Variant report

Variant	nsv978603
Chromosome Location	chr18:12039958-12046831
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	CEBPB	chr18:12039777-12039991	HepG2	liver:	n/a	chr18:12039845-12039856
2	CEBPB	chr18:12046531-12046750	HepG2	liver:	n/a	chr18:12046686-12046697 chr18:12046684-12046695 chr18:12046686-12046697
3	CEBPB	chr18:12039763-12039999	IMR90	lung:	n/a	chr18:12039845-12039856
4	CEBPB	chr18:12041488-12041922	IMR90	lung:	n/a	n/a
5	CEBPB	chr18:12041661-12041872	A549	lung:	n/a	n/a
6	CHD2	chr18:12044269-12044270	HepG2	liver:	n/a	n/a
7	CTCF	chr18:12046466-12046681	HepG2	liver:	n/a	chr18:12046573-12046591
8	CTCF	chr18:12046543-12046603	MCF-7	breast:	n/a	chr18:12046573-12046591
9	CTCF	chr18:12046540-12046690	GM12869	blood:	n/a	chr18:12046573-12046591
10	CTCF	chr18:12046460-12046610	GM12873	blood:	n/a	chr18:12046573-12046591
11	CTCF	chr18:12046520-12046670	WERI-Rb-1	eye:	n/a	chr18:12046573-12046591
12	CTCF	chr18:12046480-12046630	HRPEpiC	eye:	n/a	chr18:12046573-12046591
13	CTCF	chr18:12045595-12045687	Lung_OC	lung:	n/a	n/a
14	CTCF	chr18:12046540-12046635	GM12891	blood:	n/a	chr18:12046573-12046591
15	CTCF	chr18:12046541-12046628	MCF-7	breast:	n/a	chr18:12046573-12046591
16	CTCF	chr18:12040160-12040310	AG09319	gingival:	n/a	n/a
17	CTCF	chr18:12046660-12046810	GM12871	blood:	n/a	n/a
18	CTCF	chr18:12046280-12046430	HepG2	liver:	n/a	n/a
19	CTCF	chr18:12046460-12046610	NHEK	skin:	n/a	chr18:12046573-12046591
20	CTCF	chr18:12046540-12046690	K562	blood:	n/a	chr18:12046573-12046591
21	CTCF	chr18:12046540-12046616	MCF-7	breast:	n/a	chr18:12046573-12046591
22	CTCF	chr18:12046310-12047405	A549	lung:	n/a	chr18:12046573-12046591 chr18:12047090-12047103
23	CTCF	chr18:12046540-12046690	HepG2	liver:	n/a	chr18:12046573-12046591
24	CTCF	chr18:12046700-12046850	GM12864	blood:	n/a	n/a
25	CTCF	chr18:12046507-12046649	Hela-S3	cervix:	n/a	chr18:12046573-12046591
26	CTCF	chr18:12046525-12046629	MCF-7	breast:	n/a	chr18:12046573-12046591
27	CTCF	chr18:12046558-12046582	MCF-7	breast:	n/a	n/a
28	CTCF	chr18:12046520-12046670	HepG2	liver:	n/a	chr18:12046573-12046591
29	CTCF	chr18:12046416-12046712	H1-hESC	embryonic stem cell:	n/a	chr18:12046573-12046591
30	CTCF	chr18:12046480-12046630	Hela-S3	cervix:	n/a	chr18:12046573-12046591
31	CTCF	chr18:12046460-12046610	HCPEpiC	choroid plexus:	n/a	chr18:12046573-12046591
32	CTCF	chr18:12041120-12041270	HPF	lung:	n/a	n/a
33	CTCF	chr18:12046524-12046603	HepG2	liver:	n/a	chr18:12046573-12046591
34	CTCF	chr18:12041720-12041870	HCPEpiC	choroid plexus:	n/a	n/a
35	CTCF	chr18:12046550-12046595	A549	lung:	n/a	chr18:12046573-12046591
36	CTCF	chr18:12046460-12046610	GM12875	blood:	n/a	chr18:12046573-12046591
37	CTCF	chr18:12046493-12046671	H1-hESC	embryonic stem cell:	n/a	chr18:12046573-12046591
38	CTCF	chr18:12046440-12046590	GM12873	blood:	n/a	n/a
39	E2F4	chr18:12041553-12041954	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr18:12045432-12045744	MCF10A-Er-Src	breast:	n/a	chr18:12045561-12045572
41	FOS	chr18:12045419-12045737	MCF10A-Er-Src	breast:	n/a	chr18:12045561-12045572
42	FOS	chr18:12045423-12045744	MCF10A-Er-Src	breast:	n/a	chr18:12045561-12045572
43	FOS	chr18:12041548-12041964	MCF10A-Er-Src	breast:	n/a	chr18:12041721-12041732
44	FOS	chr18:12041553-12041963	MCF10A-Er-Src	breast:	n/a	chr18:12041721-12041732
45	FOS	chr18:12045433-12045745	MCF10A-Er-Src	breast:	n/a	chr18:12045561-12045572
46	FOS	chr18:12045503-12045715	HUVEC	blood vessel:	n/a	chr18:12045561-12045572
47	FOS	chr18:12041521-12041918	HUVEC	blood vessel:	n/a	chr18:12041721-12041732
48	FOS	chr18:12041561-12041978	MCF10A-Er-Src	breast:	n/a	chr18:12041721-12041732
49	FOS	chr18:12041550-12041923	MCF10A-Er-Src	breast:	n/a	chr18:12041721-12041732
50	FOSL2	chr18:12041595-12041837	A549	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:12041672-12041722	HL-60	blood:	n/a
2	chr18:12041356-12041406	HCM	heart:	n/a
3	chr18:12041356-12041406	NHDF-neo	bronchial:	n/a
4	chr18:12041672-12041722	HEEpiC	esophagus:	n/a
5	chr18:12041356-12041406	GM19239	blood:	n/a
6	chr18:12041356-12041406	HNPCEpiC	eye:	n/a
7	chr18:12041672-12041722	BJ	skin:	n/a
8	chr18:12041672-12041722	HCT-116	colon:	n/a
9	chr18:12041672-12041722	AG09309	skin:	n/a
10	chr18:12041672-12041722	HRE	kidney:	n/a
11	chr18:12041672-12041722	ovcar-3	ovarian:	n/a
12	chr18:12041672-12041722	NH-A	brain:	n/a
13	chr18:12041356-12041406	AG09309	skin:	n/a
14	chr18:12041356-12041406	CMK	blood:	n/a
15	chr18:12041672-12041722	HCPEpiC	choroid plexus:	n/a
16	chr18:12041356-12041406	BE2_C	brain:	n/a
17	chr18:12041356-12041406	HMEC	breast:	n/a
18	chr18:12041672-12041722	NHBE	bronchial:	n/a
19	chr18:12041356-12041406	HCF	heart:	n/a
20	chr18:12041356-12041406	U87	brain:	n/a
21	chr18:12041672-12041722	Hepatocyte	liver:	n/a
22	chr18:12041672-12041722	U87	brain:	n/a
23	chr18:12041672-12041722	RPTEC	kidney:	n/a
24	chr18:12041672-12041722	LNCaP	prostate:	n/a
25	chr18:12041672-12041722	NB4	blood:	n/a
26	chr18:12041672-12041722	PANC-1	pancreas:	n/a
27	chr18:12041672-12041722	HRCEpiC	kidney:	n/a
28	chr18:12041356-12041406	HAEpiC	amniotic membrane:	n/a
29	chr18:12041672-12041722	AG04449	skin:	fetal
30	chr18:12041672-12041722	HCM	heart:	n/a
31	chr18:12041672-12041722	HMEC	breast:	n/a
