Variant report

Variant	nsv574749
Chromosome Location	chr17:33684035-33768199
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:863)
CpG islands
(count:2384)
Chromatin interactive
region (count:9)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:863 , 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	chr17:33760160-33760916	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr17:33760159-33760921	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF3	chr17:33760267-33760589	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr17:33760593-33760991	K562	blood:	n/a	n/a
6	ATF3	chr17:33760640-33760960	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr17:33760631-33760858	K562	blood:	n/a	n/a
8	ATF3	chr17:33760478-33761048	A549	lung:	n/a	n/a
9	ATF3	chr17:33760190-33760966	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr17:33700735-33700996	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr17:33759792-33760985	H1-hESC	embryonic stem cell:	n/a	chr17:33760771-33760785
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	chr17:33717723-33718092	HepG2	liver:	n/a	chr17:33717904-33717917 chr17:33717904-33717917 chr17:33717905-33717916
21	CEBPB	chr17:33717731-33718093	A549	lung:	n/a	chr17:33717904-33717917 chr17:33717904-33717917 chr17:33717905-33717916
22	CEBPB	chr17:33701339-33701878	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr17:33698339-33698621	HepG2	liver:	n/a	chr17:33698439-33698450
24	CEBPB	chr17:33731395-33731702	A549	lung:	n/a	n/a
25	CEBPB	chr17:33717739-33718092	Hela-S3	cervix:	n/a	chr17:33717904-33717917 chr17:33717904-33717917 chr17:33717905-33717916
26	CEBPB	chr17:33760651-33760906	K562	blood:	n/a	n/a
27	CEBPB	chr17:33717673-33718118	A549	lung:	n/a	chr17:33717904-33717917 chr17:33717904-33717917 chr17:33717905-33717916
28	CEBPB	chr17:33698317-33698552	A549	lung:	n/a	chr17:33698439-33698450
29	CEBPB	chr17:33760660-33760956	A549	lung:	n/a	n/a
30	CEBPB	chr17:33717633-33718161	A549	lung:	n/a	chr17:33717904-33717917 chr17:33717904-33717917 chr17:33717905-33717916
31	CEBPB	chr17:33731440-33731698	IMR90	lung:	n/a	n/a
32	CEBPB	chr17:33700361-33701097	GM12878	blood:	n/a	n/a
33	CEBPB	chr17:33717812-33718023	K562	blood:	n/a	chr17:33717904-33717917 chr17:33717904-33717917 chr17:33717905-33717916
34	CEBPB	chr17:33760241-33760955	IMR90	lung:	n/a	n/a
35	CEBPB	chr17:33698406-33698449	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr17:33700583-33700911	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr17:33759330-33759655	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr17:33760263-33760970	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr17:33731382-33731714	HepG2	liver:	n/a	n/a
40	CEBPB	chr17:33701311-33701959	IMR90	lung:	n/a	n/a
41	CEBPB	chr17:33717748-33718067	H1-hESC	embryonic stem cell:	n/a	chr17:33717904-33717917 chr17:33717904-33717917 chr17:33717905-33717916
42	CEBPB	chr17:33717804-33717994	MCF-7	breast:	n/a	chr17:33717904-33717917 chr17:33717904-33717917 chr17:33717905-33717916
43	CEBPB	chr17:33731441-33731629	K562	blood:	n/a	n/a
44	CEBPB	chr17:33760228-33760918	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr17:33760228-33761108	A549	lung:	n/a	chr17:33761021-33761029
46	CEBPB	chr17:33717720-33718093	IMR90	lung:	n/a	chr17:33717904-33717917 chr17:33717904-33717917 chr17:33717905-33717916
47	CEBPB	chr17:33760621-33760983	A549	lung:	n/a	n/a
48	CEBPB	chr17:33717730-33718103	K562	blood:	n/a	chr17:33717904-33717917 chr17:33717904-33717917 chr17:33717905-33717916
49	CHD1	chr17:33701236-33701436	GM12878	blood:	n/a	n/a
50	CHD1	chr17:33700415-33700981	GM12878	blood:	n/a	n/a

