| Tag | Content |
|---|
EnhancerAtlas ID | HS184-02663 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr1:223871140-223872340 | 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 |
| GH01I223684 | chr1 | 223872021 | 223872150 |
| Enhancer Sequence | AAAATGTTTG CGACTACAAC TTAAACCAAG ACAACCTAAG GATTTCGAGA AGCAGTAAGA 60
GTATCCAGAG AAAATAGTAA CTTAGATGCA GCCAATACAA GCTCAAGACT GAGAGTCTGC 120
AAATCTAGAT TCCAGCCTCT GCTCTGCCAC ATTCTTGAGT GACCTGGAGA AGTCACTTTA 180
ACCCTGGGTC TTCCTGTGCT CATCTGACAC AGAGGGCATG GGAGCCTGGA GCCCAGCCCT 240
CCTGTGCACC CTGTCTAGCT ACACTTCTCT GGAGGCGAAA GGCTGCTGGG CATTGAACAC 300
AGCTATCAGC CTGGGAGCTG GGCCGAGCCT CACCAGGGAA TAGTGAGGGG CTCCCTGCTC 360
CGACAGCACA CAGGTGCACA CACACGCCTG CTCATCAGGT CCCCGGCTGA CCCCTTTACA 420
CACACCATCT CCTGCTTCTG CAACAATGCC GTGCAATAGC AACTATCACC AGCCACATTC 480
TACAGGTGAG AAAGCTGAGC TTCATCCACA GTTCCTCAGT AGCAGGAGTA GGATTGGAAC 540
CCAAGTGTGT TAGCTAAAAG CCCACACATT TATCCAAGAT ACCATATTGA CACTGTTTAA 600
AGTGACAAAC GATCACTTTA TGTAGAATGC ACCCAGGGAG TTGAACTGAT GGAGTCTGCA 660
TTCTTGTCAC AGAGTCCACT CTCCCCTCCA CATCTCCCCC TTAGCCCCAA CACAGGACTG 720
CTGGGTTCCT CTGCTAGTCC CAGGTGAGAT ACTCTCTCAC CTTCCAGCAG CAGGTAACAA 780
GGACCAGGAG GCACCAGAGA CAAACCCAGC TCCTCACTGC AGCCAGCAAG GGAATATGGC 840
CTCTCAGAGC AGCTGGGATT CTAGCCAGCT GAAATTAAAC TGCGCAGCGA CAGCAGTCAG 900
AGGTAACTCA TGTTAAAGGT ATCAGTGATG GCTCCAGCAA CTGGTGGTCT CTGCTGCCCC 960
CTAGATGTCT GTTTCCTCCA ACAGGCCTCA GATTAATTTA AAACCAAGTG CTTGGTGTAA 1020
TATTGCATAG TAACACTCTT TTCCTGCTTC ATCAATCATG CATTTATCCT ACCTTTCCTG 1080
TGTGGACTGT AAGTAGTTGG CAAGGCAATG CTCTTCTTAA GAATTGCAGC AAATAGGAGA 1140
ACAAGTGATA GAGGAGTCAC CGTCTGGCAA CCCTTAATGA CATAATGAGT CTAGGTAGCC 1200
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