| Tag | Content |
|---|
EnhancerAtlas ID | HS003-30792 | Organism | Homo sapiens | Tissue/cell | A549 | Coordinate | chr22:19691080-19692430 | SNPs | | Number: 2 | 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 |
| GH22I019704 | chr22 | 19691577 | 19692323 |
| Enhancer Sequence | TTATGATTAA TTATTATTAT TATTATTTTT TGAGACAGAG TCTTGCTCTG TCCCCCAGGC 60
TGGAGTGCAA TGGCGCAATC TCGGCTCACT GCAACCTCCA CCTCCTGGGT TCAAGTGATT 120
CTCCTGCCTC AGCCTCCCCA GTGGCTGGGA TTACAGGTGT GCGCCACAAC GCCTAGCTAA 180
TTTTTGTATT TTTAGTAGAG ATGGGGTTTC ACCATGATGG CCAGGCTGAT CTCAAACTCC 240
TGACCTCAAG TGATCCACCT GCCTCGGCCT CCAAAAGTGT TGGGATTATA GGTGTGAGCC 300
ACTGCGCCCG ACTGATTAAT TTTTAAAAAT CACAGTGGGT AGCTAGTATT TGTGGAGCCC 360
CTTCTCTGAG GCCCCGTGGT CCCATCTGGA CCTCGCTGCA CTGGGGAGCC ACCTTCCACT 420
GTTGTCCCAC TGTACGGATG AGGAGCCCAA GCTCTGGTCC AGGTGTGAGC AAGTGACAAG 480
GAGCCAAGGA GCCCTTCCCT TCACAGGTGC TTCCCTGCAG GTGGGGTGGC CAGGTGTCCT 540
CAGACCGGGT GGCTCTCCCT CAGGGACCGG GGTGGGGCAG GAAGGAGGAA GGAGTTGTTG 600
CGCATTCGGC ACAACCCATG CCTGCTCTGC TGCCAGCCGC GTGGAAGCTT GATTGCCATA 660
CAGCACAGAC TGCTGCCTTT CTATGTTGCT GACTGTTTTT AAAGAGGGGT TTTGGGAGGG 720
GTGGTATGAA ATTGATTGTT TCTCTCTTTC CTCATTACTG TTCGCACCTA TTTTGGGTGT 780
TTTGTTTTTC CCTGTGCTTC CTGTCCTCTG TGCACTAGGG AAGCCTCTCA AATGGCAACA 840
GAAAGTGGTT GGTTTCTTTG AAGAGCATTT GAACTGAGTG AATTTTCAAA AAGCGTGGCA 900
TTGACAGAAC AATGAAAGTC CCAGGATAAA GTCCAGGCCA GTTGCCATGA CAGACGGCAT 960
CTGTTGTTGA CAGAAACATG GAGCCAGGCT GAAACTCCGG CGGCAGGAGG GCTGCGCACC 1020
TGGGCAGGGC AGTGCCGAGC ACAGCTCCCA GTTTGGGTAG CCAGTGGGAC TGGGTCTGGT 1080
ACCAGCCTTG ATTTCGGACT GGAGCAGAGT CACCCAGTTG TGCCTCTGTT TTGTTTTCTG 1140
TGGAGCAGTG GGGGGCCCAC CACACCCCTC CTCGTGGCTT CATTAGCCTC TTCTTGCCTG 1200
AACCAGGGAT AATGGTGAGG TGATGCCAAG GAACATGGTG GATGCAGCTC TGCCTCCAGA 1260
GTCAGCCAGC AGCAAGAACG AGCCATGCAC CATCACTGCT GCAGTGACCG GACTGCACCC 1320
CGCAGAGCTC TGATCGCCTC TCTGGGGGCT 1350
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