Variant report

Variant	nsv883413
Chromosome Location	chr6:4371622-4474114
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:920)
CpG islands
(count:366)
Chromatin interactive
region (count:29)
LncRNA
region (count:58)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:920 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:4459423-4459617	K562	blood:	n/a	n/a
2	ARID3A	chr6:4420426-4420740	K562	blood:	n/a	n/a
3	ARID3A	chr6:4459428-4459682	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:4371555-4372189	K562	blood:	n/a	n/a
5	ATF1	chr6:4441484-4441571	K562	blood:	n/a	n/a
6	ATF1	chr6:4388922-4389146	K562	blood:	n/a	n/a
7	ATF1	chr6:4431662-4431756	K562	blood:	n/a	n/a
8	ATF1	chr6:4371386-4372137	K562	blood:	n/a	n/a
9	ATF1	chr6:4380295-4380488	K562	blood:	n/a	n/a
10	ATF1	chr6:4420436-4420836	K562	blood:	n/a	n/a
11	ATF1	chr6:4459328-4459665	K562	blood:	n/a	n/a
12	ATF1	chr6:4382623-4382877	K562	blood:	n/a	n/a
13	ATF1	chr6:4436128-4436625	K562	blood:	n/a	n/a
14	ATF1	chr6:4387606-4387797	K562	blood:	n/a	n/a
15	ATF1	chr6:4435051-4435518	K562	blood:	n/a	n/a
16	ATF2	chr6:4407962-4408329	GM12878	blood:	n/a	n/a
17	ATF3	chr6:4382602-4382869	K562	blood:	n/a	n/a
18	BACH1	chr6:4388962-4389162	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr6:4402639-4403061	H1-hESC	embryonic stem cell:	n/a	chr6:4402848-4402862
20	BACH1	chr6:4402693-4402960	K562	blood:	n/a	chr6:4402848-4402862
21	BATF	chr6:4402702-4403013	GM12878	blood:	n/a	chr6:4402851-4402862 chr6:4402852-4402862
22	BATF	chr6:4402678-4402929	GM12878	blood:	n/a	chr6:4402851-4402862 chr6:4402852-4402862
23	BATF	chr6:4407963-4408218	GM12878	blood:	n/a	chr6:4408088-4408099
24	BATF	chr6:4407908-4408272	GM12878	blood:	n/a	chr6:4408088-4408099
25	BCL11A	chr6:4407993-4408322	GM12878	blood:	n/a	n/a
26	BCLAF1	chr6:4407905-4408328	GM12878	blood:	n/a	n/a
27	BCLAF1	chr6:4408007-4408284	GM12878	blood:	n/a	n/a
28	BHLHE40	chr6:4388945-4389115	K562	blood:	n/a	n/a
29	BHLHE40	chr6:4378633-4378860	K562	blood:	n/a	n/a
30	BHLHE40	chr6:4402531-4402707	K562	blood:	n/a	n/a
31	BHLHE40	chr6:4371434-4372512	K562	blood:	n/a	n/a
32	BHLHE40	chr6:4402992-4403270	K562	blood:	n/a	n/a
33	BHLHE40	chr6:4459340-4459597	K562	blood:	n/a	n/a
34	BHLHE40	chr6:4420487-4420718	K562	blood:	n/a	n/a
35	BHLHE40	chr6:4404118-4404418	K562	blood:	n/a	chr6:4404288-4404297 chr6:4404287-4404296 chr6:4404285-4404298 chr6:4404281-4404302 chr6:4404287-4404296
36	BHLHE40	chr6:4408013-4408375	GM12878	blood:	n/a	n/a
37	CBX3	chr6:4384292-4384704	K562	blood:	n/a	n/a
38	CBX3	chr6:4371514-4372140	K562	blood:	n/a	n/a
39	CBX3	chr6:4384260-4384748	HCT-116	colon:	n/a	n/a
40	CBX3	chr6:4384289-4384651	K562	blood:	n/a	n/a
41	CBX3	chr6:4471754-4472115	K562	blood:	n/a	n/a
42	CCNT2	chr6:4378508-4378955	K562	blood:	n/a	n/a
43	CCNT2	chr6:4371578-4372104	K562	blood:	n/a	n/a
44	CCNT2	chr6:4382740-4383053	K562	blood:	n/a	n/a
45	CEBPB	chr6:4402701-4402913	IMR90	lung:	n/a	n/a
46	CEBPB	chr6:4382578-4382953	K562	blood:	n/a	chr6:4382755-4382768 chr6:4382756-4382767
47	CEBPB	chr6:4388839-4389110	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr6:4399954-4400281	K562	blood:	n/a	n/a
49	CEBPB	chr6:4384101-4384397	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr6:4395195-4395274	K562	blood:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:4427110-4427160	AG04450	lung:	fetal
2	chr6:4461158-4461208	HCM	heart:	n/a
3	chr6:4381808-4381858	HCT-116	colon:	n/a
4	chr6:4403020-4403070	AG10803	skin:	n/a
5	chr6:4381808-4381858	U87	brain:	n/a
6	chr6:4461158-4461208	RPTEC	kidney:	n/a
7	chr6:4381808-4381858	AoSMC	blood vessel:	n/a
8	chr6:4461158-4461208	SK-N-SH	brain:	n/a
9	chr6:4381808-4381858	HIPEpiC	eye:	n/a
10	chr6:4459669-4459719	AG09309	skin:	n/a
11	chr6:4459669-4459719	GM06990	blood:	n/a
