Variant report

Variant	esv3355637
Chromosome Location	chr6:149769659-149774457
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:66)
CpG islands
(count:611)
Chromatin interactive
region (count:5)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:66 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr6:149771870-149772280	H1-hESC	embryonic stem cell:	n/a	n/a
2	BRCA1	chr6:149771895-149772095	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr6:149773526-149773769	ECC-1	luminal epithelium:	n/a	n/a
4	CEBPB	chr6:149773402-149773753	ECC-1	luminal epithelium:	n/a	n/a
5	CHD2	chr6:149771773-149772058	H1-hESC	embryonic stem cell:	n/a	n/a
6	CHD2	chr6:149772508-149772792	Hela-S3	cervix:	n/a	chr6:149772657-149772667
7	E2F6	chr6:149771598-149772236	H1-hESC	embryonic stem cell:	n/a	n/a
8	E2F6	chr6:149771661-149772189	H1-hESC	embryonic stem cell:	n/a	n/a
9	EP300	chr6:149773322-149773993	ECC-1	luminal epithelium:	n/a	n/a
10	ESR1	chr6:149773436-149773808	ECC-1	luminal epithelium:	n/a	n/a
11	ESR1	chr6:149773364-149773816	ECC-1	luminal epithelium:	n/a	n/a
12	ESR1	chr6:149773317-149773816	ECC-1	luminal epithelium:	n/a	n/a
13	ESR1	chr6:149773497-149773699	ECC-1	luminal epithelium:	n/a	n/a
14	FOXA1	chr6:149770275-149770585	HepG2	liver:	n/a	n/a
15	GABPA	chr6:149771740-149772160	H1-hESC	embryonic stem cell:	n/a	n/a
16	HMGN3	chr6:149772388-149772512	K562	blood:	n/a	n/a
17	HMGN3	chr6:149772171-149772185	K562	blood:	n/a	n/a
18	HNF4A	chr6:149773237-149773530	HepG2	liver:	n/a	chr6:149773369-149773384
19	MAFK	chr6:149770394-149770438	HepG2	liver:	n/a	n/a
20	MAX	chr6:149773388-149773906	ECC-1	luminal epithelium:	n/a	n/a
21	MAX	chr6:149772401-149772790	Hela-S3	cervix:	n/a	chr6:149772703-149772713
22	MAX	chr6:149771691-149772179	H1-hESC	embryonic stem cell:	n/a	n/a
23	MAX	chr6:149771673-149772189	H1-hESC	embryonic stem cell:	n/a	n/a
24	MAZ	chr6:149772168-149772169	Hela-S3	cervix:	n/a	n/a
25	MAZ	chr6:149772414-149772820	Hela-S3	cervix:	n/a	chr6:149772703-149772713
26	MYC	chr6:149771895-149772009	MCF-7	breast:	n/a	n/a
27	NFIC	chr6:149773250-149773960	ECC-1	luminal epithelium:	n/a	n/a
28	NFIC	chr6:149773245-149774035	ECC-1	luminal epithelium:	n/a	n/a
29	POLR2A	chr6:149773559-149773586	GM12878	blood:	n/a	n/a
30	POLR2A	chr6:149770309-149770368	GM12878	blood:	n/a	n/a
31	POLR2A	chr6:149771905-149772047	MCF-7	breast:	n/a	n/a
32	POLR2A	chr6:149771732-149771737	GM12878	blood:	n/a	n/a
33	POLR2A	chr6:149771989-149773037	Hela-S3	cervix:	n/a	n/a
34	POLR2A	chr6:149771173-149771500	GM12878	blood:	n/a	n/a
35	POLR2A	chr6:149769796-149770498	GM12878	blood:	n/a	n/a
36	POLR2A	chr6:149773558-149773947	GM12878	blood:	n/a	n/a
37	POLR2A	chr6:149772412-149772835	Hela-S3	cervix:	n/a	n/a
38	POLR2A	chr6:149774322-149774390	Hela-S3	cervix:	n/a	n/a
39	POLR2A	chr6:149772303-149772310	GM12878	blood:	n/a	n/a
40	POLR2A	chr6:149770919-149771956	GM12878	blood:	n/a	n/a
41	POLR2A	chr6:149773385-149773535	GM12878	blood:	n/a	n/a
42	POLR2A	chr6:149773059-149773068	Hela-S3	cervix:	n/a	n/a
43	POLR2A	chr6:149772385-149772707	Hela-S3	cervix:	n/a	n/a
44	POLR2A	chr6:149769439-149770621	GM12878	blood:	n/a	n/a
45	POLR2A	chr6:149773078-149773102	Hela-S3	cervix:	n/a	n/a
