Variant report

Variant	nsv911625
Chromosome Location	chr19:35856925-35890205
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:568)
CpG islands
(count:61)
Chromatin interactive
region (count:10)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:568 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:35880399-35880681	K562	blood:	n/a	n/a
2	ARID3A	chr19:35879373-35880761	HepG2	liver:	n/a	n/a
3	ARID3A	chr19:35871213-35871725	HepG2	liver:	n/a	n/a
4	ARID3A	chr19:35886903-35887125	HepG2	liver:	n/a	n/a
5	ARID3A	chr19:35871270-35871889	K562	blood:	n/a	n/a
6	ARID3A	chr19:35865850-35866169	K562	blood:	n/a	n/a
7	ARID3A	chr19:35879815-35880030	K562	blood:	n/a	n/a
8	ATF1	chr19:35879415-35879568	K562	blood:	n/a	n/a
9	ATF1	chr19:35865921-35866194	K562	blood:	n/a	n/a
10	ATF1	chr19:35871331-35871743	K562	blood:	n/a	n/a
11	ATF2	chr19:35867800-35868411	GM12878	blood:	n/a	n/a
12	ATF2	chr19:35867750-35868427	GM12878	blood:	n/a	n/a
13	ATF3	chr19:35880272-35880656	K562	blood:	n/a	n/a
14	ATF3	chr19:35865963-35866126	K562	blood:	n/a	n/a
15	ATF3	chr19:35865822-35866257	K562	blood:	n/a	n/a
16	ATF3	chr19:35871366-35871742	K562	blood:	n/a	n/a
17	BACH1	chr19:35880167-35880508	K562	blood:	n/a	n/a
18	BATF	chr19:35867870-35868281	GM12878	blood:	n/a	n/a
19	BCL11A	chr19:35867927-35868350	GM12878	blood:	n/a	n/a
20	BCL3	chr19:35880476-35880817	GM12878	blood:	n/a	n/a
21	BCL3	chr19:35867838-35868337	GM12878	blood:	n/a	n/a
22	BCL3	chr19:35887917-35888406	GM12878	blood:	n/a	n/a
23	BCL3	chr19:35867879-35868288	GM12878	blood:	n/a	n/a
24	BCL3	chr19:35887977-35888372	GM12878	blood:	n/a	n/a
25	BHLHE40	chr19:35871044-35872001	K562	blood:	n/a	n/a
26	BHLHE40	chr19:35865883-35866242	K562	blood:	n/a	n/a
27	BHLHE40	chr19:35883275-35883547	K562	blood:	n/a	n/a
28	BHLHE40	chr19:35880321-35880607	K562	blood:	n/a	n/a
29	BHLHE40	chr19:35865989-35866016	GM12878	blood:	n/a	n/a
30	BHLHE40	chr19:35879520-35879925	K562	blood:	n/a	n/a
31	BHLHE40	chr19:35867943-35868341	GM12878	blood:	n/a	n/a
32	BHLHE40	chr19:35880373-35880665	HepG2	liver:	n/a	n/a
33	BHLHE40	chr19:35879537-35879888	HepG2	liver:	n/a	n/a
34	BHLHE40	chr19:35879559-35879857	HepG2	liver:	n/a	n/a
35	CBX3	chr19:35876775-35877102	K562	blood:	n/a	n/a
36	CBX3	chr19:35865901-35866279	K562	blood:	n/a	n/a
37	CBX3	chr19:35876793-35877224	HCT-116	colon:	n/a	n/a
38	CBX3	chr19:35876803-35877084	K562	blood:	n/a	n/a
39	CBX3	chr19:35871059-35871809	K562	blood:	n/a	n/a
40	CCNT2	chr19:35871129-35871769	K562	blood:	n/a	n/a
41	CCNT2	chr19:35880399-35880711	K562	blood:	n/a	n/a
42	CCNT2	chr19:35879588-35879922	K562	blood:	n/a	n/a
43	CEBPB	chr19:35864457-35864718	HepG2	liver:	n/a	n/a
44	CEBPB	chr19:35887411-35887755	A549	lung:	n/a	chr19:35887578-35887589
45	CEBPB	chr19:35870455-35870720	H1-hESC	embryonic stem cell:	n/a	chr19:35870619-35870630
46	CEBPB	chr19:35868610-35868885	H1-hESC	embryonic stem cell:	n/a	chr19:35868767-35868780
47	CEBPB	chr19:35861291-35861545	IMR90	lung:	n/a	chr19:35861400-35861411
48	CEBPB	chr19:35870443-35870805	A549	lung:	n/a	chr19:35870619-35870630
49	CEBPB	chr19:35870435-35870802	HepG2	liver:	n/a	chr19:35870619-35870630
50	CEBPB	chr19:35861266-35861524	A549	lung:	n/a	chr19:35861400-35861411

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:35861862-35861912	A549	lung:	n/a
2	chr19:35861862-35861912	AG09309	skin:	n/a
3	chr19:35861862-35861912	HPAEpiC	pulmonary alveolar:	n/a
4	chr19:35861862-35861912	NHDF-neo	bronchial:	n/a
5	chr19:35861862-35861912	HUVEC	blood vessel:	n/a
6	chr19:35861862-35861912	SK-N-MC	brain:	n/a
7	chr19:35861862-35861912	HCM	heart:	n/a
8	chr19:35861862-35861912	NT2-D1	testis:	n/a
9	chr19:35861862-35861912	SKMC	muscle:	n/a
10	chr19:35861862-35861912	HNPCEpiC	eye:	n/a
11	chr19:35861862-35861912	BJ	skin:	n/a
12	chr19:35861862-35861912	HL-60	blood:	n/a
13	chr19:35861862-35861912	HIPEpiC	eye:	n/a
14	chr19:35861862-35861912	HCF	heart:	n/a
15	chr19:35861862-35861912	SK-N-SH_RA	brain:	n/a
16	chr19:35861862-35861912	CMK	blood:	n/a
