Variant report

Variant	nsv430836
Chromosome Location	chr2:37936138-38003485
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:700)
CpG islands
(count:550)
Chromatin interactive
region (count:23)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:700 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:37940290-37940750	K562	blood:	n/a	n/a
2	ARID3A	chr2:37945884-37946232	K562	blood:	n/a	n/a
3	ARID3A	chr2:37991365-37991558	K562	blood:	n/a	n/a
4	ATF1	chr2:37938545-37938858	K562	blood:	n/a	n/a
5	ATF1	chr2:37940479-37940807	K562	blood:	n/a	n/a
6	ATF1	chr2:37945872-37946265	K562	blood:	n/a	n/a
7	ATF3	chr2:37995433-37996168	A549	lung:	n/a	n/a
8	ATF3	chr2:37995406-37996129	A549	lung:	n/a	n/a
9	BCL11A	chr2:37940546-37940813	GM12878	blood:	n/a	n/a
10	BCL11A	chr2:37962705-37962895	GM12878	blood:	n/a	n/a
11	BCL3	chr2:37995243-37996336	A549	lung:	n/a	n/a
12	BCL3	chr2:37995811-37996081	GM12878	blood:	n/a	n/a
13	BCL3	chr2:37993027-37993826	A549	lung:	n/a	chr2:37993597-37993606
14	BCL3	chr2:37995167-37996320	A549	lung:	n/a	n/a
15	BCL3	chr2:37984248-37984605	GM12878	blood:	n/a	n/a
16	BHLHE40	chr2:37938610-37938663	K562	blood:	n/a	n/a
17	BHLHE40	chr2:37945886-37946387	K562	blood:	n/a	n/a
18	BHLHE40	chr2:37991364-37991559	K562	blood:	n/a	n/a
19	CBX3	chr2:37945729-37946316	K562	blood:	n/a	n/a
20	CCNT2	chr2:37945975-37946199	K562	blood:	n/a	n/a
21	CCNT2	chr2:37940581-37940741	K562	blood:	n/a	n/a
22	CEBPB	chr2:37993064-37993861	A549	lung:	n/a	n/a
23	CEBPB	chr2:37958768-37959040	IMR90	lung:	n/a	chr2:37958919-37958930
24	CEBPB	chr2:37995096-37996236	A549	lung:	n/a	n/a
25	CEBPB	chr2:37948104-37948290	A549	lung:	n/a	n/a
26	CEBPB	chr2:37980414-37980446	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr2:37958731-37959009	MCF-7	breast:	n/a	chr2:37958919-37958930 chr2:37958758-37958766
28	CEBPB	chr2:37948155-37948260	HepG2	liver:	n/a	n/a
29	CEBPB	chr2:37958770-37959005	Hela-S3	cervix:	n/a	chr2:37958919-37958930
30	CEBPB	chr2:37995107-37996126	IMR90	lung:	n/a	n/a
31	CEBPB	chr2:37958749-37959043	HepG2	liver:	n/a	chr2:37958919-37958930 chr2:37958758-37958766
32	CEBPB	chr2:37977395-37977710	MCF-7	breast:	n/a	n/a
33	CEBPB	chr2:37977492-37977692	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr2:37962124-37962469	IMR90	lung:	n/a	n/a
35	CEBPB	chr2:37940535-37940788	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr2:37980323-37980575	A549	lung:	n/a	n/a
37	CEBPB	chr2:37979966-37980544	IMR90	lung:	n/a	n/a
38	CEBPB	chr2:37938535-37938821	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr2:37979935-37980527	HepG2	liver:	n/a	n/a
40	CEBPB	chr2:37945981-37946153	K562	blood:	n/a	n/a
41	CEBPB	chr2:37977474-37977568	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr2:37977457-37977649	K562	blood:	n/a	n/a
43	CEBPB	chr2:37995436-37996046	A549	lung:	n/a	n/a
44	CEBPB	chr2:37995384-37995863	MCF-7	breast:	n/a	n/a
45	CEBPB	chr2:37958826-37959080	K562	blood:	n/a	chr2:37958919-37958930
46	CEBPB	chr2:37980380-37980532	K562	blood:	n/a	n/a
47	CEBPB	chr2:37938554-37939655	IMR90	lung:	n/a	chr2:37939317-37939329
48	CEBPB	chr2:37940527-37940702	K562	blood:	n/a	n/a
49	CEBPB	chr2:37995121-37995973	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr2:37940453-37940854	IMR90	lung:	n/a	n/a

