Variant report

Variant	esv3322429
Chromosome Location	chr6:167663221-167823962
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2085)
CpG islands
(count:4580)
Chromatin interactive
region (count:30)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2085 , 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	chr6:167704338-167705733	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:167699867-167700232	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:167809998-167810531	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:167702230-167702578	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:167722138-167722657	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:167811767-167812223	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:167762709-167763005	HepG2	liver:	n/a	n/a
8	ARID3A	chr6:167723215-167724601	HepG2	liver:	n/a	n/a
9	ARID3A	chr6:167682223-167682912	HepG2	liver:	n/a	n/a
10	ARID3A	chr6:167754780-167756165	HepG2	liver:	n/a	n/a
11	ATF1	chr6:167702337-167702425	K562	blood:	n/a	n/a
12	ATF1	chr6:167727339-167727444	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	chr6:167702257-167702472	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	chr6:167764960-167765154	H1-hESC	embryonic stem cell:	n/a	n/a
18	BATF	chr6:167801477-167801674	GM12878	blood:	n/a	n/a
19	BATF	chr6:167726056-167726329	GM12878	blood:	n/a	n/a
20	BATF	chr6:167765430-167765771	GM12878	blood:	n/a	n/a
21	BATF	chr6:167765440-167765736	GM12878	blood:	n/a	n/a
22	BATF	chr6:167764807-167765183	GM12878	blood:	n/a	n/a
23	BATF	chr6:167726053-167726251	GM12878	blood:	n/a	n/a
24	BATF	chr6:167785311-167785621	GM12878	blood:	n/a	n/a
25	BATF	chr6:167702166-167702414	GM12878	blood:	n/a	n/a
26	BCL11A	chr6:167799353-167799569	GM12878	blood:	n/a	n/a
27	BCL11A	chr6:167800632-167800815	GM12878	blood:	n/a	n/a
28	BCL11A	chr6:167801474-167801790	GM12878	blood:	n/a	n/a
29	BCL11A	chr6:167801472-167801775	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	chr6:167754879-167756141	HepG2	liver:	n/a	n/a
34	BHLHE40	chr6:167732490-167732554	GM12878	blood:	n/a	n/a
35	BHLHE40	chr6:167814832-167815507	HepG2	liver:	n/a	chr6:167815146-167815155 chr6:167815144-167815157 chr6:167815147-167815156 chr6:167815140-167815161 chr6:167815146-167815155
36	BHLHE40	chr6:167810045-167810579	HepG2	liver:	n/a	n/a
37	BHLHE40	chr6:167723198-167723690	HepG2	liver:	n/a	n/a
38	BHLHE40	chr6:167704696-167705644	HepG2	liver:	n/a	n/a
39	BHLHE40	chr6:167691769-167691891	K562	blood:	n/a	chr6:167691854-167691867
40	BHLHE40	chr6:167815066-167815240	K562	blood:	n/a	chr6:167815146-167815155 chr6:167815144-167815157 chr6:167815147-167815156 chr6:167815140-167815161 chr6:167815146-167815155
41	BHLHE40	chr6:167699851-167700081	HepG2	liver:	n/a	n/a
42	BHLHE40	chr6:167755635-167755964	HepG2	liver:	n/a	n/a
43	BHLHE40	chr6:167702264-167702463	HepG2	liver:	n/a	n/a
44	BHLHE40	chr6:167785339-167785655	HepG2	liver:	n/a	n/a
45	BHLHE40	chr6:167811642-167812135	HepG2	liver:	n/a	n/a
46	BHLHE40	chr6:167764785-167765457	GM12878	blood:	n/a	n/a
47	BHLHE40	chr6:167702270-167702451	K562	blood:	n/a	n/a
48	BHLHE40	chr6:167733370-167733629	HepG2	liver:	n/a	n/a
49	BHLHE40	chr6:167722070-167722725	HepG2	liver:	n/a	chr6:167722523-167722539
50	BHLHE40	chr6:167811648-167812302	HepG2	liver:	n/a	n/a

(count:4580 , 50 per page) page: 1 2 3 4 5 6 7 ... 92

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:167705750-167705800	AoSMC	blood vessel:	n/a
2	chr6:167786642-167786692	HIPEpiC	eye:	n/a
3	chr6:167765215-167765265	HepG2	liver:	n/a
4	chr6:167738592-167738642	HCT-116	colon:	n/a
5	chr6:167813372-167813422	K562	blood:	n/a
6	chr6:167705750-167705800	AoSMC	blood vessel:	n/a
7	chr6:167786642-167786692	HIPEpiC	eye:	n/a
8	chr6:167765215-167765265	HepG2	liver:	n/a
9	chr6:167738592-167738642	HCT-116	colon:	n/a
10	chr6:167813372-167813422	K562	blood:	n/a
11	chr6:167738277-167738327	AG10803	skin:	n/a
12	chr6:167734054-167734104	NB4	blood:	n/a
13	chr6:167704769-167704819	HL-60	blood:	n/a
14	chr6:167718461-167718511	HCF	heart:	n/a
15	chr6:167789539-167789589	HRCEpiC	kidney:	n/a
16	chr6:167764967-167765017	SK-N-SH_RA	brain:	n/a
17	chr6:167786059-167786109	SK-N-MC	brain:	n/a
18	chr6:167738592-167738642	SAEC	small airway:	n/a
