Tag | Content |
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EnhancerAtlas ID | HS026-01749 | Organism | Homo sapiens | Tissue/cell | CNCC | Coordinate | chr1:92076830-92078090 | SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 92077041 | 92077526 | chr1 | 92077685 | 92077999 |
| | Number: 1 | ID | Chromosome | Start | End |
GH01I091608 | chr1 | 92074061 | 92078134 |
| Enhancer Sequence | TATTCCATGC ATCGCAAAGT CAAATTTAAC ATTTTGCTTT TTTCTATTAT ATATAATAAA 60 CTTATTTGCT CACTTCTAAC ATTTGTCATT TTCAGCCTTC ATTTTACCAG CACAGACTCT 120 AGCTCTCGGT ATTTGGGCCT TAAGATCTTC ACAAACAAAC AAATCTTTCT GAAATAGAAA 180 AAAAAAAAAA CAGACCCAAA AATCTAACAC TATAGTGACC TCCTACTAGG CTTTAAGTTT 240 AAACGGATTA GGGCAGGAAG TTTTACGTTC CTGTCGTATT TGCTGAAGGT GTATGGCAGG 300 GTGCGGCGCC TGTTGCAGGA TTCCAGCAGG GCCTGCCCTG GCTCCCCAGG GCTTTGCAAG 360 GAAGCTGGAG AAGTCCGCCA CCTCGCTGTC ACTGCACATC AGTAGACCCC TATCCCCACC 420 CGCAAACTCA GGGCACCCAC AGTCTCTCCA AGGACTGCAG TTTTGTCGCC AGATTGTGGG 480 AACATCTGTC TTGAATCTAA AGAGACAAAA CAGATGGGCT TGGTTTCGGA GTTCCGCCCA 540 CTCCCCAGTG TGCTGTTGTT AGTGACCACA GGAGTGGGAG CAGTCCAGAG AGGTTCAGCC 600 CAGGAACTCA TTAAACTAAG CTCCTCCGAA AGGCACCTTC CAGTGTGGAT GGGGGCAAGG 660 AGGGAGGAGG GCAACTGGGG CCCAGCAGAA CTCCTTCCTC CCAGAGCCCT TACAAAGGCA 720 AGGGAGGTCG GCCTGGGCCA AGCTCCCCGC CCACCCTCCC AGCTTTGCAC CCCCTTCTCA 780 GCCAGACCCA CTGCCCTCTC ACAATGCAGA AATGAAGATG GAAGGAAACA GGGAACATGC 840 AACCGCCAGA CTCCCTCTGG AGCCCAAGTA ACTGTTCCAC AGTGTGCATA AAGGGGCCAA 900 GCTGGTGCTC CTCCGGCTTG ATGGAGTTGG TCAGTAGAAA CTAGGATGTC CCAACCTTGT 960 GATCCGTGGT CCATGCAGCA CATTGTAGAG ACATTGGTTG ACTTTTCCAT GAGTTAAACC 1020 CTGTCTGGGG ATGGCATCCC AGACCCAGTC CGGAATGAAG GACATGACTG AGTAATAAGG 1080 GGACTGTGTG CTTAACAGAA GACATGACTG AGTAATAAGG GGGCTGTGTG GTTAATAGAA 1140 GCCCTGTGTT GCCGAATCAG GCTCACACTG GAGCCATGCA GCACCTCACA AGGGGAGCTG 1200 AACTCCGACA AGCACCACCG CCCTGATGTG CAACTGTGTT GAACAGCCTG GCCTAGAGCA 1260
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