Tag | Content |
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EnhancerAtlas ID | HS161-02269 |
Organism | Homo sapiens |
Tissue/cell | PC3 |
Coordinate | chr10:119173470-119174730 |
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) |
Crx | MA0467.1 | chr10:119173708-119173719 | AAGAGGATTAG | + | 6.62 | IRF1 | MA0050.2 | chr10:119174695-119174716 | AAAAAAAAAAAGAAAGAAAGA | - | 6.25 |
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| Number: 1 | ID | Chromosome | Start | End |
GH10I117414 | chr10 | 119173581 | 119173650 |
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Enhancer Sequence | TTTTCATTTC TCATGGAAAT TTGGAGATTT GGCCACATCA TGTATCTTTC CTCATTTATC 60 TCCTGTCTGG GCTCTGGAAA CTTGCCAGGC TTTGACTCTT GGATGACTGT ATGGGGCACA 120 GTTCCTGCTC CTTCCTTGCC CTGGAATCTT TCTCAATCAA TGTTTGTTTT AAAGAATCAC 180 AAAGCTGGAA CGTCCCTACA GGTTCTCTGG GTTCAAACCC TCATTTGTCA GTGGAGGAAA 240 GAGGATTAGG GAGGAGGAGG TGACTTACCC TATGTCATGT GGATCACCAG TGATGTGGGT 300 GGGAAAAGAG CCCAGGTCTT CTTCCTCCTG GTTTAGTGCC CCTGTTCAGC CCTTGGGGAC 360 AAGTGGCCAT CATCCTCCTC CTAAAAATTG AGACCTTCTT AAGAGATGTG TTTGATTCAC 420 CTCAAAGGTC ATCAGCCCTT ACTTTTCTTT CCTGTCTCAG CCAAGGCAAA TGTTTACCTT 480 GCAAAAGTGG AATTAGATCC AGAGTGGTTC CTCTTGGCTT ACATGGTATT TAAATGTCTC 540 TGTCTTTGTC CTCTGTGACT TTTCCTCATG GCCTTGCTGT GGTTGCAGCT GTTTTAAGAG 600 ATGCCTGCAC AAAGTCATTC ACCTAAGTGG GAGTTCAAAA AGGACACTTA TTTTCAATGT 660 TGGCTGGTTA CTTTTTTAAA GCCTTTTACC GCAAGGTAGA GGAAAAACAG CTTGGGGTGC 720 ATTTTTTGTC AAGCATGGTC ACAGATAATA CCAGTATTAA CAGTTTGACA TATGTGTAAT 780 CCCCTGACTG TCCCAGAGAA AAGGTGCGGG GTAGCAGCCA TGAGCCATTT GCAGAGGGGG 840 ATGCCACACT GCACTGGGCA CTGGGCCAGG ATTAGCCGAT ATTTTCAATT GTTTTAATTT 900 TTTAAAATTT ATTTTGCATT AGAAAATAGC CAAGCATAGG CTGGGCGCGA TGGCTCACGC 960 CTGTAATCCC AGCACTTTGG GAGGCCAGGG CGGGTGGATT ACCTGAGGTC AGGAGTTCGA 1020 GACTAGCTTG ACCAACATAA AGAAACTCCT TTTCTACTAA AAATACAAAA TTAGCCAGGC 1080 ATGACGGCAC ATGCCTGTAA TCTTAGCTAC TCAGGAGGCT GAGGCAGGAG AATCGCTTGA 1140 ATCCGGGAGG CGGAGGTTGC AGTGAGCCGA GATCGTGCGA TTGCACTCTA GCCTGGGCAA 1200 CAAGAGTGAA ACTCCATCTC AAAAAAAAAA AAAAAAGAAA GAAAGAAAAT AAAATAGCCA 1260
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