Variant report

Variant	nsv1049442
Chromosome Location	chr10:55638740-55681002
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	ARID3A	chr10:55653961-55654284	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:55646406-55646955	HepG2	liver:	n/a	n/a
3	CCNT2	chr10:55664795-55664881	K562	blood:	n/a	n/a
4	CEBPB	chr10:55654044-55654416	HepG2	liver:	n/a	n/a
5	CEBPB	chr10:55659265-55659499	IMR90	lung:	n/a	n/a
6	CEBPB	chr10:55657552-55657619	HepG2	liver:	n/a	n/a
7	CEBPB	chr10:55646454-55646819	A549	lung:	n/a	chr10:55646779-55646790 chr10:55646779-55646792
8	CEBPB	chr10:55646415-55646944	HepG2	liver:	n/a	chr10:55646779-55646790 chr10:55646779-55646792
9	CEBPB	chr10:55646463-55646995	MCF-7	breast:	n/a	chr10:55646779-55646790 chr10:55646779-55646792
10	CEBPB	chr10:55646576-55646910	A549	lung:	n/a	chr10:55646779-55646790 chr10:55646779-55646792
11	CEBPB	chr10:55646421-55646815	HepG2	liver:	n/a	chr10:55646779-55646790 chr10:55646779-55646792
12	CEBPB	chr10:55678641-55678961	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr10:55656136-55656417	A549	lung:	n/a	chr10:55656227-55656238
14	CEBPB	chr10:55646449-55646949	MCF-7	breast:	n/a	chr10:55646779-55646790 chr10:55646779-55646792
15	CEBPB	chr10:55656183-55656384	HepG2	liver:	n/a	chr10:55656227-55656238
16	CEBPB	chr10:55646486-55646676	HepG2	liver:	n/a	n/a
17	CEBPB	chr10:55646412-55647027	Hela-S3	cervix:	n/a	chr10:55646779-55646790 chr10:55646779-55646792
18	CTCF	chr10:55678580-55678730	SK-N-SH_RA	brain:	n/a	n/a
19	CTCF	chr10:55666460-55666610	HepG2	liver:	n/a	n/a
20	CTCF	chr10:55678560-55678710	HEK293	kidney:	n/a	n/a
21	CTCF	chr10:55678560-55678710	BE2_C	brain:	n/a	n/a
22	CTCF	chr10:55646969-55647023	LNCaP	prostate:	n/a	n/a
23	CTCF	chr10:55646956-55646959	Hela-S3	cervix:	n/a	n/a
24	CTCF	chr10:55646990-55647090	GM12878	blood:	n/a	n/a
25	CTCF	chr10:55678600-55678750	NHEK	skin:	n/a	n/a
26	CTCF	chr10:55646963-55647043	LNCaP	prostate:	n/a	n/a
27	CTCF	chr10:55678600-55678750	MCF-7	breast:	n/a	n/a
28	CTCF	chr10:55678580-55678730	HEEpiC	esophagus:	n/a	n/a
29	CTCF	chr10:55678540-55678690	HepG2	liver:	n/a	n/a
30	CTCF	chr10:55678520-55678670	SAEC	small airway:	n/a	n/a
31	CTCF	chr10:55646960-55647049	Hela-S3	cervix:	n/a	n/a
32	CTCF	chr10:55678640-55678790	Caco-2	colon:	n/a	n/a
33	CTCF	chr10:55678560-55678710	MCF-7	breast:	n/a	n/a
34	EP300	chr10:55641543-55642284	SK-N-SH	brain:	n/a	chr10:55641556-55641564 chr10:55641570-55641577
35	EP300	chr10:55653949-55654286	HepG2	liver:	n/a	chr10:55654059-55654069
36	EP300	chr10:55641813-55642147	SK-N-SH_RA	brain:	n/a	n/a
37	EP300	chr10:55641810-55642123	SK-N-SH_RA	brain:	n/a	n/a
38	FOS	chr10:55664307-55665089	MCF10A-Er-Src	breast:	n/a	chr10:55664737-55664746 chr10:55664736-55664748 chr10:55664739-55664746 chr10:55664738-55664747 chr10:55664738-55664746
39	FOS	chr10:55658313-55658631	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr10:55663546-55665144	MCF10A-Er-Src	breast:	n/a	chr10:55664737-55664746 chr10:55664736-55664748 chr10:55663741-55663749 chr10:55664739-55664746 chr10:55663740-55663749 chr10:55663741-55663748 chr10:55664738-55664747 chr10:55663741-55663750 chr10:55664738-55664746
41	FOS	chr10:55663468-55665128	MCF10A-Er-Src	breast:	n/a	chr10:55664737-55664746 chr10:55664736-55664748 chr10:55663741-55663749 chr10:55664739-55664746 chr10:55663740-55663749 chr10:55663741-55663748 chr10:55664738-55664747 chr10:55663741-55663750 chr10:55664738-55664746
42	FOS	chr10:55663419-55665425	MCF10A-Er-Src	breast:	n/a	chr10:55664737-55664746 chr10:55664736-55664748 chr10:55663741-55663749 chr10:55664739-55664746 chr10:55663740-55663749 chr10:55663741-55663748 chr10:55664738-55664747 chr10:55663741-55663750 chr10:55664738-55664746
43	FOS	chr10:55653979-55654362	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr10:55658429-55658616	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr10:55663536-55663975	MCF10A-Er-Src	breast:	n/a	chr10:55663741-55663749 chr10:55663740-55663749 chr10:55663741-55663748 chr10:55663741-55663750
