Variant report

Variant	nsv901873
Chromosome Location	chr14:47136591-47366340
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:306)
CpG islands
(count:122)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr14:47227696-47227775	K562	blood:	n/a	n/a
2	ATF2	chr14:47238352-47238954	GM12878	blood:	n/a	n/a
3	ATF2	chr14:47238421-47238949	GM12878	blood:	n/a	n/a
4	BACH1	chr14:47354811-47355132	K562	blood:	n/a	n/a
5	BACH1	chr14:47354745-47355139	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr14:47144126-47144310	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr14:47238467-47238929	GM12878	blood:	n/a	chr14:47238736-47238744
8	BATF	chr14:47238445-47238909	GM12878	blood:	n/a	chr14:47238736-47238744
9	BATF	chr14:47356425-47356723	GM12878	blood:	n/a	chr14:47356567-47356578
10	BATF	chr14:47356455-47356637	GM12878	blood:	n/a	chr14:47356567-47356578
11	BCL11A	chr14:47287397-47287658	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCL11A	chr14:47238500-47238903	GM12878	blood:	n/a	chr14:47238829-47238838 chr14:47238615-47238624
13	BCLAF1	chr14:47238310-47239094	GM12878	blood:	n/a	chr14:47238829-47238838 chr14:47238615-47238624
14	BHLHE40	chr14:47238505-47238975	GM12878	blood:	n/a	n/a
15	BHLHE40	chr14:47243207-47243216	GM12878	blood:	n/a	n/a
16	BRCA1	chr14:47303861-47303947	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr14:47303627-47303827	HepG2	liver:	n/a	chr14:47303681-47303692
18	CEBPB	chr14:47362102-47362436	HepG2	liver:	n/a	chr14:47362259-47362270
19	CEBPB	chr14:47150417-47150717	IMR90	lung:	n/a	n/a
20	CEBPB	chr14:47163064-47163185	HepG2	liver:	n/a	n/a
21	CEBPB	chr14:47353274-47353450	A549	lung:	n/a	n/a
22	CEBPB	chr14:47362170-47362344	H1-hESC	embryonic stem cell:	n/a	chr14:47362259-47362270
23	CEBPB	chr14:47280156-47280467	HepG2	liver:	n/a	chr14:47280326-47280337 chr14:47280326-47280339 chr14:47280326-47280339
24	CEBPB	chr14:47191649-47191654	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr14:47217051-47217222	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr14:47362090-47362394	IMR90	lung:	n/a	chr14:47362259-47362270
27	CEBPB	chr14:47191227-47191420	HepG2	liver:	n/a	chr14:47191326-47191337
28	CEBPB	chr14:47362166-47362402	A549	lung:	n/a	chr14:47362259-47362270
29	CEBPB	chr14:47204885-47205091	A549	lung:	n/a	n/a
30	CEBPB	chr14:47163162-47163272	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr14:47150385-47150700	HepG2	liver:	n/a	n/a
32	CEBPB	chr14:47237873-47237945	H1-hESC	embryonic stem cell:	n/a	chr14:47237881-47237890 chr14:47237881-47237890 chr14:47237879-47237892 chr14:47237881-47237890
33	CEBPB	chr14:47303607-47303836	A549	lung:	n/a	chr14:47303681-47303692
34	CEBPB	chr14:47184230-47184309	H1-hESC	embryonic stem cell:	n/a	chr14:47184272-47184283
35	CEBPB	chr14:47288797-47289144	HepG2	liver:	n/a	chr14:47288961-47288972
36	CEBPB	chr14:47288787-47289125	A549	lung:	n/a	chr14:47288961-47288972
37	CEBPB	chr14:47353249-47353482	HepG2	liver:	n/a	n/a
38	CEBPB	chr14:47184168-47184434	HepG2	liver:	n/a	chr14:47184272-47184283
39	CEBPB	chr14:47150439-47150659	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr14:47150425-47150718	A549	lung:	n/a	n/a
41	CHD1	chr14:47251413-47251417	GM12878	blood:	n/a	n/a
42	CHD1	chr14:47238985-47239024	GM12878	blood:	n/a	n/a
