Tag | Content |
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EnhancerAtlas ID | HS087-00041 |
Organism | Homo sapiens |
Tissue/cell | HEK293T |
Coordinate | chr1:992890-995570 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF14 | MA0740.1 | chr1:995224-995238 | AGGTGGGCGTGGCG | - | 6.25 | KLF14 | MA0740.1 | chr1:995005-995019 | CGGGGGGCGTGGCC | - | 6.32 | KLF16 | MA0741.1 | chr1:994765-994776 | GCCCCGCCCCC | + | 6.02 | KLF16 | MA0741.1 | chr1:995007-995018 | GGGGGCGTGGC | - | 6.62 | KLF5 | MA0599.1 | chr1:994760-994770 | GCCCCGCCCC | + | 6.02 | KLF5 | MA0599.1 | chr1:994765-994775 | GCCCCGCCCC | + | 6.02 | Nr2f6(var.2) | MA0728.1 | chr1:992918-992933 | GAGGTCAGGAGTTCA | + | 6.22 | Nr2f6(var.2) | MA0728.1 | chr1:993254-993269 | GAGGTCAGGAGTTCA | + | 6.22 | SP1 | MA0079.4 | chr1:995225-995240 | GGTGGGCGTGGCGAA | - | 6.2 | SP1 | MA0079.4 | chr1:995006-995021 | GGGGGGCGTGGCCTC | - | 7.17 | SP3 | MA0746.2 | chr1:994764-994777 | CGCCCCGCCCCCC | + | 6.11 | SP3 | MA0746.2 | chr1:995006-995019 | GGGGGGCGTGGCC | - | 7.22 | SP3 | MA0746.2 | chr1:995225-995238 | GGTGGGCGTGGCG | - | 7.52 | SP4 | MA0685.1 | chr1:995223-995240 | CAGGTGGGCGTGGCGAA | - | 6.13 | SP4 | MA0685.1 | chr1:995004-995021 | CCGGGGGGCGTGGCCTC | - | 6.26 | SP8 | MA0747.1 | chr1:995006-995018 | GGGGGGCGTGGC | - | 6.44 | SP8 | MA0747.1 | chr1:995225-995237 | GGTGGGCGTGGC | - | 6.62 | ZNF263 | MA0528.1 | chr1:993742-993763 | GAAGCATGAGCAGGGGGAGGG | + | 6.18 | Zfx | MA0146.2 | chr1:992894-992908 | GAGGCCGAGGCGGG | - | 6.01 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_24070 | chr1:995142-995502 | Colon_Crypt_2 | SE_24817 | chr1:994228-995515 | Colon_Crypt_3 | SE_34539 | chr1:993520-995869 | HCT-116 | SE_65935 | chr1:993812-995036 | Pancreatic_islets | SE_65935 | chr1:995102-996141 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr1 | 993716 | 993800 | chr1 | 993400 | 993707 | chr1 | 993800 | 994951 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I001059 | chr1 | 993741 | 993890 |
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Enhancer Sequence | TTGGGAGGCC GAGGCGGGTG GATCACCTGA GGTCAGGAGT TCAAGACGAG CCTGGCCAAC 60 ATGGTGAAAC CCTGTCTCTC CTAAAATACA AAAACTGGCT GGGCATGATG GTGGGTGCCT 120 GTAGTCCCAG CTACTCCGGA GGCTGAGACG GGAGAATTGC TTGAACCCAG GAGACGGTGG 180 TTGCAGTGAG CCGAGATCAC GCCATTGCAC TCCAGCCTCA GTGGCTGAAG GAGACTCCGT 240 CTCAAAAAAA AAAAGAAAAA AGAAAACCAC AAAAACATCG AAATAAAATA ACACCAATGG 300 CTGGGCACAT TGGCTCATGC CTATAATCCC AGCACTTTGG GAGGCTGAGG CAGGCGGATC 360 ACCTGAGGTC AGGAGTTCAA CACCAGACTG GCCAACATGG TGAAACCCTG TATCTACTAA 420 AAACACAAAC ATCTGGGCGT GGTGGCAGGT ATCTGTAATC CCAGTTACTC GGGAGGCTGA 480 GGCACGAGAA