Tag | Content |
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EnhancerAtlas ID | HS104-29433 | Organism | Homo sapiens | Tissue/cell | HUVEC | Coordinate | chr19:33963170-33965560 | 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 |
chr19 | 33963705 | 33963779 | chr19 | 33963844 | 33964533 |
| | Number: 1 | ID | Chromosome | Start | End |
GH19I033472 | chr19 | 33963218 | 33965499 |
| Enhancer Sequence | TTGTAGTGAG CCATGATTAC AACACTGCAT TCCAGCCTGG GCAAGAGCAT AAGACCCTGT 60 CTCTAAAAAG AGAACTTGGG GCAGAAGTCA GCTCAGGCTC TTTGGCCAGG AAAAAACGTG 120 CCAGGAAATG TGGGCACTGC ACAGCCTCAC AGAGAGTCCC CAGCTCATGG CCACGCTGTG 180 GGCATCAACA TGCCTGGAGG CTGCTCAAAC AGACAGGGAG GCTGGGAGGC AAAGTCTCCT 240 ACCCCATGTA GGCCTACTCT CCTGCTACAG ACCAAAAATC ACAAAAAGTA GATGAGGCAA 300 AGATGTACTT GTGCAACCTT ATTTTTTTCC TTAAACATTC ACAAGTCACA GCACTGCCTC 360 TGAGCATTAA ACCCTGAATT AAGATATCAA TTAACTGAGA TCTAAACACT CCACTGATTA 420 AAATAGTAGT GAGACAAGGA TGAAGGATTT CCAAAATCAG CCTCTAAGCA TCAAAGTGGC 480 ACCGTGTTGA ACAAAACTCA TTTAAAGGGC CAGGAATTCC ATCTCTCCTG GAGATGGATG 540 TGCAGGGAAT GATTCTATTG GAGCCAGGTG GGCGGGAATT CAACACCACT GAACCCGCAA 600 CAACTATCCC TCCCACACTC CATGACCCAG TGATGCAAAG GATAAAATCC CACAAGGGGA 660 AGGACAGAAA GAAAAGAGCT GGTTGGAATT ACATATCCTC TGGGGAATCA ATCAATAAGT 720 CCTCTCCAAG AAACCAAAGC CATGAAGAAA ATGATGGTTT AGCTCAGCTG CGAGCTGAGT 780 GTGCCTGAAA CCTAGCCAGG GACGGGCAGA CGTGGGGCAG AGGTCCACCT CCACGCTGGA 840 CCAGGGCCTG GCCACGCCTT TCCTTCTGTC TGATGCTCCC ACATCCATCT CCTGCCTCCT 900 GGCGCGCAGT GACTCAAGTT CTCACTCTCC CCTAGGAGTC CCACTTCCCA TGTGGCTTTC 960 TTGCTGGCGT AGGGTTAAAT GCCTATTCAT GAGGACACAA AGATGAGCAA TGCTACTGGA 1020 ATCCTTTTCA CAGACACACC GAGAATTTAG GTCATCATCT ACGTATCTTT TCTAATTTGG 1080 GACATGTTAC CCAGGATGTA GAATCCTGGG ACACGTCTAC CTGTGAACCA ACCACAGCTT 1140 CCCATCTCCT GTGCACACAG AGAGGCCGGG GAGCAGAAAT AGACATGTTA CCCACCGCCT 1200 GATTAATGCA TGCAGGACAC TTTTCGTTCT GTGTAATTAA CAGCTCTAAA ACCGGCAGAT 1260 GACTCAATTT AACACAGTCT CGCTTAAAAC CCAAGAAGGC ACACGGCAAT TGCTGACACG 1320 CCTGCTCTCC CCTGACGCTT CCAGAGGTAC TTAACCGAAA CCCAAGGCAC TGAGCTATCA 1380 GGTGGTATGA AAGCATCTCC TTTTATTTCC CACCTTGCCT TCAGATCAAT TTAATCATCT 1440 GCAAAACAGT AAAGCAGAAC CACAGCCTAA ATTATGGAAG TAAGATGCCT GCTCTTTTGA 1500 AGTTTCAACT TTTGACCTTC ACATTCAAAC TGCACTACCC AGCACAAGAA AAGAAATTAT 1560 CCAGTTATGA TCTCATGTTT GTGGGGAAGA GTATGATTAT AGAGGAATTT ACAGGCAATC 1620 AAAAAGGCGC TCCTTGAGAG AATGGAAAAC AATAAAACAG TCACAGGAAG GAAATGAATG 1680 ACAGCCGAAC AAAAATGAGA AAGCGAGTTT GCCTGTGCTA GGAGAGGCTG CTTGCTGCCT 1740 TCCAATCAAG ACAGGCTCCT GAGGAACCCT GTGTCCCCAG CCAAGCTGCT AGCAGAAGCT 1800 GGGGTGCATG TGGGTGCCAA GGAAGCCAAG CATCTGCCCC CTGGTTCTCC ACCCTACTAT 1860 ACCCTGGCCC CAGCACAAGA CCATTCCAAG GGTGCTGGAC CGTACGTTCA GTGGGACCAG 1920 CAGTGAGCTG GGAGGATGAC TGACACTCAG GCAGCCCCAC TCCACGGGTG CCCCCTCAGA 1980 GCTGCAAGGA GCAGTGCAAG AGCCTGGGAT CAACAGTCTG GGCTCAACTG GCATTTTCTT 2040 GGGCAAGTCA CTAACTTCCC TGTACCTCAG TTTCTTCATC TGTAGCATGG AAATAACTAG 2100 AACACTTACC TAATACACCA CAAATATCTT TAAATACAGT GACATGTGTT AAGTGCTTAG 2160 CACAACACCT TGTACACATG GAGTCTCAAC AGGTGACAGT CAGTGTTATC AAGATGTGCC 2220 AGGCTGCAGC CTGGCTAACA TGATGAAACC CCATCTCTAC TAAAAATGCA AAAAGTAGCC 2280 GGGCATGGTG GTGCGCACCT GTAGTGGGGA GGCGGGGGCT GAGGCACAAG AATCACGTGA 2340 ACCCGGGAGG CGGAGGTTGC AGTGAGCCAA GATCATGCCA TTGTACTCCA 2390
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