Variant report

Variant	nsv538545
Chromosome Location	chr6:167570212-167832936
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3490)
CpG islands
(count:7637)
Chromatin interactive
region (count:43)
LncRNA
region (count:35)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3490 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:167645950-167646149	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:167809998-167810531	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:167651727-167651738	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:167754780-167756165	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:167637599-167638030	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:167702230-167702578	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:167722138-167722657	HepG2	liver:	n/a	n/a
8	ARID3A	chr6:167811767-167812223	HepG2	liver:	n/a	n/a
9	ARID3A	chr6:167723215-167724601	HepG2	liver:	n/a	n/a
10	ARID3A	chr6:167699867-167700232	HepG2	liver:	n/a	n/a
11	ARID3A	chr6:167628930-167629130	HepG2	liver:	n/a	n/a
12	ARID3A	chr6:167682223-167682912	HepG2	liver:	n/a	n/a
13	ARID3A	chr6:167762709-167763005	HepG2	liver:	n/a	n/a
14	ARID3A	chr6:167632046-167632420	HepG2	liver:	n/a	n/a
15	ARID3A	chr6:167629415-167629646	HepG2	liver:	n/a	n/a
16	ARID3A	chr6:167629887-167630151	HepG2	liver:	n/a	n/a
17	ARID3A	chr6:167652605-167653007	HepG2	liver:	n/a	n/a
18	ARID3A	chr6:167655013-167655211	HepG2	liver:	n/a	n/a
19	ARID3A	chr6:167633428-167633974	HepG2	liver:	n/a	n/a
20	ARID3A	chr6:167704338-167705733	HepG2	liver:	n/a	n/a
21	ARID3A	chr6:167624462-167624811	HepG2	liver:	n/a	n/a
22	ATF1	chr6:167727339-167727444	K562	blood:	n/a	n/a
23	ATF1	chr6:167702337-167702425	K562	blood:	n/a	n/a
24	ATF2	chr6:167651500-167652487	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF2	chr6:167625939-167626508	GM12878	blood:	n/a	n/a
26	ATF2	chr6:167626020-167626431	GM12878	blood:	n/a	n/a
27	ATF2	chr6:167764830-167765266	H1-hESC	embryonic stem cell:	n/a	n/a
28	ATF2	chr6:167641353-167641826	H1-hESC	embryonic stem cell:	n/a	n/a
29	ATF2	chr6:167641333-167641936	H1-hESC	embryonic stem cell:	n/a	n/a
30	ATF2	chr6:167764810-167765270	H1-hESC	embryonic stem cell:	n/a	n/a
31	ATF2	chr6:167576782-167577257	H1-hESC	embryonic stem cell:	n/a	n/a
32	BACH1	chr6:167754224-167754403	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr6:167577029-167577525	H1-hESC	embryonic stem cell:	n/a	n/a
34	BACH1	chr6:167702257-167702472	H1-hESC	embryonic stem cell:	n/a	n/a
35	BACH1	chr6:167631950-167632087	H1-hESC	embryonic stem cell:	n/a	n/a
36	BACH1	chr6:167641591-167641850	H1-hESC	embryonic stem cell:	n/a	n/a
37	BACH1	chr6:167764960-167765154	H1-hESC	embryonic stem cell:	n/a	n/a
38	BACH1	chr6:167637370-167637829	H1-hESC	embryonic stem cell:	n/a	n/a
39	BATF	chr6:167785311-167785621	GM12878	blood:	n/a	n/a
40	BATF	chr6:167596405-167596715	GM12878	blood:	n/a	n/a
41	BATF	chr6:167765430-167765771	GM12878	blood:	n/a	n/a
42	BATF	chr6:167625959-167626402	GM12878	blood:	n/a	n/a
43	BATF	chr6:167625794-167626502	GM12878	blood:	n/a	n/a
44	BATF	chr6:167726053-167726251	GM12878	blood:	n/a	n/a
45	BATF	chr6:167764807-167765183	GM12878	blood:	n/a	n/a
46	BATF	chr6:167765440-167765736	GM12878	blood:	n/a	n/a
47	BATF	chr6:167702166-167702414	GM12878	blood:	n/a	n/a
48	BATF	chr6:167726056-167726329	GM12878	blood:	n/a	n/a
49	BATF	chr6:167801477-167801674	GM12878	blood:	n/a	n/a
50	BATF	chr6:167631870-167632155	GM12878	blood:	n/a	n/a

