Variant report

Variant	rs10873724
Chromosome Location	chr1:76291986-76291987
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 93 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:85)

rs_ID	r²[population]
rs10782556	0.81[ASN][1000 genomes]
rs10873727	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10873728	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10873735	0.81[ASN][1000 genomes]
rs10873738	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10873739	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11161602	0.81[ASN][1000 genomes]
rs11161700	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11161704	0.94[ASN][1000 genomes]
rs11161790	0.89[ASN][1000 genomes]
rs11161795	0.89[ASN][1000 genomes]
rs1144328	0.93[ASN][1000 genomes]
rs1144331	0.94[ASN][1000 genomes]
rs1144333	0.94[ASN][1000 genomes]
rs1144337	0.94[ASN][1000 genomes]
rs1144338	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1144339	0.94[ASN][1000 genomes]
rs1144341	0.94[ASN][1000 genomes]
rs1144342	0.94[ASN][1000 genomes]
rs1146592	0.82[ASN][1000 genomes]
rs1146593	0.84[ASN][1000 genomes]
rs1146602	0.87[ASN][1000 genomes]
rs1146613	0.81[ASN][1000 genomes]
rs1146616	0.89[ASN][1000 genomes]
rs1146625	0.84[ASN][1000 genomes]
rs1146645	0.93[ASN][1000 genomes]
rs1146647	0.93[ASN][1000 genomes]
rs1146648	0.80[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1146649	0.92[ASN][1000 genomes]
rs1146651	0.94[ASN][1000 genomes]
rs1146652	0.94[ASN][1000 genomes]
rs1146656	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11579355	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12021750	0.81[ASN][1000 genomes]
rs12024086	0.89[ASN][1000 genomes]
rs12024645	0.81[ASN][1000 genomes]
rs12033058	0.81[ASN][1000 genomes]
rs12033059	0.81[ASN][1000 genomes]
rs12045363	0.81[ASN][1000 genomes]
rs12076093	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12078151	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12081710	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12090712	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12385715	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12401729	0.90[ASN][1000 genomes]
rs12403889	0.90[ASN][1000 genomes]
rs12405178	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12407107	0.81[ASN][1000 genomes]
rs1250881	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1250882	0.94[ASN][1000 genomes]
rs1251270	0.94[ASN][1000 genomes]
rs1251272	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1251273	0.94[ASN][1000 genomes]
rs1251274	0.94[ASN][1000 genomes]
rs1251275	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12564772	0.81[ASN][1000 genomes]
rs12703	0.93[ASN][1000 genomes]
rs12748900	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17097634	0.81[ASN][1000 genomes]
rs1767459	0.81[ASN][1000 genomes]
rs1770513	0.81[ASN][1000 genomes]
rs1812589	0.97[ASN][1000 genomes]
rs2012536	0.93[ASN][1000 genomes]
rs2131558	0.81[ASN][1000 genomes]
rs34045364	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs34177389	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs34486572	0.81[ASN][1000 genomes]
rs35591768	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs36054685	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3737574	0.81[ASN][1000 genomes]
rs4347163	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4949884	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs5019550	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs56350137	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs5745314	0.81[ASN][1000 genomes]
rs5745327	0.93[ASN][1000 genomes]
rs5745334	0.81[ASN][1000 genomes]
rs5745343	0.94[ASN][1000 genomes]
rs5745354	0.94[ASN][1000 genomes]
rs5745392	0.94[ASN][1000 genomes]
rs58552356	0.83[ASN][1000 genomes]
rs61676733	0.90[ASN][1000 genomes]
rs7514912	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7525919	0.81[ASN][1000 genomes]
rs7548391	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv519329	chr1:75830438-76358591	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	nsv1014072	chr1:76200531-76460726	Genic enhancers Enhancers Strong transcription Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
3	nsv535005	chr1:76200531-76460726	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
4	esv1795237	chr1:76268573-76383565	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	esv1800125	chr1:76269439-76379497	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	esv1799260	chr1:76269439-76383297	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
7	esv1847721	chr1:76269439-76383565	Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
8	nsv1466	chr1:76280957-76299478	ZNF genes & repeats Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 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	chr1:76262600-76294600	Weak transcription	Primary B cells from cord blood	blood
2	chr1:76263000-76296200	Weak transcription	Ovary	ovary
3	chr1:76282200-76295200	Weak transcription	Right Ventricle	heart
4	chr1:76289400-76295200	Weak transcription	Skeletal Muscle Female	skeletal muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links