Variant report

Variant	nsv1024654
Chromosome Location	chr6:167662500-167818861
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2076)
CpG islands
(count:4584)
Chromatin interactive
region (count:28)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2076 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:167702230-167702578	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:167811767-167812223	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:167704338-167705733	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:167762709-167763005	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:167722138-167722657	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:167723215-167724601	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:167682223-167682912	HepG2	liver:	n/a	n/a
8	ARID3A	chr6:167754780-167756165	HepG2	liver:	n/a	n/a
9	ARID3A	chr6:167699867-167700232	HepG2	liver:	n/a	n/a
10	ARID3A	chr6:167809998-167810531	HepG2	liver:	n/a	n/a
11	ATF1	chr6:167727339-167727444	K562	blood:	n/a	n/a
12	ATF1	chr6:167702337-167702425	K562	blood:	n/a	n/a
13	ATF2	chr6:167764830-167765266	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr6:167764810-167765270	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr6:167764960-167765154	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr6:167754224-167754403	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr6:167702257-167702472	H1-hESC	embryonic stem cell:	n/a	n/a
18	BATF	chr6:167765430-167765771	GM12878	blood:	n/a	n/a
19	BATF	chr6:167765440-167765736	GM12878	blood:	n/a	n/a
20	BATF	chr6:167785311-167785621	GM12878	blood:	n/a	n/a
21	BATF	chr6:167702166-167702414	GM12878	blood:	n/a	n/a
22	BATF	chr6:167764807-167765183	GM12878	blood:	n/a	n/a
23	BATF	chr6:167726056-167726329	GM12878	blood:	n/a	n/a
24	BATF	chr6:167801477-167801674	GM12878	blood:	n/a	n/a
25	BATF	chr6:167726053-167726251	GM12878	blood:	n/a	n/a
26	BCL11A	chr6:167801474-167801790	GM12878	blood:	n/a	n/a
27	BCL11A	chr6:167799353-167799569	GM12878	blood:	n/a	n/a
28	BCL11A	chr6:167801472-167801775	GM12878	blood:	n/a	n/a
29	BCL11A	chr6:167800632-167800815	GM12878	blood:	n/a	n/a
30	BCL11A	chr6:167801917-167802109	GM12878	blood:	n/a	n/a
31	BCL3	chr6:167710341-167710705	GM12878	blood:	n/a	n/a
32	BCLAF1	chr6:167764829-167765189	GM12878	blood:	n/a	chr6:167764879-167764888 chr6:167765036-167765044
33	BHLHE40	chr6:167722070-167722725	HepG2	liver:	n/a	chr6:167722523-167722539
34	BHLHE40	chr6:167764869-167765070	K562	blood:	n/a	n/a
35	BHLHE40	chr6:167755531-167755951	HepG2	liver:	n/a	n/a
36	BHLHE40	chr6:167764785-167765457	GM12878	blood:	n/a	n/a
37	BHLHE40	chr6:167815066-167815240	K562	blood:	n/a	chr6:167815146-167815155 chr6:167815144-167815157 chr6:167815147-167815156 chr6:167815140-167815161 chr6:167815146-167815155
38	BHLHE40	chr6:167723177-167724281	HepG2	liver:	n/a	n/a
39	BHLHE40	chr6:167691769-167691891	K562	blood:	n/a	chr6:167691854-167691867
40	BHLHE40	chr6:167811648-167812302	HepG2	liver:	n/a	n/a
41	BHLHE40	chr6:167682232-167682824	HepG2	liver:	n/a	n/a
42	BHLHE40	chr6:167702270-167702451	K562	blood:	n/a	n/a
43	BHLHE40	chr6:167733370-167733629	HepG2	liver:	n/a	n/a
44	BHLHE40	chr6:167785339-167785655	HepG2	liver:	n/a	n/a
45	BHLHE40	chr6:167702264-167702463	HepG2	liver:	n/a	n/a
46	BHLHE40	chr6:167733252-167733970	HepG2	liver:	n/a	n/a
47	BHLHE40	chr6:167723198-167723690	HepG2	liver:	n/a	n/a
48	BHLHE40	chr6:167722146-167722527	HepG2	liver:	n/a	n/a
49	BHLHE40	chr6:167814832-167815507	HepG2	liver:	n/a	chr6:167815146-167815155 chr6:167815144-167815157 chr6:167815147-167815156 chr6:167815140-167815161 chr6:167815146-167815155
50	BHLHE40	chr6:167755635-167755964	HepG2	liver:	n/a	n/a

