Variant report

Variant	esv1850963
Chromosome Location	chr4:95146281-95175682
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	chr4:95175178-95175378	K562	blood:	n/a	n/a
2	BHLHE40	chr4:95165619-95165782	GM12878	blood:	n/a	n/a
3	CEBPB	chr4:95158043-95158356	HepG2	liver:	n/a	chr4:95158238-95158249
4	CEBPB	chr4:95157038-95157401	IMR90	lung:	n/a	chr4:95157074-95157083 chr4:95157221-95157234 chr4:95157072-95157083 chr4:95157222-95157233
5	CEBPB	chr4:95158074-95158320	A549	lung:	n/a	chr4:95158238-95158249
6	CEBPB	chr4:95157165-95157365	HepG2	liver:	n/a	chr4:95157221-95157234 chr4:95157222-95157233
7	CEBPB	chr4:95158050-95158343	IMR90	lung:	n/a	chr4:95158238-95158249
8	CHD2	chr4:95153576-95153591	GM12878	blood:	n/a	n/a
9	CTCF	chr4:95164020-95164170	AG09309	skin:	n/a	n/a
10	CTCF	chr4:95166440-95166590	BE2_C	brain:	n/a	n/a
11	CTCF	chr4:95146206-95146296	K562	blood:	n/a	n/a
12	E2F4	chr4:95170378-95170555	MCF10A-Er-Src	breast:	n/a	n/a
13	E2F4	chr4:95159206-95159406	MCF10A-Er-Src	breast:	n/a	n/a
14	E2F4	chr4:95169102-95169197	MCF10A-Er-Src	breast:	n/a	n/a
15	ELK1	chr4:95160320-95160334	GM12878	blood:	n/a	n/a
16	EP300	chr4:95172563-95172677	GM12878	blood:	n/a	n/a
17	FOS	chr4:95172356-95172634	MCF10A-Er-Src	breast:	n/a	n/a
18	FOS	chr4:95172332-95172605	MCF10A-Er-Src	breast:	n/a	n/a
19	FOS	chr4:95172409-95172535	MCF10A-Er-Src	breast:	n/a	n/a
20	FOS	chr4:95172290-95172601	MCF10A-Er-Src	breast:	n/a	n/a
21	FOXA1	chr4:95171258-95171563	T-47D	breast:	n/a	n/a
22	IRF3	chr4:95165987-95166017	GM12878	blood:	n/a	n/a
23	IRF3	chr4:95148629-95148648	GM12878	blood:	n/a	n/a
24	JUN	chr4:95165726-95165832	H1-hESC	embryonic stem cell:	n/a	n/a
25	JUN	chr4:95157367-95157625	HepG2	liver:	n/a	chr4:95157513-95157522
26	JUN	chr4:95147309-95147343	HepG2	liver:	n/a	n/a
27	JUND	chr4:95157435-95157602	HepG2	liver:	n/a	chr4:95157513-95157522
28	JUND	chr4:95162606-95162631	HepG2	liver:	n/a	n/a
29	MAFF	chr4:95158435-95158785	HepG2	liver:	n/a	chr4:95158610-95158628
30	MAFF	chr4:95158449-95158800	K562	blood:	n/a	chr4:95158610-95158628
31	MAFF	chr4:95170514-95170779	HepG2	liver:	n/a	chr4:95170611-95170629
32	MAFK	chr4:95170562-95170578	K562	blood:	n/a	n/a
33	MAFK	chr4:95158439-95158804	HepG2	liver:	n/a	chr4:95158612-95158627 chr4:95158611-95158625 chr4:95158612-95158623 chr4:95158612-95158628 chr4:95158613-95158624 chr4:95158612-95158623 chr4:95158613-95158624
34	MAFK	chr4:95149357-95149545	IMR90	lung:	n/a	n/a
35	MAFK	chr4:95170554-95170759	HepG2	liver:	n/a	chr4:95170615-95170629 chr4:95170617-95170628 chr4:95170612-95170628 chr4:95170616-95170627 chr4:95170617-95170628
36	MAFK	chr4:95158443-95158786	Hela-S3	cervix:	n/a	chr4:95158612-95158627 chr4:95158611-95158625 chr4:95158612-95158623 chr4:95158612-95158628 chr4:95158613-95158624 chr4:95158612-95158623 chr4:95158613-95158624
37	MAFK	chr4:95158441-95158805	IMR90	lung:	n/a	chr4:95158612-95158627 chr4:95158611-95158625 chr4:95158612-95158623 chr4:95158612-95158628 chr4:95158613-95158624 chr4:95158612-95158623 chr4:95158613-95158624
38	MAFK	chr4:95149712-95149904	HepG2	liver:	n/a	n/a
39	MAFK	chr4:95158476-95158803	K562	blood:	n/a	chr4:95158612-95158627 chr4:95158611-95158625 chr4:95158612-95158623 chr4:95158612-95158628 chr4:95158613-95158624 chr4:95158612-95158623 chr4:95158613-95158624
40	MAFK	chr4:95158437-95158802	HepG2	liver:	n/a	chr4:95158612-95158627 chr4:95158611-95158625 chr4:95158612-95158623 chr4:95158612-95158628 chr4:95158613-95158624 chr4:95158612-95158623 chr4:95158613-95158624
41	MAFK	chr4:95149479-95149916	HepG2	liver:	n/a	n/a
42	MAZ	chr4:95172248-95172262	HepG2	liver:	n/a	n/a
43	NFIC	chr4:95146595-95147026	ECC-1	luminal epithelium:	n/a	n/a
44	NFYA	chr4:95174280-95174522	K562	blood:	n/a	chr4:95174376-95174391 chr4:95174380-95174392 chr4:95174379-95174389 chr4:95174376-95174391 chr4:95174377-95174391
45	NFYA	chr4:95172748-95172875	GM12878	blood:	n/a	n/a
46	POLR2A	chr4:95148708-95148968	Hela-S3	cervix:	n/a	n/a
47	POLR2A	chr4:95151905-95152519	K562	blood:	n/a	n/a
48	POLR2A	chr4:95148797-95148801	HepG2	liver:	n/a	n/a
49	POLR2A	chr4:95164922-95164951	HepG2	liver:	n/a	n/a
50	POLR2A	chr4:95155935-95156798	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:95151162..95153621-chr4:95153761..95157182,3	MCF-7	breast:
2	chr4:95129534..95131597-chr4:95158313..95160306,3	K562	blood:
3	chr4:95138512..95140147-chr4:95160968..95162982,2	K562	blood:
4	chr4:95129050..95131907-chr4:95154706..95157143,2	K562	blood:
5	chr4:89205783..89207731-chr4:95150954..95153219,2	K562	blood:
6	chr4:95136830..95141746-chr4:95150101..95153393,4	K562	blood:
7	chr4:95149538..95151966-chr4:95163560..95166301,2	K562	blood:
8	chr4:95127789..95130549-chr4:95156882..95159861,2	MCF-7	breast:
