Tag | Content |
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EnhancerAtlas ID | HS029-10621 |
Organism | Homo sapiens |
Tissue/cell | CUTLL1 |
Coordinate | chr3:15501820-15503580 |
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 | STAT3 | MA0144.2 | chr3:15501929-15501940 | CTTCTGGGAAA | + | 6.62 |
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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 | AGTCACATTC TGGCTGGCAG AAAAGCACCA GAACAAAAGC CATCTAACAG GAAGTGAGGA 60 AAGAGAAAAA AAGATGGGGA CTGAGAAGAG AAATAGGTAA GGATCCCTTC TTCTGGGAAA 120 ATAGCGAGGG GTGGGTTTGG AGGCCAGCCA GTCATTGGTG TCAGGCAGTA TGACATCTGG 180 GGCAGCCAGG GGCTGGGAAC ACAGTTCACA GATCCAGAAG GGCAGGAAAT AAAATGACCC 240 CAGGGGAGAG ATCTGGCCAG GACCCCAGGG AAAACACTGC AGTCGGAGGA GACTGAACTT 300 TCCTGAGCGA GTTGACAGGT ATTCGTACAA TCAGAATGCT GACAGCATGA GGGGAAGGGC 360 ACTGTGCCAA TATCTTATCC TAAGTTATGG TTGTTTGTTC TAACAAGAAA TACAAATATA 420 ATTCTGTAGG AAGAGCTCCA GTCTGTGTTC TGATATTTTC AGAAGAGCCC AGAGAGACAG 480 GGAATCCACC AGGCTAGGAA TATTCTGGGT AATTAAGCAC TTGGGGAAAT TGAAGTGGAA 540 AAGCTCTGTG ACCAAGAATA TGAGGGTGGC ATTGGAACAG CCTTCCAGAA GGCTCTGTGA 600 CCCCAACAAC TCCTCCAGAA CCATGGCCTG AGAGACAGTC AGGAGTTTGT CCCATTAGCT 660 GCTGATGAAT GGTGAGGCTG AGATTTGAAT TCATGTTTTA CTTAACACTA TGCTGTTCAA 720 AAGACAAATG TCCAAGAATA CTGATGCTCT CAGGAAGCTG GCAATTCCCA GGTACCACGT 780 TGATTCACTT ATACTCTGTC TGGGTACAGG AAGGACTCAG CCAAATTTGT AATTTGATTA 840 TTGCAAATTA CATCCTAAAG GCATTTTGCC TTTATTCCCC CCCCGACCTC TTAGCCCCTC 900 TTACCCTCTA ACTCAGATAA GTACAAAGCT CTCACCCTTT CCACCTCCCC CAGCACCATC 960 TGGTCCCACA GAGCTGGGCA CCAGAAACCG AGGTCACCTC CCAACAGGAT GTGGCAGGGA 1020 GCCTGCTGCC ACCACTGCAG TTTCCCTGCA GCTTCCTCCC AGTTGCTGCA GGGCATCTGT 1080 TACCCCTGCC TGTTTTCTGC CAGGCTATAC TAAAGGACTC AGCAACCTGA ACTTCCCCAC 1140 CCTGACCTCT GGGAGATCAT GTCTCAGCTG GGTTTCATCG CCACCCCCTG CAGCCAGAGG 1200 ACCTGGCTCT CCATCTTTTC CCAGGCAGGC TCCCGCTTCC ATTGGCTGCC TCAGTGGGAA 1260 AGGATCAGGA AAGGGGAATC TAGGAGAGGG CAGAGGAACC AGCACAACAA CCTCTAGGGC 1320 CGCCTGGCTG ACACTCACCC ATTCTGGACC AGGGTGGCCC CCAGTCACTG CTGTGACCTT 1380 GCAGGCATCA CTTCTCTTTG AGGTTCAAGA TTCTTTTCTC TAAGGGGAGG GTAGGACTAG 1440 ACCAGGGGAG TTTTAACCTG TGGTCTACAG AGGCCAAGGC TATCTCACGA TGGCGCTGGG 1500 ACAGGGGTTC TGGAACCCTG GGAAACAGGG TGCAAAACCT TGGATGTAGG TATATACAGT 1560 TTTTTCCCCC CCGAGAATGG GTTTGGGACT TTCATCAGAC TGTCAAAGGT AGTGTCAGGA 1620 ACCAATTTGG GGGGCCTAGT CCAACTCTGG ATGATTATCC AACTGGTCCC AGGCACAGGG 1680 ATAACTTATT TATTTATTTA TTTATTTATT TATTTATTTA TTTATTTATT TTTGAGATGG 1740 AGTCTTACTC TGTCGCCCAG 1760
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