Variant report

Variant	rs28695426
Chromosome Location	chr15:56054727-56054728
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:56053448..56056343-chr15:56061329..56062999,2	K562	blood:

Extended variants
information (count: 59 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs11071205	0.81[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs11071206	0.98[ASN][1000 genomes]
rs11071207	0.81[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs11071208	0.81[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs11071209	0.81[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs11630006	0.81[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs11630082	0.95[ASN][1000 genomes]
rs11635384	0.95[ASN][1000 genomes]
rs11635386	0.95[ASN][1000 genomes]
rs12324528	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12911233	0.85[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs16976527	0.95[ASN][1000 genomes]
rs16976529	0.95[ASN][1000 genomes]
rs2018522	0.81[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs55729352	0.85[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs58587583	0.81[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs60285843	0.81[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs62043930	0.83[ASN][1000 genomes]
rs6493816	0.86[ASN][1000 genomes]
rs6493817	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6493818	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6493819	0.81[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7161830	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7165205	0.81[AFR][1000 genomes];0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7165214	0.81[AFR][1000 genomes];0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7165438	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7165837	0.98[ASN][1000 genomes]
rs7166279	0.85[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs7167653	0.81[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7170400	0.82[AMR][1000 genomes]
rs7175125	0.98[ASN][1000 genomes]
rs7176575	0.81[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7177532	0.81[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7178078	0.81[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7178119	0.81[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7178959	0.98[ASN][1000 genomes]
rs7179170	0.81[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7179377	0.81[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7181777	0.85[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs7181910	0.96[ASN][1000 genomes]
rs8025157	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs8025162	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs8025491	0.92[ASN][1000 genomes]
rs8027296	0.94[ASN][1000 genomes]
rs8028734	0.87[ASN][1000 genomes]
rs8029134	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8029241	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8029388	0.84[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs8029451	0.81[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs8029572	0.84[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs8029665	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8033057	0.85[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs8040736	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1043789	chr15:55400872-56092454	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
2	nsv457157	chr15:55722213-56255774	Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv569539	chr15:55722213-56255774	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
4	nsv833017	chr15:55965957-56157912	Weak transcription Genic enhancers Strong transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
5	esv3366380	chr15:56003224-56141650	Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
6	nsv1052495	chr15:56013617-56102164	Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs28695426	PRTG	cis	Adipose Subcutaneous	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:56051200-56058600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links