Variant report

Variant	rs2223329
Chromosome Location	chr1:186705404-186705405
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10737269	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10752971	0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10752973	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10752974	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10798055	0.98[EUR][1000 genomes]
rs10798057	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10911922	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1158042	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1158043	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12029765	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12116711	0.92[EUR][1000 genomes]
rs12117451	0.96[EUR][1000 genomes]
rs12119919	0.96[EUR][1000 genomes]
rs12124257	0.80[CEU][hapmap]
rs12144220	0.96[EUR][1000 genomes]
rs12239324	1.00[ASN][1000 genomes]
rs16825688	1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs1980454	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2205951	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2223310	1.00[JPT][hapmap]
rs2223330	1.00[EUR][1000 genomes]
rs3218622	1.00[CHB][hapmap]
rs4648259	1.00[CHB][hapmap]
rs4648282	0.83[ASN][1000 genomes]
rs4648284	0.83[ASN][1000 genomes]
rs4648298	1.00[JPT][hapmap]
rs4650701	1.00[EUR][1000 genomes]
rs4650705	1.00[JPT][hapmap]
rs56337220	1.00[ASN][1000 genomes]
rs61516014	0.83[ASN][1000 genomes]
rs6425049	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6660635	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6663605	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6688484	0.92[EUR][1000 genomes]
rs6692679	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6695425	1.00[JPT][hapmap]
rs6696144	1.00[ASN][1000 genomes]
rs689462	1.00[JPT][hapmap]
rs689468	0.83[ASN][1000 genomes]
rs689470	1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs74134717	0.83[ASN][1000 genomes]
rs74134991	1.00[ASN][1000 genomes]
rs74134997	1.00[ASN][1000 genomes]
rs7418312	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7516460	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7520374	0.83[ASN][1000 genomes]
rs7523981	0.96[EUR][1000 genomes]
rs7532307	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7554410	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7555275	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs766400	0.98[EUR][1000 genomes]
rs964570	0.98[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1004481	chr1:186095854-186750968	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
2	nsv535223	chr1:186095854-186750968	Strong transcription Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
3	esv2762854	chr1:186547101-186847574	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
4	nsv872590	chr1:186557453-187500338	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
5	nsv466261	chr1:186652395-186742947	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
6	nsv548405	chr1:186652395-186742947	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:186704000-186707600	Enhancers	NHEK	skin
2	chr1:186704200-186709400	Enhancers	HMEC	breast
3	chr1:186705000-186706400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr1:186705200-186707000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr1:186705400-186706200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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