Variant report

Variant	rs6696222
Chromosome Location	chr1:224052248-224052249
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs10503144	1.00[ASN][1000 genomes]
rs12059128	1.00[ASN][1000 genomes]
rs12059770	1.00[ASN][1000 genomes]
rs12060361	1.00[ASN][1000 genomes]
rs12080250	1.00[ASN][1000 genomes]
rs12091841	1.00[ASN][1000 genomes]
rs12564557	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12565202	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12565573	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12565967	1.00[ASN][1000 genomes]
rs12566817	1.00[ASN][1000 genomes]
rs16841190	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16842162	1.00[ASN][1000 genomes]
rs16842229	0.87[ASN][1000 genomes]
rs16842257	1.00[ASN][1000 genomes]
rs16842326	1.00[ASN][1000 genomes]
rs16842343	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28370159	1.00[ASN][1000 genomes]
rs28370170	1.00[ASN][1000 genomes]
rs34683843	1.00[ASN][1000 genomes]
rs36032024	1.00[ASN][1000 genomes]
rs3885657	1.00[ASN][1000 genomes]
rs41303996	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58774026	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61823581	1.00[ASN][1000 genomes]
rs61823583	1.00[ASN][1000 genomes]
rs61823585	1.00[ASN][1000 genomes]
rs61823587	1.00[ASN][1000 genomes]
rs61823591	1.00[ASN][1000 genomes]
rs61824003	1.00[ASN][1000 genomes]
rs61824008	1.00[ASN][1000 genomes]
rs6604724	1.00[ASN][1000 genomes]
rs6604727	1.00[ASN][1000 genomes]
rs6604728	1.00[ASN][1000 genomes]
rs6604729	1.00[ASN][1000 genomes]
rs6604730	1.00[ASN][1000 genomes]
rs6658954	1.00[ASN][1000 genomes]
rs6678365	1.00[ASN][1000 genomes]
rs6682964	1.00[ASN][1000 genomes]
rs6685557	1.00[ASN][1000 genomes]
rs6691315	1.00[ASN][1000 genomes]
rs6694960	1.00[ASN][1000 genomes]
rs6700366	1.00[ASN][1000 genomes]
rs73116425	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73116447	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73116451	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73116456	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7331	1.00[ASN][1000 genomes]
rs7515821	0.81[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7528455	1.00[ASN][1000 genomes]
rs7530328	1.00[ASN][1000 genomes]
rs7533551	1.00[ASN][1000 genomes]
rs7535882	1.00[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	esv3361888	chr1:223725597-224114846	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
2	esv34082	chr1:223851018-224144509	Enhancers Genic enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
3	nsv1008800	chr1:223904653-224061032	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
4	esv2757772	chr1:223935220-224363163	Genic enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
5	esv2759000	chr1:223935220-224363163	Enhancers Weak transcription Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
6	esv1793921	chr1:224048131-224105965	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv945313	chr1:224048561-224060636	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region	3 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	chr1:224051800-224052400	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr1:224052000-224052400	ZNF genes & repeats	Spleen	Spleen
3	chr1:224052000-224052600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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