Variant report

Variant	rs10938793
Chromosome Location	chr4:20314411-20314412
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10516351	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10805216	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10938794	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12233914	0.83[AMR][1000 genomes]
rs12508158	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12511950	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12646142	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12648551	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1344849	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs16869521	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs16869526	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1853386	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs3945867	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4697157	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs55911061	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs58086451	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs61333152	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs66478358	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs66615925	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs66875143	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs66960874	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs66981451	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs67264035	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs67506381	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs72619155	0.86[AMR][1000 genomes];0.85[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	nsv593792	chr4:20275477-20362716	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv593793	chr4:20282334-20333722	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv878740	chr4:20292239-20333722	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:20291800-20319000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr4:20299400-20319000	Weak transcription	NHLF	lung
3	chr4:20301400-20316800	Weak transcription	NHDF-Ad	bronchial
4	chr4:20306200-20325600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr4:20309600-20314800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr4:20310000-20315000	Weak transcription	Fetal Lung	lung
7	chr4:20312400-20317000	Weak transcription	Colon Smooth Muscle	Colon
8	chr4:20313000-20318600	Weak transcription	Brain Angular Gyrus	brain
9	chr4:20313600-20319000	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr4:20314000-20318600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr4:20314000-20319000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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

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