Variant report

Variant	nsv526402
Chromosome Location	chr11:68201295-68217420
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:68214779-68214979	HepG2	liver:	n/a	n/a
2	ATF1	chr11:68204745-68205239	K562	blood:	n/a	n/a
3	ATF2	chr11:68214666-68215081	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr11:68214457-68214918	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr11:68204884-68205173	K562	blood:	n/a	n/a
6	ATF3	chr11:68204935-68205156	K562	blood:	n/a	n/a
7	BACH1	chr11:68207128-68207263	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr11:68214626-68214918	H1-hESC	embryonic stem cell:	n/a	n/a
9	BHLHE40	chr11:68204728-68205480	K562	blood:	n/a	n/a
10	BHLHE40	chr11:68214718-68215037	GM12878	blood:	n/a	n/a
11	BHLHE40	chr11:68214716-68214964	K562	blood:	n/a	n/a
12	BRCA1	chr11:68214814-68214858	GM12878	blood:	n/a	n/a
13	BRCA1	chr11:68214812-68214871	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr11:68214751-68215024	H1-hESC	embryonic stem cell:	n/a	n/a
15	CBX3	chr11:68204635-68205503	K562	blood:	n/a	n/a
16	CCNT2	chr11:68204961-68205464	K562	blood:	n/a	n/a
17	CEBPB	chr11:68214741-68214941	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr11:68204983-68205065	A549	lung:	n/a	n/a
19	CEBPB	chr11:68214720-68215022	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr11:68214833-68214942	K562	blood:	n/a	n/a
21	CHD2	chr11:68214777-68214839	K562	blood:	n/a	n/a
22	CHD2	chr11:68214646-68214907	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr11:68214787-68214903	Hela-S3	cervix:	n/a	n/a
24	CHD2	chr11:68214819-68214939	HepG2	liver:	n/a	n/a
25	CHD2	chr11:68214806-68215042	GM12878	blood:	n/a	n/a
26	CHD2	chr11:68216192-68216201	Hela-S3	cervix:	n/a	n/a
27	CTCF	chr11:68214697-68214971	HepG2	liver:	n/a	chr11:68214857-68214870 chr11:68214856-68214872 chr11:68214862-68214869 chr11:68214850-68214871 chr11:68214855-68214873
28	CTCF	chr11:68214737-68215012	Kidney_OC	kidney:	n/a	chr11:68214857-68214870 chr11:68214856-68214872 chr11:68214862-68214869 chr11:68214850-68214871 chr11:68214855-68214873
29	CTCF	chr11:68214654-68215085	K562	blood:	n/a	chr11:68214857-68214870 chr11:68214856-68214872 chr11:68214862-68214869 chr11:68214850-68214871 chr11:68214855-68214873
30	CTCF	chr11:68214780-68214930	K562	blood:	n/a	chr11:68214857-68214870 chr11:68214856-68214872 chr11:68214862-68214869 chr11:68214850-68214871 chr11:68214855-68214873
31	CTCF	chr11:68214820-68214970	GM12871	blood:	n/a	chr11:68214857-68214870 chr11:68214856-68214872 chr11:68214862-68214869 chr11:68214850-68214871 chr11:68214855-68214873
32	CTCF	chr11:68209460-68209610	Caco-2	colon:	n/a	chr11:68209522-68209531
33	CTCF	chr11:68214780-68214930	GM06990	blood:	n/a	chr11:68214857-68214870 chr11:68214856-68214872 chr11:68214862-68214869 chr11:68214850-68214871 chr11:68214855-68214873
34	CTCF	chr11:68214780-68214930	HCT-116	colon:	n/a	chr11:68214857-68214870 chr11:68214856-68214872 chr11:68214862-68214869 chr11:68214850-68214871 chr11:68214855-68214873
35	CTCF	chr11:68214628-68215191	HCT-116	colon:	n/a	chr11:68214857-68214870 chr11:68214856-68214872 chr11:68214862-68214869 chr11:68214850-68214871 chr11:68214855-68214873
36	CTCF	chr11:68205040-68205190	NB4	blood:	n/a	n/a
37	CTCF	chr11:68209440-68209590	BJ	skin:	n/a	chr11:68209522-68209531
38	CTCF	chr11:68214800-68214950	HCFaa	heart:	n/a	chr11:68214857-68214870 chr11:68214856-68214872 chr11:68214862-68214869 chr11:68214850-68214871 chr11:68214855-68214873
39	CTCF	chr11:68209380-68209530	SK-N-SH_RA	brain:	n/a	n/a
40	CTCF	chr11:68214705-68215055	Spleen_OC	spleen:	n/a	chr11:68214857-68214870 chr11:68214856-68214872 chr11:68214862-68214869 chr11:68214850-68214871 chr11:68214855-68214873
41	CTCF	chr11:68214820-68214970	HUVEC	blood vessel:	n/a	chr11:68214857-68214870 chr11:68214856-68214872 chr11:68214862-68214869 chr11:68214850-68214871 chr11:68214855-68214873
