Tag | Content |
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EnhancerAtlas ID | HS184-06846 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr11:124514030-124515090 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MYB | MA0100.3 | chr11:124514829-124514839 | ACCAACTGTC | + | 6.02 |
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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 |
GH11I124642 | chr11 | 124512712 | 124515190 |
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Enhancer Sequence | AAAATTATCT TAGGCAAATC AGCTTTAACA TAGGAAATGA TAGAAGGTGC CACTGAAGCC 60 TCACAGTAGA ATCTCATGAA GACTAGAAAA TGGGAATAAA AAATCTATTA AGTCACCCTA 120 CTTCTTCCAC ACCCAGAAGA CAAAGTGGAA CCATGTGCAC CAGCCAGGGT CATAATGAAG 180 ATCACAGTAA CAACGCCACA GGAAAGAGTC TGTGGTGAGA AAAAAAAAAA AAAAAAAAAA 240 CTAGCCTGAA GCTCAACAGG GAGCAATGCT AATAACAGTC CCTCAAGTCA AGGGAATTTT 300 CTCAAAATGG CAGTTTGCTG AGAATTCTTG CAGCAATTCA CTTTTTCATT GACTGCACTA 360 TTATATACTC GCCACATGGG GGCACCGGCG TACTCCACAC CCACATGAAA TTCCTGTTTT 420 CCTAATCTGA GATACAGTGG GGCGCTAATC CGTCTCCCAC AGTGGCTGGT AGAAATACTG 480 CGGCTAATAA AGGCGTGGAC CAGCCAAAGA ATATAAAGCT GGCCACGCTC ACAAATAACA 540 TGCTGCAGTT TGTGGTCTGT TCAACTGTTC CTCCAAATCC CTATTTAAAA ACCACACTCC 600 TTGGGACTCC AGCCCCTAGC CTCTTGCTGT TTCGCTCTCA GGCTCCAGGT GGCCTTTCTG 660 CTAATAAGTC TGGGATACAC GTGTCCAGCC CTGGTCTCTC CGTGGAACTC ACATCCTCCA 720 TCTCTAGCTG TACTCTAGTC ACTGCAACCA TCATTTCAAA CTTAGCACTT CTATGAAGCC 780 AGTTCCTCTT TCCTTACAGA CCAACTGTCC CTCCAGATCT TCTGATTTCT CTCATCAACA 840 ATATTCAACA CTAACATTAT CTGGTATGTT CCCGGCTTTC CATGGATGAA CTCATTCAAT 900 ATTTAAAATA ACAAAGAGTT CAGTATCGTG TTCGAAATCA CGTGGCTCAG GAGGTGTCAC 960 AGCTAGCATC TGAATGCACT TAGTCTAGCT CAGACTCAGT CTGAACCATG ACGCTGTCAT 1020 GCTGGGTATT TCCCTTTGAA GGGATATGTT TATATTTCCA 1060
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