| Tag | Content |
|---|
EnhancerAtlas ID | HS044-13134 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr9:3793550-3795220 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Znf423 | MA0116.1 | chr9:3794955-3794970 | GGAACCCAAGGTGTA | + | 6.03 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I003793 | chr9 | 3793474 | 3794554 |
|
Enhancer Sequence | AGATCAAATG GCTTTCTTAA AGTTGCATAG CTAGTGAGGA GAGGATCTTG GATTTGAACC 60
AACCCTCCCC AAAACATGTT CCCATAGGCT ATAGGAGGGC CTCTCTCCTT TATCTTCTAT 120
TGCACCTCAT GAATCCTCAA GCAGTGAAAA CGCCACTCTG GTTTCCCTTT TCTGGGTTTT 180
ACAGGCTATG TGGAACTAGT ACAAAACAAC TAGAAAGGCT TTATTTTTAA CTAAAGGCTG 240
CCTGCCCTAC CTCTGCCAAA ACCTTCACAA CTTGTACAGA GGGTGAGTTT AGGGACAGGA 300
AATGTGTGTA TCTCCTTTAT CACTTCATTT CATTACGTGT CCTCATTGGT AAATATTACT 360
GAAAATCTAC CATCAGACTG GCCTGAGAAC TGGGGGCTTA AAACAATGAG CAGAGAAAAT 420
ATTTGGTAAA CTTGAGTAAG AAAATCTCCT TTGATTTTCC AGTGTCTATC CTCAAGCTTG 480
TGAGCACAGG CTCAGTTCAG AAAAGCCCTA AGCAGGCCAC CTCCCACAAT TCTTAGGGGA 540
AGTGTAACTC GATCATCCAG TTATACATCC TATCCCTGCT CCTCTCTAGT CCTCGCTAAT 600
TGCTCCTCAT TACATACTTC AAGAATTCCT TTCTGTCTGG GATGTGTGTT CAGAAAACAC 660
ATTGTGTTTT GTCTTCTCGT GGGCTCATTA GCATTTGCTA AAGGAAGCAG CAGAGCTTGG 720
AGCCCTCTGA TCTCCTAGAA AGGCCGGACG CTCGTTTGTT TGCCTCACTG AATTTCCTCT 780
ACTCTGTTTG CTTTCTCTGT TTGGACACCT CAACTTCATC AGGAGCTAGG GGCAGCCATC 840
CTGGGATTGG ATAAAAAGTA TTTCTTTTCT CTTTGTTCAG GTACCTTGTA CTTTGGCAGC 900
CTGAAAGAGT GCTTGCTGAG TGTGCTAAAA GCTCAATTTA TGTTGCTTTT TCCTTTTTGC 960
ATTGCTTCAG TGCAAGCTGT ATTTTATGAA GGTTCGGTGG CATTTTCCAA AGTAGAAAGT 1020
AAGCACTCTC CCTGTATTCT TTATATATAT AATCTGAGCA CCTCTGAATT TTTAACACAA 1080
TGTCTTCTGC CCCATTGGTG CATGCAATAT TTATTAACCA ACTGCAAGTT TCTATTTCAC 1140
CAACTTTTTG ATTGATTTCC TCTTGATGGT CACTAGAGAC ATAAATAACT ATGTGATTCA 1200
AGCTTTTTGT TTGCCCATAT CTTTTTTCTA GACATGTCTT TTTGCTTTGG CCCTGCTGCT 1260
CTTTCCACAA CAATACCGTA CAGTTCAGTG CTGTTAAGAG TTGCTAGGTT GGATCACATT 1320
TAAGGGGAGA GTACCGTCCC CAGGAATGTT TCAAAGACCT TTGGAAAAAC ATGTGTTGGC 1380
AAGAGTAATA ATGAGCAGAA AGTCAGGAAC CCAAGGTGTA TATGCATGAT TCCCCCATCA 1440
GTATCCTTGG GGAGGTTACT TCCCTTCTCT GCCTCTCAGT TGTGCCAGCT CTAAAATGAA 1500
AATATTTTAC CAGATCACAT CCTGTAATTC TTTCTTCATT TTGTCTCATC AACTGTTTGT 1560
TGGTTTGGAG CTACAGAGAT GAGATGAATT TTGTTGATAT ACAAATTGAA GAAAGCTGGA 1620
TTTGATCTTC ATTTAGCCTT GCTTTCCTCC CACCACCCCC AACAAATGGT 1670
|
