Variant report

Variant	nsv515973
Chromosome Location	chr11:75569267-75832315
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1887)
CpG islands
(count:735)
Chromatin interactive
region (count:163)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1887 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:75784907-75786000	K562	blood:	n/a	n/a
2	ARID3A	chr11:75607891-75608210	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:75578851-75579162	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:75825160-75825598	K562	blood:	n/a	n/a
5	ARID3A	chr11:75578850-75579151	K562	blood:	n/a	n/a
6	ATF1	chr11:75785533-75785799	K562	blood:	n/a	n/a
7	ATF1	chr11:75657979-75658367	K562	blood:	n/a	n/a
8	ATF2	chr11:75773730-75774230	GM12878	blood:	n/a	n/a
9	ATF2	chr11:75619524-75620170	GM12878	blood:	n/a	n/a
10	ATF2	chr11:75619674-75620057	GM12878	blood:	n/a	n/a
11	ATF2	chr11:75584014-75585266	GM12878	blood:	n/a	n/a
12	ATF2	chr11:75602768-75603323	GM12878	blood:	n/a	n/a
13	ATF2	chr11:75657668-75658357	GM12878	blood:	n/a	n/a
14	ATF2	chr11:75773537-75774294	GM12878	blood:	n/a	n/a
15	ATF3	chr11:75741214-75741818	A549	lung:	n/a	n/a
16	BACH1	chr11:75746098-75746443	H1-hESC	embryonic stem cell:	n/a	chr11:75746263-75746277
17	BACH1	chr11:75661955-75662107	K562	blood:	n/a	n/a
18	BACH1	chr11:75746064-75746454	K562	blood:	n/a	chr11:75746263-75746277
19	BATF	chr11:75619655-75620120	GM12878	blood:	n/a	chr11:75619903-75619914 chr11:75619858-75619869 chr11:75619889-75619900
20	BATF	chr11:75604406-75604655	GM12878	blood:	n/a	n/a
21	BATF	chr11:75773809-75774206	GM12878	blood:	n/a	n/a
22	BATF	chr11:75584403-75584837	GM12878	blood:	n/a	n/a
23	BATF	chr11:75613336-75613623	GM12878	blood:	n/a	n/a
24	BATF	chr11:75584383-75585199	GM12878	blood:	n/a	n/a
25	BATF	chr11:75583968-75584354	GM12878	blood:	n/a	n/a
26	BATF	chr11:75584848-75585162	GM12878	blood:	n/a	n/a
27	BATF	chr11:75636517-75636757	GM12878	blood:	n/a	n/a
28	BATF	chr11:75619654-75620057	GM12878	blood:	n/a	chr11:75619903-75619914 chr11:75619858-75619869 chr11:75619889-75619900
29	BATF	chr11:75773817-75774236	GM12878	blood:	n/a	n/a
30	BCL11A	chr11:75619720-75620078	GM12878	blood:	n/a	n/a
31	BCL11A	chr11:75584419-75585119	GM12878	blood:	n/a	n/a
32	BCL3	chr11:75741198-75741802	A549	lung:	n/a	n/a
33	BCL3	chr11:75741125-75742309	A549	lung:	n/a	n/a
34	BCLAF1	chr11:75602943-75603559	GM12878	blood:	n/a	n/a
35	BCLAF1	chr11:75773476-75774274	GM12878	blood:	n/a	n/a
36	BCLAF1	chr11:75584271-75584825	GM12878	blood:	n/a	n/a
37	BHLHE40	chr11:75583838-75585192	GM12878	blood:	n/a	n/a
38	BHLHE40	chr11:75826721-75826921	K562	blood:	n/a	n/a
39	BHLHE40	chr11:75785317-75785442	K562	blood:	n/a	n/a
40	BHLHE40	chr11:75657668-75657728	K562	blood:	n/a	n/a
41	BHLHE40	chr11:75578988-75579093	K562	blood:	n/a	n/a
42	BHLHE40	chr11:75630681-75631056	GM12878	blood:	n/a	n/a
43	BHLHE40	chr11:75773815-75774217	GM12878	blood:	n/a	n/a
44	BRCA1	chr11:75578944-75579078	H1-hESC	embryonic stem cell:	n/a	n/a
45	CBX3	chr11:75759934-75760178	K562	blood:	n/a	n/a
46	CBX3	chr11:75759787-75760141	HCT-116	colon:	n/a	n/a
47	CBX3	chr11:75759787-75760240	K562	blood:	n/a	n/a
48	CBX3	chr11:75759830-75760251	HCT-116	colon:	n/a	n/a
49	CCNT2	chr11:75785551-75785880	K562	blood:	n/a	n/a
50	CCNT2	chr11:75607865-75607888	K562	blood:	n/a	n/a

