| Tag | Content |
|---|
EnhancerAtlas ID | HS044-13457 | Organism | Homo sapiens | Tissue/cell | Fetal_kidney | Coordinate | chr9:90851460-90853130 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RFX2 | MA0600.2 | chr9:90852459-90852475 | TGTTGCTATGAAAACC | + | 6.1 |
| | | 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 |
| GH09I088237 | chr9 | 90851577 | 90853295 |
| Enhancer Sequence | ACACAAACAA CAGAACCATT GTCCTACAAT GATACTACAG TTTACCTCCC AGCTGGTGGT 60
GGTATCCGGG AGTCAGAAGT GTTAGATTGT AAAAAATGAT GTGTCTTAGA ATGGACAATG 120
CAATTCAATC AGCAGATGGC CAGAAGAATG GAGCCGGAAC AGGCTGACAG AAATGCTCAC 180
AGGTGGCTTC TTGGGTCGTT ATGAAACAGC TCCTGGGACC TGTCTTAAAT GGATGCGTCA 240
CATGGTGCTT CTCCCCATAT GGCCAGAGTC AGGGCAGTTG AATTCCCAGG TTTCCAGGTT 300
TACACCACAG CTGCAGACAT CACAGAGGAG GAAAGCAAGT GGTGGTCCAG ATACAAAAAT 360
ACTCTCAGGC CTGCGAGCAG CCTGCAACGG CCGAAGCGCC CCGGAAAGGA GAGCTCATCA 420
CGCCTCGTGT CCTGCCAGCC CACTAGGCCC TCGGCCAGGC CTCCAGACTC GGCCAACTGT 480
CTCCTGCCCC AGACCTCGTG CTCTCCCCAG CTCTGAGCAC AGACTGAGGC AGCCTCTTGT 540
TCTCCAGGCA CAGAGATGGT GGTAGGCTGT GAACAGCCAA AGCCAGAGAA GCAGCCTGTC 600
TAGGCTACTC CACAGGTGTA GAAATATGGA GGTCTCCCAC TTCCCAGAGC CAAGGTGAAT 660
TGCAGGGTAA TTTGAGGCTG ACAGACCGGT ATGCAGGGAC GTTCCTCCAT GGCCTCCCAT 720
GACAGGCTCT GCAGTGCTGG AGGACAGCCA TACATATTTG TCCAGTTGCA TAGTTCGGGC 780
TTGTGAAAAT CAGAACTGAG AAATAAGCTC TTTATTCTCT TTCCAAAAAC AATGCTTGAA 840
CTCTGACTTC TGCCCCCCCT CCACCTCATT TCTGCTCGAT TTTCAATCTG TTTTCTATTA 900
TTTTCACTTC ACATCCCTGT GCAGACTTTG CTAGAAATGC AGTGAGTCCA GGTCAAAAAA 960
CAATCAGCGC ATTATGCTGA ACGTATCTGA ATACCTCCTT GTTGCTATGA AAACCTACTC 1020
ATTCTGGGGA CTGATTTGAG GCCACTCCTG GCCTTGCTGA GGTGCTCCTC CTCCCAACAG 1080
AGAACAGCCT GGCCTTCAGA AGCATGTCTT GTGTCTTGGA GTCACCTGGT ATATCCCTAG 1140
GCAGGGCCCC GTCCACACAG CCAGGAGTGG CTGGGTTAGT CCCCCAGTGA ACCAGCAGCC 1200
ACCTCCCTCC CTGGCTGTTT TTCTAGACCT GCCCTCTGCC CAGGGGCTGC ATGTATATTT 1260
GCCGCTTCCC CAAAAGGGGG CATTTCCCAC CGTTCTGGAA TTCTTGATTA TGCATGCATC 1320
TGTGCGTGTG AAGCCAACCC AGTTGCCTGG CACTTTTCAT ACTGTTCCAA CCAGCTGTTT 1380
CCAGTCGGTC AGAGTTTCAG CTGGGTTAGC TGTTTCTTCT CTCCTGGACG TGTAGTGCAG 1440
TCTGTACTAT TTAGACCCTG GTGTCTGCTT GTTTAATCAA TGCTGGAGAC ACGTGGGAAA 1500
TAGAGATGAC CCTGTTCTGA ACCGGTTAGG TGGTATGGGC ACCAGTAGGG CCTCAGGAGG 1560
AAACTTAGCC TTTGAGGAAA CCGAGGAGGG TGCACCTGTA CAGGGTGGTG CTTCCAGCTA 1620
AGGAAGTGTG GGGAGATGCT GCCACGGCTG CTCCATGTCT TTCACTTGTA 1670
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