Variant report

Variant	nsv438281
Chromosome Location	chr2:30406902-30418294
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:235)
CpG islands
(count:61)
Chromatin interactive
region (count:18)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:235 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:30408132-30408440	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:30414637-30415306	K562	blood:	n/a	n/a
3	ARID3A	chr2:30415863-30416374	K562	blood:	n/a	n/a
4	ATF1	chr2:30414653-30415109	K562	blood:	n/a	n/a
5	BHLHE40	chr2:30414296-30415431	K562	blood:	n/a	n/a
6	BHLHE40	chr2:30416113-30416537	K562	blood:	n/a	n/a
7	CBX3	chr2:30412685-30413072	K562	blood:	n/a	n/a
8	CBX3	chr2:30415869-30416358	K562	blood:	n/a	n/a
9	CBX3	chr2:30414283-30415080	K562	blood:	n/a	n/a
10	CCNT2	chr2:30415989-30416483	K562	blood:	n/a	n/a
11	CCNT2	chr2:30414518-30415088	K562	blood:	n/a	chr2:30414743-30414752 chr2:30414764-30414773
12	CEBPB	chr2:30408085-30408440	A549	lung:	n/a	chr2:30408306-30408317
13	CEBPB	chr2:30407996-30408528	MCF-7	breast:	n/a	chr2:30408306-30408317
14	CEBPB	chr2:30408089-30408389	HepG2	liver:	n/a	chr2:30408306-30408317
15	CEBPB	chr2:30413143-30413358	A549	lung:	n/a	n/a
16	CEBPB	chr2:30408042-30408496	HepG2	liver:	n/a	chr2:30408306-30408317
17	CEBPB	chr2:30408145-30408489	K562	blood:	n/a	chr2:30408306-30408317
18	CEBPB	chr2:30413242-30413243	K562	blood:	n/a	n/a
19	CEBPB	chr2:30407992-30408541	MCF-7	breast:	n/a	chr2:30408306-30408317
20	CEBPB	chr2:30413207-30413376	IMR90	lung:	n/a	n/a
21	CEBPB	chr2:30408129-30408435	Hela-S3	cervix:	n/a	chr2:30408306-30408317
22	CEBPB	chr2:30414479-30415082	K562	blood:	n/a	n/a
23	CEBPB	chr2:30414474-30414883	K562	blood:	n/a	n/a
24	CEBPB	chr2:30413141-30413404	HepG2	liver:	n/a	n/a
25	CEBPB	chr2:30407965-30408535	A549	lung:	n/a	chr2:30408306-30408317
26	CEBPB	chr2:30408127-30408379	HepG2	liver:	n/a	chr2:30408306-30408317
27	CEBPB	chr2:30408121-30408434	IMR90	lung:	n/a	chr2:30408306-30408317
28	CEBPB	chr2:30408082-30408432	HepG2	liver:	n/a	chr2:30408306-30408317
29	CEBPD	chr2:30414492-30415191	K562	blood:	n/a	n/a
30	CEBPD	chr2:30408125-30408416	HepG2	liver:	n/a	n/a
31	CEBPD	chr2:30414558-30415177	K562	blood:	n/a	n/a
32	CHD2	chr2:30414540-30415056	K562	blood:	n/a	n/a
33	CTCF	chr2:30417320-30417470	WERI-Rb-1	eye:	n/a	n/a
34	CTCF	chr2:30418160-30418310	GM12873	blood:	n/a	n/a
35	CTCF	chr2:30408540-30408690	A549	lung:	n/a	n/a
36	CUX1	chr2:30414580-30414976	K562	blood:	n/a	n/a
37	E2F4	chr2:30408132-30408361	MCF10A-Er-Src	breast:	n/a	n/a
38	E2F6	chr2:30414680-30414832	K562	blood:	n/a	n/a
39	E2F6	chr2:30413561-30413931	H1-hESC	embryonic stem cell:	n/a	n/a
40	E2F6	chr2:30415935-30416173	K562	blood:	n/a	n/a
41	EGR1	chr2:30414571-30415054	K562	blood:	n/a	n/a
42	EP300	chr2:30408151-30408428	HepG2	liver:	n/a	n/a
43	EP300	chr2:30415851-30416430	K562	blood:	n/a	chr2:30415951-30415965 chr2:30415857-30415871
44	EP300	chr2:30414611-30415558	K562	blood:	n/a	n/a
45	EP300	chr2:30414507-30414965	K562	blood:	n/a	n/a
46	FOS	chr2:30408004-30408474	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr2:30407042-30407241	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr2:30407032-30407258	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr2:30408014-30408465	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr2:30408095-30408448	MCF10A-Er-Src	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:30415987-30416037	GM12891	blood:	n/a
2	chr2:30415987-30416037	AG04449	skin:	fetal
3	chr2:30415987-30416037	HRE	kidney:	n/a
4	chr2:30415987-30416037	PrEC	prostate:	n/a
5	chr2:30415987-30416037	BE2_C	brain:	n/a
6	chr2:30415987-30416037	HMEC	breast:	n/a
7	chr2:30415987-30416037	NHDF-neo	bronchial:	n/a
8	chr2:30415987-30416037	HCM	heart:	n/a
9	chr2:30415987-30416037	AG04450	lung:	fetal
10	chr2:30415987-30416037	HAEpiC	amniotic membrane:	n/a
11	chr2:30415987-30416037	LNCaP	prostate:	n/a
12	chr2:30415987-30416037	K562	blood:	n/a
13	chr2:30415987-30416037	HRCEpiC	kidney:	n/a
