Variant report

Variant	nsv1028156
Chromosome Location	chr6:167680557-167772833
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1468)
CpG islands
(count:2566)
Chromatin interactive
region (count:20)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1468 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:167754780-167756165	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:167723215-167724601	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:167682223-167682912	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:167699867-167700232	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:167704338-167705733	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:167762709-167763005	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:167702230-167702578	HepG2	liver:	n/a	n/a
8	ARID3A	chr6:167722138-167722657	HepG2	liver:	n/a	n/a
9	ATF1	chr6:167727339-167727444	K562	blood:	n/a	n/a
10	ATF1	chr6:167702337-167702425	K562	blood:	n/a	n/a
11	ATF2	chr6:167764830-167765266	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr6:167764810-167765270	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr6:167702257-167702472	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr6:167754224-167754403	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr6:167764960-167765154	H1-hESC	embryonic stem cell:	n/a	n/a
16	BATF	chr6:167764807-167765183	GM12878	blood:	n/a	n/a
17	BATF	chr6:167765440-167765736	GM12878	blood:	n/a	n/a
18	BATF	chr6:167726053-167726251	GM12878	blood:	n/a	n/a
19	BATF	chr6:167765430-167765771	GM12878	blood:	n/a	n/a
20	BATF	chr6:167726056-167726329	GM12878	blood:	n/a	n/a
21	BATF	chr6:167702166-167702414	GM12878	blood:	n/a	n/a
22	BCL3	chr6:167710341-167710705	GM12878	blood:	n/a	n/a
23	BCLAF1	chr6:167764829-167765189	GM12878	blood:	n/a	chr6:167764879-167764888 chr6:167765036-167765044
24	BHLHE40	chr6:167764869-167765070	K562	blood:	n/a	n/a
25	BHLHE40	chr6:167733252-167733970	HepG2	liver:	n/a	n/a
26	BHLHE40	chr6:167723198-167723690	HepG2	liver:	n/a	n/a
27	BHLHE40	chr6:167722146-167722527	HepG2	liver:	n/a	n/a
28	BHLHE40	chr6:167732490-167732554	GM12878	blood:	n/a	n/a
29	BHLHE40	chr6:167702270-167702451	K562	blood:	n/a	n/a
30	BHLHE40	chr6:167722070-167722725	HepG2	liver:	n/a	chr6:167722523-167722539
31	BHLHE40	chr6:167754879-167756141	HepG2	liver:	n/a	n/a
32	BHLHE40	chr6:167704696-167705644	HepG2	liver:	n/a	n/a
33	BHLHE40	chr6:167682232-167682824	HepG2	liver:	n/a	n/a
34	BHLHE40	chr6:167733370-167733629	HepG2	liver:	n/a	n/a
35	BHLHE40	chr6:167723177-167724281	HepG2	liver:	n/a	n/a
36	BHLHE40	chr6:167691769-167691891	K562	blood:	n/a	chr6:167691854-167691867
37	BHLHE40	chr6:167755531-167755951	HepG2	liver:	n/a	n/a
38	BHLHE40	chr6:167702264-167702463	HepG2	liver:	n/a	n/a
39	BHLHE40	chr6:167699851-167700081	HepG2	liver:	n/a	n/a
40	BHLHE40	chr6:167755635-167755964	HepG2	liver:	n/a	n/a
41	BHLHE40	chr6:167764785-167765457	GM12878	blood:	n/a	n/a
42	BRCA1	chr6:167722055-167722521	HepG2	liver:	n/a	n/a
43	BRCA1	chr6:167764922-167765205	H1-hESC	embryonic stem cell:	n/a	n/a
44	BRCA1	chr6:167750805-167750846	HepG2	liver:	n/a	n/a
45	CBX3	chr6:167702109-167702642	K562	blood:	n/a	n/a
46	CBX3	chr6:167708857-167709379	K562	blood:	n/a	n/a
47	CBX3	chr6:167708762-167709384	K562	blood:	n/a	n/a
48	CEBPB	chr6:167693339-167693586	A549	lung:	n/a	chr6:167693472-167693481 chr6:167693471-167693482 chr6:167693470-167693481
49	CEBPB	chr6:167705074-167705472	HepG2	liver:	n/a	chr6:167705263-167705276 chr6:167705265-167705274 chr6:167705263-167705274
50	CEBPB	chr6:167723167-167723598	HepG2	liver:	n/a	n/a

