Tag | Content |
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EnhancerAtlas ID | HS055-04686 |
Organism | Homo sapiens |
Tissue/cell | FT33 |
Coordinate | chr2:205706640-205709610 |
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) |
HSF1 | MA0486.2 | chr2:205706722-205706735 | TTCCAGAAGGTTC | + | 6.15 | ZNF263 | MA0528.1 | chr2:205708107-205708128 | TCCTCTTCTCTCCTCTCCTCT | - | 6.63 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I204842 | chr2 | 205706833 | 205708592 |
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Enhancer Sequence | AACATTGTAG GAATATGTGA AATTGAATAG CAAACTCAAT TTAGATGAGT TCACATGAAT 60 AACATACTTC AGGTTGGTAA TATTCCAGAA GGTTCAACTG CCTCATAGAA AATTAAATCT 120 CTGAAAAATT CCCCGACTAA AAATCATTTG AAAATTCTAA TTTTTTCTAA TTATTTGGAT 180 TTTCTTATGT TAGATTTCAT TTCATGGAAG GATATTGAGT TTGTGTATAT TCCTGTGTGT 240 GAACATGTGC TTGTGTGTGC TCTTAATAGC GGTTATTTTT CAAAGCAATA GTCTTTCAAG 300 CCTTTCTCTA ATCTCTCCAG CATCTAAAAT GAGGTGATAT AAAACTCCCA GGTGGGTACT 360 AAATATTAGA TTTGTTGACA CCAGCATGGG TGCTTGAGTG GTAGTGGGAA AAAGAAAAAT 420 GATTGTCTAG AGTTTGTATG CTACAGAATT GAGGTGGTTT CAGCTGCTTT CATTTCCTTT 480 AAAGAATAAT ATTGTTTTTT TCAAATGAGG AGGATTAAGT AAGCACCTTA AAAAAAGAGG 540 AGCAATATAT TGACAACATC TGGTATGAAG AGTTATTATA AAAGGTAAGA GGATCTGTGC 600 CAGAAAAAGA ATGGAGAGGG AGATTCTCTC TAATAAATAA ATTTCTTTTA AATGTGCCTA 660 AAACATTAAG GGGGTTTTTC CCATTTAAAT TTATCTTTGA AAACTCCCTA GAGAAGGAGA 720 GTGGTTTCTG TAACAGCTGG TTAGAATTGC TGAGCAAATG TCTGGAAAAG ATGATTTTGA 780 AACAATGTGT TTTGTAATGT TTAAACATTT TACATTTTTG TTGAAACCTG ACTTCTGATG 840 AAGAAAATCG CTCTGTACAG CAGGCCTGCG CTGTGGGCTG CTTTTCTGCT TTCTCTAGAG 900 CTGAGTCACT GAGGACTGCT ACCTTAGCTC CTCAAAGCTG TTAAATTTCT CGAAGGGAAG 960 CTGAGTCATT AGGAAATGTA CCAGAATAGG AGAAAGTAGG TCATTTTGCT AGACTTGGCA 1020 AAACTTTCAT CAGCTTCAGA TTCGCAAGAT CTGCAGTTCT CAAACTCCAG GGTTAATCAG 1080 AATCTCCTGG AGGGCTTATT CAAACATGCG TGTCTGGGCC CTCCTGGCAG AGTTCCTGAT 1140 TCAGTAGGTC TGAGCTGAGC CCCGAGGATC TGTATTTCTG ACAGGTTCCT AGGTGAAGGT 1200 GATGCCGCTA AACCTCGGCC CATACTTTGA GAATTGTTAC ACTAGTGAAA GCTTGGAGAG 1260 AAAAAAAAAA TTAGACAAGC