Variant report

Variant	nsv457725
Chromosome Location	chr17:33664044-33774159
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1089)
CpG islands
(count:3055)
Chromatin interactive
region (count:14)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1089 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr17:33760648-33760943	K562	blood:	n/a	n/a
2	ATF2	chr17:33760159-33760921	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr17:33760160-33760916	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr17:33668688-33669050	GM12878	blood:	n/a	n/a
5	ATF2	chr17:33668590-33669116	GM12878	blood:	n/a	n/a
6	ATF3	chr17:33760267-33760589	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr17:33760631-33760858	K562	blood:	n/a	n/a
8	ATF3	chr17:33760190-33760966	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr17:33760593-33760991	K562	blood:	n/a	n/a
10	ATF3	chr17:33760478-33761048	A549	lung:	n/a	n/a
11	ATF3	chr17:33760640-33760960	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr17:33673564-33673712	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr17:33672911-33673111	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr17:33759792-33760985	H1-hESC	embryonic stem cell:	n/a	chr17:33760771-33760785
15	BACH1	chr17:33700735-33700996	H1-hESC	embryonic stem cell:	n/a	n/a
16	BATF	chr17:33760581-33760913	GM12878	blood:	n/a	chr17:33760774-33760785 chr17:33760775-33760785
17	BATF	chr17:33760594-33760881	GM12878	blood:	n/a	chr17:33760774-33760785 chr17:33760775-33760785
18	BATF	chr17:33668595-33669032	GM12878	blood:	n/a	n/a
19	BATF	chr17:33668673-33668963	GM12878	blood:	n/a	n/a
20	BCL11A	chr17:33668550-33669051	GM12878	blood:	n/a	n/a
21	BCL11A	chr17:33668612-33668946	GM12878	blood:	n/a	n/a
22	BCL3	chr17:33760474-33760983	A549	lung:	n/a	chr17:33760774-33760783 chr17:33760773-33760782
23	BCLAF1	chr17:33700435-33700893	GM12878	blood:	n/a	n/a
24	BCLAF1	chr17:33668581-33669130	GM12878	blood:	n/a	n/a
25	BHLHE40	chr17:33700507-33700933	GM12878	blood:	n/a	n/a
26	BHLHE40	chr17:33731448-33731557	GM12878	blood:	n/a	n/a
27	BHLHE40	chr17:33668628-33669113	GM12878	blood:	n/a	n/a
28	BHLHE40	chr17:33765638-33765645	HepG2	liver:	n/a	n/a
29	BRCA1	chr17:33700927-33700952	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr17:33760228-33761108	A549	lung:	n/a	chr17:33761021-33761029
31	CEBPB	chr17:33717739-33718092	Hela-S3	cervix:	n/a	chr17:33717904-33717917 chr17:33717904-33717917 chr17:33717905-33717916
32	CEBPB	chr17:33760228-33760918	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr17:33665288-33665615	HepG2	liver:	n/a	chr17:33665455-33665466
34	CEBPB	chr17:33717730-33718103	K562	blood:	n/a	chr17:33717904-33717917 chr17:33717904-33717917 chr17:33717905-33717916
35	CEBPB	chr17:33717812-33718023	K562	blood:	n/a	chr17:33717904-33717917 chr17:33717904-33717917 chr17:33717905-33717916
36	CEBPB	chr17:33731441-33731629	K562	blood:	n/a	n/a
37	CEBPB	chr17:33760241-33760955	IMR90	lung:	n/a	n/a
38	CEBPB	chr17:33760263-33760970	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr17:33760651-33760906	K562	blood:	n/a	n/a
40	CEBPB	chr17:33673144-33673435	HepG2	liver:	n/a	chr17:33673292-33673303 chr17:33673367-33673378
41	CEBPB	chr17:33698317-33698552	A549	lung:	n/a	chr17:33698439-33698450
42	CEBPB	chr17:33717723-33718092	HepG2	liver:	n/a	chr17:33717904-33717917 chr17:33717904-33717917 chr17:33717905-33717916
43	CEBPB	chr17:33665282-33665555	IMR90	lung:	n/a	chr17:33665455-33665466
44	CEBPB	chr17:33673203-33673334	HepG2	liver:	n/a	chr17:33673292-33673303
45	CEBPB	chr17:33701311-33701959	IMR90	lung:	n/a	n/a
46	CEBPB	chr17:33681594-33681772	HepG2	liver:	n/a	chr17:33681650-33681661
47	CEBPB	chr17:33717748-33718067	H1-hESC	embryonic stem cell:	n/a	chr17:33717904-33717917 chr17:33717904-33717917 chr17:33717905-33717916
48	CEBPB	chr17:33673192-33673389	Hela-S3	cervix:	n/a	chr17:33673292-33673303 chr17:33673367-33673378
49	CEBPB	chr17:33700583-33700911	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr17:33700361-33701097	GM12878	blood:	n/a	n/a

