Variant report

Variant	esv988312
Chromosome Location	chr8:47750639-47776253
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	BACH1	chr8:47770297-47770313	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr8:47750627-47750683	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr8:47771804-47772479	IMR90	lung:	n/a	chr8:47771968-47771977 chr8:47771966-47771979 chr8:47771966-47771977 chr8:47771968-47771977 chr8:47771966-47771977 chr8:47771968-47771977 chr8:47771967-47771978 chr8:47771966-47771979 chr8:47771966-47771979 chr8:47771968-47771977
4	CEBPB	chr8:47754786-47755004	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr8:47771818-47772113	K562	blood:	n/a	chr8:47771968-47771977 chr8:47771966-47771979 chr8:47771966-47771977 chr8:47771968-47771977 chr8:47771966-47771977 chr8:47771968-47771977 chr8:47771967-47771978 chr8:47771966-47771979 chr8:47771966-47771979 chr8:47771968-47771977
6	CEBPB	chr8:47766223-47766564	HepG2	liver:	n/a	chr8:47766390-47766401
7	CEBPB	chr8:47771800-47772449	HepG2	liver:	n/a	chr8:47771968-47771977 chr8:47771966-47771979 chr8:47771966-47771977 chr8:47771968-47771977 chr8:47771966-47771977 chr8:47771968-47771977 chr8:47771967-47771978 chr8:47771966-47771979 chr8:47771966-47771979 chr8:47771968-47771977
8	CEBPB	chr8:47753754-47755047	HepG2	liver:	n/a	n/a
9	CEBPB	chr8:47755769-47755984	A549	lung:	n/a	n/a
10	CEBPB	chr8:47757331-47758282	HepG2	liver:	n/a	n/a
11	CEBPB	chr8:47752270-47752699	IMR90	lung:	n/a	n/a
12	CEBPB	chr8:47752209-47752790	A549	lung:	n/a	n/a
13	CEBPB	chr8:47772797-47772971	HepG2	liver:	n/a	n/a
14	CEBPB	chr8:47753716-47755048	A549	lung:	n/a	n/a
15	CEBPB	chr8:47750894-47751193	IMR90	lung:	n/a	chr8:47751033-47751044
16	CEBPB	chr8:47769177-47769401	A549	lung:	n/a	n/a
17	CEBPB	chr8:47767015-47767397	IMR90	lung:	n/a	chr8:47767152-47767163
18	CEBPB	chr8:47754666-47755099	MCF-7	breast:	n/a	n/a
19	CEBPB	chr8:47760294-47760574	HepG2	liver:	n/a	chr8:47760422-47760435 chr8:47760424-47760433 chr8:47760423-47760434 chr8:47760424-47760433 chr8:47760424-47760433 chr8:47760424-47760433 chr8:47760422-47760435 chr8:47760422-47760433 chr8:47760422-47760435 chr8:47760422-47760433
20	CEBPB	chr8:47757356-47758245	A549	lung:	n/a	n/a
21	CEBPB	chr8:47766294-47766573	K562	blood:	n/a	chr8:47766390-47766401
22	CEBPB	chr8:47767893-47768218	HepG2	liver:	n/a	n/a
23	CEBPB	chr8:47766240-47766570	A549	lung:	n/a	chr8:47766390-47766401
24	CEBPB	chr8:47750993-47751208	A549	lung:	n/a	chr8:47751033-47751044
25	CEBPB	chr8:47775654-47775901	HepG2	liver:	n/a	n/a
26	CEBPB	chr8:47760243-47760576	K562	blood:	n/a	chr8:47760422-47760435 chr8:47760424-47760433 chr8:47760423-47760434 chr8:47760424-47760433 chr8:47760424-47760433 chr8:47760424-47760433 chr8:47760422-47760435 chr8:47760422-47760433 chr8:47760422-47760435 chr8:47760422-47760433
27	CEBPB	chr8:47775705-47775883	A549	lung:	n/a	n/a
28	CEBPB	chr8:47773608-47774441	A549	lung:	n/a	n/a
29	CEBPB	chr8:47767029-47767606	A549	lung:	n/a	chr8:47767152-47767163
30	CEBPB	chr8:47770756-47771098	HepG2	liver:	n/a	chr8:47770927-47770938
31	CEBPB	chr8:47754701-47755059	IMR90	lung:	n/a	n/a
32	CEBPB	chr8:47773617-47773955	IMR90	lung:	n/a	n/a
33	CEBPB	chr8:47760272-47760591	A549	lung:	n/a	chr8:47760422-47760435 chr8:47760424-47760433 chr8:47760423-47760434 chr8:47760424-47760433 chr8:47760424-47760433 chr8:47760424-47760433 chr8:47760422-47760435 chr8:47760422-47760433 chr8:47760422-47760435 chr8:47760422-47760433
