| Tag | Content |
|---|
EnhancerAtlas ID | HS044-08630 | Organism | Homo sapiens | Tissue/cell | Fetal_kidney | Coordinate | chr22:41984560-41985720 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SPDEF | MA0686.1 | chr22:41985107-41985118 | CACATCCGGGT | - | 6.32 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GTTAGCCAGA CTGATCTAGA ATTCCTGACC TCAGGTGATC TGCCCACCAT GGCCTCCCAA 60
AGTGCTGGGA TTACAGGCGT GACCCACAAG CAAATGGCCC ACCTTTGCTC CAGTCCTGCT 120
ATCTTCCTCC CGGATCCACC CCTGCAGGAA GGCCTCCAGG GCCCAAGCCA GGGCAACTTC 180
ACCACAGAGG ATGGGGAGGG GCATTCGGGA CCTAAGAGAG GAGGCTAAGA CCTGGGTTCC 240
CATCAGCCAC TGCCCAGTAA AGCCCATCCC ACTGCTCCCC CACGCTAGGA GACCTGTTGG 300
TTGGTCCTTG AGGCCCCCAG ACTGGAGGGT GGGTTACCCA CAGGGAGGGC ATGAATGAAG 360
CCTGCTTACT GATGCATCCA GCTGGTGAGG GGGCTTTTGG GGACTCACTC ACAATGAGAC 420
CCAATGGGAG AAAAACTGAG CAGAGGTAAG AGGCTCAACA CAGCGAGAGT CTTTAGAAGA 480
AAACTAGACT CTTACCCTCA CTATTCCTCA GTGTCCTCAC AGCAAACAGG CTAGGCCTGG 540
AGCCTCTCAC ATCCGGGTGG GTAGAGCTCA TAAACGAATT TGAAAAGAAG CCCTCTCTGC 600
TCCACGACTG GGGGTGGAAG GTAAAGTGGG TGATGGGGCT TCAGAAACTA GACCCAGTCC 660
CAGGCCTGCA AAGGTCGGGG TGGGAAGACT CCGAGACGCC CTGTCTCCCA CCAGATGATG 720
ACTGACGCTT GGCTGTGTGC TTGTGTGCCT GGAACCCCGG TTCAGAAGCC AGCTCCGACC 780
ACTGGTGTGT CGTAGGGCTG AACTAGGGTG GGATCCCCAG CTCAGGAGGC GGGGGCGTCC 840
GTGAGCCAGG CCTTAGCGGC GTGTGACAGC CTCCGGGGAG GGAGGGAGCT AGGCCCCTGC 900
TCGCAGCCTC CTCCCTCCAG TACTGGATCC AACCCCAGCA CTCCCAAGCA GAACACAGGC 960
AAGGACGCTG CGGGGTCAGT GACGTGAGGG CCAGGTCCCC TCACTCCCGG TGGGTGGCCC 1020
CGGATGTCAG GGGGCCGGGT ACCGCCGCAT CCCACACTCG GTCCCCGGGT GTCCACGGTC 1080
ACGCTGCTGC AGACCCCACA CTCAGCCTCG GGGGTGTCCG CGTGACACTC CCGGTGGGAG 1140
CTTCCAATCT TCAGGGTCCT 1160
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