(count:2384 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:33760293-33760343	AG10803	skin:	n/a
2	chr17:33759484-33759534	ProgFib	skin:	n/a
3	chr17:33698288-33698338	HRPEpiC	eye:	n/a
4	chr17:33731014-33731064	H1-hESC	embryonic stem cell:	embryo
5	chr17:33701529-33701579	GM12891	blood:	n/a
6	chr17:33760293-33760343	AG10803	skin:	n/a
7	chr17:33759484-33759534	ProgFib	skin:	n/a
8	chr17:33698288-33698338	HRPEpiC	eye:	n/a
9	chr17:33731014-33731064	H1-hESC	embryonic stem cell:	embryo
10	chr17:33701529-33701579	GM12891	blood:	n/a
11	chr17:33700801-33700851	SK-N-SH	brain:	n/a
12	chr17:33700759-33700809	HCM	heart:	n/a
13	chr17:33734847-33734897	Hepatocyte	liver:	n/a
14	chr17:33759648-33759698	GM19239	blood:	n/a
15	chr17:33700180-33700230	AoSMC	blood vessel:	n/a
16	chr17:33700295-33700345	RPTEC	kidney:	n/a
17	chr17:33759965-33760015	AoSMC	blood vessel:	n/a
18	chr17:33763575-33763625	U87	brain:	n/a
19	chr17:33760419-33760469	AG04449	skin:	fetal
20	chr17:33700745-33700795	HepG2	liver:	n/a
21	chr17:33700745-33700795	HRPEpiC	eye:	n/a
22	chr17:33760230-33760280	NB4	blood:	n/a
23	chr17:33700513-33700563	IMR90	lung:	fetal
24	chr17:33759965-33760015	PANC-1	pancreas:	n/a
25	chr17:33759573-33759623	NH-A	brain:	n/a
26	chr17:33701529-33701579	IMR90	lung:	fetal
27	chr17:33700180-33700230	HCM	heart:	n/a
28	chr17:33700230-33700280	HMEC	breast:	n/a
29	chr17:33759965-33760015	HRCEpiC	kidney:	n/a
30	chr17:33731014-33731064	HL-60	blood:	n/a
31	chr17:33700817-33700867	NHBE	bronchial:	n/a
32	chr17:33759957-33760007	AG09319	gingival:	n/a
33	chr17:33760230-33760280	HepG2	liver:	n/a
34	chr17:33734481-33734531	AoSMC	blood vessel:	n/a
35	chr17:33760230-33760280	AG10803	skin:	n/a
36	chr17:33738370-33738420	MCF-7	breast:	n/a
37	chr17:33760230-33760280	SK-N-MC	brain:	n/a
38	chr17:33734664-33734714	SK-N-SH	brain:	n/a
39	chr17:33700745-33700795	K562	blood:	n/a
40	chr17:33738370-33738420	AG10803	skin:	n/a
41	chr17:33700513-33700563	HIPEpiC	eye:	n/a
42	chr17:33700513-33700563	NB4	blood:	n/a
43	chr17:33760293-33760343	GM19239	blood:	n/a
44	chr17:33700230-33700280	NHBE	bronchial:	n/a
45	chr17:33700295-33700345	PFSK-1	brain:	n/a
46	chr17:33760230-33760280	HCPEpiC	choroid plexus:	n/a
47	chr17:33763575-33763625	Caco-2	colon:	n/a
48	chr17:33700801-33700851	HUVEC	blood vessel:	n/a
49	chr17:33701350-33701400	MCF-7	breast:	n/a
50	chr17:33700747-33700797	U87	brain:	n/a

(count:9 , 50 per page) page: 1

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

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

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

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
ENSG00000146834	chromatin interactions
ENSG00000078487	chromatin interactions
ENSG00000267102	chromatin interactions
ENSG00000267547	chromatin interactions
ENSG00000267711	chromatin interactions
ENSG00000172716	chromatin interactions

Extended variants
information (count: 3110 )
Associated
traits (count: 117 )

