Variant report

Variant	nsv1002272
Chromosome Location	chr4:49081001-49309842
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:9934)
CpG islands
(count:976)
Chromatin interactive
region (count:1)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:9934 , 50 per page) page: 1 2 3 4 5 6 7 ... 199

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:49112366-49112562	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:49099072-49099244	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:49154831-49157744	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:49149318-49150059	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:49290236-49290256	K562	blood:	n/a	n/a
6	ARID3A	chr4:49219672-49219782	K562	blood:	n/a	n/a
7	ARID3A	chr4:49107140-49107875	HepG2	liver:	n/a	n/a
8	ARID3A	chr4:49109281-49110893	HepG2	liver:	n/a	n/a
9	ARID3A	chr4:49111528-49111563	HepG2	liver:	n/a	n/a
10	ARID3A	chr4:49291177-49291344	K562	blood:	n/a	n/a
11	ATF1	chr4:49148799-49149989	K562	blood:	n/a	n/a
12	ATF1	chr4:49111368-49111728	K562	blood:	n/a	n/a
13	ATF1	chr4:49140067-49140092	K562	blood:	n/a	n/a
14	ATF1	chr4:49158063-49158263	K562	blood:	n/a	n/a
15	ATF1	chr4:49163055-49163411	K562	blood:	n/a	n/a
16	ATF1	chr4:49120008-49120552	K562	blood:	n/a	n/a
17	ATF1	chr4:49126584-49126957	K562	blood:	n/a	n/a
18	ATF1	chr4:49150936-49153536	K562	blood:	n/a	n/a
19	ATF1	chr4:49093328-49093478	K562	blood:	n/a	n/a
20	ATF1	chr4:49110185-49110828	K562	blood:	n/a	n/a
21	ATF1	chr4:49114188-49114560	K562	blood:	n/a	n/a
22	ATF1	chr4:49120865-49121692	K562	blood:	n/a	n/a
23	ATF1	chr4:49099067-49099261	K562	blood:	n/a	n/a
24	ATF1	chr4:49291140-49291510	K562	blood:	n/a	n/a
25	ATF1	chr4:49104617-49104920	K562	blood:	n/a	n/a
26	ATF1	chr4:49121975-49123219	K562	blood:	n/a	n/a
27	ATF1	chr4:49112358-49112551	K562	blood:	n/a	n/a
28	ATF1	chr4:49118726-49119093	K562	blood:	n/a	n/a
29	ATF1	chr4:49168855-49169084	K562	blood:	n/a	n/a
30	ATF1	chr4:49109270-49109652	K562	blood:	n/a	n/a
31	ATF1	chr4:49093788-49094700	K562	blood:	n/a	n/a
32	ATF1	chr4:49106177-49107831	K562	blood:	n/a	n/a
33	ATF1	chr4:49142534-49142590	K562	blood:	n/a	n/a
34	ATF1	chr4:49117835-49117841	K562	blood:	n/a	n/a
35	ATF1	chr4:49101009-49102452	K562	blood:	n/a	n/a
36	ATF1	chr4:49105237-49105606	K562	blood:	n/a	n/a
37	ATF1	chr4:49147847-49148046	K562	blood:	n/a	n/a
38	ATF1	chr4:49154859-49157591	K562	blood:	n/a	n/a
39	ATF3	chr4:49156156-49156703	HCT-116	colon:	n/a	n/a
40	ATF3	chr4:49107079-49107836	H1-hESC	embryonic stem cell:	n/a	n/a
41	ATF3	chr4:49151701-49151864	GM12878	blood:	n/a	n/a
42	ATF3	chr4:49163110-49163368	K562	blood:	n/a	chr4:49163223-49163236
43	ATF3	chr4:49142496-49142609	K562	blood:	n/a	n/a
44	ATF3	chr4:49120637-49121281	HCT-116	colon:	n/a	n/a
45	ATF3	chr4:49151473-49151931	H1-hESC	embryonic stem cell:	n/a	n/a
46	BACH1	chr4:49289396-49289534	K562	blood:	n/a	n/a
47	BACH1	chr4:49291317-49291355	K562	blood:	n/a	n/a
48	BATF	chr4:49199682-49200057	GM12878	blood:	n/a	n/a
49	BATF	chr4:49252453-49252649	GM12878	blood:	n/a	n/a
50	BATF	chr4:49260971-49261375	GM12878	blood:	n/a	n/a