19	chr6:167704188-167704238	RPTEC	kidney:	n/a
20	chr6:167794374-167794424	SK-N-SH	brain:	n/a
21	chr6:167761204-167761254	Hepatocyte	liver:	n/a
22	chr6:167797877-167797927	Caco-2	colon:	n/a
23	chr6:167704673-167704723	Jurkat	blood:	n/a
24	chr6:167734054-167734104	SAEC	small airway:	n/a
25	chr6:167765215-167765265	HL-60	blood:	n/a
26	chr6:167792741-167792791	HAEpiC	amniotic membrane:	n/a
27	chr6:167739618-167739668	NB4	blood:	n/a
28	chr6:167791024-167791074	K562	blood:	n/a
29	chr6:167770239-167770289	MCF-7	breast:	n/a
30	chr6:167798410-167798460	AG09309	skin:	n/a
31	chr6:167734054-167734104	GM12878	blood:	n/a
32	chr6:167813338-167813388	NB4	blood:	n/a
33	chr6:167814257-167814307	IMR90	lung:	fetal
34	chr6:167786642-167786692	SK-N-SH	brain:	n/a
35	chr6:167761204-167761254	BE2_C	brain:	n/a
36	chr6:167709720-167709770	GM06990	blood:	n/a
37	chr6:167786059-167786109	IMR90	lung:	fetal
38	chr6:167810043-167810093	Hepatocyte	liver:	n/a
39	chr6:167738342-167738392	NH-A	brain:	n/a
40	chr6:167813267-167813317	A549	lung:	n/a
41	chr6:167738592-167738642	MCF10A-Er-Src	breast:	n/a
42	chr6:167810343-167810393	AG10803	skin:	n/a
43	chr6:167813372-167813422	GM12878	blood:	n/a
44	chr6:167791114-167791164	SK-N-MC	brain:	n/a
45	chr6:167680447-167680497	HCT-116	colon:	n/a
46	chr6:167762783-167762833	GM06990	blood:	n/a
47	chr6:167813267-167813317	SKMC	muscle:	n/a
48	chr6:167764620-167764670	MCF10A-Er-Src	breast:	n/a
49	chr6:167738592-167738642	GM06990	blood:	n/a
50	chr6:167764967-167765017	PrEC	prostate:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:167715327..167717333-chr6:167717541..167719931,2	MCF-7	breast:
2	chr6:167736614..167738249-chr6:167740426..167742938,2	K562	blood:
3	chr6:167703616..167705764-chr6:167717598..167719278,2	MCF-7	breast:
4	chr6:167743283..167745523-chr6:167751106..167753120,2	K562	blood:
5	chr6:167823826..167826272-chr6:167829672..167831832,2	K562	blood:
6	chr6:167818746..167821496-chr6:167831177..167833070,2	K562	blood:
7	chr6:167669951..167671777-chr6:167683631..167687000,3	K562	blood:
8	chr6:167662732..167663315-chr6:167819023..167819880,2	K562	blood:
9	chr6:167662535..167665478-chr6:167668701..167671430,2	K562	blood:
10	chr6:167187967..167188932-chr6:167764453..167765086,2	K562	blood:
11	chr6:167631751..167632287-chr6:167701939..167702527,2	MCF-7	breast:
12	chr6:167715327..167717333-chr6:167717541..167719931,2	MCF-7	breast:
13	chr6:167743283..167745523-chr6:167751106..167753120,2	K562	blood:
14	chr6:167702039..167702568-chr6:167764606..167765474,2	MCF-7	breast:
15	chr6:167813417..167815135-chr6:167817698..167819518,2	K562	blood:
16	chr6:167662732..167663315-chr6:167819023..167819880,2	K562	blood:
17	chr6:167813417..167815135-chr6:167817698..167819518,2	K562	blood:
18	chr6:167744023..167747282-chr6:167750789..167753119,3	K562	blood:
19	chr6:167734899..167737753-chr6:167743376..167745822,2	MCF-7	breast:
20	chr6:167699179..167702166-chr6:167703091..167705361,2	K562	blood:
21	chr6:167734899..167737753-chr6:167743376..167745822,2	MCF-7	breast:
22	chr6:167736614..167738249-chr6:167740426..167742938,2	K562	blood:
23	chr1:28836187..28837925-chr6:167694572..167696254,2	K562	blood:
24	chr6:167631565..167632072-chr6:167702069..167702692,3	K562	blood:
25	chr6:167668192..167671777-chr6:167684157..167687082,3	K562	blood:
26	chr6:167636874..167638495-chr6:167694115..167696567,2	K562	blood:
27	chr6:167615262..167616947-chr6:167733556..167735117,2	MCF-7	breast:
28	chr6:167662535..167665478-chr6:167668701..167671430,2	K562	blood:
29	chr6:167744023..167747282-chr6:167750789..167753119,3	K562	blood:
30	chr6:167702039..167702568-chr6:167764606..167765474,2	MCF-7	breast:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TCP10-2	chr6:167810373-167814438	ucscGeneNc_uc003qvx_1
2	lnc-TCP10-1	chr6:167787839-167789289	NONHSAT116097
3	lnc-TCP10-1	chr6:167786578-167786848	NONHSAT116097
4	lnc-TTLL2-1	chr6:167803650-167803969	XLOC_005541
5	lnc-TCP10-3	chr6:167823155-167825466	ucscGeneNc_uc003qvy_1
6	lnc-TCP10-2	chr6:167821589-167821728	ucscGeneNc_uc003qvx_1
7	lnc-UNC93A-3	chr6:167764976-167765446	NONHSAT116095
8	lnc-TCP10-2	chr6:167822441-167822752	ucscGeneNc_uc003qvx_1
9	lnc-TTLL2-1	chr6:167804760-167804979	XLOC_005541
