Variant report

Variant	nsv997975
Chromosome Location	chr3:177664921-177719623
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	ATF2	chr3:177719561-177720036	GM12878	blood:	n/a	n/a
2	BCL11A	chr3:177719612-177719946	GM12878	blood:	n/a	n/a
3	BHLHE40	chr3:177684381-177684528	HepG2	liver:	n/a	n/a
4	CEBPB	chr3:177664416-177665132	IMR90	lung:	n/a	chr3:177664995-177665006 chr3:177664579-177664588 chr3:177664579-177664588 chr3:177664993-177665006 chr3:177664945-177664956 chr3:177664944-177664955 chr3:177664551-177664563 chr3:177664995-177665006 chr3:177664993-177665004
5	CEBPB	chr3:177695627-177695962	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr3:177695571-177696022	IMR90	lung:	n/a	n/a
7	CEBPB	chr3:177710879-177711150	K562	blood:	n/a	chr3:177710999-177711010 chr3:177710998-177711009
8	CEBPB	chr3:177664797-177665136	A549	lung:	n/a	chr3:177664995-177665006 chr3:177664993-177665006 chr3:177664945-177664956 chr3:177664944-177664955 chr3:177664995-177665006 chr3:177664993-177665004
9	CEBPB	chr3:177665648-177665684	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr3:177695460-177696133	A549	lung:	n/a	n/a
11	CEBPB	chr3:177695640-177695965	A549	lung:	n/a	n/a
12	CEBPB	chr3:177710821-177711139	K562	blood:	n/a	chr3:177710999-177711010 chr3:177710998-177711009
13	CEBPB	chr3:177664762-177665224	MCF-7	breast:	n/a	chr3:177664995-177665006 chr3:177664993-177665006 chr3:177664945-177664956 chr3:177664944-177664955 chr3:177664995-177665006 chr3:177664993-177665004
14	CEBPB	chr3:177711874-177711898	K562	blood:	n/a	n/a
15	CEBPB	chr3:177664724-177665185	A549	lung:	n/a	chr3:177664995-177665006 chr3:177664993-177665006 chr3:177664945-177664956 chr3:177664944-177664955 chr3:177664995-177665006 chr3:177664993-177665004
16	CEBPB	chr3:177710838-177711139	HepG2	liver:	n/a	chr3:177710999-177711010 chr3:177710998-177711009
17	CEBPB	chr3:177687543-177687646	IMR90	lung:	n/a	n/a
18	CEBPB	chr3:177711800-177711977	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr3:177664830-177665120	HepG2	liver:	n/a	chr3:177664995-177665006 chr3:177664993-177665006 chr3:177664945-177664956 chr3:177664944-177664955 chr3:177664995-177665006 chr3:177664993-177665004
20	CEBPB	chr3:177709192-177709234	HepG2	liver:	n/a	chr3:177709202-177709215
21	CEBPB	chr3:177695645-177695997	A549	lung:	n/a	n/a
22	CEBPB	chr3:177664375-177665182	Hela-S3	cervix:	n/a	chr3:177664995-177665006 chr3:177664579-177664588 chr3:177664579-177664588 chr3:177664993-177665006 chr3:177664945-177664956 chr3:177664944-177664955 chr3:177664551-177664563 chr3:177664995-177665006 chr3:177664993-177665004
23	CEBPB	chr3:177695470-177695978	HCT-116	colon:	n/a	n/a
24	CHD2	chr3:177717923-177717952	K562	blood:	n/a	n/a
25	CTCF	chr3:177683100-177683250	HCT-116	colon:	n/a	n/a
26	CTCF	chr3:177683020-177683170	MCF-7	breast:	n/a	n/a
27	CTCF	chr3:177683110-177683160	K562	blood:	n/a	n/a
28	CTCF	chr3:177683020-177683170	HVMF	connective:	n/a	n/a
29	CTCF	chr3:177682720-177682870	HUVEC	blood vessel:	n/a	n/a
30	CTCF	chr3:177683020-177683170	HPAF	blood vessel:	n/a	n/a
31	CTCF	chr3:177683020-177683170	AoAF	blood vessel:	n/a	n/a
32	CTCF	chr3:177683000-177683150	HMEC	breast:	n/a	n/a
33	CTCF	chr3:177718261-177718276	LNCaP	prostate:	n/a	n/a
34	CTCF	chr3:177683080-177683230	HMF	breast:	n/a	n/a
35	CTCF	chr3:177699060-177699210	BE2_C	brain:	n/a	n/a
36	CTCF	chr3:177683080-177683230	HEK293	kidney:	n/a	n/a
37	CTCF	chr3:177709309-177709314	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr3:177682940-177683090	HPAF	blood vessel:	n/a	n/a
39	CTCF	chr3:177683040-177683190	GM12873	blood:	n/a	n/a
40	CTCF	chr3:177710400-177710550	HCPEpiC	choroid plexus:	n/a	n/a
41	CTCF	chr3:177683080-177683230	GM12873	blood:	n/a	n/a
42	CTCF	chr3:177709140-177709290	A549	lung:	n/a	n/a
43	CTCF	chr3:177683080-177683230	GM12875	blood:	n/a	n/a
44	CTCF	chr3:177702478-177702505	MCF-7	breast:	n/a	n/a
45	CTCF	chr3:177683000-177683150	HCFaa	heart:	n/a	n/a
