Variant report

Variant	nsv604051
Chromosome Location	chr6:79691175-79728328
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	chr6:79718377-79718449	K562	blood:	n/a	n/a
2	CCNT2	chr6:79722163-79722350	K562	blood:	n/a	n/a
3	CEBPB	chr6:79709474-79709816	IMR90	lung:	n/a	n/a
4	CEBPB	chr6:79709498-79709824	K562	blood:	n/a	n/a
5	CEBPB	chr6:79695188-79695197	K562	blood:	n/a	n/a
6	CTCF	chr6:79712802-79712919	Medullo	brain:	n/a	n/a
7	CTCF	chr6:79712760-79712910	HMF	breast:	n/a	n/a
8	CTCF	chr6:79699083-79699139	Lung_OC	lung:	n/a	n/a
9	CTCF	chr6:79712800-79712950	BE2_C	brain:	n/a	n/a
10	CTCF	chr6:79715175-79715235	Spleen_OC	spleen:	n/a	n/a
11	CTCF	chr6:79712846-79712902	HepG2	liver:	n/a	n/a
12	CTCF	chr6:79721124-79721268	GM12878	blood:	n/a	n/a
13	CTCF	chr6:79712760-79712910	GM12875	blood:	n/a	n/a
14	CTCF	chr6:79712831-79712918	NHEK	skin:	n/a	n/a
15	CUX1	chr6:79722376-79722441	K562	blood:	n/a	n/a
16	E2F4	chr6:79693917-79694087	MCF10A-Er-Src	breast:	n/a	n/a
17	E2F4	chr6:79697023-79697272	MCF10A-Er-Src	breast:	n/a	n/a
18	FAM48A	chr6:79691151-79691267	GM12878	blood:	n/a	n/a
19	FOS	chr6:79714879-79715034	MCF10A-Er-Src	breast:	n/a	chr6:79714906-79714917 chr6:79714902-79714911
20	FOS	chr6:79709555-79709757	MCF10A-Er-Src	breast:	n/a	n/a
21	FOS	chr6:79714716-79715141	HUVEC	blood vessel:	n/a	chr6:79714906-79714917 chr6:79714902-79714911
22	FOS	chr6:79714825-79714969	MCF10A-Er-Src	breast:	n/a	chr6:79714906-79714917 chr6:79714902-79714911
23	FOS	chr6:79714802-79715049	MCF10A-Er-Src	breast:	n/a	chr6:79714906-79714917 chr6:79714902-79714911
24	GATA2	chr6:79714796-79715161	HUVEC	blood vessel:	n/a	chr6:79714901-79714911
25	GATA3	chr6:79712794-79713100	SH-SY5Y	brain:	n/a	n/a
26	GATA3	chr6:79725193-79725323	SH-SY5Y	brain:	n/a	chr6:79725302-79725309
27	GATA3	chr6:79720780-79720811	SH-SY5Y	brain:	n/a	n/a
28	GATA3	chr6:79714617-79715747	SK-N-SH	brain:	n/a	chr6:79715466-79715473 chr6:79714901-79714911
29	IRF1	chr6:79707426-79707567	K562	blood:	n/a	chr6:79707476-79707490
30	IRF1	chr6:79716591-79716604	K562	blood:	n/a	n/a
31	IRF1	chr6:79726408-79726497	K562	blood:	n/a	chr6:79726486-79726493
32	IRF1	chr6:79709660-79709796	K562	blood:	n/a	n/a
33	IRF1	chr6:79722967-79723206	K562	blood:	n/a	chr6:79723023-79723034 chr6:79723025-79723035 chr6:79723021-79723035
34	KAP1	chr6:79719038-79719541	K562	blood:	n/a	n/a
35	MAFF	chr6:79703711-79704020	K562	blood:	n/a	chr6:79703861-79703879
36	MAFF	chr6:79721757-79721934	K562	blood:	n/a	n/a
37	MAFF	chr6:79721716-79721953	HepG2	liver:	n/a	n/a
38	MAFF	chr6:79711187-79711475	HepG2	liver:	n/a	chr6:79711321-79711339
39	MAFF	chr6:79711157-79711494	K562	blood:	n/a	chr6:79711321-79711339
40	MAFF	chr6:79703716-79704019	HepG2	liver:	n/a	chr6:79703861-79703879
41	MAFF	chr6:79704755-79704955	HepG2	liver:	n/a	chr6:79704866-79704884
42	MAFK	chr6:79703699-79704043	HepG2	liver:	n/a	chr6:79703863-79703878
43	MAFK	chr6:79697720-79697806	H1-hESC	embryonic stem cell:	n/a	n/a
44	MAFK	chr6:79721732-79721932	Hela-S3	cervix:	n/a	chr6:79721841-79721855 chr6:79721842-79721853 chr6:79721842-79721853 chr6:79721843-79721854 chr6:79721842-79721858 chr6:79721843-79721854
45	MAFK	chr6:79716443-79716614	HepG2	liver:	n/a	n/a
46	MAFK	chr6:79721707-79722024	HepG2	liver:	n/a	chr6:79721841-79721855 chr6:79721842-79721853 chr6:79721842-79721853 chr6:79721843-79721854 chr6:79721842-79721858 chr6:79721843-79721854
47	MAFK	chr6:79703700-79704018	IMR90	lung:	n/a	chr6:79703863-79703878
48	MAFK	chr6:79721770-79721957	K562	blood:	n/a	chr6:79721841-79721855 chr6:79721842-79721853 chr6:79721842-79721853 chr6:79721843-79721854 chr6:79721842-79721858 chr6:79721843-79721854
49	MAFK	chr6:79711174-79711491	HepG2	liver:	n/a	chr6:79711323-79711338
50	MAFK	chr6:79721750-79722006	HepG2	liver:	n/a	chr6:79721841-79721855 chr6:79721842-79721853 chr6:79721842-79721853 chr6:79721843-79721854 chr6:79721842-79721858 chr6:79721843-79721854

