Tag | Content |
---|
EnhancerAtlas ID | HS087-08443 | Organism | Homo sapiens | Tissue/cell | HEK293T | Coordinate | chr16:89779230-89781540 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr16:89781361-89781376 | TGAACTCCTGACCTT | - | 6.04 | Zfx | MA0146.2 | chr16:89779905-89779919 | CCCGCCTCGGCCTC | + | 6.01 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr16 | 89780012 | 89780093 | chr16 | 89780875 | 89780932 |
| Enhancer Sequence | GGAGAAAGAG GAGGGGAGCC ATCTGGGGTG GGCTGCAACA TCTGCCCCTT CTTGCCTGCC 60 CTTCCAAAAC ACAGGTTTTG GCCAGGTGCA GTGGCTCCCG CCTCTAATGC CAGCACTTTA 120 GGAGGCTAAG GCCGGGCGGA TCACCTGAGG TCAGGAGTTC GAGACCAGCC TGGCCAACAT 180 GGTGAAACTC TGTCTCTACT AAAAATACAA AAATTAGCTG GGCATGGTGC ACACTTGTAA 240 TCCCAGCTAC TCGGGAGGCT GAGGCAGAAT AGCTTGATCC CGGGAGGTGA TGCAGTGAGC 300 CGAGATCTGG CCACTGCACT CCAGCTGGGG TGATAGAGTG AGACTCTGTC TCAAAAAAAC 360 AAAACCAAAA CAAAAAATAA CAAAAAGAAA GAAAACACAG GTTTTGGTAT TGCCAGGACT 420 TTTGGTTTTT CTTTTTTTCT TTTTTTTTTT GAGACGGAGT CTCGCTCTGT CGCCCAGGCT 480 GGAGCGCAGT GGCGCAATCT CGGCTCACTG CAAACTCCGC CTCCCGGGTT CATGCCATTC 540 TCCTGCCTCA GCCTCCTGAG TAGCTGGGAC TACAGGTGCC CGCCACTATG CCCGGCTAAT 600 TTTTTGTATT TTTAGTAGAG ACGGGGTTTC ACCGCATTAA CCAGGATGGT CTTGATCTCC 660 TGACCTCGTG ATCCACCCGC CTCGGCCTCC CAAAGTACTG GGATTACAGG CGTGAGCTAC 720 CGCGCCCGGC CGGACTTTTG GTTTTTCAAG AGAAGCTGGA CCACTGGACT TCTATGGAGA 780 TCCGTTATAT GTGTTTGGCA ACAGTATGAA TCTTGTTAAA GCAAGCTTGT GCAACAATCC 840 GAGGCTGTAT GACTTCGAAT GTGGCCCAAC ACAAATTCCT AAACTTTCTT AAAACATCAC 900 TGAGGGCTGG GCACGGTGGC TCACGCCTGT AATCCCAGCA CTTTGGGAGG ATGAGGCAGG 960 CGGATAATGA GGTCAGGAGA TTGAGACCAT CCTGGCTAAC ATGGTGAAAC CCCGTCTCTA 1020 TTAAAAATAC AAAAAATTAG CCGGGTGTGG TGGCATGTGC CTGTGCTCCA GCCTGGGTGA 1080 TAGAGACTCT GTCTCAAAAA ATCACTGAGG TTTTTTTGCA AAATTTTTTT TTTTGAGTCA 1140 GTCTCATTCT GTCGCCCAGG CTGGAGTGCA GTGACACAAT CTCAACTCAC TGCAACCTCC 1200 GCCTCCTGGG TTCAAGTGAT TCTCCTGCCT CAGCCTCCCG AGTAGCTGGG ATTACAGGCA 1260 TGTGACACCA CGCCCAGCTA ATTTTTGTAT TTTTTAGTAG AGATGGGGTT TCATCATGTT 1320 GGCCAGGCTG ATCTCGAACT CCTGACCTCA GGTAATCTGC CCGCCTTGGC CTTCCAAAGT 1380 GCTGGGATTA CAGGCGGGAG CCACTGCGCC CAGCCTTGCA ATTTTTTTTT TTAAGCTCAT 1440 CGGCTGTTGT TAGTGTTAGC GTATTTTATG TGTGGCCCAA GACAATTCTT CCAGTGTGGC 1500 CCAGGGAAGG CAAAAGATTG GACACCCCTG CTTTAAAGGC ACTATGTGGG TCAAACAGCC 1560 AGATTAGTCT GTGACCCATG AAAGGAAGAA GTGTCCTGTC TCCTTTATAC AGTTCCCAAC 1620 AGCCACTCCA CCTTGAAAGC TTTGTTCCCT CGTACCTTCC CACTGTCAGG GACAATGGAG 1680 GACAAGGAGG AAAGTCAGAG CCTGACGCCT GGCCACCCTG CCCTGAAGCC ACATTGCAGA 1740 AACAAGGGGA CTGGGAAGCC AGGCCCCGCC AGAGCAGGGG CAGGAGGAGT GGACCCTTCT 1800 CGTCTCTCCC ACTTGGGAGT CACTGGGCTT TTTGCATTTG TGTCTTTGTA TCTTTCATCA 1860 GTTCTAGACA ACTGTCTGCC ATTCTAACTT CTAATAATGC CTCTCTCCCA TTTTCTTTCT 1920 TCTTTTTTTT TGAGCCGGAG TCTCGCTCTG TTGCTAGGCT GGAGTGCAGT GGCACGATCT 1980 TGGCTCACTG CAACCTCCAC CTCCTGGGTT CAAGCGATTC TCCTGCCTCA GCCTCCCAAG 2040 TAGCTGGGGT TACAGGCACG CGCCACCATG CCCAGCTAAG TTTTGTATTT TTAGTAGAGA 2100 TGGGGTTTCA CCATGTTAGC CAGGCTGGTC TTGAACTCCT GACCTTGTGA TCTGCCTGCC 2160 TTGGCCTCCC TCCCATTTTC TTTCTGGAAC TCCAACGAAC ACGTTAGGCT TTCCATCTCT 2220 TGTTTTCTGT CTTTATTTTT TGTTTCTGTA ATTCATTCTA GCTATCTTTT GACCTTTTTT 2280 CCAATACATG AATTTGCTCT TCAGCTATAT 2310
|
| |
|
|
|