Variant report

Variant	nsv1026715
Chromosome Location	chr9:266044-459077
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1764)
CpG islands
(count:122)
Chromatin interactive
region (count:96)
LncRNA
region (count:30)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1764 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:267916-268404	K562	blood:	n/a	n/a
2	ARID3A	chr9:371491-371553	K562	blood:	n/a	n/a
3	ARID3A	chr9:272758-273406	K562	blood:	n/a	chr9:273064-273079
4	ARID3A	chr9:272095-272522	K562	blood:	n/a	n/a
5	ARID3A	chr9:336046-336405	HepG2	liver:	n/a	n/a
6	ATF1	chr9:312958-313372	K562	blood:	n/a	n/a
7	ATF1	chr9:428430-428702	K562	blood:	n/a	n/a
8	ATF1	chr9:272781-273161	K562	blood:	n/a	n/a
9	ATF1	chr9:270753-271026	K562	blood:	n/a	n/a
10	ATF1	chr9:272150-272512	K562	blood:	n/a	n/a
11	ATF2	chr9:272650-273286	GM12878	blood:	n/a	n/a
12	ATF2	chr9:272677-273240	GM12878	blood:	n/a	n/a
13	ATF2	chr9:297286-297859	GM12878	blood:	n/a	n/a
14	ATF3	chr9:272081-272576	K562	blood:	n/a	n/a
15	ATF3	chr9:326568-327022	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr9:450112-450344	H1-hESC	embryonic stem cell:	n/a	n/a
17	BATF	chr9:278668-278987	GM12878	blood:	n/a	n/a
18	BATF	chr9:297422-297902	GM12878	blood:	n/a	chr9:297684-297695 chr9:297685-297695
19	BATF	chr9:297420-297885	GM12878	blood:	n/a	chr9:297684-297695 chr9:297685-297695
20	BCL11A	chr9:331212-331567	H1-hESC	embryonic stem cell:	n/a	n/a
21	BCLAF1	chr9:297419-297950	GM12878	blood:	n/a	chr9:297687-297696 chr9:297688-297697
22	BCLAF1	chr9:272677-273191	GM12878	blood:	n/a	chr9:272862-272871
23	BCLAF1	chr9:297343-297922	GM12878	blood:	n/a	chr9:297687-297696 chr9:297688-297697
24	BCLAF1	chr9:307023-307293	GM12878	blood:	n/a	n/a
25	BCLAF1	chr9:272658-273387	GM12878	blood:	n/a	chr9:272862-272871
26	BHLHE40	chr9:439327-439591	HepG2	liver:	n/a	n/a
27	BHLHE40	chr9:270725-270976	GM12878	blood:	n/a	n/a
28	BHLHE40	chr9:272179-272510	K562	blood:	n/a	n/a
29	BHLHE40	chr9:297517-297717	K562	blood:	n/a	n/a
30	CBX3	chr9:456299-456866	HCT-116	colon:	n/a	n/a
31	CBX3	chr9:272119-272641	K562	blood:	n/a	n/a
32	CCNT2	chr9:270745-270945	K562	blood:	n/a	n/a
33	CCNT2	chr9:312627-313052	K562	blood:	n/a	n/a
34	CCNT2	chr9:373782-374327	K562	blood:	n/a	chr9:373878-373898
35	CCNT2	chr9:272149-272834	K562	blood:	n/a	n/a
36	CCNT2	chr9:371246-371675	K562	blood:	n/a	n/a
37	CEBPB	chr9:272749-273224	K562	blood:	n/a	chr9:273149-273160
38	CEBPB	chr9:272157-272436	K562	blood:	n/a	n/a
39	CEBPB	chr9:347670-348082	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr9:436508-436820	HepG2	liver:	n/a	chr9:436672-436681 chr9:436672-436683 chr9:436670-436681
41	CEBPB	chr9:289229-289501	K562	blood:	n/a	chr9:289375-289386
42	CEBPB	chr9:377556-377839	A549	lung:	n/a	n/a
43	CEBPB	chr9:272832-273310	K562	blood:	n/a	chr9:273149-273160
44	CEBPB	chr9:278053-278054	K562	blood:	n/a	n/a
45	CEBPB	chr9:436525-436849	A549	lung:	n/a	chr9:436672-436681 chr9:436672-436683 chr9:436670-436681
46	CEBPB	chr9:437428-438537	Hela-S3	cervix:	n/a	chr9:437615-437626 chr9:437615-437626
47	CEBPB	chr9:437658-437967	A549	lung:	n/a	n/a
48	CEBPB	chr9:347684-348092	A549	lung:	n/a	n/a
49	CEBPB	chr9:416846-416891	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr9:437611-438522	IMR90	lung:	n/a	chr9:437615-437626 chr9:437615-437626

