Variant report

Variant	nsv1011085
Chromosome Location	chr1:158703583-158845135
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:684)
CpG islands
(count:1037)
Chromatin interactive
region (count:43)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:684 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:158769460-158770024	K562	blood:	n/a	n/a
2	ARID3A	chr1:158825932-158825957	K562	blood:	n/a	n/a
3	ARID3A	chr1:158788979-158789707	K562	blood:	n/a	n/a
4	ARID3A	chr1:158704604-158704729	K562	blood:	n/a	n/a
5	ARID3A	chr1:158709982-158710193	K562	blood:	n/a	n/a
6	ATF1	chr1:158789343-158789721	K562	blood:	n/a	n/a
7	ATF1	chr1:158769556-158769886	K562	blood:	n/a	n/a
8	ATF2	chr1:158789360-158789737	GM12878	blood:	n/a	n/a
9	ATF2	chr1:158800775-158801330	GM12878	blood:	n/a	n/a
10	ATF2	chr1:158800669-158801400	GM12878	blood:	n/a	n/a
11	ATF3	chr1:158769474-158769844	K562	blood:	n/a	n/a
12	ATF3	chr1:158789352-158789686	K562	blood:	n/a	n/a
13	BACH1	chr1:158737227-158737232	K562	blood:	n/a	n/a
14	BACH1	chr1:158805878-158806042	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr1:158805801-158806172	K562	blood:	n/a	n/a
16	BCLAF1	chr1:158800861-158801338	GM12878	blood:	n/a	n/a
17	BHLHE40	chr1:158788081-158788271	K562	blood:	n/a	n/a
18	BHLHE40	chr1:158788978-158789714	K562	blood:	n/a	n/a
19	BHLHE40	chr1:158726549-158726678	K562	blood:	n/a	chr1:158726580-158726593 chr1:158726576-158726597
20	BHLHE40	chr1:158800659-158801366	GM12878	blood:	n/a	n/a
21	CBX3	chr1:158769307-158769963	K562	blood:	n/a	n/a
22	CBX3	chr1:158788999-158790050	K562	blood:	n/a	n/a
23	CBX3	chr1:158797558-158797934	K562	blood:	n/a	n/a
24	CBX3	chr1:158798388-158798797	K562	blood:	n/a	n/a
25	CBX3	chr1:158808484-158808794	K562	blood:	n/a	n/a
26	CBX3	chr1:158808439-158808799	K562	blood:	n/a	n/a
27	CCNT2	chr1:158769560-158769964	K562	blood:	n/a	n/a
28	CCNT2	chr1:158789159-158789743	K562	blood:	n/a	n/a
29	CEBPB	chr1:158804453-158804753	K562	blood:	n/a	n/a
30	CEBPB	chr1:158791602-158791765	K562	blood:	n/a	n/a
31	CEBPB	chr1:158722946-158723214	HepG2	liver:	n/a	chr1:158723040-158723051 chr1:158723037-158723054 chr1:158723040-158723053
32	CEBPB	chr1:158789146-158789635	K562	blood:	n/a	n/a
33	CEBPB	chr1:158749817-158749847	K562	blood:	n/a	n/a
34	CEBPB	chr1:158776989-158777341	IMR90	lung:	n/a	chr1:158777157-158777168 chr1:158777157-158777168
35	CEBPB	chr1:158803073-158803345	HepG2	liver:	n/a	chr1:158803197-158803208
36	CEBPB	chr1:158803107-158803362	K562	blood:	n/a	chr1:158803197-158803208
37	CEBPB	chr1:158719042-158719256	HepG2	liver:	n/a	chr1:158719183-158719196 chr1:158719183-158719194
38	CEBPB	chr1:158722945-158723184	H1-hESC	embryonic stem cell:	n/a	chr1:158723040-158723051 chr1:158723037-158723054 chr1:158723040-158723053
39	CEBPB	chr1:158769583-158769879	K562	blood:	n/a	n/a
40	CEBPB	chr1:158722942-158723176	Hela-S3	cervix:	n/a	chr1:158723040-158723051 chr1:158723037-158723054 chr1:158723040-158723053
41	CEBPB	chr1:158800950-158801174	K562	blood:	n/a	n/a
42	CEBPB	chr1:158787677-158787924	K562	blood:	n/a	n/a
43	CEBPB	chr1:158749660-158749862	HepG2	liver:	n/a	chr1:158749776-158749789 chr1:158749776-158749787 chr1:158749777-158749788
44	CEBPB	chr1:158763468-158763735	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr1:158722871-158723208	K562	blood:	n/a	chr1:158723040-158723051 chr1:158723037-158723054 chr1:158723040-158723053
46	CEBPB	chr1:158711092-158711357	K562	blood:	n/a	n/a
47	CEBPB	chr1:158754063-158754299	A549	lung:	n/a	chr1:158754205-158754216
48	CEBPB	chr1:158754057-158754293	HepG2	liver:	n/a	chr1:158754205-158754216
49	CEBPB	chr1:158803069-158803328	A549	lung:	n/a	chr1:158803197-158803208
50	CEBPB	chr1:158779741-158779957	K562	blood:	n/a	n/a

