Variant report

Variant	rs7017170
Chromosome Location	chr8:19603700-19603701
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10104473	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12375275	0.93[CHB][hapmap];0.90[ASN][1000 genomes]
rs12549679	0.89[ASN][1000 genomes]
rs13249203	0.92[ASN][1000 genomes]
rs13264159	0.89[ASN][1000 genomes]
rs13279183	0.90[ASN][1000 genomes]
rs17091266	0.89[ASN][1000 genomes]
rs28660470	0.89[ASN][1000 genomes]
rs28717065	0.87[ASN][1000 genomes]
rs34347433	0.90[ASN][1000 genomes]
rs34909571	0.90[ASN][1000 genomes]
rs35174554	0.87[ASN][1000 genomes]
rs35192805	0.90[ASN][1000 genomes]
rs35403757	0.92[ASN][1000 genomes]
rs6586862	0.94[CHB][hapmap];0.90[ASN][1000 genomes]
rs67841905	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6999967	0.92[ASN][1000 genomes]
rs6999968	0.90[ASN][1000 genomes]
rs71510659	0.90[ASN][1000 genomes]
rs7814601	0.90[ASN][1000 genomes]
rs7832074	0.94[CHB][hapmap];0.90[ASN][1000 genomes]
rs7832946	0.82[ASN][1000 genomes]
rs7834607	0.82[ASN][1000 genomes]
rs7845430	0.94[CHB][hapmap];0.90[ASN][1000 genomes]
rs9693642	0.90[ASN][1000 genomes]
rs9694733	0.90[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	nsv949636	chr8:18957705-19664732	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
2	nsv948861	chr8:19199688-19609029	Strong transcription Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv949304	chr8:19199688-19625912	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer 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	11 gene(s)	inside rSNPs	diseases
4	nsv890625	chr8:19368697-19799641	Strong transcription Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
5	nsv1021575	chr8:19430653-19623452	Enhancers Active TSS Weak transcription Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	nsv1021731	chr8:19515149-19643313	Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
7	nsv610759	chr8:19561997-20068842	Enhancers Strong transcription Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:19588600-19613400	Weak transcription	Pancreas	Pancrea
2	chr8:19601800-19604600	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
3	chr8:19602400-19604600	ZNF genes & repeats	Primary T helper naive cells fromperipheralblood	blood
4	chr8:19602400-19604800	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
5	chr8:19602400-19605400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
6	chr8:19602800-19603800	ZNF genes & repeats	Primary T helper naive cells from peripheral blood	blood
7	chr8:19603000-19604600	ZNF genes & repeats	Hela-S3	cervix
8	chr8:19603000-19605400	ZNF genes & repeats	Primary B cells from cord blood	blood
9	chr8:19603000-19605600	ZNF genes & repeats	A549	lung
10	chr8:19603200-19604000	ZNF genes & repeats	Left Ventricle	heart
11	chr8:19603400-19603800	ZNF genes & repeats	Primary T helper 17 cells PMA-I stimulated	--
12	chr8:19603600-19604000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr8:19603600-19604400	Weak transcription	Aorta	Aorta

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