Variant report

Variant	esv3444563
Chromosome Location	chr18:44541054-44558652
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:435)
CpG islands
(count:978)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:435 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL11A	chr18:44549353-44549656	GM12878	blood:	n/a	n/a
2	BCL11A	chr18:44555313-44555571	GM12878	blood:	n/a	n/a
3	BHLHE40	chr18:44552793-44553372	HepG2	liver:	n/a	n/a
4	BHLHE40	chr18:44547816-44548107	HepG2	liver:	n/a	n/a
5	BHLHE40	chr18:44553731-44554022	HepG2	liver:	n/a	n/a
6	BHLHE40	chr18:44546870-44547457	HepG2	liver:	n/a	n/a
7	CEBPB	chr18:44540976-44541166	K562	blood:	n/a	n/a
8	CTCF	chr18:44552256-44552456	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr18:44552308-44552416	Gliobla	brain:	n/a	n/a
10	CTCF	chr18:44550232-44550622	K562	blood:	n/a	n/a
11	CTCF	chr18:44551550-44551578	LNCaP	prostate:	n/a	n/a
12	CTCF	chr18:44551620-44551770	SK-N-SH_RA	brain:	n/a	n/a
13	CTCF	chr18:44551208-44551848	K562	blood:	n/a	n/a
14	CTCF	chr18:44550236-44550581	K562	blood:	n/a	n/a
15	CTCF	chr18:44551620-44551770	AG10803	skin:	n/a	n/a
16	CTCF	chr18:44547080-44547230	HEK293	kidney:	n/a	n/a
17	CTCF	chr18:44557382-44557538	LNCaP	prostate:	n/a	n/a
18	CTCF	chr18:44557309-44557626	K562	blood:	n/a	n/a
19	CTCF	chr18:44557269-44557573	K562	blood:	n/a	n/a
20	CTCF	chr18:44551296-44551735	K562	blood:	n/a	n/a
21	CTCF	chr18:44547060-44547210	WI-38	lung:	n/a	n/a
22	CTCF	chr18:44552060-44552210	HFF-Myc	foreskin:	n/a	n/a
23	CTCF	chr18:44557427-44557512	GM20000	blood:	n/a	n/a
24	CTCF	chr18:44556144-44556568	K562	blood:	n/a	n/a
25	CTCF	chr18:44551620-44551770	HepG2	liver:	n/a	n/a
26	CTCF	chr18:44554460-44554610	AoAF	blood vessel:	n/a	n/a
27	CTCF	chr18:44552060-44552210	HepG2	liver:	n/a	n/a
28	CTCF	chr18:44552363-44552374	A549	lung:	n/a	n/a
29	CTCF	chr18:44545700-44545850	HBMEC	blood vessel:	n/a	n/a
30	CTCF	chr18:44544285-44544576	K562	blood:	n/a	n/a
31	CTCF	chr18:44547060-44547210	HAc	cerebellar:	n/a	n/a
32	CTCF	chr18:44547080-44547230	HBMEC	blood vessel:	n/a	n/a
33	CTCF	chr18:44546424-44546457	LNCaP	prostate:	n/a	n/a
34	CTCF	chr18:44552060-44552210	HA-sp	spinal cord:	n/a	n/a
35	CTCF	chr18:44554040-44554190	HA-sp	spinal cord:	n/a	n/a
36	CTCF	chr18:44547060-44547210	GM12868	blood:	n/a	n/a
37	CTCF	chr18:44545599-44545658	LNCaP	prostate:	n/a	n/a
38	CTCF	chr18:44546361-44546519	HepG2	liver:	n/a	n/a
39	CTCF	chr18:44551498-44551626	LNCaP	prostate:	n/a	n/a
40	CTCF	chr18:44546352-44546572	K562	blood:	n/a	n/a
41	CTCF	chr18:44551620-44551770	HEEpiC	esophagus:	n/a	n/a
42	CTCF	chr18:44546374-44546519	Gliobla	brain:	n/a	n/a
43	CTCF	chr18:44557203-44557231	Kidney_OC	kidney:	n/a	n/a
44	CTCF	chr18:44557210-44557657	K562	blood:	n/a	n/a
45	CTCF	chr18:44544278-44544695	K562	blood:	n/a	n/a
46	CTCF	chr18:44546337-44546544	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr18:44545720-44545870	HepG2	liver:	n/a	n/a
48	CTCF	chr18:44557477-44557530	Kidney_OC	kidney:	n/a	n/a
49	CTCF	chr18:44547060-44547210	GM12867	blood:	n/a	n/a
50	CTCF	chr18:44556180-44556382	K562	blood:	n/a	n/a

