Variant report

Variant	rs1948827
Chromosome Location	chr4:127773003-127773004
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:127695737..127697601-chr4:127770299..127773125,2	K562	blood:
2	chr4:127716621..127718255-chr4:127771445..127774248,2	K562	blood:
3	chr4:127771990..127773680-chr4:127776900..127779323,2	K562	blood:
4	chr4:127771841..127773556-chr4:127876449..127879979,3	K562	blood:

Extended variants
information (count: 82 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:77)

rs_ID	r²[population]
rs1014773	0.87[ASN][1000 genomes]
rs10461207	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10857117	0.87[ASN][1000 genomes]
rs11098891	1.00[CHB][hapmap];0.87[ASN][1000 genomes]
rs11098892	0.87[ASN][1000 genomes]
rs11098893	0.87[ASN][1000 genomes]
rs11098896	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11098898	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1157308	0.87[ASN][1000 genomes]
rs1167190	1.00[ASN][1000 genomes]
rs11935382	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11940501	0.87[ASN][1000 genomes]
rs11941222	1.00[ASN][1000 genomes]
rs12163770	0.87[ASN][1000 genomes]
rs12503440	0.87[ASN][1000 genomes]
rs12504330	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12507115	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12647109	0.87[ASN][1000 genomes]
rs12650177	0.87[ASN][1000 genomes]
rs13111309	0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs13112652	0.87[ASN][1000 genomes]
rs13114412	0.91[AFR][1000 genomes]
rs13143010	0.87[ASN][1000 genomes]
rs13148138	0.87[ASN][1000 genomes]
rs13152826	0.87[ASN][1000 genomes]
rs1393991	0.81[CEU][hapmap];1.00[CHB][hapmap];0.89[YRI][hapmap];0.87[AFR][1000 genomes];0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1393993	0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1503604	0.87[ASN][1000 genomes]
rs1503605	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1503606	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1503608	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1503610	0.87[ASN][1000 genomes]
rs1503611	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1503612	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1503614	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1503631	0.87[ASN][1000 genomes]
rs1532768	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1604719	0.87[ASN][1000 genomes]
rs1604724	0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17011528	1.00[ASN][1000 genomes]
rs17203028	1.00[ASN][1000 genomes]
rs1875740	0.82[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs1955281	0.87[ASN][1000 genomes]
rs1976483	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2013778	1.00[CHB][hapmap];0.87[ASN][1000 genomes]
rs2013864	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2089061	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2134641	0.87[ASN][1000 genomes]
rs2134645	0.87[ASN][1000 genomes]
rs2174184	0.87[ASN][1000 genomes]
rs2391099	1.00[CHB][hapmap];0.83[YRI][hapmap];0.83[AFR][1000 genomes]
rs28666008	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28742896	1.00[ASN][1000 genomes]
rs28811377	1.00[ASN][1000 genomes]
rs28876486	1.00[ASN][1000 genomes]
rs2893192	0.87[ASN][1000 genomes]
rs4834142	0.87[ASN][1000 genomes]
rs4834147	0.94[AFR][1000 genomes]
rs55791209	1.00[ASN][1000 genomes]
rs62324217	1.00[ASN][1000 genomes]
rs6534583	0.87[AFR][1000 genomes];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6812442	0.87[ASN][1000 genomes]
rs6829454	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6830097	0.87[ASN][1000 genomes]
rs6848985	0.87[AFR][1000 genomes];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6856064	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7654869	0.87[ASN][1000 genomes]
rs7672155	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7676848	0.87[ASN][1000 genomes]
rs7681140	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7686181	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7691822	1.00[ASN][1000 genomes]
rs7694861	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7696445	0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7696767	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs969315	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs986907	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	nsv879912	chr4:127706053-127775563	Weak transcription ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv428773	chr4:127760014-127913973	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Strong transcription Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:127770200-127773200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr4:127770200-127773400	Enhancers	NH-A	brain
3	chr4:127770200-127773400	Enhancers	NHDF-Ad	bronchial
4	chr4:127770600-127773400	Enhancers	HMEC	breast
5	chr4:127771400-127773200	Enhancers	K562	blood
6	chr4:127772400-127773400	Weak transcription	HSMM	muscle
7	chr4:127772800-127777800	Weak transcription	NHEK	skin
8	chr4:127772800-127792000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr4:127773000-127777200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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