Tag | Content |
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EnhancerAtlas ID | HS105-52733 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr22:28424570-28425900 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr22:28424603-28424621 | GGAAGGGAAGAAGGATGA | + | 6.08 | EWSR1-FLI1 | MA0149.1 | chr22:28424599-28424617 | GGTAGGAAGGGAAGAAGG | + | 6.67 | Tcf12 | MA0521.1 | chr22:28424645-28424656 | AACAGCTGCTG | + | 6.32 |
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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 |
GH22I028026 | chr22 | 28422486 | 28427373 |
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Enhancer Sequence | TTGGCAGCTC TCTCCTGTGA AGGACTTGAG GTAGGAAGGG AAGAAGGATG AGGGAGGCTA 60 CAACCCAAGA TGGCCAACAG CTGCTGCATA GGCACACAGA CGTCTCATCC CTTCCAAAGT 120 TTCTCCACCC ATGTTAAGAA TTTAAGTTTA GCACTATTCT TCCCACTTTA CTCCAAACAA 180 CAGAAACCCA CCAGTTGTTC AGTGCCTTCC ACACATTAAG TCGGTCAGTG TGTTATTTAT 240 ACATTGGCTC CTTTATTCCC ACATTACAGG AACCCTGCAG GGTAAGAAGC CATCCCCATT 300 TCACAGATGA CGAGACTGAG GCTGACAGAG GTGAAACTGC CTCCCTAGTG TCCTACAGCT 360 TGTGAGTGGC AAGGCCAGAG GCTGCACTCT GAGCTCTTCA CACTCTAGTT TATCACCACA 420 GCCTGCATCA CCTGGTGGAG GTAAGTGTCA CCTGCCTTCA CTGGCTGAGA AGTTGGCAGA 480 GCAAGAACAT GTGTCCAGGC CCAATCCCAG GCCTCCGCAA ACCTGGTTGC ATCCCTACAT 540 GAAACCAAAA GCCATGAGGG ACACCTGTGA AGGTGGCTGG GAAGAAGGAA CTAAGGGTGA 600 ACTAGCTTGA AGTTTTGGCC TCCTTACAAC CAGGCTGCCA GCTCCTACAT CCCCTGCCCT 660 TGGCTCCCTT CCCACTCAAC TCAGCCCTGG GAAAGTCAAC ACACATTTGT CACCCTGACA 720 GCACAATAAT GAGAGGAAAC CAGGGCCTGG AGTAGGAACA GACAGGGCGC ACAATGCCCT 780 GCACAGCAGG GCTGCCAAGC AGAGGCTGCC TCCCACCCAG TGCACAGTCA CTTCCTGCCT 840 GTGTTCTAGG GTCAACCAGC TGCCCTTTAA AGGCAGGCCT TCAGGCTGTG GCAGGGACCT 900 AGGGAGTCTG TGATATCTTT CCAAAGAGGT CTATCAAAAT GTACTCCTAG GTTGTTGCCA 960 GGCAACCAAA CAACAGTGGG ACAGGTGTCC CTCAACCCCA ACCGCCTGCC CTGTTTATCC 1020 GGACCCAGCT CAGGTGTCAC TCCTAAGAAA AAGATGAAGG GGTGTGCTGG CTTGGAAATT 1080 TCAAACTCGA TTCATCTTAA AGCCATTAAG GCCTATTTGG TCAAGTGACA GGGAACTGAG 1140 GTCTTGGCAC AGACGGGTGA GCCTGGGTCT GGATGAGTGC ATTCCTAGGC CCAGTTTCTC 1200 CCTCCAACAG CACTAGCATT CTCACTCTCC CTGACCTCCC CGAATCTCAG GCCAGGAAGT 1260 CAGTGCAGGT ACCTGGCCCA GGAGTTACCT GCAGAAGCTG GCAAAGAAGT ATGTGAAGTT 1320 GCTCTGGCTT 1330
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