CTTCCCCAAA GGTTTGGCAG TCAGCTTCAT AGTTGGATGG 1320 AGGAGGACAC TACCATTTAT TAATCACTAG ATACTGTCCC AGTCTTGACA TTCAATCTTC 1380 CATCCAATTC TGTAACATGA GTCATGGTAT ATCTATGCTG CATAATCATC TGTACAGAAC 1440 TCACAGAACT CAGTTAGTTT GTTTCCTTCC TCTTCTCTCC TCTCCTCTCC TTTTTCTTTT 1500 TTTTCTCCAT TGCCCTGGCT GAGGTACAGT GGCGTGATCT TGGTTGACTG CAACCTCCAC 1560 CTGTGGGGTT CAAGTGACTC TCCTGCCTCA GCCTCTTGAG TAGCTGGGAC TACAGGTTCA 1620 CACCATCACA CCTGGCTAAT TTTTGTATTT TCATTAGGGA CGAGGTTTCG CCATGTTAGC 1680 CAGGCCGGTC TCAAACTGCT GACCTCCTCA GCTTCGCAAA GTGCTGGGAT TACAGATGTG 1740 AGCCACCGCG CCCAGTCCAG AACTCAGTTT CCATAATCAA CCTGCCCAGA GTTTAAAGCC 1800 AGAGAAGCAG GTGCATCTGA ATTTCTGCCT TTGTCTGTTT AGATCTAAAG GTTCAACTCT 1860 TTCTATCAAA ACATACTTTT GTACTTGTTC TCAACGTGTC TTTATTTCCT CTTCTTTTTC 1920 ATTCATACAT GTTATTCAGA GGATCTCAAA ATTCTTTGGA GTTTTACAAA GGAAAAGTTC 1980 AATTTCCAAA ATTTTTTTGC GACCTGACAT CCCCTACTAT CAGGTAACAC TAATTTATTT 2040 AATATTGACT TTGCTTATGA GTAATGGCAA TGCACAAAGC TGATGAAAGC CGAAATTCCA 2100 TCAGATGGAT TTAGCAAATT AACAGGAGAG AGAAACTACT TAGTTTGTGA GAAACTACTC 2160 GTTTGTAAAC TATGCAAAAA GGATAGACAT TGTCTTACCT AATCACAAAT AAGCCTTTCC 2220 CAAAGGAAGT GGTTACCTTT TAAATGTGTG CACTTATGTT TGTTTTTAAT CCAAATTTGT 2280 GCCAAGGAAT TATGTAATTA TTATTTCTGT ACAAAAGTTA CTTAGCCATT CCTAAATTAT 2340 CATTCATTGA TGTCTGAGAG TAAATAATTT TAGTACCACT ACGATTAAAT TGTAGCAGGA 2400 AAAAAAACTA TGAAATAGAC TCATTCTGAG TCATTGCTTA TAGCCATTTA AAGTTGATTA 2460 GCAATGTTAG TTTAGGAGAT GTAAAAATGC AAAATTTTAT TTTTAAGTTA TAATATTTTA 2520 ATTTGTAATT TCAATGAGCT ATAAAGGAAT GTTTATATTT ATGGAAACTC TATGAAATAT 2580 AAAGAAATGC TCTCACAGAT GTCATTTTAG ATATATTAAG TCTGCTAAAT TCAAATAAAA 2640 GTTTTGGTAC TAACGTGTGA GCACCTGGAT GGCGGGGGCT GGGTGTTATA TATTTTTACA 2700 TCGAAGATGA AGTCCTGCAT AGTGACTTGC ATGTGAATAG GAGTCAGGAA GCATTGACCA 2760 AATGATAAAG CATTGCTCCA GCTGAGTTAC AGGCCTATTC TTTTTAGCTC AAATCAACCC 2820 ATTAAATTAT TTGTGAGATA AAATTTTTCT CAAGTGTATT TTTCCAATAA GAACTTGAAA 2880 AAGTTGTACG TTTTATTTTA TTTGAAAATG TATTAATAAC TTTACACTAT TGACTTTCTC 2940 CTTTCATATA TTTTTAAATA TGAGAAGGCT 2970
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