Tag | Content |
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EnhancerAtlas ID | HS093-20119 |
Organism | Homo sapiens |
Tissue/cell | HL-60 |
Coordinate | chr21:35347760-35349200 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr21:35348775-35348793 | CCCTGCTGCCCTCCTTCC | - | 6.45 | MEF2C | MA0497.1 | chr21:35348667-35348682 | ATCTATTTTTGGCCT | - | 6.87 | RREB1 | MA0073.1 | chr21:35348906-35348926 | ACCCACCCCACCCCCCGCCC | + | 7.13 | Stat6 | MA0520.1 | chr21:35348175-35348190 | GGTTCTCAGGAAACG | - | 6.75 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_56093 | chr21:35338449-35351194 | u87 | SE_67857 | chr21:35338449-35351194 | u87 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH21I033975 | chr21 | 35347200 | 35350635 |
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Enhancer Sequence | AAGAGTAGCT AGAATTGTTT TAGTCTGTGT ATAGTGAGTT GAATATCTGA AACCTCTGTG 60 AGTCTGTTTC TTTTGTCTGC TAGCCCTACT CATGGCGTCA TGTTTTCCTG GATGTTTAGT 120 TGGTTGTCTT TGAATATGTC CAACTCCAGT TATTTCTGGG AATACCCAAA GGCACACCTG 180 TTCACTATCA CCCAGTGAAC TGCCATGTGT TTGTCTCCTG TCATGGTAAC ATTTGCATTC 240 AGGGAGAGGC CTCTGCTCTC TGCAGAACAG TGTGAAATCA CCTCATTTTT GCCTTCAATG 300 AAGGTTGTCT CTTGCTGGTC ACCACCACTT CCTCAAATGA CTAATGCCAC TCTTGCTCAC 360 AGTGCTAAGG CGCTAAGGAG TTTTCAGAGG GCTAGAGTGA TTCTGCATCC TCTGGGGTTC 420 TCAGGAAACG AGGCCACAGG GCCATCTGTG CATGAGTGAC AGTGGGGTGG GGTGGATGAG 480 CAGTGGCAGT GGTGGGCACC TATGCTGCTG GCGCCACAGC TTTTTATATC TTGGTGAAAA 540 CAACGCCTTG CGTTTTCACT TGTAGATTCT CCGGCTACAT TCCACAAGAA CAAATTCTGG 600 TCACAGAGGC CAGAGTAGAC TATCAGTGTA ATGGCCCTTC CCCTTTGATG ATAGCAGCTT 660 TTTTCGGGGG AGCAGGGGTG GCCAAACTTC CTAGCCTTAT TTTATCTTCC TTTCTAGTTC 720 TCCCCAGAGG CTGCTGGGTC CACCTCTCCC TCTGCCAGAC AGACAGGCTC AGACATGCAA 780 GAACGGAAGG GGGTGTGGGG GTTGGTGGGA GGATTAAGTT GGGGAAAGCC AGTCTTGTCT 840 TTGTAGATTA CCAGAACTGA CACACGTACA CACACGTACA CTCACTCACT CACTCACTCA 900 TCTATTCATC TATTTTTGGC CTAAGTGCCT TTGGACACTT CTTCGGAAAA GCACATGAAC 960 TCTTCGGAGT CTCCTGTTCC ACTTGGTAAA TTTCCTATAG CCACGCACTG AAAGTCCCTG 1020 CTGCCCTCCT TCCTCTGAGC TTGTGGGGCC CACAGATCCC CTGCTCCACT TCCTGCTTCA 1080 TTTCAGCTGA TGGTGAGTCC AGGGCAGGCT TGTAGGAAGG GCGGGCTAGG CGTGGGGAAC 1140 TGCAGCACCC ACCCCACCCC CCGCCCCAGT GCTTGTTGCC CCAGCCTCTG TCTCCCTCGC 1200 TGTGCCCTTC CCTTAAGCCC CACTCTTGGC CTCCCCAAAG ACAGAGTTTG TTCTGTTTTT 1260 ATTGATAGGA TGACACTCCC TCGTTCTAAT ACCATCTGAA TGCCTGAGCA ATTACATCTT 1320 ACAACCTCAT GAAAAACACA GCAGCTTGTC ACGATGAATG ATGTTACCGT GAATAATGCA 1380 GTTTTGAGTT CAAACTCCTT CTTATTCCAA GAATGAGTAA ATATCCCTAT TCCCTCCCCT 1440
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