Tag | Content |
---|
EnhancerAtlas ID | HS047-00487 | Organism | Homo sapiens | Tissue/cell | Fetal_placenta | Coordinate | chr1:21778760-21781110 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr1:21779734-21779755 | TTCCCTCTCCCTCCCTGCTCT | - | 6.16 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 21780356 | 21780793 | chr1 | 21779612 | 21779713 |
| | Number: 1 | ID | Chromosome | Start | End |
GH01I021449 | chr1 | 21776247 | 21781693 |
| Enhancer Sequence | GGTCATAGAA TTGGTTCAGT GGTTGTGAGT TCAGCAACCC AAGAGTGTCT TATCTGAAAT 60 ACCACGAGGA ATGCCTGGAC ACAGTAGACA AAGGTTGTTC AACTGGATGC CTTAGGATAC 120 ATGCTACCAA AAACAAAGTA GCTGAAAAGG AACCAGAATA ACAGAATATC AGAGCCAGAG 180 GAACATTTGG AGGTAATTCA GTACCTCCTC CTTTTCAACC TACAGGGGAG ATAGTGGAAC 240 AGAAGCAGAA ATGGGCCTGC CTGCTGTGCC CAAAATTCAT TGGAGATTAT TGCGGTGAAG 300 AATTTCATTT ATGATGAAGG AGAATTAAAT CCCCGTCAGT TTAAATTCAG GCAGGTTTAT 360 TGAAAAGGTG AAGAAGCGTC TTGCAGAAGC AAAGCGTGGC TGAGGCTTGT GGGCTTTGGG 420 AAAATGAGCA GCTGACAGTG GCTGATGCTG CCCCTGACTC TGGGACCATG TGGTCTCTTG 480 TTCCCTGAGA GCATCTCTTC TATTCTCTTG CATCTTCCCT CAGCCTGGCA GTCTCTGTAT 540 AATCTTCAAC ACATAATCGA GCAAGGCTGT GCCAGCCCCA ATGCCACCTG GCACTTTAGG 600 TCAAATTAGG AAGGCATGAA ATAAACTGGC CCTTTATAAT ACAGCTGTTG GAACCACAGT 660 TGAAAGTACA ATATCTTGAC TCCTGGGTTA GTGCTTTATG CTGAGCTTTT TTTTCTGAAT 720 ATGAGCACAG ACTTTGGAAT ATTAGTGTCA CCTAGCGTTA TTAGCTAGTA TTCTCCTTTT 780 GTTTCCCCAT GACATCCCCT CCTTCTTCCC ACAGATCCAC TGTCCGCTCA TTTCCATCCT 840 GTCTCATGCC ACTCGGGGCT CGTCCCTTCT AGAATGCATT CCTGGCTCCC CTGCATGCAC 900 ACTTCCAGTT AGGTTTAGCA ATGGAGGGCA CCTGATGGAG CCTGGAAGTG AGAGGAAGGT 960 GAGGTCTGTA TTTCTTCCCT CTCCCTCCCT GCTCTGGCAC TGAGTATCTG GCAATAGCTG 1020 CATCTGTCTA TTACTTCAGT GGCCACTCTT CCACAGCCCC AGTTCTCAGT GGGTCCCATA 1080 GCATTATTTA CCTTTGTTCC TTTAGCTCCC ATCAAGGAAG ATCCAGAGAC ATTCTCCTTA 1140 CCAAGACGTT AAGAAATGCA CAGGTGAGGA GAACAGCGGC ATGCGTGTAA AGGTCCTGTG 1200 GCACCCATCC TCTGCAGGCT GGAGGTCATG GCGGGAGATG CTGCATGGAT TTGCCCTCCC 1260 CGCTGTCAGT GAGAACAACA GGGTTCTGGA AGAGTAGAGG ACAGGCCATG GGACTTGGCC 1320 ATCTAGAGAT AAGGCGGGAG GGATTTCCTT GAGAGGCAGG GATATGTGGT GGTTACTAAT 1380 CATTCGAATC ATTGTGAGGT GTCTGGGAAT GTAATGGATG GGAAATCTAC TAAGAAATCA 1440 ACTTAGTAAT AATTAGAAAA GCTCTAGTTC TGAGGACAGA GACCTGATGG AGTCACCATA 1500 GTGGGAATTT ATGACCTGGC ATCCGGTTCA GATACCTGGA GCTTCTTGAG TGAGGGAAGA 1560 TTGGATCCCT TGAGGAAGAG TGAAGCCTTC AATGCTGCCA CCAGTGTATG CTGTAAATCT 1620 TCCTCCAGGC CTTCCCCAGA AGGCCCTGAA GCCATTTATG TGGGTGACTG AGGAAAGGGA 1680 AATACTCAGA GCTTCTGTGG CTTGTTGGAT TCTGGCTCTG AAGAATGCTA AACTAAGGGC 1740 ACCTGTGGTG GCCATGAAAA TGCACTACTT GCATCTCCAG CTGCAGGAGG CCTAACGAAT 1800 CAGCAGCCCC AGCTGCTACA CTCCGAATGG AGGACTTGAT GACATTTCCC CTGGATCTGC 1860 ACTAGCCCAT GAGGAGGAAA GCCTCCTATC AAGTCCTCCC AGCAGAACAC CCATGATGAC 1920 TCATGAGGAT GTTGAAAGTG TTTTCCTGTG TCAACTGTGA CTTTCTTTCT TCAAAGTCTG 1980 TTTTGTTCCT GCACATTAAC TGATTTATAT CAAATAAGAG AATAAATGCC TAGACTCCCA 2040 TGAGTCTATC TTTTACTGAT AAACTCAATA GTTCTGAGGA CGGAAGCCTG ATGGAGTCAG 2100 TATAGGGGGA ATTTATAACC TGGCATCCAG TTCAGAGACT TGGAGCTTCT TGACTGAGGG 2160 GAGATCGGGT CCCTTTGGGG AAGAAGGAAG CCTTCAATGT TGTCACAAGT GTATCCTGGA 2220 AATCTTCCTC TAAGCCTTCC TAGAGAGACC TGATAATATG ACTTATGATA CAGTGACCCC 2280 AAATTCAGGG TGTTCTTGTC TACTCTCAAG AATGCAATAT CTTCTTCCTC TGAATTGAAC 2340 GTAGTACCAA 2350
|
| |
|
|
|