46	CTCF	chr3:177683080-177683230	NHEK	skin:	n/a	n/a
47	CTCF	chr3:177683080-177683230	BE2_C	brain:	n/a	n/a
48	CTCF	chr3:177683080-177683230	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr3:177683000-177683150	GM12874	blood:	n/a	n/a
50	CTCF	chr3:177677020-177677170	BE2_C	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:177696327-177696377	GM06990	blood:	n/a
2	chr3:177700638-177700688	Hepatocyte	liver:	n/a
3	chr3:177700638-177700688	HUVEC	blood vessel:	n/a
4	chr3:177700638-177700688	PFSK-1	brain:	n/a
5	chr3:177696327-177696377	GM19239	blood:	n/a
6	chr3:177696327-177696377	NT2-D1	testis:	n/a
7	chr3:177700638-177700688	NT2-D1	testis:	n/a
8	chr3:177696327-177696377	A549	lung:	n/a
9	chr3:177700638-177700688	GM12891	blood:	n/a
10	chr3:177700638-177700688	HL-60	blood:	n/a
11	chr3:177700638-177700688	HRE	kidney:	n/a
12	chr3:177700638-177700688	MCF-7	breast:	n/a
13	chr3:177696327-177696377	PrEC	prostate:	n/a
14	chr3:177700638-177700688	HCT-116	colon:	n/a
15	chr3:177696327-177696377	HCT-116	colon:	n/a
16	chr3:177700638-177700688	IMR90	lung:	fetal
17	chr3:177696327-177696377	AG10803	skin:	n/a
18	chr3:177700638-177700688	A549	lung:	n/a
19	chr3:177700638-177700688	HCF	heart:	n/a
20	chr3:177700638-177700688	NHDF-neo	bronchial:	n/a
21	chr3:177700638-177700688	NB4	blood:	n/a
22	chr3:177700638-177700688	HEEpiC	esophagus:	n/a
23	chr3:177696327-177696377	MCF-7	breast:	n/a
24	chr3:177696327-177696377	NHBE	bronchial:	n/a
25	chr3:177700638-177700688	RPTEC	kidney:	n/a
26	chr3:177696327-177696377	HRE	kidney:	n/a
27	chr3:177700638-177700688	HRPEpiC	eye:	n/a
28	chr3:177696327-177696377	HRPEpiC	eye:	n/a
29	chr3:177700638-177700688	PrEC	prostate:	n/a
30	chr3:177696327-177696377	HL-60	blood:	n/a
31	chr3:177696327-177696377	BE2_C	brain:	n/a
32	chr3:177696327-177696377	NH-A	brain:	n/a
33	chr3:177700638-177700688	T-47D	breast:	n/a
34	chr3:177696327-177696377	GM12878	blood:	n/a
35	chr3:177696327-177696377	ECC-1	luminal epithelium:	n/a
36	chr3:177696327-177696377	SK-N-SH_RA	brain:	n/a
37	chr3:177696327-177696377	U87	brain:	n/a
38	chr3:177696327-177696377	K562	blood:	n/a
39	chr3:177696327-177696377	AG04449	skin:	fetal
40	chr3:177700638-177700688	GM12892	blood:	n/a
41	chr3:177700638-177700688	SK-N-SH_RA	brain:	n/a
42	chr3:177700638-177700688	Jurkat	blood:	n/a
43	chr3:177700638-177700688	Hela-S3	cervix:	n/a
44	chr3:177696327-177696377	HEK293	kidney:	embryo
45	chr3:177700638-177700688	H1-hESC	embryonic stem cell:	embryo
46	chr3:177696327-177696377	HIPEpiC	eye:	n/a
47	chr3:177696327-177696377	AG04450	lung:	fetal
48	chr3:177700638-177700688	AoSMC	blood vessel:	n/a
49	chr3:177700638-177700688	SK-N-MC	brain:	n/a
50	chr3:177700638-177700688	Caco-2	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:177532426..177535224-chr3:177663514..177665237,2	MCF-7	breast:
2	chr3:177684306..177686654-chr3:177686995..177689814,2	MCF-7	breast:
3	chr3:177709402..177711641-chr3:177711937..177714399,2	K562	blood:
4	chr3:177709402..177711641-chr3:177711937..177714399,2	K562	blood:
5	chr3:177684306..177686654-chr3:177686995..177689814,2	MCF-7	breast:
6	chr3:177076309..177079025-chr3:177709045..177711034,2	K562	blood:

Variant related genes	Relation type
ENSG00000270321	TF binding region
ENSG00000270321	CpG island
ENSG00000231574	chromatin interactions

Extended variants
