Variant report

Variant	nsv550949
Chromosome Location	chr10:55662089-55725234
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	chr10:55717206-55717861	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:55710160-55710468	HepG2	liver:	n/a	chr10:55710189-55710205
3	ARID3A	chr10:55724313-55724586	HepG2	liver:	n/a	n/a
4	ARID3A	chr10:55699363-55700282	HepG2	liver:	n/a	n/a
5	BACH1	chr10:55701395-55701491	K562	blood:	n/a	n/a
6	CCNT2	chr10:55664795-55664881	K562	blood:	n/a	n/a
7	CEBPB	chr10:55712025-55712195	HepG2	liver:	n/a	chr10:55712071-55712082
8	CEBPB	chr10:55713525-55713758	HepG2	liver:	n/a	chr10:55713605-55713616
9	CEBPB	chr10:55694537-55694784	HepG2	liver:	n/a	chr10:55694635-55694646
10	CEBPB	chr10:55699537-55699743	HepG2	liver:	n/a	n/a
11	CEBPB	chr10:55699503-55699807	HepG2	liver:	n/a	n/a
12	CEBPB	chr10:55716794-55717575	Hela-S3	cervix:	n/a	chr10:55717377-55717388 chr10:55716937-55716949
13	CEBPB	chr10:55704126-55704331	HepG2	liver:	n/a	chr10:55704166-55704177 chr10:55704168-55704179 chr10:55704166-55704179
14	CEBPB	chr10:55678641-55678961	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr10:55717275-55717435	HepG2	liver:	n/a	chr10:55717377-55717388
16	CEBPB	chr10:55717230-55717393	HepG2	liver:	n/a	chr10:55717377-55717388
17	CEBPB	chr10:55710123-55710465	IMR90	lung:	n/a	chr10:55710241-55710252 chr10:55710258-55710269 chr10:55710279-55710290 chr10:55710280-55710291 chr10:55710279-55710292 chr10:55710242-55710253 chr10:55710241-55710252 chr10:55710241-55710254 chr10:55710281-55710290
18	CEBPB	chr10:55710220-55710433	H1-hESC	embryonic stem cell:	n/a	chr10:55710241-55710252 chr10:55710258-55710269 chr10:55710279-55710290 chr10:55710280-55710291 chr10:55710279-55710292 chr10:55710242-55710253 chr10:55710241-55710252 chr10:55710241-55710254 chr10:55710281-55710290
19	CEBPB	chr10:55717174-55717552	HepG2	liver:	n/a	chr10:55717377-55717388
20	CEBPB	chr10:55710096-55710489	HepG2	liver:	n/a	chr10:55710241-55710252 chr10:55710258-55710269 chr10:55710279-55710290 chr10:55710280-55710291 chr10:55710279-55710292 chr10:55710242-55710253 chr10:55710241-55710252 chr10:55710241-55710254 chr10:55710281-55710290
21	CEBPB	chr10:55710156-55710453	A549	lung:	n/a	chr10:55710241-55710252 chr10:55710258-55710269 chr10:55710279-55710290 chr10:55710280-55710291 chr10:55710279-55710292 chr10:55710242-55710253 chr10:55710241-55710252 chr10:55710241-55710254 chr10:55710281-55710290
22	CEBPB	chr10:55713444-55713755	Hela-S3	cervix:	n/a	chr10:55713605-55713616
23	CTCF	chr10:55678600-55678750	MCF-7	breast:	n/a	n/a
24	CTCF	chr10:55678580-55678730	SK-N-SH_RA	brain:	n/a	n/a
25	CTCF	chr10:55678540-55678690	HepG2	liver:	n/a	n/a
26	CTCF	chr10:55719419-55719460	Medullo	brain:	n/a	n/a
27	CTCF	chr10:55678580-55678730	HEEpiC	esophagus:	n/a	n/a
28	CTCF	chr10:55666460-55666610	HepG2	liver:	n/a	n/a
29	CTCF	chr10:55678640-55678790	Caco-2	colon:	n/a	n/a
30	CTCF	chr10:55678600-55678750	NHEK	skin:	n/a	n/a
31	CTCF	chr10:55678560-55678710	MCF-7	breast:	n/a	n/a
32	CTCF	chr10:55678520-55678670	SAEC	small airway:	n/a	n/a
33	CTCF	chr10:55678560-55678710	HEK293	kidney:	n/a	n/a
34	CTCF	chr10:55678560-55678710	BE2_C	brain:	n/a	n/a
35	E2F4	chr10:55697826-55698005	MCF10A-Er-Src	breast:	n/a	n/a
36	E2F4	chr10:55717355-55717615	MCF10A-Er-Src	breast:	n/a	n/a
37	EP300	chr10:55717073-55717524	SK-N-SH_RA	brain:	n/a	n/a
38	EP300	chr10:55717064-55717685	HepG2	liver:	n/a	n/a
39	EP300	chr10:55717585-55717940	SK-N-SH_RA	brain:	n/a	n/a
40	EP300	chr10:55699362-55699839	HepG2	liver:	n/a	chr10:55699679-55699688
41	EP300	chr10:55717076-55717564	HepG2	liver:	n/a	n/a
42	EP300	chr10:55717131-55717551	MCF-7	breast:	n/a	n/a
43	EP300	chr10:55717249-55717575	Hela-S3	cervix:	n/a	n/a
44	EP300	chr10:55717156-55717571	SK-N-SH_RA	brain:	n/a	n/a
45	EP300	chr10:55717110-55717476	HepG2	liver:	n/a	n/a
46	EP300	chr10:55716954-55718034	SK-N-SH	brain:	n/a	n/a
47	EP300	chr10:55717572-55717908	SK-N-SH_RA	brain:	n/a	n/a
48	EP300	chr10:55697634-55697654	GM12878	blood:	n/a	n/a
49	EP300	chr10:55699389-55699847	HepG2	liver:	n/a	chr10:55699679-55699688
50	ESR1	chr10:55717174-55717455	ECC-1	luminal epithelium:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:55685173-55685223	HMEC	breast:	n/a
2	chr10:55685173-55685223	NH-A	brain:	n/a
3	chr10:55685173-55685223	U87	brain:	n/a
4	chr10:55685173-55685223	AG04450	lung:	fetal
5	chr10:55685173-55685223	AG10803	skin:	n/a
6	chr10:55685173-55685223	BE2_C	brain:	n/a
7	chr10:55685173-55685223	HEK293	kidney:	embryo
8	chr10:55685173-55685223	SK-N-SH	brain:	n/a
9	chr10:55685173-55685223	HepG2	liver:	n/a
10	chr10:55685173-55685223	Hepatocyte	liver:	n/a
11	chr10:55685173-55685223	RPTEC	kidney:	n/a
12	chr10:55685173-55685223	AG04449	skin:	fetal
13	chr10:55685173-55685223	HUVEC	blood vessel:	n/a
14	chr10:55685173-55685223	IMR90	lung:	fetal
15	chr10:55685173-55685223	GM12878	blood:	n/a
16	chr10:55685173-55685223	HRPEpiC	eye:	n/a
17	chr10:55685173-55685223	HPAEpiC	pulmonary alveolar:	n/a
18	chr10:55685173-55685223	BJ	skin:	n/a
19	chr10:55685173-55685223	HRCEpiC	kidney:	n/a
20	chr10:55685173-55685223	T-47D	breast:	n/a
21	chr10:55685173-55685223	NB4	blood:	n/a
22	chr10:55685173-55685223	MCF10A-Er-Src	breast:	n/a
23	chr10:55685173-55685223	HCT-116	colon:	n/a
24	chr10:55685173-55685223	GM12892	blood:	n/a
