Variant report

Variant	rs1874616
Chromosome Location	chr15:49802271-49802272
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 119 )
Associated
traits (count: 7 )

rSNPs within LD-proxies of this variant (count:115)

rs_ID	r²[population]
rs10047970	0.88[ASW][hapmap];0.98[LWK][hapmap];1.00[YRI][hapmap];0.80[AFR][1000 genomes]
rs10083602	0.87[AFR][1000 genomes]
rs10519224	0.82[JPT][hapmap]
rs10519225	0.82[JPT][hapmap]
rs1057636	0.84[AFR][1000 genomes]
rs1057638	0.84[AFR][1000 genomes]
rs1072726	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10851479	0.82[JPT][hapmap]
rs11070699	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs11070706	0.82[JPT][hapmap]
rs11632674	0.96[YRI][hapmap];0.85[AFR][1000 genomes]
rs11637582	0.82[CEU][hapmap];0.82[JPT][hapmap]
rs11855798	0.82[JPT][hapmap]
rs11858411	0.82[JPT][hapmap]
rs12050614	0.82[JPT][hapmap]
rs12148764	0.82[JPT][hapmap]
rs12232355	0.82[JPT][hapmap]
rs12438856	0.82[AFR][1000 genomes]
rs12440099	0.92[AFR][1000 genomes]
rs12442143	0.84[AFR][1000 genomes]
rs12591659	0.82[JPT][hapmap]
rs12595692	0.81[JPT][hapmap]
rs12902794	0.83[YRI][hapmap]
rs12902960	0.81[JPT][hapmap]
rs12908624	0.82[JPT][hapmap]
rs12908635	0.82[JPT][hapmap]
rs12916839	0.82[JPT][hapmap]
rs1354920	0.82[YRI][hapmap]
rs1395901	0.82[JPT][hapmap]
rs1395902	0.85[AFR][1000 genomes]
rs1532955	0.94[ASW][hapmap];0.98[LWK][hapmap];0.96[YRI][hapmap]
rs1546424	0.80[YRI][hapmap]
rs1546425	0.81[YRI][hapmap]
rs1605477	0.87[AFR][1000 genomes]
rs1605478	0.85[AFR][1000 genomes]
rs1605479	0.87[AFR][1000 genomes]
rs16962528	0.84[AFR][1000 genomes]
rs16973952	0.84[AFR][1000 genomes]
rs17402115	0.82[JPT][hapmap]
rs17478694	0.82[JPT][hapmap]
rs17478785	0.82[JPT][hapmap]
rs17479589	0.82[JPT][hapmap]
rs1874612	0.90[AFR][1000 genomes]
rs1874615	0.94[ASW][hapmap];1.00[LWK][hapmap];0.81[MKK][hapmap];1.00[YRI][hapmap]
rs1911612	0.82[JPT][hapmap]
rs1911614	0.94[ASW][hapmap];1.00[LWK][hapmap];0.81[MKK][hapmap];0.96[YRI][hapmap];0.85[AFR][1000 genomes]
rs1976551	0.82[CEU][hapmap];0.82[JPT][hapmap]
rs2007474	0.87[AFR][1000 genomes]
rs2202714	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs2413946	0.84[AFR][1000 genomes]
rs2413953	0.94[ASW][hapmap];1.00[LWK][hapmap];0.81[MKK][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes]
rs2413954	0.86[YRI][hapmap]
rs2413957	0.84[AFR][1000 genomes]
rs2413958	0.82[LWK][hapmap];0.83[MKK][hapmap]
rs2413959	0.83[AFR][1000 genomes]
rs28788326	0.87[AFR][1000 genomes]
rs28815194	0.87[AFR][1000 genomes]
rs28822970	0.86[AFR][1000 genomes]
rs28836194	0.87[AFR][1000 genomes]
rs28842346	0.85[AFR][1000 genomes]
rs28871940	0.87[AFR][1000 genomes]
rs2899433	0.85[LWK][hapmap];0.81[MKK][hapmap];0.90[YRI][hapmap]
rs2899434	0.82[JPT][hapmap]
rs34127708	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4303431	0.96[YRI][hapmap];0.87[AFR][1000 genomes]
rs4350524	0.94[ASW][hapmap]
rs4389093	0.82[JPT][hapmap]
rs4480740	0.82[JPT][hapmap]
rs4774539	0.80[YRI][hapmap]
rs4775811	0.84[AFR][1000 genomes]
rs4775815	0.94[ASW][hapmap];0.98[LWK][hapmap];0.81[MKK][hapmap];0.96[YRI][hapmap]
rs56335122	0.87[AFR][1000 genomes]
