Variant report

Variant	nsv605259
Chromosome Location	chr6:166936021-166952981
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:47)
CpG islands
(count:305)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:47 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr6:166944351-166944586	HepG2	liver:	n/a	chr6:166944492-166944505
2	CEBPB	chr6:166944203-166944657	MCF-7	breast:	n/a	chr6:166944492-166944505
3	CEBPB	chr6:166941347-166941459	A549	lung:	n/a	chr6:166941381-166941392
4	CEBPB	chr6:166941237-166941545	HepG2	liver:	n/a	chr6:166941381-166941392
5	CUX1	chr6:166952954-166952957	K562	blood:	n/a	n/a
6	EP300	chr6:166944560-166944604	K562	blood:	n/a	n/a
7	FAM48A	chr6:166943316-166943473	GM12878	blood:	n/a	n/a
8	FOS	chr6:166944246-166944450	MCF10A-Er-Src	breast:	n/a	chr6:166944335-166944346
9	FOS	chr6:166944273-166944473	MCF10A-Er-Src	breast:	n/a	chr6:166944335-166944346
10	FOS	chr6:166944276-166944493	MCF10A-Er-Src	breast:	n/a	chr6:166944335-166944346
11	FOSL2	chr6:166944193-166944559	MCF-7	breast:	n/a	chr6:166944335-166944346
12	FOSL2	chr6:166944244-166944422	A549	lung:	n/a	chr6:166944335-166944346
13	FOSL2	chr6:166944031-166944524	MCF-7	breast:	n/a	chr6:166944335-166944346
14	FOXA1	chr6:166952908-166953073	T-47D	breast:	n/a	n/a
15	FOXA2	chr6:166944026-166944550	A549	lung:	n/a	n/a
16	FOXA2	chr6:166944092-166944506	A549	lung:	n/a	n/a
17	JUN	chr6:166944250-166944328	HepG2	liver:	n/a	n/a
18	JUND	chr6:166948621-166948827	HepG2	liver:	n/a	chr6:166948728-166948737
19	JUND	chr6:166944395-166944398	K562	blood:	n/a	n/a
20	JUND	chr6:166944221-166944392	HepG2	liver:	n/a	chr6:166944337-166944348 chr6:166944335-166944346
21	MAFK	chr6:166949549-166949682	HepG2	liver:	n/a	n/a
22	MAFK	chr6:166949562-166949634	HepG2	liver:	n/a	n/a
23	MAX	chr6:166943592-166944659	HCT-116	colon:	n/a	chr6:166944338-166944347
24	MAX	chr6:166943700-166944608	MCF-7	breast:	n/a	chr6:166944338-166944347
25	MAX	chr6:166943797-166943846	HepG2	liver:	n/a	n/a
26	MYC	chr6:166944334-166944468	MCF-7	breast:	n/a	chr6:166944338-166944347
27	MYC	chr6:166944348-166944501	MCF10A-Er-Src	breast:	n/a	n/a
28	POLR2A	chr6:166951253-166951675	H1-neurons	neurons:	n/a	n/a
29	POLR2A	chr6:166943749-166944181	HCT-116	colon:	n/a	n/a
30	POLR2A	chr6:166943909-166943950	ProgFib	skin:	n/a	n/a
31	POLR2A	chr6:166944141-166944501	HCT-116	colon:	n/a	n/a
32	POLR2A	chr6:166951326-166951697	H1-neurons	neurons:	n/a	n/a
33	POLR2A	chr6:166943904-166943959	MCF-7	breast:	n/a	n/a
34	POLR2A	chr6:166950515-166950555	HUVEC	blood vessel:	n/a	n/a
35	POLR2A	chr6:166943744-166944126	HCT-116	colon:	n/a	n/a
36	STAT3	chr6:166944436-166944480	MCF10A-Er-Src	breast:	n/a	n/a
37	STAT3	chr6:166949022-166949096	MCF10A-Er-Src	breast:	n/a	n/a
38	TAL1	chr6:166943264-166943307	K562	blood:	n/a	n/a
39	USF1	chr6:166952977-166953312	SK-N-SH_RA	brain:	n/a	n/a
40	USF1	chr6:166943727-166944061	A549	lung:	n/a	chr6:166943893-166943904
41	USF1	chr6:166943744-166943990	A549	lung:	n/a	chr6:166943893-166943904
42	USF1	chr6:166943770-166943988	A549	lung:	n/a	chr6:166943893-166943904
43	USF1	chr6:166943492-166944393	HCT-116	colon:	n/a	chr6:166943893-166943904
44	USF1	chr6:166943530-166944655	HCT-116	colon:	n/a	chr6:166943893-166943904
45	USF1	chr6:166943755-166944004	A549	lung:	n/a	chr6:166943893-166943904
46	USF1	chr6:166943795-166943994	HepG2	liver:	n/a	chr6:166943893-166943904
47	USF2	chr6:166943796-166943978	HepG2	liver:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:166944283-166944333	HCF	heart:	n/a
2	chr6:166944375-166944425	CMK	blood:	n/a
3	chr6:166944191-166944241	AG09319	gingival:	n/a
4	chr6:166944708-166944758	MCF10A-Er-Src	breast:	n/a
5	chr6:166944191-166944241	Hela-S3	cervix:	n/a
6	chr6:166944375-166944425	AG04450	lung:	fetal
7	chr6:166944768-166944818	HMEC	breast:	n/a
8	chr6:166944768-166944818	BJ	skin:	n/a
9	chr6:166944375-166944425	NHBE	bronchial:	n/a
10	chr6:166944283-166944333	A549	lung:	n/a
11	chr6:166944768-166944818	SKMC	muscle:	n/a
12	chr6:166944768-166944818	K562	blood:	n/a
13	chr6:166944283-166944333	AG04450	lung:	fetal
14	chr6:166944375-166944425	ECC-1	luminal epithelium:	n/a
15	chr6:166944768-166944818	SK-N-SH	brain:	n/a
16	chr6:166944708-166944758	CMK	blood:	n/a
17	chr6:166944768-166944818	IMR90	lung:	fetal
18	chr6:166944191-166944241	SKMC	muscle:	n/a
19	chr6:166944768-166944818	AoSMC	blood vessel:	n/a
20	chr6:166944191-166944241	HRCEpiC	kidney:	n/a
21	chr6:166944283-166944333	GM12892	blood:	n/a
22	chr6:166944191-166944241	PFSK-1	brain:	n/a
23	chr6:166944708-166944758	AoSMC	blood vessel:	n/a
24	chr6:166944283-166944333	HRCEpiC	kidney:	n/a
25	chr6:166944375-166944425	AG09309	skin:	n/a
26	chr6:166944283-166944333	HMEC	breast:	n/a
27	chr6:166944768-166944818	HCF	heart:	n/a
28	chr6:166944708-166944758	PrEC	prostate:	n/a
29	chr6:166944375-166944425	HEK293	kidney:	embryo
30	chr6:166944768-166944818	LNCaP	prostate:	n/a
31	chr6:166944708-166944758	ProgFib	skin:	n/a
32	chr6:166944191-166944241	HIPEpiC	eye:	n/a
33	chr6:166944768-166944818	HCT-116	colon:	n/a
34	chr6:166944708-166944758	U87	brain:	n/a
35	chr6:166944768-166944818	MCF10A-Er-Src	breast:	n/a
36	chr6:166944283-166944333	HIPEpiC	eye:	n/a
