Variant report

Variant	nsv1009680
Chromosome Location	chr2:52185751-52307426
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	BACH1	chr2:52196504-52196867	K562	blood:	n/a	n/a
2	BACH1	chr2:52196504-52196856	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr2:52208991-52209296	H1-hESC	embryonic stem cell:	n/a	chr2:52209155-52209169
4	BACH1	chr2:52185802-52185829	K562	blood:	n/a	n/a
5	BATF	chr2:52304385-52304596	GM12878	blood:	n/a	n/a
6	BRCA1	chr2:52259388-52259484	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr2:52222380-52222693	A549	lung:	n/a	chr2:52222524-52222537 chr2:52222524-52222535
8	CEBPB	chr2:52257247-52257351	A549	lung:	n/a	n/a
9	CEBPB	chr2:52221635-52221866	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr2:52227686-52227965	IMR90	lung:	n/a	n/a
11	CEBPB	chr2:52194035-52194142	H1-hESC	embryonic stem cell:	n/a	chr2:52194121-52194132
12	CEBPB	chr2:52222480-52222649	K562	blood:	n/a	chr2:52222524-52222537 chr2:52222524-52222535
13	CEBPB	chr2:52222336-52222779	IMR90	lung:	n/a	chr2:52222749-52222761 chr2:52222524-52222537 chr2:52222524-52222535
14	CEBPB	chr2:52284303-52284564	A549	lung:	n/a	chr2:52284412-52284421 chr2:52284412-52284423 chr2:52284410-52284423 chr2:52284410-52284421
15	CEBPB	chr2:52231382-52231629	HepG2	liver:	n/a	n/a
16	CEBPB	chr2:52215249-52215477	A549	lung:	n/a	n/a
17	CEBPB	chr2:52284272-52284554	IMR90	lung:	n/a	chr2:52284412-52284421 chr2:52284412-52284423 chr2:52284410-52284423 chr2:52284410-52284421
18	CEBPB	chr2:52222385-52222704	HepG2	liver:	n/a	chr2:52222524-52222537 chr2:52222524-52222535
19	CEBPB	chr2:52194008-52194207	A549	lung:	n/a	chr2:52194121-52194132
20	CEBPB	chr2:52262546-52262937	Hela-S3	cervix:	n/a	chr2:52262762-52262773
21	CEBPB	chr2:52282155-52282341	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr2:52263141-52263506	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr2:52231435-52231623	A549	lung:	n/a	n/a
24	CEBPB	chr2:52193961-52194229	Hela-S3	cervix:	n/a	chr2:52194121-52194132
25	CEBPB	chr2:52215321-52215434	HepG2	liver:	n/a	n/a
26	CEBPB	chr2:52193951-52194247	HepG2	liver:	n/a	chr2:52194121-52194132
27	CEBPB	chr2:52306793-52307085	HepG2	liver:	n/a	chr2:52306925-52306936 chr2:52306927-52306936
28	CEBPB	chr2:52203479-52204403	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr2:52284332-52284595	HepG2	liver:	n/a	chr2:52284412-52284421 chr2:52284412-52284423 chr2:52284410-52284423 chr2:52284410-52284421
30	CEBPB	chr2:52222367-52222678	H1-hESC	embryonic stem cell:	n/a	chr2:52222524-52222537 chr2:52222524-52222535
31	CEBPB	chr2:52306763-52307073	IMR90	lung:	n/a	chr2:52306925-52306936 chr2:52306927-52306936
32	CEBPB	chr2:52222401-52222715	Hela-S3	cervix:	n/a	chr2:52222524-52222537 chr2:52222524-52222535
33	CEBPB	chr2:52262597-52262865	HepG2	liver:	n/a	chr2:52262762-52262773
34	CEBPB	chr2:52193973-52194288	IMR90	lung:	n/a	chr2:52194121-52194132
35	CTCF	chr2:52224825-52224978	Gliobla	brain:	n/a	n/a
36	CTCF	chr2:52261840-52261990	AG10803	skin:	n/a	n/a
37	CTCF	chr2:52261800-52261950	HMEC	breast:	n/a	n/a
38	CTCF	chr2:52217860-52218010	BE2_C	brain:	n/a	n/a
39	CTCF	chr2:52224800-52224950	HMF	breast:	n/a	n/a
40	CTCF	chr2:52224840-52224990	HCT-116	colon:	n/a	n/a
41	CTCF	chr2:52224740-52224890	RPTEC	kidney:	n/a	n/a
42	CTCF	chr2:52261884-52261929	Pancreas_OC	pancreas:	n/a	n/a
43	CTCF	chr2:52261800-52261950	AoAF	blood vessel:	n/a	n/a
44	CTCF	chr2:52224864-52224968	K562	blood:	n/a	n/a
45	CTCF	chr2:52192460-52192610	HBMEC	blood vessel:	n/a	n/a
46	CTCF	chr2:52261877-52261988	HUVEC	blood vessel:	n/a	n/a
47	CTCF	chr2:52224820-52224970	WERI-Rb-1	eye:	n/a	n/a
48	CTCF	chr2:52224820-52224970	AoAF	blood vessel:	n/a	n/a
49	CTCF	chr2:52261820-52261970	AoAF	blood vessel:	n/a	n/a
50	CTCF	chr2:52224800-52224950	HPAF	blood vessel:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:52235062-52235112	PrEC	prostate:	n/a
2	chr2:52221668-52221718	H1-hESC	embryonic stem cell:	embryo
