGGGAAAG CCCAGGAAGG AGCCCGGGCC ACGTGGAGGA 300 GAGGCAGGTG GGAGGAGGCA GGAGAGAGCA AGGCTGCCCA GGACAATGGA GCGGGACCGG 360 AGGAGACGCG GGGAGGGACG CGGGCCAGGG GTGCGGTGGG GGGCACGGGG TGGAACTCCG 420 GGTCCCGTAG GGCGGGGTGG GGGAGTGGGT GGGGGGATGG CCCACCTGCC GTGGGAGCGG 480 GTCCGGAGGA AGCTAGGGTC TCGGGGTGGG AAGTGCTGTG TAGAAGCGAG CGCAAGAGGC 540 GAGAGGAAGC GCGGCGGGGC GGCCCCTGTC CCAGCCTCAC CCCCATCCCC CCAAGTCTCG 600 CACCCCGGTC CGCCCCAGCT TCCGGCTCCG CAGGTGCCGC CTTTGAGGGC CGCCGCTCGC 660 AGTTTACCGC GGAGCCGGAG CCAGAGCCCC TTCCCCGCGG CGAGGAACTG CCTCTGCGTC 720 TCGTAAAAGG GGTCTGGGCC TGGGGGGCGG CGGCCTCCGT CGCCATGGAA ACCGGGGCGG 780 GGAGGCGGCG GCCCGGAGAG CCCCATGCAC TTTGCATACC ATTGCAGGTT CCTCCCCTTG 840 GGCCCCGCCA GCCTCGCTGG GCCCGCCTCT CTCTCCGCCC CTCCTCCCCA AACCCATCAC 900 CCTTGCCTTT ATTTGTCTTA AATTTATTTT AAAATGTATT TATTTATTTT TTTCAAACAG 960 GATCTCGCTC TGTCACCCAG GCCAGAGTGC AGTGGTGCGA TCATGACTCT CTACAGCCTT 1020 CCATCTCCCC AGGCTCAGGT GATCCTCCCA CCCCAGTTTC CCAATAGCTG GGACCACCAC 1080 GCCTGGCTAA TTTTGTGTGT GTGTGTGGTG ATGTCGCCCT CTGTCACCCA GGCTGGAGTG 1140 CCGTGGCCAG ATCTTGGCCC ACTGCAACCT CCGCCTCCCA GGTTCAAGCA ATTCTCCTGC 1200 CTTAGCCTCC TGAGTAGCTG GGATTACAGG CGCGTGCCAT CACACCCGGC TAATTTTTTT 1260 GGTATTTTTA GTAGAGACGG GGTTTCACCA CGTTGACCAG GCTGATCTCA AACTCCTGAC 1320 CTCGTGATCT GCCTGCCTCA GCCTCCCAAA GTGCTGAGAT TACAGGCGTG AGCCACCGTG 1380 CCTGGCAATG CCCGGCAATT TTTGTATTAT AGAGACAGGG TCTTGCCATG TTGCCCAGGC 1440 TGGTGTTAAA CTCCTGGACT CAAACAACCT GCCCACCTCC GCCTCCCAAA GTGTTAGGAT 1500 TACAGGCATG AGCCACTGCA CTCGGCCACC CCTGCCTTTA AAAGTCACCT CCTCCAGGAA 1560 GCTTTCAGCC ACCACCACCA CGCCCGGTGG CACCACTGAC ACTTCATAAC AATAATAATT 1620 CATCATCACT GTGATCGTGG CTAGGCTTGG CTGAGCTTTG TCTCTGTGCT TCCTTCACCC 1680 CCATCTTCTT CTGTCCTCAT ACCAACCCTG TATGGAGAGG CCACTTTTGT CGATATTTAC 1740 AAATGAGAAA ACTAAAGCTG GTAGGGGGTC TGCTCAAGGT CTCACACCTG GAAAATTCCC 1800 TCCTCATTCT AGTCTCAGTG TTCTCATTTG TAAAAAGGGA AGCTCGCACC AGGCGCTTGC 1860 CGAGTGACCA CGCAAGGGTG GGAATGAGAC CGCAGGTTTG TCTGAGCAGG GGCTGAGTGT 1920 GGCATTCTGA CTCTGAAGGC CTGTAGTCAG GGTATGCATG CTCTAGTTCA CCTCAGCCCG 1980 GCTGCGTCAC ACCCCCACTC TGTCCCCCAG TGCATCCCCA CCCTTGGGAC CCTAAGTGAA 2040 TCTCTCCAGA CCAAGCTCCT AGTGACTCAA GAGACATCTC TAAGGGGTCT TCCAGCTCTG 2100 CCATTCTGAA GTCTTAGCTT ATTGAGAGGG TGACTCCTTG TGCTGTCTCC CTCCTCTGAC 2160 TGGATGCTCC TGGGGGTGAG GGGCTGTGCC TCTCCTGTCA GACGGGACAC TGCTAAGGGT 2220 TAGGACACCT CTGTCACTCC CCTAGGTCTG TGGTCACTAG AAATGCCCAA ATCCAGGCTG 2280 AAGGCTGACC ATGTCTCTCC AAGCACAAGC ACACCCCAAG GTGCCCCAGT CCCTTGTCCT 2340 GATCCTGAGA TCTGAGGTCT ACAGGACTGG GTTCTTGGTG GGGAAACCTC CAGCTCTGCC 2400 ATAAAAAGAA AGCCTCATCC CAGACCTTCA GACCCGTTCC AGCACAGGCT CAGAAGAGGA 2460 GAAATGGGCC CAGAGACAAC TTCCAGGGCA GCAACACCAC AATCATCATC CCTTCTATTT 2520 AGTGATCTTG GCTATGTGCC CAAAACCTTT TTTTTTGAGA CAGAGTGTCA CTCTGTCGCC 2580 CAGGCTAGCG TGCAGTGGCA TGATCTCAGC CCACTGCAAC CTTCATCTCC TGGGTTCAAG 2640 TGATTCTCCT GCCTCAGCCT CCTGAGTAGC TGAGATTACA GGCATGCGCC ACCATGCCCA 2700 GCTGATTTTT GTATTTTTAG 2720
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