Variant report

Variant	rs12665235
Chromosome Location	chr6:128059880-128059881
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 49 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10872324	1.00[CEU][hapmap];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11753398	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11961168	1.00[CEU][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11967147	1.00[CEU][hapmap];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12191259	1.00[CEU][hapmap]
rs12194548	0.86[CEU][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12214409	0.94[CEU][hapmap];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12660845	0.81[ASN][1000 genomes]
rs12661098	0.81[ASN][1000 genomes]
rs12661121	0.84[ASN][1000 genomes]
rs12665648	0.81[ASN][1000 genomes]
rs13215234	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13219045	0.83[CEU][hapmap];0.89[AMR][1000 genomes];0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17055025	0.81[ASN][1000 genomes]
rs199148	0.82[ASN][1000 genomes]
rs269992	0.80[ASN][1000 genomes]
rs270009	0.80[ASN][1000 genomes]
rs270010	0.82[ASN][1000 genomes]
rs58586522	0.81[ASN][1000 genomes]
rs59993660	0.84[ASN][1000 genomes]
rs669722	0.80[ASN][1000 genomes]
rs68018843	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6902009	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6902933	0.81[ASN][1000 genomes]
rs6905527	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6934865	0.95[ASN][1000 genomes]
rs6935256	1.00[CEU][hapmap]
rs6939770	0.88[CEU][hapmap];0.86[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6940280	0.88[CEU][hapmap];0.81[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7744896	1.00[CEU][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7768836	1.00[CEU][hapmap]
rs7772357	1.00[CEU][hapmap]
rs7774647	0.92[ASN][1000 genomes]
rs9482835	0.92[ASN][1000 genomes]
rs9491858	0.92[ASN][1000 genomes]
rs9491859	0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv886638	chr6:127954614-128087172	Enhancers Strong transcription Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv886639	chr6:127954614-128109244	Strong transcription Weak transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv886640	chr6:127961263-128096587	Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv886641	chr6:127971136-128085283	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv886642	chr6:127971136-128096587	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv886643	chr6:127971136-128109244	Strong transcription Enhancers Weak transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv886644	chr6:127976408-128109244	Weak transcription Genic enhancers Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv886645	chr6:127977160-128085283	Strong transcription Enhancers Weak transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
9	nsv886646	chr6:127977160-128087172	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
10	nsv886647	chr6:127977160-128109244	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
11	nsv886648	chr6:127983009-128109244	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
12	nsv830799	chr6:128033100-128194511	Genic enhancers Enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
13	nsv518548	chr6:128046713-128062827	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:128039800-128069200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
2	chr6:128045600-128069200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr6:128047200-128082400	Weak transcription	Primary T cells fromperipheralblood	blood
4	chr6:128047600-128060800	Weak transcription	Thymus	Thymus
5	chr6:128055200-128069000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
6	chr6:128056400-128060400	Enhancers	Primary T helper cells PMA-I stimulated	--
7	chr6:128056800-128069200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
8	chr6:128058400-128060200	Enhancers	Primary T helper cells fromperipheralblood	blood
9	chr6:128058600-128060400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
10	chr6:128058600-128060800	Weak transcription	Primary T cells from cord blood	blood
11	chr6:128058600-128061200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
12	chr6:128058800-128068800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
13	chr6:128059200-128060400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr6:128059400-128060400	Weak transcription	Fetal Thymus	thymus
15	chr6:128059800-128060600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood

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