Variant report

Variant	esv3374188
Chromosome Location	chr6:149770709-149773207
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:43)
CpG islands
(count:491)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:43 , 50 per page) page: 1

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	CHD2	chr6:149772508-149772792	Hela-S3	cervix:	n/a	chr6:149772657-149772667
4	CHD2	chr6:149771773-149772058	H1-hESC	embryonic stem cell:	n/a	n/a
5	E2F6	chr6:149771661-149772189	H1-hESC	embryonic stem cell:	n/a	n/a
6	E2F6	chr6:149771598-149772236	H1-hESC	embryonic stem cell:	n/a	n/a
7	GABPA	chr6:149771740-149772160	H1-hESC	embryonic stem cell:	n/a	n/a
8	HMGN3	chr6:149772388-149772512	K562	blood:	n/a	n/a
9	HMGN3	chr6:149772171-149772185	K562	blood:	n/a	n/a
10	MAX	chr6:149771673-149772189	H1-hESC	embryonic stem cell:	n/a	n/a
11	MAX	chr6:149772401-149772790	Hela-S3	cervix:	n/a	chr6:149772703-149772713
12	MAX	chr6:149771691-149772179	H1-hESC	embryonic stem cell:	n/a	n/a
13	MAZ	chr6:149772414-149772820	Hela-S3	cervix:	n/a	chr6:149772703-149772713
14	MAZ	chr6:149772168-149772169	Hela-S3	cervix:	n/a	n/a
15	MYC	chr6:149771895-149772009	MCF-7	breast:	n/a	n/a
16	POLR2A	chr6:149772412-149772835	Hela-S3	cervix:	n/a	n/a
17	POLR2A	chr6:149770919-149771956	GM12878	blood:	n/a	n/a
18	POLR2A	chr6:149773059-149773068	Hela-S3	cervix:	n/a	n/a
19	POLR2A	chr6:149772303-149772310	GM12878	blood:	n/a	n/a
20	POLR2A	chr6:149772385-149772707	Hela-S3	cervix:	n/a	n/a
21	POLR2A	chr6:149771989-149773037	Hela-S3	cervix:	n/a	n/a
22	POLR2A	chr6:149771891-149771904	MCF-7	breast:	n/a	n/a
23	POLR2A	chr6:149771173-149771500	GM12878	blood:	n/a	n/a
24	POLR2A	chr6:149772064-149772251	GM12878	blood:	n/a	n/a
25	POLR2A	chr6:149771743-149771871	GM12878	blood:	n/a	n/a
26	POLR2A	chr6:149771732-149771737	GM12878	blood:	n/a	n/a
27	POLR2A	chr6:149771905-149772047	MCF-7	breast:	n/a	n/a
28	POLR2A	chr6:149772582-149772879	Hela-S3	cervix:	n/a	n/a
29	POLR2A	chr6:149773078-149773102	Hela-S3	cervix:	n/a	n/a
30	POLR2A	chr6:149770891-149772320	GM12878	blood:	n/a	n/a
31	RCOR1	chr6:149772619-149772622	Hela-S3	cervix:	n/a	n/a
32	RCOR1	chr6:149771947-149771965	Hela-S3	cervix:	n/a	n/a
33	SMARCB1	chr6:149771406-149773213	Hela-S3	cervix:	n/a	n/a
34	SMC3	chr6:149772110-149772264	Hela-S3	cervix:	n/a	n/a
35	TEAD4	chr6:149771829-149772097	H1-hESC	embryonic stem cell:	n/a	n/a
36	TFAP2C	chr6:149771572-149773122	Hela-S3	cervix:	n/a	n/a
37	USF1	chr6:149771807-149772073	H1-hESC	embryonic stem cell:	n/a	n/a
38	USF1	chr6:149771818-149772097	SK-N-SH_RA	brain:	n/a	n/a
39	USF1	chr6:149771755-149772090	H1-hESC	embryonic stem cell:	n/a	n/a
40	USF2	chr6:149771855-149772075	H1-hESC	embryonic stem cell:	n/a	n/a
41	ZKSCAN1	chr6:149772612-149772801	Hela-S3	cervix:	n/a	n/a
42	ZNF143	chr6:149772104-149772292	H1-hESC	embryonic stem cell:	n/a	n/a
43	ZNF143	chr6:149772584-149772590	Hela-S3	cervix:	n/a	n/a