(count:976 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:49308684-49308734	MCF-7	breast:	n/a
2	chr4:49159508-49159558	SAEC	small airway:	n/a
3	chr4:49163276-49163326	HepG2	liver:	n/a
4	chr4:49237109-49237159	GM12878	blood:	n/a
5	chr4:49236405-49236455	AG09319	gingival:	n/a
6	chr4:49163755-49163805	GM19239	blood:	n/a
7	chr4:49237497-49237547	HPAEpiC	pulmonary alveolar:	n/a
8	chr4:49163276-49163326	GM12891	blood:	n/a
9	chr4:49164979-49165029	HEEpiC	esophagus:	n/a
10	chr4:49163558-49163608	NH-A	brain:	n/a
11	chr4:49163276-49163326	PrEC	prostate:	n/a
12	chr4:49308567-49308617	NH-A	brain:	n/a
13	chr4:49297073-49297123	GM12878	blood:	n/a
14	chr4:49308684-49308734	NB4	blood:	n/a
15	chr4:49272914-49272964	PFSK-1	brain:	n/a
16	chr4:49163276-49163326	T-47D	breast:	n/a
17	chr4:49159508-49159558	GM12878	blood:	n/a
18	chr4:49237497-49237547	HCPEpiC	choroid plexus:	n/a
19	chr4:49204696-49204746	LNCaP	prostate:	n/a
20	chr4:49166489-49166539	SAEC	small airway:	n/a
21	chr4:49237109-49237159	HRPEpiC	eye:	n/a
22	chr4:49163276-49163326	BE2_C	brain:	n/a
23	chr4:49163755-49163805	AG04450	lung:	fetal
24	chr4:49237109-49237159	MCF10A-Er-Src	breast:	n/a
25	chr4:49163558-49163608	IMR90	lung:	fetal
26	chr4:49159508-49159558	LNCaP	prostate:	n/a
27	chr4:49237109-49237159	SKMC	muscle:	n/a
28	chr4:49159508-49159558	NHBE	bronchial:	n/a
29	chr4:49236405-49236455	IMR90	lung:	fetal
30	chr4:49237109-49237159	HCM	heart:	n/a
31	chr4:49272914-49272964	U87	brain:	n/a
32	chr4:49166489-49166539	HIPEpiC	eye:	n/a
33	chr4:49163558-49163608	U87	brain:	n/a
34	chr4:49308567-49308617	HRCEpiC	kidney:	n/a
35	chr4:49163558-49163608	BJ	skin:	n/a
36	chr4:49204696-49204746	Hela-S3	cervix:	n/a
37	chr4:49308684-49308734	HNPCEpiC	eye:	n/a
38	chr4:49236405-49236455	PANC-1	pancreas:	n/a
39	chr4:49166489-49166539	GM12892	blood:	n/a
40	chr4:49236405-49236455	HAEpiC	amniotic membrane:	n/a
41	chr4:49308684-49308734	HPAEpiC	pulmonary alveolar:	n/a
42	chr4:49204696-49204746	HepG2	liver:	n/a
43	chr4:49163755-49163805	HPAEpiC	pulmonary alveolar:	n/a
44	chr4:49204696-49204746	RPTEC	kidney:	n/a
45	chr4:49164979-49165029	HRCEpiC	kidney:	n/a
46	chr4:49289994-49290044	Hela-S3	cervix:	n/a
47	chr4:49303202-49303252	HNPCEpiC	eye:	n/a
48	chr4:49163276-49163326	HEK293	kidney:	embryo
49	chr4:49303202-49303252	AG09309	skin:	n/a
50	chr4:49164979-49165029	NT2-D1	testis:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:89879085..89879687-chr4:49152239..49152833,2	MCF-7	breast:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OCIAD2-9	chr4:49244726-49244948	NONHSAT096322
2	lnc-CWH43-5	chr4:49248618-49248710	NONHSAT096324
3	lnc-CWH43-4	chr4:49248038-49248555	NONHSAT096323
4	lnc-OCIAD2-9	chr4:49246290-49246387	NONHSAT096322
5	lnc-OCIAD2-9	chr4:49239669-49239711	NONHSAT096322
6	lnc-OCIAD2-9	chr4:49239116-49239167	NONHSAT096322
7	lnc-CWH43-5	chr4:49248783-49248932	NONHSAT096324
8	lnc-OCIAD2-9	chr4:49240040-49240093	NONHSAT096322
9	lnc-OCIAD2-6	chr4:49221527-49221803	NONHSAT096315
10	lnc-OCIAD2-7	chr4:49231590-49233301	NONHSAT096320
11	lnc-OCIAD2-9	chr4:49241263-49241308	NONHSAT096322
12	lnc-OCIAD2-5	chr4:49214268-49214641	NONHSAT096314
13	lnc-CWH43-2	chr4:49175125-49175286	NONHSAT096308
14	lnc-CWH43-2	chr4:49171338-49171778	NONHSAT096308