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:426894-426944	T-47D	breast:	n/a
2	chr9:273072-273122	NHBE	bronchial:	n/a
3	chr9:273072-273122	IMR90	lung:	fetal
4	chr9:426894-426944	GM06990	blood:	n/a
5	chr9:273072-273122	GM19239	blood:	n/a
6	chr9:426894-426944	HL-60	blood:	n/a
7	chr9:426894-426944	HMEC	breast:	n/a
8	chr9:273072-273122	ECC-1	luminal epithelium:	n/a
9	chr9:426894-426944	NB4	blood:	n/a
10	chr9:426894-426944	BE2_C	brain:	n/a
11	chr9:273072-273122	HRPEpiC	eye:	n/a
12	chr9:273072-273122	GM12878	blood:	n/a
13	chr9:273072-273122	HCF	heart:	n/a
14	chr9:273072-273122	ProgFib	skin:	n/a
15	chr9:273072-273122	AG04450	lung:	fetal
16	chr9:426894-426944	HCM	heart:	n/a
17	chr9:426894-426944	LNCaP	prostate:	n/a
18	chr9:273072-273122	SK-N-SH	brain:	n/a
19	chr9:273072-273122	A549	lung:	n/a
20	chr9:426894-426944	K562	blood:	n/a
21	chr9:273072-273122	BJ	skin:	n/a
22	chr9:426894-426944	NHDF-neo	bronchial:	n/a
23	chr9:426894-426944	SKMC	muscle:	n/a
24	chr9:273072-273122	BE2_C	brain:	n/a
25	chr9:426894-426944	SK-N-MC	brain:	n/a
26	chr9:273072-273122	Jurkat	blood:	n/a
27	chr9:426894-426944	HRE	kidney:	n/a
28	chr9:426894-426944	HNPCEpiC	eye:	n/a
29	chr9:273072-273122	SK-N-MC	brain:	n/a
30	chr9:426894-426944	HIPEpiC	eye:	n/a
31	chr9:273072-273122	NT2-D1	testis:	n/a
32	chr9:426894-426944	GM19239	blood:	n/a
33	chr9:426894-426944	AoSMC	blood vessel:	n/a
34	chr9:426894-426944	IMR90	lung:	fetal
35	chr9:273072-273122	GM06990	blood:	n/a
36	chr9:273072-273122	ovcar-3	ovarian:	n/a
37	chr9:426894-426944	SAEC	small airway:	n/a
38	chr9:273072-273122	K562	blood:	n/a
39	chr9:273072-273122	CMK	blood:	n/a
40	chr9:426894-426944	PFSK-1	brain:	n/a
41	chr9:273072-273122	AG09309	skin:	n/a
42	chr9:273072-273122	HAEpiC	amniotic membrane:	n/a
43	chr9:273072-273122	T-47D	breast:	n/a
44	chr9:426894-426944	HRCEpiC	kidney:	n/a
45	chr9:426894-426944	A549	lung:	n/a
46	chr9:426894-426944	GM12891	blood:	n/a
47	chr9:273072-273122	MCF10A-Er-Src	breast:	n/a
48	chr9:426894-426944	PANC-1	pancreas:	n/a
49	chr9:273072-273122	HCT-116	colon:	n/a
50	chr9:273072-273122	SK-N-SH_RA	brain:	n/a

