Tag | Content |
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EnhancerAtlas ID | HS184-13256 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr17:28579940-28581040 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxo1 | MA0480.1 | chr17:28580822-28580833 | TCTTGTTTACA | + | 6.02 | GFI1 | MA0038.2 | chr17:28580142-28580154 | TAAATCACTGCA | + | 6.92 |
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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 |
GH17I030253 | chr17 | 28580138 | 28581001 |
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Enhancer Sequence | GCAACAAAAG TTCTGTCCGC TCAAAGGTCA ACCAGTGCGT ATTATTTAAA ACTAAAATAC 60 TGCATCCTAA GTGAGTGCTT CCTGAAAAAC TAAGCATCTG CCTTCCCAAA AAGGAGCTTT 120 CAGCAAGCAG GAGAGCAGAC TAGGGAACAC CACACTGTTT GAGACATTAG TCGTCCCTTC 180 CCTCACCACA ATGCAGGCTG AATAAATCAC TGCAGTGGCC CTGGGCAGTT AGGCAGGTGA 240 AGGATAGAAG CAGATTCATG TAATAAAATT CTGTGTCCTT TCAACAATAC TATCACCATA 300 CAATCAAATG AATCTTCAAA GAATGCTCCC AGAAGATGGA CAATAAGTAC ATCTACACTA 360 TCTTGTTCCA AAAGCATATC AGATTAAGTC CTCACAAATT AAAATTCCTA TCAATTGTAA 420 CCCACCCTTT CAATGTCCCT GCCAAGAGGA CCCGCCTTGA TTAGTCTCTC TCTTCAGGAT 480 ATGAGTTCTT TGGGGACCCA CAAAAACCTC ACAGTCTAGG TAGCTGCCAA GTAATTGCGC 540 CCTATGTAGA TAATGAACTT GTGGCTGCCG TAACTGTTGA CACTGTGTGT CTTGGAGTTT 600 GACTGAGAAG ATTAGGATCA GTGTGTCTGA AACCTGTGTA GGAAGCAGCA AAGCACCGGC 660 TCAGGCAGGA TTCGGCTGGC CCTTTTGACT TGCGGGAAGG TGCAGCTCCT AACCCTTAGA 720 CACACTGGCC GTGAGACACA AGCATTCCAA GGAAAAAAGA AAAGAAAACA AAATAAAAAC 780 CTGCTCCAGG GATCCCAAGG TTACACTGAG TGAAACACAG ACAAATAGAT AAAGTCAGCT 840 TTAGGAACTA AGGTGAAATT AAATTTTGTT TAAACTTTAA TGTCTTGTTT ACATGCGATG 900 AGAAAGAAAG AAAAGTGAAC AGTCCTCAAA ACAAAACACC TCAAACCAAC CAACCAACCA 960 AAAAACACTG GCAACGTTTC TGTATTTTGT AACAGAAAGG GTAGGGTCAG TCTGTAAAGG 1020 GAAAAACAGT GTCTGTGAAT ATAGCTGTAG ACAGGTTAGG TGAAATTCAT TCAGAAACAG 1080 AAGAGTTTCA AATGGGCTAG 1100
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