| Tag | Content |
|---|
EnhancerAtlas ID | HS053-04049 | Organism | Homo sapiens | Tissue/cell | Foreskin_keratinocyte | Coordinate | chr1:233742660-233744080 | | | 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 |
| GH01I233607 | chr1 | 233743341 | 233743490 |
| Enhancer Sequence | AATAATAATA ATAATAACAC TAGGAGGTGC ATGTTAGGGA CCTAGTGAAT AACAACACTA 60
GGAGGTGCAT GTTAGGGACC CAGTGACTCA AACAGAGAGC ATGTGTAGCA TGAATTCAGA 120
TGGAGGAGAG ATGGGTTTTT GCATGTTTAC GTAGTTAAAG GAGGTTACCT GAAGGGCCAA 180
TTCGAATGGG ATCTTGAAGT AACGGAAAGT TCCAGTGAAA GTGGCACTGA AGAGGGAAGG 240
AACAGAACTG TTCTAGGATC TAAGGGAGTT GCTAATGTAG CAAACTCAAA ACTGTATGGA 300
GTGAATGTTT GCAGATCTCA TTCAGGCACT AGAATTCAGC AGGAGGAAGT GGTGAATCCC 360
AGTGTCCCCA GATCTGAAAA ATTTTTTTCT GAATATGCAG GTTCCTGAAA AGATAAAAAG 420
CTGACCTTCA GCATCAAACT ACCCTCTGCT GGCAAGCTTC CTGATGCCAC ACAGTGCCCT 480
GTGTTTGTGC TGCTGACACG TGTCACATGC AAATACAGTG GTTTATGAAG TGTATTGCCC 540
AGTGTTGTCA AAGAGCTTAC AGCTCAGGTG CTGTTCATCC AGGTGTCAGC CCAGTGCCCA 600
TAAGACTCAG TGCACAGATA ATAACTGGCA GCCAGGGCTA GACTGCTCCA GGAGGCAAAA 660
AAGATCATCC ATCTTTTGTG TTCTTTCTCT TTTTCAGCAT CAAGGCCACC GCCCCCGATA 720
TAGTCATGGT CTGAAATCGT GGGAGCAAAC AAGTGTGGGC GAGCCCATTC CAAGCGCTGA 780
CACATAGGGC CTGTTTGGGA GAAAGCAATG AGGCAGCTGA GTGAATATTG AGATGACCAT 840
CTCACTTCAG CACGGGAGTA CTCTGAGGAC AGGGAGGGTG GGAGAGTGCA TGGCTGGGCT 900
GGGGACACCT TCCAAATATG CATGACAGGA CAGAGCAGTG GATGGCATTG GAATACCCTC 960
AGCTCCTCCC CCTGTCATTT GATCTGTTTC TCATCCATCT TTCTTCACTT GCTTCTAGGA 1020
CAGCCCTTTC TTCTTTTCCT TCCTCTCCTT ACCTCTCATA CCCATGGAGT ATGTGTTGAA 1080
TGAGACATGA GCAGGGACCA ATTATGATTT AACACTCACA GGCAAAGTGT GATTGGAGGG 1140
CATGGGTAAG AGACAGTGAT GAAGGCAGGA AAATGATAAG CATCACTCAG GCCACCGGTG 1200
GTCAGGCCAC CATGGGCCTG TGTGGGCAGG AAGAGGATAT GAAGGGGCAT CATCTGTCAC 1260
TGCTGCCTCC TGGCAGGCCC TGTCTGGAGG CTGAGCCCTG ATCTGCACAC CTCAGAGCAT 1320
AGCCACCTTA CCACAATAAG AGGAGTTGGC AACACCCTCA GCCAAAGGTA ACAGAGAAGC 1380
TGAGCGCCTG CTCCGTCTGT ATTCCCTGAC AACTGGACGT 1420
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