Variant report

Variant	nsv872762
Chromosome Location	chr1:190389741-190510003
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	chr1:190422723-190422890	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:190412968-190413009	HepG2	liver:	n/a	n/a
3	ATF1	chr1:190503941-190504004	K562	blood:	n/a	n/a
4	ATF1	chr1:190468018-190468035	K562	blood:	n/a	n/a
5	BACH1	chr1:190400937-190401001	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr1:190444539-190444919	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr1:190486481-190486484	K562	blood:	n/a	n/a
8	BRCA1	chr1:190448178-190448180	H1-hESC	embryonic stem cell:	n/a	n/a
9	CBX3	chr1:190405748-190406186	HCT-116	colon:	n/a	n/a
10	CEBPB	chr1:190482496-190482946	HepG2	liver:	n/a	chr1:190482774-190482783 chr1:190482774-190482783 chr1:190482773-190482784 chr1:190482774-190482783 chr1:190482772-190482785
11	CEBPB	chr1:190444799-190445222	A549	lung:	n/a	chr1:190444996-190445005 chr1:190444996-190445005 chr1:190444996-190445005 chr1:190444996-190445005
12	CEBPB	chr1:190482561-190482944	IMR90	lung:	n/a	chr1:190482774-190482783 chr1:190482774-190482783 chr1:190482773-190482784 chr1:190482774-190482783 chr1:190482772-190482785
13	CEBPB	chr1:190444800-190445186	HepG2	liver:	n/a	chr1:190444996-190445005 chr1:190444996-190445005 chr1:190444996-190445005 chr1:190444996-190445005
14	CEBPB	chr1:190394686-190395016	HepG2	liver:	n/a	chr1:190394836-190394849 chr1:190394838-190394847 chr1:190394836-190394847
15	CEBPB	chr1:190397535-190397821	HepG2	liver:	n/a	chr1:190397680-190397689 chr1:190397680-190397689 chr1:190397678-190397689 chr1:190397679-190397690 chr1:190397680-190397689 chr1:190397680-190397689
16	CEBPB	chr1:190444814-190445176	A549	lung:	n/a	chr1:190444996-190445005 chr1:190444996-190445005 chr1:190444996-190445005 chr1:190444996-190445005
17	CEBPB	chr1:190500757-190501016	HepG2	liver:	n/a	chr1:190500851-190500862
18	CEBPB	chr1:190397520-190397814	K562	blood:	n/a	chr1:190397680-190397689 chr1:190397680-190397689 chr1:190397678-190397689 chr1:190397679-190397690 chr1:190397680-190397689 chr1:190397680-190397689
19	CEBPB	chr1:190497113-190497229	HepG2	liver:	n/a	chr1:190497165-190497176
20	CEBPB	chr1:190394699-190395026	IMR90	lung:	n/a	chr1:190394836-190394849 chr1:190394838-190394847 chr1:190394836-190394847
21	CEBPB	chr1:190482603-190482902	Hela-S3	cervix:	n/a	chr1:190482774-190482783 chr1:190482774-190482783 chr1:190482773-190482784 chr1:190482774-190482783 chr1:190482772-190482785
22	CEBPB	chr1:190482634-190482949	H1-hESC	embryonic stem cell:	n/a	chr1:190482774-190482783 chr1:190482774-190482783 chr1:190482773-190482784 chr1:190482774-190482783 chr1:190482772-190482785
23	CEBPB	chr1:190444847-190445175	K562	blood:	n/a	chr1:190444996-190445005 chr1:190444996-190445005 chr1:190444996-190445005 chr1:190444996-190445005
24	CEBPB	chr1:190444781-190445213	MCF-7	breast:	n/a	chr1:190444996-190445005 chr1:190444996-190445005 chr1:190444996-190445005 chr1:190444996-190445005
25	CEBPB	chr1:190447237-190447354	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr1:190444708-190445343	A549	lung:	n/a	chr1:190444996-190445005 chr1:190444996-190445005 chr1:190444996-190445005 chr1:190444996-190445005
27	CEBPB	chr1:190397512-190397820	A549	lung:	n/a	chr1:190397680-190397689 chr1:190397680-190397689 chr1:190397678-190397689 chr1:190397679-190397690 chr1:190397680-190397689 chr1:190397680-190397689
28	CEBPB	chr1:190397507-190397871	IMR90	lung:	n/a	chr1:190397680-190397689 chr1:190397680-190397689 chr1:190397678-190397689 chr1:190397679-190397690 chr1:190397680-190397689 chr1:190397680-190397689
29	CEBPB	chr1:190444631-190445184	H1-hESC	embryonic stem cell:	n/a	chr1:190444996-190445005 chr1:190444996-190445005 chr1:190444996-190445005 chr1:190444996-190445005
30	CEBPB	chr1:190444837-190445233	MCF-7	breast:	n/a	chr1:190444996-190445005 chr1:190444996-190445005 chr1:190444996-190445005 chr1:190444996-190445005
