Variant report

Variant	nsv592852
Chromosome Location	chr3:191073228-191093310
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:238)
CpG islands
(count:122)
Chromatin interactive
region (count:19)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:238 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:191084522-191084823	K562	blood:	n/a	n/a
2	ATF2	chr3:191073077-191073657	GM12878	blood:	n/a	n/a
3	ATF2	chr3:191073184-191073591	GM12878	blood:	n/a	n/a
4	BACH1	chr3:191084611-191084798	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr3:191077719-191077728	K562	blood:	n/a	n/a
6	BATF	chr3:191073229-191073582	GM12878	blood:	n/a	n/a
7	BATF	chr3:191073214-191073692	GM12878	blood:	n/a	n/a
8	BCL11A	chr3:191073268-191073474	GM12878	blood:	n/a	n/a
9	BHLHE40	chr3:191077897-191077906	GM12878	blood:	n/a	n/a
10	BHLHE40	chr3:191078418-191078441	GM12878	blood:	n/a	n/a
11	CBX3	chr3:191074379-191075227	HCT-116	colon:	n/a	n/a
12	CEBPB	chr3:191081900-191082043	H1-hESC	embryonic stem cell:	n/a	chr3:191081913-191081924
13	CEBPB	chr3:191075765-191076112	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr3:191078435-191078827	ECC-1	luminal epithelium:	n/a	chr3:191078657-191078668
15	CEBPB	chr3:191087382-191087710	H1-hESC	embryonic stem cell:	n/a	chr3:191087666-191087678
16	CEBPB	chr3:191091115-191091465	IMR90	lung:	n/a	n/a
17	CEBPB	chr3:191078366-191079000	HCT-116	colon:	n/a	chr3:191078657-191078668
18	CEBPB	chr3:191074423-191075056	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr3:191078410-191078922	HCT-116	colon:	n/a	chr3:191078657-191078668
20	CEBPB	chr3:191086006-191086268	A549	lung:	n/a	n/a
21	CEBPB	chr3:191087379-191087710	K562	blood:	n/a	chr3:191087666-191087678
22	CEBPB	chr3:191078519-191078784	HepG2	liver:	n/a	chr3:191078657-191078668
23	CEBPB	chr3:191086030-191086258	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr3:191085954-191086285	IMR90	lung:	n/a	n/a
25	CEBPB	chr3:191081892-191081981	HepG2	liver:	n/a	chr3:191081913-191081924
26	CEBPB	chr3:191078463-191078784	MCF-7	breast:	n/a	chr3:191078657-191078668
27	CEBPB	chr3:191078400-191078886	ECC-1	luminal epithelium:	n/a	chr3:191078657-191078668
28	CHD2	chr3:191074858-191075140	Hela-S3	cervix:	n/a	n/a
29	CTCF	chr3:191087500-191087650	HPF	lung:	n/a	n/a
30	E2F4	chr3:191074719-191075036	MCF10A-Er-Src	breast:	n/a	n/a
31	EBF1	chr3:191077503-191077610	GM12878	blood:	n/a	n/a
32	EBF1	chr3:191073206-191074715	GM12878	blood:	n/a	chr3:191074290-191074299 chr3:191074290-191074299 chr3:191074288-191074301
33	EBF1	chr3:191076788-191077221	GM12878	blood:	n/a	n/a
34	ELK4	chr3:191074340-191074578	Hela-S3	cervix:	n/a	n/a
35	EP300	chr3:191073219-191073768	GM12878	blood:	n/a	n/a
36	EP300	chr3:191087183-191087965	SK-N-SH	brain:	n/a	n/a
37	EP300	chr3:191074122-191074965	ECC-1	luminal epithelium:	n/a	chr3:191074757-191074764
38	EP300	chr3:191084525-191084840	K562	blood:	n/a	n/a
39	EP300	chr3:191073204-191073728	GM12878	blood:	n/a	n/a
40	EP300	chr3:191087418-191087757	SK-N-SH_RA	brain:	n/a	n/a
41	EP300	chr3:191087395-191087681	SK-N-SH_RA	brain:	n/a	n/a
42	EP300	chr3:191078336-191078936	ECC-1	luminal epithelium:	n/a	chr3:191078839-191078853 chr3:191078348-191078362
43	ESR1	chr3:191074391-191074665	ECC-1	luminal epithelium:	n/a	n/a
44	FOS	chr3:191076741-191077072	MCF10A-Er-Src	breast:	n/a	chr3:191076923-191076932 chr3:191076921-191076928 chr3:191076922-191076933
45	FOS	chr3:191084439-191084904	HUVEC	blood vessel:	n/a	chr3:191084667-191084677
46	FOS	chr3:191078567-191078726	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr3:191081085-191081506	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr3:191074461-191075193	HUVEC	blood vessel:	n/a	n/a
49	FOS	chr3:191073694-191073996	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr3:191074363-191075181	MCF10A-Er-Src	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:191086850-191086900	GM12878	blood:	n/a
2	chr3:191075822-191075872	HEK293	kidney:	embryo
3	chr3:191086850-191086900	SK-N-SH_RA	brain:	n/a
4	chr3:191086850-191086900	AG04450	lung:	fetal
5	chr3:191075822-191075872	GM12892	blood:	n/a
6	chr3:191075822-191075872	NHBE	bronchial:	n/a
7	chr3:191086850-191086900	BE2_C	brain:	n/a
8	chr3:191086850-191086900	HCPEpiC	choroid plexus:	n/a