(count:735 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:75678837-75678887	HCT-116	colon:	n/a
2	chr11:75772645-75772695	AG04449	skin:	fetal
3	chr11:75772747-75772797	NH-A	brain:	n/a
4	chr11:75678837-75678887	HCT-116	colon:	n/a
5	chr11:75772645-75772695	AG04449	skin:	fetal
6	chr11:75772747-75772797	NH-A	brain:	n/a
7	chr11:75831715-75831765	PFSK-1	brain:	n/a
8	chr11:75771707-75771757	HCF	heart:	n/a
9	chr11:75772645-75772695	ProgFib	skin:	n/a
10	chr11:75772645-75772695	Jurkat	blood:	n/a
11	chr11:75736215-75736265	Hepatocyte	liver:	n/a
12	chr11:75772747-75772797	ProgFib	skin:	n/a
13	chr11:75649913-75649963	AoSMC	blood vessel:	n/a
14	chr11:75736215-75736265	PrEC	prostate:	n/a
15	chr11:75589353-75589403	CMK	blood:	n/a
16	chr11:75584802-75584852	HCPEpiC	choroid plexus:	n/a
17	chr11:75772747-75772797	HRE	kidney:	n/a
18	chr11:75649913-75649963	NH-A	brain:	n/a
19	chr11:75678837-75678887	SK-N-SH	brain:	n/a
20	chr11:75589770-75589820	NT2-D1	testis:	n/a
21	chr11:75797825-75797875	SK-N-SH_RA	brain:	n/a
22	chr11:75736215-75736265	HepG2	liver:	n/a
23	chr11:75649913-75649963	HNPCEpiC	eye:	n/a
24	chr11:75678837-75678887	SAEC	small airway:	n/a
25	chr11:75772645-75772695	ovcar-3	ovarian:	n/a
26	chr11:75678837-75678887	SKMC	muscle:	n/a
27	chr11:75584802-75584852	HRCEpiC	kidney:	n/a
28	chr11:75772645-75772695	BJ	skin:	n/a
29	chr11:75589770-75589820	PrEC	prostate:	n/a
30	chr11:75771707-75771757	HCT-116	colon:	n/a
31	chr11:75678837-75678887	HepG2	liver:	n/a
32	chr11:75589770-75589820	HIPEpiC	eye:	n/a
33	chr11:75649913-75649963	PANC-1	pancreas:	n/a
34	chr11:75772747-75772797	MCF-7	breast:	n/a
35	chr11:75589770-75589820	LNCaP	prostate:	n/a
36	chr11:75589770-75589820	MCF10A-Er-Src	breast:	n/a
37	chr11:75772747-75772797	SAEC	small airway:	n/a
38	chr11:75649913-75649963	GM19239	blood:	n/a
39	chr11:75799276-75799326	NH-A	brain:	n/a
40	chr11:75831715-75831765	NT2-D1	testis:	n/a
41	chr11:75589353-75589403	PANC-1	pancreas:	n/a
42	chr11:75678837-75678887	AG09319	gingival:	n/a
43	chr11:75584802-75584852	NHDF-neo	bronchial:	n/a
44	chr11:75736215-75736265	SAEC	small airway:	n/a
45	chr11:75678837-75678887	HRPEpiC	eye:	n/a
46	chr11:75678837-75678887	NHBE	bronchial:	n/a
47	chr11:75797825-75797875	CMK	blood:	n/a
48	chr11:75797825-75797875	HRCEpiC	kidney:	n/a
49	chr11:75772645-75772695	IMR90	lung:	fetal
50	chr11:75799276-75799326	HIPEpiC	eye:	n/a

