Variant report

Variant	rs502174
Chromosome Location	chr11:102682503-102682504
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs1010698	0.83[CEU][hapmap];0.89[CHB][hapmap];0.93[JPT][hapmap];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10791596	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10895364	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10895365	0.85[AFR][1000 genomes];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10895366	0.85[EUR][1000 genomes]
rs11225434	0.83[AFR][1000 genomes];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1144396	0.95[CEU][hapmap];0.89[CHB][hapmap];0.93[JPT][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1144397	0.84[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs1144398	0.86[AFR][1000 genomes]
rs12792871	0.84[CEU][hapmap];0.85[EUR][1000 genomes]
rs12801529	0.81[AFR][1000 genomes];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12804136	0.82[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2097248	0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2155013	0.89[CHB][hapmap];0.93[JPT][hapmap];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2212637	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4754884	0.89[CHB][hapmap];0.88[JPT][hapmap];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs520540	0.84[CEU][hapmap];0.89[CHB][hapmap];0.88[JPT][hapmap];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs526215	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs565082	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs575027	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs591058	0.83[CEU][hapmap];0.89[CHB][hapmap];0.86[JPT][hapmap];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs595840	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs602128	0.84[CEU][hapmap];0.89[CHB][hapmap];0.81[JPT][hapmap];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs617819	0.82[ASN][1000 genomes]
rs632478	0.82[ASN][1000 genomes]
rs633962	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs635746	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs639752	0.83[CEU][hapmap];0.89[CHB][hapmap];0.93[JPT][hapmap];0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs645419	0.83[CEU][hapmap];0.89[CHB][hapmap];0.85[JPT][hapmap];0.82[ASN][1000 genomes]
rs6590993	0.83[AFR][1000 genomes];0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6590994	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs666734	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs678815	0.84[CEU][hapmap];0.89[CHB][hapmap];0.81[JPT][hapmap];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs679620	0.89[CHB][hapmap];0.81[JPT][hapmap];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7117013	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7118731	0.88[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs7126392	0.82[AFR][1000 genomes];0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs756544	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7926920	0.83[CEU][hapmap];0.89[CHB][hapmap];0.93[JPT][hapmap];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7946057	0.81[AFR][1000 genomes];0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv898335	chr11:102682285-102866158	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:102678800-102690000	Weak transcription	Gastric	stomach
2	chr11:102679000-102690400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr11:102681000-102682600	Enhancers	Stomach Mucosa	stomach
4	chr11:102681600-102682600	Enhancers	Duodenum Mucosa	Duodenum
5	chr11:102681600-102682600	Enhancers	Fetal Intestine Small	intestine
6	chr11:102681600-102682600	Enhancers	NHEK	skin
7	chr11:102681600-102682800	Enhancers	Fetal Intestine Large	intestine
8	chr11:102681800-102683800	Weak transcription	HMEC	breast
9	chr11:102682200-102685000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links