Tag | Content |
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EnhancerAtlas ID | HS099-10440 | Organism | Homo sapiens | Tissue/cell | HSMMtube | Coordinate | chr18:43858020-43859550 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr18:43859358-43859376 | GGAAGGAGGCAAGGGTGG | + | 6.06 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 1 | ID | Chromosome | Start | End |
GH18I046278 | chr18 | 43858581 | 43858730 |
| Enhancer Sequence | CCCTTCCTCG GCCTCTGACC AGCTGCAGCT GTGGCAGGCA GTTCTGTGTG AGCTTGGACT 60 CATGCTGACA GCACCCCGAT TTCCATCACA CGGAGTGCAT CATTCAGATT TCTATTTCAG 120 CTCCTCCTCC GAAGTCCCAG GAGTCTGTTT GGCTTGTGTG ACTCAAGCAG AGCCCAGAAA 180 TTAGGGGAGT TAATGGCCCT GGGACAACCC TCAACAATGG AGGATGGGAG CCGGTAGACA 240 TATGCCCCAG CCTCTTTGAG TTGGACAGTT CTGGGAAGCA TTCTGTATGT TTTTCAGGAG 300 ATCCCAGCGG AATTGAGCCC CCATTGCTCA TGGCAGTGAC TTTGATGATG GACCTTATAT 360 TGGCTTTTCC TCCTCACTCT CACTTTTTCA TTCTCCTCAA TTCCTCACTT CTATGTCCTG 420 AGATCAACTC CCAGTTAAAC CACCTGCATC TAAATCCTTG TCTCAATCTC TGCTCCTAGG 480 AGAATTCAAA CTAAGACAGG AAGGAAAAGG TCAAGTTCAC TCTGAGCTTG ACGTGCTGAA 540 GAGACATCCC GTGGAAATGT GCAGCAGGCA GTGGCCACGT GACTTTTGGA GATGCTGATT 600 TATGTATCAG CATGTGGTGA CAGATAAAAC CACAGGCTAG AGAAAATGCA TTCCTAAGAG 660 GCCAGTGCAG AGGCATCCTT CCAAGGCAGG GGTTCTCAAC CACGAGCCAT TTTACCCCCC 720 AGTAAATATT TGGCAATGCC CGAGGACATT TTTGGTTGTC ACAACGGGAA CAGGAACCTG 780 CTACTGGCAT CTAATGAGTA GAGGTGAAGG ATGCTGCTGA ACATCCTACA GTGCACAGGT 840 CAGAACCCCA TAACAAAGAA TGATCCAGCC CAAAATATCA CTAGTGCCGA GGCTGAGAAA 900 CCTGTTCTAA GGGCATTGCA AAGTACCATG AGAGTGATGC TGTGAAAGCT GGTTTCACAT 960 AGCCAGAGGG GCCAGCAGGC AGTGCTGCAG GGGCCATGGG AAGTAAGAAC CAATTATTGC 1020 CCATTGAGCT CAGCACCATG GGGCAGAAGC CAGTGCCTTG AAGGCAGTCG ATGAAGATGA 1080 GTACAGACTC TTTCCAGGAG CTTTGAGGGG AAGGAAAAGA GCAAGTGTTT GGGCTTAGCC 1140 AGAAGGAGCT GTAGAGTCAA GGAAGAGTTT TAAAAGATAC TGGAATGATA AACATCCTGT 1200 ATATGCTGAT GACAAAGCAC CAGTTGGGAC ACCAGAAAGG GATGACTGAT GGAAGAGAGA 1260 GAGCCCCGGG ACATAATGTG GTACTCAAAG CCAGATGAAC TAACTTGGAT CAGGTAAGGA 1320 AAACCTTCCC TGGAAGCTGG AAGGAGGCAA GGGTGGGCAT AGTTATACCT ACAGTTGTCA 1380 GGGAGGAAGG GTAGACTGTC GAGAGAGTTA ACCTGTGAGC CTTTTTTGTT CTTTGCTTGT 1440 TTTGCAGGCT ATAAGTGCAG AAGTGATAAG GTAGGAGGCC TGGTATTAAT ACCTCCTTGT 1500 TGATTGATTA CATATGGTGG TTTACTGCAG 1530
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