Variant report

Variant	esv2763473
Chromosome Location	chr5:99883352-99907664
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	BATF	chr5:99886169-99886390	GM12878	blood:	n/a	n/a
2	BCL11A	chr5:99886437-99886629	GM12878	blood:	n/a	n/a
3	BCLAF1	chr5:99886248-99886772	GM12878	blood:	n/a	n/a
4	CEBPB	chr5:99898160-99898375	A549	lung:	n/a	n/a
5	CEBPB	chr5:99886551-99886855	IMR90	lung:	n/a	n/a
6	CEBPB	chr5:99890906-99891108	IMR90	lung:	n/a	n/a
7	CEBPB	chr5:99891070-99891104	A549	lung:	n/a	n/a
8	CTCF	chr5:99887980-99888130	HCPEpiC	choroid plexus:	n/a	n/a
9	CTCF	chr5:99887640-99887790	MCF-7	breast:	n/a	n/a
10	CTCF	chr5:99888018-99888146	HUVEC	blood vessel:	n/a	n/a
11	EP300	chr5:99886098-99886830	SK-N-SH_RA	brain:	n/a	n/a
12	EP300	chr5:99886267-99886815	GM12878	blood:	n/a	n/a
13	EP300	chr5:99886115-99886784	SK-N-SH_RA	brain:	n/a	n/a
14	FOS	chr5:99888941-99889172	MCF10A-Er-Src	breast:	n/a	n/a
15	FOS	chr5:99905262-99905455	MCF10A-Er-Src	breast:	n/a	n/a
16	FOS	chr5:99889046-99889246	HUVEC	blood vessel:	n/a	n/a
17	FOS	chr5:99886601-99886799	MCF10A-Er-Src	breast:	n/a	n/a
18	FOSL2	chr5:99888900-99889354	SK-N-SH	brain:	n/a	chr5:99889279-99889291 chr5:99889281-99889289
19	FOXA1	chr5:99903943-99904338	T-47D	breast:	n/a	n/a
20	FOXA1	chr5:99903947-99904326	T-47D	breast:	n/a	n/a
21	GATA3	chr5:99886343-99887055	SK-N-SH	brain:	n/a	chr5:99886779-99886787
22	GATA3	chr5:99886061-99887100	SK-N-SH	brain:	n/a	chr5:99886779-99886787
23	GATA3	chr5:99904154-99904290	MCF-7	breast:	n/a	n/a
24	GATA3	chr5:99904015-99904439	T-47D	breast:	n/a	n/a
25	GATA3	chr5:99896221-99896840	MCF-7	breast:	n/a	n/a
26	GATA3	chr5:99903439-99903758	SH-SY5Y	brain:	n/a	n/a
27	GATA3	chr5:99896001-99896767	MCF-7	breast:	n/a	n/a
28	GATA3	chr5:99903963-99904413	T-47D	breast:	n/a	n/a
29	IKZF1	chr5:99886181-99886863	GM12878	blood:	n/a	n/a
30	IKZF1	chr5:99902244-99902411	GM12878	blood:	n/a	n/a
31	IRF4	chr5:99886311-99886729	GM12878	blood:	n/a	n/a
32	IRF4	chr5:99886343-99886729	GM12878	blood:	n/a	n/a
33	JUND	chr5:99889025-99889180	HepG2	liver:	n/a	chr5:99889087-99889098
34	MAFF	chr5:99904338-99904500	HepG2	liver:	n/a	n/a
35	MAFF	chr5:99898663-99898863	K562	blood:	n/a	chr5:99898724-99898742
36	MAFF	chr5:99883180-99883397	HepG2	liver:	n/a	chr5:99883308-99883326
37	MAFF	chr5:99898326-99898869	HepG2	liver:	n/a	chr5:99898724-99898742
38	MAFK	chr5:99898342-99898841	HepG2	liver:	n/a	chr5:99898727-99898736 chr5:99898726-99898736
39	MAFK	chr5:99898351-99898884	HepG2	liver:	n/a	chr5:99898727-99898736 chr5:99898726-99898736
40	MAFK	chr5:99883192-99883392	HepG2	liver:	n/a	chr5:99883310-99883326 chr5:99883310-99883321 chr5:99883309-99883323 chr5:99883311-99883322 chr5:99883310-99883321
41	MAFK	chr5:99904317-99904493	HepG2	liver:	n/a	n/a
42	MAFK	chr5:99907625-99907791	HepG2	liver:	n/a	chr5:99907736-99907745
43	MAFK	chr5:99898358-99898862	IMR90	lung:	n/a	chr5:99898727-99898736 chr5:99898726-99898736
44	MEF2A	chr5:99886517-99887005	SK-N-SH	brain:	n/a	chr5:99886793-99886810 chr5:99886795-99886809 chr5:99886868-99886877 chr5:99886867-99886878 chr5:99886863-99886884
45	MEF2A	chr5:99886184-99886726	GM12878	blood:	n/a	n/a
46	MEF2A	chr5:99886168-99886684	GM12878	blood:	n/a	n/a
47	NFIC	chr5:99886162-99886771	GM12878	blood:	n/a	n/a
48	NFYB	chr5:99886176-99886719	GM12878	blood:	n/a	n/a
49	PBX3	chr5:99886394-99886574	GM12878	blood:	n/a	n/a
50	PBX3	chr5:99886391-99886983	SK-N-SH	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:99886768-99886818	AG04449	skin:	fetal
2	chr5:99886768-99886818	HCT-116	colon:	n/a
3	chr5:99886768-99886818	HCM	heart:	n/a
4	chr5:99886768-99886818	NB4	blood:	n/a
5	chr5:99886768-99886818	AG04450	lung:	fetal
6	chr5:99886768-99886818	BE2_C	brain:	n/a
7	chr5:99886768-99886818	AoSMC	blood vessel:	n/a
8	chr5:99886768-99886818	LNCaP	prostate:	n/a
9	chr5:99886768-99886818	MCF-7	breast:	n/a
10	chr5:99886768-99886818	HIPEpiC	eye:	n/a
11	chr5:99886768-99886818	HRCEpiC	kidney:	n/a
12	chr5:99886768-99886818	IMR90	lung:	fetal
13	chr5:99886768-99886818	HUVEC	blood vessel:	n/a
14	chr5:99886768-99886818	A549	lung:	n/a
15	chr5:99886768-99886818	PANC-1	pancreas:	n/a
16	chr5:99886768-99886818	MCF10A-Er-Src	breast:	n/a
17	chr5:99886768-99886818	HAEpiC	amniotic membrane:	n/a
18	chr5:99886768-99886818	HMEC	breast:	n/a
19	chr5:99886768-99886818	HL-60	blood:	n/a
20	chr5:99886768-99886818	HCPEpiC	choroid plexus:	n/a
21	chr5:99886768-99886818	GM12892	blood:	n/a
22	chr5:99886768-99886818	SKMC	muscle:	n/a
23	chr5:99886768-99886818	GM12891	blood:	n/a
24	chr5:99886768-99886818	K562	blood:	n/a
25	chr5:99886768-99886818	HRPEpiC	eye:	n/a
26	chr5:99886768-99886818	RPTEC	kidney:	n/a
27	chr5:99886768-99886818	HNPCEpiC	eye:	n/a
28	chr5:99886768-99886818	SK-N-MC	brain:	n/a