37	chr6:166944191-166944241	Caco-2	colon:	n/a
38	chr6:166944283-166944333	HCM	heart:	n/a
39	chr6:166944283-166944333	HepG2	liver:	n/a
40	chr6:166944708-166944758	Caco-2	colon:	n/a
41	chr6:166944283-166944333	IMR90	lung:	fetal
42	chr6:166944283-166944333	Jurkat	blood:	n/a
43	chr6:166944708-166944758	T-47D	breast:	n/a
44	chr6:166944768-166944818	Hepatocyte	liver:	n/a
45	chr6:166944375-166944425	HNPCEpiC	eye:	n/a
46	chr6:166944708-166944758	AG04449	skin:	fetal
47	chr6:166944283-166944333	RPTEC	kidney:	n/a
48	chr6:166944191-166944241	K562	blood:	n/a
49	chr6:166944768-166944818	HPAEpiC	pulmonary alveolar:	n/a
50	chr6:166944768-166944818	SAEC	small airway:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:166950092..166951979-chr6:166959386..166961071,2	K562	blood:
2	chr6:166938386..166940136-chr6:166942749..166944700,2	K562	blood:
3	chr6:166935159..166937591-chr6:166943431..166946372,2	K562	blood:
4	chr6:166938386..166940136-chr6:166942749..166944700,2	K562	blood:
5	chr6:166932943..166934797-chr6:166936117..166937896,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000269048	TF binding region
ENSG00000269048	CpG island
ENSG00000269048	chromatin interactions

Extended variants
information (count: 795 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs743980	chr6:166936021-166936022	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs185889542	chr6:166936035-166936036	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs535796551	chr6:166936043-166936044	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs531375923	chr6:166936065-166936066	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs192027961	chr6:166936066-166936067	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs575206087	chr6:166936074-166936075	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs545545163	chr6:166936089-166936090	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs386708484	chr6:166936092-166936093	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs754491	chr6:166936094-166936095	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs529197382	chr6:166936095-166936096	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs186665885	chr6:166936131-166936132	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs547634109	chr6:166936139-166936140	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs181768009	chr6:166936189-166936190	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs529537135	chr6:166936244-166936245	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs544890934	chr6:166936247-166936248	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs557105860	chr6:166936253-166936254	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs77389751	chr6:166936254-166936255	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs3799658	chr6:166936266-166936267	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs559291331	chr6:166936281-166936282	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs566944536	chr6:166936288-166936289	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs532913150	chr6:166936293-166936294	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs56868569	chr6:166936304-166936305	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs568265800	chr6:166936306-166936307	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs535707927	chr6:166936318-166936319	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs12189583	chr6:166936344-166936345	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs12189584	chr6:166936347-166936348	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs186192681	chr6:166936395-166936396	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs150555021	chr6:166936396-166936397	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs139524693	chr6:166936409-166936410	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs763188	chr6:166936412-166936413	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs743978	chr6:166936429-166936430	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs190606447	chr6:166936512-166936513	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs182876621	chr6:166936516-166936517	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs555491796	chr6:166936518-166936519	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs573904401	chr6:166936526-166936527	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs544551949	chr6:166936527-166936528	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs563177413	chr6:166936529-166936530	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs578214223	chr6:166936530-166936531	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs149261331	chr6:166936542-166936543	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs115577151	chr6:166936549-166936550	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs743977	chr6:166936612-166936613	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs549509141	chr6:166936616-166936617	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs561831400	chr6:166936622-166936623	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs144444812	chr6:166936626-166936627	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs550528911	chr6:166936630-166936631	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs569117555	chr6:166936638-166936639	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs539392462	chr6:166936664-166936665	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs188019531	chr6:166936688-166936689	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs191241758	chr6:166936700-166936701	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs533600352	chr6:166936790-166936791	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:90)