(count:2566 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:167738425-167738475	AG04450	lung:	fetal
2	chr6:167763320-167763370	HCT-116	colon:	n/a
3	chr6:167709720-167709770	HCM	heart:	n/a
4	chr6:167739618-167739668	BJ	skin:	n/a
5	chr6:167738425-167738475	AG04450	lung:	fetal
6	chr6:167763320-167763370	HCT-116	colon:	n/a
7	chr6:167709720-167709770	HCM	heart:	n/a
8	chr6:167739618-167739668	BJ	skin:	n/a
9	chr6:167708827-167708877	HEK293	kidney:	embryo
10	chr6:167705750-167705800	K562	blood:	n/a
11	chr6:167763320-167763370	PANC-1	pancreas:	n/a
12	chr6:167738277-167738327	HPAEpiC	pulmonary alveolar:	n/a
13	chr6:167738594-167738644	GM06990	blood:	n/a
14	chr6:167705253-167705303	NH-A	brain:	n/a
15	chr6:167738592-167738642	NH-A	brain:	n/a
16	chr6:167763975-167764025	GM06990	blood:	n/a
17	chr6:167705253-167705303	GM19239	blood:	n/a
18	chr6:167764146-167764196	HNPCEpiC	eye:	n/a
19	chr6:167765110-167765160	HPAEpiC	pulmonary alveolar:	n/a
20	chr6:167765215-167765265	NH-A	brain:	n/a
21	chr6:167705253-167705303	GM12892	blood:	n/a
22	chr6:167700000-167700050	H1-hESC	embryonic stem cell:	embryo
23	chr6:167768382-167768432	T-47D	breast:	n/a
24	chr6:167709720-167709770	AG10803	skin:	n/a
25	chr6:167705253-167705303	HCPEpiC	choroid plexus:	n/a
26	chr6:167705253-167705303	RPTEC	kidney:	n/a
27	chr6:167764967-167765017	AG09309	skin:	n/a
28	chr6:167763975-167764025	HCM	heart:	n/a
29	chr6:167727700-167727750	PrEC	prostate:	n/a
30	chr6:167765110-167765160	SK-N-SH	brain:	n/a
31	chr6:167704673-167704723	AG04450	lung:	fetal
32	chr6:167763819-167763869	AG09319	gingival:	n/a
33	chr6:167763975-167764025	HRE	kidney:	n/a
34	chr6:167756099-167756149	NB4	blood:	n/a
35	chr6:167761204-167761254	HCPEpiC	choroid plexus:	n/a
36	chr6:167727700-167727750	AG09309	skin:	n/a
37	chr6:167753807-167753857	HEK293	kidney:	embryo
38	chr6:167717313-167717363	AG09309	skin:	n/a
39	chr6:167764620-167764670	HUVEC	blood vessel:	n/a
40	chr6:167763819-167763869	Caco-2	colon:	n/a
41	chr6:167764146-167764196	AG09309	skin:	n/a
42	chr6:167765110-167765160	CMK	blood:	n/a
43	chr6:167739618-167739668	HCM	heart:	n/a
44	chr6:167768382-167768432	SAEC	small airway:	n/a
45	chr6:167700000-167700050	HCM	heart:	n/a
46	chr6:167704188-167704238	GM06990	blood:	n/a
47	chr6:167700000-167700050	IMR90	lung:	fetal
48	chr6:167738592-167738642	HCT-116	colon:	n/a
49	chr6:167738594-167738644	SK-N-MC	brain:	n/a
50	chr6:167763819-167763869	GM12878	blood:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:167743283..167745523-chr6:167751106..167753120,2	K562	blood:
2	chr6:167744023..167747282-chr6:167750789..167753119,3	K562	blood:
3	chr6:167744023..167747282-chr6:167750789..167753119,3	K562	blood:
4	chr6:167743283..167745523-chr6:167751106..167753120,2	K562	blood:
5	chr6:167734899..167737753-chr6:167743376..167745822,2	MCF-7	breast:
6	chr6:167736614..167738249-chr6:167740426..167742938,2	K562	blood:
7	chr6:167734899..167737753-chr6:167743376..167745822,2	MCF-7	breast:
8	chr6:167715327..167717333-chr6:167717541..167719931,2	MCF-7	breast:
9	chr6:167703616..167705764-chr6:167717598..167719278,2	MCF-7	breast:
10	chr6:167187967..167188932-chr6:167764453..167765086,2	K562	blood:
11	chr6:167702039..167702568-chr6:167764606..167765474,2	MCF-7	breast:
12	chr6:167715327..167717333-chr6:167717541..167719931,2	MCF-7	breast:
13	chr6:167615262..167616947-chr6:167733556..167735117,2	MCF-7	breast:
14	chr6:167631751..167632287-chr6:167701939..167702527,2	MCF-7	breast:
15	chr6:167699179..167702166-chr6:167703091..167705361,2	K562	blood:
16	chr6:167631565..167632072-chr6:167702069..167702692,3	K562	blood:
17	chr6:167736614..167738249-chr6:167740426..167742938,2	K562	blood:
18	chr1:28836187..28837925-chr6:167694572..167696254,2	K562	blood:
19	chr6:167702039..167702568-chr6:167764606..167765474,2	MCF-7	breast:
20	chr6:167636874..167638495-chr6:167694115..167696567,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UNC93A-3	chr6:167764293-167764966	NONHSAT116095
2	lnc-UNC93A-3	chr6:167764976-167765446	NONHSAT116095
3	lnc-UNC93A-2	chr6:167760960-167761541	NONHSAT116094