TCGCTTGAAC CCGGGAGGCG GAGGTTGCAG TGAGCCGCGA TTGCACCACT 540 GCACTCCAGC GTGGGCGACA GAGCGCGACT CCGTTTCAAA AAAAAAATGA AAAGATAATA 600 CCCACAAGCT CCACACCCAG GAGGTCCCAT GCGTCTGAGT GTTTGCTTTC TGGGCTTTTC 660 ATCACCTGGT CCTCTGGGGA TATGCTGACC GACCCTGTGT GCCTGGCAGG TGTCAGGCAC 720 TGGGGGTCGG GGAGGAGAGA GTCCAGGAGC GGTGGCCACA CACAGGTCGC TGACGGTGGG 780 GGGCCAGGGT GGGGGCAGAC TAACTTTGGT TTTCAGGAAA GGTCCAGAGA AAACACGCCC 840 AAACCCAGAC CCGAAGCATG AGCAGGGGGA GGGCAGGTGA GGAGGCCAGA GGCGGGGCAT 900 GTGGTGTGGG TCCATTGGAC GGTGTGCAGG GCCCTGTGGC TTGACAAAGG GATCTTTCAG 960 CAGGAAGCGG AGGCGTAGGA GCGGCCAGAG GCCAGCGTGC AGGACAGAGG CCACAGGTCA 1020 GAGCAGCAGA GGCTGGACAG AGATGGGCAG GGCAGGTCCA GTGGGGCTGC GTGGGCCTGG 1080 GGAAGAGAGC TGGGGGTGCT GCCTGAGGAG CTGTGGGAGG CTCCTGGAGG GCTCCAAGCA 1140 GGAGGCCACC AGATTTCATG AAGACGCCCC TGGCTAGGAC AGGGTGCTAG GCTGCAGGGG 1200 GAGCAGAGGG AGGGATTTGG GGGAGAATGG GCGGGTCGAG GGGGGTGAGA AGAGGCGCTC 1260 AGGGACGTGG AGATGGAGCT GGAGGCACCG GAGCTTTGGG TGGATTCGCC CTGATGCGTC 1320 TGGAGGGATG GCTGGGCTGG GGAAGCTGGG GTTCCCTGAG TGGGGTCCAG GGGGCCGAGG 1380 GGTGCCAGGC AGGGAGAGGC TGGGCTGAAG CCTGAGGCAG GTGCTCCTGC TGGGTGTTGC 1440 CTAGGAGAGG AGAAAAAGCC CCGACGCCAG AAATGGAGGA GGGAGGAGGA CCTCGGAGGG 1500 GAGGAGGAGG GTGCGCAGAA CCAGGAGAGG CAGTTTGGGG AGCAACCGCT GCGGAGCGCG 1560 CAGGACCCAG AGGACTCAAA GGGGACCTGG AGGGTGACGA GGCCTTCCGT GGCCGGGGGT 1620 GAGGAGGAGG GAAGCCGCGC GGGCGGAGAG GCGCTGGTGG GTCCCAGGTT GGAGGCTGTG 1680 GGTCTGAGAG GCGAAGCCCA GGGGAGCCCG GGGCCACCGC TGAAAAGGAT GGCAGCTGAG 1740 CGCAGGCGAG GGAGAGGCGC GCGTGTCCGG GACAGACCGC GGTGGGAGCT CGACTCCGGA 1800 AACCGGCGGG CCTGGGGCTG GGACCTACAG GGAGGCGGAC GCGGCACAGC CAGGGAGGTC 1860 GGTCCCGCGG GCCCCGCCCC GCCCCCCAGC CTGGAGCGCC CCCCTCCGGC CCCGGTCCGC 1920 AGTGGAGGCG GCCCCGGAAA AGCCAGAGGG TCTTGGAATG GAGGGCGGGA CGGAGCCGCC 1980 TGCAACGCCC GCGACCCGCG ACCCGGCTGC CCGCGGGACC CCCGGCTCTG AAGCGGGGAC 2040 GGCCGGAGCT TCCGCCTGCA GCCCAAACTC CCAGGCGCCC GGCAAGAGTG GCGGGCGCGG 2100 ACCCTTTAAG AAGGCCGGGG GGCGTGGCCT CGGGGCGTGG CCCGGGGCGT GGCATCGGGG 2160 CGAGGCTTCG GGGGCGGAGC CCAGGCAGCG CCTTCGCGGA GTTGCCGGAG GGTGCGGCCG 2220 CCCAGAGCGC ACCCCGAGCG CCGGCGAGCG GCGCGGTGAG ACCCTCGTGC AGGTGAGCCC 2280 GGCGCACGGC GGCCCAGAAT CCTGGACCCC AGGAGAAGCG TCTACGGCCC CGACAGGTGG 2340 GCGTGGCGAA ATGCCACCCG GGCCCTCCTC GCGCTCCCAG CTGGGTCACG CCTCAGACCC 2400 GGGGTCCTGG ACGCCTGCCC CCCTCCACCC GCAGGCCCTG CCAGGACACT TTGGTCCCTG 2460 GCCCGCCAGG CCTGGCCTCA CTCAGGCTTG GCTGTGGGGT CAGAGTCGGG CAGAACGGAA 2520 CCAACAGTCC TGGCAGGCCC AGGCGGTTGG AGGAGAAGTG GTCGGCTCTG GACACCTTTG 2580 TTGTTTTTTG TTTTTTGTTT TTGAGATGGC GTCTCACTGT GTCACCCAGG CTGGAGTGCA 2640 CTGGCGCGGT CTTGGCTCAC TGCAACCTCC ACCTCCCGGG 2680
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