Variant report

Variant	rs72825999
Chromosome Location	chr17:33808695-33808696
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs12449487	0.86[EUR][1000 genomes]
rs12451876	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12936256	0.86[EUR][1000 genomes]
rs12936954	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12937961	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12939675	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12949245	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12953115	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2304967	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs34048495	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs34121367	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs34620580	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs34646901	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs34656640	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs34734788	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs34747751	0.94[EUR][1000 genomes]
rs34787927	0.81[EUR][1000 genomes]
rs35057074	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs35210090	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs35367381	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs35563348	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs35863546	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs3744372	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4239251	0.87[EUR][1000 genomes]
rs55668225	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs56033496	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs56061417	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs67338337	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs67536209	0.82[EUR][1000 genomes]
rs72826000	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8064887	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs8065289	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs8066132	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs8072477	0.85[EUR][1000 genomes]
rs8079653	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs8082478	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1055936	chr17:33327166-33884184	Strong transcription Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Genic enhancers Active TSS 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	112 gene(s)	inside rSNPs	diseases
2	nsv543317	chr17:33327166-33884184	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers 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	112 gene(s)	inside rSNPs	diseases
3	nsv534371	chr17:33456878-34094068	Strong transcription Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	137 gene(s)	inside rSNPs	diseases
4	nsv574741	chr17:33552275-33827134	Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	72 gene(s)	inside rSNPs	diseases
5	nsv1056116	chr17:33691457-33815452	Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:33800400-33809400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr17:33801800-33809400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr17:33807000-33809600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr17:33807000-33809600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
5	chr17:33807000-33811000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
6	chr17:33807200-33809200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
7	chr17:33807200-33809200	Weak transcription	Dnd41	blood
8	chr17:33807200-33809600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
9	chr17:33807200-33810000	Weak transcription	GM12878-XiMat	blood
10	chr17:33807200-33810200	Weak transcription	Primary T cells from cord blood	blood
11	chr17:33807200-33810400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
12	chr17:33807200-33811200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
13	chr17:33807200-33812800	Weak transcription	Primary T helper cells PMA-I stimulated	--
14	chr17:33807400-33811400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
15	chr17:33808200-33810000	Strong transcription	Primary T helper cells fromperipheralblood	blood
16	chr17:33808400-33809800	Strong transcription	Primary T cells fromperipheralblood	blood
17	chr17:33808600-33812800	Weak transcription	Primary T helper naive cells from peripheral blood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links