(count:3055 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:33759986-33760036	T-47D	breast:	n/a
2	chr17:33760293-33760343	ovcar-3	ovarian:	n/a
3	chr17:33672713-33672763	GM06990	blood:	n/a
4	chr17:33673476-33673526	HMEC	breast:	n/a
5	chr17:33759573-33759623	HCM	heart:	n/a
6	chr17:33759986-33760036	T-47D	breast:	n/a
7	chr17:33760293-33760343	ovcar-3	ovarian:	n/a
8	chr17:33672713-33672763	GM06990	blood:	n/a
9	chr17:33673476-33673526	HMEC	breast:	n/a
10	chr17:33759573-33759623	HCM	heart:	n/a
11	chr17:33701350-33701400	RPTEC	kidney:	n/a
12	chr17:33759573-33759623	HNPCEpiC	eye:	n/a
13	chr17:33760230-33760280	HepG2	liver:	n/a
14	chr17:33673036-33673086	NH-A	brain:	n/a
15	chr17:33673708-33673758	HCM	heart:	n/a
16	chr17:33672921-33672971	HL-60	blood:	n/a
17	chr17:33760527-33760577	NT2-D1	testis:	n/a
18	chr17:33760293-33760343	CMK	blood:	n/a
19	chr17:33738370-33738420	Hela-S3	cervix:	n/a
20	chr17:33678143-33678193	HEK293	kidney:	embryo
21	chr17:33700295-33700345	NH-A	brain:	n/a
22	chr17:33763575-33763625	HCM	heart:	n/a
23	chr17:33760249-33760299	HEEpiC	esophagus:	n/a
24	chr17:33672921-33672971	NB4	blood:	n/a
25	chr17:33721242-33721292	ECC-1	luminal epithelium:	n/a
26	chr17:33701353-33701403	H1-hESC	embryonic stem cell:	embryo
27	chr17:33701321-33701371	Hela-S3	cervix:	n/a
28	chr17:33698288-33698338	ECC-1	luminal epithelium:	n/a
29	chr17:33701776-33701826	AG10803	skin:	n/a
30	chr17:33679797-33679847	ProgFib	skin:	n/a
31	chr17:33704726-33704776	BE2_C	brain:	n/a
32	chr17:33673590-33673640	GM19239	blood:	n/a
33	chr17:33760419-33760469	BJ	skin:	n/a
34	chr17:33738370-33738420	GM12892	blood:	n/a
35	chr17:33760527-33760577	K562	blood:	n/a
36	chr17:33734847-33734897	MCF10A-Er-Src	breast:	n/a
37	chr17:33673476-33673526	A549	lung:	n/a
38	chr17:33759957-33760007	AG04449	skin:	fetal
39	chr17:33760230-33760280	AG04450	lung:	fetal
40	chr17:33698288-33698338	AG04449	skin:	fetal
41	chr17:33731014-33731064	HUVEC	blood vessel:	n/a
42	chr17:33759957-33760007	HCM	heart:	n/a
43	chr17:33734481-33734531	NHDF-neo	bronchial:	n/a
44	chr17:33673590-33673640	Caco-2	colon:	n/a
45	chr17:33700759-33700809	HRPEpiC	eye:	n/a
46	chr17:33672921-33672971	SAEC	small airway:	n/a
47	chr17:33700230-33700280	HL-60	blood:	n/a
