Variant report

Variant	esv3394919
Chromosome Location	chr3:195680455-195688753
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:676)
CpG islands
(count:488)
Chromatin interactive
region (count:11)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:676 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:195687778-195688031	K562	blood:	n/a	n/a
2	ATF1	chr3:195681353-195681596	K562	blood:	n/a	n/a
3	ATF2	chr3:195681259-195681587	GM12878	blood:	n/a	n/a
4	ATF3	chr3:195681303-195681452	K562	blood:	n/a	n/a
5	BATF	chr3:195682768-195683488	GM12878	blood:	n/a	n/a
6	BATF	chr3:195680472-195680694	GM12878	blood:	n/a	n/a
7	BATF	chr3:195682771-195683491	GM12878	blood:	n/a	n/a
8	BATF	chr3:195681129-195681669	GM12878	blood:	n/a	n/a
9	BATF	chr3:195688640-195688926	GM12878	blood:	n/a	n/a
10	BATF	chr3:195681681-195681957	GM12878	blood:	n/a	n/a
11	BCL11A	chr3:195681171-195681812	GM12878	blood:	n/a	chr3:195681302-195681315 chr3:195681417-195681426
12	BCL11A	chr3:195681118-195681900	GM12878	blood:	n/a	chr3:195681302-195681315 chr3:195681417-195681426
13	BCL11A	chr3:195680283-195680924	GM12878	blood:	n/a	chr3:195680659-195680668
14	BCL11A	chr3:195682872-195683277	GM12878	blood:	n/a	n/a
15	BCL11A	chr3:195681860-195682057	GM12878	blood:	n/a	n/a
16	BCL11A	chr3:195682895-195683356	GM12878	blood:	n/a	n/a
17	BCL11A	chr3:195680538-195680860	GM12878	blood:	n/a	chr3:195680659-195680668
18	BCL3	chr3:195681285-195681563	GM12878	blood:	n/a	chr3:195681302-195681315 chr3:195681417-195681426
19	BCLAF1	chr3:195681253-195681686	GM12878	blood:	n/a	chr3:195681302-195681315 chr3:195681417-195681426
20	BCLAF1	chr3:195681279-195681563	GM12878	blood:	n/a	chr3:195681302-195681315 chr3:195681417-195681426
21	BHLHE40	chr3:195681214-195681663	GM12878	blood:	n/a	chr3:195681296-195681312 chr3:195681304-195681320
22	BHLHE40	chr3:195681210-195681587	K562	blood:	n/a	chr3:195681296-195681312 chr3:195681304-195681320
23	BHLHE40	chr3:195681203-195681678	HepG2	liver:	n/a	chr3:195681296-195681312 chr3:195681304-195681320
24	BRCA1	chr3:195681377-195681604	Hela-S3	cervix:	n/a	n/a
25	CBX3	chr3:195680129-195680896	K562	blood:	n/a	n/a
26	CBX3	chr3:195687930-195689486	K562	blood:	n/a	n/a
27	CBX3	chr3:195681209-195681715	K562	blood:	n/a	n/a
28	CBX3	chr3:195681152-195682264	K562	blood:	n/a	n/a
29	CCNT2	chr3:195682412-195682541	K562	blood:	n/a	n/a
30	CCNT2	chr3:195681222-195681599	K562	blood:	n/a	n/a
31	CEBPB	chr3:195681244-195681840	GM12878	blood:	n/a	n/a
32	CEBPB	chr3:195681388-195681580	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr3:195681219-195681730	K562	blood:	n/a	n/a
34	CEBPB	chr3:195680276-195680721	K562	blood:	n/a	n/a
35	CEBPD	chr3:195681081-195681739	K562	blood:	n/a	n/a
36	CHD1	chr3:195681413-195681628	GM12878	blood:	n/a	n/a
37	CHD2	chr3:195681301-195681610	Hela-S3	cervix:	n/a	n/a
38	CHD2	chr3:195681358-195681608	GM12878	blood:	n/a	n/a
39	CREB1	chr3:195681284-195681534	GM12878	blood:	n/a	n/a
40	CREB1	chr3:195681296-195681494	K562	blood:	n/a	n/a
41	CREB1	chr3:195681315-195681561	H1-hESC	embryonic stem cell:	n/a	n/a
42	CREB1	chr3:195681279-195681557	K562	blood:	n/a	n/a
43	CREB1	chr3:195681268-195681489	A549	lung:	n/a	n/a
44	CREB1	chr3:195681295-195681566	GM12878	blood:	n/a	n/a
45	CREB1	chr3:195681297-195681526	HepG2	liver:	n/a	n/a
46	CREB1	chr3:195681317-195681541	HepG2	liver:	n/a	n/a
47	CREB1	chr3:195681328-195681466	A549	lung:	n/a	n/a
48	CREB1	chr3:195681318-195681559	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr3:195681417-195681479	Pancreas_OC	pancreas:	n/a	n/a
50	CTCF	chr3:195681406-195681496	GM12878	blood:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:195682365-195682415	PrEC	prostate:	n/a
2	chr3:195683635-195683685	SK-N-SH_RA	brain:	n/a
3	chr3:195681091-195681141	K562	blood:	n/a
4	chr3:195682595-195682645	HPAEpiC	pulmonary alveolar:	n/a
5	chr3:195681091-195681141	H1-hESC	embryonic stem cell:	embryo
6	chr3:195682595-195682645	HIPEpiC	eye:	n/a
7	chr3:195687741-195687791	U87	brain:	n/a