34	CEBPB	chr8:47771800-47772967	A549	lung:	n/a	chr8:47771968-47771977 chr8:47771966-47771979 chr8:47771966-47771977 chr8:47771968-47771977 chr8:47771966-47771977 chr8:47771968-47771977 chr8:47771967-47771978 chr8:47771966-47771979 chr8:47771966-47771979 chr8:47771968-47771977
35	CEBPB	chr8:47766213-47766559	IMR90	lung:	n/a	chr8:47766390-47766401
36	CEBPB	chr8:47770771-47771000	A549	lung:	n/a	chr8:47770927-47770938
37	CEBPB	chr8:47767862-47768307	A549	lung:	n/a	n/a
38	CEBPB	chr8:47773629-47774333	HepG2	liver:	n/a	n/a
39	CEBPB	chr8:47750868-47751216	HepG2	liver:	n/a	chr8:47751033-47751044
40	CEBPB	chr8:47752236-47752796	HepG2	liver:	n/a	n/a
41	CEBPB	chr8:47760261-47760601	IMR90	lung:	n/a	chr8:47760422-47760435 chr8:47760424-47760433 chr8:47760423-47760434 chr8:47760424-47760433 chr8:47760424-47760433 chr8:47760424-47760433 chr8:47760422-47760435 chr8:47760422-47760433 chr8:47760422-47760435 chr8:47760422-47760433
42	CEBPB	chr8:47767024-47767380	HepG2	liver:	n/a	chr8:47767152-47767163
43	CEBPB	chr8:47752678-47752878	K562	blood:	n/a	n/a
44	CTCF	chr8:47750714-47750872	GM12878	blood:	n/a	n/a
45	E2F4	chr8:47752325-47752839	MCF10A-Er-Src	breast:	n/a	n/a
46	E2F4	chr8:47765631-47765852	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr8:47754699-47755316	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr8:47751530-47752792	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr8:47761743-47762073	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr8:47751690-47752756	MCF10A-Er-Src	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:47751623-47751673	HEEpiC	esophagus:	n/a
2	chr8:47751953-47752003	ECC-1	luminal epithelium:	n/a
3	chr8:47751953-47752003	A549	lung:	n/a
4	chr8:47751623-47751673	H1-hESC	embryonic stem cell:	embryo
5	chr8:47761906-47761956	HRE	kidney:	n/a
6	chr8:47751953-47752003	SK-N-SH_RA	brain:	n/a
7	chr8:47751494-47751544	ovcar-3	ovarian:	n/a
8	chr8:47751623-47751673	AoSMC	blood vessel:	n/a
9	chr8:47751494-47751544	HPAEpiC	pulmonary alveolar:	n/a
10	chr8:47751953-47752003	HEK293	kidney:	embryo
11	chr8:47751623-47751673	Hepatocyte	liver:	n/a
12	chr8:47761906-47761956	SK-N-MC	brain:	n/a
13	chr8:47751953-47752003	MCF10A-Er-Src	breast:	n/a
14	chr8:47761906-47761956	MCF-7	breast:	n/a
15	chr8:47761906-47761956	HRCEpiC	kidney:	n/a
16	chr8:47751623-47751673	T-47D	breast:	n/a
17	chr8:47751494-47751544	A549	lung:	n/a
18	chr8:47751623-47751673	CMK	blood:	n/a
19	chr8:47751623-47751673	BJ	skin:	n/a
20	chr8:47751494-47751544	AG04450	lung:	fetal
21	chr8:47761906-47761956	AG09319	gingival:	n/a
22	chr8:47751953-47752003	Hela-S3	cervix:	n/a
23	chr8:47751953-47752003	BJ	skin:	n/a
24	chr8:47751623-47751673	GM19239	blood:	n/a
25	chr8:47761906-47761956	HAEpiC	amniotic membrane:	n/a
26	chr8:47751623-47751673	HPAEpiC	pulmonary alveolar:	n/a
27	chr8:47751953-47752003	NHBE	bronchial:	n/a
28	chr8:47751623-47751673	HMEC	breast:	n/a
29	chr8:47751623-47751673	GM12892	blood:	n/a
30	chr8:47761906-47761956	HNPCEpiC	eye:	n/a
31	chr8:47751623-47751673	PrEC	prostate:	n/a
32	chr8:47751953-47752003	NH-A	brain:	n/a
33	chr8:47751623-47751673	HAEpiC	amniotic membrane:	n/a
34	chr8:47751623-47751673	GM12878	blood:	n/a
35	chr8:47761906-47761956	GM12892	blood:	n/a
36	chr8:47761906-47761956	A549	lung:	n/a
37	chr8:47751953-47752003	CMK	blood:	n/a
38	chr8:47751494-47751544	GM12891	blood:	n/a
39	chr8:47761906-47761956	HRPEpiC	eye:	n/a
40	chr8:47761906-47761956	NB4	blood:	n/a
41	chr8:47751494-47751544	AoSMC	blood vessel:	n/a