(count:491 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:149772854-149772904	MCF10A-Er-Src	breast:	n/a
2	chr6:149772854-149772904	AG04450	lung:	fetal
3	chr6:149772707-149772757	RPTEC	kidney:	n/a
4	chr6:149772854-149772904	MCF10A-Er-Src	breast:	n/a
5	chr6:149772854-149772904	AG04450	lung:	fetal
6	chr6:149772707-149772757	RPTEC	kidney:	n/a
7	chr6:149771807-149771857	HIPEpiC	eye:	n/a
8	chr6:149772150-149772200	HCF	heart:	n/a
9	chr6:149772854-149772904	IMR90	lung:	fetal
10	chr6:149772150-149772200	RPTEC	kidney:	n/a
11	chr6:149771845-149771895	SK-N-SH	brain:	n/a
12	chr6:149772346-149772396	GM12891	blood:	n/a
13	chr6:149772716-149772766	MCF-7	breast:	n/a
14	chr6:149772854-149772904	HUVEC	blood vessel:	n/a
15	chr6:149772892-149772942	ovcar-3	ovarian:	n/a
16	chr6:149771807-149771857	RPTEC	kidney:	n/a
17	chr6:149772716-149772766	AG04449	skin:	fetal
18	chr6:149772892-149772942	CMK	blood:	n/a
19	chr6:149772150-149772200	ProgFib	skin:	n/a
20	chr6:149772150-149772200	BJ	skin:	n/a
21	chr6:149772707-149772757	ovcar-3	ovarian:	n/a
22	chr6:149772707-149772757	GM12891	blood:	n/a
23	chr6:149772854-149772904	AG04449	skin:	fetal
24	chr6:149772346-149772396	MCF-7	breast:	n/a
25	chr6:149771807-149771857	HepG2	liver:	n/a
26	chr6:149771845-149771895	HRE	kidney:	n/a
27	chr6:149772716-149772766	K562	blood:	n/a
28	chr6:149772346-149772396	T-47D	breast:	n/a
29	chr6:149771807-149771857	Hepatocyte	liver:	n/a
30	chr6:149771807-149771857	BJ	skin:	n/a
31	chr6:149772346-149772396	H1-hESC	embryonic stem cell:	embryo
32	chr6:149772150-149772200	HepG2	liver:	n/a
33	chr6:149772346-149772396	HEEpiC	esophagus:	n/a
34	chr6:149772707-149772757	AG09319	gingival:	n/a
35	chr6:149772707-149772757	LNCaP	prostate:	n/a
36	chr6:149772346-149772396	HCT-116	colon:	n/a
37	chr6:149772892-149772942	HMEC	breast:	n/a
38	chr6:149771807-149771857	BE2_C	brain:	n/a
39	chr6:149772346-149772396	HIPEpiC	eye:	n/a
40	chr6:149772346-149772396	AG09319	gingival:	n/a
41	chr6:149772716-149772766	HIPEpiC	eye:	n/a
42	chr6:149772854-149772904	BJ	skin:	n/a
43	chr6:149771807-149771857	HPAEpiC	pulmonary alveolar:	n/a
44	chr6:149771845-149771895	HPAEpiC	pulmonary alveolar:	n/a
45	chr6:149772716-149772766	SK-N-SH	brain:	n/a
46	chr6:149771807-149771857	IMR90	lung:	fetal
47	chr6:149772150-149772200	NB4	blood:	n/a
48	chr6:149772892-149772942	HEK293	kidney:	embryo
49	chr6:149772892-149772942	SK-N-SH_RA	brain:	n/a
50	chr6:149772346-149772396	AG04449	skin:	fetal

(count:3 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 99 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:99 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs146019021	chr6:149770766-149770767	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs191844941	chr6:149770795-149770796	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs533359932	chr6:149770797-149770798	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs111323265	chr6:149770829-149770830	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs141743176	chr6:149770870-149770871	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs535716929	chr6:149770873-149770874	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs555661994	chr6:149770875-149770876	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs116305016	chr6:149770877-149770878	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs532601038	chr6:149770896-149770897	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs368404967	chr6:149770920-149770921	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs184977260	chr6:149770935-149770936	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs554309582	chr6:149770937-149770938	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs560179533	chr6:149770939-149770940	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs190268674	chr6:149770966-149770967	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs115463986	chr6:149770988-149770989	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs117638213	chr6:149771008-149771009	Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs3222365	chr6:149771019-149771020	Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs539953907	chr6:149771020-149771021	Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs375644717	chr6:149771040-149771041	Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs182053497	chr6:149771044-149771045	Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs371954872	chr6:149771061-149771062	Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs34037220	chr6:149771062-149771063	Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs61206923	chr6:149771063-149771064	Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs626755	chr6:149771064-149771065	Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs55845807	chr6:149771092-149771093	Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs61009180	chr6:149771093-149771094	Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs573894844	chr6:149771095-149771096	Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs376889920	chr6:149771100-149771101	Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs376783766	chr6:149771103-149771104	Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs370823630	chr6:149771105-149771106	Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs552295847	chr6:149771130-149771131	Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs376965754	chr6:149771141-149771142	Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs187662760	chr6:149771155-149771156	Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs530921665	chr6:149771246-149771247	Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs544644171	chr6:149771300-149771301	Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs564328806	chr6:149771337-149771338	Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs412746	chr6:149771344-149771345	Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs546795921	chr6:149771377-149771378	Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs560287315	chr6:149771406-149771407	Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Enhancers Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs374656417	chr6:149771472-149771473	Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Enhancers Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs370405209	chr6:149771483-149771484	Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Enhancers Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs529473850	chr6:149771503-149771504	Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Enhancers Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs116831134	chr6:149771537-149771538	Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Enhancers Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs76605937	chr6:149771659-149771660	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs368031027	chr6:149771664-149771665	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs537438541	chr6:149771689-149771690	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs116615164	chr6:149771717-149771718	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs113491906	chr6:149771727-149771728	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs571164448	chr6:149771780-149771781	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs527633563	chr6:149771811-149771812	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:83)

