| Tag | Content |
|---|
EnhancerAtlas ID | HS098-37747 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr3:13936170-13937800 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MAX | MA0058.3 | chr3:13936215-13936225 | ACCACGTGCT | + | 6.02 | | Myod1 | MA0499.1 | chr3:13936440-13936453 | AGCAACAGCTGCA | - | 6.64 |
|
| | 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 |
| GH03I013894 | chr3 | 13936421 | 13938350 |
|
Enhancer Sequence | GGAGCTCTGC CCATCTTAGG GAGGGGAAAC GGCTCCAGAG GCTAGACCAC GTGCTCAACG 60
CCACACAGCC AGCGGAAAAA GCAGAGGGCC AGGCGTTTTT GCAAACATGC TGGTTTAATC 120
CTCTGTGTGC GCCTCCATAC ACAGGGTCCT GACCTCGCTG TCCGCTCACT CGGGTGTCCC 180
TTGCGTCCAC ACTCCGCCTT ACACACAAAG GGCTCTCAAC AAGTGCTCAC TGGCCCCTAA 240
TCCTCCCGCC GGGCCCGGGA GAGCAGAATT AGCAACAGCT GCATTTTGCA GATGGGGAGA 300
CTCAGATGTG CGAGGGCTAC CCCAGGGCAT CCAGGTGTGA TGTGGGGGTC CCGAGACGCG 360
TCGCCAAGTC AAGATACCCC GGAGCTCAGT TCGTTCCTCA GCCTGAGCGG TGCCCACGAT 420
GATGGAAGAC TTTGCAAGAC CCCTCCTGGG TCGTTTCGAA CCGAGCTGCC CTAGAGCTGT 480
CGGGTAGGTG AGGGGGAGAC AGGTGCACGA GCTGACCTCG TAGGTGACCG AAGAAGGGGA 540
GGGAAGCAGG CCCGATGGAG CCGACCTGTA CCCGACGCAA CCCGCTGTGG GCCGAAACGG 600
GAGCTAAGCC AGATGGAACA AACGACCCCC AACCCGAGCC CGGCGGGGCG AACAGGACAT 660
CCCGCGTTGT TCCACCTGCC AAAGAGGGCG AGCGCGCGGG CCGATCGGAG CAGAGCGAGA 720
GGGCGGGGCC AAGCGGAGCG GATGGGGCCA AGTGGACGAG CCGAGGGAGT GGGGCGCAGC 780
CGAAAGTAGC CGAGTGAAGC CGAACAGAGA CGAGGCGCGG GTCGGGTGGT GCCAAGCGGA 840
AATGAGTGGG GCCGAGCGGG GCAGGGTGGA GCCGAGCGGA GCCGGGTGGA GCCGAGCGGA 900
GCCGAGCGAG TGAGAAGCCG GAGGCCGAGA GGGCCGGGCC GACTTGAAGA GGTGGGGATT 960
GCTGAGGGCT GGTCTGTCGG CTCTGGAAAT CCTGTCATAC TGTCACTTTT GGATTCCGCC 1020
GTTTCCGTCC CAACGGAAAA CTGGGGCTCC TGGATTCCCC TGACCCGAGT TGTAACCACC 1080
GACGAGAATC TTTTTCACTG GCGGCCTCGG CGTCGGCATT TTATAAAATG AGAGCGGGGA 1140
GGGCGGCCGA AGACGAGTGT GCGGAGCCTT AGGCCCCCCG CTCGGGTCCG CTTTTCGTAT 1200
ATTCGGGTAG GATCGGATGT GGTGTCTTCC GTTGAAGTCC CTCGGCTCCA GTTCACCTGG 1260
GAGCGGGTGG GGGTTCTGGG GAATGTCACT TTAAAGACTT TGCTTTTGGG GAACGGTCCT 1320
GGCGCCTCCT GTGTAGATGC TGTCACTTGA GGTCTAGAAA GGGTCAGTGC GTGACGCAAC 1380
GGACGCCGGG GAAGCCTGGT CTGGATCCCG AAGTCCAGCT CGTTTACCTG CAACAGGCTG 1440
GAGGTCCCTG CAGCCTGGCT GTGAAGGAAT TTTACCCGGG GGGCTGCGCC TCTGCCCTTA 1500
CCAGGGCAAC CTCACTGAGC CCCACTGTTT ATATCTGTAA GATGAGGAAA GCGATGCCTT 1560
CCTCTCAGGC TGCTGTGCAG CTGGATGGGG TGGGGGCTCT GTATTTTGAC AGTGTTATCA 1620
TGTAGTCATA 1630
|
