Variant report

Variant	nsv1060969
Chromosome Location	chr16:46463770-46607439
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:855)
CpG islands
(count:672)
Chromatin interactive
region (count:11)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr16:46498944-46499144	K562	blood:	n/a	n/a
2	ATF1	chr16:46499905-46500324	K562	blood:	n/a	n/a
3	BACH1	chr16:46530728-46530816	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr16:46530690-46530890	K562	blood:	n/a	n/a
5	BATF	chr16:46464835-46465139	GM12878	blood:	n/a	n/a
6	BATF	chr16:46497607-46498499	GM12878	blood:	n/a	n/a
7	BATF	chr16:46464603-46465194	GM12878	blood:	n/a	n/a
8	BATF	chr16:46465420-46465657	GM12878	blood:	n/a	n/a
9	BATF	chr16:46466860-46467142	GM12878	blood:	n/a	n/a
10	BATF	chr16:46464146-46464430	GM12878	blood:	n/a	n/a
11	BATF	chr16:46499548-46500481	GM12878	blood:	n/a	n/a
12	BATF	chr16:46490523-46490744	GM12878	blood:	n/a	n/a
13	BATF	chr16:46498790-46499489	GM12878	blood:	n/a	n/a
14	BATF	chr16:46498510-46500501	GM12878	blood:	n/a	n/a
15	BATF	chr16:46468387-46468633	GM12878	blood:	n/a	n/a
16	BATF	chr16:46491560-46491719	GM12878	blood:	n/a	n/a
17	BATF	chr16:46468429-46468661	GM12878	blood:	n/a	n/a
18	BATF	chr16:46465288-46465597	GM12878	blood:	n/a	n/a
19	BCL11A	chr16:46497586-46500478	GM12878	blood:	n/a	n/a
20	BCL11A	chr16:46493297-46493565	GM12878	blood:	n/a	n/a
21	BCL11A	chr16:46464241-46464460	GM12878	blood:	n/a	n/a
22	BCL11A	chr16:46492046-46492424	GM12878	blood:	n/a	n/a
23	BCL11A	chr16:46492177-46492356	GM12878	blood:	n/a	n/a
24	BCL11A	chr16:46464900-46465146	GM12878	blood:	n/a	n/a
25	BCL11A	chr16:46466521-46466834	GM12878	blood:	n/a	n/a
26	BCL11A	chr16:46466605-46467158	GM12878	blood:	n/a	n/a
27	BCL11A	chr16:46464605-46465237	GM12878	blood:	n/a	n/a
28	BCL11A	chr16:46499718-46500387	GM12878	blood:	n/a	n/a
29	BCL11A	chr16:46465436-46465679	GM12878	blood:	n/a	n/a
30	BCL11A	chr16:46466938-46467211	GM12878	blood:	n/a	n/a
31	BCLAF1	chr16:46588341-46588614	GM12878	blood:	n/a	n/a
32	BHLHE40	chr16:46492587-46492815	HepG2	liver:	n/a	n/a
33	BHLHE40	chr16:46493982-46494279	HepG2	liver:	n/a	n/a
34	BHLHE40	chr16:46464582-46464779	HepG2	liver:	n/a	n/a
35	BHLHE40	chr16:46499569-46500280	HepG2	liver:	n/a	n/a
36	BHLHE40	chr16:46498816-46499197	HepG2	liver:	n/a	n/a
37	BHLHE40	chr16:46603093-46603220	K562	blood:	n/a	n/a
38	BHLHE40	chr16:46464889-46465093	HepG2	liver:	n/a	n/a
39	BHLHE40	chr16:46467079-46467322	HepG2	liver:	n/a	n/a
40	BRCA1	chr16:46498742-46498822	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr16:46553053-46553266	Hela-S3	cervix:	n/a	chr16:46553164-46553181 chr16:46553167-46553180
42	CEBPB	chr16:46534572-46534639	HepG2	liver:	n/a	n/a
43	CEBPB	chr16:46500020-46500158	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr16:46553020-46553329	HepG2	liver:	n/a	chr16:46553164-46553181 chr16:46553167-46553180
45	CEBPB	chr16:46607214-46607273	K562	blood:	n/a	n/a
46	CEBPD	chr16:46499727-46500511	K562	blood:	n/a	n/a
47	CEBPD	chr16:46498833-46499417	K562	blood:	n/a	n/a
48	CHD1	chr16:46500186-46500234	GM12878	blood:	n/a	n/a
49	CHD1	chr16:46498962-46499438	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr16:46588360-46588510	GM12865	blood:	n/a	n/a

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:46588509-46588559	AoSMC	blood vessel:	n/a
2	chr16:46588509-46588559	AoSMC	blood vessel:	n/a
3	chr16:46603021-46603071	AG04450	lung:	fetal
4	chr16:46603321-46603371	AG10803	skin:	n/a
5	chr16:46603321-46603371	PrEC	prostate:	n/a
6	chr16:46603015-46603065	AoSMC	blood vessel:	n/a
7	chr16:46604297-46604347	HUVEC	blood vessel:	n/a
8	chr16:46588509-46588559	NT2-D1	testis:	n/a
9	chr16:46603059-46603109	AG09309	skin:	n/a
10	chr16:46465353-46465403	HIPEpiC	eye:	n/a
11	chr16:46603259-46603309	ECC-1	luminal epithelium:	n/a
12	chr16:46603059-46603109	K562	blood:	n/a
13	chr16:46465353-46465403	PANC-1	pancreas:	n/a
14	chr16:46603191-46603241	PANC-1	pancreas:	n/a
15	chr16:46489157-46489207	BJ	skin:	n/a
16	chr16:46603021-46603071	AG10803	skin:	n/a
17	chr16:46603059-46603109	NB4	blood:	n/a
18	chr16:46604297-46604347	MCF10A-Er-Src	breast:	n/a
