| Tag | Content |
|---|
EnhancerAtlas ID | HS184-02779 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr1:228632940-228634040 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MIXL1 | MA0662.1 | chr1:228633152-228633162 | GTTAATTAGA | - | 6.02 |
| | | 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 |
| GH01I228445 | chr1 | 228633222 | 228634355 |
| Enhancer Sequence | GGATTGCTTG AGCCAGGAGT TTTGAAGCCA CAGTGAGCCT GATTAGGCGG CAGAGCTAGA 60
CCCCGTCTCA GCAAAACAAA AACAAAACAA AAACAAAAGC AAAGGTGCTT CCAACAATCA 120
GGGTGATCCT AAAATGACAG AGCAGCGTTT TGAAAATACC TCCCCGGGGC TGCAATGTGA 180
CCATTTGAGC ACTAAAAACA ACCATACAAA TGGTTAATTA GAACATGCCC CATTTATAAA 240
AGGAGGAAAG TTAACATACA CGTTTCTAAT AAGACAACAA AAGGATGGAA ATAACATTGT 300
GTTGAATTTT TGTTGATTTT GTTAAAAAGG AGCGCGTTGA CACATAGGGG GATTTTGTTT 360
CTTTAAGTTC ATGTCTGTTT ATATAAAGTT TAGGTCTGGG TGTGTGTGTG TACCTGTGTA 420
AGCAGGAAAG AGTAAACAAA ATCGAGAGCC CGGGACAAAT GCACTTAAGA AGGGGCGACG 480
GGAGGGCCAG GCTCGCCGGG CTGAGTGCTG AGGAGGGGGC GCGTCCCACC CATGCAAGCC 540
CGGAACAAAG GCGCCTGTCA CTCGTCACTC TCCACGCGGG CTGGCTCTGG AAAGCCCAAA 600
GGAAAAAACC CTCACTTTCA GGAAGAATAA GCCTCAGCCC ATGTATCTAG GGAACACGTG 660
ATGCTGCAAG AAACCAGTGA CTTAACGCGT GTAAAAGCAG GAGAGCGTCA GAGGTTCTGA 720
CCCCGGGGGA GGAGCAGACC CGCGGCAGCG TGCGGAGACT TAGCGGGCGG AATCTGCCAC 780
CAACGCAACC TGGCCCAGAG GTTTTGAACT GACCAACTGG GAGACGTCCC CGAGCTTGAA 840
TAAGGGCCTC AAAAGCTTAG CGTTTTATGC AGAGTCGCAA CCACCCAGCG CTGGGAACCT 900
GAGCCTGCAC AACCCACTAG AAAGCACCCG TGACCGTCCC CTGCGCCCGT TATCCCTGCG 960
CCCCGCACCC CTGTATCCCC GGCTTCTCTG CAGCTGTACA CCCTGCACTG CGGCGCCCCC 1020
CAGTCCCGCT GTCCGCTCCA TCGCGCAGGT CTCCAAAACG AATCCCGGCT TGGAGGGGCT 1080
CAGCGGCCCT GGGCCTGTGC 1100
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