Tag | Content |
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EnhancerAtlas ID | HS184-19504 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr22:41405280-41405930 |
Target genes | |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
E2F6 | MA0471.1 | chr22:41405697-41405708 | GGGCGGGAAGA | + | 6.14 | ESR2 | MA0258.2 | chr22:41405669-41405684 | GGGCCAAGCTGACCT | - | 6.52 |
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| 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 |
GH22I041008 | chr22 | 41404931 | 41406002 |
|
Enhancer Sequence | TTTTTTTTTT TTTTTTTTTG AGCCTCTATG CCCCAGGCTC AAGCAATCCT GCCTATGTTG 60 CTCAGGCTGA CCTCACACTC CTGGGCTCAA GCCATCTTCC ACCTCAGCCT CCCAAAGTGC 120 TAGGGTTACA TGCATGAGCC ATCACATCTG GCTCCCACGG GGGGTTTTGT AAACTGAACA 180 AAGGGAGCTC CCTTTCCCCA GCAATTCATC CCTGGAGTCC ATATGAACCA ATGTTCCTCA 240 TTTACAGCAG AAAAAGCAGC TTCCCATGCT CTAACCCCTG CCTGCTCCTC AGCTGAATGA 300 GGCTGACAGG TGCACACCCT GCAGCATCCT GCACCTCACC AGGTAAACAG GCCTGAAAGA 360 GGGAGGCCAT GGGTGTGGGC ACAGGCTCAG GGCCAAGCTG ACCTCGCAAA GGCTGAGGGG 420 CGGGAAGAAC AGGAGGAAGT GTGGGCAATG GGGAGCTGCT GGGTCTGGAG CAATTACCAT 480 TGCCACATGG TGAAGACACC AGCCCAGAGG CTGACCTGGG GCTGAGCAGA GCCCAGCAGT 540 AGGGTAGGAA GGGGCCCACC CTTGCTCCTC CAGCTCCCTT TTCTCCCCAC CCCTCAACCC 600 CAAACTCTGT CCCTCCTCCT CACTGCCCTG CTGTCAGTTC ACCTCCTTTA 650
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