Tag | Content |
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EnhancerAtlas ID | HS034-29515 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr8:102091430-102094360 |
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 | CTTTGGCCTC CAAAACAGCA GCCCCACCTG GTATTGAAGG GCCGGTGTGT AAACAACCTT 60 CCTTCTATCT TATCCTGGCT GGGTTTATCA GATTTGACTC ACTCCCTGGA GCCCCTTGCA 120 AGGACTGGGC TGGGATTGCA GGGCTGAGCA GGAACCGGCT TCTCTAGCCT CTTCAGGGAA 180 GGGCCTTCTA AACTCCACTC TGCCCCATAC CCTCCAGCTA GAAACCCAGC CTCCTGCCTT 240 TGGGGAATAT AGCCCCAGTA AGGGCTCAGT GTCTTTTCCA CAAGCTCTTT TCCTATGGCC 300 TTTAGGGGCA CATGACTTTG AGGAAACCAG ACAGCTGGGG GGGACATGAG AATCAGGGCC 360 AGTGCTTGCA GGAAAGAAAG CAAACGCTCT GAATGTGAGC CAGATGGCAG GTCCCCCACA 420 CAAGGCAGGG GGCTCAAGAA CACTTCCTTT CATGCTAGCA GTACTAGCTG CTCCCACCTT 480 TGTGAAATGC ATTTTTGAAA GCAGAACAAA TGATCATTTA ATTTGAGAAG CCCACACCTC 540 TTAATACTCA TAGTATTTTC ACCATCATCC TGGCCCCTGG TCAGCTGGAA GAGCAGCAGG 600 GGAGGGGAAG CATCACTTTG GTTTCTACCT CCCAGCTGGG GCAGGTGCAA GGCAGCGCAC 660 TCCATCAGCT CCTTGCCCAG AAGGGCAAAA TGATGTCTCC TTTCTCCCTC TCTTCCTCTT 720 TCCCTCTCTC CCTCCCTCCT TCCTTCCCTC TTTCCTTTCC TCCCTTCCAA CATTTTTTGA 780 GTGAGGATCT TCTGCCAGAC ATTGTGCAAA ATTCGGGGAA TCCAAGGTAC AGAGAGGAGG 840 CCTGGCTCTG CCCTCCTGGC CCTTCCAGTC CAGTGGGGAG GAGAGGCCTC TTGCCAAGAC 900 ATGGCAGCTG TGAGGAATGC TACAAAGAGT TTCTGGGTCC TGCGGGGTGG AGTGACTGGA 960 GTGACTGAAG TTACCCGCCT GGGTGGGGTG GGAACAGGAC AGGCTGTCCT GGAAAAGTGA 1020 TGTTTGGGCT GATACCAGAA GGGGCAAACG CGGGATGGAA GTGACGGCAT CCCAGGTAGA 1080 GGAGAGGGCC TGGGCAATGG CTGTGAGGGA GAGCTCAGGA AATGGGAAGG CCACCAGTGT 1140 GGCCCAGGGC AGAGAGGTCA GGGGACCAGG CAGGAGACAG GATGTGGGGG GAGGCCAGTG 1200 CAGAGCACCT GGGCCACAGC CACGGGTCAA GTTCGTGTTT ATGCTGGGAG CCTGGGGAAG 1260 CCGGCGAGAG ACTGGAGTAG GAGTGGCCTT CAGGTCTTGG GGCGCCCAGT ACAGTGCAAG 1320 TGATGGGCTG GGGCCCCTCC GCCCTCCTTG TCAAGCAGTG TCCACGGATA AGGGCGTCCC 1380 GGGGCGGGGG GGGGACGTGG GCGAGGAGAT GGTGGAGCTG GGGGAAGGGA CAGGGACAGA 1440 AGGCAGAAGA GTCACCCTCA GCGTCACCTT CTCTCCCCTC CCTACTCCGG AGGCCAAGCG 1500 CCCCAGCGGG AGGCTTCCCT GCCCGCCTCG GCCTCGCTTA CACCGCAGGT GCTGTGAGTC 1560 ACCCACCTGC GTGGTGAGTC AGGGGAGGAG GCCGAGAAGG CAGGTGGGCG GCGCGGCAGG 1620 GCGCCGGGCT TCGCGGGGAG GGGAGCGCTG TCTCCCCACG CGCCCCTCCC CCACGAGCGG 1680 CTTCCAGAAA CCCGTTTGCC CATCCCCGGC AGGAGGCCTC CGCCCGGCTT CTCGCTCCCT 1740 CTTCCCTCTC CCCGACCCCC TCCCGGGCTG TCAGCCGACT GCCACCGTCA CCATGGCTAC 1800 GCGGCTCCCG CTCAGTTCCA CAGTCAGCAG GAGTCGAGCA GGGGAGGCGG CTGTCTCCTT 1860 GGTCTTCCTG CTGCACCGGG TTCTTTGAAA ATCAGCTCCT GACTGCATGT TGCGGATTCC 1920 AGGCCCAGCC CCCTTACCTG GAAGGCTCAC CTTGAAAGAC GGCAGGATGA GACCAGGAAA 1980 CGGGGCCACA GGCATACCAA GGAAGCTTAT TTTGCCTGGC TTCCCTTTTT AAGCACGGAT 2040 GCATACCGGT GTGTTGGACA TGACTGATGA ACCAAGATTT GAGGAAGGCC ACCCACTGAG 2100 TGACTGGAGG TAGACGTGGA AGGCTTTGGT TGCCATAGGC AACTTGGGGC CAGAAAGACC 2160 TGGATTCAAA TTCTGGCACT TATCAAAGGG ATAAAGTGGG ACAAACAATT TTACCTTGCT 2220 GGGCCTCAGT CTCCTCATCT GTAAAATACG GATAATCCCC CCTTGGTAGA TTGGGATGAG 2280 GATTAAAGAT AATGCATGCA AAATATTTGG CACGTAGCAG GTGCTACCAA ATGCTTATTG 2340 TTGTTGTTAT TACGGAGTTC AGAGCCCTTT GAGATGCTCC ACAAGTGTTT GCTGATTTGA 2400 GGGTGGCACA AAAGGCAGTT TTCCCCAACA CCAATTGAAA GACTCCTTGG AGTGTGAATT 2460 TCAAGATGGT GGGGTACAGC AATTTCTACC CTCTCGTCGA AAGTCTCATC TCTGCTGGGA 2520 GACTGTGTGA CCCAGAACCA CAGTATAGGA AGATGGTGGA AGGTGAAGGC ATGAGCAGAG 2580 AAGAAGGGAG GTCCAAGCTG AGTGCCTAGG AACAGGGGTG GCCTACATCA GAGAGGCCAG 2640 TTGCTATGGC CCATAGAACC TTGCTAGGTC TCAAGGACTG GGGCATTAGC TGCTGTGGAA 2700 GGGAGTAAGG TGAACACAGA GGCATTATTT AGAAGTGTTT ACAAGTATTT ACAACAGGCA 2760 GACAGACTTG CAGGTCTCAA GCCCTACCCA CTTCTGCAGG AGAGGAAGTT TATTTTCTAG 2820 AGAAATTGGA CCAGAGACTT CGTGCTAATA ATACCAGGTT CAGAGGGAGG CTGCGATGGG 2880 GTGAGTTTGC ACAATGAGTG AGTGCTTCCC TGACCTAGCC TTAGAACAAC 2930
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