Tag | Content |
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EnhancerAtlas ID | HS102-11207 | Organism | Homo sapiens | Tissue/cell | HuCCT1 | Coordinate | chr18:47685150-47686600 | 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 |
GH18I050157 | chr18 | 47683898 | 47689095 |
| Enhancer Sequence | GAGCCGGTGT TCTCTGAGGC AGGAGCTACA GTTATCAACC TCCTGGCACA TTGTGGAAAG 60 CTGTTGAGCA TCTGATGATG GGGTAAGAAT GATAATGTGT ATGGATTACC ATGAAGTCCT 120 CTAGATTAAA CATGAATCTA CGCCTGTGCT ACCCTACACC ACGATGTTTG CCGTTATCAT 180 TATTAATGGA CACTTCCAAA TGAGAGCAGG CTGCACAAAG CCCTGCAAAT TCTACAGCTC 240 CTTTCATGCA TGAAGACTAA CAACCATGAG AGACAAAGGT TTAAACTCGT TATCCTGGGG 300 AGACTCCCAG AGAAGTCAAA CAGGTTTGTC CAGAGCTGTC AATCACTTCT GAAAATAAAC 360 AGACCTAGTT GAGAAGGTGC ACAGCCAGCC TCAAAGGTTA ACCAAACCCA CAGTTAACCC 420 AGGGAAGATC TCCTGACTCC TAAGAAATCA TGCAAAGGTT GAAGCAACTG ATTTACGCCC 480 CCGCCAACTG CCACCCCTCT GCCATCAAAG AAAATATGCT TTCCTCTACT TTCTAACTCT 540 GATATTTGAT TATTTCAACC CCTGCAGAAA ATCTCTCAGA TACCAATCCC CTGGCATGTT 600 CAAGGAGCTT TCACATGTTT ATTACCTTCT TCAACCCTCA CACCCATCTT TCCCAGGCTG 660 GGCCTAAATA TACAACCCAG GAAACTCAAG CTGAGAGACG TTAGTGACAT TCAGTCACCC 720 ACGGGAGAGC AGTCAACTAA AGCTCCCAGC TCCAGGTGCT CTGCAGCCCC CAGGCCACCG 780 TGCTTCTCAT GCTCACAGTG GCTTTCTCTG CCCACATCAT GTCAAATCCC AAATCCTCCC 840 CCACAGACTT GTCTCCCAAC TGTCCCAAAA GGAATCTTCT ATTCTAAGAA AAAGTCCCTT 900 TGCCATCCCG CACCTCCAGG CCTCTATGAT GCCCCACGCC GCCAGCAACC AGCTCCCCTC 960 TCTCCCAGTG TTTGTTACTC AAGGTCTTCA CGTTCCACTG TTTAGTCTCC TCCTGCATCC 1020 TCCCCAGCAC CCCCACGCCA CTGATATCAT GCTGCACATT CCGTGTGGCA CTGCCTGTGC 1080 TGCTGCTGCC CTATCCAAGA CTGAGCTTCA GATGGCAGGA ACCCTGCTGC CCAACCCTCA 1140 CCCTCCCTTG CAGAACAGGC ACAGGCACAC AGACGCTCCA CATGAACAAC GTAGCAACAC 1200 TGGATCCTGG AGAGTCACAA GTTGGACAGT ACTCACGCAG ACGTGATGGC ATGGCCAGGG 1260 GTGCAAATGG CTCCCCTCTG TCCATGGGAC CACATGCTAA CACGCACAAC GTACCACAGT 1320 CAACACTTCC CAGCGGATGA TAAAACACCA AGCAAGAATA TCCACCGTAA GCATGGAAGC 1380 AGAAACAACG GGGCTGCCCG GGTGCACCTA TGACCCTAAC GTAGGGTCAG TGAGGGTAGC 1440 TGCTCTCTCG 1450
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