Tag | Content |
---|
EnhancerAtlas ID | HS042-00713 | Organism | Homo sapiens | Tissue/cell | Fetal_brain | Coordinate | chr1:18116160-18118560 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myog | MA0500.1 | chr1:18117658-18117669 | GACAGCTGCAG | + | 6.62 | NFYB | MA0502.1 | chr1:18117068-18117083 | CTGATTGGTCCATGG | - | 6.98 | Tcf12 | MA0521.1 | chr1:18117658-18117669 | GACAGCTGCAG | + | 6.14 | ZBTB18 | MA0698.1 | chr1:18117399-18117412 | GCACATCTGGCTG | - | 6 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GACATCATCA TCTCCATTTT GTAGGTAAGA AACTTGGGTT CAGAGAGGTT GAGTAATTTA 60 CTCTAGGTCA CACAGCTGTT TGTGCCTAGA GGTGGGAGAA AGAGAGATAA CATTTTCCAA 120 GTACCTGCTA AATGCCTGGC TCTGACCATA CCGTTGTTAT AGGACCTTTG GGGTGTCATT 180 TTTCTGGCTG GAAACCTCTG TGGCTGGTGG CACCTTTGCC TGAGTTTTGC TTAGGCCTGC 240 TGGGCTCATT TCACGCACTC AGCCTGGAAG GCTGCACTTG GCTCATGCCA CTGGCCTGGG 300 TCCCACGCCT GCCAAGGGAG AGTCAAGTGT GGAATGGCAA GGGGTGTGTG AGCAAGCGTG 360 GTGTGTGGCC ACTGCACACA GTCAGACATG CCAGCTGCTG CAGTGGGGCA GGCAGCTCTG 420 GGTGCCAGCA CAGGTGCCAG CTCTCTGTGG GTCTGTGGCT GGACCAGGTG TACCACAAGC 480 AGCTTCCACG GCTGGCACCG GGGAACACAA AGGCACTCGG AAGCTTGGAG ATGCCAGGAA 540 CCACAGGGCC CCAGTGAGGG AGTCACAGCC CTGGCATGGG GAGCTCCCAG GTCTGGGCTC 600 CCTGAAGGGC CACAGCTCTT CTCTTCTTCT CTTCACCTGC AATGTGGTGA GCAAGGGTCA 660 TGTTTCAGCC CTGTTTGTGT TACAGCTCTT TTAGCCTCAT TCAGTGGTTC CCAAGTTCTT 720 GTCCCATGCC CTGGAAGAAT GAGATAGGCA GACAAACAGA AGGTGAGCAA GACGAAGAGG 780 AGCTTTATTG AGCAAATATA GCTCAGTGGA GGCCCTGGAG TGGGTAACTC CTCTCTGCAG 840 CCTGTTGTCC CGATGTCTGC TCAGCTCTGG CTGATCCCAG GGCTTTTATG GGCCTCAGAA 900 AGTGCATGCT GATTGGTCCA TGGGCACCCA TGGGCGGGCC CAGAAAAGGC ACCACAAGTT 960 CCCACTCTGT GAGACTGGCA TCTGGCCCCC AGCCTTCAGG TCCTCCCTGA TCTGAAGGTG 1020 GGGCCTCACC AGGGACCCAC CCCCTTCTAC CCAGGAAACT GTCTGCCTCC TGCTGCTGTT 1080 CATAGTGCCC CAGGCTGTAG GTGCCAAGGG GCACCTGCAG GCCAGTGCCA AGTTGCCCTT 1140 AGCCCTCCCT TGGCTTCCCT CCTGTGCTCA TCAGCATCCA AAATTCAGAG GGGGCTGAGG 1200 CAGCAGGAGG CTGGTGTGTC AGCACTTTCC TGACCGTGTG CACATCTGGC TGGGCTGTGA 1260 CAGGGCCTGG GCTTGGCCTT GACTTTGCTC TGAGATTGGA GCAGATGCTA ACAGCAGGGG 1320 GAAGCCAGGC AGTGGGAGCA GGCTTTTCTG AGCCTATGAG GGTTGGGGGG AGGGGGCCTT 1380 CCTGGGCCCC TAAGAGTGCA GAGATGACTG GGTGGCTGCA GCTGTGCCTG GCAGGGGGTG 1440 GGGCCGGGCT CCTGCCTACT CCATGGAGCA GGAGGCCTGG GTCTGCTGCC ATAGTTCAGA 1500 CAGCTGCAGC GGCACCCAGG GATCTCCTGC CCCAACTCGG AAGGGGCAGG CCTCCTGCTT 1560 GTCCCCAGCT CCCGCCAGCT CCACGGAGTG TACAGCCCTG GCCACGCCTC CCTGCTGCAG 1620 CAGGCGTGAT GGCAGCAGCT GCTTCAGATG GCTCGCTGCT GCCATCACCT TGATACCACC 1680 TCATTGGCTA CGAAGAGGAA ACTGTGTTCA CAGAATAGTA AACTGAGACT CAGAGATGAG 1740 AAGCAGCTTT CCAGGGCCAC ACAATTAGGG AGTGGAAGAT CCGGGATTTG AACACAGGTC 1800 TGTGTGAATC CTAGGCACAT TCTCTTGCCA CCACCCCAGC AGCAATTTCC TTTATTTTGA 1860 GTCAGCTCAA GTGCCTGGTG GTGGCTCTGA GGTCTGCATC GGGCACATCG GGGTGCAGAG 1920 TGAATGTGGG TTCCCCTGGC AGATGCCTCC CTGAGGGGCC ATCAGCATGG TGAGGAGGCT 1980 GGCTAGATCA AGCCGCCCTG CGAGTGGGCA CCGGGCCATG GGCACCAGGC CCCGAAGCCA 2040 GCCTGATTTG CCTGTGGAAC GAGGAGGGTG ATGTTTTATG CATGGTGCCT AATTTTGCCC 2100 TGGCAGTCTC TGGCTATATT TAACACCATT AATCATTATT GTTGGCTCCC AGGGGGATGG 2160 ATCCCTGATT AGTGTCAGAA ACACATCTTA TGAGGAAGAG AGAGGGAAAA AATAAGAGCT 2220 TCACCCCCAA CTTGATTTCT TCCAACTGAA GCCGGGACTC CCATTCCTGC CACCATCTCT 2280 TTGCTATCTG CAGAGTTTGT GACTTGTGGC ATCCTTGGCT TGGGATCCTG CCCCCCCTCA 2340 TCAACCCCAT CAGGAACCCT TATCATTGGG GCTGGAGCCA GGGCCTCTTA ACCCCAATGG 2400
|
| |
|
|
|