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

Chromatin state (count:368 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:149762600-149770800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr6:149762800-149771000	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr6:149763200-149771000	Weak transcription	Fetal Intestine Small	intestine
4	chr6:149763200-149771400	Weak transcription	Pancreas	Pancrea
5	chr6:149764800-149771400	Weak transcription	Spleen	Spleen
6	chr6:149765200-149771400	Weak transcription	Brain Anterior Caudate	brain
7	chr6:149766000-149771400	Weak transcription	Right Atrium	heart
8	chr6:149766200-149771000	Weak transcription	GM12878-XiMat	blood
9	chr6:149766200-149771200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr6:149766600-149773000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
11	chr6:149766800-149771000	Weak transcription	Fetal Heart	heart
12	chr6:149766800-149771400	Weak transcription	Left Ventricle	heart
13	chr6:149766800-149771600	Weak transcription	Lung	lung
14	chr6:149767400-149772800	Weak transcription	HepG2	liver
15	chr6:149768400-149771600	Strong transcription	Primary T helper cells PMA-I stimulated	--
16	chr6:149768400-149779400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
17	chr6:149768600-149771600	Weak transcription	Gastric	stomach
18	chr6:149769600-149771400	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
19	chr6:149769600-149782800	Strong transcription	Primary B cells from peripheral blood	blood
20	chr6:149769600-149787200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
21	chr6:149769800-149771400	Strong transcription	Primary T cells fromperipheralblood	blood
22	chr6:149769800-149779800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
23	chr6:149770000-149773000	Weak transcription	Primary B cells from cord blood	blood
24	chr6:149770000-149779600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
25	chr6:149770000-149785200	Strong transcription	Primary T helper cells fromperipheralblood	blood
26	chr6:149770400-149771400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr6:149770400-149771600	Weak transcription	Esophagus	oesophagus
28	chr6:149771000-149771200	Enhancers	Hela-S3	cervix
29	chr6:149771000-149771400	Active TSS	Rectal Mucosa Donor 29	rectum
30	chr6:149771000-149771400	Enhancers	Rectal Mucosa Donor 31	rectum
31	chr6:149771000-149771600	Enhancers	Brain Angular Gyrus	brain
32	chr6:149771000-149771600	Bivalent Enhancer	Fetal Intestine Small	intestine
33	chr6:149771000-149771600	Strong transcription	GM12878-XiMat	blood
34	chr6:149771000-149771800	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
35	chr6:149771000-149773400	Enhancers	Fetal Heart	heart
36	chr6:149771200-149771400	Enhancers	Duodenum Mucosa	Duodenum
37	chr6:149771200-149771600	Enhancers	Breast Myoepithelial Primary Cells	Breast
38	chr6:149771200-149771600	Bivalent Enhancer	Brain Inferior Temporal Lobe	brain
39	chr6:149771200-149771600	Enhancers	Colonic Mucosa	Colon
40	chr6:149771200-149771600	Enhancers	Placenta Amnion	Placenta Amnion
41	chr6:149771200-149771800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
42	chr6:149771200-149771800	Bivalent Enhancer	Stomach Mucosa	stomach
43	chr6:149771200-149772000	Flanking Active TSS	Hela-S3	cervix
44	chr6:149771400-149771600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
45	chr6:149771400-149771600	Bivalent/Poised TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr6:149771400-149771600	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr6:149771400-149771600	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr6:149771400-149771600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr6:149771400-149771600	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr6:149771400-149771600	Bivalent Enhancer	Adipose Nuclei	Adipose

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