8	chr3:195683635-195683685	HUVEC	blood vessel:	n/a
9	chr3:195687741-195687791	ovcar-3	ovarian:	n/a
10	chr3:195688021-195688071	AG09309	skin:	n/a
11	chr3:195683635-195683685	NH-A	brain:	n/a
12	chr3:195681091-195681141	T-47D	breast:	n/a
13	chr3:195681400-195681450	AG09319	gingival:	n/a
14	chr3:195683635-195683685	Jurkat	blood:	n/a
15	chr3:195682595-195682645	AG10803	skin:	n/a
16	chr3:195681400-195681450	PrEC	prostate:	n/a
17	chr3:195682365-195682415	HCF	heart:	n/a
18	chr3:195682595-195682645	SK-N-SH	brain:	n/a
19	chr3:195681400-195681450	HNPCEpiC	eye:	n/a
20	chr3:195681400-195681450	H1-hESC	embryonic stem cell:	embryo
21	chr3:195681091-195681141	HNPCEpiC	eye:	n/a
22	chr3:195688021-195688071	HepG2	liver:	n/a
23	chr3:195688021-195688071	HCT-116	colon:	n/a
24	chr3:195682365-195682415	T-47D	breast:	n/a
25	chr3:195688021-195688071	BJ	skin:	n/a
26	chr3:195682326-195682376	SK-N-MC	brain:	n/a
27	chr3:195683635-195683685	HRPEpiC	eye:	n/a
28	chr3:195687741-195687791	HRE	kidney:	n/a
29	chr3:195681400-195681450	NHBE	bronchial:	n/a
30	chr3:195681091-195681141	PrEC	prostate:	n/a
31	chr3:195683635-195683685	PrEC	prostate:	n/a
32	chr3:195683635-195683685	NB4	blood:	n/a
33	chr3:195681400-195681450	NHDF-neo	bronchial:	n/a
34	chr3:195682595-195682645	HL-60	blood:	n/a
35	chr3:195682365-195682415	RPTEC	kidney:	n/a
36	chr3:195681091-195681141	Caco-2	colon:	n/a
37	chr3:195682365-195682415	HUVEC	blood vessel:	n/a
38	chr3:195682595-195682645	ECC-1	luminal epithelium:	n/a
39	chr3:195683635-195683685	ProgFib	skin:	n/a
40	chr3:195681400-195681450	HEK293	kidney:	embryo
41	chr3:195688021-195688071	H1-hESC	embryonic stem cell:	embryo
42	chr3:195681400-195681450	AG09309	skin:	n/a
43	chr3:195682595-195682645	BE2_C	brain:	n/a
44	chr3:195681400-195681450	BJ	skin:	n/a
45	chr3:195682365-195682415	HAEpiC	amniotic membrane:	n/a
46	chr3:195687741-195687791	IMR90	lung:	fetal
47	chr3:195682326-195682376	U87	brain:	n/a
48	chr3:195682365-195682415	NT2-D1	testis:	n/a
49	chr3:195687741-195687791	HCF	heart:	n/a
50	chr3:195682326-195682376	HCT-116	colon:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr3:195416074..195419636-chr3:195682871..195685500,3	K562	blood:
2	chr3:195679870..195682569-chr3:197379763..197382610,2	K562	blood:
3	chr3:195361738..195362245-chr3:195681393..195681916,2	HCT-116	colon:
4	chr3:195620748..195623057-chr3:195678515..195681386,2	K562	blood:
5	chr3:195361732..195362263-chr3:195681373..195681896,2	MCF-7	breast:
6	chr3:195620748..195623055-chr3:195679886..195681403,2	K562	blood:
7	chr3:195639677..195641924-chr3:195679365..195681428,2	MCF-7	breast:
8	chr3:195645901..195648267-chr3:195679890..195681479,3	MCF-7	breast:
9	chr3:195679874..195682569-chr3:197381110..197382679,2	K562	blood:
10	chr3:195636473..195638760-chr3:195679951..195681488,2	MCF-7	breast:
11	chr3:195419233..195421889-chr3:195682348..195684419,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TNK2-6	chr3:195688656-195689069	expReg_chr3_13675_-

No data

Variant related genes	Relation type
ENSG00000260261	TF binding region
ENSG00000260261	CpG island
ENSG00000266730	chromatin interactions
ENSG00000242086	chromatin interactions
ENSG00000061938	chromatin interactions
ENSG00000273009	chromatin interactions

Extended variants
information (count: 520 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:520 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs201324279	chr3:195680476-195680477	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs368815166	chr3:195680573-195680574	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs113451307	chr3:195680650-195680651	Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs2259641	chr3:195680864-195680865	Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs200622078	chr3:195680891-195680892	Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs2259679	chr3:195681085-195681086	Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs553098579	chr3:195681126-195681127	Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs376514731	