Tag | Content |
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EnhancerAtlas ID | HS074-08216 |
Organism | Homo sapiens |
Tissue/cell | GM19239 |
Coordinate | chr2:25139510-25141180 |
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) |
PPARG | MA0066.1 | chr2:25139822-25139842 | CTGGGTGACAGTGAACCAGT | + | 6.35 |
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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: 2 | ID | Chromosome | Start | End |
GH02I024919 | chr2 | 25139891 | 25140364 | GH02I024917 | chr2 | 25140470 | 25140869 |
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Enhancer Sequence | ATTGCACTCC AGCCTGGCAA CAAAGCAAGA CTCCGTCTCA AAAAAAAAAA GAACCTGGGA 60 CTGGCTAATG CATGGCCTGA AGAGATATGA CTGGTGTTTC CACCTAGTCA ATGACCAGAA 120 ACTCACAGCC CCCTCTACAG AGATTTGGGG TGGGGACGGC AGGGCAGCAC ATAGCCACTG 180 TCTCCAGGAG GTGGGGTGGG AAGCAAAGCT CCTGCTCTCA GGCAGCTCTC AGTGCTCCAA 240 GGAACATACA CAAATGAGCC CTGGGCTGGG GGTCAATGCC TGGGCTCCCG TCCTGTTTCT 300 GCCACCAAAG TGCTGGGTGA CAGTGAACCA GTTATCACTC ATCTCTGTTT CCTCCTCTGT 360 AAAATGGGTA GTCTGGGCTA GATGCCCTGC CAGGCCCTGC CTATGTTAAC ATCCTCTACC 420 CATTTCTAGA ACAAATCAGC AGGATGAGAC ATGAGTGGAG AAATCAGCAG AGGAGTGGAA 480 GATTCTGTCT GTCCACCCTG GGCCTGCACA TAGCACCTGG TCTCCAGGAC CCAGGCACTG 540 ACCTCCATGG CTGCTAGAGG CTCACGTCAG TCAGCAAGGA TTCTGGGCAC GCCCTGCCTC 600 TCCTGACACC CAGAAGGTCA CCGCTTCAGA GCTGACTCTA CCCCAGCCCC ACTAACCACA 660 GAACAGAGCT GGCGTGGGAG TTAAGACATC TCTACCAGAC AGAGCACTGC AGGGGCAGGA 720 AGTGGGGGAG CCTCTCTTGA CCATCATTGG CACGAGGCTG GCAGGCTGGG CACCAAACCC 780 AGATGCAGAC ATCTCCGCCT CATTCTCTGG TCACCGGCTT GCTGGCTCCC CAGGGACACA 840 CACTGCCTAC TGTCCCTCAG GTCCCCTGGT CTCTGCAGCC CCTGAGGGCC TGGCACTTGG 900 TGGGAACACA ATACTATAAT AGTTAAGCTG AGGCCGAAAT TCCACCCCTT CCAGTAGAAA 960 GCGTGCTCCA GGACCAGCAG AATGCGTGCT TTAGGACCAG GAGACCCTAC GTCACAGTGG 1020 CCGGCATGAC TGTCCCCATT TGCATCCCCA CACCACACCT TCAGTGGGGA GACCACCATT 1080 CTCCACTTCA TAGAACTCCC CAGGCACCCC GAGCTCCCGG AGGCAGGAAA TATGACAACT 1140 GCGTCTTCCC TCTGTGCAGC CCTTCACGTA TCCTAATGCG CTTTCCCCCA CATCTCCTGC 1200 AATCCTGACA ACAACCGTGT CATGCAGGCA GAGCGGACGT TATCCCCATT TGACAAAGGG 1260 GCACTGAGTC CACACAGCTA GTCAGTGCTG GGGAGAGATG GGAATCAAGG AGCCCTCTTC 1320 CCAAGGGAGG TCCTCCTTGC CAGGGTCACT GACAGGGAAT GGCCAGGACA ATGCTGCCTC 1380 AAGACCAGCC CTGGGTGGGC CTTCCTGTCA CACACTTAGA CTGGGCACAG GTGAAGAGTG 1440 GCCCTGAGGC CCAATGCCCT GACATCCTCC TTTCCCTGGG GCCAAGCACA GGCAGACTCC 1500 GGGTAATGGC ACAGGGGTGA AAAGGCAGGG ACTAGGGAGA GAGGTGAGAG CCCCGGAGGC 1560 CCCCAGGACA CATTTTGACT CAAAGGCAAA GCAAACAGCA ACTCCAACAG GTCCCAAGTT 1620 GGTGAGAGCT GCAGGAGAGG ACGCTGTGGG GGGACAGTGG GCAGGACTCA 1670
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