46	POLR2A	chr6:149770891-149772320	GM12878	blood:	n/a	n/a
47	POLR2A	chr6:149771743-149771871	GM12878	blood:	n/a	n/a
48	POLR2A	chr6:149771891-149771904	MCF-7	breast:	n/a	n/a
49	POLR2A	chr6:149772064-149772251	GM12878	blood:	n/a	n/a
50	POLR2A	chr6:149772582-149772879	Hela-S3	cervix:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:149772892-149772942	PANC-1	pancreas:	n/a
2	chr6:149772892-149772942	PANC-1	pancreas:	n/a
3	chr6:149770103-149770153	HRCEpiC	kidney:	n/a
4	chr6:149769803-149769853	HEEpiC	esophagus:	n/a
5	chr6:149769803-149769853	NT2-D1	testis:	n/a
6	chr6:149772854-149772904	CMK	blood:	n/a
7	chr6:149769803-149769853	CMK	blood:	n/a
8	chr6:149772716-149772766	AG09319	gingival:	n/a
9	chr6:149771807-149771857	HepG2	liver:	n/a
10	chr6:149771807-149771857	AG04450	lung:	fetal
11	chr6:149772892-149772942	HIPEpiC	eye:	n/a
12	chr6:149771845-149771895	HRPEpiC	eye:	n/a
13	chr6:149772716-149772766	HAEpiC	amniotic membrane:	n/a
14	chr6:149772892-149772942	HRE	kidney:	n/a
15	chr6:149772716-149772766	Hela-S3	cervix:	n/a
16	chr6:149771845-149771895	PrEC	prostate:	n/a
17	chr6:149772150-149772200	ovcar-3	ovarian:	n/a
18	chr6:149772346-149772396	U87	brain:	n/a
19	chr6:149771845-149771895	NB4	blood:	n/a
20	chr6:149772707-149772757	HCM	heart:	n/a
21	chr6:149770103-149770153	CMK	blood:	n/a
22	chr6:149772892-149772942	Hela-S3	cervix:	n/a
23	chr6:149770103-149770153	SK-N-SH	brain:	n/a
24	chr6:149772150-149772200	GM12892	blood:	n/a
25	chr6:149772854-149772904	GM12878	blood:	n/a
26	chr6:149772346-149772396	ECC-1	luminal epithelium:	n/a
27	chr6:149772707-149772757	AG10803	skin:	n/a
28	chr6:149772854-149772904	HL-60	blood:	n/a
29	chr6:149772716-149772766	PANC-1	pancreas:	n/a
30	chr6:149771807-149771857	ProgFib	skin:	n/a
31	chr6:149772854-149772904	Hela-S3	cervix:	n/a
32	chr6:149772892-149772942	AG09309	skin:	n/a
33	chr6:149770103-149770153	HRE	kidney:	n/a
34	chr6:149771807-149771857	Hela-S3	cervix:	n/a
35	chr6:149772150-149772200	ProgFib	skin:	n/a
36	chr6:149772707-149772757	HCF	heart:	n/a
37	chr6:149772150-149772200	HRE	kidney:	n/a
38	chr6:149771807-149771857	SAEC	small airway:	n/a
39	chr6:149772707-149772757	AG09319	gingival:	n/a
40	chr6:149770103-149770153	MCF10A-Er-Src	breast:	n/a
41	chr6:149771845-149771895	U87	brain:	n/a
42	chr6:149772346-149772396	HCT-116	colon:	n/a
43	chr6:149772892-149772942	Caco-2	colon:	n/a
44	chr6:149772716-149772766	PrEC	prostate:	n/a
45	chr6:149772150-149772200	Jurkat	blood:	n/a
46	chr6:149772716-149772766	AG04450	lung:	fetal
47	chr6:149771807-149771857	HMEC	breast:	n/a
48	chr6:149772707-149772757	MCF-7	breast:	n/a
49	chr6:149771807-149771857	GM12892	blood:	n/a
50	chr6:149772716-149772766	Caco-2	colon:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr6:149767445..149770252-chr6:149772541..149774258,2	MCF-7	breast:
2	chr6:149764839..149766396-chr6:149774052..149775951,2	MCF-7	breast:
3	chr6:149769726..149773853-chr6:149775332..149778151,3	K562	blood:
4	chr6:149399709..149402380-chr6:149772394..149774498,2	K562	blood:
5	chr6:149767445..149770252-chr6:149772541..149774258,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZC3H12D-9	chr6:149769570-149770516	NONHSAT115500

