| Tag | Content |
|---|
EnhancerAtlas ID | HS037-21118 | Organism | Homo sapiens | Tissue/cell | ESC | Coordinate | chr2:175594150-175595800 | 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 |
| GH02I174729 | chr2 | 175594641 | 175595128 |
| Enhancer Sequence | GTCGGTGATA TGCCGGGGAC ACCCGAGTCC CAGCCAGGAA GTGCCCAGGG AGGAATGAAC 60
CAGACCTATG GGAAGGAACA AGTGAGTCCT GCCAATGCAA CCCCTGTCCT CCCTTTAAAA 120
AAAAATGACA ATTAAGCTTA ATGAAGGTAT TTGCAATTGA ACCATGGATC TAAAAAGGTA 180
AAAGTGGGGG AAAGTTAAGA GTTTCTAATT ATAAGCATCA TCTTCCTGAA ACTCTCACTT 240
TTACCCTTAA TTCAGAAAAG ACACGTGGCT CTTAACCTCC TATGTACTTG TGTTGCAGGT 300
GGTGTCTTTG GTGGCTGTTC ACCCTTCCAC AGTAAACATG CTTGGGAAGC AACTTTGCCA 360
AAAGCCTTCG GACAGTCCAG CGTCAACACC GCAAGCCAAG TGGTAAGGCC CGCGGGGACA 420
GAACCGTCGG ACCCTGGTGG CGAATCTGGG ATGGATGAAT TCGTTGCTGT TGCGGCGGGC 480
GGTGTTGGCA GGAGCGCTAG ATTTGCTCGG GTTGGAGTGT GAGATGTTCC CTTCCGCCGA 540
AGGAGCCCAT GCAGACAGGG CTAGATGTAC CTTCTGCAGC TTCTGCAGCG ACTTGAGGCG 600
CGTCGCTGCT AGAGGGTCCT GGTGCCCTCG GCGTGCGTGA GGTGCTGTGT GTCCCTCCCC 660
ACCCCCCGTA CAATCCTCCC CGTAACTGGG CAGTGGAATC GGTGGGCACT GGAAGGACCC 720
GACGCAGGTG ATGGGATGCA GCGCTTCCAG GTGGTGACCC CGGCTGGACG TGCGTGGGTG 780
CGAACTGCCA CCCGGGCTGG GGCCAGCTTG CTGCGCCGCT GCCTCCGCAA GCCCTCCCAG 840
CCCGGAGCTG AGTCTGACGA GGATTTCTTA CGCGTTCAAG CGAGTGTGGA GCGGCGAGGC 900
AGTGCACTTG CCCCATAGCT CCCGCGCTGG GAAACCCGGA GGGGAGGGGC TGTGGAGGGC 960
GGGAGCCCCG GGCAGTAGGT CTGTGCTTCT TCCTTGGTCC CATTACACGG GAAGGGCAAG 1020
GTGACGCCAC TCAGCCACGC AGGCCTCGCA TTGGTGCCTT CCCTTCCCTA GCCAGGACGC 1080
GGCTATTAAA CGCTGCTTTT AGCCGATTGT ATTTCCTGTC TTTGAATCCG TTTTCTTTCT 1140
CCTCTCTGGT TGGTTGGTTC TAGCTCTAAG CCCATCAAAG ACTTTAAGGA TCCTACACAG 1200
AGTGCTGCAG GCTCCCTTTG TCAGAATTGG GGCCCCTAGG AGCTGAGTGC GGCAGGTTTC 1260
GCCTGTTCCT GGAGCTCGTA GTCAGGGTCG CTAGTGCACT GCCACTCTGA GGACTGGACG 1320
GAGTTCCAGA CCTGCCTCCG GGGACCTCCT GCGTGAGGGC GGAGGCCCTT TCATGACCGT 1380
GAGATGCTCC GGGCCTTCCT GGTCAGCATG AGCTGCAGCC TCCACGCTGG GGCCTCCTGC 1440
CAAGTCCCGG GCTTTGGTGA CTTAAGTGCC TTTTGCAGTC TCACCACCCA GGGAAAATTT 1500
ATAGCGGTGT GGATTGAATT TTTGTTTTAA GTCTGATTGT GTTCTTTAAT CTTGCTAAGG 1560
GAATCGCTAA GGGTAGCCAT TAAATTATTT TGTGTCGTTT AATTTGATTT TCCCATAGGT 1620
ACCCAATAGG ACAGCTTAGG ATGAGAGCAC 1650
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