42	chr8:47751623-47751673	Jurkat	blood:	n/a
43	chr8:47751953-47752003	HCPEpiC	choroid plexus:	n/a
44	chr8:47751623-47751673	U87	brain:	n/a
45	chr8:47751953-47752003	K562	blood:	n/a
46	chr8:47751953-47752003	Hepatocyte	liver:	n/a
47	chr8:47761906-47761956	HMEC	breast:	n/a
48	chr8:47751623-47751673	SK-N-SH	brain:	n/a
49	chr8:47761906-47761956	U87	brain:	n/a
50	chr8:47751953-47752003	GM19239	blood:	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-1134I14.8.1-3	chr8:47754972-47755048	NR_027013
2	lnc-RP11-1134I14.8.1-3	chr8:47759598-47759722	ENSG00000253314.1
3	lnc-RP11-1134I14.8.1-3	chr8:47755811-47755918	ENSG00000253314.1
4	lnc-RP11-1134I14.8.1-3	chr8:47754972-47755048	ENSG00000253314.1
5	lnc-RP11-1134I14.8.1-3	chr8:47766092-47766216	NONHSAT126424
6	lnc-RP11-1134I14.8.1-3	chr8:47765729-47765991	NONHSAT126423
7	lnc-RP11-1134I14.8.1-3	chr8:47752517-47752557	ENSG00000253314.1
8	lnc-RP11-1134I14.8.1-3	chr8:47752667-47752748	ENSG00000253314.1
9	lnc-RP11-1134I14.8.1-3	chr8:47752508-47752557	NR_027013
10	lnc-RP11-1134I14.8.1-3	chr8:47752667-47752748	ENSG00000253314.1
11	lnc-RP11-1134I14.8.1-3	chr8:47752667-47752748	ENSG00000253314.1
12	lnc-RP11-1134I14.8.1-3	chr8:47760406-47760523	NONHSAT126421
13	lnc-RP11-1134I14.8.1-3	chr8:47765729-47765929	NR_027013
14	lnc-RP11-1134I14.8.1-3	chr8:47766092-47766220	NONHSAT126423
15	lnc-RP11-1134I14.8.1-3	chr8:47757651-47757703	NONHSAT126421
16	lnc-RP11-1134I14.8.1-3	chr8:47752486-47752557	NONHSAT126419
17	lnc-RP11-1134I14.8.1-3	chr8:47752667-47752748	NR_027013
18	lnc-RP11-1134I14.8.1-3	chr8:47754972-47755048	NONHSAT126415
19	lnc-RP11-1134I14.8.1-3	chr8:47759598-47759688	ENSG00000253314.1
20	lnc-RP11-1134I14.8.1-3	chr8:47759598-47759722	NONHSAT126421
21	lnc-RP11-1134I14.8.1-3	chr8:47757651-47757703	ENSG00000253314.1
22	lnc-RP11-1134I14.8.1-3	chr8:47757651-47757703	ENSG00000253314.1
23	lnc-RP11-1134I14.8.1-3	chr8:47752667-47752748	NONHSAT126415
24	lnc-RP11-1134I14.8.1-3	chr8:47754972-47755048	NONHSAT126419
25	lnc-RP11-1134I14.8.1-3	chr8:47754972-47755048	ENSG00000253314.1
26	lnc-RP11-1134I14.8.1-3	chr8:47753899-47753974	NONHSAT126421
27	lnc-RP11-1134I14.8.1-3	chr8:47760406-47761152	NONHSAT126420
28	lnc-RP11-1134I14.8.1-3	chr8:47753899-47753974	NR_027013
29	lnc-RP11-1134I14.8.1-3	chr8:47766386-47767407	NONHSAT126421
30	lnc-RP11-1134I14.8.1-3	chr8:47762290-47762365	NR_027013
31	lnc-RP11-1134I14.8.1-3	chr8:47752667-47752748	ENSG00000253314.1
32	lnc-RP11-1134I14.8.1-3	chr8:47759598-47759722	NONHSAT126420
33	lnc-RP11-1134I14.8.1-3	chr8:47765729-47765833	ENSG00000253314.1
34	lnc-RP11-1134I14.8.1-3	chr8:47754972-47755048	ENSG00000253314.1
35	lnc-RP11-1134I14.8.1-3	chr8:47762290-47762365	ENSG00000253314.1
36	lnc-RP11-1134I14.8.1-3	chr8:47760406-47761152	NR_027013
37	lnc-RP11-1134I14.8.1-3	chr8:47765729-47765929	ENSG00000253314.1
38	lnc-RP11-1134I14.8.1-3	chr8:47762290-47762365	NONHSAT126420
39	lnc-RP11-1134I14.8.1-3	chr8:47761071-47761152	ENSG00000253314.1
40	lnc-RP11-1134I14.8.1-3	chr8:47760406-47761152	ENSG00000253314.1
41	lnc-RP11-1134I14.8.1-3	chr8:47752667-47752748	NONHSAT126419
42	lnc-RP11-1134I14.8.1-3	chr8:47752508-47752557	NONHSAT126421
43	lnc-RP11-1134I14.8.1-3	chr8:47759598-47759722	NONHSAT126415
44	lnc-RP11-1134I14.8.1-3	chr8:47752438-47752557	ENSG00000253314.1
45	lnc-RP11-1134I14.8.1-3	chr8:47760406-47760523	ENSG00000253314.1
46	lnc-RP11-1134I14.8.1-3	chr8:47753899-47753974	NONHSAT126420
47	lnc-RP11-1134I14.8.1-3	chr8:47757651-47757703	NONHSAT126419
