| Tag | Content |
|---|
EnhancerAtlas ID | HS147-00046 | Organism | Homo sapiens | Tissue/cell | NHEK | Coordinate | chr1:1160090-1162630 | 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 |
| chr1 | 1160713 | 1160888 | | chr1 | 1161319 | 1161601 |
| Enhancer Sequence | GACCAGCTTG GGCAACATAG GGAGACCCCA CCTCTACAAA AACAATTACG AAAATTCGCC 60
AGGCGCGGTG GCGTGCACCT GTGGTTTCAG CTACTCAAGA GGCTGAGGTG GGAGGCCTCC 120
CGAACCTGGA ATGCGAAGGT TGCAGTGAAC TGTGATCACA CCACTGCACT CCAGCCTGGG 180
CGGCATACCG AGACCCTGAC TCAAAACAAG ACAAAACAAA ATCCTTCATA TAAATTTAAG 240
TTGTGAGATT TAGGAAGAAG ACCGTGTGGG GACTTAACAT TGTGTGCAAG GATGGAAGAG 300
ACCACAGACT TGGGGGATAG GGACACAGAC TGGGGACACG GGGCCAGCGC AGGCCAGGTC 360
AGGAGGCCAC AGGCCCCAGG ACAGGTCACT CCCGTCCCAG CTTCAGAGCT CGGCTTCACC 420
ATTATGTCTT TGTGGAAGCC ACAGGCTCCT ACCCCTGCTG CAGCCGCCCG TGTCCTGAGC 480
TCACCTGTTG GAAACTTAAC CCCCAGGGCA ACAGCACTGG GAGGCAGGGC TTCCAGAGGT 540
GCGAGGTCTT GAGACCCCGG CTGGTGCGTT TGCCGGAGGC ATCCCCGAGA GTAGGGTGCC 600
CTGGCCCCTT GCCTCTATGC TCCGCTCAGG GGCAGCCGCG GCCACGTTAT GAGGTGGCAA 660
GCAGGCCCTC GTCAGGCAGG TGTGGCCTCT GGGACCTGGG CCAGGCAAGC TTCGAGGGTG 720
CACACACCGC AGGCACGGCT CAGAAGCACT GGGCAGAGAT CCTCATGGAA GAAGGCCAGG 780
CTGCCGCTCA CACGCGCCCC TCCCTCAGCA GCCGCAGCAG CCCAGAGGTG GACGGGCCTG 840
GGAGGCACCC TCAGCTCCAC AGTCCCCAAA ACACACCGGC TGGGGACGGG GCCACCCGGG 900
TGGCCATGTG GCAGGTGGGG CACCTGGTGG GTCTCACGTG GACACGTGCA TCCTCGAATG 960
CTCCGGTCAC GCTCCACACG CGCCACAGAC ACAGGCCACA CGCTCCACAC GCCACAGACA 1020
CGGGCCACAC ACTCCACATG CCACAGACAC GGGCCACACA CTCCACACGC TCTACACACT 1080
CCACAGACAC AGACACACAC GAGGCAGAGC AAAAAGCAAA AAGGTGGAAA GAAACCACAT 1140
GGCGCAGGAT TCCAGTCAAG ATGTCGGCAA GGAGTCACTC ATCCAAACTC AGGTGCCTGA 1200
AGACACGGCT GCAGGGCGGT GCACGTACAT GGAGCTGGCA CGCACACACG CAAGTGCACA 1260
GGCCGGTACC CACGTGTACA CAGCACACAC ACGTGAACAG GGCTGGCAGA ACACAGATGT 1320
GACTGGGCTG GTGCACACAC GCATGTTATC AAGTTCTGGC TCCTGAGAGA ACAAGGGCAA 1380
GACGCCCAGT GCCCAGACCC TGGCTTCCAG CTCCAGCCAC GGGAGACAGG GCTTCCTGGA 1440
AAGGCGGCAG CTATTGCACT GGGGCAGGTG GCACGGAGGC GAGCCCAGAG CATCTCACCG 1500
TGCCAGGAAG CGGGAAGGAA AGCCTGGAGC ATCTCGTGGT GCAGGGAAGC GGGAAGGAAG 1560
TGAAGCTCAA AAGCCCCTAG GACAGGGCAC CTCCCCTCTG GATGCTCTTT CCAGAAACCC 1620
TCAACCCTGT ACGGTCAGGA GGAAACATGG CACCTCCCCT CTGGGGGCTC TTTCCAGAAA 1680
CCCTCAACCC TGTACGGTCA GGAGAAAACA CATCCCACAA GCCCAAACTG AGGGACAGCC 1740
TAAAACCTCC TACCCAGCCC TTCTCAGAAC TGTTACGTCC TCACAAAAAC GGGAGAGTCT 1800
GAGACACCGT TCCAGCCCAG AGGAGACAGA GGAGACAGGA CAGCTGAGTG AACGTGGGTC 1860
CTGGAGGGAC GGGGCCCTAC GCAGGAGAAG GGCGAGAAGG GACCCGCGTG TGGGAAGGGA 1920
AGTCTAAACA CCCACAGCGG CCGCTGTCGC CGCTCGGCGC AGGAGTCAGG GAGACCCGGA 1980
GACCTGCTGT TACTTCCCAC TCCCCATGCC CACCTCCTCA AACGAGACAG CTTGGGGTTT 2040
CGTTACAGGC ACCAAAAAGA AACCCCGGTC CAGCTGGAGA CGCACCGAGC AGAAGCCTCA 2100
ACTCCCCTCG CCCAGGCGTG CAGCCCACCC CCAGCACCGG CTGAGCAGGG ACGGGGACCC 2160
TTCCCCTGTG ATGCCGCGAG CCAGGCCTTC GTGAGCTCAG GGGTGGTGAA CCTGACAGGC 2220
CCCAGGGGCA CCAGCAGCCT CTTCGTGGGT TGGTCAGCTC ACCACCAAGT GAACTCAGGC 2280
CACGCAAGGA CCCCCGAACC GTACCATCTG AGGAGAGGTG CAAGGGGACA CCACACCTGG 2340
TGCCCAGGTC CTCCAGCTGG CACCGTGCCT CCGTCCCACC AGCTCACCTG TGCTCCGCCC 2400
GAAAGCCTGG ATCCTCAGGG CCCTCCCGCC TGGCCCTCAG CCCAAGGGCC GTGGCACAGC 2460
CAGACCAGTC CTCACACCTT TCCTACCTGC TCCTGCACCC CAGGACCCCA GCCCTGCCCA 2520
ATCCCCTTGC TCACCAGCTT 2540
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