Tag | Content |
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EnhancerAtlas ID | HS098-36068 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr21:44846070-44846880 |
Target genes | |
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) |
KLF4 | MA0039.3 | chr21:44846519-44846530 | CCACACCCTGC | + | 6.62 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_11196 | chr21:44843317-44848801 | CD20 | SE_34640 | chr21:44836922-44847063 | HeLa | SE_52671 | chr21:44845571-44847049 | Small_Intestine | SE_58455 | chr21:44763901-44850830 | Ly1 | SE_59568 | chr21:44816711-44859975 | Ly3 | SE_62541 | chr21:44767678-44851140 | Tonsil |
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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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Enhancer Sequence | ACCTGCGGGG CCGCACAGAG CTCAGAGCCC ACCAGCGCCC CCGCCGCCCG CGGTCGGCTC 60 CATCCGTGCC CGCGGAGCCC CCAGTCCCCA CGGGACGCAG GGACCTGCTC CCACGCCTGT 120 CGCCCCCACT CTATCCACGG GCCCCTCCAG CCCCGTGGGA GGTGTGGACC CGCCCCCGCC 180 GCCCGCTCCA CCCGGACCCC CGACCCTCTT GAGCCCCGCG GGGCGCACGG ACCCGCTCTC 240 ATAGAGGCCC CTGCCGCCCG AGTCCGGTTC CGTCCCGATC CCGGGACCCC CTGAGCCGGG 300 ATTCCACACT CGCCTCCCGC CGCCCGCTGT CGGTTCCGTC CCCACCCTCG ACCCCTTTAG 360 CACCTCTGGG CGCGGACCCG CTCCCACACC TGGCCCTGCC ACCCGAGGTC GGCTCGATCC 420 GGATCCCAGG ACCGTCCCCT GCCCCGCTCC CACACCCTGC CCCCGCCGCC CGCGATCCGT 480 CCGGTCCCCA CCCCCGACAT CCCAGGCACC TCGGGGATCG CGGACCCGCC CCCCACACCC 540 GGTATCTCCG CCCGCGGTCG GCTCCAACCT GACCCCCGGC TCCCCAGCCC CTGAGCCCCG 600 CGGACTCACT CCTACCCCGG CCCCCCAACA AAGGGGAGCC CGAGGGCGGC CAGGCCGCCA 660 ACCCCGCCCG CGAACCCCGC GCGCGCAAGG CCAGGGACCC TGCGCGGTGG CTGCAACCCC 720 GAGCCCCGGC CCGGCGCCCG CGCGGAGCCC CCACGGCGGC CACCTCCGCC CGCCCGGAGC 780 CCGCCGCTGC CGCCGCTGCC GCCGCTGCCG 810
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