9	chr4:95151162..95153621-chr4:95153761..95157182,3	MCF-7	breast:
10	chr4:95167803..95169759-chr4:95172973..95174736,2	K562	blood:
11	chr4:95157684..95160378-chr4:95163793..95166793,3	K562	blood:
12	chr4:95132907..95134525-chr4:95158211..95160242,2	K562	blood:
13	chr4:95127424..95132801-chr4:95147153..95153356,7	K562	blood:
14	chr4:95149746..95151767-chr4:95154549..95156118,2	K562	blood:
15	chr4:95149746..95151767-chr4:95154549..95156118,2	K562	blood:
16	chr4:95157684..95160378-chr4:95163793..95166793,3	K562	blood:
17	chr4:95133025..95135753-chr4:95158742..95161544,2	K562	blood:
18	chr4:95129080..95131009-chr4:95145514..95147582,2	MCF-7	breast:
19	chr4:95149538..95151966-chr4:95163560..95166301,2	K562	blood:

Variant related genes	Relation type
SMARCAD1	TF binding region
ENSG00000246541	chromatin interactions
ENSG00000163104	chromatin interactions
ENSG00000246375	chromatin interactions
ENSG00000163644	chromatin interactions

Extended variants
information (count: 1221 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:1221 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2664871	chr4:95146281-95146282	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs184736007	chr4:95146285-95146286	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs115484243	chr4:95146297-95146298	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs189611316	chr4:95146308-95146309	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs568240324	chr4:95146317-95146318	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs536854860	chr4:95146373-95146374	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs180768162	chr4:95146415-95146416	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs147946963	chr4:95146450-95146451	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs386400847	chr4:95146451-95146452	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs398107672	chr4:95146452-95146453	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs369016718	chr4:95146456-95146457	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs567448241	chr4:95146506-95146507	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs570178502	chr4:95146526-95146527	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs112078463	chr4:95146527-95146528	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs558969892	chr4:95146536-95146537	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs368017848	chr4:95146594-95146595	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs186366306	chr4:95146599-95146600	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs549404759	chr4:95146654-95146655	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs190767436	chr4:95146661-95146662	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs139441785	chr4:95146669-95146670	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs181582274	chr4:95146720-95146721	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs538113966	chr4:95146757-95146758	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs186780316	chr4:95146844-95146845	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs139948330	chr4:95146851-95146852	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs2664872	chr4:95146952-95146953	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs558909789	chr4:95147004-95147005	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs374413095	chr4:95147031-95147032	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs2632401	chr4:95147055-95147056	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs561842163	chr4:95147059-95147060	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs530697341	chr4:95147173-95147174	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs550815722	chr4:95147202-95147203	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs12647120	chr4:95147217-95147218	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs116697560	chr4:95147221-95147222	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs74975674	chr4:95147229-95147230	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs201013072	chr4:95147258-95147259	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs373127175	chr4:95147262-95147263	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs11723410	chr4:95147276-95147277	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs534711902	chr4:95147283-95147284	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs555203609	chr4:95147284-95147285	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs371482856	chr4:95147315-95147316	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs140729712	chr4:95147337-95147338	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs201116246	