Tag | Content |
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EnhancerAtlas ID | HS055-00354 |
Organism | Homo sapiens |
Tissue/cell | FT33 |
Coordinate | chr1:90439360-90441910 |
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) |
IRF1 | MA0050.2 | chr1:90440648-90440669 | AGTAAGAAAATGAAAGTTGAA | - | 6.05 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I089973 | chr1 | 90438738 | 90442095 |
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Enhancer Sequence | ACACTGAGGC ACTCCAGGAA AGGGAGTGTT TATCATAGAT ACACAAACTG GAACCAGAAA 60 ACTGTTCGGG GATTGAGGGA GCTCTAGGGA CTGGCTGTTT CCTTTATCTT TCTCATAGCC 120 AGGATCATCT CCCTCTTGTT ATCTTTCTGC TTTTTTCCTA TGAAGTGTCT GCTCTGTCTT 180 CCCTCTTTAT CAAGAGGCCA ATCCCGGCCG GGCGCGGTGG CCTGTAATCT CAGCACTTTG 240 GGCGGATCGT GAGGTCAAGA GATGGAGACC ATCCTGAACA ACATGGTGAA ACCCCATCTC 300 TACTAAAAAA AAAATACAAA AATTAGCCGG GTGTGGGGGT GCACACCTGT AGTCCCAGCT 360 ACTCAGGAGG CTGAAGCAGG AGAATCGCTT GAACCCGGGA GGCAGAGGTT GCAGTGAGCT 420 GAGAATGTGC CACTGCACTC CAGCCTTGCG ACAGAGTGAG ACTTCATCTC AACAAAAAAA 480 AAAAAAGAAA AAAAAAAGAA AAAAAAAGAG GCCAATCCCT CAATCCAAAT GCCTGAGAGA 540 GCAAGTCCAG TTGCCTTTGT TCCGTGAGGC TACCCTTTGG GTAGAGCTCT TTGCCCAAGG 600 CATCTTCATG AGTCATTAAC CAACTGATGG AAAGGCTGCC TCAGGCCAGG TGTCTACCTC 660 TGGTCCACTT AGGGTCCCTT GTGCGTAGAC ACCAGCCTAA GGTAACTTCC TGATCCTGGG 720 GATTATGGAT GTGGCAGTTT ATACTAAAAG CAACTGTTGG ATGACAGTGC CTAGGATCTG 780 CATTTAGTCT GAGTCCCAAT GCGATCACAT GCCTAATTTG TTTGACCAGT CAGCGCTCAG 840 ATTTCTTCCT CTGTAAATAG GGGATAATAA TGAAACCAAC TTCACAAAGT TGTAGTGAGG 900 CTCCAACAGG GTAATATATT AGTGAAAGGG CTTTGTAAAC TATTAAATAT TATACGAATG 960 ATATTATTAT CAAAAAGAGA TAACCTCTTA AGCCATTTTG ACCCCTTTGG GTTCTCAGGC 1020 TAGTCATTCA TCTTAAAAAG GAACATGGCA GGGAACAAAT GGGGAGTGTC AGGGGGCCGG 1080 GAATCTCTTG TTACCCTCTG TTAAGGGATG TCCAAGGACA GCTAGCTGGG AGTCTTGGGC 1140 CTCAGGGCAT CACAAGGCTC TGGGTTCTTG ATGTGTATAT GTATAAAATG AGGGGGAATA 1200 GAGGACCCCT TTTCTCCTTG CCTCTAGTGA CACATCCCTT TTCATTGATA ACCCCTCCAA 1260 ATTTCTTTAA AGAGAAAAGG AGACGAGAAG TAAGAAAATG AAAGTTGAAA AGAGAGAGGT 1320 GATGGTGACT AGGCAGAAGT AATAAGATAC TGGGTGTGAG TTCCCTAGAA GGGCTGGGCA 1380 GTTCAGCTCA CAGAACTGAA TTGCTGGGGA ATTTTGGCTC ACAACTAAAC ATCCTGCAGC 1440 TGCCAGTAAA TGGCAACCCC TTTGTATGAA ATGTGGCCCT GACCTTGGGC AGAGCTCCAT 1500 CTGAGCACCC CTGGACCCCC TGACTCACTG CTGAAGTAGC TAAATGAGGG TGGAGCACTG 1560 GACGGAGTAC AGTGGCTTTG TAATTAAGTT TACCAAGTCC CTCATTGCAC AAGGGGAAAG 1620 ATGGAAAAGA GGTTGGAGAG ATACTTCTTT AATAAGATCC CTGTCCCAAA TCTGAAACCT 1680 AGGTCCTGTT TGAGTAGGCT CAAGTTGCTC ATATCTAGGC TGTCATGTAA AAATGATCTG 1740 TGTGCTCCAG AAATTTATAA TTTATTCATA AAAACACATT TTCAAAAACA TACTGCAAAC 1800 TGGAATGTTT TGGTGCAGCA CAGACTAGCT ATTAAATTCC GATGGCCTAG ATGGGCCTCT 1860 GCAGAGCCAT GTGGTGTGAG AAGATTAAAT AGGGAGGAAG AAAAGTAGAA GCAAACTTTT 1920 GATATGTTCC TTTGAGAAGA GTATAGGAAG GTCAAGCAAG GGGAGATAGG GAAGTGAAGA 1980 AGTCGATGAA TCATTCTCCT CTATATTTGG CTAATTTCCT CATTGGCATT GGCAGATATG 2040 ACTTCCAAGT TCCGGGGTCC TGACTTTCTT TTTCCAGGGT TTTTCATTCT CTGTTAATTA 2100 GGACATTGGA AGAATTGTCA TGATAATTAT AATGTCTAGA CTAGGGGAAC TACAGGAGGC 2160 AATAAGAGAA TATTTAATTG CAGAGCTGAG AAGACACATG AAGATGACAT GATTGTGTAA 2220 GTCTCTCCTT AGAACAATGC CACACGGAGC TGTGTTTCAC AGGTGCTCTG ACATTGCCTC 2280 TTATGTAAGG GGACTCTTTG GTGTTTTCTC TGAGCATTTA GGGTTTTCAA AATTCCCATT 2340 TCCTCCAGAA GATACTAAGG ATCTGCAGAA AAAGCAGGGC TGCAGTACTC TGATGTTTAT 2400 CAGCTTTACC CTCAGAGTCT GTCATTGTAA AGGTAGGGAT GGATGCTCTC AGAGTTTCTT 2460 GCCCAGACTA AAAGACACCT GCTGATTCCT TTGGAGAGGT AGGAAAAATG ATCAGGCAGG 2520 GAAATCTCTT ACCTTGCCAA GTTTGGTCAT 2550
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