Variant report

Variant	esv1805898
Chromosome Location	chr19:21233245-21256249
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:44)
CpG islands
(count:61)
Chromatin interactive
region (count:7)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:44 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr19:21253959-21254016	H1-hESC	embryonic stem cell:	n/a	chr19:21253998-21254009
2	CEBPB	chr19:21253847-21254163	IMR90	lung:	n/a	chr19:21253998-21254009
3	CEBPB	chr19:21253892-21254156	HepG2	liver:	n/a	chr19:21253998-21254009
4	CEBPB	chr19:21253004-21253205	K562	blood:	n/a	n/a
5	CEBPB	chr19:21235748-21236054	K562	blood:	n/a	n/a
6	CEBPB	chr19:21235801-21235931	K562	blood:	n/a	n/a
7	CEBPB	chr19:21253957-21254166	K562	blood:	n/a	chr19:21253998-21254009
8	CEBPD	chr19:21235821-21236083	K562	blood:	n/a	n/a
9	CEBPD	chr19:21256240-21256511	K562	blood:	n/a	n/a
10	CTCF	chr19:21240303-21240329	LNCaP	prostate:	n/a	n/a
11	CTCF	chr19:21240248-21240355	GM13977	blood:	n/a	n/a
12	GATA2	chr19:21235714-21236087	K562	blood:	n/a	n/a
13	JUND	chr19:21253978-21254163	HepG2	liver:	n/a	n/a
14	KAP1	chr19:21243924-21244064	K562	blood:	n/a	n/a
15	NFYB	chr19:21235656-21235858	K562	blood:	n/a	n/a
16	POLR2A	chr19:21239021-21239098	MCF-7	breast:	n/a	n/a
17	POLR2A	chr19:21245750-21245791	GM12878	blood:	n/a	n/a
18	POLR2A	chr19:21240744-21240959	K562	blood:	n/a	n/a
19	POLR2A	chr19:21246736-21246843	MCF10A-Er-Src	breast:	n/a	n/a
20	POLR2A	chr19:21240931-21240937	HepG2	liver:	n/a	n/a
21	POLR2A	chr19:21243703-21243894	K562	blood:	n/a	n/a
22	POLR2A	chr19:21255858-21256000	MCF-7	breast:	n/a	n/a
23	POLR2A	chr19:21244873-21244890	HepG2	liver:	n/a	n/a
24	POLR2A	chr19:21252404-21252604	MCF10A-Er-Src	breast:	n/a	n/a
25	POLR2A	chr19:21244710-21244865	HepG2	liver:	n/a	n/a
26	POLR2A	chr19:21234368-21234555	MCF-7	breast:	n/a	n/a
27	POLR2A	chr19:21252825-21252940	H1-hESC	embryonic stem cell:	n/a	n/a
28	POLR2A	chr19:21243003-21243177	HepG2	liver:	n/a	n/a
29	POLR2A	chr19:21241318-21244493	K562	blood:	n/a	n/a
30	POLR2A	chr19:21240881-21240923	HepG2	liver:	n/a	n/a
31	POLR2A	chr19:21244309-21244601	GM12878	blood:	n/a	n/a
32	POLR2A	chr19:21239908-21240232	HepG2	liver:	n/a	n/a
33	POLR2A	chr19:21251376-21251435	GM12878	blood:	n/a	n/a
34	POLR2A	chr19:21239198-21239232	MCF-7	breast:	n/a	n/a
35	POLR2A	chr19:21244656-21244674	HepG2	liver:	n/a	n/a
36	POLR2A	chr19:21243413-21243534	GM12878	blood:	n/a	n/a
37	POLR2A	chr19:21243948-21244321	MCF10A-Er-Src	breast:	n/a	n/a
38	RFX5	chr19:21241251-21241412	K562	blood:	n/a	n/a
39	RFX5	chr19:21256153-21256175	K562	blood:	n/a	n/a
40	SETDB1	chr19:21248138-21248462	U2OS	brain:	n/a	n/a
41	SRF	chr19:21239130-21239264	GM12878	blood:	n/a	n/a
42	SRF	chr19:21239152-21239242	GM12878	blood:	n/a	n/a
43	STAT3	chr19:21246414-21246572	MCF10A-Er-Src	breast:	n/a	n/a
44	TAL1	chr19:21235773-21236087	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:21240978-21241028	IMR90	lung:	fetal