12	chr6:4427110-4427160	AoSMC	blood vessel:	n/a
13	chr6:4428712-4428762	T-47D	breast:	n/a
14	chr6:4428712-4428762	ECC-1	luminal epithelium:	n/a
15	chr6:4427110-4427160	PANC-1	pancreas:	n/a
16	chr6:4403020-4403070	GM12878	blood:	n/a
17	chr6:4459669-4459719	GM12878	blood:	n/a
18	chr6:4459669-4459719	K562	blood:	n/a
19	chr6:4427110-4427160	PrEC	prostate:	n/a
20	chr6:4403020-4403070	HRCEpiC	kidney:	n/a
21	chr6:4461158-4461208	SK-N-MC	brain:	n/a
22	chr6:4461158-4461208	NHDF-neo	bronchial:	n/a
23	chr6:4428712-4428762	MCF10A-Er-Src	breast:	n/a
24	chr6:4427110-4427160	LNCaP	prostate:	n/a
25	chr6:4403020-4403070	HRPEpiC	eye:	n/a
26	chr6:4459669-4459719	NHDF-neo	bronchial:	n/a
27	chr6:4403020-4403070	NH-A	brain:	n/a
28	chr6:4459669-4459719	PrEC	prostate:	n/a
29	chr6:4403020-4403070	HIPEpiC	eye:	n/a
30	chr6:4428712-4428762	GM12891	blood:	n/a
31	chr6:4428712-4428762	RPTEC	kidney:	n/a
32	chr6:4428712-4428762	HCPEpiC	choroid plexus:	n/a
33	chr6:4461158-4461208	GM06990	blood:	n/a
34	chr6:4461158-4461208	ovcar-3	ovarian:	n/a
35	chr6:4428712-4428762	MCF-7	breast:	n/a
36	chr6:4459669-4459719	T-47D	breast:	n/a
37	chr6:4461158-4461208	H1-hESC	embryonic stem cell:	embryo
38	chr6:4459669-4459719	NH-A	brain:	n/a
39	chr6:4403020-4403070	BE2_C	brain:	n/a
40	chr6:4461158-4461208	SK-N-SH_RA	brain:	n/a
41	chr6:4461158-4461208	AG09319	gingival:	n/a
42	chr6:4428712-4428762	HCT-116	colon:	n/a
43	chr6:4403020-4403070	GM19239	blood:	n/a
44	chr6:4459669-4459719	Caco-2	colon:	n/a
45	chr6:4403020-4403070	HCF	heart:	n/a
46	chr6:4381808-4381858	GM19239	blood:	n/a
47	chr6:4403020-4403070	MCF10A-Er-Src	breast:	n/a
48	chr6:4428712-4428762	IMR90	lung:	fetal
49	chr6:4461158-4461208	HUVEC	blood vessel:	n/a
50	chr6:4461158-4461208	HEK293	kidney:	embryo

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:4473560..4475868-chr6:4477837..4480497,2	MCF-7	breast:
2	chr6:4445245..4447675-chr6:4451631..4454250,2	K562	blood:
3	chr6:4368833..4371140-chr6:4377835..4379659,2	MCF-7	breast:
4	chr6:4371859..4373766-chr6:4377826..4380202,2	MCF-7	breast:
5	chr6:4423287..4425558-chr6:4426635..4429033,2	K562	blood:
6	chr6:4445245..4447675-chr6:4451631..4454250,2	K562	blood:
7	chr6:4324445..4326506-chr6:4412431..4414561,2	MCF-7	breast:
8	chr6:4401256..4404324-chr6:4774451..4776953,3	MCF-7	breast:
9	chr6:4365852..4368376-chr6:4465065..4467160,2	MCF-7	breast:
10	chr6:4429968..4432992-chr6:4433898..4437374,3	MCF-7	breast:
11	chr6:4432640..4435847-chr6:4435972..4439530,3	MCF-7	breast:
12	chr6:4398942..4400523-chr6:4402964..4405624,2	K562	blood:
13	chr6:4436749..4438740-chr6:4557869..4560584,2	MCF-7	breast:
14	chr6:4368958..4371929-chr6:4378307..4380468,2	K562	blood:
15	chr6:4398942..4400523-chr6:4402964..4405624,2	K562	blood:
16	chr6:4457494..4459250-chr6:4462928..4465436,2	MCF-7	breast:
17	chr6:4401718..4402258-chr6:4475763..4476371,2	MCF-7	breast:
18	chr6:4432640..4435847-chr6:4435972..4439530,3	MCF-7	breast:
19	chr6:4443894..4445765-chr6:4448052..4449778,2	MCF-7	breast:
20	chr6:4457494..4459250-chr6:4462928..4465436,2	MCF-7	breast:
21	chr6:4458091..4459630-chr6:4459877..4462370,2	MCF-7	breast:
22	chr6:4429968..4432992-chr6:4433898..4437374,3	MCF-7	breast:
23	chr6:4371859..4373766-chr6:4377826..4380202,2	MCF-7	breast:
24	chr6:4443894..4445765-chr6:4448052..4449778,2	MCF-7	breast:
25	chr6:4458091..4459630-chr6:4459877..4462370,2	MCF-7	breast:
26	chr6:4401864..4404753-chr6:4405538..4407059,2	MCF-7	breast:
27	chr6:4368958..4371929-chr6:4378307..4380468,2	K562	blood:
28	chr6:4401864..4404753-chr6:4405538..4407059,2	MCF-7	breast:
29	chr6:4465798..4468788-chr6:4591118..4593386,2	MCF-7	breast:

(count:58 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C6orf201-21	chr6:4401562-4401936	NONHSAT107419
2	lnc-C6orf201-21	chr6:4396599-4397931	NONHSAT107419
