Variant report

Variant	nsv517210
Chromosome Location	chr6:167683069-167778498
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1402)
CpG islands
(count:2567)
Chromatin interactive
region (count:20)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1402 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:167704338-167705733	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:167699867-167700232	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:167723215-167724601	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:167702230-167702578	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:167754780-167756165	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:167722138-167722657	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:167762709-167763005	HepG2	liver:	n/a	n/a
8	ATF1	chr6:167727339-167727444	K562	blood:	n/a	n/a
9	ATF1	chr6:167702337-167702425	K562	blood:	n/a	n/a
10	ATF2	chr6:167764830-167765266	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr6:167764810-167765270	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr6:167702257-167702472	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr6:167764960-167765154	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr6:167754224-167754403	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr6:167702166-167702414	GM12878	blood:	n/a	n/a
16	BATF	chr6:167726056-167726329	GM12878	blood:	n/a	n/a
17	BATF	chr6:167764807-167765183	GM12878	blood:	n/a	n/a
18	BATF	chr6:167726053-167726251	GM12878	blood:	n/a	n/a
19	BATF	chr6:167765440-167765736	GM12878	blood:	n/a	n/a
20	BATF	chr6:167765430-167765771	GM12878	blood:	n/a	n/a
21	BCL3	chr6:167710341-167710705	GM12878	blood:	n/a	n/a
22	BCLAF1	chr6:167764829-167765189	GM12878	blood:	n/a	chr6:167764879-167764888 chr6:167765036-167765044
23	BHLHE40	chr6:167764785-167765457	GM12878	blood:	n/a	n/a
24	BHLHE40	chr6:167702270-167702451	K562	blood:	n/a	n/a
25	BHLHE40	chr6:167723198-167723690	HepG2	liver:	n/a	n/a
26	BHLHE40	chr6:167722070-167722725	HepG2	liver:	n/a	chr6:167722523-167722539
27	BHLHE40	chr6:167704696-167705644	HepG2	liver:	n/a	n/a
28	BHLHE40	chr6:167702264-167702463	HepG2	liver:	n/a	n/a
29	BHLHE40	chr6:167691769-167691891	K562	blood:	n/a	chr6:167691854-167691867
30	BHLHE40	chr6:167722146-167722527	HepG2	liver:	n/a	n/a
31	BHLHE40	chr6:167733252-167733970	HepG2	liver:	n/a	n/a
32	BHLHE40	chr6:167732490-167732554	GM12878	blood:	n/a	n/a
33	BHLHE40	chr6:167755635-167755964	HepG2	liver:	n/a	n/a
34	BHLHE40	chr6:167723177-167724281	HepG2	liver:	n/a	n/a
35	BHLHE40	chr6:167733370-167733629	HepG2	liver:	n/a	n/a
36	BHLHE40	chr6:167755531-167755951	HepG2	liver:	n/a	n/a
37	BHLHE40	chr6:167699851-167700081	HepG2	liver:	n/a	n/a
38	BHLHE40	chr6:167764869-167765070	K562	blood:	n/a	n/a
39	BHLHE40	chr6:167754879-167756141	HepG2	liver:	n/a	n/a
40	BRCA1	chr6:167722055-167722521	HepG2	liver:	n/a	n/a
41	BRCA1	chr6:167764922-167765205	H1-hESC	embryonic stem cell:	n/a	n/a
42	BRCA1	chr6:167750805-167750846	HepG2	liver:	n/a	n/a
43	CBX3	chr6:167702109-167702642	K562	blood:	n/a	n/a
44	CBX3	chr6:167708857-167709379	K562	blood:	n/a	n/a
45	CBX3	chr6:167708762-167709384	K562	blood:	n/a	n/a
46	CEBPB	chr6:167705019-167705507	HepG2	liver:	n/a	chr6:167705263-167705276 chr6:167705265-167705274 chr6:167705263-167705274
47	CEBPB	chr6:167722086-167722440	HepG2	liver:	n/a	n/a
48	CEBPB	chr6:167693339-167693586	A549	lung:	n/a	chr6:167693472-167693481 chr6:167693471-167693482 chr6:167693470-167693481
49	CEBPB	chr6:167755617-167756086	HepG2	liver:	n/a	n/a
50	CEBPB	chr6:167705190-167705356	K562	blood:	n/a	chr6:167705263-167705276 chr6:167705265-167705274 chr6:167705263-167705274

