Tag | Content |
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EnhancerAtlas ID | HS105-52417 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr22:20946000-20946660 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF13 | MA0657.1 | chr22:20946521-20946539 | TGGAAAGGGGCGTGGCTG | - | 6.03 | KLF14 | MA0740.1 | chr22:20946524-20946538 | AAAGGGGCGTGGCT | - | 6.63 | SP1 | MA0079.4 | chr22:20946525-20946540 | AAGGGGCGTGGCTGA | - | 6.04 | SP4 | MA0685.1 | chr22:20946523-20946540 | GAAAGGGGCGTGGCTGA | - | 6.57 | ZIC3 | MA0697.1 | chr22:20946384-20946399 | GCACTGCGGGGGGTG | - | 6.44 | ZIC4 | MA0751.1 | chr22:20946384-20946399 | GCACTGCGGGGGGTG | - | 6.28 |
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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 |
GH22I020591 | chr22 | 20946281 | 20946550 |
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Enhancer Sequence | ATGCTGCCCC CGGCGGGACA GGCAGACAAG GAGGGCACCG CCCCGGGCCT AGGCGGGTCT 60 CCGTCCTGGG GCAGGGGAAG AGCTCAGCAT GGCAGGACCT AGCGTGGGCT TGCTGCCCTG 120 TGTCCTCCCT GAGCCCAGGC AGGTGCTGGA GTTCATGTGC TGCGTTTCTG CTCTGCGGGC 180 CGCCGCCGTG TTCAGGCGCT TGGGGAGGCA GGGCAGGCCT AGGGCCCTGT GGCTGGGCTC 240 ACCCTTGTTC TCCCACTTCA GATGCTCGAT CTTCTAGTGG AGCTTGGCCA GCAACTCCAA 300 GGACTGCTGC TGTAGGAACT GCAGGCCCAG GTCCAAGTCC AGGATCTGCC TCTGCTGGTC 360 GATCTGGACA CCCACAGACC GGCGGCACTG CGGGGGGTGC GACGTAACCT GAGATCCCGG 420 GGACCAGCTG GGAGGCTAGC TCGCACGGCT CATGTCGCCA CCCCCAACTA CACAGCCGCT 480 GCCACTGCAC CCTGGCTCAG TGGCCATGCT GCCCGTCACA ATGGAAAGGG GCGTGGCTGA 540 GGAGCAGGGT GGGCAGCTGG GGCAGGGCCT GTGGCTGGCT CTTCCTGGGT GAGTACAGTC 600 TGATTTAAAA GGCACCCAGG GCTGGGCACG GTGGCTCATG CCTATAATCC CAGCACTTTG 660
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