No data

Variant related genes	Relation type
ENSG00000249079	TF binding region
ENSG00000221747	TF binding region
ENSG00000266337	TF binding region
ENSG00000248946	TF binding region
ENSG00000249828	TF binding region
ENSG00000222437	TF binding region
ENSG00000237961	TF binding region
ENSG00000268736	TF binding region
SNX18P23	TF binding region
ENSG00000221415	TF binding region
ENSG00000249079	CpG island
ENSG00000221747	CpG island
ENSG00000266337	CpG island
ENSG00000248946	CpG island
ENSG00000249828	CpG island
ENSG00000222437	CpG island
ENSG00000237961	CpG island
ENSG00000268736	CpG island
SNX18P23	CpG island
ENSG00000221415	CpG island

Extended variants
information (count: 20613 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:20613 , 50 per page) page: 1 2 3 4 5 6 7 ... 413

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs142487645	chr4:49085026-49085027	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs554172585	chr4:49085033-49085034	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs186246310	chr4:49085053-49085054	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs145964890	chr4:49085054-49085055	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs371885275	chr4:49085075-49085076	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs574217614	chr4:49085086-49085087	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs550807857	chr4:49085147-49085148	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs191170405	chr4:49085172-49085173	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs535942757	chr4:49085177-49085178	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs530059993	chr4:49085179-49085180	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs139834896	chr4:49085193-49085194	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs552765017	chr4:49085195-49085196	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs112568200	chr4:49085236-49085237	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs533729561	chr4:49085242-49085243	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs552000454	chr4:49085250-49085251	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs543125001	chr4:49085328-49085329	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs183288647	chr4:49085353-49085354	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs188216722	chr4:49085355-49085356	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs574352922	chr4:49085366-49085367	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs141530646	chr4:49085392-49085393	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs6825482	chr4:49085414-49085415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs150799479	chr4:49085424-49085425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs569409338	chr4:49085445-49085446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs573629476	chr4:49085459-49085460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs566304470	chr4:49085462-49085463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs540934708	chr4:49085467-49085468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs375220612	chr4:49085485-49085486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs565439574	chr4:49085499-49085500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs200011430	chr4:49085511-49085512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs190566368	chr4:49085547-49085548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs183150418	chr4:49085578-49085579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs369492388	chr4:49085599-49085600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs562867619	chr4:49085610-49085611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs187686317	chr4:49085639-49085640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs530086540	chr4:49085666-49085667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs192650485	chr4:49085700-49085701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs536778608	chr4:49085705-49085706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs560010718	chr4:49085711-49085712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs527535010	chr4:49085726-49085727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs149934387	chr4:49085849-49085850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs144987326	chr4:49085870-49085871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs531435729	chr4:49085904-49085905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs534944509	chr4:49085962-49085963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs534512426	chr4:49085975-49085976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs549832368	chr4:49085977-49085978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs568103759	chr4:49085984-49085985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs184322712	chr4:49085992-49085993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs553445262	chr4:49086025-49086026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs565689956	chr4:49086028-49086029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs558959387	chr4:49086051-49086052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