32	chr18:12041672-12041722	GM19239	blood:	n/a
33	chr18:12041356-12041406	NB4	blood:	n/a
34	chr18:12041672-12041722	MCF-7	breast:	n/a
35	chr18:12041672-12041722	SKMC	muscle:	n/a
36	chr18:12041356-12041406	Hela-S3	cervix:	n/a
37	chr18:12041672-12041722	Jurkat	blood:	n/a
38	chr18:12041356-12041406	HRPEpiC	eye:	n/a
39	chr18:12041356-12041406	PFSK-1	brain:	n/a
40	chr18:12041672-12041722	PrEC	prostate:	n/a
41	chr18:12041356-12041406	ovcar-3	ovarian:	n/a
42	chr18:12041356-12041406	SKMC	muscle:	n/a
43	chr18:12041672-12041722	K562	blood:	n/a
44	chr18:12041672-12041722	HUVEC	blood vessel:	n/a
45	chr18:12041356-12041406	SK-N-SH_RA	brain:	n/a
46	chr18:12041356-12041406	MCF10A-Er-Src	breast:	n/a
47	chr18:12041672-12041722	Hela-S3	cervix:	n/a
48	chr18:12041672-12041722	MCF10A-Er-Src	breast:	n/a
49	chr18:12041356-12041406	K562	blood:	n/a
50	chr18:12041356-12041406	NHBE	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr18:11907841..11909998-chr18:12042409..12044684,2	MCF-7	breast:
2	chr18:11992964..11995381-chr18:12038056..12040567,2	MCF-7	breast:
3	chr18:12035639..12037274-chr18:12041657..12044195,2	MCF-7	breast:
4	chr18:12038572..12040680-chr18:12043555..12046070,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000266995	TF binding region
ENSG00000266995	CpG island
ENSG00000266995	chromatin interactions
ENSG00000273141	chromatin interactions
ENSG00000154889	chromatin interactions
ENSG00000266955	chromatin interactions

Extended variants
information (count: 261 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:261 , 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	rs187388555	chr18:12040011-12040012	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs567512059	chr18:12040014-12040015	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs374223434	chr18:12040047-12040048	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs578010714	chr18:12040070-12040071	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs545217062	chr18:12040144-12040145	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs560100750	chr18:12040150-12040151	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs573550891	chr18:12040197-12040198	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs190611526	chr18:12040219-12040220	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs368200687	chr18:12040222-12040223	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs371387675	chr18:12040272-12040273	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs375422558	chr18:12040273-12040274	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs55754026	chr18:12040282-12040283	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs562594667	chr18:12040283-12040284	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs56319012	chr18:12040284-12040285	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs28540878	chr18:12040306-12040307	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs561215361	chr18:12040312-12040313	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs531923871	chr18:12040339-12040340	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs550304526	chr18:12040367-12040368	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs534628946	chr18:12040374-12040375	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs146658277	chr18:12040401-12040402	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs372062592	chr18:12040422-12040423	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs547547240	chr18:12040428-12040429	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs565655063	chr18:12040472-12040473	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs529682773	chr18:12040481-12040482	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs543893708	chr18:12040510-12040511	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs548223700	chr18:12040514-12040515	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs182900084	chr18:12040536-12040537	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs536949375	chr18:12040537-12040538	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs558712579	chr18:12040538-12040539	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs4797611	chr18:12040540-12040541	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs538727081	chr18:12040541-12040542	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs8086525	chr18:12040602-12040603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs553822567	chr18:12040612-12040613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs368336859	chr18:12040641-12040642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs572222562	chr18:12040654-12040655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs10530914	chr18:12040658-12040659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs368215391	chr18:12040659-12040660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs398059051	chr18:12040664-12040665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs528503490	chr18:12040762-12040763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs545082681	chr18:12040796-12040797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs140423561	chr18:12040820-12040821	