31	CEBPB	chr1:190448377-190448519	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr1:190444585-190445212	IMR90	lung:	n/a	chr1:190444996-190445005 chr1:190444996-190445005 chr1:190444996-190445005 chr1:190444996-190445005
33	CEBPB	chr1:190463528-190463986	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr1:190482588-190482907	A549	lung:	n/a	chr1:190482774-190482783 chr1:190482774-190482783 chr1:190482773-190482784 chr1:190482774-190482783 chr1:190482772-190482785
35	CEBPB	chr1:190482609-190482928	K562	blood:	n/a	chr1:190482774-190482783 chr1:190482774-190482783 chr1:190482773-190482784 chr1:190482774-190482783 chr1:190482772-190482785
36	CHD1	chr1:190448119-190448317	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD1	chr1:190508485-190508604	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD1	chr1:190447111-190447248	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD1	chr1:190444232-190444267	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr1:190444200-190444215	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD2	chr1:190447252-190447284	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD2	chr1:190448095-190448332	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTBP2	chr1:190447174-190448394	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr1:190405820-190405970	HCT-116	colon:	n/a	chr1:190405933-190405949 chr1:190405927-190405948 chr1:190405934-190405947 chr1:190405935-190405945 chr1:190405932-190405950
45	CTCF	chr1:190405900-190406050	NHDF-neo	bronchial:	n/a	chr1:190405933-190405949 chr1:190405927-190405948 chr1:190405934-190405947 chr1:190405935-190405945 chr1:190405932-190405950
46	CTCF	chr1:190422700-190422850	NHDF-neo	bronchial:	n/a	n/a
47	CTCF	chr1:190422760-190422910	AG04450	lung:	n/a	chr1:190422882-190422892 chr1:190422874-190422895 chr1:190422881-190422894 chr1:190422880-190422896 chr1:190422879-190422897
48	CTCF	chr1:190405880-190406030	MCF-7	breast:	n/a	chr1:190405933-190405949 chr1:190405927-190405948 chr1:190405934-190405947 chr1:190405935-190405945 chr1:190405932-190405950
49	CTCF	chr1:190447320-190447470	HBMEC	blood vessel:	n/a	n/a
50	CTCF	chr1:190405860-190406010	GM12865	blood:	n/a	chr1:190405933-190405949 chr1:190405927-190405948 chr1:190405934-190405947 chr1:190405935-190405945 chr1:190405932-190405950

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:190444825-190444875	IMR90	lung:	fetal
2	chr1:190447603-190447653	HEK293	kidney:	embryo
3	chr1:190446829-190446879	GM06990	blood:	n/a
4	chr1:190444825-190444875	IMR90	lung:	fetal
5	chr1:190447603-190447653	HEK293	kidney:	embryo
6	chr1:190446829-190446879	GM06990	blood:	n/a
7	chr1:190447232-190447282	HUVEC	blood vessel:	n/a
8	chr1:190446829-190446879	ProgFib	skin:	n/a
9	chr1:190444387-190444437	SK-N-SH_RA	brain:	n/a
10	chr1:190444825-190444875	LNCaP	prostate:	n/a
11	chr1:190448126-190448176	PrEC	prostate:	n/a
12	chr1:190446756-190446806	H1-hESC	embryonic stem cell:	embryo
13	chr1:190444761-190444811	HEK293	kidney:	embryo
14	chr1:190447232-190447282	HIPEpiC	eye:	n/a
15	chr1:190447640-190447690	HUVEC	blood vessel:	n/a
16	chr1:190446756-190446806	ovcar-3	ovarian:	n/a
17	chr1:190447290-190447340	BE2_C	brain:	n/a
18	chr1:190447640-190447690	HIPEpiC	eye:	n/a
19	chr1:190444776-190444826	SK-N-MC	brain:	n/a
20	chr1:190447640-190447690	MCF-7	breast:	n/a
21	chr1:190444776-190444826	GM06990	blood:	n/a
22	chr1:190444825-190444875	HCM	heart:	n/a
23	chr1:190447290-190447340	U87	brain:	n/a
24	chr1:190444666-190444716	GM12892	blood:	n/a
25	chr1:190446829-190446879	AG09309	skin:	n/a
26	chr1:190445197-190445247	U87	brain:	n/a
27	chr1:190447290-190447340	HPAEpiC	pulmonary alveolar:	n/a
28	chr1:190444666-190444716	HCT-116	colon:	n/a
29	chr1:190445197-190445247	HMEC	breast:	n/a
30	chr1:190448126-190448176	AoSMC	blood vessel:	n/a
31	chr1:190444387-190444437	NH-A	brain:	n/a
32	chr1:190444776-190444826	NHDF-neo	bronchial:	n/a
33	chr1:190444776-190444826	HCPEpiC	choroid plexus:	n/a
34	chr1:190447232-190447282	SAEC	small airway:	n/a
35	chr1:190446756-190446806	T-47D	breast:	n/a
36	chr1:190448126-190448176	NT2-D1	testis:	n/a
37	chr1:190445197-190445247	HCPEpiC	choroid plexus:	n/a