(count:2567 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:167739618-167739668	GM06990	blood:	n/a
2	chr6:167738277-167738327	U87	brain:	n/a
3	chr6:167739618-167739668	H1-hESC	embryonic stem cell:	embryo
4	chr6:167708827-167708877	ECC-1	luminal epithelium:	n/a
5	chr6:167717196-167717246	MCF10A-Er-Src	breast:	n/a
6	chr6:167739618-167739668	GM06990	blood:	n/a
7	chr6:167738277-167738327	U87	brain:	n/a
8	chr6:167739618-167739668	H1-hESC	embryonic stem cell:	embryo
9	chr6:167708827-167708877	ECC-1	luminal epithelium:	n/a
10	chr6:167717196-167717246	MCF10A-Er-Src	breast:	n/a
11	chr6:167738342-167738392	IMR90	lung:	fetal
12	chr6:167717313-167717363	BE2_C	brain:	n/a
13	chr6:167695026-167695076	Caco-2	colon:	n/a
14	chr6:167695026-167695076	HL-60	blood:	n/a
15	chr6:167765215-167765265	AG10803	skin:	n/a
16	chr6:167710360-167710410	AoSMC	blood vessel:	n/a
17	chr6:167708827-167708877	T-47D	breast:	n/a
18	chr6:167703894-167703944	HRPEpiC	eye:	n/a
19	chr6:167717313-167717363	SKMC	muscle:	n/a
20	chr6:167738592-167738642	ProgFib	skin:	n/a
21	chr6:167764523-167764573	ECC-1	luminal epithelium:	n/a
22	chr6:167710360-167710410	HAEpiC	amniotic membrane:	n/a
23	chr6:167717196-167717246	AG09309	skin:	n/a
24	chr6:167717196-167717246	RPTEC	kidney:	n/a
25	chr6:167738342-167738392	Caco-2	colon:	n/a
26	chr6:167756099-167756149	MCF10A-Er-Src	breast:	n/a
27	chr6:167703894-167703944	HRE	kidney:	n/a
28	chr6:167738592-167738642	H1-hESC	embryonic stem cell:	embryo
29	chr6:167717196-167717246	HRE	kidney:	n/a
30	chr6:167764620-167764670	Caco-2	colon:	n/a
31	chr6:167703591-167703641	GM19239	blood:	n/a
32	chr6:167734054-167734104	GM12891	blood:	n/a
33	chr6:167703591-167703641	HCPEpiC	choroid plexus:	n/a
34	chr6:167765110-167765160	PFSK-1	brain:	n/a
35	chr6:167770239-167770289	AG10803	skin:	n/a
36	chr6:167705750-167705800	AG04450	lung:	fetal
37	chr6:167756099-167756149	CMK	blood:	n/a
38	chr6:167734054-167734104	BE2_C	brain:	n/a
39	chr6:167703591-167703641	MCF10A-Er-Src	breast:	n/a
40	chr6:167765215-167765265	Caco-2	colon:	n/a
41	chr6:167738425-167738475	ProgFib	skin:	n/a
42	chr6:167768382-167768432	HEK293	kidney:	embryo
43	chr6:167738277-167738327	GM12892	blood:	n/a
44	chr6:167756099-167756149	HRCEpiC	kidney:	n/a
45	chr6:167709720-167709770	HNPCEpiC	eye:	n/a
46	chr6:167704673-167704723	SK-N-MC	brain:	n/a
47	chr6:167762783-167762833	PANC-1	pancreas:	n/a
48	chr6:167764967-167765017	AG04450	lung:	fetal
49	chr6:167764967-167765017	GM12892	blood:	n/a
50	chr6:167704769-167704819	AG09319	gingival:	n/a

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

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

(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-2	chr6:167760960-167761541	NONHSAT116094
3	lnc-UNC93A-3	chr6:167764976-167765446	NONHSAT116095

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
ENSG00000112494	chromatin interactions
ENSG00000180198	chromatin interactions