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs554549822	chr18:12040826-12040827	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs144136089	chr18:12040867-12040868	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs543804026	chr18:12040904-12040905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs2851918	chr18:12040933-12040934	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs575428915	chr18:12040958-12040959	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs532622715	chr18:12040964-12040965	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs541663247	chr18:12040995-12040996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs150985151	chr18:12041024-12041025	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs34966148	chr18:12041025-12041026	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Intellectual disability	22102821	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Acute myeloid leukemia	16864856	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Kartagener syndrome	16639409	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Cancer	21183584	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Human rectal carcinomas	16397240	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16272173	CNVD
Colorectal cancer	19150955	CNVD
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
Autism	20808228	CNVD
lymphocytic leukemia	21291569	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	17377590	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Developmental delay	21147756	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16620391	CNVD
Myelofibrosis	22110671	CNVD
Retinoblastoma	21504564	CNVD
Glioma	17123091	CNVD
Neurodevelopmental disorder	22521361	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Autism	20531469	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:87 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:12039200-12040800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr18:12039400-12040200	Enhancers	HepG2	liver
3	chr18:12039400-12041000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr18:12039400-12041000	Weak transcription	HSMM	muscle
5	chr18:12039400-12041000	Weak transcription	NHDF-Ad	bronchial
6	chr18:12039400-12041000	Weak transcription	Osteobl	bone
7	chr18:12039400-12041200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr18:12039400-12041200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr18:12039400-12041200	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr18:12039400-12041200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr18:12039400-12041200	Weak transcription	A549	lung
12	chr18:12039400-12041200	Weak transcription	HMEC	breast
13	chr18:12039400-12041200	Weak transcription	HSMMtube	muscle
14	chr18:12039400-12041200	Weak transcription	NH-A	brain
15	chr18:12039400-12041200	Weak transcription	NHLF	lung
16	chr18:12039400-12041400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr18:12039400-12041400	Weak transcription	NHEK	skin
18	chr18:12039400-12042600	Weak transcription	GM12878-XiMat	blood
19	chr18:12039400-12044800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr18:12039400-12045800	Weak transcription	Pancreas	Pancrea
21	chr18:12039400-12047000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr18:12039400-12047400	Weak transcription	Gastric	stomach
23	chr18:12039400-12048400	Weak transcription	Right Ventricle	heart
24	chr18:12039600-12041000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr18:12039800-12041000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr18:12039800-12041000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr18:12040800-12041600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr18:12041000-12041600	Enhancers	HSMM	muscle
29	chr18:12041000-12042400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr18:12041000-12042400	Enhancers	NHDF-Ad	bronchial
31	chr18:12041000-12042400	Enhancers	Osteobl	bone
32	chr18:12041000-12042600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr18:12041000-12042800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr18:12041000-12042800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr18:12041200-12042000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr18:12041200-12042000	Enhancers	HSMMtube	muscle
37	chr18:12041200-12042000	Enhancers	NH-A	brain
38	chr18:12041200-12042200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr18:12041200-12042200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr18:12041200-12042200	Enhancers	Muscle Satellite Cultured Cells	--
41	chr18:12041200-12042400	Enhancers	HMEC	breast
42	chr18:12041200-12042600	Enhancers	A549	lung
43	chr18:12041200-12042600	Enhancers	NHLF	lung
44	chr18:12041400-12041600	Enhancers	Hela-S3	cervix
45	chr18:12041400-12042000	Enhancers	NHEK	skin
46	chr18:12041400-12042400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr18:12042000-12044400	Weak transcription	NH-A	brain
48	chr18:12042000-12048600	Weak transcription	HSMMtube	muscle
49	chr18:12042400-12044400	Weak transcription	Osteobl	bone
50	chr18:12042400-12045200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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