42	CTCF	chr11:68214780-68214930	GM12866	blood:	n/a	chr11:68214857-68214870 chr11:68214856-68214872 chr11:68214862-68214869 chr11:68214850-68214871 chr11:68214855-68214873
43	CTCF	chr11:68214716-68215014	A549	lung:	n/a	chr11:68214857-68214870 chr11:68214856-68214872 chr11:68214862-68214869 chr11:68214850-68214871 chr11:68214855-68214873
44	CTCF	chr11:68214800-68214950	GM12869	blood:	n/a	chr11:68214857-68214870 chr11:68214856-68214872 chr11:68214862-68214869 chr11:68214850-68214871 chr11:68214855-68214873
45	CTCF	chr11:68214715-68215054	GM12878	blood:	n/a	chr11:68214857-68214870 chr11:68214856-68214872 chr11:68214862-68214869 chr11:68214850-68214871 chr11:68214855-68214873
46	CTCF	chr11:68205280-68205430	HPAF	blood vessel:	n/a	n/a
47	CTCF	chr11:68214717-68215033	A549	lung:	n/a	chr11:68214857-68214870 chr11:68214856-68214872 chr11:68214862-68214869 chr11:68214850-68214871 chr11:68214855-68214873
48	CTCF	chr11:68214780-68214930	HEK293	kidney:	n/a	chr11:68214857-68214870 chr11:68214856-68214872 chr11:68214862-68214869 chr11:68214850-68214871 chr11:68214855-68214873
49	CTCF	chr11:68214800-68214950	HCPEpiC	choroid plexus:	n/a	chr11:68214857-68214870 chr11:68214856-68214872 chr11:68214862-68214869 chr11:68214850-68214871 chr11:68214855-68214873
50	CTCF	chr11:68214653-68215007	K562	blood:	n/a	chr11:68214857-68214870 chr11:68214856-68214872 chr11:68214862-68214869 chr11:68214850-68214871 chr11:68214855-68214873

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:68216423-68216473	AG10803	skin:	n/a
2	chr11:68205335-68205385	MCF10A-Er-Src	breast:	n/a
3	chr11:68216423-68216473	AG10803	skin:	n/a
4	chr11:68205335-68205385	MCF10A-Er-Src	breast:	n/a
5	chr11:68207228-68207278	NB4	blood:	n/a
6	chr11:68214299-68214349	MCF10A-Er-Src	breast:	n/a
7	chr11:68216546-68216596	Hepatocyte	liver:	n/a
8	chr11:68205840-68205890	NT2-D1	testis:	n/a
9	chr11:68208313-68208363	HepG2	liver:	n/a
10	chr11:68205561-68205611	AG09319	gingival:	n/a
11	chr11:68207327-68207377	HRPEpiC	eye:	n/a
12	chr11:68205561-68205611	HRE	kidney:	n/a
13	chr11:68206125-68206175	SAEC	small airway:	n/a
14	chr11:68201305-68201355	PrEC	prostate:	n/a
15	chr11:68201305-68201355	GM12892	blood:	n/a
16	chr11:68205335-68205385	HUVEC	blood vessel:	n/a
17	chr11:68205926-68205976	AG09319	gingival:	n/a
18	chr11:68204497-68204547	HRPEpiC	eye:	n/a
19	chr11:68205840-68205890	MCF-7	breast:	n/a
20	chr11:68207327-68207377	GM12891	blood:	n/a
21	chr11:68213980-68214030	H1-hESC	embryonic stem cell:	embryo
22	chr11:68216546-68216596	HAEpiC	amniotic membrane:	n/a
23	chr11:68205840-68205890	HRE	kidney:	n/a
24	chr11:68205561-68205611	GM12878	blood:	n/a
25	chr11:68205561-68205611	SK-N-SH	brain:	n/a
26	chr11:68205840-68205890	MCF10A-Er-Src	breast:	n/a
27	chr11:68205561-68205611	HIPEpiC	eye:	n/a
28	chr11:68216546-68216596	NHDF-neo	bronchial:	n/a
29	chr11:68201305-68201355	NB4	blood:	n/a
30	chr11:68205594-68205644	SKMC	muscle:	n/a
31	chr11:68207327-68207377	SK-N-SH_RA	brain:	n/a
32	chr11:68205561-68205611	GM12891	blood:	n/a
33	chr11:68216423-68216473	AG04450	lung:	fetal
34	chr11:68216788-68216838	HRCEpiC	kidney:	n/a
35	chr11:68205594-68205644	LNCaP	prostate:	n/a
36	chr11:68206027-68206077	K562	blood:	n/a
37	chr11:68205594-68205644	HCM	heart:	n/a
38	chr11:68204497-68204547	BE2_C	brain:	n/a
39	chr11:68216328-68216378	AG10803	skin:	n/a
40	chr11:68205335-68205385	T-47D	breast:	n/a
41	chr11:68216328-68216378	H1-hESC	embryonic stem cell:	embryo
42	chr11:68205926-68205976	SK-N-MC	brain:	n/a
43	chr11:68207228-68207278	HRPEpiC	eye:	n/a
44	chr11:68213980-68214030	RPTEC	kidney:	n/a
45	chr11:68216328-68216378	ovcar-3	ovarian:	n/a
46	chr11:68205335-68205385	NB4	blood:	n/a
47	chr11:68204497-68204547	Hepatocyte	liver:	n/a
48	chr11:68216328-68216378	GM12878	blood:	n/a