29	chr5:99886768-99886818	Hela-S3	cervix:	n/a
30	chr5:99886768-99886818	Jurkat	blood:	n/a
31	chr5:99886768-99886818	T-47D	breast:	n/a
32	chr5:99886768-99886818	ProgFib	skin:	n/a
33	chr5:99886768-99886818	SK-N-SH_RA	brain:	n/a
34	chr5:99886768-99886818	CMK	blood:	n/a
35	chr5:99886768-99886818	HepG2	liver:	n/a
36	chr5:99886768-99886818	Caco-2	colon:	n/a
37	chr5:99886768-99886818	PFSK-1	brain:	n/a
38	chr5:99886768-99886818	ovcar-3	ovarian:	n/a
39	chr5:99886768-99886818	AG10803	skin:	n/a
40	chr5:99886768-99886818	HEEpiC	esophagus:	n/a
41	chr5:99886768-99886818	SK-N-SH	brain:	n/a
42	chr5:99886768-99886818	GM19239	blood:	n/a
43	chr5:99886768-99886818	Hepatocyte	liver:	n/a
44	chr5:99886768-99886818	HRE	kidney:	n/a
45	chr5:99886768-99886818	PrEC	prostate:	n/a
46	chr5:99886768-99886818	HEK293	kidney:	embryo
47	chr5:99886768-99886818	AG09309	skin:	n/a
48	chr5:99886768-99886818	HPAEpiC	pulmonary alveolar:	n/a
49	chr5:99886768-99886818	GM12878	blood:	n/a
50	chr5:99886768-99886818	ECC-1	luminal epithelium:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:99901928..99904752-chr5:99911773..99913756,2	MCF-7	breast:
2	chr5:99880455..99883115-chr5:99884041..99887018,2	MCF-7	breast:

Variant related genes	Relation type
FAM174A	TF binding region
FAM174A	CpG island

Extended variants
information (count: 973 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:973 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17447375	chr5:99883352-99883353	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs17447382	chr5:99883371-99883372	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs10477616	chr5:99883381-99883382	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs547744307	chr5:99883417-99883418	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs181468390	chr5:99883431-99883432	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs186052960	chr5:99883456-99883457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs552430021	chr5:99883481-99883482	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs540841696	chr5:99883491-99883492	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs559528362	chr5:99883538-99883539	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs538033102	chr5:99883573-99883574	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs26026	chr5:99883577-99883578	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs569329753	chr5:99883620-99883621	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs536756884	chr5:99883632-99883633	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs554640918	chr5:99883639-99883640	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs556469836	chr5:99883689-99883690	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs570276727	chr5:99883714-99883715	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs573172634	chr5:99883726-99883727	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs154712	chr5:99883729-99883730	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs142103175	chr5:99883758-99883759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs577165434	chr5:99883789-99883790	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs544354379	chr5:99883855-99883856	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs569713907	chr5:99883943-99883944	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs572428588	chr5:99884197-99884198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs151178653	chr5:99884278-99884279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs182901204	chr5:99884290-99884291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs466613	chr5:99884308-99884309	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs560024623	chr5:99884316-99884317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs527267823	chr5:99884373-99884374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs551931971	chr5:99884419-99884420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs369935039	chr5:99884475-99884476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs570825356	chr5:99884476-99884477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs553386982	chr5:99884488-99884489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs535138945	chr5:99884489-99884490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs531645729	chr5:99884527-99884528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs372422521	chr5:99884578-99884579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs186710705	chr5:99884593-99884594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs140295346	chr5:99884626-99884627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs35756724	chr5:99884667-99884668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs535678074	