Variant report

Variant	rs415276
Chromosome Location	chr8:50841799-50841800
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 133 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:131)

rs_ID	r²[population]
rs10086004	0.85[EUR][1000 genomes]
rs10089399	0.85[EUR][1000 genomes]
rs10090657	0.85[EUR][1000 genomes]
rs10092384	0.85[EUR][1000 genomes]
rs10504092	0.85[EUR][1000 genomes]
rs1074385	0.86[EUR][1000 genomes]
rs11785147	0.85[EUR][1000 genomes]
rs12542041	0.85[EUR][1000 genomes]
rs13251355	0.86[EUR][1000 genomes]
rs13264385	0.81[EUR][1000 genomes]
rs13267366	0.84[CEU][hapmap]
rs1352112	0.85[EUR][1000 genomes]
rs1352117	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];0.95[EUR][1000 genomes]
rs1385311	0.84[CEU][hapmap]
rs1385974	0.85[EUR][1000 genomes]
rs1385975	0.85[EUR][1000 genomes]
rs1385976	0.84[EUR][1000 genomes]
rs1486241	0.85[EUR][1000 genomes]
rs1486242	0.85[EUR][1000 genomes]
rs1486243	0.85[EUR][1000 genomes]
rs1486245	0.83[EUR][1000 genomes]
rs1486251	0.85[EUR][1000 genomes]
rs1486252	0.85[EUR][1000 genomes]
rs1486258	0.84[TSI][hapmap];0.81[EUR][1000 genomes]
rs1552372	0.85[EUR][1000 genomes]
rs1580468	0.86[EUR][1000 genomes]
rs167629	0.92[CEU][hapmap];0.88[EUR][1000 genomes]
rs167630	0.84[CEU][hapmap]
rs16913838	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs16913881	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs16913981	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs17674783	0.85[EUR][1000 genomes]
rs17747294	0.85[EUR][1000 genomes]
rs17747567	0.85[EUR][1000 genomes]
rs17747896	0.85[EUR][1000 genomes]
rs17747929	0.85[EUR][1000 genomes]
rs182646	0.92[CEU][hapmap];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2129162	0.86[EUR][1000 genomes]
rs2129165	0.86[EUR][1000 genomes]
rs2170953	0.87[TSI][hapmap]
rs2200494	0.90[CEU][hapmap];1.00[GIH][hapmap];0.96[TSI][hapmap];0.98[EUR][1000 genomes]
rs223081	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2306742	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2385544	0.85[EUR][1000 genomes]
rs2385545	0.85[EUR][1000 genomes]
rs2385546	0.86[EUR][1000 genomes]
rs2385547	0.86[EUR][1000 genomes]
rs2385548	0.86[EUR][1000 genomes]
rs2385554	0.87[TSI][hapmap];0.82[EUR][1000 genomes]
rs2449957	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]
rs2449958	0.92[CEU][hapmap];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2449959	0.84[EUR][1000 genomes]
rs2450285	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2450288	0.89[CEU][hapmap];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2450291	1.00[CEU][hapmap];0.98[EUR][1000 genomes]
rs2628417	0.92[CEU][hapmap];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2630550	0.92[CEU][hapmap];0.87[EUR][1000 genomes]
rs318860	0.90[CEU][hapmap];1.00[GIH][hapmap];0.96[TSI][hapmap];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs318862	0.92[CEU][hapmap];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs318864	0.92[CEU][hapmap];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs318870	0.92[CEU][hapmap];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs318871	0.92[CEU][hapmap];0.83[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs318872	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]
rs318873	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[TSI][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]
rs318875	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]
rs318877	0.92[CEU][hapmap];0.88[EUR][1000 genomes]
