Variant report

Variant	rs6962479
Chromosome Location	chr7:122248201-122248202
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs1010498	0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10266303	0.96[ASN][1000 genomes]
rs11763594	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12706423	0.98[ASN][1000 genomes]
rs12706424	0.98[ASN][1000 genomes]
rs13222290	0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13222449	0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13236662	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17144588	0.91[ASN][1000 genomes]
rs1990350	0.92[ASN][1000 genomes]
rs28565406	0.98[ASN][1000 genomes]
rs28671172	0.96[ASN][1000 genomes]
rs34009656	0.96[ASN][1000 genomes]
rs34208874	0.98[ASN][1000 genomes]
rs35131640	0.98[ASN][1000 genomes]
rs35147547	0.92[ASN][1000 genomes]
rs35345335	0.98[ASN][1000 genomes]
rs35778660	0.98[ASN][1000 genomes]
rs4131663	0.98[ASN][1000 genomes]
rs4521704	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4604372	0.98[ASN][1000 genomes]
rs55913030	0.87[ASN][1000 genomes]
rs6466825	0.98[ASN][1000 genomes]
rs6944494	0.98[ASN][1000 genomes]
rs6952217	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6954625	0.98[ASN][1000 genomes]
rs6956116	0.84[EUR][1000 genomes]
rs6959395	0.98[ASN][1000 genomes]
rs6962798	0.91[ASN][1000 genomes]
rs6964649	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7781627	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7782215	0.96[ASN][1000 genomes]
rs7791524	0.98[ASN][1000 genomes]
rs7808115	0.98[ASN][1000 genomes]
rs7809699	0.98[ASN][1000 genomes]
rs7810271	0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1017029	chr7:121958574-122338623	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv532178	chr7:122203056-122978846	Enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:122217600-122265600	Weak transcription	Aorta	Aorta
2	chr7:122237600-122258800	Weak transcription	Pancreas	Pancrea
3	chr7:122238000-122257200	Weak transcription	Fetal Lung	lung
4	chr7:122240400-122256200	Weak transcription	Liver	Liver
5	chr7:122245000-122254800	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr7:122246000-122248400	Weak transcription	Stomach Smooth Muscle	stomach
7	chr7:122246800-122254000	Weak transcription	Left Ventricle	heart

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links