Tag | Content |
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EnhancerAtlas ID | HS116-06494 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr11:62165390-62166530 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr11:62166368-62166379 | AGTGACTCATG | + | 6.14 | Mecom | MA0029.1 | chr11:62166245-62166259 | TGTTGTCTTATCTC | - | 6.16 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_26858 | chr11:62165319-62171408 | Esophagus | SE_30860 | chr11:62165065-62171276 | Fetal_Muscle |
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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 |
GH11I062394 | chr11 | 62161921 | 62170750 |
|
Enhancer Sequence | AATTGTTCAA ATCCAGCACC TTTCTTACTG GCACTGCTTG CTGGGTAGTT AGGGCCCCGG 60 GCCCCTCGGC GTCGCATCTT CTGCTTGTCA GGCTGCCCCT CGTTGAGTGA GGGAAGCACC 120 TGGCTGAACA CCACCACAGG CGCTGGGGGC CAGGCCGACC ATTTCAAACA GAAATGTCGA 180 CACCCTGCCA CCGCAGGAGC CATGCAGCGC TGGCCTGTGG GCTGGGGAGG GTTTGGAAAG 240 GGAAATATGG GTTGTGCCAA AGCACAAGGC CCCACCCAGA AGTTTGGCAA AGGGTGACTT 300 GGAGTGAGAA GAGCAGGTGG GGAGCAAGTC CACCCTGCGC CACCACCAGG AAAGGACCTG 360 CCCCCACCCT TCCTCAGCGG CCTCTTCCCA GGTCACTTCC CCTCATACAA AAAGCGTGTG 420 TGCTCCCTTC CCAGCTCCCC TCACCTCAGC CTTTCCCACA CAGCTAGGAG CCAGAGCTAC 480 CCCACGTGCT TGTTGGCCAA AGGGCCACTT TCAGAAGTGT TTACAAATTA CCCCAGGTGG 540 AGGCCACTCA CACCAAATCC AGGAACATTT ACCTCGGGCA TAGAACCACA TTCCCTGGCT 600 ACCCAGTGAA GATCCCCGGG GGCTCGAACC CCCAAATTCT CCCAACTTTC TTTGCAGACA 660 CCAAGTATTT CATCTTTTTT AAAAGTAAGA AACACCAAGG CCAGTTCCCC TCCTCCTCCC 720 ATCTGCTCCC CGCCCCTCCC CTGGGCCCAC TCCCGCTAGC GGCGGCGGCT CATTGCAGGC 780 CGGCATGTCT CCCCGGTGAC CTCACCCCAG ATCTGGCCTT TCTCTGTCAG GCCTCACAAT 840 CTTCCGGGCC ATCTTTGTTG TCTTATCTCT GGCTTTGGCA CAAATATCAC ACCCTGGATG 900 CCTCATGACT AAAAGTCCAT CACTTTCCCC AAGCCCTTTC CCTGTCTTCC CTAGAAATTC 960 CAATATATGG CCAGGCGCAG TGACTCATGC CTGTAATCTC AGTTCTTTGG GAGGCCAAGA 1020 CAGGCAGATG ACCTGAGGTT AGGAGTTGAA GACCAACCTG GCCAACATGG TGAAACCCCG 1080 TGTCTACTAA AAATACAGAA TTAGCTGGAC GTGGTGGTGC AAAACCCCGT GTCTACTAAA 1140
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