Tag | Content |
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EnhancerAtlas ID | HS139-08392 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr11:479150-480340 |
Target genes | Number: 27 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
E2F6 | MA0471.1 | chr11:480205-480216 | TCTTCCCGCCC | - | 6.14 | E2F6 | MA0471.1 | chr11:480262-480273 | TCTTCCCGCCC | - | 6.14 | E2F6 | MA0471.1 | chr11:480319-480330 | TCTTCCCGCCC | - | 6.14 | INSM1 | MA0155.1 | chr11:480081-480093 | TGACCCCTGACA | - | 6.18 | SOX10 | MA0442.2 | chr11:479653-479664 | GTCTTTGTTTT | - | 6.14 | ZIC3 | MA0697.1 | chr11:479288-479303 | GAGCTGCGGGGGGTC | - | 6.03 | ZIC4 | MA0751.1 | chr11:479288-479303 | GAGCTGCGGGGGGTC | - | 6.16 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_05234 | chr11:478630-480362 | Brain_Cingulate_Gyrus | SE_06093 | chr11:478471-480357 | Brain_Hippocampus_Middle |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I000478 | chr11 | 478472 | 480362 |
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Enhancer Sequence | AGGTAAGCTG TTTTTCTGGG TTGGATACCT GGGAACTTAG GTGACAGTGT GGCCCCAGGC 60 ATGGTGACAA AGGAGGCCTT GCCCACACAG CCCTCGAGTG ATGGGAGGAA GCAGGGCTAG 120 ACCCCCACAA AGTAGGCCGA GCTGCGGGGG GTCTCCAGGA GCATCTGTGC GGCCCTTGAG 180 TGATGGGGGG CAGCAAAGCT AGACCTTCAA AACGTAGGCC GAGCTGCGGG GGGCCTCCAG 240 GAGCATCTGC TGGTGGGGCG CTGACTGTGG CCATTTAGCA GGGCCACACT TAAGGAGGGC 300 AGGGCCAGTG GTGCAGGCAC AGAAGAGGGC AGGGCCAGTG GTGCAGCTGC CAGGGTGGCT 360 TTGCCCACAG CTGTCGTATC TGAGTGCTGG TGGGGACTGG GCGTGAAGGG AGCCGCAAGT 420 CAGGTCCTGC GATGCAGGCC AGCGTCTGCA TGGCCGGGGC AAATCTGGGC CTCAGAGGGG 480 ACCCCAGCGC CAAGAGGGAC GGGGTCTTTG TTTTTGTGTT TTGTGGTTGA CCAGTGTGAC 540 TGTGTGTGCT TCTTCCCCAT CCTGACCACA TTCTGCAAGA CGAGCAGGGT GCAGGTGGGA 600 GACGCAGCTC CTTTGTAAAT CCTGGGTCAG GCTGTGTTGC TGCTGCAAAT GCCTACTTTA 660 TTAATACTCT TTGTTCTGTT TAACTTAGTG TAAACACACA TTTTTGGGGC TGTCTTCAGC 720 TTACAAAGGA CTTTATTATT CCCAATCTTA AAACTCCATC AGTGCATGAT GAGATTTTTT 780 ATCATCGTGG CAAAATTGAC TTTTCTGAGG CAGTGTACAT TCTGTGAATT TTAGCATTTG 840 TGTAGACTTC TAGAAACACA ATTAGGACGC ACAAGAATTC CACTGGCCCT AAAACTCCTT 900 TGTGTTACCC CTTGGTAGTC ATACCCGGCC CTGACCCCTG ACAGCTGGTG AGGGTTCGCT 960 TCTGTCTCTT CTAGAATGGA ATCGTGGGGT GGGCAGCCTC TTCCCACCCT GCACAGTGCC 1020 TCTGAGGTTC ACCCAGGATC ATGCGGTGGG CAGCCTCTTC CCGCCCTGCA CAGTGCCTCT 1080 GAGGTTCACC CAGGATCATG CGGTGTGCAG CCTCTTCCCG CCCTGCACAG TGCCTCTGAG 1140 GTTCACCCAG GATCATGCGG TGGGCAGCCT CTTCCCGCCC TGCACAGTGC 1190
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