Tag | Content |
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EnhancerAtlas ID | HS049-03152 | Organism | Homo sapiens | Tissue/cell | Fetal_spinal_cord | Coordinate | chr17:5568230-5569560 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr17 | 5568492 | 5568883 | chr17 | 5568934 | 5569003 |
| Enhancer Sequence | CGGTATTTTA AAATCATTAG ATTTCACATA TAAATCCGAT GTTCTGAATT TTATCTTAAA 60 ATATAGGGTG ATCCGGCAAC AATTGGACCT ATACTCCTGC CTGTTTCAGA GCCTCCTAGG 120 CAATTCCAGC TGGAGGTGGA ACGTTCCCAG GTGAGGTAGG CCCTGCAGAC GTGGGAGTGG 180 GGTCACTGTC ACCCAAAAGG AGGAGCATCG GCTTTTTAGA CCGGGGCCTG AGGAGCCCCC 240 AAGGGAAGTG TCTGAACCAC GCAGGTTCCT TACAGTCTTG AGCTCAGATT TAACTTGACA 300 AGTGCTGAGT GCAGCGGGAC TCTTAGCCAC ATTGATCCGG ACACTAAACT CCTATTAATG 360 TAGTCAGAGA AAGCAATTGC TTTCTTGGCA GCCACATGCG GCTGGCGGCT CGCACAGACC 420 TTGCAGTCAG ATGGAGACAC CAGGACCGCC CCGTGGGAGC AGCTGTGAGC TAAGACTTCC 480 GCGCCTGGGT ATCCAGCCTC AGTGCAGGCT TCACGCTCTG GCTCTGTCAG TGTGGACTGT 540 CACTTTAGCT GCCAGCCTTT CCTGTGAGTG GCATCCTCAG CTGTCCCCTG CACTGGCCCC 600 TTGGCATTTT CCTAACCCCT ACACAAAAGG GCAGCGGGAT CTTGGCTAGG GGGCTCAGAG 660 CAATGCTCCC TGCTCCCCAA TTTGGCCTTC CCTGCTAACA TCCCCTTCCC TGGTGTTCTG 720 ACCCTTTTTG GCTTCCTCCC TCAGCACATG CAGGCCCCCC CCCCATGCTC TGTTTTGGAT 780 GTGTCTTCCT GGTGCTCCCT CCTCAGGCTC ACTCCAGTGG ACATGATTTT GCTTCTGACC 840 TCTGGACTTA TGCACCTTTG CCAGGCCCAA CAGCTTCTCC CTTTTTCGTG CTATGTGGGG 900 ACTGTGACGG CCAGGACCCC TTCCCAGCCC CCGCAGCGCC CCCCTCAGTC ACCAAAGTCT 960 GTCTTTTTTA CTCTCTGATA TCTTCGAAGT TGTCCATTTC TTTCACCCCC AGTGCCATGC 1020 GTGTCCAGCC CAATCTCTCA CCTGGCTGCT CCCAGAGCCT CTGACCTGTA CTCCCTGCCT 1080 CCAGGCTTTT CGCCTCCAGC CCACTTTCCA ACAGCAGCCG GAGAGCTCTC TTCAGAGGAC 1140 AAACCTGACC ATGGCAACTC TGTCCAGAAT CCTTCAATGC ATCGTTCCGG ATTTCAAGAT 1200 GAAGCCTGAG TTCCAGGCAG TTCCAGACTT GGCCCCGGTT CTCTCCTCCA GCCTCATGGC 1260 TCCCCGCATC CATCCCCCAG TCCATGTTCT GGCCATACTG GTCCATTTGC AGCACGCTTG 1320 CTTCCTCTGA 1330
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