| Tag | Content |
|---|
EnhancerAtlas ID | HS139-38117 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr3:112851020-112852550 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gfi1b | MA0483.1 | chr3:112852462-112852473 | TGCTGAGATTT | - | 6.32 | | MEF2A | MA0052.3 | chr3:112851890-112851902 | TCTAAAAATAGC | + | 6.52 | | MEF2B | MA0660.1 | chr3:112851890-112851902 | TCTAAAAATAGC | + | 6.22 | | MEF2C | MA0497.1 | chr3:112851888-112851903 | GATCTAAAAATAGCC | + | 6.76 | | Znf423 | MA0116.1 | chr3:112851923-112851938 | GGCCCCTAAGGGTCC | + | 6.41 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr3 | 112851372 | 112851820 | | chr3 | 112851887 | 112852230 |
|
Enhancer Sequence | TTTTTAATTT TGATCAGCAT CTTCCAGATC TTCAGAGTAA TAAATGCTGA TTAGAGAAAA 60
CGTTGAAAGA AAAGTATAAA GAAGCAGGAA ATATTATCTA TGATTCCACT GCCCAGTGTC 120
ACTCACTGTT AACTTTGGTA CAGTTCCTTT GAGTCCTCTC TCCATCTTTC TTTTTCATTG 180
TATAGGTAAG ATCACACTAT ATAATTCTGT AATGCAATTG TATGCAACTC TATAAAGTAG 240
GTATTATATA ATCAAATAGA ACACTTACGC AACCAGTATT TTCATATACT CTACTTTTTA 300
AGAGAAAGAA GTAAAGGACA ACAAAAAGGT GATAGACCTA ATTTATTTCA AAAACCCAAA 360
CAAAACACTG CCAGGCTGTG GCCTGTGGTT GCTATAAATT CCTTTCTGTT TTCCACCCCT 420
TTTCCATCTA CAGCATTAGG ATTGATTTCC ATTTTCTTGA CCACAATGAT GATTCACAAG 480
CATCACAGAT TAAAGGATGT TTAACGACAC TTCCCTCCTT TGGCTTGCAC TTGGACAGGC 540
CAGCACTTGA GCAGGCCAGA CTATGGGACC ACTCAGTGGA CATCAGAAAC AGGAGACGAA 600
CCACATCTCC CTCCTGTGGC CTGGATGGTG TTCCAATTTC CTCTTTTGGT CATTCTTGCT 660
GGCTCTACAG TAGCCCTCTT GTCTCTAGGA TCTAAATTTC AGGCCTTCCT TCTCTGCAGC 720
CCTTAGACAC TTCTCTGACT AACCATAGAC TATGTGGAAA ATGGTAGCTG GATTGCCTTT 780
GGGTGGAGTC CTTGCCCTGT GGCATAGGAA ACAAAGGAAA GGAGAGAGAT GCCCTTTGAG 840
ATTAATGAAA ATGCTCTCAG CCAAATAAGA TCTAAAAATA GCCTCCCTGT GATATGAACG 900
CGTGGCCCCT AAGGGTCCTA AAGAGAGAGC TAGGGGAGGT TCAGCTGGCC ACAGAGATGC 960
TAAAGGTCAG GAGCAGACTT TTAGGGTTTG CTGTTTTATA GGTTTAAAGA CCAGGTCTGT 1020
GTTTTGATAA TTGAACTTGC TAATAGCTGG CCACTTGAGT TGCTTCTTCC AGCTCTTTGT 1080
TTGTTTTAAA TAAAGAGATT CAGCCAGTAA TAATGGGAAG AGCTGCAAAT GACTTCCCCA 1140
GTTGGGAGTG CCTGCTTGTT TTTCCTTCTG CCTGGGCATG CTGATGTGCA GGCCACACTC 1200
ACAGACTCAC ACGTCTGAGG AGATAGCCCA AGGGAGCCCT CGGTTTGTAT ATTTATATAG 1260
GATGTGTGTA TAAGAATGTG TTCAAGTATC AAAATACATA GGTAACCATG GGTGAAAAGA 1320
GGAATTCTGT TGCAAGAATT TAAATATACT GTTTCTCGTA CATTTATGTC TTCATTCATT 1380
CCTTTAACAG ACACTTATTG AGCACCTGCT GTGAGAAGCA CTGTGCTATT TGCTGGGAGA 1440
CATGCTGAGA TTTCTAAAAA AGTGGGCCTT TATTTCTCCC CCTTCAGAAG CTTTCCATCC 1500
AGTGGGGGCA CTATCTGATC ATTCATTAAA 1530
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