Variant report

Variant	nsv946443
Chromosome Location	chr1:158905154-158911493
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	FOS	chr1:158907779-158908113	MCF10A-Er-Src	breast:	n/a	chr1:158907885-158907894 chr1:158907995-158908007 chr1:158907997-158908005 chr1:158907993-158908004
2	FOS	chr1:158907748-158908108	MCF10A-Er-Src	breast:	n/a	chr1:158907885-158907894 chr1:158907995-158908007 chr1:158907997-158908005 chr1:158907993-158908004
3	FOS	chr1:158907814-158908129	MCF10A-Er-Src	breast:	n/a	chr1:158907885-158907894 chr1:158907995-158908007 chr1:158907997-158908005 chr1:158907993-158908004
4	MAFF	chr1:158908556-158908721	K562	blood:	n/a	chr1:158908634-158908652
5	MAFF	chr1:158908514-158908737	HepG2	liver:	n/a	chr1:158908634-158908652
6	MAFK	chr1:158908468-158908794	HepG2	liver:	n/a	chr1:158908635-158908650 chr1:158908635-158908651 chr1:158908638-158908652 chr1:158908640-158908651 chr1:158908639-158908650
7	MAFK	chr1:158908590-158908821	IMR90	lung:	n/a	chr1:158908635-158908650 chr1:158908635-158908651 chr1:158908638-158908652 chr1:158908640-158908651 chr1:158908639-158908650
8	MAFK	chr1:158908118-158908258	HepG2	liver:	n/a	n/a
9	MAFK	chr1:158908591-158908754	Hela-S3	cervix:	n/a	chr1:158908635-158908650 chr1:158908635-158908651 chr1:158908638-158908652 chr1:158908640-158908651 chr1:158908639-158908650
10	MAFK	chr1:158908535-158908792	HepG2	liver:	n/a	chr1:158908635-158908650 chr1:158908635-158908651 chr1:158908638-158908652 chr1:158908640-158908651 chr1:158908639-158908650
11	MAX	chr1:158907797-158908067	NB4	blood:	n/a	chr1:158907922-158907932
12	MYC	chr1:158907799-158908091	NB4	blood:	n/a	chr1:158907922-158907932
13	MYC	chr1:158907855-158908067	MCF10A-Er-Src	breast:	n/a	chr1:158907922-158907932
14	MYC	chr1:158907810-158908099	MCF10A-Er-Src	breast:	n/a	chr1:158907922-158907932
15	STAT3	chr1:158907771-158908074	MCF10A-Er-Src	breast:	n/a	n/a
16	STAT3	chr1:158907859-158908044	MCF10A-Er-Src	breast:	n/a	n/a
17	STAT3	chr1:158907798-158908051	MCF10A-Er-Src	breast:	n/a	n/a
18	TAL1	chr1:158909068-158909368	K562	blood:	n/a	n/a
19	TEAD4	chr1:158909027-158909391	K562	blood:	n/a	n/a
20	TEAD4	chr1:158909018-158909393	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:158905479-158905529	T-47D	breast:	n/a
2	chr1:158905479-158905529	GM12878	blood:	n/a
3	chr1:158905479-158905529	CMK	blood:	n/a
4	chr1:158905479-158905529	H1-hESC	embryonic stem cell:	embryo
5	chr1:158905479-158905529	BJ	skin:	n/a
6	chr1:158911377-158911427	HMEC	breast:	n/a
7	chr1:158911377-158911427	HepG2	liver:	n/a
8	chr1:158905479-158905529	NH-A	brain:	n/a
9	chr1:158905479-158905529	SAEC	small airway:	n/a
10	chr1:158905479-158905529	HEEpiC	esophagus:	n/a
11	chr1:158911377-158911427	PANC-1	pancreas:	n/a
12	chr1:158905479-158905529	HMEC	breast:	n/a
13	chr1:158911377-158911427	HEEpiC	esophagus:	n/a
14	chr1:158911377-158911427	NHDF-neo	bronchial:	n/a
15	chr1:158905479-158905529	HIPEpiC	eye:	n/a
16	chr1:158911377-158911427	HRPEpiC	eye:	n/a
17	chr1:158911377-158911427	BE2_C	brain:	n/a
18	chr1:158905479-158905529	HRCEpiC	kidney:	n/a
19	chr1:158905479-158905529	SK-N-SH	brain:	n/a
20	chr1:158911377-158911427	SK-N-SH_RA	brain:	n/a
21	chr1:158905479-158905529	ProgFib	skin:	n/a
22	chr1:158911377-158911427	SK-N-SH	brain:	n/a
23	chr1:158905479-158905529	PrEC	prostate:	n/a
24	chr1:158911377-158911427	GM06990	blood:	n/a
25	chr1:158905479-158905529	AG09309	skin:	n/a
26	chr1:158905479-158905529	Hela-S3	cervix:	n/a
27	chr1:158905479-158905529	AG04449	skin:	fetal
28	chr1:158905479-158905529	GM06990	blood:	n/a
29	chr1:158911377-158911427	ProgFib	skin:	n/a
30	chr1:158905479-158905529	LNCaP	prostate:	n/a
31	chr1:158911377-158911427	CMK	blood:	n/a
32	chr1:158905479-158905529	Hepatocyte	liver:	n/a
33	chr1:158911377-158911427	HEK293	kidney:	embryo
34	chr1:158905479-158905529	PANC-1	pancreas:	n/a
35	chr1:158911377-158911427	LNCaP	prostate:	n/a
36	chr1:158911377-158911427	Caco-2	colon:	n/a
37	chr1:158911377-158911427	Hepatocyte	liver:	n/a
38	chr1:158905479-158905529	HCT-116	colon:	n/a
39	chr1:158905479-158905529	Jurkat	blood:	n/a
40	chr1:158911377-158911427	ovcar-3	ovarian:	n/a
41	chr1:158905479-158905529	U87	brain:	n/a
42	chr1:158905479-158905529	PFSK-1	brain:	n/a
43	chr1:158905479-158905529	SK-N-SH_RA	brain:	n/a
44	chr1:158905479-158905529	HL-60	blood:	n/a
45	chr1:158911377-158911427	SK-N-MC	brain:	n/a
46	chr1:158905479-158905529	AoSMC	blood vessel:	n/a
47	chr1:158911377-158911427	T-47D	breast:	n/a
48	chr1:158911377-158911427	AG09309	skin:	n/a
49	chr1:158911377-158911427	AG10803	skin:	n/a
50	chr1:158911377-158911427	AG09319	gingival:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:158909146..158911653-chr1:158916474..158918051,2	K562	blood:

Variant related genes	Relation type
PYHIN1	TF binding region
PYHIN1	CpG island

Extended variants
