Tag | Content |
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EnhancerAtlas ID | HS105-11645 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr10:104748280-104750110 |
SNPs | Number: 2 | 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 | chr10:104749287-104749298 | GGTGACTCATG | + | 6.62 | Foxd3 | MA0041.1 | chr10:104749884-104749896 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr10:104749888-104749900 | GTTTGTTTGTTT | + | 6.32 | JUND | MA0491.1 | chr10:104749287-104749298 | GGTGACTCATG | + | 6.02 | MEF2C | MA0497.1 | chr10:104748483-104748498 | TACCTAAAAATAGCA | + | 6.24 |
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| Number: 1 | ID | Chromosome | Start | End |
GH10I102987 | chr10 | 104747537 | 104749886 |
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Enhancer Sequence | ATACAAAGTA TAGACCTTTT CCCCAGAAGT ATGCATACAC ACACATACTT TGGCATACAG 60 TTTGAGTGAA TGTCTCGTTC TGCAGCTGCC CTAGAGCATC CAGGGACCTC AGCTCATCAT 120 TTGCTAACTT TACCAAATGA TGGGTTAAAA TTCTCTTCCT TGGTAAAATT CTGCCCACAC 180 CCTATCTTTT GGGCACTTAA TTATACCTAA AAATAGCATT GAGAAAAGCA GCTATTTCAT 240 CCACAATTAG AGAATATTCT TGAGTCCAGC ATCAAAGCCA TTATGGTGCT TTGATCAATA 300 AGTTTGTTCT CCACGGAAGT GAGGCTTAAT GGCTTAGGTG ACCGACTAAC TTTCTCCTTA 360 GTTGCTCTAG AAGTCACCTG TGAATGAGCC CTTTCAAAGG GAATGATTTT GACTTCTGAA 420 AACTTAAGCA GATTAGAAGC CTTGAGTATA GGATTTAGAA TAAGAAGTAC TCAGTAGTAA 480 CCCTGGTTGT CTAACTACAC AGGCTTGTAT GATTTGAACT TTTGTTGTTG TTGCTCTTCT 540 GGTTTCCTTA AACACCAGAC AGATCCGATT ACAATTCTAA ATATTTAGTT CTGTGCAAAC 600 AGGAACAGCT CAACAGTTCA CCTTCACTGA GTAACGTATG TCTATTTAGA TAAGCAAACT 660 ACTGTTGCAA AAACCCTGGC AAAATGTCAG GATGAGCAGG GGAAACTTTC ATTATCTTTT 720 CAGCCATCCG AACAGTTCCC CAAGAATCGG ACATTTTTGA GACTTAACTA GTCAAGGTTA 780 AATTACTCAT TGTTCAGTGA GTAAATTCTG TCTAAAGACT TAGCTGGGGT CGTCTTTATT 840 TTATTTTTTT CATTCTTCTT TTTTTTTGGA GGTTACTTCA ACAAATAAAG TTTTATTTTT 900 ATTTAGGCTT TCCTTGTATT TTAGGGAAGA GAAAATATTT GCTTTATGTT CTTAAAGTGA 960 GTTTAAAAAA AAAATGGTAC ATTTAAAGAT AGTTTGGGGA CGGGCATGGT GACTCATGCC 1020 TGTAATCCCA GCACTTTGGG AGGCTGAGGC GGGCGGATCA CCTTAGGTCA AGAGTTCGAG 1080 ACCAGCCTGG CCAACATGGC GAAACCCGAT CTCTACTAAA AATACAAAAA TTAGCCAGGC 1140 ATGGTGGCGC ATCCTTGTGG TCCCAGCTAC TTGGGAGGCT GAGGCAGGAG AATTGTTTGA 1200 CCCAGGAGAC GGAGGTTGCA GTGAGCTGAG ATGGCACCAC TGCACTCCAG CCTGGGCGAC 1260 AGAGTGAGAA TCCTATCTCA AAATAAAATA CAATTTGGGG TTTCTTAATG CCTATACTCC 1320 TTTGTTTAAC TATAGGGCTT CTAGTTCTTT AAAGATGATT AGTGATTGTA CAAAAGGTAT 1380 AATATAATAA TTATAACAGC CTCTTACTTT TCATATCCAT TAAACTTTTT TTTTTTTTTG 1440 AGACAGAGTC TGGCTCTGTC ACCCAGGCTG CAGTGCAGTG GTGCAATCTC GTCTCACTGC 1500 AACCTCTCCC TCCCCGGTTC AAGCGATTCT CATGCCTCAG CCTCCCAAGT AGCTGGGATT 1560 ATAGGCATGT GCCACCACAC CTGGCTAATT CTTTGTTGTT TTTTGTTTGT TTGTTTGTTT 1620 TTAGTAGAGA TAGGGTTTCA TTATGTTGGC CAGGCTGATC TCGAACTCCT CACCTCAGGT 1680 GATCCGCCTG CCTTGGCTTC CCAAAGTGCT GGGATTACAG GTGTGAGCCA CCGCGCCCGG 1740 TTTAAGCCAC CGTGCCCGGT CTTAAACTTT CAAGTAGACA GGACACACTG GCTACTTGTG 1800 TGCCCCCAGA TGTATAGAAT TATGTTACTA 1830
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