| Tag | Content |
|---|
EnhancerAtlas ID | HS182-19051 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr6:109561100-109562170 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr6:109561945-109561963 | TGAAGGAAGGAAAGTAAG | + | 6.04 | | NR2C2 | MA0504.1 | chr6:109561797-109561812 | TGACCTCTGACCCTC | - | 7.34 | | Nr2f6 | MA0677.1 | chr6:109561797-109561811 | TGACCTCTGACCCT | - | 6.93 | | Rxra | MA0512.2 | chr6:109561797-109561811 | TGACCTCTGACCCT | - | 6.73 | | STAT3 | MA0144.2 | chr6:109561663-109561674 | CTTCTGGGAAA | + | 6.62 | | ZBTB18 | MA0698.1 | chr6:109562064-109562077 | GAACATCTGGCTA | - | 6.15 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_00650 | chr6:109556393-109565577 | Adipose_Nuclei |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr6 | 109561585 | 109561717 | | chr6 | 109561733 | 109561874 | | chr6 | 109561956 | 109562129 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH06I109235 | chr6 | 109557181 | 109562202 |
|
Enhancer Sequence | CCTCAGTCAC TGGGCCCCAG GAGACAGAAA GGAGCAGGGC TGAGAGGGAC GACATGCTCC 60
AGGGCTCATG TCACACTGAT ATGTGCGCCA GGAATGACCG CCCATGTACT CCTAAAGTTC 120
AACCCACCCA CCAGTTCAGT CAAGAATTAT GCTTTTAATT CTTCATGTTT GGCCACTGAA 180
GATCAAATCC ACCATGATAA CAGGATTTCA GTACAACAGG CTCTTTCCAG TTACGACAGA 240
CAAAGATGTC CAGGCTCTTG ATAAGAAACA AAAGTTCCTT TGACTTCTCT TGCGAGGACC 300
GAAGAGATAA ATGTTTTCTT TGTGATCTGT TGAAATGTTT ATATAGACTT GAAAAAACAA 360
CTAACAGTCA TTCTGTGCTC TGGTTCCCTG GAAGGTTTCT CATGATCTCC CCTTCAATAG 420
CTAGAGGGCT TGTGTGTCAG GGAACAAAGA ATTAAGACAC TTTAAGCGAT AAAAATCCTA 480
GTGCAACACT CAGAGGCAGA TCGTGGGCTT GAGGGGGCCG GAGGGGTGCG AGGCAGGTGC 540
TTTGACTGAG GAGCAGGTGC TGCCTTCTGG GAAAGCCTAG TGGAGACAGA AGCAGGAGCA 600
GGAAGCCCTG CCAGGGAAGG CCCAGTTTCT TCCTTGCTCT CCTGAGGTAC AAGGGACAGC 660
ACGGCCCCTG CATTTTCATT TCTCAGGGCC AAAGACCTGA CCTCTGACCC TCTACCCACT 720
CTGGTGACCT GCACGCTAAA TTGGGTGGTT TCTGACTAAA ACAGGCTTAA GCCAAGAATT 780
GGGATTTTAC TCCCAGGGGC ATTTCTGCGT CACCCACTGG GTGCAGGGGA TGTGGTGCAG 840
GACCCTGAAG GAAGGAAAGT AAGCAAGTGA AACAAATGAC TTTTCTAAGT GGTAGACCTT 900
GAGGAAACTG CATTTAGCAG CAGAGACAGC CCTGAGTTCC TAACAGGAAA CCACTAGGAT 960
GCAAGAACAT CTGGCTAGGA AAATGCCAGA CAAGCCCCAG AGGAAGAAAT CATTACTCAG 1020
GGTAATCAAG TAACCCATAA CCTGTATTTT CTCTTCCTTT TGGCATCACT 1070
|
