Variant report

Variant	rs73122446
Chromosome Location	chr1:224283292-224283293
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:224281326..224283671-chr1:224300267..224301796,2	K562	blood:

Variant related genes	Relation type
ENSG00000143756	Chromatin interaction

Extended variants
information (count: 87 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:83)

rs_ID	r²[population]
rs10737430	1.00[ASN][1000 genomes]
rs10737435	1.00[ASN][1000 genomes]
rs10737437	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10753448	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10753453	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10799483	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10799486	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10916326	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10916388	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11804140	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13313058	1.00[ASN][1000 genomes]
rs1586888	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1602706	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1891738	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1891739	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2035897	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2048994	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2172359	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2404844	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2404845	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2404846	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2404847	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2896986	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4353057	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4653565	1.00[ASN][1000 genomes]
rs4653955	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4653956	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4653985	1.00[EUR][1000 genomes]
rs56718298	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs56887412	1.00[ASN][1000 genomes]
rs57138220	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs57746928	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs57823919	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs58090997	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59018039	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs59368039	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs59518883	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs59819476	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60013765	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs60381264	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs60432349	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs60643079	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs60972853	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61074366	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61144016	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61347348	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61495337	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6426108	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6426112	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6426162	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6659249	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6663997	1.00[ASN][1000 genomes]
rs6668856	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6668862	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6670475	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6670483	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6670591	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6671784	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6679683	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6687331	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6689914	1.00[ASN][1000 genomes]
rs6689922	1.00[ASN][1000 genomes]
rs6690358	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6690543	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6702019	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6704386	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73120501	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73122403	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73122404	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73122411	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73122413	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73122436	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73122438	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73122441	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73124453	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73126416	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7526301	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7535007	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7537121	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs908796	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs937155	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs969008	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs969009	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	nsv427941	chr1:224085052-224363163	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
4	nsv832692	chr1:224206536-224407717	Strong transcription Enhancers Flanking Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:224282200-224283400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr1:224283200-224284000	Enhancers	Stomach Mucosa	stomach

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