3	lnc-C6orf201-21	chr6:4404826-4405130	NONHSAT107419
4	lnc-C6orf201-21	chr6:4402442-4402570	NONHSAT107419
5	lnc-C6orf201-20	chr6:4392903-4393826	NONHSAT107417
6	lnc-C6orf201-21	chr6:4395892-4396201	NONHSAT107419
7	lnc-C6orf201-22	chr6:4428383-4428687	NONHSAT107410
8	lnc-C6orf201-20	chr6:4383203-4383512	NONHSAT107417
9	lnc-C6orf201-21	chr6:4405580-4406503	NONHSAT107419
10	lnc-C6orf201-22	chr6:4426308-4426556	NONHSAT107410
11	lnc-C6orf201-22	chr6:4423935-4424072	NONHSAT107410
12	lnc-C6orf201-20	chr6:4390443-4390705	NONHSAT107417
13	lnc-CDYL-3	chr6:4467041-4467252	XLOC_005140
14	lnc-CDYL-21	chr6:4417111-4417210	NONHSAT107425
15	lnc-C6orf201-22	chr6:4426677-4426939	NONHSAT107410
16	lnc-C6orf201-20	chr6:4371497-4371760	NONHSAT107406
17	lnc-C6orf201-21	chr6:4401250-4401464	NONHSAT107419
18	lnc-C6orf201-22	chr6:4423011-4423314	NONHSAT107410
19	lnc-CDYL-20	chr6:4450612-4450707	NONHSAT107428
20	lnc-C6orf201-22	chr6:4425993-4426121	NONHSAT107410
21	lnc-CDYL-20	chr6:4449786-4449885	NONHSAT107428
22	lnc-C6orf201-20	chr6:4386777-4387080	NONHSAT107417
23	lnc-C6orf201-21	chr6:4400384-4400521	NONHSAT107419
24	lnc-C6orf201-21	chr6:4400025-4400116	NONHSAT107419
25	lnc-CDYL-3	chr6:4466645-4466838	XLOC_005140
26	lnc-C6orf201-22	chr6:4425113-4425487	NONHSAT107410
27	lnc-C6orf201-20	chr6:4392149-4392453	NONHSAT107417
28	lnc-C6orf201-20	chr6:4388348-4388486	NONHSAT107417
29	lnc-C6orf201-20	chr6:4392663-4392785	NONHSAT107417
30	lnc-C6orf201-20	chr6:4382355-4382635	NONHSAT107406
31	lnc-C6orf201-21	chr6:4403126-4403388	NONHSAT107419
32	lnc-C6orf201-20	chr6:4387336-4387427	NONHSAT107417
33	lnc-C6orf201-20	chr6:4388879-4389253	NONHSAT107417
34	lnc-C6orf201-22	chr6:4424582-4424720	NONHSAT107410
35	lnc-C6orf201-22	chr6:4423570-4423661	NONHSAT107410
36	lnc-C6orf201-20	chr6:4388567-4388781	NONHSAT107417
37	lnc-CDYL-20	chr6:4451509-4451702	NONHSAT107428
38	lnc-C6orf201-21	chr6:4405340-4405462	NONHSAT107419
39	lnc-CDYL-21	chr6:4421551-4421814	NONHSAT107425
40	lnc-C6orf201-22	chr6:4420566-4421476	NONHSAT107410
41	lnc-C6orf201-21	chr6:4399466-4399769	NONHSAT107419
42	lnc-C6orf201-20	chr6:4383602-4383650	NONHSAT107406
43	lnc-CDYL-19	chr6:4472090-4472135	NONHSAT107434
44	lnc-C6orf201-22	chr6:4424801-4425015	NONHSAT107410
45	lnc-C6orf201-22	chr6:4429137-4430060	NONHSAT107410
46	lnc-CDYL-20	chr6:4454691-4454883	NONHSAT107428
47	lnc-C6orf201-20	chr6:4383171-4383281	NONHSAT107406
48	lnc-C6orf201-22	chr6:4428897-4429019	NONHSAT107410
49	lnc-CDYL-20	chr6:4449532-4449651	NONHSAT107428
50	lnc-C6orf201-20	chr6:4387701-4387838	NONHSAT107417

No data

Variant related genes	Relation type
RNA5SP202	TF binding region
RNA5SP202	CpG island
ENSG00000153046	chromatin interactions
ENSG00000236336	chromatin interactions
ENSG00000201185	chromatin interactions

Extended variants
information (count: 4393 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:4393 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9502168	chr6:4371622-4371623	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs76926903	chr6:4371649-4371650	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
3	rs560953762	chr6:4371659-4371660	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
4	rs114574401	chr6:4371670-4371671	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
5	rs546508701	chr6:4371693-4371694	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
6	rs560434405	chr6:4371707-4371708	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
