| Tag | Content |
|---|
EnhancerAtlas ID | HS182-09014 | Organism | Homo sapiens | Tissue/cell | Spleen | Coordinate | chr17:7972140-7973250 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxo1 | MA0480.1 | chr17:7973151-7973162 | TCCTGTTTACT | + | 6.32 |
| | | 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 |
| GH17I008068 | chr17 | 7971936 | 7973154 |
| Enhancer Sequence | ATACAATGTC TGTAATCTAC AGATAACATA ACCGATTAGA TTAGGGGTTG ATCTTTAACT 60
ACCAGGCCCG GGGTGTGGCG CAGGGCTGCC TGCCTGTGGA TTTCATTTCT GCCTTAGTTT 120
TTACTTCTTC TTTCTTTGGA GGCAGAAATT GGGCATAAGA CAATATGAGG GGTGGTCTCC 180
TCCCTTATTC TGGCCCCATG GACGTGGTGA TGGGCTGCCC TTCCCCAGTT TCTGCCCAAT 240
GCCTGCCCTC TCCTGTGCCC CCACTCCAGC TCACTCAGAC ACCCAGCCTA GACAGCCCCA 300
TCTTCCTGCC CAGTGACCCC AGCTGAAGAC TGGTTCCTGG CCAAGACCTG GGTGTGACCC 360
TGAAAGTTCC TGTTGCACAA GACGGTCACT CATCTACTTC AAACCCACTT TGTGGTGGAG 420
CTTTTGCTTT GTCCATGCTG TGGCAGCTGC CCATGAGCCA CCCATTTTCA AGGCAGGGAG 480
GAGCCCTCCT CTCAGTGCCC ACAGCTGTGG GAGACCCGGG GCTGCCTGAT CTGACCTCTG 540
ACTCCGGCTT CCCCTTTCTT CTGCACCTTC CACATCAACA TCCAGCCCGC ACTGGGCTCT 600
TTGTACCAGG AAAGCTCATC CACCAGGTCA AGGCCCTGGA GGCCTGGGAT CTTGGGGTGA 660
GCACAGAGGG CCTGGGGAGG CCTGAGATTT GGTCCAGAGC CCCTCCTAGC AGCAGGAGTG 720
GGCTCTCTGC TCATTACAGT CAACATTGTT GGGACAGATG GGCTGCCTGG AGCTGATCAC 780
CAAAGGGCTG GCAGCTGCCA GCTACCACTC CCTCTACCTG TCCCACCAGC TGGCTGACTT 840
CAAGGTCCAG GACCTCGCCC GCTACTACAC TCCAGATCTG GGCAGCCATA GAGAGGTGAC 900
ACTCCCCTGG GGCCTGAGGG CTCCAACCCT CTCACCCTCG GCTAGACCCC TGTTGGTTTA 960
TTCAACCTTC CCCCAGCCTC CTTCCCAAAC ACACTGCTGT CTCCAAGCCC TTCCTGTTTA 1020
CTCTTGATCC TTCCCAGCTG TGTTGGGAAG TTATTTAACC TCTCTGTGCC TGTTTCCTCA 1080
TCTGACAATG GGGTAATAAG AGCACCTATG 1110
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