Tag | Content |
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EnhancerAtlas ID | HS034-15114 | Organism | Homo sapiens | Tissue/cell | ECC-1 | Coordinate | chr19:33496020-33497440 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Lhx3 | MA0135.1 | chr19:33496801-33496814 | TAATTAATTATTT | + | 6.71 | Lhx3 | MA0135.1 | chr19:33496797-33496810 | TAATTAATTAATT | + | 6.78 | Lhx3 | MA0135.1 | chr19:33496798-33496811 | AATTAATTAATTA | - | 6.78 | Nr2f6(var.2) | MA0728.1 | chr19:33496103-33496118 | GAGGTCAGGAGTTCA | + | 6.22 | POU6F1 | MA0628.1 | chr19:33496799-33496809 | ATTAATTAAT | + | 6.02 | POU6F1 | MA0628.1 | chr19:33496799-33496809 | ATTAATTAAT | - | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr19 | 33496859 | 33496909 | chr19 | 33496943 | 33497026 |
| Enhancer Sequence | CAAGAAAGAT CTATTCTGGC CAGGCGTGGT GGCTCATGCC TCTAATCCCA GCACTTTGGG 60 AGGCCGAGGT GGGCGGATCA CCTGAGGTCA GGAGTTCAAG ACCAGCCTGG CCAACATGGC 120 AAAAGCCCAT CTCTACCAAA AATACAAAAT TAGCCAGGTG TGGTGGTGCA CGCCTATAAT 180 CCCAGCTACT CCGGAGGCTG AGGCAGGAGA ATCACTTGAA CCCGGGAAGC AGAGGCTGCA 240 GTGAGCCGAG ATCTCGCCAC TGCACTCCAG CCTGGGCGAC AGAGTGAGAT TCTGTCTCAA 300 AAAAAAAAAA AAAAAAAAAA AAATCTCAAT CCGTCTGCTC CAATGGAAAT TTTCATGCTG 360 CAGCCTTCCT CTGACTTCTT TGTAGTTTAG AAAATTAACT GTCCAAAGCG CTAACTGACA 420 ATCAATCTGG AACTGAAATA GAATCTCTCA TATGAATCCC ATCCAACTGG TTCCTCTGGT 480 TTTGTTGCTG AGCAAAAAAA AAAAAAAAAA AGCCCTGCCC TGCGGAGGGA TGGCACCTGC 540 TGTTTTGAGC TGCGAGCTCC ATGGGGGTTC CCTCACACTC CCCACTGTTC TCCTACTTGC 600 TTCATTTCGT CTATAGTTTG TCTCCATTGA TATAATCTCA GAGACAGGAC ACAGAGTGCC 660 TGCCTAAGAT TCCTCAGAAA GATGAGTCCA GAAAAAAGAT TTACAGCAAA AGAAATCAAC 720 TCATACTTGG AATCTTAGCA TATCGCTTCA TCCCGATAGA CCAATCTTTT ATTTTTTTAA 780 TTAATTAATT ATTTTTTGGG ACAGGGTCTT GCTCTGTCGC CCAAGCTGGA GTGCAATGGC 840 GCGATCTTGG CTTACCACAA CCTCGGCTGA TCCTTCTGTC TCAGCCTCCC AAGTAGCTGA 900 GACTACAGGC ATGCACCACC AGGCCCAGCT AACTTTTGTA CTTTTTGTAG AGATGGAGTT 960 TCGCCTTGTT GCCCAGACTG ATCTCAAATT CCTGGGCTCC AGCAATCCAC CCACCTCAGC 1020 CTCCTAAAGT GCTGGGATTA CAGGCATGAG CCACCATGCC CAGCCTATTT CATTAATTTA 1080 AAAAAAAAAA ATTCTTTTTA GGGATGGAGT CTTACTCTGT CACCCAGGCT AGAGTACAGT 1140 GGTGCAATCA TAGCTCACTG CAGCCTCAAA CTCCTGGGCT TAAGTGATCT TCCCGTCTTA 1200 GCCACTGGAG TAGCTGGAAC TACGGGCATA CACCACCACG CCTGGCTAAT TTTTAAATAT 1260 TTTGTAGAGA TGGGGTCCTC CTGTGTGGCC CAGGCTGGTA GGACCAATCA TTATAACATC 1320 AGAAATTTCA CGATGAGTCA AAGTGGCAAA GCTATGGTTC TTCACAAGCT TGCAGGGCAA 1380 AGTGATATCA AACAATGATC CACACGGGTG GAAGGGGATC 1420
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