Variant report

Variant	rs6883216
Chromosome Location	chr5:150944455-150944456
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:150942025..150944523-chr5:150961662..150964571,2	K562	blood:

Extended variants
information (count: 65 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:64)

rs_ID	r²[population]
rs10039591	0.87[ASN][1000 genomes]
rs10044120	0.90[ASN][1000 genomes]
rs10052817	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10054406	0.81[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10060613	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10060662	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10069540	0.82[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10069901	0.82[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10071034	0.90[ASN][1000 genomes]
rs10072841	0.90[ASN][1000 genomes]
rs10074454	0.85[ASN][1000 genomes]
rs10079712	0.90[ASN][1000 genomes]
rs10085060	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11746958	0.90[ASN][1000 genomes]
rs11750312	0.90[ASN][1000 genomes]
rs13158643	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13166858	0.90[ASN][1000 genomes]
rs13167092	0.90[ASN][1000 genomes]
rs13187324	0.90[ASN][1000 genomes]
rs1432862	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1432866	0.90[ASN][1000 genomes]
rs1541909	0.88[ASN][1000 genomes]
rs1835944	0.90[ASN][1000 genomes]
rs2163769	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2304053	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2304054	0.82[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs28449749	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs34335300	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs34346367	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs35211425	0.88[ASN][1000 genomes]
rs35908499	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs35957412	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3734055	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3734057	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3734058	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3734059	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3734060	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4314387	0.90[ASN][1000 genomes]
rs4320248	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4376256	0.90[ASN][1000 genomes]
rs4416593	0.90[ASN][1000 genomes]
rs4416594	0.90[ASN][1000 genomes]
rs4416595	0.88[ASN][1000 genomes]
rs4452546	0.90[ASN][1000 genomes]
rs6859217	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6878528	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6878532	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6878556	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6878627	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6880902	0.87[ASN][1000 genomes]
rs6883153	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7709576	0.88[ASN][1000 genomes]
rs7710596	0.89[ASN][1000 genomes]
rs7719117	0.90[ASN][1000 genomes]
rs7726769	0.82[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7727173	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7732813	0.88[ASN][1000 genomes]
rs7737011	0.90[ASN][1000 genomes]
rs7737419	0.90[ASN][1000 genomes]
rs9324698	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9324699	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9324700	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9918229	0.90[ASN][1000 genomes]
rs9918283	0.90[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	esv20633	chr5:150941705-150955343	Strong transcription Enhancers Genic enhancers Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:150908200-150948000	Strong transcription	HMEC	breast
2	chr5:150918200-150945400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr5:150934200-150949600	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr5:150937000-150948600	Weak transcription	Right Atrium	heart
5	chr5:150937600-150948600	Weak transcription	Adipose Nuclei	Adipose
6	chr5:150942600-150948400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr5:150942800-150945000	Weak transcription	Esophagus	oesophagus
8	chr5:150943200-150945200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
9	chr5:150943400-150945400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr5:150944000-150945400	Weak transcription	NHEK	skin
11	chr5:150944000-150948400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links