Tag | Content |
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EnhancerAtlas ID | HS187-16700 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr3:15502420-15503380 |
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) |
PROP1 | MA0715.1 | chr3:15502649-15502660 | TAATTTGATTA | - | 6.02 |
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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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Enhancer Sequence | CCCCAACAAC TCCTCCAGAA CCATGGCCTG AGAGACAGTC AGGAGTTTGT CCCATTAGCT 60 GCTGATGAAT GGTGAGGCTG AGATTTGAAT TCATGTTTTA CTTAACACTA TGCTGTTCAA 120 AAGACAAATG TCCAAGAATA CTGATGCTCT CAGGAAGCTG GCAATTCCCA GGTACCACGT 180 TGATTCACTT ATACTCTGTC TGGGTACAGG AAGGACTCAG CCAAATTTGT AATTTGATTA 240 TTGCAAATTA CATCCTAAAG GCATTTTGCC TTTATTCCCC CCCCGACCTC TTAGCCCCTC 300 TTACCCTCTA ACTCAGATAA GTACAAAGCT CTCACCCTTT CCACCTCCCC CAGCACCATC 360 TGGTCCCACA GAGCTGGGCA CCAGAAACCG AGGTCACCTC CCAACAGGAT GTGGCAGGGA 420 GCCTGCTGCC ACCACTGCAG TTTCCCTGCA GCTTCCTCCC AGTTGCTGCA GGGCATCTGT 480 TACCCCTGCC TGTTTTCTGC CAGGCTATAC TAAAGGACTC AGCAACCTGA ACTTCCCCAC 540 CCTGACCTCT GGGAGATCAT GTCTCAGCTG GGTTTCATCG CCACCCCCTG CAGCCAGAGG 600 ACCTGGCTCT CCATCTTTTC CCAGGCAGGC TCCCGCTTCC ATTGGCTGCC TCAGTGGGAA 660 AGGATCAGGA AAGGGGAATC TAGGAGAGGG CAGAGGAACC AGCACAACAA CCTCTAGGGC 720 CGCCTGGCTG ACACTCACCC ATTCTGGACC AGGGTGGCCC CCAGTCACTG CTGTGACCTT 780 GCAGGCATCA CTTCTCTTTG AGGTTCAAGA TTCTTTTCTC TAAGGGGAGG GTAGGACTAG 840 ACCAGGGGAG TTTTAACCTG TGGTCTACAG AGGCCAAGGC TATCTCACGA TGGCGCTGGG 900 ACAGGGGTTC TGGAACCCTG GGAAACAGGG TGCAAAACCT TGGATGTAGG TATATACAGT 960
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