Tag | Content |
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EnhancerAtlas ID | HS094-40084 |
Organism | Homo sapiens |
Tissue/cell | hMADS-3 |
Coordinate | chr8:22598720-22600110 |
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) |
Myod1 | MA0499.1 | chr8:22599480-22599493 | AGGGACAGCTGCT | - | 7.52 | Myog | MA0500.1 | chr8:22599483-22599494 | GACAGCTGCTG | + | 6.14 | Tcf12 | MA0521.1 | chr8:22599483-22599494 | GACAGCTGCTG | + | 6.02 |
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| Number: 1 | ID | Chromosome | Start | End |
GH08I022741 | chr8 | 22599459 | 22607261 |
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Enhancer Sequence | AAGCCAGCTG CCATCTCTGC TGAGCTGCCG TTCTCACGTG CCTTGGTCAT GCCAAGGCCT 60 GTGTGGTGGG CCTTCGTGTC CCTGCCTGCC TTCGTCAACC CAGATTCATT TGTCTGAGCC 120 AACGGAAGAG TGAATGTGGC CCACCAGGGC CTGCTGGGGT CCAAGGCCCT GCCACTGTCT 180 GCCAGGCCCA GGGCTTGTTC TCATTCTGTT GTGGCACTTT TTACAGTGCT CAGCAGGCAA 240 ATGCCAATCC GGGAAGTTTG ACAATCATAG CAAAAAAACC CTGAGCCTGT GCTCAGTGAA 300 CTCCACCTGG AGCTCACAGT TGGTCCCATG TCCCGGGAAT GCTTTGGGTA CTGACAGAGC 360 CCCAGGGAGA GGAAGGGAGG CCCACTGCTC TCTCAGGCAA GTGACCCAGC GGAACCTGGG 420 TCACTGTGCC ACCCCATCAG TGGGTGGCTG TCTGTTAAGG GCCGCTCAGC TGAGCCCCAC 480 AGGTGGTGGG AAGGTTTGTG TGCAGAGGAG GAACCCTGAC TGTCTTGGAA GCCAGCGCCA 540 CCGTCCCCCC GGCAGGCAGG AGAGCGGGGT TGGGGGCAGC CCATACTGCT TGGCTTCCAG 600 TCCCCATGGG GAACATCGCC TGTTTCAGAG TATGTTGAAA TGAGTCTTTG CACAACCATG 660 ACAAGGGCCC AGCTGTTCCT GGTGACAGTG CGCAGGGACA CGAGGAGATG GGAGGAAAGG 720 GGACAGGGTC ACAGCAGAGG GAGGGACCCA AAGAGGATCA AGGGACAGCT GCTGGCTCCC 780 CAGGCCTCCC TATCTGGGGC TCCCCTGCCT CCTTCCAATC AAAGCCCACC GTGCTCTAGG 840 TCCAGGGCAG GGCCTCACCC TCGAAGCTAG GCCTTCAGAG GCCTTCCTCT GAGGAGTCTG 900 GGATTCTAGG ACACCAGGCC CACCCCTAGG CTGTGCCATG GGAAGCTAAG AGAAACTTCT 960 CCCTAGAACT TTTTGCTGTG AGCAGTTAAT TGCCCTGGCA TCTGAGGCTG CTGTGCACAC 1020 AAGCAAGGGG CCTTTAATGA ATGCAAACGA CAGCTGATTA ATCTGCCAGC TCTTGCGCCC 1080 CTGGTCCTTG CTGTGGGGTC TGGCTACGCT CCATTCAGCC TCGATGGCCT GCACCAGCGG 1140 GGTGGGCTCC AACCTATTAC CAGTGGCGCT GCCAGCCCTA ATGGGAAAGA GGGTGAGACC 1200 CCTCCCCTCC TCTGCCCCCA TCGGCCTGTG GTCCTGTCAA GCATGAGAGG CTCTTGGGAC 1260 TGGCCCTGGA AGTGTGGGCT TGCCCCTGCT GGACTTTGTC ACTGGGTGTT TCCTATAGTG 1320 ATGTGGTCAC CCCTCTGGGG ACAGAAGGGG GATGATGACA AGGGGAGTGC TGTCTAGCTG 1380 CTCAGTGGGA 1390
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