information (count: 255 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:255 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548147345	chr1:158905179-158905180	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs386635957	chr1:158905206-158905207	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs1633278	chr1:158905207-158905208	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs188539834	chr1:158905208-158905209	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs572076982	chr1:158905217-158905218	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs12087637	chr1:158905261-158905262	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs545616756	chr1:158905266-158905267	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs77751301	chr1:158905366-158905367	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs148301378	chr1:158905416-158905417	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs181415705	chr1:158905451-158905452	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs186868381	chr1:158905453-158905454	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs562349881	chr1:158905455-158905456	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs529561829	chr1:158905469-158905470	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs370162950	chr1:158905480-158905481	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs542172554	chr1:158905487-158905488	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs560319466	chr1:158905494-158905495	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs527763224	chr1:158905563-158905564	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs12073719	chr1:158905587-158905588	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs527369304	chr1:158905619-158905620	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs141550322	chr1:158905625-158905626	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs377504019	chr1:158905629-158905630	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs116617418	chr1:158905733-158905734	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs191763752	chr1:158905768-158905769	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs568317244	chr1:158905769-158905770	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs535404081	chr1:158905778-158905779	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs116554597	chr1:158905794-158905795	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs550368958	chr1:158905913-158905914	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs370305504	chr1:158905948-158905949	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs71632647	chr1:158906002-158906003	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs182348832	chr1:158906096-158906097	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs150903697	chr1:158906119-158906120	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs113460160	chr1:158906120-158906121	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs575733111	chr1:158906123-158906124	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs544368905	chr1:158906131-158906132	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs556350942	chr1:158906187-158906188	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs575061866	chr1:158906227-158906228	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs542186309	chr1:158906350-158906351	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs560534416	chr1:158906358-158906359	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs537576947	chr1:158906366-158906367	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs572388371	chr1:158906388-158906389	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs546229543	chr1:158906391-158906392	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs1633279	chr1:158906410-158906411	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs531864314	chr1:158906414-158906415	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs6664820	chr1:158906416-158906417	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs568006420	chr1:158906438-158906439	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs529168354	chr1:158906480-158906481	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs547423606	chr1:158906482-158906483	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs1633280	chr1:158906555-158906556	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs538997333	chr1:158906572-158906573	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs12089154	chr1:158906637-158906638	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:109)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Non-small cell lung cancer	21385341	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Systemic lupus erythematosus	19220326	CNVD
Systemic lupus erythematosus	19287148	CNVD
Glomerulonephritis	19341492	CNVD
Systemic lupus erythematosus	18559452	CNVD
Systemic autoimmune disease	17597778	CNVD