46	FOS	chr10:55652926-55653126	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr10:55653960-55654359	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr10:55653970-55654389	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr10:55646473-55646903	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr10:55654064-55654410	MCF10A-Er-Src	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:55651840-55651890	MCF10A-Er-Src	breast:	n/a
2	chr10:55651840-55651890	MCF10A-Er-Src	breast:	n/a
3	chr10:55651840-55651890	ECC-1	luminal epithelium:	n/a
4	chr10:55651840-55651890	NT2-D1	testis:	n/a
5	chr10:55651840-55651890	HL-60	blood:	n/a
6	chr10:55651840-55651890	ovcar-3	ovarian:	n/a
7	chr10:55651840-55651890	AG09319	gingival:	n/a
8	chr10:55651840-55651890	Caco-2	colon:	n/a
9	chr10:55651840-55651890	HRCEpiC	kidney:	n/a
10	chr10:55651840-55651890	MCF-7	breast:	n/a
11	chr10:55651840-55651890	T-47D	breast:	n/a
12	chr10:55651840-55651890	GM06990	blood:	n/a
13	chr10:55651840-55651890	HRPEpiC	eye:	n/a
14	chr10:55651840-55651890	LNCaP	prostate:	n/a
15	chr10:55651840-55651890	SK-N-MC	brain:	n/a
16	chr10:55651840-55651890	Hepatocyte	liver:	n/a
17	chr10:55651840-55651890	PANC-1	pancreas:	n/a
18	chr10:55651840-55651890	NH-A	brain:	n/a
19	chr10:55651840-55651890	CMK	blood:	n/a
20	chr10:55651840-55651890	HEEpiC	esophagus:	n/a
21	chr10:55651840-55651890	U87	brain:	n/a
22	chr10:55651840-55651890	AG09309	skin:	n/a
23	chr10:55651840-55651890	HRE	kidney:	n/a
24	chr10:55651840-55651890	HPAEpiC	pulmonary alveolar:	n/a
25	chr10:55651840-55651890	H1-hESC	embryonic stem cell:	embryo
26	chr10:55651840-55651890	AoSMC	blood vessel:	n/a
27	chr10:55651840-55651890	SK-N-SH_RA	brain:	n/a
28	chr10:55651840-55651890	GM12878	blood:	n/a
29	chr10:55651840-55651890	HMEC	breast:	n/a
30	chr10:55651840-55651890	SK-N-SH	brain:	n/a
31	chr10:55651840-55651890	SKMC	muscle:	n/a
32	chr10:55651840-55651890	A549	lung:	n/a
33	chr10:55651840-55651890	HAEpiC	amniotic membrane:	n/a
34	chr10:55651840-55651890	BJ	skin:	n/a
35	chr10:55651840-55651890	HepG2	liver:	n/a
36	chr10:55651840-55651890	BE2_C	brain:	n/a
37	chr10:55651840-55651890	AG04449	skin:	fetal
38	chr10:55651840-55651890	HCF	heart:	n/a
39	chr10:55651840-55651890	ProgFib	skin:	n/a
40	chr10:55651840-55651890	Jurkat	blood:	n/a
41	chr10:55651840-55651890	HNPCEpiC	eye:	n/a
42	chr10:55651840-55651890	NHDF-neo	bronchial:	n/a
43	chr10:55651840-55651890	HCPEpiC	choroid plexus:	n/a
44	chr10:55651840-55651890	NB4	blood:	n/a
45	chr10:55651840-55651890	SAEC	small airway:	n/a
46	chr10:55651840-55651890	RPTEC	kidney:	n/a
47	chr10:55651840-55651890	GM19239	blood:	n/a
48	chr10:55651840-55651890	HCM	heart:	n/a
49	chr10:55651840-55651890	AG04450	lung:	fetal
50	chr10:55651840-55651890	HIPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:55658704..55661053-chr10:55661936..55664959,3	K562	blood:
2	chr10:55658704..55661053-chr10:55661936..55664959,3	K562	blood:

Variant related genes	Relation type
PCDH15	TF binding region
PCDH15	CpG island

Extended variants
information (count: 1074 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:1074 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11003908	chr10:55645842-55645843	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs200588561	chr10:55645859-55645860	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs552108602	chr10:55645945-55645946	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs181319591	chr10:55645949-55645950	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs10825150	chr10:55645953-55645954	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs565649435	chr10:55645986-55645987	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs186937361	chr10:55646002-55646003	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs547253476	chr10:55646081-55646082	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs1900433	chr10:55646100-55646101	