No data

Variant related genes	Relation type
ZC3H12D	TF binding region
ZC3H12D	CpG island
ENSG00000178199	chromatin interactions

Extended variants
information (count: 201 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:201 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548685370	chr6:149769716-149769717	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
2	rs534051485	chr6:149769779-149769780	Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs187572257	chr6:149769790-149769791	Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs73779356	chr6:149769795-149769796	Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs557540905	chr6:149769847-149769848	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs573481848	chr6:149769881-149769882	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs535978977	chr6:149769907-149769908	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs539708725	chr6:149769918-149769919	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
9	rs553659723	chr6:149769923-149769924	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs572737144	chr6:149769953-149769954	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
11	rs527368013	chr6:149769960-149769961	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
12	rs541467636	chr6:149769968-149769969	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
13	rs12197676	chr6:149769973-149769974	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs574948518	chr6:149769994-149769995	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
15	rs2789496	chr6:149770043-149770044	Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs564091998	chr6:149770046-149770047	Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
17	rs191612075	chr6:149770066-149770067	Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
18	rs62621196	chr6:149770067-149770068	Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs540557204	chr6:149770072-149770073	Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
20	rs528483409	chr6:149770073-149770074	Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
21	rs564858138	chr6:149770116-149770117	Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
22	rs548648368	chr6:149770149-149770150	Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
23	rs568466398	chr6:149770158-149770159	Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
24	rs237005	chr6:149770179-149770180	Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs141428605	chr6:149770188-149770189	Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
26	rs184089438	chr6:149770194-149770195	Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
27	rs188529647	chr6:149770196-149770197	Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
28	rs553383951	chr6:149770200-149770201	Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
29	rs567202675	chr6:149770221-149770222	Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
30	rs535752060	chr6:149770252-149770253	Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
31	rs554903076	chr6:149770268-149770269	Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
32	rs541708572	chr6:149770299-149770300	Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
33	rs6908378	chr6:149770327-149770328	Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs569556089	chr6:149770366-149770367	Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
35	rs557862429	chr6:149770382-149770383	Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
36	rs76214745	chr6:149770383-149770384	Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
37	rs60382924	chr6:149770443-149770444	Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs560183601	chr6:149770444-149770445	Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
39	rs529154551	chr6:149770555-149770556	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs57506869	chr6:149770591-149770592	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs138129073	chr6:149770597-149770598	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs376380343	chr6:149770621-149770622	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs562027162	chr6:149770659-149770660	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs805027	chr6:149770676-149770677	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs146019021	chr6:149770766-149770767	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs191844941	chr6:149770795-149770796	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs533359932	chr6:149770797-149770798	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs111323265	chr6:149770829-149770830	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs141743176	chr6:149770870-149770871	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs535716929	chr6:149770873-149770874	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:414 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:149753400-149770000	Weak transcription	Primary T helper cells fromperipheralblood	blood
2	chr6:149762600-149770800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr6:149762800-149771000	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr6:149763200-149770000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr6:149763200-149771000	Weak transcription	Fetal Intestine Small	intestine
6	chr6:149763200-149771400	Weak transcription	Pancreas	Pancrea
7	chr6:149764800-149771400	Weak transcription	Spleen	Spleen
8	chr6:149765200-149771400	Weak transcription	Brain Anterior Caudate	brain
9	chr6:149766000-149771400	Weak transcription	Right Atrium	heart
10	chr6:149766200-149771000	Weak transcription	GM12878-XiMat	blood
11	chr6:149766200-149771200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr6:149766600-149769800	Weak transcription	Primary T cells fromperipheralblood	blood
13	chr6:149766600-149773000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
14	chr6:149766800-149771000	Weak transcription	Fetal Heart	heart
15	chr6:149766800-149771400	Weak transcription	Left Ventricle	heart
16	chr6:149766800-149771600	Weak transcription	Lung	lung
17	chr6:149767400-149772800	Weak transcription	HepG2	liver
18	chr6:149768400-149771600	Strong transcription	Primary T helper cells PMA-I stimulated	--
19	chr6:149768400-149779400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
20	chr6:149768600-149771600	Weak transcription	Gastric	stomach
21	chr6:149769000-149769800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
22	chr6:149769600-149770000	Strong transcription	Primary B cells from cord blood	blood
23	chr6:149769600-149771400	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
24	chr6:149769600-149782800	Strong transcription	Primary B cells from peripheral blood	blood
25	chr6:149769600-149787200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr6:149769800-149770000	Enhancers	Brain Inferior Temporal Lobe	brain
27	chr6:149769800-149770200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
28	chr6:149769800-149770400	Enhancers	Cortex derived primary cultured neurospheres	brain
29	chr6:149769800-149771400	Strong transcription	Primary T cells fromperipheralblood	blood
30	chr6:149769800-149779800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
31	chr6:149770000-149770200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr6:149770000-149770400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr6:149770000-149770400	Bivalent Enhancer	Fetal Muscle Leg	muscle
34	chr6:149770000-149773000	Weak transcription	Primary B cells from cord blood	blood
35	chr6:149770000-149779600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
36	chr6:149770000-149785200	Strong transcription	Primary T helper cells fromperipheralblood	blood
37	chr6:149770200-149770400	Enhancers	Esophagus	oesophagus
38	chr6:149770400-149771400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr6:149770400-149771600	Weak transcription	Esophagus	oesophagus
40	chr6:149771000-149771200	Enhancers	Hela-S3	cervix
41	chr6:149771000-149771400	Active TSS	Rectal Mucosa Donor 29	rectum
42	chr6:149771000-149771400	Enhancers	Rectal Mucosa Donor 31	rectum
43	chr6:149771000-149771600	Enhancers	Brain Angular Gyrus	brain
44	chr6:149771000-149771600	Bivalent Enhancer	Fetal Intestine Small	intestine
45	chr6:149771000-149771600	Strong transcription	GM12878-XiMat	blood
46	chr6:149771000-149771800	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
47	chr6:149771000-149773400	Enhancers	Fetal Heart	heart
48	chr6:149771200-149771400	Enhancers	Duodenum Mucosa	Duodenum
49	chr6:149771200-149771600	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr6:149771200-149771600	Bivalent Enhancer	Brain Inferior Temporal Lobe	brain

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