48	lnc-RP11-1134I14.8.1-3	chr8:47757651-47757703	NONHSAT126420
49	lnc-RP11-1134I14.8.1-3	chr8:47753899-47753974	ENSG00000253314.1
50	lnc-RP11-1134I14.8.1-3	chr8:47759598-47759722	NONHSAT126419

Variant related genes	Relation type
LINC00293	TF binding region
ENSG00000254118	TF binding region
LINC00293	CpG island
ENSG00000254118	CpG island

Extended variants
information (count: 672 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs557742883	chr8:47750674-47750675	Inactive region	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
2	rs561094766	chr8:47750727-47750728	Inactive region	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
3	rs117596029	chr8:47750728-47750729	Inactive region	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
4	rs191343551	chr8:47750890-47750891	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs551906588	chr8:47750892-47750893	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs118158448	chr8:47750999-47751000	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs556953511	chr8:47751020-47751021	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs183923810	chr8:47751035-47751036	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs75287549	chr8:47751047-47751048	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs542379348	chr8:47751088-47751089	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs536375191	chr8:47751112-47751113	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs11994320	chr8:47751125-47751126	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs112286882	chr8:47751138-47751139	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs528526089	chr8:47751160-47751161	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs190605632	chr8:47751166-47751167	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
16	rs374713735	chr8:47751410-47751411	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs556954559	chr8:47751433-47751434	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs145138527	chr8:47751448-47751449	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs542716760	chr8:47751464-47751465	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs560981529	chr8:47751484-47751485	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs528256074	chr8:47751494-47751495	ZNF genes & repeats Enhancers	CpG island	2 gene(s)	Overlapped CNVs	n/a
22	rs564986954	chr8:47751495-47751496	ZNF genes & repeats Enhancers	CpG island	2 gene(s)	Overlapped CNVs	n/a
23	rs146881571	chr8:47751536-47751537	ZNF genes & repeats Enhancers	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
24	rs182334017	chr8:47751624-47751625	ZNF genes & repeats Enhancers	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
25	rs532471076	chr8:47751675-47751676	ZNF genes & repeats Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
26	rs550677526	chr8:47751702-47751703	ZNF genes & repeats Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
27	rs569205880	chr8:47751727-47751728	ZNF genes & repeats Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
28	rs140741357	chr8:47751754-47751755	ZNF genes & repeats Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
29	rs187415289	chr8:47751763-47751764	ZNF genes & repeats Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
30	rs566626292	chr8:47751766-47751767	ZNF genes & repeats Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
31	rs189839174	chr8:47751792-47751793	ZNF genes & repeats Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