25	chr10:55685173-55685223	NHBE	bronchial:	n/a
26	chr10:55685173-55685223	LNCaP	prostate:	n/a
27	chr10:55685173-55685223	Jurkat	blood:	n/a
28	chr10:55685173-55685223	MCF-7	breast:	n/a
29	chr10:55685173-55685223	HIPEpiC	eye:	n/a
30	chr10:55685173-55685223	AoSMC	blood vessel:	n/a
31	chr10:55685173-55685223	AG09319	gingival:	n/a
32	chr10:55685173-55685223	HCM	heart:	n/a
33	chr10:55685173-55685223	H1-hESC	embryonic stem cell:	embryo
34	chr10:55685173-55685223	GM19239	blood:	n/a
35	chr10:55685173-55685223	Caco-2	colon:	n/a
36	chr10:55685173-55685223	ProgFib	skin:	n/a
37	chr10:55685173-55685223	HEEpiC	esophagus:	n/a
38	chr10:55685173-55685223	HRE	kidney:	n/a
39	chr10:55685173-55685223	ECC-1	luminal epithelium:	n/a
40	chr10:55685173-55685223	HL-60	blood:	n/a
41	chr10:55685173-55685223	PFSK-1	brain:	n/a
42	chr10:55685173-55685223	NT2-D1	testis:	n/a
43	chr10:55685173-55685223	HNPCEpiC	eye:	n/a
44	chr10:55685173-55685223	A549	lung:	n/a
45	chr10:55685173-55685223	ovcar-3	ovarian:	n/a
46	chr10:55685173-55685223	SAEC	small airway:	n/a
47	chr10:55685173-55685223	K562	blood:	n/a
48	chr10:55685173-55685223	NHDF-neo	bronchial:	n/a
49	chr10:55685173-55685223	CMK	blood:	n/a
50	chr10:55685173-55685223	AG09309	skin:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:55658704..55661053-chr10:55661936..55664959,3	K562	blood:

Variant related genes	Relation type
PCDH15	TF binding region
PCDH15	CpG island

Extended variants
information (count: 1653 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:1653 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2921923	chr10:55662089-55662090	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs372633424	chr10:55662091-55662092	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs537236300	chr10:55662111-55662112	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs188498601	chr10:55662137-55662138	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs567427500	chr10:55662141-55662142	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs138693449	chr10:55662152-55662153	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs11003924	chr10:55662156-55662157	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs181309259	chr10:55662183-55662184	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs11003925	chr10:55662226-55662227	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs557820869	chr10:55662253-55662254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs115883679	chr10:55662263-55662264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs543630629	chr10:55662272-55662273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs369800796	chr10:55662282-55662283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs557666552	chr10:55662302-55662303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs186711742	chr10:55662304-55662305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs566128035	chr10:55662325-55662326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs543274914	chr10:55662350-55662351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs190418484	chr10:55662357-55662358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs528053060	chr10:55662358-55662359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs182006672	chr10:55662366-55662367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs564971909	chr10:55662389-55662390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs141125688	chr10:55662399-55662400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs539921175	chr10:55662416-55662417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs187612596	chr10:55662430-55662431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs2921922	chr10:55662434-55662435	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs370804669	chr10:55662464-55662465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs570116923	chr10:55662467-55662468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs75973846	chr10:55662558-55662559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs555737741	chr10:55662564-55662565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs77947769	chr10:55662610-55662611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs528448015	chr10:55662617-55662618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs574286178	chr10:55662686-55662687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs192006402	chr10:55662704-55662705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs571588904	chr10:55662706-55662707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs112216606	chr10:55662743-55662744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs77889682	chr10:55662773-55662774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs535024160	chr10:55662790-55662791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs201990327	chr10:55662793-55662794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs386743898	chr10:55662794-55662795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs185084457	chr10:55662796-55662797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs111859932	chr10:55662836-55662837	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs537514881	chr10:55662841-55662842	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs557292233	chr10:55662908-55662909	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs367879932	chr10:55662919-55662920	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs368234589	chr10:55662941-55662942	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs199868166	chr10:55662948-55662949	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs200140818	chr10:55662972-55662973	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs369120466	chr10:55662977-55662978	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs137968290	chr10:55662987-55662988	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs370178425	chr10:55662997-55662998	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Obesity	21956041	CNVD
