| Tag | Content |
|---|
EnhancerAtlas ID | HS139-12502 | Organism | Homo sapiens | Tissue/cell | Myotube | Coordinate | chr12:53524590-53525670 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Mafb | MA0117.2 | chr12:53525277-53525289 | AAAATGCTGACA | + | 6.62 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr12 | 53524797 | 53524847 | | chr12 | 53525610 | 53525670 |
| Enhancer Sequence | CCTACTAGTA GTCACTCTCC ATGTCCCGAA AACCTCCCAG CCTTGGGCAA CCACTGATTT 60
ACTTTCTGGA TATTTCTTTT CTTTTTCTTT TTTCTGTTTT TTTTTTTGAG ACAAGGTCTC 120
ATTCTGTCAC CCAGACAGTG GTTTCTGGGT ACAGTGGTGC CATCATAGCT CACTGCGACA 180
TTGAACTCCT CGCACAAGCA ATCCTCCTAC CTCAGTCTCC TGAGTAGCGG AGACCACAGG 240
TGCACACCAC CACACCCAGC TAGATTTTGT ACTTAAAAAA TTATTTTTGT AGAGATGGGG 300
TTTTGCCATG TTGCCAAGCT GGTCTCAAAC TCCTGGGCTC AAGTGATCTG CCCACCTCAG 360
CCTCCCAAAG TGCTGGGATT ACAGGCATGA GCCACCATGC ATGGCCTATT CTGGATATTT 420
CACATAAATG AAATCAGGCA TCAGTGGTGG GGATGGCTAC AGGCCAGGGC TGCTGACTGA 480
CAAGCTAGGA GAGGGCCCAG TGCCCAGAAT CTTGGTGGGC GCTGCTGAAG CACCGCCTAC 540
ACCATGCCTC TCTCTGCCAC CTCCTTGGAG CGTTTTGAGC AGCTGCACGA GATGTGCCTC 600
CAAGGGGTGC ACTAGTGGCT GCTGGGTATG GCAGGGACCC AGGAGAAGCT GATCAGAGAT 660
TTTGATGAAA AGCAACAGGA AGCAAACAAA ATGCTGACAC AGATGGAGGA GGAACTACAT 720
TATGCACCCG TATCTTTCCA TAACCCCATG ATGTCTAAGC TTCAAGACTA TCAGAAGGAC 780
CTTGCCCAAT TCCATCTGGA GGCAAGAAGT ACACCTTTGC AGCCATGCCT GGGGACCGAG 840
GAGACATGAA ATATGGCACA TATGCTGTAG AGAATGAGCA TATGAATAGG CTACAGTCTC 900
AAAGGGCAAT GCTTCTCCAA GGCACCAAAA GCCTGGGCCG GGCCACCCAA GAGACTGACC 960
AGATTGGCTC AGAAATCTCA GAAGAGCTGG GGAACCAACG GGACCAGTGA GAACGTACCA 1020
AGAGTACACT GGGAAACGCA AGTGAAAACT TGTTCAAAAG TCGAAAGATT CTCTCTTCTA 1080
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