32	rs534125200	chr8:47751807-47751808	ZNF genes & repeats Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
33	rs181598011	chr8:47751812-47751813	ZNF genes & repeats Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
34	rs369029842	chr8:47751832-47751833	ZNF genes & repeats Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
35	rs185368521	chr8:47751873-47751874	ZNF genes & repeats Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
36	rs144603025	chr8:47751890-47751891	ZNF genes & repeats Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
37	rs190231018	chr8:47751940-47751941	ZNF genes & repeats Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
38	rs182165140	chr8:47751953-47751954	ZNF genes & repeats Enhancers	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
39	rs530792379	chr8:47751954-47751955	ZNF genes & repeats Enhancers	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
40	rs36108918	chr8:47751978-47751979	ZNF genes & repeats Enhancers	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
41	rs28675351	chr8:47751993-47751994	ZNF genes & repeats Enhancers	TF binding region CpG island	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs554659843	chr8:47752029-47752030	Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
43	rs573013111	chr8:47752033-47752034	Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
44	rs540412068	chr8:47752126-47752127	Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
45	rs565116324	chr8:47752127-47752128	Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
46	rs528927841	chr8:47752132-47752133	Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
47	rs544458094	chr8:47752186-47752187	Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
48	rs116358189	chr8:47752221-47752222	Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
49	rs529987695	chr8:47752228-47752229	Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
50	rs548223125	chr8:47752230-47752231	Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Lung cancer	18438408	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
abnormal development	18461090	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Medulloblastoma	20607354	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	20409316	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Tetralogy of Fallot	22912587	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:47751400-47752000	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
2	chr8:47751400-47753800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr8:47753200-47753800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
4	chr8:47754000-47755000	Enhancers	Placenta	Placenta
5	chr8:47755000-47757000	Weak transcription	Placenta	Placenta
6	chr8:47757000-47758200	Enhancers	Placenta	Placenta
7	chr8:47758200-47759400	Weak transcription	Placenta	Placenta
8	chr8:47759200-47761400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
9	chr8:47760000-47760400	Active TSS	Fetal Heart	heart
10	chr8:47761400-47762000	Weak transcription	Placenta	Placenta
11	chr8:47762000-47763400	Enhancers	Placenta	Placenta
12	chr8:47763400-47767400	Weak transcription	Placenta	Placenta
13	chr8:47764200-47764400	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
14	chr8:47765200-47765400	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
15	chr8:47767400-47767800	Enhancers	Placenta	Placenta

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