49	chr11:68216546-68216596	PrEC	prostate:	n/a
50	chr11:68214299-68214349	HRE	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:68189170..68193221-chr11:68199268..68202860,4	MCF-7	breast:
2	chr11:68210143..68211930-chr11:68216141..68218232,2	K562	blood:
3	chr11:68194684..68197011-chr11:68198113..68201482,3	K562	blood:
4	chr11:68198542..68202152-chr11:68203500..68206057,4	K562	blood:
5	chr11:68108795..68110881-chr11:68215051..68217783,2	MCF-7	breast:
6	chr11:68199257..68202152-chr11:68202690..68206057,4	K562	blood:
7	chr11:68214438..68216560-chr11:68227072..68229013,2	MCF-7	breast:
8	chr11:68192944..68194475-chr11:68202719..68205051,2	K562	blood:
9	chr11:68199257..68202152-chr11:68202690..68206057,4	K562	blood:
10	chr11:67980019..67981960-chr11:68214785..68216375,2	MCF-7	breast:
11	chr11:68192236..68194475-chr11:68203551..68205457,2	K562	blood:
12	chr11:68210143..68211930-chr11:68216141..68218232,2	K562	blood:
13	chr11:68204961..68210848-chr11:68212670..68216087,6	K562	blood:
14	chr11:67976075..67978498-chr11:68214944..68216504,2	MCF-7	breast:
15	chr11:68209498..68212492-chr11:68216141..68219004,3	K562	blood:
16	chr11:68213038..68215869-chr11:68227703..68229994,2	K562	blood:
17	chr11:68209498..68212492-chr11:68216141..68219004,3	K562	blood:
18	chr11:68206590..68210286-chr11:68212679..68215708,3	K562	blood:
19	chr11:68170884..68173607-chr11:68215077..68217390,2	MCF-7	breast:
20	chr11:68037835..68039908-chr11:68205347..68207124,2	MCF-7	breast:
21	chr11:68214551..68216392-chr11:68225423..68227032,2	MCF-7	breast:
22	chr11:68206590..68210286-chr11:68212679..68215708,3	K562	blood:
23	chr11:68216085..68219220-chr11:68223663..68227582,3	K562	blood:
24	chr11:67980477..67985206-chr11:68208162..68213238,5	MCF-7	breast:
25	chr11:68214975..68217976-chr11:68221508..68224126,3	K562	blood:
26	chr11:68198542..68202152-chr11:68203500..68206057,4	K562	blood:
27	chr11:68200745..68203688-chr11:68203810..68206580,3	MCF-7	breast:
28	chr11:68204961..68210848-chr11:68212670..68216087,6	K562	blood:
29	chr11:68198567..68200565-chr11:68200854..68203104,2	K562	blood:
30	chr11:68214931..68216465-chr11:68218868..68221338,2	K562	blood:
31	chr11:68024574..68025128-chr11:68214513..68215078,2	MCF-7	breast:
32	chr11:68151226..68152155-chr11:68214483..68215186,2	MCF-7	breast:
33	chr11:68038613..68041081-chr11:68205366..68206871,2	K562	blood:

Variant related genes	Relation type
LRP5	TF binding region
LRP5	CpG island
ENSG00000171067	chromatin interactions
ENSG00000110066	chromatin interactions
ENSG00000110075	chromatin interactions
ENSG00000162337	chromatin interactions

Extended variants
information (count: 777 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:777 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3736228	chr11:68201295-68201296	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
2	rs147637431	chr11:68201296-68201297	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs148685646	chr11:68201315-68201316	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs116068042	chr11:68201316-68201317	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs367615138	chr11:68201317-68201318	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs545461250	chr11:68201320-68201321	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs563578294	chr11:68201321-68201322	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs564282815	chr11:68201339-68201340	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs530922432	chr11:68201341-68201342	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs375245638	chr11:68201355-68201356	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs141169902	chr11:68201356-68201357	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs370759725	chr11:68201357-68201358	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs150717018	