Variant report

Variant	rs72810811
Chromosome Location	chr2:76727665-76727666
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs10496204	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10519330	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11126536	0.94[ASN][1000 genomes]
rs11126537	0.94[ASN][1000 genomes]
rs11126538	0.94[ASN][1000 genomes]
rs11679162	0.94[ASN][1000 genomes]
rs12474459	0.94[ASN][1000 genomes]
rs12623421	0.95[ASN][1000 genomes]
rs13002864	0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs13010949	0.81[ASN][1000 genomes]
rs13011427	0.94[ASN][1000 genomes]
rs13012727	0.94[ASN][1000 genomes]
rs13033650	0.94[ASN][1000 genomes]
rs13033844	0.81[ASN][1000 genomes]
rs13034021	0.87[ASN][1000 genomes]
rs17012831	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17491623	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17517504	0.94[ASN][1000 genomes]
rs2091716	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2178520	0.95[ASN][1000 genomes]
rs2222848	0.90[ASN][1000 genomes]
rs2860769	0.94[ASN][1000 genomes]
rs2860770	0.95[ASN][1000 genomes]
rs34117684	0.86[ASN][1000 genomes]
rs34475125	0.94[ASN][1000 genomes]
rs35041598	0.94[ASN][1000 genomes]
rs35289637	0.94[ASN][1000 genomes]
rs35683467	0.86[ASN][1000 genomes]
rs35822600	0.94[ASN][1000 genomes]
rs36064715	0.94[ASN][1000 genomes]
rs55718418	0.90[ASN][1000 genomes]
rs55765515	0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs55799622	0.83[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs60507784	0.86[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs62166048	0.85[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs62167487	0.89[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs62167489	0.89[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs6547087	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72809040	0.93[ASN][1000 genomes]
rs72809043	0.93[ASN][1000 genomes]
rs72809046	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72809050	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72809069	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72810819	0.94[ASN][1000 genomes]
rs72810824	0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7422459	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7424489	0.94[ASN][1000 genomes]
rs7585094	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[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	nsv874317	chr2:76554077-76890567	Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr2:76720000-76728800	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr2:76727400-76728200	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr2:76727600-76728000	Enhancers	iPS-18 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links