(count:163 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr11:75645975..75650713-chr11:75652976..75655754,4	K562	blood:
2	chr11:75525323..75528172-chr11:75603103..75604687,2	K562	blood:
3	chr11:75701857..75704473-chr11:75717022..75719427,2	MCF-7	breast:
4	chr11:75751052..75753833-chr11:75757773..75759280,2	MCF-7	breast:
5	chr11:75817536..75821071-chr11:75829941..75832993,4	MCF-7	breast:
6	chr11:75701857..75704473-chr11:75717022..75719427,2	MCF-7	breast:
7	chr11:75663345..75665731-chr11:75679525..75682423,2	MCF-7	breast:
8	chr11:75817741..75819762-chr11:75822475..75824409,2	MCF-7	breast:
9	chr11:75766818..75769750-chr11:75773214..75775149,2	MCF-7	breast:
10	chr11:75648758..75651551-chr11:75653084..75655719,3	MCF-7	breast:
11	chr11:75823480..75825443-chr11:75829721..75831691,3	K562	blood:
12	chr11:75572105..75574188-chr11:75575421..75577310,2	K562	blood:
13	chr11:75693505..75695019-chr11:75700477..75702152,2	MCF-7	breast:
14	chr11:75741432..75743179-chr11:75743618..75746649,3	MCF-7	breast:
15	chr11:75751015..75753754-chr11:75754593..75756274,2	K562	blood:
16	chr11:75599406..75601050-chr11:75607902..75610678,2	MCF-7	breast:
17	chr11:75747230..75749357-chr11:75750035..75751551,2	K562	blood:
18	chr11:75822862..75824965-chr11:75825307..75828253,2	MCF-7	breast:
19	chr11:75562235..75563926-chr11:75568149..75570504,2	MCF-7	breast:
20	chr11:75663345..75665731-chr11:75679525..75682423,2	MCF-7	breast:
21	chr11:75776976..75780489-chr11:75783161..75785961,4	K562	blood:
22	chr11:75817536..75821071-chr11:75829941..75832993,4	MCF-7	breast:
23	chr11:75596310..75598967-chr11:75601075..75603866,2	K562	blood:
24	chr11:75527717..75529229-chr11:75577673..75580461,2	MCF-7	breast:
25	chr11:75784443..75786135-chr11:75795046..75797035,2	K562	blood:
26	chr11:75694721..75696566-chr11:75699250..75701587,2	K562	blood:
27	chr11:75593236..75595084-chr11:75596698..75599353,2	K562	blood:
28	chr11:75818203..75819720-chr11:75822712..75825166,2	K562	blood:
29	chr11:75663693..75667116-chr11:75675374..75678918,4	MCF-7	breast:
30	chr11:75599026..75601409-chr11:75602652..75605269,2	MCF-7	breast:
31	chr11:75479334..75480245-chr11:75578518..75579248,2	K562	blood:
32	chr11:75796883..75799472-chr11:75836520..75838163,2	K562	blood:
33	chr11:75523919..75526976-chr11:75573533..75576982,4	MCF-7	breast:
34	chr11:75705127..75707335-chr11:75709352..75710974,2	K562	blood:
35	chr11:75806084..75808673-chr11:75812097..75814529,2	K562	blood:
36	chr11:75572105..75574188-chr11:75575421..75577310,2	K562	blood:
37	chr11:75761226..75763293-chr11:75765586..75768192,3	K562	blood:
38	chr11:75817741..75819762-chr11:75822475..75824409,2	MCF-7	breast:
39	chr11:75654690..75656388-chr11:75656892..75658413,2	MCF-7	breast:
40	chr11:75808133..75810411-chr11:75817807..75820091,2	K562	blood:
41	chr11:75607077..75608544-chr11:75862937..75863839,5	K562	blood:
42	chr11:75632402..75634534-chr11:75653760..75656009,2	MCF-7	breast:
43	chr11:75551619..75553508-chr11:75579174..75581979,3	MCF-7	breast:
44	chr11:75736549..75740161-chr11:75742024..75745000,3	K562	blood:
45	chr11:75632402..75634534-chr11:75653760..75656009,2	MCF-7	breast:
46	chr11:75523214..75528138-chr11:75567466..75570910,7	MCF-7	breast:
47	chr11:75524219..75527964-chr11:75564659..75570839,6	MCF-7	breast:
48	chr11:75676550..75678071-chr14:20809872..20811501,5	MCF-7	breast:
49	chr11:75773281..75776298-chr11:75779635..75783081,3	K562	blood:
50	chr11:75788595..75790602-chr11:75807460..75809496,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DGAT2-4	chr11:75797169-75797314	ucscGeneNc_uc001oxi_1
2	lnc-DGAT2-4	chr11:75770005-75770066	ucscGeneNc_uc001oxi_1
3	lnc-DGAT2-3	chr11:75694431-75694868	NONHSAT023145
4	lnc-WNT11-5	chr11:75653173-75653479	NONHSAT023144
5	lnc-DGAT2-3	chr11:75672507-75672593	NONHSAT023145
6	lnc-WNT11-3	chr11:75830027-75830331	ucscGeneNc_uc009yui_1
7	lnc-DGAT2-4	chr11:75799554-75803311	ucscGeneNc_uc001oxi_1
8	lnc-DGAT2-1	chr11:75626175-75626257	ENSG00000255081.1
9	lnc-DGAT2-4	chr11:75792352-75792613	ucscGeneNc_uc001oxi_1
10	lnc-MAP6-6	chr11:75622248-75622672	NONHSAT023140
11	lnc-DGAT2-1	chr11:75625245-75625632	ENSG00000255081.1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	UVRAG	hsa-miR-32-5p	chr11:75672491-75672512

