| Tag | Content |
|---|
EnhancerAtlas ID | HS105-38443 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr19:3115470-3117130 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF14 | MA0740.1 | chr19:3115528-3115542 | TGGGGGGCGTGGCC | - | 6.83 | | KLF16 | MA0741.1 | chr19:3115530-3115541 | GGGGGCGTGGC | - | 6.62 | | SP1 | MA0079.4 | chr19:3115529-3115544 | GGGGGGCGTGGCCAC | - | 6.95 | | SP3 | MA0746.2 | chr19:3115529-3115542 | GGGGGGCGTGGCC | - | 7.22 | | SP4 | MA0685.1 | chr19:3115527-3115544 | GTGGGGGGCGTGGCCAC | - | 6.63 | | SP8 | MA0747.1 | chr19:3115529-3115541 | GGGGGGCGTGGC | - | 6.44 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr19 | 3115690 | 3115804 | | chr19 | 3115813 | 3115992 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I003116 | chr19 | 3116204 | 3116686 |
|
Enhancer Sequence | AGATTTATCT CTAAGTATGT GTGAGCCAGG GCCACACAGG GAAGGAGCTG TGGGGGTGTG 60
GGGGGCGTGG CCACATCCAT CCAGACCGGC AGCCGAAGAG ACCTGGCAGG GAGGACATTT 120
GACAGGGCCT CCAGGACGGG CCGGGGGCCT GGTTGGAGCC AGCATGGGGC TGGGGTCTGG 180
AGTGCTGGCC GGAGCAGGGG GTGCCGCATG GTGCGGGAGG GGTCATAGGG ACTGAGGCTG 240
CCAGGGGAGG GGGCTCATGG GGACCGAGGC TGTGAGGGGA GGAGGGGTCA TAGGGACCGA 300
GGCTGTGAGG GGAGGGGGGG GGTCACGGGG ACCGAGGCTG TGAGTGGAGG AGGGGTCATA 360
GGGACTGAGT GGGGAGGAGG GGTCATAGGG ACTGAGGCTG TGAGGGGAGG AGGGGTCATA 420
GGGGCCGAGG CTGTCAGGGA AGAGGGGTCA TGGGGACCGA GGCTGTGAGG GGAGGAGGGG 480
TCGTGGGGAC CGAGGCTTTG AGGGGAGGAG GGGTCATAGG GACTGAGTGG GGAGGAGGGC 540
TCCAGGCTGG GGTGGAGGAG CTGGGTGGTG TGGGGTGGAT TCTGTTCTTC ACGGGCTGCC 600
CCTGCGGATC CTGCTGGGCC TCCGGGGCTC CAGGTCCACT GTGGCTGGGG GCCGGCCAGC 660
AGAGCCGGGT TCTCCCTGGG GACCCTCAGT GGGTCCTGTG TCTGGTAGGC TGCTCAGCTG 720
GCTGGACTCT GCTGTCCCTG GGAACGTGGA CCCTGCCTGC CTGTCTCCTG GCCCCATATA 780
ACATCTCCAG CGCTGAGGTC CCGGCTTTAT GCGTGCCTGT CCTGGGCTGC TGGTGTCGGG 840
CGTGAGACTC CCACCGCAGG CCTTATTCCC GCCCAGTGCT GGAGGCCAGA AGGCTGAGAT 900
GCAGGTGTGG GCCGGGCCAG GTCCTTCTGA GGCTGAGGGG ATCTGCCCAG GCCTCACTCG 960
GCTCCTAGTG GCGGCCGCAT CCTTGGCATC CTTGGCATCC TTGGCATCCT TGGCTTGTGG 1020
CCGGGTTGCC TCATCCCTGC CCCCATCCTC ATGCAGCGTC CTCCCCGCCT GCGCCTTTGC 1080
CTCTGTTCTC TTATAACCTG TCCTTGGCCA GGGCCACCCT ACCTCTGTGT GACGTTATCC 1140
TAACCAGTGA CATCCGCACA GACCCTGTTT CCAGATCAGA GCCGTCCCCG GGTTCTGGTG 1200
TTCGTGCGTG TGGGGCGCTA GACGGCTCTG TCCTGGAGGG CCTCGCGGTG GCTCCGGTTG 1260
CGGGTGCCTT CTCCTGCAGT GCAAGCTCGC CCTGGCACTG GCCCTCATGA GGGAATGACG 1320
CCTCCCTGCC AGGGTGTCCC CACCCAGCTG GTGCACTGCC GAGGCCATTG TGAGGGTTCC 1380
GGGAAGTCTG TGGGGTTTTC CTCGAGAGCC CTGCCTTGAG ACCCACCCCA GGGCTGGGGG 1440
TGCCACCCCC TGCCATCTGC CTGTTCTCCC CACCCGTCCT CCCAGCTCGG CCTCCCAGCG 1500
CAGGCAGGGA GGATGCGGCG TGAAGATGGA GGCAGGGATG GAGCAATGTG GCCACAAGCC 1560
AAGGAATGCC AAGCTCTGGG ATGGTTCCCG GGGACCCGAG CAGGCGCTGG GCCCTCAGAA 1620
GCTGCGGTGT CCTCTCTGGA CATGGGCGAT GGTGTATATT 1660
|
