Variant report

Variant	rs68039795
Chromosome Location	chr11:56677107-56677108
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10501359	0.81[ASN][1000 genomes]
rs11228836	0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11603620	0.91[ASN][1000 genomes]
rs12272961	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12282767	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12416998	0.91[ASN][1000 genomes]
rs12419314	0.80[ASN][1000 genomes]
rs12805799	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1613887	0.81[ASN][1000 genomes]
rs1622278	0.92[ASN][1000 genomes]
rs17640838	0.86[ASN][1000 genomes]
rs17640885	0.96[ASN][1000 genomes]
rs1783444	0.81[ASN][1000 genomes]
rs1783445	0.81[ASN][1000 genomes]
rs1783446	0.81[ASN][1000 genomes]
rs1783447	0.81[ASN][1000 genomes]
rs1783450	0.80[ASN][1000 genomes]
rs1783451	0.81[ASN][1000 genomes]
rs1783459	0.82[ASN][1000 genomes]
rs1783465	0.81[ASN][1000 genomes]
rs1792494	0.81[ASN][1000 genomes]
rs1792495	0.81[ASN][1000 genomes]
rs1792496	0.81[ASN][1000 genomes]
rs1792498	0.81[ASN][1000 genomes]
rs1792499	0.81[ASN][1000 genomes]
rs1793426	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1892787	0.81[ASN][1000 genomes]
rs1938751	0.80[ASN][1000 genomes]
rs1938753	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1938759	0.96[ASN][1000 genomes]
rs1938760	0.96[ASN][1000 genomes]
rs2226850	0.80[ASN][1000 genomes]
rs2226851	0.80[ASN][1000 genomes]
rs2374	0.81[ASN][1000 genomes]
rs4939095	0.80[ASN][1000 genomes]
rs4939097	0.80[ASN][1000 genomes]
rs523098	0.81[ASN][1000 genomes]
rs56210588	0.80[ASN][1000 genomes]
rs7111113	0.94[ASN][1000 genomes]
rs7118645	0.96[ASN][1000 genomes]
rs7119402	0.91[ASN][1000 genomes]
rs731744	0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs737368	0.87[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs7930832	0.80[ASN][1000 genomes]
rs7940288	0.86[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7943283	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7947879	0.96[ASN][1000 genomes]
rs947805	0.89[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs947806	0.86[AFR][1000 genomes];0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv468577	chr11:56503728-56704042	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases
2	nsv555101	chr11:56503728-56704042	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases
3	nsv469960	chr11:56605222-56704042	Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv1045889	chr11:56624365-56737435	Flanking Active TSS Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv520375	chr11:56669830-56704042	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:56673600-56677400	Weak transcription	Rectal Mucosa Donor 29	rectum
2	chr11:56674600-56677600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr11:56674600-56677800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr11:56675600-56677200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr11:56675600-56677200	Weak transcription	NHEK	skin
6	chr11:56676600-56678200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr11:56676600-56678200	Enhancers	Rectal Mucosa Donor 31	rectum
8	chr11:56676600-56679200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr11:56676600-56679200	Enhancers	HMEC	breast
10	chr11:56676800-56677400	Flanking Active TSS	A549	lung
11	chr11:56677000-56678200	Enhancers	Fetal Intestine Large	intestine

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