Tag | Content |
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EnhancerAtlas ID | HS105-15246 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr11:75473820-75474780 |
Target genes | |
SNPs | Number: 1 | 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 |
|
| 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 | CTACTGCTGA ATAATAATTG TCATTTTAGG TGTCTGTTTC TTCCCCCAGA ATGCCCCTAA 60 GGAGCAAGAA CTGTACCCAC AGCACCCAGC ACAAGGATGG GGGGTCTCAG GAAAGGTCGG 120 CCAGATAGAA GGGCAGATGA GAAATGAATG TACTGGGAGC TCTCTGTGTA ATATCCCCTC 180 CCCCACCCTC ACCCCACCCC CCAATTCCTG CAGGGAAGAG GCCTTGAGAG AGTTGAGTAA 240 GAAATAAGCA GGCAGAATGA TGCAAGGGGA GCTGTCTGTA CACATTGCAA CAGAACTTTC 300 TAAAACAAGC CTGGGGCTGC TCCCAAGGGT CTCAGTCCTG CCCTATTCCT CTACTGTCAT 360 CCAGACCTGT CACACAAGAT AGGGCCAAAG GCCATTACCA AGCTCTGCTA AGGCCTGACC 420 TTAGAGCTGG GAGGTCTGTG CTCTTGGGTT CTGGTTTGAA ACCCGGAGCC ATCTTCAATC 480 ACCCCCTTCC TTCCTTTCAG CCCTACATCC ATGCCATCAA ATCCTAGAGA CTCTAAAGCT 540 TCAGCATCTC TCAAAATCAC CCTCGCTTCT CTTTTGCCTT GCCACCCCTT CAGTTCAGGC 600 TCTGTCGTCA TTATCTCTCT CCTTCCTCTC ATCTGCCTCC CTCCCTTCCA TCCAATATCA 660 CCCAGGTCCC TGTGGGTTGT CTGTGCCCCT TCAGCAAAGG CCACAGCTTC CATGTGGCAG 720 CCCTCTCCGC TCAGCCCCCA TTGCACCTGC AGTGTCCTTC TCTTAGTCCT TCAGGCCAGA 780 TCCCCTGTGA GGTGACTAGT CCTGGGCTAC TGCACCATCC CTTGAGTTTT CTCTATAGCC 840 TGCTTACATC TTTGCAAACA GTCTTTGTAT TAAACTGTCC TCAAATTACC CAGTTTGGGT 900 GGGCTGTTTC CCATAGGGAC ACTGACTAAT ATAAGGTAGA GGTAGTTAGG AAGGGTGCCA 960
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