Tag | Content |
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EnhancerAtlas ID | HS184-32002 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chrX:13687300-13687820 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chrX:13687531-13687552 | AACCAGTTTCAGTTTGTTTTT | + | 6 | Mecom | MA0029.1 | chrX:13687746-13687760 | TTTTGTCTTATCTT | - | 6.53 |
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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 |
GH0XI013667 | chrX | 13685850 | 13688710 |
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Enhancer Sequence | TTTATTTTTG GAATATACCA TATTCACTTT TGAAATGCAG GTAAACAGAT ACAGGTAGCT 60 CCCCGGCAGC TACTTTTACA ACTTCAGAGT GATGTCATAA CTCACGAAAT TCCCCTTTGT 120 AGACTGAAAC AAAAAATTCA GAAATTTCCA AGGTGCCGGT GAGGCCCTGA GTCATCTGGC 180 TGGATTCCAC CTAACGCGCC TATCTGTGAA TGATTGAAGA CAGAGCTGCA AAACCAGTTT 240 CAGTTTGTTT TTTTTTCTCT AACCACAGCA CACCCAGGCA CTTGTCCAAC AGTTTCCCAC 300 GTAGCTCTTC CCCATGGCGT GTGACTTCAT GTGCGTGTCA GTTGGGAAGA GCTAAAAGTC 360 AAAGTTCACC CATGTCTAGC AGAAAAGGAC TTGAAGATTT TACATGGACT GTGTGTTGGT 420 GTTTATGAGT CCACCAGGCC ATCTTGTTTT GTCTTATCTT TTCAGACCGA GGATTTCTAT 480 TCCTTCAGTT TTGTTTTCTT TCAGCAGATG GGCTTTTGTC 520
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