rs318884	0.92[CEU][hapmap];0.88[EUR][1000 genomes]
rs318885	0.90[CEU][hapmap];1.00[GIH][hapmap];0.96[TSI][hapmap];0.88[EUR][1000 genomes]
rs318888	0.92[CEU][hapmap];0.88[EUR][1000 genomes]
rs318890	0.90[CEU][hapmap];1.00[GIH][hapmap];0.96[TSI][hapmap];0.88[EUR][1000 genomes]
rs318893	0.84[CEU][hapmap]
rs318894	0.80[CEU][hapmap];0.81[GIH][hapmap];0.83[TSI][hapmap]
rs318902	0.80[CEU][hapmap];0.81[GIH][hapmap];0.83[TSI][hapmap]
rs318903	0.80[CEU][hapmap];0.81[GIH][hapmap];0.83[TSI][hapmap]
rs318905	0.84[CEU][hapmap]
rs318906	0.84[CEU][hapmap]
rs318908	0.84[CEU][hapmap]
rs318910	0.80[CEU][hapmap];0.81[GIH][hapmap];0.83[TSI][hapmap]
rs318911	0.84[CEU][hapmap]
rs318912	0.84[CEU][hapmap]
rs365318	0.90[CEU][hapmap];1.00[GIH][hapmap];0.96[TSI][hapmap];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs366526	0.92[CEU][hapmap];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs380279	0.92[CEU][hapmap];0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs3812426	0.82[EUR][1000 genomes]
rs384406	0.92[CEU][hapmap];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs391798	0.92[CEU][hapmap];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs402156	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs406337	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs417918	0.80[CEU][hapmap]
rs436688	0.97[EUR][1000 genomes]
rs4377975	0.86[EUR][1000 genomes]
rs4383988	0.85[EUR][1000 genomes]
rs4460388	0.81[EUR][1000 genomes]
rs4584153	0.85[EUR][1000 genomes]
rs55920504	0.86[EUR][1000 genomes]
rs57585353	0.85[EUR][1000 genomes]
rs58254228	1.00[ASN][1000 genomes]
rs58597929	0.86[EUR][1000 genomes]
rs59405147	0.84[EUR][1000 genomes]
rs60061614	0.85[EUR][1000 genomes]
rs60356093	1.00[ASN][1000 genomes]
rs61374770	1.00[ASN][1000 genomes]
rs6472674	1.00[JPT][hapmap]
rs6472722	0.84[CEU][hapmap]
rs6984738	0.81[EUR][1000 genomes]
rs6988557	1.00[JPT][hapmap]
rs7002909	0.81[EUR][1000 genomes]
rs7008924	0.85[EUR][1000 genomes]
rs7013903	0.85[EUR][1000 genomes]
rs72638307	0.85[EUR][1000 genomes]
rs72638311	0.85[EUR][1000 genomes]
rs72638312	0.85[EUR][1000 genomes]
rs72638332	0.85[EUR][1000 genomes]
rs72638338	0.86[EUR][1000 genomes]
rs73569315	1.00[ASN][1000 genomes]
rs73569317	1.00[ASN][1000 genomes]
rs73584754	1.00[ASN][1000 genomes]
rs73584759	1.00[ASN][1000 genomes]
rs73584763	1.00[ASN][1000 genomes]
rs73584765	0.91[ASN][1000 genomes]
rs73584771	1.00[ASN][1000 genomes]
rs73677815	1.00[ASN][1000 genomes]
rs7825552	0.85[EUR][1000 genomes]
rs9298228	0.85[EUR][1000 genomes]
rs9298229	0.85[EUR][1000 genomes]
rs964011	0.85[EUR][1000 genomes]
rs967109	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs967110	0.92[CEU][hapmap];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs967116	0.90[CEU][hapmap];1.00[GIH][hapmap];0.96[TSI][hapmap];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9886451	0.85[EUR][1000 genomes]
rs993552	0.84[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3353749	chr8:50530807-51139242	Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv916392	chr8:50827638-51395140	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr8:50832000-50841800	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr8:50838600-50854400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr8:50838800-50853200	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr8:50841600-50842000	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr8:50841600-50842200	Enhancers	HUES48 Cell Line	embryonic stem cell

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