Tag | Content |
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EnhancerAtlas ID | HS134-00412 |
Organism | Homo sapiens |
Tissue/cell | Mesendoderm |
Coordinate | chr1:18975600-18977020 |
Target genes | |
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) |
NFE2L1 | MA0089.2 | chr1:18976337-18976352 | ACTGCTGTGTCATTC | - | 6.2 | Nfe2l2 | MA0150.2 | chr1:18976339-18976354 | TGCTGTGTCATTCTG | - | 6.95 | ZNF263 | MA0528.1 | chr1:18976624-18976645 | GGAGGAGGGTGAGGGGAAGAA | + | 7.84 |
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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: 3 | ID | Chromosome | Start | End |
GH01I018649 | chr1 | 18976241 | 18976390 | GH01I018652 | chr1 | 18976454 | 18976529 | GH01I018650 | chr1 | 18976581 | 18976730 |
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Enhancer Sequence | CATCTGGCCA TTTTACAGAT GGAAAAGCTC AGGTCCAGAG GGAGTGACAT GAGTGAGGCC 60 AATGGAGGGG AAGGCCACTC TGGTCTGCTG ACAGTTATGT GCGGGTACAG GAGCAAAACG 120 GACTGGTGGA AGCTTTGCTC CCAGGAATTA GGAAGGCATG GGATAAGGAC AGCCATGGGA 180 ATGAGGCCTT TCCCCATGCT GGCAGTTCAT CGCCCTTCGT GTTTAATGTG ACACATGCCT 240 TAAAGTTCTG ATTCACAGAG GGGGAGACTG AGGCACAGAG AGTTGATTAG CCCAAGGAAG 300 TAAGGGGAGG AGGGTCCCCT TCTAACAGGC TCTGCAGGAC TCTGACACCT TTGCCCTAAG 360 AAGCCTGAAG GGCAGCAAGA ATCTCCTCTT CTTACCCCAT CTGGACAATT GCAGCCCCCA 420 TCCCCCTCCC CCGTTCTTCA TAAACCCCAG ATTCTCAGGT CCAGGGGAGA CTGTGGTTCA 480 AGCCATTGCC ACACCCACCC CACCCCGCTA TCACCCACAC TCCCAGCACC CATAAGCACC 540 TACTGGGATC TCAAGCCCTG CTAGATGCCA CAAACTTGGC CTGCTGAAGG GTTAGTCTGT 600 CCACCATCCG GGGAACTGTC CTTTCAACAG CAAGGGAAAA TAAAGCCCAG AGGGAAAAGA 660 ATCACAGATT GTGGTTAGGG TTGGAATTCA GATCCTCATG TAAATGGCCC CATGCAGAGG 720 CCCTAGCCTG AGCACTAACT GCTGTGTCAT TCTGGAAGAG CCGCTTCATG TCTCTGGCCC 780 CTGGTCCTTT TGTCTGAACA ATGGCAAGGC AGGATCCACC TAGTGGTTTT CAAACTGTGT 840 TCCATGGAGT CCTGGGATTC TCAGCCTCAG GGGCCATCCT TTGAGCTGTA ATACTCTGGG 900 CGTGTGTTTA GTGGAGGGGA AGCAGTGAAA AAACAGCCTG TTTCCCCATG GATAGAGGAA 960 ACTCCGGGGA GGCAGGGCTT TGTCCTGGGA AGAGCAAGGA CCACTTCCCA TCCAAGGCTA 1020 CTCTGGAGGA GGGTGAGGGG AAGAAGCTCT GTATACTCCT GGAATCAGAG CCCTCAGGCT 1080 GTGGTTATTG GTCTTCAGAG ATAAGGTGAT AACTGCTTAT CTGGTGACAA ATGATTATCC 1140 TCCTCTTCTA TTCCTCTGAT TAGGGAACTT TCTCTCCTGG CTGGGAGGTC TCTTTGGAAA 1200 AAGGGCAGGG CTGGTCAAGA GACACTGACA TCTGCCTCTT CAGTCCCTGC CCGGCTTGCT 1260 GTGTGACCAG AAAGCAGTTA CACACTCTGT GCTTCATTTT GGGGCCTGGT GGAGCAGCTG 1320 GCTTGCAATG CCATCCTGGG ATGGTGCTGG AAGGAGGATT CAATGCAGCC TGTGGGGGAT 1380 GGAAGGAGCA GGAGGGCAGA GGGCGGAGGA CAGAGGGCTG 1420
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