Tag | Content |
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EnhancerAtlas ID | HS098-26714 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr19:1725290-1726660 |
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 |
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| 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 |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I001725 | chr19 | 1725277 | 1726482 |
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Enhancer Sequence | GGCAAATTTT TGTAGATATG GGTGGGGTGG GTCTCGCTAT GTTGTCCGGA CTGGTCTCTT 60 AACTCCAGGC CTCAAGCGAT CCTCCCGCCT CGGACTCCCA CAGCGCTGGG ATCACAGCCT 120 CCCCCCGCCC CGAGGTAGCG GGTGGTGGGA ACGGGATTGG AATCCCGACT GTGGGGCCCC 180 TGCGGCCACC TCCAGGATAC AGCGGACCCC GATGAAGCCC TGGCCTGGGT GCTGGGGGAG 240 GCTCCGCGGC GCGGTCCCGC AGGCGGGAGG CGATGCTGCC GACGCTATTG CTGCCATTAC 300 TATTACGGAG AGATGGGGCG GGGCGGGAGC ACCGGGCCCT TCCCGGAAGC CCTTCCTGAG 360 CTTATTCAGT GCCTGGGGCC GCGGCGATCG ATGACAGCTG GGCGCCGGCC GAGCCCCCTC 420 CGGGCCGCGC GGGGGCGCAT GCGCGGGGCC GCGGGATCGA TCGGCCGCGC TCGGGCCTCC 480 CCGCACCCGC CCGACCCCGC CCCCCCGGCT CGTTGCCCGG CAACCTCTGC CCGGCGCGCT 540 CCCATTGGCT GGCGGCGGCC CGGGCCCCGG CCGCGCGTGG TCACTTGGTC AGCGCGGGCT 600 CGGCGTGGCC GGGGGCCTGG CTCCGGGCGC GGGTCGATGC CGCCTCGCAT CTGACCTTTC 660 CCGGCGCGGG GAGGGGGCCC GAGAGGATGG AGAGAGCTGG ACCATCTTGG AAGAAAACTT 720 TATTGACCCG TCTCTTATCT TGGGGACGCA CGGTTCCAGC GGCGGGGGGC GAGGGTACGG 780 CTGGGTGGGG GCAGGGGCGG CCAGGACCTT CCTCCCGGAC ATGCACGGAC CCCCTGACCG 840 CCGCCCCGGC CATCTCCCTG GGCGGGCTGC TCTCCATTCC CTAGACAGGA AAATTGAGGC 900 TCACGAGGGC CCGGGGATTA CCCAAGGCGC AAAGGGTTTA TGAGGTGCAA GGGGCCTGGA 960 GCCCAGAGAG TGTGGCTCGA GGGCTTCAGA CTCTCTCTGC CACGCCGTGC TGACATCTGC 1020 ACCCTCCAAG CAAAGCTAAA ACATCTTCCC GCGTTGCTGG GTCCCACACC GTCGCAGCCT 1080 GGAACCCACC ACCCCATAAG GAGGGACCGT TCCTTAAATT GAAATGCGAT GTTGAACAGC 1140 CACGAAAAAG GACGAAATCG TGTCCTTTAC AGCAACATAC GTGCAGCTGG AGGCCATTAT 1200 CCTAAGCGAA TGAAAGCAGA AACAGAAAAC CAAGTACCCA TGTTCTCGCT TATCAGTGGA 1260 GGCTAAACAT TGGGTACTCA TGGACACGAG GATGGGAATA ATAGACCCTG AGGACTTCTA 1320 AATCGGGGAA GGTGGGGGAC AGGGGCTGAG AAACTCCTGG GTACCATGCT 1370
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