Tag | Content |
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EnhancerAtlas ID | HS167-07196 |
Organism | Homo sapiens |
Tissue/cell | Retina |
Coordinate | chr8:102091480-102093770 |
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 | AAACAACCTT CCTTCTATCT TATCCTGGCT GGGTTTATCA GATTTGACTC ACTCCCTGGA 60 GCCCCTTGCA AGGACTGGGC TGGGATTGCA GGGCTGAGCA GGAACCGGCT TCTCTAGCCT 120 CTTCAGGGAA GGGCCTTCTA AACTCCACTC TGCCCCATAC CCTCCAGCTA GAAACCCAGC 180 CTCCTGCCTT TGGGGAATAT AGCCCCAGTA AGGGCTCAGT GTCTTTTCCA CAAGCTCTTT 240 TCCTATGGCC TTTAGGGGCA CATGACTTTG AGGAAACCAG ACAGCTGGGG GGGACATGAG 300 AATCAGGGCC AGTGCTTGCA GGAAAGAAAG CAAACGCTCT GAATGTGAGC CAGATGGCAG 360 GTCCCCCACA CAAGGCAGGG GGCTCAAGAA CACTTCCTTT CATGCTAGCA GTACTAGCTG 420 CTCCCACCTT TGTGAAATGC ATTTTTGAAA GCAGAACAAA TGATCATTTA ATTTGAGAAG 480 CCCACACCTC TTAATACTCA TAGTATTTTC ACCATCATCC TGGCCCCTGG TCAGCTGGAA 540 GAGCAGCAGG GGAGGGGAAG CATCACTTTG GTTTCTACCT CCCAGCTGGG GCAGGTGCAA 600 GGCAGCGCAC TCCATCAGCT CCTTGCCCAG AAGGGCAAAA TGATGTCTCC TTTCTCCCTC 660 TCTTCCTCTT TCCCTCTCTC CCTCCCTCCT TCCTTCCCTC TTTCCTTTCC TCCCTTCCAA 720 CATTTTTTGA GTGAGGATCT TCTGCCAGAC ATTGTGCAAA ATTCGGGGAA TCCAAGGTAC 780 AGAGAGGAGG CCTGGCTCTG CCCTCCTGGC CCTTCCAGTC CAGTGGGGAG GAGAGGCCTC 840 TTGCCAAGAC ATGGCAGCTG TGAGGAATGC TACAAAGAGT TTCTGGGTCC TGCGGGGTGG 900 AGTGACTGGA GTGACTGAAG TTACCCGCCT GGGTGGGGTG GGAACAGGAC AGGCTGTCCT 960 GGAAAAGTGA TGTTTGGGCT GATACCAGAA GGGGCAAACG CGGGATGGAA GTGACGGCAT 1020 CCCAGGTAGA GGAGAGGGCC TGGGCAATGG CTGTGAGGGA GAGCTCAGGA AATGGGAAGG 1080 CCACCAGTGT GGCCCAGGGC AGAGAGGTCA GGGGACCAGG CAGGAGACAG GATGTGGGGG 1140 GAGGCCAGTG CAGAGCACCT GGGCCACAGC CACGGGTCAA GTTCGTGTTT ATGCTGGGAG 1200 CCTGGGGAAG CCGGCGAGAG ACTGGAGTAG GAGTGGCCTT CAGGTCTTGG GGCGCCCAGT 1260 ACAGTGCAAG TGATGGGCTG GGGCCCCTCC GCCCTCCTTG TCAAGCAGTG TCCACGGATA 1320 AGGGCGTCCC GGGGCGGGGG GGGGACGTGG GCGAGGAGAT GGTGGAGCTG GGGGAAGGGA 1380 CAGGGACAGA AGGCAGAAGA GTCACCCTCA GCGTCACCTT CTCTCCCCTC CCTACTCCGG 1440 AGGCCAAGCG CCCCAGCGGG AGGCTTCCCT GCCCGCCTCG GCCTCGCTTA CACCGCAGGT 1500 GCTGTGAGTC ACCCACCTGC GTGGTGAGTC AGGGGAGGAG GCCGAGAAGG CAGGTGGGCG 1560 GCGCGGCAGG GCGCCGGGCT TCGCGGGGAG GGGAGCGCTG TCTCCCCACG CGCCCCTCCC 1620 CCACGAGCGG CTTCCAGAAA CCCGTTTGCC CATCCCCGGC AGGAGGCCTC CGCCCGGCTT 1680 CTCGCTCCCT CTTCCCTCTC CCCGACCCCC TCCCGGGCTG TCAGCCGACT GCCACCGTCA 1740 CCATGGCTAC GCGGCTCCCG CTCAGTTCCA CAGTCAGCAG GAGTCGAGCA GGGGAGGCGG 1800 CTGTCTCCTT GGTCTTCCTG CTGCACCGGG TTCTTTGAAA ATCAGCTCCT GACTGCATGT 1860 TGCGGATTCC AGGCCCAGCC CCCTTACCTG GAAGGCTCAC CTTGAAAGAC GGCAGGATGA 1920 GACCAGGAAA CGGGGCCACA GGCATACCAA GGAAGCTTAT TTTGCCTGGC TTCCCTTTTT 1980 AAGCACGGAT GCATACCGGT GTGTTGGACA TGACTGATGA ACCAAGATTT GAGGAAGGCC 2040 ACCCACTGAG TGACTGGAGG TAGACGTGGA AGGCTTTGGT TGCCATAGGC AACTTGGGGC 2100 CAGAAAGACC TGGATTCAAA TTCTGGCACT TATCAAAGGG ATAAAGTGGG ACAAACAATT 2160 TTACCTTGCT GGGCCTCAGT CTCCTCATCT GTAAAATACG GATAATCCCC CCTTGGTAGA 2220 TTGGGATGAG GATTAAAGAT AATGCATGCA AAATATTTGG CACGTAGCAG GTGCTACCAA 2280 ATGCTTATTG 2290
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