Tag | Content |
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EnhancerAtlas ID | HS158-00655 | Organism | Homo sapiens | Tissue/cell | Pancreas | Coordinate | chr1:16417230-16419640 | 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 | ATTCTAACTG TGCAACTCCT AGGCCTGGGT TCCCTTGGCT GGCAATGTGG AGGGAAATGG 60 GTGTGGGTAG GTGGGTGCAG GCTCCACATG CTCTTCACTT GGCAAGAGGG AGAGGGGACC 120 TACCCCCTTC CTCCATCTGT CCTGGCCTCT CTTCCACCTC CCAACCCCAC CAAAGGCAGG 180 TCCTGCAAGG AAGCATCCCT TTCTGACTCC AGAACTCCTC CGTGGGCTGC AATGACTCTC 240 TTGGGTCTAA CCTGAGTCCT TCCTACTTTG GGTACAGACT GCTTCCTCTC CACCTGCCTG 300 CTGGGCTGGC AGATGGCAGC CACCTCTATC AAGACCCCCA ACGCTTCAGT GATGTGGAAA 360 AGAGGGGTCA CCAACCCCTC TTGCAGGGCA TCATCCTTTC TGGGCCAGGG GTGCCCTAAA 420 TCTCTGCCAG CCTCCCCTGC AAAAGGAACT GCAGCTCCTC ACACTCCAGG GCTGCTGTGG 480 GCACGTGAGG GAAATCAGGC AGAGAGGAAA TCAGACATCG GGTTCTAAGC AAAGACCTGC 540 AGTCGTCCTC TTCTGGTCAC CCCTTCAGTC TCGTGCCCTG TCCCAGCGGA GCCAGAACCT 600 TGAATGCCAA CTGGGCCAGG CAGGAACAGC CAGCCTCTCC TGGCACACCT GGCCAGGTGA 660 GCAGGTGATG AAGCCAAGAG CCAGCTCATC ACTTGGGTGT AAACAACTGC CCAGTGGGAG 720 GTTGGCAGCC ACCTCCTCTG CTCTATCCCC AGTCCCTGCC CCGTGAGCCC CGCCTACCCA 780 GAGAAAGAGG GTGTCCCAAC TTGTTGGAGG AGTTTCCATC CCACATCGGT GCCTGGTGCC 840 TGTACTGGGT GTGTGTGGGG GACTCTGATG GGGGCCCACA ACGGATCTTT GTCCTCCAGA 900 CCTGCGCCCC TCACTGTCCG GGAGGTGCCC AGCTCTTTGG AATGCCAAGG CCCCTGTCTC 960 ACCCACCCAC CCCAGATGGC TTTGCCATTC CCTCCCAGGG CCCTCGCCAG CACAACAGAG 1020 CAAGGGCCGT CTGGGAACTA GGTCGTGCCT TAAGCGGAGG GAGCTTGGCT CTCTCTACCC 1080 ACCAGCTGAG AGCTGTGTCC CTTGGAAGAA GGCGTGCAGT TCCAGGTTTC CAGAAGGAGG 1140 ACGAAAACAG ACCTCCACTG AGCACTTGGC CCCGATGCCC TGCATTTGAC AGATGTTGCC 1200 TGGAAGACAG ATACTGCCAC CCTCACTTTA AAGATGGAGA AACTGAGGCA AGACCACCAA 1260 TTCCATGAAG GCTGGGACCT TCTCTGCCTT GTTTGCTCCC GGCACACAGC AAGATCTCAA 1320 GGTGTACTTG TGGAAGGGAT GAATGGGGTT CGGAGAGGGC AAGTGACGTG GCCAAGGTCA 1380 CACAGCCAGA AAGGAGCTCA ACTGGGGATA ATTCAGGCCG GTTTGAACCC TAAACTCAGG 1440 CTGCTTCTGA GACCCACCCA CCGAGGTGGA GGCATCACAC CTGCCCACAT GAACGTGCAC 1500 CCACCCCGCT GTCAGAGTCC TGCTCACACA CATATACACA TCTACACCTG TGTGGGTCCA 1560 CCCAGGCACA CAGCCCCCAC CCACACCACT CAAGCCCATG CAAAGGGCCC TCCCACCATC 1620 ACCTCCCAGT CACCCTCTTA GACACCCCTC CCTTTCCTGA GGTGTGCGTC TTCCTTCGTA 1680 TCAATGAGCA GTAAATCCAG CTTTGTCCAG GTGTGTTTCT GGTGGTCTTT GGAAGTCTGT 1740 GGGTACACAG ACTTCCTTCT GTGCTGTTCT CACACCCTCC TTGTCACCAC CCCCTCCTCC 1800 ACACCTGAGA GGCAGGATGG TACATGCCCT CTTCCACCCC CACAGCCCTG GTGCCTTCTC 1860 TGCCTCTCCA GGCCTAGCAG TTGCACTGGC ACCACCGCTG TTCCGGAGAA GGCTAGAGAG 1920 TCACAGAACG TCACTTCTGG AAGGGCATCC CCCCAGCATA TAGAGGGTCA GTCTCAAGCC 1980 CAAAGAACGC AGCACCCTGC CTGCGGCGAT GGAGCTGACA CCTGGGCAGC ATTGGGGGAG 2040 CAAGGGGCTG GGCTGCCTGC AAGGTGATCC CATGGTGCAG GACCGGCTCG CTACTGTGTC 2100 ACGTGGTCCA GCCTCCGGAG CAGCTGAAAG TGTAGACCGG AGAGGGAGGC CCAAACCCCA 2160 GGATCTCCTC CTCCTGCTTT GTGCACTCCC AGATCTGCCT GGGGACCAGC TGGGGTCTCA 2220 GCTCCCTGGG CTGTGGGGCG GGGGCCTTGT TCTCCAGAGC GGGCTGAACC TGGAATGGGC 2280 CCTGGTTCTC TACTAATAAA GGGCCCACTA GGCAGAGGTG GTTAAGGAGG CCCAGAGGAC 2340 CCCTAGGAGG TCCAGGTGGC ATGTACTGGA CTCTGTGCCT GAGCCTGTAC ACTGAGTTTT 2400 CCATTTGACC 2410
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