Variant report

Variant	nsv428657
Chromosome Location	chr16:47748036-47913816
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:747)
CpG islands
(count:244)
Chromatin interactive
region (count:30)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:747 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:47765182-47765217	HepG2	liver:	n/a	n/a
2	BATF	chr16:47895897-47896215	GM12878	blood:	n/a	n/a
3	BHLHE40	chr16:47907555-47907562	K562	blood:	n/a	n/a
4	BHLHE40	chr16:47813767-47813947	GM12878	blood:	n/a	n/a
5	BHLHE40	chr16:47765191-47765357	HepG2	liver:	n/a	n/a
6	BHLHE40	chr16:47813447-47813875	K562	blood:	n/a	n/a
7	CEBPB	chr16:47766276-47767103	IMR90	lung:	n/a	n/a
8	CEBPB	chr16:47881169-47881481	IMR90	lung:	n/a	n/a
9	CEBPB	chr16:47771267-47771329	HepG2	liver:	n/a	chr16:47771281-47771292
10	CEBPB	chr16:47765466-47765614	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr16:47833134-47833268	HepG2	liver:	n/a	chr16:47833192-47833203
12	CEBPB	chr16:47818412-47818616	HepG2	liver:	n/a	chr16:47818508-47818521 chr16:47818508-47818519
13	CEBPB	chr16:47881196-47881475	HepG2	liver:	n/a	n/a
14	CEBPB	chr16:47811075-47811358	IMR90	lung:	n/a	n/a
15	CEBPB	chr16:47750530-47750729	IMR90	lung:	n/a	n/a
16	CEBPB	chr16:47862073-47862353	IMR90	lung:	n/a	chr16:47862210-47862221
17	CEBPB	chr16:47759946-47760213	Hela-S3	cervix:	n/a	chr16:47760059-47760070
18	CEBPB	chr16:47760046-47760135	K562	blood:	n/a	chr16:47760059-47760070
19	CEBPB	chr16:47862202-47862240	K562	blood:	n/a	chr16:47862210-47862221
20	CEBPB	chr16:47833173-47833237	H1-hESC	embryonic stem cell:	n/a	chr16:47833192-47833203
21	CEBPB	chr16:47750580-47750608	K562	blood:	n/a	n/a
22	CEBPB	chr16:47759880-47760251	IMR90	lung:	n/a	chr16:47760059-47760070
23	CEBPB	chr16:47818450-47818575	K562	blood:	n/a	chr16:47818508-47818521 chr16:47818508-47818519
24	CEBPB	chr16:47766293-47766687	A549	lung:	n/a	n/a
25	CEBPB	chr16:47759875-47760252	A549	lung:	n/a	chr16:47760059-47760070
26	CEBPB	chr16:47766318-47766903	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr16:47767953-47768022	HepG2	liver:	n/a	n/a
28	CEBPB	chr16:47766385-47766714	A549	lung:	n/a	n/a
29	CEBPB	chr16:47881134-47881427	MCF-7	breast:	n/a	n/a
30	CEBPB	chr16:47862090-47862402	HepG2	liver:	n/a	chr16:47862210-47862221
31	CEBPB	chr16:47902767-47903011	IMR90	lung:	n/a	n/a
32	CEBPB	chr16:47765039-47765748	IMR90	lung:	n/a	n/a
33	CEBPB	chr16:47902775-47903019	HepG2	liver:	n/a	n/a
34	CEBPB	chr16:47771177-47771470	IMR90	lung:	n/a	chr16:47771281-47771292
35	CEBPB	chr16:47759897-47760258	HepG2	liver:	n/a	chr16:47760059-47760070
36	CEBPB	chr16:47813817-47813941	IMR90	lung:	n/a	n/a
37	CEBPB	chr16:47761111-47761277	HepG2	liver:	n/a	chr16:47761188-47761199
38	CEBPB	chr16:47799940-47800063	IMR90	lung:	n/a	n/a
39	CHD2	chr16:47808668-47808804	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr16:47907440-47907590	GM12873	blood:	n/a	n/a
41	CTCF	chr16:47808640-47808790	WI-38	lung:	n/a	n/a
42	CTCF	chr16:47808672-47808776	NHEK	skin:	n/a	n/a
43	CTCF	chr16:47907440-47907590	HBMEC	blood vessel:	n/a	n/a
44	CTCF	chr16:47808674-47808732	LNCaP	prostate:	n/a	n/a
45	CTCF	chr16:47868708-47868758	HUVEC	blood vessel:	n/a	n/a
46	CTCF	chr16:47907500-47907650	GM12864	blood:	n/a	n/a
47	CTCF	chr16:47881700-47881850	SAEC	small airway:	n/a	n/a
48	CTCF	chr16:47907420-47907570	Caco-2	colon:	n/a	n/a
49	CTCF	chr16:47907284-47907799	HCT-116	colon:	n/a	n/a
50	CTCF	chr16:47766720-47766870	HCPEpiC	choroid plexus:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:47760096-47760146	K562	blood:	n/a
2	chr16:47882395-47882445	RPTEC	kidney:	n/a
3	chr16:47814576-47814626	AG09309	skin:	n/a
4	chr16:47760096-47760146	HCPEpiC	choroid plexus:	n/a
5	chr16:47882395-47882445	BJ	skin:	n/a
6	chr16:47882395-47882445	GM06990	blood:	n/a
7	chr16:47814576-47814626	HNPCEpiC	eye:	n/a
8	chr16:47882395-47882445	PrEC	prostate:	n/a
9	chr16:47814576-47814626	AG09319	gingival:	n/a
10	chr16:47766189-47766239	Jurkat	blood:	n/a
11	chr16:47766189-47766239	NB4	blood:	n/a
12	chr16:47882395-47882445	GM12891	blood:	n/a
13	chr16:47882395-47882445	HRE	kidney:	n/a
14	chr16:47766189-47766239	GM06990	blood:	n/a
15	chr16:47760096-47760146	CMK	blood:	n/a
16	chr16:47760096-47760146	AG09309	skin:	n/a
17	chr16:47814576-47814626	AG04450	lung:	fetal
18	chr16:47882395-47882445	Jurkat	blood:	n/a
19	chr16:47766189-47766239	AoSMC	blood vessel:	n/a
20	chr16:47814576-47814626	HCT-116	colon:	n/a
21	chr16:47766189-47766239	BE2_C	brain:	n/a
