Tag | Content |
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EnhancerAtlas ID | HS139-08382 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr11:268740-269600 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr11:269490-269511 | GTGTGGTTTCAGTTCCTGTTT | + | 6 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_16128 | chr11:267513-270474 | CD4_Naive_Primary_7pool | SE_21864 | chr11:267477-270412 | CD8_Naive_7pool | SE_22226 | chr11:267090-270596 | CD8_Naive_8pool | SE_28519 | chr11:268667-269561 | Fetal_Intestine | SE_52556 | chr11:267492-273530 | Small_Intestine | SE_61820 | chr11:266425-273086 | Toledo | SE_62809 | chr11:266595-290841 | Tonsil |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH11I000266 | chr11 | 266649 | 273455 |
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Enhancer Sequence | GATCCGCCCG CCTCTGCCTC CCAAAGTGCT GGGATCACAG ATATGAGCCA CCGCGCCCCG 60 CCCTTGGCAC TGTTTAATCC ATGTGTTGTT TATTTATGTA TCCTGTTTAT TTTCTGTCTC 120 CCAACAAAGA CGTAGCTCCT TCTGGGTAGG GCATTTTGTT CATGCTCTCA GATGCCGCCT 180 ACCGCCCTAG AGCAGGAAAT AGCGGTCAGC GCCAGCTGTG AGGAGCACAG CATTGCGGCC 240 AACACAGGAG GCACTGACCA CGGGGCAGGC GCTATTTAAA AATCGTGGCA AAGGATCAGA 300 CGTAACAGAA CTCTTTTTGT TTTAATCATT TTTAAGTGTG CAGTTCAATG ATGTTAGTTA 360 CATGCACAAT ATTGTGTAAC CATCACCACT ATTTCCAAAA TCCTTTCTAT CCGTCAGACA 420 GAAACTCCGT CCCCATTAAA CAGCAACTCT GCATTCCTCC GTCCCCCCAG CCTCTGGTCA 480 CGTGTCTCAT CTACTTTCAG TCTCTACGGA TTTGCCTGTT CTAATTATTT CATAGAAGTG 540 GATTCATACA GTACGTGTCC TTCTGTGTCA GGTTCATGTC ACTCAGCGTG ATGTGCCCAA 600 GGTTCACCCA TGCGTCGGGC TCTCATTCCT GAATCGCATT TCTCTGTACG GATAGACTGA 660 GTTTTGTTTG TCTGTTCACC TGTTTAGGAA CACTTGGTTG CTTCCACATT TTGACTGTTA 720 TGAATAACGC TACTAGCAAA GTGAACACGA GTGTGGTTTC AGTTCCTGTT TTCAATTCTT 780 CCGCGTCTTT TAAGAAAAAA CAAACTGTTT TCAACAGTTG CATCATTTTA CCGTCCCACC 840 AGCAACATGG GAGGCTTCCC 860
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