19	chr16:46603059-46603109	GM12891	blood:	n/a
20	chr16:46603191-46603241	HCT-116	colon:	n/a
21	chr16:46602737-46602787	BJ	skin:	n/a
22	chr16:46603321-46603371	SK-N-MC	brain:	n/a
23	chr16:46489157-46489207	HRCEpiC	kidney:	n/a
24	chr16:46603191-46603241	HEEpiC	esophagus:	n/a
25	chr16:46489157-46489207	HIPEpiC	eye:	n/a
26	chr16:46603259-46603309	HRE	kidney:	n/a
27	chr16:46465353-46465403	SAEC	small airway:	n/a
28	chr16:46604297-46604347	BE2_C	brain:	n/a
29	chr16:46603191-46603241	HRPEpiC	eye:	n/a
30	chr16:46603059-46603109	NT2-D1	testis:	n/a
31	chr16:46603021-46603071	BJ	skin:	n/a
32	chr16:46603259-46603309	NH-A	brain:	n/a
33	chr16:46465353-46465403	HNPCEpiC	eye:	n/a
34	chr16:46603259-46603309	HPAEpiC	pulmonary alveolar:	n/a
35	chr16:46603321-46603371	SAEC	small airway:	n/a
36	chr16:46588509-46588559	HRPEpiC	eye:	n/a
37	chr16:46602737-46602787	GM06990	blood:	n/a
38	chr16:46603191-46603241	CMK	blood:	n/a
39	chr16:46588509-46588559	GM12891	blood:	n/a
40	chr16:46603321-46603371	BE2_C	brain:	n/a
41	chr16:46604297-46604347	HCPEpiC	choroid plexus:	n/a
42	chr16:46465353-46465403	HPAEpiC	pulmonary alveolar:	n/a
43	chr16:46603015-46603065	HepG2	liver:	n/a
44	chr16:46603021-46603071	U87	brain:	n/a
45	chr16:46603059-46603109	HL-60	blood:	n/a
46	chr16:46603059-46603109	HNPCEpiC	eye:	n/a
47	chr16:46588509-46588559	HAEpiC	amniotic membrane:	n/a
48	chr16:46603321-46603371	Hepatocyte	liver:	n/a
49	chr16:46603191-46603241	HNPCEpiC	eye:	n/a
50	chr16:46604297-46604347	GM12892	blood:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:46588378..46588920-chr16:46662972..46663507,2	K562	blood:
2	chr16:46530274..46532917-chr16:46535064..46536684,2	K562	blood:
3	chr16:46603053..46604562-chr16:46606887..46609535,2	MCF-7	breast:
4	chr16:46589331..46591714-chr16:46654314..46656100,2	K562	blood:
5	chr16:46607322..46610381-chr16:46616231..46620606,3	K562	blood:
6	chr16:46530274..46532917-chr16:46535064..46536684,2	K562	blood:
7	chr16:46598432..46601412-chr16:46613348..46615647,2	K562	blood:
8	chr11:125334060..125334821-chr16:46593821..46594420,2	HCT-116	colon:
9	chr16:46588077..46588805-chr16:46640597..46641513,2	MCF-7	breast:
10	chr16:46511252..46512930-chr16:46534367..46536672,2	K562	blood:
11	chr16:46601237..46602830-chr16:46605603..46608385,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SHCBP1-3	chr16:46512241-46512351	NONHSAT142250
2	lnc-SHCBP1-3	chr16:46508034-46508241	NONHSAT142250
3	lnc-SHCBP1-3	chr16:46509678-46509906	NONHSAT142250
4	lnc-SHCBP1-4	chr16:46477853-46478542	ucscGeneNc_uc002eex_1
5	lnc-ORC6-4	chr16:46605449-46606048	NONHSAT142252

No data

Variant related genes	Relation type
RNU6-845P	TF binding region
ENSG00000261356	TF binding region
ANKRD26P1	TF binding region
ENSG00000260251	TF binding region
RNU6-845P	CpG island
ENSG00000261356	CpG island
ANKRD26P1	CpG island
ENSG00000260251	CpG island
ENSG00000260251	chromatin interactions
ENSG00000261239	chromatin interactions
ENSG00000171241	chromatin interactions
GJA1	miRNA target sites
UTRN	miRNA target sites

Extended variants
information (count: 1924 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:1924 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs368529688	chr16:46463776-46463777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs200538348	chr16:46463781-46463782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs527433265	chr16:46463782-46463783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs552208235	chr16:46463812-46463813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs374883673	chr16:46463863-46463864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs564371358	chr16:46463872-46463873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs62021701	chr16:46463889-46463890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs62021702	chr16:46463892-46463893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs370268496	chr16:46463901-46463902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs62021703	chr16:46463911-46463912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs549779545	