17	chr19:35861862-35861912	HepG2	liver:	n/a
18	chr19:35861862-35861912	AG09319	gingival:	n/a
19	chr19:35861862-35861912	Jurkat	blood:	n/a
20	chr19:35861862-35861912	AoSMC	blood vessel:	n/a
21	chr19:35861862-35861912	ProgFib	skin:	n/a
22	chr19:35861862-35861912	HMEC	breast:	n/a
23	chr19:35861862-35861912	AG04449	skin:	fetal
24	chr19:35861862-35861912	GM19239	blood:	n/a
25	chr19:35861862-35861912	H1-hESC	embryonic stem cell:	embryo
26	chr19:35861862-35861912	NHBE	bronchial:	n/a
27	chr19:35861862-35861912	ECC-1	luminal epithelium:	n/a
28	chr19:35861862-35861912	U87	brain:	n/a
29	chr19:35861862-35861912	Hepatocyte	liver:	n/a
30	chr19:35861862-35861912	SAEC	small airway:	n/a
31	chr19:35861862-35861912	AG04450	lung:	fetal
32	chr19:35861862-35861912	BE2_C	brain:	n/a
33	chr19:35861862-35861912	HRPEpiC	eye:	n/a
34	chr19:35861862-35861912	RPTEC	kidney:	n/a
35	chr19:35861862-35861912	HEK293	kidney:	embryo
36	chr19:35861862-35861912	GM12892	blood:	n/a
37	chr19:35861862-35861912	T-47D	breast:	n/a
38	chr19:35861862-35861912	GM12891	blood:	n/a
39	chr19:35861862-35861912	AG10803	skin:	n/a
40	chr19:35861862-35861912	HRCEpiC	kidney:	n/a
41	chr19:35861862-35861912	HRE	kidney:	n/a
42	chr19:35861862-35861912	K562	blood:	n/a
43	chr19:35861862-35861912	GM12878	blood:	n/a
44	chr19:35861862-35861912	PFSK-1	brain:	n/a
45	chr19:35861862-35861912	Hela-S3	cervix:	n/a
46	chr19:35861862-35861912	HAEpiC	amniotic membrane:	n/a
47	chr19:35861862-35861912	HEEpiC	esophagus:	n/a
48	chr19:35861862-35861912	HCPEpiC	choroid plexus:	n/a
49	chr19:35861862-35861912	PrEC	prostate:	n/a
50	chr19:35861862-35861912	ovcar-3	ovarian:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr19:35881601..35884861-chr19:35885155..35888151,3	K562	blood:
2	chr19:35866654..35868491-chr19:35868954..35871337,2	K562	blood:
3	chr19:35885081..35886581-chr6:162062521..162064392,2	K562	blood:
4	chr19:35885135..35886720-chr19:35887964..35890211,2	K562	blood:
5	chr19:35881601..35884861-chr19:35885155..35888151,3	K562	blood:
6	chr19:35865310..35868154-chr19:35869837..35872073,2	K562	blood:
7	chr19:35885135..35886720-chr19:35887964..35890211,2	K562	blood:
8	chr19:35864467..35867206-chr19:35939200..35941045,2	MCF-7	breast:
9	chr19:35866654..35868491-chr19:35868954..35871337,2	K562	blood:
10	chr19:35865310..35868154-chr19:35869837..35872073,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPR42-2	chr19:35870421-35870690	NONHSAT065830
2	lnc-GPR42-2	chr19:35871954-35872278	NONHSAT065830

No data

Variant related genes	Relation type
EEF1A1P7	TF binding region
GPR42	TF binding region
ENSG00000205786	TF binding region
EEF1A1P7	CpG island
GPR42	CpG island
ENSG00000205786	CpG island
ENSG00000126262	chromatin interactions

Extended variants
information (count: 1157 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:1157 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10401894	chr19:35860422-35860423	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs4806139	chr19:35860458-35860459	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs55802006	chr19:35860462-35860463	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs571265023	chr19:35860495-35860496	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs192527563	chr19:35860508-35860509	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs75694299	chr19:35860547-35860548	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs184801435	chr19:35860585-35860586	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs150424296	chr19:35860631-35860632	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs138239795	chr19:35860635-35860636	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs544661220	chr19:35860648-35860649	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs569652713	chr19:35860661-35860662	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs117745285	chr19:35860672-35860673	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs2312584	chr19:35860689-35860690	