| Tag | Content |
|---|
EnhancerAtlas ID | HS182-22480 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chrX:53115850-53116950 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chrX:53116738-53116756 | ACTGCCTTCCTGCCTCCC | - | 6.09 | | EWSR1-FLI1 | MA0149.1 | chrX:53116742-53116760 | CCTTCCTGCCTCCCTCCA | - | 6.15 | | ZNF740 | MA0753.2 | chrX:53115948-53115961 | GTGGGGGGGGTGG | - | 7.52 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH0XI053087 | chrX | 53115801 | 53115970 | | GH0XI053086 | chrX | 53116059 | 53118781 |
|
Enhancer Sequence | GCGCATTTCC AGGCTTGTGT TGGGAGCAGA GCATGAAGTG AACAGTGTGC TCTCTGAGTC 60
CAGAAAAGGG TGCAGCCAGT TCTACCTCAA GAATCGGGGT GGGGGGGGTG GCGGGGGAAG 120
AGCTAGAGGA AAAAGGTGAC ATTTGAACTG GAGGATGCAT TCACACTGAG GAGCTTTATG 180
GAGCATTCTC CGTGGAGTGG ATCATCTGAA CAAGGACCTG GAAGGGTGAA AATGCATCGT 240
AGGTTGGGCA GGGTTTCCAA AATTATGTCC TGAGGATCAC TCACCAGATC TGAAAGCTGC 300
TTCCCACAAA AGGTTTCAGT GGTCGTATAT GTTGGACAAG TACTGCATAT AGTAATACCC 360
TCTTGTAGAG TCACATTAGC ACCTTAAAGG CTCTGAGAAT AACACGAGAA TTATAAAGGT 420
GCTGAGAAGT ACTCAGATGG GAGGTGGAAG GGGCAGGAAA ATCAACTACT CTTCGGGTTT 480
TTTTGGCTAT GGGGTCCCTG GCAAACTTCC ATTGAGGGCA AGGCCAGGGC ACTAAGGGAA 540
GAGGAATGAA TGTGGAGCCT CAATCTAGAC ATGTTCAGGT AGGAGAGAGA AACAGGGATT 600
CTCAGTTCTC TTCCCCTCCC ACCTGATGGC ATCTCTTTTC TCAGAAGGGG AGGCAGAGCT 660
ATCTGCCCAG CCCTGAGGGT GGGAGTGGGG GTGGGGAATT GGGTTGCAGA ACACAAACTA 720
GGGCCTCTTT GGATCAGACT GGGGGAGAAA GCGAGGAAGC TGCCTGGAGA TGAATAGGTT 780
TATTCAGCTG AGGTCAGAGC TCAGGAAGAG ACACACATTG AGGAGTACAA GGGGGAGAAA 840
AAGCTACTAT CAGAGATGTA TCAGTTTTGA CAGAGGCAGG GATCCCACAC TGCCTTCCTG 900
CCTCCCTCCA TCTCCCTCTC ATTCTGTGGG CTTGCTTGAG TACACCCACA CACACTCTTG 960
GCTGTTTGTT CCAAGCAGAG GCGCTGACAA GTTGTCCCAG GCCGCTAAAA ACCCTGGCTA 1020
TGGTCTCTGT TCCCTTTTAG AGTGACACCT ATCTGCTCAT CTAACTGCCT TCCTCCATTT 1080
CCCCTTCCTT GCTTCTCCCC 1100
|
