Tag | Content |
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EnhancerAtlas ID | HS098-22112 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr16:67440350-67441660 |
Target genes | Number: 17 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr16:67441065-67441084 | AGACCACCAGATGGCATCA | + | 6.08 | Nfe2l2 | MA0150.2 | chr16:67441506-67441521 | TGCTAAGTCATTGTT | - | 6.36 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_29769 | chr16:67439428-67441964 | Fetal_Muscle |
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| Number: 1 | ID | Chromosome | Start | End |
GH16I067403 | chr16 | 67436954 | 67442064 |
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Enhancer Sequence | GAGGGAGAAA CAGTAGAGAG AGCATTAGCC CAAGAAGCTG GGCTGGAGCC CAGGGCCTGT 60 GTCTGCAGCC AAGTTTCAGC ACAGGGGGAG TAGGCTGCGA CAGCTACTCT GCTGGGGAAA 120 CTGGGGTCCT AGCACAATAG AGATGGGCAG TGGGGAGAGG GTGGGAGTGG GCTGCTGTCT 180 CAAAGCCCAA AGCAAACCCT GGCCCTAGAC TGGCCAGGAC AAGGTAGGAG GGCCCAGGAT 240 TTATTCAGGA CACAGTGCTG CTGCCTGTAA CTCAAAGTGC TGTCTTCACA GCCATCACAG 300 TTAAACCCAA TAAGACATGT TCTCATCTGG TAACAATATC AGGCTGGGGC CAGAGTGATG 360 AGAACACATG CTGATTCTGT TAGGATTAGT CACCTCCTTC CTGAGGTCCA AATGCAAGTG 420 TCAGACACCC CCGCTATCCT TTGCTCAGGG AAACGGGGAA TGGGGTGCCC AGAAGGAGGA 480 TCTGCCCTCT CCCCCACGGT GGACAGAAAA TCCCTTTAGG ACTGGGGGAG TCTGAAGCTC 540 TGCCCCATGC TGCCTGAGGG TTCTCAGCTG GGGAGGGGCC AGCACATGTG AGGAAGGGAA 600 GGATTCCTCT TTAGTTCCCT TCAGCAGCAG AAATGACCAC GTTTCTCTAA GTAAATCTGG 660 GCCTGGTGTA CAGTTTTGTA CAGAAAGGTG GGCTAACGCC CTTGGACTCA GAGCCAGACC 720 ACCAGATGGC ATCAACCACC CCCTCCACCC GCCACCCTCT AGCCGGACAG CTGGCCCAGG 780 GTCCAGGGAT GAATGCCAGG CAAGAAGGGG TAGGCTACAG GAGGAAGACC CCCATCCCCA 840 GGATATGGGC CCAAGATGGG ACAACAGCTC AGGCAGGCAG CGCCACACCT GGGAGACAGG 900 CCAGCTCTGC GCTCATGGTG GGAAGGCCAG GAGCTGGGAC TAAAACCCTG GTAGCTGAAC 960 TCTCCTTTCA GGAGCCCCTG CCCATGAGAC AGGGAACCTA AGCAGAAAGG GTGCCGCAGA 1020 CCCCGACTCA GTGCATCTTC CTGGATCACC TTTCTCACTT CTCAATCCAC AGAATGAGGC 1080 TTGATCTTCA GAGCCAACTG CAAGGGTTGC CTCATCCAGG AAGCTTTCCC TGATGCCCTG 1140 AGTCAGGGGG CCCTTATGCT AAGTCATTGT TGGGCAAATT ACTTTGCCAT TTGGGACGCT 1200 TTGCAATCCT CATGTCTGCC CTCATTAGGA CAACTTTCCC CAAAGGCAGC AAATGTGCTG 1260 GGTGGGGTTT ATTCATCTCT GTCCCCTATG TCCCTTCCCC CAGGCACCCA 1310
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