Variant report

Variant	rs7431849
Chromosome Location	chr3:111322854-111322855
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs11914473	0.94[ASN][1000 genomes]
rs1513328	0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs16858327	0.88[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.91[LWK][hapmap];0.91[MEX][hapmap];0.85[MKK][hapmap];1.00[TSI][hapmap];0.83[YRI][hapmap]
rs16858329	0.88[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.91[LWK][hapmap];0.91[MEX][hapmap];0.86[MKK][hapmap];1.00[TSI][hapmap];0.83[YRI][hapmap];0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2895386	0.93[ASN][1000 genomes]
rs3733176	0.88[ASW][hapmap];0.95[CEU][hapmap];0.85[CHB][hapmap];0.91[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.90[MEX][hapmap];0.95[TSI][hapmap];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs56172864	0.94[ASN][1000 genomes]
rs56306480	0.94[ASN][1000 genomes]
rs57067927	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs57501419	0.96[ASN][1000 genomes]
rs57831621	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6763322	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6765832	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6768092	0.94[ASN][1000 genomes]
rs6770144	0.83[ASW][hapmap];1.00[CEU][hapmap];0.92[CHB][hapmap];0.91[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.95[TSI][hapmap];0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6770679	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6771309	0.88[ASW][hapmap];1.00[CEU][hapmap];0.92[CHB][hapmap];0.91[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6780210	0.88[ASW][hapmap];1.00[CEU][hapmap];0.92[CHB][hapmap];0.91[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6780729	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6787870	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6801876	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73230132	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73230143	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73852844	0.94[ASN][1000 genomes]
rs73852849	0.94[ASN][1000 genomes]
rs7637536	0.82[ASN][1000 genomes]
rs9819529	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9858544	1.00[ASW][hapmap];1.00[CEU][hapmap];0.92[CHB][hapmap];0.88[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.98[LWK][hapmap];1.00[MEX][hapmap];0.99[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[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	nsv997756	chr3:111226058-111376585	Active TSS Enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs7431849	CD200	cis	parietal	SCAN

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:111299400-111328600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr3:111314000-111326800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
3	chr3:111314200-111323400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr3:111314200-111327200	Strong transcription	Primary T cells fromperipheralblood	blood
5	chr3:111314400-111324000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
6	chr3:111314400-111328600	Weak transcription	Thymus	Thymus
7	chr3:111314800-111323000	Weak transcription	NHEK	skin
8	chr3:111315600-111323400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr3:111317600-111323000	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr3:111317800-111326000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
11	chr3:111318600-111326800	Strong transcription	Primary T cells from cord blood	blood
12	chr3:111318800-111323200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
13	chr3:111321000-111323000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr3:111321000-111323200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr3:111321600-111325200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr3:111321600-111326200	Strong transcription	Fetal Thymus	thymus
17	chr3:111321600-111328200	Genic enhancers	Primary T helper cells PMA-I stimulated	--
18	chr3:111322000-111323200	Genic enhancers	Primary T helper cells fromperipheralblood	blood
19	chr3:111322000-111324000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
20	chr3:111322200-111323600	Enhancers	Primary B cells from cord blood	blood
21	chr3:111322200-111323600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
22	chr3:111322200-111323800	Enhancers	Primary B cells from peripheral blood	blood
23	chr3:111322400-111325200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
24	chr3:111322600-111323400	Genic enhancers	Dnd41	blood
25	chr3:111322600-111324400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr3:111322600-111326600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
27	chr3:111322800-111323000	Enhancers	Primary T helper naive cells from peripheral blood	blood
28	chr3:111322800-111323200	Genic enhancers	Primary T helper 17 cells PMA-I stimulated	--
29	chr3:111322800-111323200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr3:111322800-111324800	Enhancers	Osteobl	bone

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links