Tag | Content |
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EnhancerAtlas ID | HS110-04795 |
Organism | Homo sapiens |
Tissue/cell | KATO3 |
Coordinate | chr8:102090890-102093550 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr8:102092128-102092146 | CCTTTCTCCCTCTCTTCC | - | 6.12 | EWSR1-FLI1 | MA0149.1 | chr8:102092155-102092173 | CTCTCCCTCCCTCCTTCC | - | 6.39 | EWSR1-FLI1 | MA0149.1 | chr8:102092171-102092189 | CCTTCCCTCTTTCCTTTC | - | 6.62 | EWSR1-FLI1 | MA0149.1 | chr8:102092163-102092181 | CCCTCCTTCCTTCCCTCT | - | 6.84 | EWSR1-FLI1 | MA0149.1 | chr8:102092159-102092177 | CCCTCCCTCCTTCCTTCC | - | 7.97 | EWSR1-FLI1 | MA0149.1 | chr8:102092167-102092185 | CCTTCCTTCCCTCTTTCC | - | 8.45 | RFX1 | MA0509.2 | chr8:102093215-102093231 | CGTCACCATGGCTACG | - | 6.68 | RFX1 | MA0509.2 | chr8:102093215-102093231 | CGTCACCATGGCTACG | + | 6.69 | RFX2 | MA0600.2 | chr8:102093215-102093231 | CGTCACCATGGCTACG | + | 6.39 | RFX2 | MA0600.2 | chr8:102093215-102093231 | CGTCACCATGGCTACG | - | 6.63 | ZNF263 | MA0528.1 | chr8:102092159-102092180 | CCCTCCCTCCTTCCTTCCCTC | - | 6.25 | ZNF263 | MA0528.1 | chr8:102092175-102092196 | CCCTCTTTCCTTTCCTCCCTT | - | 6.45 | ZNF263 | MA0528.1 | chr8:102092163-102092184 | CCCTCCTTCCTTCCCTCTTTC | - | 6.48 | ZNF263 | MA0528.1 | chr8:102092131-102092152 | TTCTCCCTCTCTTCCTCTTTC | - | 6.61 | ZNF263 | MA0528.1 | chr8:102092143-102092164 | TCCTCTTTCCCTCTCTCCCTC | - | 6.67 | ZNF263 | MA0528.1 | chr8:102092128-102092149 | CCTTTCTCCCTCTCTTCCTCT | - | 6.69 | ZNF263 | MA0528.1 | chr8:102092155-102092176 | CTCTCCCTCCCTCCTTCCTTC | - | 7.08 | ZNF263 | MA0528.1 | chr8:102092147-102092168 | CTTTCCCTCTCTCCCTCCCTC | - | 7.1 | ZNF263 | MA0528.1 | chr8:102092151-102092172 | CCCTCTCTCCCTCCCTCCTTC | - | 8.27 | Zfx | MA0146.2 | chr8:102092951-102092965 | CCCGCCTCGGCCTC | + | 6.01 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_25430 | chr8:102089963-102095749 | DND41 | SE_27458 | chr8:102090078-102093744 | Esophagus | SE_36229 | chr8:102091981-102094113 | HMEC | SE_64657 | chr8:102092135-102093972 | NHEK |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr8 | 102092221 | 102093367 | chr8 | 102092753 | 102093116 |
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| Number: 1 | ID | Chromosome | Start | End |
GH08I101077 | chr8 | 102089241 | 102094190 |
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Enhancer Sequence | TGAGTTGGCT TCAGGGTGGT TTATGAAGCA GAGAAGTAAA ATGCTTTACT AAGTCACATG 60 GCTAGAGAAT GCATTTAACT TGCATTATAC ATTTAGACAC CTTTCTCTGG TAGGACTGAC 120 TCAGAGCCCA TTTAAAATAA ATTCAAGGCC GGGTGTGGTA GCTCATGCCT GTAATCCTAG 180 CACTTTGAGA GGCCAAGGCA GGAAGATAGC TCGAGTCCAG GAGTTTGAGA CTAGCCTGGA 240 CAACACAGTG AGACCCCCGT CTACAAAACA ACAAAATAAA ATAAAATTAG CTGGGTGTTG 300 TGGCATGCAC CTGTGGTCCC AGCTACTCAG GGGGCTGAGG CAGGAAGATC