chr16:46463937-46463938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs368917230	chr16:46463942-46463943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs372213757	chr16:46463962-46463963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs375238913	chr16:46463974-46463975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs372122725	chr16:46463997-46463998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs62021704	chr16:46464006-46464007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs568205003	chr16:46464007-46464008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs201970693	chr16:46464018-46464019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs62021705	chr16:46464024-46464025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs113578909	chr16:46464045-46464046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs535532592	chr16:46464047-46464048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs112963462	chr16:46464048-46464049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs77738754	chr16:46464061-46464062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs9745935	chr16:46464062-46464063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs566975925	chr16:46464067-46464068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs534370153	chr16:46464069-46464070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs74622494	chr16:46464086-46464087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs111726586	chr16:46464116-46464117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs72814895	chr16:46464125-46464126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs559023988	chr16:46464126-46464127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs111939471	chr16:46464127-46464128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs147033621	chr16:46464128-46464129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs561909943	chr16:46464129-46464130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs74951682	chr16:46464149-46464150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs149530170	chr16:46464158-46464159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs75102124	chr16:46464166-46464167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs77436372	chr16:46464184-46464185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs78402865	chr16:46464203-46464204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs77122918	chr16:46464208-46464209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs150681635	chr16:46464220-46464221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs113070023	chr16:46464224-46464225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs140912609	chr16:46464230-46464231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs577447654	chr16:46464241-46464242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs76397119	chr16:46464245-46464246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs537897244	chr16:46464265-46464266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs369671420	chr16:46464275-46464276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs371450295	chr16:46464283-46464284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs111584259	chr16:46464285-46464286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs201001747	chr16:46464292-46464293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs560141089	chr16:46464305-46464306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	22958593	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Wilms tumour	21544195	CNVD
Cancer	20164920	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16702952	CNVD
Medulloblastoma	16968546	CNVD
Prostate cancer	19242612	CNVD
Cancer	22429812	CNVD
Ewing''s sarcoma	21437220	CNVD
Ewing''s sarcoma	22429812	CNVD
Melanoma	18172304	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Multiple myeloma	21628407	CNVD
Autism	19955444	CNVD
Schizophrenia	19955444	CNVD
Renal cell carcinoma	18765545	CNVD
Sudden cardiac death	19188705	CNVD
Multiple myeloma	16616336	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	21364760	CNVD
