Variant report

Variant	rs10742756
Chromosome Location	chr11:45454283-45454284
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10160422	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10742753	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10742754	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10742755	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10769141	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1156593	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1156594	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1387055	1.00[EUR][1000 genomes]
rs1488662	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1873055	0.88[AFR][1000 genomes]
rs1906582	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1906584	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1906585	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2044872	0.91[EUR][1000 genomes]
rs2044874	0.88[AFR][1000 genomes]
rs2044875	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2167377	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4497379	0.89[EUR][1000 genomes]
rs6485624	1.00[EUR][1000 genomes]
rs7126146	0.85[EUR][1000 genomes]
rs7929511	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7929683	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7942441	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7951748	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7951947	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs896345	1.00[EUR][1000 genomes]
rs985140	0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530619	chr11:45294176-45553928	Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv1045831	chr11:45419113-45580407	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv1049520	chr11:45430802-45494235	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
4	nsv541026	chr11:45430802-45494235	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:45436400-45456800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr11:45447800-45462400	Weak transcription	Fetal Brain Male	brain
3	chr11:45453800-45454800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

what's new

Quick links