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:38001560-38001610	A549	lung:	n/a
2	chr2:38001560-38001610	A549	lung:	n/a
3	chr2:37962248-37962298	HCM	heart:	n/a
4	chr2:37962248-37962298	HRCEpiC	kidney:	n/a
5	chr2:38001560-38001610	T-47D	breast:	n/a
6	chr2:37993353-37993403	H1-hESC	embryonic stem cell:	embryo
7	chr2:37948491-37948541	Caco-2	colon:	n/a
8	chr2:37997383-37997433	HCPEpiC	choroid plexus:	n/a
9	chr2:37985316-37985366	LNCaP	prostate:	n/a
10	chr2:37997383-37997433	AG04449	skin:	fetal
11	chr2:38001560-38001610	HEEpiC	esophagus:	n/a
12	chr2:37985316-37985366	HIPEpiC	eye:	n/a
13	chr2:37962248-37962298	GM12891	blood:	n/a
14	chr2:37969786-37969836	MCF-7	breast:	n/a
15	chr2:37996000-37996050	HNPCEpiC	eye:	n/a
16	chr2:37993353-37993403	Caco-2	colon:	n/a
17	chr2:38001560-38001610	SK-N-SH_RA	brain:	n/a
18	chr2:37985316-37985366	BJ	skin:	n/a
19	chr2:37993353-37993403	SK-N-SH	brain:	n/a
20	chr2:37997383-37997433	SK-N-SH_RA	brain:	n/a
21	chr2:37997383-37997433	PANC-1	pancreas:	n/a
22	chr2:37969786-37969836	NB4	blood:	n/a
23	chr2:38001560-38001610	MCF10A-Er-Src	breast:	n/a
24	chr2:37985316-37985366	HCM	heart:	n/a
25	chr2:37996000-37996050	SK-N-MC	brain:	n/a
26	chr2:37962248-37962298	LNCaP	prostate:	n/a
27	chr2:37948491-37948541	HepG2	liver:	n/a
28	chr2:37996000-37996050	BJ	skin:	n/a
29	chr2:37993353-37993403	LNCaP	prostate:	n/a
30	chr2:37938640-37938690	Jurkat	blood:	n/a
31	chr2:37997383-37997433	HEEpiC	esophagus:	n/a
32	chr2:37938640-37938690	HCF	heart:	n/a
33	chr2:37997383-37997433	PFSK-1	brain:	n/a
34	chr2:37948491-37948541	HCF	heart:	n/a
35	chr2:37993353-37993403	U87	brain:	n/a
36	chr2:37997383-37997433	AG09309	skin:	n/a
37	chr2:37962248-37962298	MCF10A-Er-Src	breast:	n/a
38	chr2:37985316-37985366	U87	brain:	n/a
39	chr2:37948491-37948541	U87	brain:	n/a
40	chr2:37948491-37948541	GM19239	blood:	n/a
41	chr2:37969786-37969836	SKMC	muscle:	n/a
42	chr2:37948491-37948541	GM12892	blood:	n/a
43	chr2:37962248-37962298	NT2-D1	testis:	n/a
44	chr2:37985316-37985366	Hepatocyte	liver:	n/a
45	chr2:37969786-37969836	Hela-S3	cervix:	n/a
46	chr2:37969786-37969836	LNCaP	prostate:	n/a