Oral squamous cell carcinoma	17134496	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Cancer	22183965	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Breast cancer	16272173	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:2051 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:49085000-49085400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr4:49085400-49093200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr4:49087400-49093200	Weak transcription	Left Ventricle	heart
4	chr4:49089800-49090000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr4:49090000-49093200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr4:49093000-49095200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
7	chr4:49093200-49093600	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells	blood
8	chr4:49093200-49093600	ZNF genes & repeats	Right Atrium	heart
9	chr4:49093200-49093600	ZNF genes & repeats	Osteobl	bone
10	chr4:49093200-49094000	ZNF genes & repeats	Hela-S3	cervix
11	chr4:49093200-49094200	Flanking Bivalent TSS/Enh	Gastric	stomach
12	chr4:49093200-49094600	ZNF genes & repeats	HSMMtube	muscle
13	chr4:49093200-49094600	ZNF genes & repeats	NHEK	skin
14	chr4:49093200-49094800	ZNF genes & repeats	HMEC	breast
15	chr4:49093200-49095000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
16	chr4:49093200-49095000	ZNF genes & repeats	ES-WA7 Cell Line	embryonic stem cell
17	chr4:49093200-49095000	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
18	chr4:49093200-49095000	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
19	chr4:49093200-49095000	ZNF genes & repeats	Primary B cells from peripheral blood	blood
20	chr4:49093200-49095000	ZNF genes & repeats	Primary T cells fromperipheralblood	blood
21	chr4:49093200-49095000	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
22	chr4:49093200-49095000	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
23	chr4:49093200-49095000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr4:49093200-49095000	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr4:49093200-49095000	ZNF genes & repeats	Brain Anterior Caudate	brain
26	chr4:49093200-49095000	ZNF genes & repeats	Brain Hippocampus Middle	brain
27	chr4:49093200-49095000	ZNF genes & repeats	Brain Dorsolateral Prefrontal Cortex	brain
28	chr4:49093200-49095000	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
29	chr4:49093200-49095000	ZNF genes & repeats	Fetal Muscle Trunk	muscle
30	chr4:49093200-49095000	ZNF genes & repeats	Placenta	Placenta
31	chr4:49093200-49095000	ZNF genes & repeats	Fetal Stomach	stomach
32	chr4:49093200-49095000	ZNF genes & repeats	Pancreas	Pancrea
33	chr4:49093200-49095000	ZNF genes & repeats	Rectal Mucosa Donor 31	rectum
34	chr4:49093200-49095000	ZNF genes & repeats	Small Intestine	intestine
35	chr4:49093200-49095000	ZNF genes & repeats	Stomach Smooth Muscle	stomach
36	chr4:49093200-49095000	ZNF genes & repeats	Dnd41	blood
37	chr4:49093200-49095000	ZNF genes & repeats	HUVEC	blood vessel
38	chr4:49093200-49095000	ZNF genes & repeats	K562	blood
39	chr4:49093200-49095000	ZNF genes & repeats	NHDF-Ad	bronchial
40	chr4:49093200-49095200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
41	chr4:49093200-49095200	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr4:49093200-49095200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr4:49093200-49095200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr4:49093200-49095200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr4:49093200-49095200	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr4:49093200-49095200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
47	chr4:49093200-49095200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
48	chr4:49093200-49095200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
49	chr4:49093200-49095200	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
50	chr4:49093200-49095200	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell

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