No data

Variant related genes	Relation type
UNC93A	TF binding region
TTLL2	TF binding region
ENSG00000217447	TF binding region
UNC93A	CpG island
TTLL2	CpG island
ENSG00000217447	CpG island
ENSG00000180198	chromatin interactions
ENSG00000112494	chromatin interactions

Extended variants
information (count: 4559 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:4559 , 50 per page) page: 1 2 3 4 5 6 7 ... 92

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs407663	chr6:167680557-167680558	Flanking Active TSS Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs369321395	chr6:167680577-167680578	Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs116703541	chr6:167680589-167680590	Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs565670059	chr6:167680613-167680614	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs9348252	chr6:167680626-167680627	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs448509	chr6:167680649-167680650	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs569603319	chr6:167680661-167680662	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs149577722	chr6:167680666-167680667	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs558234801	chr6:167680690-167680691	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs570485441	chr6:167680699-167680700	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs556747732	chr6:167680715-167680716	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs367106	chr6:167680728-167680729	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs73033171	chr6:167680770-167680771	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs73790103	chr6:167680798-167680799	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs114251647	chr6:167680799-167680800	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs578243306	chr6:167680823-167680824	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs575610669	chr6:167680838-167680839	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs73255003	chr6:167680874-167680875	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs564266541	chr6:167680887-167680888	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs572883589	chr6:167680920-167680921	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs9366128	chr6:167680925-167680926	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs368147768	chr6:167680933-167680934	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs559220234	chr6:167680983-167680984	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs529940362	chr6:167680987-167680988	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs548037435	chr6:167680991-167680992	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs563512359	chr6:167681012-167681013	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs530496096	chr6:167681036-167681037	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs552229334	chr6:167681049-167681050	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs570595548	chr6:167681064-167681065	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs534591281	chr6:167681066-167681067	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs111897839	chr6:167681124-167681125	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs425237	chr6:167681136-167681137	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs536157167	chr6:167681148-167681149	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs188133508	chr6:167681156-167681157	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs575771014	chr6:167681163-167681164	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs539677547	chr6:167681167-167681168	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs115795696	chr6:167681196-167681197	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs573048039	chr6:167681232-167681233	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs540187715	chr6:167681243-167681244	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs561755406	chr6:167681247-167681248	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs574608854	chr6:167681288-167681289	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs542131362	chr6:167681374-167681375	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs147227398	chr6:167681382-167681383	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs377511	chr6:167681389-167681390	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs552442520	chr6:167681398-167681399	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs385410	chr6:167681399-167681400	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs454264	chr6:167681408-167681409	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs386708574	chr6:167681411-167681412	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs149896510	chr6:167681413-167681414	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs535131773	chr6:167681448-167681449	Weak transcription Enhancers	TF binding 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
