Tag | Content |
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EnhancerAtlas ID | HS092-10324 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr11:106857850-106860430 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr11:106858160-106858175 | GAGGTCAGGAGTTCA | + | 6.22 | ONECUT1 | MA0679.1 | chr11:106860379-106860393 | AAAAAATCAATAAA | + | 6.89 | ONECUT2 | MA0756.1 | chr11:106860379-106860393 | AAAAAATCAATAAA | + | 7.52 | ONECUT3 | MA0757.1 | chr11:106860379-106860393 | AAAAAATCAATAAA | + | 8.12 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I106987 | chr11 | 106858408 | 106860050 |
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Enhancer Sequence | CTCAAGGCCT CATCAAAGCA TTGATCCATT ACAGCCAAGG ATGAATTCTT GGGGAATACG 60 AATGTAATAC AAACCCTTCA AGATGTGAGG CAGCATGGTA GCCTTCTACC TCTAAAAAGG 120 CAATCTGCAG AAAGGGTCTA GCATAGTGCT GATACCTAAG AAGCAGTTAA TAAGTATCAA 180 TTTCCAATTG CTAATCCTTC AAAGTGGCTG TCTTAAAAAT ATATCGTCTA AAGGAGACCC 240 CAGGAGCTGG GCACTCTGGC TCACGCCTGT AATCCCAGCA CTTTGGGAGG CCGAGGCACG 300 TGGATCACTT GAGGTCAGGA GTTCAAGACC ATCCTTGCCA AATTGGTGAA ACCCTGTCTC 360 TACTAAAAGT ACCAAAAATT AGGCGAGCAT GGTGGTACAT GCCTGTAGTC CCAGCTGCCT 420 GGGAGGCTGA GGCATAAGAA TTGCTTGAAC CCAGGAGGCA GAGGTTGCAG TGAGCCAAGA 480 TCACCCCCAC TGCACTCCAT TCTGGGTGAC TGAGTGAGAC TCTGCCTCAA AAAAAAAAAA 540 AAAAAGACAC CAGAGGTCTA TGTCAAATCT CACTTAGACC CACTCCATGT CCACCTCTTC 600 ATAAAAACAT CCAAGACAGA TGTAACACTC TCCCTACCTA ACACTCTTCG AATCTTTAAC 660 ATCCTCCTTG GTAGGCAATG GTTAAAGTTA GAGGAAAGTG AGCTTAAATT GAATCAAGGG 720 CATCTACTGA GATCTACTCT ACATTACCAC GTAGGAGAAC CCTTTCACCA CACAAATCTA 780 AGGCCTCAGA TACCTACTGC ACATTAGCCA AACCAATTCA CAAATTAATT TTAGGAGGAA 840 TCAGCTTCCA AGTGTTCAAA GGAGAGGTAC AGAGCAACTT CTTTCAGCAG CTGCTTTTCA 900 CTTATACCAG GCCTCAGACT GGCACAAATG TTTCTACTCA TCCAAACAGA CTCAAAGCAG 960 AGTAAATGGT ATGCACCTAG GAAAGAAAAA TCATTCCTGA ACGAAGAGGC AATGGAATGG 1020 TTAAGAAATC TAAAGAGAAT GAATCAGACA TAGTGATCCT AGTGCACACA GAAAGCATGC 1080 TTTAACAACC TAGTCCATGA CCAATCTAAA TCCAATCATC ATCAGTCACT AGCTCAGTAC 1140 CCCTTGGATC TGGGCCTCTT GCACTGGCTT GGCAGTTCCT GAGCTAAGAT AACTTTCCCC 1200 TTGGCAACAA ACTGAAAAGG CAGTGGATAT CCACAGAGGG ATGATCCTTC CAATAACCTC 1260 TGGTCATAAA ACATGGAACA GAAAGCAGGA ACTAGAGTGT ACAGGGCCAG TTAAGACCAG 1320 AATGACCTCA TTTGTACAAA AGGACATTTT TTTTTCTGTA CCAGGAATTT CCCAGTCATT 1380 AAAAAGCACA TATTTGTGAA AGGAGTTAAG CCTTTTAAAG ATCTAGCTTT TTTCTTGTGT 1440 GAAGCAATTA CTTCCACTCC CAGCAGGAGT TAAATTTATA GTTTCCACAT ACATTAAAAA 1500 GAAATGTTCT CTGAGCACAT CCAACAAAGC TTCAGGTTGA TAAAGCATTT ATGCACTTCC 1560 TATTTCTTGC CAAAGTGGGC AGGCACATTC TAATAGCCTA AACCACAAGC ATAGAGGCTG 1620 ACTGCACAGC ATCTCCTAAC TTCAGCAATC CAAGACTGAC TTCAACACAG CCCTGGCCCC 1680 TCCGAATATC TTATCACCAT GGATTCATTC CAGTTTTCAG AGTGTGTCTG AAGGCCTCAA 1740 CCCATGGCCT GATCAGTGAG AGACAAATTC ACATAATCTC AGCCTCTCTG ACCTGAGTAA 1800 AAAGCATGAA GTGAAGACCC ACAAACGGGC CAAAGCCTTC CATCAGATGA TTTCTGCCTC 1860 TGGGGTGGTA GGGTCCAGCT CTCAACAAAC TTTTATTAAG TGTCCATGTA TGCCAGTGAT 1920 GCAAGTCAAT GTAGATCAGT GGGAACAACA AGGGCTTTGA AAACATGCAG ACTGTCTATC 1980 CTCTTCTTTA AGAATGCAGC TCCATAACTG GCTCCTACTT AAGAGAACCA TCCAACATTC 2040 TACAGGCCAA GATCCCAGTC CTCTTATGTG CATCTGTCCT TTTCTGCAAG GAGTTTGGAA 2100 AGATGATTTA GAAAAGAGGT TTTAAAGTCA AACTGAATTC AAAAGCAAGT TCTATGACTC 2160 ACTAGCTAGA TGACCTTGGG CAATTTACTT AAGCTCTTCT GAAACAAGAT TCCTTATGCG 2220 TACCTTATTT TTTTTTTAGT TAAATGATCT TTTTAATTTT TTTATTATTA TACTTTAAGT 2280 TCTGGGATAC AAGTACAGAA TGTGCAGGTT TGTTACATAT GTGTACCTTA TTTTTATGGG 2340 AATGCACTGA AATAATTAGA GCAACATCTC TGACACACAG TCGGTGTGTA ATAAATGAGA 2400 GATATGGCTA TGCTAAGCTG AAAAACATGG TTCCTACCCT CAGGAGTCTC ATAATCTAAT 2460 GTAGGAACAC AGACTTCAAT TAGAAAACTC ATCCCACAGG TGTAATGTTT CAAGATCTTC 2520 ATCATCGAAA AAAAATCAAT AAAGCTACCG ATACTTCTCA TTATGAGAAG TTGACACCAA 2580
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