43	CTCF	chr14:47184860-47185010	AG09309	skin:	n/a	n/a
44	CTCF	chr14:47344468-47344503	Lung_OC	lung:	n/a	n/a
45	CTCF	chr14:47338869-47338905	GM13976	blood:	n/a	n/a
46	CTCF	chr14:47255117-47255134	Medullo	brain:	n/a	n/a
47	CTCF	chr14:47268380-47268530	GM12865	blood:	n/a	n/a
48	CTCF	chr14:47155900-47156050	NB4	blood:	n/a	n/a
49	CTCF	chr14:47242592-47242640	LNCaP	prostate:	n/a	n/a
50	CTCF	chr14:47205542-47205579	Lung_OC	lung:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:47310377-47310427	NB4	blood:	n/a
2	chr14:47311141-47311191	T-47D	breast:	n/a
3	chr14:47310377-47310427	BJ	skin:	n/a
4	chr14:47311141-47311191	SK-N-MC	brain:	n/a
5	chr14:47310377-47310427	PANC-1	pancreas:	n/a
6	chr14:47310377-47310427	AG09309	skin:	n/a
7	chr14:47311141-47311191	AoSMC	blood vessel:	n/a
8	chr14:47311141-47311191	HepG2	liver:	n/a
9	chr14:47311141-47311191	Jurkat	blood:	n/a
10	chr14:47311141-47311191	HRE	kidney:	n/a
11	chr14:47311141-47311191	SK-N-SH	brain:	n/a
12	chr14:47311141-47311191	NB4	blood:	n/a
13	chr14:47310377-47310427	Hepatocyte	liver:	n/a
14	chr14:47311141-47311191	NT2-D1	testis:	n/a
15	chr14:47311141-47311191	HMEC	breast:	n/a
16	chr14:47311141-47311191	HUVEC	blood vessel:	n/a
17	chr14:47311141-47311191	GM12892	blood:	n/a
18	chr14:47311141-47311191	H1-hESC	embryonic stem cell:	embryo
19	chr14:47311141-47311191	AG09309	skin:	n/a
20	chr14:47311141-47311191	HNPCEpiC	eye:	n/a
21	chr14:47310377-47310427	HRCEpiC	kidney:	n/a
22	chr14:47310377-47310427	HL-60	blood:	n/a
23	chr14:47311141-47311191	NH-A	brain:	n/a
24	chr14:47310377-47310427	H1-hESC	embryonic stem cell:	embryo
25	chr14:47310377-47310427	Hela-S3	cervix:	n/a
26	chr14:47310377-47310427	AG09319	gingival:	n/a
27	chr14:47310377-47310427	HNPCEpiC	eye:	n/a
28	chr14:47310377-47310427	SK-N-SH_RA	brain:	n/a
29	chr14:47311141-47311191	HCT-116	colon:	n/a
30	chr14:47311141-47311191	HCM	heart:	n/a
31	chr14:47310377-47310427	T-47D	breast:	n/a
32	chr14:47310377-47310427	AG04450	lung:	fetal
33	chr14:47311141-47311191	LNCaP	prostate:	n/a
34	chr14:47311141-47311191	GM19239	blood:	n/a
35	chr14:47311141-47311191	GM12878	blood:	n/a
36	chr14:47310377-47310427	GM12891	blood:	n/a
37	chr14:47310377-47310427	K562	blood:	n/a
38	chr14:47311141-47311191	U87	brain:	n/a
39	chr14:47310377-47310427	NT2-D1	testis:	n/a
40	chr14:47311141-47311191	AG04449	skin:	fetal
41	chr14:47310377-47310427	GM12878	blood:	n/a
42	chr14:47310377-47310427	HUVEC	blood vessel:	n/a
43	chr14:47310377-47310427	NHDF-neo	bronchial:	n/a
44	chr14:47311141-47311191	HRCEpiC	kidney:	n/a
45	chr14:47311141-47311191	AG10803	skin:	n/a
46	chr14:47311141-47311191	PANC-1	pancreas:	n/a
47	chr14:47310377-47310427	MCF10A-Er-Src	breast:	n/a
48	chr14:47310377-47310427	PFSK-1	brain:	n/a
49	chr14:47310377-47310427	HCM	heart:	n/a
50	chr14:47310377-47310427	Caco-2	colon:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:47190435..47193179-chr14:47198084..47200809,2	MCF-7	breast:
2	chr14:47229054..47230571-chr14:47239361..47241042,2	K562	blood:
3	chr14:47196544..47199011-chr14:47199972..47202196,2	K562	blood:
4	chr14:47229054..47230571-chr14:47239361..47241042,2	K562	blood:
5	chr14:47196544..47199011-chr14:47199972..47202196,2	K562	blood:
6	chr14:47190435..47193179-chr14:47198084..47200809,2	MCF-7	breast:

No data

Variant related genes	Relation type
MDGA2	TF binding region
MDGA2	CpG island

Extended variants
information (count: 2619 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:2619 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2219684	chr14:47136591-47136592	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs565624856	chr14:47136622-47136623	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs575493641	chr14:47136623-47136624	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs559985880	chr14:47136685-47136686	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs145596151	chr14:47136745-47136746	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs577453140	chr14:47136762-47136763	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs544432763	chr14:47136813-47136814	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs192097543	chr14:47136817-47136818	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs553355430	chr14:47136886-47136887	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs183468308	chr14:47136893-47136894	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs10134490	chr14:47136903-47136904	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs188519944	chr14:47136976-47136977	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs527654944	chr14:47137001-47137002	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs545792491	chr14:47137026-47137027	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs371605334	chr14:47137033-47137034	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs541811822	chr14:47137035-47137036	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs1381642	chr14:47137095-47137096	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs550046873	chr14:47137142-47137143	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs568251506	chr14:47137143-47137144	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs191848499	chr14:47137214-47137215	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs547442697	chr14:47137215-47137216	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs147708928	chr14:47137218-47137219	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs79352668	chr14:47137234-47137235	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs184086115	chr14:47137303-47137304	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs76835833	chr14:47137336-47137337	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs556350783	chr14:47137345-47137346	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs186928195	chr14:47137360-47137361	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs564447989	chr14:47137385-47137386	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs544704037	chr14:47137396-47137397	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs377519712	chr14:47137417-47137418	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs1381641	chr14:47137435-47137436	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs572430910	chr14:47137469-47137470	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs546206212	chr14:47137512-47137513	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs191392777	chr14:47137556-47137557	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs146495905	chr14:47137581-47137582	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs185874002	chr14:47137627-47137628	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs375627920	chr14:47137683-47137684	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs543699942	chr14:47137728-47137729	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs561886040	chr14:47137747-47137748	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs34674898	chr14:47137826-47137827	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs28728204	chr14:47137855-47137856	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs547258528	chr14:47137884-47137885	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs559426203	chr14:47137910-47137911	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs549266219	chr14:47137969-47137970	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs138730573	chr14:47137981-47137982	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs148938258	chr14:47137988-47137989	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs528381963	chr14:47137989-47137990	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs569266305	chr14:47138041-47138042	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs559266673	chr14:47138062-47138063	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs538150168	chr14:47138091-47138092	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21785460	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21858162	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Renal cell carcinoma	18194544	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	19907438	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:136 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:47124800-47142000	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr14:47136400-47138400	Enhancers	Fetal Intestine Large	intestine
3	chr14:47139600-47140000	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr14:47140000-47141200	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr14:47141200-47142000	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr14:47141400-47141600	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr14:47141400-47142000	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr14:47141400-47142200	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr14:47142000-47142200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr14:47142000-47142200	Enhancers	Rectal Mucosa Donor 31	rectum
11	chr14:47142200-47142400	Weak transcription	Rectal Mucosa Donor 31	rectum
12	chr14:47142200-47143200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr14:47142200-47143600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr14:47143200-47143400	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr14:47143600-47144000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr14:47143600-47144000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
17	chr14:47143800-47144200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
18	chr14:47163000-47163800	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr14:47186400-47187400	Enhancers	Sigmoid Colon	Sigmoid Colon
20	chr14:47186600-47187000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr14:47186600-47187000	Enhancers	NH-A	brain
22	chr14:47186600-47187600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr14:47197800-47200400	Weak transcription	Rectal Mucosa Donor 29	rectum
24	chr14:47200400-47200600	Enhancers	Rectal Mucosa Donor 29	rectum
25	chr14:47200600-47203800	Active TSS	Rectal Mucosa Donor 29	rectum
26	chr14:47201000-47202200	Enhancers	Fetal Intestine Small	intestine
27	chr14:47201800-47203800	Active TSS	Rectal Mucosa Donor 31	rectum
28	chr14:47202200-47203800	Active TSS	Fetal Intestine Small	intestine
29	chr14:47202400-47202800	Enhancers	Fetal Intestine Large	intestine
30	chr14:47202400-47203800	Active TSS	Duodenum Mucosa	Duodenum
31	chr14:47202800-47203200	Active TSS	Fetal Intestine Large	intestine
32	chr14:47203000-47203600	Active TSS	Colonic Mucosa	Colon
33	chr14:47203200-47203600	Flanking Active TSS	Fetal Intestine Large	intestine
34	chr14:47203200-47203600	Active TSS	Rectal Smooth Muscle	rectum
35	chr14:47203200-47203600	Active TSS	Sigmoid Colon	Sigmoid Colon
36	chr14:47203600-47203800	Active TSS	Fetal Intestine Large	intestine
37	chr14:47203800-47204200	Enhancers	Fetal Intestine Large	intestine
38	chr14:47215000-47216400	Enhancers	Fetal Intestine Large	intestine
39	chr14:47215000-47217200	Enhancers	Fetal Intestine Small	intestine
40	chr14:47216600-47217000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr14:47217000-47220800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr14:47220800-47221200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr14:47221200-47224200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr14:47224200-47224800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr14:47238200-47238400	Enhancers	GM12878-XiMat	blood
46	chr14:47238400-47238600	Flanking Active TSS	GM12878-XiMat	blood
47	chr14:47238400-47239000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr14:47238600-47239400	Enhancers	GM12878-XiMat	blood
49	chr14:47250200-47250600	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr14:47250200-47250600	ZNF genes & repeats	Liver	Liver

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