(count:1037 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:158747277-158747327	SK-N-MC	brain:	n/a
2	chr1:158799935-158799985	AG10803	skin:	n/a
3	chr1:158724057-158724107	HEK293	kidney:	embryo
4	chr1:158799935-158799985	HepG2	liver:	n/a
5	chr1:158737599-158737649	ovcar-3	ovarian:	n/a
6	chr1:158724057-158724107	HAEpiC	amniotic membrane:	n/a
7	chr1:158799935-158799985	HCF	heart:	n/a
8	chr1:158724057-158724107	CMK	blood:	n/a
9	chr1:158809049-158809099	LNCaP	prostate:	n/a
10	chr1:158747277-158747327	AG10803	skin:	n/a
11	chr1:158723939-158723989	HCF	heart:	n/a
12	chr1:158736112-158736162	AG09319	gingival:	n/a
13	chr1:158724794-158724844	SK-N-MC	brain:	n/a
14	chr1:158746611-158746661	NHDF-neo	bronchial:	n/a
15	chr1:158736112-158736162	ECC-1	luminal epithelium:	n/a
16	chr1:158737599-158737649	HRCEpiC	kidney:	n/a
17	chr1:158817808-158817858	PANC-1	pancreas:	n/a
18	chr1:158736312-158736362	PANC-1	pancreas:	n/a
19	chr1:158737591-158737641	GM19239	blood:	n/a
20	chr1:158809049-158809099	NH-A	brain:	n/a
21	chr1:158724362-158724412	HRE	kidney:	n/a
22	chr1:158737591-158737641	NT2-D1	testis:	n/a
23	chr1:158747277-158747327	HL-60	blood:	n/a
24	chr1:158746611-158746661	SK-N-SH	brain:	n/a
25	chr1:158724362-158724412	HRCEpiC	kidney:	n/a
26	chr1:158737820-158737870	HRPEpiC	eye:	n/a
27	chr1:158724362-158724412	GM12892	blood:	n/a
28	chr1:158748156-158748206	Hela-S3	cervix:	n/a
29	chr1:158817808-158817858	SK-N-SH_RA	brain:	n/a
30	chr1:158725300-158725350	HCF	heart:	n/a
31	chr1:158737820-158737870	ProgFib	skin:	n/a
32	chr1:158748156-158748206	Caco-2	colon:	n/a
33	chr1:158746611-158746661	Hepatocyte	liver:	n/a
34	chr1:158800024-158800074	MCF10A-Er-Src	breast:	n/a
35	chr1:158748156-158748206	NHBE	bronchial:	n/a
36	chr1:158748156-158748206	AG09309	skin:	n/a
37	chr1:158725300-158725350	HIPEpiC	eye:	n/a
38	chr1:158748156-158748206	ProgFib	skin:	n/a
39	chr1:158809049-158809099	BJ	skin:	n/a
40	chr1:158809049-158809099	PANC-1	pancreas:	n/a
41	chr1:158737820-158737870	HMEC	breast:	n/a
42	chr1:158817808-158817858	HCPEpiC	choroid plexus:	n/a
43	chr1:158724362-158724412	BE2_C	brain:	n/a
44	chr1:158724057-158724107	Caco-2	colon:	n/a
45	chr1:158800024-158800074	NT2-D1	testis:	n/a
46	chr1:158748156-158748206	NHDF-neo	bronchial:	n/a
47	chr1:158737820-158737870	AG04450	lung:	fetal
48	chr1:158817808-158817858	GM12892	blood:	n/a
49	chr1:158748156-158748206	SK-N-MC	brain:	n/a
50	chr1:158800024-158800074	AG04450	lung:	fetal

