Variant report

Variant	rs72811894
Chromosome Location	chr2:49070423-49070424
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs10187109	0.94[ASN][1000 genomes]
rs10210521	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10210646	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12469769	0.82[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs12477968	0.82[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs12478030	0.82[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs13001380	0.88[ASN][1000 genomes]
rs13418054	0.85[ASN][1000 genomes]
rs17037665	0.82[AMR][1000 genomes]
rs17037685	0.85[ASN][1000 genomes]
rs17037688	0.82[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs17037700	0.82[ASN][1000 genomes]
rs34307840	0.88[ASN][1000 genomes]
rs34682390	0.84[ASN][1000 genomes]
rs35457516	0.85[ASN][1000 genomes]
rs35486816	0.85[ASN][1000 genomes]
rs4254550	0.88[ASN][1000 genomes]
rs4271811	0.83[ASN][1000 genomes]
rs4325806	0.94[ASN][1000 genomes]
rs4462824	0.86[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs4499466	0.82[ASN][1000 genomes]
rs55649687	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs55671226	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs55671322	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs56406984	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61349130	0.99[ASN][1000 genomes]
rs62137442	0.90[ASN][1000 genomes]
rs62137443	0.92[ASN][1000 genomes]
rs6419618	0.94[ASN][1000 genomes]
rs6708130	0.82[ASN][1000 genomes]
rs72811865	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72811866	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72811883	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72811897	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs72811898	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs72811899	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72813703	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72813705	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72813714	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs72823278	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs72823284	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs72823285	0.82[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs72823286	0.85[ASN][1000 genomes]
rs733726	0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1002793	chr2:48771220-49466550	ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
2	nsv1004965	chr2:48796170-49443587	Bivalent Enhancer Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv535684	chr2:48796170-49443587	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv498119	chr2:48808834-49422647	Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
5	nsv998864	chr2:49015878-49230000	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:48994600-49080200	Weak transcription	Stomach Smooth Muscle	stomach
2	chr2:49068800-49071600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr2:49069000-49071200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr2:49069000-49071200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr2:49069200-49071200	Weak transcription	HMEC	breast
6	chr2:49070400-49071800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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