Tag | Content |
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EnhancerAtlas ID | HS040-00607 | Organism | Homo sapiens | Tissue/cell | Esophagus | Coordinate | chr1:16417220-16419640 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TCTCCCTACA ATTCTAACTG TGCAACTCCT AGGCCTGGGT TCCCTTGGCT GGCAATGTGG 60 AGGGAAATGG GTGTGGGTAG GTGGGTGCAG GCTCCACATG CTCTTCACTT GGCAAGAGGG 120 AGAGGGGACC TACCCCCTTC CTCCATCTGT CCTGGCCTCT CTTCCACCTC CCAACCCCAC 180 CAAAGGCAGG TCCTGCAAGG AAGCATCCCT TTCTGACTCC AGAACTCCTC CGTGGGCTGC 240 AATGACTCTC TTGGGTCTAA CCTGAGTCCT TCCTACTTTG GGTACAGACT GCTTCCTCTC 300 CACCTGCCTG CTGGGCTGGC AGATGGCAGC CACCTCTATC AAGACCCCCA ACGCTTCAGT 360 GATGTGGAAA AGAGGGGTCA CCAACCCCTC TTGCAGGGCA TCATCCTTTC TGGGCCAGGG 420 GTGCCCTAAA TCTCTGCCAG CCTCCCCTGC AAAAGGAACT GCAGCTCCTC ACACTCCAGG 480 GCTGCTGTGG GCACGTGAGG GAAATCAGGC AGAGAGGAAA TCAGACATCG GGTTCTAAGC 540 AAAGACCTGC AGTCGTCCTC TTCTGGTCAC CCCTTCAGTC TCGTGCCCTG TCCCAGCGGA 600 GCCAGAACCT TGAATGCCAA CTGGGCCAGG CAGGAACAGC CAGCCTCTCC TGGCACACCT 660 GGCCAGGTGA GCAGGTGATG AAGCCAAGAG CCAGCTCATC ACTTGGGTGT AAACAACTGC 720 CCAGTGGGAG GTTGGCAGCC ACCTCCTCTG CTCTATCCCC AGTCCCTGCC CCGTGAGCCC 780 CGCCTACCCA GAGAAAGAGG GTGTCCCAAC TTGTTGGAGG AGTTTCCATC CCACATCGGT 840 GCCTGGTGCC TGTACTGGGT GTGTGTGGGG GACTCTGATG GGGGCCCACA ACGGATCTTT 900 GTCCTCCAGA CCTGCGCCCC TCACTGTCCG GGAGGTGCCC AGCTCTTTGG AATGCCAAGG 960 CCCCTGTCTC ACCCACCCAC CCCAGATGGC TTTGCCATTC CCTCCCAGGG CCCTCGCCAG 1020 CACAACAGAG CAAGGGCCGT CTGGGAACTA GGTCGTGCCT TAAGCGGAGG GAGCTTGGCT 1080 CTCTCTACCC ACCAGCTGAG AGCTGTGTCC CTTGGAAGAA GGCGTGCAGT TCCAGGTTTC 1140 CAGAAGGAGG ACGAAAACAG ACCTCCACTG AGCACTTGGC CCCGATGCCC TGCATTTGAC 1200 AGATGTTGCC TGGAAGACAG ATACTGCCAC CCTCACTTTA AAGATGGAGA AACTGAGGCA 1260 AGACCACCAA TTCCATGAAG GCTGGGACCT TCTCTGCCTT GTTTGCTCCC GGCACACAGC 1320 AAGATCTCAA GGTGTACTTG TGGAAGGGAT GAATGGGGTT CGGAGAGGGC AAGTGACGTG 1380 GCCAAGGTCA CACAGCCAGA AAGGAGCTCA ACTGGGGATA ATTCAGGCCG GTTTGAACCC 1440 TAAACTCAGG CTGCTTCTGA GACCCACCCA CCGAGGTGGA GGCATCACAC CTGCCCACAT 1500 GAACGTGCAC CCACCCCGCT GTCAGAGTCC TGCTCACACA CATATACACA TCTACACCTG 1560 TGTGGGTCCA CCCAGGCACA CAGCCCCCAC CCACACCACT CAAGCCCATG CAAAGGGCCC 1620 TCCCACCATC ACCTCCCAGT CACCCTCTTA GACACCCCTC CCTTTCCTGA GGTGTGCGTC 1680 TTCCTTCGTA TCAATGAGCA GTAAATCCAG CTTTGTCCAG GTGTGTTTCT GGTGGTCTTT 1740 GGAAGTCTGT GGGTACACAG ACTTCCTTCT GTGCTGTTCT CACACCCTCC TTGTCACCAC 1800 CCCCTCCTCC ACACCTGAGA GGCAGGATGG TACATGCCCT CTTCCACCCC CACAGCCCTG 1860 GTGCCTTCTC TGCCTCTCCA GGCCTAGCAG TTGCACTGGC ACCACCGCTG TTCCGGAGAA 1920 GGCTAGAGAG TCACAGAACG TCACTTCTGG AAGGGCATCC CCCCAGCATA TAGAGGGTCA 1980 GTCTCAAGCC CAAAGAACGC AGCACCCTGC CTGCGGCGAT GGAGCTGACA CCTGGGCAGC 2040 ATTGGGGGAG CAAGGGGCTG GGCTGCCTGC AAGGTGATCC CATGGTGCAG GACCGGCTCG 2100 CTACTGTGTC ACGTGGTCCA GCCTCCGGAG CAGCTGAAAG TGTAGACCGG AGAGGGAGGC 2160 CCAAACCCCA GGATCTCCTC CTCCTGCTTT GTGCACTCCC AGATCTGCCT GGGGACCAGC 2220 TGGGGTCTCA GCTCCCTGGG CTGTGGGGCG GGGGCCTTGT TCTCCAGAGC GGGCTGAACC 2280 TGGAATGGGC CCTGGTTCTC TACTAATAAA GGGCCCACTA GGCAGAGGTG GTTAAGGAGG 2340 CCCAGAGGAC CCCTAGGAGG TCCAGGTGGC ATGTACTGGA CTCTGTGCCT GAGCCTGTAC 2400 ACTGAGTTTT CCATTTGACC 2420
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