information (count: 1294 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:1294 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16828811	chr3:177664921-177664922	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs535435450	chr3:177664922-177664923	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs371267226	chr3:177664966-177664967	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs543311733	chr3:177664968-177664969	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs35491071	chr3:177664987-177664988	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs76974489	chr3:177665063-177665064	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs558028352	chr3:177665079-177665080	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs556880479	chr3:177665089-177665090	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs578209106	chr3:177665095-177665096	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs367550942	chr3:177665182-177665183	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs727335	chr3:177665203-177665204	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs542486822	chr3:177665216-177665217	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs559514049	chr3:177665246-177665247	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs563951858	chr3:177665260-177665261	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs572808853	chr3:177665270-177665271	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs141307247	chr3:177665290-177665291	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs150186403	chr3:177665308-177665309	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs113666405	chr3:177665328-177665329	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs148893036	chr3:177665347-177665348	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs528125072	chr3:177665382-177665383	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs551559881	chr3:177665411-177665412	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs186327262	chr3:177665431-177665432	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs530562350	chr3:177665451-177665452	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs558371184	chr3:177665467-177665468	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs530853779	chr3:177665496-177665497	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs550489296	chr3:177665505-177665506	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs567207896	chr3:177665607-177665608	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs535496458	chr3:177665636-177665637	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs375526284	chr3:177665668-177665669	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs548919775	chr3:177665727-177665728	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs566174667	chr3:177665745-177665746	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs141661176	chr3:177665816-177665817	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs534776253	chr3:177665845-177665846	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs558354100	chr3:177665868-177665869	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs143599452	chr3:177665884-177665885	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs537638696	chr3:177665893-177665894	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs557730279	chr3:177665932-177665933	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs369611156	chr3:177666053-177666054	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs542645300	chr3:177666054-177666055	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs559348715	chr3:177666080-177666081	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs572909038	chr3:177666143-177666144	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs201872779	chr3:177666161-177666162	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs544747467	chr3:177666203-177666204	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs113086848	chr3:177666206-177666207	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs555052525	chr3:177666209-177666210	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs371876790	chr3:177666212-177666213	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs143609896	chr3:177666234-177666235	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs550351927	chr3:177666245-177666246	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs147196183	chr3:177666248-177666249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs138706328	chr3:177666272-177666273	Weak transcription Enhancers	n/a	n/a	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
