| Tag | Content |
|---|
EnhancerAtlas ID | HS147-34351 | Organism | Homo sapiens | Tissue/cell | NHEK | Coordinate | chr5:137576350-137578680 | 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 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH05I138241 | chr5 | 137577221 | 137578130 |
| Enhancer Sequence | TTTTTACTGC TTTGTCCTAC TGTCCTCTGA GATAAACTTT AAGCATGAGA AACTTTAAGC 60
ATGTAGATTT TGTGGTCAGA CAGATCTGGA TACAAATCAT GACTCTTTGG GTAATCAGGA 120
AAATGAACTC ACTAACTATT TCAAACAGTG AGAATTTAAT ACTGTGGCTA TGTAAGTGAT 180
GGAAGAACTG AGAAGCCAAA CAGGGGAAAC GGGGGCAACC CAGAGATTAG CAAGAACAGG 240
AAACCACTAC CATCCCTAGT GTGGGGCCAG ATGAAGGAGA TGGAGCCAGA AGCTGCCAAG 300
GCTGTGGGTC TCCTAGCTTC TCCTGTCCTC CCACCCTCAG TCTGTGCCTG TGGCTCCCGT 360
TGTCCAAACC CAGCCAAAAG CCAGCTGACA AGGGAGCCTG GGAAATGCAG CCTGCCTGGG 420
GATGGGATGG GGATGGAGTG TAGGGGTAGC CCACATGTGA CACAGAGTAT TAGAAGGAGA 480
GCAATGGATC TGAAGGCAAA CAGACAAATG ATGAGCCCAG CTCTTGCTAG TTTCAAGTTC 540
CTCCTTTATA ACACGATTTC TATCTCACAG GGTTGTTGTG AGAATTAAAT GAGTAAATGT 600
AAGTAAAATG TTAGCACAGT TCCTGGCACC TAGTATGGAG GCAGCTACAA CTAACTTTCC 660
CCTAGATGGG AAAACCAAGG TTCAGACACA TTAATCTGTG CAAGGAAAAA GCATGGGAAG 720
CTGGGAGATC AGTGTGATCT TGGGCAAGTC ATTTCTCTGA GTCTCAGTTT CCCCACCCTA 780
CCAACTCCCT GGGCTGCTAA GGGGATTCAT TCCTTGGGCA GATATGTACT GAGCACTTGC 840
ATCTTCCAGG CACTTTGGGT GCAGGTACAC AAGGCAGATC CACTAAGTCC CGCTCTTCTG 900
GGGTTTACAG TCTGGACGGG ATAAAGATAC TGTAGAGAAC CTTCTATAGA TCACTTTATA 960
GTGTCACTGT GATAAATGCC ATGAAGTGCT GTGAGGGTGG GTGACACGGT GGTCTGGCCT 1020
GGTCTAGGGA GGTCAGGGCG GCTTCCCTGT GACTTCGGCT GGACCTGCAG CATGAGCTGG 1080
CTGAGCGTGT TGTACAGCCT GGGCCGAGAG CGCTGGGAAC AGCACCAGGG ACTCTTTGGA 1140
ATGTTTAAAC GTTAACCCAG CCGTCGGCAT CGCGCCCCTG GCCTACCCTA AGCCAGGCCG 1200
CGATGCTCGC GCCTCCGAGG GCCTCCCGCA GTCAAGCCGG GACCTCGCCC AGCAAGGACT 1260
CCAGGGCTGC CCAGGCAGGG GCGCCCGTCC GGCACCGGAC TCCCGCCCTG GGCCCAGCTC 1320
CGGCGCTCGG CCAGCCCCGT GCCCCGGGCG GCCGCTGATA GTCGGCTAAT GCGTATCGAA 1380
TTTTTGTGGA GTTCGGCCCG CGCAGAGTGC GCGCGGAGGC GCTGCCCGAG CCTCTTAATT 1440
CCCTTTGCAT CGATCCTGCC GTTAATGACA TAACCTTCTC CCCTAATTAA CTGACAACTG 1500
CATTAGGCGG CGCGCCTCCG CCGCACGCCG CCCACAGCTT CCCCCACGCA GTTCCGCCCG 1560
CGCCGGTGCG GGGCTGGGGC GCAGCGGCTC CGCCTGGACT CAACTCAGGG TCCGGCTGCC 1620
GTGGTGGAGG GGAGAGGATA GTGTTTCAGG ATCGGGATGC CCCTGCCATC CATATCAGCT 1680
CAATAAACAT TTGCCGTTAT TTATATTGTT GTTGTTTACC TCTTTGCCAC TTAACATACT 1740
GTAGCTTACT GTTTCATTAC AACGACCCAA GAGGCAGAGA GTGGAAATTG GGGCTTGGAG 1800
AGGTGGAGGG ACTTCGGCAA TAACCACGAA TGTGCAGCAA GCTACTGGGG GAGGCGGGAC 1860
TCCCACCCTC CTAAGCAGCC TGGGACTCCA AGTTTGTACT GTTAAGCCCT AGGCTACCCT 1920
CCAACGTGTA ATTTAGACCC TACTAAAGCT ATTACATGCA AAGTGCTTAG CAGAGTACCT 1980
GGCAGATAAT GAGCACTCAA TAAATTTTAG TATGTCAGGC TAATTTACGG AAATACTAAT 2040
TTGTGTTTAT TCTCCTTTGC CTCCCTTTTT CTGGATGGCC AGTTCAGTCA AGTGGCCAGG 2100
TTTTCTAATT ACTTGGGCAG CAGAGAAAGC AGAGGCAGTG GGCTTGGTCT CTTGCCAATT 2160
CAAACACAGG AGTCCCAAAT TTTGTGTAAT TTAAAGGATC ATTTATCTCT TACACACACA 2220
CACACACACA CACACACACA CACACACGCG CGCTATATGC TGGAACCAGG TCAGGACTTA 2280
ACCTCAATTT CATTTGTAAA ATACAAACAC TTTGCCAGGC ACAGTGGCTC 2330
|
| |
|
|
|
