Variant report

Variant	rs60308761
Chromosome Location	chr22:30927422-30927423
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 79 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:77)

rs_ID	r²[population]
rs1001409	0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1008801	0.88[ASN][1000 genomes]
rs11912737	0.86[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs13053262	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13053759	0.84[AMR][1000 genomes]
rs13054004	0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13054381	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs13750	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs16988720	0.86[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs17670707	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17670808	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17738527	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17738540	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1859479	0.86[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs1986969	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2023967	0.91[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2189835	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2412989	0.86[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs2412990	0.86[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs35102600	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35530794	0.88[ASN][1000 genomes]
rs35841307	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4602314	0.88[ASN][1000 genomes]
rs6518693	0.86[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs6518695	0.86[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs7284873	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7285878	0.81[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs7286523	0.88[ASN][1000 genomes]
rs7286807	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7287003	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7287135	0.86[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs7287596	0.86[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs7289277	0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs7289820	0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs7289828	0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7291870	0.86[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs7292573	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs737942	0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs8136225	0.86[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs8136992	0.87[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs8137267	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs8137718	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs8138759	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs8141108	0.86[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs8141286	0.86[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs8141318	0.88[ASN][1000 genomes]
rs8141428	0.84[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs8141671	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs886615	0.86[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs886616	0.86[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs886617	0.86[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs9306262	0.86[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs9606735	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9606736	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9606738	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9606739	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9606744	0.86[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs9606745	0.86[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs9606746	0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9606747	0.86[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs9606749	0.86[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs9608935	0.88[ASN][1000 genomes]
rs9608936	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9608938	0.88[ASN][1000 genomes]
rs9608940	0.88[ASN][1000 genomes]
rs9608941	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9608942	0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs9608944	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9608946	0.81[EUR][1000 genomes]
rs9608955	0.80[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9608956	0.84[AMR][1000 genomes]
rs9608960	0.86[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs9608964	0.84[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs9608966	0.86[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs9608967	0.86[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs9608968	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9608972	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[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	nsv829171	chr22:30598030-31043578	Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
2	nsv915818	chr22:30708245-31346302	Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	82 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:30914400-30933400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr22:30922200-30927800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr22:30925400-30928000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links