Variant report

Variant	rs11206942
Chromosome Location	chr1:57440321-57440322
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs11206954	0.89[ASN][1000 genomes]
rs11206955	0.82[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs11810899	0.86[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs12035887	0.89[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs12036280	0.93[ASN][1000 genomes]
rs12062362	0.87[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs12082861	0.83[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs12118564	0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs12144161	0.87[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs1329448	0.86[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs1329451	0.89[ASN][1000 genomes]
rs17114695	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17114816	0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs1831871	0.87[ASN][1000 genomes]
rs1854508	0.86[ASN][1000 genomes]
rs2026083	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3738558	0.89[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs3754268	0.83[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs3768209	0.85[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs3768211	0.89[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs3820579	0.89[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs3820581	0.89[ASN][1000 genomes]
rs4912420	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4912422	0.83[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs6668180	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6668269	0.84[ASN][1000 genomes]
rs6676740	0.81[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs6679906	0.85[ASN][1000 genomes]
rs697580	0.88[ASN][1000 genomes]
rs706353	0.85[ASN][1000 genomes]
rs706357	0.85[ASN][1000 genomes]
rs706360	0.84[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs72917455	0.94[ASN][1000 genomes]
rs7533953	0.90[ASN][1000 genomes]
rs944923	0.86[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	nsv869295	chr1:56894955-57656562	Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs11206942	C8B	cis	Whole Blood	GTEx

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:57434000-57445800	Weak transcription	Pancreas	Pancrea
2	chr1:57439600-57440400	Enhancers	HepG2	liver
3	chr1:57439600-57441200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
4	chr1:57439800-57440400	Enhancers	Liver	Liver
5	chr1:57439800-57440400	Enhancers	HMEC	breast

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links