7	rs532188522	chr6:4371826-4371827	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs147841050	chr6:4371886-4371887	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs117292204	chr6:4371891-4371892	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs115505519	chr6:4371896-4371897	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs548162825	chr6:4371942-4371943	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs116332457	chr6:4371947-4371948	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs139477784	chr6:4371985-4371986	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs553686911	chr6:4372020-4372021	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs573507620	chr6:4372021-4372022	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs373432039	chr6:4372026-4372027	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs563079968	chr6:4372033-4372034	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs559145332	chr6:4372062-4372063	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs73717307	chr6:4372069-4372070	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs544301170	chr6:4372127-4372128	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs180967143	chr6:4372170-4372171	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs574480339	chr6:4372203-4372204	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs548785520	chr6:4372221-4372222	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs373483950	chr6:4372228-4372229	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs375421928	chr6:4372247-4372248	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs548504097	chr6:4372334-4372335	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs532479256	chr6:4372335-4372336	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs568625363	chr6:4372387-4372388	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs562706563	chr6:4372436-4372437	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs531406731	chr6:4372501-4372502	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs548320533	chr6:4372555-4372556	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs568194744	chr6:4372663-4372664	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs369611658	chr6:4372668-4372669	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs114882033	chr6:4372724-4372725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs199726433	chr6:4372728-4372729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs547414475	chr6:4372752-4372753	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs567041490	chr6:4372769-4372770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs9504064	chr6:4372852-4372853	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs185150372	chr6:4372882-4372883	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs558835178	chr6:4372893-4372894	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs568218490	chr6:4372990-4372991	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs145005163	chr6:4373006-4373007	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs144963727	chr6:4373009-4373010	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs570155115	chr6:4373024-4373025	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs574641809	chr6:4373078-4373079	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs190431084	chr6:4373101-4373102	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs539132095	chr6:4373102-4373103	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs556013157	chr6:4373196-4373197	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs9405232	chr6:4373213-4373214	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs377747326	chr6:4373238-4373239	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

Disease	PMID	Source
Developmental delay	19490664	CNVD
Cancer	21183584	CNVD
Multiple Epiphyseal Dysplasia	20877625	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Glaucoma	18694899	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Cancer	20164920	CNVD