rs57421305	0.88[AFR][1000 genomes]
rs57997677	0.92[AFR][1000 genomes]
rs58284238	0.84[AFR][1000 genomes]
rs58410445	0.84[AFR][1000 genomes]
rs60216777	0.83[AFR][1000 genomes]
rs62009983	0.90[AFR][1000 genomes]
rs62009985	0.92[AFR][1000 genomes]
rs62021583	0.87[AFR][1000 genomes]
rs62021584	0.87[AFR][1000 genomes]
rs6493371	0.88[ASW][hapmap];1.00[LWK][hapmap];0.81[MKK][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes]
rs6493372	0.82[JPT][hapmap]
rs6493376	0.96[YRI][hapmap];0.85[AFR][1000 genomes]
rs67916122	0.92[AFR][1000 genomes]
rs68095295	0.92[AFR][1000 genomes]
rs7162351	0.90[AFR][1000 genomes]
rs7162792	0.90[AFR][1000 genomes]
rs7162800	1.00[YRI][hapmap];0.90[AFR][1000 genomes]
rs7166498	0.88[ASW][hapmap];0.98[LWK][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes]
rs7167041	0.88[ASW][hapmap];0.98[LWK][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes]
rs7168031	0.87[AFR][1000 genomes]
rs7170426	0.88[ASW][hapmap];0.98[LWK][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes]
rs7174135	0.82[JPT][hapmap]
rs7176350	0.92[AFR][1000 genomes]
rs7177247	0.92[AFR][1000 genomes]
rs7178194	0.90[AFR][1000 genomes]
rs7181916	0.86[AFR][1000 genomes]
rs7182072	0.84[AFR][1000 genomes]
rs733097	0.94[ASW][hapmap];1.00[LWK][hapmap];0.81[MKK][hapmap];0.96[YRI][hapmap];0.82[AFR][1000 genomes]
rs753857	0.84[ASW][hapmap];0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap];0.90[YRI][hapmap];0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8026236	0.82[AFR][1000 genomes]
rs8030761	0.87[AFR][1000 genomes]
rs8032688	0.82[JPT][hapmap]
rs8032952	0.82[AFR][1000 genomes]
rs8033476	0.89[CEU][hapmap];0.82[JPT][hapmap];0.87[MEX][hapmap];0.86[TSI][hapmap]
rs8034473	0.80[YRI][hapmap]
rs8035468	0.96[YRI][hapmap];0.85[AFR][1000 genomes]
rs8040436	0.80[YRI][hapmap]
rs906419	0.86[AFR][1000 genomes]
rs9302148	0.84[AFR][1000 genomes]
rs9920722	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs9972329	0.88[ASW][hapmap];0.98[LWK][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes]
rs9972429	0.85[AFR][1000 genomes]
rs9972565	0.84[AFR][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	nsv9263	chr15:49734435-49809465	Active TSS Genic enhancers Weak transcription Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
2	nsv1043119	chr15:49760222-49844366	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
3	nsv1039185	chr15:49786255-49844366	Strong transcription Weak transcription Enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv569392	chr15:49789413-49926300	ZNF genes & repeats Flanking Active TSS Strong transcription Weak transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases

mRNA abundance (count:7)

SNP	Gene	Cis/trans	Tissue	Source
rs1874616	DTWD1	Cis_1M	lymphoblastoid	RTeQTL
rs1874616	GALK2	Cis_1M	lymphoblastoid	RTeQTL
rs1874616	CTDSPL2	cis	cerebellum	SCAN
rs1874616	DTWD1	cis	cerebellum	SCAN
rs1874616	SPATA5L1	cis	parietal	SCAN
rs1874616	MAP1A	cis	cerebellum	SCAN
rs1874616	CATSPER2P1	cis	cerebellum	SCAN

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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