Variant report

Variant	nsv593072
Chromosome Location	chr3:195946535-195950490
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:100)
CpG islands
(count:184)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:100 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr3:195946516-195946940	GM12878	blood:	n/a	n/a
2	BHLHE40	chr3:195946147-195946748	GM12878	blood:	n/a	n/a
3	CEBPB	chr3:195947840-195948176	ECC-1	luminal epithelium:	n/a	n/a
4	CEBPB	chr3:195946582-195946893	HepG2	liver:	n/a	n/a
5	CEBPB	chr3:195946212-195946790	IMR90	lung:	n/a	n/a
6	CHD1	chr3:195946518-195946606	GM12878	blood:	n/a	n/a
7	CHD2	chr3:195946790-195946792	HepG2	liver:	n/a	n/a
8	CHD2	chr3:195946307-195946566	GM12878	blood:	n/a	n/a
9	CTCF	chr3:195946480-195946630	GM12873	blood:	n/a	n/a
10	CTCF	chr3:195946420-195946570	HBMEC	blood vessel:	n/a	n/a
11	CTCF	chr3:195950280-195950430	MCF-7	breast:	n/a	n/a
12	CTCF	chr3:195946500-195946650	GM06990	blood:	n/a	n/a
13	CTCF	chr3:195946580-195946730	NB4	blood:	n/a	n/a
14	CTCF	chr3:195946460-195946610	HCPEpiC	choroid plexus:	n/a	n/a
15	CTCF	chr3:195946552-195946661	GM12892	blood:	n/a	n/a
16	CTCF	chr3:195946440-195946590	GM12865	blood:	n/a	n/a
17	CTCF	chr3:195946420-195946570	GM12873	blood:	n/a	n/a
18	CTCF	chr3:195946525-195946671	Gliobla	brain:	n/a	n/a
19	CTCF	chr3:195946400-195946550	SK-N-SH_RA	brain:	n/a	n/a
20	CTCF	chr3:195946540-195946690	GM12878	blood:	n/a	n/a
21	CTCF	chr3:195946420-195946570	BE2_C	brain:	n/a	n/a
22	CTCF	chr3:195946541-195946681	NHEK	skin:	n/a	n/a
23	CTCF	chr3:195946420-195946570	GM12874	blood:	n/a	n/a
24	CTCF	chr3:195946570-195946684	GM12878	blood:	n/a	n/a
25	CTCF	chr3:195946460-195946610	GM12872	blood:	n/a	n/a
26	CTCF	chr3:195946460-195946610	HMEC	breast:	n/a	n/a
27	CTCF	chr3:195946460-195946610	HFF-Myc	foreskin:	n/a	n/a
28	CTCF	chr3:195946440-195946590	AG10803	skin:	n/a	n/a
29	CTCF	chr3:195946601-195946649	GM12891	blood:	n/a	n/a
30	CTCF	chr3:195946420-195946570	HMF	breast:	n/a	n/a
31	CTCF	chr3:195946455-195946783	GM12878	blood:	n/a	n/a
32	CTCF	chr3:195946440-195946590	GM12873	blood:	n/a	n/a
33	CTCF	chr3:195946480-195946630	HCFaa	heart:	n/a	n/a
34	CTCF	chr3:195946520-195946670	HMEC	breast:	n/a	n/a
35	CTCF	chr3:195946587-195946689	GM19238	blood:	n/a	n/a
36	CTCF	chr3:195946400-195946550	HepG2	liver:	n/a	n/a
37	CUX1	chr3:195946281-195946638	GM12878	blood:	n/a	n/a
38	EBF1	chr3:195946044-195946806	GM12878	blood:	n/a	chr3:195946560-195946571
39	EBF1	chr3:195946201-195946754	GM12878	blood:	n/a	chr3:195946560-195946571
40	EBF1	chr3:195946152-195946826	GM12878	blood:	n/a	chr3:195946560-195946571
41	EGR1	chr3:195950169-195950411	K562	blood:	n/a	n/a
42	ELF1	chr3:195946285-195947144	GM12878	blood:	n/a	n/a
43	ELK1	chr3:195946227-195946841	GM12878	blood:	n/a	n/a
44	EP300	chr3:195946249-195946551	GM12878	blood:	n/a	n/a
45	EP300	chr3:195945960-195946942	SK-N-SH	brain:	n/a	n/a
46	FOS	chr3:195949849-195950067	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr3:195947632-195947643	MCF10A-Er-Src	breast:	n/a	n/a
48	FOXA1	chr3:195950082-195950467	T-47D	breast:	n/a	n/a
49	FOXA1	chr3:195946598-195946862	HepG2	liver:	n/a	n/a
50	FOXA1	chr3:195946551-195946813	HepG2	liver:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:195946851-195946901	AG09319	gingival:	n/a
2	chr3:195946851-195946901	AG09319	gingival:	n/a
3	chr3:195946921-195946971	NH-A	brain:	n/a
4	chr3:195947062-195947112	SAEC	small airway:	n/a
5	chr3:195947062-195947112	Caco-2	colon:	n/a
6	chr3:195947062-195947112	NHBE	bronchial:	n/a
7	chr3:195946921-195946971	GM12891	blood:	n/a
8	chr3:195946921-195946971	SK-N-SH	brain:	n/a
9	chr3:195946851-195946901	GM12891	blood:	n/a
10	chr3:195947062-195947112	Hela-S3	cervix:	n/a
11	chr3:195946921-195946971	T-47D	breast:	n/a
12	chr3:195946851-195946901	HAEpiC	amniotic membrane:	n/a
13	chr3:195946921-195946971	HepG2	liver:	n/a
14	chr3:195946851-195946901	T-47D	breast:	n/a
15	chr3:195946921-195946971	MCF-7	breast:	n/a
16	chr3:195946921-195946971	RPTEC	kidney:	n/a
17	chr3:195946921-195946971	AG04450	lung:	fetal
