Tag | Content |
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EnhancerAtlas ID | HS065-03012 |
Organism | Homo sapiens |
Tissue/cell | GM18508 |
Coordinate | chr2:73234120-73235420 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr2:73234539-73234560 | ATCCCTCCCTCCTCATCCTTC | - | 6.22 |
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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 |
GH02I073007 | chr2 | 73234314 | 73235209 |
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Enhancer Sequence | ATCTTCACTT TGGGCCTCCT CCTTCAGAGT ATTCTAACTG CTGCAGAGAG ATGAGGTCTC 60 AATCTGGGAG AGAGGCACCC CCAAATATCT CAGTCTGCTT GGCCAGAAGT GGAACATGAA 120 CAGCTGAAGA TAAAGGCAGG AGGGGTAAGG CCACTGCCAC AGTTCTGTGT ACGATGATAT 180 CAGGACTCAG AACTGAGCAA GCCCCCACCC CCTTGGCCAC CTCCCATACA AAACTGACTC 240 AAACTACAGG AGAAAGGTTT TTTTAAAAGC GTGGGAAACC TGGAGAGGAA ATGGGGTATG 300 CGTCAAAACA ATTGGGTGGT AAAACTGAAG CCAGGGGAAG ACTAGGGCGA ACTGTCTTGT 360 TCGCCAAGAT AATGGAAATA ATCATCCCTC TCACCCTTCA CCCCATTTCT GCTTGGCTAA 420 TCCCTCCCTC CTCATCCTTC AGGTTTCAGT TTAGGCGTCA CTTCCTCCAG GATGTCTCCT 480 CTGACCCTCA CAGTGAGGTT AGGTCTGTCA CGCGCTCTCC GGCACCCTGC ATGCCTTCTC 540 TGTACCATTC ACCTCATCAG CAAAAAGCTG TGGAAAGTTT ATCTTCCTCG AGAGCTTCTA 600 TAAGCTTCAG AGAAATGAGG CCCCTCCACG CTGCCTCCCC ACATACCCGG GAGCCTCCCA 660 GGTAGAGCAA GTGTCTTTAC ATCTCATCCC CTTCCGCCAC ACTGACTCGC TCAACTCCAA 720 AATGTTCCTC TTTGTCATCC ACCATGGGCC GCAGTACCCC AACACACAAC AATTGTCCTG 780 TTTTTTCCTT CTACTGTGTC TCCATCTTCT GATTTATGTG GCTAATGATC TGAAAGTTAC 840 ACTTCAGTGT ATAAGGGGTG TTGCTACTTA AAGGATGTCA GCCAGTTAAA GAAAATCTCT 900 GTCAAATGAA TGTTTACCCC AGACCGGTCA ATTCTAGCTT CACTGGAGCG ACACCTCCTG 960 TGTGGTGAGC TAGGTCAACA TGGCTGGGGT CTGGTAATGC TGGAGGAAGG CCAGGGAGAA 1020 CATTGGGATT GGGATTTAAA TGTGCAAAAA AGCAGAGGAG GGATGAGGCG GCTTGGGAGA 1080 TGTCAGGAGG GCCCTGGGAA ACACCCCTGG AGATGAAGTG GCCGACACCA GCATCTTCTG 1140 ATACTTAGAG TCTCTAAGCC CATGTGATCA CCTGTGTGTT AAAATGAAGG AGTGCAAAGT 1200 ACAGAGTCCA AGTTCTTAAT GTCTCAAGAC AGAAATCGGA TTTAGACTTA ACCTAAGGCC 1260 ACCAGACCCA ATAACTAGGT GTTCATGGTC TGCCCTCCTT 1300
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