3	chr2:52272404-52272454	ECC-1	luminal epithelium:	n/a
4	chr2:52221668-52221718	BJ	skin:	n/a
5	chr2:52272404-52272454	MCF10A-Er-Src	breast:	n/a
6	chr2:52235062-52235112	CMK	blood:	n/a
7	chr2:52235062-52235112	HCPEpiC	choroid plexus:	n/a
8	chr2:52221668-52221718	PrEC	prostate:	n/a
9	chr2:52234104-52234154	Caco-2	colon:	n/a
10	chr2:52281777-52281827	NT2-D1	testis:	n/a
11	chr2:52281777-52281827	AG10803	skin:	n/a
12	chr2:52235062-52235112	AG10803	skin:	n/a
13	chr2:52221668-52221718	U87	brain:	n/a
14	chr2:52281777-52281827	HEEpiC	esophagus:	n/a
15	chr2:52235062-52235112	BJ	skin:	n/a
16	chr2:52281777-52281827	SK-N-SH	brain:	n/a
17	chr2:52221668-52221718	CMK	blood:	n/a
18	chr2:52272404-52272454	U87	brain:	n/a
19	chr2:52281777-52281827	MCF-7	breast:	n/a
20	chr2:52272404-52272454	NB4	blood:	n/a
21	chr2:52221668-52221718	AG09309	skin:	n/a
22	chr2:52272404-52272454	Hepatocyte	liver:	n/a
23	chr2:52281777-52281827	HRPEpiC	eye:	n/a
24	chr2:52234104-52234154	AG09309	skin:	n/a
25	chr2:52272404-52272454	IMR90	lung:	fetal
26	chr2:52281777-52281827	HepG2	liver:	n/a
27	chr2:52281777-52281827	Caco-2	colon:	n/a
28	chr2:52272404-52272454	BE2_C	brain:	n/a
29	chr2:52234104-52234154	CMK	blood:	n/a
30	chr2:52235062-52235112	SKMC	muscle:	n/a
31	chr2:52235062-52235112	HCF	heart:	n/a
32	chr2:52272404-52272454	AG04450	lung:	fetal
33	chr2:52235062-52235112	SK-N-SH_RA	brain:	n/a
34	chr2:52272404-52272454	MCF-7	breast:	n/a
35	chr2:52221668-52221718	HCT-116	colon:	n/a
36	chr2:52221668-52221718	HCF	heart:	n/a
37	chr2:52272404-52272454	HRE	kidney:	n/a
38	chr2:52221668-52221718	HRE	kidney:	n/a
39	chr2:52221668-52221718	RPTEC	kidney:	n/a
40	chr2:52281777-52281827	GM12891	blood:	n/a
41	chr2:52272404-52272454	HAEpiC	amniotic membrane:	n/a
42	chr2:52235062-52235112	H1-hESC	embryonic stem cell:	embryo
43	chr2:52281777-52281827	PANC-1	pancreas:	n/a
44	chr2:52235062-52235112	NH-A	brain:	n/a
45	chr2:52272404-52272454	ovcar-3	ovarian:	n/a
46	chr2:52272404-52272454	AG09319	gingival:	n/a
47	chr2:52221668-52221718	SAEC	small airway:	n/a
48	chr2:52221668-52221718	ovcar-3	ovarian:	n/a
49	chr2:52281777-52281827	MCF10A-Er-Src	breast:	n/a
50	chr2:52221668-52221718	NHBE	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:52239790..52242380-chr2:52244407..52246519,2	K562	blood:
2	chr2:52261393..52263430-chr2:52272675..52274372,2	K562	blood:
3	chr2:50763606..50764181-chr2:52224822..52225393,2	MCF-7	breast:
4	chr2:50973459..50974271-chr2:52224493..52225477,4	MCF-7	breast:
5	chr2:52261393..52263430-chr2:52272675..52274372,2	K562	blood:
6	chr2:52239790..52242380-chr2:52244407..52246519,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHAC2-11	chr2:52302622-52302775	NONHSAT070666
2	lnc-CHAC2-11	chr2:52298493-52298559	NONHSAT070666
3	lnc-CHAC2-11	chr2:52304140-52304335	NONHSAT070666

Variant related genes	Relation type
ZNF863P	TF binding region
ZNF863P	CpG island

Extended variants
information (count: 2640 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:2640 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs537927802	chr2:52185786-52185787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs74759494	chr2:52185801-52185802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs77388900	chr2:52185811-52185812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs201616849	chr2:52185825-52185826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs188456166	chr2:52185831-52185832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs193038011	chr2:52185833-52185834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs142871993	chr2:52185848-52185849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs34925056	chr2:52185858-52185859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs368663315	chr2:52185859-52185860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs555766584	