| Tag | Content |
|---|
EnhancerAtlas ID | HS060-08664 | Organism | Homo sapiens | Tissue/cell | GM12891 | Coordinate | chr12:111493960-111495450 | | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr12 | 111494792 | 111495250 | | chr12 | 111494325 | 111494437 | | chr12 | 111494439 | 111495312 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH12I111055 | chr12 | 111493558 | 111496432 |
| Enhancer Sequence | TTGGATGGAT CTGTCAGGGA AGGAGGATGC TAGAGACGAG GACTGTTCTT AACATGTGTG 60
ACTGCATGTG TCTCTGTAAA CGCAGCAGTC ATTTGTTGCT GGGTAGCAAG CCACCCCAAA 120
CTTAGTGGAC AGAAACAACT CTTGTATACC TGATTCTGTG GGCTGGAATT AGGACGGAGC 180
CCAGTTGGTT CAGCTTGTCC CCACTCCATG ATAGCTGTGG CTTCATCTGG GCAGATTCAA 240
CATTTGCGGG TAATTTGACA ACTCCCACAT CTGGCAATTG ATGCTGGCTG TTGGCTGGAA 300
CCTCAGCTAC CTGTGGGAAC CCCAGTTTAT GGCCTCTCTG CAGGGTCTCT CTGTGTGTTC 360
TCCTTTGGGC TTCCTCACAG CATGGTGGCT GGGTTCCGAG AGGCAACATC CTGAGAGAGC 420
CAGGTGGAAG TGCAGGTGTT TTCATGCTCT TGCCTTGCAA GTTGCTAGTA TCACTTCCAT 480
CTACTCTGCT GATTGGGGCA GTAACAAAGG TGGGCCCAGG TTCAAAGGGA GGAGGACGTA 540
GATCCCACCA CTGGGTGGAA GGAGTGTCAA GGTCACCTTG CAGGAAGCCT TGGTGGCGAG 600
GGATATTATG GCAGCCATCT TTAGAAAAGA CAGTTGGCTA CAGTGAGGGC GATGGTGGTG 660
GTGATTCAGG TGACTCAGGC TGGTTGTGAC AGGCTGTAAA GGGAGCCAGT GCGGCAGGAA 720
GTGGCTGAGC AGGAGAGTAG ATGTGACAGG AGGTTGTGTG AGGTGAGTTG GTGTGACAGG 780
AAGTAGCCAA GTAGGGAGTG GGTGTGACAG GAGGATGTGT GGGGGACAGA GTGTAACAAG 840
CGGTGGCCAA GCTGGAATGG TTGTGACAAG AGGTTGTGTG AGGGAATTCA GTGTGACAGG 900
AGATTGTGTG GGGGAGTGTG ACAGGAAGTG GCCAAGTAGG GAGTGAGTGT GACAGAAAAT 960
GGCCAAGCTG CAATGGTTGT GACGGGAGGT TGTGTGACGA GAGTGAGTAT GACAGGAAAT 1020
GGCCTGAGCT GCAGTGGGTG TGATAGGAAG TGGCCCAGTA GCAAGTAAGT GTGACAAGAA 1080
ATTGTGTGGG GGAGTCAGTA TGACAGGAAG TTACCAAGCT GGAGTGGATG TTACAGGAAG 1140
CTGTGTGAGG GCAATGGGTG TGGCAGGAGA TTATGTGAGG GAAGTTAGTG GGACAGAGAC 1200
GGCTATGTGA GTGGAGTGGA GTGGGTGTGA CAGGAAGTGG CCACTGGAGA TCTGGCTTTG 1260
TCTGCCATGA TGGAAGTGGG CCTGCCAGTG ACAGGGCCCT AGATGCTGAC AGCACCACCT 1320
TTCCTTGCTT TCCAAGCTGC CCTCTTGAGG GCCTCAGGGT GACCAGGCCG ATTCCAACGT 1380
GGGGACCCAG ACCTCCTTAC ACGGGCCCCA TCTTTCTCCC TGCCCTAGCC TCCACCATCT 1440
TCCTGTCTTC CTGTGGGCCC CTCGCTCCCC ACTTCTGCCA GCAGCCTCCC 1490
|
| |
|
|
|