Variant related genes	Relation type
RNA5SP344	TF binding region
ENSG00000255081	TF binding region
UVRAG	TF binding region
ENSG00000254915	TF binding region
PPP1R1AP1	TF binding region
RNA5SP344	CpG island
ENSG00000255081	CpG island
UVRAG	CpG island
ENSG00000254915	CpG island
PPP1R1AP1	CpG island
ENSG00000255081	chromatin interactions
ENSG00000254814	chromatin interactions
ENSG00000062282	chromatin interactions
ENSG00000223013	chromatin interactions
ENSG00000247867	chromatin interactions
ENSG00000158636	chromatin interactions
ENSG00000198382	chromatin interactions
ENSG00000255507	chromatin interactions
ENSG00000149257	chromatin interactions
ENSG00000149273	chromatin interactions
ENSG00000254915	chromatin interactions
ENSG00000206941	chromatin interactions
ENSG00000150456	chromatin interactions

Extended variants
information (count: 9460 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:9460 , 50 per page) page: 1 2 3 4 5 6 7 ... 190

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7119809	chr11:75569267-75569268	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs12285184	chr11:75569276-75569277	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs538750242	chr11:75569288-75569289	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs371390107	chr11:75569315-75569316	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs139642838	chr11:75569316-75569317	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs149982061	chr11:75569349-75569350	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs192038397	chr11:75569441-75569442	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs146558813	chr11:75569465-75569466	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs117632611	chr11:75569467-75569468	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs556557921	chr11:75569488-75569489	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs141275987	chr11:75569492-75569493	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs561368576	chr11:75569556-75569557	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs368435354	chr11:75569600-75569601	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs538191156	chr11:75569609-75569610	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs182977725	chr11:75569689-75569690	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs143697375	chr11:75569703-75569704	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs540275289	chr11:75569739-75569740	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs553606759	chr11:75569797-75569798	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs566554510	chr11:75569813-75569814	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs576737845	chr11:75569829-75569830	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs545465726	chr11:75569866-75569867	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs562170493	chr11:75569874-75569875	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs115824232	chr11:75569911-75569912	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs542155021	chr11:75569927-75569928	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs146838524	chr11:75569933-75569934	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs376432988	chr11:75569969-75569970	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs114339401	chr11:75569998-75569999	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs115568358	chr11:75570011-75570012	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs371223674	chr11:75570036-75570037	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs374291102	chr11:75570056-75570057	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs140672452	chr11:75570097-75570098	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs186661808	chr11:75570136-75570137	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs143783178	chr11:75570141-75570142	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs148161186	chr11:75570147-75570148	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs190709705	chr11:75570158-75570159	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs141123517	chr11:75570192-75570193	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs367825335	chr11:75570288-75570289	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs567199641	chr11:75570313-75570314	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs568233109	chr11:75570329-75570330	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs368205709	chr11:75570335-75570336	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs182687429	chr11:75570370-75570371	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs11603892	chr11:75570407-75570408	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs150085804	chr11:75570498-75570499	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs12287106	chr11:75570529-75570530	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs555727729	chr11:75570535-75570536	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs575229240	chr11:75570537-75570538	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs561342458	chr11:75570539-75570540	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs540939646	chr11:75570554-75570555	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs555729811	chr11:75570559-75570560	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs138672623	chr11:75570580-75570581	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:110)