2	chr19:21240978-21241028	LNCaP	prostate:	n/a
3	chr19:21240978-21241028	H1-hESC	embryonic stem cell:	embryo
4	chr19:21240978-21241028	GM19239	blood:	n/a
5	chr19:21240978-21241028	HRE	kidney:	n/a
6	chr19:21240978-21241028	HEK293	kidney:	embryo
7	chr19:21240978-21241028	ECC-1	luminal epithelium:	n/a
8	chr19:21240978-21241028	HRCEpiC	kidney:	n/a
9	chr19:21240978-21241028	NHBE	bronchial:	n/a
10	chr19:21240978-21241028	HCT-116	colon:	n/a
11	chr19:21240978-21241028	HIPEpiC	eye:	n/a
12	chr19:21240978-21241028	HL-60	blood:	n/a
13	chr19:21240978-21241028	SAEC	small airway:	n/a
14	chr19:21240978-21241028	BE2_C	brain:	n/a
15	chr19:21240978-21241028	RPTEC	kidney:	n/a
16	chr19:21240978-21241028	Hepatocyte	liver:	n/a
17	chr19:21240978-21241028	BJ	skin:	n/a
18	chr19:21240978-21241028	Caco-2	colon:	n/a
19	chr19:21240978-21241028	PANC-1	pancreas:	n/a
20	chr19:21240978-21241028	AG04450	lung:	fetal
21	chr19:21240978-21241028	NT2-D1	testis:	n/a
22	chr19:21240978-21241028	GM06990	blood:	n/a
23	chr19:21240978-21241028	NH-A	brain:	n/a
24	chr19:21240978-21241028	HNPCEpiC	eye:	n/a
25	chr19:21240978-21241028	HAEpiC	amniotic membrane:	n/a
26	chr19:21240978-21241028	HEEpiC	esophagus:	n/a
27	chr19:21240978-21241028	AoSMC	blood vessel:	n/a
28	chr19:21240978-21241028	AG04449	skin:	fetal
29	chr19:21240978-21241028	PFSK-1	brain:	n/a
30	chr19:21240978-21241028	Jurkat	blood:	n/a
31	chr19:21240978-21241028	PrEC	prostate:	n/a
32	chr19:21240978-21241028	HMEC	breast:	n/a
33	chr19:21240978-21241028	ovcar-3	ovarian:	n/a
34	chr19:21240978-21241028	NHDF-neo	bronchial:	n/a
35	chr19:21240978-21241028	GM12892	blood:	n/a
36	chr19:21240978-21241028	HRPEpiC	eye:	n/a
37	chr19:21240978-21241028	K562	blood:	n/a
38	chr19:21240978-21241028	SKMC	muscle:	n/a
39	chr19:21240978-21241028	ProgFib	skin:	n/a
40	chr19:21240978-21241028	MCF10A-Er-Src	breast:	n/a
41	chr19:21240978-21241028	HCPEpiC	choroid plexus:	n/a
42	chr19:21240978-21241028	HUVEC	blood vessel:	n/a
43	chr19:21240978-21241028	A549	lung:	n/a
44	chr19:21240978-21241028	GM12878	blood:	n/a
45	chr19:21240978-21241028	NB4	blood:	n/a
46	chr19:21240978-21241028	Hela-S3	cervix:	n/a
47	chr19:21240978-21241028	AG09309	skin:	n/a
48	chr19:21240978-21241028	HCF	heart:	n/a
49	chr19:21240978-21241028	HCM	heart:	n/a
50	chr19:21240978-21241028	SK-N-SH_RA	brain:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:21230722..21233642-chr19:21264436..21267129,2	K562	blood:
2	chr17:41381927..41383535-chr19:21236269..21237789,2	MCF-7	breast:
3	chr19:21246343..21248444-chr19:21263959..21266875,2	K562	blood:
4	chr17:41398648..41400647-chr19:21234769..21236289,5	MCF-7	breast:
5	chr17:41381905..41383742-chr19:21236269..21237789,3	K562	blood:
6	chr19:21236568..21238876-chr19:21241377..21243478,2	K562	blood:
7	chr19:21238270..21239771-chr19:21264302..21266943,2	K562	blood:

