Tag | Content |
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EnhancerAtlas ID | HS052-03040 | Organism | Homo sapiens | Tissue/cell | Fibroblast_foreskin | Coordinate | chr1:183679780-183681940 | 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: 2 | ID | Chromosome | Start | End |
GH01I183712 | chr1 | 183681261 | 183681410 | GH01I183711 | chr1 | 183680981 | 183681130 |
| Enhancer Sequence | GAAGCAAGGA CATTCTTCAC ATGGTGGCAG GAGAGGGAGA GAGCACACAG GGGAAACTGC 60 CACTTTTGAA GTATCAGATC TCATGAGAAC TCCCTCACTA TCAAGAGAAC AGCATGGGAA 120 AACTGCCCCC ACGATCCAGT CACCTCCCAC CAGGTACAAT TTGAGATGAG ATTTGGGTGA 180 GAACACAGAG TCAAACCATA TCACCAGGAT CACAGAAGTA GTGGAAGTGG ATAACTAGAA 240 GGAAAAGGGC AAAAATCCCT TGCTTATCTG GGTGCCATCT TTCTCTTGGC CCTTGATGCT 300 TTCCAGATGT GACATGCTTA CATATGTCTT CTCTCTCCTG AGCTACACTT CTGCATCTTT 360 GGAGGCCTCT CACTTGGGAT GTCTCTGCTT TACCCTTCTT TGAATTTATC CTGAGCTCCT 420 GCTCCTGGAG GTTGACCCCA CAACCTGTTA TTGAGTCAGC CCTTTTAGGC CGGGTCACAC 480 ACGATGTCTC AAGGCTGGGT TACCCTTTGC AGTGTGCACT CAGATCCTGG GCAACTCACA 540 TCGTTATGCA AAGGGTAGCC TGCTGCACAC CCTCTGCACT CTACTTTTGC ACACTGGTTC 600 CAACCAACTC TTCAGTGAGA AGCAGAACCC AAGCTCTGTG TTCATAGGCA CCCAGATTCC 660 AGAGGACATC TGTCATTTTC TCTCATGAAC TGTCCCTGGA TGTAGTTCAA TGACATTCAG 720 CCCATGGAGC CTGCAGTCTC TCCCAGCCTC AGTGAGCAGT TTTCTGGGAG CCCTCCAACT 780 CTCCCACCCA CCACTGCACT TAATGAGTAT GTAGGAGGTG TTGGGGGGTG AGGTGACAGA 840 GAAGCACTCT AGAGAGGAGT GAAATACTAT AGCCCACTCT TACTGGGTCT TTCCAACCGC 900 CTCTTAAGAT TAGTAAGGTT GAATGGGGTA CAAAGGTGAG AGTCTAGGGG CCTTTAGTTT 960 TCCCCTTGGA AAGCCTTGGA GGGGAATTCA TTCCATGTCC TGTTATAATT ATCTGGAGAG 1020 GTCAGCTCTA CATTCAATTG AACCTGTGAG TGGATTTGGC AACTGTCTTG AGCTTAGCCC 1080 TGGTTGCCAT AACTCATTAA GTTTCTCACA AGCATTTACT ATGTTAACAG AACGCTGGGA 1140 ATGGGGTGTG GGGGCGGGCG GAGAAGAAGA AGACATTCAC AGTTAACACC TCTGATGACA 1200 TCTCTGATAG CAAATAGATA CTATTACAAG ACTCTATCCA CCCAAGAGCT AAATCGTTAG 1260 TCACAGATGC AAAGTGCTGT GTGGTCTTGA GTAAGCCTCT CAGTTTTCCC ATCTATAAAT 1320 CTAGAGTAGC AGTGCAGATT TACTTGGCAA GGTTTTTCTG AGGATTAAAG TACCCTAAAT 1380 CATGTAATTA AAATGAACAT AAAGTATTTT CCAAATTTGA AGAGCCATGG AAATGAGAAA 1440 AATAATTACT AAGAGACCCA GTGAGGGGCT ATGTTTGAAC TGTTGGCCAT TCCTTGGGCA 1500 GTAGTAATTT CCTGGCAGGA ACTGGCCTGG GAGGGCCCTT GACAGATGTT GCACAGAACT 1560 AGTTTAAGAA GGGCTGACTG GCATGTGGTT TTTATTTTAT CTTTGTAAAG CTACAGTGTG 1620 AGGCCTGTGA CAGCAGGAGG AGGCCGTGAG GTATTCACTT GACAGCCTGC CATTGTCAAC 1680 TCTAATGGGA GAGAAACTTC AGTGGCTAGA AGGGCAGCCT CAGGTTGTAA GCGATTCATT 1740 TTTAGTTCAG CTGCAATAAC TCCTGCTGGT GATTTAATCC TGTGACTTAG GAACTCTTCG 1800 TGTGTGCTTG AGTGAATGAA TAAAAGAGAG ACAGAGTGAG AGAGAGAGAG AGTGTGTGTG 1860 TGTGCACGTG TGCACACATG CACACACATT CATGTGAACA ATTTCTATTC ACTCACTTGT 1920 GATTACCAAT GGGCCACATT CTATTTAGGT TTTGGAGGCT TGGCATGAAG CATGTTTTGC 1980 TAGGATGATT TGTTTTTTGG ACAAGGAAGC TAACATGGTA AGTCATATGA TAATTTAGTT 2040 TATGTCTTCA TTGTTGCAGA GTTTGGCTGA TAGCAAGGGC AGTCGAGAAT GATAGTCTCA 2100 TATAGACCTT AATCCCAGCT CCTAAAGTAG AATGGAATTG TGGAAATCAA GTTTTCTGGT 2160
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