Variant report

Variant	rs10749934
Chromosome Location	chr11:108901267-108901268
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:108899961..108902009-chr11:108909481..108912314,2	K562	blood:

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10749932	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10749933	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10789708	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10789709	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10890931	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10890932	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11212864	0.93[AMR][1000 genomes];0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1396910	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1509708	0.80[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1509710	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1912234	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1912235	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1912236	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2136532	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2136533	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2136534	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2175173	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4370904	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4586113	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6589047	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7126518	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7927284	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7927428	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7930665	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7930745	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7938927	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7942258	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7948895	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7952458	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1040650	chr11:108859584-109174553	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv898390	chr11:108893765-109003536	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	esv1815918	chr11:108900487-108948487	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:108894200-108903800	Weak transcription	Osteobl	bone
2	chr11:108899000-108904200	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr11:108900800-108901400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr11:108901000-108904000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr11:108901000-108908800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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