Variant report

Variant	nsv966666
Chromosome Location	chr6:150092480-150114661
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:59)
CpG islands
(count:0)
Chromatin interactive
region (count:24)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:59 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr6:150092348-150092664	K562	blood:	n/a	n/a
2	BACH1	chr6:150092456-150092554	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL3	chr6:150100819-150100990	GM12878	blood:	n/a	n/a
4	CCNT2	chr6:150095023-150095118	K562	blood:	n/a	n/a
5	CEBPB	chr6:150102851-150103103	IMR90	lung:	n/a	chr6:150102954-150102965
6	CEBPB	chr6:150102851-150103107	K562	blood:	n/a	chr6:150102954-150102965
7	CEBPB	chr6:150098433-150098649	IMR90	lung:	n/a	n/a
8	CEBPB	chr6:150102801-150103114	HepG2	liver:	n/a	chr6:150102954-150102965
9	CEBPB	chr6:150106213-150106402	K562	blood:	n/a	n/a
10	CTCF	chr6:150099418-150099462	Lung_OC	lung:	n/a	n/a
11	EBF1	chr6:150112228-150112457	GM12878	blood:	n/a	chr6:150112332-150112341 chr6:150112330-150112343 chr6:150112332-150112342
12	EP300	chr6:150111030-150111045	GM12878	blood:	n/a	n/a
13	FOXA2	chr6:150114116-150114316	A549	lung:	n/a	n/a
14	GATA3	chr6:150110877-150111207	MCF-7	breast:	n/a	n/a
15	GATA3	chr6:150110906-150111113	MCF-7	breast:	n/a	n/a
16	GATA3	chr6:150110939-150111116	SH-SY5Y	brain:	n/a	n/a
17	IRF1	chr6:150103335-150103555	K562	blood:	n/a	n/a
18	JUND	chr6:150101428-150101459	K562	blood:	n/a	n/a
19	MAFK	chr6:150105148-150105183	K562	blood:	n/a	n/a
20	MAFK	chr6:150092382-150092592	IMR90	lung:	n/a	chr6:150092522-150092531 chr6:150092521-150092531 chr6:150092515-150092535 chr6:150092525-150092536 chr6:150092520-150092535
21	MAFK	chr6:150092349-150092667	HepG2	liver:	n/a	chr6:150092522-150092531 chr6:150092521-150092531 chr6:150092515-150092535 chr6:150092525-150092536 chr6:150092520-150092535
22	MAFK	chr6:150092408-150092608	HepG2	liver:	n/a	chr6:150092522-150092531 chr6:150092521-150092531 chr6:150092515-150092535 chr6:150092525-150092536 chr6:150092520-150092535
23	NR2F2	chr6:150106569-150106940	K562	blood:	n/a	n/a
24	NR2F2	chr6:150106550-150107026	K562	blood:	n/a	n/a
25	POLR2A	chr6:150104550-150105539	K562	blood:	n/a	n/a
26	POLR2A	chr6:150104006-150104025	HUVEC	blood vessel:	n/a	n/a
27	POLR2A	chr6:150107986-150108033	ProgFib	skin:	n/a	n/a
28	POLR2A	chr6:150105800-150105878	HepG2	liver:	n/a	n/a
29	POLR2A	chr6:150098222-150098279	MCF10A-Er-Src	breast:	n/a	n/a
30	POLR2A	chr6:150112577-150112662	K562	blood:	n/a	n/a
31	POLR2A	chr6:150095528-150095667	HepG2	liver:	n/a	n/a
32	POLR2A	chr6:150104426-150104812	PFSK-1	brain:	n/a	n/a
33	POLR2A	chr6:150104961-150105078	ProgFib	skin:	n/a	n/a
34	POLR2A	chr6:150100242-150101254	K562	blood:	n/a	n/a
35	POLR2A	chr6:150111009-150111052	MCF-7	breast:	n/a	n/a
36	POLR2A	chr6:150111065-150111074	MCF-7	breast:	n/a	n/a
37	POLR2A	chr6:150111896-150111979	K562	blood:	n/a	n/a
38	POLR2A	chr6:150097454-150097678	HepG2	liver:	n/a	n/a
39	POLR2A	chr6:150102831-150102854	K562	blood:	n/a	n/a
40	POLR2A	chr6:150101236-150101241	MCF-7	breast:	n/a	n/a
41	POLR2A	chr6:150105659-150105666	MCF-7	breast:	n/a	n/a
42	POLR2A	chr6:150104608-150104626	HepG2	liver:	n/a	n/a
43	POLR2A	chr6:150100281-150100339	ProgFib	skin:	n/a	n/a
44	POLR2A	chr6:150112081-150112390	K562	blood:	n/a	n/a
45	POLR2A	chr6:150096573-150096728	K562	blood:	n/a	n/a
46	POLR2A	chr6:150104683-150104980	MCF-7	breast:	n/a	n/a
47	POLR2A	chr6:150111984-150112372	K562	blood:	n/a	n/a
48	POLR2A	chr6:150113806-150113822	HepG2	liver:	n/a	n/a
49	POLR2A	chr6:150113776-150113809	K562	blood:	n/a	n/a
50	POLR2A	chr6:150109103-150109227	HepG2	liver:	n/a	n/a