38	chr1:190444387-190444437	GM12892	blood:	n/a
39	chr1:190444666-190444716	GM12878	blood:	n/a
40	chr1:190444825-190444875	NH-A	brain:	n/a
41	chr1:190447232-190447282	GM06990	blood:	n/a
42	chr1:190447640-190447690	PFSK-1	brain:	n/a
43	chr1:190448126-190448176	SK-N-MC	brain:	n/a
44	chr1:190444387-190444437	PANC-1	pancreas:	n/a
45	chr1:190447232-190447282	GM12892	blood:	n/a
46	chr1:190447290-190447340	HIPEpiC	eye:	n/a
47	chr1:190447232-190447282	HRE	kidney:	n/a
48	chr1:190444776-190444826	SK-N-SH_RA	brain:	n/a
49	chr1:190446829-190446879	NHBE	bronchial:	n/a
50	chr1:190444387-190444437	AG10803	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:190476606..190478933-chr1:190479727..190481548,2	MCF-7	breast:
2	chr1:190476606..190478933-chr1:190479727..190481548,2	MCF-7	breast:
3	chr1:190481525..190484334-chr1:190501308..190503770,2	K562	blood:
4	chr1:187382637..187383516-chr1:190422637..190423274,2	MCF-7	breast:
5	chr1:190405958..190408213-chr1:190432999..190435234,2	K562	blood:
6	chr1:190405958..190408213-chr1:190432999..190435234,2	K562	blood:
7	chr1:190443878..190446178-chr1:190461343..190463264,2	K562	blood:
8	chr1:190481525..190484334-chr1:190501308..190503770,2	K562	blood:
9	chr1:190429891..190431427-chr1:190443822..190445349,2	MCF-7	breast:
10	chr1:190456328..190457105-chr20:42218949..42219566,2	Hela-S3	cervix:
11	chr1:190378593..190380350-chr1:190390238..190392382,2	K562	blood:
12	chr1:190438085..190440650-chr1:190553313..190555425,2	K562	blood:
13	chr1:190342576..190343250-chr1:190405276..190406393,5	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RGS18-5	chr1:190449475-190449865	XLOC_000505
2	lnc-RGS18-5	chr1:190449475-190450667	XLOC_000505
3	lnc-RGS18-5	chr1:190449475-190449865	XLOC_000505
4	lnc-RGS18-5	chr1:190447593-190447761	XLOC_000505
5	lnc-RGS18-5	chr1:190444999-190445131	NONHSAT008496
6	lnc-RGS18-5	chr1:190462968-190463427	ENSG00000241505
7	lnc-RGS18-5	chr1:190448171-190448270	XLOC_000505
8	lnc-RGS18-5	chr1:190449509-190449554	ENSG00000241505
9	lnc-RGS18-5	chr1:190449475-190449779	NONHSAT008496
10	lnc-RGS18-5	chr1:190462968-190463251	XLOC_000505
11	lnc-RGS18-5	chr1:190445011-190445157	NONHSAT008495
12	lnc-RGS18-5	chr1:190448212-190448255	NONHSAT008497
13	lnc-RGS18-5	chr1:190447681-190447761	XLOC_000505
14	lnc-RGS18-5	chr1:190446965-190447761	NONHSAT008497
15	lnc-RGS18-5	chr1:190449475-190449704	XLOC_000505
16	lnc-RGS18-5	chr1:190448136-190448270	XLOC_000505
17	lnc-RGS18-5	chr1:190449475-190450523	XLOC_000505
18	lnc-RGS18-5	chr1:190447888-190448066	NONHSAT008498
19	lnc-RGS18-5	chr1:190447939-190447943	XLOC_000505
20	lnc-RGS18-5	chr1:190448171-190448271	XLOC_000505
21	lnc-RGS18-5	chr1:190447390-190447622	XLOC_000505
22	lnc-RGS18-5	chr1:190448212-190448270	XLOC_000505
23	lnc-RGS18-5	chr1:190447329-190447761	NONHSAT008498
24	lnc-RGS18-5	chr1:190449475-190450669	XLOC_000505
25	lnc-RGS18-5	chr1:190447611-190447761	XLOC_000505
26	lnc-RGS18-5	chr1:190447356-190447622	XLOC_000505
27	lnc-RGS18-5	chr1:190444703-190444884	NONHSAT008495
28	lnc-RGS18-5	chr1:190449475-190450669	XLOC_000505
29	lnc-RGS18-5	chr1:190448171-190448270	XLOC_000505
30	lnc-RGS18-5	chr1:190447753-190447761	XLOC_000505

Variant related genes	Relation type
ENSG00000237457	TF binding region
ENSG00000241505	TF binding region
BRINP3	TF binding region
ENSG00000237457	CpG island
ENSG00000241505	CpG island
BRINP3	CpG island
ENSG00000162670	chromatin interactions
PDLIM5	miRNA target sites
FECH	miRNA target sites
NRAS	miRNA target sites
PRNP	miRNA target sites

Extended variants
