Variant report

Variant	nsv1018258
Chromosome Location	chr9:27234184-27292709
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	chr9:27276433-27276779	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:27261532-27261892	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:27276480-27276766	K562	blood:	n/a	n/a
4	BHLHE40	chr9:27281155-27281334	K562	blood:	n/a	n/a
5	BHLHE40	chr9:27261364-27261936	HepG2	liver:	n/a	n/a
6	BRCA1	chr9:27261881-27262104	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr9:27238842-27239132	HepG2	liver:	n/a	chr9:27238966-27238975
8	CEBPB	chr9:27248839-27249287	IMR90	lung:	n/a	chr9:27249140-27249151 chr9:27248881-27248898
9	CEBPB	chr9:27272984-27273198	A549	lung:	n/a	chr9:27273158-27273171
10	CEBPB	chr9:27261315-27261855	HepG2	liver:	n/a	n/a
11	CEBPB	chr9:27261315-27262115	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr9:27258771-27259071	K562	blood:	n/a	chr9:27258921-27258932 chr9:27258921-27258934 chr9:27258921-27258934
13	CEBPB	chr9:27258775-27259094	HepG2	liver:	n/a	chr9:27258921-27258932 chr9:27258921-27258934 chr9:27258921-27258934
14	CEBPB	chr9:27261286-27261670	MCF-7	breast:	n/a	n/a
15	CEBPB	chr9:27248999-27249274	HepG2	liver:	n/a	chr9:27249140-27249151
16	CEBPB	chr9:27248970-27249261	A549	lung:	n/a	chr9:27249140-27249151
17	CEBPB	chr9:27258776-27259077	A549	lung:	n/a	chr9:27258921-27258932 chr9:27258921-27258934 chr9:27258921-27258934
18	CTCF	chr9:27276287-27276294	GM12878	blood:	n/a	n/a
19	CTCF	chr9:27247724-27247959	H1-hESC	embryonic stem cell:	n/a	chr9:27247863-27247873 chr9:27247860-27247881 chr9:27247858-27247876 chr9:27247861-27247870 chr9:27247859-27247875
20	CTCF	chr9:27247820-27247970	GM12866	blood:	n/a	chr9:27247863-27247873 chr9:27247860-27247881 chr9:27247858-27247876 chr9:27247861-27247870 chr9:27247859-27247875
21	CTCF	chr9:27276240-27276390	GM12874	blood:	n/a	n/a
22	CTCF	chr9:27247800-27247950	HRE	kidney:	n/a	chr9:27247863-27247873 chr9:27247860-27247881 chr9:27247858-27247876 chr9:27247861-27247870 chr9:27247859-27247875
23	CTCF	chr9:27246980-27247130	GM12873	blood:	n/a	n/a
24	CTCF	chr9:27276560-27276710	AoAF	blood vessel:	n/a	chr9:27276618-27276636 chr9:27276620-27276633 chr9:27276619-27276635 chr9:27276624-27276633 chr9:27276613-27276634
25	CTCF	chr9:27276540-27276690	GM12864	blood:	n/a	chr9:27276618-27276636 chr9:27276620-27276633 chr9:27276619-27276635 chr9:27276624-27276633 chr9:27276613-27276634
26	CTCF	chr9:27247670-27248050	K562	blood:	n/a	chr9:27247863-27247873 chr9:27247860-27247881 chr9:27247858-27247876 chr9:27247861-27247870 chr9:27247859-27247875
27	CTCF	chr9:27260640-27260790	HBMEC	blood vessel:	n/a	n/a
28	CTCF	chr9:27276518-27276685	GM19239	blood:	n/a	chr9:27276618-27276636 chr9:27276620-27276633 chr9:27276619-27276635 chr9:27276624-27276633 chr9:27276613-27276634
29	CTCF	chr9:27276500-27276650	HBMEC	blood vessel:	n/a	chr9:27276618-27276636 chr9:27276620-27276633 chr9:27276619-27276635 chr9:27276624-27276633 chr9:27276613-27276634
30	CTCF	chr9:27247568-27248191	HCT-116	colon:	n/a	chr9:27247863-27247873 chr9:27247860-27247881 chr9:27247858-27247876 chr9:27247861-27247870 chr9:27247859-27247875
31	CTCF	chr9:27276500-27276650	GM12874	blood:	n/a	chr9:27276618-27276636 chr9:27276620-27276633 chr9:27276619-27276635 chr9:27276624-27276633 chr9:27276613-27276634
32	CTCF	chr9:27277193-27277248	GM20000	blood:	n/a	n/a
33	CTCF	chr9:27247720-27247870	HFF	foreskin:	n/a	chr9:27247861-27247870
34	CTCF	chr9:27276560-27276710	GM12870	blood:	n/a	chr9:27276618-27276636 chr9:27276620-27276633 chr9:27276619-27276635 chr9:27276624-27276633 chr9:27276613-27276634
35	CTCF	chr9:27260620-27260770	HEEpiC	esophagus:	n/a	n/a
36	CTCF	chr9:27276560-27276710	NHEK	skin:	n/a	chr9:27276618-27276636 chr9:27276620-27276633 chr9:27276619-27276635 chr9:27276624-27276633 chr9:27276613-27276634
37	CTCF	chr9:27247756-27247977	Lung_OC	lung:	n/a	chr9:27247863-27247873 chr9:27247860-27247881 chr9:27247858-27247876 chr9:27247861-27247870 chr9:27247859-27247875
38	CTCF	chr9:27276500-27276650	HRE	kidney:	n/a	chr9:27276618-27276636 chr9:27276620-27276633 chr9:27276619-27276635 chr9:27276624-27276633 chr9:27276613-27276634
