Tag | Content |
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EnhancerAtlas ID | HS146-00671 | Organism | Homo sapiens | Tissue/cell | NHDF | Coordinate | chr1:92076930-92078130 | 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 | ATTTTACCAG CACAGACTCT AGCTCTCGGT ATTTGGGCCT TAAGATCTTC ACAAACAAAC 60 AAATCTTTCT GAAATAGAAA AAAAAAAAAA CAGACCCAAA AATCTAACAC TATAGTGACC 120 TCCTACTAGG CTTTAAGTTT AAACGGATTA GGGCAGGAAG TTTTACGTTC CTGTCGTATT 180 TGCTGAAGGT GTATGGCAGG GTGCGGCGCC TGTTGCAGGA TTCCAGCAGG GCCTGCCCTG 240 GCTCCCCAGG GCTTTGCAAG GAAGCTGGAG AAGTCCGCCA CCTCGCTGTC ACTGCACATC 300 AGTAGACCCC TATCCCCACC CGCAAACTCA GGGCACCCAC AGTCTCTCCA AGGACTGCAG 360 TTTTGTCGCC AGATTGTGGG AACATCTGTC TTGAATCTAA AGAGACAAAA CAGATGGGCT 420 TGGTTTCGGA GTTCCGCCCA CTCCCCAGTG TGCTGTTGTT AGTGACCACA GGAGTGGGAG 480 CAGTCCAGAG AGGTTCAGCC CAGGAACTCA TTAAACTAAG CTCCTCCGAA AGGCACCTTC 540 CAGTGTGGAT GGGGGCAAGG AGGGAGGAGG GCAACTGGGG CCCAGCAGAA CTCCTTCCTC 600 CCAGAGCCCT TACAAAGGCA AGGGAGGTCG GCCTGGGCCA AGCTCCCCGC CCACCCTCCC 660 AGCTTTGCAC CCCCTTCTCA GCCAGACCCA CTGCCCTCTC ACAATGCAGA AATGAAGATG 720 GAAGGAAACA GGGAACATGC AACCGCCAGA CTCCCTCTGG AGCCCAAGTA ACTGTTCCAC 780 AGTGTGCATA AAGGGGCCAA GCTGGTGCTC CTCCGGCTTG ATGGAGTTGG TCAGTAGAAA 840 CTAGGATGTC CCAACCTTGT GATCCGTGGT CCATGCAGCA CATTGTAGAG ACATTGGTTG 900 ACTTTTCCAT GAGTTAAACC CTGTCTGGGG ATGGCATCCC AGACCCAGTC CGGAATGAAG 960 GACATGACTG AGTAATAAGG GGACTGTGTG CTTAACAGAA GACATGACTG AGTAATAAGG 1020 GGGCTGTGTG GTTAATAGAA GCCCTGTGTT GCCGAATCAG GCTCACACTG GAGCCATGCA 1080 GCACCTCACA AGGGGAGCTG AACTCCGACA AGCACCACCG CCCTGATGTG CAACTGTGTT 1140 GAACAGCCTG GCCTAGAGCA AAGTCACCAG GATCACCAAG TAAAGCTTCC CTTATTTGAA 1200
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