Variant report

Variant	nsv967094
Chromosome Location	chr3:178976467-178978666
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr3:178977798-178978001	K562	blood:	n/a	n/a
2	BACH1	chr3:178977747-178978398	K562	blood:	n/a	n/a
3	BACH1	chr3:178977174-178977262	K562	blood:	n/a	n/a
4	BHLHE40	chr3:178978584-178978761	GM12878	blood:	n/a	n/a
5	CBX3	chr3:178977713-178978308	K562	blood:	n/a	n/a
6	CCNT2	chr3:178978613-178979465	K562	blood:	n/a	chr3:178979263-178979272
7	CEBPB	chr3:178977748-178978451	K562	blood:	n/a	chr3:178978270-178978281
8	CEBPB	chr3:178978151-178978413	IMR90	lung:	n/a	chr3:178978270-178978281
9	CEBPB	chr3:178977750-178978649	K562	blood:	n/a	chr3:178978270-178978281
10	CEBPB	chr3:178978195-178978464	A549	lung:	n/a	chr3:178978270-178978281
11	CEBPB	chr3:178978117-178978469	HepG2	liver:	n/a	chr3:178978270-178978281
12	CHD2	chr3:178977582-178977934	K562	blood:	n/a	n/a
13	E2F6	chr3:178977678-178979605	K562	blood:	n/a	chr3:178979088-178979097 chr3:178979089-178979096 chr3:178979089-178979096 chr3:178979089-178979096
14	E2F6	chr3:178978580-178979371	K562	blood:	n/a	chr3:178979088-178979097 chr3:178979089-178979096 chr3:178979089-178979096 chr3:178979089-178979096
15	E2F6	chr3:178978388-178979369	H1-hESC	embryonic stem cell:	n/a	chr3:178979088-178979097 chr3:178979089-178979096 chr3:178979089-178979096 chr3:178979089-178979096
16	E2F6	chr3:178977853-178978074	K562	blood:	n/a	n/a
17	ELF1	chr3:178977571-178977954	K562	blood:	n/a	chr3:178977787-178977800
18	ELF1	chr3:178978651-178979430	K562	blood:	n/a	chr3:178979336-178979345 chr3:178979261-178979273 chr3:178979004-178979017 chr3:178979196-178979205
19	EP300	chr3:178977773-178978098	K562	blood:	n/a	n/a
20	GTF2F1	chr3:178977119-178977129	H1-hESC	embryonic stem cell:	n/a	n/a
21	HA-E2F1	chr3:178978522-178979654	MCF-7	breast:	n/a	chr3:178979088-178979097 chr3:178979089-178979096 chr3:178979089-178979096 chr3:178979089-178979096
22	HCFC1	chr3:178977712-178977940	K562	blood:	n/a	n/a
23	HCFC1	chr3:178978484-178979457	K562	blood:	n/a	n/a
24	HEY1	chr3:178977793-178978395	K562	blood:	n/a	n/a
25	IRF1	chr3:178978390-178978684	K562	blood:	n/a	n/a
26	IRF1	chr3:178976899-178977207	K562	blood:	n/a	n/a
27	IRF1	chr3:178976915-178977118	K562	blood:	n/a	n/a
28	JUN	chr3:178976743-178978188	K562	blood:	n/a	n/a
29	JUN	chr3:178977791-178977942	K562	blood:	n/a	n/a
30	JUND	chr3:178977740-178978122	K562	blood:	n/a	chr3:178977939-178977950
31	JUND	chr3:178978622-178979591	K562	blood:	n/a	chr3:178979356-178979365
32	JUND	chr3:178977793-178977958	HepG2	liver:	n/a	chr3:178977939-178977950
33	KAP1	chr3:178978348-178978497	K562	blood:	n/a	n/a
34	MAX	chr3:178977727-178978129	K562	blood:	n/a	n/a
35	MAX	chr3:178978656-178979495	A549	lung:	n/a	chr3:178979295-178979305
36	MAX	chr3:178977829-178978055	K562	blood:	n/a	n/a
37	MAX	chr3:178978371-178979455	K562	blood:	n/a	chr3:178979295-178979305
38	MAX	chr3:178978625-178979566	HepG2	liver:	n/a	chr3:178979295-178979305
39	MAX	chr3:178978552-178979560	A549	lung:	n/a	chr3:178979295-178979305
40	MAX	chr3:178978587-178979507	MCF-7	breast:	n/a	chr3:178979295-178979305
41	MAX	chr3:178976675-178976913	K562	blood:	n/a	n/a
42	MAX	chr3:178978651-178979547	ECC-1	luminal epithelium:	n/a	chr3:178979295-178979305
43	MAX	chr3:178978642-178979499	K562	blood:	n/a	chr3:178979295-178979305
44	MAX	chr3:178977736-178978103	K562	blood:	n/a	n/a
45	MAZ	chr3:178978660-178979677	IMR90	lung:	n/a	chr3:178979295-178979305
46	MAZ	chr3:178976740-178976774	K562	blood:	n/a	n/a
47	MAZ	chr3:178978470-178979536	K562	blood:	n/a	chr3:178979295-178979305
48	MYC	chr3:178977749-178978098	K562	blood:	n/a	n/a
49	MYC	chr3:178978627-178979671	K562	blood:	n/a	chr3:178979295-178979305
50	MYC	chr3:178978605-178979527	K562	blood:	n/a	chr3:178979295-178979305