chr2:52185901-52185902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs577238063	chr2:52185922-52185923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs544565549	chr2:52185926-52185927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs199766406	chr2:52185956-52185957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs144117148	chr2:52185957-52185958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs116300390	chr2:52185969-52185970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs573480948	chr2:52186012-52186013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs540514569	chr2:52186042-52186043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs12469398	chr2:52186043-52186044	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs549255494	chr2:52186124-52186125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs79444278	chr2:52186145-52186146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs551077048	chr2:52186156-52186157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs562937080	chr2:52186213-52186214	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs533373072	chr2:52186215-52186216	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs551751427	chr2:52186247-52186248	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs528614296	chr2:52186284-52186285	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs566818196	chr2:52186318-52186319	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs182313504	chr2:52186325-52186326	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs376768504	chr2:52186326-52186327	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs185231038	chr2:52186327-52186328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs151078658	chr2:52186332-52186333	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs374239099	chr2:52186333-52186334	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs114252608	chr2:52186368-52186369	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs75439001	chr2:52186372-52186373	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs74467060	chr2:52186399-52186400	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs577274888	chr2:52186412-52186413	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs538296186	chr2:52186435-52186436	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs114788410	chr2:52186474-52186475	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs146027583	chr2:52186521-52186522	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs540900462	chr2:52186536-52186537	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs555757854	chr2:52186552-52186553	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs190089979	chr2:52186616-52186617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs529746965	chr2:52186629-52186630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs138822596	chr2:52186651-52186652	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs373429821	chr2:52186656-52186657	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs80205746	chr2:52186657-52186658	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs114903627	chr2:52186660-52186661	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs181165057	chr2:52186683-52186684	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs7609543	chr2:52186748-52186749	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs554129611	chr2:52186774-52186775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs527616019	chr2:52186805-52186806	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	16272173	CNVD
Lung cancer	17297452	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Schizophrenia	20433910	CNVD
Autism	21701786	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Austim spectrum disorder	21302340	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	20553308	CNVD
Autism	22241247	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Retinoblastoma	22278416	CNVD
