Tag | Content |
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EnhancerAtlas ID | HS187-20938 | Organism | Homo sapiens | Tissue/cell | Th1 | Coordinate | chr6:27759100-27760770 | 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 |
GH06I027791 | chr6 | 27758905 | 27762526 |
| Enhancer Sequence | GAAGTCATAC GACTGAAACT TGAAACAGCA GACTGGGTCC CACCGAGATT TGAACTCGGA 60 TCGCTGGATT CAGAGTCCAG AGTGCTGACC ATTACACCAT GGGGCCAAGT TCTTAGCGAT 120 TTTCCCTGAA TTCTTTCATG ACCTAGTTCT TCCTTTCTAA AGTCTGATGT GGTTTTCCAA 180 TGTCAGCACA CCCCACCCTT CGCACCCCAG ACCTTTCCTT CCAGGGGGTT CAGAAACTTG 240 GTGCCCCCTC GGGCTTCTGT TTCTTCACTG GAAAAAAAGT GAAGTCGTCG AACAAAACCG 300 AGCCCTTATC GTGTGCCAGG TTTTGTGACT AGTGTTCTGT ATTGTTACCT CATGGAACGC 360 TCACAGTAAC CTGGTGAGAT GCGAACTATT GTCTTTATTT TACAGGTGAG GAGCCTGTGA 420 GAGACCTGAG ATCTTTTATT CTGCTTTGTG ATCAGATCCT ATTGCTTTCA CAAAAAAACG 480 TCGTTTATTA GGGGTGGTGT ATGGCGCGTT TGAGGACGTG CGTGGAAAGA TTTTCCCAAG 540 TTGCAGAGGA GACGTTGGTG TTTACGGAAA ACTGAAATAA GTGAACTTGC AAGACAAGAC 600 TGGAGGAAAA TCCCAGCATT CCTGGGAGCT CAACTGAGGG GGCGAAGGGA AGGGGAAAAG 660 GAATGCCCCT CGGGAGTTTC CCGGGATAGC GCGCGGCCCC ACGGGCTTCC TACTGCCGGC 720 TCACCAACGG GAAATATGCG CAGGGGAGAC TCCCAAACGG ACACAAAAAA GATTCCTCAT 780 CCCTGCTTCT CATACCCCCT TTTTCGCACA TACACAGGAG CCCATACTGT GAAAATCCAC 840 CCCCTACACC ACAGCTGATT GCTGCGATGG GTCTCTGGGG ATGTTCTCAG TCGGCCCTAC 900 CCTAGCATCT TTATAAACGC CTCCTGGTGG CTTTTAGCTG AGTAGGAGCG CCACGATATT 960 CAGTACACAT TTAGAAGCGA GCGCTTCAGC AATTTCCTTG TGGTAGAGAG GAATGCAGCT 1020 CTGCTCCAAG TAGTTTAACC TAGATTCGAC GCCTGTTCAT GGACAGCGTG CTTAGTGCAA 1080 ATTGAATGTA ACAGTTTGCA GGTTGGGGTT GGTTTCCGGG ATTTCAGATT TTTAAACGGA 1140 CACACCGACA CTCTGGAAGT GGTCTTCGAG GACCGCATGC TCCCTCTTGT GGATGACAAC 1200 AGTTCCCAAC GCCAAACAAA CAAGAAAACC ACAACCCAGT AACTCTCCCT GCAAATACAG 1260 GCTTCTTTTT ATCAGGATTC CTGCTGGATT TCTTTGCAAC GGAATTTTTG CAACTGGCTG 1320 TCATTAGGCA AAATCTTTAA ATTCAGTGTT TTCTGGAAAG CTGGGTTGGG AGTGTTCCTC 1380 AATCTTAGAC TAGGTCTATG AGAAACAAAT TCACCGTCCA AACCCAAAGA ATGGACTCAG 1440 AGACCCGGAG AACAGCAAAA GTGAGAGTTT AACGACGATC TTGCAAGATC GGTTGTCTGA 1500 TGAGCGGGCA CACCCAGCAC ACTTTGAACA ACCGATTTAT CCCGTGGTGC GCAGGTCCCT 1560 CCCCGGGTTC CTCACAGGGT GAGTACTATG GGGTCACAAC CTTCCCGGAT GTCGCCTATT 1620 GATTGTTGGT TAGAGGCTTT AGGTGTTTCT TTAGGGTTGT CTTGCTGCAT 1670
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