Colorectal cancer	21297112	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Myelodysplastic syndrome	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21364760	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	22495311	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
small cell lung cancer	20016488	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
dysmorphism	22105932	CNVD
psychomotor delay	22105932	CNVD
Ovarian cancer	19193619	CNVD
Osteosarcoma	16790693	CNVD
Hepatocellular carcinoma	16750200	CNVD
Schizophrenia	20967226	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD

Chromatin state (count:757 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:4359600-4374600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr6:4368000-4372600	Enhancers	NHLF	lung
3	chr6:4368400-4371800	Enhancers	Skeletal Muscle Female	skeletal muscle
4	chr6:4368600-4372400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr6:4368800-4373800	Enhancers	Left Ventricle	heart
6	chr6:4369000-4371800	Enhancers	Psoas Muscle	Psoas
7	chr6:4369400-4372200	Enhancers	Fetal Muscle Leg	muscle
8	chr6:4369400-4372400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr6:4369400-4372400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr6:4369400-4372400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr6:4369600-4373400	Enhancers	Right Ventricle	heart
12	chr6:4369800-4372200	Enhancers	HSMMtube	muscle
13	chr6:4370200-4372400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr6:4370400-4372200	Enhancers	Muscle Satellite Cultured Cells	--
15	chr6:4370400-4372200	Enhancers	HSMM	muscle
16	chr6:4370400-4372400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr6:4370400-4372400	Enhancers	NH-A	brain
18	chr6:4370400-4372600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr6:4370600-4372400	Enhancers	NHDF-Ad	bronchial
20	chr6:4370600-4372400	Enhancers	Osteobl	bone
21	chr6:4370600-4372600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr6:4370600-4373200	Weak transcription	Fetal Muscle Trunk	muscle
23	chr6:4370600-4373600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr6:4371000-4372000	Enhancers	A549	lung
25	chr6:4371000-4372400	Enhancers	Right Atrium	heart
26	chr6:4371200-4372000	Enhancers	Spleen	Spleen
27	chr6:4371400-4372200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr6:4371400-4372400	Flanking Active TSS	K562	blood
29	chr6:4371600-4371800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr6:4371600-4371800	Enhancers	HUVEC	blood vessel
31	chr6:4371600-4372000	Enhancers	Aorta	Aorta
32	chr6:4371600-4372000	Enhancers	Skeletal Muscle Male	skeletal muscle
33	chr6:4371600-4379000	Enhancers	Fetal Heart	heart
34	chr6:4371800-4372400	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
35	chr6:4371800-4372800	Weak transcription	Psoas Muscle	Psoas
36	chr6:4371800-4376800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr6:4372000-4372400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
38	chr6:4372000-4373400	Enhancers	Duodenum Mucosa	Duodenum
39	chr6:4372200-4373200	Weak transcription	Fetal Muscle Leg	muscle
40	chr6:4372400-4372600	Enhancers	K562	blood
41	chr6:4372400-4373200	Enhancers	Skeletal Muscle Female	skeletal muscle
42	chr6:4372400-4375000	Enhancers	Skeletal Muscle Male	skeletal muscle
43	chr6:4372400-4380800	Weak transcription	Right Atrium	heart
44	chr6:4372600-4374600	Weak transcription	K562	blood
45	chr6:4372800-4373000	Enhancers	Psoas Muscle	Psoas
46	chr6:4373200-4374400	Weak transcription	Skeletal Muscle Female	skeletal muscle
47	chr6:4373200-4374600	Enhancers	Fetal Muscle Trunk	muscle
48	chr6:4373200-4375200	Enhancers	Fetal Muscle Leg	muscle
49	chr6:4373400-4380600	Weak transcription	Right Ventricle	heart
50	chr6:4373600-4373800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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