39	CTCF	chr9:27276500-27276650	GM12870	blood:	n/a	chr9:27276618-27276636 chr9:27276620-27276633 chr9:27276619-27276635 chr9:27276624-27276633 chr9:27276613-27276634
40	CTCF	chr9:27276460-27276610	Caco-2	colon:	n/a	n/a
41	CTCF	chr9:27276540-27276690	HMF	breast:	n/a	chr9:27276618-27276636 chr9:27276620-27276633 chr9:27276619-27276635 chr9:27276624-27276633 chr9:27276613-27276634
42	CTCF	chr9:27276540-27276690	HFF-Myc	foreskin:	n/a	chr9:27276618-27276636 chr9:27276620-27276633 chr9:27276619-27276635 chr9:27276624-27276633 chr9:27276613-27276634
43	CTCF	chr9:27247800-27247950	HCFaa	heart:	n/a	chr9:27247863-27247873 chr9:27247860-27247881 chr9:27247858-27247876 chr9:27247861-27247870 chr9:27247859-27247875
44	CTCF	chr9:27276392-27276851	GM12878	blood:	n/a	chr9:27276618-27276636 chr9:27276620-27276633 chr9:27276619-27276635 chr9:27276624-27276633 chr9:27276613-27276634
45	CTCF	chr9:27276520-27276670	NHLF	lung:	n/a	chr9:27276618-27276636 chr9:27276620-27276633 chr9:27276619-27276635 chr9:27276624-27276633 chr9:27276613-27276634
46	CTCF	chr9:27276503-27276692	NHEK	skin:	n/a	chr9:27276618-27276636 chr9:27276620-27276633 chr9:27276619-27276635 chr9:27276624-27276633 chr9:27276613-27276634
47	CTCF	chr9:27247820-27247970	SAEC	small airway:	n/a	chr9:27247863-27247873 chr9:27247860-27247881 chr9:27247858-27247876 chr9:27247861-27247870 chr9:27247859-27247875
48	CTCF	chr9:27247240-27247390	BE2_C	brain:	n/a	chr9:27247243-27247252
49	CTCF	chr9:27247760-27247910	HVMF	connective:	n/a	chr9:27247863-27247873 chr9:27247860-27247881 chr9:27247858-27247876 chr9:27247861-27247870 chr9:27247859-27247875
50	CTCF	chr9:27276580-27276730	GM12878	blood:	n/a	chr9:27276618-27276636 chr9:27276620-27276633 chr9:27276619-27276635 chr9:27276624-27276633 chr9:27276613-27276634

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:27248473-27248523	HEK293	kidney:	embryo
2	chr9:27282580-27282630	AoSMC	blood vessel:	n/a
3	chr9:27248473-27248523	HRE	kidney:	n/a
4	chr9:27292606-27292656	GM19239	blood:	n/a
5	chr9:27248473-27248523	ECC-1	luminal epithelium:	n/a
6	chr9:27282776-27282826	HCPEpiC	choroid plexus:	n/a
7	chr9:27282776-27282826	PANC-1	pancreas:	n/a
8	chr9:27248473-27248523	U87	brain:	n/a
9	chr9:27292606-27292656	SK-N-SH_RA	brain:	n/a
10	chr9:27282580-27282630	HPAEpiC	pulmonary alveolar:	n/a
11	chr9:27248473-27248523	BJ	skin:	n/a
12	chr9:27282580-27282630	HCT-116	colon:	n/a
13	chr9:27282776-27282826	NH-A	brain:	n/a
14	chr9:27292606-27292656	NT2-D1	testis:	n/a
15	chr9:27292606-27292656	Caco-2	colon:	n/a
16	chr9:27282776-27282826	U87	brain:	n/a
17	chr9:27248473-27248523	LNCaP	prostate:	n/a
18	chr9:27248473-27248523	ovcar-3	ovarian:	n/a
19	chr9:27282580-27282630	HAEpiC	amniotic membrane:	n/a
20	chr9:27248473-27248523	HRCEpiC	kidney:	n/a
21	chr9:27282580-27282630	GM06990	blood:	n/a
22	chr9:27248473-27248523	HCPEpiC	choroid plexus:	n/a
23	chr9:27282776-27282826	HMEC	breast:	n/a
24	chr9:27282776-27282826	ovcar-3	ovarian:	n/a
25	chr9:27282580-27282630	Hepatocyte	liver:	n/a
26	chr9:27282776-27282826	BJ	skin:	n/a
27	chr9:27248473-27248523	HCF	heart:	n/a
28	chr9:27292606-27292656	K562	blood:	n/a
29	chr9:27282580-27282630	HCM	heart:	n/a
30	chr9:27282580-27282630	HRPEpiC	eye:	n/a
31	chr9:27282776-27282826	GM12891	blood:	n/a
32	chr9:27282776-27282826	AG10803	skin:	n/a
33	chr9:27282580-27282630	GM12892	blood:	n/a
34	chr9:27282580-27282630	HRCEpiC	kidney:	n/a
35	chr9:27282776-27282826	MCF-7	breast:	n/a
36	chr9:27282776-27282826	GM06990	blood:	n/a
37	chr9:27282776-27282826	IMR90	lung:	fetal
38	chr9:27282776-27282826	T-47D	breast:	n/a
39	chr9:27282776-27282826	ProgFib	skin:	n/a
40	chr9:27282776-27282826	HL-60	blood:	n/a
41	chr9:27292606-27292656	Jurkat	blood:	n/a
42	chr9:27248473-27248523	HCT-116	colon:	n/a
43	chr9:27248473-27248523	Hepatocyte	liver:	n/a
44	chr9:27282580-27282630	AG04449	skin:	fetal
45	chr9:27292606-27292656	HCM	heart:	n/a
46	chr9:27282580-27282630	NHBE	bronchial:	n/a
47	chr9:27248473-27248523	HepG2	liver:	n/a
48	chr9:27282580-27282630	GM19239	blood:	n/a
49	chr9:27282776-27282826	LNCaP	prostate:	n/a
50	chr9:27282776-27282826	HCT-116	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:27247423..27248703-chr9:27275999..27276820,3	MCF-7	breast:
2	chr9:27033540..27034483-chr9:27275947..27276717,3	MCF-7	breast:
3	chr9:27275368..27278167-chr9:27278207..27280246,2	MCF-7	breast:
4	chr9:27275368..27278167-chr9:27278207..27280246,2	MCF-7	breast:
5	chr9:27033902..27034442-chr9:27247489..27248319,2	MCF-7	breast:
6	chr9:27280860..27282970-chr9:27289180..27290823,2	K562	blood:
7	chr9:27247560..27248337-chr9:27547652..27548456,2	MCF-7	breast:
8	chr9:27033503..27034503-chr9:27276144..27277065,4	K562	blood:
9	chr9:27247423..27248703-chr9:27275999..27276820,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C9orf11-1	chr9:27253207-27253263	l_3745_NR_026687
2	lnc-C9orf11-1	chr9:27270766-27270922	l_3745_NR_026687
3	lnc-C9orf11-1	chr9:27272328-27272791	NONHSAT130610
4	lnc-C9orf11-1	chr9:27248693-27248766	NONHSAT130610
5	lnc-C9orf11-1	chr9:27270426-27270613	l_3745_NR_026687
6	lnc-C9orf11-1	chr9:27266962-27267108	l_3745_NR_026687
7	lnc-C9orf11-1	chr9:27264088-27264284	l_3745_NR_026687
8	lnc-C9orf11-1	chr9:27251828-27252034	NONHSAT130610
9	lnc-C9orf11-1	chr9:27253207-27253263	NONHSAT130610
10	lnc-C9orf11-1	chr9:27272328-27272791	l_3745_NR_026687
11	lnc-C9orf11-1	chr9:27265780-27265948	l_3745_NR_026687
12	lnc-C9orf11-1	chr9:27252710-27252801	l_3745_NR_026687
13	lnc-TEK-2	chr9:27245472-27245673	XLOC_007307
14	lnc-C9orf11-1	chr9:27252710-27252801	NONHSAT130610
15	lnc-C9orf11-1	chr9:27251828-27252034	l_3745_NR_026687
16	lnc-C9orf11-1	chr9:27267549-27267774	NONHSAT130610
17	lnc-C9orf11-1	chr9:27248410-27248517	l_3745_NR_026687
18	lnc-MOB3B-1	chr9:27292411-27292485	NONHSAT130613
19	lnc-C9orf11-1	chr9:27267549-27267774	l_3745_NR_026687
20	lnc-C9orf11-1	chr9:27268359-27268726	NONHSAT130610
21	lnc-C9orf11-1	chr9:27268359-27268726	l_3745_NR_026687
22	lnc-C9orf11-1	chr9:27265780-27265948	NONHSAT130610
23	lnc-C9orf11-1	chr9:27258419-27258515	NONHSAT130610
24	lnc-C9orf11-1	chr9:27261925-27262086	NONHSAT130610
25	lnc-C9orf11-1	chr9:27270766-27270922	NONHSAT130610
26	lnc-C9orf11-1	chr9:27264088-27264284	NONHSAT130610
27	lnc-TEK-2	chr9:27245986-27246282	XLOC_007307
28	lnc-C9orf11-1	chr9:27237388-27237508	NONHSAT130610
29	lnc-C9orf11-1	chr9:27248693-27248766	l_3745_NR_026687
30	lnc-C9orf11-1	chr9:27270426-27270613	NONHSAT130610
31	lnc-C9orf11-1	chr9:27266962-27267108	NONHSAT130610
32	lnc-C9orf11-1	chr9:27248410-27248517	NONHSAT130610
33	lnc-C9orf11-1	chr9:27261925-27262086	l_3745_NR_026687
34	lnc-C9orf11-1	chr9:27235684-27235760	l_3745_NR_026687
35	lnc-C9orf11-1	chr9:27237388-27237508	l_3745_NR_026687
36	lnc-C9orf11-1	chr9:27258419-27258515	l_3745_NR_026687
37	lnc-C9orf11-1	chr9:27235682-27235760	NONHSAT130610

Variant related genes	Relation type
LINC00032	TF binding region
LINC00032	CpG island
ENSG00000231459	chromatin interactions
ATP6V1B2	miRNA target sites

Extended variants
information (count: 1257 )
Associated
traits (count: 124 )

Variant overlapped rSNPs/rCNVs (count:1257 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576126241	chr9:27235690-27235691	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs12341363	chr9:27235707-27235708	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs372259306	chr9:27235710-27235711	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs557139335	chr9:27235728-27235729	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs200537554	chr9:27235734-27235735	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs538864358	chr9:27235756-27235757	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs2208634	chr9:27237399-27237400	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs549268882	chr9:27237400-27237401	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs142593490	chr9:27237415-27237416	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs556857103	chr9:27237434-27237435	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs574891706	chr9:27237442-27237443	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs542282647	chr9:27237484-27237485	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs560485969	chr9:27237494-27237495	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs376568044	chr9:27245512-27245513	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs570365264	chr9:27245532-27245533	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs528344920	