Tag | Content |
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EnhancerAtlas ID | HS139-23997 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr17:73599390-73600720 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr17:73600624-73600642 | CCCTCCCTCCCTCCCTCC | - | 6.03 | KLF14 | MA0740.1 | chr17:73600548-73600562 | TGCCACGCCCCTCC | + | 6.06 | Myog | MA0500.1 | chr17:73599715-73599726 | CAGCAGCTGTC | - | 6.14 | SP3 | MA0746.2 | chr17:73600548-73600561 | TGCCACGCCCCTC | + | 6.08 | Tcf12 | MA0521.1 | chr17:73599715-73599726 | CAGCAGCTGTC | - | 6.02 | ZNF263 | MA0528.1 | chr17:73599517-73599538 | CCCTCTCTCTCCTCGTCCTCT | - | 6.73 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_23082 | chr17:73597298-73601104 | Colon_Crypt_1 | SE_24179 | chr17:73599887-73600883 | Colon_Crypt_2 | SE_52698 | chr17:73599237-73601046 | Small_Intestine |
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| Number: 2 | ID | Chromosome | Start | End |
GH17I075603 | chr17 | 73599888 | 73600030 | GH17I075604 | chr17 | 73600161 | 73600310 |
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Enhancer Sequence | CAGGTGGGGC CCAGCACCTC GGGGCAGGAC TGACAAGGAG GCCACCGGGA GTGACTGGCA 60 GCCCCGGGGG TCCTTCTGAT TGGAGATGGA CTCACTCTGC CCAGGACTGG GCCTAGCACC 120 CAACCCTCCC TCTCTCTCCT CGTCCTCTCA TCCTCTCTCT CTCTCTCTTT CTCTCTCCAT 180 CTCACTCTCT TCTACCATTC ACCATCCCTC CACGCATTCG TCATTTCTTC TCCTCTCTGC 240 AAACCTCTCC TGTGCTGATG CCTGGGCACC AGAGATGAGG TGGGAGCAGT ACCTGCCCTA 300 GGCGGGGCTC ACGGTCTAGT GCCCACAGCA GCTGTCCAGG GAGTGCAGGC TGAAGCAGTG 360 AGATGGCAGG GGGGACGGAG TGAGAAAAGA GCCTCTCAGA AGGGCAGGAG GGGCGGGGAG 420 GGGCGGGGTG GCACATGGAG CTGCCAGGAA CCCCAGAGGC AGCTCTGTTC CCAGAGTTCA 480 GAAACCTCCA AGAAAAGCTG GTGGCATTGT CCGTTTTGTT GTTTGCCTAT CTGGCCTTTG 540 GCTATTGACT GGATGGCATC TTGGGAATCC TCTGAAGGGC TGGAGTTTAC CCCAAGCACA 600 GGGACAGAGG GAGCAGGTGG AGTCACTTCT CGTTGATGTC CAGCTGAGCT GGGCTGGTGG 660 CTGCCTCAGA AGGGAGGGGG CAGCTACTAG GAGCAGCAGC CTCACCCCAG GGCTCTGTGG 720 ACCTCCTTAG CCTGTGATGG CCTTGGCAAT GGGGATGGCC TGGTTGGGGG ACTGAGCAAA 780 AGGCAGGCAG TAGGGATGGG TGTTCCCAGC CTTGAGTCAG ATCCTGAGAA GCTCCAGGGC 840 GGGGCACGTT CTGTCTCTGC CATCTGGAAA CCTACCAGCT ACAGCAATTG TCACCTCCAA 900 CAAGAACCCC TGAGCCCGGA AGCTGGGTGA GAGGAACCTC CAGGTACAAC TCTCCACCCA 960 GCACAGACCA GGTCTGCTGA TCTGTGCCAT TCCCTGATGC ACTGTGGCAT CCCGTGACCA 1020 CAGACTGTCA CCCACATCCC CAGAACCTGC ACGGTGCTTG CTTGGTACAG ACTAACTACT 1080 GAGTGTCCAT TAAGCCAAAC TGGTACCACC ATCTGGACCT GTGAAATGTC CTTCAACACT 1140 CCCCCACCCA CCCCTTCCTG CCACGCCCCT CCCTCCCTTC CACGTCCCTC CCTCCCACGC 1200 CCCTCCCTCC CTTCCATGCC CCTCCCTTCC ACACCCCTCC CTCCCTCCCT CCCACAAACT 1260 TGTCTTGAGA CCTACTGTGT TGGGTGGCGA GGAGACGAAG GCCTTGGGAA CCACATTCCT 1320 GTTGCTCCCG 1330
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