information (count: 2760 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:2760 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6678713	chr1:190389741-190389742	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs574043508	chr1:190389743-190389744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs147005292	chr1:190389758-190389759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs559740736	chr1:190389820-190389821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs527597631	chr1:190389853-190389854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs182703301	chr1:190389872-190389873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs137932952	chr1:190389944-190389945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs533186876	chr1:190389988-190389989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs187948038	chr1:190389999-190390000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs34146065	chr1:190390029-190390030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs192027395	chr1:190390054-190390055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs535132206	chr1:190390056-190390057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs1157187	chr1:190390066-190390067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs565303028	chr1:190390079-190390080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs535008334	chr1:190390116-190390117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs561265779	chr1:190390171-190390172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs531609844	chr1:190390198-190390199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs183346906	chr1:190390204-190390205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs550018394	chr1:190390206-190390207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs376685554	chr1:190390227-190390228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs115047329	chr1:190390258-190390259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs16832316	chr1:190390297-190390298	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs369183729	chr1:190390301-190390302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs537693141	chr1:190390309-190390310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs557272113	chr1:190390421-190390422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs538744992	chr1:190390441-190390442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs149891626	chr1:190390446-190390447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs34998352	chr1:190390447-190390448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs3079089	chr1:190390451-190390452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs78369563	chr1:190390457-190390458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs141956681	chr1:190390607-190390608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs189153126	chr1:190390626-190390627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs114712910	chr1:190390658-190390659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs192415741	chr1:190390683-190390684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs78653112	chr1:190390687-190390688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs564444529	chr1:190390689-190390690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs186600028	chr1:190390794-190390795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs549951042	chr1:190390809-190390810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs115584307	chr1:190390811-190390812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs544703051	chr1:190390820-190390821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs143100467	chr1:190390844-190390845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs564876980	chr1:190390845-190390846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs536271455	chr1:190390848-190390849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs191405529	chr1:190390875-190390876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs565416017	chr1:190390888-190390889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs373331065	chr1:190390924-190390925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs148222519	chr1:190390977-190390978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs80138477	chr1:190391067-190391068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs554238638	chr1:190391112-190391113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs150884229	chr1:190391135-190391136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	20688739	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21611746	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17899364	CNVD
