| Tag | Content |
|---|
EnhancerAtlas ID | HS139-19653 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr15:89424960-89427270 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Lhx3 | MA0135.1 | chr15:89426254-89426267 | AATTAATTAATTA | - | 6.78 | | Lhx3 | MA0135.1 | chr15:89426253-89426266 | AAATTAATTAATT | + | 6.92 | | POU6F1 | MA0628.1 | chr15:89426255-89426265 | ATTAATTAAT | + | 6.02 | | POU6F1 | MA0628.1 | chr15:89426255-89426265 | ATTAATTAAT | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GGGGAGAGAC AGGGTGCAGA TGAGACCTGC TGAAGCACAT CTGTACCCCT GCAAGGGCCA 60
CCGCACACCC TCATCCACGG CTCCTACAGG CTCAGATTGC AAAAATGGCC ACCATGCTCC 120
ACCCCTCCCT GTATCCACAT GCTCTGCAAT GTGACTTTGC ATCTCCTTCC ATCAAGAGAT 180
GACAGTTATT CCCCCACCCC CTTGAATCTG TGCTGGCCTT GCCACTTGCT TGACCAACTG 240
AATGCCTTGG AAGTGACTGT TATCCATCAT GCCTGCTCTG AGCATAGGTC CCAGGGGGCC 300
TTGCTGCTTC CACTCTTTTT TTAGGACTTT GCCAGCCACC ATGAGCACAT GGCCAGGCTT 360
GCCTGCTAGA GGATGAGAGA ATACACAGAA CAGAGACAGG GCGCCCCAGC TGAGGCCATC 420
CTACAGCAAC CAGCCCCCAG CTGACCTGCC CACCATGGGC AGGCACATCT GCAAGACCCA 480
ACCGCAAGAC CTGAAGAAAT GGAGCCCACT CCAAAATGCT GACCCACAGA ATCATGAGCT 540
AAACAAATGG CTGTCATCCT AAAGAAGTCA CTAAGTTTTG GGTGGTTTGC TATGCATAAA 600
ATCTAACCAA TGGAGCAGGC AACAAGAGCC ACCCCACATG AGGTACATGG CCAGGACAAG 660
TGGCCCTGAT AGGGATCCGT CGGAGTTTCC TTCCCCACCA CACTGGCCAG AGGACAGCAC 720
AGCCCTGGCT TTACTCTCTG GTCCAGCTGT CCACCATAAC TCTTCCCAAA TACGGAGCAG 780
CCTACTGAGC TAAGGGCAGA ACTTCTAAAG GAGACTACGC TCACGGCTCA GAGTTACAAA 840
TACACACAGA ACTCAACATG CAACAAAAGA ATCAAGTTCA TAGGCTAAGG CTGCCTCATC 900
TTTAACTTGG GAGCCCCTGT TGGGACCTCA CTGATTCATT CTCTTGGGTC TAGACTTCAA 960
GACATGCTTG ATTTACTCAA GGTGGGGACA GGGGCCAGGC ACGGTGGTTC ACGCTTATAA 1020
TCCCAACACT TTGAGAGGCC AGGACAGGAG GATCGCTTCA GCCCAGGAGT TTGAGACCAG 1080
CCTGGGCAAT AAAGTGAGAC CCTGTCTCTA CAAAAAAATT TTTAAAACTA GCTGAGTATG 1140
GTGGTAGATG CTTGTGGTCC CAGCTACTCG GGAGGCTGAG GTGGGAGTAT TGTTTCAGCC 1200
CAGAAGTCAA GGCTGCAGTG AGTCATGATC GCACCACTGC ATTCCAAACT GGGTGAGAGA 1260
GCAAGACTCT GTTGCCAAAA ACAAAATAAA AACAAATTAA TTAATTAAAA AGGTGGAGGC 1320
AAGGGGACAG CCTCATGGGT AAGCAGGAGA CAGACAGGGA GGTTCCCTGT AGAGGAATCG 1380
TGCTAAAAAA GAGCTATACC TAATGTAGCA GATTGCCATA TGCAGAAGTC TCCAAGTGTG 1440
GCCCTCGGGC CAGCAGCATT AGCATCACCA GGAATTTGTC AGAAATGCAC ATTGTGGGGT 1500
CCCAGTGCCT CAGAGACTCT GGGAATGGGG TCCAGCCTCC AGGGGACTTT CAGGCTCATT 1560
CAGATTAGAG CTGTCCTGCT CTGCAGAGGC AGTAGGTACA GAGGTTTGGA GTCAGGCAAT 1620
TCGGGCTTGC CCTTGGTTCC ACCTTTTCCC AGCTGTGTAA TCCAGGGAAG TCAAGACTCA 1680
GCTTCCCCAT TTGTAGAATG GGTTAATTAC AGTCCCTACA GAGGGCTGTG GTAAGGTTCA 1740
AATCAGGTAA GGCAGGATGC CTGGCACACA GAAAGTGTCC AATAAATATG AAGCAGGGCT 1800
ATCATTTAGG GGCCACTTCC TTGGTTCTTC CCAACTCTCT TAAGTAAACT ACCTTTGAAG 1860
CTTTAACCTG AATAAAATGA AAATGTACAT CCATATGATA AAATACTATA CAGCCATGTA 1920
AAATAATCTG GTAGATGTAC ATTCAATCAT TGACTTAGAA AACGAGTTCT ATTCTATGAG 1980
GTGATAAGGG AGAATACAAA AATCACATGT ATGACATGAG CTGGTTTTTG TTGGAGAAAG 2040
TTTTCTAAAT CATAAAAGAA TGGCTCAGCT AGGTGCAGTG GCTCACGCCT GTAATCCTAG 2100
CACTTTGGGA GGCCAAGGCG GGCAGATCAC TTGAGGCCAC GAGTTCGAGA CTAGCGTGGC 2160
CAACACGGTG AAGCCCCATC TCTACTAAAA ATACAAAAAT TAGCTGGGCA CAGTGGTGCA 2220
CGCCTGTAGT CTCAGCTAAC TCAGGAGGCT AAAGTGGAAG GATCTCTTGA GCCCAGGAGG 2280
CAGAAGTTGC AGTGAGCCGA GATCACACCA 2310
|