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs551980006	chr19:35860699-35860700	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs78095447	chr19:35860701-35860702	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs190002424	chr19:35860805-35860806	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs77640168	chr19:35860816-35860817	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs78070184	chr19:35861286-35861287	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs567471205	chr19:35861317-35861318	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs537097344	chr19:35861436-35861437	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs114061824	chr19:35861443-35861444	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs369726033	chr19:35861493-35861494	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs8103476	chr19:35861506-35861507	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs112640961	chr19:35861541-35861542	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs546398882	chr19:35861630-35861631	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs558728245	chr19:35861642-35861643	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs10652244	chr19:35861651-35861652	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs10651644	chr19:35861652-35861653	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs372771664	chr19:35861653-35861654	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs397813321	chr19:35861654-35861655	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs200728205	chr19:35861656-35861657	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs370397611	chr19:35861689-35861690	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs11881816	chr19:35861695-35861696	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs12973766	chr19:35861715-35861716	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs112288237	chr19:35861718-35861719	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs543890872	chr19:35861720-35861721	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs560908307	chr19:35861771-35861772	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs187268583	chr19:35861862-35861863	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
39	rs567614052	chr19:35861875-35861876	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
40	rs189196514	chr19:35861879-35861880	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
41	rs416849	chr19:35861905-35861906	Inactive region	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs566764985	chr19:35861908-35861909	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
43	rs554277618	chr19:35861991-35861992	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs566554920	chr19:35862047-35862048	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs539837910	chr19:35862126-35862127	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs201135977	chr19:35862159-35862160	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs573179967	chr19:35862164-35862165	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs201724750	chr19:35862191-35862192	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs111392142	chr19:35864214-35864215	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs560490467	chr19:35864224-35864225	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	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
Adenoid cystic carcinoma	18698036	CNVD
Ductal carcinoma	22052326	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21858162	CNVD
Breast cancer	17603634	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
renal disease	20603712	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Ovarian cancer	21397856	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Ovarian cancer	20844748	CNVD
Non-small cell lung cancer	21829676	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cancer	21183584	CNVD
Honadal dysgenesis	21048976	CNVD
Neurodevelopmental disorder	22521361	CNVD