(count:4584 , 50 per page) page: 1 2 3 4 5 6 7 ... 92

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:167816104-167816154	AG10803	skin:	n/a
2	chr6:167756099-167756149	GM19239	blood:	n/a
3	chr6:167753807-167753857	ECC-1	luminal epithelium:	n/a
4	chr6:167764523-167764573	PANC-1	pancreas:	n/a
5	chr6:167737937-167737987	HepG2	liver:	n/a
6	chr6:167680447-167680497	GM19239	blood:	n/a
7	chr6:167765110-167765160	AG04450	lung:	fetal
8	chr6:167703591-167703641	Hela-S3	cervix:	n/a
9	chr6:167705750-167705800	ovcar-3	ovarian:	n/a
10	chr6:167816104-167816154	AG10803	skin:	n/a
11	chr6:167756099-167756149	GM19239	blood:	n/a
12	chr6:167753807-167753857	ECC-1	luminal epithelium:	n/a
13	chr6:167764523-167764573	PANC-1	pancreas:	n/a
14	chr6:167737937-167737987	HepG2	liver:	n/a
15	chr6:167680447-167680497	GM19239	blood:	n/a
16	chr6:167765110-167765160	AG04450	lung:	fetal
17	chr6:167703591-167703641	Hela-S3	cervix:	n/a
18	chr6:167705750-167705800	ovcar-3	ovarian:	n/a
19	chr6:167705253-167705303	HCPEpiC	choroid plexus:	n/a
20	chr6:167792181-167792231	SAEC	small airway:	n/a
21	chr6:167789539-167789589	ECC-1	luminal epithelium:	n/a
22	chr6:167718461-167718511	NT2-D1	testis:	n/a
23	chr6:167763819-167763869	HCPEpiC	choroid plexus:	n/a
24	chr6:167809876-167809926	GM12892	blood:	n/a
25	chr6:167808366-167808416	BE2_C	brain:	n/a
26	chr6:167794506-167794556	BE2_C	brain:	n/a
27	chr6:167734054-167734104	Caco-2	colon:	n/a
28	chr6:167786592-167786642	NHDF-neo	bronchial:	n/a
29	chr6:167709720-167709770	HRCEpiC	kidney:	n/a
30	chr6:167786642-167786692	HIPEpiC	eye:	n/a
31	chr6:167803413-167803463	ovcar-3	ovarian:	n/a
32	chr6:167770239-167770289	AG09319	gingival:	n/a
33	chr6:167789539-167789589	GM12892	blood:	n/a
34	chr6:167705253-167705303	HL-60	blood:	n/a
35	chr6:167738342-167738392	ECC-1	luminal epithelium:	n/a
36	chr6:167763819-167763869	A549	lung:	n/a
37	chr6:167703894-167703944	SK-N-SH	brain:	n/a
38	chr6:167705253-167705303	ovcar-3	ovarian:	n/a
39	chr6:167764620-167764670	IMR90	lung:	fetal
40	chr6:167708827-167708877	GM06990	blood:	n/a
41	chr6:167808551-167808601	HCT-116	colon:	n/a
42	chr6:167814314-167814364	BJ	skin:	n/a
43	chr6:167709720-167709770	HCM	heart:	n/a
44	chr6:167813267-167813317	GM06990	blood:	n/a
45	chr6:167738594-167738644	SKMC	muscle:	n/a
46	chr6:167764967-167765017	HNPCEpiC	eye:	n/a
47	chr6:167718461-167718511	HRCEpiC	kidney:	n/a
48	chr6:167709720-167709770	AG04450	lung:	fetal
49	chr6:167753807-167753857	Jurkat	blood:	n/a
