Tag | Content |
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EnhancerAtlas ID | HS023-24531 |
Organism | Homo sapiens |
Tissue/cell | CD8+ |
Coordinate | chr8:102092070-102094290 |
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 | GCAGGTGCAA GGCAGCGCAC TCCATCAGCT CCTTGCCCAG AAGGGCAAAA TGATGTCTCC 60 TTTCTCCCTC TCTTCCTCTT TCCCTCTCTC CCTCCCTCCT TCCTTCCCTC TTTCCTTTCC 120 TCCCTTCCAA CATTTTTTGA GTGAGGATCT TCTGCCAGAC ATTGTGCAAA ATTCGGGGAA 180 TCCAAGGTAC AGAGAGGAGG CCTGGCTCTG CCCTCCTGGC CCTTCCAGTC CAGTGGGGAG 240 GAGAGGCCTC TTGCCAAGAC ATGGCAGCTG TGAGGAATGC TACAAAGAGT TTCTGGGTCC 300 TGCGGGGTGG AGTGACTGGA GTGACTGAAG TTACCCGCCT GGGTGGGGTG GGAACAGGAC 360 AGGCTGTCCT GGAAAAGTGA TGTTTGGGCT GATACCAGAA GGGGCAAACG CGGGATGGAA 420 GTGACGGCAT CCCAGGTAGA GGAGAGGGCC TGGGCAATGG CTGTGAGGGA GAGCTCAGGA 480 AATGGGAAGG CCACCAGTGT GGCCCAGGGC AGAGAGGTCA GGGGACCAGG CAGGAGACAG 540 GATGTGGGGG GAGGCCAGTG CAGAGCACCT GGGCCACAGC CACGGGTCAA GTTCGTGTTT 600 ATGCTGGGAG CCTGGGGAAG CCGGCGAGAG ACTGGAGTAG GAGTGGCCTT CAGGTCTTGG 660 GGCGCCCAGT ACAGTGCAAG TGATGGGCTG GGGCCCCTCC GCCCTCCTTG TCAAGCAGTG 720 TCCACGGATA AGGGCGTCCC GGGGCGGGGG GGGGACGTGG GCGAGGAGAT GGTGGAGCTG 780 GGGGAAGGGA CAGGGACAGA AGGCAGAAGA GTCACCCTCA GCGTCACCTT CTCTCCCCTC 840 CCTACTCCGG AGGCCAAGCG CCCCAGCGGG AGGCTTCCCT GCCCGCCTCG GCCTCGCTTA 900 CACCGCAGGT GCTGTGAGTC ACCCACCTGC GTGGTGAGTC AGGGGAGGAG GCCGAGAAGG 960 CAGGTGGGCG GCGCGGCAGG GCGCCGGGCT TCGCGGGGAG GGGAGCGCTG TCTCCCCACG 1020 CGCCCCTCCC CCACGAGCGG CTTCCAGAAA CCCGTTTGCC CATCCCCGGC AGGAGGCCTC 1080 CGCCCGGCTT CTCGCTCCCT CTTCCCTCTC CCCGACCCCC TCCCGGGCTG TCAGCCGACT 1140 GCCACCGTCA CCATGGCTAC GCGGCTCCCG CTCAGTTCCA CAGTCAGCAG GAGTCGAGCA 1200 GGGGAGGCGG CTGTCTCCTT GGTCTTCCTG CTGCACCGGG TTCTTTGAAA ATCAGCTCCT 1260 GACTGCATGT TGCGGATTCC AGGCCCAGCC CCCTTACCTG GAAGGCTCAC CTTGAAAGAC 1320 GGCAGGATGA GACCAGGAAA CGGGGCCACA GGCATACCAA GGAAGCTTAT TTTGCCTGGC 1380 TTCCCTTTTT AAGCACGGAT GCATACCGGT GTGTTGGACA TGACTGATGA ACCAAGATTT 1440 GAGGAAGGCC ACCCACTGAG TGACTGGAGG TAGACGTGGA AGGCTTTGGT TGCCATAGGC 1500 AACTTGGGGC CAGAAAGACC TGGATTCAAA TTCTGGCACT TATCAAAGGG ATAAAGTGGG 1560 ACAAACAATT TTACCTTGCT GGGCCTCAGT CTCCTCATCT GTAAAATACG GATAATCCCC 1620 CCTTGGTAGA TTGGGATGAG GATTAAAGAT AATGCATGCA AAATATTTGG CACGTAGCAG 1680 GTGCTACCAA ATGCTTATTG TTGTTGTTAT TACGGAGTTC AGAGCCCTTT GAGATGCTCC 1740 ACAAGTGTTT GCTGATTTGA GGGTGGCACA AAAGGCAGTT TTCCCCAACA CCAATTGAAA 1800 GACTCCTTGG AGTGTGAATT TCAAGATGGT GGGGTACAGC AATTTCTACC CTCTCGTCGA 1860 AAGTCTCATC TCTGCTGGGA GACTGTGTGA CCCAGAACCA CAGTATAGGA AGATGGTGGA 1920 AGGTGAAGGC ATGAGCAGAG AAGAAGGGAG GTCCAAGCTG AGTGCCTAGG AACAGGGGTG 1980 GCCTACATCA GAGAGGCCAG TTGCTATGGC CCATAGAACC TTGCTAGGTC TCAAGGACTG 2040 GGGCATTAGC TGCTGTGGAA GGGAGTAAGG TGAACACAGA GGCATTATTT AGAAGTGTTT 2100 ACAAGTATTT ACAACAGGCA GACAGACTTG CAGGTCTCAA GCCCTACCCA CTTCTGCAGG 2160 AGAGGAAGTT TATTTTCTAG AGAAATTGGA CCAGAGACTT CGTGCTAATA ATACCAGGTT 2220
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