| Tag | Content |
|---|
EnhancerAtlas ID | HS139-42793 | Organism | Homo sapiens | Tissue/cell | Myotube | Coordinate | chr5:1227310-1228800 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| POU2F2 | MA0507.1 | chr5:1227700-1227713 | AACATTTGCATAT | + | 6.21 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr5 | 1227409 | 1227924 | | chr5 | 1228000 | 1228400 |
| Enhancer Sequence | CAGTTACCAT TGCTAAGCGC CTGCAGTGTA CTGGAAGTGT CTGGCACTAG CCTCCCTTAA 60
ACTCAGCTGC TCCACGCTGG GGCAAAGCTG GGGAGGCCCC CACCTGGGGT GCTGCTGAGG 120
AGGGAGAACA GCCCTGCCCG CCAGCTGCGC GGGGACTTCA GGGCTGCTCC ACTCATGAAC 180
GACTCTACCA TCAATCTCCT GATGCAAGCC ACCGGGTTGC ATGTCATGAA ACATCCAAGT 240
TTATTTAACT CACACACTTC CTAAGGGCCG TGCCATCAGC ATTCTCACCC TGTGTGTGAA 300
CATGCCCTTC ACTTTGTCTC GCTGTGAGGA TCACTCATTG ATGATTTTGA AAACAAGATA 360
TAATTAAGAA GCAGGTACTG TGTAGCTTTT AACATTTGCA TATACTCATG ACTACCAAAG 420
GCGAATATTA TTTGCTCTCC CATTCATAAG TATTCAACTA CATAAATGTT CTCTTCAAAG 480
CTAAGACTTG TAAAGCAACA TTGTAACAGA ATGTAGCAAA ACGTTGCGGT AAAGATTTAC 540
AGTGATTTTC TCACACCTAT GACATTTCAT GGCAGCTGCT TTATTACACA TTCAGCGTCT 600
TTAAATCAAA GGAACGTAGA CTCGTAAATG CCAAGCGATG GGTTCAGGCC AGCTGCCCGG 660
GACACTCTAA CACTTGCTGT GGTTTAAGGT TTCAACCCAG GAAGCTTTTA TGACTAAGCT 720
GGTGGCCCTG GGCTGGCTGT GTCCACACAC GTGAGGTCAC TCATCAAGCG CGCCCCCTCC 780
CCGCTACTTC CTGCCTCCGG TGTTCAACCG ACTTCTGTAT CTGGTAGGTG CTGTTGAGAT 840
CTGTGGATTC TTGCACCAAA AACGACACTG TATTAATTAC TATGGCTTCT TCGTTAGTCT 900
CGACGCCTAG TAGTAGAGCA AGGCCTTTTT TTTTTATTCT TTGAACTTTT GCCAGCTGCT 960
ACTTTTCCTC TGAGCTTTAC ACCAGGTTGT CAATTTCCAG AAGAGATTCT TCGGCGCTCC 1020
CTTGGCCCTG TGCTGCTTTC TACACTGCCC GGGGGGAGTT TCCACCTTGA CGGCCTTCAC 1080
GCCTTGGAGG CAGTGCCCAG GCAGTGGGGG CTGGCACTGG AGCACCATCT GCCGTCTGCA 1140
CCCTCGCGGC TCCCGGCTCG GTCTCCTTTC TGCCTTCCTG CGGGTCTCTC CATCATGACC 1200
CTGGGCGTGT CTCTGGTTGA TTCTCAGCAA TCCCTGGCTT TTGCCGCTGC TCTGAGCAGA 1260
GCCTGCTTCT CCTCTGCATT TGCTCAGTGG CTGCACTGCG GCCTCTGCAT CTCTCAGCCT 1320
CGTGTGGTGG GGTGCAGGTT TCTCTCGATC CTGCGTGGAT CGATTGTAAC AGCAGCCAGC 1380
CGTTCACAGC CACCTTTCCC GTCTTCGGCA GACACCACTG CGTCCTCCAT GCTTATGAAC 1440
GACTGCTAAA CTTCACGTAA TTGTTAAAAC TAGGAGCTGC AGCCTGGGCA 1490
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