Variant report

Variant	rs1014773
Chromosome Location	chr4:127675927-127675928
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:127661132..127664302-chr4:127673229..127676858,3	K562	blood:

Extended variants
information (count: 90 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:80)

rs_ID	r²[population]
rs10461207	0.87[ASN][1000 genomes]
rs10857116	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10857117	1.00[ASN][1000 genomes]
rs11098891	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11098892	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11098893	0.94[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs11098896	0.87[ASN][1000 genomes]
rs11098898	0.87[ASN][1000 genomes]
rs1157308	0.99[AFR][1000 genomes];0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1167190	0.87[ASN][1000 genomes]
rs11935382	0.87[ASN][1000 genomes]
rs11940501	1.00[ASN][1000 genomes]
rs11941222	0.87[ASN][1000 genomes]
rs12163770	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12503440	1.00[ASN][1000 genomes]
rs12504330	0.87[ASN][1000 genomes]
rs12507115	0.87[ASN][1000 genomes]
rs12647109	1.00[ASN][1000 genomes]
rs12650177	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13111309	0.87[ASN][1000 genomes]
rs13112652	1.00[ASN][1000 genomes]
rs13143010	1.00[ASN][1000 genomes]
rs13148138	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13152826	0.99[AFR][1000 genomes];0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1393991	1.00[CHB][hapmap];0.87[ASN][1000 genomes]
rs1503604	1.00[ASN][1000 genomes]
rs1503605	0.87[ASN][1000 genomes]
rs1503606	0.87[ASN][1000 genomes]
rs1503608	0.87[ASN][1000 genomes]
rs1503610	1.00[ASN][1000 genomes]
rs1503611	0.87[ASN][1000 genomes]
rs1503614	0.87[ASN][1000 genomes]
rs1503631	1.00[ASN][1000 genomes]
rs1532768	0.87[ASN][1000 genomes]
rs1587744	0.87[ASN][1000 genomes]
rs1604719	1.00[ASN][1000 genomes]
rs1604724	0.87[ASN][1000 genomes]
rs17011528	0.87[ASN][1000 genomes]
rs17203028	0.87[ASN][1000 genomes]
rs1875740	1.00[ASN][1000 genomes]
rs1948827	0.87[ASN][1000 genomes]
rs1955281	0.99[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1976483	0.87[ASN][1000 genomes]
rs2013778	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs2013864	0.87[ASN][1000 genomes]
rs2089061	0.87[ASN][1000 genomes]
rs2134641	1.00[ASN][1000 genomes]
rs2134645	1.00[ASN][1000 genomes]
rs2174183	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2174184	1.00[ASN][1000 genomes]
rs2391099	1.00[CHB][hapmap]
rs28666008	0.87[ASN][1000 genomes]
rs28742896	0.87[ASN][1000 genomes]
rs28811377	0.87[ASN][1000 genomes]
rs28876486	0.87[ASN][1000 genomes]
rs2893192	1.00[ASN][1000 genomes]
rs4618330	0.95[AFR][1000 genomes];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4834142	1.00[ASN][1000 genomes]
rs5004421	0.83[EUR][1000 genomes]
rs55791209	0.87[ASN][1000 genomes]
rs62324217	0.87[ASN][1000 genomes]
rs6534583	0.87[ASN][1000 genomes]
rs6812442	0.99[AFR][1000 genomes];0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6829454	0.87[ASN][1000 genomes]
rs6830097	1.00[ASN][1000 genomes]
rs6835402	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6848985	0.87[ASN][1000 genomes]
rs6856064	0.87[ASN][1000 genomes]
rs6858446	0.89[EUR][1000 genomes]
rs7654869	1.00[ASN][1000 genomes]
rs7672155	0.87[ASN][1000 genomes]
rs7676848	1.00[ASN][1000 genomes]
rs7681140	0.87[ASN][1000 genomes]
rs7686181	0.87[ASN][1000 genomes]
rs7691822	0.87[ASN][1000 genomes]
rs7694861	0.87[ASN][1000 genomes]
rs7696445	0.87[ASN][1000 genomes]
rs7696767	0.87[ASN][1000 genomes]
rs969315	0.87[ASN][1000 genomes]
rs986907	0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1012833	chr4:127468474-127760933	Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv537242	chr4:127468474-127760933	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv524850	chr4:127470903-127768849	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1007477	chr4:127561735-127726291	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv537244	chr4:127561735-127726291	Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv879907	chr4:127646765-127709859	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
7	nsv879908	chr4:127646765-127749390	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
8	nsv879909	chr4:127646765-127792639	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	nsv879910	chr4:127646765-127805466	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
10	nsv879911	chr4:127646765-127835677	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:127671800-127677000	Enhancers	K562	blood
2	chr4:127672200-127677200	Weak transcription	Fetal Lung	lung
3	chr4:127673600-127680800	Weak transcription	Fetal Heart	heart

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links