50	chr6:167789539-167789589	Hepatocyte	liver:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:167703616..167705764-chr6:167717598..167719278,2	MCF-7	breast:
2	chr6:167668192..167671777-chr6:167684157..167687082,3	K562	blood:
3	chr6:167736614..167738249-chr6:167740426..167742938,2	K562	blood:
4	chr6:167734899..167737753-chr6:167743376..167745822,2	MCF-7	breast:
5	chr6:167631565..167632072-chr6:167702069..167702692,3	K562	blood:
6	chr6:167702039..167702568-chr6:167764606..167765474,2	MCF-7	breast:
7	chr6:167813417..167815135-chr6:167817698..167819518,2	K562	blood:
8	chr6:167744023..167747282-chr6:167750789..167753119,3	K562	blood:
9	chr6:167631751..167632287-chr6:167701939..167702527,2	MCF-7	breast:
10	chr6:167662535..167665478-chr6:167668701..167671430,2	K562	blood:
11	chr6:167662535..167665478-chr6:167668701..167671430,2	K562	blood:
12	chr6:167187967..167188932-chr6:167764453..167765086,2	K562	blood:
13	chr6:167636874..167638495-chr6:167694115..167696567,2	K562	blood:
14	chr6:167662732..167663315-chr6:167819023..167819880,2	K562	blood:
15	chr6:167743283..167745523-chr6:167751106..167753120,2	K562	blood:
16	chr6:167615262..167616947-chr6:167733556..167735117,2	MCF-7	breast:
17	chr6:167734899..167737753-chr6:167743376..167745822,2	MCF-7	breast:
18	chr6:167813417..167815135-chr6:167817698..167819518,2	K562	blood:
19	chr6:167715327..167717333-chr6:167717541..167719931,2	MCF-7	breast:
20	chr6:167669951..167671777-chr6:167683631..167687000,3	K562	blood:
21	chr6:167699179..167702166-chr6:167703091..167705361,2	K562	blood:
22	chr6:167702039..167702568-chr6:167764606..167765474,2	MCF-7	breast:
23	chr6:167736614..167738249-chr6:167740426..167742938,2	K562	blood:
24	chr6:167818746..167821496-chr6:167831177..167833070,2	K562	blood:
25	chr6:167744023..167747282-chr6:167750789..167753119,3	K562	blood:
26	chr6:167743283..167745523-chr6:167751106..167753120,2	K562	blood:
27	chr6:167715327..167717333-chr6:167717541..167719931,2	MCF-7	breast:
28	chr1:28836187..28837925-chr6:167694572..167696254,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TCP10-2	chr6:167810373-167814438	ucscGeneNc_uc003qvx_1
2	lnc-TTLL2-1	chr6:167804760-167804979	XLOC_005541
3	lnc-TTLL2-1	chr6:167803650-167803969	XLOC_005541
4	lnc-UNC93A-2	chr6:167760960-167761541	NONHSAT116094
5	lnc-UNC93A-3	chr6:167764293-167764966	NONHSAT116095
6	lnc-TCP10-1	chr6:167786578-167786848	NONHSAT116097
7	lnc-TCP10-1	chr6:167787839-167789289	NONHSAT116097
8	lnc-UNC93A-3	chr6:167764976-167765446	NONHSAT116095

