Variant report

Variant	rs2012736
Chromosome Location	chr2:234622379-234622380
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	chr2:234616675..234619386-chr2:234621500..234623443,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000224814	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:77)

rs_ID	r²[population]
rs1018124	0.82[ASN][1000 genomes]
rs10929293	0.85[ASN][1000 genomes]
rs12052787	0.82[ASN][1000 genomes]
rs12463641	0.85[ASN][1000 genomes]
rs12463910	0.85[ASN][1000 genomes]
rs12466779	0.85[ASN][1000 genomes]
rs12466997	0.82[ASN][1000 genomes]
rs12468274	0.85[ASN][1000 genomes]
rs12468356	0.85[ASN][1000 genomes]
rs12468543	0.83[ASN][1000 genomes]
rs12475068	0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs12475934	0.85[ASN][1000 genomes]
rs12477216	0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs12479045	0.83[ASN][1000 genomes]
rs12479208	0.85[ASN][1000 genomes]
rs17862867	0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs17862868	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17862869	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17862870	0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs17862871	0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs17862872	0.83[ASN][1000 genomes]
rs17862878	0.83[ASN][1000 genomes]
rs17863790	0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs17863791	0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs17863798	0.83[ASN][1000 genomes]
rs17864696	0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs17864697	0.83[ASN][1000 genomes]
rs17864705	0.83[ASN][1000 genomes]
rs17868333	0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs17868334	0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs17868335	0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs17874943	0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs2003569	0.82[ASN][1000 genomes]
rs2011219	0.85[ASN][1000 genomes]
rs2013018	0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs2013021	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs2013030	0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs2885295	0.85[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs28898595	0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs28898596	0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs28898605	0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs28898615	0.85[ASN][1000 genomes]
rs28898621	0.83[ASN][1000 genomes]
rs28899186	0.85[ASN][1000 genomes]
rs28899187	0.85[ASN][1000 genomes]
rs28899189	0.83[ASN][1000 genomes]
rs28899191	0.83[ASN][1000 genomes]
rs3732217	0.96[AFR][1000 genomes];0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs3732218	0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs3732219	0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs3732220	0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs3732221	0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs3755320	0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs3755321	0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs3755322	0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs3755323	0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs3771342	0.83[ASN][1000 genomes]
rs3796088	0.83[ASN][1000 genomes]
rs3806591	0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs3806593	0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs3806594	0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs3806595	0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs3892170	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3893334	0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs4556969	0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs4663326	0.85[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs4663945	0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs4663964	0.83[ASN][1000 genomes]
rs4663966	0.83[ASN][1000 genomes]
rs4663968	0.82[ASN][1000 genomes]
rs5020121	0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs62191916	0.83[ASN][1000 genomes]
rs62191917	0.83[ASN][1000 genomes]
rs62191918	0.83[ASN][1000 genomes]
rs7420193	0.82[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs904855	0.85[ASN][1000 genomes]
rs904856	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 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	nsv428072	chr2:234393609-234624769	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
3	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
4	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
5	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
6	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
7	nsv963781	chr2:234618109-234626863	Enhancers Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
8	nsv876017	chr2:234618243-234626972	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
9	esv3382515	chr2:234620643-234626555	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
10	esv3448604	chr2:234622257-234628221	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:234617800-234631600	Weak transcription	Gastric	stomach
2	chr2:234619800-234623000	Enhancers	Thymus	Thymus
3	chr2:234620400-234659200	Weak transcription	Colonic Mucosa	Colon
4	chr2:234620600-234652200	Weak transcription	Esophagus	oesophagus
5	chr2:234621400-234625800	Weak transcription	Liver	Liver
6	chr2:234621800-234622600	Weak transcription	A549	lung
7	chr2:234621800-234626200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr2:234622200-234625400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr2:234622200-234625600	Weak transcription	NHEK	skin
10	chr2:234622200-234627400	Weak transcription	Fetal Intestine Small	intestine

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links