chr3:195681213-195681214	Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs577694784	chr3:195681304-195681305	Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs545629243	chr3:195681341-195681342	Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs557496553	chr3:195681375-195681376	Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs2257543	chr3:195681385-195681386	Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs2257542	chr3:195681387-195681388	Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs2261195	chr3:195681394-195681395	Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs576310164	chr3:195681396-195681397	Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs2257541	chr3:195681397-195681398	Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs376366431	chr3:195681403-195681404	Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs375520639	chr3:195681404-195681405	Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs543307097	chr3:195681423-195681424	Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs149766478	chr3:195681432-195681433	Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs190677064	chr3:195681457-195681458	Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs561736529	chr3:195681481-195681482	Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs58263594	chr3:195681482-195681483	Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs2261192	chr3:195681490-195681491	Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
25	rs541002362	chr3:195681523-195681524	Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs200198464	chr3:195681527-195681528	Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs58923551	chr3:195681545-195681546	Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs373036306	chr3:195681549-195681550	Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs533023370	chr3:195681558-195681559	Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs3844935	chr3:195681636-195681637	Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs552023672	chr3:195681640-195681641	Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs570102655	chr3:195681680-195681681	Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs139415898	chr3:195681690-195681691	Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs549446854	chr3:195681701-195681702	Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs201973699	chr3:195681706-195681707	Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs567926075	chr3:195681714-195681715	Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs4927811	chr3:195681902-195681903	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs4927812	chr3:195681904-195681905	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs375444999	chr3:195681953-195681954	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs369167251	chr3:195682039-195682040	Weak transcription Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs200007926	chr3:195682077-195682078	Weak transcription Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs552939256	chr3:195682098-195682099	Weak transcription Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs201335223	chr3:195682102-195682103	Weak transcription Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs201963939	chr3:195682106-195682107	Weak transcription Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs557551051	chr3:195682108-195682109	Weak transcription Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs200191712	chr3:195682112-195682113	Weak transcription Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs12386334	chr3:195682116-195682117	Weak transcription Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs112788096	chr3:195682140-195682141	Weak transcription Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs113786804	chr3:195682145-195682146	Weak transcription Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs112616969	chr3:195682146-195682147	Weak transcription Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:81)