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs190184914	chr10:55646118-55646119	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs372944554	chr10:55646218-55646219	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs16937813	chr10:55646297-55646298	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs36171553	chr10:55646356-55646357	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs147934011	chr10:55646378-55646379	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs11003909	chr10:55646396-55646397	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs75914599	chr10:55646400-55646401	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs35714117	chr10:55646401-55646402	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs555189512	chr10:55646410-55646411	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs11003910	chr10:55646422-55646423	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs572779428	chr10:55646475-55646476	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs182301329	chr10:55646487-55646488	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs187360631	chr10:55646528-55646529	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs560719082	chr10:55646540-55646541	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs576780889	chr10:55646567-55646568	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs545469896	chr10:55646585-55646586	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs562647256	chr10:55646611-55646612	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs41487044	chr10:55646644-55646645	Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs141748135	chr10:55646647-55646648	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs74137226	chr10:55646650-55646651	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs2069217	chr10:55646762-55646763	Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs2069216	chr10:55646825-55646826	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs2069215	chr10:55646846-55646847	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs539069421	chr10:55646878-55646879	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs77538645	chr10:55646895-55646896	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs147114602	chr10:55646897-55646898	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs72794910	chr10:55646914-55646915	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs555074991	chr10:55646917-55646918	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs568671052	chr10:55646927-55646928	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs534347559	chr10:55646937-55646938	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs554487012	chr10:55646990-55646991	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs377479582	chr10:55647081-55647082	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs534573248	chr10:55647087-55647088	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs75865308	chr10:55647095-55647096	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs545812116	chr10:55647103-55647104	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs140943685	chr10:55647114-55647115	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs563651759	chr10:55647183-55647184	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs180731864	chr10:55654000-55654001	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs186164075	chr10:55654018-55654019	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs548670905	chr10:55654065-55654066	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs368580130	chr10:55654080-55654081	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Obesity	21956041	CNVD
Developmental delay	21948486	CNVD
Intellectual disability	21948486	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16272173	CNVD
Metanephric adenoma	20802469	CNVD
Autism	20841430	CNVD
Mental retardation	17124404	CNVD
Epilepsy	20923578	CNVD
Prostate cancer	16573809	CNVD