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
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
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
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Testicular germ cell tumor	18059402	CNVD
Developmental delay	21147756	CNVD
Chordoma	18071362	CNVD
Glioblastoma multiforme	19435819	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Epilepsy	22083797	CNVD
Myelofibrosis	22110671	CNVD
chordoma	19801981	CNVD
Myxofibrosarcoma	16751306	CNVD
Autism	17483303	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute myeloid leukemia	19651601	CNVD
Sudden cardiac death	19188705	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Ependymoma	20639864	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:482 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:166901000-166954800	Weak transcription	Rectal Smooth Muscle	rectum
2	chr6:166902200-166954400	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr6:166902600-166952800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
4	chr6:166909600-166943800	Weak transcription	Colonic Mucosa	Colon
5	chr6:166913000-166952000	Weak transcription	Primary T cells from cord blood	blood
6	chr6:166916200-166954200	Weak transcription	Right Atrium	heart
7	chr6:166916400-166940400	Weak transcription	Fetal Heart	heart
8	chr6:166921400-166943600	Weak transcription	Fetal Lung	lung
9	chr6:166921600-166937400	Weak transcription	Fetal Brain Male	brain
10	chr6:166923000-166937200	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr6:166923000-166940400	Weak transcription	Aorta	Aorta
12	chr6:166923000-166943800	Weak transcription	Sigmoid Colon	Sigmoid Colon
13	chr6:166923200-166940200	Weak transcription	Ovary	ovary
14	chr6:166923200-166943200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr6:166923200-166943800	Weak transcription	Duodenum Smooth Muscle	Duodenum
16	chr6:166923600-166936800	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr6:166923800-166944400	Weak transcription	Psoas Muscle	Psoas
18	chr6:166923800-166953000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr6:166925000-166940400	Weak transcription	Adipose Nuclei	Adipose
20	chr6:166927200-166938000	Weak transcription	Stomach Smooth Muscle	stomach
21	chr6:166928400-166938400	Weak transcription	Right Ventricle	heart
22	chr6:166928800-166936800	Weak transcription	Skeletal Muscle Male	skeletal muscle
23	chr6:166928800-166943400	Weak transcription	Fetal Brain Female	brain
24	chr6:166929000-166938000	Weak transcription	Primary neutrophils fromperipheralblood	blood
25	chr6:166929000-166943400	Weak transcription	Liver	Liver
26	chr6:166929400-166943000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr6:166929600-166937400	Weak transcription	HUVEC	blood vessel
28	chr6:166929600-166938200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr6:166929600-166942800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
30	chr6:166929600-166954000	Weak transcription	HSMM	muscle
31	chr6:166929600-166955600	Weak transcription	HMEC	breast
32	chr6:166930200-166944000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr6:166930400-166937400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr6:166930400-166937400	Weak transcription	Brain Hippocampus Middle	brain
35	chr6:166930400-166937400	Weak transcription	Spleen	Spleen
36	chr6:166930400-166938600	Weak transcription	Brain Cingulate Gyrus	brain
37	chr6:166930400-166940200	Weak transcription	Brain Angular Gyrus	brain
38	chr6:166930400-166940400	Weak transcription	NHDF-Ad	bronchial
39	chr6:166930400-166943000	Weak transcription	Brain Anterior Caudate	brain
40	chr6:166930400-166943800	Weak transcription	Esophagus	oesophagus
41	chr6:166930400-166954200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr6:166930400-166957800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr6:166930600-166937800	Weak transcription	NHLF	lung
44	chr6:166930600-166942800	Weak transcription	Brain Substantia Nigra	brain
45	chr6:166931600-166941600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr6:166931600-166943200	Weak transcription	Brain Germinal Matrix	brain
47	chr6:166932000-166941400	Strong transcription	Muscle Satellite Cultured Cells	--
48	chr6:166932200-166941800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr6:166932400-166940400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr6:166932400-166948600	Weak transcription	Primary B cells from cord blood	blood

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