47	chr2:37985316-37985366	ECC-1	luminal epithelium:	n/a
48	chr2:38001560-38001610	PFSK-1	brain:	n/a
49	chr2:37996000-37996050	Jurkat	blood:	n/a
50	chr2:37969786-37969836	HCM	heart:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:37984227..37987177-chr2:37987780..37989668,2	MCF-7	breast:
2	chr2:37903809..37907927-chr2:37994371..37997035,4	MCF-7	breast:
3	chr2:37965210..37967124-chr2:37973295..37975217,2	MCF-7	breast:
4	chr2:37958368..37961673-chr2:37962589..37965814,3	K562	blood:
5	chr2:37897696..37900309-chr2:37936640..37940177,3	MCF-7	breast:
6	chr2:37984227..37987177-chr2:37987780..37989668,2	MCF-7	breast:
7	chr2:37887391..37889613-chr2:38000617..38003018,2	K562	blood:
8	chr2:37993752..37996799-chr2:38014077..38017922,3	MCF-7	breast:
9	chr2:37992911..37994888-chr2:37999261..38002227,2	MCF-7	breast:
10	chr2:37987301..37989251-chr2:37993852..37996621,2	K562	blood:
11	chr2:37896203..37899196-chr2:37994735..37996425,2	MCF-7	breast:
12	chr2:37992694..37995245-chr2:38016725..38019213,2	MCF-7	breast:
13	chr2:37944151..37947328-chr2:37948654..37951437,3	K562	blood:
14	chr2:37992911..37994888-chr2:37999261..38002227,2	MCF-7	breast:
15	chr2:37993452..37995079-chr2:37996632..37998258,2	K562	blood:
16	chr2:37987301..37989251-chr2:37993852..37996621,2	K562	blood:
17	chr2:37944151..37947328-chr2:37948654..37951437,3	K562	blood:
18	chr2:37958368..37961444-chr2:37963169..37965814,4	K562	blood:
19	chr2:38000546..38002739-chr2:38022244..38024636,2	MCF-7	breast:
20	chr2:37931880..37933672-chr2:37934871..37936423,2	MCF-7	breast:
21	chr2:37993452..37995079-chr2:37996632..37998258,2	K562	blood:
22	chr2:37995679..37997775-chr2:38028677..38031407,2	MCF-7	breast:
23	chr2:37961835..37963512-chr2:37971098..37973001,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM82A1-3	chr2:37974117-37974189	XLOC_001431
2	lnc-FAM82A1-3	chr2:37971476-37971786	XLOC_001431
3	lnc-PRKD3-1	chr2:37945761-37945925	NONHSAT070138
4	lnc-PRKD3-1	chr2:37956390-37956510	NONHSAT070138
5	lnc-PRKD3-1	chr2:37945761-37945925	NONHSAT070140
6	lnc-PRKD3-1	chr2:37956758-37956921	NONHSAT070140

