Tag | Content |
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EnhancerAtlas ID | HS127-05976 |
Organism | Homo sapiens |
Tissue/cell | Macrophage |
Coordinate | chr11:75473590-75474780 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr11:75474300-75474318 | ACCCCCTTCCTTCCTTTC | - | 6.14 | EWSR1-FLI1 | MA0149.1 | chr11:75474451-75474469 | TCTGCCTCCCTCCCTTCC | - | 6.44 | EWSR1-FLI1 | MA0149.1 | chr11:75474304-75474322 | CCTTCCTTCCTTTCAGCC | - | 6.65 | EWSR1-FLI1 | MA0149.1 | chr11:75474455-75474473 | CCTCCCTCCCTTCCATCC | - | 6.72 | HNF4G | MA0484.1 | chr11:75474199-75474214 | TAGGGCCAAAGGCCA | + | 6.38 | ZNF263 | MA0528.1 | chr11:75473993-75474014 | TCCCCTCCCCCACCCTCACCC | - | 6.14 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_00075 | chr11:75470367-75491042 | Adipose_Nuclei |
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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 |
GH11I075762 | chr11 | 75473541 | 75474676 |
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Enhancer Sequence | TAAAAATACA AAAAAAAAAT TAGCTGGATG TGGTGGCGGG CGCCTGTAGT CCCAGCTACT 60 TGGGAGGCTG AGGCAGGAGA ATGGCGTGAA CCCGGGAGGT GGAGCTTGTA GTGAGCCGAG 120 ATTGTGCCAC TGCACTCCAG CCTGGGCGAC AGAACGAGAC TCCGTCTCAA AAAAAAAAAA 180 AAGAAAAAAG AAAAAAAGAA ATGGTTTCAC TGCTTTTAAA AAGCTAGAAA CTACTGCTGA 240 ATAATAATTG TCATTTTAGG TGTCTGTTTC TTCCCCCAGA ATGCCCCTAA GGAGCAAGAA 300 CTGTACCCAC AGCACCCAGC ACAAGGATGG GGGGTCTCAG GAAAGGTCGG CCAGATAGAA 360 GGGCAGATGA GAAATGAATG TACTGGGAGC TCTCTGTGTA ATATCCCCTC CCCCACCCTC 420 ACCCCACCCC CCAATTCCTG CAGGGAAGAG GCCTTGAGAG AGTTGAGTAA GAAATAAGCA 480 GGCAGAATGA TGCAAGGGGA GCTGTCTGTA CACATTGCAA CAGAACTTTC TAAAACAAGC 540 CTGGGGCTGC TCCCAAGGGT CTCAGTCCTG CCCTATTCCT CTACTGTCAT CCAGACCTGT 600 CACACAAGAT AGGGCCAAAG GCCATTACCA AGCTCTGCTA AGGCCTGACC TTAGAGCTGG 660 GAGGTCTGTG CTCTTGGGTT CTGGTTTGAA ACCCGGAGCC ATCTTCAATC ACCCCCTTCC 720 TTCCTTTCAG CCCTACATCC ATGCCATCAA ATCCTAGAGA CTCTAAAGCT TCAGCATCTC 780 TCAAAATCAC CCTCGCTTCT CTTTTGCCTT GCCACCCCTT CAGTTCAGGC TCTGTCGTCA 840 TTATCTCTCT CCTTCCTCTC ATCTGCCTCC CTCCCTTCCA TCCAATATCA CCCAGGTCCC 900 TGTGGGTTGT CTGTGCCCCT TCAGCAAAGG CCACAGCTTC CATGTGGCAG CCCTCTCCGC 960 TCAGCCCCCA TTGCACCTGC AGTGTCCTTC TCTTAGTCCT TCAGGCCAGA TCCCCTGTGA 1020 GGTGACTAGT CCTGGGCTAC TGCACCATCC CTTGAGTTTT CTCTATAGCC TGCTTACATC 1080 TTTGCAAACA GTCTTTGTAT TAAACTGTCC TCAAATTACC CAGTTTGGGT GGGCTGTTTC 1140 CCATAGGGAC ACTGACTAAT ATAAGGTAGA GGTAGTTAGG AAGGGTGCCA 1190
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