48	chr17:33734764-33734814	HMEC	breast:	n/a
49	chr17:33700295-33700345	HPAEpiC	pulmonary alveolar:	n/a
50	chr17:33760293-33760343	HRE	kidney:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:33663634..33666079-chr17:33669263..33671638,2	K562	blood:
2	chr17:33726969..33729366-chr17:33731337..33733299,2	K562	blood:
3	chr17:33676876..33678377-chr17:33681878..33683602,2	K562	blood:
4	chr17:33749302..33751373-chr17:33754505..33756544,2	K562	blood:
5	chr17:33676876..33678377-chr17:33681878..33683602,2	K562	blood:
6	chr17:33675973..33676543-chr19:47291156..47291826,2	NB4	blood:
7	chr17:33700355..33701212-chr7:100026345..100027279,2	NB4	blood:
8	chr17:33760769..33763748-chr17:33765471..33767342,2	MCF-7	breast:
9	chr17:33691774..33694475-chr17:33701256..33703274,2	K562	blood:
10	chr17:33749302..33751373-chr17:33754505..33756544,2	K562	blood:
11	chr17:33729515..33731700-chr17:33736981..33738686,2	K562	blood:
12	chr17:33760769..33763748-chr17:33765471..33767342,2	MCF-7	breast:
13	chr17:33729515..33731700-chr17:33736981..33738686,2	K562	blood:
14	chr17:33769997..33772468-chr17:33774210..33776177,2	K562	blood:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLFN12-6	chr17:33689786-33690011	NONHSAT053086
2	lnc-SLFN13-1	chr17:33758902-33759093	NONHSAT053095
3	lnc-SLFN12-6	chr17:33687038-33687390	NONHSAT053086
4	lnc-SLFN12-1	chr17:33736621-33737247	NONHSAT053094
5	lnc-SLFN12-2	chr17:33730856-33731392	ENSG00000267547.1
6	lnc-SLFN13-1	chr17:33759207-33759276	NONHSAT053095
7	lnc-SLFN13-1	chr17:33759924-33760184	NONHSAT053095
8	lnc-SLFN12-5	chr17:33694285-33694719	NONHSAT053088
9	lnc-SLFN12-1	chr17:33736484-33736787	ENSG00000267745.1
10	lnc-SLFN12-4	chr17:33774005-33774433	NONHSAT053096
11	lnc-SLFN12-5	chr17:33693966-33694313	NONHSAT053087
12	lnc-SLFN12-3	chr17:33729955-33730025	ENSG00000267711.1
13	lnc-SLFN5-2	chr17:33671250-33671583	NONHSAT053085
14	lnc-SLFN11-1	chr17:33704435-33704697	NONHSAT053089
15	lnc-SLFN12-1	chr17:33733703-33734610	ENSG00000267745.1
16	lnc-SLFN12-5	chr17:33690641-33690845	NONHSAT053087
17	lnc-SLFN12-5	chr17:33700493-33700639	NONHSAT053088
18	lnc-SLFN12-1	chr17:33733967-33734837	NONHSAT053093
19	lnc-SLFN12-3	chr17:33727897-33728219	ENSG00000267711.1

