Variant report

Variant	rs6684696
Chromosome Location	chr1:158197221-158197222
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 132 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:124)

rs_ID	r²[population]
rs11264929	0.89[ASN][1000 genomes]
rs11264930	0.84[ASN][1000 genomes]
rs12040592	0.92[ASN][1000 genomes]
rs12726365	0.92[ASN][1000 genomes]
rs1622565	0.90[ASN][1000 genomes]
rs1622690	0.90[ASN][1000 genomes]
rs1633135	0.90[ASN][1000 genomes]
rs1633136	0.91[ASN][1000 genomes]
rs1633137	0.91[ASN][1000 genomes]
rs1633138	0.91[ASN][1000 genomes]
rs1633141	0.92[ASN][1000 genomes]
rs1633142	0.92[ASN][1000 genomes]
rs1633143	0.92[ASN][1000 genomes]
rs1633158	0.98[ASN][1000 genomes]
rs1633159	0.97[ASN][1000 genomes]
rs1633160	0.98[ASN][1000 genomes]
rs1633161	0.98[ASN][1000 genomes]
rs1690782	0.90[ASN][1000 genomes]
rs1690783	0.92[ASN][1000 genomes]
rs1748377	0.91[ASN][1000 genomes]
rs1748378	0.90[ASN][1000 genomes]
rs1748379	0.88[ASN][1000 genomes]
rs1748380	0.91[ASN][1000 genomes]
rs1748381	0.91[ASN][1000 genomes]
rs1748382	0.91[ASN][1000 genomes]
rs1748383	0.91[ASN][1000 genomes]
rs1748386	0.92[ASN][1000 genomes]
rs1748387	0.92[ASN][1000 genomes]
rs1748395	0.92[ASN][1000 genomes]
rs2518477	0.92[ASN][1000 genomes]
rs3018315	0.90[ASN][1000 genomes]
rs33998633	0.92[ASN][1000 genomes]
rs34261126	0.92[ASN][1000 genomes]
rs34768799	0.92[ASN][1000 genomes]
rs35043390	0.92[ASN][1000 genomes]
rs35200730	0.92[ASN][1000 genomes]
rs35717739	0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35860011	0.92[ASN][1000 genomes]
rs36120073	0.92[ASN][1000 genomes]
rs372403	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs374513	0.98[ASN][1000 genomes]
rs374686	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs379522	0.91[ASN][1000 genomes]
rs380015	0.91[ASN][1000 genomes]
rs380314	0.98[ASN][1000 genomes]
rs380382	0.98[ASN][1000 genomes]
rs383688	0.98[ASN][1000 genomes]
rs383819	0.92[ASN][1000 genomes]
rs384378	0.83[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs384414	0.92[ASN][1000 genomes]
rs392249	0.92[ASN][1000 genomes]
rs392333	0.98[ASN][1000 genomes]
rs394591	0.98[ASN][1000 genomes]
rs394823	0.91[ASN][1000 genomes]
rs395614	0.99[ASN][1000 genomes]
rs399687	0.98[ASN][1000 genomes]
rs401904	0.91[ASN][1000 genomes]
rs402135	0.98[ASN][1000 genomes]
rs402699	0.92[ASN][1000 genomes]
rs404278	0.99[ASN][1000 genomes]
rs406361	0.90[ASN][1000 genomes]
rs406558	0.99[ASN][1000 genomes]
rs407309	0.92[ASN][1000 genomes]
rs410919	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs411088	0.91[ASN][1000 genomes]
rs411395	0.98[ASN][1000 genomes]
rs412713	0.91[ASN][1000 genomes]
rs413557	0.98[ASN][1000 genomes]
rs420074	0.98[ASN][1000 genomes]
rs421484	0.92[ASN][1000 genomes]
rs421719	0.96[ASN][1000 genomes]
rs422617	0.98[ASN][1000 genomes]
rs423405	0.97[ASN][1000 genomes]
rs427275	0.99[ASN][1000 genomes]
rs429201	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs429379	0.99[ASN][1000 genomes]
rs432627	0.83[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs434232	0.98[ASN][1000 genomes]
rs434570	0.96[ASN][1000 genomes]
rs435349	0.98[ASN][1000 genomes]
rs437721	0.91[ASN][1000 genomes]
rs440862	0.91[ASN][1000 genomes]
rs440955	0.89[ASN][1000 genomes]
rs442076	0.92[ASN][1000 genomes]
rs442575	0.99[ASN][1000 genomes]
rs442713	0.98[ASN][1000 genomes]
rs449838	0.92[ASN][1000 genomes]
rs454825	0.88[ASN][1000 genomes]
rs583775	0.97[ASN][1000 genomes]
rs584126	0.98[ASN][1000 genomes]
rs590018	0.92[ASN][1000 genomes]
rs594364	0.92[ASN][1000 genomes]
rs594840	0.92[ASN][1000 genomes]
rs607550	0.92[ASN][1000 genomes]
rs607948	0.92[ASN][1000 genomes]
rs607982	0.90[ASN][1000 genomes]
rs608279	0.90[ASN][1000 genomes]
rs611532	0.99[ASN][1000 genomes]
rs620699	0.92[ASN][1000 genomes]
rs621880	0.92[ASN][1000 genomes]
rs622707	0.92[ASN][1000 genomes]
rs651780	0.91[ASN][1000 genomes]
rs652269	0.88[ASN][1000 genomes]
rs652786	0.91[ASN][1000 genomes]
rs6661098	1.00[ASN][1000 genomes]
rs6677683	0.90[ASN][1000 genomes]
rs6680015	0.84[EUR][1000 genomes]
rs6690078	0.90[ASN][1000 genomes]
rs670766	0.88[ASN][1000 genomes]
rs690734	0.91[ASN][1000 genomes]
rs690837	0.92[ASN][1000 genomes]
rs690984	0.92[ASN][1000 genomes]
rs691174	0.92[ASN][1000 genomes]
rs691175	0.92[ASN][1000 genomes]
rs691240	0.90[ASN][1000 genomes]
rs691306	0.92[ASN][1000 genomes]
rs691314	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs691318	0.92[ASN][1000 genomes]
rs691368	0.86[ASN][1000 genomes]
rs691935	0.90[ASN][1000 genomes]
rs691983	0.92[ASN][1000 genomes]
rs692052	0.88[ASN][1000 genomes]
rs692564	0.91[ASN][1000 genomes]
rs71515589	0.92[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	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
8	esv1850818	chr1:158192339-158200312	Weak transcription ZNF genes & repeats	lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:158194200-158198400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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