Cancer	21183584	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	18768390	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	18940311	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18945720	CNVD
Schizophrenia	19571808	CNVD
Prostate cancer	16573809	CNVD
Neuroticism	17667963	CNVD
Schizophrenia	19443537	CNVD
Schizophrenia	19546859	CNVD
Autism	17322880	CNVD
Lung cancer	17086460	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Hereditary non-polyposis colorectal cancer	19566914	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Bipolar disorder	19114987	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:150 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:52182000-52186400	Weak transcription	NHDF-Ad	bronchial
2	chr2:52182600-52186200	Weak transcription	Osteobl	bone
3	chr2:52186200-52188400	Enhancers	Osteobl	bone
4	chr2:52186400-52186600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr2:52186400-52188400	Enhancers	NHDF-Ad	bronchial
6	chr2:52186600-52187200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr2:52187200-52188400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr2:52187200-52188400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr2:52187400-52188200	Enhancers	NH-A	brain
10	chr2:52188000-52188400	Enhancers	HMEC	breast
11	chr2:52188400-52192200	Weak transcription	Osteobl	bone
12	chr2:52192200-52192600	Enhancers	Osteobl	bone
13	chr2:52192200-52192800	Enhancers	Pancreatic Islets	Pancreatic Islet
14	chr2:52203000-52204400	Enhancers	Hela-S3	cervix
15	chr2:52203800-52204200	Enhancers	Osteobl	bone
16	chr2:52206600-52207000	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr2:52207000-52207400	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr2:52209000-52209400	Active TSS	A549	lung
19	chr2:52214000-52214400	Enhancers	Fetal Brain Male	brain
20	chr2:52217800-52218000	Enhancers	Left Ventricle	heart
21	chr2:52217800-52218600	Enhancers	Fetal Heart	heart
22	chr2:52218000-52225800	Weak transcription	Left Ventricle	heart
23	chr2:52218600-52220800	Weak transcription	Fetal Heart	heart
24	chr2:52220800-52222400	Enhancers	NHDF-Ad	bronchial
25	chr2:52220800-52222800	Enhancers	Fetal Heart	heart
26	chr2:52221000-52222400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr2:52221000-52222600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr2:52221000-52222600	Enhancers	NHLF	lung
29	chr2:52221000-52222800	Enhancers	NH-A	brain
30	chr2:52221000-52222800	Enhancers	Osteobl	bone
31	chr2:52221200-52221400	Enhancers	Fetal Brain Male	brain
32	chr2:52221200-52222200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr2:52221200-52222400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr2:52221200-52222400	Enhancers	Hela-S3	cervix
35	chr2:52221400-52222400	Weak transcription	Fetal Brain Male	brain
36	chr2:52221400-52224200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr2:52221600-52222400	Enhancers	Muscle Satellite Cultured Cells	--
38	chr2:52221600-52222800	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr2:52221800-52223800	Enhancers	HUVEC	blood vessel
40	chr2:52222200-52222600	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr2:52222200-52223800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr2:52222400-52222600	Enhancers	Fetal Brain Male	brain
43	chr2:52222400-52223600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr2:52222400-52223600	Weak transcription	Muscle Satellite Cultured Cells	--
45	chr2:52222400-52223600	Weak transcription	NHDF-Ad	bronchial
46	chr2:52222400-52225400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr2:52222600-52223600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr2:52222600-52223800	Weak transcription	NHLF	lung
49	chr2:52222800-52223200	Weak transcription	NH-A	brain
50	chr2:52222800-52223200	Weak transcription	Osteobl	bone

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