(count:7637 , 50 per page) page: 1 2 3 4 5 6 7 ... 153

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:167584900-167584950	T-47D	breast:	n/a
2	chr6:167652028-167652078	PFSK-1	brain:	n/a
3	chr6:167623149-167623199	AG10803	skin:	n/a
4	chr6:167705750-167705800	HEEpiC	esophagus:	n/a
5	chr6:167653907-167653957	BE2_C	brain:	n/a
6	chr6:167813267-167813317	PANC-1	pancreas:	n/a
7	chr6:167680455-167680505	MCF-7	breast:	n/a
8	chr6:167763758-167763808	T-47D	breast:	n/a
9	chr6:167814397-167814447	AG09309	skin:	n/a
10	chr6:167680447-167680497	Hela-S3	cervix:	n/a
11	chr6:167591040-167591090	MCF10A-Er-Src	breast:	n/a
12	chr6:167709720-167709770	HEEpiC	esophagus:	n/a
13	chr6:167584900-167584950	T-47D	breast:	n/a
14	chr6:167652028-167652078	PFSK-1	brain:	n/a
15	chr6:167623149-167623199	AG10803	skin:	n/a
16	chr6:167705750-167705800	HEEpiC	esophagus:	n/a
17	chr6:167653907-167653957	BE2_C	brain:	n/a
18	chr6:167813267-167813317	PANC-1	pancreas:	n/a
19	chr6:167680455-167680505	MCF-7	breast:	n/a
20	chr6:167763758-167763808	T-47D	breast:	n/a
21	chr6:167814397-167814447	AG09309	skin:	n/a
22	chr6:167680447-167680497	Hela-S3	cervix:	n/a
23	chr6:167591040-167591090	MCF10A-Er-Src	breast:	n/a
24	chr6:167709720-167709770	HEEpiC	esophagus:	n/a
25	chr6:167587692-167587742	K562	blood:	n/a
26	chr6:167635072-167635122	HRCEpiC	kidney:	n/a
27	chr6:167590911-167590961	LNCaP	prostate:	n/a
28	chr6:167587558-167587608	HAEpiC	amniotic membrane:	n/a
29	chr6:167764523-167764573	AoSMC	blood vessel:	n/a
30	chr6:167584900-167584950	H1-hESC	embryonic stem cell:	embryo
31	chr6:167756099-167756149	U87	brain:	n/a
32	chr6:167704188-167704238	HCT-116	colon:	n/a
33	chr6:167622441-167622491	Hepatocyte	liver:	n/a
34	chr6:167571630-167571680	ECC-1	luminal epithelium:	n/a
35	chr6:167589323-167589373	T-47D	breast:	n/a
36	chr6:167763975-167764025	K562	blood:	n/a
37	chr6:167738592-167738642	H1-hESC	embryonic stem cell:	embryo
38	chr6:167789539-167789589	NT2-D1	testis:	n/a
39	chr6:167649256-167649306	GM19239	blood:	n/a
40	chr6:167709720-167709770	PFSK-1	brain:	n/a
41	chr6:167738592-167738642	GM06990	blood:	n/a
42	chr6:167704673-167704723	NT2-D1	testis:	n/a
43	chr6:167622441-167622491	A549	lung:	n/a
44	chr6:167792741-167792791	Caco-2	colon:	n/a
45	chr6:167738592-167738642	PrEC	prostate:	n/a
46	chr6:167764967-167765017	AoSMC	blood vessel:	n/a
47	chr6:167704188-167704238	HCM	heart:	n/a
48	chr6:167803413-167803463	ovcar-3	ovarian:	n/a
49	chr6:167792741-167792791	AG04450	lung:	fetal
50	chr6:167727700-167727750	ECC-1	luminal epithelium:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr6:167631565..167632072-chr6:167702069..167702692,3	K562	blood:
2	chr6:167620399..167623068-chr6:167623897..167626646,2	K562	blood:
3	chr6:167636874..167638495-chr6:167694115..167696567,2	K562	blood:
4	chr6:167744023..167747282-chr6:167750789..167753119,3	K562	blood:
5	chr6:167703616..167705764-chr6:167717598..167719278,2	MCF-7	breast:
6	chr6:167823826..167826272-chr6:167829672..167831832,2	K562	blood:
7	chr6:167623945..167626187-chr6:168297648..168300373,2	K562	blood:
8	chr6:167668192..167671777-chr6:167684157..167687082,3	K562	blood:
9	chr6:167743283..167745523-chr6:167751106..167753120,2	K562	blood:
10	chr6:167615262..167616947-chr6:167733556..167735117,2	MCF-7	breast:
11	chr6:167702039..167702568-chr6:167764606..167765474,2	MCF-7	breast:
12	chr6:167823826..167826272-chr6:167829672..167831832,2	K562	blood:
13	chr6:167573482..167576354-chr6:167702662..167705429,2	K562	blood:
14	chr6:167662535..167665478-chr6:167668701..167671430,2	K562	blood:
15	chr6:167818746..167821496-chr6:167831177..167833070,2	K562	blood:
16	chr6:167615262..167616947-chr6:167733556..167735117,2	MCF-7	breast:
17	chr6:167623779..167626117-chr6:167629928..167632260,2	MCF-7	breast:
18	chr6:167662732..167663315-chr6:167819023..167819880,2	K562	blood:
19	chr6:167636874..167638495-chr6:167694115..167696567,2	K562	blood:
20	chr6:167702039..167702568-chr6:167764606..167765474,2	MCF-7	breast:
21	chr6:167813417..167815135-chr6:167817698..167819518,2	K562	blood:
22	chr6:167736614..167738249-chr6:167740426..167742938,2	K562	blood:
23	chr6:167699179..167702166-chr6:167703091..167705361,2	K562	blood:
24	chr6:167734899..167737753-chr6:167743376..167745822,2	MCF-7	breast:
25	chr6:167744023..167747282-chr6:167750789..167753119,3	K562	blood:
26	chr6:167813417..167815135-chr6:167817698..167819518,2	K562	blood:
27	chr6:167571310..167572911-chr6:167574419..167576239,2	K562	blood:
28	chr1:28836187..28837925-chr6:167694572..167696254,2	K562	blood:
29	chr6:167187967..167188932-chr6:167764453..167765086,2	K562	blood:
30	chr20:57615578..57617834-chr6:167831422..167833295,2	MCF-7	breast:
31	chr6:167743283..167745523-chr6:167751106..167753120,2	K562	blood:
32	chr6:167715327..167717333-chr6:167717541..167719931,2	MCF-7	breast:
33	chr6:167631565..167632072-chr6:167702069..167702692,3	K562	blood:
34	chr6:167662732..167663315-chr6:167819023..167819880,2	K562	blood:
35	chr6:167631751..167632287-chr6:167701939..167702527,2	MCF-7	breast:
36	chr6:167669951..167671777-chr6:167683631..167687000,3	K562	blood:
37	chr6:167662535..167665478-chr6:167668701..167671430,2	K562	blood:
38	chr6:167736614..167738249-chr6:167740426..167742938,2	K562	blood:
39	chr6:167623779..167626117-chr6:167629928..167632260,2	MCF-7	breast:
40	chr6:167818746..167821496-chr6:167831177..167833070,2	K562	blood:
41	chr6:167631751..167632287-chr6:167701939..167702527,2	MCF-7	breast:
42	chr6:167734899..167737753-chr6:167743376..167745822,2	MCF-7	breast:
43	chr6:167715327..167717333-chr6:167717541..167719931,2	MCF-7	breast:

(count:35 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPR31-3	chr6:167582786-167583034	FPKM1_group_28907_transcript_1
2	lnc-CCR6-2	chr6:167584159-167584210	NONHSAT116087
3	lnc-TCP10L2-1	chr6:167577889-167578048	NONHSAT116082
4	lnc-UNC93A-3	chr6:167764293-167764966	NONHSAT116095
5	lnc-TCP10-3	chr6:167823155-167825466	ucscGeneNc_uc003qvy_1
6	lnc-UNC93A-1	chr6:167659275-167659404	XLOC_005540
7	lnc-CCR6-1	chr6:167575369-167575443	NONHSAT116084
8	lnc-CCR6-2	chr6:167584146-167584210	NONHSAT116086
9	lnc-TCP10L2-1	chr6:167578697-167578796	NONHSAT116082
10	lnc-TTLL2-1	chr6:167804760-167804979	XLOC_005541
11	lnc-UNC93A-2	chr6:167760960-167761541	NONHSAT116094
12	lnc-GPR31-1	chr6:167651156-167651293	XLOC_005921
13	lnc-TCP10-3	chr6:167825862-167825976	ucscGeneNc_uc003qvy_1
14	lnc-UNC93A-3	chr6:167764976-167765446	NONHSAT116095
15	lnc-GPR31-1	chr6:167653636-167653833	XLOC_005921
16	lnc-TCP10-2	chr6:167810373-167814438	ucscGeneNc_uc003qvx_1
17	lnc-TTLL2-1	chr6:167803650-167803969	XLOC_005541
18	lnc-CCR6-2	chr6:167585632-167586297	NONHSAT116086
19	lnc-CCR6-1	chr6:167579265-167579394	NONHSAT116084
20	lnc-TCP10-1	chr6:167787839-167789289	NONHSAT116097
21	lnc-UNC93A-1	chr6:167655379-167655453	XLOC_005540
22	lnc-GPR31-1	chr6:167650996-167651293	XLOC_005921
23	lnc-GPR31-3	chr6:167582786-167583124	NONHSAT116085
24	lnc-TCP10-2	chr6:167821589-167821728	ucscGeneNc_uc003qvx_1
25	lnc-TCP10-2	chr6:167822441-167822752	ucscGeneNc_uc003qvx_1
26	lnc-CCR6-2	chr6:167591872-167592248	NONHSAT116087
27	lnc-GPR31-1	chr6:167653688-167653968	XLOC_005921
28	lnc-GPR31-3	chr6:167583147-167583385	FPKM1_group_28907_transcript_1
29	lnc-TCP10-3	chr6:167826637-167827774	ucscGeneNc_uc003qvy_1
30	lnc-TCP10-1	chr6:167786578-167786848	NONHSAT116097
31	lnc-CCR6-2	chr6:167590485-167590622	NONHSAT116087
32	lnc-GPR31-3	chr6:167583039-167583124	FPKM1_group_28907_transcript_1
33	lnc-GPR31-2	chr6:167571213-167571283	l_3324_chr6:167571212-167573961_ovary
34	lnc-GPR31-3	chr6:167583147-167583385	NONHSAT116085
35	lnc-GPR31-2	chr6:167573626-167573961	l_3324_chr6:167571212-167573961_ovary