Ewing''s sarcoma	17952124	CNVD
Myelofibrosis	22110671	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:170 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:46462800-46466200	Weak transcription	Right Atrium	heart
2	chr16:46488800-46489200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr16:46488800-46489400	Active TSS	ES-I3 Cell Line	embryonic stem cell
4	chr16:46492000-46492200	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr16:46494400-46497600	Weak transcription	Brain Angular Gyrus	brain
6	chr16:46495200-46497600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr16:46495400-46496000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr16:46496000-46497600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr16:46497600-46500400	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
10	chr16:46497600-46500400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
11	chr16:46497600-46500400	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr16:46497600-46500400	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
13	chr16:46497600-46500400	ZNF genes & repeats	Adipose Nuclei	Adipose
14	chr16:46497600-46500400	ZNF genes & repeats	Brain Angular Gyrus	brain
15	chr16:46497600-46500400	ZNF genes & repeats	Brain Substantia Nigra	brain
16	chr16:46497600-46500400	ZNF genes & repeats	Duodenum Mucosa	Duodenum
17	chr16:46497600-46500400	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
18	chr16:46497600-46500400	ZNF genes & repeats	Fetal Brain Male	brain
19	chr16:46497600-46500400	ZNF genes & repeats	Fetal Lung	lung
20	chr16:46497600-46500400	ZNF genes & repeats	Rectal Mucosa Donor 29	rectum
21	chr16:46497600-46500600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr16:46497600-46500600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
23	chr16:46497600-46500600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
24	chr16:46497600-46500600	ZNF genes & repeats	Liver	Liver
25	chr16:46497600-46500600	ZNF genes & repeats	Fetal Kidney	kidney
26	chr16:46497800-46498800	ZNF genes & repeats	ES-WA7 Cell Line	embryonic stem cell
27	chr16:46497800-46500400	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr16:46497800-46500400	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
29	chr16:46497800-46500400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr16:46497800-46500400	ZNF genes & repeats	Primary T cells from cord blood	blood
31	chr16:46497800-46500400	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 1	blood
32	chr16:46497800-46500400	ZNF genes & repeats	Brain Anterior Caudate	brain
33	chr16:46497800-46500400	ZNF genes & repeats	Brain Inferior Temporal Lobe	brain
34	chr16:46497800-46500400	ZNF genes & repeats	Skeletal Muscle Female	skeletal muscle
35	chr16:46497800-46500400	ZNF genes & repeats	GM12878-XiMat	blood
36	chr16:46497800-46500400	ZNF genes & repeats	K562	blood
37	chr16:46497800-46500400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
38	chr16:46497800-46500600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
39	chr16:46497800-46500600	ZNF genes & repeats	Fetal Heart	heart
40	chr16:46497800-46500600	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
41	chr16:46497800-46500600	ZNF genes & repeats	HUVEC	blood vessel
42	chr16:46497800-46500800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
43	chr16:46498000-46500600	ZNF genes & repeats	Brain Hippocampus Middle	brain
44	chr16:46498400-46500200	ZNF genes & repeats	Brain Dorsolateral Prefrontal Cortex	brain
45	chr16:46498600-46500400	ZNF genes & repeats	Primary T killer memory cells from peripheral blood	blood
46	chr16:46498800-46500400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr16:46498800-46500400	ZNF genes & repeats	Primary T helper naive cells from peripheral blood	blood
48	chr16:46498800-46500400	ZNF genes & repeats	NH-A	brain
49	chr16:46499000-46500400	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
50	chr16:46499000-46500400	ZNF genes & repeats	Aorta	Aorta

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links