14	chr2:30415987-30416037	Jurkat	blood:	n/a
15	chr2:30415987-30416037	AG09309	skin:	n/a
16	chr2:30415987-30416037	GM19239	blood:	n/a
17	chr2:30415987-30416037	HCPEpiC	choroid plexus:	n/a
18	chr2:30415987-30416037	AG09319	gingival:	n/a
19	chr2:30415987-30416037	SK-N-MC	brain:	n/a
20	chr2:30415987-30416037	BJ	skin:	n/a
21	chr2:30415987-30416037	HEK293	kidney:	embryo
22	chr2:30415987-30416037	Hepatocyte	liver:	n/a
23	chr2:30415987-30416037	AoSMC	blood vessel:	n/a
24	chr2:30415987-30416037	U87	brain:	n/a
25	chr2:30415987-30416037	NT2-D1	testis:	n/a
26	chr2:30415987-30416037	ovcar-3	ovarian:	n/a
27	chr2:30415987-30416037	HCT-116	colon:	n/a
28	chr2:30415987-30416037	Caco-2	colon:	n/a
29	chr2:30415987-30416037	HepG2	liver:	n/a
30	chr2:30415987-30416037	A549	lung:	n/a
31	chr2:30415987-30416037	H1-hESC	embryonic stem cell:	embryo
32	chr2:30415987-30416037	HRPEpiC	eye:	n/a
33	chr2:30415987-30416037	ECC-1	luminal epithelium:	n/a
34	chr2:30415987-30416037	HIPEpiC	eye:	n/a
35	chr2:30415987-30416037	PANC-1	pancreas:	n/a
36	chr2:30415987-30416037	GM06990	blood:	n/a
37	chr2:30415987-30416037	GM12878	blood:	n/a
38	chr2:30415987-30416037	ProgFib	skin:	n/a
39	chr2:30415987-30416037	NH-A	brain:	n/a
40	chr2:30415987-30416037	Hela-S3	cervix:	n/a
41	chr2:30415987-30416037	AG10803	skin:	n/a
42	chr2:30415987-30416037	HCF	heart:	n/a
43	chr2:30415987-30416037	PFSK-1	brain:	n/a
44	chr2:30415987-30416037	T-47D	breast:	n/a
45	chr2:30415987-30416037	SK-N-SH	brain:	n/a
46	chr2:30415987-30416037	NB4	blood:	n/a
47	chr2:30415987-30416037	NHBE	bronchial:	n/a
48	chr2:30415987-30416037	SK-N-SH_RA	brain:	n/a
49	chr2:30415987-30416037	RPTEC	kidney:	n/a
50	chr2:30415987-30416037	HL-60	blood:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:30415618..30417667-chr2:30452873..30455930,4	K562	blood:
2	chr2:30415467..30417118-chr2:30453057..30455723,2	K562	blood:
3	chr2:30400952..30403280-chr2:30405755..30407533,2	MCF-7	breast:
4	chr2:30405584..30407720-chr2:30454665..30456695,2	K562	blood:
5	chr2:30407485..30409523-chr2:30412863..30415112,2	K562	blood:
6	chr2:30414974..30417455-chr2:30421362..30423390,2	K562	blood:
7	chr2:30408028..30410165-chr2:30454230..30456153,2	K562	blood:
8	chr2:30415995..30419383-chr2:30883156..30885905,4	K562	blood:
9	chr2:30414606..30417729-chr2:30883474..30885497,4	K562	blood:
10	chr2:30412652..30418181-chr2:30474392..30478394,5	K562	blood:
11	chr2:30413233..30414815-chr2:30417588..30419624,2	K562	blood:
12	chr2:30413233..30414815-chr2:30417588..30419624,2	K562	blood:
13	chr2:30414847..30417455-chr2:30420606..30423390,3	K562	blood:
14	chr2:30415427..30416932-chr2:30426631..30428336,2	K562	blood:
15	chr2:30407485..30409523-chr2:30412863..30415112,2	K562	blood:
16	chr2:30417149..30419073-chr2:30452087..30455593,3	K562	blood:
17	chr2:30401585..30406142-chr2:30413640..30418582,6	K562	blood:
18	chr2:30408028..30410032-chr2:30453305..30455730,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ALK-4	chr2:30413665-30413701	NONHSAT069892

No data

Variant related genes	Relation type
ENSG00000207187	TF binding region
ENSG00000207187	CpG island
ENSG00000213626	chromatin interactions

Extended variants
information (count: 446 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:446 , 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	rs4264597	chr2:30406902-30406903	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs565566521	chr2:30406909-30406910	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs533002121	chr2:30406929-30406930	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs540210394	chr2:30406936-30406937	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs115173852	chr2:30406974-30406975	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs187336321	chr2:30407003-30407004	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs73923280	chr2:30407081-30407082	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs73923281	chr2:30407082-30407083	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs531516196	