chr9:27245541-27245542	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs546220804	chr9:27245548-27245549	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs570884299	chr9:27245555-27245556	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs538353200	chr9:27245566-27245567	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs369612363	chr9:27245585-27245586	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs568853094	chr9:27245595-27245596	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs373302727	chr9:27245605-27245606	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs375158738	chr9:27245634-27245635	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs554845063	chr9:27245635-27245636	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs573613526	chr9:27245642-27245643	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs144539229	chr9:27245653-27245654	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs368546740	chr9:27246018-27246019	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs74685567	chr9:27246019-27246020	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs78873333	chr9:27246026-27246027	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
30	rs539393411	chr9:27246040-27246041	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
31	rs187106372	chr9:27246042-27246043	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
32	rs577601377	chr9:27246045-27246046	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs17834925	chr9:27246055-27246056	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs1885382	chr9:27246116-27246117	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs574907806	chr9:27246117-27246118	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs541922054	chr9:27246135-27246136	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
37	rs199873969	chr9:27246149-27246150	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
38	rs1885381	chr9:27246151-27246152	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs57082575	chr9:27246160-27246161	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
40	rs367979816	chr9:27246170-27246171	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
41	rs572664709	chr9:27246245-27246246	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
42	rs542515470	chr9:27247600-27247601	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs568238136	chr9:27247608-27247609	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs535710105	chr9:27247665-27247666	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs535245685	chr9:27247670-27247671	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs12238077	chr9:27247792-27247793	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs116017306	chr9:27247797-27247798	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs151013929	chr9:27247813-27247814	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs377341821	chr9:27247822-27247823	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs545807886	chr9:27247834-27247835	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:124)

Disease	PMID	Source
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Medulloblastoma	21979893	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
Melanoma	18172304	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
Oral squamous cell carcinoma	17134496	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
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	21668985	CNVD
Myelodysplastic syndrome	21251322	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	18803288	CNVD
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Acute myeloid leukemia	19651601	CNVD
Coronary Disease	20032323	CNVD
Squamous cell cancer	20885788	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21732550	CNVD
Gastric cancer	22539939	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Metastatic melanoma	18483359	CNVD
Non-small cell lung cancer	20864512	CNVD
Cervical cancer	21062161	CNVD
Acute myeloid leukemia	16864856	CNVD
Glioblastoma	17090523	CNVD
Lung cancer	16773561	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16774939	CNVD
Bladder cancer	19088036	CNVD
