Variant report

Variant	rs406337
Chromosome Location	chr8:50843082-50843083
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 103 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:99)

rs_ID	r²[population]
rs10086004	0.83[EUR][1000 genomes]
rs10089399	0.83[EUR][1000 genomes]
rs10090657	0.83[EUR][1000 genomes]
rs10092384	0.83[EUR][1000 genomes]
rs10504092	0.87[EUR][1000 genomes]
rs1074385	0.84[EUR][1000 genomes]
rs11781675	0.81[EUR][1000 genomes]
rs11785147	0.83[EUR][1000 genomes]
rs12542041	0.83[EUR][1000 genomes]
rs13251355	0.84[EUR][1000 genomes]
rs1352112	0.83[EUR][1000 genomes]
rs1352117	0.93[EUR][1000 genomes]
rs1385974	0.83[EUR][1000 genomes]
rs1385975	0.83[EUR][1000 genomes]
rs1385976	0.83[EUR][1000 genomes]
rs1486241	0.83[EUR][1000 genomes]
rs1486242	0.83[EUR][1000 genomes]
rs1486243	0.83[EUR][1000 genomes]
rs1486245	0.85[EUR][1000 genomes]
rs1486251	0.83[EUR][1000 genomes]
rs1486252	0.83[EUR][1000 genomes]
rs1552372	0.83[EUR][1000 genomes]
rs1580468	0.84[EUR][1000 genomes]
rs167629	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs172758	0.80[EUR][1000 genomes]
rs17674783	0.87[EUR][1000 genomes]
rs17747294	0.87[EUR][1000 genomes]
rs17747567	0.87[EUR][1000 genomes]
rs17747896	0.87[EUR][1000 genomes]
rs17747929	0.87[EUR][1000 genomes]
rs182646	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2129162	0.84[EUR][1000 genomes]
rs2129165	0.84[EUR][1000 genomes]
rs2200494	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs223081	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2385544	0.87[EUR][1000 genomes]
rs2385545	0.83[EUR][1000 genomes]
rs2385546	0.84[EUR][1000 genomes]
rs2385547	0.84[EUR][1000 genomes]
rs2385548	0.84[EUR][1000 genomes]
rs2385554	0.81[EUR][1000 genomes]
rs2449957	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2449958	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2449959	0.86[EUR][1000 genomes]
rs2450285	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2450288	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2450291	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2628417	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2630550	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs28869911	0.81[EUR][1000 genomes]
rs318860	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs318862	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs318864	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs318870	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs318871	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs318872	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs318873	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs318875	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs318877	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs318884	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs318885	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs318888	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs318890	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs318893	0.81[EUR][1000 genomes]
rs318894	0.81[EUR][1000 genomes]
rs365318	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs366526	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs380279	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs3812426	0.81[EUR][1000 genomes]
rs384406	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs391798	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs402156	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs415276	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs417918	0.81[EUR][1000 genomes]
rs436688	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs4377975	0.88[EUR][1000 genomes]
rs4383988	0.83[EUR][1000 genomes]
rs4584153	0.83[EUR][1000 genomes]
rs55920504	0.88[EUR][1000 genomes]
rs57585353	0.87[EUR][1000 genomes]
rs58597929	0.88[EUR][1000 genomes]
rs59405147	0.86[EUR][1000 genomes]
rs60061614	0.87[EUR][1000 genomes]
rs7008924	0.83[EUR][1000 genomes]
rs7013903	0.83[EUR][1000 genomes]
rs72638307	0.87[EUR][1000 genomes]
rs72638311	0.87[EUR][1000 genomes]
rs72638312	0.87[EUR][1000 genomes]
rs72638332	0.87[EUR][1000 genomes]
rs72638338	0.88[EUR][1000 genomes]
rs7825552	0.83[EUR][1000 genomes]
rs9298228	0.83[EUR][1000 genomes]
rs9298229	0.83[EUR][1000 genomes]
rs964011	0.83[EUR][1000 genomes]
rs967109	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs967110	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs967116	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9886451	0.83[EUR][1000 genomes]
rs993552	0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 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
3	nsv971234	chr8:50842641-50848642	Weak transcription Enhancers	n/a	n/a	inside rSNPs	n/a
4	esv3333208	chr8:50843000-50843165	Weak transcription Enhancers	n/a	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:50838600-50854400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr8:50838800-50853200	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr8:50841800-50844000	Enhancers	Dnd41	blood
4	chr8:50842200-50850400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links