chr2:30407083-30407084	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs531623638	chr2:30407086-30407087	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs571204663	chr2:30407136-30407137	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs552230978	chr2:30407139-30407140	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs149949870	chr2:30407173-30407174	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs144144719	chr2:30407175-30407176	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs536724376	chr2:30407229-30407230	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs190090248	chr2:30407241-30407242	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs576542306	chr2:30407258-30407259	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs4952105	chr2:30407284-30407285	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs139474282	chr2:30407309-30407310	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs144198185	chr2:30407344-30407345	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs565053200	chr2:30407387-30407388	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs540246223	chr2:30407413-30407414	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs76348484	chr2:30407431-30407432	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs75767060	chr2:30407455-30407456	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs553250344	chr2:30407463-30407464	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs542666608	chr2:30407492-30407493	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs181837953	chr2:30407511-30407512	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs562432843	chr2:30407525-30407526	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs1355207	chr2:30407566-30407567	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs79807509	chr2:30407583-30407584	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs146561060	chr2:30407588-30407589	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs73923282	chr2:30407610-30407611	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs60709715	chr2:30407712-30407713	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs4023909	chr2:30407713-30407714	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs386417896	chr2:30407714-30407715	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs554317438	chr2:30407738-30407739	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs397707243	chr2:30407739-30407740	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs150724492	chr2:30407762-30407763	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs60178145	chr2:30407771-30407772	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs201572885	chr2:30407772-30407773	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs185852288	chr2:30407779-30407780	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs536359360	chr2:30407787-30407788	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs556662368	chr2:30407792-30407793	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs190273940	chr2:30407844-30407845	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs539254551	chr2:30407886-30407887	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs372421895	chr2:30407895-30407896	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs549041192	chr2:30407915-30407916	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs141286960	chr2:30407972-30407973	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs572797353	chr2:30408029-30408030	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs13014039	chr2:30408040-30408041	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Cancer	16751803	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	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
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Autism	22495311	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	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
Medulloblastoma	16968546	CNVD