No data

Variant related genes	Relation type
ENSG00000267547	TF binding region
SLFN11	TF binding region
ENSG00000267315	TF binding region
ENSG00000267271	TF binding region
SLFN12	TF binding region
SLFN13	TF binding region
ENSG00000267745	TF binding region
ENSG00000267648	TF binding region
ENSG00000267711	TF binding region
ENSG00000267102	TF binding region
ENSG00000267547	CpG island
SLFN11	CpG island
ENSG00000267315	CpG island
ENSG00000267271	CpG island
SLFN12	CpG island
SLFN13	CpG island
ENSG00000267745	CpG island
ENSG00000267648	CpG island
ENSG00000267711	CpG island
ENSG00000267102	CpG island
ENSG00000267102	chromatin interactions
ENSG00000267271	chromatin interactions
ENSG00000172716	chromatin interactions
ENSG00000267711	chromatin interactions
ENSG00000146834	chromatin interactions
ENSG00000078487	chromatin interactions
ENSG00000267547	chromatin interactions
ENSG00000154760	chromatin interactions

Extended variants
information (count: 4273 )
Associated
traits (count: 118 )

Variant overlapped rSNPs/rCNVs (count:4273 , 50 per page) page: 1 2 3 4 5 6 7 ... 86

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1548182	chr17:33664044-33664045	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs190084878	chr17:33664049-33664050	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs537288643	chr17:33664095-33664096	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs557121263	chr17:33664098-33664099	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs573811796	chr17:33664200-33664201	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs1546583	chr17:33664242-33664243	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs371988118	chr17:33664328-33664329	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs116207468	chr17:33664362-33664363	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs114620712	chr17:33664378-33664379	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs181248647	chr17:33664394-33664395	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs9898340	chr17:33664441-33664442	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs542846501	chr17:33664565-33664566	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs554896158	chr17:33664598-33664599	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs577815513	chr17:33664752-33664753	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs543607116	chr17:33664762-33664763	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs144993381	chr17:33664782-33664783	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs529529784	chr17:33664798-33664799	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs186138132	chr17:33664804-33664805	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs11655688	chr17:33664818-33664819	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
20	rs528131641	chr17:33664844-33664845	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs551497535	chr17:33664848-33664849	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs8068794	chr17:33664879-33664880	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs530638803	chr17:33664955-33664956	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs371523222	chr17:33664991-33664992	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs550467683	chr17:33665019-33665020	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs4795071	chr17:33665043-33665044	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs536135069	chr17:33665052-33665053	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs149090616	chr17:33665123-33665124	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs533113256	chr17:33665138-33665139	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs565729367	chr17:33665150-33665151	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs369254985	chr17:33665158-33665159	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs576684236	chr17:33665220-33665221	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs372237044	chr17:33665244-33665245	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs534743277	chr17:33665267-33665268	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs557735059	chr17:33665278-33665279	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs62079535	chr17:33665329-33665330	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs543915420	chr17:33665358-33665359	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs74369373	chr17:33665366-33665367	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs115894876	chr17:33665406-33665407	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs116292116	chr17:33665416-33665417	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs528796227	chr17:33665424-33665425	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs143696063	chr17:33665441-33665442	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs148113656	chr17:33665448-33665449	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs530494670	chr17:33665465-33665466	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs117343677	chr17:33665466-33665467	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs567333735	chr17:33665474-33665475	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs190945856	chr17:33665483-33665484	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs77652400	chr17:33665504-33665505	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs78571462	chr17:33665505-33665506	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs546488333	chr17:33665517-33665518	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:118)

