Tag | Content |
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EnhancerAtlas ID | HS184-16230 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr2:44108800-44110120 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
LMX1B | MA0703.2 | chr2:44109238-44109249 | ATTTTAATTAA | + | 6.62 | MEF2A | MA0052.3 | chr2:44110099-44110111 | GCTAAAAATAAA | + | 6.04 | TFAP2A | MA0003.3 | chr2:44109824-44109835 | TGCCTGAGGCA | - | 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 |
GH02I043881 | chr2 | 44108361 | 44109566 |
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Enhancer Sequence | TTGAGCCACC GCACTCCAGC CTGGTGACAG AGCGATACTC TGTCTCAAAA AAAAAAAAAA 60 AAAACCCAAG GCTCTCGAGG CATGCATGCT GTTCAGCGAG CCCTGCCCTG CATTGCGAAA 120 GGGTAGAGAT TTGTTTATTT GTCAGTATTG AAAGCATGGC TTGCAAAGTT TTCCTGTTAA 180 GAGTCAGATA GTAAATATTT GGGACTTCGT GGGCCTTATA GGCTCTGCTG CAATTACTTA 240 ACTCTGCTGT TACAGTGTGA GAGCAGCTGT AGACTATAGT AACGTACAGC CGGTGTGGCT 300 GTCTTCTAAG AAAGTATTAT TTACAAAAAC AGGCAGGTTG CTAGATTTGA CCTGAGGGTG 360 TAGTTTGCAG AGCCTTGGTA AAGGTTTTCA AATTTGCATT TTAAGCCCTC CAATTTCAAG 420 TTATGCTATT GGTGGGGAAT TTTAATTAAA CAGAAAATAA TCACCAATAT TGGCTCAAAT 480 ATTTCCTGAT TTAAAAAAAA ATCTGCTCTT GTTCCTATAA ATAGTATATA AGATGTAATC 540 TTGCCCTGGG TTAAACCAGT CTACAGAGGT AGATCTCGCA TTTGCTTTTG TTTTCTTCTA 600 CTTCAACTCT TGTCATGATC CCAAATTAAA CAACTAGCAA CAGAAATGTT CAAATCTGTC 660 AAATCCAAGT GTTAACAGAC CTGGGACCAG GGGTTCCTCA TAGTGGCTTA GCACAGCATA 720 CAGACCACTT TCCTTTGGCC CAACCGGCCT TGGGGTCTGG AGCACCAAAC AGGCCCTGAG 780 GAAGCGTGCA AGGAACTGGA ATGCGGGGAA AGTGATGAAA TATTTTGTTG GTTGGCCTTT 840 GCTTGTTTGC AAAATATATC CAATGCTCAC ACCTGAGAGA CAACAGACAT CCTTATTTGT 900 GAATAGTCTG CACTAGATAA TTCAGATTTC AAGTCATCTG TCATTCGTAC TTGATAATGA 960 TTTGTTCTTC ATTTAAAGTG GCCTGGGTAC AGAGCAACAT CCCCTGTCTT TATCACATGA 1020 GCTCTGCCTG AGGCAGCTTC AGCAGGTAGG CAGGCAGGCA GATGGAGCAC AGCCCATTCT 1080 CTGCTGGTGC ACTAGGAACA GCAGCACGTG TGGTGTTAGC AGCTAATAAT TAAAACAACG 1140 TTTAAGCAGT GGGTTGAGAT TTTTAAACAC AAACCAACTC AAAAACACTT CTCTGCTTTC 1200 TATGTAATAG TGCTCACATC ATTTGTATGA TTGTCTCGTC TCTTTAAAAT TGGAAATATT 1260 CTTGTTTCCC CAAACTGCTA ATAAGCTCTA CTGACCCATG CTAAAAATAA AGCTCTTTCG 1320
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