Variant report

Variant	nsv1064831
Chromosome Location	chr17:33676494-33768199
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:895)
CpG islands
(count:2504)
Chromatin interactive
region (count:12)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:895 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

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	ATF3	chr17:33760593-33760991	K562	blood:	n/a	n/a
5	ATF3	chr17:33760478-33761048	A549	lung:	n/a	n/a
6	ATF3	chr17:33760640-33760960	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr17:33760267-33760589	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr17:33760631-33760858	K562	blood:	n/a	n/a
9	ATF3	chr17:33760190-33760966	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr17:33759792-33760985	H1-hESC	embryonic stem cell:	n/a	chr17:33760771-33760785
11	BACH1	chr17:33700735-33700996	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr17:33760581-33760913	GM12878	blood:	n/a	chr17:33760774-33760785 chr17:33760775-33760785
13	BATF	chr17:33760594-33760881	GM12878	blood:	n/a	chr17:33760774-33760785 chr17:33760775-33760785
14	BCL3	chr17:33760474-33760983	A549	lung:	n/a	chr17:33760774-33760783 chr17:33760773-33760782
15	BCLAF1	chr17:33700435-33700893	GM12878	blood:	n/a	n/a
16	BHLHE40	chr17:33700507-33700933	GM12878	blood:	n/a	n/a
17	BHLHE40	chr17:33765638-33765645	HepG2	liver:	n/a	n/a
18	BHLHE40	chr17:33731448-33731557	GM12878	blood:	n/a	n/a
19	BRCA1	chr17:33700927-33700952	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr17:33760241-33760955	IMR90	lung:	n/a	n/a
21	CEBPB	chr17:33698339-33698621	HepG2	liver:	n/a	chr17:33698439-33698450
22	CEBPB	chr17:33717723-33718092	HepG2	liver:	n/a	chr17:33717904-33717917 chr17:33717904-33717917 chr17:33717905-33717916
23	CEBPB	chr17:33731395-33731702	A549	lung:	n/a	n/a
24	CEBPB	chr17:33760228-33761108	A549	lung:	n/a	chr17:33761021-33761029
25	CEBPB	chr17:33717633-33718161	A549	lung:	n/a	chr17:33717904-33717917 chr17:33717904-33717917 chr17:33717905-33717916
26	CEBPB	chr17:33760228-33760918	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr17:33760660-33760956	A549	lung:	n/a	n/a
28	CEBPB	chr17:33681594-33681772	HepG2	liver:	n/a	chr17:33681650-33681661
29	CEBPB	chr17:33717673-33718118	A549	lung:	n/a	chr17:33717904-33717917 chr17:33717904-33717917 chr17:33717905-33717916
30	CEBPB	chr17:33717730-33718103	K562	blood:	n/a	chr17:33717904-33717917 chr17:33717904-33717917 chr17:33717905-33717916
31	CEBPB	chr17:33759330-33759655	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr17:33701311-33701959	IMR90	lung:	n/a	n/a
33	CEBPB	chr17:33760621-33760983	A549	lung:	n/a	n/a
34	CEBPB	chr17:33698406-33698449	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr17:33717731-33718093	A549	lung:	n/a	chr17:33717904-33717917 chr17:33717904-33717917 chr17:33717905-33717916
36	CEBPB	chr17:33760651-33760906	K562	blood:	n/a	n/a
37	CEBPB	chr17:33717720-33718093	IMR90	lung:	n/a	chr17:33717904-33717917 chr17:33717904-33717917 chr17:33717905-33717916
38	CEBPB	chr17:33717804-33717994	MCF-7	breast:	n/a	chr17:33717904-33717917 chr17:33717904-33717917 chr17:33717905-33717916
39	CEBPB	chr17:33701339-33701878	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr17:33717748-33718067	H1-hESC	embryonic stem cell:	n/a	chr17:33717904-33717917 chr17:33717904-33717917 chr17:33717905-33717916
41	CEBPB	chr17:33731440-33731698	IMR90	lung:	n/a	n/a
42	CEBPB	chr17:33731382-33731714	HepG2	liver:	n/a	n/a
43	CEBPB	chr17:33760263-33760970	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr17:33700583-33700911	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr17:33698317-33698552	A549	lung:	n/a	chr17:33698439-33698450
46	CEBPB	chr17:33681579-33681723	IMR90	lung:	n/a	chr17:33681650-33681661
47	CEBPB	chr17:33717812-33718023	K562	blood:	n/a	chr17:33717904-33717917 chr17:33717904-33717917 chr17:33717905-33717916
48	CEBPB	chr17:33731441-33731629	K562	blood:	n/a	n/a
49	CEBPB	chr17:33717739-33718092	Hela-S3	cervix:	n/a	chr17:33717904-33717917 chr17:33717904-33717917 chr17:33717905-33717916
50	CEBPB	chr17:33700361-33701097	GM12878	blood:	n/a	n/a

