| Tag | Content |
|---|
EnhancerAtlas ID | HS139-25726 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr19:1725240-1726720 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF5 | MA0599.1 | chr19:1725604-1725614 | GGGGCGGGGC | - | 6.02 | | NRF1 | MA0506.1 | chr19:1725724-1725735 | GCGCATGCGCG | + | 6.02 | | REST | MA0138.2 | chr19:1725505-1725526 | AGCCCTGGCCTGGGTGCTGGG | - | 6.23 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr19 | 1725845 | 1726600 | | chr19 | 1725719 | 1725877 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I001725 | chr19 | 1725277 | 1726482 |
|
Enhancer Sequence | CTCCTGCTTC AGCCTCCCAA ATCATTGGGA CCAAAGGCAC CACCACGCCT GGCAAATTTT 60
TGTAGATATG GGTGGGGTGG GTCTCGCTAT GTTGTCCGGA CTGGTCTCTT AACTCCAGGC 120
CTCAAGCGAT CCTCCCGCCT CGGACTCCCA CAGCGCTGGG ATCACAGCCT CCCCCCGCCC 180
CGAGGTAGCG GGTGGTGGGA ACGGGATTGG AATCCCGACT GTGGGGCCCC TGCGGCCACC 240
TCCAGGATAC AGCGGACCCC GATGAAGCCC TGGCCTGGGT GCTGGGGGAG GCTCCGCGGC 300
GCGGTCCCGC AGGCGGGAGG CGATGCTGCC GACGCTATTG CTGCCATTAC TATTACGGAG 360
AGATGGGGCG GGGCGGGAGC ACCGGGCCCT TCCCGGAAGC CCTTCCTGAG CTTATTCAGT 420
GCCTGGGGCC GCGGCGATCG ATGACAGCTG GGCGCCGGCC GAGCCCCCTC CGGGCCGCGC 480
GGGGGCGCAT GCGCGGGGCC GCGGGATCGA TCGGCCGCGC TCGGGCCTCC CCGCACCCGC 540
CCGACCCCGC CCCCCCGGCT CGTTGCCCGG CAACCTCTGC CCGGCGCGCT CCCATTGGCT 600
GGCGGCGGCC CGGGCCCCGG CCGCGCGTGG TCACTTGGTC AGCGCGGGCT CGGCGTGGCC 660
GGGGGCCTGG CTCCGGGCGC GGGTCGATGC CGCCTCGCAT CTGACCTTTC CCGGCGCGGG 720
GAGGGGGCCC GAGAGGATGG AGAGAGCTGG ACCATCTTGG AAGAAAACTT TATTGACCCG 780
TCTCTTATCT TGGGGACGCA CGGTTCCAGC GGCGGGGGGC GAGGGTACGG CTGGGTGGGG 840
GCAGGGGCGG CCAGGACCTT CCTCCCGGAC ATGCACGGAC CCCCTGACCG CCGCCCCGGC 900
CATCTCCCTG GGCGGGCTGC TCTCCATTCC CTAGACAGGA AAATTGAGGC TCACGAGGGC 960
CCGGGGATTA CCCAAGGCGC AAAGGGTTTA TGAGGTGCAA GGGGCCTGGA GCCCAGAGAG 1020
TGTGGCTCGA GGGCTTCAGA CTCTCTCTGC CACGCCGTGC TGACATCTGC ACCCTCCAAG 1080
CAAAGCTAAA ACATCTTCCC GCGTTGCTGG GTCCCACACC GTCGCAGCCT GGAACCCACC 1140
ACCCCATAAG GAGGGACCGT TCCTTAAATT GAAATGCGAT GTTGAACAGC CACGAAAAAG 1200
GACGAAATCG TGTCCTTTAC AGCAACATAC GTGCAGCTGG AGGCCATTAT CCTAAGCGAA 1260
TGAAAGCAGA AACAGAAAAC CAAGTACCCA TGTTCTCGCT TATCAGTGGA GGCTAAACAT 1320
TGGGTACTCA TGGACACGAG GATGGGAATA ATAGACCCTG AGGACTTCTA AATCGGGGAA 1380
GGTGGGGGAC AGGGGCTGAG AAACTCCTGG GTACCATGCT TAGCACCTGG ATGACGACGG 1440
GATCGGTCAT ATCCCAAACC TCAGCATCAC ACCATATACC 1480
|