(count:96 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr9:347951..349550-chr9:363997..366575,2	MCF-7	breast:
2	chr9:268889..271022-chr9:277493..279614,2	K562	blood:
3	chr9:347477..348464-chr9:378346..378946,4	MCF-7	breast:
4	chr9:284961..287002-chr9:306876..309185,2	K562	blood:
5	chr9:347287..349476-chr9:362112..363970,2	MCF-7	breast:
6	chr9:277861..283096-chr9:291676..296273,5	K562	blood:
7	chr5:96288877..96289613-chr9:429812..430395,2	MCF-7	breast:
8	chr9:318530..320927-chr9:322721..325349,2	K562	blood:
9	chr9:347287..349476-chr9:362112..363970,2	MCF-7	breast:
10	chr9:441366..444017-chr9:451304..454209,2	MCF-7	breast:
11	chr9:276314..278461-chr9:285139..287718,2	K562	blood:
12	chr9:288365..290115-chr9:299185..301598,2	MCF-7	breast:
13	chr9:452598..454624-chr9:456757..459664,2	MCF-7	breast:
14	chr9:316274..318543-chr9:331270..334145,2	MCF-7	breast:
15	chr9:347437..348401-chr9:378296..379161,3	MCF-7	breast:
16	chr12:21809676..21810203-chr9:455132..455632,2	NB4	blood:
17	chr9:283346..286966-chr9:287946..290894,7	K562	blood:
18	chr9:324085..328451-chr9:329787..332698,3	K562	blood:
19	chr9:276314..278461-chr9:285139..287718,2	K562	blood:
20	chr9:454517..457686-chr9:460777..463722,3	K562	blood:
21	chr9:441366..444017-chr9:451304..454209,2	MCF-7	breast:
22	chr9:385756..386457-chr9:1008777..1009377,2	MCF-7	breast:
23	chr9:326951..329483-chr9:330404..332162,2	K562	blood:
24	chr9:276287..280123-chr9:282139..284880,4	K562	blood:
25	chr9:350965..353575-chr9:397923..399924,2	K562	blood:
26	chr9:271874..274602-chr9:275665..279412,3	K562	blood:
27	chr9:387700..389795-chr9:395557..397565,2	MCF-7	breast:
28	chr9:303334..306488-chr9:313112..315414,3	MCF-7	breast:
29	chr9:347437..348401-chr9:378296..379161,3	MCF-7	breast:
30	chr9:214682..216322-chr9:293864..296795,2	MCF-7	breast:
31	chr9:265556..268525-chr9:268878..270498,2	K562	blood:
32	chr9:214996..215595-chr9:307020..307600,2	MCF-7	breast:
33	chr9:214091..217459-chr9:295851..299102,3	MCF-7	breast:
34	chr9:275975..278627-chr9:279451..282123,3	K562	blood:
35	chr9:385789..386423-chr9:612104..612846,2	K562	blood:
36	chr9:457391..459101-chr9:460366..462265,2	MCF-7	breast:
37	chr9:316274..318543-chr9:331270..334145,2	MCF-7	breast:
38	chr9:331276..333871-chr9:335644..338943,3	MCF-7	breast:
39	chr9:270180..272736-chr9:272837..274435,2	K562	blood:
