Variant report

Variant	rs34048495
Chromosome Location	chr17:33794280-33794281
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs12449487	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12451876	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12937961	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12949245	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12953115	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs34121367	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs34734788	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs34787927	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs35057074	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs35210090	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35563348	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs35863546	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4239251	0.82[EUR][1000 genomes]
rs56061417	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs67536209	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72825999	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs72826000	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs8066132	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[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	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
6	esv3432530	chr17:33738621-33802241	Flanking Active TSS Strong transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:33788400-33794400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr17:33788600-33794400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr17:33788600-33794600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
4	chr17:33791200-33801200	Weak transcription	Dnd41	blood
5	chr17:33793800-33797000	Enhancers	Primary T cells fromperipheralblood	blood
6	chr17:33793800-33797000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
7	chr17:33793800-33797400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
8	chr17:33794000-33796000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
9	chr17:33794000-33796200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
10	chr17:33794000-33796800	Enhancers	Primary T killer memory cells from peripheral blood	blood
11	chr17:33794000-33797200	Enhancers	Hela-S3	cervix
12	chr17:33794000-33797400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
13	chr17:33794200-33796000	Enhancers	Primary T helper cells fromperipheralblood	blood
14	chr17:33794200-33796200	Enhancers	Primary T cells from cord blood	blood
15	chr17:33794200-33796200	Enhancers	Primary T helper cells PMA-I stimulated	--
16	chr17:33794200-33797000	Enhancers	Primary T helper naive cells from peripheral blood	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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