Variant report

Variant	nsv1056126
Chromosome Location	chr16:47658705-47738655
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:472)
CpG islands
(count:122)
Chromatin interactive
region (count:30)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:472 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:47703753-47704095	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:47658634-47659953	K562	blood:	n/a	n/a
3	ARID3A	chr16:47690725-47691453	HepG2	liver:	n/a	n/a
4	ARID3A	chr16:47667679-47668530	HepG2	liver:	n/a	n/a
5	ARID3A	chr16:47698347-47698941	HepG2	liver:	n/a	chr16:47698627-47698643
6	ATF1	chr16:47658917-47659475	K562	blood:	n/a	n/a
7	BHLHE40	chr16:47668708-47668902	K562	blood:	n/a	n/a
8	BHLHE40	chr16:47668062-47668411	HepG2	liver:	n/a	n/a
9	BHLHE40	chr16:47658711-47659466	K562	blood:	n/a	n/a
10	CBX3	chr16:47658890-47659582	K562	blood:	n/a	n/a
11	CCNT2	chr16:47658728-47659261	K562	blood:	n/a	n/a
12	CEBPB	chr16:47667650-47667860	K562	blood:	n/a	chr16:47667751-47667762 chr16:47667749-47667762 chr16:47667749-47667762
13	CEBPB	chr16:47678634-47678969	Hela-S3	cervix:	n/a	chr16:47678857-47678870
14	CEBPB	chr16:47667940-47668470	A549	lung:	n/a	n/a
15	CEBPB	chr16:47668025-47668345	HepG2	liver:	n/a	n/a
16	CEBPB	chr16:47690989-47691318	HepG2	liver:	n/a	n/a
17	CEBPB	chr16:47667652-47668462	HepG2	liver:	n/a	chr16:47667751-47667762 chr16:47667749-47667762 chr16:47667749-47667762
18	CEBPB	chr16:47667582-47668346	A549	lung:	n/a	chr16:47667751-47667762 chr16:47667749-47667762 chr16:47667749-47667762
19	CEBPB	chr16:47682841-47682939	K562	blood:	n/a	n/a
20	CEBPB	chr16:47667887-47668556	A549	lung:	n/a	n/a
21	CEBPB	chr16:47692576-47692824	A549	lung:	n/a	n/a
22	CEBPB	chr16:47692634-47692817	K562	blood:	n/a	n/a
23	CEBPD	chr16:47658822-47659377	K562	blood:	n/a	n/a
24	CEBPD	chr16:47658800-47659507	K562	blood:	n/a	n/a
25	CTCF	chr16:47694520-47694670	GM12878	blood:	n/a	n/a
26	CTCF	chr16:47694560-47694710	GM12872	blood:	n/a	n/a
27	CTCF	chr16:47728520-47728670	GM12869	blood:	n/a	chr16:47728576-47728589
28	CTCF	chr16:47728560-47728710	HCPEpiC	choroid plexus:	n/a	chr16:47728576-47728589
29	CTCF	chr16:47728700-47728850	HCT-116	colon:	n/a	n/a
30	CTCF	chr16:47694540-47694690	HPAF	blood vessel:	n/a	n/a
31	CTCF	chr16:47728614-47728666	GM13976	blood:	n/a	n/a
32	CTCF	chr16:47694580-47694730	HepG2	liver:	n/a	n/a
33	CTCF	chr16:47728520-47728670	GM12864	blood:	n/a	chr16:47728576-47728589
34	CTCF	chr16:47728589-47728627	GM10248	blood:	n/a	n/a
35	CTCF	chr16:47728572-47728719	A549	lung:	n/a	chr16:47728576-47728589
36	CTCF	chr16:47728580-47728730	WERI-Rb-1	eye:	n/a	n/a
37	CTCF	chr16:47728580-47728730	GM12866	blood:	n/a	n/a
38	CTCF	chr16:47728640-47728790	HBMEC	blood vessel:	n/a	n/a
39	CTCF	chr16:47728598-47728697	GM12891	blood:	n/a	n/a
40	CTCF	chr16:47731240-47731390	GM12869	blood:	n/a	n/a
41	CTCF	chr16:47728528-47728799	K562	blood:	n/a	chr16:47728576-47728589
42	CTCF	chr16:47728560-47728710	Caco-2	colon:	n/a	chr16:47728576-47728589
43	CTCF	chr16:47728592-47728717	GM12878	blood:	n/a	n/a
44	CTCF	chr16:47728560-47728710	GM12874	blood:	n/a	chr16:47728576-47728589
45	CTCF	chr16:47728453-47728794	HepG2	liver:	n/a	chr16:47728576-47728589
46	CTCF	chr16:47728610-47728680	GM13977	blood:	n/a	n/a
47	CTCF	chr16:47728640-47728790	HMEC	breast:	n/a	n/a
48	CTCF	chr16:47728720-47728870	HFF-Myc	foreskin:	n/a	n/a
49	CTCF	chr16:47728624-47728709	Fibrobl	skin:	n/a	n/a
50	CTCF	chr16:47660820-47660970	HPAF	blood vessel:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:47733368-47733418	GM12892	blood:	n/a
2	chr16:47677874-47677924	ECC-1	luminal epithelium:	n/a
3	chr16:47677874-47677924	BJ	skin:	n/a
4	chr16:47677874-47677924	GM12892	blood:	n/a
5	chr16:47677874-47677924	PFSK-1	brain:	n/a
6	chr16:47677874-47677924	NH-A	brain:	n/a
7	chr16:47677874-47677924	CMK	blood:	n/a
8	chr16:47733368-47733418	H1-hESC	embryonic stem cell:	embryo
9	chr16:47733368-47733418	HMEC	breast:	n/a
10	chr16:47677874-47677924	AG09319	gingival:	n/a