40	chr9:418287..419917-chr9:426635..429458,2	MCF-7	breast:
41	chr9:213410..215081-chr9:270583..272682,2	MCF-7	breast:
42	chr9:385566..386417-chr9:764222..764740,2	MCF-7	breast:
43	chr9:303334..306488-chr9:313112..315414,3	MCF-7	breast:
44	chr1:27191066..27191830-chr9:408050..409042,2	NB4	blood:
45	chr9:347797..348410-chr9:459774..460369,2	MCF-7	breast:
46	chr9:454476..456616-chr9:461041..463916,2	MCF-7	breast:
47	chr9:347478..348338-chr9:806313..807172,2	MCF-7	breast:
48	chr9:217275..219531-chr9:301975..303827,2	MCF-7	breast:
49	chr9:268983..271562-chr9:284279..286719,2	MCF-7	breast:
50	chr9:288330..291260-chr9:302503..304653,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C9orf66-2	chr9:454304-454606	ENSG00000227155.1
2	lnc-C9orf66-1	chr9:272905-273002	ENSG00000235880.1
3	lnc-C9orf66-2	chr9:454304-454606	ENSG00000227155.3
4	lnc-C9orf66-2	chr9:456201-456703	ENSG00000227155.3
5	lnc-C9orf66-2	chr9:456915-457047	ENSG00000227155.3
6	lnc-C9orf66-2	chr9:456201-456703	ENSG00000227155.3
7	lnc-C9orf66-1	chr9:267966-268273	ENSG00000235880.1
8	lnc-C9orf66-2	chr9:456915-457047	ENSG00000227155.3
9	lnc-C9orf66-2	chr9:456211-456703	ENSG00000227155.3
10	lnc-C9orf66-2	chr9:457004-457047	ENSG00000227155.3
11	lnc-C9orf66-2	chr9:456201-456703	ENSG00000227155.3
12	lnc-C9orf66-2	chr9:454432-454606	ENSG00000227155.3
13	lnc-C9orf66-2	chr9:454585-454606	ENSG00000227155.3
14	lnc-C9orf66-2	chr9:458117-458281	ENSG00000227155.3
15	lnc-C9orf66-2	chr9:456201-456703	ENSG00000227155.3
16	lnc-C9orf66-2	chr9:456518-456703	ENSG00000227155.3
17	lnc-C9orf66-2	chr9:458370-458423	ENSG00000227155.3
18	lnc-C9orf66-2	chr9:456915-457047	ENSG00000227155.3
19	lnc-C9orf66-2	chr9:454447-454606	ENSG00000227155.3
20	lnc-C9orf66-2	chr9:454457-454606	ENSG00000227155.3
21	lnc-C9orf66-2	chr9:456530-456703	ENSG00000227155.3
22	lnc-C9orf66-2	chr9:456915-457047	ENSG00000227155.3
23	lnc-C9orf66-2	chr9:456201-456703	ENSG00000227155.3
24	lnc-C9orf66-2	chr9:456201-456988	ENSG00000227155.3
25	lnc-C9orf66-2	chr9:456204-456703	ENSG00000227155.3
26	lnc-C9orf66-2	chr9:456545-456703	ENSG00000227155.3
27	lnc-C9orf66-2	chr9:456521-456703	ENSG00000227155.3
28	lnc-C9orf66-2	chr9:454576-454606	ENSG00000227155.3
29	lnc-C9orf66-2	chr9:456201-456703	ENSG00000227155.3
30	lnc-C9orf66-2	chr9:456201-456358	ENSG00000227155.1