Non-small cell lung cancer	19010865	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Trisomy 5 syndrome	21098271	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Lung adenocarcinoma	17086460	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:531 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:190379400-190420000	Weak transcription	Fetal Intestine Large	intestine
2	chr1:190397600-190413000	Weak transcription	Fetal Intestine Small	intestine
3	chr1:190407800-190408200	Enhancers	Fetal Heart	heart
4	chr1:190411000-190425600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr1:190411400-190411800	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr1:190411400-190412000	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr1:190412200-190412800	Active TSS	Placenta	Placenta
8	chr1:190412800-190413200	Enhancers	Placenta	Placenta
9	chr1:190413000-190414000	ZNF genes & repeats	Fetal Intestine Small	intestine
10	chr1:190414000-190419200	Weak transcription	Fetal Intestine Small	intestine
11	chr1:190414600-190415000	Enhancers	H1 Cell Line	embryonic stem cell
12	chr1:190414600-190415000	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr1:190419200-190419400	Enhancers	Fetal Intestine Small	intestine
14	chr1:190419200-190420800	Enhancers	Duodenum Mucosa	Duodenum
15	chr1:190419400-190419800	Weak transcription	Fetal Intestine Small	intestine
16	chr1:190419800-190420800	Enhancers	Fetal Intestine Small	intestine
17	chr1:190420000-190422000	Enhancers	Fetal Intestine Large	intestine
18	chr1:190420400-190421000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr1:190420800-190421600	Weak transcription	Fetal Intestine Small	intestine
20	chr1:190421400-190422200	Enhancers	HepG2	liver
21	chr1:190421400-190424200	Weak transcription	Cortex derived primary cultured neurospheres	brain
22	chr1:190421600-190422800	Strong transcription	Fetal Intestine Small	intestine
23	chr1:190421800-190422200	Enhancers	Placenta	Placenta
24	chr1:190422000-190438400	Weak transcription	Fetal Intestine Large	intestine
25	chr1:190422800-190438800	Weak transcription	Fetal Intestine Small	intestine
26	chr1:190423800-190424000	Enhancers	Fetal Heart	heart
27	chr1:190436200-190436600	Enhancers	Fetal Heart	heart
28	chr1:190438400-190439000	Active TSS	Fetal Intestine Large	intestine
29	chr1:190438800-190439400	Enhancers	Fetal Intestine Small	intestine
30	chr1:190439000-190440200	Weak transcription	Fetal Intestine Large	intestine
31	chr1:190439400-190441200	Weak transcription	Fetal Intestine Small	intestine
32	chr1:190440000-190440200	Enhancers	Rectal Mucosa Donor 29	rectum
33	chr1:190440000-190448800	Active TSS	Duodenum Mucosa	Duodenum
34	chr1:190440200-190448800	Active TSS	Fetal Intestine Large	intestine
35	chr1:190440600-190441000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr1:190440800-190448600	Active TSS	Rectal Mucosa Donor 31	rectum
37	chr1:190440800-190448800	Active TSS	Rectal Mucosa Donor 29	rectum
38	chr1:190441000-190445800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr1:190441200-190441800	Active TSS	Brain Germinal Matrix	brain
40	chr1:190441200-190443600	Active TSS	Brain Inferior Temporal Lobe	brain
41	chr1:190441200-190448600	Active TSS	Fetal Intestine Small	intestine
42	chr1:190441200-190448600	Active TSS	Right Atrium	heart
43	chr1:190441400-190444600	Active TSS	Brain Angular Gyrus	brain
44	chr1:190441400-190445600	Active TSS	Brain Anterior Caudate	brain
45	chr1:190441800-190442200	Active TSS	Fetal Lung	lung
46	chr1:190441800-190442600	Weak transcription	Brain Germinal Matrix	brain
47	chr1:190442200-190442400	Bivalent/Poised TSS	Fetal Lung	lung
48	chr1:190442600-190443800	Active TSS	Fetal Stomach	stomach
49	chr1:190442600-190445000	Active TSS	Cortex derived primary cultured neurospheres	brain
50	chr1:190442600-190445200	Active TSS	Brain Germinal Matrix	brain

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