No data

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:150068365..150071134-chr6:150101769..150103680,2	K562	blood:
2	chr6:150103642..150105538-chr6:150109602..150112158,2	K562	blood:
3	chr6:150085048..150087027-chr6:150091947..150093777,2	MCF-7	breast:
4	chr6:150092888..150094576-chr6:150096247..150098891,2	K562	blood:
5	chr6:150103684..150106554-chr6:150183972..150185592,2	MCF-7	breast:
6	chr6:150080535..150082998-chr6:150090034..150092678,2	MCF-7	breast:
7	chr6:150069990..150071882-chr6:150109798..150112486,2	MCF-7	breast:
8	chr6:150075712..150077814-chr6:150098516..150101508,2	K562	blood:
9	chr6:150066753..150069159-chr6:150105236..150106762,2	K562	blood:
10	chr6:150103039..150105538-chr6:150109602..150113560,4	K562	blood:
11	chr6:150068651..150072384-chr6:150088938..150093926,7	K562	blood:
12	chr6:150073818..150075342-chr6:150092909..150094549,2	K562	blood:
13	chr6:150103039..150105538-chr6:150109602..150113560,4	K562	blood:
14	chr6:150069279..150071165-chr6:150089916..150092656,2	MCF-7	breast:
15	chr6:150055968..150058286-chr6:150092691..150095282,2	K562	blood:
16	chr6:150092888..150094576-chr6:150096247..150098891,2	K562	blood:
17	chr6:150103186..150105713-chr6:150110065..150112313,2	MCF-7	breast:
18	chr6:150070320..150072055-chr6:150100262..150102859,2	K562	blood:
19	chr6:150088901..150091246-chr6:150095391..150098115,2	MCF-7	breast:
20	chr6:150103642..150105538-chr6:150109602..150112158,2	K562	blood:
21	chr6:150075319..150077363-chr6:150091174..150093691,2	MCF-7	breast:
22	chr6:150069126..150071489-chr6:150107300..150111812,4	K562	blood:
23	chr6:150103186..150105713-chr6:150110065..150112313,2	MCF-7	breast:
24	chr1:16160895..16163789-chr6:150103318..150105332,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000219433	TF binding region
ENSG00000179743	chromatin interactions
ENSG00000268592	chromatin interactions
ENSG00000120253	chromatin interactions
ENSG00000120256	chromatin interactions
ENSG00000120265	chromatin interactions

Extended variants
information (count: 881 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:881 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs572252478	chr6:150092574-150092575	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs111907716	chr6:150092579-150092580	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs561980906	chr6:150092599-150092600	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs180783698	chr6:150092715-150092716	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs534889166	chr6:150092722-150092723	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs532931432	chr6:150092727-150092728	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs554482078	chr6:150092773-150092774	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs562974813	chr6:150092796-150092797	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs9766214	chr6:150092809-150092810	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs150765962	chr6:150092818-150092819	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs543141708	chr6:150092841-150092842	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs548270945	chr6:150092844-150092845	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs568568006	chr6:150092863-150092864	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs537170250	chr6:150092888-150092889	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs557391276	chr6:150092915-150092916	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs577522537	chr6:150092934-150092935	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs75330085	chr6:150092954-150092955	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs573569010	chr6:150092982-150092983	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs183962982	chr6:150093016-150093017	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs188642280	chr6:150093028-150093029	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs181120098	chr6:150093114-150093115	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs368798530	chr6:150093169-150093170	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs543991160	chr6:150093175-150093176	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs576489884	chr6:150093255-150093256	Strong transcription Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs563788811	chr6:150093267-150093268	Strong transcription Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs552610304	chr6:150093268-150093269	Strong transcription Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs533003108	chr6:150093280-150093281	Strong transcription Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs545399531	chr6:150093281-150093282	Strong transcription Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs540027239	chr6:150093283-150093284	Strong transcription Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs560048317	chr6:150093372-150093373	Strong transcription Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs529153037	chr6:150093382-150093383	Strong transcription Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs549231308	chr6:150093426-150093427	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs185719393	chr6:150093441-150093442	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs191727706	chr6:150093476-150093477	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs181793028	chr6:150093546-150093547	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs73779556	chr6:150093592-150093593	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs35408417	chr6:150093617-150093618	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs3805748	chr6:150093678-150093679	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs3805749	chr6:150093682-150093683	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs542496441	chr6:150093701-150093702	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs558170673	chr6:150093744-150093745	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs553589844	chr6:150093812-150093813	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs567202075	chr6:150093875-150093876	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs147577776	chr6:150093891-150093892	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs140298308	chr6:150093892-150093893	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs555994803	chr6:150093919-150093920	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs575144197	chr6:150093925-150093926	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs11155681	chr6:150093968-150093969	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs11155682	chr6:150093981-150093982	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs551133684	chr6:150093988-150093989	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
Autism	22495311	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
Melanoma	18172304	CNVD
Cancer	21637783	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
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	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
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Soft tissue tumor	16732325	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
Cancer	17160897	CNVD
Breast cancer	17417639	CNVD
Breast cancer	17850661	CNVD
Renal cell carcinoma	18765545	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Ovarian neoplasms	16753589	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20556506	CNVD
Hirschsprung''s Disease	21712996	CNVD
Testicular germ cell tumor	18059402	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD
Lung adenocarcinoma	21935476	CNVD

