| Tag | Content |
|---|
EnhancerAtlas ID | HS044-13677 | Organism | Homo sapiens | Tissue/cell | Fetal_kidney | Coordinate | chr9:129444530-129446360 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr9:129445183-129445204 | AAAAAAAAAAAGAAAGAAAGA | - | 6.25 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CTCCCTCTGC AAGGAGCCAC TTCCCCCGAT ATTGTAGATA CCATCCCCCA GGTGTCGGCT 60
GGAATGTGTG TCTCATTCAT GCCTCTGACT GTCCCTTCTA AAGCTGCAGC CCCATCTCTC 120
TTCCCTGTCT TCACTCTTCT TTGCCTTGTA GTCACCATTC GTCATACTCT GTATGAAATG 180
GATTTATCTA CGTGTTAAAA TAGATCAGTG TTACTGTCCT TCCGCCTATG AGAATGTCCT 240
CCACGGGTAA GAAGGAACTG GGGGTGGGGG CATTGGGAGG GGCTGTCTCT CTTCTCACTG 300
CTCTAGCCCC GCCTCCAGAC AGCGCCGGCC CGCACATAGT AGACGCTAAA GAAATATTTG 360
TGGGGCCGTG TGCGGTGGCT CACGCCTGTA ATCCCAACGC TTTGAGAGCC CTAGGTGGGG 420
GGATCACGAG GTCAGGAGAT CGAGACCAGC CTGGCTAACA TGGTGAAACC CCATCTCTAC 480
TAAAAATACA AATATTAGCC GGGCGCGGTG GCGCCTGCCT GTAGTCCCAG CTACTCGGGA 540
GGGTAAGGTA GGAGAATCGC TTGAACCCAG GAGGCGGAGG TTGCAATGAG CTGAGATCAC 600
GCCACTGCAC TCCAGCCTGG GTGACAGAGA GGCACTCTGT CTGAAAAAAA AAAAAAAAAA 660
AAAAGAAAGA AAGAAATATT TGTGGAATCG CCAAATGTGC ATGTGGGCCT CCCTGGCCAG 720
GCTGGCCTGG GATGGCTCCC CGGGCTCCCG GCTGTGCCCG TCCCTCCCTG TCCCTGGCCC 780
GTGACCTCCA GCCCCGGCTG GGGGCTCCCG ACAGCGCCCC TGGCGCGGAT CAAAGGGCCG 840
AGGGGCCGGC GGCCCCGCAC AGCTGCGGGC CGCAGGAAGC GCAGGGGCAG CCCTCGCTGC 900
AGGCCCGGCC CCGACGCGGC GAGGAGGCCG GGGGAGGCCG GGAGGCTGGG AGAGGCCCCG 960
CGAGGCCCGC AGAGCGCGCC CGTCTCGCCG CGCATTCCAG CCGCGTGATT GACGCGCGTA 1020
CCGGGGCCCC CGCCCGCGGC TCCCGCCGCC GCCCGCCCGG CCCGCGGCCG CCGCATCAAA 1080
GCAGATGTTT GCAGCTGGTT TGAGTTGGAT CCCCATCAAC AGGCCCTTTT TTGTCTCAAA 1140
ATAAAAAACA GCTACGCCCG GAATGATAAG GACGCGGCAG GCACGTGGGG GAGATGTCAG 1200
CGAGTCCGGC AGGGAGGAGG CCGGGCGGCT CCCTCTCTAA GTGACAGGCT GACTCTAGCA 1260
GCAGCAGCCG TGACCCCCAG AGTGTCTAGG GTCCTGTCGC CTAGCTCCTG TGAACTGCAG 1320
CTCATCCTTC AGCCGGCATC ATCAGAGCCC CGTCCCGCCC ACAACCATAA CCTCAGCCAC 1380
CACACTGAGC GCTTACTGTC CGACATGCTC TACAGCCTGC CATCCTGGGC ACCTCGCCAC 1440
CAGCCTAGGG AGGAGGTGTG ACACAGGAAG GTCAATACAT TATGATGATT ACCCATAAGG 1500
TGGGAATTGG GGTCACCAGT TTTCAAATGG GAAAACCAGT TCAGAGAGCG GAGAGGGCTT 1560
GTCCCAAGTC AGGCAGCTAG GAAGTGGCAG AGCCGGGATT TAAATCCATT CCTTCTGCTC 1620
CAGAACCGGG TTCTTAGGTA TGTGTTATGT CACCTTTTCC AAGAAGTCCC CAGATAGACT 1680
CTTGGTGCTT TCTGTGCCTC TCTGCTTGCC CAGCATGCCC CAGTACCCCA TCCAAGCACG 1740
TGTCCTACGG GATGAGATTC TAACTCCATG CCCCAAGTCC ATGAGCCCAG CCCAGAGTCA 1800
GCCTCCATGG GTGTTTGCTG GGTGAATGTG 1830
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