| Tag | Content |
|---|
EnhancerAtlas ID | HS139-08601 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr11:8402840-8404810 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Ar | MA0007.3 | chr11:8403196-8403213 | TGGAACACCCTGTCCCT | - | 6.17 | | Myod1 | MA0499.1 | chr11:8402995-8403008 | AGGGACAGCTGCT | - | 7.52 | | Myog | MA0500.1 | chr11:8402998-8403009 | GACAGCTGCTG | + | 6.14 | | TFAP2A | MA0003.3 | chr11:8403940-8403951 | TGCCTCAGGCA | + | 6.02 | | Tcf12 | MA0521.1 | chr11:8402998-8403009 | GACAGCTGCTG | + | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 4 | Chromosome | Start | End |
| chr11 | 8403838 | 8404574 | | chr11 | 8402971 | 8403080 | | chr11 | 8403565 | 8403708 | | chr11 | 8403765 | 8403833 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I008382 | chr11 | 8403915 | 8404755 |
|
Enhancer Sequence | AATCTAACTT GCAAAGGCAG TTGTGGGGAC TGCTACATAA TTAGTAAGGG GTATTCCAAG 60
TAATCTGTCA GCCGAGAGTC TCCTGGCTGC CCCTTCCCCA CTCCATTGTG GCTAAGGGTT 120
AGGGCTCCTG CTGTTGACCC ACGGAGAATG AAAGCAGGGA CAGCTGCTGG GGCTGTGAGT 180
GACTAAGCCA CAAGAGCCTG TGCCTGCCCT GATCCCCAAA TAAGGATCCC ACAGGCGGAA 240
GGTTTATCCC ACAGTGAACA TCCTGAATGC AGAAACATGA GAGATCACCT AGCACCCAGC 300
ACCCCACTTG TAGCCGACAC CCCACCTGGC TTCTGGTCTA GTGAGCACCG AGCAGCTGGA 360
ACACCCTGTC CCTGGGCCTT GCTGTACAGT GAGGGGCTGG ACTACCTCTC ACCCTTTACA 420
CCTCCAACGA TGCCTGTCAT TATTTCTTTT GTGAGCTCTG TGTTTTGAAA TATTTTATTA 480
CCCAAAAACT TTAGGTGAGT GTGGTCTGAG CCATTTCACT ATAGGCAGAT ACGCTTTTTC 540
CATTATGTTC CTTGCAATTT GGAAATAGCC TACAGATCCC TTTAGTTTGG GGCCCAGATA 600
GGAAACAGAC ACGTTGCATG TCAGGATTAC CTGGGGAGCT TCTGAGACCC AGAAGGGAAG 660
GGCCAGAGCA ATCTCTGCTG AGACCTCCTT CCCACCCATA TCCCTCTGTA ACCACAGTAT 720
GCACCGTGCC TCTCCCACAC CACACCTCTT CCCAACTCCT GCCTCGCCCC CACCCCCACA 780
TCCTACGGCT TATGTACCAG CACACCCTTG CCACCCACAT CCACTCCACT CCACGAGGTC 840
AGTCCACATG AAGGGACATC CTGCAGCGAG GAACATCGGA GGACCGCAGG GCCCGGCTGC 900
TGTGTCACGC TACATTGGGG TGACACTTGG GATTTGGGCC TGGCGCTCAT CACACTGGAC 960
ATGTGGCATC TTGCTGGGCA GCTGCCGCCA CAGCCCCTGG CTGACCAGAG GCTGCACAGT 1020
CGCTGATGGT AGCTGGGGAG CAGAAGCCCT GGAAATGAAA GTGAGAGGCA AGGACATCAG 1080
AAATGATGCA TCTGAGCCTC TGCCTCAGGC AAAGAGCCAC AAGTGGACAA GGACATGTGT 1140
GAACACTCCT GGGAATTCTC AGAGATGTTC AGGGGAGGGC GCTCAGAGTC TTCCCTGCAA 1200
AAGACTCAGA TTCCTGATAG TAGCATGGGG AGAGAGGGCT CAGAGCCATT CCATTTAGGC 1260
AAAGAAGTTA ATGTGCCCCA GTGCCTGTGG GCGGGAGGCG TGGGGACATG CAGCTTACAC 1320
AGACACAGAC CACACCTGCG CTCACCCTGT TTGGAGGGTC CAGGACAGGT CCTGTGTGAG 1380
GTTGCCAAAC CTCTCCTGTT TCCCACCGCC ACCCCAGCAG GAGCTAAGCC ACTAAGGCAT 1440
CCTCTGGCAA GCAGGCCTGT AATTCGGTTT GTGCCTTCTT CCCTCCCCAT ATATCTCAGT 1500
GGATAATTAG CAAGACCGAT ACTTAAGGAA AATGAGTGTG TCTTCCTGGA TAATCTCAGG 1560
GCTCTGTGAC TCAGACCCAA CCCCAGAGCG CTGACTCAAC ACACTCTCTG TTGCTCCCCA 1620
CAGGCAACAC ACTGCAAAAA GCCTCTTTAG CAGTCACTGA AAGTCCACCA CAAGGACACT 1680
GATAGGAAAA TAACCATGCT TCAGGGACAC ATTGTCATTA AAGCCTGTCC TGGTAAACTC 1740
AAACTAGATT GTCCACGAAT CCCTGTTAAC AGGAACACAA TGGACTGCAG TGACAGACGC 1800
ACAGTGTTCC GAGGACTGGG GGTGACGGGC CACACTTGGA GGTCTGACTT CAATTTTGGA 1860
AAAAGACCCA GATGAACTAG AATGAAGGGC CTAGAAACAT GTCACTAAGG AAGAGTCCAA 1920
GAGACATGGG GATGTTTAGC CTGAAGAAGG CACACAGGGC TGTGGGAATT 1970
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