9	chr3:191075822-191075872	AG10803	skin:	n/a
10	chr3:191086850-191086900	Hepatocyte	liver:	n/a
11	chr3:191075822-191075872	MCF10A-Er-Src	breast:	n/a
12	chr3:191086850-191086900	LNCaP	prostate:	n/a
13	chr3:191086850-191086900	NB4	blood:	n/a
14	chr3:191075822-191075872	GM12878	blood:	n/a
15	chr3:191075822-191075872	HRPEpiC	eye:	n/a
16	chr3:191075822-191075872	AG04449	skin:	fetal
17	chr3:191086850-191086900	PrEC	prostate:	n/a
18	chr3:191075822-191075872	HepG2	liver:	n/a
19	chr3:191086850-191086900	PANC-1	pancreas:	n/a
20	chr3:191086850-191086900	HL-60	blood:	n/a
21	chr3:191075822-191075872	HRE	kidney:	n/a
22	chr3:191086850-191086900	HRPEpiC	eye:	n/a
23	chr3:191086850-191086900	CMK	blood:	n/a
24	chr3:191075822-191075872	ProgFib	skin:	n/a
25	chr3:191086850-191086900	U87	brain:	n/a
26	chr3:191086850-191086900	HMEC	breast:	n/a
27	chr3:191086850-191086900	NT2-D1	testis:	n/a
28	chr3:191075822-191075872	K562	blood:	n/a
29	chr3:191075822-191075872	GM12891	blood:	n/a
30	chr3:191075822-191075872	PFSK-1	brain:	n/a
31	chr3:191086850-191086900	HAEpiC	amniotic membrane:	n/a
32	chr3:191086850-191086900	HUVEC	blood vessel:	n/a
33	chr3:191075822-191075872	NT2-D1	testis:	n/a
34	chr3:191086850-191086900	AG04449	skin:	fetal
35	chr3:191086850-191086900	MCF-7	breast:	n/a
36	chr3:191075822-191075872	AG09319	gingival:	n/a
37	chr3:191086850-191086900	HepG2	liver:	n/a
38	chr3:191075822-191075872	A549	lung:	n/a
39	chr3:191086850-191086900	HRCEpiC	kidney:	n/a
40	chr3:191075822-191075872	HEEpiC	esophagus:	n/a
41	chr3:191075822-191075872	HAEpiC	amniotic membrane:	n/a
42	chr3:191086850-191086900	HCF	heart:	n/a
43	chr3:191075822-191075872	HUVEC	blood vessel:	n/a
44	chr3:191086850-191086900	K562	blood:	n/a
45	chr3:191086850-191086900	NH-A	brain:	n/a
46	chr3:191075822-191075872	HIPEpiC	eye:	n/a
47	chr3:191086850-191086900	HNPCEpiC	eye:	n/a
48	chr3:191075822-191075872	Jurkat	blood:	n/a
49	chr3:191086850-191086900	HPAEpiC	pulmonary alveolar:	n/a
50	chr3:191075822-191075872	HRCEpiC	kidney:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:191079003..191081290-chr3:191082916..191084769,2	K562	blood:
2	chr3:191080948..191083585-chr3:191091535..191093381,2	K562	blood:
3	chr3:191079200..191081290-chr3:191083269..191086255,2	K562	blood:
4	chr3:191084566..191087269-chr3:191092450..191094970,3	MCF-7	breast:
5	chr3:191049478..191053328-chr3:191074760..191077632,3	K562	blood:
6	chr3:191079200..191081290-chr3:191083269..191086255,2	K562	blood:
7	chr3:191084566..191087269-chr3:191092450..191094970,3	MCF-7	breast:
8	chr3:191080948..191083585-chr3:191091535..191093381,2	K562	blood:
9	chr3:191049298..191052407-chr3:191074621..191077632,4	K562	blood:
10	chr3:191071589..191073614-chr3:191084774..191087547,2	K562	blood:
11	chr3:191089153..191091755-chr3:191092405..191093970,2	K562	blood:
12	chr3:191059352..191062066-chr3:191073918..191075676,3	K562	blood:
13	chr3:191089153..191091755-chr3:191092405..191093970,2	K562	blood:
14	chr3:191072104..191073931-chr3:191077551..191079300,2	K562	blood:
15	chr3:191059352..191066044-chr3:191070268..191075568,9	K562	blood:
16	chr3:191045177..191046733-chr3:191083021..191085089,2	K562	blood:
17	chr3:191071589..191073614-chr3:191084774..191087547,2	K562	blood:
18	chr3:191060607..191064094-chr3:191071227..191073545,3	K562	blood:
19	chr3:191079003..191081290-chr3:191082916..191084769,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PYDC2-7	chr3:191089936-191090896	NONHSAT093966

No data

Variant related genes	Relation type
CCDC50	TF binding region
CCDC50	CpG island
ENSG00000152492	chromatin interactions

Extended variants
information (count: 835 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:835 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs523270	chr3:191073228-191073229	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs558525209	chr3:191073333-191073334	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs184812349	chr3:191073343-191073344	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs533982166	chr3:191073354-191073355	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs369724323	chr3:191073459-191073460	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs115160635	chr3:191073463-191073464	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs573826513	