Tag | Content |
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EnhancerAtlas ID | HS024-15560 |
Organism | Homo sapiens |
Tissue/cell | Cerebellum |
Coordinate | chr8:102091150-102094100 |
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 | CTACAAAACA ACAAAATAAA ATAAAATTAG CTGGGTGTTG TGGCATGCAC CTGTGGTCCC 60 AGCTACTCAG GGGGCTGAGG CAGGAAGATC TCATGAGTCT GGGAGGTCGA AGCTGCAGTG 120 AGCCTTGATT GCAACACTGC ACTCCAGCCT GGGCAACAGA GCAAAACCCA TTTTGAAAAA 180 TCAAAAATAA AAATAATAAA ATAAATTCAA GAAAATGACA GTTGGGCTCC TCTGTCTTCG 240 TCTGGTTTCT AACAGGACTT CTCCTATTCC AATGGATGTT CTTTGGCCTC CAAAACAGCA 300 GCCCCACCTG GTATTGAAGG GCCGGTGTGT AAACAACCTT CCTTCTATCT TATCCTGGCT 360 GGGTTTATCA GATTTGACTC ACTCCCTGGA GCCCCTTGCA AGGACTGGGC TGGGATTGCA 420 GGGCTGAGCA GGAACCGGCT TCTCTAGCCT CTTCAGGGAA GGGCCTTCTA AACTCCACTC 480 TGCCCCATAC CCTCCAGCTA GAAACCCAGC CTCCTGCCTT TGGGGAATAT AGCCCCAGTA 540 AGGGCTCAGT GTCTTTTCCA CAAGCTCTTT TCCTATGGCC TTTAGGGGCA CATGACTTTG 600 AGGAAACCAG ACAGCTGGGG GGGACATGAG AATCAGGGCC AGTGCTTGCA GGAAAGAAAG 660 CAAACGCTCT GAATGTGAGC CAGATGGCAG GTCCCCCACA CAAGGCAGGG GGCTCAAGAA 720 CACTTCCTTT CATGCTAGCA GTACTAGCTG CTCCCACCTT TGTGAAATGC ATTTTTGAAA 780 GCAGAACAAA TGATCATTTA ATTTGAGAAG CCCACACCTC TTAATACTCA TAGTATTTTC 840 ACCATCATCC TGGCCCCTGG TCAGCTGGAA GAGCAGCAGG GGAGGGGAAG CATCACTTTG 900 GTTTCTACCT CCCAGCTGGG GCAGGTGCAA GGCAGCGCAC TCCATCAGCT CCTTGCCCAG 960 AAGGGCAAAA TGATGTCTCC TTTCTCCCTC TCTTCCTCTT TCCCTCTCTC CCTCCCTCCT 1020 TCCTTCCCTC TTTCCTTTCC TCCCTTCCAA CATTTTTTGA GTGAGGATCT TCTGCCAGAC 1080 ATTGTGCAAA ATTCGGGGAA TCCAAGGTAC AGAGAGGAGG CCTGGCTCTG CCCTCCTGGC 1140 CCTTCCAGTC CAGTGGGGAG GAGAGGCCTC TTGCCAAGAC ATGGCAGCTG TGAGGAATGC 1200 TACAAAGAGT TTCTGGGTCC TGCGGGGTGG AGTGACTGGA GTGACTGAAG TTACCCGCCT 1260 GGGTGGGGTG GGAACAGGAC AGGCTGTCCT GGAAAAGTGA TGTTTGGGCT GATACCAGAA 1320 GGGGCAAACG CGGGATGGAA GTGACGGCAT CCCAGGTAGA GGAGAGGGCC TGGGCAATGG 1380 CTGTGAGGGA GAGCTCAGGA AATGGGAAGG CCACCAGTGT GGCCCAGGGC AGAGAGGTCA 1440 GGGGACCAGG CAGGAGACAG GATGTGGGGG GAGGCCAGTG CAGAGCACCT GGGCCACAGC 1500 CACGGGTCAA GTTCGTGTTT ATGCTGGGAG CCTGGGGAAG CCGGCGAGAG ACTGGAGTAG 1560 GAGTGGCCTT CAGGTCTTGG GGCGCCCAGT ACAGTGCAAG TGATGGGCTG GGGCCCCTCC 1620 GCCCTCCTTG TCAAGCAGTG TCCACGGATA AGGGCGTCCC GGGGCGGGGG GGGGACGTGG 1680 GCGAGGAGAT GGTGGAGCTG GGGGAAGGGA CAGGGACAGA AGGCAGAAGA GTCACCCTCA 1740 GCGTCACCTT CTCTCCCCTC CCTACTCCGG AGGCCAAGCG CCCCAGCGGG AGGCTTCCCT 1800 GCCCGCCTCG GCCTCGCTTA CACCGCAGGT GCTGTGAGTC ACCCACCTGC GTGGTGAGTC 1860 AGGGGAGGAG GCCGAGAAGG CAGGTGGGCG GCGCGGCAGG GCGCCGGGCT TCGCGGGGAG 1920 GGGAGCGCTG TCTCCCCACG CGCCCCTCCC CCACGAGCGG CTTCCAGAAA CCCGTTTGCC 1980 CATCCCCGGC AGGAGGCCTC CGCCCGGCTT CTCGCTCCCT CTTCCCTCTC CCCGACCCCC 2040 TCCCGGGCTG TCAGCCGACT GCCACCGTCA CCATGGCTAC GCGGCTCCCG CTCAGTTCCA 2100 CAGTCAGCAG GAGTCGAGCA GGGGAGGCGG CTGTCTCCTT GGTCTTCCTG CTGCACCGGG 2160 TTCTTTGAAA ATCAGCTCCT GACTGCATGT TGCGGATTCC AGGCCCAGCC CCCTTACCTG 2220 GAAGGCTCAC CTTGAAAGAC GGCAGGATGA GACCAGGAAA CGGGGCCACA GGCATACCAA 2280 GGAAGCTTAT TTTGCCTGGC TTCCCTTTTT AAGCACGGAT GCATACCGGT GTGTTGGACA 2340 TGACTGATGA ACCAAGATTT GAGGAAGGCC ACCCACTGAG TGACTGGAGG TAGACGTGGA 2400 AGGCTTTGGT TGCCATAGGC AACTTGGGGC CAGAAAGACC TGGATTCAAA TTCTGGCACT 2460 TATCAAAGGG ATAAAGTGGG ACAAACAATT TTACCTTGCT GGGCCTCAGT CTCCTCATCT 2520 GTAAAATACG GATAATCCCC CCTTGGTAGA TTGGGATGAG GATTAAAGAT AATGCATGCA 2580 AAATATTTGG CACGTAGCAG GTGCTACCAA ATGCTTATTG TTGTTGTTAT TACGGAGTTC 2640 AGAGCCCTTT GAGATGCTCC ACAAGTGTTT GCTGATTTGA GGGTGGCACA AAAGGCAGTT 2700 TTCCCCAACA CCAATTGAAA GACTCCTTGG AGTGTGAATT TCAAGATGGT GGGGTACAGC 2760 AATTTCTACC CTCTCGTCGA AAGTCTCATC TCTGCTGGGA GACTGTGTGA CCCAGAACCA 2820 CAGTATAGGA AGATGGTGGA AGGTGAAGGC ATGAGCAGAG AAGAAGGGAG GTCCAAGCTG 2880 AGTGCCTAGG AACAGGGGTG GCCTACATCA GAGAGGCCAG TTGCTATGGC CCATAGAACC 2940 TTGCTAGGTC 2950
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