Tag | Content |
---|
EnhancerAtlas ID | HS055-01542 |
Organism | Homo sapiens |
Tissue/cell | FT33 |
Coordinate | chr11:66724220-66725790 |
Target genes | Number: 11 | Name | Ensembl ID |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GFI1 | MA0038.2 | chr11:66724249-66724261 | TGCTGTGATTTA | - | 6.27 | Gfi1b | MA0483.1 | chr11:66724249-66724260 | TGCTGTGATTT | - | 6.62 | PLAG1 | MA0163.1 | chr11:66725522-66725536 | GGGGCGCTCGGGGG | + | 6.13 |
|
| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_34745 | chr11:66723671-66727204 | HeLa |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TCTCCTCTCT CTCGCTTTAG TGTGTGGTTT GCTGTGATTT ACTGGCCTCT ACTGAACTTC 60 CTCTTCCATG TCCTCCTAGG GCCAATACCT CACCCACTAG GCTCTCTACA AACATCTGCA 120 GCAGGCTGCC TTGCTGCTTA GGTTTTGTTT ATTTTCTCTC TCCCCCAATG GGTTTGTCAG 180 CAGTTGCAGG ACAAGGATTG ACCTCATCGC CCACGCTGTC TCTCGGCCCA GTGTAGGGAT 240 AGGAACACTG TAGGTGTGCA AAAGAATGTG ATTAAGAGTT CAACAGTTAA GGAGAGCCTG 300 CAGGCAGGAA GCTGTAGCTG CAAGTGAGAG AAATGCTGAG CACATCCACC CCCAGCACAA 360 GTGTTTGCAT CACATACAGG GAAAGGGTGC CTTGGGGGAG GCCAGCCAGG GCTGATGGTG 420 GCAGTGGGTA CGGGAGCAAT AGGGAGGCAG ATGGCAGGCA CTCTGGAGGT TCTGGTTGTC 480 ATCAGCAAGT GTTGGTACTT CTCTGAGCCT GTTTTCTCAG CTGGAGAACG GGTAAGGAGC 540 CCAGGCCTAC CTCTTCTCAC AAAATAAAGA CACAATCTGA TTTTTTAGAA TTTCAGACGA 600 GGCACGCCTG TAATCTCAGC ACTTTGGGAA GCCAGGGCAG GCCGCTCGCT TGAGCGTAGG 660 AGTTCGAGAC CAGCCTGGGC AACATGACGG AACCTCGTCT CTACCAAAAA ATACAAAAAT 720 TAGCTAGGCG TGGTGGCGCC CGCCTGTAGT CCCAGCACTG GGGGACTGTG GCAGGAGGGT 780 CGCTTGAGCC CGGGAGGTCG AGACTGCAGT GAGCCGAGAT CGCGCCACTG CACTCCAGCC 840 TGGGTGGGTG ACAGCAAGAC CCTGTCTAAA AAAGAAAAGA AAACAAAAGA ATCTCAAAGT 900 TGCCAGGGAC CTAGGGACTT GGCTTCCGAC TCTGATGCGC TTTGTAAACT ACTAAAAGCT 960 GGAGAAATAA GGGGCTGAGC CCAGCCCCAC CTCCTGAATG AGCGGCCTTG GGCGAATCAC 1020 TGCGTCTGGG CGCCTGGAGC TTCCCCGTCT GAAACAAAGT AGAGGATCCT ACGGGAGGCG 1080 GAGTGCGAGA GCAAGGAACA AGGAAAGCCC TCGCCTTACA CGCCGCGGCT TCCTGCAGAG 1140 CTGAGCCACA TCCAGTACGA TGGGGACAAC TTGGGCTCCC GATCCTGACA GACTTGGGTT 1200 CGAACCCTCA GGGACCTCGC GCGAGGCGCT TTAGTCAGTT TCTCCATCTG CAAAATGGGC 1260 CCGAGAGCAA GAATGAGGCA GCCCGCAGGC GGACGCTGCG GAGGGGCGCT CGGGGGCTGC 1320 AGCCGGGGGC GGGTCCGGGG GCGGGTCCAG CCGGCCGAGC CCCCGCGCGA GGGGGAGGGG 1380 CGCCGTCCGC TGCGTCGCGT CGCGCACCGC GCACAGCCCG TCGCTGTCTC CTCCAGCCGT 1440 CACTCGCGGA GCCCGCGCCG CCTTTGCGCG CGCGACCCTT ACATAAGCGT CCCTCGCAGC 1500 GGTGCCGGCG CACGTCCACC CGCTCCGACC CGCCGCGGGA AGAGGACCGT GCGGAGCGCG 1560 GCGGACACTC 1570
|