Tag | Content |
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EnhancerAtlas ID | HS051-14139 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr19:33269700-33270850 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EBF1 | MA0154.3 | chr19:33270397-33270411 | ATCCCCTTGGGAAT | + | 6.08 | TCF7L2 | MA0523.1 | chr19:33269867-33269881 | AAACATCAAAGAAG | + | 6.08 |
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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 |
GH19I032779 | chr19 | 33269938 | 33270656 |
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Enhancer Sequence | CGGATGACCC TGGAACATTC TATTCCCTTT TATTTTCGTA TTAAAAAGTT CTGTCTTGTC 60 TCCTGTTCTG TTAAAATGCC CTTTACTTAG AACCCACTGA TTAAACAACA TCAGTTATCC 120 TGTCAGTCTC CTGTGGGTTT CAGGGAACTT TGAGGTAATT CAGGATTAAA CATCAAAGAA 180 GGCTTTGAGT TCCTTAGGGA CACAGGGATG ACCTGGTGAT CCTGGGACCC TCCCCCTTGA 240 CTGCGCAGAG GTCCAGCATT GGCTGCACTG CGTCCAAAGC CTGGGGAACC CTGTGCTGTC 300 ATTTCTGGCG AGATAGCCAA GGCAGCCTGG AGGAGAGGCA CCCTTTCCTT AAGGATGGCC 360 AGTCAGAGAC CCGCATTGCC GCATCCCCAA ACCTCACTTG GGACTATGAT AACGACTGTC 420 ACAATGTGGG CAGAGGGGCA CAGGGACCTT GGCTCATTGC CAGGGGCCAG GTGTCCCACT 480 AGCCTCCTCT GTGTGACACC TGTGGTTTTC TTTTCCTGTC TTTTTGTCTC GCTGATGGAG 540 TTGCTCAAGC CTGTAAGTAC CAGTAAGCGG TTGTATTTCT TTCTCCTCGG GCCTGTTCCT 600 TCATATAACT CATTTGGAAA CCCCCAAGTT ACAGTACATT CTGGAAGAGG TCACCCCAGA 660 TGCAGTCTTT CCCATTCCAG GATCACATAC CACCAGGATC CCCTTGGGAA TCCTGGATAC 720 TTGGGTAGCA GAGGAAGTGG CGGGGCCCAC ACCCAGGTTT AAGGGCTCTC CTAGTGAAAT 780 TCTCTCTCTT AATTTTTGGG TGTTCAAGAG AAACTGCTCT GTTTTGCTAA GGGCTTCTGG 840 AGGTGGCAAG GCAGCCTGGA TTGGGCTGAG ATCGTGTTTC TAAGCTGGTG CCAGCTTCCG 900 CCCAGCCCGT GGAAATATGC TAGGTGGTGG GTGAGTCTCA ACTCTGTGTG TTGACCCTCG 960 CAGCATTATT TTCAGGAGGC TTTTGGACTT TGACAATGCA GCCATATGTG CTGCGGGGAG 1020 TACTTTCATA ACTGGTTAAG ATGTCCTGAG CATAGGAGGG TGGAGTGGTA CCTGCTTGCC 1080 ACTCACGTCA TCTCTGATAT TTAATGTACC CTGGAGCTCT CTCTGCAGTT CTTTGTCTTT 1140 CCTTCTTCTG 1150
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