| Tag | Content |
|---|
EnhancerAtlas ID | HS053-29232 | Organism | Homo sapiens | Tissue/cell | Foreskin_keratinocyte | Coordinate | chr4:17068660-17070480 | 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 |
| GH04I017065 | chr4 | 17066956 | 17069852 |
| Enhancer Sequence | CTCATAATAT AAAAAGATTC TGATTCTATT CCCTATTCCT ATCCAGGCAG AGTTACCAGC 60
TACAGTGATG CAGTTTATTC ACTGCCAAAA TATGCCTGCC TTAGGGAGTG AGTCAGGGCC 120
AAAATCCCTC ACTGCATGCG AGTCATGACT CAGGCTGACA TTTACCTAGA GGAGAGAAGG 180
ATCACATTTC ACTGTTATTC GTCCAGAAAA GTTCCTTTTT CCTAATTTAC AAAAAGGCTG 240
ATGCCTGGCC CAAATTTAAG GTCCCACTGA GAACGGAGAC TTGGCCAAGA TGCCATCCAG 300
TTTACTGTGC TCCCCACAGC CTGTCTAGCT CTCTCTTGCC AACCAGGATC CTCTTCCCCA 360
AAGTTCCACG GATGGAGCTC TAGTTCCTTG ACTTCTAGTT GATCTTCTGC TCGGAATAGA 420
CTGATTATCC CAAAGCTATC CAGGTACCTG TAGTCTCTGC TACACTCTCA GAGCATTTAC 480
ACCAAAAATA GGCAGTTCCA ACGTGTCTTT GGTATAGGAT TTGCTAAGTC GTGAGTGATG 540
TACATTTGAA GTAGTCCCTG GCTCAGAGTG CCTAGATATG GAACTTTCTG TCAGATATTG 600
ACAACCTGAG ATGATTTGAG GGCAAGGGAT GGGTGGGGAA CTGGTTGCTA CAGGTGTGAA 660
AGCATTAACT CTGGTCTCAC TTTGTCCACC ACTTCCTGAG TTTGGAAACT GAAAGCATGG 720
CCATTTAGAA CCTCTGTTCC CTGGAAGCTA AGAGCCAGAT CATAATTCTT CATAGAAGGC 780
TGATGAGGCT TCCCAGTACC CTCTTCATTA AGCTCCTCTG TCTCCCTACC TCCCTCATTC 840
CCTACCCTTA GTCCCAACAC CAAACCATAT TTCCACAGCC CCACTCAGGC AATCTGAACC 900
CTTTCTGGCT AATTCCAAAA TTGCCAGGAG ATTTGTTTCT GATAAAAGAA ACTCACTCTC 960
TGATGTTGCT TCTAGGTGCC TTTTCTTAAT AAATAGGCAA GATCATGACA TGCATCTTAG 1020
CCACATAAGA AATTAGTAGA AAATGAACAA AATCAAAACA GCACGGGCTT CAGGGTCAGA 1080
CAGAACTGAG TTCAGTGCTA GAATAGCTAA TTATTAGCTG TGTGTCCTTG AACAAGTTAC 1140
TTCACATCTC TGAGTCTCAA TTTCAAAACA TGTAATATTG AGGGTACCAA TAATTATCTC 1200
CAAGTGTTGT CATGAAGATG AAAGTAGGGT CCCCTACAAA AAGTGCCCCA TGTAGTTGCT 1260
GGCAAAGAAG AAGTACTGGA TGAAGCACTT GGAGGAATTG GAAAGACTAC CTCTGCCTGG 1320
CTTGTTTCCT TATCCAAAAG GAGCCCACAG AGCAGCTGAT TCCAGAGAGA ATTCACTGAT 1380
GAATTTGTAC GCTGACTTCC CCCATCTGAT AGTATGCAAC AAAGGAATAA TACTTATGTA 1440
GATATGTGTT TGAAGCACCA TTTGCCATCA ACATGAACAT AAAGAACCTA TTAGACTCTA 1500
AATACCTCAT GTAAGCTAAA TTACTCATCT GCACACTGTG GCAAAGACTT GCCTTGGAAT 1560
TAGGCACTCA ACTTCTAAGT CTGGCTCTGC CTGTCATCAA TCATGTGTCC TCGGATCAGT 1620
CACACCCTTG CAAAATCACA ACTTTGCAAA CAAATGTTTG CAAGAAACAG ATAAAATCAT 1680
TGATGTGGGA TACAACATAG AGAAGAGGCT CAATATATTA GAATTCTCTA CAGTTTTTTT 1740
GTAGATCAAT AGTGCCAAAT TTACAAACTG TGAGATGACA CCAACTGTAC CCTGAACTGT 1800
TATTTCAAAT CCTTTATTCT 1820
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