Tag | Content |
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EnhancerAtlas ID | HS139-34945 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr22:23492900-23494640 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Klf1 | MA0493.1 | chr22:23494327-23494338 | AGCCACACCCT | + | 6.02 | PPARG | MA0066.1 | chr22:23493983-23494003 | TTGGGGAACAGTGACCCACA | + | 6.15 |
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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 |
GH22I023152 | chr22 | 23494440 | 23496429 |
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Enhancer Sequence | TTTCCTCTGT CTGGAATGTC TTTCCTAATC CCCTCGCTTC CCCTTCCCCT TCCCCTTCAG 60 GTCTCAGCGT GTCAAGTCCT CTGGGAGCCT TCTCTGACCC CCCACTACCC TTGCCCCTGG 120 ACTGGGGAGG GTACCCCTCC TGGGTGCTCT TGTGCCCCCA AGAACTTATC TCACAGAATT 180 GCAGGCTGGA TTCCTCACTA GACCTAGCCC AAGAGGGCGA GGGCTGTGTC TGTCCTCTTC 240 CTGCCGCGGC AGCTCCTGCC ACCACTGGCA GAGGGATTGT GAAATAGTCA TTCCTTCTTT 300 TAACAAATAG GTACAAGGGC CTGCTTTTGC CCCTCTTCCT AAGGAGCTCA TAGTCTGCTC 360 AGGGAGTTGG CTGAGCTCAC AGGGGTCACA GAGGTGCGAT GAGGCTGCCA GAGAGCGCAG 420 CTAGAGGTTC CCAAACTGCA CAGAGTGGGT GAGGCAGAGC TGAGATCAGA ATAGCCGAAG 480 TGGCCATGGT GGTGGGATGA GAGTAATGGC ATCTGTTGGG GAATGCTGGT GCCATATCAG 540 GTGCTTCACA CAGATGATCT CCCTGATCCC TTATGGCAGC ACTGGAGGTG GGGAAACTGA 600 GGATCAGAGG GTACCTGCTG TAAGACCTTG TCAACACCTT TACTCATTCA TAGGAGAAAT 660 GGAGTCAGAA CGAAAGGGCC CTCTGGGAGC AGGGTAGACA CAATCCCTGC TCTCACGGAC 720 CTGGCAAGGT GACCTGCAGC CCAGGTCACC AGGTGACACA GTGGTGCCCT CTTGCTGTCT 780 GCAGGCAGAG GAAGTGCCTG TCAGATATTT ACCCAGGTTG GTTGCTGTGA CCATTTGGCT 840 CCTTGGGGAT GAGCTGCAAA AACTCTTAAA GTGTTGTCAA CAGTCCCAGG AAGCTGGGAC 900 AATGGCACCT GTAGTCCCAG TTACTCAGGA GGCTGAGGTG GGAGGATCAC TCGAGCCAAG 960 GAGTTTGAGA CTACTAGCCT GGGCAACACA GCGAGACCCT GTCTCTAAAA AAATAATAAA 1020 CAGTCCGAGA AACGCCTCTG CACAGAGTGT AGGACACACA GAGGGTGAGG GTGGCGGCTG 1080 CTCTTGGGGA ACAGTGACCC ACAGAGAGCC CAAGAACCTC AGAGCCGATT TGCCTCAAGC 1140 CACAGCCCGG ATGCATAGAG CCTCAGCCCT GTTCGGGGTG TGCCCCTTGG CCTGTCGGAC 1200 CCTTACAGAT CTCTAAGTGA GCAGGGCACG GTGGTGTCAT GGTCAGGGAG TGCCTGCTTG 1260 CAAGAGGCCG GAGCCCACAT CGGCGCACAG CCCCGGGGGT GCATAGGAGG GTGAGGGGCT 1320 GCCCGTCCCT TTTGCCGGGG TCTCCCTGCA CGTGGACCCT GTGTCTGCAC CCTCAGCACA 1380 GCTCCCGGAC AGCACAGACG TGCCCACGGC TGTTGGTTGG TTACCACAGC CACACCCTGG 1440 CCTCCTGCCT CTGCCCCTCC ACCTGTGACT CGGCCTCTTG TTATGCCCAT TCCTAATTCT 1500 CAGGATGGGG ACTTTGGCCA AATATGGTGA GGGGTGCAGC TCTAGGGGCA GCAGAGTCTC 1560 CAGCCTCTCC CGTCTCCCCT CTGGGGACTG TGAAGGGGGA ACACAGTGTC TCAGCAGGGT 1620 GGCCCATCCT GTGTCCAGGA GTGAGGGGTG TCTCACCAGC AGAGAGCTCA GGGAAGGAAG 1680 GGGCTGTGAG TGTCTGAAGA CACCCTGGAA GGCATGCCCG ACGGCAACAC GGCCATATTT 1740
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