No data

Variant related genes	Relation type
UNC93A	TF binding region
TCP10	TF binding region
TTLL2	TF binding region
ENSG00000217447	TF binding region
UNC93A	CpG island
TCP10	CpG island
TTLL2	CpG island
ENSG00000217447	CpG island
ENSG00000112494	chromatin interactions
ENSG00000180198	chromatin interactions

Extended variants
information (count: 7334 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:7334 , 50 per page) page: 1 2 3 4 5 6 7 ... 147

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs559110454	chr6:167662510-167662511	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs368202125	chr6:167662517-167662518	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs577281735	chr6:167662518-167662519	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs138733626	chr6:167662536-167662537	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs186139188	chr6:167662541-167662542	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs530648662	chr6:167662554-167662555	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs543359273	chr6:167662569-167662570	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs561226396	chr6:167662578-167662579	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs573195298	chr6:167662587-167662588	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs542912059	chr6:167662599-167662600	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs560878857	chr6:167662603-167662604	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs191653115	chr6:167662609-167662610	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs183215501	chr6:167662624-167662625	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs71553158	chr6:167662650-167662651	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs370753316	chr6:167662673-167662674	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs564618848	chr6:167662703-167662704	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs10455812	chr6:167662738-167662739	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs186495465	chr6:167662746-167662747	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs546982468	chr6:167662761-167662762	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs117509938	chr6:167662768-167662769	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs530280914	chr6:167662769-167662770	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs190919900	chr6:167662849-167662850	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs368771739	chr6:167662852-167662853	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs570115077	chr6:167662853-167662854	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs540969929	chr6:167662874-167662875	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs59744400	chr6:167662875-167662876	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs9459945	chr6:167662893-167662894	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs552832057	chr6:167662914-167662915	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs143650303	chr6:167662965-167662966	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs535172778	chr6:167662971-167662972	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs553356743	chr6:167663002-167663003	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs574786285	chr6:167663020-167663021	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs62437250	chr6:167663025-167663026	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs554873240	chr6:167663046-167663047	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs7748959	chr6:167663080-167663081	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs543199847	chr6:167663089-167663090	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs59458610	chr6:167663092-167663093	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs200248508	chr6:167663108-167663109	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs576524961	chr6:167663151-167663152	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs540727850	chr6:167663175-167663176	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs2989562	chr6:167663178-167663179	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs28402977	chr6:167663184-167663185	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs146245257	chr6:167663235-167663236	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs139265225	chr6:167663238-167663239	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs141692876	chr6:167663242-167663243	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs182131653	chr6:167663243-167663244	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs7749161	chr6:167663244-167663245	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs7748106	chr6:167663264-167663265	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs547132409	chr6:167663268-167663269	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs73033153	chr6:167663296-167663297	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1271 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:167654800-167664800	Weak transcription	Right Atrium	heart
2	chr6:167660800-167662800	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr6:167660800-167663800	Enhancers	H1 Cell Line	embryonic stem cell
4	chr6:167661000-167662800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
5	chr6:167661000-167663000	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr6:167661200-167662800	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr6:167661200-167662800	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr6:167661200-167662800	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr6:167661200-167663400	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr6:167661200-167663600	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr6:167661200-167663600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr6:167661200-167663600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr6:167661200-167663600	Enhancers	HepG2	liver
14	chr6:167661200-167664000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr6:167661600-167662600	Enhancers	H9 Cell Line	embryonic stem cell
16	chr6:167662200-167662800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr6:167662200-167662800	Enhancers	Fetal Brain Male	brain
18	chr6:167662400-167662600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr6:167662400-167662600	Enhancers	Brain Anterior Caudate	brain
20	chr6:167662400-167662600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
21	chr6:167662400-167662800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr6:167662600-167663000	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr6:167662800-167663800	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr6:167663200-167663400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr6:167663400-167663600	Bivalent Enhancer	Right Ventricle	heart
26	chr6:167663600-167666400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr6:167663600-167668000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr6:167663600-167668000	Weak transcription	HepG2	liver
29	chr6:167663800-167664000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
30	chr6:167663800-167667000	Weak transcription	H1 Cell Line	embryonic stem cell
31	chr6:167664000-167665000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr6:167664000-167666800	Weak transcription	HUES6 Cell Line	embryonic stem cell
33	chr6:167664800-167665200	Bivalent Enhancer	Right Ventricle	heart
34	chr6:167665000-167665200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr6:167666400-167667200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr6:167666800-167667800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
37	chr6:167667000-167667200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
38	chr6:167667200-167668000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
39	chr6:167667800-167668000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
40	chr6:167667800-167668400	ZNF genes & repeats	Spleen	Spleen
41	chr6:167668000-167668400	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr6:167668000-167668800	Enhancers	HepG2	liver
43	chr6:167668400-167669800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr6:167668800-167669200	Weak transcription	HepG2	liver
45	chr6:167669200-167673000	Enhancers	HepG2	liver
46	chr6:167669800-167670000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr6:167669800-167670000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr6:167670000-167671600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr6:167671600-167672200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr6:167672200-167672600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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