| Tag | Content |
|---|
EnhancerAtlas ID | HS044-10865 | Organism | Homo sapiens | Tissue/cell | Fetal_kidney | Coordinate | chr5:167761340-167762390 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr5a2 | MA0505.1 | chr5:167762007-167762022 | CCTGACCTTGAAGTT | - | 6.78 |
| | | 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 |
| GH05I168333 | chr5 | 167760729 | 167762465 |
| Enhancer Sequence | CTCTGCCCCA CCCCCACTGC ACTCTGGCAA CAGGTCTCGA GAGACATTGC AACCTTGTGC 60
ATTATAGAGA CTTGCAAATG CTGGCCTCTC TAACCGGAGT TATCTTTCCT GCTCTCTTCA 120
CCTACTTACA CCTACTCATC CTTCAGCCCT GAGTTTAATC ACACTCACTT GGGAAGCCTT 180
CTATAACTGT GAGGAGTAAG ATCAGACCCT CCCCCCTCCA CCCCCATTTA CAGTCTCATG 240
CTCCTGTGTG CTGCTGCTTT GTAGAATTGC CCAAATTATT TCTGTGTCTG CCTTCTCTAC 300
TGCACTGCAA GCTCCTTAAG GACAGGGGAC TCTGGCTGTT TACCACAAAA CTGTATCCTC 360
AGTGCCTGGC TCTAGTGAGT TCTGAACATA TATTTTGGGC AACTGAATGA ATCAATGACT 420
CTCCTGCTAA GCAGCAATGC TTCTCCCAAG AACAAGGGTT AGGCCCAGCT TCCAGCAGGG 480
AGGCAGCTGA GGATGTGACT GAGCGCCTGA GCGCCTGGAG CCCAGCTGAA GAAGCTGATT 540
GGTGGGATGG AATGCTACCG GTCCCTCTGG TATCCTGGAT ACGGAGAGGG TGGGAATGTA 600
AACTGGGCCC AGAGGCTGAA TTCTTGAAAT TTCACTGCAG CCTAGGAGGA GCCTGCAGGG 660
AAGTGAACCT GACCTTGAAG TTCTAGCCTT GATTTTTTTC CCCTCTAAAA AAAAAATAAG 720
ATAAAAGGTG CAATCATGCA ACACATTCTT TCTGAGGGAG CTGTGAGGTG AGGGCTTTCT 780
AAGTCCCTCA AAAGTCACTT CTAAGTCACT TCTAAGTCCA CTCATCACCC AGGCCTACTT 840
TTTGCTGGTG CAGGTGCATC TTCCAAGGTT TCTCGGCATT GCACACCCTA GAGGAGTTGA 900
AGTTCCTGGT GGGTACTTCT TGGGTGCTAG CAGAGACATC CCAGCAGCAG TTCTCCTAAT 960
GAGGTGTCAC AGAAGATAAT ATCAAGTGTT TATTGAACAT CTAGGCCAGC CATGGCGGCT 1020
CACACCTGTA ATCCTAGCTC TTAGGGAGGC 1050
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