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
Chordoma	18071362	CNVD
Glioblastoma multiforme	19435819	CNVD
Developmental delay	21147756	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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1094 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:167678400-167682400	Enhancers	Fetal Intestine Small	intestine
2	chr6:167679000-167683200	Enhancers	Duodenum Mucosa	Duodenum
3	chr6:167680200-167680800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr6:167680200-167681000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr6:167680200-167681000	Enhancers	Fetal Kidney	kidney
6	chr6:167680200-167681000	Enhancers	Fetal Muscle Leg	muscle
7	chr6:167680200-167682000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr6:167680200-167682400	Enhancers	HepG2	liver
9	chr6:167680400-167680600	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr6:167680400-167680600	Enhancers	Sigmoid Colon	Sigmoid Colon
11	chr6:167680400-167680800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr6:167680400-167681000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr6:167680400-167681800	Enhancers	Esophagus	oesophagus
14	chr6:167680400-167682000	Enhancers	Fetal Thymus	thymus
15	chr6:167680400-167682400	Enhancers	Fetal Intestine Large	intestine
16	chr6:167680400-167682600	Enhancers	Stomach Mucosa	stomach
17	chr6:167680600-167680800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
18	chr6:167680600-167681000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr6:167680600-167681200	Enhancers	Gastric	stomach
20	chr6:167680600-167681400	Weak transcription	Sigmoid Colon	Sigmoid Colon
21	chr6:167680800-167681000	Enhancers	Rectal Mucosa Donor 29	rectum
22	chr6:167680800-167681800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr6:167680800-167682200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr6:167680800-167682600	Enhancers	Rectal Mucosa Donor 31	rectum
25	chr6:167681000-167681600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr6:167681000-167682200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr6:167681000-167682600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr6:167681000-167682800	Weak transcription	Fetal Kidney	kidney
29	chr6:167681000-167684600	Weak transcription	Rectal Mucosa Donor 29	rectum
30	chr6:167681200-167681600	Weak transcription	Gastric	stomach
31	chr6:167681400-167681800	Enhancers	Sigmoid Colon	Sigmoid Colon
32	chr6:167681600-167681800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr6:167681600-167681800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr6:167681600-167681800	Enhancers	Gastric	stomach
35	chr6:167681600-167682400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr6:167681600-167682800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr6:167681600-167682800	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr6:167681600-167683000	Enhancers	Placenta Amnion	Placenta Amnion
39	chr6:167681800-167682200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr6:167681800-167682400	Enhancers	Liver	Liver
41	chr6:167681800-167682400	Weak transcription	Esophagus	oesophagus
42	chr6:167681800-167684400	Weak transcription	Gastric	stomach
43	chr6:167681800-167689000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr6:167682000-167682400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr6:167682000-167682400	Enhancers	Sigmoid Colon	Sigmoid Colon
46	chr6:167682200-167682400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr6:167682200-167682600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr6:167682200-167682600	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr6:167682200-167682800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr6:167682400-167682800	Enhancers	iPS-18 Cell Line	embryonic stem cell

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