Variant report

Variant	rs3732217
Chromosome Location	chr2:234628270-234628271
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 85 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:76)

rs_ID	r²[population]
rs1018124	0.81[ASN][1000 genomes]
rs10929293	0.84[ASN][1000 genomes]
rs12052787	0.81[ASN][1000 genomes]
rs12463641	0.83[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs12463910	0.83[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs12466779	0.83[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs12466997	0.81[ASN][1000 genomes]
rs12468274	0.83[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs12468356	0.83[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs12468543	0.83[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs12475068	0.83[ASN][1000 genomes]
rs12475934	0.83[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs12477216	0.83[ASN][1000 genomes]
rs12479045	0.82[ASN][1000 genomes]
rs12479208	0.83[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs17862867	0.83[ASN][1000 genomes]
rs17862868	0.96[AFR][1000 genomes];0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs17862869	0.86[AFR][1000 genomes];0.86[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs17862870	0.83[ASN][1000 genomes]
rs17862871	0.83[ASN][1000 genomes]
rs17862872	0.83[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs17862878	0.82[ASN][1000 genomes]
rs17863790	0.83[ASN][1000 genomes]
rs17863791	0.83[ASN][1000 genomes]
rs17863798	0.83[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs17864696	0.83[ASN][1000 genomes]
rs17864697	0.82[ASN][1000 genomes]
rs17864705	0.82[ASN][1000 genomes]
rs17868333	0.83[ASN][1000 genomes]
rs17868334	0.83[ASN][1000 genomes]
rs17868335	0.83[ASN][1000 genomes]
rs17874943	0.83[ASN][1000 genomes]
rs2003569	0.81[ASN][1000 genomes]
rs2011219	0.83[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs2012736	0.96[AFR][1000 genomes];0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2013018	0.83[ASN][1000 genomes]
rs2013021	0.83[ASN][1000 genomes]
rs2013030	0.83[ASN][1000 genomes]
rs2885295	0.82[ASN][1000 genomes]
rs28898595	0.83[ASN][1000 genomes]
rs28898596	0.83[ASN][1000 genomes]
rs28898605	0.83[ASN][1000 genomes]
rs28898615	0.83[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs28898621	0.83[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs28899186	0.83[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs28899187	0.83[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs28899189	0.83[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs28899191	0.83[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs3732218	0.83[ASN][1000 genomes]
rs3732219	0.83[ASN][1000 genomes]
rs3732220	0.83[ASN][1000 genomes]
rs3732221	0.83[ASN][1000 genomes]
rs3755320	0.83[ASN][1000 genomes]
rs3755321	0.83[ASN][1000 genomes]
rs3755322	0.83[ASN][1000 genomes]
rs3755323	0.83[ASN][1000 genomes]
rs3771342	0.82[ASN][1000 genomes]
rs3796088	0.80[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs3806591	0.83[ASN][1000 genomes]
rs3806593	0.83[ASN][1000 genomes]
rs3806594	0.83[ASN][1000 genomes]
rs3806595	0.83[ASN][1000 genomes]
rs3892170	0.92[AFR][1000 genomes];0.86[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs3893334	0.83[ASN][1000 genomes]
rs4556969	0.83[ASN][1000 genomes]
rs4663326	0.82[ASN][1000 genomes]
rs4663945	0.83[ASN][1000 genomes]
rs4663964	0.83[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs4663966	0.83[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs4663968	0.83[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs5020121	0.83[ASN][1000 genomes]
rs62191916	0.83[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs62191917	0.83[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs62191918	0.80[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs904855	0.83[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs904856	0.83[AMR][1000 genomes];0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529419	chr2:234229606-234670426	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
2	nsv1010936	chr2:234549011-234640221	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
3	nsv1013712	chr2:234558457-235495825	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription 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	41 gene(s)	inside rSNPs	diseases
4	nsv532476	chr2:234595695-235134381	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
5	esv2760615	chr2:234613030-234640233	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
6	esv3460836	chr2:234623884-234634466	Enhancers ZNF genes & repeats Strong transcription Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island lncRNA	4 gene(s)	inside rSNPs	diseases
7	esv3460837	chr2:234624010-234634422	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats	TF binding region CpG island lncRNA	4 gene(s)	inside rSNPs	diseases
8	nsv979187	chr2:234627363-234628474	Weak transcription Enhancers Active TSS Strong transcription	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases
9	esv3429693	chr2:234627837-234638254	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:234617800-234631600	Weak transcription	Gastric	stomach
2	chr2:234620400-234659200	Weak transcription	Colonic Mucosa	Colon
3	chr2:234620600-234652200	Weak transcription	Esophagus	oesophagus
4	chr2:234626000-234634600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr2:234626200-234649600	Weak transcription	Rectal Mucosa Donor 29	rectum
6	chr2:234626600-234628600	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr2:234626600-234668400	Weak transcription	NHEK	skin
8	chr2:234627200-234630000	Active TSS	Liver	Liver
9	chr2:234627600-234629000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr2:234627600-234637200	Weak transcription	Duodenum Mucosa	Duodenum
11	chr2:234627800-234636000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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