| Tag | Content |
|---|
EnhancerAtlas ID | HS052-18026 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr19:1725210-1726750 |
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 | CTGGTCTCCA ACTCCTGGCC TCAAATAATC CTCCTGCTTC AGCCTCCCAA ATCATTGGGA 60
CCAAAGGCAC CACCACGCCT GGCAAATTTT TGTAGATATG GGTGGGGTGG GTCTCGCTAT 120
GTTGTCCGGA CTGGTCTCTT AACTCCAGGC CTCAAGCGAT CCTCCCGCCT CGGACTCCCA 180
CAGCGCTGGG ATCACAGCCT CCCCCCGCCC CGAGGTAGCG GGTGGTGGGA ACGGGATTGG 240
AATCCCGACT GTGGGGCCCC TGCGGCCACC TCCAGGATAC AGCGGACCCC GATGAAGCCC 300
TGGCCTGGGT GCTGGGGGAG GCTCCGCGGC GCGGTCCCGC AGGCGGGAGG CGATGCTGCC 360
GACGCTATTG CTGCCATTAC TATTACGGAG AGATGGGGCG GGGCGGGAGC ACCGGGCCCT 420
TCCCGGAAGC CCTTCCTGAG CTTATTCAGT GCCTGGGGCC GCGGCGATCG ATGACAGCTG 480
GGCGCCGGCC GAGCCCCCTC CGGGCCGCGC GGGGGCGCAT GCGCGGGGCC GCGGGATCGA 540
TCGGCCGCGC TCGGGCCTCC CCGCACCCGC CCGACCCCGC CCCCCCGGCT CGTTGCCCGG 600
CAACCTCTGC CCGGCGCGCT CCCATTGGCT GGCGGCGGCC CGGGCCCCGG CCGCGCGTGG 660
TCACTTGGTC AGCGCGGGCT CGGCGTGGCC GGGGGCCTGG CTCCGGGCGC GGGTCGATGC 720
CGCCTCGCAT CTGACCTTTC CCGGCGCGGG GAGGGGGCCC GAGAGGATGG AGAGAGCTGG 780
ACCATCTTGG AAGAAAACTT TATTGACCCG TCTCTTATCT TGGGGACGCA CGGTTCCAGC 840
GGCGGGGGGC GAGGGTACGG CTGGGTGGGG GCAGGGGCGG CCAGGACCTT CCTCCCGGAC 900
ATGCACGGAC CCCCTGACCG CCGCCCCGGC CATCTCCCTG GGCGGGCTGC TCTCCATTCC 960
CTAGACAGGA AAATTGAGGC TCACGAGGGC CCGGGGATTA CCCAAGGCGC AAAGGGTTTA 1020
TGAGGTGCAA GGGGCCTGGA GCCCAGAGAG TGTGGCTCGA GGGCTTCAGA CTCTCTCTGC 1080
CACGCCGTGC TGACATCTGC ACCCTCCAAG CAAAGCTAAA ACATCTTCCC GCGTTGCTGG 1140
GTCCCACACC GTCGCAGCCT GGAACCCACC ACCCCATAAG GAGGGACCGT TCCTTAAATT 1200
GAAATGCGAT GTTGAACAGC CACGAAAAAG GACGAAATCG TGTCCTTTAC AGCAACATAC 1260
GTGCAGCTGG AGGCCATTAT CCTAAGCGAA TGAAAGCAGA AACAGAAAAC CAAGTACCCA 1320
TGTTCTCGCT TATCAGTGGA GGCTAAACAT TGGGTACTCA TGGACACGAG GATGGGAATA 1380
ATAGACCCTG AGGACTTCTA AATCGGGGAA GGTGGGGGAC AGGGGCTGAG AAACTCCTGG 1440
GTACCATGCT TAGCACCTGG ATGACGACGG GATCGGTCAT ATCCCAAACC TCAGCATCAC 1500
ACCATATACC CATGGAACAA ACCCGCATAT GTACTCCTGA 1540
|
