Tag | Content |
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EnhancerAtlas ID | HS024-10699 |
Organism | Homo sapiens |
Tissue/cell | Cerebellum |
Coordinate | chr21:37621800-37623450 |
Target genes | Number: 10 | Name | Ensembl ID |
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SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH21I036250 | chr21 | 37623021 | 37623170 |
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Enhancer Sequence | TTGAGTCTCT AAAGCATTTC TGCGAGACAG CTCATCTCTG TTCTGCTTTT AGCGGTGCCT 60 GTCAAACATG GCCCCATCAG AGTGGAATGT CAGGGTGCCT TTGAGTTCTT AAACCAAAAA 120 CGCACAACTG TGAATATTTA TATTATAGTT TAGTCTTTGG TTTTCAGTGT CTGCCTCAGA 180 AGGCTGTAGG CGCAGGACTC GGTCGCTCAC CATCTGTGTT ACTGTGTGTG GCATCTCAGA 240 ATTATCTGCC ACATCTGACA TCAGTTGAGA GCCCCCAGGT GCCAGATGTG GCCGCAGGGA 300 TGAGCCTTGC CATCCTGCAT TTAGGTACCA CGGTGCGTTG TTGGCCTCCA GACATTCTGT 360 CGGTTCCTAG GGTGCCAAGG GAATTCTGTA TTTCAAGCTC CTATAAGAAC CTGCTCTTAA 420 AAAGATTCAG AAAACCTTTT TTCTCACTCA GAAAAAAAGA TTTTCTAAAC CTTTTTTAGG 480 GGAGCTTCCT GTAGCACTCA GCCTCTCTGA GCCTCCATTT CCTCGTCTGT TAAACCAGGC 540 TGTGGCTAGC ATCCTGTCCT CATGGGTTGA GGGAAAGAGT AATTACGATA AAGGCCGATG 600 CTCATTAGGC ACTTAACTCC TAGCCCTCCC TGAGGAACCC AGGGCCGGGG AGCGGGACCC 660 CACATTAGTC CCTCTAGAGC AGAAGCCATG GTGGAAAAGA GGGGACAGCT CCATTGCTGG 720 CTCAGTTGTA TCTAATGTGA AATAAACATG GGCGGTTGTC ACAGGAAGCG CTGGGTAAAT 780 CCGTCTCTTC GACAGACATT TTGTGCCTGC TGCCACGCAC CAGGCTCTCT TGCTTTACCG 840 GTGGACAAGA GAGATGAAGT CCCTGCCCCT GTGGCAGAGG CAGACATTAA CTGGCAGTGT 900 AATAACGATG TGAGCAGGGC TTCAAAGAAA CACAGGGTTT CCTGAGAGTG TGTGAACAGG 960 AGGCCTGGCC TGACCTGGGG TTCCTGAGGC GGCATGGCTT AGCTGAGGCC CCAGGCGGAG 1020 AGGATTTAAC TACGGTGGGC ACTGCAGGCT GAGAGAGCGG TAGGATTTAC AGAGCGAGAA 1080 ACGTGGCGGG AACACAGAGA AATTCATAAG TAGCAAAACA GAGGGTGCTG AGTGACATCA 1140 GGACCATGTT ACAGGTTTAA ATTGATTACC TGATAAAATT AGTTAAATGG TGCTTATTTC 1200 TGGAAATTGA GCAACAACTT TCCTAATGAA TATAAGCCCT TCCGCAGCAG ATGGAGTCAG 1260 GCTGAGGCTG TGGGGTTTCC AGATGGAAGC AGTGCTGCAA AGCCTTGCCC GGCTTCCTGC 1320 AAGACCCCCA CTGTGCTCAC AGCAGCAAGG GTGATATTCA TCGTCTCCCG AGATGCTCCT 1380 GGCCAATCGA GCTGGCCATC CGTCTCTCCA CCTTGGCTGC TCACTGCCCC TTCCCCCCGC 1440 CGGCATGACA CGCCAACATC ACACATCTAG CTCCTTGCGG AAAGGGTTTG ATTCCTCCCA 1500 TTGCTGGGAT CCACCCATCA GGGAAGCACC TCAGCACAAC ATTGGGCACA AACATGACAG 1560 GGTCCTTGCT CTCGGTATGG ACAGCAGTGG TGGTTCAATG TATATGATGC CATAGCCCCA 1620 ATATTACTCT GCAGTAACTT TTTTTTCCCT 1650
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