chr3:191073478-191073479	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs559989338	chr3:191073490-191073491	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs386669594	chr3:191073493-191073494	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs115364607	chr3:191073495-191073496	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs1850961	chr3:191073498-191073499	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs565481030	chr3:191073629-191073630	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs372054910	chr3:191073631-191073632	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs527982893	chr3:191073635-191073636	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs540697661	chr3:191073655-191073656	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs192671	chr3:191073706-191073707	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs187722196	chr3:191073707-191073708	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs549873876	chr3:191073709-191073710	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs550594118	chr3:191073796-191073797	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs569868925	chr3:191073824-191073825	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs140974398	chr3:191073871-191073872	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs567599170	chr3:191073878-191073879	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs9985271	chr3:191073897-191073898	Enhancers Weak transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs373748452	chr3:191073913-191073914	Enhancers Weak transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs552710127	chr3:191073925-191073926	Enhancers Weak transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs75755521	chr3:191073968-191073969	Enhancers Weak transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs534899229	chr3:191073973-191073974	Enhancers Weak transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs538318439	chr3:191073980-191073981	Enhancers Weak transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs553763447	chr3:191074015-191074016	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs372357389	chr3:191074026-191074027	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs560506983	chr3:191074056-191074057	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs558258809	chr3:191074084-191074085	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs375268201	chr3:191074125-191074126	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs536346677	chr3:191074170-191074171	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs293815	chr3:191074201-191074202	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs293816	chr3:191074245-191074246	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs115958511	chr3:191074271-191074272	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs559085924	chr3:191074297-191074298	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs572683802	chr3:191074300-191074301	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs372723882	chr3:191074371-191074372	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs114389764	chr3:191074427-191074428	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs556147152	chr3:191074504-191074505	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs560889433	chr3:191074505-191074506	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs529668335	chr3:191074521-191074522	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs149775832	chr3:191074533-191074534	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs293817	chr3:191074538-191074539	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs543349517	chr3:191074562-191074563	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs78393737	chr3:191074569-191074570	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs552118114	chr3:191074587-191074588	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs146773939	chr3:191074628-191074629	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	16608533	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
Parkinson disease	21907011	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	16751803	CNVD
abnormal development	18461090	CNVD