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:158763178..158764363-chr1:158967947..158968721,3	MCF-7	breast:
2	chr1:158722697..158725195-chr1:158729520..158731092,2	K562	blood:
3	chr1:158779601..158781616-chr1:158791201..158793222,2	K562	blood:
4	chr1:158699118..158701949-chr1:158709331..158711984,2	K562	blood:
5	chr1:158812790..158814752-chr1:158826099..158828358,2	K562	blood:
6	chr1:158702009..158703945-chr1:158717255..158718973,2	K562	blood:
7	chr1:158757287..158759072-chr1:158760688..158763230,2	K562	blood:
8	chr1:158711568..158713375-chr1:158713499..158715477,2	K562	blood:
9	chr1:158653549..158656527-chr1:158701529..158703994,2	K562	blood:
10	chr1:158733358..158736133-chr1:158736433..158738088,2	K562	blood:
11	chr1:158843130..158845633-chr1:158845939..158848183,3	K562	blood:
12	chr1:158757057..158758976-chr1:158767246..158769366,2	K562	blood:
13	chr1:158770831..158772373-chr1:158787697..158790487,2	K562	blood:
14	chr1:158701358..158703864-chr1:158711036..158713684,2	K562	blood:
15	chr1:158801901..158804321-chr1:158817913..158819439,2	K562	blood:
16	chr1:158842732..158844535-chr1:158852060..158853613,2	MCF-7	breast:
17	chr1:158812214..158814009-chr1:158818009..158819946,2	K562	blood:
18	chr1:158770831..158772373-chr1:158787697..158790487,2	K562	blood:
19	chr1:158821520..158824176-chr1:158832622..158835555,2	K562	blood:
20	chr1:158768206..158768907-chr1:158968540..158969106,3	MCF-7	breast:
21	chr1:158771201..158773385-chr1:158776168..158777671,2	K562	blood:
22	chr1:158820836..158822483-chr1:158829667..158831273,2	K562	blood:
23	chr1:158843130..158845633-chr1:158846139..158848183,2	K562	blood:
24	chr1:158651114..158653909-chr1:158727740..158729801,2	K562	blood:
25	chr1:158701755..158705583-chr1:158706296..158709041,3	K562	blood:
26	chr1:158704822..158706927-chr1:158777581..158780196,2	K562	blood:
27	chr1:158801901..158804321-chr1:158817913..158819439,2	K562	blood:
28	chr1:158821520..158824176-chr1:158832622..158835555,2	K562	blood:
29	chr1:158748328..158750308-chr1:158751698..158753611,2	K562	blood:
30	chr1:158701755..158705583-chr1:158706296..158709041,3	K562	blood:
31	chr1:158715265..158717778-chr1:158778694..158781362,2	K562	blood:
32	chr1:158697116..158699497-chr1:158702619..158704927,2	K562	blood:
33	chr1:158779601..158781616-chr1:158791201..158793222,2	K562	blood:
34	chr1:158757057..158758976-chr1:158767246..158769366,2	K562	blood:
35	chr1:158748328..158750308-chr1:158751698..158753611,2	K562	blood:
36	chr1:158820836..158822483-chr1:158829667..158831273,2	K562	blood:
37	chr1:158757287..158759072-chr1:158760688..158763230,2	K562	blood:
38	chr1:158702009..158703945-chr1:158717255..158718973,2	K562	blood:
39	chr1:158812790..158814752-chr1:158826099..158828358,2	K562	blood:
40	chr1:158735490..158738266-chr1:158739766..158741760,2	K562	blood:
41	chr1:158696982..158701883-chr1:158702210..158705771,7	K562	blood:
42	chr1:158812214..158814009-chr1:158818009..158819946,2	K562	blood:
43	chr1:158771201..158773385-chr1:158776168..158777671,2	K562	blood:

No data

Variant related genes	Relation type
OR6N2	TF binding region
OR2AQ1P	TF binding region
OR6K5P	TF binding region
OR10AA1P	TF binding region
ENSG00000229849	TF binding region
OR6N1	TF binding region
MNDA	TF binding region
OR6K6	TF binding region
OR6N2	CpG island
OR2AQ1P	CpG island
OR6K5P	CpG island
OR10AA1P	CpG island
ENSG00000229849	CpG island
OR6N1	CpG island
MNDA	CpG island
OR6K6	CpG island
ENSG00000226949	chromatin interactions
ENSG00000180433	chromatin interactions
ENSG00000180409	chromatin interactions
ENSG00000163554	chromatin interactions
ENSG00000197403	chromatin interactions

Extended variants
information (count: 4472 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:4472 , 50 per page) page: 1 2 3 4 5 6 7 ... 90

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs369140416	chr1:158703602-158703603	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs11265055	chr1:158703650-158703651	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs74122440	chr1:158703655-158703656	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs188017421	chr1:158703716-158703717	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs2078721	chr1:158703726-158703727	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs529962464	chr1:158703736-158703737	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs1429853	chr1:158703742-158703743	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs191414818	chr1:158703769-158703770	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs566783328	chr1:158703791-158703792	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs374951856	chr1:158703828-158703829	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs533724079	chr1:158703840-158703841	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs184804804	chr1:158703860-158703861	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs570417206	chr1:158703884-158703885	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs376660862	chr1:158703890-158703891	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs534276529	chr1:158703913-158703914	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs556015207	chr1:158703989-158703990	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs60908588	chr1:158704009-158704010	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs189774942	chr1:158704060-158704061	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs558041192	chr1:158704076-158704077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs554793364	chr1:158704120-158704121	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs1429854	chr1:158704144-158704145	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs540197954	chr1:158704164-158704165	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs565264864	chr1:158704219-158704220	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs532428775	chr1:158704301-158704302	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs145108540	chr1:158704303-158704304	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs181790734	chr1:158704369-158704370	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs12408501	chr1:158704370-158704371	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs548409698	chr1:158704388-158704389	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs566746405	chr1:158704424-158704425	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs326010	chr1:158704433-158704434	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs142828070	chr1:158704436-158704437	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs151034010	chr1:158704501-158704502	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs16840777	chr1:158704511-158704512	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs11265056	chr1:158704553-158704554	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs12076675	chr1:158704573-158704574	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs536417793	chr1:158704600-158704601	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs12072162	chr1:158704636-158704637	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs10908693	chr1:158704649-158704650	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs545116665	chr1:158704656-158704657	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs534481131	chr1:158704708-158704709	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs529759195	chr1:158704715-158704716	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs559033052	chr1:158704882-158704883	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs577158784	chr1:158704920-158704921	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs565280731	chr1:158704978-158704979	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs12127259	chr1:158704995-158704996	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs575009720	chr1:158705009-158705010	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs76658598	chr1:158705066-158705067	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs560374151	chr1:158705070-158705071	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs186572643	chr1:158705074-158705075	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs552445192	chr1:158705089-158705090	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:115)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Non-small cell lung cancer	21385341	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	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
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
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Systemic lupus erythematosus	19220326	CNVD
Systemic lupus erythematosus	19287148	CNVD
Glomerulonephritis	19341492	CNVD
Systemic lupus erythematosus	18559452	CNVD
Systemic autoimmune disease	17597778	CNVD
Glomerulonephritis	17008540	CNVD
Glomerulonephritis	16482158	CNVD
Soft tissue tumor	16732325	CNVD
Cancer	17060936	CNVD
Lung cancer	16740712	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Breast cancer	21045282	CNVD
Cancer	20164920	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Follicular lymphoma	18703704	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Intracranial ependymoma	16609018	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	17440070	CNVD