22	chr16:47760096-47760146	A549	lung:	n/a
23	chr16:47882395-47882445	GM12892	blood:	n/a
24	chr16:47760096-47760146	GM06990	blood:	n/a
25	chr16:47766189-47766239	HUVEC	blood vessel:	n/a
26	chr16:47814576-47814626	HMEC	breast:	n/a
27	chr16:47760096-47760146	ProgFib	skin:	n/a
28	chr16:47760096-47760146	HNPCEpiC	eye:	n/a
29	chr16:47760096-47760146	LNCaP	prostate:	n/a
30	chr16:47760096-47760146	SKMC	muscle:	n/a
31	chr16:47882395-47882445	H1-hESC	embryonic stem cell:	embryo
32	chr16:47882395-47882445	BE2_C	brain:	n/a
33	chr16:47814576-47814626	K562	blood:	n/a
34	chr16:47766189-47766239	SK-N-MC	brain:	n/a
35	chr16:47766189-47766239	NHBE	bronchial:	n/a
36	chr16:47760096-47760146	H1-hESC	embryonic stem cell:	embryo
37	chr16:47882395-47882445	A549	lung:	n/a
38	chr16:47760096-47760146	GM12891	blood:	n/a
39	chr16:47814576-47814626	IMR90	lung:	fetal
40	chr16:47766189-47766239	HCF	heart:	n/a
41	chr16:47882395-47882445	HCF	heart:	n/a
42	chr16:47882395-47882445	HMEC	breast:	n/a
43	chr16:47760096-47760146	MCF10A-Er-Src	breast:	n/a
44	chr16:47760096-47760146	HL-60	blood:	n/a
45	chr16:47814576-47814626	U87	brain:	n/a
46	chr16:47814576-47814626	Jurkat	blood:	n/a
47	chr16:47882395-47882445	HUVEC	blood vessel:	n/a
48	chr16:47766189-47766239	MCF10A-Er-Src	breast:	n/a
49	chr16:47766189-47766239	HepG2	liver:	n/a
50	chr16:47766189-47766239	GM19239	blood:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:47749783..47754089-chr16:47757775..47760980,3	K562	blood:
2	chr16:47898981..47901770-chr16:47903295..47905311,2	MCF-7	breast:
3	chr16:47898981..47901770-chr16:47903295..47905311,2	MCF-7	breast:
4	chr16:47743169..47744769-chr16:47758952..47760563,2	K562	blood:
5	chr16:47853395..47855870-chr16:47906219..47908579,2	MCF-7	breast:
6	chr16:47761277..47762823-chr16:47767710..47769287,2	K562	blood:
7	chr16:47748542..47750702-chr16:47752632..47756051,3	MCF-7	breast:
8	chr16:47850878..47851398-chr2:135208123..135208687,2	MCF-7	breast:
9	chr16:47705945..47707735-chr16:47749048..47750835,2	K562	blood:
10	chr16:47735369..47737433-chr16:47748955..47750476,2	K562	blood:
11	chr16:47902554..47904960-chr16:47904969..47907935,2	MCF-7	breast:
12	chr16:47878462..47880186-chr16:47883805..47885785,2	K562	blood:
13	chr16:47749922..47751934-chr16:47754227..47756860,2	K562	blood:
14	chr16:47853395..47855870-chr16:47906219..47908579,2	MCF-7	breast:
15	chr16:47902554..47904960-chr16:47904969..47907935,2	MCF-7	breast:
16	chr16:47878462..47880186-chr16:47883805..47885785,2	K562	blood:
17	chr16:47817919..47820643-chr16:47820665..47822436,2	K562	blood:
18	chr16:47817919..47820643-chr16:47820665..47822436,2	K562	blood:
19	chr16:47749922..47751934-chr16:47754227..47756860,2	K562	blood:
20	chr16:47819570..47821548-chr16:47825325..47827450,2	K562	blood:
21	chr16:47779892..47782625-chr16:47790853..47792797,2	K562	blood:
22	chr16:47761277..47762823-chr16:47767710..47769287,2	K562	blood:
23	chr16:47748542..47750702-chr16:47752632..47756051,3	MCF-7	breast:
24	chr16:47740356..47742078-chr16:47745865..47748205,2	K562	blood:
25	chr16:47779892..47782625-chr16:47790853..47792797,2	K562	blood:
26	chr16:47739084..47740587-chr16:47746132..47748221,2	MCF-7	breast:
27	chr16:47788304..47791051-chr16:47793224..47795920,2	K562	blood:
28	chr16:47748038..47749649-chr16:47753215..47755119,2	MCF-7	breast:
29	chr16:47819570..47821548-chr16:47825325..47827450,2	K562	blood:
30	chr16:47748038..47749649-chr16:47753215..47755119,2	MCF-7	breast:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PHKB-7	chr16:47880608-47881067	l_1318_chr16:47873310-47881874_testes
2	lnc-PHKB-7	chr16:47873311-47873777	l_1318_chr16:47873310-47881874_testes
3	lnc-PHKB-7	chr16:47881150-47881874	l_1318_chr16:47873310-47881874_testes
4	lnc-PHKB-6	chr16:47761228-47761433	l_1317_chr16:47755114-47761433_testes
5	lnc-PHKB-2	chr16:47758479-47758757	ENSG00000261231.2
6	lnc-PHKB-2	chr16:47848541-47848654	ENSG00000261231.2
7	lnc-PHKB-7	chr16:47878779-47878887	l_1318_chr16:47873310-47881874_testes
8	lnc-PHKB-2	chr16:47913110-47913346	ENSG00000261231.2
9	lnc-PHKB-2	chr16:47897357-47897510	ENSG00000261231.2
10	lnc-PHKB-6	chr16:47760335-47760434	l_1317_chr16:47755114-47761433_testes
11	lnc-PHKB-2	chr16:47897357-47897510	ENSG00000261231.2
12	lnc-PHKB-2	chr16:47892490-47893840	ENSG00000261231.2
13	lnc-PHKB-7	chr16:47880417-47880591	l_1318_chr16:47873310-47881874_testes
14	lnc-PHKB-6	chr16:47755115-47755212	l_1317_chr16:47755114-47761433_testes