Autism	19653912	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cervical cancer	21062161	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Austim spectrum disorder	21302340	CNVD
Lung cancer	19547694	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Cancer	20164919	CNVD
Myelofibrosis	22110671	CNVD
Optic atrophy	21457585	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-small cell lung cancer	21829676	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Esophageal cancer	20955586	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:891 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:191050200-191074800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr3:191060600-191074800	Weak transcription	Primary B cells from cord blood	blood
3	chr3:191062000-191075600	Weak transcription	K562	blood
4	chr3:191062200-191075400	Weak transcription	Fetal Brain Female	brain
5	chr3:191063000-191076600	Weak transcription	Brain Substantia Nigra	brain
6	chr3:191068600-191073800	Weak transcription	NHLF	lung
7	chr3:191068600-191074600	Weak transcription	Fetal Stomach	stomach
8	chr3:191068600-191075000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr3:191068600-191075000	Weak transcription	Aorta	Aorta
10	chr3:191068600-191076600	Weak transcription	Fetal Kidney	kidney
11	chr3:191068800-191073400	Weak transcription	Osteobl	bone
12	chr3:191068800-191073600	Weak transcription	HSMM	muscle
13	chr3:191068800-191075400	Enhancers	Colon Smooth Muscle	Colon
14	chr3:191068800-191078800	Weak transcription	Fetal Brain Male	brain
15	chr3:191069400-191074200	Enhancers	HUVEC	blood vessel
16	chr3:191069400-191075000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr3:191069600-191073400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr3:191069800-191096000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
19	chr3:191070800-191073800	Enhancers	Primary B cells from peripheral blood	blood
20	chr3:191071000-191074800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr3:191071000-191076000	Weak transcription	Primary T cells from cord blood	blood
22	chr3:191071000-191088400	Weak transcription	Brain Inferior Temporal Lobe	brain
23	chr3:191071200-191073800	Weak transcription	Muscle Satellite Cultured Cells	--
24	chr3:191071200-191074000	Weak transcription	Fetal Muscle Leg	muscle
25	chr3:191071200-191076800	Weak transcription	H9 Cell Line	embryonic stem cell
26	chr3:191071200-191078800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr3:191071200-191078800	Weak transcription	Lung	lung
28	chr3:191071200-191114000	Weak transcription	Colonic Mucosa	Colon
29	chr3:191071400-191073400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr3:191071400-191073600	Weak transcription	HUES6 Cell Line	embryonic stem cell
31	chr3:191071400-191073600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr3:191071400-191073600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr3:191071400-191073600	Enhancers	Fetal Heart	heart
34	chr3:191071400-191073800	Weak transcription	Duodenum Smooth Muscle	Duodenum
35	chr3:191071400-191074000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
36	chr3:191071400-191074200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
37	chr3:191071400-191074200	Weak transcription	Cortex derived primary cultured neurospheres	brain
38	chr3:191071400-191074200	Weak transcription	Right Atrium	heart
39	chr3:191071400-191074400	Weak transcription	Stomach Mucosa	stomach
40	chr3:191071400-191074800	Weak transcription	Duodenum Mucosa	Duodenum
41	chr3:191071400-191075000	Weak transcription	Fetal Lung	lung
42	chr3:191071400-191075800	Weak transcription	Rectal Mucosa Donor 29	rectum
43	chr3:191071400-191078400	Weak transcription	Fetal Intestine Small	intestine
44	chr3:191071400-191078800	Weak transcription	Gastric	stomach
45	chr3:191071400-191078800	Weak transcription	Pancreas	Pancrea
46	chr3:191071400-191078800	Weak transcription	Spleen	Spleen
47	chr3:191071400-191094200	Weak transcription	Small Intestine	intestine
48	chr3:191071400-191097400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr3:191071400-191100000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr3:191071600-191074400	Weak transcription	A549	lung

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