Variant report

Variant	rs12002215
Chromosome Location	chr9:3372925-3372926
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 101 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:89)

rs_ID	r²[population]
rs10117357	0.92[CEU][hapmap];1.00[JPT][hapmap];0.93[AFR][1000 genomes];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10117431	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10124292	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10124295	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[YRI][hapmap];0.97[AFR][1000 genomes];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10511447	0.88[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs10814019	0.83[AFR][1000 genomes];0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10814038	1.00[YRI][hapmap];0.83[AFR][1000 genomes]
rs10814039	0.94[YRI][hapmap]
rs10814097	0.88[JPT][hapmap]
rs10971534	0.83[ASN][1000 genomes]
rs10971535	0.83[ASN][1000 genomes]
rs10971599	1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs10971661	0.96[YRI][hapmap]
rs10971665	0.89[CHB][hapmap];0.92[YRI][hapmap]
rs10971667	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs10971806	0.92[CEU][hapmap]
rs10972081	0.81[EUR][1000 genomes]
rs11536748	0.87[EUR][1000 genomes]
rs12115798	0.88[CHB][hapmap];0.88[JPT][hapmap]
rs12335763	0.94[YRI][hapmap]
rs12337095	0.81[CHB][hapmap]
rs12338587	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12338746	0.83[ASN][1000 genomes]
rs12338927	0.87[EUR][1000 genomes]
rs12340535	0.92[CEU][hapmap];1.00[CHB][hapmap];0.88[JPT][hapmap];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12341652	0.92[CEU][hapmap];0.90[CHB][hapmap];0.89[JPT][hapmap];0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12341737	0.92[CEU][hapmap];1.00[CHB][hapmap];0.88[JPT][hapmap];0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12343385	0.92[CEU][hapmap]
rs12346432	0.92[CEU][hapmap];0.90[CHB][hapmap];0.89[JPT][hapmap];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12347068	1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs12347811	0.91[CEU][hapmap];0.83[EUR][1000 genomes]
rs12347985	0.92[CEU][hapmap]
rs12554323	0.85[CEU][hapmap];0.88[CHB][hapmap];0.88[JPT][hapmap];0.83[EUR][1000 genomes]
rs13283163	0.88[CHB][hapmap]
rs13286511	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13290412	0.84[CEU][hapmap];0.90[CHB][hapmap];0.89[JPT][hapmap];0.83[ASN][1000 genomes]
rs13298219	0.92[CEU][hapmap];0.90[CHB][hapmap];0.89[JPT][hapmap]
rs13298908	0.92[CEU][hapmap];0.83[EUR][1000 genomes]
rs13300358	0.89[JPT][hapmap]
rs13302664	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13302841	0.88[JPT][hapmap]
rs1348369	1.00[YRI][hapmap];0.84[AFR][1000 genomes]
rs16917371	1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs16924266	0.85[CEU][hapmap];0.89[JPT][hapmap];0.81[EUR][1000 genomes]
rs1998976	1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[JPT][hapmap];0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2000216	0.81[YRI][hapmap]
rs2986682	0.83[ASN][1000 genomes]
rs34086781	0.81[EUR][1000 genomes]
rs34123151	0.81[EUR][1000 genomes]
rs34233417	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs34708788	0.81[EUR][1000 genomes]
rs35244433	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs35545940	0.87[EUR][1000 genomes]
rs35625648	0.81[EUR][1000 genomes]
rs35824006	0.83[ASN][1000 genomes]
rs35945655	0.85[AFR][1000 genomes];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3758195	0.91[CEU][hapmap]
rs3758196	0.92[CEU][hapmap];1.00[CHB][hapmap];0.88[JPT][hapmap];0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4237147	0.96[YRI][hapmap]
rs4741825	0.92[CEU][hapmap];0.84[YRI][hapmap];0.89[EUR][1000 genomes]
rs4741826	0.89[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs4741829	0.92[CEU][hapmap];0.84[EUR][1000 genomes]
rs56829164	0.83[ASN][1000 genomes]
rs57004251	0.83[EUR][1000 genomes]
rs6476451	0.83[EUR][1000 genomes]
rs66463406	0.94[AFR][1000 genomes];0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66763574	0.87[EUR][1000 genomes]
rs7021584	0.88[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs7022682	0.82[JPT][hapmap];0.83[ASN][1000 genomes]
rs7026530	1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs7028812	0.85[CEU][hapmap];0.88[JPT][hapmap];0.81[EUR][1000 genomes]
rs7029544	1.00[JPT][hapmap];0.87[YRI][hapmap];0.83[ASN][1000 genomes]
rs7040113	0.85[CEU][hapmap]
rs7041836	0.92[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7043493	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[YRI][hapmap];0.98[AFR][1000 genomes];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7045360	1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs71506638	0.83[ASN][1000 genomes]
rs71506639	0.83[EUR][1000 genomes]
rs71506645	0.81[EUR][1000 genomes]
rs768485	0.88[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs7850570	0.84[AFR][1000 genomes]
rs7858850	0.83[ASN][1000 genomes]
rs7860163	0.83[ASN][1000 genomes]
rs7864459	0.88[CHB][hapmap];0.88[JPT][hapmap]
rs7869854	0.88[JPT][hapmap];0.96[YRI][hapmap];0.83[ASN][1000 genomes]
rs7870914	0.83[ASN][1000 genomes]
rs7875889	1.00[YRI][hapmap];0.83[AFR][1000 genomes]
rs9298952	1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs9695619	0.92[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv892086	chr9:3012276-3410838	Bivalent Enhancer ZNF genes & repeats Strong transcription Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv1032921	chr9:3139007-3502815	Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv539940	chr9:3139007-3502815	Strong transcription Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
4	nsv531566	chr9:3288211-3545454	Weak transcription Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
5	nsv892089	chr9:3290569-3578094	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
6	nsv916259	chr9:3308176-4296711	Enhancers ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
7	nsv1034280	chr9:3319718-3491987	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
8	nsv539942	chr9:3319718-3491987	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
9	nsv1028815	chr9:3319718-3584455	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
10	nsv466091	chr9:3349487-3389660	Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
11	nsv613146	chr9:3349487-3389660	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
12	nsv613147	chr9:3368111-3440355	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:3288200-3378400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
2	chr9:3337800-3388800	Weak transcription	Primary T cells fromperipheralblood	blood
3	chr9:3341200-3397600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
4	chr9:3351000-3408200	Weak transcription	Fetal Intestine Small	intestine
5	chr9:3355000-3383800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr9:3359400-3383200	Weak transcription	Primary T cells from cord blood	blood
7	chr9:3359400-3387600	Weak transcription	Primary hematopoietic stem cells	blood
8	chr9:3359600-3383800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr9:3359800-3384000	Weak transcription	Primary B cells from cord blood	blood
10	chr9:3364200-3397200	Weak transcription	Left Ventricle	heart
11	chr9:3364800-3393800	Weak transcription	Adipose Nuclei	Adipose
12	chr9:3367600-3384800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
13	chr9:3367800-3383800	Weak transcription	Cortex derived primary cultured neurospheres	brain
14	chr9:3369200-3377600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr9:3369400-3398400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links