No.	Distal block	Cell Line	Cell type
1	chr6:79715703..79719532-chr6:79722802..79725708,3	K562	blood:
2	chr6:79720377..79723032-chr6:79723737..79726706,2	K562	blood:
3	chr6:79696346..79699328-chr6:79702014..79705060,3	K562	blood:
4	chr6:79712764..79715566-chr6:79719156..79721327,2	K562	blood:
5	chr6:79705477..79707613-chr6:79708103..79710185,2	K562	blood:
6	chr6:79710026..79712564-chr6:79720572..79723552,2	K562	blood:
7	chr6:79721662..79723988-chr6:79780005..79781950,2	K562	blood:
8	chr6:79715998..79718423-chr6:79786608..79788657,2	K562	blood:
9	chr6:79715703..79719532-chr6:79722802..79725708,3	K562	blood:
10	chr6:79712764..79715566-chr6:79719156..79721327,2	K562	blood:
11	chr6:79705477..79707613-chr6:79708103..79710185,2	K562	blood:
12	chr6:79706595..79709353-chr6:79719320..79721938,2	K562	blood:
13	chr6:79690140..79691957-chr6:79692625..79694281,2	MCF-7	breast:
14	chr6:79727066..79729124-chr6:79732429..79734345,2	K562	blood:
15	chr6:79720377..79723032-chr6:79723737..79726706,2	K562	blood:
16	chr6:79704207..79706109-chr6:79716156..79718775,2	K562	blood:
17	chr6:79704207..79706109-chr6:79716156..79718775,2	K562	blood:
18	chr6:79696346..79699328-chr6:79702014..79705060,3	K562	blood:
19	chr6:79710026..79712564-chr6:79720572..79723552,2	K562	blood:
20	chr6:79706595..79709353-chr6:79719320..79721938,2	K562	blood:

Variant related genes	Relation type
PHIP	TF binding region
ENSG00000146247	chromatin interactions

