Tag | Content |
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EnhancerAtlas ID | HS139-12376 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr12:50506280-50507460 |
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) |
Zfx | MA0146.2 | chr12:50506901-50506915 | CCCGCCTCGGCCTC | + | 6.01 | Zfx | MA0146.2 | chr12:50507329-50507343 | CCCGCCTCGGCCTC | + | 6.01 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_06595 | chr12:50491342-50507397 | Brain_Hippocampus_Middle | SE_07621 | chr12:50502758-50507167 | Brain_Hippocampus_Middle_150 | SE_28375 | chr12:50500665-50507198 | Fetal_Intestine | SE_29325 | chr12:50495292-50507023 | Fetal_Intestine_Large | SE_53026 | chr12:50502834-50507248 | Small_Intestine | SE_65813 | chr12:50502724-50507642 | Pancreatic_islets |
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Enhancer Sequence | GTCAGTCTTG CTAGAGCTCA GCGCTAATCC TGTCAAACCT CGACTCCTGC CTGGCGTCTC 60 GACCCTCCAC GCTCCAACTC TGCCTCTTCC TTGCTCTATA GACCTCTGCG TCCTGATAAG 120 TGGCTCTCCG GGGCACCCTT CGTGCATATC GGCTATCCAG CTCCACCTCT TGACCGCTTT 180 CACTTCCTGG AATGCTCTCA CTGCTCCTCT TCTCCAGGCC ATCCTTCTAA AAAGACAGTT 240 CCACTCCCAC CCCGATTCCC ACCCCTACAC CTTTCTGCTA AGTTTTCTCA AGCCCCCACC 300 CTGTCTTTGA GCTGTTGTCT CTGAACTCTC ACAGTGCCTC TCCATGAGAC CATAAGCTCC 360 TGTATGACAG AAGCCATGTT CTTTTTAGCG GCCTCCGTAG CATGATGTAC GTTATGTTAT 420 GTTATGTTAT GTTATGTTAT GTTATGTTAT TTTGAGACAG GGTCTTGCTT TGTCGCTCAG 480 GCTGCAGGTG TGCGCCACCA CGCCCGGGTA ATTTTTAAAA AAAGGTTTTT TTTTTGTTGT 540 TGTTGTTGTT GTTTTTAAAT AGAGAAAAGG TCTCCCTATG TTGCCCAACC TGGTCTCCAA 600 CTCCTGAGCT CAAGCCATCC TCCCGCCTCG GCCTCCCAAA GTGTTGGGAT TACCGGCGTG 660 AGCCACCGTA CCCGGCCGAT GTACTACTCT CTAAGTGCCA AACAAAAAGT AGATAAAAGA 720 TGATGGATAC CTTAAAAGCC CTGAGTTGAC CACTATGCAG TGTATGCATG TAACAAAATC 780 GCACTTCTAC CCATACGTTT ACGCAATTTT TTTTTTTTTT TTTTGAGACG GAGTCTTGCT 840 CTGTCGCCCA GGCTGGGGTC CCGTGGCGGG ATCTCGGCTC ACTACAAGCT CCGCCTTCCG 900 GGTTCATGCC ATTCTCCTGC CTCAGCCTCC AGAGTAGCTG GGACTACAGG TGCCCGCCAC 960 CACGCCCGGC TAATTTTTTG TGTTTTTAGT AGAGATGGGG TTTCACTGTG TTAGCCAGGA 1020 TGGTCTCGAT ATCCTGACCT CGTGATCCAC CCGCCTCGGC CTCCCAAAGT GCTGGGATTA 1080 CAGGCGTGAG CCACTGTACC CGGCCGTTAT TTTATTTATT TATTTATTTG TTTGTTATTT 1140 TATTTATTTT TTTGAGACGG AGTCTCGCCC TGTCGCCCAG 1180
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