chr5:99884730-99884731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs548650168	chr5:99884753-99884754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs566895045	chr5:99884838-99884839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs190645752	chr5:99884853-99884854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs73774435	chr5:99884871-99884872	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs73774436	chr5:99884889-99884890	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs116242263	chr5:99884892-99884893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs553266715	chr5:99884895-99884896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs113416728	chr5:99884965-99884966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs574676670	chr5:99885051-99885052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs182938304	chr5:99885067-99885068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs553827395	chr5:99885097-99885098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Ovarian cancer	21720365	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:269 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:99871800-99886400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr5:99871800-99886400	Weak transcription	Lung	lung
3	chr5:99871800-99886800	Weak transcription	Pancreas	Pancrea
4	chr5:99871800-99889400	Weak transcription	Spleen	Spleen
5	chr5:99871800-99890200	Weak transcription	Gastric	stomach
6	chr5:99872400-99886200	Weak transcription	Small Intestine	intestine
7	chr5:99872400-99931400	Weak transcription	Aorta	Aorta
8	chr5:99872600-99886400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr5:99872600-99922800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr5:99872800-99886200	Weak transcription	HSMMtube	muscle
11	chr5:99872800-99886200	Weak transcription	Osteobl	bone
12	chr5:99872800-99886400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr5:99872800-99902000	Weak transcription	HSMM	muscle
14	chr5:99872800-99916200	Weak transcription	Ovary	ovary
15	chr5:99873000-99886400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
16	chr5:99873400-99897000	Weak transcription	Primary T cells from cord blood	blood
17	chr5:99873400-99916200	Weak transcription	Fetal Stomach	stomach
18	chr5:99873400-99930600	Weak transcription	NH-A	brain
19	chr5:99873600-99883800	Weak transcription	Brain Germinal Matrix	brain
20	chr5:99873800-99886400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr5:99874000-99886200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
22	chr5:99874000-99897800	Weak transcription	Adipose Nuclei	Adipose
23	chr5:99875600-99887600	Weak transcription	Fetal Brain Male	brain
24	chr5:99878400-99885800	Weak transcription	Skeletal Muscle Female	skeletal muscle
25	chr5:99878400-99886400	Weak transcription	HMEC	breast
26	chr5:99878400-99930600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr5:99878600-99886400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr5:99878800-99886000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr5:99879600-99886200	Weak transcription	NHEK	skin
30	chr5:99879600-99897600	Weak transcription	Primary B cells from cord blood	blood
31	chr5:99880600-99897800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
32	chr5:99881000-99886000	Weak transcription	Muscle Satellite Cultured Cells	--
33	chr5:99882200-99886400	Weak transcription	Fetal Muscle Leg	muscle
34	chr5:99882200-99886400	Weak transcription	Skeletal Muscle Male	skeletal muscle
35	chr5:99882200-99887000	Weak transcription	Psoas Muscle	Psoas
36	chr5:99882200-99899200	Weak transcription	Left Ventricle	heart
37	chr5:99882400-99886400	Weak transcription	Fetal Lung	lung
38	chr5:99882800-99888800	Weak transcription	Primary hematopoietic stem cells	blood
39	chr5:99883200-99884000	Enhancers	HUVEC	blood vessel
40	chr5:99883800-99884000	Enhancers	Brain Germinal Matrix	brain
41	chr5:99884000-99910400	Weak transcription	HUVEC	blood vessel
42	chr5:99885200-99887400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
43	chr5:99885800-99886000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr5:99885800-99886600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr5:99885800-99887200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr5:99885800-99887200	Enhancers	NHDF-Ad	bronchial
47	chr5:99885800-99887800	Enhancers	Skeletal Muscle Female	skeletal muscle
48	chr5:99886000-99886600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr5:99886000-99886800	Enhancers	Muscle Satellite Cultured Cells	--
50	chr5:99886000-99887800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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