Tag | Content |
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EnhancerAtlas ID | HS105-20618 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr12:115214500-115215750 |
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 | chr12:115214704-115214715 | GGTGACTCATG | + | 6.62 | JUND | MA0491.1 | chr12:115214704-115214715 | GGTGACTCATG | + | 6.02 | MEF2A | MA0052.3 | chr12:115214807-115214819 | ACTAAAAATAGA | + | 6.27 | MEF2B | MA0660.1 | chr12:115214807-115214819 | ACTAAAAATAGA | + | 6.32 | MEF2C | MA0497.1 | chr12:115214805-115214820 | CTACTAAAAATAGAA | + | 6.57 |
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| Number: 2 | ID | Chromosome | Start | End |
GH12I114777 | chr12 | 115215149 | 115216000 | GH12I114772 | chr12 | 115210706 | 115214582 |
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Enhancer Sequence | CTGAAAAATT AGATGAGTGT GGTGGCGTAC ACCTGAGGTC CCAGCTACGC AGGAAGCTGA 60 AGTGGGGCAA TCACTCGAGT CTAGGTGGTC AAGGATGCAG TGAGCTGAGA TCACACCACT 120 GCATTCCAGC CTGGGTGCAG AGCGAGATCC TGTCTCAAAA AATAAAATAA AATAAAATAA 180 AAATAAATAA ATAAGGCCGG GCACGGTGAC TCATGCCTGT AATCCCAGCA CTTTGGGAGG 240 CTGAGGTGGG TAAATCACGA GGTCGAGATC GAGACCATCC AGGTCAACGT GGTGAAACCC 300 TGTCTCTACT AAAAATAGAA AAATTAGCTA CTCCAGAGGC TGAGGCAGGA GAATCACTTG 360 AACCCGGGAG GCAGAGGTTG CAGTGAGCCG AAATTGTGCC ACTGCACTCC AGCCTGACGA 420 CAGAGCAAGA CTCCATCTTA AGAATGAATA AATAAATAAA TAGGCAAAGG GATTTTCAAG 480 ACACTTCACA GAAGGAGCTA TGTGAATAGT CAAAAAGCAC CTTAAAAAAT AACTACATCA 540 TGAATCATCA GGAAAATAAA AATTAAAACC ACAATGTGGT ACCACTCATA ATGTGATACC 600 ACAGCGATGG CTGAAATTAA AGACTGGTCA TTCCAAGTGT TGAGGAAAAT GGGGAGCAAC 660 TGGAATGTTC CAACTCTGCT GGTGGGAATG CAAAATTAGA TCGCCAGTGT TGGAGAACGT 720 TTGTCAGTTT CTTCCAACAG TTTGCTTTTG TAATTAAAAA AATGAAAACA GCTTTTAAAA 780 TCCTCCAGTG GCCTCACATG GCATTCAAAT AAAATCCAAA CGTTTTCTTT TTTTCTTTTT 840 AAATTTTTCT AAAATTTTAA TTATAAATCC AAACTTTGAT CTGTGTCCTA CAAAGCCTCT 900 AGTTCACGCC CCTGCAGCCA CACAGCACCT GGTTCTGATC TTTAAGTGGA GAAGGCACCT 960 TTGCTCTTCC CTCTGCCTGG TGGTCTCTCC TGAGCCCTTC CTAGGATGGA CTCCATGACC 1020 AAGTCTCTCC TCAGATGTCC TCTCCGTACA AAGAAGGTGT TCCTGTCCCT CACCATTTCC 1080 TTTACTGTGT CTTATTTACC TCTGAAAATC TCCTATGAAT TTGCCTGCCA TCTGCCTCCA 1140 CTCTCCCAGC TCTTCCAATG AGGAAGGAGG CTCCAGGAGG GCGGGAACAC CATTTCTCTG 1200 TTTAGCACTG TGCCCCATAA CGCAGCTCCC AGCACATAGT AGGACCTTCA 1250
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