Tag | Content |
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EnhancerAtlas ID | HS006-10622 |
Organism | Homo sapiens |
Tissue/cell | Astrocyte |
Coordinate | chr13:26759680-26761960 |
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 | AGACTATCCT GGCCAACATG GTGAAACCCC GTCTCTACTA AAAATACAAA AAATTAGCCT 60 GGCGTGGTGG CAGGCGCCTG TTATCACAGC TACTTGGGAG GCTGAGGCAG GAGAATCGCT 120 TGAACCCGGG AGGCGGAGGT TGCAGTGAGC CGAGATCGTG CCACTGCACT CCAGCCTGGG 180 CAAAACGAGC GAAACCCTGT CTCAAAAAAA AGTTGTTACT TAAAGTAATG CATTGTCAAC 240 AGAAGTGTAG AGGCCATGAT TCTAAACTTG TGTTCTCTAC GCCTAACTAC GAACCTTGTG 300 CCTTTCCAAA ACCAAAGGTC ACACTTCTGG AAAGTTCCTT CCTCCCTCAC ATTCAATATC 360 TATTTAGAGA ACACACACTA TGTCCTAGCT TCTGCTAGGT TCTGAAAATA CAGTAAGAGG 420 CAAAAGAGCC ATAGCCCCTC CCACCCCGTG CCCTTATGAA ACTTGCAGTC TACATAAACA 480 TAGATATGAA ACAAACACAA AATGTATGTT TTAACCCTAA AATGCGATAG GGAAGCCAGT 540 CAGACGATTT ACTCGGGAGT AAGAATTCAG GTCATTCACC AAGGCGCCCA TGTCAAAGCT 600 TCATCACCCG CCTCGCGGCC CTAAAACGTG TCAGAGTCAT GATACACACA ACGCAGAGGA 660 AAAGTTCAAA AACAGATCTT AAAAAGAGAA GTGAAAGCAA GCGATCAAAA CATTTCTGGA 720 AATCTGACAC ATCTGGAGTG CCGTGTGGAG ACGCCAGGGC GCGTGGAGCT TTGAGCAGTT 780 AAAAACCCAG ACCGGGAGGC CAGTGCGTGT GTAAGACCGC GTTTCTCTGC AAGGCTGTCC 840 CGCGGCAGGA ACGCGCTCGT TGGGCCGCAG AGCAAGAGCG GGACGCGCCG GGGGGCGTCT 900 GCGTGGCACG TGGGCCCCGC AGCCAGTCGC GCTACCGACT GGCAGTCAGC GGAGACGCTT 960 CGGAGCAGGT CTGTTAGGGC GCGCGCACAC ACATGCACGT GCACGAGCGC ACGTACACGC 1020 GCACACCGCC AGCGCGGACC CTGACGGGGC CGAGCCTCGG AATTGGGCCT CCTCGGCCGC 1080 CGTCGTCTTC TCAGCTCTCA CAGGGCCCGC AGCGGCGCTA TACCTTCGGC CACAGGTAGC 1140 GCGTTCCTTC GCTGTGCTGA CCGTCGATCC CGGGGGCGCT AGAGCGCCGG CTCCGGGGAG 1200 GGCAGGGAAG CGTCAGGGAC CTTTCTTCTT CTTTTTTTTT TTTTCTTTTT TTGAGACGGA 1260 GTCTCGTTCT GTCGCCCAGG CTGGAGTGTA GTGGCGCGAT CTCGGCTCAC TGCAATTTCC 1320 GCCTCCCAGG TTCACGCCAT TCTCCTGCCT CAGCCTCCCG AGTAGCTGGG ACTACAGGCG 1380 CCCGCCACCA CGCCCGGCTA ATTTTGTGTA TTTTTAGTAG AGACGGGGTT TCACCGTGTT 1440 AGCCAGGATG GTCTCGATCT CCTGACTTCG TGATCCACCC ACCTCGGCCT CCCAAAGTGC 1500 TGAGATTACA GGCATGAGCC ACCGCGCCCG GCAAGCGTCA GGGACCTTTC TAGAGCCTTG 1560 CTTGGCCTGA GGTCCGGGAC TGGGGCTGTC CCCGCTTCCT GTTTCTGCCA TCAGTGGGGC 1620 CACAGGCCTG AAGACGGCTT GTACCGCCAC CTTGGGCGCC TCTGCTCCTG GCTGCGACGT 1680 GGGGCGTCCT AGCCTTCGGA CCGGGAACCT GATAGGAGAC GAATAGAAAG GGGGAAAGCC 1740 CTGGAAAATT AAGCCGGCAC AAGAAGGGGG AAACGTTTGG AGGTCAGGCA AGGCTGATGG 1800 CCTTGGGGAT CGCGGAGCAG GAGGCTTACT GGGATGTCCA GTGTGAGAAT GTCAGCCCGT 1860 GAGCTCTGGT GTGCAAGAAA AATGCCTCTT TTCTGGATTT CAGGTGAATT TCTGACTCCT 1920 CTGGGCTACA TACGACCACC CTTCCCTGGC CCCCTCTGGT GAACTGGTTA TAAAAGAAAA 1980 ATTACCCTAG TTCTTCCTGC GGTCCCCTCC CCAGGGATTA GGCCAAGTTC TGGAAGCTTA 2040 TTGGGTGACT TAGTGGGTAT GTTAATGGTT AAGTAACGTA CCCAAGGTCT TATTGCCAAT 2100 CAGTGGCAAA GTCAGGATTC AAATGCAGAT CTCTTGGACT CCAGAGGCTG GAGTTTATTA 2160 AATGTTTAGC CCCAGCTCTA TTTGATTTTG GGGGTTTTTT AAGACAGTCT CTATCTGTTG 2220 CCCAGGATGG AGTGCAGTGG TGCAATCTTA GCTCACTGCA GCCTTGAACT GTTGGGCTTA 2280
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