Tag | Content |
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EnhancerAtlas ID | HS129-21799 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr20:3523710-3526400 |
Target genes | Number: 16 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr20:3524915-3524926 | AGTGACTCATG | + | 6.14 | Nr2f6(var.2) | MA0728.1 | chr20:3525797-3525812 | GAGGTCAGGAGTTCA | + | 6.22 | SOX10 | MA0442.2 | chr20:3524701-3524712 | AAAACAAAGCA | + | 6.02 | Sox6 | MA0515.1 | chr20:3524827-3524837 | CCATTGTTTT | + | 6.02 | TP53 | MA0106.3 | chr20:3526357-3526375 | GACATGTCTGTGCTTGTG | - | 6.02 |
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| Number: 1 | ID | Chromosome | Start | End |
GH20I003541 | chr20 | 3521922 | 3527004 |
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Enhancer Sequence | TACATCTCCA ATCAAATGTC ACCTCTTCTA AGAGGCCTTC CTTTCACCCT TTCTAAAGTA 60 GCACCTTCTG TTCTTTCCCT CTGCTCTCTT TCCCTTCATA GCATTTGTCT CTACCTGGCA 120 TTACGTATAC ACACACCTGT GTGGGGAGTA TCTGGGCTTA TCTGTTGTTT TTCTAATGTG 180 AACTACATGA AGGCAGGGAC ATAGTCTTAT TCACTGTTGT ATTCCTGGTA CCTAGAACAG 240 TGACTCACAT GTAGTAAGTG CTTAGTAAAT ATTTGTTAGT TGAATACATA GTAGAAAATG 300 CATCACTGTT TTGTAACTCC TGGAGCACCA GAGTTTCAGA GTTCCTAGAG TTCTGTCTTC 360 ATATTAAAAA TTGAAGGGCG AGGCGTGGTG GCTCACACCT GTAATCCCAG CACTTTGGGA 420 GGCCGAGGTG GGCGGATTGC CTGAGGTTAG GAGTTCAAGA CCAGTCTGGC CAACATGGTG 480 AAACCCCGTC TCTACTAAAA ATACAAAAAA AATCATCTGG GCATGGTGGG GTGCGCCTGT 540 AATCCTAGCT ACTGAGGAGG CTGAGGCAGG GGAATTGCTT AAACCAGGGA GGTGGAGGTT 600 GCGGTGAGCC GAGATTGTGC CACTGCACTC CAGCCTAGGT GACAGAACAA GACTCGGTCT 660 CAAGAAAAAA AAAAAAAATG AATGAAGGGC CAGGCACAGT GGCTCAGGCC TGTAACCCCA 720 ACACTTTGTG AGGCCGAGGC AGGAGAATTA CTTGATCCCA GGAGTTCAAG ACCAGCCTGG 780 GCAACAGGGT GAGACCTCAT CTGTACAAAA AGTCTTAAAA ATTAACCAGC CATGGTGGTG 840 TGTGCCTGTA GTCCCAGTCA CTCAGGAGGC TGAGGTGGGA AGATTTCTTG AGCCCAGGAG 900 GTCAAGACTG CAGTGAGCTG TGATCATGCC ACTGCACTCT AGCTTGGGCT AGACCTTGGG 960 TCTAGCTAGA CCTTGGGTGA GACCTTGTCT CAAAACAAAG CAAAACAAAA GGAACGAAAA 1020 TCCCTTCCCC TCCTCATTTT CATTCCTTGC TTATGGATTC TTCCAGCCAT TTTTGTATGC 1080 ATTTATATAG GTATGTGTAA GTGTACACAT GTACGGTCCA TTGTTTTGCA GCTTGCTTCT 1140 CCCCCATGCC CTTATCAGAA TGCCTGTTGA GCTTCTTGTT AGTCCCGCAG ACCTAGGTAA 1200 TATGCAGTGA CTCATGCAGT CAGATTTCTG GGCATGAGCA TTTAGATGGG TTTCAACCTG 1260 TTGCCATCTG AACAGTGCTG TGGTTCGCAT TCTTGTATAT TGGTCATCGT GTACATGAGC 1320 AAGTATTTCT TCTACAAAGA AATAGAATTG CTAGGTCAGA GTGAATGAGC ATGAGGTTGT 1380 GTGTCTGGGA CAGATTGCGT AGGGCCTGGC AAGGATATAG GCTTTTACCA AATGTGGTGG 1440 TGGTGGTGGT GGTGGTGGTG AATCAATAAT GGGGCAAAAA TCATGGACAT ATGAAGAAAT 1500 GCAACAGCAG GTAGACATAA GAAAAACAAT TAACCTCAGG AGTAAAAAGA ACTCAGAACC 1560 ACAATTTAAA AATTGCTTTT TACTTATTAA ATTAACAAAA TTAAAATAGA ACTAGTAGTC 1620 CTTGCTGTTG GCAGAGTGAA GTGGGATGGA CCCTTCATTC TGTATTGATA CGATTTCAAA 1680 TCACATATCT CTTCTGGAAA GCAAGTTGGT ATTATGGCTC TAGAGTCTTA AAGGCATCAT 1740 TTAGACCCTT TTACTCAGTA AGGTTTTTTT TTTTTTTTTT ACCAGTCACA CAACAAACAT 1800 TTAGAATCCG TCATGTGCTG GGTTGTGAGT GAGGTCTTAA GAAGAACCTA GGGAGCTTTT 1860 AATGATATAG AAAATGCGTT AAGTTTTATT TGTAAAATGG AATATACAAT GTAAATAACA 1920 TCAATTAGGC TAAGAAAATG CATCAGAATA CTAACAGTGT TGGAGTTATG GGTGTTTGTT 1980 TAGCTTCTTC GTATTCTTAT ATAAATATTT TATATAAAAT ATCTTGGGCA CAATGGCTCA 2040 CGCCTGTAGT CCCTACATTT TGGGAGGCCG AGGTGGGTGG ATCACCTGAG GTCAGGAGTT 2100 CAAGACCAGC CTGGCCTACA TGATGAAATG CTGTCTCTAC TAAAACTATA AAAAATTAGC 2160 TGGGCATGGT GGTGGGCACC TGTAATCCCA GCTACTCAGG AGGCTGATGC AGGAGAATCG 2220 CTTGAACCCC GGGACGCAGA GATTGTACTG AGATTGCACC ACTGCACTCC AGCCTGGGCA 2280 ACAAGAGCGA AACTCTGTCT CAAAAAAAAA AAAAAAAACA ACAAAAACCT CATGTCTTTC 2340 AGCAATATAT GTGTGGTATT CATCACTCAT AAAATTTGTT ACTTTATGTG ATTGTGGAGG 2400 TTTATTTTTT CAAAGAAGCA GTATAAAAAG TTTTATAAGA AAAAGAATAG GGCCATTGAT 2460 TTCAAATCTC ATTAGAAATA CAACTCAGAA TAAAGGAAGC CTAGCAAAAG ATTCAGATCT 2520 GTTCCTCAAG GATCCAGAAC TGATAGGGTA GCACTGTGTG TTTATCACAG GAATTTGCCT 2580 GTCTTCCTGG ATGTGGTTTT TAAATTTTAA GGACGGATTT GTTTTTAATT TCTGTCTGCT 2640 ACAATTTGAC ATGTCTGTGC TTGTGCTTCC CTCTATAAGA AGTGTGTTTT 2690
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