Cancer	20164920	CNVD
Endometrial cancer	19261849	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21611746	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	20164919	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:276 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:177661200-177665800	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr3:177662600-177666400	Weak transcription	Fetal Thymus	thymus
3	chr3:177663200-177665400	Enhancers	Fetal Lung	lung
4	chr3:177663200-177666800	Weak transcription	Primary B cells from cord blood	blood
5	chr3:177663600-177665600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr3:177663800-177665400	Enhancers	Muscle Satellite Cultured Cells	--
7	chr3:177663800-177666000	Enhancers	Adipose Nuclei	Adipose
8	chr3:177663800-177666000	Enhancers	Osteobl	bone
9	chr3:177663800-177666800	Weak transcription	Thymus	Thymus
10	chr3:177664000-177665400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr3:177664000-177666200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
12	chr3:177664000-177666400	Weak transcription	Dnd41	blood
13	chr3:177664200-177666000	Enhancers	Hela-S3	cervix
14	chr3:177664400-177665200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr3:177664600-177665000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr3:177664800-177665200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr3:177664800-177665200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
18	chr3:177665000-177665400	Enhancers	Liver	Liver
19	chr3:177665000-177665600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr3:177665200-177666000	Enhancers	Monocytes-CD14+_RO01746	blood
21	chr3:177665400-177666600	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr3:177665600-177666200	Weak transcription	HSMM	muscle
23	chr3:177665800-177666200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr3:177666200-177667200	Enhancers	HSMM	muscle
25	chr3:177666400-177666600	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr3:177666400-177666800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr3:177666400-177667400	Enhancers	Fetal Muscle Leg	muscle
28	chr3:177666400-177667400	Enhancers	HSMMtube	muscle
29	chr3:177666400-177667600	Enhancers	Fetal Thymus	thymus
30	chr3:177666400-177668000	Enhancers	Dnd41	blood
31	chr3:177666600-177666800	Enhancers	Muscle Satellite Cultured Cells	--
32	chr3:177666600-177668400	Enhancers	Primary B cells from peripheral blood	blood
33	chr3:177666800-177667600	Enhancers	Thymus	Thymus
34	chr3:177666800-177668000	Enhancers	Primary B cells from cord blood	blood
35	chr3:177675000-177675800	Enhancers	Pancreatic Islets	Pancreatic Islet
36	chr3:177677000-177677400	Active TSS	Colon Smooth Muscle	Colon
37	chr3:177677000-177678000	Enhancers	Stomach Smooth Muscle	stomach
38	chr3:177677200-177677800	Enhancers	Primary B cells from cord blood	blood
39	chr3:177677400-177678400	Enhancers	Colon Smooth Muscle	Colon
40	chr3:177677600-177678800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr3:177677600-177678800	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr3:177677800-177678000	Enhancers	Fetal Lung	lung
43	chr3:177677800-177678200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr3:177677800-177678200	Enhancers	NH-A	brain
45	chr3:177677800-177678600	Enhancers	Muscle Satellite Cultured Cells	--
46	chr3:177677800-177678600	Enhancers	Duodenum Smooth Muscle	Duodenum
47	chr3:177677800-177678800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr3:177677800-177678800	Enhancers	Adipose Nuclei	Adipose
49	chr3:177677800-177678800	Enhancers	Fetal Stomach	stomach
50	chr3:177677800-177678800	Enhancers	HSMM	muscle

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