Tag | Content |
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EnhancerAtlas ID | HS102-09819 | Organism | Homo sapiens | Tissue/cell | HuCCT1 | Coordinate | chr17:16185400-16186890 | 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 |
chr17 | 16186785 | 16186836 | chr17 | 16185602 | 16186232 |
| | Number: 1 | ID | Chromosome | Start | End |
GH17I016280 | chr17 | 16184313 | 16186737 |
| Enhancer Sequence | TTTCGAGAAT AATTCACCCT ACAGAAGCTA TCTGAGCATC ACCAGACAGG GTCTTCCTGG 60 GAATTAGCAC ATATCCCAAA TTTCCTTCAG CTTTGCCTGC CCACAGTCCC CTGAAAGCCC 120 TCCCTTTTTC TGGGTGTGAG AGGAATGGCT GGGCATCCCT TGGCTTATCC TCCTTCTTGC 180 CCACCATAGC CAGCATCTCA GAGTGAACAT GCACGAGGGA GGTAGAAAGA CTCCATATCC 240 TTGTTCTTTA CAACTTAGAA AAGCCTAAGT TATAGGAGAG AGATAGCACA ATGGAATGCT 300 GAATTAGAGG TAAATAATTG GTCTGTTTTT TTTTCACCAG TCTAGTTACT ACTATTATGT 360 AAAATATCTA ATTTTACATA CCCTAAACAC CCATACCCAA ACACCTTGAC AAAGGAATCA 420 TTTTACCTCC CAAACATAGT CAGTGTTGAT TTCACAAAAT ATCCCTAGAA TTACTCTTTC 480 TGAGGCTAAC AGGACTACTT AGATGGTTCC TAAAGTCCCT TCTAACTCCT GCATTCTCTG 540 GTTAATGAAT CAGCATTAGT CATGTGGAAG GAAGGTATCC TCCTCAAACT CTTTTTAAGA 600 ATGATCTCAA GGAATCCAGA GTGCTCATTA AGTTGGTGAA AGAGTCAGTG CAGAATGCAG 660 CTCATACATA TATCCTGATG TGATGTTGGC ACCTCTCAAG AAGCTGGGAA AGATGTCCAG 720 GCTGGTCATA GGACTCAGCC CCTATTATGG GTCCAGCAGC CAGTAATAGT AAGCAATGTC 780 TACTTCAAAA GATATCTCTG GCCAGGTGCA GTGGCTCAAT CCCAGCACTT TGGGAAGCTG 840 AAGCGGGAGC ATCACTTGAG CCCAGGAGTA CAAGACCAGC CTGGGCAACA TGGCGAGACC 900 CCATGTCTAC CAAAAAAGAA TTTTTTTTTT TTTTTAGACA GATTCTCACT CTGTTGCCCA 960 GGTTGGAGTG CAATGGCATG ATCTTGGCTC ACTGCAACTT CTGCCTCCTG GGTTTAAGCG 1020 ATTCTCCTGC CTCAGCCTCC CGAGTAGCTG GGATTACAGT CACACATCAC CATGCCCAGC 1080 TAATTTTTGT ATTTTTAGTA GAGGTGGGAT TTCACCATGT TGGCCAGGAT GGTGTCTAAC 1140 TTCTGACCTC AGGTGATCTG CCAGTCTCAG CCTCCCAAAG TGCTGGGATT ACAGGCGTGA 1200 GCCACTGTGC CTGGCCAAAA CAATTGTTTT AATTAGCTGG CCGTGGTTGT GCATGCCTGT 1260 AGTCCCAGCT ACTCAAGAGG CTGAGGAAGG AGGATTGCCT GATCCTAGGA GGTTGAGGCT 1320 GCAGTGAGCT GTGTTTGCAC CACTGCACTC CAGCCTGGAT GACAGAGCAA GACCCTATTT 1380 CAAAAAAAAA AAGATATTTC TGAGGAGCCA TGCTCATTCA AGACTCACTG CTCTTAGAAG 1440 AGGTGTTAAT CTGGCCAGGT GCCGTGGCTC ACACCTGTAA TCTGAGCACT 1490
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