| Tag | Content |
|---|
EnhancerAtlas ID | HS184-19168 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr22:19679020-19679940 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr22 | 19679200 | 19679849 | | chr22 | 19679104 | 19679921 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH22I019691 | chr22 | 19678730 | 19680090 |
| Enhancer Sequence | TTTGGAAATT ATCCGAAAGG TAAAAATAAA AACAGAAGCA AGTAATATGC CTTGTTACTG 60
CTCCTTAATT AGGTAAGAGC CTCATTTCTT GGGCTGCTGG GATGTAAATT CTGCATAAAA 120
TGGCTGGCTT TCTTTTTAAG GCTTTGCAGC AGTGTTAACA TTCGGCTGCC AACTAAGTCG 180
ATTTTAATCG CCTTTACAGG AACCTTCACT TTTTCTGTTT GTTCCATTCC ACTCTTTCCT 240
CAGTGGATAA TCCCGCATGT TAAGATTCCT GTGCAGCCGA GGGAGGCGGC TTTTGGCCGG 300
GAGCTTGTGC TCTGGGTGTG AGCGTGGCTG TTGGGAACGC CTTCTGCTCA GAATTCCGTG 360
GTCTCAGCAG ATCGTTCAGT CTAGCCACTG GGACGGGGCC GACCGCACAC TGCTGGACCT 420
CTGAGCGGAA GATGTGTGAG GTTAGGAGGG AAGGAATAAA CAAAGTCGCC TTCTTCCCTG 480
CTGACCTGCC TTGGTATGTC ACCATTACTC AGCTCCTTAC AGAACAGGAG CTTCAAGCTT 540
TCACCGGACA GGCTGGCTTC TTCCCGGGAG CCCCCGCCCA AGGTGGGGCC TGGTGGGGTG 600
GGGCCACCAT CGCTGCTGGA AGCTTTAGCT CTTTTCCCTC AGCTTGGCCT CCTTTGGCAA 660
CTAATTTTTT AACTTTTTCT AATAGGTAAC AGAGTCCCAA GATTCCAAGT TCCAGGAGCA 720
TGAAAGGACT CACTTGTGGA GATTCCTGCC TGGGGCTCCC ACCCACCTAA GGAATGCCAT 780
CCTTGTCACC GGCTCACGGG GCAGCTCTTT GGTATCCTTC CAGGGTGGTG TGTACAAGTA 840
CAGGCACATG GATGCATGGA TGCATGAGCA TTTTTTTCTT TTGCCGACAT ATTAATACAC 900
CCGGCAGCAC TCTAGGCCCA 920
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