Tag | Content |
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EnhancerAtlas ID | HS139-21062 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr16:56904650-56906260 |
Target genes | Number: 23 | Name | Ensembl ID |
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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 | chr16:56905438-56905449 | CTGCAGCTGTC | - | 6.62 | Tcf12 | MA0521.1 | chr16:56905438-56905449 | CTGCAGCTGTC | - | 6.14 | ZNF263 | MA0528.1 | chr16:56904661-56904682 | GGAGGAGGGGGACATGGAGGT | + | 6.24 |
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| Number: 1 | ID | Chromosome | Start | End |
GH16I056871 | chr16 | 56905112 | 56905513 |
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Enhancer Sequence | GAGGAGGCCA TGGAGGAGGG GGACATGGAG GTGGTCACGT GGAGAAGCGG GGGTTGCCAG 60 GCCTGGGCCC TCCCTGGTCC TCTGCCTTTT CTTTTTCTTT TCTTTTTTTT TTTTTGAGAC 120 AGAATCTCGC TCGATGTCCA TGCTGGAGTG CAGTGGTACC ATCTCGGCTC ACTGCAACCT 180 CCATCTCCCA GGTTCAAGAG ATTCTCCTGC CTCAGCCTCC CGAGTAGCTG GGATTACAGG 240 CACCTGCCAC CACACCTGGC TAATTTTTAT ATTGTTTGTA GAGACGGGGT TTCACCATGT 300 TGGTCAGGCT GGTCTCAAAC TCTTGACCTC AAGTGATCTG CCCGCCTTGG CCTCCCAAAG 360 TGCTGGGATT ACAGGTGTGA GCCACTGTGC CCTGCTGCTT TGTATCTCTT GTGTGACAAC 420 CTAGGTCCAC ATGGCCCAGG GTGGGCATGG TGGCTCAGGG GGCCGGGCAC CCAGACTCCT 480 TCCATCTTGT GCTCCCTCCA TCCCTGCGCC GTGGCCTTTG TCCACCTGGT CCACCATACC 540 CACATCCCCT CCAGTCAGAG GGAAAGCAAA GAAGGGGGAA ATGAAAGGGA GGGAATTCCC 600 TTTTCTCTTT CTTTTTATGG CACCATCTGG AAGTTTCACT ATCGCTGTCA CACATGGCTG 660 CGAGGGAGCC TGGGGAGGTG TGGCCTTCAA CTGAATCATG GATCCTGCTG GCAGACTCAG 720 CCGGACAGGC CCTACAGGCA GGGCAGGACC TGGCCCCTGC AGCCTGTCCT CTCCCCGCAT 780 TTTCTGACCT GCAGCTGTCA GAGGGTGTCC TCCTTGCTCT TCCTTGGATG CCCTGAGCTG 840 AATTCCCTGG ACAGTTCTCT GGCTTGTTCA TTCTCCCACT TAAGGTGTCT GCTAAACACC 900 TTCTCTCTGG TGACACCTTC CCAGGTCATC CTGCTAAATG AGCTCCACCC AGTCCCCATC 960 ACACTCCCTC TTCTTTATTT ATTTATTTAT TTATTTATTT TTGAGATGGA GTCTCGTTCT 1020 GTCACCTAGG CTGGGGTGCA GAGGCGTGAT CTCGGCTCAC TGCAACCTCC GCCTCCTCGT 1080 CTCAAGCAAT TCTCCTGCCT CAGCCTCCCA AGTAGCTAGG ATTACAGACA CCCACCACCA 1140 TGCCTGGCTA ATTTTTGTAT TTTTAGTATA GACGGGGTTT CACCATGTTG GCCAGGCTGA 1200 TCTCGAACTC CTGACCTCAG GTGATCCGCC CACCTCGGTC TCCCAAAATG CTGAGATTAC 1260 AGGTTTGAGC CACTGTTTCC GGCCTGTATT TTTAGTAGAG ACAGAGTTTC CCCATGTTGG 1320 CCAGGCTGGT CTCAAACTCC TGACCTCAGG TGATCCGCCC ACCTCGGCCT CCCAAACCTC 1380 TTCTTACTTT AAATTCATCC TCCTTATTTA TCAGCCAAGA CAAGAGGCTT TGGCGGTCTT 1440 GTTCACTGCT ATATTCCCAA CTCCTTGAAC AGATCCTGCT GCATAATGGG TGTTGAATGA 1500 ATGAGTGAGT GAATAATGGA GAAACGGGCC CTGGGCAAAT CATTTTCTGG CGGGGCTTCC 1560 CAGAGAGGTA GAACAAAACT ATCTGACCTC TGGGGTCCTT CGCCCCCTCC 1610
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