No data

Variant related genes	Relation type
ENSG00000236572	TF binding region
CDC42EP3	TF binding region
ENSG00000236572	CpG island
CDC42EP3	CpG island
ENSG00000163171	chromatin interactions
ENSG00000236572	chromatin interactions
ACVR2B	miRNA target sites

Extended variants
information (count: 4577 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:4577 , 50 per page) page: 1 2 3 4 5 6 7 ... 92

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12185537	chr2:37936138-37936139	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs576719362	chr2:37936148-37936149	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs17021243	chr2:37936162-37936163	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs555603019	chr2:37936165-37936166	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs573945886	chr2:37936170-37936171	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs558971657	chr2:37936197-37936198	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs7585397	chr2:37936201-37936202	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs568080229	chr2:37936220-37936221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs149723233	chr2:37936236-37936237	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs369750827	chr2:37936238-37936239	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs146512631	chr2:37936255-37936256	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs12185713	chr2:37936256-37936257	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs141053018	chr2:37936312-37936313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs531404033	chr2:37936318-37936319	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs553563272	chr2:37936368-37936369	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs144773358	chr2:37936378-37936379	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs549436130	chr2:37936405-37936406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs568077041	chr2:37936414-37936415	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs148114121	chr2:37936447-37936448	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs17021244	chr2:37936581-37936582	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs181268294	chr2:37936607-37936608	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs12621199	chr2:37936625-37936626	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs141871891	chr2:37936626-37936627	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs570235217	chr2:37936636-37936637	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs537658029	chr2:37936673-37936674	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs555962547	chr2:37936699-37936700	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs574031646	chr2:37936717-37936718	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs563740765	chr2:37936729-37936730	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs541563713	chr2:37936736-37936737	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs575531293	chr2:37936765-37936766	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs185605923	chr2:37936836-37936837	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs11899876	chr2:37936871-37936872	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs564059554	chr2:37936904-37936905	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs531367720	chr2:37936918-37936919	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs576158367	chr2:37936920-37936921	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs578101951	chr2:37936927-37936928	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs543725499	chr2:37936928-37936929	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs375323298	chr2:37936940-37936941	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs367855931	chr2:37936945-37936946	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs543195710	chr2:37936952-37936953	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs77275413	chr2:37936953-37936954	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs564855595	chr2:37936960-37936961	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs547509973	chr2:37936992-37936993	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs190021892	chr2:37937009-37937010	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs183028928	chr2:37937020-37937021	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs574823766	chr2:37937039-37937040	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs187563294	chr2:37937053-37937054	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs532243211	chr2:37937064-37937065	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs537770865	chr2:37937067-37937068	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs549310599	chr2:37937074-37937075	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
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
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Bladder cancer	21909424	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Non-small cell lung cancer	18927303	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Neurocytoma	17123091	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21364760	CNVD

Chromatin state (count:973 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:37917200-37938000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr2:37917200-37938800	Weak transcription	Aorta	Aorta
3	chr2:37927000-37937800	Weak transcription	NHLF	lung
4	chr2:37932800-37936400	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr2:37933400-37936200	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr2:37933400-37937800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr2:37934200-37937800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr2:37934200-37938200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr2:37934400-37937600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr2:37934400-37938000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr2:37934400-37938000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
12	chr2:37934400-37938000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr2:37934400-37938000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr2:37934400-37938000	Weak transcription	Osteobl	bone
15	chr2:37934400-37938200	Weak transcription	Primary T cells fromperipheralblood	blood
16	chr2:37934400-37938200	Weak transcription	Placenta	Placenta
17	chr2:37934400-37938400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
18	chr2:37934600-37937400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr2:37934600-37937800	Weak transcription	NHDF-Ad	bronchial
20	chr2:37934600-37938200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr2:37934600-37938200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr2:37934800-37938000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
23	chr2:37934800-37938000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr2:37935000-37936200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
25	chr2:37935000-37937600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
26	chr2:37935000-37938200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr2:37935200-37937600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
28	chr2:37935400-37936800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr2:37935600-37936800	Enhancers	Lung	lung
30	chr2:37935600-37938000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
31	chr2:37935800-37936200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr2:37935800-37936400	Enhancers	Fetal Heart	heart
33	chr2:37935800-37937600	Weak transcription	Muscle Satellite Cultured Cells	--
34	chr2:37935800-37938000	Weak transcription	Primary hematopoietic stem cells	blood
35	chr2:37935800-37938000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr2:37935800-37938200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
37	chr2:37935800-37938200	Weak transcription	Fetal Thymus	thymus
38	chr2:37936000-37936200	Enhancers	HSMM	muscle
39	chr2:37936000-37936400	Enhancers	Right Ventricle	heart
40	chr2:37936000-37937400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr2:37936000-37938200	Weak transcription	Primary B cells from peripheral blood	blood
42	chr2:37936000-37938200	Weak transcription	GM12878-XiMat	blood
43	chr2:37936000-37938400	Weak transcription	Fetal Lung	lung
44	chr2:37936200-37936400	Enhancers	Monocytes-CD14+_RO01746	blood
45	chr2:37936200-37937400	Weak transcription	HSMM	muscle
46	chr2:37936200-37937800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr2:37936200-37937800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
48	chr2:37936400-37938000	Weak transcription	Primary monocytes fromperipheralblood	blood
49	chr2:37936400-37938000	Weak transcription	Monocytes-CD14+_RO01746	blood
50	chr2:37936400-37945200	Weak transcription	Fetal Heart	heart

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