Tag | Content |
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EnhancerAtlas ID | HS047-08617 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr12:112007200-112008760 |
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: 2 | Chromosome | Start | End |
chr12 | 112007759 | 112007843 | chr12 | 112007223 | 112007484 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I111569 | chr12 | 112007197 | 112009194 |
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Enhancer Sequence | TTATTTCCTC ATATTCCAGC ATACACTAGA GTAGTAAAGG AGAAAAAAAA GGCCAGTCGC 60 AGTGGCCCAC ACCTGCAATC CCAGCACTCT GGGAGGCCAA GGTGAGTCCA GGAATTTGAG 120 ACCAGCCTGG ACAACATGGC GAAATCTCGT CTCTACAGAA AGTTTTAAAA ATTAGGCAGG 180 TGTGGTGGCT CATGCCTACA GTTCCAGTTA CTTGGGAGCT GAGGTGGGAG GATCACTTAA 240 GCCCAGGAAG TCGAGGCTGC AGTGAGCCAG GATCATGCCA CTGGACTCCA GCCTGAGTGA 300 CAGAGCGAGA CCCTGTCTTA AAACACCACC ACCACCACCA CACTCTTCAT ATGAAGTTTT 360 ACCCCTTCAG TGCCTTTACC CCTTGAGTCC CTCTAGAGAA AGGGATAAAA GGCTTGGTCA 420 TGAAGCCATG AACAACTAGA TCCAACCTAG ACACACCAAA AAATCCAAAC AACTCAGGTA 480 GAAAAGGATC TTAGGGCTCT AGTCCCATGC TGTCCAAGAG AACTTTGTAC AATGATGAAG 540 ATGTCCTATG TCATGCTGTC CAATATTGCA GCCATTAGGC ACATGTGGCA GCTAAGCACT 600 TGAAATACGA TTAGTATGGC TGAGGAACTG AAATATTTAA ATTTTAATCA ACATAATTTT 660 AAATTTAAAG AACCATGTGT GGAAGTAGCC ACAATACTGG ACAGTGCCCA TTCCCATCTT 720 CTCGAGTTCT CCAGACAGTA AGCCACCCCC TTCCACGGCA TTCATATCAC CTCTGACTTA 780 TGCACCAAGA ATGCTTCCTG ACAGGAAACT CAAGTCTCTC CCAACGATCT ACCCGTTGCT 840 CATAAACTTA TCCCTTTCTG GAGGCCACAA AACAATTGTA TTCCCCTTCA AAAGACTATC 900 AGTGGAGGAG AGGGGAGTAT AGCTGAAACA ACGTTGGCCA TTTACTGATA ACTGCTAAAG 960 CTGAGTGACA GGTACATAAG ATTCATCCAG CTGTTCTCTT TCTAAATACG TTGAAATTTT 1020 ACATTTTAAA AACCTTATTA GCGTTTACTT TAAGCTCATT TCATTTTCTA ACTGAAACAT 1080 ATTCTTCCAA ATGTGTTTCC TTACTTTCAG TGAGGACCCC CTCCAATTCT TCTATCACAC 1140 TGTGAACCAA ATTTTTTCTA CATACACCAT GTGTATAGCA ATCCCTGTAC TTTAGCACAA 1200 ACTCTTCCCG CCTGGAACTT CCTCCTCTCT TCATGGCCTT ACTGAAAACT GCTTATCTTC 1260 CTTGAAGATC CATCTCAACT CTCATTATTT TGAAGCCCTT TTTCTTCACT GCCCACCCAT 1320 GGCAGTCCCC TCCCAGTGCT ACCAATTTAA ACTATCTGCA TGCCTGCCTT CTCTACTACA 1380 CTGGGTAACC TGGAAGCAGA GATAATGTTT CATTCATCTT TGTCTCTGTC CTAGTCTGAC 1440 AGCATCAAAT GTGTAATGAA TTAATGAATA TACAAACTTA ATGAAACGCT AAACTGTAGC 1500 CATTCATACT GTACTACCCC AAGCCCATCA ATACCACTTT TCAACCTTAA CTTGCTGGTG 1560
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