Variant report

Variant	rs2094297
Chromosome Location	chr10:96423456-96423457
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 90 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:78)

rs_ID	r²[population]
rs1409654	1.00[CEU][hapmap]
rs1575935	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1810769	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1854033	0.93[AFR][1000 genomes]
rs2094295	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2296679	1.00[CEU][hapmap]
rs2296682	1.00[CEU][hapmap]
rs2296684	1.00[CEU][hapmap]
rs2901782	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4451645	0.84[YRI][hapmap]
rs55673362	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55697065	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55761123	1.00[AMR][1000 genomes]
rs55783943	0.86[AFR][1000 genomes]
rs55902049	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55925546	0.86[AFR][1000 genomes]
rs56024124	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56113807	1.00[AMR][1000 genomes]
rs56188429	0.86[AFR][1000 genomes]
rs56248909	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56281613	0.93[AFR][1000 genomes]
rs56778943	0.86[AFR][1000 genomes]
rs57096906	0.86[AFR][1000 genomes]
rs57108647	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57257088	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57501369	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57713587	1.00[AMR][1000 genomes]
rs57802384	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58262373	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58430331	0.86[AFR][1000 genomes]
rs58643119	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58691803	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58984186	0.89[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs59080023	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59955762	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59962294	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60231225	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60234155	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61093485	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61410136	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61668937	0.86[AFR][1000 genomes]
rs7088972	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74150807	0.86[AFR][1000 genomes]
rs74150809	0.86[AFR][1000 genomes]
rs74150810	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74150811	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74150813	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74150814	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74150816	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74150822	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74150830	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74150837	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74150849	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74150850	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74150854	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74150887	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74150888	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74150889	0.82[AFR][1000 genomes]
rs74150890	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74150892	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74150893	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74150894	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74150895	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74150897	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74150902	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74152304	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74152308	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74152309	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74152310	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74152320	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74152341	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74152353	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74152363	1.00[AMR][1000 genomes]
rs74152371	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74152374	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7902619	0.83[AMR][1000 genomes]
rs7912667	1.00[CEU][hapmap]
rs7923806	1.00[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	nsv497859	chr10:96058024-97027747	Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
2	nsv934280	chr10:96401297-96540495	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
3	nsv1040106	chr10:96405296-96514994	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
4	nsv1040976	chr10:96405296-96516804	Weak transcription Active TSS Strong transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
5	nsv551954	chr10:96405329-96521249	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	nsv522538	chr10:96405329-96547463	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
7	nsv1049225	chr10:96405502-96516804	Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
8	nsv1052478	chr10:96406313-96516804	ZNF genes & repeats Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
9	nsv1037516	chr10:96407511-96516804	Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
10	nsv1047944	chr10:96407825-96563288	Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
11	nsv1050653	chr10:96407825-96634161	Active TSS Enhancers ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
12	nsv1049341	chr10:96416809-96471236	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:96422200-96423800	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chr10:96422600-96423600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr10:96422600-96423800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr10:96422800-96423600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr10:96422800-96423800	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr10:96422800-96423800	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr10:96423000-96424000	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr10:96423200-96423600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
9	chr10:96423200-96424200	Weak transcription	Gastric	stomach
10	chr10:96423400-96423600	Enhancers	Rectal Mucosa Donor 31	rectum
11	chr10:96423400-96423800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr10:96423400-96424000	Enhancers	Stomach Mucosa	stomach

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links