Variant report

Variant	rs4986187
Chromosome Location	chr18:44872493-44872494
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs1019989	0.89[GIH][hapmap];0.82[TSI][hapmap]
rs1583387	0.93[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs28450247	0.92[AFR][1000 genomes]
rs4986188	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4986211	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6507728	0.90[AFR][1000 genomes];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7235455	0.89[GIH][hapmap];0.82[TSI][hapmap]
rs7239378	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs8094937	0.96[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9947662	0.82[EUR][1000 genomes]
rs9952058	0.82[CEU][hapmap];0.86[YRI][hapmap]
rs9953407	0.92[AFR][1000 genomes]
rs9959021	0.90[CEU][hapmap];0.82[YRI][hapmap];0.88[AFR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv833641	chr18:44815063-45020202	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA miRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:44871800-44872800	Enhancers	Pancreas	Pancrea
2	chr18:44871800-44873600	Enhancers	Brain Germinal Matrix	brain
3	chr18:44872000-44872800	Enhancers	Fetal Brain Male	brain
4	chr18:44872400-44872600	Enhancers	HSMM	muscle

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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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