| Tag | Content |
|---|
EnhancerAtlas ID | HS044-10178 | Organism | Homo sapiens | Tissue/cell | Fetal_kidney | Coordinate | chr5:1227280-1228690 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| POU2F2 | MA0507.1 | chr5:1227700-1227713 | AACATTTGCATAT | + | 6.21 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr5 | 1227409 | 1227924 | | chr5 | 1228000 | 1228400 |
| Enhancer Sequence | TTGCCCGCCG ATGCCTTGCC CACCGAAACC CAGTTACCAT TGCTAAGCGC CTGCAGTGTA 60
CTGGAAGTGT CTGGCACTAG CCTCCCTTAA ACTCAGCTGC TCCACGCTGG GGCAAAGCTG 120
GGGAGGCCCC CACCTGGGGT GCTGCTGAGG AGGGAGAACA GCCCTGCCCG CCAGCTGCGC 180
GGGGACTTCA GGGCTGCTCC ACTCATGAAC GACTCTACCA TCAATCTCCT GATGCAAGCC 240
ACCGGGTTGC ATGTCATGAA ACATCCAAGT TTATTTAACT CACACACTTC CTAAGGGCCG 300
TGCCATCAGC ATTCTCACCC TGTGTGTGAA CATGCCCTTC ACTTTGTCTC GCTGTGAGGA 360
TCACTCATTG ATGATTTTGA AAACAAGATA TAATTAAGAA GCAGGTACTG TGTAGCTTTT 420
AACATTTGCA TATACTCATG ACTACCAAAG GCGAATATTA TTTGCTCTCC CATTCATAAG 480
TATTCAACTA CATAAATGTT CTCTTCAAAG CTAAGACTTG TAAAGCAACA TTGTAACAGA 540
ATGTAGCAAA ACGTTGCGGT AAAGATTTAC AGTGATTTTC TCACACCTAT GACATTTCAT 600
GGCAGCTGCT TTATTACACA TTCAGCGTCT TTAAATCAAA GGAACGTAGA CTCGTAAATG 660
CCAAGCGATG GGTTCAGGCC AGCTGCCCGG GACACTCTAA CACTTGCTGT GGTTTAAGGT 720
TTCAACCCAG GAAGCTTTTA TGACTAAGCT GGTGGCCCTG GGCTGGCTGT GTCCACACAC 780
GTGAGGTCAC TCATCAAGCG CGCCCCCTCC CCGCTACTTC CTGCCTCCGG TGTTCAACCG 840
ACTTCTGTAT CTGGTAGGTG CTGTTGAGAT CTGTGGATTC TTGCACCAAA AACGACACTG 900
TATTAATTAC TATGGCTTCT TCGTTAGTCT CGACGCCTAG TAGTAGAGCA AGGCCTTTTT 960
TTTTTATTCT TTGAACTTTT GCCAGCTGCT ACTTTTCCTC TGAGCTTTAC ACCAGGTTGT 1020
CAATTTCCAG AAGAGATTCT TCGGCGCTCC CTTGGCCCTG TGCTGCTTTC TACACTGCCC 1080
GGGGGGAGTT TCCACCTTGA CGGCCTTCAC GCCTTGGAGG CAGTGCCCAG GCAGTGGGGG 1140
CTGGCACTGG AGCACCATCT GCCGTCTGCA CCCTCGCGGC TCCCGGCTCG GTCTCCTTTC 1200
TGCCTTCCTG CGGGTCTCTC CATCATGACC CTGGGCGTGT CTCTGGTTGA TTCTCAGCAA 1260
TCCCTGGCTT TTGCCGCTGC TCTGAGCAGA GCCTGCTTCT CCTCTGCATT TGCTCAGTGG 1320
CTGCACTGCG GCCTCTGCAT CTCTCAGCCT CGTGTGGTGG GGTGCAGGTT TCTCTCGATC 1380
CTGCGTGGAT CGATTGTAAC AGCAGCCAGC 1410
|
| |
|
|
|