TCATGAGTCT 360 GGGAGGTCGA AGCTGCAGTG AGCCTTGATT GCAACACTGC ACTCCAGCCT GGGCAACAGA 420 GCAAAACCCA TTTTGAAAAA TCAAAAATAA AAATAATAAA ATAAATTCAA GAAAATGACA 480 GTTGGGCTCC TCTGTCTTCG TCTGGTTTCT AACAGGACTT CTCCTATTCC AATGGATGTT 540 CTTTGGCCTC CAAAACAGCA GCCCCACCTG GTATTGAAGG GCCGGTGTGT AAACAACCTT 600 CCTTCTATCT TATCCTGGCT GGGTTTATCA GATTTGACTC ACTCCCTGGA GCCCCTTGCA 660 AGGACTGGGC TGGGATTGCA GGGCTGAGCA GGAACCGGCT TCTCTAGCCT CTTCAGGGAA 720 GGGCCTTCTA AACTCCACTC TGCCCCATAC CCTCCAGCTA GAAACCCAGC CTCCTGCCTT 780 TGGGGAATAT AGCCCCAGTA AGGGCTCAGT GTCTTTTCCA CAAGCTCTTT TCCTATGGCC 840 TTTAGGGGCA CATGACTTTG AGGAAACCAG ACAGCTGGGG GGGACATGAG AATCAGGGCC 900 AGTGCTTGCA GGAAAGAAAG CAAACGCTCT GAATGTGAGC CAGATGGCAG GTCCCCCACA 960 CAAGGCAGGG GGCTCAAGAA CACTTCCTTT CATGCTAGCA GTACTAGCTG CTCCCACCTT 1020 TGTGAAATGC ATTTTTGAAA GCAGAACAAA TGATCATTTA ATTTGAGAAG CCCACACCTC 1080 TTAATACTCA TAGTATTTTC ACCATCATCC TGGCCCCTGG TCAGCTGGAA GAGCAGCAGG 1140 GGAGGGGAAG CATCACTTTG GTTTCTACCT CCCAGCTGGG GCAGGTGCAA GGCAGCGCAC 1200 TCCATCAGCT CCTTGCCCAG AAGGGCAAAA TGATGTCTCC TTTCTCCCTC TCTTCCTCTT 1260 TCCCTCTCTC CCTCCCTCCT TCCTTCCCTC TTTCCTTTCC TCCCTTCCAA CATTTTTTGA 1320 GTGAGGATCT TCTGCCAGAC ATTGTGCAAA ATTCGGGGAA TCCAAGGTAC AGAGAGGAGG 1380 CCTGGCTCTG CCCTCCTGGC CCTTCCAGTC CAGTGGGGAG GAGAGGCCTC TTGCCAAGAC 1440 ATGGCAGCTG TGAGGAATGC TACAAAGAGT TTCTGGGTCC TGCGGGGTGG AGTGACTGGA 1500 GTGACTGAAG TTACCCGCCT GGGTGGGGTG GGAACAGGAC AGGCTGTCCT GGAAAAGTGA 1560 TGTTTGGGCT GATACCAGAA GGGGCAAACG CGGGATGGAA GTGACGGCAT CCCAGGTAGA 1620 GGAGAGGGCC TGGGCAATGG CTGTGAGGGA GAGCTCAGGA AATGGGAAGG CCACCAGTGT 1680 GGCCCAGGGC AGAGAGGTCA GGGGACCAGG CAGGAGACAG GATGTGGGGG GAGGCCAGTG 1740 CAGAGCACCT GGGCCACAGC CACGGGTCAA GTTCGTGTTT ATGCTGGGAG CCTGGGGAAG 1800 CCGGCGAGAG ACTGGAGTAG GAGTGGCCTT CAGGTCTTGG GGCGCCCAGT ACAGTGCAAG 1860 TGATGGGCTG GGGCCCCTCC GCCCTCCTTG TCAAGCAGTG TCCACGGATA AGGGCGTCCC 1920 GGGGCGGGGG GGGGACGTGG GCGAGGAGAT GGTGGAGCTG GGGGAAGGGA CAGGGACAGA 1980 AGGCAGAAGA GTCACCCTCA GCGTCACCTT CTCTCCCCTC CCTACTCCGG AGGCCAAGCG 2040 CCCCAGCGGG AGGCTTCCCT GCCCGCCTCG GCCTCGCTTA CACCGCAGGT GCTGTGAGTC 2100 ACCCACCTGC GTGGTGAGTC AGGGGAGGAG GCCGAGAAGG CAGGTGGGCG GCGCGGCAGG 2160 GCGCCGGGCT TCGCGGGGAG GGGAGCGCTG TCTCCCCACG CGCCCCTCCC CCACGAGCGG 2220 CTTCCAGAAA CCCGTTTGCC CATCCCCGGC AGGAGGCCTC CGCCCGGCTT CTCGCTCCCT 2280 CTTCCCTCTC CCCGACCCCC TCCCGGGCTG TCAGCCGACT GCCACCGTCA CCATGGCTAC 2340 GCGGCTCCCG CTCAGTTCCA CAGTCAGCAG GAGTCGAGCA GGGGAGGCGG CTGTCTCCTT 2400 GGTCTTCCTG CTGCACCGGG TTCTTTGAAA ATCAGCTCCT GACTGCATGT TGCGGATTCC 2460 AGGCCCAGCC CCCTTACCTG GAAGGCTCAC CTTGAAAGAC GGCAGGATGA GACCAGGAAA 2520 CGGGGCCACA GGCATACCAA GGAAGCTTAT TTTGCCTGGC TTCCCTTTTT AAGCACGGAT 2580 GCATACCGGT GTGTTGGACA TGACTGATGA ACCAAGATTT GAGGAAGGCC ACCCACTGAG 2640 TGACTGGAGG TAGACGTGGA 2660
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