No data

Variant related genes	Relation type
DOCK8	TF binding region
ENSG00000235880	TF binding region
ENSG00000227155	TF binding region
DOCK8	CpG island
ENSG00000235880	CpG island
ENSG00000227155	CpG island
ENSG00000107099	chromatin interactions
ENSG00000235880	chromatin interactions
ENSG00000183784	chromatin interactions
ENSG00000226403	chromatin interactions
ENSG00000227155	chromatin interactions

Extended variants
information (count: 10719 )
Associated
traits (count: 118 )

Variant overlapped rSNPs/rCNVs (count:10719 , 50 per page) page: 1 2 3 4 5 6 7 ... 215

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535265730	chr9:266073-266074	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs184180978	chr9:266087-266088	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs369750330	chr9:266120-266121	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs2021977	chr9:266121-266122	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs12342002	chr9:266165-266166	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs543432922	chr9:266182-266183	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs564710337	chr9:266192-266193	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs373280792	chr9:266196-266197	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs113882242	chr9:266226-266227	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs116244962	chr9:266234-266235	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs76047579	chr9:266235-266236	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs189671137	chr9:266239-266240	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs549572146	chr9:266241-266242	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs561397516	chr9:266273-266274	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs561751211	chr9:266318-266319	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs192847536	chr9:266325-266326	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs140578086	chr9:266364-266365	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs368006763	chr9:266365-266366	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs3046373	chr9:266395-266396	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs77919192	chr9:266431-266432	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs116829386	chr9:266479-266480	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs538974918	chr9:266484-266485	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs547381918	chr9:266503-266504	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs573851	chr9:266505-266506	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs78244574	chr9:266528-266529	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs13292783	chr9:266543-266544	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs575765518	chr9:266569-266570	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs184688768	chr9:266609-266610	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs558569472	chr9:266610-266611	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs73374506	chr9:266611-266612	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs114488420	chr9:266629-266630	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs189576655	chr9:266646-266647	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs540232062	chr9:266650-266651	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs572756570	chr9:266667-266668	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs543279838	chr9:266678-266679	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs561460956	chr9:266705-266706	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs11788947	chr9:266708-266709	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs540054087	chr9:266782-266783	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs663327	chr9:266786-266787	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs570221148	chr9:266793-266794	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs663309	chr9:266795-266796	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs180875311	chr9:266837-266838	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs186571919	chr9:266847-266848	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs565663860	chr9:266875-266876	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs536123882	chr9:266890-266891	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs374687502	chr9:266893-266894	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs202046056	chr9:266913-266914	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs548021815	chr9:266920-266921	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs569510615	chr9:266961-266962	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs562302927	chr9:266971-266972	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:118)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	20164920	CNVD
Ovarian cancer	21720365	CNVD
Myelofibrosis	22110671	CNVD
Lynch syndrome	18415027	CNVD
Retinoblastoma	21504564	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	22286061	CNVD
Williams-beuren syndrome	18553513	CNVD
Disorders of sex development	21048976	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
prenatal diagnosis	20453657	CNVD
Gastric cancer	16715143	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Intracranial aneurysm	16715129	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Disorders of sex development	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Sudden cardiac death	19188705	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21952639	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
abnormal development	18461090	CNVD
Honadal dysgenesis	21048976	CNVD
Medulloblastoma	21979893	CNVD
Lung cancer	16740712	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Schizophrenia	20967226	CNVD
Lung cancer	18438408	CNVD
Autism	20531469	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Developmental delay	20808231	CNVD
Obesity	20808231	CNVD
Myelodysplastic syndrome	21251322	CNVD
Primary immunodeficiency	22942019	CNVD
Melanoma	20877625	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Breast cancer	21364760	CNVD
Bipolar disorder	19114987	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:2525 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:255000-268600	Weak transcription	Spleen	Spleen
2	chr9:255000-270400	Weak transcription	Pancreas	Pancrea
3	chr9:255000-271800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr9:258400-271400	Weak transcription	Primary B cells from peripheral blood	blood
5	chr9:259200-269200	Weak transcription	Primary B cells from cord blood	blood
6	chr9:260200-268200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
7	chr9:260400-269600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr9:264600-268600	Weak transcription	Thymus	Thymus
9	chr9:264800-268000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
10	chr9:264800-268200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
11	chr9:264800-268400	Weak transcription	Primary T cells from cord blood	blood
12	chr9:265000-268000	Weak transcription	Primary T helper cells PMA-I stimulated	--
13	chr9:265400-268200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr9:265600-266200	Enhancers	Stomach Mucosa	stomach
15	chr9:265600-268000	Weak transcription	Primary hematopoietic stem cells	blood
16	chr9:265600-268600	Enhancers	Primary neutrophils fromperipheralblood	blood
17	chr9:265600-272600	Enhancers	Primary monocytes fromperipheralblood	blood
18	chr9:265800-266400	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chr9:265800-266400	Enhancers	K562	blood
20	chr9:265800-267800	Enhancers	Monocytes-CD14+_RO01746	blood
21	chr9:265800-268000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr9:265800-268200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr9:265800-268400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr9:266000-270400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
25	chr9:266000-281600	Weak transcription	Adipose Nuclei	Adipose
26	chr9:266200-268400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr9:266200-268600	Weak transcription	Stomach Mucosa	stomach
28	chr9:266400-268000	Weak transcription	K562	blood
29	chr9:266400-271800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
30	chr9:267800-269400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
31	chr9:268000-268400	Enhancers	K562	blood
32	chr9:268000-268800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr9:268000-268800	Enhancers	Primary T helper cells PMA-I stimulated	--
34	chr9:268000-269000	Enhancers	Primary hematopoietic stem cells	blood
35	chr9:268000-269000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
36	chr9:268200-268400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
37	chr9:268200-268600	Enhancers	Primary hematopoietic stem cells short term culture	blood
38	chr9:268200-268800	Enhancers	Primary T helper naive cells from peripheral blood	blood
39	chr9:268200-268800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
40	chr9:268200-268800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
41	chr9:268200-268800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr9:268200-268800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr9:268200-269000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
44	chr9:268200-269400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr9:268400-268800	Enhancers	Primary T helper cells fromperipheralblood	blood
46	chr9:268400-268800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr9:268400-268800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr9:268400-269000	Enhancers	Primary T cells from cord blood	blood
49	chr9:268400-269000	Flanking Active TSS	K562	blood
50	chr9:268600-268800	Enhancers	Primary T cells fromperipheralblood	blood

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