Tag | Content |
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EnhancerAtlas ID | HS051-07177 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr13:26759800-26761040 |
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) |
IRF1 | MA0050.2 | chr13:26760361-26760382 | AAAAGAGAAGTGAAAGCAAGC | - | 6.18 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr13 | 26760200 | 26760326 | chr13 | 26760531 | 26760858 |
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| Number: 1 | ID | Chromosome | Start | End |
GH13I026185 | chr13 | 26759591 | 26762164 |
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Enhancer Sequence | TGAACCCGGG AGGCGGAGGT TGCAGTGAGC CGAGATCGTG CCACTGCACT CCAGCCTGGG 60 CAAAACGAGC GAAACCCTGT CTCAAAAAAA AGTTGTTACT TAAAGTAATG CATTGTCAAC 120 AGAAGTGTAG AGGCCATGAT TCTAAACTTG TGTTCTCTAC GCCTAACTAC GAACCTTGTG 180 CCTTTCCAAA ACCAAAGGTC ACACTTCTGG AAAGTTCCTT CCTCCCTCAC ATTCAATATC 240 TATTTAGAGA ACACACACTA TGTCCTAGCT TCTGCTAGGT TCTGAAAATA CAGTAAGAGG 300 CAAAAGAGCC ATAGCCCCTC CCACCCCGTG CCCTTATGAA ACTTGCAGTC TACATAAACA 360 TAGATATGAA ACAAACACAA AATGTATGTT TTAACCCTAA AATGCGATAG GGAAGCCAGT 420 CAGACGATTT ACTCGGGAGT AAGAATTCAG GTCATTCACC AAGGCGCCCA TGTCAAAGCT 480 TCATCACCCG CCTCGCGGCC CTAAAACGTG TCAGAGTCAT GATACACACA ACGCAGAGGA 540 AAAGTTCAAA AACAGATCTT AAAAAGAGAA GTGAAAGCAA GCGATCAAAA CATTTCTGGA 600 AATCTGACAC ATCTGGAGTG CCGTGTGGAG ACGCCAGGGC GCGTGGAGCT TTGAGCAGTT 660 AAAAACCCAG ACCGGGAGGC CAGTGCGTGT GTAAGACCGC GTTTCTCTGC AAGGCTGTCC 720 CGCGGCAGGA ACGCGCTCGT TGGGCCGCAG AGCAAGAGCG GGACGCGCCG GGGGGCGTCT 780 GCGTGGCACG TGGGCCCCGC AGCCAGTCGC GCTACCGACT GGCAGTCAGC GGAGACGCTT 840 CGGAGCAGGT CTGTTAGGGC GCGCGCACAC ACATGCACGT GCACGAGCGC ACGTACACGC 900 GCACACCGCC AGCGCGGACC CTGACGGGGC CGAGCCTCGG AATTGGGCCT CCTCGGCCGC 960 CGTCGTCTTC TCAGCTCTCA CAGGGCCCGC AGCGGCGCTA TACCTTCGGC CACAGGTAGC 1020 GCGTTCCTTC GCTGTGCTGA CCGTCGATCC CGGGGGCGCT AGAGCGCCGG CTCCGGGGAG 1080 GGCAGGGAAG CGTCAGGGAC CTTTCTTCTT CTTTTTTTTT TTTTCTTTTT TTGAGACGGA 1140 GTCTCGTTCT GTCGCCCAGG CTGGAGTGTA GTGGCGCGAT CTCGGCTCAC TGCAATTTCC 1200 GCCTCCCAGG TTCACGCCAT TCTCCTGCCT CAGCCTCCCG 1240
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