10	lnc-UNC93A-2	chr6:167760960-167761541	NONHSAT116094
11	lnc-UNC93A-3	chr6:167764293-167764966	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
ENSG00000180198	chromatin interactions
ENSG00000112494	chromatin interactions

Extended variants
information (count: 7557 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:7557 , 50 per page) page: 1 2 3 4 5 6 7 ... 152

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs146245257	chr6:167663235-167663236	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs139265225	chr6:167663238-167663239	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs141692876	chr6:167663242-167663243	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs182131653	chr6:167663243-167663244	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs7749161	chr6:167663244-167663245	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs7748106	chr6:167663264-167663265	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs547132409	chr6:167663268-167663269	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs73033153	chr6:167663296-167663297	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs568336157	chr6:167663299-167663300	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs535822564	chr6:167663300-167663301	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs117701027	chr6:167663334-167663335	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs150544069	chr6:167663352-167663353	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs7769055	chr6:167663360-167663361	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs139508648	chr6:167663372-167663373	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs551927221	chr6:167663406-167663407	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs373147864	chr6:167663411-167663412	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs4302650	chr6:167663436-167663437	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs4326217	chr6:167663463-167663464	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs575920527	chr6:167663514-167663515	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs149677924	chr6:167663517-167663518	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs7749762	chr6:167663578-167663579	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs563176305	chr6:167663585-167663586	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs28611126	chr6:167663610-167663611	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs28593008	chr6:167663613-167663614	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs7773576	chr6:167663636-167663637	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs555300175	chr6:167663659-167663660	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs545897079	chr6:167663663-167663664	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs62437251	chr6:167663715-167663716	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs376624481	chr6:167663718-167663719	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs540609231	chr6:167663723-167663724	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs568527911	chr6:167663735-167663736	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs529411185	chr6:167663739-167663740	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs147771402	chr6:167663815-167663816	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs186531362	chr6:167663818-167663819	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs140194211	chr6:167663959-167663960	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs558442510	chr6:167663964-167663965	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs570282033	chr6:167663969-167663970	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs534487839	chr6:167663997-167663998	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs145618818	chr6:167664004-167664005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs571293052	chr6:167664009-167664010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs538624823	chr6:167664049-167664050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs541606024	chr6:167664053-167664054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs556876847	chr6:167664117-167664118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs147723917	