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:178977073-178977123	HRCEpiC	kidney:	n/a
2	chr3:178976891-178976941	HUVEC	blood vessel:	n/a
3	chr3:178977073-178977123	AG04450	lung:	fetal
4	chr3:178977073-178977123	AG09309	skin:	n/a
5	chr3:178977073-178977123	SK-N-SH_RA	brain:	n/a
6	chr3:178976891-178976941	U87	brain:	n/a
7	chr3:178977073-178977123	HAEpiC	amniotic membrane:	n/a
8	chr3:178976891-178976941	IMR90	lung:	fetal
9	chr3:178976891-178976941	PFSK-1	brain:	n/a
10	chr3:178976891-178976941	AG09309	skin:	n/a
11	chr3:178976891-178976941	H1-hESC	embryonic stem cell:	embryo
12	chr3:178977073-178977123	GM06990	blood:	n/a
13	chr3:178976891-178976941	T-47D	breast:	n/a
14	chr3:178977073-178977123	MCF-7	breast:	n/a
15	chr3:178977073-178977123	ProgFib	skin:	n/a
16	chr3:178976891-178976941	GM19239	blood:	n/a
17	chr3:178976891-178976941	HCPEpiC	choroid plexus:	n/a
18	chr3:178977073-178977123	AG04449	skin:	fetal
19	chr3:178977073-178977123	HCF	heart:	n/a
20	chr3:178976891-178976941	HPAEpiC	pulmonary alveolar:	n/a
21	chr3:178976891-178976941	AG10803	skin:	n/a
22	chr3:178976891-178976941	PANC-1	pancreas:	n/a
23	chr3:178977073-178977123	NHBE	bronchial:	n/a
24	chr3:178977073-178977123	MCF10A-Er-Src	breast:	n/a
25	chr3:178976891-178976941	HRE	kidney:	n/a
26	chr3:178977073-178977123	BE2_C	brain:	n/a
27	chr3:178976891-178976941	Jurkat	blood:	n/a
28	chr3:178976891-178976941	ProgFib	skin:	n/a
29	chr3:178976891-178976941	AoSMC	blood vessel:	n/a
30	chr3:178976891-178976941	K562	blood:	n/a
31	chr3:178977073-178977123	HNPCEpiC	eye:	n/a
32	chr3:178977073-178977123	NH-A	brain:	n/a
33	chr3:178977073-178977123	K562	blood:	n/a
34	chr3:178977073-178977123	HRE	kidney:	n/a
35	chr3:178976891-178976941	MCF-7	breast:	n/a
36	chr3:178976891-178976941	HIPEpiC	eye:	n/a
37	chr3:178977073-178977123	HL-60	blood:	n/a
38	chr3:178977073-178977123	PrEC	prostate:	n/a
39	chr3:178977073-178977123	NHDF-neo	bronchial:	n/a
40	chr3:178976891-178976941	BE2_C	brain:	n/a
41	chr3:178976891-178976941	SK-N-MC	brain:	n/a
42	chr3:178976891-178976941	HCT-116	colon:	n/a
43	chr3:178976891-178976941	RPTEC	kidney:	n/a
44	chr3:178976891-178976941	AG09319	gingival:	n/a
45	chr3:178976891-178976941	HNPCEpiC	eye:	n/a
46	chr3:178976891-178976941	GM06990	blood:	n/a
47	chr3:178976891-178976941	A549	lung:	n/a
48	chr3:178976891-178976941	HRCEpiC	kidney:	n/a
49	chr3:178976891-178976941	MCF10A-Er-Src	breast:	n/a
50	chr3:178976891-178976941	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:178863877..178866682-chr3:178977686..178979355,3	K562	blood:
2	chr3:178866930..178870480-chr3:178976906..178979282,3	K562	blood:
3	chr3:178977469..178980839-chr3:179038593..179042214,6	K562	blood:
4	chr3:178863877..178868371-chr3:178977065..178980370,6	K562	blood:
5	chr3:178977854..178979821-chr3:179040251..179043018,2	MCF-7	breast:
6	chr3:178971723..178977145-chr3:178977567..178980865,6	K562	blood:
7	chr3:178977431..178979193-chr3:179039095..179041437,2	MCF-7	breast:
8	chr3:178976479..178980556-chr3:178981755..178985679,10	K562	blood:
9	chr3:178865885..178868102-chr3:178977747..178979601,3	MCF-7	breast:
10	chr3:178978041..178980864-chr3:179039699..179042008,3	K562	blood:
11	chr3:178787758..178789707-chr3:178977770..178980269,2	MCF-7	breast:
12	chr3:178978446..178980464-chr3:179279567..179281993,2	K562	blood:
13	chr3:178976102..178980828-chr3:178981002..178985885,12	K562	blood:
14	chr3:178971723..178977145-chr3:178977567..178980865,6	K562	blood:

