| Tag | Content |
|---|
EnhancerAtlas ID | HS044-10917 | Organism | Homo sapiens | Tissue/cell | Fetal_kidney | Coordinate | chr5:176119960-176120940 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxo1 | MA0480.1 | chr5:176120021-176120032 | TGTAAACAGCA | - | 6.14 |
| | | 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 |
| GH05I176692 | chr5 | 176119654 | 176120597 |
| Enhancer Sequence | CTAAGAGGCA CAATCAATAC AGCGCACACA CATCATCGTC TTTCATTGCA AACGATAAAA 60
GTGTAAACAG CAGGGGTGGC GGCAGCTCTG GAGGCTGCAG TGGGGGCAGG GCGGGCTGCC 120
ACCACTTCCC TGACTGTCAC CCTTCTTCTG GGACACAGGG CTCTTCCAGG TGCGAGCGGG 180
AGTGCCTTCC CCACTCTGGG GAGTGGCACC CCTCATTAAA GCCCATTCAG GGAAGTGGTT 240
TTTCCTGTTT TTGCTTCCAG ATGCAGCAAC CCCAGTTTCT TTAACCCGAC TTCAGAAATC 300
CAATTTGTCC TCTGTACTTT AAAAGCTTTT CCCTTGCTTC CCCTGCATCC AAAATACAGA 360
GCTAGGGGTG GCTTCTGGTG GCAGAAGAAC TTGTTGGGGT TTTGCCTGTC ACAAGCCCAT 420
GAACTGACCT CGACCCCATT TTAACCCCAG CTCTTGACAG CCAACTTCTT TCGCCACCTG 480
TCCAGCCTGC CACCCACAGC TTTTCTTGGA ACGTGCACAG AAACCATTAT ATCCCCAGCT 540
CCCACACACT CCCGGCGACG ACTTCCTCAA ACTAGTTACT TAATGAACGT CATCCAATTC 600
CGATTCCGTC TTGCTGTAGT CTCATTTGCG AAAGCCAATC TGCTTTATGA TTCTAACCTC 660
TGGCTAGCAA CTGCTCCCAA TTTCATGTCA TCCATAAACT TGATGAACGA TTAGCTTGCT 720
TCTCTGCAGT CATTCATTTA TTTATTCAAC CGGTATTTAG TGAGCGCCTA CTGGATGCTG 780
GGTGCTGGAT ACAGAGTTAC AGGAGACGCA GGTCCTGGGC TGAAGAGACT CCTGTGGGGA 840
GGCGGAGCCC ACGTGAAAAT GGTTCCCATT TATGTGATCT GTGCTCAACT GGGGCAGGGG 900
AGAGAGCCAG CTCCTTCTTG GTGCGGGGGG CGGGGGGCAG TTTACATTTG CCTGAAGATG 960
CTGGAGGGGA TTTTGGCAGC 980
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