15	lnc-ABCC12-1	chr16:47883225-47883859	XLOC_011928
16	lnc-PHKB-7	chr16:47876426-47877035	l_1318_chr16:47873310-47881874_testes

No data

Variant related genes	Relation type
ENSG00000261231	TF binding region
ENSG00000260497	TF binding region
ENSG00000261231	CpG island
ENSG00000260497	CpG island
ENSG00000261231	chromatin interactions
ENSG00000260497	chromatin interactions
KLF6	miRNA target sites

Extended variants
information (count: 4522 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:4522 , 50 per page) page: 1 2 3 4 5 6 7 ... 91

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs377335408	chr16:47748240-47748241	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs557544944	chr16:47748280-47748281	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs573925018	chr16:47748301-47748302	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs571554993	chr16:47748327-47748328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs542911314	chr16:47748339-47748340	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs553294750	chr16:47748381-47748382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs186335273	chr16:47748518-47748519	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs112149949	chr16:47748519-47748520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs199698811	chr16:47748533-47748534	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs540630670	chr16:47748552-47748553	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs563999421	chr16:47748576-47748577	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs577686466	chr16:47748601-47748602	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs543190291	chr16:47748602-47748603	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs563473932	chr16:47748603-47748604	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs529144787	chr16:47748629-47748630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs191585598	chr16:47748630-47748631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs548736857	chr16:47748640-47748641	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs559692738	chr16:47748718-47748719	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs367557127	chr16:47748778-47748779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs528446689	chr16:47748794-47748795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs9328600	chr16:47748806-47748807	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs116554690	chr16:47748835-47748836	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs553960620	chr16:47748888-47748889	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs537537063	chr16:47748921-47748922	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs180711914	chr16:47748927-47748928	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs567510617	chr16:47748950-47748951	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs536459023	chr16:47748963-47748964	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs144618133	chr16:47748966-47748967	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs138525186	chr16:47749044-47749045	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs371657781	chr16:47749053-47749054	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs185321327	chr16:47749090-47749091	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs116116622	chr16:47749152-47749153	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs577591994	chr16:47749164-47749165	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs543498146	chr16:47749190-47749191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs572183877	chr16:47749214-47749215	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs370730164	chr16:47749261-47749262	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs563412229	chr16:47749293-47749294	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs573837329	chr16:47749303-47749304	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs542845585	chr16:47749320-47749321	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs559656565	chr16:47749341-47749342	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs201348261	chr16:47749353-47749354	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs536321621	chr16:47749354-47749355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs190900103	chr16:47749365-47749366	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs139274658	chr16:47749400-47749401	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs565279407	chr16:47749459-47749460	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs202126644	chr16:47749513-47749514	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs375255565	chr16:47749518-47749519	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs530850396	chr16:47749572-47749573	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs551013855	chr16:47749671-47749672	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs183321517	chr16:47749808-47749809	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
