Variant report

Variant	rs4268330
Chromosome Location	chr1:215999810-215999811
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:215996903..215999986-chr1:216001908..216004780,3	K562	blood:

Extended variants
information (count: 65 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs10082095	0.87[CEU][hapmap];0.88[CHB][hapmap];0.85[JPT][hapmap];0.83[AFR][1000 genomes];0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10082147	0.88[CEU][hapmap];0.82[CHB][hapmap];0.86[JPT][hapmap];0.83[AFR][1000 genomes];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10779661	0.87[CEU][hapmap];0.94[CHB][hapmap];0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10864203	0.89[CHB][hapmap];0.95[ASN][1000 genomes]
rs10864205	0.88[CEU][hapmap];0.89[CHB][hapmap];0.86[JPT][hapmap];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10864207	0.91[CEU][hapmap];0.94[CHB][hapmap];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10864208	0.91[CEU][hapmap];0.94[CHB][hapmap]
rs11120635	0.94[CHB][hapmap]
rs11120646	0.81[AFR][1000 genomes];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11120649	0.83[AFR][1000 genomes];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11120651	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11120653	0.87[CEU][hapmap];0.94[CHB][hapmap];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11120664	0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11120666	0.87[CEU][hapmap];0.94[CHB][hapmap];0.85[JPT][hapmap];0.98[ASN][1000 genomes]
rs11120684	0.88[CHB][hapmap]
rs11526532	1.00[CHB][hapmap]
rs11579793	0.87[CEU][hapmap];0.88[CHB][hapmap]
rs12029340	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12037661	1.00[CHB][hapmap];0.85[JPT][hapmap]
rs12042414	0.99[ASN][1000 genomes]
rs12043203	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12046040	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12049039	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12049485	0.92[CEU][hapmap];0.88[CHB][hapmap];0.80[JPT][hapmap];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12404720	0.92[ASN][1000 genomes]
rs12567496	0.91[CHB][hapmap]
rs12724961	0.88[CHB][hapmap];0.86[JPT][hapmap]
rs12725398	0.89[CHB][hapmap];0.94[ASN][1000 genomes]
rs1547765	0.88[CEU][hapmap];0.83[CHB][hapmap];0.92[JPT][hapmap];0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1934425	0.89[ASN][1000 genomes]
rs1934429	0.88[CEU][hapmap];0.94[CHB][hapmap];0.80[JPT][hapmap];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1934432	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1972368	0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2027355	0.83[CEU][hapmap];0.94[CHB][hapmap];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2364866	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs28477637	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs34007298	0.87[ASN][1000 genomes]
rs3884585	0.88[CEU][hapmap];0.94[CHB][hapmap];0.85[JPT][hapmap];0.82[AFR][1000 genomes];0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4143467	0.99[ASN][1000 genomes]
rs4284237	0.82[CHB][hapmap]
rs4330894	0.88[CEU][hapmap];0.89[CHB][hapmap];0.82[AFR][1000 genomes];0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4363405	0.94[CHB][hapmap]
rs4375238	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4390149	0.87[CEU][hapmap];0.88[CHB][hapmap];0.85[JPT][hapmap];0.83[AFR][1000 genomes];0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4405115	0.94[CHB][hapmap]
rs4528089	0.83[AFR][1000 genomes];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4528090	0.88[CEU][hapmap];0.94[CHB][hapmap];0.86[JPT][hapmap];0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4545310	0.88[CEU][hapmap];0.94[CHB][hapmap];0.92[JPT][hapmap];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4571939	0.83[CHB][hapmap];0.86[JPT][hapmap];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4607850	0.81[EUR][1000 genomes]
rs6540912	0.87[CEU][hapmap];0.88[CHB][hapmap];0.82[AFR][1000 genomes];0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6701765	0.94[CHB][hapmap]
rs71639583	0.89[ASN][1000 genomes]
rs721099	0.87[ASN][1000 genomes]
rs7516792	0.83[AFR][1000 genomes];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7556611	0.87[CEU][hapmap];0.88[CHB][hapmap];0.85[JPT][hapmap];0.83[AFR][1000 genomes];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs975994	0.87[CHB][hapmap]
rs9887827	0.87[CEU][hapmap];0.88[CHB][hapmap];0.85[JPT][hapmap];0.83[AFR][1000 genomes];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv430324	chr1:215649163-216082605	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
2	nsv1006504	chr1:215890460-216642124	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv535288	chr1:215890460-216642124	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
4	nsv949671	chr1:215942740-216120815	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv549192	chr1:215967857-216034753	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv1012279	chr1:215982058-216035558	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv832548	chr1:215987089-216175724	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:215987200-216007400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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