chr11:68201381-68201382	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs139201002	chr11:68201470-68201471	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs571793094	chr11:68201492-68201493	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs532932645	chr11:68201500-68201501	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs184447584	chr11:68201609-68201610	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs189021331	chr11:68201644-68201645	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs536653660	chr11:68201660-68201661	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs554915669	chr11:68201676-68201677	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs567238807	chr11:68201792-68201793	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs534589593	chr11:68201805-68201806	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs201597699	chr11:68201819-68201820	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs552777201	chr11:68201838-68201839	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs375289404	chr11:68201861-68201862	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs67156850	chr11:68201862-68201863	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs367860156	chr11:68201864-68201865	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs113061887	chr11:68201865-68201866	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs545211070	chr11:68201872-68201873	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs536161257	chr11:68201921-68201922	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs575600678	chr11:68201951-68201952	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs543062395	chr11:68201972-68201973	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs561230139	chr11:68201973-68201974	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs372635577	chr11:68202007-68202008	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs591511	chr11:68202027-68202028	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs573611044	chr11:68202055-68202056	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs193258297	chr11:68202095-68202096	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs565381899	chr11:68202100-68202101	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs532752988	chr11:68202113-68202114	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs146610414	chr11:68202139-68202140	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs563418942	chr11:68202149-68202150	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs528275136	chr11:68202228-68202229	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs185450573	chr11:68202233-68202234	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs548602458	chr11:68202237-68202238	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs189138021	chr11:68202302-68202303	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs140113831	chr11:68202304-68202305	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs376861290	chr11:68202305-68202306	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs181547914	chr11:68202310-68202311	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs375940168	chr11:68202322-68202323	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs571409701	chr11:68202332-68202333	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Metanephric adenoma	20802469	CNVD
Chordoma	21602918	CNVD
Melanoma	18172304	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	22860045	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	21399695	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21373257	CNVD
speech delay	21373257	CNVD
small cell lung cancer	17426248	CNVD
Gastric cancer	18160780	CNVD
