Tag | Content |
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EnhancerAtlas ID | HS184-14360 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr17:77824490-77825870 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOS | MA0476.1 | chr17:77824591-77824602 | TGTGACTCATC | + | 6.14 | JUND | MA0491.1 | chr17:77824591-77824602 | TGTGACTCATC | + | 6.14 | Myod1 | MA0499.1 | chr17:77825753-77825766 | AGGGGCAGCTGCT | - | 6.18 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_27416 | chr17:77824455-77826074 | Esophagus | SE_28334 | chr17:77824306-77825602 | Fetal_Intestine | SE_32172 | chr17:77824473-77825355 | Gastric | SE_62183 | chr17:77773273-77827285 | Toledo |
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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 |
GH17I079849 | chr17 | 77823291 | 77825909 |
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Enhancer Sequence | GTTGCACCTC CCCAGGTCAC CAGCAGCTGA GCAACTTACT CATGTGGGAG GAATGCCCCT 60 GCAAGTGGGG TGCACCCCAG TGACTTGCGT GTCAGACTAG ATGTGACTCA TCTACTTGTC 120 CTAGACAGCC TTGTCTTCAG CTTCGTGTGG GAGCCTCTAT GGGCCTTGGG TCCTAATACC 180 TAGTAGAGTC TCTGTTCCTC CCAGCTTGCC CCGTGAGCCA CCCAGGCAGA GGTCCAGATC 240 CACGGGGACT GACCTGACAG AACTCTTGGC CATGGCCAGT TAGGACTGTT GAGACAAGTA 300 GGAGCTGGGG CGCTGCACAC CTGCTGACTG TCCCTCTGCC ATGTGGAAGC AGGAGCATGG 360 TGTGGTAAGA GCCAGACGGA CCCAGGCTTC TCCCCGCTCT CCCGCCGGCC ACCGGCGTGA 420 CTCCGAGCAC CAGTGTATTC ATCTGCAAAG GGGAGAGGAG ACTTTCTAGG CTCAACACCC 480 TAAGAAGTCC TCTGACATCC AAGGCCCTGC CTCATGTGTC CCCGTGACCT CCTGGCTTTC 540 TTTTCCACCC CTCTCTCCCT TATACACTCT GTTCTGGGCA CACGGGCTCC TCCACTAATC 600 CTCAAACACT GACTTGGTGT TGCCTCAGGG CCTTTGAACT GACTGTAGCC ACCACTTGGA 660 ATGTTCTTTC TCCAATAACT GCATGGTTCT TTTTCACTCA AGTCTTTACT CAAATGTCAT 720 CTTTGTAATG AGCTGGCCCT GACCACCTGA TCACTACGGT CCCAGCCCTG TCCCCACCAA 780 CACTCCCAAT CTCCTTATTC CTGCTTACAT AGCACCCTCA CCTCCTTACA GACAGTATCC 840 TCTGGATGTT GATGGTGTTT CCAGCCTGCA TCTCCTGTTG GAACATAAGA GCTGCAAGCG 900 TCGGGGCGTG TCCACACCCT TGTCCGACGT GTCCCTGGCA TCTGGCACAG TGCCCAGCAC 960 GTACCTGTCA GATGAATGTT GAATTAATAG GATTTGTGTG AGGACCGAGT GAGCTCACAC 1020 AGCCAGATGA AGCTGGTCCA CCCGTACGGG CTGGCAAGAG CCGTTGGCCA CATTCTCAGA 1080 CATTTTGTGA ACCCGTTGTT GAACCCAGCC ATGATTACAA ATTAAATGAT TGGCATTTAC 1140 AATTAAATTA TGTAAAGAAC AACAATAATA AATGCTCACT ACTGACTCCT TCCTAGTGAT 1200 TTCCTCAGAT TCACATGTTC CCGGGTTCTT TGTGTCCCCT GTGTGTGGTG GAAAACGCCA 1260 CGCAGGGGCA GCTGCTGCTG CACATCTCGG CCCAATTCTG CCTTCAGCGC TGTCCTAATG 1320 GTAGCTTGAA GCCAGCTATG GCTGGAGCTT TTACTCAACA GAAATTGGTA AACACGACAA 1380
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