Tag | Content |
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EnhancerAtlas ID | HS092-38566 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr9:113939840-113942130 |
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 | chr9:113941253-113941274 | TTTGGCTTTCTGTTTTTGTTT | + | 6.35 | MEF2C | MA0497.1 | chr9:113941370-113941385 | TGCTATTTTTGTATT | - | 6.33 | SOX10 | MA0442.2 | chr9:113941495-113941506 | TGCTTTGTTTT | - | 6.02 | Sox6 | MA0515.1 | chr9:113940737-113940747 | AAAACAATGG | - | 6.02 |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I111178 | chr9 | 113940496 | 113941293 |
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Enhancer Sequence | CTTCTCCCTG TCTATTCATA CCTAAAGCAC TTTATCTGTC AGTTACACTT CCAGGATGAA 60 CCATCCTATT TTCCTTTTAC TCATTTTCCA GTTTTCTACA ACTCTTCTAT GAATAGACGC 120 TTACATCTGG CAAAGGGGTA GACAATGACA GCTTCACATA TCTTATTGTC ACCATTCTGT 180 AGAAATGTAA CTTATTTTAG AAATGGCTAG TTTTCTATTT TCCACTGATA TTAAGTACCT 240 TGCACAAATG TACCTCTTTG ATAAAGAATT AGGGACTATA GTTATTAAAA TAATATTAAA 300 AATAATGTAA TATATTTCAA ATTGTAGTTT CACTATAAAT TAGTCTTTAA AATTTTTAAC 360 TACGTTTTCA CATAATTTGG ATATTTTTGG ATTAAGATTT TAGAAATTAC TGTATATTGT 420 AGCCAAAATT CTTAAACAGC CTTTCTATAT TTTCTAGTGG GAAGGACAAG CCTTATTCCA 480 TTTTTGTGGC ATATTGTCAC TATTTTTAAT TTTTAAAAAT TATGTCACTA TTTTATAAAT 540 TTTCAAAATT GTCACTTTTA TAAATTTAAA ATTATGTTAC TATTTTGTAA ATTTTTAAAA 600 TTGTACAAAT TGTTCTGTAA CTCCTGTCAC AATTTCACAT CTGTGCCTAA GAAATTATGT 660 AAATTAAGCA ATGCTGTTTA ACAAACACAA AGTTTTTTTT ATTTTATGAA ATATAACCTC 720 TTATATGTAG GGCAAAACTA AAAAGTTAAA AAAGTTATAG ACCGGCAGCT GGTGAAGAAA 780 TACACTAGAA ACTCTGCCGA GTTAAAAAAT TATAGAAGCT GAAGTCTGAC TCATAAGATG 840 TGTTTTCCCA ATGTCAGGTT AATAATTTTG TGTGTCTGGC ACTGTGGTTT AACTGTAAAA 900 ACAATGGAAC TCCATCAAGT TGGGATTGTG TGGGGGAAGG CAAGAAGAAA GCAGTGAGGG 960 GTAAGGAGGA TATGATTTTA ACATCTGAAA CTCAACTCTA TAATGAGAAA CAGGGGAGAC 1020 ATGATGTCAT ACTGTAGAAG GTTGCTCCAC TGTATTTTTT TTTTTTCCAG GCTGGCTTGA 1080 CCTGAGGTTT TCAACAAAGT CCAGATGGAA TTGAGGGAGA AACGTGTGTG TGTGTGTGTG 1140 CGTGTGTGCG TGAGTGTGTG TGTGTGTGTA GGATTTAAAG CAGGGGGTTT CTCACTCATG 1200 AATTTAACAT GCTTGGATTT AATGCAGACC AAACACGGCC ACCTCATTAT TCCCTCCTCC 1260 TCGCTTCCTT ACCCCAAACC TTTTAACCTC CCTCCGAATC GACAGGATGC CATCTGGTCT 1320 GGTTAGTCTC CTGATCACTA ACTGAAGGAG GTTCTTTAAT TCTTACTGAT GAGGAAGTCA 1380 TTTATCATTT TTTCATCAAC TCTAAGACTC AGGTTTGGCT TTCTGTTTTT GTTTTATTTT 1440 CATATTTTAA TCTCTGAAAT TTCGATGGGT CTTACAATCA AGCATGCATT ATAGTTTAAT 1500 TGGCAAAGCT TTCTTGTTTT ATTCTTCATC TGCTATTTTT GTATTTTCCT TATTGGAACA 1560 TAAAATAATG CTGCATTCAC TATCAATGTT GCCCTAGAAT TTATGAAATA TGATAGCTCT 1620 AATGATGGTG ACTGATGAGG CAGATGGGTT TTATTTGCTT TGTTTTGCTT TATTTGGTTT 1680 TTATTCTGGA GTGACCTCTC AATTTAAGAA GAAACCTAAA AAGAAAGTCA CCTAGGAGCT 1740 GATCTCTGTT CTGTGAAAGT TCACCTGTGT GGTTCCTCTT GATTATGCAA ATATAAAAGC 1800 AGTAGTCACT TTTCACCTAG AAGAAAGGTT GCCCCTCCTC TGCAAAGCTT TATGAAGAGA 1860 ATGTATCACC CTGCATAAGA AGCTCAGGTT TTTCAAAGAG GAAAGAATGA ATAATCCAGA 1920 CCCTATTCCC TCAAAATCCA AGGTTAGGGA ACTACAGGGC AAGAGATGCT GAAAGAAAAT 1980 GATAGTAAGC ACACCAAAGA GAAATTGAAA AAATAATAAT GATAATTGGC TTTTCTTATG 2040 TAGGTGCCAC AAACTCAAGG CAAGCCTAAT TTTAAGGGGG AAAGACTGAG ATAGGAAGCC 2100 CTGCAGACTT AGCCACTCTG GCATAGTATT AGAAGGACAA TGACCTGAAT AGAACATCTG 2160 GTAGACCAAC CAGGAACCAT TGCAGTGCTG GCAGGAATCC AGACCATCCA CAGCGTTTTC 2220 TCAACCGCAA GCTGAGCAGA ACAAGCTTTA CCATAGCAAT AAGACACAAA AAGCAGTAGC 2280 GCCAGTGGAT 2290
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