chr6:167664156-167664157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs546493074	chr6:167664167-167664168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs7753298	chr6:167664193-167664194	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs58903661	chr6:167664199-167664200	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs540814573	chr6:167664235-167664236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs563093483	chr6:167664243-167664244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs562194062	chr6:167664265-167664266	Weak transcription	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:1287 , 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	chr6:167660800-167663800	Enhancers	H1 Cell Line	embryonic stem cell
3	chr6:167661200-167663400	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr6:167661200-167663600	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr6:167661200-167663600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr6:167661200-167663600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr6:167661200-167663600	Enhancers	HepG2	liver
8	chr6:167661200-167664000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr6:167662800-167663800	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr6:167663200-167663400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr6:167663400-167663600	Bivalent Enhancer	Right Ventricle	heart
12	chr6:167663600-167666400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr6:167663600-167668000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr6:167663600-167668000	Weak transcription	HepG2	liver
15	chr6:167663800-167664000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
16	chr6:167663800-167667000	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr6:167664000-167665000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr6:167664000-167666800	Weak transcription	HUES6 Cell Line	embryonic stem cell
19	chr6:167664800-167665200	Bivalent Enhancer	Right Ventricle	heart
20	chr6:167665000-167665200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr6:167666400-167667200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr6:167666800-167667800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
23	chr6:167667000-167667200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
24	chr6:167667200-167668000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr6:167667800-167668000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
26	chr6:167667800-167668400	ZNF genes & repeats	Spleen	Spleen
27	chr6:167668000-167668400	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr6:167668000-167668800	Enhancers	HepG2	liver
29	chr6:167668400-167669800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr6:167668800-167669200	Weak transcription	HepG2	liver
31	chr6:167669200-167673000	Enhancers	HepG2	liver
32	chr6:167669800-167670000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr6:167669800-167670000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr6:167670000-167671600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr6:167671600-167672200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr6:167672200-167672600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr6:167672600-167672800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr6:167672800-167680200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr6:167673000-167674000	Weak transcription	HepG2	liver
40	chr6:167674000-167675000	Enhancers	HepG2	liver
41	chr6:167675000-167678600	Weak transcription	HepG2	liver
42	chr6:167678400-167679600	Enhancers	Fetal Intestine Large	intestine
43	chr6:167678400-167682400	Enhancers	Fetal Intestine Small	intestine
44	chr6:167678600-167679800	Enhancers	HepG2	liver
45	chr6:167678800-167679000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr6:167678800-167679400	Enhancers	Fetal Kidney	kidney
47	chr6:167678800-167679800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr6:167679000-167679600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr6:167679000-167679800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr6:167679000-167683200	Enhancers	Duodenum Mucosa	Duodenum

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