Tag | Content |
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EnhancerAtlas ID | HS092-38840 | Organism | Homo sapiens | Tissue/cell | HFF | Coordinate | chr9:129293220-129295480 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr9 | 129294120 | 129294170 | chr9 | 129294211 | 129295157 | chr9 | 129295182 | 129295387 |
| | Number: 1 | ID | Chromosome | Start | End |
GH09I126530 | chr9 | 129293168 | 129297039 |
| Enhancer Sequence | GTTGCATGGG ACATACTTAT ACTAAAAACT TATTCCTGGT TCATATGAAA TTCACCTGCC 60 CTGGTGTATG CCATCTGGCA ACCCTAGCCT TGGGTTCCAA ACAGGGTCCA GCAGGCTGAA 120 CAGGGACATC CCAGTTTTCC CACCTCAAAG CAAAACTGAG TCCATGAAGA AAAGAGTGCT 180 TTGTGCTGGG CTGGGAACAA TGCTTGCCTG GCCATCAGCT AGCTGTGTGA CAAACTCGTC 240 CCATCTCCTC TCTGAACCCC AGTTTTCCTA TCTGTGAATT GGGGGTTGGG TGAGATCTGA 300 GGCCTGCAGG AGGGAAGGAA GCCGCCCAGC TCCGGCAGCC CTGAGCGAGT CTTTCTGGGT 360 CTCACCCTCT CCTGTCTTTG CAAGCCTCCC AGATTACTGA GCCGGTCCCT GCTTTATGAT 420 AAGGAAGCTG AGGCTCCAAG GGAGGACGTG CCTGGCTGGG TCACCCAACA AGCACGCAGA 480 CAAAAACACT CAGAAATTTC AGTTGGATTT TCTTGTTAAG CACCAAACTG TTCACCGCAG 540 GGAGAATCGG GACTTTGCAG GTTTCCTTGA TGTTTGCTTT ACAGTTTACT ACCGTGTGTT 600 TTGATGACCT GGGGTAGAGG ATAAATTTTT GGGAACTTTG GCCGTTCAAA GTCGGGACTT 660 GTGGGCCTGG CTCTCCCCAG CCAGCTTGGG TCCAGGCCCC GGAGATGTGG GGTTTCCCAG 720 ACCTCTCACC TCCTGCATTG AGCTTGGGGA AATGGCCTCA GAGGCTCCTA TGAGACCTCA 780 GACTGCTGGC CCTACTGGGG TGGCTTAGCC CCTGCTCCAC ACGGCAGGGC TGGGCAGGCA 840 CAGGGATCTA CTAATTCAGA TCATGTTCTC AGAGGAGAAT ACCACTTCTC AAGGGAGTGT 900 CCCCATTCCC GCTGCACCCA AACCACATCC CTGCCCCGGG TGCTGGCATT GCCCTCCTGG 960 CCAAAACCCA GTTAGGGGCT GCCAACCTGT TTCTTACAGC TCCTCAGAGG ATGGTTCTCT 1020 TACTATCTCA GTCCAAACCC CTCCTTCAGC CAGTTCTTTT TCCTATCCTC CTTAACTCCC 1080 TCCTGCTGTA GGAGAAATCT TTTTGTTCCT GCTGAGCCTC CAGGGAGACA GGGAACAGCT 1140 GGTCAGCATC TGGTGCTCTC CATTAGCCAG GACTCCTGCC CCCTGGGCCT TCCGCTCCCC 1200 GGGCAGAATA ACTCTGCTTC CTCTAACCTT TCGGCTGGGT CCCGTGCTCC AGGGCTTTCA 1260 TCATGTCCTT CATACCTCTG AAGCCACTCC AGGCTCCCTG GCCCTCCTGT GGCTTCTGTT 1320 GGGCCCTGCC AGGCGGGCCA GCCAGGGCAG GGGCAGAGGG CGAATGACCC TCTCCCCTCC 1380 CAGCCCAGAG AAGCGGGGGG TGCGGGCAGC CATGTCTGGG GAAGGAGGCA GATGTCACAG 1440 CTGTGCCAGG TTCCTCCTAC TGCAGGGTGA GCCTGAGCTT GTCTTCTGGA AAATGCGGAC 1500 TGATGCCCTT TCTGCAAGGT TTGGTAAGAG GATGCCATGT GGTGGTACGG GTAGAGCCCC 1560 CTGCCTCTGT TCCAGGCCAC CCTGAACTTC TCTTTCCCCA TTGGATGACC TTGGATAAAT 1620 GACCTCACTT CTCAAACCTC AGCTTTTTCA TCTGTAAAGG GGTAGTTAGG AAGATTCTAG 1680 AGATAAGGTC CTAATGAGCC TGGCCCTGAC CCACAGCGAG AGCTGTGCGG GGCCCATATT 1740 TTCAGCGACA TTATCTCTGT TTTATTGTTA GTCATCTCAG GCCAGGAATG TGCACACCCA 1800 GGGGCTCAGC TGTCTGGCTT TGCTCGACCC TAGAGTCCTG GATTCTGAGC CTGTTGGATT 1860 CTGCTGCAGC CTGCTCCTAC CTAGGAAAGG AGGGGTCTGT AAACACGGCC GAGTTAGCTC 1920 TTCCTCCGCA ACACTTCCAA AATCCATTTG GGGATCTCCT CTTTCCAGAA GCTTCCGAGG 1980 CCCCAGTGAG ATGTCTCTGC CAGCCACAGG GGCACAGGAG GGCTAAATCC AGTGGCCCTC 2040 TCCCTTCTCT CCCTAGCTTG GGTTCCTTTG TGCCACCCCG CGAGCGGGGT GTGTGTGCCC 2100 CAAGCCGACA TGGGCACCTA CAGATGAGGC CTGGTGGGCT GAACCGTCCA CACTCAGCAT 2160 TTACAGACTT GAATGAAAAC CGAGCTCACA GAAGCTCCAG CCACCATCCT GGCCTCAGGT 2220 CACGTCCCTT AGAGACCCAC CGCTGTGAAG GTGTCCCAGA 2260
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