Tag | Content |
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EnhancerAtlas ID | HS059-29407 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr20:61958180-61959300 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxo1 | MA0480.1 | chr20:61958338-61958349 | TCCTGTTTACT | + | 6.32 | ZNF263 | MA0528.1 | chr20:61959278-61959299 | TCTTTTCTCTTCCCCTCCTCA | - | 6.2 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH20I063326 | chr20 | 61957403 | 61958904 |
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Enhancer Sequence | TGCATTTCCA ACACCCACCA GCCAACCAAA GGTGGGGGAG CGAAGGGTGC AAGCCCCACA 60 TGCAACCACT CAGGGACTTC CTACTGACAG CTCAGGGACT TCCTACTGAC CACCTAGGGA 120 CTTCCTGTTG ACAGCCCACA GACTTCCTGT TGACAGCTTC CTGTTTACTG GCCTGGAACT 180 TCCTGTTGAC CCCCCTAGGG ACTTCCTGGT GACAGCCCAT GGACTTCCTG TTGACCACCC 240 AAGGACTTCC TGTCGCTCTC CCAGGGACTT CCTGTTGACT GCCAGGGACT TCCTGTTTAC 300 CACTCAGGGA CTTTCTGTTG ACTGCCCAGG GACTTGTGTT TACCACTCAG GGACTTCCTG 360 TTGACGGCCC GGGGACTTCC TGTTGACCGC TCAGAGACTT CCTGTTGGCC ACTCAGGGAC 420 TTCCTATTGA CCACCCAGGG ACTTCCTATT GACCACTCAG GGACTTCCCA TTTGTTGTTG 480 GAGGCCTGTT CTGAGCTGGG AGCTTGGTGT TGGTGCTAGT ACAAGAGAGT GTAGCTAAGG 540 GCTGGTTCTG CACCTCTCCC AACCCCACCC AGGACAGACG TGGTGGAGGG GAGGTGGTGG 600 GGCGGCAGGC TCCATGGAGG GTAGGGGGAC AGACGTGGGA GATGGGGGTG TAGTGTCCCC 660 TGGGGGATGC CTTGGCCTTC AGCAGCTCCA TGGGCCCCCC CTTAGGTGGG CTCCAGGTTC 720 ACCAAGGAGC TGGGGAGGTG GAAGAAGACA GAAGACGGCA GGGAAGTGCC AGCACAGGCC 780 TGACCCGGGC CCGGGGCCCG GGAGGGGTCT GTTCTCTGGG CAGTGTCCCA CACCCGCCAT 840 CTCCCCTAGC ACAAAATCTA CAGCCAGAGG CAAGTCCTTT GTGGCACAAG TTCCAGCCCC 900 ACTCAGGACT CTGCTGCAGA ACCGAGCCTC TCACATGCCT GCTCTCGGGT GCAGGCGAGG 960 ACCACAGGCT CCTAGGATCT GGGAATTTGG GATGGGGCTT TCACACCGCC ACTGTGGCTA 1020 TCAGGCTGCC TGAGTGAGGA TCCACCTCAG GGCCATCTCA CACTTGTCAC GTGTGGTCTC 1080 AGGCCATCTC TGCTGACTTC TTTTCTCTTC CCCTCCTCAT 1120
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