(count:2504 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:33759512-33759562	ProgFib	skin:	n/a
2	chr17:33701321-33701371	HIPEpiC	eye:	n/a
3	chr17:33700295-33700345	PrEC	prostate:	n/a
4	chr17:33759512-33759562	ProgFib	skin:	n/a
5	chr17:33701321-33701371	HIPEpiC	eye:	n/a
6	chr17:33700295-33700345	PrEC	prostate:	n/a
7	chr17:33678143-33678193	HEK293	kidney:	embryo
8	chr17:33700801-33700851	HCPEpiC	choroid plexus:	n/a
9	chr17:33678143-33678193	SK-N-MC	brain:	n/a
10	chr17:33760527-33760577	HCM	heart:	n/a
11	chr17:33700817-33700867	HRCEpiC	kidney:	n/a
12	chr17:33701321-33701371	ProgFib	skin:	n/a
13	chr17:33721242-33721292	HRCEpiC	kidney:	n/a
14	chr17:33759957-33760007	NT2-D1	testis:	n/a
15	chr17:33700801-33700851	GM12891	blood:	n/a
16	chr17:33700230-33700280	HNPCEpiC	eye:	n/a
17	chr17:33760293-33760343	SK-N-SH	brain:	n/a
18	chr17:33700513-33700563	RPTEC	kidney:	n/a
19	chr17:33700747-33700797	AG09319	gingival:	n/a
20	chr17:33760419-33760469	HepG2	liver:	n/a
21	chr17:33721242-33721292	SK-N-SH	brain:	n/a
22	chr17:33700759-33700809	BE2_C	brain:	n/a
23	chr17:33759648-33759698	HAEpiC	amniotic membrane:	n/a
24	chr17:33700513-33700563	HAEpiC	amniotic membrane:	n/a
25	chr17:33700817-33700867	Hela-S3	cervix:	n/a
26	chr17:33700513-33700563	T-47D	breast:	n/a
27	chr17:33700745-33700795	ProgFib	skin:	n/a
28	chr17:33760230-33760280	GM12892	blood:	n/a
29	chr17:33701321-33701371	NH-A	brain:	n/a
30	chr17:33759512-33759562	HMEC	breast:	n/a
31	chr17:33701321-33701371	GM12878	blood:	n/a
32	chr17:33704726-33704776	SK-N-MC	brain:	n/a
33	chr17:33700230-33700280	HCT-116	colon:	n/a
34	chr17:33700817-33700867	HMEC	breast:	n/a
35	chr17:33700757-33700807	IMR90	lung:	fetal
36	chr17:33734847-33734897	ProgFib	skin:	n/a
37	chr17:33704726-33704776	GM19239	blood:	n/a
38	chr17:33759929-33759979	A549	lung:	n/a
39	chr17:33734481-33734531	NHDF-neo	bronchial:	n/a
40	chr17:33700745-33700795	ECC-1	luminal epithelium:	n/a
41	chr17:33700801-33700851	SK-N-SH_RA	brain:	n/a
42	chr17:33759484-33759534	AG04450	lung:	fetal
43	chr17:33760293-33760343	HCF	heart:	n/a
44	chr17:33700747-33700797	HEEpiC	esophagus:	n/a
45	chr17:33700747-33700797	GM12878	blood:	n/a
46	chr17:33731014-33731064	RPTEC	kidney:	n/a
47	chr17:33760527-33760577	BE2_C	brain:	n/a
48	chr17:33734664-33734714	HPAEpiC	pulmonary alveolar:	n/a
49	chr17:33734481-33734531	GM12891	blood:	n/a
50	chr17:33701529-33701579	NH-A	brain:	n/a

(count:12 , 50 per page) page: 1

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

(count:17 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 3459 )
Associated
traits (count: 117 )