Extended variants
information (count: 1256 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:1256 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10943611	chr6:79691175-79691176	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs539469705	chr6:79691179-79691180	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs555978353	chr6:79691216-79691217	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs143085621	chr6:79691242-79691243	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs77398006	chr6:79691251-79691252	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs181058622	chr6:79691284-79691285	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs572367459	chr6:79691291-79691292	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs75462615	chr6:79691332-79691333	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs76062709	chr6:79691393-79691394	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs185923429	chr6:79691410-79691411	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs550158557	chr6:79691457-79691458	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs147492147	chr6:79691556-79691557	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs559982728	chr6:79691558-79691559	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs112250917	chr6:79691597-79691598	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs118136130	chr6:79691719-79691720	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs140497553	chr6:79691732-79691733	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs545739031	chr6:79691745-79691746	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs149310358	chr6:79691746-79691747	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs190382388	chr6:79691754-79691755	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs547713428	chr6:79691760-79691761	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs570767280	chr6:79691772-79691773	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs539020623	chr6:79691804-79691805	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs556124387	chr6:79691834-79691835	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs576026594	chr6:79691872-79691873	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs183384302	chr6:79691966-79691967	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs555075929	chr6:79691971-79691972	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs575690189	chr6:79691983-79691984	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs144576498	chr6:79692004-79692005	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs187130165	chr6:79692005-79692006	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs575917596	chr6:79692041-79692042	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs191177616	chr6:79692076-79692077	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs112741997	chr6:79692089-79692090	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs542991026	chr6:79692099-79692100	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs563718344	chr6:79692117-79692118	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs529342104	chr6:79692135-79692136	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs543124821	chr6:79692143-79692144	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs559936169	chr6:79692148-79692149	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs148484465	chr6:79692176-79692177	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs142493554	chr6:79692187-79692188	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs570606369	chr6:79692364-79692365	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs182550903	chr6:79692380-79692381	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs9343859	chr6:79692399-79692400	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs530932944	chr6:79692419-79692420	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs540770834	chr6:79692430-79692431	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs187686106	chr6:79692434-79692435	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs535108308	chr6:79692448-79692449	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs367884914	chr6:79692454-79692455	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs113766513	chr6:79692532-79692533	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs372610239	chr6:79692576-79692577	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs555040045	chr6:79692577-79692578	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Follicular lymphoma	17699855	CNVD
Breast cancer	17133270	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Developmental delay	21147756	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Salivary gland tumor	18059337	CNVD
Lung cancer	16773561	CNVD
Glioblastoma multiforme	22286061	CNVD
Urothelial cell carcinoma	18451213	CNVD
Prostate cancer	16461572	CNVD
Mental retardation	21045960	CNVD
Obesity	21045960	CNVD
learning difficulties	21045960	CNVD
Prostate cancer	17245344	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Cancer	20164920	CNVD
Burkitt''s lymphoma	20823134	CNVD
Ductal carcinoma	22052326	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	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	chr6:79648800-79714400	Weak transcription	Gastric	stomach
2	chr6:79649000-79715200	Weak transcription	Stomach Mucosa	stomach
3	chr6:79658600-79695000	Weak transcription	Pancreas	Pancrea
4	chr6:79659200-79702800	Weak transcription	Psoas Muscle	Psoas
5	chr6:79659400-79702400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr6:79659400-79707000	Weak transcription	Esophagus	oesophagus
7	chr6:79659600-79704000	Weak transcription	Lung	lung
8	chr6:79659600-79707000	Weak transcription	Spleen	Spleen
9	chr6:79659800-79702600	Weak transcription	Right Ventricle	heart
10	chr6:79659800-79703400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr6:79659800-79704000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr6:79659800-79707000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr6:79664200-79695000	Weak transcription	Fetal Stomach	stomach
14	chr6:79664200-79698000	Weak transcription	Fetal Intestine Small	intestine
15	chr6:79664200-79702400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr6:79669800-79707000	Weak transcription	Aorta	Aorta
17	chr6:79671600-79693200	Weak transcription	Thymus	Thymus
18	chr6:79672800-79702600	Weak transcription	Placenta Amnion	Placenta Amnion
19	chr6:79675200-79693200	Weak transcription	Colonic Mucosa	Colon
20	chr6:79675200-79702200	Weak transcription	Brain Angular Gyrus	brain
21	chr6:79675200-79704600	Weak transcription	Small Intestine	intestine
22	chr6:79675400-79691800	Weak transcription	Skeletal Muscle Male	skeletal muscle
23	chr6:79675400-79695000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr6:79675800-79706800	Weak transcription	NHEK	skin
25	chr6:79676000-79694000	Weak transcription	HSMMtube	muscle
26	chr6:79676000-79703600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
27	chr6:79676600-79691200	Weak transcription	NHLF	lung
28	chr6:79676600-79691400	Weak transcription	Osteobl	bone
29	chr6:79678400-79691400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr6:79679000-79692000	Weak transcription	A549	lung
31	chr6:79679200-79691600	Weak transcription	HUVEC	blood vessel
32	chr6:79679200-79698800	Weak transcription	Brain Substantia Nigra	brain
33	chr6:79679800-79702600	Weak transcription	Brain Cingulate Gyrus	brain
34	chr6:79680000-79702200	Weak transcription	Stomach Smooth Muscle	stomach
35	chr6:79681400-79691200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr6:79687000-79692200	Strong transcription	Primary T killer memory cells from peripheral blood	blood
37	chr6:79687000-79695200	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr6:79687000-79698800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
39	chr6:79687000-79709400	Strong transcription	Duodenum Mucosa	Duodenum
40	chr6:79687000-79714400	Strong transcription	Liver	Liver
41	chr6:79687000-79715800	Strong transcription	Primary T cells fromperipheralblood	blood
42	chr6:79687000-79715800	Strong transcription	Primary T helper cells fromperipheralblood	blood
43	chr6:79687000-79736000	Strong transcription	HUES6 Cell Line	embryonic stem cell
44	chr6:79687000-79736200	Strong transcription	Primary monocytes fromperipheralblood	blood
45	chr6:79687200-79692200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
46	chr6:79687200-79692200	Strong transcription	Primary T killer naive cells fromperipheralblood	blood
47	chr6:79687200-79692200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr6:79687200-79692200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr6:79687200-79692200	Strong transcription	HSMM	muscle
50	chr6:79687200-79695000	Strong transcription	Primary T helper memory cells from peripheral blood 1	blood

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