Tag | Content |
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EnhancerAtlas ID | HS105-21526 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr13:26759830-26761080 |
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 | CGAGATCGTG CCACTGCACT CCAGCCTGGG CAAAACGAGC GAAACCCTGT CTCAAAAAAA 60 AGTTGTTACT TAAAGTAATG CATTGTCAAC AGAAGTGTAG AGGCCATGAT TCTAAACTTG 120 TGTTCTCTAC GCCTAACTAC GAACCTTGTG CCTTTCCAAA ACCAAAGGTC ACACTTCTGG 180 AAAGTTCCTT CCTCCCTCAC ATTCAATATC TATTTAGAGA ACACACACTA TGTCCTAGCT 240 TCTGCTAGGT TCTGAAAATA CAGTAAGAGG CAAAAGAGCC ATAGCCCCTC CCACCCCGTG 300 CCCTTATGAA ACTTGCAGTC TACATAAACA TAGATATGAA ACAAACACAA AATGTATGTT 360 TTAACCCTAA AATGCGATAG GGAAGCCAGT CAGACGATTT ACTCGGGAGT AAGAATTCAG 420 GTCATTCACC AAGGCGCCCA TGTCAAAGCT TCATCACCCG CCTCGCGGCC CTAAAACGTG 480 TCAGAGTCAT GATACACACA ACGCAGAGGA AAAGTTCAAA AACAGATCTT AAAAAGAGAA 540 GTGAAAGCAA GCGATCAAAA CATTTCTGGA AATCTGACAC ATCTGGAGTG CCGTGTGGAG 600 ACGCCAGGGC GCGTGGAGCT TTGAGCAGTT AAAAACCCAG ACCGGGAGGC CAGTGCGTGT 660 GTAAGACCGC GTTTCTCTGC AAGGCTGTCC CGCGGCAGGA ACGCGCTCGT TGGGCCGCAG 720 AGCAAGAGCG GGACGCGCCG GGGGGCGTCT GCGTGGCACG TGGGCCCCGC AGCCAGTCGC 780 GCTACCGACT GGCAGTCAGC GGAGACGCTT CGGAGCAGGT CTGTTAGGGC GCGCGCACAC 840 ACATGCACGT GCACGAGCGC ACGTACACGC GCACACCGCC AGCGCGGACC CTGACGGGGC 900 CGAGCCTCGG AATTGGGCCT CCTCGGCCGC CGTCGTCTTC TCAGCTCTCA CAGGGCCCGC 960 AGCGGCGCTA TACCTTCGGC CACAGGTAGC GCGTTCCTTC GCTGTGCTGA CCGTCGATCC 1020 CGGGGGCGCT AGAGCGCCGG CTCCGGGGAG GGCAGGGAAG CGTCAGGGAC CTTTCTTCTT 1080 CTTTTTTTTT TTTTCTTTTT TTGAGACGGA GTCTCGTTCT GTCGCCCAGG CTGGAGTGTA 1140 GTGGCGCGAT CTCGGCTCAC TGCAATTTCC GCCTCCCAGG TTCACGCCAT TCTCCTGCCT 1200 CAGCCTCCCG AGTAGCTGGG ACTACAGGCG CCCGCCACCA CGCCCGGCTA 1250
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