Variant report

Variant	rs6506651
Chromosome Location	chr18:9329122-9329123
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr18:9328376..9330058-chr18:9340619..9342360,2	K562	blood:
2	chr18:9320913..9322639-chr18:9326828..9329816,2	K562	blood:

Extended variants
information (count: 86 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:79)

rs_ID	r²[population]
rs1046483	0.93[ASN][1000 genomes]
rs10502391	0.86[ASN][1000 genomes]
rs1114591	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11659948	0.86[ASN][1000 genomes]
rs12326829	0.86[ASN][1000 genomes]
rs1443597	0.86[ASN][1000 genomes]
rs1443598	0.86[ASN][1000 genomes]
rs16954886	0.86[ASN][1000 genomes]
rs16954905	0.86[ASN][1000 genomes]
rs16954914	0.86[ASN][1000 genomes]
rs17498752	0.86[ASN][1000 genomes]
rs17498969	0.86[ASN][1000 genomes]
rs17499116	0.86[ASN][1000 genomes]
rs1899668	0.86[ASN][1000 genomes]
rs2120316	0.86[ASN][1000 genomes]
rs28520663	0.86[ASN][1000 genomes]
rs28619483	0.93[ASN][1000 genomes]
rs28637808	0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2864515	0.82[ASN][1000 genomes]
rs28820062	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28844999	0.88[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3213925	0.86[ASN][1000 genomes]
rs3744822	0.86[ASN][1000 genomes]
rs3744823	0.86[ASN][1000 genomes]
rs4356535	0.86[ASN][1000 genomes]
rs4449017	0.83[ASN][1000 genomes]
rs4490062	0.82[ASN][1000 genomes]
rs5011606	0.86[ASN][1000 genomes]
rs56996721	0.82[ASN][1000 genomes]
rs57567668	0.93[ASN][1000 genomes]
rs59018067	0.86[ASN][1000 genomes]
rs59616258	0.86[ASN][1000 genomes]
rs59633812	0.86[ASN][1000 genomes]
rs59864974	0.93[ASN][1000 genomes]
rs60119987	0.86[ASN][1000 genomes]
rs60143204	0.82[ASN][1000 genomes]
rs60354371	0.86[ASN][1000 genomes]
rs62085951	0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62087470	0.80[ASN][1000 genomes]
rs7229105	0.82[ASN][1000 genomes]
rs7234017	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7235358	0.86[ASN][1000 genomes]
rs7237039	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7242002	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7242624	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72937244	0.82[ASN][1000 genomes]
rs72937245	0.82[ASN][1000 genomes]
rs72937248	0.82[ASN][1000 genomes]
rs72937250	0.82[ASN][1000 genomes]
rs72937258	0.86[ASN][1000 genomes]
rs72937259	0.86[ASN][1000 genomes]
rs72937263	0.86[ASN][1000 genomes]
rs72937267	0.86[ASN][1000 genomes]
rs72937270	0.86[ASN][1000 genomes]
rs72937287	0.86[ASN][1000 genomes]
rs72937291	0.86[ASN][1000 genomes]
rs72937297	0.86[ASN][1000 genomes]
rs72937301	0.86[ASN][1000 genomes]
rs72937302	0.86[ASN][1000 genomes]
rs72939207	0.86[ASN][1000 genomes]
rs72939211	0.86[ASN][1000 genomes]
rs72939216	0.86[ASN][1000 genomes]
rs72939219	0.86[ASN][1000 genomes]
rs72939220	0.86[ASN][1000 genomes]
rs72939221	0.86[ASN][1000 genomes]
rs72939224	0.86[ASN][1000 genomes]
rs72939227	0.86[ASN][1000 genomes]
rs72939230	0.86[ASN][1000 genomes]
rs72939231	0.86[ASN][1000 genomes]
rs72939232	0.86[ASN][1000 genomes]
rs72939235	0.86[ASN][1000 genomes]
rs72939239	0.86[ASN][1000 genomes]
rs7506375	0.86[ASN][1000 genomes]
rs8089057	0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8096630	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8098516	0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8098544	0.86[ASN][1000 genomes]
rs8099583	0.86[ASN][1000 genomes]
rs9748485	0.82[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	nsv916373	chr18:9026803-9592201	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS 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	nsv1056407	chr18:9144345-9553764	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
3	nsv458023	chr18:9240413-9357786	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
4	nsv576447	chr18:9240413-9357786	ZNF genes & repeats Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
5	nsv1062025	chr18:9287249-9552470	Flanking Active TSS Strong transcription Bivalent/Poised TSS Active TSS Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
6	nsv543643	chr18:9287249-9552470	ZNF genes & repeats Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
7	nsv909365	chr18:9299538-9400422	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:9320200-9333800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr18:9320600-9333400	Weak transcription	Aorta	Aorta
3	chr18:9321800-9333600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr18:9321800-9333600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr18:9324400-9333400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr18:9324600-9329400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr18:9324600-9334000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr18:9327400-9333400	Weak transcription	Placenta	Placenta
9	chr18:9328600-9329600	Enhancers	Muscle Satellite Cultured Cells	--

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