Variant report

Variant	esv1829875
Chromosome Location	chr11:100803267-100806544
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:100803313-100803463	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:100803246-100803827	K562	blood:	n/a	n/a
3	ATF1	chr11:100803319-100803533	K562	blood:	n/a	n/a
4	CTCF	chr11:100803320-100803470	HL-60	blood:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
5	CTCF	chr11:100803300-100803450	AG04450	lung:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
6	CTCF	chr11:100803239-100803510	ECC-1	luminal epithelium:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
7	CTCF	chr11:100803240-100803390	A549	lung:	n/a	n/a
8	CTCF	chr11:100803300-100803450	GM12866	blood:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
9	CTCF	chr11:100803380-100803530	GM06990	blood:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
10	CTCF	chr11:100803380-100803530	HMF	breast:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
11	CTCF	chr11:100803380-100803530	HEK293	kidney:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
12	CTCF	chr11:100803340-100803490	WERI-Rb-1	eye:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
13	CTCF	chr11:100803340-100803490	HPAF	blood vessel:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
14	CTCF	chr11:100803340-100803490	SK-N-SH_RA	brain:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
15	CTCF	chr11:100803328-100803526	LNCaP	prostate:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
16	CTCF	chr11:100803360-100803510	BJ	skin:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
17	CTCF	chr11:100803300-100803522	HepG2	liver:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
18	CTCF	chr11:100803340-100803490	HRPEpiC	eye:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
19	CTCF	chr11:100803300-100803508	A549	lung:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
20	CTCF	chr11:100803360-100803510	WI-38	lung:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
21	CTCF	chr11:100803360-100803510	GM12873	blood:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
22	CTCF	chr11:100803396-100803472	MCF-7	breast:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
23	CTCF	chr11:100803320-100803470	GM12871	blood:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
24	CTCF	chr11:100803340-100803490	GM12875	blood:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
25	CTCF	chr11:100803340-100803490	AG09319	gingival:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
26	CTCF	chr11:100803340-100803490	HCPEpiC	choroid plexus:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
27	CTCF	chr11:100803310-100803558	GM12878	blood:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
28	CTCF	chr11:100803300-100803450	GM12873	blood:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
29	CTCF	chr11:100803380-100803530	BE2_C	brain:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
30	CTCF	chr11:100803400-100803550	AoAF	blood vessel:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
31	CTCF	chr11:100803060-100803726	A549	lung:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
32	CTCF	chr11:100803191-100803730	MCF-7	breast:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
33	CTCF	chr11:100803320-100803470	HPAF	blood vessel:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
34	CTCF	chr11:100803261-100803556	HepG2	liver:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
35	CTCF	chr11:100803257-100803663	T-47D	breast:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
36	CTCF	chr11:100803360-100803510	GM12868	blood:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
37	CTCF	chr11:100803145-100803724	HCT-116	colon:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
38	CTCF	chr11:100803360-100803510	MCF-7	breast:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
39	CTCF	chr11:100803385-100803493	Lung_OC	lung:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
40	CTCF	chr11:100803330-100803529	LNCaP	prostate:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
41	CTCF	chr11:100803340-100803490	HVMF	connective:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
42	CTCF	chr11:100803192-100803564	Spleen_OC	spleen:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
43	CTCF	chr11:100803400-100803550	RPTEC	kidney:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
44	CTCF	chr11:100803369-100803495	HepG2	liver:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
45	CTCF	chr11:100803196-100803604	A549	lung:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
46	CTCF	chr11:100803400-100803550	HCPEpiC	choroid plexus:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
47	CTCF	chr11:100803340-100803490	RPTEC	kidney:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
48	CTCF	chr11:100803340-100803490	GM12864	blood:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
49	CTCF	chr11:100803340-100803490	AG09309	skin:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
50	CTCF	chr11:100803300-100803450	HFF	foreskin:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429

No.	Distal block	Cell Line	Cell type
1	chr11:100805825..100807914-chr11:100811015..100813625,3	K562	blood:
2	chr11:100448550..100449412-chr11:100802794..100803475,2	K562	blood:
3	chr11:100446552..100447865-chr11:100802950..100803911,5	K562	blood:
4	chr11:100446930..100447515-chr11:100802994..100803615,2	MCF-7	breast:
5	chr11:100802948..100803667-chr11:101307051..101307600,2	K562	blood:
6	chr11:100447225..100447948-chr11:100803021..100803878,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000238388	TF binding region

