Variant report

Variant	rs7075138
Chromosome Location	chr10:90140199-90140200
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs10887807	0.86[ASN][1000 genomes]
rs11202705	0.81[ASN][1000 genomes]
rs11202722	0.84[ASN][1000 genomes]
rs11202726	0.88[ASN][1000 genomes]
rs11202731	0.92[ASN][1000 genomes]
rs11202734	0.93[AFR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11528433	0.80[ASN][1000 genomes]
rs11598623	0.88[ASN][1000 genomes]
rs12217988	0.93[AFR][1000 genomes];0.80[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12219831	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12220632	0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12221213	0.85[ASN][1000 genomes]
rs12569922	0.87[ASN][1000 genomes]
rs12572813	0.80[ASN][1000 genomes]
rs1582223	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1582224	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1613409	0.89[AFR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1648512	0.92[ASN][1000 genomes]
rs1648523	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17111200	0.87[ASN][1000 genomes]
rs1774970	0.95[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1774971	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2241515	0.82[ASN][1000 genomes]
rs3740279	0.90[ASN][1000 genomes]
rs3781201	0.86[ASN][1000 genomes]
rs55749454	0.85[ASN][1000 genomes]
rs57949777	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs59184458	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs59482232	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs61260851	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7073755	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7097606	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs74149704	0.89[ASN][1000 genomes]
rs74149712	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs74149714	0.98[AFR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs74149715	0.98[AFR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs752709	0.88[ASN][1000 genomes]
rs792224	0.84[ASN][1000 genomes]
rs792225	0.92[ASN][1000 genomes]
rs792227	0.90[ASN][1000 genomes]
rs792228	0.93[ASN][1000 genomes]
rs792229	0.86[ASN][1000 genomes]
rs792232	0.84[AFR][1000 genomes];0.80[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs792234	0.82[AFR][1000 genomes]
rs880793	0.83[ASN][1000 genomes]
rs880794	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv895879	chr10:90015725-90219298	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv482385	chr10:90066140-90259751	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv948664	chr10:90076715-90517150	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv1054984	chr10:90122512-90278038	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:90135800-90144800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr10:90136000-90140400	Weak transcription	Primary B cells from cord blood	blood
3	chr10:90139200-90140200	Enhancers	Dnd41	blood
4	chr10:90139800-90144000	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr10:90139800-90144200	Weak transcription	Duodenum Mucosa	Duodenum
6	chr10:90139800-90144200	Weak transcription	Fetal Thymus	thymus
7	chr10:90139800-90144600	Weak transcription	Small Intestine	intestine
8	chr10:90139800-90144600	Weak transcription	Thymus	Thymus
9	chr10:90139800-90144800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr10:90139800-90144800	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr10:90139800-90145200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr10:90139800-90145200	Weak transcription	NHDF-Ad	bronchial
13	chr10:90139800-90146400	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr10:90140000-90143200	Weak transcription	Fetal Intestine Large	intestine
15	chr10:90140000-90143200	Weak transcription	Fetal Intestine Small	intestine
16	chr10:90140000-90144600	Weak transcription	A549	lung
17	chr10:90140000-90144600	Weak transcription	HMEC	breast
18	chr10:90140000-90145400	Weak transcription	Osteobl	bone

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