18	chr3:195946851-195946901	NT2-D1	testis:	n/a
19	chr3:195946921-195946971	MCF10A-Er-Src	breast:	n/a
20	chr3:195947062-195947112	HEK293	kidney:	embryo
21	chr3:195946851-195946901	PrEC	prostate:	n/a
22	chr3:195946921-195946971	BE2_C	brain:	n/a
23	chr3:195946851-195946901	HepG2	liver:	n/a
24	chr3:195947062-195947112	GM12878	blood:	n/a
25	chr3:195946851-195946901	K562	blood:	n/a
26	chr3:195946921-195946971	NHBE	bronchial:	n/a
27	chr3:195947062-195947112	CMK	blood:	n/a
28	chr3:195947062-195947112	HUVEC	blood vessel:	n/a
29	chr3:195947062-195947112	HIPEpiC	eye:	n/a
30	chr3:195946851-195946901	NH-A	brain:	n/a
31	chr3:195946851-195946901	Caco-2	colon:	n/a
32	chr3:195946921-195946971	GM12892	blood:	n/a
33	chr3:195947062-195947112	ECC-1	luminal epithelium:	n/a
34	chr3:195947062-195947112	GM12891	blood:	n/a
35	chr3:195947062-195947112	HRE	kidney:	n/a
36	chr3:195947062-195947112	SK-N-SH	brain:	n/a
37	chr3:195946851-195946901	HNPCEpiC	eye:	n/a
38	chr3:195947062-195947112	HCF	heart:	n/a
39	chr3:195946921-195946971	NT2-D1	testis:	n/a
40	chr3:195946851-195946901	MCF-7	breast:	n/a
41	chr3:195946921-195946971	HMEC	breast:	n/a
42	chr3:195946921-195946971	HEEpiC	esophagus:	n/a
43	chr3:195947062-195947112	HNPCEpiC	eye:	n/a
44	chr3:195947062-195947112	HRPEpiC	eye:	n/a
45	chr3:195947062-195947112	NB4	blood:	n/a
46	chr3:195946921-195946971	PANC-1	pancreas:	n/a
47	chr3:195947062-195947112	NHDF-neo	bronchial:	n/a
48	chr3:195947062-195947112	AG04450	lung:	fetal
49	chr3:195946921-195946971	HCT-116	colon:	n/a
50	chr3:195947062-195947112	HPAEpiC	pulmonary alveolar:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:195945138..195947988-chr3:195949670..195951213,2	MCF-7	breast:
2	chr3:195947010..195950626-chr3:195954155..195955751,3	K562	blood:
3	chr3:195943354..195945789-chr3:195947655..195950538,2	K562	blood:
4	chr3:195942995..195944795-chr3:195945273..195947923,2	MCF-7	breast:
5	chr3:195807479..195809245-chr3:195949684..195952002,2	MCF-7	breast:
6	chr3:195945138..195947988-chr3:195949670..195951213,2	MCF-7	breast:

No data

Variant related genes	Relation type
SLC51A	TF binding region
SLC51A	CpG island
ENSG00000163959	chromatin interactions
ENSG00000072274	chromatin interactions

Extended variants
information (count: 182 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:182 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11185518	chr3:195946535-195946536	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs116861666	chr3:195946571-195946572	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs560125071	chr3:195946576-195946577	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs116735912	chr3:195946618-195946619	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs555085631	chr3:195946621-195946622	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs564412317	chr3:195946631-195946632	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs368091634	chr3:195946698-195946699	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs34752214	chr3:195946707-195946708	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs531468772	chr3:195946729-195946730	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs199735066	chr3:195946753-195946754	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs186233989	chr3:195946759-195946760	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs371959864	chr3:195946771-195946772	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs376218632	chr3:195946778-195946779	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs190705620	chr3:195946827-195946828	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs535536498	chr3:195946843-195946844	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs566190462	chr3:195946855-195946856	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs574805912	chr3:195946869-195946870	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs558028383	chr3:195946885-195946886	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs537048041	chr3:195946922-195946923	