Variant report

Variant	rs231286
Chromosome Location	chr8:113840219-113840220
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10081489	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10106945	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10216504	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10216505	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12334432	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13261060	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs1549354	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17652171	0.88[CHB][hapmap];0.88[JPT][hapmap]
rs1991136	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1991137	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2113666	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2161925	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap]
rs2194598	0.85[ASN][1000 genomes]
rs231279	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs231281	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs231285	0.88[CEU][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs231289	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs231316	1.00[CEU][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs231319	0.94[CEU][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2355821	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2432737	0.80[CHB][hapmap];0.89[JPT][hapmap]
rs2432738	0.80[CHB][hapmap];0.89[JPT][hapmap]
rs2432739	0.80[CHB][hapmap];0.89[JPT][hapmap]
rs2432742	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2446470	0.80[CHB][hapmap];0.89[JPT][hapmap];0.89[ASN][1000 genomes]
rs2446471	0.80[CHB][hapmap];0.89[JPT][hapmap];0.89[ASN][1000 genomes]
rs2446472	0.80[CHB][hapmap];0.89[JPT][hapmap]
rs2511531	0.80[CHB][hapmap];0.89[JPT][hapmap]
rs2511532	0.80[CHB][hapmap];0.89[JPT][hapmap]
rs2511534	0.89[JPT][hapmap]
rs4567066	0.89[JPT][hapmap]
rs4876480	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs57897007	0.80[ASN][1000 genomes]
rs61291053	0.82[ASN][1000 genomes]
rs61584754	0.87[ASN][1000 genomes]
rs6999481	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7004983	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7005129	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs72678452	0.80[ASN][1000 genomes]
rs72678454	0.80[ASN][1000 genomes]
rs72680285	0.87[ASN][1000 genomes]
rs73700769	0.80[ASN][1000 genomes]
rs7817596	0.82[CHB][hapmap];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7817836	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7832050	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap]
rs889987	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.87[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs9297478	0.80[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap]
rs9297479	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap]
rs9297480	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2753595	chr8:113283214-114190390	Enhancers Weak transcription Active TSS Strong transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
2	nsv534270	chr8:113585830-113979075	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	3 gene(s)	inside rSNPs	diseases
3	esv2754315	chr8:113736824-114048824	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv524089	chr8:113761143-113852777	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
5	nsv891326	chr8:113777669-114091732	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv891327	chr8:113828980-114109342	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:113838800-113855800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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