Variant report

Variant	rs491394
Chromosome Location	chr7:78482180-78482181
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs1207820	0.92[YRI][hapmap];0.94[AFR][1000 genomes];0.83[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs12670051	0.85[ASN][1000 genomes]
rs1928911	0.85[ASN][1000 genomes]
rs1928912	0.85[ASN][1000 genomes]
rs2065198	0.88[ASN][1000 genomes]
rs472023	0.86[CEU][hapmap];0.92[YRI][hapmap]
rs4730552	0.89[ASN][1000 genomes]
rs474780	0.87[ASN][1000 genomes]
rs488478	0.87[YRI][hapmap];0.90[AFR][1000 genomes];0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs492944	0.92[YRI][hapmap]
rs504216	0.85[CEU][hapmap];0.96[YRI][hapmap]
rs508142	0.88[ASN][1000 genomes]
rs508841	0.81[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs514025	0.80[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs514156	0.95[YRI][hapmap];0.97[AFR][1000 genomes];0.84[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs514951	0.84[YRI][hapmap];0.86[AFR][1000 genomes];0.80[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs516085	0.96[ASN][1000 genomes]
rs522601	0.97[AFR][1000 genomes];0.84[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs527231	0.89[ASN][1000 genomes]
rs529602	0.96[ASN][1000 genomes]
rs535355	0.91[CEU][hapmap];0.92[YRI][hapmap]
rs535451	0.86[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs541737	0.98[AFR][1000 genomes];0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs546953	0.92[YRI][hapmap]
rs550607	0.86[CEU][hapmap];0.92[YRI][hapmap]
rs552822	0.88[YRI][hapmap];0.93[AFR][1000 genomes];0.83[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs564808	0.89[ASN][1000 genomes]
rs571376	0.96[ASN][1000 genomes]
rs571502	0.81[YRI][hapmap];0.86[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs576744	0.88[YRI][hapmap];0.92[AFR][1000 genomes];0.83[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs578047	0.91[ASN][1000 genomes]
rs578326	0.92[YRI][hapmap];0.97[AFR][1000 genomes];0.84[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs6950191	0.84[ASN][1000 genomes]
rs7794352	0.85[ASN][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	nsv607657	chr7:78329795-78483211	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv949647	chr7:78406281-78495913	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv1024961	chr7:78432257-78483201	Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:78478600-78484600	Enhancers	Muscle Satellite Cultured Cells	--
2	chr7:78478600-78484600	Enhancers	HSMM	muscle
3	chr7:78479800-78482400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr7:78481000-78482200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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