chr4:95147373-95147374	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs376715102	chr4:95147380-95147381	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs200948051	chr4:95147383-95147384	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs368809274	chr4:95147392-95147393	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs537626552	chr4:95147397-95147398	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs199979749	chr4:95147402-95147403	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs539162347	chr4:95147410-95147411	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs577058645	chr4:95147416-95147417	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs545488452	chr4:95147424-95147425	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
primary effusion lymphomas	17116491	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal cancer	21851588	CNVD
Cancer	19907438	CNVD
Prostate cancer	16573809	CNVD
Multiple myeloma	16616336	CNVD

Chromatin state (count:926 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:95129800-95161800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr4:95130000-95148000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr4:95130000-95176000	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr4:95130200-95162600	Weak transcription	Pancreas	Pancrea
5	chr4:95130200-95162600	Weak transcription	Small Intestine	intestine
6	chr4:95130200-95164000	Weak transcription	Spleen	Spleen
7	chr4:95130200-95193000	Weak transcription	Right Ventricle	heart
8	chr4:95130200-95194000	Weak transcription	Gastric	stomach
9	chr4:95130200-95198200	Weak transcription	Colonic Mucosa	Colon
10	chr4:95130400-95152000	Weak transcription	Brain Angular Gyrus	brain
11	chr4:95130600-95151600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr4:95131200-95164400	Weak transcription	Colon Smooth Muscle	Colon
13	chr4:95131600-95148600	Weak transcription	Pancreatic Islets	Pancreatic Islet
14	chr4:95131600-95157200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
15	chr4:95131600-95198200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
16	chr4:95131800-95161600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
17	chr4:95131800-95169200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr4:95133600-95148000	Weak transcription	Lung	lung
19	chr4:95134800-95162400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr4:95134800-95162800	Weak transcription	Hela-S3	cervix
21	chr4:95135000-95147800	Weak transcription	Rectal Smooth Muscle	rectum
22	chr4:95135200-95148000	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr4:95135200-95162600	Weak transcription	Placenta Amnion	Placenta Amnion
24	chr4:95135200-95162800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr4:95135800-95160200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
26	chr4:95136400-95148400	Weak transcription	Cortex derived primary cultured neurospheres	brain
27	chr4:95136400-95157600	Weak transcription	Stomach Smooth Muscle	stomach
28	chr4:95136600-95164800	Weak transcription	Fetal Brain Male	brain
29	chr4:95136600-95174400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr4:95136800-95147800	Weak transcription	Sigmoid Colon	Sigmoid Colon
31	chr4:95136800-95162600	Weak transcription	Brain Inferior Temporal Lobe	brain
32	chr4:95137200-95148000	Weak transcription	Skeletal Muscle Male	skeletal muscle
33	chr4:95137400-95147800	Weak transcription	Skeletal Muscle Female	skeletal muscle
34	chr4:95137400-95148000	Weak transcription	Left Ventricle	heart
35	chr4:95137400-95150600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr4:95137400-95162400	Weak transcription	Ovary	ovary
37	chr4:95137400-95162600	Weak transcription	Thymus	Thymus
38	chr4:95137400-95162800	Weak transcription	Psoas Muscle	Psoas
39	chr4:95137600-95162600	Weak transcription	Aorta	Aorta
40	chr4:95138000-95161400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
41	chr4:95138200-95146400	Weak transcription	Fetal Intestine Large	intestine
42	chr4:95138200-95148000	Weak transcription	Brain Germinal Matrix	brain
43	chr4:95138200-95162400	Weak transcription	HSMMtube	muscle
44	chr4:95138400-95164200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
45	chr4:95138600-95148600	Weak transcription	Fetal Kidney	kidney
46	chr4:95138800-95161600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
47	chr4:95138800-95214400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr4:95139200-95149600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr4:95139400-95147400	Weak transcription	HMEC	breast
50	chr4:95140200-95167000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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