Schizophrenia	19329560	CNVD
Heart failure	18772530	CNVD
Heart failure	18854381	CNVD
Hyperglycemia	19060297	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Glioblastoma multiforme	22286061	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Usher syndrome	20538994	CNVD
Glioblastoma multiforme	17002787	CNVD
Colorectal cancer	16774939	CNVD
Autism	20858243	CNVD
Breast cancer	22522925	CNVD
Usher type I cohort	17277737	CNVD
Usher type I cohort	21436283	CNVD
Leukemia	21357790	CNVD
Medulloblastoma	22832581	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:57 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:55645800-55646600	Enhancers	Liver	Liver
2	chr10:55646000-55646800	Enhancers	Fetal Intestine Small	intestine
3	chr10:55646000-55647000	Enhancers	Rectal Mucosa Donor 31	rectum
4	chr10:55646200-55646600	Enhancers	Fetal Intestine Large	intestine
5	chr10:55646200-55646600	Active TSS	A549	lung
6	chr10:55646200-55647200	Enhancers	HepG2	liver
7	chr10:55646600-55646800	Enhancers	Duodenum Mucosa	Duodenum
8	chr10:55646600-55647000	Flanking Active TSS	Liver	Liver
9	chr10:55646600-55647000	Enhancers	Rectal Mucosa Donor 29	rectum
10	chr10:55646600-55647000	Flanking Active TSS	A549	lung
11	chr10:55646800-55647000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr10:55647000-55647200	Enhancers	A549	lung
13	chr10:55654000-55654200	Enhancers	Fetal Intestine Small	intestine
14	chr10:55654000-55654600	Enhancers	HepG2	liver
15	chr10:55654000-55655000	Enhancers	Stomach Smooth Muscle	stomach
16	chr10:55654200-55658400	Weak transcription	Fetal Intestine Small	intestine
17	chr10:55658200-55658600	Enhancers	Fetal Kidney	kidney
18	chr10:55658200-55658600	Enhancers	NHEK	skin
19	chr10:55658200-55658800	Enhancers	Fetal Intestine Large	intestine
20	chr10:55658400-55658600	Enhancers	Fetal Intestine Small	intestine
21	chr10:55658600-55659000	Weak transcription	Fetal Kidney	kidney
22	chr10:55658600-55659400	Weak transcription	Fetal Intestine Small	intestine
23	chr10:55658600-55663000	Weak transcription	NHEK	skin
24	chr10:55658800-55659200	Weak transcription	Fetal Intestine Large	intestine
25	chr10:55659000-55660600	Enhancers	Fetal Kidney	kidney
26	chr10:55659200-55660600	Enhancers	Fetal Intestine Large	intestine
27	chr10:55659400-55660200	Enhancers	Colon Smooth Muscle	Colon
28	chr10:55659400-55660600	Enhancers	Fetal Intestine Small	intestine
29	chr10:55659800-55660200	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
30	chr10:55659800-55660400	Enhancers	Fetal Stomach	stomach
31	chr10:55660600-55661800	Weak transcription	Fetal Intestine Small	intestine
32	chr10:55660600-55661800	Weak transcription	Fetal Kidney	kidney
33	chr10:55661400-55662200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr10:55662000-55662200	Enhancers	Fetal Intestine Small	intestine
35	chr10:55662000-55662200	Enhancers	Fetal Kidney	kidney
36	chr10:55662800-55663200	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr10:55662800-55663200	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr10:55662800-55663200	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr10:55662800-55664000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr10:55662800-55664400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr10:55663000-55665200	Enhancers	NHEK	skin
42	chr10:55663200-55664400	Enhancers	HMEC	breast
43	chr10:55664000-55664200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr10:55664000-55665000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr10:55664200-55665400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr10:55664400-55664800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr10:55664400-55664800	Active TSS	HMEC	breast
48	chr10:55664400-55665000	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr10:55664800-55665200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr10:55664800-55665400	Enhancers	HMEC	breast

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