Colorectal cancer	16272173	CNVD
Melanoma	16977458	CNVD
Glioblastoma multiforme	17369134	CNVD
Chagasic megaesophagus	20163722	CNVD
Melanoma	19566914	CNVD
Squamous cell cancer	19047905	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Hodgkin''s lymphoma	18179710	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21858162	CNVD
Pancreatic cancer	21811587	CNVD
Barrett''s syndrome	19417022	CNVD
Myelofibrosis	22110671	CNVD
Urothelial cell carcinoma	18451213	CNVD
polycythaemia	22829968	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21364760	CNVD
Glioblastoma multiforme	21525872	CNVD
Epilepsy	22083797	CNVD
Cancer	22183965	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Cancer	21215367	CNVD
Renal cell carcinoma	21215367	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:207 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:27247600-27248200	Enhancers	Stomach Mucosa	stomach
2	chr9:27247600-27248600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr9:27247600-27249400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr9:27247800-27248600	Enhancers	Placenta	Placenta
5	chr9:27247800-27249000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr9:27247800-27249200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr9:27247800-27249200	Enhancers	NHEK	skin
8	chr9:27247800-27249400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr9:27247800-27249400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr9:27247800-27249400	Enhancers	Muscle Satellite Cultured Cells	--
11	chr9:27247800-27249400	Enhancers	Osteobl	bone
12	chr9:27248000-27248800	Enhancers	Hela-S3	cervix
13	chr9:27248200-27249400	Enhancers	HSMM	muscle
14	chr9:27248400-27249200	Enhancers	Placenta Amnion	Placenta Amnion
15	chr9:27249000-27249200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr9:27259400-27259600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr9:27260200-27260600	Enhancers	Lung	lung
18	chr9:27260600-27262200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
19	chr9:27260800-27262400	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr9:27261000-27262000	Enhancers	HepG2	liver
21	chr9:27261000-27262200	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr9:27261000-27262200	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr9:27261200-27261400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr9:27261200-27261400	Enhancers	Placenta	Placenta
25	chr9:27261200-27261800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr9:27261200-27262200	Enhancers	H1 Cell Line	embryonic stem cell
27	chr9:27261200-27262200	Enhancers	Hela-S3	cervix
28	chr9:27261400-27261800	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr9:27261400-27262200	Enhancers	Gastric	stomach
30	chr9:27261600-27261800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr9:27261600-27261800	Enhancers	Stomach Mucosa	stomach
32	chr9:27261600-27262000	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr9:27261600-27262200	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr9:27261800-27262200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr9:27261800-27262200	Enhancers	NHEK	skin
36	chr9:27262000-27262200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr9:27262000-27262200	Enhancers	Placenta	Placenta
38	chr9:27262200-27262400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr9:27266800-27267000	Enhancers	Pancreas	Pancrea
40	chr9:27269600-27270400	Enhancers	Stomach Mucosa	stomach
41	chr9:27270000-27270400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr9:27270400-27272800	Weak transcription	Stomach Mucosa	stomach
43	chr9:27272600-27273000	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr9:27272600-27273000	Enhancers	Fetal Intestine Large	intestine
45	chr9:27272600-27274600	Enhancers	Fetal Intestine Small	intestine
46	chr9:27272800-27273600	Enhancers	Stomach Mucosa	stomach
47	chr9:27273000-27276000	Weak transcription	HUES48 Cell Line	embryonic stem cell
48	chr9:27273000-27278200	Weak transcription	Fetal Intestine Large	intestine
49	chr9:27273600-27276200	Weak transcription	Stomach Mucosa	stomach
50	chr9:27274600-27276000	Weak transcription	Fetal Intestine Small	intestine

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