Tag | Content |
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EnhancerAtlas ID | HS068-04601 | Organism | Homo sapiens | Tissue/cell | GM18526 | Coordinate | chr5:139106730-139107900 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EHF | MA0598.2 | chr5:139107828-139107840 | GACTTCCGGGTT | - | 6.14 | ELF1 | MA0473.2 | chr5:139107828-139107840 | GACTTCCGGGTT | - | 6.74 | ELF3 | MA0640.1 | chr5:139107827-139107840 | TGACTTCCGGGTT | - | 6.27 | ELF4 | MA0641.1 | chr5:139107828-139107840 | GACTTCCGGGTT | - | 6.18 | Nr2f6(var.2) | MA0728.1 | chr5:139107661-139107676 | TGAACTCCTGACCTC | - | 6.22 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CACCCAGGCT GGAGTGCAGT GGGGTAATCT CGGCTCCCTG CAACCTCCGC CTCCCGGGTT 60 CAAGCGATTA TCCCACCTCA GCCTCCCGAG TAGCTGGGAT TACAGGTGCG CACTACTACG 120 CCTGAGTAAT TTTTGTATTT TTAGTAGAGA CGGGGTTTCA TCATGTTGGT CAGGCTGGTC 180 TCAAACTCCT GACCTCGTGA TCCGTCTGCC TGGGCCTCCC AAAGTGCTGG GATTAAAGGC 240 GTGAGCCACC GTGCCTAGCC TTTTTTTGGA GATGGAGTTT CGCCCTTGTT GCCCAGGCTG 300 GAGCACAGTG GCGTGATCTC AGCTCACTGC AACCTCTGCC TCCCGGGTTC AAGCGATTCT 360 CTTGTCTCAG CCTCCTGAGT AGCTGGGATT ACAGGTGCGT GCCACCACAC CCAGCTAATT 420 TTTTGTATTT TTAGTATAGA CAGGGTTTCA CCATGTTGGC CAGGCTGGTC TCGAACTCCT 480 GACTTCAGGT GATCCAGCCA CCTTGGCCTC CCAAAGTGCT GGGATTATAG TGTGAGCCAC 540 TGCCCTTTTG TTTTGTTTTT TTAAGAGACA AGGTCTCACC CTGTTGCCAG GGTGGAGTGC 600 AGTGGCAGGA TCTTGGCTCA CTGCAACCTC AATCTCCCAC GCTCAAGTGA TCCTCCCACC 660 TCAGCCTTCT GAGTAGTGGG GACTACTGGT GCGTGCCACC ATGCTCAGCT AATTTTTTTT 720 TTTTTTTTTG AGACGGTGTC TCACTCTGTC GCCCAGGCTG GAGTGCAGTG ACGCAATCTT 780 GGCCCACTGC AAGCTCTGCC TCCTGGGTTC ATGCCATTCT CCTGCCTCAG CCTCCCCAGT 840 AGCTGGGACT ACAGGCGCCG GCCACCACGC CAGCTAATTT TTTTGTATTT TTAGTAGAGA 900 CGGGGTTTCA CCGTGTTAGC CAGGATGCTC TTGAACTCCT GACCTCGTGA TCCATCCGCC 960 TCGGCCTCCC AAAGTGCTGG GATTACAGGT GTGAGTCACT GTGCCTGGCC TAATTTTTTT 1020 TTTTTTTTTT TGAGATGGAG TCTTGCTCTG TCGCCCAGGT TGGAGTGCAT GGCGCGATCT 1080 GGGCTCACTG CAATCCCTGA CTTCCGGGTT CACGCCGTTC TCCTGCCTCA GCCTCCCAAG 1140 TAGCTGGGAC TACAGGTGCC TGCAAGCAAG 1170
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