Variant report

Variant	rs7701296
Chromosome Location	chr5:108460725-108460726
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10035284	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10055161	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10063768	0.82[EUR][1000 genomes]
rs10066375	0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10067445	0.81[AFR][1000 genomes];0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10074150	0.82[ASN][1000 genomes]
rs10074425	0.82[ASN][1000 genomes]
rs10080132	0.81[ASN][1000 genomes]
rs10213898	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10214383	0.81[AFR][1000 genomes];0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10214384	0.81[AFR][1000 genomes];0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1036214	0.83[ASN][1000 genomes]
rs10477438	0.80[ASN][1000 genomes]
rs10477951	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10477955	0.80[ASN][1000 genomes]
rs11746231	0.80[AFR][1000 genomes]
rs11750370	0.80[AFR][1000 genomes]
rs11952637	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11957989	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs17161612	0.83[ASN][1000 genomes]
rs17407717	0.80[AFR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17450490	0.86[AFR][1000 genomes];0.80[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs28759518	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs3814065	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4130644	0.80[AFR][1000 genomes]
rs4957568	0.81[AFR][1000 genomes];0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4957569	0.81[AFR][1000 genomes];0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4957797	0.83[EUR][1000 genomes]
rs6861626	0.80[ASN][1000 genomes]
rs6869357	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6873546	0.81[AFR][1000 genomes];0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6883750	0.81[AFR][1000 genomes];0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6894117	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs72796593	0.82[ASN][1000 genomes]
rs72796595	0.82[ASN][1000 genomes]
rs72796596	0.82[ASN][1000 genomes]
rs9326764	0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830443	chr5:108326491-108496723	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
2	nsv882692	chr5:108391660-108474166	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv882693	chr5:108391660-108502493	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
4	nsv882694	chr5:108391660-108524416	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
5	nsv4953	chr5:108443905-108488747	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv1027163	chr5:108445447-108839913	Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
7	esv2756048	chr5:108448101-108542101	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:108442000-108497400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr5:108456800-108472800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr5:108458800-108461000	Weak transcription	HMEC	breast
4	chr5:108459600-108461200	Enhancers	Dnd41	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links