Glomerulonephritis	17008540	CNVD
Glomerulonephritis	16482158	CNVD
Soft tissue tumor	16732325	CNVD
Cancer	17060936	CNVD
Lung cancer	16740712	CNVD
Breast cancer	21045282	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Cancer	20164920	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Follicular lymphoma	18703704	CNVD
Pancreatic cancer	17952125	CNVD
Myelofibrosis	22110671	CNVD
Intracranial ependymoma	16609018	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:69 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:158902200-158907800	Weak transcription	Thymus	Thymus
2	chr1:158902200-158920000	Weak transcription	Primary B cells from peripheral blood	blood
3	chr1:158904200-158905400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
4	chr1:158904200-158912000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr1:158904400-158905800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
6	chr1:158904400-158905800	Enhancers	Primary T helper cells fromperipheralblood	blood
7	chr1:158904400-158906600	Weak transcription	Primary B cells from cord blood	blood
8	chr1:158904400-158906800	Weak transcription	Primary T cells from cord blood	blood
9	chr1:158904800-158905400	Weak transcription	Primary T cells fromperipheralblood	blood
10	chr1:158904800-158905400	Enhancers	Primary T helper naive cells from peripheral blood	blood
11	chr1:158904800-158905600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr1:158904800-158905800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
13	chr1:158904800-158906800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
14	chr1:158904800-158906800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr1:158905000-158905600	Enhancers	Primary T helper cells PMA-I stimulated	--
16	chr1:158905000-158905600	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
17	chr1:158905000-158905600	Enhancers	Primary T killer memory cells from peripheral blood	blood
18	chr1:158905000-158905800	Genic enhancers	Primary T helper 17 cells PMA-I stimulated	--
19	chr1:158905000-158905800	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
20	chr1:158905400-158905600	Genic enhancers	Primary T cells fromperipheralblood	blood
21	chr1:158905400-158906600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
22	chr1:158905400-158907000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
23	chr1:158905600-158906600	Weak transcription	Primary T helper cells PMA-I stimulated	--
24	chr1:158905600-158906800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
25	chr1:158905600-158908800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr1:158905600-158921800	Strong transcription	Primary T cells fromperipheralblood	blood
27	chr1:158905600-158922000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
28	chr1:158905800-158906200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
29	chr1:158905800-158906600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
30	chr1:158905800-158906600	Weak transcription	Primary T helper cells fromperipheralblood	blood
31	chr1:158905800-158906800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
32	chr1:158905800-158930200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
33	chr1:158906200-158908000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
34	chr1:158906600-158907000	Genic enhancers	Primary T helper memory cells from peripheral blood 2	blood
35	chr1:158906600-158907200	Strong transcription	Primary B cells from cord blood	blood
36	chr1:158906600-158907800	Strong transcription	Primary T helper cells PMA-I stimulated	--
37	chr1:158906600-158909600	Strong transcription	Primary T helper naive cells from peripheral blood	blood
38	chr1:158906600-158919600	Strong transcription	Primary T helper cells fromperipheralblood	blood
39	chr1:158906800-158907000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
40	chr1:158906800-158907000	Genic enhancers	Primary T helper 17 cells PMA-I stimulated	--
41	chr1:158906800-158908000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr1:158906800-158908200	Strong transcription	Primary T killer memory cells from peripheral blood	blood
43	chr1:158906800-158909400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
44	chr1:158906800-158910000	Strong transcription	Primary T cells from cord blood	blood
45	chr1:158907000-158909400	Strong transcription	Primary T helper memory cells from peripheral blood 2	blood
46	chr1:158907000-158909600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
47	chr1:158907000-158919200	Strong transcription	Primary T helper memory cells from peripheral blood 1	blood
48	chr1:158907200-158918200	Weak transcription	Primary B cells from cord blood	blood
49	chr1:158907800-158908200	Genic enhancers	Primary T helper cells PMA-I stimulated	--
50	chr1:158908000-158908400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links