Variant report

Variant	rs4873382
Chromosome Location	chr8:50727949-50727950
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 142 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:141)

rs_ID	r²[population]
rs10086004	0.98[ASN][1000 genomes]
rs10089399	0.98[ASN][1000 genomes]
rs10090657	0.98[ASN][1000 genomes]
rs10092384	0.98[ASN][1000 genomes]
rs10107423	0.98[ASN][1000 genomes]
rs10111730	0.98[ASN][1000 genomes]
rs1038534	0.98[ASN][1000 genomes]
rs10504093	0.86[CHB][hapmap]
rs1074385	0.98[ASN][1000 genomes]
rs10957620	0.98[ASN][1000 genomes]
rs10957679	0.87[ASN][1000 genomes]
rs10957682	0.87[ASN][1000 genomes]
rs1157932	0.86[CHB][hapmap]
rs11777957	0.86[CHB][hapmap]
rs11781675	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11783631	0.86[CHB][hapmap]
rs11785147	0.98[ASN][1000 genomes]
rs11786939	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11787050	0.87[ASN][1000 genomes]
rs12541363	0.84[CHB][hapmap]
rs12542041	0.95[ASN][1000 genomes]
rs12542687	0.84[ASN][1000 genomes]
rs12545695	0.83[ASN][1000 genomes]
rs12547245	0.95[ASN][1000 genomes]
rs12677051	0.98[ASN][1000 genomes]
rs13251355	0.98[ASN][1000 genomes]
rs13255117	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13261298	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13267366	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs1352112	0.98[ASN][1000 genomes]
rs1352113	0.85[ASN][1000 genomes]
rs1385974	0.98[ASN][1000 genomes]
rs1385975	0.98[ASN][1000 genomes]
rs1385976	0.86[ASN][1000 genomes]
rs1385980	0.84[ASN][1000 genomes]
rs1385982	0.86[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1486241	0.98[ASN][1000 genomes]
rs1486242	0.98[ASN][1000 genomes]
rs1486243	0.98[ASN][1000 genomes]
rs1486251	0.98[ASN][1000 genomes]
rs1486252	0.98[ASN][1000 genomes]
rs1486253	0.98[ASN][1000 genomes]
rs1486254	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1486263	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs1552371	0.85[ASN][1000 genomes]
rs1552372	0.98[ASN][1000 genomes]
rs1552373	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1552375	0.97[ASN][1000 genomes]
rs1552377	0.95[ASN][1000 genomes]
rs1552378	0.83[ASN][1000 genomes]
rs1552379	0.83[ASN][1000 genomes]
rs1580468	0.98[ASN][1000 genomes]
rs1586364	0.87[ASN][1000 genomes]
rs1601569	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs16912794	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs16913087	0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs16913172	0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs16913461	0.86[AFR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs16913472	0.86[AFR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs16913475	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs16913687	0.87[ASN][1000 genomes]
rs16914039	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs170331	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs1906014	0.83[ASN][1000 genomes]
rs1906015	0.93[ASN][1000 genomes]
rs1979535	0.98[ASN][1000 genomes]
rs1994344	0.98[ASN][1000 genomes]
rs2129162	0.98[ASN][1000 genomes]
rs2129164	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2129165	0.94[ASN][1000 genomes]
rs2247368	1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs2385545	0.98[ASN][1000 genomes]
rs2385546	0.98[ASN][1000 genomes]
rs2385547	0.98[ASN][1000 genomes]
rs2385548	0.86[ASN][1000 genomes]
rs2385696	0.86[CHB][hapmap]
rs2449960	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs2450286	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs2450287	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2450290	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs28869911	0.81[ASN][1000 genomes]
rs318850	0.83[ASN][1000 genomes]
rs318854	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs318858	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs318859	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs318861	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs318874	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs4242456	0.86[CHB][hapmap]
rs4339657	0.97[ASN][1000 genomes]
rs4383988	0.98[ASN][1000 genomes]
rs4584153	0.98[ASN][1000 genomes]
rs4873113	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4873114	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4873116	0.86[AFR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4873118	0.87[ASN][1000 genomes]
rs4873119	0.87[ASN][1000 genomes]
rs4873120	0.86[CHB][hapmap]
rs4873123	0.86[CHB][hapmap]
rs4873379	0.82[ASN][1000 genomes]
rs4873383	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4873388	0.86[AFR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4873391	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4873392	0.87[ASN][1000 genomes]
rs55636909	0.92[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs55879210	0.87[ASN][1000 genomes]
rs56659775	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs57462717	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs58764084	0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs59379959	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs59848488	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs60213702	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs60631955	0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs61662535	0.98[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6472721	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6988440	0.84[ASN][1000 genomes]
rs6994224	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7004973	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs7008449	0.83[ASN][1000 genomes]
rs7008924	0.97[ASN][1000 genomes]
rs7013903	0.98[ASN][1000 genomes]
rs73582706	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73582713	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73582718	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73582724	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73582755	0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73582756	0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73676017	0.86[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs73676077	0.83[ASN][1000 genomes]
rs7388392	0.95[ASN][1000 genomes]
rs7825552	0.98[ASN][1000 genomes]
rs7826013	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7828311	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7828900	0.84[CHB][hapmap]
rs7834858	0.97[AMR][1000 genomes]
rs9298228	0.98[ASN][1000 genomes]
rs9298229	0.98[ASN][1000 genomes]
rs964011	0.98[ASN][1000 genomes]
rs967107	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs974740	0.87[ASN][1000 genomes]
rs974742	0.87[ASN][1000 genomes]
rs9886451	0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 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

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:50725000-50729400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr8:50725200-50728400	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr8:50725200-50729000	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr8:50725200-50729000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr8:50725200-50729200	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr8:50725200-50729400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr8:50725400-50729200	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr8:50725800-50728600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr8:50725800-50728600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr8:50726000-50728400	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr8:50727200-50732600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr8:50727600-50728600	Weak transcription	NHDF-Ad	bronchial

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links