Tag | Content |
---|
EnhancerAtlas ID | HS108-16657 | Organism | Homo sapiens | Tissue/cell | K562 | Coordinate | chr17:33212970-33215160 | SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 1 | ID | Chromosome | Start | End |
GH17I034886 | chr17 | 33213881 | 33214030 |
| Enhancer Sequence | AAGCCTACAG TGAGCTGTGA TGGCACCACT GCACTCCAGC CTGGGAGACA GAGGAAGAAC 60 TTGTCTCTAA AAACTAAAAA CACCTTGTTT CCCCCTCTAT ACATTATACA TGGCGTCAAT 120 GTAAGGATAA AGGAAATCAC ATATGTTTTA ACAGGGTGGC ATATTGTACA CTGTTTCAGT 180 TCAAATACCA GCCCAGCTAC TGGAAGGCTG TGTGGCCTTC GACAAGTCAT TTGACTTCCC 240 TCAGCTTCAG TCCTCATCTG TAAAATCAGA ATAGGAATAG TACCCATCCC ACAAGTGTTT 300 GTGGGTATTC ATAGTGATAT TACATTTAAA GTGCATAGAA GAATACCTGA CACATAGAGA 360 GCCCAGAACA AATTATTGGA GTGGTTGTCA AGCATTGTTA CTTGTCCTGT GCTTGGCACG 420 TCTTAGGCAC TCTTCTCAAA CATGTCGGTT CCCCATGTTT GCTCCCCGCT GGAAGAGACA 480 GCACAGGAGT CCTGGGCAAT GGCAGCCTAG GCACCCACAG CCACCGCTGT GTAGCCAGGT 540 AGGCAGCACT GATCCTGGGC TTAATTTGGA GTAAGGATGG GGATGGAGGG GGGTACAATC 600 TGGACAGGGA AAGGGCAGGG AGGAGATCAG ACTAGTGGGA GCCCAGAGCT TAGGCAAGGC 660 AGGCTCCGGA TCTCAGGGCT GTGACTTAAC AGAGCTGATA TACCCAAAAA TGTGGGTCTT 720 CACCCTTGGC AATTCTGAGA AGAGATGCCC AGCAGCCCTG ACTTTGAAAT GTGCTCCACT 780 CAATTGTGAA TGAATAATTT ACAGTCTTTG ATCTTATATT GCTGAGAAGG AGAGGGAGAA 840 GACCATGAGG GCATCGGGTA CAAGAAGATG AGAAAGTAAA AGAGGAAATA ACTTAACCCT 900 CTCTGGCCTA TCTGAACTTT CAAGTCTCCC TGAGAGACGA CTGGCAGAGT CTGGCACTGG 960 AAAGCCTGCT GATTCCTTCC TGTCGGGGCC CGTGCACCCC GGGTAGCAAG AGCCACGTGA 1020 ACACATTTGG GTTAGTGTGT CAATAAGATT AGCAGGAAAG AAAAAGGAGA AGTTGTCAGC 1080 ATGTGAGACA TAAAGGTGTA AAGCTTTTAT CAGTATTGCC AAATGGCTTC AGTCTCCCCG 1140 ACCTAGATCC CATCGCTCCT GCTGACAAAC CACTCTTTTT CTTCATTCAG AAAACACTGA 1200 TACAGCCCTT TTTCCACCAG CCTGTGGGTG TGAATGACAT GAACAACACC CAAATATTGC 1260 AAGTTCCAAG CACCTATCTG CCAACTCAGG GGATCTCAAT CCTTTGCAAA CCCCTCTCCC 1320 ACTCCTGGGA GCCCCAAGAG GCCTCTCACC ACGGATTGGG CTGGGTTTCC ACTCTCTAGT 1380 TTGCTCTGCA TGTGGCTTTG TTCTCCCAAG ACATCTGCAA ATTGGCTATG ACAAAAAACA 1440 TTCACTAAAT GAGCTTGTTA AAAGTCATAG TATTATTTTA ACCAAATAGT TTTGAGCACC 1500 GACTTTGTAG CCGGCACTGG GCTAAGAGCT CAGCCTGCTC CTCCAAGGGA AAAAAAGTCA 1560 CCCATGCCCT GTCCAGGGGC TGCAAGGAGG GTGCCCACCA GGGTGCTGCT TGGGCACCAA 1620 AGGCTTAGAG AGTTGATGAA ATAATGTTTT GTCCACACAC ACAGCTTTTG CTCTCTGGAG 1680 ACGCTTGGCA CACCAAAGTC ACTTGGTTTA GAGGGGTTCA CACACCCATT CCCAGAATGA 1740 CTGCCCCTCT GTTTCTCAGG CAGTCTGCAG CAGCCAGACC TCAAGGCTAG ACCTTTTCAG 1800 CCCCCATGAT GAATTCTCTC TCAGGGACCC CACTGTCCCC CAGCACCCTG GTCTCCACTG 1860 CCCCTCCCTC TTGTCCAGCA GACACAACTC TAAATATGTG TCACCCTATT TTGTGTCACC 1920 CTATTTGTAG ACAGAATTCA GTGCTTGTCC CCCACAAAAT CTTTTTCTTC CACGAATCCA 1980 TGAATGCAAA CAGGTCCTTG GGCTAAGAGG GGTCATTACC ATACATGCCA GCTTCATCAG 2040 AATCTCCGCT CTGGCCTGGC CGACCCAGAG CCTGCTGCCT CCCTCAGCAC CAGGAGCTCT 2100 GTCCTGATTG ACAGGCCCTA GTGGGAAAAA GCCACTGGGG CTCAAGGCTA GGATGAAAGC 2160 CCACTTCAAC GACATTGCCT CTCCTCCCAG 2190
|
| |
|
|
|