Tag | Content |
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EnhancerAtlas ID | HS177-17960 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH_RA |
Coordinate | chr5:78104640-78105820 |
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) |
Myog | MA0500.1 | chr5:78105497-78105508 | CTGCAGCTGTC | - | 6.62 | Nr5a2 | MA0505.1 | chr5:78105626-78105641 | CCTGGCCTTGAACCC | - | 6.86 | Tcf12 | MA0521.1 | chr5:78105497-78105508 | CTGCAGCTGTC | - | 6.14 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH05I078809 | chr5 | 78105283 | 78108146 |
|
Enhancer Sequence | ACAGGATGGC CCCCTGGGCT CCCTCTGCTC GGGTCAACGA TGTGTGACTT TTTGCTGGAC 60 ACGGGGTGTC TAGGGCAGCA CACAGCAAGA CGCCAATATG TGTTAGCTGT GCCATGTGCC 120 CTACTTTTGA TTTCTCAACT AGTCAGAGCT AAGATGTTAA TGAAATCTAC AGGCTTTCAT 180 CTCAGATAAC GGATTTGCAA AACAGACATG TATAAATGAC AAACTGTGTT TCAGCCACTG 240 TGCTGGGAGG GATACAGAGA TGAATGGACA GATGTCCAGG TCCCTGTCTT GGACAGATTC 300 AGCATCTAAC AAAGAATGTG AATAAATAAC TCTATCATAA TGGGCTAGAG CTACAGGTGC 360 ATAGAACACG CTGAGCGGGC ACCGAGGGGG TTGCAATCAG TATGCAATCC TGCCAGGAAA 420 GGTGGTGGTC AGAGCGGCTG GGAAGGACTT GCCAAGGAAG CTTACATTTG AACTGGATCT 480 CAAAGAACAA GCCAGATTTT ACCAGGCACA GAAAGGCAGG AAAGGTCACT TGGGCAACGG 540 GAACAGCATG AGGAAAAGCA CGGCAGCACA TTGGTGGTGT AGGTGTCTTG TGACAGAGCT 600 TTCGGCACAT AACACAGTGC CTCTCTTCTC TGTCTACAAC AAAGGCCAGC CCCGTGGAGA 660 GCTAAAAAGA GTGAGGAACA ACAGGCAGAC AGATGATCCT GGAGCACGTT CAGGGAGGAG 720 GGCAGGAGCC AGGTCTGGCT CAGCTCCCCA AGTCAGCGGC ACTTCTTGCC TTCAGCTGAA 780 GCTGGGAGAC CCATCCTACG GTCAGGCTGA GGGCCGCCAG AGCCTGCGGC CAGGCCTAAC 840 ACTAGGCAGA GACGACTCTG CAGCTGTCTG CTCACACTCA CTGCCAGTCA CGCTTCACTC 900 CACTTTCCTG CTCTGAAAAT CACGTCCTGG CAACCTGCCC ATCGGACCTG GAGCCAGCCT 960 TGCCCTCTCC ACTGCGGGCC TGTAGGCCTG GCCTTGAACC CCAGCCTGCT GACATGCTTC 1020 TCAAGCTACA GGCCCATTGC TTTGGCCCTC TGATTCTGGC TGACCATGGG CCACAGAGAG 1080 GAATAGGGGG CAGCTGATGC TGGCAGTTGT AGACTGCACA AGCAGGACCC ATCTCTGGGC 1140 CCTTTCCATC AAGCCTGGTC TGGTGGCCAG TGTGGTGGGC 1180
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