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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Glioblastoma multiforme	21080181	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Melanoma	18172304	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
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21482786	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	16608533	CNVD
Usher syndrome	18421352	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Ovarian cancer	21240255	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Melanoma	20877625	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Glioblastoma multiforme	22122801	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:4904 , 50 per page) page: 1 2 3 4 5 6 7 ... 99

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:75535400-75579000	Weak transcription	Fetal Intestine Large	intestine
2	chr11:75535800-75573800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
3	chr11:75538800-75591400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr11:75544000-75584000	Weak transcription	Small Intestine	intestine
5	chr11:75547600-75600000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
6	chr11:75549800-75602800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr11:75552000-75580000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr11:75553800-75600800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
9	chr11:75557400-75586800	Weak transcription	Ovary	ovary
10	chr11:75558400-75602800	Weak transcription	Fetal Muscle Trunk	muscle
11	chr11:75559800-75575600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
12	chr11:75560200-75579400	Weak transcription	Pancreas	Pancrea
13	chr11:75561200-75584200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
14	chr11:75561200-75584800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr11:75561200-75584800	Weak transcription	Lung	lung
16	chr11:75561400-75569400	Weak transcription	Liver	Liver
17	chr11:75561400-75578400	Weak transcription	Duodenum Mucosa	Duodenum
18	chr11:75561600-75573400	Weak transcription	Left Ventricle	heart
19	chr11:75561800-75572000	Weak transcription	Primary T helper cells PMA-I stimulated	--
20	chr11:75561800-75574200	Weak transcription	Cortex derived primary cultured neurospheres	brain
21	chr11:75561800-75576400	Weak transcription	HUES48 Cell Line	embryonic stem cell
22	chr11:75562000-75573400	Weak transcription	Primary T helper cells fromperipheralblood	blood
23	chr11:75562000-75586400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
24	chr11:75562200-75569400	Weak transcription	Placenta Amnion	Placenta Amnion
25	chr11:75562200-75569600	Weak transcription	NHLF	lung
26	chr11:75562200-75569800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr11:75562200-75585800	Weak transcription	Fetal Brain Male	brain
28	chr11:75562200-75590800	Weak transcription	Thymus	Thymus
29	chr11:75562400-75569400	Weak transcription	HSMM	muscle
30	chr11:75562400-75573400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr11:75562400-75579400	Weak transcription	Fetal Thymus	thymus
32	chr11:75562600-75569800	Weak transcription	Brain Anterior Caudate	brain
33	chr11:75562600-75578400	Weak transcription	Brain Inferior Temporal Lobe	brain
34	chr11:75562600-75579000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
35	chr11:75562600-75580000	Weak transcription	Fetal Lung	lung
36	chr11:75562600-75584800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr11:75562600-75591400	Weak transcription	Sigmoid Colon	Sigmoid Colon
38	chr11:75562600-75630400	Weak transcription	Rectal Mucosa Donor 31	rectum
39	chr11:75562800-75569400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr11:75562800-75569400	Weak transcription	Duodenum Smooth Muscle	Duodenum
41	chr11:75562800-75569400	Weak transcription	Skeletal Muscle Male	skeletal muscle
42	chr11:75562800-75569600	Weak transcription	Fetal Heart	heart
43	chr11:75562800-75569600	Weak transcription	Pancreatic Islets	Pancreatic Islet
44	chr11:75562800-75573400	Weak transcription	Brain Hippocampus Middle	brain
45	chr11:75562800-75577800	Weak transcription	Brain Cingulate Gyrus	brain
46	chr11:75562800-75578000	Weak transcription	Brain Angular Gyrus	brain
47	chr11:75562800-75578000	Weak transcription	Brain Substantia Nigra	brain
48	chr11:75562800-75578000	Weak transcription	Colon Smooth Muscle	Colon
49	chr11:75562800-75578000	Weak transcription	Rectal Smooth Muscle	rectum
50	chr11:75562800-75610800	Weak transcription	HSMMtube	muscle

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