Tag | Content |
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EnhancerAtlas ID | HS092-15159 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr13:102780080-102782370 |
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) |
FOSL1 | MA0477.1 | chr13:102781160-102781171 | GGTGACTCATG | + | 6.62 | JUND | MA0491.1 | chr13:102781160-102781171 | GGTGACTCATG | + | 6.02 | Stat4 | MA0518.1 | chr13:102780346-102780360 | CTTCCAGGAAAGAG | + | 6.49 | ZNF410 | MA0752.1 | chr13:102782028-102782045 | GCCTATTGTGGGATGGG | - | 6.36 |
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| Number: 1 | ID | Chromosome | Start | End |
GH13I102128 | chr13 | 102780442 | 102781560 |
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Enhancer Sequence | TCCTCACCAC TGAGCAATGC CAATGACTTG AATGAAGTGA CTAAAATAAA TTAACACGAG 60 TGGTGTTCAC AATGAGATTG TTAGAAGTGC TACATATTTT TTAACAATGA TTCTTTTGCA 120 TCATGTTAGC TATGGAGTCT CAGCTGGCAG CTATCAGCTG TCTCTAGCTG TAAATGACAG 180 CACAAGTGAG CAGGGCTCAC CTACACTTGC TCTGCTCCCA CTGATCCCTC CATCCCCATC 240 TCGCAGCGGT GGGGAAGCAC CTGCCCCTTC CAGGAAAGAG AACACCTTTC TGAACACTGC 300 CTGCCCCAGC TCTCACAGAG AGGCAGTGGG TTCAGTGTCA TAATGCGGTC TTCACTCCAC 360 ATCCCGGATA TCCAATCCTG ACTACACCCC TTACTAACAA GGGAACCTTG GACACGTTGC 420 TTAACTTCTC TGTGCCTCGG CTTTCTCATC TATAAAAAAG ATGATGATAG AAGCATTTAA 480 TCCATAAGGC TGTTGAGAGG GTGGATCCTT CAAATAGTAG CCCATACTAG GAGCTCAGTA 540 GCTGTCGGCT AATATCATTA CTTTTATCAT TAACACTATC TCCCAGGAAA GGTTAGCCAT 600 TCAGGAACTC CAGCCCCAGT AAGAAGGTGG ACAAATATGC CTGTGGCTGA CAAGTGGATT 660 GGCCAAGTAG AGGTAGGAGG TCCCCGCGGT GTTACTGTTA ACAGAAAGCT GAAGTTGATT 720 CTGTAATTCC CATTTGGCTC TGAACCCACA TTCTATTGAA AGGAAGTTTA AACTTGTTCT 780 AGCAAATCAA ACTTACTGGG CTTTTAACCA CATGACTCAC CCCAATGTGA GTGCTAATTC 840 TGAAAAACTC CACCCTCACT TCCCCATGAA CACATGTTAT CACTCTAGAG TCACTGAAAA 900 CAGACAAAGG GAAATGAAGC ATGAAGCTCA TTCTAGGTCA CTGGCAAACG TATGTGAAAA 960 AGTGCTGTCT TCTGAAGAGA AGTGATTTAT GTTGGAAAAG GTTAATGGCA TTCTCTTTGA 1020 CATAGGCAGG CTTTTCAGTA ATACTGAGTT CTCTTAAAAT TTAAAAATTA GGCTGGGCAA 1080 GGTGACTCAT GCATGTAATC CCAGCACTTT GGGAGGCTAA GGCAGGCGGA TCACTTGAGG 1140 TCAGGAGTTC GAGACCAGCC TGACTAACAC GGTGAAACCC TGTCTCTACC AAAAATACAA 1200 AAATTAGCCT GGCATTGTGG CAGGCGCCTG TAATCTCAGA TAGTTGGGAG GCTGAGGCAG 1260 GAGAATCGCT TGAACCAGGG AGGTGGAAGT TGCAGAAGTT GCACTCTAGC CTGGGCAACA 1320 AGAGTCAAAC TGTGTCTCAA AATAAATAAA TTAATTAAAA AATACAAAAC TTAGCCGGGT 1380 GTAGTGGAGT GCACTTCTGG TCCCAGATAC TCAGGAGGCT GAGGCAGGAG AATCACTTGA 1440 ACTCGGGAAG CAGAAGCTGT AGTGAGCTGA AAGCACACCA CTGCACTCCA GCCTGAGTGA 1500 CAGAGTGAGA CTCCATCTCA AAAAAAAGAA AGAAAGAAAG AAAGAAATTA AAACTTCCCT 1560 TTAAGGATTT TTTTTCACTC CATGTTGAAC TGATTACTGA GGACATTGAC TAAACTTTGA 1620 AGCAGAGCAG TTCATTAATA AATTTGATGT GATACAGTTT TACATGTTTA GAAGAATTCC 1680 ACAGAGTGGA CGAGCGTTGA ACCTGGCATC AATTCTCTCC TTTAGCAAAA CTTGGAAAAA 1740 TATTGATATT AAAACTCTGT TACTATTGGA AGAGATTTCT GTCTCTATTT GACACGAATA 1800 AAGAAATGTA TATTACATGA GTATTTCCCT TCCTCAATTC CTTACAATGT GTACACACTA 1860 GTTCTCTTTG GGAAGAAACA AGCCAAGCAC AAGTTTCAAA AAATTCTTAC TGATAATGCA 1920 CACAGGAAGG GGAACATCAC ACACCGGGGC CTATTGTGGG ATGGGGGTAG GGGGGAGGGA 1980 TAGCATTAGG AGATATACCT AATGTAAATG ATGAGTTAAT GGGTGCAGCA CACCAACATG 2040 GCACATGTAT ACATATGTAA CAAACCTGCA CATTGTACAC ATGTACCCTA AAAGTATAAT 2100 AATAAAAAAA AAGAATTAAG AGCCAACCTG GTAAATTAAA GTTCTCCATT GCAGATCTAT 2160 TCTATTGGGT AATAAAATGT GCTTTCCTTG GGCCAAAATC AGCAATAGAG TGTTACATTA 2220 GTTTCCTGTT GCTCCTGTAA CAAATCACCA CAAATGTAGC AGCTTAAAAC TACATAAATT 2280 TATTATCTTA 2290
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