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
Colorectal cancer	19359472	CNVD
Olfactory neuroblastoma	18408657	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17133270	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:725 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:47733800-47750200	Weak transcription	Brain Germinal Matrix	brain
2	chr16:47745600-47750800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr16:47746000-47748800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr16:47746200-47748400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr16:47746200-47748400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr16:47746200-47748400	Enhancers	HMEC	breast
7	chr16:47746400-47748400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr16:47746400-47748400	Enhancers	NHEK	skin
9	chr16:47746600-47748400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr16:47746800-47748200	Enhancers	HUVEC	blood vessel
11	chr16:47747000-47749800	Weak transcription	Placenta	Placenta
12	chr16:47747400-47755000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr16:47748000-47753800	Weak transcription	Stomach Mucosa	stomach
14	chr16:47748400-47749800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr16:47748400-47749800	Weak transcription	HMEC	breast
16	chr16:47748400-47750400	Weak transcription	NHEK	skin
17	chr16:47748400-47752200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr16:47748800-47749800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr16:47749400-47749800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr16:47749800-47750000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr16:47749800-47750000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr16:47749800-47750800	Enhancers	Placenta	Placenta
23	chr16:47749800-47751000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr16:47749800-47751200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr16:47749800-47751200	Enhancers	HMEC	breast
26	chr16:47750000-47750600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr16:47750400-47751200	Enhancers	NHEK	skin
28	chr16:47750600-47751200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr16:47750600-47751400	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr16:47750800-47751800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
31	chr16:47751000-47755000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr16:47751800-47752400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
33	chr16:47752200-47752400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr16:47753000-47753400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr16:47753000-47753800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr16:47753400-47760000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr16:47753800-47756400	Enhancers	Stomach Mucosa	stomach
38	chr16:47753800-47757800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr16:47755000-47755400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr16:47755400-47757000	Enhancers	Fetal Brain Male	brain
41	chr16:47755400-47765400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr16:47755800-47756200	Enhancers	Breast Myoepithelial Primary Cells	Breast
43	chr16:47755800-47756600	Enhancers	Fetal Brain Female	brain
44	chr16:47756400-47761800	Weak transcription	Stomach Mucosa	stomach
45	chr16:47757000-47757800	Weak transcription	Fetal Brain Male	brain
46	chr16:47757800-47758000	Enhancers	Fetal Brain Male	brain
47	chr16:47757800-47758600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr16:47757800-47758600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr16:47758000-47763600	Weak transcription	Fetal Brain Male	brain
50	chr16:47758800-47759600	Enhancers	Placenta	Placenta

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links