Extended variants
information (count: 4603 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:4603 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4710230	chr6:167683069-167683070	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs544557509	chr6:167683083-167683084	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs77663979	chr6:167683084-167683085	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs572371741	chr6:167683089-167683090	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs542975956	chr6:167683090-167683091	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs59489215	chr6:167683163-167683164	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs1736599	chr6:167683244-167683245	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs1736600	chr6:167683252-167683253	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs200873286	chr6:167683258-167683259	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs1736601	chr6:167683260-167683261	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs2092092	chr6:167683267-167683268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
12	rs375259980	chr6:167683295-167683296	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs191243050	chr6:167683331-167683332	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs539213330	chr6:167683338-167683339	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs386708576	chr6:167683354-167683355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs548990243	chr6:167683355-167683356	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs1757120	chr6:167683392-167683393	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs537642543	chr6:167683404-167683405	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs35874140	chr6:167683422-167683423	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs570969923	chr6:167683459-167683460	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs555048330	chr6:167683534-167683535	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs185086240	chr6:167683563-167683564	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs189706204	chr6:167683580-167683581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs80101451	chr6:167683593-167683594	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs542644127	chr6:167683594-167683595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs554959572	chr6:167683595-167683596	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs372191	chr6:167683611-167683612	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs62437258	chr6:167683628-167683629	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs183429044	chr6:167683632-167683633	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs75570977	chr6:167683663-167683664	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs576961766	chr6:167683700-167683701	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs187704252	chr6:167683736-167683737	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs559919938	chr6:167683742-167683743	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs373771495	chr6:167683754-167683755	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs191993585	chr6:167683761-167683762	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs548611300	chr6:167683806-167683807	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs567403159	chr6:167683845-167683846	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs397728	chr6:167683846-167683847	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs368772439	chr6:167683871-167683872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs75570424	chr6:167683872-167683873	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs538477349	chr6:167683881-167683882	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs113397013	chr6:167683894-167683895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs431415	chr6:167683914-167683915	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs377524910	chr6:167683919-167683920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs113084757	chr6:167683945-167683946	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs563069085	chr6:167683995-167683996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs139187833	chr6:167683996-167683997	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs576624080	chr6:167684019-167684020	Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs73790122	chr6:167684021-167684022	Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs143059003	chr6:167684022-167684023	Weak transcription Genic enhancers 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:1044 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:167679000-167683200	Enhancers	Duodenum Mucosa	Duodenum
2	chr6:167681000-167684600	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr6:167681800-167684400	Weak transcription	Gastric	stomach
4	chr6:167681800-167689000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr6:167682600-167684200	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr6:167682600-167684800	Weak transcription	Stomach Mucosa	stomach
7	chr6:167682800-167683800	Weak transcription	Esophagus	oesophagus
8	chr6:167682800-167684000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr6:167682800-167684200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr6:167682800-167688000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr6:167682800-167688400	Enhancers	Fetal Intestine Large	intestine
12	chr6:167682800-167688600	Enhancers	Fetal Intestine Small	intestine
13	chr6:167683000-167688000	Weak transcription	Placenta Amnion	Placenta Amnion
14	chr6:167683000-167688800	Enhancers	HepG2	liver
15	chr6:167683000-167690200	Weak transcription	Liver	Liver
16	chr6:167683200-167683600	Weak transcription	Duodenum Mucosa	Duodenum
17	chr6:167683600-167687000	Enhancers	Duodenum Mucosa	Duodenum
18	chr6:167683800-167685600	Enhancers	Esophagus	oesophagus
19	chr6:167684000-167684600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr6:167684200-167685000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr6:167684200-167687000	Enhancers	Rectal Mucosa Donor 31	rectum
22	chr6:167684400-167685200	Enhancers	Gastric	stomach
23	chr6:167684400-167685600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr6:167684600-167684800	Enhancers	Rectal Mucosa Donor 29	rectum
25	chr6:167684600-167685000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr6:167684800-167685200	Weak transcription	Rectal Mucosa Donor 29	rectum
27	chr6:167684800-167687000	Enhancers	Stomach Mucosa	stomach
28	chr6:167685000-167686600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr6:167685000-167691800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr6:167685200-167685600	Weak transcription	Gastric	stomach
31	chr6:167685200-167685600	Enhancers	Rectal Mucosa Donor 29	rectum
32	chr6:167685200-167685800	Enhancers	Fetal Heart	heart
33	chr6:167685600-167685800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr6:167685600-167685800	Enhancers	Gastric	stomach
35	chr6:167685600-167686600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr6:167685600-167688000	Weak transcription	Esophagus	oesophagus
37	chr6:167685800-167686600	Weak transcription	Gastric	stomach
38	chr6:167685800-167691600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr6:167686000-167686800	Weak transcription	Small Intestine	intestine
40	chr6:167686600-167687000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr6:167686600-167687000	Enhancers	Gastric	stomach
42	chr6:167686600-167687200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr6:167687000-167688600	Weak transcription	Gastric	stomach
44	chr6:167687000-167690400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr6:167688000-167689200	Enhancers	Placenta Amnion	Placenta Amnion
46	chr6:167688000-167689400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr6:167688000-167689400	Enhancers	Esophagus	oesophagus
48	chr6:167688000-167691600	Weak transcription	H9 Cell Line	embryonic stem cell
49	chr6:167688200-167688400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr6:167688400-167689200	Enhancers	Lung	lung

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