Variant report

Variant	rs4682057
Chromosome Location	chr3:111465647-111465648
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs10212300	0.95[ASN][1000 genomes]
rs10470303	0.96[CHB][hapmap];0.91[JPT][hapmap];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10934106	0.95[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs10934107	0.96[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs11710738	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11711582	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12330761	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs12490166	0.95[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs12490595	0.99[ASN][1000 genomes]
rs12496925	0.99[ASN][1000 genomes]
rs12496971	0.99[ASN][1000 genomes]
rs12497012	0.91[ASN][1000 genomes]
rs13069980	1.00[ASN][1000 genomes]
rs13074817	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs13079085	0.95[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs2137595	0.88[EUR][1000 genomes]
rs4284954	0.95[CHB][hapmap];0.95[JPT][hapmap];0.99[ASN][1000 genomes]
rs4413291	0.88[EUR][1000 genomes]
rs4431081	0.95[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs4682298	0.80[AFR][1000 genomes]
rs4682299	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4682303	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs4682305	0.96[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs56028731	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62273780	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62275532	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6438008	0.96[ASN][1000 genomes]
rs6438009	0.96[ASN][1000 genomes]
rs6764720	0.86[ASN][1000 genomes]
rs6768713	0.95[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs6777540	0.96[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs6784753	0.95[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6786386	0.96[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs6786612	0.96[CHB][hapmap];0.91[JPT][hapmap];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6788543	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6790072	0.95[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs6790079	0.95[ASN][1000 genomes]
rs6792493	0.85[ASN][1000 genomes]
rs6796087	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6802995	0.96[ASN][1000 genomes]
rs7427201	0.95[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs7609653	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7614443	0.95[ASN][1000 genomes]
rs955381	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs959540	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9818574	0.96[CHB][hapmap];0.91[JPT][hapmap];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9823974	0.96[CHB][hapmap];0.91[JPT][hapmap];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9825915	0.94[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs9834030	0.95[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs9838371	0.95[ASN][1000 genomes]
rs9863403	0.95[ASN][1000 genomes]
rs9868171	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9868909	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9870823	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv460821	chr3:110637471-111501097	Enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv591275	chr3:110637471-111501097	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv829676	chr3:111464087-111619200	Genic enhancers Strong transcription Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:111458000-111467000	Weak transcription	Right Ventricle	heart
2	chr3:111458600-111467200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr3:111458800-111466800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr3:111459000-111466400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr3:111459000-111466400	Weak transcription	NHDF-Ad	bronchial
6	chr3:111459000-111466600	Weak transcription	Stomach Mucosa	stomach
7	chr3:111459200-111466400	Weak transcription	Gastric	stomach
8	chr3:111459200-111466600	Weak transcription	Osteobl	bone
9	chr3:111462400-111466800	Weak transcription	Liver	Liver
10	chr3:111462600-111467000	Weak transcription	Fetal Kidney	kidney
11	chr3:111462600-111468000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr3:111462600-111468000	Weak transcription	Stomach Smooth Muscle	stomach
13	chr3:111463000-111469600	Weak transcription	Adipose Nuclei	Adipose
14	chr3:111463800-111468200	Weak transcription	Colon Smooth Muscle	Colon
15	chr3:111464000-111467000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr3:111465000-111466200	Weak transcription	NHEK	skin
17	chr3:111465000-111466400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr3:111465000-111466400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr3:111465000-111466400	Weak transcription	NH-A	brain
20	chr3:111465000-111469200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chr3:111465200-111466200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr3:111465200-111466400	Weak transcription	HMEC	breast
23	chr3:111465200-111468000	Weak transcription	HUES48 Cell Line	embryonic stem cell
24	chr3:111465200-111468200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr3:111465200-111468400	Weak transcription	H1 Cell Line	embryonic stem cell
26	chr3:111465400-111469600	Weak transcription	A549	lung
27	chr3:111465400-111470400	Weak transcription	Hela-S3	cervix
28	chr3:111465600-111466000	ZNF genes & repeats	HepG2	liver

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links