(count:978 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:44557635-44557685	HNPCEpiC	eye:	n/a
2	chr18:44547161-44547211	T-47D	breast:	n/a
3	chr18:44557635-44557685	HNPCEpiC	eye:	n/a
4	chr18:44547161-44547211	T-47D	breast:	n/a
5	chr18:44544982-44545032	NT2-D1	testis:	n/a
6	chr18:44543259-44543309	BE2_C	brain:	n/a
7	chr18:44557635-44557685	RPTEC	kidney:	n/a
8	chr18:44557819-44557869	BJ	skin:	n/a
9	chr18:44547161-44547211	A549	lung:	n/a
10	chr18:44557673-44557723	NH-A	brain:	n/a
11	chr18:44555308-44555358	HRE	kidney:	n/a
12	chr18:44557732-44557782	U87	brain:	n/a
13	chr18:44545794-44545844	Hepatocyte	liver:	n/a
14	chr18:44551719-44551769	ProgFib	skin:	n/a
15	chr18:44551719-44551769	NB4	blood:	n/a
16	chr18:44551732-44551782	HL-60	blood:	n/a
17	chr18:44555308-44555358	BJ	skin:	n/a
18	chr18:44557647-44557697	LNCaP	prostate:	n/a
19	chr18:44557819-44557869	GM12891	blood:	n/a
20	chr18:44541383-44541433	AG09319	gingival:	n/a
21	chr18:44545794-44545844	RPTEC	kidney:	n/a
22	chr18:44545807-44545857	HCPEpiC	choroid plexus:	n/a
23	chr18:44557635-44557685	AG09319	gingival:	n/a
24	chr18:44557732-44557782	HCPEpiC	choroid plexus:	n/a
25	chr18:44557673-44557723	GM06990	blood:	n/a
26	chr18:44553084-44553134	GM12892	blood:	n/a
27	chr18:44557819-44557869	HCF	heart:	n/a
28	chr18:44557819-44557869	AG09309	skin:	n/a
29	chr18:44557819-44557869	SK-N-SH_RA	brain:	n/a
30	chr18:44545807-44545857	ovcar-3	ovarian:	n/a
31	chr18:44545807-44545857	BE2_C	brain:	n/a
32	chr18:44557647-44557697	AG04450	lung:	fetal
33	chr18:44544982-44545032	HCPEpiC	choroid plexus:	n/a
34	chr18:44543612-44543662	HCM	heart:	n/a
35	chr18:44557819-44557869	HNPCEpiC	eye:	n/a
36	chr18:44557647-44557697	NT2-D1	testis:	n/a
37	chr18:44557819-44557869	SKMC	muscle:	n/a
38	chr18:44551719-44551769	HCPEpiC	choroid plexus:	n/a
39	chr18:44545807-44545857	HAEpiC	amniotic membrane:	n/a
40	chr18:44543259-44543309	H1-hESC	embryonic stem cell:	embryo
41	chr18:44547161-44547211	HRE	kidney:	n/a
42	chr18:44557635-44557685	HRPEpiC	eye:	n/a
43	chr18:44543259-44543309	GM12878	blood:	n/a
44	chr18:44543612-44543662	AG04450	lung:	fetal
45	chr18:44557673-44557723	AG04450	lung:	fetal
46	chr18:44557647-44557697	HPAEpiC	pulmonary alveolar:	n/a
47	chr18:44557635-44557685	NHBE	bronchial:	n/a
48	chr18:44557732-44557782	SK-N-SH_RA	brain:	n/a
49	chr18:44551719-44551769	NHBE	bronchial:	n/a
50	chr18:44551732-44551782	NHDF-neo	bronchial:	n/a

No data

Variant related genes	Relation type
TCEB3CL2	TF binding region
TCEB3CL	TF binding region
TCEB3C	TF binding region
TCEB3CL2	CpG island
TCEB3CL	CpG island
TCEB3C	CpG island