Variant overlapped rSNPs/rCNVs (count:3110 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7211677	chr17:33684035-33684036	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs184176856	chr17:33684036-33684037	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs573511701	chr17:33684097-33684098	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs7212322	chr17:33684107-33684108	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs552833542	chr17:33684110-33684111	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs572880005	chr17:33684114-33684115	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs368883832	chr17:33684158-33684159	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs371807963	chr17:33684159-33684160	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs7216624	chr17:33684184-33684185	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs35291259	chr17:33684193-33684194	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs398030713	chr17:33684195-33684196	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs60376888	chr17:33684196-33684197	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs62079544	chr17:33684197-33684198	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs564711311	chr17:33684215-33684216	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs556985949	chr17:33684227-33684228	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs575185368	chr17:33684260-33684261	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs555433947	chr17:33684262-33684263	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs137898106	chr17:33684325-33684326	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs537935785	chr17:33684335-33684336	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs563701952	chr17:33684400-33684401	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs529315029	chr17:33684417-33684418	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs187085669	chr17:33684418-33684419	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs372064467	chr17:33684441-33684442	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs142649240	chr17:33684463-33684464	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs191895203	chr17:33684507-33684508	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs565689634	chr17:33684532-33684533	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs537744343	chr17:33684553-33684554	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs551038747	chr17:33684568-33684569	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs567939968	chr17:33684612-33684613	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs535904088	chr17:33684653-33684654	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs552914115	chr17:33684677-33684678	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs534646260	chr17:33684699-33684700	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs370874584	chr17:33684705-33684706	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs538314672	chr17:33684794-33684795	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs558342568	chr17:33684838-33684839	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs201837167	chr17:33684842-33684843	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs575046160	chr17:33684862-33684863	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs543996209	chr17:33684867-33684868	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs112625740	chr17:33684945-33684946	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs561066783	chr17:33684955-33684956	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs182750635	chr17:33685027-33685028	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs542683369	chr17:33685055-33685056	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs559669731	chr17:33685068-33685069	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs28532779	chr17:33685099-33685100	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs187340748	chr17:33685219-33685220	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs73992746	chr17:33685305-33685306	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs565190674	chr17:33685307-33685308	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs565375529	chr17:33685322-33685323	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs191871001	chr17:33685345-33685346	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs376317480	chr17:33685387-33685388	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:2048 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:33673800-33689800	Weak transcription	Gastric	stomach
2	chr17:33673800-33699800	Weak transcription	Ovary	ovary
3	chr17:33674000-33686400	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr17:33674000-33695600	Weak transcription	Colonic Mucosa	Colon
5	chr17:33674000-33695600	Weak transcription	Placenta	Placenta
6	chr17:33674000-33698600	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr17:33674200-33686000	Weak transcription	Brain Hippocampus Middle	brain
8	chr17:33674200-33699800	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr17:33674400-33693600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
10	chr17:33674600-33694600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
11	chr17:33675000-33686600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
12	chr17:33675000-33688400	Weak transcription	Colon Smooth Muscle	Colon
13	chr17:33675600-33684400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr17:33675800-33687800	Strong transcription	Dnd41	blood
15	chr17:33675800-33694000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr17:33675800-33699800	Weak transcription	Rectal Smooth Muscle	rectum
17	chr17:33676000-33687600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
18	chr17:33676000-33689600	Weak transcription	Primary neutrophils fromperipheralblood	blood
19	chr17:33676000-33689600	Weak transcription	Stomach Smooth Muscle	stomach
20	chr17:33676400-33684800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
21	chr17:33677600-33684800	Strong transcription	Monocytes-CD14+_RO01746	blood
22	chr17:33677600-33691400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr17:33677600-33691400	Strong transcription	Primary monocytes fromperipheralblood	blood
24	chr17:33677800-33684200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
25	chr17:33678200-33687800	Weak transcription	Skeletal Muscle Female	skeletal muscle
26	chr17:33678400-33700000	Weak transcription	Esophagus	oesophagus
27	chr17:33678600-33687400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr17:33678800-33684800	Strong transcription	Primary B cells from peripheral blood	blood
29	chr17:33679800-33684400	Strong transcription	Adipose Nuclei	Adipose
30	chr17:33680000-33687600	Weak transcription	Thymus	Thymus
31	chr17:33680000-33689400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr17:33680000-33695600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr17:33680200-33685800	Weak transcription	Primary T cells from cord blood	blood
34	chr17:33680200-33687800	Weak transcription	Aorta	Aorta
35	chr17:33680400-33687400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
36	chr17:33681200-33684400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
37	chr17:33681200-33684600	Strong transcription	Fetal Thymus	thymus
38	chr17:33681400-33691000	Strong transcription	HUVEC	blood vessel
39	chr17:33681600-33684600	Strong transcription	Primary hematopoietic stem cells	blood
40	chr17:33681800-33686600	Weak transcription	Duodenum Smooth Muscle	Duodenum
41	chr17:33682000-33697600	Weak transcription	Osteobl	bone
42	chr17:33682200-33691600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr17:33682200-33694400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
44	chr17:33682400-33686400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr17:33682600-33685200	Strong transcription	NHDF-Ad	bronchial
46	chr17:33682600-33688400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
47	chr17:33682800-33684400	Strong transcription	Primary T helper cells fromperipheralblood	blood
48	chr17:33682800-33685800	Weak transcription	Primary T cells fromperipheralblood	blood
49	chr17:33683000-33685800	Weak transcription	Primary T helper cells PMA-I stimulated	--
50	chr17:33683000-33686400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood

The 2.0 version of rSNPBase

Variant report

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