Tag | Content |
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EnhancerAtlas ID | HS092-13527 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr12:116821750-116824000 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr12:116823227-116823248 | CTTTTCTTTTTCTTTTTCTTT | + | 6.02 | IRF1 | MA0050.2 | chr12:116823233-116823254 | TTTTTCTTTTTCTTTTTTTTT | + | 6.09 | SPI1 | MA0080.4 | chr12:116823103-116823117 | AGAAAGAGGAAGTT | + | 6.7 | SPIC | MA0687.1 | chr12:116823103-116823117 | AGAAAGAGGAAGTT | + | 6.24 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I116380 | chr12 | 116818006 | 116824100 |
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Enhancer Sequence | TGTTGGCCAG GCTGGTCTTG AACTCCTGGC CTCAAGCGAT CCTCTGGCCT CAGCCTCCCA 60 AAATGCTGGG ATTACAGGAA TGAGCCACCA TGCCCAGACC AAGGCGAGCC TTAAATCCAG 120 TGTGAGTGTC CTAAAGAAAG CTAGAGAAGG ACCTAGAGAC TGTGAGGATA GAGGTCGACA 180 TTGGAGTGAT GCAGCCGCGA GCTAAGGAAC TCCAGGAGCC ACCAGAAGCT GGAAGGATAC 240 TGGAAGTGAC ATTTTGATTT TGGACTTCTG GCCTCCAGAA CTGGGAGAGT AACACATTTC 300 TGTTGTTTTC AGCCATGCAG TGTGCGGTAA TTTGTTACAG TAGCCACAAG AAACTAATAT 360 GCTTTGCAAA GCATGTGTCA ATGATCCCAT TTTACAGATA GGAAAACCAA GGCACAGCGA 420 GGGAAAATTT GCCTAAAAAT CACACAGTTG GTTGGAAGTG AAGCCAGGAT TCCAGCCCAG 480 GTCTGTGTGA TTCCAGCACC TGGACCCTGG ACCACCGAGT TCACAGAGAA GGGACATTTC 540 TGCAGGGGAG AGCTGTGGTC AAAGAGAGGA ATAAAGGCAA GTGTTGGCTT CCTCAGAAAG 600 CGGCAAACAG ACCGGCAAGG AAGCTGTGGC AAGGGGTCTG GGAGATGGGA CCCACTGTCT 660 CAGACATCTT CCCCTAGGCT TAGAGTCCAC ATCAGGGAAG GGTTGCTGAG AATTCCACTG 720 GAGTGTCTCC CAACCCCTCC CCCACCCCTC AATCTGGAGA GCCAGGTGGT TATGAGACAA 780 AGAAGCAAAG GACCTCTGGT CACAGCTGAC CAGAACATTC TTCCTGTCTG GGAGCTGCCC 840 TGATCTTGCA GTGGGCAGTG AGCTACTACA CCTGCCCTCT GGGAGGCTGA GTATTTACCT 900 AGAGGCACTG CTGGGGCTGC CGGCCTGGGA GCAAAATTTA AGGAGGCACT TGTTCTCAGG 960 GCCATGCATG ATGTTCAGGG TCGTGACTTG CGTGAACCTG AGAATGAGCG CCTCCTTAAA 1020 AATTGCACCT GGTTTGCCTG GCCCTATTCC TGGCCCCACC CCAGGGGTAA TTTATCAGAG 1080 GAACAGAGGG TATTTGGGGT CCATTGGCAG CTGGTAGGTG CAGAGTCACA CAGACCTGGG 1140 CTTGAATACT GACTTCAGTC ACTTAATAGC TGGGTGACCA TGTATGGGTC TATTCTTTTA 1200 CTTGAGCTCA GTTTTCTCAT CTATAAAATG GGGATTATAG AATAAAACTG ACCTCATAGG 1260 TGGTTGTGGG ATTAAATGAA GAGTGTCCAC ATAAAGTACC CGGCACTCAG TAATGTTAGC 1320 TTATTATTAT CTTTTTTTTT TTTTTGGCAG CTTAGAAAGA GGAAGTTCGT GGGTTGCAAA 1380 GTGAGTAATG GCTGCATCTG GGAGCTGATC AAAGGTGGCC AGCCAAGTTG AGTAGCCAGT 1440 TCGGTGTATG AGACTTAACA ACACTGGTAA TTTCTTTCTT TTCTTTTTCT TTTTCTTTTT 1500 TTTTTTTTTT TTTTTTTTGA GGCACTCTGT TGCCCAGGCT GGAGTGCGGT GGCGTGATCT 1560 TGGCTCACTG CAATGTCTGC CTCCCAGGTT CAAGCGATTC TCCTGCTTCC GCCTCCTAAG 1620 TAGCTGGAAC TACAGGCACA CGCCACCAGG CCCAGCTAAT TTTTGTATTT TTTAGTACAG 1680 ACAGAATTTC ACCATGTTAG CCAGGCTGGT CTCGAACTCC TGACCTCAGG TGACCCACCC 1740 GCCTCAGCCT CCAAAGGTGC TGGGACTGCG CCTGGCCAAC ACTGGAAATT TCTTGTTTAA 1800 GAAAATTCCA AGCTCATACT GGGAGGGCGA GGCCAGGACA TGAGGCTGCA GTGGACATCC 1860 ATAGCTGCAG GGAGCCTCAC TCGCTAGGCT CTTCCACATG TGTGAAGCCA TCACATTCCT 1920 CTAGGCACCG CCCAGGACAT CTCCTGCTGG AGGAGCGTTA GAGAGTGTCC CGGCTCCCCC 1980 TAGATCCACC TCTGACCATC TGATCTGGTT ACTTCCTAAC GTCCTGTTTG TTTTCCTCTA 2040 AACCAGAGAG AACGTTGAGC TGGGTCATTG GCGATAAGGG CAGGTTGGGT TGAGCAACCG 2100 AATCTGTTCC TTATCCAAGC AACAGATCTT TTCTAAAGTT CAGCTCTGGT CGGATCCACT 2160 GCCCACGAAG CGGTTCATAC AGCCACCACC ATCAGTTCAT GATTCTCCAC GCCAACAACA 2220 GCATGTGCTT CACTAGCCTC CACAAATGCT 2250
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