Extended variants
information (count: 408 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:408 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs368204218	chr18:44541114-44541115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs187865568	chr18:44541138-44541139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs547606020	chr18:44541167-44541168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs377567695	chr18:44541183-44541184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs149800236	chr18:44541218-44541219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs192432077	chr18:44541219-44541220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs548955188	chr18:44541238-44541239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs568806444	chr18:44541249-44541250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs537925416	chr18:44541254-44541255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs535570622	chr18:44541257-44541258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs577831159	chr18:44541279-44541280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs533948828	chr18:44541292-44541293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs574983911	chr18:44541310-44541311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs549070328	chr18:44541384-44541385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs183914784	chr18:44541402-44541403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs562876539	chr18:44541420-44541421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs576390602	chr18:44541496-44541497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs545400778	chr18:44541502-44541503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs188466166	chr18:44541524-44541525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs527781362	chr18:44541537-44541538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs145787418	chr18:44541551-44541552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs193019460	chr18:44541560-44541561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs373212764	chr18:44541564-44541565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs184816110	chr18:44541591-44541592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs550235204	chr18:44541595-44541596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs568820181	chr18:44541600-44541601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs1942248	chr18:44541614-44541615	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs551380887	chr18:44541617-44541618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs554420636	chr18:44541626-44541627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs60844368	chr18:44541649-44541650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs56974235	chr18:44541652-44541653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs188646713	chr18:44541655-44541656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs191611933	chr18:44541665-44541666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs554003822	chr18:44541710-44541711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs113417822	chr18:44541716-44541717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs183712835	chr18:44541727-44541728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs72919273	chr18:44541735-44541736	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs386802913	chr18:44541736-44541737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs576308086	chr18:44541739-44541740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs146881768	chr18:44541754-44541755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs377733969	chr18:44541755-44541756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs2156047	chr18:44541763-44541764	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs558919024	chr18:44541773-44541774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs530724384	chr18:44541777-44541778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs541175370	chr18:44541810-44541811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs561125206	chr18:44541820-44541821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs148529143	chr18:44541830-44541831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs189611846	chr18:44541832-44541833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs142832071	chr18:44541836-44541837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs532847115	chr18:44541857-44541858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
lymphocytic leukemia	21291569	CNVD
Barrett''s syndrome	19417022	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
18q deletion syndrome	19533772	CNVD
Acute myeloid leukemia	16864856	CNVD
Colorectal cancer	21102417	CNVD
Colorectal cancer	20709793	CNVD
Pancreatic cancer	21811562	CNVD
Basal cell lymphoma	21115979	CNVD
Mucosa-associated lymphoid tissue lymphomas	21459788	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
colon cancer	17210682	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	16573809	CNVD
Autism	16446308	CNVD
Colorectal cancer	19359472	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	18056178	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
small cell lung cancer	20016488	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Colorectal cancer	21297112	CNVD
Breast cancer	17603634	CNVD
Thyroid cancer	19087340	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Colorectal cancer	19150955	CNVD
Acute myeloid leukemia	21251322	CNVD
Colorectal cancer	16912164	CNVD
Lung cancer	18438408	CNVD
Seminomas	18059402	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
prenatal diagnosis	22389664	CNVD
Medulloblastoma	16783165	CNVD
Neuroblastoma	21508638	CNVD
Myelofibrosis	22110671	CNVD
Multiple myeloma	16461302	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Pilomyxoid astrocytoma	17436254	CNVD
Mental retardation	21062444	CNVD
Cancer	21183584	CNVD
Burkitt''s lymphoma	18698080	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Cancer	17160897	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Gastric cancer	16891809	CNVD
Idiopathic thrombocytopenic purpura	19566914	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16774939	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Lung cancer	21569311	CNVD
small cell lung cancer	17426248	CNVD
Cancer	20164919	CNVD
Intellectual disability	21811512	CNVD
Lung adenocarcinoma	21935476	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21509527	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:46 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:44538200-44551600	Weak transcription	Gastric	stomach
2	chr18:44544400-44545000	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr18:44545000-44545200	Enhancers	H1 Cell Line	embryonic stem cell
4	chr18:44545000-44545200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr18:44545000-44545200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr18:44545000-44545200	ZNF genes & repeats	Ovary	ovary
7	chr18:44545200-44547200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr18:44545200-44552000	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr18:44546400-44547000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr18:44547000-44547400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr18:44547000-44547400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr18:44547000-44547400	ZNF genes & repeats	Fetal Stomach	stomach
13	chr18:44547200-44547400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr18:44547200-44547400	ZNF genes & repeats	Fetal Brain Female	brain
15	chr18:44547200-44547400	Bivalent Enhancer	HepG2	liver
16	chr18:44547400-44552000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr18:44547400-44552000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr18:44550200-44556600	Weak transcription	Fetal Lung	lung
19	chr18:44551600-44551800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr18:44551600-44551800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr18:44551800-44553000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr18:44551800-44553000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr18:44552000-44552200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr18:44552000-44552200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr18:44552000-44552400	Enhancers	H1 Cell Line	embryonic stem cell
26	chr18:44552000-44552400	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr18:44552000-44552400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr18:44552200-44552400	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr18:44552400-44555000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
30	chr18:44553000-44553200	Enhancers	Right Ventricle	heart
31	chr18:44553000-44553600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr18:44553000-44553600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr18:44553200-44562600	Weak transcription	Right Ventricle	heart
34	chr18:44553600-44554000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr18:44553600-44555000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr18:44554000-44555400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr18:44554000-44555400	ZNF genes & repeats	Stomach Smooth Muscle	stomach
38	chr18:44554600-44555400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
39	chr18:44555000-44555400	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
40	chr18:44555000-44555400	Genic enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr18:44555000-44555400	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
42	chr18:44555200-44555400	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr18:44555400-44560000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr18:44555400-44560000	Weak transcription	Duodenum Smooth Muscle	Duodenum
45	chr18:44555400-44561400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr18:44555400-44563200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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