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs570344834	chr3:195946946-195946947	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs150808995	chr3:195946947-195946948	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs537715389	chr3:195947009-195947010	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs9825083	chr3:195947029-195947030	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs546657301	chr3:195947031-195947032	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs1696075	chr3:195947035-195947036	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs74766584	chr3:195947049-195947050	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs34387857	chr3:195947062-195947063	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs541581700	chr3:195947063-195947064	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs59792018	chr3:195947079-195947080	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs180732234	chr3:195947110-195947111	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs545991823	chr3:195947126-195947127	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs564095994	chr3:195947134-195947135	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs185522009	chr3:195947135-195947136	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs543297203	chr3:195947149-195947150	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs561386215	chr3:195947181-195947182	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs143587618	chr3:195947196-195947197	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs546941879	chr3:195947222-195947223	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs112960794	chr3:195947248-195947249	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs532854519	chr3:195947286-195947287	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs551975436	chr3:195947339-195947340	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs535427810	chr3:195947371-195947372	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs550162167	chr3:195947383-195947384	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs557264238	chr3:195947393-195947394	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs537778868	chr3:195947401-195947402	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs556088276	chr3:195947415-195947416	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs567908664	chr3:195947417-195947418	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs9844310	chr3:195947462-195947463	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs146425508	chr3:195947463-195947464	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs374541764	chr3:195947508-195947509	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs545149510	chr3:195947516-195947517	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
Cancer	16751803	CNVD
abnormal development	18461090	CNVD
Autism	19653912	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Cervical cancer	21062161	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Austim spectrum disorder	21302340	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	16397240	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
speech impairment	20736978	CNVD
Intracranial aneurysm	16715129	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Mental retardation	17124404	CNVD
Congenital anomalies of the kidney and urinary tract	20299530	CNVD
Developmental delay	21147756	CNVD
Breast cancer	21509527	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Neurodevelopmental disorder	16760732	CNVD
Schizophrenia	22118685	CNVD
Schizophrenia	22958593	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20970697	CNVD
Mental retardation	19951919	CNVD
Autism	20970697	CNVD
Developmental delay	18471269	CNVD
Intellectual disability	22045946	CNVD
Breast cancer	21045282	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian cancer	20844748	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Uveal melanoma	20484589	CNVD
3q29 microdeletion syndrome	20500065	CNVD
Biliary cancer	20453639	CNVD
