Tag | Content |
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EnhancerAtlas ID | HS048-19938 | Organism | Homo sapiens | Tissue/cell | Fetal_small_intestine | Coordinate | chr2:27204560-27205470 | 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 |
GH02I026981 | chr2 | 27204798 | 27205970 |
| Enhancer Sequence | CCTACCTTGA AAAGGTGCTG GGCCTCTAAG GAGCCTCCAC GTGTCAGCCA GTGGCTTCTG 60 TGGTCTCAGC TTGTCACAAA AGAGTGGCAC CCAGCCAGCA GCCCTCCTCC ACCTACACTC 120 CAGTAGTGTT CAAAATCCAA GGAGGCCCAT CTTCCCAGGC TTGACAGTCG ACTCTTAGAT 180 GTGCTGTTGC GTGAGTCTGG TGGTTTCCAA CTCTCTGAGC AGATCCCTAC TGAGCCATGC 240 CTCTCTGGCC TCTGTGAGTG AAGGTTCTTC CTCCAGACAG ATAGAGTCCC TTGCTAGGAA 300 TGCAGTTTTG TGAGTGGAGC TTGGGTTCTA CTCATTTTGT GAGGGTTCCA GCCCTCATCT 360 CCTCCACAAG GTGCTTTGTG CAGTGTACAA AGTGTACAAC TGTTTATAAC AGCCCTGTTT 420 CTCTCTTGCC TATTATGAAA CTTGGCCTAA AGTCCTTTCC TCCTCTGACC CCTCTCTTTC 480 TCATGTCCTC CTAGATCATT CACTTTGACT CTGACCCTGT CTAACACCCT GGGTTGTGGT 540 CTTTATTCCA CCTGCTGGAT TCACATTACT TTCATGCTGC ACAACTGAAG CCATTTACAC 600 AGCTCACCAT GCAAAGCAGC CACAGGGGCT GATAGCAGGG GACTTAACTA GGTGGGAATA 660 TGTGGAAAGT CAGGTGCAGG AGTCAACCTG TGGAAACGGA AAAGCTAGGG CTGCTTTCTT 720 TCCAGGGCCT TACACTGACA TTACCTTGCC TGGACATTTT GTAGTCCCGT TTCATGAAAG 780 CCAGGACCTA AGCAGAAGTA TGGCTCCCTG CCAGTCCCTA CCAGGAAGGA ACAAACAGCT 840 TGCAGTACAG GCCTCAAGCC AGGTGGGGCA GGAGCAAAAG TGCATTGTGT TGCCTGTGGA 900 ATTAAATGGA 910
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