Tag | Content |
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EnhancerAtlas ID | HS059-33292 | Organism | Homo sapiens | Tissue/cell | GM12878 | Coordinate | chr3:137765560-137767100 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Pou2f3 | MA0627.1 | chr3:137766481-137766497 | GTGAATTTGCATAAAA | - | 7.1 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGAGAGGGTC CCACTTCATG ATGTCCGTAT GAAACAAGGT CATGGAGAAT CCTTTGAATT 60 TACTTCCACA AATATTTCTT TGAGTACCTA TTTTGTGCCA GGTGCCACAA CATGTATAAA 120 GATGAATAAG GAAGAAAAGA GAAGGATCAT TTGTCGAGAT TCTGGTCTGC TATGCAATGT 180 GCTGATGCCA TTCTGGGGAC TTGGAAGCAT TCATCTCATT CCATTCCCAT AACTACCTCC 240 CAAAGCATCT TTATCACAGT TACAGCTGAG GAAACTGAGG CTTGGGGAGG TTACCTGACT 300 TGCCCAGTCA TTCATCTAGT AGTTACTGGT GCTAGGATCT GAATCATGTC TGTCTGACTC 360 AAAGCCCATG TTTCAATTCT CCTGACATGA GACCAATTGA GAAGTATGGT TCACAAGCTG 420 GGGAGGGTGT CTTGGGAAAT TTTGAGGCGG GGCACTTCCT AGCCCAGCGT GTGAAAGCAG 480 GCCAGTTACT AACCTGTCTT AGCCTCAGCA GCCCAGTCAA CAGAGGCCAA TACCTACCTT 540 GCAAGGTTGT TGTGAGGATT AAAGATAATG GGTAAAGCAT CCAGCACACA GTATGTGGTC 600 TATGAAGAAT AGCTATGTTA TTCAGAGCTA CGTAAAAAAT TACCATTTCT CAAAGAGGCA 660 GGAGCTATTT TCTGATACAG TGAATTCTTG GAACTTGCAA CGGGTGTGTA TTATGAAATT 720 TAGGATCTAA GCTAGCAAGA CTTTGCTATA CGGCTTTGAG AAGGTATATG GTTGTCGCAA 780 AAATCTCAGG AGACTCTGCA AGATAAGAAA ATCTCAAAGC AGAGGCAAGT TCAGAGACTT 840 GCTTTCCTAC TCCTGAATCT TCATTCAGCT GAGCTAATGG CCAGGAATGA CAAGAGGACT 900 CACCATTGTT TGAGCCTGCC TGTGAATTTG CATAAAATGT GATTTAAAAC AAAAACATAA 960 CCAAGGATCT GGCCCCCAGG AATAGTCAAG GTATCTGCAG TGAGTAGAAG ACTATTATTT 1020 ATACTGCCTG GAATCCCACC ACAAATCTTT ACAGAAACGC ACAAACTCAC ATTGGATCAG 1080 GCTTTTGTTG GTCTCCAGGG AATGCTGACT TTGTTTATTA ATGCCACAAC AAACGTGTCT 1140 CTGAATAAGG GAACTGACAG GACACCCGTC TCTGCATTGA AACCTGATTA AAAGCAAGTC 1200 CAGCCCCTTC TAGTCTCTCA GGAGTCTTCA CAGTTTCTAA GCTGTCCTTT GTGAGTCAGT 1260 GATGTCGATG GCAGGAAAAC TCCATCCTTG TTTCTTTGGG TGATAATCCA CACATCACAG 1320 CATGAATACT CAAGCTCTCA CACGAAGCAA TGGTCTGCCT CCCAAATAGA AAGAAGGAGA 1380 GTTGCCTAAG TGGAAGGACT TGATAGGAGC TGAAAATGCA GCCCCATGAC ACCCAGTCCT 1440 CCTCTAATAA AGGTTTTTCC CTATCTCCTG TCACTGATGC TGCAAATTCT ACTCTGGAGG 1500 CAGAGTGGCA TCGGCAGGCA GCACTTCCTG AACCTTTCCA 1540
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