Tag | Content |
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EnhancerAtlas ID | HS101-42449 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr8:62408420-62411010 |
Target genes | |
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) |
FOSL1 | MA0477.1 | chr8:62408723-62408734 | GATGAGTCACT | - | 6.02 | HLTF | MA0109.1 | chr8:62409190-62409200 | ATATAAGGTT | - | 6.02 | JUND | MA0491.1 | chr8:62408723-62408734 | GATGAGTCACT | - | 6.32 | REST | MA0138.2 | chr8:62408887-62408908 | GCAGCTGTCCAAGGTGCTGGA | - | 9.67 |
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| Number: 1 | ID | Chromosome | Start | End |
GH08I061496 | chr8 | 62408560 | 62409159 |
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Enhancer Sequence | GATACAGGAT AGTGCTAAGG TGGCCAGTTT TAGAAACCTT GGCACAAGAG GAATCTGGCT 60 AGCCTTGGCT GGGCAGGTGT GGGAGGGCTA AAAGGTACTT GTGTCTACTC TGGTGGCTCC 120 AGGAGAAAGA ATCAGAAATT GTACATAGAA GTTTAGAAAG GGCAGAGCTG AGTTCAATGT 180 AAGGAAGAAT TTTCTAGCTG AGTTGACTGT TTAGGGGCAT GGAGGAGCAG GTTCCTCAAG 240 TTAGTTATGT TCAAGAAGAG GCTGCACAAC TCCTTACTGA AGATTTCCTA TCAGGTTGGT 300 CTAGATGAGT CACTGTTTCC CTCTAACTCT GTGGCTGTGG TTCTCATGCC ATGTTGTGAA 360 ATAAAGTGAA GTCATATGAC AGAAGGTAAA TGGAGTTTAA GGTCTGTAAA AGTAGATGGC 420 CATCAGTATT TTCCTTTTCC ACAGGGTCCG TAGGTCAAAG CAGGAAGGCA GCTGTCCAAG 480 GTGCTGGAGG GAGGTTGGCC TGTGTCTCTG GTTGTGCTCT CTTGGTTGTC TTCATGCTTG 540 CTGTTTGTTT TAATGCCTCT GGATTTTCTG CTTTCCTGTT CCTCGTACAA ACCTACACTT 600 CTCCCTTCCC CACATGCACA CTGGGCCTTA AACTAAAACA AAGAGAAAAA TGCACTGGAA 660 ATGTGTTAGG GGGCTGGGGC TAAACTACAA CCTAGAGCTT CCTTCCTCTG CCCTATCCCA 720 GCAATAAGTG AGTCCATGAG TCCATTTTGC TTTCAAAGGT TCAGCTTGGT ATATAAGGTT 780 GGACTGTTTG AATGGATTGA TAGTTACAGT AGAAATAAAT TTTTTTGAGA CACTTGTACT 840 GATTTGCTTC TTGATTTCTT AATTTTATCC TTTCTACAGT ACATACATAT CTTGAAAGGA 900 GACAGGAATC TTAGGCAAAA CAACAGTGAT TTTTATGGTG AGGTGGAAGG AACACTCGAT 960 GTTTTAGCTA AACGCTTCTG TGGCCTTTGG TATACCCAGG AACTGTGGGT TGGTAATAAA 1020 CCTGTCAACA TCTCCACTTT CTATTTGTGT TGCCTTCTAT ACATCATATG ACTTCTCAGT 1080 CCCTTAGTTT TTTAGATGGA AAAAACTAAG GGTTGTGAAA ATGAAATGTT AATATATGTC 1140 AATGTAAATA CATGTTAATA TACAACTATG GGTTATGAAA ATGAAATAAG CTAATATAGG 1200 TCAAGAACTT CTTAGAACAA TACCATGCAC AAACATAGTG TTTTAGTATG TTGTGTTGAG 1260 GGGGTCCTCA AGACCACCCT TTTCTGTATT TGATAATTTT GATAATGTCT TCCTAACTTA 1320 CTAGAAAGAC CCACAGGACA CAGAAAAGTT GTTAAGACTG ACAGTTGTGG TTTACTACAG 1380 AAAAGGATAT AGATTGCAAT CAGGAATGGA AAGCCATGCA TAAGGAGGAG TCCAGGAAGG 1440 ACCAGCTGTA AGTTTCCAGT TGTCCTTCCA GTAAAATCAC ATGAACAGAA CTTAATTCTC 1500 TTAGCAATGA TGTGTGACAA CATCTGCAAA GTGTTGTCAA CCAAGGAGGT TCATCTGTGC 1560 CCTGGTGTCC AGGTTTTTAT TGGGGGGGGG GTGTCAGTCT CATGGGCATG CAGTACCTTT 1620 GTGACTGACC TTAACAGCTC AGTCCTCAGC CTTCCACCAT TCCCTCTTGT TACCAGGCCC 1680 CACCACTTAC TTACTCAAAG TTAGTCTTTG GGTCAGGGGT TTCCTCAGTA TTGTCCCTTC 1740 ATGGTTCATC AGAAAGATGT TACCAGAAAG TGGTCCCAAT TCAGACCCCA AGAGAGGGGT 1800 TCTTGGATCT CATGCAAGAA AGAATTCAGG GGAAGTCCAT AGAGTAAAGT GAAAGCAAGT 1860 TTATTAAGAA AGTAAAGGAA TAAAAGAATG TCTACACCAT AGAAAGAGCA GCTCTGAGGG 1920 CTGCTGGTTG CCCATTCTTA CGGTTATTTC TTGATTATAT GCTAAGCAAG GGGTAGATTA 1980 TTCATGCCTC CGCTTTTTAG ACCATATAGG TTAACTTCCT GATGTTGCTA TGGCATCTGT 2040 AAACTGTCAT GGTGCTGGTG GGAGTGTAGC AGTGAAGATG GCTGGAAATC ACTCTCATCG 2100 CCGTCTTGGT TTCGGTGGGT TTTGTCTGGC TTTTTTACTA CAACGTGTTT TATCAGCAAG 2160 GACTTTATGA TCTGTATCTT TTGCTAACCT CCTATCTCAT TCTGTGACTA AGAATGCCTT 2220 AACCTTCTGG GAATGCATCT CAGCAGGCTT TAGCCTTATT TTACCCAGCC CCTATTTAAG 2280 ATGGAGTTGC TCTGGTTCAA GCACCTCTGA CACTCTTACT GCCTTAAAAG GGTCAAACTG 2340 ATACAGTGTG ACCTAAAGCC CAGACATACA AAACCAAGCA TGCACTATAA ATCACACTGT 2400 TAGCATAAAC TACTTGGCAT GAAGTCAGGT CTCAGATATA CAAAGATCTC CTTATCAGGT 2460 AGACTACTCT AAGGGCTCAG AGGAGCCAAA GGCCAGTCTT GAAAACTTGT AATGTGTAGG 2520 GTTTGGGCAC CCCAGGTCTA CCGAGTTAAC AATTTACTGC ACATATATGT AAGTTTTACT 2580 TATTTGAACA 2590
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