Disease	PMID	Source
Melanoma	18172304	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Ewing''s sarcoma	21437220	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Moyamoya disease	22323933	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21781307	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	17603634	CNVD
T-cell lymphomas	19863542	CNVD
Cancer	16751803	CNVD
Chordoma	21602918	CNVD
Neurofibromatosis	20686819	CNVD
Peripheral nerve sheath tumors	20686819	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	17897457	CNVD
Neuroblastoma	17327916	CNVD
Breast cancer	21264507	CNVD
Endometrial cancer	22040021	CNVD
Neuroblastoma	21484798	CNVD
Breast cancer	22028636	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute myeloid leukemia	20724749	CNVD
Breast cancer	21858162	CNVD
Breast cancer	16397240	CNVD
Myxofibrosarcoma	16751306	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17157792	CNVD
Bladder cancer	19088036	CNVD
Gastric cancer	17167181	CNVD
Breast cancer	19287154	CNVD
Leukemia	20874852	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Neuroblastoma	18664255	CNVD
Neuroblastoma	17533364	CNVD
Human rectal carcinomas	16397240	CNVD
Meningioma	19431122	CNVD
Neurocytoma	17123091	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Lung cancer	21911935	CNVD
Breast cancer	22048815	CNVD
Cervical cancer	21062161	CNVD
Colorectal cancer	22860045	CNVD
Ductal carcinoma	18381933	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16417655	CNVD
Renal cysts	20603712	CNVD
Epilepsy	21858020	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Autism	20587423	CNVD
Renal cysts	20587423	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Mayer-Rokitansky-Kuster-Hauser syndrome	19889212	CNVD
Endometrial cancer	23636398	CNVD
Urothelial cell carcinoma	18451213	CNVD
Gastric cancer	24379144	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Gastric cancer	18160780	CNVD
Hepatocellular carcinoma	16785998	CNVD
Breast cancer	17850661	CNVD
Primary lung adenocarcinoma	16799635	CNVD
HIV/AIDS	18848619	CNVD
Rheumatoid arthritis	19220326	CNVD
Rheumatoid arthritis	18848619	CNVD
Systemic lupus erythematosus	19220326	CNVD
Systemic lupus erythematosus	18848619	CNVD
Type 1 diabetes	19220326	CNVD
HIV/AIDS	17330138	CNVD
Basal cell lymphoma	17053054	CNVD
Autism	19955444	CNVD
Schizophrenia	19955444	CNVD
Acute monocytic leukemia	16498392	CNVD
Breast cancer	20409316	CNVD
Myelodysplastic syndrome	18663149	CNVD
Breast cancer	17457667	CNVD
Breast cancer	16951389	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Lung cancer	19153074	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Breast cancer	20932292	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Recurrent pregnancy loss	19789632	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:2637 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:33641200-33668600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr17:33653000-33671200	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr17:33660200-33668000	Weak transcription	Primary T cells fromperipheralblood	blood
4	chr17:33661200-33668000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
5	chr17:33664400-33664600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr17:33667600-33668400	Enhancers	Monocytes-CD14+_RO01746	blood
7	chr17:33668000-33668800	ZNF genes & repeats	Primary Natural Killer cells fromperipheralblood	blood
8	chr17:33668000-33669400	Enhancers	Primary T cells fromperipheralblood	blood
9	chr17:33668000-33670000	ZNF genes & repeats	Primary B cells from peripheral blood	blood
10	chr17:33668000-33670800	Enhancers	Primary B cells from cord blood	blood
11	chr17:33668000-33672400	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr17:33668200-33668400	Enhancers	GM12878-XiMat	blood
13	chr17:33668200-33670000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
14	chr17:33668200-33670400	Enhancers	Primary T helper cells PMA-I stimulated	--
15	chr17:33668400-33668800	Flanking Active TSS	GM12878-XiMat	blood
16	chr17:33668400-33669000	Active TSS	Monocytes-CD14+_RO01746	blood
17	chr17:33668400-33669600	Enhancers	Primary T helper cells fromperipheralblood	blood
18	chr17:33668400-33669800	Enhancers	Dnd41	blood
19	chr17:33668400-33670000	Enhancers	Primary T helper naive cells from peripheral blood	blood
20	chr17:33668400-33670200	Enhancers	Primary T killer memory cells from peripheral blood	blood
21	chr17:33668600-33669200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
22	chr17:33668600-33669200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
23	chr17:33668600-33669200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
24	chr17:33668600-33669800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
25	chr17:33668800-33669000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
26	chr17:33668800-33669000	Enhancers	GM12878-XiMat	blood
27	chr17:33669000-33669400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
28	chr17:33669000-33669400	Flanking Active TSS	GM12878-XiMat	blood
29	chr17:33669000-33669400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
30	chr17:33669000-33670000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
31	chr17:33669000-33670600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
32	chr17:33669200-33672200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr17:33669200-33672400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
34	chr17:33669200-33672400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
35	chr17:33669400-33669600	Enhancers	Monocytes-CD14+_RO01746	blood
36	chr17:33669400-33669800	Flanking Bivalent TSS/Enh	GM12878-XiMat	blood
37	chr17:33669400-33671200	Weak transcription	Primary T cells fromperipheralblood	blood
38	chr17:33669400-33672200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
39	chr17:33669600-33670000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
40	chr17:33669600-33672200	Weak transcription	Primary T helper cells fromperipheralblood	blood
41	chr17:33669800-33670000	Bivalent Enhancer	GM12878-XiMat	blood
42	chr17:33669800-33672200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
43	chr17:33669800-33672400	Weak transcription	Dnd41	blood
44	chr17:33670000-33671400	Enhancers	Monocytes-CD14+_RO01746	blood
45	chr17:33670000-33672200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
46	chr17:33670000-33672400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
47	chr17:33670000-33672600	Weak transcription	Primary B cells from peripheral blood	blood
48	chr17:33670000-33672600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
49	chr17:33670200-33671800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
50	chr17:33670400-33671600	Weak transcription	Primary T helper cells PMA-I stimulated	--

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