(count:1 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF430-1	chr19:21246730-21247067	NONHSAT063682

No data

Variant related genes	Relation type
ENSG00000265650	TF binding region
VN1R80P	TF binding region
ZNF430	TF binding region
ENSG00000265650	CpG island
VN1R80P	CpG island
ZNF430	CpG island
ENSG00000265650	chromatin interactions
ENSG00000236383	chromatin interactions
ENSG00000160352	chromatin interactions

Extended variants
information (count: 926 )
Associated
traits (count: 38 )

Variant overlapped rSNPs/rCNVs (count:926 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13345915	chr19:21233245-21233246	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs150388609	chr19:21233301-21233302	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs12609167	chr19:21233388-21233389	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs190936155	chr19:21233406-21233407	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs141576246	chr19:21233409-21233410	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs528397507	chr19:21233410-21233411	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs73531882	chr19:21233429-21233430	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs111276502	chr19:21233503-21233504	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs547225742	chr19:21233525-21233526	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs530656697	chr19:21233618-21233619	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs10416383	chr19:21233662-21233663	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs35781160	chr19:21233673-21233674	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs375514629	chr19:21233702-21233703	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs138029563	chr19:21233750-21233751	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs182821728	chr19:21233758-21233759	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs369493354	chr19:21233817-21233818	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs187778569	chr19:21233826-21233827	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs546303476	chr19:21233828-21233829	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs562214087	chr19:21233882-21233883	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs149499700	chr19:21233911-21233912	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs192872949	chr19:21233958-21233959	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs183142742	chr19:21233959-21233960	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs568768457	chr19:21233963-21233964	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs537645650	chr19:21233995-21233996	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs12052091	chr19:21234122-21234123	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs577429077	chr19:21234125-21234126	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs200351502	chr19:21234151-21234152	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs4530295	chr19:21234163-21234164	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs62122606	chr19:21234180-21234181	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs539893845	chr19:21234184-21234185	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs375880562	chr19:21234234-21234235	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs573221660	chr19:21234241-21234242	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs144042364	chr19:21234242-21234243	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs561692265	chr19:21234259-21234260	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs544239313	chr19:21234343-21234344	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs549573032	chr19:21234369-21234370	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs563912194	chr19:21234371-21234372	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs532943120	chr19:21234372-21234373	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs187235301	chr19:21234451-21234452	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs75731933	chr19:21234458-21234459	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs528930315	chr19:21234514-21234515	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs548656025	chr19:21234517-21234518	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs370510374	chr19:21234537-21234538	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs564154607	chr19:21234569-21234570	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs192045231	chr19:21234575-21234576	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs563200525	chr19:21234703-21234704	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs532769382	chr19:21234728-21234729	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs142761050	chr19:21234775-21234776	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs201673648	chr19:21234797-21234798	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs571083045	chr19:21234798-21234799	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:38)

Disease	PMID	Source
Medulloblastoma	16783165	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Prostate cancer	16573809	CNVD
Chordoma	18071362	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
ovarian endometriomas	16273235	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Cervical cancer	21063398	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Lung cancer	18438408	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Colorectal cancer	20459617	CNVD
small cell lung cancer	20016488	CNVD
Ductal carcinoma	22052326	CNVD

Chromatin state (count:783 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:21204400-21264800	Weak transcription	Right Ventricle	heart
2	chr19:21204600-21239800	Weak transcription	Colon Smooth Muscle	Colon
3	chr19:21206200-21241600	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr19:21207200-21239400	Weak transcription	Hela-S3	cervix
5	chr19:21209200-21235600	Weak transcription	Stomach Smooth Muscle	stomach
6	chr19:21211400-21235400	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr19:21212000-21241400	Weak transcription	Fetal Heart	heart
8	chr19:21220400-21235200	Weak transcription	NHDF-Ad	bronchial
9	chr19:21221400-21242000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr19:21222400-21242200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr19:21223000-21244200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr19:21223400-21235600	Weak transcription	NH-A	brain
13	chr19:21225200-21234200	Weak transcription	A549	lung
14	chr19:21225600-21237200	Weak transcription	HUVEC	blood vessel
15	chr19:21227400-21241400	ZNF genes & repeats	GM12878-XiMat	blood
16	chr19:21227800-21247200	Weak transcription	HepG2	liver
17	chr19:21228000-21233600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr19:21228800-21235400	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr19:21229600-21235600	Weak transcription	Brain Substantia Nigra	brain
20	chr19:21229800-21235400	Weak transcription	Brain Anterior Caudate	brain
21	chr19:21230600-21235600	Weak transcription	Brain Cingulate Gyrus	brain
22	chr19:21230600-21248400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr19:21230800-21233400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr19:21230800-21233400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr19:21230800-21233400	Weak transcription	Fetal Muscle Leg	muscle
26	chr19:21230800-21233600	Weak transcription	Duodenum Smooth Muscle	Duodenum
27	chr19:21230800-21233600	Weak transcription	Esophagus	oesophagus
28	chr19:21230800-21234000	Weak transcription	Placenta Amnion	Placenta Amnion
29	chr19:21230800-21234200	Weak transcription	Fetal Muscle Trunk	muscle
30	chr19:21230800-21234600	Strong transcription	Primary T helper naive cells from peripheral blood	blood
31	chr19:21230800-21235200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr19:21230800-21235400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
33	chr19:21230800-21235400	Weak transcription	Pancreatic Islets	Pancreatic Islet
34	chr19:21230800-21235400	Weak transcription	Rectal Smooth Muscle	rectum
35	chr19:21230800-21235400	Weak transcription	HSMM	muscle
36	chr19:21230800-21235600	Weak transcription	HUES48 Cell Line	embryonic stem cell
37	chr19:21230800-21235600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr19:21230800-21235600	Weak transcription	Brain Angular Gyrus	brain
39	chr19:21230800-21235600	Weak transcription	Left Ventricle	heart
40	chr19:21230800-21235600	Weak transcription	NHEK	skin
41	chr19:21230800-21235800	Weak transcription	Brain Inferior Temporal Lobe	brain
42	chr19:21230800-21237000	Weak transcription	Brain Hippocampus Middle	brain
43	chr19:21230800-21238600	Weak transcription	NHLF	lung
44	chr19:21230800-21240400	Weak transcription	HSMMtube	muscle
45	chr19:21230800-21243000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr19:21231000-21235600	Weak transcription	HMEC	breast
47	chr19:21231000-21238200	Weak transcription	Stomach Mucosa	stomach
48	chr19:21231000-21239000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr19:21231600-21233800	ZNF genes & repeats	Fetal Intestine Large	intestine
50	chr19:21231600-21234400	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links