11	chr16:47733368-47733418	HL-60	blood:	n/a
12	chr16:47677874-47677924	HCPEpiC	choroid plexus:	n/a
13	chr16:47733368-47733418	AG04449	skin:	fetal
14	chr16:47733368-47733418	NB4	blood:	n/a
15	chr16:47733368-47733418	T-47D	breast:	n/a
16	chr16:47733368-47733418	HIPEpiC	eye:	n/a
17	chr16:47677874-47677924	T-47D	breast:	n/a
18	chr16:47677874-47677924	IMR90	lung:	fetal
19	chr16:47733368-47733418	HEK293	kidney:	embryo
20	chr16:47733368-47733418	HNPCEpiC	eye:	n/a
21	chr16:47733368-47733418	AG09309	skin:	n/a
22	chr16:47733368-47733418	HRE	kidney:	n/a
23	chr16:47677874-47677924	HRE	kidney:	n/a
24	chr16:47733368-47733418	AoSMC	blood vessel:	n/a
25	chr16:47733368-47733418	HCPEpiC	choroid plexus:	n/a
26	chr16:47677874-47677924	SK-N-MC	brain:	n/a
27	chr16:47733368-47733418	SAEC	small airway:	n/a
28	chr16:47677874-47677924	Hela-S3	cervix:	n/a
29	chr16:47733368-47733418	ovcar-3	ovarian:	n/a
30	chr16:47677874-47677924	HUVEC	blood vessel:	n/a
31	chr16:47677874-47677924	NHDF-neo	bronchial:	n/a
32	chr16:47677874-47677924	BE2_C	brain:	n/a
33	chr16:47677874-47677924	GM12878	blood:	n/a
34	chr16:47677874-47677924	Caco-2	colon:	n/a
35	chr16:47677874-47677924	HEEpiC	esophagus:	n/a
36	chr16:47677874-47677924	AoSMC	blood vessel:	n/a
37	chr16:47733368-47733418	GM12878	blood:	n/a
38	chr16:47677874-47677924	HEK293	kidney:	embryo
39	chr16:47677874-47677924	SK-N-SH_RA	brain:	n/a
40	chr16:47677874-47677924	AG10803	skin:	n/a
41	chr16:47677874-47677924	AG04449	skin:	fetal
42	chr16:47733368-47733418	GM12891	blood:	n/a
43	chr16:47733368-47733418	HRPEpiC	eye:	n/a
44	chr16:47733368-47733418	Hepatocyte	liver:	n/a
45	chr16:47733368-47733418	AG10803	skin:	n/a
46	chr16:47733368-47733418	ProgFib	skin:	n/a
47	chr16:47733368-47733418	NHDF-neo	bronchial:	n/a
48	chr16:47733368-47733418	HUVEC	blood vessel:	n/a
49	chr16:47733368-47733418	SK-N-MC	brain:	n/a
50	chr16:47733368-47733418	NT2-D1	testis:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr16:47691613..47697230-chr16:47697697..47701033,5	K562	blood:
2	chr16:47705945..47707735-chr16:47749048..47750835,2	K562	blood:
3	chr16:47689743..47692961-chr16:47700339..47703493,3	K562	blood:
4	chr16:47727162..47730087-chr16:47731751..47735128,4	K562	blood:
5	chr16:47671896..47674537-chr16:47675667..47678409,3	K562	blood:
6	chr16:47657682..47661918-chr16:47662510..47665105,4	K562	blood:
7	chr16:47680750..47683336-chr16:47685961..47688381,2	K562	blood:
8	chr16:47684293..47686207-chr16:47688405..47690926,2	K562	blood:
9	chr16:47727162..47730087-chr16:47731751..47735128,4	K562	blood:
10	chr16:47648657..47650524-chr16:47658477..47661384,2	K562	blood:
11	chr16:47735369..47737433-chr16:47748955..47750476,2	K562	blood:
12	chr16:47178385..47180317-chr16:47705518..47707688,2	K562	blood:
13	chr16:47652198..47653880-chr16:47657938..47660462,2	K562	blood:
14	chr16:47680750..47683336-chr16:47685961..47688381,2	K562	blood:
15	chr16:47493375..47499099-chr16:47656022..47661380,7	K562	blood:
16	chr16:47504741..47507121-chr16:47699160..47701122,2	K562	blood:
17	chr16:47671896..47674537-chr16:47675667..47678409,3	K562	blood:
18	chr16:47691613..47697230-chr16:47697697..47701033,5	K562	blood:
19	chr16:47652839..47655718-chr16:47656564..47660553,3	K562	blood:
20	chr16:47674595..47678731-chr16:47680937..47684112,3	K562	blood:
21	chr16:47689743..47692961-chr16:47700339..47703493,3	K562	blood:
22	chr16:47673393..47675073-chr16:47721240..47723950,2	K562	blood:
23	chr16:47001442..47003182-chr16:47662025..47664778,2	K562	blood:
24	chr16:47687860..47689573-chr16:47695289..47697558,2	K562	blood:
25	chr16:47687860..47689573-chr16:47695289..47697558,2	K562	blood:
26	chr16:47673393..47675073-chr16:47721240..47723950,2	K562	blood:
27	chr16:47657682..47661918-chr16:47662510..47665105,4	K562	blood:
28	chr16:47668276..47670957-chr16:47675128..47677879,2	K562	blood:
29	chr16:47674595..47678731-chr16:47680937..47684112,3	K562	blood:
30	chr16:47668276..47670957-chr16:47675128..47677879,2	K562	blood:

No data

Variant related genes	Relation type
PHKB	TF binding region
PHKB	CpG island
ENSG00000102893	chromatin interactions
ENSG00000129636	chromatin interactions

Extended variants
information (count: 2525 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:2525 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577457175	chr16:47658775-47658776	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs572483588	chr16:47658776-47658777	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs546520793	chr16:47658781-47658782	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs369626050	chr16:47658813-47658814	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs80030177	chr16:47658820-47658821	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs75047828	chr16:47658823-47658824	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs550225153	chr16:47658898-47658899	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs372911313	chr16:47658926-47658927	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs560669075	chr16:47658975-47658976	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs8049167	chr16:47659020-47659021	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs542693622	chr16:47659021-47659022	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs546382224	chr16:47659056-47659057	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs34923617	chr16:47659099-47659100	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs377510803	chr16:47659104-47659105	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs538536339	chr16:47659106-47659107	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs552479583	chr16:47659242-47659243	Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs571182840	chr16:47659320-47659321	Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs111865404	chr16:47659351-47659352	Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs75457345	chr16:47659360-47659361	Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs538264953	chr16:47659378-47659379	Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs555054677	chr16:47659386-47659387	Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs574995629	chr16:47659429-47659430	Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs534331000	chr16:47659650-47659651	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs77612530	chr16:47659688-47659689	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs529153648	chr16:47659706-47659707	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs554068989	chr16:47659726-47659727	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs544059722	chr16:47659732-47659733	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs373391681	chr16:47659752-47659753	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs377380585	chr16:47659766-47659767	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs371229555	chr16:47659821-47659822	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs139244326	chr16:47659835-47659836	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs562357382	chr16:47659852-47659853	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs563210342	chr16:47659901-47659902	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs532989713	chr16:47659961-47659962	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs11865330	chr16:47660021-47660022	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs11862281	chr16:47660034-47660035	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs376756730	chr16:47660058-47660059	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs371910583	chr16:47660061-47660062	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs529739785	chr16:47660110-47660111	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs35712081	chr16:47660121-47660122	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs376888527	chr16:47660142-47660143	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs546706341	chr16:47660235-47660236	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs560075463	chr16:47660243-47660244	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs73534789	chr16:47660249-47660250	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs552160912	chr16:47660251-47660252	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs569137715	chr16:47660326-47660327	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs538201572	chr16:47660386-47660387	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs548593062	chr16:47660422-47660423	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs189158476	chr16:47660455-47660456	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs74016211	chr16:47660481-47660482	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:63)