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

Chromatin state (count:633 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:195647200-195681200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr3:195648600-195680600	Weak transcription	Pancreas	Pancrea
3	chr3:195656600-195681000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr3:195657800-195681400	Weak transcription	GM12878-XiMat	blood
5	chr3:195659600-195681200	Weak transcription	Brain Hippocampus Middle	brain
6	chr3:195659600-195685600	Weak transcription	Small Intestine	intestine
7	chr3:195660000-195681200	Weak transcription	Colonic Mucosa	Colon
8	chr3:195660400-195680600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr3:195660600-195681200	Weak transcription	Rectal Mucosa Donor 29	rectum
10	chr3:195661200-195681000	Weak transcription	Ovary	ovary
11	chr3:195661800-195681200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr3:195663400-195681200	Weak transcription	Left Ventricle	heart
13	chr3:195663600-195681000	Weak transcription	Fetal Brain Female	brain
14	chr3:195663600-195681200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr3:195663600-195681200	Weak transcription	Skeletal Muscle Female	skeletal muscle
16	chr3:195663800-195682000	Weak transcription	Skeletal Muscle Male	skeletal muscle
17	chr3:195664400-195681200	Weak transcription	Osteobl	bone
18	chr3:195665000-195681200	Weak transcription	Placenta	Placenta
19	chr3:195665200-195691800	Weak transcription	HSMMtube	muscle
20	chr3:195665400-195681400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr3:195665400-195685200	Weak transcription	Aorta	Aorta
22	chr3:195667200-195681200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
23	chr3:195667400-195680800	Weak transcription	Right Ventricle	heart
24	chr3:195667400-195681200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr3:195667400-195681200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr3:195667400-195681200	Weak transcription	Brain Anterior Caudate	brain
27	chr3:195667400-195681200	Weak transcription	Brain Cingulate Gyrus	brain
28	chr3:195667400-195681200	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr3:195667400-195681200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
30	chr3:195667400-195681400	Weak transcription	Primary B cells from peripheral blood	blood
31	chr3:195667400-195681400	Weak transcription	Brain Substantia Nigra	brain
32	chr3:195667400-195684200	Weak transcription	Spleen	Spleen
33	chr3:195667400-195686200	Weak transcription	Rectal Mucosa Donor 31	rectum
34	chr3:195667600-195681200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
35	chr3:195667600-195681200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr3:195667600-195681200	Weak transcription	Esophagus	oesophagus
37	chr3:195667600-195681400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr3:195667600-195681600	Weak transcription	Fetal Intestine Large	intestine
39	chr3:195667800-195681200	Weak transcription	Sigmoid Colon	Sigmoid Colon
40	chr3:195668000-195681200	Weak transcription	Lung	lung
41	chr3:195668200-195682200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
42	chr3:195669000-195680800	Weak transcription	Thymus	Thymus
43	chr3:195670800-195680800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr3:195671400-195681000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr3:195671600-195681000	Weak transcription	Brain Germinal Matrix	brain
46	chr3:195671600-195681000	Weak transcription	Dnd41	blood
47	chr3:195671600-195681200	Weak transcription	Cortex derived primary cultured neurospheres	brain
48	chr3:195671800-195681200	Weak transcription	H1 Cell Line	embryonic stem cell
49	chr3:195671800-195681200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
50	chr3:195671800-195681200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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