| Tag | Content |
|---|
EnhancerAtlas ID | HS098-37041 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr22:38590380-38591180 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr22:38590451-38590469 | GGAAGGAGGAGAGGTAGG | + | 6.22 | | RARA(var.2) | MA0730.1 | chr22:38590692-38590709 | TGACCTTGTCGTGACCG | - | 6.22 | | ZNF263 | MA0528.1 | chr22:38590886-38590907 | GGGGGTGGGGAGGGGGGGGAG | + | 6.14 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_28874 | chr22:38589495-38590460 | Fetal_Intestine_Large | | SE_41851 | chr22:38590334-38590886 | LNCaP |
|
| | 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 |
| GH22I038194 | chr22 | 38590407 | 38590608 |
|
Enhancer Sequence | AGGCTAGGAG GGCTGAAGCC ATTTGCTTCA GAGGGAGGGG ATGGGGACTG GGGTGTGGGC 60
ATGGGGATTC TGGAAGGAGG AGAGGTAGGT TTAGGGCAAG ACAAAGGACA GCCTCTGAAG 120
GGACTGGGAG GGAGAGGGAA GGGCAGGTGC AGAGGGTCGA GGCAGTGCCT ATCACATGGC 180
CTCTGCTTCC TCTGGAAGTG GCAGGAGAGC AGGTTCGATG GAGATGAGGA TGAAGGCCTG 240
CGGATGAAGG AGAAAGGCGA GTACTCCAGG GATTCCTGGC AGCTCTGAGG ATCTGGCTGT 300
GACTGGAGAA GATGACCTTG TCGTGACCGC AGCTGTTGTT GCAGTGGTGG TTGTGGTCGC 360
GATGGTGGCT TCTCTCCAGA AGCCAGAGCA GCTGGCATGC AGGAGTGAAG TGCACGGAGC 420
AGCAGTGCCC CAGCGATGGT TTTACAGGCT TGGCACAAAA GGACTCAGAC CAGGGCTGGC 480
ACATCTCCAG GTATATTGAA GCTGCTGGGG GTGGGGAGGG GGGGGAGGTT TTAGAGGGAA 540
AATGATGGAG GGCTGGGGAA AAATGGAGCA TGTGCAGTAC TGTTTCAGGT TCCTAAAATA 600
TCAGTTTGCA AACATAAAAA TGTATTCTCT AAAATAGGCA AAGCACACGA ACAAAAGAAG 660
AAAAAACCCA ACTGGTTAAC AAGCAAATGG GAATGTGTTC AAGCTCATTC CTATTCAGAG 720
AAATGCAAAT TTAAATACAA TAACGTCATT TGCCTAGGAA ATTAGCAGAG CTTAGACAAT 780
GAAAACTCCC AGTGTTGGTG 800
|
