Tag | Content |
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EnhancerAtlas ID | HS092-29666 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr3:194084540-194086910 |
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) |
NR2F1 | MA0017.2 | chr3:194084707-194084720 | CAGAGGTCAAGCG | + | 6.64 | RREB1 | MA0073.1 | chr3:194086108-194086128 | TGTTGGTTGGTGGGTTGGGA | - | 6.56 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_63431 | chr3:194084376-194118088 | NCI-H69 |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I194364 | chr3 | 194084977 | 194086825 |
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Enhancer Sequence | GCACCCTAAG ACATGGTGAG AAAAAAATTA AATTAAAATT AAAATGAAGG AGCTGTGGAT 60 GAATAAATAA CCAGAGGAGG AGATGCTGTG AGGAGTCTAC AATCACTTTC CTAGCATCCC 120 TGAAGGGCTG CCACGGGATA CAGAAAGAAC CTAGCTCAGT GTGGCTTCAG AGGTCAAGCG 180 GGTGCAGAAG TTATAGAGTA GCAGATTTCA GTTCACACTG AAAATGGGCA ACCTCACAGA 240 GGGAGTAAGC TCACTGTCAC TGGAAGCAAT CAAGCAGAGG CTAAAGCAAT CACTTGGCAA 300 GCAAGCTGTA GAGAAGACTC CCATGCCTGG TAGGGTATTG GACTGGAAGA CAACTGGTGT 360 CCTGTCCATT CCTAAGACCT TAGGATTCTA AGGCTGAGTT TCAGGGCATG AGAAAACAAT 420 CTGTCCACCA AGACAACGGT GCCTGTACTC TTAGGGGTCT GCGTGGACAG TGTGGGTATT 480 TGCCCATCTC TTTGGTGTAA GTGTACGTGA GATATTTACT GCCTGGGCTG ACGTGCAAAA 540 GGTGGAGCTT GAATTGCTCC TGGAGACAAG CTGGCTGGCA CTTATATTTA ATGTACACTC 600 ATATACCCAG CATGCTTCAA AACGGTGTCA CAGCCCAAGT GTCAGAGACT AAATTAAGTG 660 CATGTCACCT GGCCAGCCCA GGGCAATCTT GAGTTTCCCC ATCTATGAAG GACAGTGTAG 720 GATGAGGCAC CCTCTGAGGA CCCATCTTTA TGTGGCTTTC TAGGAGTCTG CACTCCCCAG 780 CTGGGGAGGG GCATCAAGCC AGCCCAGGAA GGGCTTGTGC CAGGGAAGGT GCCCCTTGAC 840 CTGAGAGGAC TGCACAGATA ATTCCCTATG GGAACAGGGC CACCACTGTC TAAAATGGGC 900 CACACTCAGC ATGACAAATA TTGCAAGAAT TTGCAGATTT TCCTCTGTAT AAATCCTCAC 960 ATCTGCAAAG CCCATCCCAG CACCACATGC AGCAGTTTCC TGTTTTCCAG CACTTTCCAC 1020 TGCTGTGGCT GGCGGCCAGG GCTCCACAGG GCCTCCAAAG TGCTCCCCTG AAACCCGGCT 1080 GCAAAGCCCG CAGGGGAGGG AGGGGCCACA GAACCAGGAC TGACAGCTGG GCCCTTGGAT 1140 TCTCAGCATG TGATGCCAGC TCCTGCAGTG GCCACAGCCT CTAGGAGCCC AGCACCTGGA 1200 GGCCTAATAG CCCACGCTGC CTGGTGCTGC TTGGCAGCTC TGACAGATGG CAGTTAAAGG 1260 GCCACAAAGC TGCCCTAATT ATAACTTCTC CCCCAGGCAG CCGAGAGCGT CGTCAATCAC 1320 TTCAGTGACT CAGTCCAGCC CCTGTCCAGC TCCTGGGAAG GGGGAATAGC CTGGTGTCTA 1380 TCACTGGCCC ATGAAGTCAG CAAGCCGAGC AGACAAACCG AAGGACAGCC TGACAGCTCT 1440 CCTGGGCGCT CTGATGCATT CCCTCCCCGT GAGCAGAAGT GCACGAACCA GGGCTCTCGG 1500 CTTTGGGTCT CAGCAGAAGC ACCGTGACTC ACGAGCAAAC GCGTAATTAG CCTCGAAGCC 1560 CTGGGCTTTG TTGGTTGGTG GGTTGGGACG TTTTTGGTTT AATACCATCG TTCACATTCC 1620 CTGAACACGA GGTTTCCTGG AAGGAGACTC CTCCTTATTT TAATGACACA GAGCATAACT 1680 TTTGGAGGGA GGCTGGAAGA CCAGCGTTCT ACTCTGGTTG ACACTAAGTT GAAGTGTGAG 1740 CTTAGGGAAA TTCTCCAGGC CTCAGTTTCC CCTTCAGTAA AGACGTCCAA GGGCCCTTGG 1800 AGCTCTGCTA TCTTCTGATG TGAGGCAGGA AGGAAATTTG GCCTGAAGCC CCTCATTCTC 1860 CTCATCTTCT CTTCCCCAGA GGACCTGCTG GACCTCCAGC AGGGCCGCCC GGCCCGGCTC 1920 CAGCTTCATG CTGAGGCCTG AGGAACTCAT GCCCATCTTT TCAGGCCCAC CTGCCTCCAA 1980 GTTTCCCAGC CAGGGCAATC CCACTTAGTA ATCAGCATGT CCGCACACAG CCAATAGCCG 2040 TTCCATGGAA CCCAGGGACT GGGAGGGGCC TCTGGGAGCT TCTGGTCCTG CCCACTCCCA 2100 GTGCACCTGG GGAAACTGAG ACCCAGAGAG GGGCTGTCTC TCCCTGGCTT CTCCCTTCTC 2160 CCCACAGAGG GCTGCCCAGT CATGGCCTTG TCTGCAGAGA GATGTCACCC AACAAGCCTG 2220 AGGGCTCCCG AGGAAGATGT CAGGCTTGGA GCAGCCAGGG TCTGTCCCCA CTGCCCACAG 2280 CTGGTGCTGA CCTCAATCAC GCGCTCATGG GGGCTCAGGC CAGTGGGTCT GCCTGAGAGG 2340 CTTGGCCTGA AGCTCGGGCC TCCGTGCCTC 2370
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