Lung cancer	21569311	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:680 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:68176000-68210400	Strong transcription	HepG2	liver
2	chr11:68182000-68204400	Strong transcription	Stomach Smooth Muscle	stomach
3	chr11:68182800-68222200	Weak transcription	Small Intestine	intestine
4	chr11:68197400-68201800	Strong transcription	H1 Cell Line	embryonic stem cell
5	chr11:68197400-68203600	Weak transcription	K562	blood
6	chr11:68197400-68204000	Strong transcription	Adipose Nuclei	Adipose
7	chr11:68197400-68204000	Weak transcription	HMEC	breast
8	chr11:68197400-68204200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
9	chr11:68197400-68204200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr11:68197400-68204400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr11:68197400-68204600	Weak transcription	Psoas Muscle	Psoas
12	chr11:68197400-68204600	Weak transcription	NH-A	brain
13	chr11:68197400-68204600	Weak transcription	NHLF	lung
14	chr11:68197400-68207600	Weak transcription	Primary B cells from cord blood	blood
15	chr11:68197400-68208000	Strong transcription	Cortex derived primary cultured neurospheres	brain
16	chr11:68197400-68208800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr11:68197400-68210600	Strong transcription	Dnd41	blood
18	chr11:68197400-68214400	Strong transcription	Fetal Intestine Small	intestine
19	chr11:68197400-68214600	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr11:68197400-68214800	Weak transcription	Brain Cingulate Gyrus	brain
21	chr11:68197400-68216400	Strong transcription	Rectal Mucosa Donor 29	rectum
22	chr11:68197400-68217800	Strong transcription	Liver	Liver
23	chr11:68197600-68203000	Strong transcription	HUES6 Cell Line	embryonic stem cell
24	chr11:68197600-68203200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr11:68197600-68203400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr11:68197600-68203600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr11:68197600-68203800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
28	chr11:68197600-68204200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr11:68197600-68204200	Strong transcription	Duodenum Mucosa	Duodenum
30	chr11:68197600-68204400	Weak transcription	Muscle Satellite Cultured Cells	--
31	chr11:68197600-68204400	Weak transcription	Skeletal Muscle Female	skeletal muscle
32	chr11:68197600-68204400	Weak transcription	Stomach Mucosa	stomach
33	chr11:68197600-68204600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
34	chr11:68197600-68204600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr11:68197600-68204600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr11:68197600-68204600	Strong transcription	Duodenum Smooth Muscle	Duodenum
37	chr11:68197600-68204600	Strong transcription	Pancreas	Pancrea
38	chr11:68197600-68204800	Weak transcription	Primary hematopoietic stem cells	blood
39	chr11:68197600-68204800	Weak transcription	Osteobl	bone
40	chr11:68197600-68206200	Weak transcription	Fetal Kidney	kidney
41	chr11:68197600-68207000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
42	chr11:68197600-68207400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
43	chr11:68197600-68207600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr11:68197600-68208400	Strong transcription	Fetal Brain Female	brain
45	chr11:68197600-68210800	Strong transcription	Brain Germinal Matrix	brain
46	chr11:68197600-68217800	Strong transcription	Fetal Intestine Large	intestine
47	chr11:68197600-68227000	Weak transcription	Brain Hippocampus Middle	brain
48	chr11:68197800-68204000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr11:68197800-68204600	Strong transcription	Fetal Stomach	stomach
50	chr11:68197800-68204600	Strong transcription	Gastric	stomach

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