Tag | Content |
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EnhancerAtlas ID | HS139-21680 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr16:81725450-81726760 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GLIS3 | MA0737.1 | chr16:81725511-81725525 | CTTAGTGGGGGGCC | - | 6.08 | Sox3 | MA0514.1 | chr16:81726590-81726600 | CCTTTGTTTT | + | 6.02 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_27561 | chr16:81725435-81732612 | Esophagus | SE_31652 | chr16:81725956-81728873 | Gastric | SE_37554 | chr16:81725043-81730268 | HSMMtube | SE_38018 | chr16:81724675-81732959 | HUVEC | SE_50750 | chr16:81724770-81728813 | Sigmoid_Colon | SE_54532 | chr16:81724445-81732958 | Stomach_Smooth_Muscle | SE_65249 | chr16:81724734-81728497 | Pancreatic_islets |
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| Number: 1 | ID | Chromosome | Start | End |
GH16I081691 | chr16 | 81725038 | 81732666 |
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Enhancer Sequence | TCCCGTGTGC ATCCCCGGAG CCCTCCCACC TGTGAGACAA ACCTCAGTTG TCCACCAAGG 60 CCTTAGTGGG GGGCCAGTCA TGTTATGGGG AAGCGAAGTC ACAGCGGGAA GACCCTGGAG 120 ACGTCGGTAC CAGCTCAGCC ACGTCCTCAG CTGTGGGACC CCTGGGGAGG CACATCTTCC 180 CTCAGAAAAA TGGGGAACTC AGGAGAACAG GGACATTGTA GGAGCTGCTT GACTGCATTG 240 TCACAAGGAT TCATGAGCTA AGAATGCAAA CAGAGCCCTC CCCATGGCTC CTGGCAGGCC 300 GTGCAGTTAT CGTCTTTTAT TATGCACCAG ATGGGAACCG TAATACCTGC CGCTCCTCTT 360 CCGAGGGCGA TAGTAAGAAT CAAAAGATAA TGCGCGTAGC ATTGCTCGCT GTGCCGTACT 420 GAGATGCTGG AAGCGCTCTA ATTACGCCCG GTACAACGCT CAGCTCAGGC TCTGCAGCAA 480 ACCTGGCCAG AAACAGACCC TCTGCCTCTC TCTTGCCGGC CCCTAGCACC ATATTGAATT 540 GATCACTGGA AACTAGAGAG AACGCTGTCT GGTGGATAAT GGCCTGAAGA GAAGGCTTTG 600 TCAAAATAAC CAGGCCCTGA AATGCCTCCA GGTCTCTTTC AAGAGGTTGG AAGGAGCAAG 660 CCTCGGGAGG CAGCTGGGGC TCTCGAAGGA GCCGATTACC AAGCGTGTTT AGGAAATGCT 720 GCCTCTGTAA GGGCACATTA CACGCAGTAA TTGCCCCATG TGCTGGCCTG GCCAGTCCCC 780 GAGGGTCCCC AGTACTTGAG GCCGGAGAAA TCCACCTCCT AAGAGGCGCT CAGTCTCAGC 840 AGAGTCGTGA CGTCATTGGC CTCAGTCCCC GTCCCCATAG GCCTGGGCGC TCTTGGCTGT 900 GGCAACTGTC TTAGAAGAAT GGTCCCCCAT GGCCGCTGAT GTGTGCAGTA ATGAGTGCCG 960 CCCGCCTTAA TCGTGGAACA ATTAATGAAC ACACCTGGGT CTCCGGAGCC CACATGCACC 1020 CACACATGCT CAGGCAGCAG CTTAGCCCCT CTTATTCACA GGTGTGGGCA CAGGGAACTT 1080 TCGGGAATGG GGGGCCCAGT GTGTTCATGT TGCTCTGATC TGCCGCCTCC TCAAAGAAGG 1140 CCTTTGTTTT GGAGCTTTGA GTGGGGACAA AATGTTGGCA TTTCACTCAC ATTCCTCTTC 1200 ATTCTTTGAA TCAGACATAA AGTCTAGACG TCCCCAGAGG TTAATCTTGG GAACATTGTG 1260 CTGTTTCCGA CGCTTCTGTT AACCGCCGTG TTTTCCCCTG TTTTTGTTGC 1310
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