Developmental delay	21948486	CNVD
Intellectual disability	21948486	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16272173	CNVD
Metanephric adenoma	20802469	CNVD
Autism	20841430	CNVD
Mental retardation	17124404	CNVD
Epilepsy	20923578	CNVD
Prostate cancer	16573809	CNVD
Schizophrenia	19329560	CNVD
Heart failure	18772530	CNVD
Heart failure	18854381	CNVD
Hyperglycemia	19060297	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Glioblastoma multiforme	22286061	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Usher syndrome	20538994	CNVD
Glioblastoma multiforme	17002787	CNVD
Colorectal cancer	16774939	CNVD
Autism	20858243	CNVD
Breast cancer	22522925	CNVD
Usher type I cohort	17277737	CNVD
Usher type I cohort	21436283	CNVD
Leukemia	21357790	CNVD
Medulloblastoma	22832581	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:68 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:55658600-55663000	Weak transcription	NHEK	skin
2	chr10:55661400-55662200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr10:55662000-55662200	Enhancers	Fetal Intestine Small	intestine
4	chr10:55662000-55662200	Enhancers	Fetal Kidney	kidney
5	chr10:55662800-55663200	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr10:55662800-55663200	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr10:55662800-55663200	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr10:55662800-55664000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr10:55662800-55664400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr10:55663000-55665200	Enhancers	NHEK	skin
11	chr10:55663200-55664400	Enhancers	HMEC	breast
12	chr10:55664000-55664200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr10:55664000-55665000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr10:55664200-55665400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr10:55664400-55664800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr10:55664400-55664800	Active TSS	HMEC	breast
17	chr10:55664400-55665000	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr10:55664800-55665200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr10:55664800-55665400	Enhancers	HMEC	breast
20	chr10:55665000-55673800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chr10:55665200-55665600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr10:55677600-55677800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr10:55677800-55683800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr10:55678400-55679000	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr10:55678600-55679000	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr10:55681000-55681400	Enhancers	Breast Myoepithelial Primary Cells	Breast
27	chr10:55681200-55681400	Enhancers	Right Atrium	heart
28	chr10:55683400-55683600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
29	chr10:55683800-55684200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr10:55683800-55684400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
31	chr10:55683800-55684600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr10:55683800-55685400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
33	chr10:55684600-55686200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr10:55685600-55685800	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr10:55685600-55685800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr10:55686000-55686200	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr10:55689800-55692200	Weak transcription	Brain Substantia Nigra	brain
38	chr10:55697400-55699600	Enhancers	HepG2	liver
39	chr10:55706600-55710400	Weak transcription	HepG2	liver
40	chr10:55710400-55712400	Enhancers	HepG2	liver
41	chr10:55711400-55711600	Enhancers	Brain Substantia Nigra	brain
42	chr10:55711400-55712000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr10:55711400-55712400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
44	chr10:55711400-55712400	Weak transcription	Gastric	stomach
45	chr10:55711600-55711800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr10:55711600-55712000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
47	chr10:55711600-55712600	ZNF genes & repeats	Brain Hippocampus Middle	brain
48	chr10:55712000-55712200	Strong transcription	ES-I3 Cell Line	embryonic stem cell
49	chr10:55712000-55712800	ZNF genes & repeats	Brain Substantia Nigra	brain
50	chr10:55712200-55714400	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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