No data

Variant related genes	Relation type
UNC93A	TF binding region
TCP10	TF binding region
TTLL2	TF binding region
ENSG00000231720	TF binding region
GPR31	TF binding region
TCP10L2	TF binding region
ENSG00000228648	TF binding region
ENSG00000216966	TF binding region
ENSG00000217447	TF binding region
UNC93A	CpG island
TCP10	CpG island
TTLL2	CpG island
ENSG00000231720	CpG island
GPR31	CpG island
TCP10L2	CpG island
ENSG00000228648	CpG island
ENSG00000216966	CpG island
ENSG00000217447	CpG island
ENSG00000216966	chromatin interactions
ENSG00000120436	chromatin interactions
ENSG00000112494	chromatin interactions
ENSG00000180198	chromatin interactions
ENSG00000101166	chromatin interactions
CYBASC3	miRNA target sites
CYB5R4	miRNA target sites

Extended variants
information (count: 11903 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:11903 , 50 per page) page: 1 2 3 4 5 6 7 ... 239

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138262241	chr6:167570221-167570222	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs555464869	chr6:167570223-167570224	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs149598520	chr6:167570246-167570247	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs144263520	chr6:167570247-167570248	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs185145891	chr6:167570249-167570250	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs563757277	chr6:167570254-167570255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs372233666	chr6:167570340-167570341	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs375648716	chr6:167570348-167570349	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs368186408	chr6:167570355-167570356	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs372047373	chr6:167570409-167570410	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs552746226	chr6:167570418-167570419	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs148093951	chr6:167570419-167570420	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs375031842	chr6:167570440-167570441	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs202061256	chr6:167570473-167570474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs528524969	chr6:167570483-167570484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs199731205	chr6:167570484-167570485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs138110561	chr6:167570520-167570521	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs35182330	chr6:167570528-167570529	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs147194973	chr6:167570529-167570530	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs554469681	chr6:167570551-167570552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs369042833	chr6:167570559-167570560	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs569690384	chr6:167570576-167570577	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs536737881	chr6:167570580-167570581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs148720450	chr6:167570584-167570585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs535333186	chr6:167570589-167570590	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs372266197	chr6:167570594-167570595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs576406275	chr6:167570598-167570599	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs375293717	chr6:167570606-167570607	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs369535042	chr6:167570632-167570633	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs35329701	chr6:167570654-167570655	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs149752894	chr6:167570685-167570686	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs144434700	chr6:167570686-167570687	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs373259365	chr6:167570695-167570696	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs372154197	chr6:167570704-167570705	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs148413899	chr6:167570712-167570713	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs369377204	chr6:167570740-167570741	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs144041703	chr6:167570755-167570756	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs373280839	chr6:167570770-167570771	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs143553061	chr6:167570789-167570790	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs190631222	chr6:167570823-167570824	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs140917572	chr6:167570864-167570865	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs563722897	chr6:167570873-167570874	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs376227230	chr6:167570876-167570877	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs118117111	chr6:167570887-167570888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs200378086	chr6:167570890-167570891	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs370151410	chr6:167570893-167570894	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs374455043	chr6:167570912-167570913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs200148167	chr6:167570914-167570915	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs143766557	chr6:167570915-167570916	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs546698033	chr6:167570918-167570919	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:2118 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:167534000-167573400	Weak transcription	Right Atrium	heart
2	chr6:167565800-167575600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr6:167566000-167575600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr6:167566800-167570600	Enhancers	Fetal Brain Male	brain
5	chr6:167567800-167571600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
6	chr6:167568000-167571000	Weak transcription	Spleen	Spleen
7	chr6:167568200-167570800	Weak transcription	Primary B cells from peripheral blood	blood
8	chr6:167568200-167571000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr6:167568200-167571000	Weak transcription	GM12878-XiMat	blood
10	chr6:167568400-167570400	Enhancers	Fetal Brain Female	brain
11	chr6:167569000-167570400	Enhancers	Brain Inferior Temporal Lobe	brain
12	chr6:167569000-167571000	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr6:167569200-167571000	Weak transcription	Primary monocytes fromperipheralblood	blood
14	chr6:167569600-167570400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr6:167569600-167571400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr6:167570200-167571000	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr6:167570400-167571400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr6:167570800-167571400	Enhancers	Esophagus	oesophagus
19	chr6:167570800-167571600	Enhancers	Primary B cells from cord blood	blood
20	chr6:167570800-167572200	Enhancers	Primary B cells from peripheral blood	blood
21	chr6:167571000-167571400	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
22	chr6:167571000-167571400	Enhancers	Primary monocytes fromperipheralblood	blood
23	chr6:167571000-167571400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
24	chr6:167571000-167571400	Enhancers	Spleen	Spleen
25	chr6:167571000-167571600	Enhancers	GM12878-XiMat	blood
26	chr6:167571000-167571800	Enhancers	Monocytes-CD14+_RO01746	blood
27	chr6:167571400-167571600	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr6:167571400-167572400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr6:167571400-167575800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr6:167572400-167573400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr6:167573400-167573800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr6:167573600-167573800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr6:167573800-167576200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr6:167573800-167577000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr6:167575400-167576600	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr6:167575400-167576800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr6:167575400-167577200	Enhancers	Fetal Intestine Small	intestine
38	chr6:167575600-167576000	Bivalent Enhancer	HepG2	liver
39	chr6:167575600-167576400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr6:167575600-167576800	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr6:167575600-167577200	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr6:167575600-167577200	Enhancers	Fetal Intestine Large	intestine
43	chr6:167575600-167579200	Enhancers	H1 Cell Line	embryonic stem cell
44	chr6:167575800-167576400	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr6:167575800-167576600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
46	chr6:167575800-167576600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr6:167575800-167576600	Enhancers	Duodenum Mucosa	Duodenum
48	chr6:167575800-167576800	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr6:167575800-167577600	Enhancers	H9 Cell Line	embryonic stem cell
50	chr6:167576000-167576600	Flanking Bivalent TSS/Enh	HepG2	liver

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