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
Prostate cancer	22341455	CNVD

Chromatin state (count:1963 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:47609600-47694400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
2	chr16:47625200-47668400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr16:47626200-47676600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
4	chr16:47626200-47677600	Weak transcription	Aorta	Aorta
5	chr16:47626400-47659800	Weak transcription	Fetal Lung	lung
6	chr16:47626400-47670400	Weak transcription	Fetal Intestine Small	intestine
7	chr16:47626600-47660800	Weak transcription	Stomach Mucosa	stomach
8	chr16:47626600-47670200	Weak transcription	Spleen	Spleen
9	chr16:47626600-47671000	Weak transcription	Esophagus	oesophagus
10	chr16:47626600-47724600	Weak transcription	Small Intestine	intestine
11	chr16:47627000-47685000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr16:47633000-47676200	Weak transcription	Rectal Smooth Muscle	rectum
13	chr16:47635000-47664800	Weak transcription	Pancreas	Pancrea
14	chr16:47635200-47684200	Weak transcription	Ovary	ovary
15	chr16:47635600-47670400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr16:47645000-47677800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr16:47645400-47670800	Weak transcription	Fetal Muscle Trunk	muscle
18	chr16:47645400-47676600	Weak transcription	Fetal Thymus	thymus
19	chr16:47645600-47667400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
20	chr16:47645600-47668400	Weak transcription	Rectal Mucosa Donor 31	rectum
21	chr16:47646000-47667800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr16:47646200-47677200	Weak transcription	HSMMtube	muscle
23	chr16:47646600-47671000	Weak transcription	Rectal Mucosa Donor 29	rectum
24	chr16:47646800-47667400	Weak transcription	Primary T helper cells PMA-I stimulated	--
25	chr16:47647000-47668200	Weak transcription	Primary T helper cells fromperipheralblood	blood
26	chr16:47647000-47669400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr16:47647200-47667200	Weak transcription	Primary T cells fromperipheralblood	blood
28	chr16:47647200-47667800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr16:47647200-47668400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
30	chr16:47647200-47668600	Weak transcription	Adipose Nuclei	Adipose
31	chr16:47647200-47675800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr16:47647400-47668400	Weak transcription	Duodenum Mucosa	Duodenum
33	chr16:47647400-47669000	Weak transcription	Dnd41	blood
34	chr16:47647400-47670800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr16:47647400-47676600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr16:47647600-47668600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
37	chr16:47647600-47670200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr16:47647600-47684200	Weak transcription	Fetal Muscle Leg	muscle
39	chr16:47647800-47668400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
40	chr16:47648200-47660000	Weak transcription	Fetal Stomach	stomach
41	chr16:47648200-47667400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
42	chr16:47648200-47668600	Weak transcription	Thymus	Thymus
43	chr16:47648400-47660800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr16:47648400-47668400	Weak transcription	Stomach Smooth Muscle	stomach
45	chr16:47649400-47660800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
46	chr16:47649400-47668400	Weak transcription	Gastric	stomach
47	chr16:47649600-47662200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
48	chr16:47649600-47667400	Weak transcription	Fetal Intestine Large	intestine
49	chr16:47649600-47667800	Weak transcription	Left Ventricle	heart
50	chr16:47649600-47668400	Weak transcription	Primary hematopoietic stem cells	blood

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