Tag | Content |
---|
EnhancerAtlas ID | HS052-31739 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr5:176521170-176522330 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr5:176522000-176522018 | GCTTCCTTCCTTCCTTCC | - | 10.05 | EWSR1-FLI1 | MA0149.1 | chr5:176522004-176522022 | CCTTCCTTCCTTCCTGCT | - | 7.69 | MAFK | MA0496.2 | chr5:176521408-176521427 | ATATCCTGTGTCAGCATTA | + | 6.2 | ZNF263 | MA0528.1 | chr5:176522003-176522024 | TCCTTCCTTCCTTCCTGCTCC | - | 7.23 |
|
| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_30460 | chr5:176520882-176523067 | Fetal_Muscle |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr5 | 176521400 | 176522200 | chr5 | 176521557 | 176522307 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH05I177093 | chr5 | 176520362 | 176528755 |
|
Enhancer Sequence | GTGAGCCCTG GAGCTGGGAG AGGCTGTGGG ATCCCACCCT TAAACCTGCA ATTCACCTCT 60 GCTCCTGACC CTGGCAAGTG ACTTCTGAGC CTCAGTTTTC CCTTGTGTCA TATGGGGTAG 120 ATAACAGTCC CTACTCCCAG CCCAAGGATT GTGGAAAGTG CCTGGCTCAT AGTCAGGGCT 180 CAATAAATCT TCACCACTGG GGTGATGATG ATGAGAAGAA TTTGGTGTGA CAGGCTTGAT 240 ATCCTGTGTC AGCATTAGTC TGTGTCAGCT TTGACTTCAC ATCTCCTTGT CAGCCTCACA 300 GGCCCTCTAC CTCCTTCCTT ATGGTTCCCC CCAGACACAC CCTCAGCCTC CCTTGGACCC 360 TCCCTAGGTC TGCCCCCCAC GTCCACTGCT GTAGGAGGAC AGCCCTTCTG CTTGCACCCA 420 GGCCCAGCCC CGGGGTGCTC TTGCTGGGCA CTCCTGCACC CCACCCATCA GGGCCTCTCC 480 TTGCAGTTCC CCAGCCCCCT CTGCAAGAAT GGCCTCCACT GCTCTTCTGC TCCTCCCCTC 540 CTCTCTACAC AGCTGGGGCC ACCTGGTGCT CCCTGGGAGG CAGGGATTGA GAAATGCACA 600 TTGTGTCATT GGCCCAGGGC CACAGGTCAG CCCCAGGGGC TCAGCCAGAG AAGCCAAAGC 660 AGCCTTCTTC CCAAGCTCCC CGGCTGCACC CGGCCTGCCG CCAGCTCCCT GAATTCCCAG 720 GCCAGTTGGA AGCCAGGCCC TGGTCAAACA GACCCCAGGG CGCCAGCCTG CTTTCCGCAC 780 CCAGAAGCTC TGACCCCATG CGGGGACTAC CGCTGACCCC TCCAGCGGCA GCTTCCTTCC 840 TTCCTTCCTG CTCCGAGCTC TTCCCCTCTC TCCTGTGTCC TGGGCCTGCC CGCTGGAAGG 900 CCTGCCTCTT AGATCCTTGA TACAGTTGCA TCCTTGCAAC TGCTGTGACA GGCAGGGTGT 960 GACCCACTGC TCTGTTTCCC ACAAGACGAA CCTGAGGTTC AGAGACGCTA GGAGACTTTT 1020 TCAAGGCCAC ACAGCCTAGC AAGGATTCAG CCCTAGACCT ACGTAGCCCT GGTCCAGTGC 1080 TGCTTGTCCT GCACCTGCCT CTGCATGCTC CCTCGTGCAG TTGGAGGGCA GCCTCTTCAC 1140 CCCGTCTGCT GCCCTTACAG 1160
|