Variant report

Variant	rs374686
Chromosome Location	chr1:158183610-158183611
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	chr1:158159135..158160992-chr1:158182164..158184743,2	K562	blood:

Extended variants
information (count: 147 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:140)

rs_ID	r²[population]
rs11264929	0.86[ASN][1000 genomes]
rs11264930	0.83[ASN][1000 genomes]
rs12040592	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs12723141	1.00[CEU][hapmap];0.82[CHB][hapmap]
rs12726365	0.98[ASN][1000 genomes]
rs1622565	0.97[ASN][1000 genomes]
rs1622690	0.97[ASN][1000 genomes]
rs1633135	0.97[ASN][1000 genomes]
rs1633136	0.97[ASN][1000 genomes]
rs1633137	0.97[ASN][1000 genomes]
rs1633138	0.97[ASN][1000 genomes]
rs1633141	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs1633142	0.99[ASN][1000 genomes]
rs1633143	0.99[ASN][1000 genomes]
rs1633149	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1633158	0.92[ASN][1000 genomes]
rs1633159	0.90[ASN][1000 genomes]
rs1633160	0.92[ASN][1000 genomes]
rs1633161	0.92[ASN][1000 genomes]
rs1690782	0.97[ASN][1000 genomes]
rs1690783	0.99[ASN][1000 genomes]
rs1748377	0.97[ASN][1000 genomes]
rs1748378	0.97[ASN][1000 genomes]
rs1748379	0.94[ASN][1000 genomes]
rs1748380	0.97[ASN][1000 genomes]
rs1748381	0.97[ASN][1000 genomes]
rs1748382	0.97[ASN][1000 genomes]
rs1748383	1.00[CHB][hapmap];0.95[JPT][hapmap];0.97[ASN][1000 genomes]
rs1748386	0.99[ASN][1000 genomes]
rs1748387	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs1748395	0.99[ASN][1000 genomes]
rs2518477	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs3018315	0.97[ASN][1000 genomes]
rs3118165	1.00[CHB][hapmap];0.96[JPT][hapmap]
rs33998633	0.99[ASN][1000 genomes]
rs34261126	0.98[ASN][1000 genomes]
rs34768799	0.99[ASN][1000 genomes]
rs35043390	0.99[ASN][1000 genomes]
rs35200730	0.99[ASN][1000 genomes]
rs35717739	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs35860011	0.99[ASN][1000 genomes]
rs36120073	0.99[ASN][1000 genomes]
rs368130	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs372403	0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs374513	0.90[CHB][hapmap];0.91[JPT][hapmap];0.92[ASN][1000 genomes]
rs377795	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs379522	0.97[ASN][1000 genomes]
rs380015	0.97[ASN][1000 genomes]
rs380314	0.92[ASN][1000 genomes]
rs380382	0.92[ASN][1000 genomes]
rs383688	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs383819	0.99[ASN][1000 genomes]
rs384378	0.92[ASN][1000 genomes]
rs384414	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs389495	1.00[CHB][hapmap];0.95[JPT][hapmap]
rs392249	0.99[ASN][1000 genomes]
rs392333	0.92[ASN][1000 genomes]
rs393304	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs394591	0.92[ASN][1000 genomes]
rs394823	0.97[ASN][1000 genomes]
rs395614	0.90[ASN][1000 genomes]
rs399687	0.92[ASN][1000 genomes]
rs401904	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs402135	0.92[ASN][1000 genomes]
rs402699	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs404278	0.90[ASN][1000 genomes]
rs406361	0.96[ASN][1000 genomes]
rs406558	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs407309	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs407980	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs410919	0.89[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs411088	0.97[ASN][1000 genomes]
rs411395	0.92[ASN][1000 genomes]
rs412713	1.00[ASN][1000 genomes]
rs413557	1.00[CHB][hapmap];0.91[JPT][hapmap];0.92[ASN][1000 genomes]
rs420074	0.92[ASN][1000 genomes]
rs421484	0.99[ASN][1000 genomes]
rs421719	0.90[ASN][1000 genomes]
rs422617	0.92[ASN][1000 genomes]
rs423405	0.90[ASN][1000 genomes]
rs427275	0.90[ASN][1000 genomes]
rs429201	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs429379	0.90[ASN][1000 genomes]
rs432627	0.90[ASN][1000 genomes]
rs434232	0.92[ASN][1000 genomes]
rs434570	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs435349	0.92[ASN][1000 genomes]
rs437721	0.97[ASN][1000 genomes]
rs440862	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs440955	0.95[ASN][1000 genomes]
rs442076	0.99[ASN][1000 genomes]
rs442575	0.90[ASN][1000 genomes]
rs442713	0.92[ASN][1000 genomes]
rs448005	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs448556	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs449838	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs454825	0.94[ASN][1000 genomes]
rs583775	0.91[ASN][1000 genomes]
rs584126	0.92[ASN][1000 genomes]
rs590018	0.82[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs592815	0.81[ASN][1000 genomes]
rs594364	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs594840	0.99[ASN][1000 genomes]
rs607550	0.99[ASN][1000 genomes]
rs607948	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs607982	0.97[ASN][1000 genomes]
rs608279	0.97[ASN][1000 genomes]
rs611532	0.90[ASN][1000 genomes]
rs614164	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs620699	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs621880	0.99[ASN][1000 genomes]
rs622707	0.99[ASN][1000 genomes]
rs623215	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs651780	0.97[ASN][1000 genomes]
rs652269	0.94[ASN][1000 genomes]
rs652786	0.97[ASN][1000 genomes]
rs6661098	0.91[ASN][1000 genomes]
rs6677683	0.96[ASN][1000 genomes]
rs6684696	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs6690078	0.96[ASN][1000 genomes]
rs670766	0.94[ASN][1000 genomes]
rs671710	0.82[ASN][1000 genomes]
rs690734	0.97[ASN][1000 genomes]
rs690837	0.99[ASN][1000 genomes]
rs690984	0.99[ASN][1000 genomes]
rs691077	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.93[YRI][hapmap]
rs691174	0.99[ASN][1000 genomes]
rs691175	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs691240	0.97[ASN][1000 genomes]
rs691306	0.99[ASN][1000 genomes]
rs691314	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs691318	0.99[ASN][1000 genomes]
rs691368	0.92[ASN][1000 genomes]
rs691551	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs691935	0.97[ASN][1000 genomes]
rs691983	0.99[ASN][1000 genomes]
rs692052	0.94[ASN][1000 genomes]
rs692564	0.97[ASN][1000 genomes]
rs71515589	0.99[ASN][1000 genomes]
rs7530662	0.82[CHB][hapmap]

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	nsv999542	chr1:158015715-158368132	Bivalent Enhancer Genic enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv872479	chr1:158118787-158484285	Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv872480	chr1:158153526-158450238	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
4	esv13585	chr1:158159222-158214160	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	esv1814455	chr1:158160528-158200312	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv508626	chr1:158161932-158242158	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	esv1845799	chr1:158175976-158230829	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	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	chr1:158182200-158184000	ZNF genes & repeats	Lung	lung
2	chr1:158182600-158183800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
3	chr1:158182600-158184200	ZNF genes & repeats	Dnd41	blood
4	chr1:158183600-158183800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin

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