Chromatin state (count:757 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:150071800-150092600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr6:150071800-150092800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr6:150071800-150100200	Weak transcription	Gastric	stomach
4	chr6:150072000-150094200	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr6:150072000-150111000	Weak transcription	Fetal Kidney	kidney
6	chr6:150072000-150152000	Weak transcription	Aorta	Aorta
7	chr6:150072400-150104600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr6:150072400-150111400	Weak transcription	Colonic Mucosa	Colon
9	chr6:150073000-150094400	Weak transcription	Lung	lung
10	chr6:150073800-150182400	Weak transcription	Fetal Brain Male	brain
11	chr6:150074200-150101000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr6:150075800-150094800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
13	chr6:150077000-150115400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
14	chr6:150077200-150118400	Weak transcription	Pancreas	Pancrea
15	chr6:150077400-150142400	Weak transcription	Fetal Heart	heart
16	chr6:150077800-150118400	Weak transcription	Psoas Muscle	Psoas
17	chr6:150078200-150092600	Weak transcription	Left Ventricle	heart
18	chr6:150081600-150101200	Weak transcription	Sigmoid Colon	Sigmoid Colon
19	chr6:150081800-150092800	Weak transcription	Spleen	Spleen
20	chr6:150081800-150092800	Weak transcription	HSMMtube	muscle
21	chr6:150082400-150092800	Weak transcription	Rectal Mucosa Donor 31	rectum
22	chr6:150083600-150092800	Weak transcription	Ovary	ovary
23	chr6:150086200-150092800	Weak transcription	Rectal Smooth Muscle	rectum
24	chr6:150087000-150093800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr6:150087000-150096600	Weak transcription	Esophagus	oesophagus
26	chr6:150087200-150095400	Strong transcription	Primary T cells from cord blood	blood
27	chr6:150087200-150154000	Weak transcription	Small Intestine	intestine
28	chr6:150087400-150134000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
29	chr6:150087600-150092600	Weak transcription	HUVEC	blood vessel
30	chr6:150087600-150117400	Weak transcription	Brain Substantia Nigra	brain
31	chr6:150087800-150092600	Weak transcription	NHLF	lung
32	chr6:150087800-150092800	Weak transcription	H1 Cell Line	embryonic stem cell
33	chr6:150087800-150092800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
34	chr6:150087800-150092800	Weak transcription	Brain Anterior Caudate	brain
35	chr6:150087800-150092800	Weak transcription	Duodenum Mucosa	Duodenum
36	chr6:150087800-150093000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr6:150087800-150093000	Weak transcription	Brain Cingulate Gyrus	brain
38	chr6:150087800-150093200	Weak transcription	HMEC	breast
39	chr6:150087800-150094000	Weak transcription	Skeletal Muscle Male	skeletal muscle
40	chr6:150087800-150101600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
41	chr6:150087800-150112000	Weak transcription	Right Ventricle	heart
42	chr6:150087800-150112400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
43	chr6:150088000-150093000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
44	chr6:150088000-150093000	Weak transcription	Fetal Lung	lung
45	chr6:150088000-150096600	Weak transcription	A549	lung
46	chr6:150088000-150096600	Weak transcription	NHEK	skin
47	chr6:150088000-150099600	Weak transcription	Brain Inferior Temporal Lobe	brain
48	chr6:150088000-150102400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr6:150088000-150111200	Weak transcription	Brain Hippocampus Middle	brain
50	chr6:150088000-150112000	Weak transcription	Colon Smooth Muscle	Colon

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