Variant related genes	Relation type
KCNMB3	TF binding region
KCNMB3	CpG island
ENSG00000121879	chromatin interactions
ENSG00000171121	chromatin interactions
ENSG00000229102	chromatin interactions
ENSG00000121864	chromatin interactions
ENSG00000240429	chromatin interactions
ENSG00000172667	chromatin interactions
ENSG00000136518	chromatin interactions

Extended variants
information (count: 105 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:105 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs557106962	chr3:178976480-178976481	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs186739496	chr3:178976543-178976544	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs542860596	chr3:178976569-178976570	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs56400023	chr3:178976591-178976592	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs528042365	chr3:178976593-178976594	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs529608361	chr3:178976596-178976597	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs150177625	chr3:178976624-178976625	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs564573834	chr3:178976640-178976641	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs115030937	chr3:178976680-178976681	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs371649923	chr3:178976688-178976689	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs7648422	chr3:178976699-178976700	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs368926867	chr3:178976700-178976701	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs200169756	chr3:178976709-178976710	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs529476096	chr3:178976727-178976728	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs375763806	chr3:178976776-178976777	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs11720871	chr3:178976777-178976778	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs566399598	chr3:178976787-178976788	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs535370021	chr3:178976788-178976789	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs558166165	chr3:178976794-178976795	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs369815460	chr3:178976795-178976796	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs11720935	chr3:178976821-178976822	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs537547233	chr3:178976901-178976902	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs371502425	chr3:178976903-178976904	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs192545252	chr3:178976983-178976984	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs571797994	chr3:178977032-178977033	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs542428624	chr3:178977053-178977054	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs552818338	chr3:178977071-178977072	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs10936996	chr3:178977074-178977075	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs12485606	chr3:178977090-178977091	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs544943213	chr3:178977109-178977110	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs2160756	chr3:178977111-178977112	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs530426893	chr3:178977145-178977146	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs372916841	chr3:178977154-178977155	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs544255358	chr3:178977159-178977160	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs149305279	chr3:178977162-178977163	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs567646802	chr3:178977178-178977179	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs529464986	chr3:178977203-178977204	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs549578596	chr3:178977216-178977217	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs552145604	chr3:178977228-178977229	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs566309451	chr3:178977299-178977300	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs528783804	chr3:178977367-178977368	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs552146320	chr3:178977370-178977371	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs562667004	chr3:178977373-178977374	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs74550828	chr3:178977388-178977389	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs535386580	chr3:178977391-178977392	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs537060218	chr3:178977393-178977394	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs557392938	chr3:178977398-178977399	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs112025995	chr3:178977426-178977427	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs536374974	chr3:178977452-178977453	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs201038141	chr3:178977469-178977470	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:75)

