Tag | Content |
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EnhancerAtlas ID | HS078-15924 |
Organism | Homo sapiens |
Tissue/cell | H2171 |
Coordinate | chr8:102091580-102094200 |
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 | GGAACCGGCT TCTCTAGCCT CTTCAGGGAA GGGCCTTCTA AACTCCACTC TGCCCCATAC 60 CCTCCAGCTA GAAACCCAGC CTCCTGCCTT TGGGGAATAT AGCCCCAGTA AGGGCTCAGT 120 GTCTTTTCCA CAAGCTCTTT TCCTATGGCC TTTAGGGGCA CATGACTTTG AGGAAACCAG 180 ACAGCTGGGG GGGACATGAG AATCAGGGCC AGTGCTTGCA GGAAAGAAAG CAAACGCTCT 240 GAATGTGAGC CAGATGGCAG GTCCCCCACA CAAGGCAGGG GGCTCAAGAA CACTTCCTTT 300 CATGCTAGCA GTACTAGCTG CTCCCACCTT TGTGAAATGC ATTTTTGAAA GCAGAACAAA 360 TGATCATTTA ATTTGAGAAG CCCACACCTC TTAATACTCA TAGTATTTTC ACCATCATCC 420 TGGCCCCTGG TCAGCTGGAA GAGCAGCAGG GGAGGGGAAG CATCACTTTG GTTTCTACCT 480 CCCAGCTGGG GCAGGTGCAA GGCAGCGCAC TCCATCAGCT CCTTGCCCAG AAGGGCAAAA 540 TGATGTCTCC TTTCTCCCTC TCTTCCTCTT TCCCTCTCTC CCTCCCTCCT TCCTTCCCTC 600 TTTCCTTTCC TCCCTTCCAA CATTTTTTGA GTGAGGATCT TCTGCCAGAC ATTGTGCAAA 660 ATTCGGGGAA TCCAAGGTAC AGAGAGGAGG CCTGGCTCTG CCCTCCTGGC CCTTCCAGTC 720 CAGTGGGGAG GAGAGGCCTC TTGCCAAGAC ATGGCAGCTG TGAGGAATGC TACAAAGAGT 780 TTCTGGGTCC TGCGGGGTGG AGTGACTGGA GTGACTGAAG TTACCCGCCT GGGTGGGGTG 840 GGAACAGGAC AGGCTGTCCT GGAAAAGTGA TGTTTGGGCT GATACCAGAA GGGGCAAACG 900 CGGGATGGAA GTGACGGCAT CCCAGGTAGA GGAGAGGGCC TGGGCAATGG CTGTGAGGGA 960 GAGCTCAGGA AATGGGAAGG CCACCAGTGT GGCCCAGGGC AGAGAGGTCA GGGGACCAGG 1020 CAGGAGACAG GATGTGGGGG GAGGCCAGTG CAGAGCACCT GGGCCACAGC CACGGGTCAA 1080 GTTCGTGTTT ATGCTGGGAG CCTGGGGAAG CCGGCGAGAG ACTGGAGTAG GAGTGGCCTT 1140 CAGGTCTTGG GGCGCCCAGT ACAGTGCAAG TGATGGGCTG GGGCCCCTCC GCCCTCCTTG 1200 TCAAGCAGTG TCCACGGATA AGGGCGTCCC GGGGCGGGGG GGGGACGTGG GCGAGGAGAT 1260 GGTGGAGCTG GGGGAAGGGA CAGGGACAGA AGGCAGAAGA GTCACCCTCA GCGTCACCTT 1320 CTCTCCCCTC CCTACTCCGG AGGCCAAGCG CCCCAGCGGG AGGCTTCCCT GCCCGCCTCG 1380 GCCTCGCTTA CACCGCAGGT GCTGTGAGTC ACCCACCTGC GTGGTGAGTC AGGGGAGGAG 1440 GCCGAGAAGG CAGGTGGGCG GCGCGGCAGG GCGCCGGGCT TCGCGGGGAG GGGAGCGCTG 1500 TCTCCCCACG CGCCCCTCCC CCACGAGCGG CTTCCAGAAA CCCGTTTGCC CATCCCCGGC 1560 AGGAGGCCTC CGCCCGGCTT CTCGCTCCCT CTTCCCTCTC CCCGACCCCC TCCCGGGCTG 1620 TCAGCCGACT GCCACCGTCA CCATGGCTAC GCGGCTCCCG CTCAGTTCCA CAGTCAGCAG 1680 GAGTCGAGCA GGGGAGGCGG CTGTCTCCTT GGTCTTCCTG CTGCACCGGG TTCTTTGAAA 1740 ATCAGCTCCT GACTGCATGT TGCGGATTCC AGGCCCAGCC CCCTTACCTG GAAGGCTCAC 1800 CTTGAAAGAC GGCAGGATGA GACCAGGAAA CGGGGCCACA GGCATACCAA GGAAGCTTAT 1860 TTTGCCTGGC TTCCCTTTTT AAGCACGGAT GCATACCGGT GTGTTGGACA TGACTGATGA 1920 ACCAAGATTT GAGGAAGGCC ACCCACTGAG TGACTGGAGG TAGACGTGGA AGGCTTTGGT 1980 TGCCATAGGC AACTTGGGGC CAGAAAGACC TGGATTCAAA TTCTGGCACT TATCAAAGGG 2040 ATAAAGTGGG ACAAACAATT TTACCTTGCT GGGCCTCAGT CTCCTCATCT GTAAAATACG 2100 GATAATCCCC CCTTGGTAGA TTGGGATGAG GATTAAAGAT AATGCATGCA AAATATTTGG 2160 CACGTAGCAG GTGCTACCAA ATGCTTATTG TTGTTGTTAT TACGGAGTTC AGAGCCCTTT 2220 GAGATGCTCC ACAAGTGTTT GCTGATTTGA GGGTGGCACA AAAGGCAGTT TTCCCCAACA 2280 CCAATTGAAA GACTCCTTGG AGTGTGAATT TCAAGATGGT GGGGTACAGC AATTTCTACC 2340 CTCTCGTCGA AAGTCTCATC TCTGCTGGGA GACTGTGTGA CCCAGAACCA CAGTATAGGA 2400 AGATGGTGGA AGGTGAAGGC ATGAGCAGAG AAGAAGGGAG GTCCAAGCTG AGTGCCTAGG 2460 AACAGGGGTG GCCTACATCA GAGAGGCCAG TTGCTATGGC CCATAGAACC TTGCTAGGTC 2520 TCAAGGACTG GGGCATTAGC TGCTGTGGAA GGGAGTAAGG TGAACACAGA GGCATTATTT 2580 AGAAGTGTTT ACAAGTATTT ACAACAGGCA GACAGACTTG 2620
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