Tag | Content |
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EnhancerAtlas ID | HS108-08562 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr11:113244130-113245180 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr11:113244769-113244790 | AAGGGGAAAATGAAACTAACC | - | 7.02 | IRF2 | MA0051.1 | chr11:113244773-113244791 | GGAAAATGAAACTAACCC | + | 6.22 | NFIC | MA0161.2 | chr11:113245131-113245142 | TGTGCCAAGTA | - | 6.32 |
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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 |
GH11I113372 | chr11 | 113243534 | 113244881 |
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Enhancer Sequence | CATAGACAGA AGGGTTGTAA TCACCCTTCT CTGAGCATGT GTCATTATGG AGGACAGGAC 60 CTTGAATTTG GGCTTGGCTC TGTCTTCGAG AGTATGTGGG TGAGTCACTA GTAGTGAACA 120 TGACTTCCCA TTCTGTCGTG GCATTATTTC CAAACTCATG GCCAGACACA ACTTGGCTCT 180 CCCATTCCTC AGGGAAGTAT GTGGCTGCCA CCACAATTCT CCCTCTCCAC ATGGGCAAAT 240 GTAGGCCGAA AGACCATCCT TCAAAGGTCT CAGAGAATCC TGGTGTTTTA GGCCAAGCCT 300 CAGCCCTGCA GTGTGTCTCT TGTCCATGAT AATAATAGCC TCACACAGGG AAGTGCTTTT 360 ATCTTCTTCA AAGGCCTTTC ATGTCAGAGA TTTCATTTCA TCTGCACAAC ATCCCTGTGA 420 GGTAGGTATT ATTATTTCCC ATTTGAAGCT AAGGGAAGAC AGGCCCGGAG ATCCAATATC 480 TTGTCCAGAA TTTCCTAAGG CTGAGCCAGT GCCAAAATCC AGCCTTTACC TTGAACCTCT 540 CTGCCCGCTG CCTGGCCCTG TCTCTCCTTT CATTAATTTT CTGGTCCAAA CTGCAACACA 600 GTCAACTAGC TAGTTCTTTT CACCTGCTCC CTGAGTGCGA AGGGGAAAAT GAAACTAACC 660 CATTTAAGGT TTTATCAGAA AGCCTCGTTA ATCCACCCGC AGTCTGTTAG ATAACAGCTT 720 AAATCTCTCC ACTGCAAAGG ATTACCTTCC CATCTGATCA GGCACAACAC ATTAGAGGAG 780 GCGTGGGGTG GGCATGAGCG TGTGGAGGCC ACGGCGCTTT CTCTGCAAAA ATGGAGATAT 840 TCAAACTTCC GGATCTGCTG TCCTCCCCCA GATGGGCTAG GAGCCCAGCA TCTGCCTGTA 900 CATCAAGCAG CTCCTCCGTG AAGTTACTTG AATGACAGCG TGTTCCTGAA AAGCTCCTCA 960 CTCACTCATT CATTCAATAT ATATTTGTCA GGCACCTACT ATGTGCCAAG TATTGTGCTA 1020 GAAAGTACAA AATGACATTG GGAAAAATGA 1050
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