Variant report

Variant	rs12631345
Chromosome Location	chr3:85440211-85440212
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:85439579..85441215-chr3:85551442..85553756,2	K562	blood:

Extended variants
information (count: 70 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs1014796	0.81[EUR][1000 genomes]
rs10865609	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11714549	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12487446	0.90[AFR][1000 genomes];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12631046	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1368741	0.89[EUR][1000 genomes]
rs1368744	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1368746	0.97[ASN][1000 genomes]
rs1368747	0.91[ASN][1000 genomes]
rs1433710	0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1433712	0.97[ASN][1000 genomes]
rs1433713	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1449403	0.81[EUR][1000 genomes]
rs1465716	0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1594795	0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1821350	0.91[ASN][1000 genomes]
rs1836131	1.00[ASN][1000 genomes]
rs1897698	1.00[ASN][1000 genomes]
rs2018416	1.00[ASN][1000 genomes]
rs2053105	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2163970	1.00[ASN][1000 genomes]
rs2326315	0.81[EUR][1000 genomes]
rs4856270	0.94[ASN][1000 genomes]
rs4856272	0.81[EUR][1000 genomes]
rs4856568	1.00[ASN][1000 genomes]
rs62250710	0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs62252517	0.81[EUR][1000 genomes]
rs6549027	0.82[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6549031	0.81[EUR][1000 genomes]
rs6762253	1.00[ASN][1000 genomes]
rs6771447	1.00[ASN][1000 genomes]
rs6772750	0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6807461	0.81[EUR][1000 genomes]
rs6809486	0.97[ASN][1000 genomes]
rs734298	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7610238	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7623369	0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7623474	0.81[EUR][1000 genomes]
rs7623947	0.81[EUR][1000 genomes]
rs7651113	0.92[AFR][1000 genomes];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9309974	0.97[ASN][1000 genomes]
rs9309975	0.97[ASN][1000 genomes]
rs9309976	0.89[ASN][1000 genomes]
rs9309978	0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9824386	1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9824840	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9830359	0.82[ASN][1000 genomes]
rs9831848	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9833972	0.94[ASN][1000 genomes]
rs9843953	0.80[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9846153	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9854888	0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9866182	1.00[ASN][1000 genomes]
rs9869121	0.84[EUR][1000 genomes]
rs9873752	0.97[ASN][1000 genomes]
rs9879417	0.97[ASN][1000 genomes]
rs989534	0.97[ASN][1000 genomes]
rs9990095	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3419993	chr3:85030343-85663403	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
2	esv2753915	chr3:85071410-85624810	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
3	nsv948806	chr3:85304744-85463443	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region miRNA	1 gene(s)	inside rSNPs	diseases
4	nsv1013407	chr3:85307022-85460325	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region miRNA	1 gene(s)	inside rSNPs	diseases
5	nsv1002238	chr3:85357855-85719373	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	1 gene(s)	inside rSNPs	diseases
6	nsv536619	chr3:85357855-85719373	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	1 gene(s)	inside rSNPs	diseases
7	nsv1008956	chr3:85394816-85460325	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region miRNA	1 gene(s)	inside rSNPs	diseases
8	nsv536620	chr3:85394816-85460325	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region miRNA	1 gene(s)	inside rSNPs	diseases
9	nsv1004254	chr3:85394816-85514910	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region miRNA	1 gene(s)	inside rSNPs	diseases
10	nsv536621	chr3:85394816-85514910	Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region miRNA	1 gene(s)	inside rSNPs	diseases
11	nsv590904	chr3:85438564-85551403	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
12	nsv590905	chr3:85438564-85797093	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	1 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	chr3:85416200-85450200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr3:85437400-85440800	Weak transcription	Brain Substantia Nigra	brain
3	chr3:85438000-85440600	Weak transcription	Brain Cingulate Gyrus	brain
4	chr3:85440200-85441200	Enhancers	Brain Hippocampus Middle	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links