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	22032731	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
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	16608533	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-small cell lung cancer	19010865	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
epilepsy	18472482	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Myxofibrosarcoma	16751306	CNVD
Parkinson disease	21907011	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21364760	CNVD
Anaplastic thyroid cancer	17989125	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Ovarian cancer	18208621	CNVD
Thyroid cancer	17317825	CNVD
Thyroid cancer	17989125	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Breast cancer	21806811	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	16751803	CNVD
abnormal development	18461090	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	19653912	CNVD
Endometrial cancer	19261849	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Prostate cancer	18632612	CNVD
Autism	20685689	CNVD

Chromatin state (count:167 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:178912400-178978600	Weak transcription	Right Ventricle	heart
2	chr3:178945800-178978400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr3:178948800-178978600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr3:178949000-178978200	Weak transcription	NHLF	lung
5	chr3:178949000-178978600	Weak transcription	Brain Cingulate Gyrus	brain
6	chr3:178949000-178978600	Weak transcription	Ovary	ovary
7	chr3:178949000-178978800	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr3:178949200-178978400	Weak transcription	Brain Anterior Caudate	brain
9	chr3:178949200-178978600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr3:178949200-178978600	Weak transcription	Osteobl	bone
11	chr3:178952000-178978400	Weak transcription	Skeletal Muscle Female	skeletal muscle
12	chr3:178952400-178978600	Weak transcription	Primary neutrophils fromperipheralblood	blood
13	chr3:178952600-178976600	Weak transcription	Colon Smooth Muscle	Colon
14	chr3:178956200-178977000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr3:178959800-178978800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr3:178963200-178978200	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr3:178963200-178978600	Weak transcription	Left Ventricle	heart
18	chr3:178963200-178978800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr3:178963800-178978800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr3:178966200-178978600	Weak transcription	HUVEC	blood vessel
21	chr3:178968800-178978400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr3:178968800-178978600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr3:178969200-178978400	Weak transcription	Primary B cells from cord blood	blood
24	chr3:178969400-178976600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr3:178969400-178978200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr3:178969600-178978600	Weak transcription	Skeletal Muscle Male	skeletal muscle
27	chr3:178972000-178978800	Weak transcription	Small Intestine	intestine
28	chr3:178974000-178976800	Active TSS	K562	blood
29	chr3:178974400-178977600	Active TSS	GM12878-XiMat	blood
30	chr3:178975000-178976800	Weak transcription	Spleen	Spleen
31	chr3:178975000-178978400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr3:178975800-178976800	Weak transcription	Pancreas	Pancrea
33	chr3:178975800-178978800	Weak transcription	Gastric	stomach
34	chr3:178976200-178977800	Enhancers	HepG2	liver
35	chr3:178976600-178976800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr3:178976600-178977200	Enhancers	Colon Smooth Muscle	Colon
37	chr3:178976800-178977000	Enhancers	Fetal Thymus	thymus
38	chr3:178976800-178977000	Enhancers	Pancreas	Pancrea
39	chr3:178976800-178977400	Flanking Active TSS	K562	blood
40	chr3:178976800-178978400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr3:178976800-178978400	Weak transcription	Stomach Smooth Muscle	stomach
42	chr3:178977000-178977600	Weak transcription	Fetal Thymus	thymus
43	chr3:178977000-178977800	Weak transcription	Pancreas	Pancrea
44	chr3:178977200-178978200	Weak transcription	Colon Smooth Muscle	Colon
45	chr3:178977400-178977600	Enhancers	K562	blood
46	chr3:178977400-178978600	Weak transcription	Brain Angular Gyrus	brain
47	chr3:178977400-178978800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
48	chr3:178977600-178977800	Enhancers	Fetal Thymus	thymus
49	chr3:178977600-178978800	Flanking Active TSS	K562	blood
50	chr3:178977600-178979000	Flanking Active TSS	GM12878-XiMat	blood

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