Leukemia	18628472	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Breast cancer	21364760	CNVD
Wilms tumour	21544195	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	18927303	CNVD
Hepatocellular carcinoma	16750200	CNVD
Lung cancer	16740712	CNVD
Hereditary gingival fibromatosis	19633868	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Tetralogy of Fallot	22912587	CNVD
Myelofibrosis	22110671	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	21339820	CNVD

Chromatin state (count:88 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:30388800-30407200	Weak transcription	Brain Hippocampus Middle	brain
2	chr2:30402400-30407800	Weak transcription	Adipose Nuclei	Adipose
3	chr2:30403400-30408200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr2:30405000-30409400	Weak transcription	K562	blood
5	chr2:30407800-30408600	Enhancers	Adipose Nuclei	Adipose
6	chr2:30407800-30408800	Enhancers	Monocytes-CD14+_RO01746	blood
7	chr2:30407800-30409000	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr2:30407800-30409000	Enhancers	Primary neutrophils fromperipheralblood	blood
9	chr2:30408200-30408600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr2:30408400-30408600	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr2:30408400-30408600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr2:30408400-30408800	Enhancers	Placenta	Placenta
13	chr2:30409400-30412200	Enhancers	K562	blood
14	chr2:30410600-30412000	Enhancers	Primary B cells from peripheral blood	blood
15	chr2:30411200-30411400	Enhancers	Primary B cells from cord blood	blood
16	chr2:30412200-30413800	Weak transcription	K562	blood
17	chr2:30413400-30413800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr2:30413600-30414000	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr2:30413600-30414200	Enhancers	H1 Cell Line	embryonic stem cell
20	chr2:30413600-30414600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr2:30413600-30415400	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr2:30413800-30414000	Enhancers	K562	blood
23	chr2:30413800-30414600	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr2:30413800-30414600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
25	chr2:30414000-30415200	Flanking Active TSS	K562	blood
26	chr2:30414200-30415400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr2:30414200-30415400	Enhancers	Fetal Heart	heart
28	chr2:30414400-30414600	Enhancers	Left Ventricle	heart
29	chr2:30414400-30415000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr2:30414400-30415400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr2:30414400-30417000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr2:30414600-30416400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
33	chr2:30414600-30416400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr2:30414800-30415000	Enhancers	Placenta	Placenta
35	chr2:30414800-30415000	Enhancers	Right Atrium	heart
36	chr2:30414800-30415600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr2:30415000-30416000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr2:30415000-30416200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr2:30415000-30416200	Weak transcription	Placenta	Placenta
40	chr2:30415000-30431400	Weak transcription	Right Atrium	heart
41	chr2:30415200-30419800	Enhancers	K562	blood
42	chr2:30415400-30416400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr2:30415400-30416400	Weak transcription	HUES6 Cell Line	embryonic stem cell
44	chr2:30415400-30417000	Weak transcription	Fetal Heart	heart
45	chr2:30415600-30416000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr2:30415600-30416400	Weak transcription	Spleen	Spleen
47	chr2:30416000-30416200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr2:30416000-30416200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
49	chr2:30416000-30416400	Enhancers	A549	lung
50	chr2:30416000-30416600	Enhancers	Muscle Satellite Cultured Cells	--

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