Endometrial cancer	23636398	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Invasive pancreatic ductal carcinoma	18765526	CNVD
Rhabdomyosarcoma	16790082	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
Gastric cancer	21811585	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Glioma	17123091	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	21569311	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:204 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:35864200-35864400	Enhancers	GM12878-XiMat	blood
2	chr19:35864200-35865800	Enhancers	Placenta Amnion	Placenta Amnion
3	chr19:35864400-35864600	Bivalent Enhancer	K562	blood
4	chr19:35864400-35865400	Weak transcription	GM12878-XiMat	blood
5	chr19:35865000-35867200	Enhancers	K562	blood
6	chr19:35865200-35866000	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
7	chr19:35865200-35866600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
8	chr19:35865400-35867200	Enhancers	Stomach Mucosa	stomach
9	chr19:35865400-35869000	Enhancers	GM12878-XiMat	blood
10	chr19:35865600-35866200	Enhancers	Ovary	ovary
11	chr19:35865600-35866400	Enhancers	HepG2	liver
12	chr19:35865800-35866000	Bivalent Enhancer	A549	lung
13	chr19:35865800-35870200	Weak transcription	Placenta Amnion	Placenta Amnion
14	chr19:35866000-35867000	Enhancers	Primary neutrophils fromperipheralblood	blood
15	chr19:35866200-35866800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
16	chr19:35866400-35866800	Weak transcription	HepG2	liver
17	chr19:35866400-35868400	Enhancers	Primary B cells from peripheral blood	blood
18	chr19:35866800-35867000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr19:35866800-35867000	Enhancers	HepG2	liver
20	chr19:35866800-35867200	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr19:35866800-35867200	Enhancers	Lung	lung
22	chr19:35866800-35867800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
23	chr19:35867000-35867800	Weak transcription	Primary neutrophils fromperipheralblood	blood
24	chr19:35867000-35868200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr19:35867000-35868200	Weak transcription	HepG2	liver
26	chr19:35867000-35868800	Enhancers	Primary B cells from cord blood	blood
27	chr19:35867200-35870200	Weak transcription	K562	blood
28	chr19:35867200-35870800	Weak transcription	Stomach Mucosa	stomach
29	chr19:35867400-35868200	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr19:35867600-35868600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr19:35867800-35868200	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr19:35867800-35868400	Enhancers	Primary monocytes fromperipheralblood	blood
33	chr19:35867800-35868400	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
34	chr19:35867800-35868600	Enhancers	Primary neutrophils fromperipheralblood	blood
35	chr19:35868000-35868200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
36	chr19:35868200-35871000	Enhancers	HepG2	liver
37	chr19:35868600-35869400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr19:35869000-35869200	Weak transcription	GM12878-XiMat	blood
39	chr19:35869200-35869400	Enhancers	Pancreatic Islets	Pancreatic Islet
40	chr19:35869200-35869800	ZNF genes & repeats	GM12878-XiMat	blood
41	chr19:35869400-35869600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr19:35869400-35870400	Weak transcription	Pancreatic Islets	Pancreatic Islet
43	chr19:35869600-35874400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr19:35869800-35871800	Weak transcription	GM12878-XiMat	blood
45	chr19:35870200-35871000	Enhancers	K562	blood
46	chr19:35870200-35873400	Enhancers	Placenta Amnion	Placenta Amnion
47	chr19:35870400-35870600	Enhancers	Pancreatic Islets	Pancreatic Islet
48	chr19:35870400-35872600	Enhancers	Rectal Smooth Muscle	rectum
49	chr19:35870600-35871000	Weak transcription	Pancreatic Islets	Pancreatic Islet
50	chr19:35870800-35872000	Enhancers	Fetal Heart	heart

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