Chromatin state (count:314 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:158692600-158735200	Weak transcription	Primary neutrophils fromperipheralblood	blood
2	chr1:158702800-158706200	Enhancers	K562	blood
3	chr1:158705600-158705800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr1:158705600-158706000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr1:158706200-158708000	Weak transcription	K562	blood
6	chr1:158708000-158708800	Enhancers	K562	blood
7	chr1:158708800-158709600	Weak transcription	K562	blood
8	chr1:158709600-158709800	Active TSS	K562	blood
9	chr1:158709800-158710000	Flanking Active TSS	K562	blood
10	chr1:158710000-158710200	Enhancers	K562	blood
11	chr1:158721800-158722200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr1:158722400-158724800	Enhancers	Fetal Heart	heart
13	chr1:158735200-158737800	Strong transcription	Primary neutrophils fromperipheralblood	blood
14	chr1:158735400-158735800	Enhancers	Fetal Stomach	stomach
15	chr1:158737800-158740000	Weak transcription	Primary neutrophils fromperipheralblood	blood
16	chr1:158739800-158740600	Enhancers	Fetal Heart	heart
17	chr1:158740000-158741800	Strong transcription	Primary neutrophils fromperipheralblood	blood
18	chr1:158740400-158741200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr1:158740600-158740800	Flanking Active TSS	Fetal Heart	heart
20	chr1:158740800-158741000	Enhancers	Fetal Heart	heart
21	chr1:158741000-158741200	Flanking Active TSS	Fetal Heart	heart
22	chr1:158741200-158744400	Enhancers	Fetal Heart	heart
23	chr1:158741800-158742000	Genic enhancers	Primary neutrophils fromperipheralblood	blood
24	chr1:158742000-158742600	Enhancers	K562	blood
25	chr1:158742000-158746000	Weak transcription	Primary neutrophils fromperipheralblood	blood
26	chr1:158746000-158747400	Strong transcription	Primary neutrophils fromperipheralblood	blood
27	chr1:158747400-158752200	Weak transcription	Primary neutrophils fromperipheralblood	blood
28	chr1:158748400-158748800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
29	chr1:158751000-158751200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr1:158752200-158753200	Enhancers	Primary neutrophils fromperipheralblood	blood
31	chr1:158752600-158753400	Enhancers	Monocytes-CD14+_RO01746	blood
32	chr1:158752800-158753000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr1:158752800-158753200	Enhancers	Primary monocytes fromperipheralblood	blood
34	chr1:158753000-158753200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr1:158763000-158763600	Enhancers	Primary neutrophils fromperipheralblood	blood
36	chr1:158763200-158763600	Enhancers	Monocytes-CD14+_RO01746	blood
37	chr1:158763400-158763600	Active TSS	Primary B cells from cord blood	blood
38	chr1:158763400-158767800	Enhancers	Primary monocytes fromperipheralblood	blood
39	chr1:158763600-158763800	Flanking Active TSS	Primary B cells from cord blood	blood
40	chr1:158763600-158765000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
41	chr1:158763600-158765000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
42	chr1:158763800-158764000	Active TSS	Primary B cells from cord blood	blood
43	chr1:158764000-158764600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr1:158764000-158765400	Enhancers	Primary B cells from cord blood	blood
45	chr1:158764800-158765600	Enhancers	Adipose Nuclei	Adipose
46	chr1:158765000-158766000	Enhancers	Monocytes-CD14+_RO01746	blood
47	chr1:158765000-158769800	Enhancers	Primary neutrophils fromperipheralblood	blood
48	chr1:158765400-158767000	Weak transcription	Primary B cells from cord blood	blood
49	chr1:158766000-158767000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
50	chr1:158766800-158767200	Enhancers	iPS-18 Cell Line	embryonic stem cell

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