3q29 microdeletion syndrome	22283845	CNVD
3q29 microdeletion syndrome	21626679	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:235 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:195944000-195950000	Weak transcription	Gastric	stomach
2	chr3:195944200-195950000	Weak transcription	Pancreas	Pancrea
3	chr3:195944200-195964000	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr3:195944800-195947000	Enhancers	Fetal Intestine Large	intestine
5	chr3:195945000-195968400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr3:195945200-195947200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr3:195945200-195947200	Enhancers	Fetal Muscle Leg	muscle
8	chr3:195945400-195946800	Flanking Active TSS	Dnd41	blood
9	chr3:195945600-195948400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
10	chr3:195945800-195946800	Flanking Active TSS	Primary B cells from cord blood	blood
11	chr3:195945800-195946800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
12	chr3:195945800-195947200	Enhancers	Fetal Muscle Trunk	muscle
13	chr3:195945800-195948000	Weak transcription	Fetal Intestine Small	intestine
14	chr3:195945800-195948600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
15	chr3:195946000-195946600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr3:195946000-195946600	Flanking Active TSS	Primary B cells from peripheral blood	blood
17	chr3:195946000-195946600	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
18	chr3:195946000-195946600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr3:195946000-195946600	Active TSS	Pancreatic Islets	Pancreatic Islet
20	chr3:195946000-195946600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
21	chr3:195946000-195946600	Flanking Active TSS	NHEK	skin
22	chr3:195946000-195946800	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
23	chr3:195946000-195946800	Flanking Active TSS	Primary T cells fromperipheralblood	blood
24	chr3:195946000-195946800	Flanking Active TSS	Primary hematopoietic stem cells	blood
25	chr3:195946000-195946800	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
26	chr3:195946000-195946800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr3:195946000-195946800	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
28	chr3:195946000-195946800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr3:195946000-195946800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr3:195946000-195946800	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
31	chr3:195946000-195946800	Flanking Active TSS	Fetal Brain Female	brain
32	chr3:195946000-195946800	Flanking Active TSS	GM12878-XiMat	blood
33	chr3:195946000-195947000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr3:195946000-195947000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr3:195946200-195946600	Enhancers	H1 Cell Line	embryonic stem cell
36	chr3:195946200-195946600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr3:195946200-195946600	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr3:195946200-195946600	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr3:195946200-195946600	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr3:195946200-195946600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr3:195946200-195946600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr3:195946200-195946600	Flanking Active TSS	Liver	Liver
43	chr3:195946200-195946600	Flanking Active TSS	Brain Angular Gyrus	brain
44	chr3:195946200-195946600	Flanking Active TSS	Brain Anterior Caudate	brain
45	chr3:195946200-195946600	Flanking Active TSS	Brain Cingulate Gyrus	brain
46	chr3:195946200-195946600	Flanking Active TSS	Brain Germinal Matrix	brain
47	chr3:195946200-195946600	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
48	chr3:195946200-195946600	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
49	chr3:195946200-195946600	Flanking Active TSS	Brain Substantia Nigra	brain
50	chr3:195946200-195946600	Flanking Active TSS	Fetal Brain Male	brain

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