Variant overlapped rSNPs/rCNVs (count:3459 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs368721086	chr17:33676521-33676522	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs530170470	chr17:33676524-33676525	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs569201826	chr17:33676528-33676529	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs79888339	chr17:33676541-33676542	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs7211866	chr17:33676586-33676587	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs572561645	chr17:33676592-33676593	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs188226594	chr17:33676601-33676602	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs115460740	chr17:33676602-33676603	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs578180248	chr17:33676605-33676606	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs543476775	chr17:33676621-33676622	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs117909950	chr17:33676622-33676623	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs6505466	chr17:33676628-33676629	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs549064100	chr17:33676636-33676637	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs559287607	chr17:33676687-33676688	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs528337232	chr17:33676689-33676690	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs375228150	chr17:33676737-33676738	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs551280037	chr17:33676753-33676754	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs145296492	chr17:33676805-33676806	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs59181907	chr17:33676818-33676819	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs201593031	chr17:33676819-33676820	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs369943687	chr17:33676820-33676821	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs398078968	chr17:33676822-33676823	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs57691946	chr17:33676827-33676828	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs76607694	chr17:33676832-33676833	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs371145228	chr17:33676873-33676874	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs7211779	chr17:33676908-33676909	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs180745404	chr17:33676941-33676942	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs377463477	chr17:33676968-33676969	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs557357861	chr17:33676981-33676982	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs7212097	chr17:33677041-33677042	Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs535565089	chr17:33677042-33677043	Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs34377059	chr17:33677109-33677110	Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs117250427	chr17:33677117-33677118	Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs184728270	chr17:33677123-33677124	Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs548641707	chr17:33677137-33677138	Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs55889228	chr17:33677147-33677148	Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs547527434	chr17:33677203-33677204	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs558052857	chr17:33677210-33677211	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs139275136	chr17:33677225-33677226	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs189171968	chr17:33677229-33677230	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs541760423	chr17:33677239-33677240	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs182069379	chr17:33677240-33677241	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs573637760	chr17:33677290-33677291	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs542643280	chr17:33677291-33677292	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs79205461	chr17:33677304-33677305	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs202222803	chr17:33677323-33677324	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs187158749	chr17:33677416-33677417	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs528161072	chr17:33677473-33677474	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs1047268	chr17:33677495-33677496	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs191495365	chr17:33677545-33677546	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:117)

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
Recurrent pregnancy loss	19789632	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	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:2168 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:33673000-33679400	Weak transcription	Lung	lung
2	chr17:33673800-33677600	Weak transcription	NHLF	lung
3	chr17:33673800-33689800	Weak transcription	Gastric	stomach
4	chr17:33673800-33699800	Weak transcription	Ovary	ovary
5	chr17:33674000-33677600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr17:33674000-33678000	Weak transcription	Aorta	Aorta
7	chr17:33674000-33678000	Weak transcription	Esophagus	oesophagus
8	chr17:33674000-33678200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr17:33674000-33678600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr17:33674000-33679400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr17:33674000-33679400	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr17:33674000-33681600	Weak transcription	Duodenum Mucosa	Duodenum
13	chr17:33674000-33682600	Weak transcription	NHDF-Ad	bronchial
14	chr17:33674000-33686400	Weak transcription	Rectal Mucosa Donor 31	rectum
15	chr17:33674000-33695600	Weak transcription	Colonic Mucosa	Colon
16	chr17:33674000-33695600	Weak transcription	Placenta	Placenta
17	chr17:33674000-33698600	Weak transcription	Muscle Satellite Cultured Cells	--
18	chr17:33674200-33677600	Weak transcription	Primary hematopoietic stem cells	blood
19	chr17:33674200-33677800	Weak transcription	HUVEC	blood vessel
20	chr17:33674200-33678200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
21	chr17:33674200-33678800	Weak transcription	Primary B cells from peripheral blood	blood
22	chr17:33674200-33679200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
23	chr17:33674200-33679200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr17:33674200-33679400	Weak transcription	Primary T cells from cord blood	blood
25	chr17:33674200-33679600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr17:33674200-33686000	Weak transcription	Brain Hippocampus Middle	brain
27	chr17:33674200-33699800	Weak transcription	Sigmoid Colon	Sigmoid Colon
28	chr17:33674400-33677800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
29	chr17:33674400-33677800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
30	chr17:33674400-33678000	Weak transcription	Primary T helper cells PMA-I stimulated	--
31	chr17:33674400-33678000	Weak transcription	Osteobl	bone
32	chr17:33674400-33678600	Weak transcription	Primary T cells fromperipheralblood	blood
33	chr17:33674400-33679000	Weak transcription	Spleen	Spleen
34	chr17:33674400-33679200	Weak transcription	Primary T helper cells fromperipheralblood	blood
35	chr17:33674400-33679400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
36	chr17:33674400-33693600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
37	chr17:33674600-33694600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
38	chr17:33674800-33677600	Weak transcription	Fetal Thymus	thymus
39	chr17:33674800-33683600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
40	chr17:33675000-33681400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr17:33675000-33686600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
42	chr17:33675000-33688400	Weak transcription	Colon Smooth Muscle	Colon
43	chr17:33675400-33677800	Weak transcription	Primary B cells from cord blood	blood
44	chr17:33675400-33678800	Weak transcription	Adipose Nuclei	Adipose
45	chr17:33675600-33684400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr17:33675800-33678000	Weak transcription	Thymus	Thymus
47	chr17:33675800-33687800	Strong transcription	Dnd41	blood
48	chr17:33675800-33694000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr17:33675800-33699800	Weak transcription	Rectal Smooth Muscle	rectum
50	chr17:33676000-33677600	Weak transcription	Primary monocytes fromperipheralblood	blood

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