Variant report

Variant	rs16835376
Chromosome Location	chr1:193418907-193418908
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10494679	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10494680	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12027971	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12035086	0.86[AFR][1000 genomes];0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12037892	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12043289	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12043960	0.85[AMR][1000 genomes]
rs12044333	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1324329	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1886294	0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1886295	0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2147304	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4474226	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4657751	0.97[EUR][1000 genomes]
rs6656737	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7417352	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7516432	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7524847	0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7528241	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7538630	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv997891	chr1:193271839-193566441	Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Weak transcription Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv1004003	chr1:193322299-193477254	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv535253	chr1:193322299-193477254	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv832159	chr1:193342434-193525072	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	nsv998663	chr1:193343230-193574004	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
6	nsv535254	chr1:193343230-193574004	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
7	nsv548661	chr1:193391298-193470234	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:193417200-193419200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
2	chr1:193417400-193419000	Enhancers	Primary B cells from peripheral blood	blood
3	chr1:193417400-193419400	Enhancers	Primary B cells from cord blood	blood
4	chr1:193417600-193419000	Enhancers	Primary T helper naive cells from peripheral blood	blood
5	chr1:193417600-193419000	Enhancers	Primary T helper cells fromperipheralblood	blood
6	chr1:193418000-193419000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr1:193418000-193419000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
8	chr1:193418000-193419000	Enhancers	Fetal Thymus	thymus
9	chr1:193418400-193419000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
10	chr1:193418600-193419000	Enhancers	Primary T helper cells PMA-I stimulated	--
11	chr1:193418600-193419800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
12	chr1:193418600-193420000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
13	chr1:193418800-193422200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
14	chr1:193418800-193425600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood

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