Tag | Content |
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EnhancerAtlas ID | HS184-22948 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr4:89241600-89242550 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr4:89242091-89242103 | GTTTGTTTGTTT | + | 6.32 | RUNX1 | MA0002.2 | chr4:89242247-89242258 | AAACCACAGAG | - | 6.14 |
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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 |
GH04I088318 | chr4 | 89239893 | 89242974 |
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Enhancer Sequence | TGGTTATATT AATGGATTAA TTCAGTTAAT CCTCACAAAA ACCTCATAAA GTAGGCAGGA 60 CCATATTCCA TTTTACAAAT GAGGAGATCA GTTCAGGAAA TTAGAACAGA GAGGTGAACT 120 AACTTAACCA AGGTGATATA GCCACTAAGT GTTGGAGTCT GACTTCAAAC ACAGTCAGTT 180 TTTATACTGC CTTGTTTGAA GCCTGGGGTG AAGATGGAGG TGGAGTGCTG TCCTGGGAGT 240 GGGGCTGAGG GATGCAGCAC TTTACAAGGG CAAAGTTTCC TACAAATCAC CTTTAAACAT 300 CTTTCTTCCT TCTCAAAGTT CACACTCACC CTGGCTGCCA AGTGCTCCCT GCTCCTCGGG 360 GCTATTGCTG TGCTGTTCTT GAGAGCTTCC TCCTTCCACC AGACAGTTTC TGTTCCCCTT 420 AGTTCTGAGA AATGTGGCCG TCCTGGCCTA GCACCCTCCT AGGAGAAGTG AAGTCCCCTG 480 CAGATCTTTC TGTTTGTTTG TTTTTCTGGA GCAAACAAGC CCTGCTTTCA ATTCAGGGAA 540 AGGTGGAAGG AGAACAGAGG TCTGGGAATG TGAAGAAGCT AAGACAGTGG ATTTGATTGG 600 GCACTTGTTT TGTTTGTGGT GTCTCAGGGA TATTCAACTG AAAAGAGAAA CCACAGAGAT 660 AGGAAGCCAG AAGAGGTTTG AAATTCTTTT GAAATACTTA CTAAATATTT GCTTTCAGAC 720 ACTTTGCAGG AGTATTCAAA CAGCATCTCC CTGTATGTTG GAAAGCAGCC CGTGTACACA 780 GCTAAATATT TTTTCTAAAT AATCTTGAAA AGGAAACTAA ACCAATCATG CATCACTGAC 840 AAAGATTTTG TCTTTTTTTT TTTTGAGACA GAGTCTCGCT GTGTCACCCA GGCTGGAGTG 900 CGGTGGCATG ATTTCAGCTC ACTGCAACCT CCACCTCCCG GGTTCAGGCG 950
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