Extended variants
information (count: 126 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:126 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs640326	chr11:100803267-100803268	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs189664927	chr11:100803279-100803280	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs565620509	chr11:100803283-100803284	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs531103992	chr11:100803286-100803287	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs6590825	chr11:100803293-100803294	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs368456746	chr11:100803295-100803296	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs12273212	chr11:100803304-100803305	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs530012106	chr11:100803483-100803484	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs17095820	chr11:100803590-100803591	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs566587723	chr11:100803632-100803633	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs534822134	chr11:100803645-100803646	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs143760798	chr11:100803656-100803657	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs571549493	chr11:100803660-100803661	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs11224521	chr11:100803717-100803718	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs558991300	chr11:100803780-100803781	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs181035022	chr11:100803781-100803782	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs112927258	chr11:100803872-100803873	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs375060905	chr11:100803877-100803878	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs573250547	chr11:100803934-100803935	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs557261474	chr11:100803958-100803959	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs79213484	chr11:100803982-100803983	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs536213558	chr11:100804061-100804062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs554625788	chr11:100804074-100804075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs626529	chr11:100804088-100804089	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs572847615	chr11:100804130-100804131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs11224522	chr11:100804309-100804310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs545624529	chr11:100804366-100804367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs541181245	chr11:100804495-100804496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs11224523	chr11:100804503-100804504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs35724249	chr11:100804525-100804526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs59173274	chr11:100804530-100804531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs397742738	chr11:100804536-100804537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs374112033	chr11:100804537-100804538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs185895333	chr11:100804551-100804552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs563381499	chr11:100804555-100804556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs11224524	chr11:100804563-100804564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs575921990	chr11:100804574-100804575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs544526488	chr11:100804595-100804596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs188892598	chr11:100804596-100804597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs182020943	chr11:100804621-100804622	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs577174122	chr11:100804687-100804688	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs12416898	chr11:100804697-100804698	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs186207209	chr11:100804707-100804708	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs563235144	chr11:100804724-100804725	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs11224525	chr11:100804762-100804763	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs551578554	chr11:100804772-100804773	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs571371682	chr11:100804779-100804780	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs527468502	chr11:100804832-100804833	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs7114062	chr11:100804914-100804915	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs140182925	chr11:100804916-100804917	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	22429812	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Melanoma	22183965	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	16790693	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Mental retardation	19966786	CNVD
Non-small cell lung cancer	21829676	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Mantle cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Intracranial aneurysm	16715129	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Urothelial carcinoma	21177765	CNVD

Chromatin state (count:56 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:100772000-100831400	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr11:100773800-100809800	Weak transcription	Left Ventricle	heart
3	chr11:100774800-100812800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr11:100784000-100808800	Weak transcription	Primary B cells from cord blood	blood
5	chr11:100785400-100838400	Weak transcription	Fetal Intestine Small	intestine
6	chr11:100786800-100806800	Weak transcription	Placenta	Placenta
7	chr11:100790200-100812600	Weak transcription	Stomach Mucosa	stomach
8	chr11:100790400-100806600	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr11:100793400-100807000	Weak transcription	Liver	Liver
10	chr11:100794200-100807000	Weak transcription	Fetal Muscle Leg	muscle
11	chr11:100794400-100812800	Weak transcription	Fetal Stomach	stomach
12	chr11:100795600-100807400	Weak transcription	Fetal Muscle Trunk	muscle
13	chr11:100797600-100811800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr11:100798600-100807600	Weak transcription	Ovary	ovary
15	chr11:100798600-100811600	Weak transcription	Fetal Lung	lung
16	chr11:100798600-100812800	Weak transcription	Brain Hippocampus Middle	brain
17	chr11:100798600-100826600	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr11:100798600-100828200	Weak transcription	Gastric	stomach
19	chr11:100798800-100807000	Weak transcription	HUES64 Cell Line	embryonic stem cell
20	chr11:100798800-100811400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr11:100798800-100832200	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr11:100799200-100804600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr11:100799200-100812800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr11:100799200-100812800	Weak transcription	Cortex derived primary cultured neurospheres	brain
25	chr11:100800200-100846600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr11:100800800-100835800	Weak transcription	Rectal Mucosa Donor 29	rectum
27	chr11:100801000-100807000	Weak transcription	Duodenum Mucosa	Duodenum
28	chr11:100801000-100809600	Weak transcription	Osteobl	bone
29	chr11:100801000-100812000	Weak transcription	Fetal Heart	heart
30	chr11:100801000-100814800	Weak transcription	HSMM	muscle
31	chr11:100801000-100819600	Weak transcription	HSMMtube	muscle
32	chr11:100801000-100823200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr11:100801000-100832400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr11:100801000-100835000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr11:100801400-100812600	Weak transcription	A549	lung
36	chr11:100801400-100833800	Weak transcription	NH-A	brain
37	chr11:100802800-100803600	Enhancers	GM12878-XiMat	blood
38	chr11:100802800-100803600	Enhancers	K562	blood
39	chr11:100803000-100803400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr11:100803000-100804000	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr11:100803000-100822600	Weak transcription	Primary B cells from peripheral blood	blood
42	chr11:100803200-100803600	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr11:100803400-100803600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr11:100803600-100806400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr11:100803600-100811000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr11:100804000-100826200	Weak transcription	HUES48 Cell Line	embryonic stem cell
47	chr11:100804200-100812800	Weak transcription	Psoas Muscle	Psoas
48	chr11:100804600-100805600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr11:100804800-100811000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
50	chr11:100805000-100807000	Weak transcription	Adipose Nuclei	Adipose

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links