Variant report

Variant	rs7678748
Chromosome Location	chr4:151968295-151968296
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:151935286..151937401-chr4:151966290..151969822,4	MCF-7	breast:

Variant related genes	Relation type
ENSG00000198589	Chromatin interaction

Extended variants
information (count: 156 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:126)

rs_ID	r²[population]
rs10000557	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs10001039	1.00[JPT][hapmap]
rs10005907	1.00[JPT][hapmap]
rs10011421	1.00[JPT][hapmap]
rs10030785	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs10032477	0.84[EUR][1000 genomes]
rs10034173	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10222881	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.91[TSI][hapmap];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1046168	1.00[JPT][hapmap];0.82[EUR][1000 genomes]
rs10857254	1.00[JPT][hapmap]
rs10857255	1.00[JPT][hapmap]
rs10964	1.00[JPT][hapmap]
rs11099781	0.90[GIH][hapmap]
rs11099782	1.00[JPT][hapmap]
rs11099783	1.00[JPT][hapmap]
rs11099788	1.00[JPT][hapmap]
rs11099795	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs1148631	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1148633	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1148634	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1148636	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1148641	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1148644	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1148646	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1148650	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1148651	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11726180	1.00[JPT][hapmap]
rs11734095	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11734586	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs11938266	1.00[JPT][hapmap]
rs11943477	1.00[JPT][hapmap]
rs1201197	0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1201199	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1201200	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1201208	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.91[TSI][hapmap];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1201209	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1201210	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.91[TSI][hapmap];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1201216	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1212119	0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12500168	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs12501829	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12507657	1.00[JPT][hapmap]
rs1273329	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1273331	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1273332	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1298678	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13123932	1.00[JPT][hapmap]
rs13125574	1.00[JPT][hapmap]
rs13146584	1.00[JPT][hapmap];0.90[EUR][1000 genomes]
rs1549512	0.90[GIH][hapmap]
rs1583188	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1583189	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1615230	0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17027155	0.83[ASN][1000 genomes]
rs17027197	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17027226	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1782365	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1878796	1.00[JPT][hapmap]
rs1975112	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2154349	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2407406	1.00[JPT][hapmap]
rs2407411	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs2407428	1.00[JPT][hapmap]
rs2407440	1.00[JPT][hapmap]
rs2897657	1.00[JPT][hapmap]
rs2897660	1.00[JPT][hapmap]
rs2912477	0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2915451	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2952814	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2952817	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2952818	0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2952819	0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3990470	0.92[ASN][1000 genomes]
rs4524364	0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4696226	1.00[JPT][hapmap];0.92[TSI][hapmap];0.87[EUR][1000 genomes]
rs4696227	0.87[EUR][1000 genomes]
rs4696229	1.00[JPT][hapmap]
rs4696235	1.00[JPT][hapmap]
rs4696237	1.00[JPT][hapmap]
rs4696648	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.91[TSI][hapmap];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4696661	0.81[EUR][1000 genomes]
rs57003564	0.83[ASN][1000 genomes]
rs57029739	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62344602	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62344619	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62344622	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62344623	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62344624	0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6535756	0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6535757	0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6535760	0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6535761	0.82[EUR][1000 genomes]
rs6535763	1.00[JPT][hapmap];0.92[TSI][hapmap];0.87[EUR][1000 genomes]
rs6535765	1.00[JPT][hapmap]
rs6535766	1.00[JPT][hapmap]
rs6812083	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6812695	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs6819599	1.00[JPT][hapmap];0.92[TSI][hapmap];0.90[EUR][1000 genomes]
rs6823953	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs6825613	1.00[JPT][hapmap]
rs6826120	0.87[EUR][1000 genomes]
rs6826863	1.00[JPT][hapmap];0.92[TSI][hapmap];0.87[EUR][1000 genomes]
rs6828937	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs6829963	1.00[JPT][hapmap]
rs6833956	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6837905	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs6839352	0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6844415	0.87[EUR][1000 genomes]
rs6847927	0.85[TSI][hapmap];0.83[EUR][1000 genomes]
rs6853215	1.00[JPT][hapmap];0.84[EUR][1000 genomes]
rs6858377	0.82[EUR][1000 genomes]
rs7436602	0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7657953	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7659146	1.00[JPT][hapmap]
rs7668154	1.00[JPT][hapmap]
rs7672381	0.86[EUR][1000 genomes]
rs7677374	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.91[TSI][hapmap];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7683092	1.00[JPT][hapmap]
rs7683377	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7684325	0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7690329	1.00[JPT][hapmap]
rs7693282	0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7697992	0.90[EUR][1000 genomes]
rs891689	1.00[CHB][hapmap];0.91[CHD][hapmap];1.00[JPT][hapmap];0.91[TSI][hapmap];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9994205	0.84[EUR][1000 genomes]
rs9999064	0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:30 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1034948	chr4:151590115-152202687	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
2	nsv537302	chr4:151590115-152202687	ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
3	nsv530159	chr4:151624865-152203910	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
4	nsv1018404	chr4:151664438-152067409	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
5	nsv1017850	chr4:151664438-152071876	Active TSS Weak transcription Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
6	esv2763837	chr4:151664438-152071888	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
7	nsv870257	chr4:151665349-152072867	Strong transcription Weak transcription Active TSS Genic enhancers Flanking Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
8	nsv1015387	chr4:151673751-152071876	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
9	nsv526976	chr4:151675819-152055073	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
10	nsv1025077	chr4:151682266-152035733	Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
11	nsv537303	chr4:151682266-152035733	Strong transcription Weak transcription Genic enhancers Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
12	nsv949066	chr4:151693149-152069566	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
13	nsv949002	chr4:151693149-152095109	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
14	nsv948719	chr4:151693149-152161625	Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
15	nsv1031720	chr4:151708502-152071876	Strong transcription Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
16	nsv880262	chr4:151712054-152519899	Enhancers Weak transcription Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
17	nsv1031516	chr4:151718614-152065644	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
18	nsv537304	chr4:151718614-152065644	Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
19	nsv1022884	chr4:151718814-152065505	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
20	nsv537305	chr4:151718814-152065505	Enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
21	nsv595689	chr4:151788955-152015704	Enhancers Active TSS Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
22	nsv595690	chr4:151788955-152109552	Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS 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	35 gene(s)	inside rSNPs	diseases
23	nsv1026416	chr4:151847403-152105879	Transcr. at gene 5' and 3' Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
24	nsv461678	chr4:151865522-151980636	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription 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	23 gene(s)	inside rSNPs	diseases
25	nsv595692	chr4:151865522-151980636	Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
26	nsv595699	chr4:151880765-151968295	Enhancers Active TSS Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
27	nsv869553	chr4:151892289-152003402	Enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
28	nsv1018797	chr4:151913585-152073419	Flanking Active TSS Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
29	nsv967953	chr4:151952005-151980912	Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
30	nsv881526	chr4:151968295-152489087	Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:151938200-151969000	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr4:151956800-151969800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr4:151961400-151968800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr4:151961600-151969200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr4:151967600-151969200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr4:151967600-151969800	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr4:151968000-151969200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr4:151968000-151969800	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr4:151968000-151970000	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr4:151968200-151970000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links