Variant report

Variant	nsv543231
Chromosome Location	chr17:16926227-16950644
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1155)
CpG islands
(count:733)
Chromatin interactive
region (count:34)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1155 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:16938055-16938383	K562	blood:	n/a	chr17:16938339-16938355
2	ARID3A	chr17:16947565-16947765	K562	blood:	n/a	n/a
3	ARID3A	chr17:16931523-16931797	HepG2	liver:	n/a	n/a
4	ARID3A	chr17:16935833-16935842	HepG2	liver:	n/a	n/a
5	ATF1	chr17:16931411-16931756	K562	blood:	n/a	chr17:16931577-16931591
6	ATF2	chr17:16945114-16945377	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr17:16948481-16948962	GM12878	blood:	n/a	n/a
8	ATF3	chr17:16931201-16932037	A549	lung:	n/a	chr17:16931577-16931590 chr17:16931578-16931588 chr17:16931579-16931590 chr17:16931578-16931591 chr17:16931579-16931590
9	ATF3	chr17:16931228-16931886	A549	lung:	n/a	chr17:16931577-16931590 chr17:16931578-16931588 chr17:16931579-16931590 chr17:16931578-16931591 chr17:16931579-16931590
10	BACH1	chr17:16945197-16945464	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr17:16948652-16948962	GM12878	blood:	n/a	n/a
12	BCL3	chr17:16946243-16947518	A549	lung:	n/a	chr17:16947227-16947236 chr17:16946450-16946459
13	BCL3	chr17:16931234-16932047	A549	lung:	n/a	n/a
14	BCL3	chr17:16931089-16932452	A549	lung:	n/a	n/a
15	BCL3	chr17:16944229-16945718	A549	lung:	n/a	n/a
16	BCLAF1	chr17:16948402-16949078	GM12878	blood:	n/a	n/a
17	BHLHE40	chr17:16945372-16945724	GM12878	blood:	n/a	chr17:16945484-16945500 chr17:16945492-16945508
18	BHLHE40	chr17:16938882-16939187	K562	blood:	n/a	n/a
19	BHLHE40	chr17:16946787-16946940	K562	blood:	n/a	n/a
20	BHLHE40	chr17:16931397-16931808	K562	blood:	n/a	n/a
21	BHLHE40	chr17:16931149-16931741	A549	lung:	n/a	n/a
22	BHLHE40	chr17:16945306-16945678	K562	blood:	n/a	chr17:16945484-16945500 chr17:16945492-16945508
23	BHLHE40	chr17:16944614-16944869	K562	blood:	n/a	n/a
24	BHLHE40	chr17:16939962-16940042	GM12878	blood:	n/a	n/a
25	BHLHE40	chr17:16931331-16931895	HepG2	liver:	n/a	n/a
26	BRCA1	chr17:16935786-16935986	HepG2	liver:	n/a	n/a
27	BRCA1	chr17:16945568-16945643	HepG2	liver:	n/a	n/a
28	BRCA1	chr17:16945406-16945615	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr17:16935408-16935596	Hela-S3	cervix:	n/a	n/a
30	BRCA1	chr17:16946847-16947072	Hela-S3	cervix:	n/a	n/a
31	BRCA1	chr17:16931320-16931889	Hela-S3	cervix:	n/a	n/a
32	CBX3	chr17:16945009-16945376	K562	blood:	n/a	n/a
33	CBX3	chr17:16931331-16931695	K562	blood:	n/a	n/a
34	CCNT2	chr17:16931456-16931742	K562	blood:	n/a	n/a
35	CCNT2	chr17:16945280-16945715	K562	blood:	n/a	n/a
36	CEBPB	chr17:16931408-16931696	HepG2	liver:	n/a	n/a
37	CEBPB	chr17:16930730-16931831	A549	lung:	n/a	n/a
38	CEBPB	chr17:16942171-16942364	Hela-S3	cervix:	n/a	chr17:16942284-16942297
39	CEBPB	chr17:16932957-16933217	A549	lung:	n/a	chr17:16933066-16933077
40	CEBPB	chr17:16932938-16933231	HepG2	liver:	n/a	chr17:16933066-16933077
41	CEBPB	chr17:16931253-16931904	A549	lung:	n/a	n/a
42	CEBPB	chr17:16931439-16931616	HepG2	liver:	n/a	n/a
43	CEBPB	chr17:16931420-16931747	K562	blood:	n/a	n/a
44	CEBPB	chr17:16945550-16945551	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr17:16931198-16931894	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr17:16932944-16933265	Hela-S3	cervix:	n/a	chr17:16933066-16933077
47	CEBPB	chr17:16933009-16933208	K562	blood:	n/a	chr17:16933066-16933077
48	CEBPB	chr17:16935944-16936069	K562	blood:	n/a	n/a
49	CEBPB	chr17:16935318-16935723	IMR90	lung:	n/a	n/a
50	CEBPB	chr17:16945498-16945589	Hela-S3	cervix:	n/a	n/a

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:16945298-16945348	HIPEpiC	eye:	n/a
2	chr17:16945298-16945348	HIPEpiC	eye:	n/a
3	chr17:16931836-16931886	MCF10A-Er-Src	breast:	n/a
4	chr17:16945301-16945351	HL-60	blood:	n/a
5	chr17:16945385-16945435	PrEC	prostate:	n/a
6	chr17:16934655-16934705	NHDF-neo	bronchial:	n/a
7	chr17:16934655-16934705	Hela-S3	cervix:	n/a
8	chr17:16946995-16947045	IMR90	lung:	fetal
9	chr17:16941778-16941828	HUVEC	blood vessel:	n/a
10	chr17:16945596-16945646	HCT-116	colon:	n/a
11	chr17:16931836-16931886	RPTEC	kidney:	n/a
12	chr17:16945596-16945646	HRE	kidney:	n/a
13	chr17:16934655-16934705	SKMC	muscle:	n/a
14	chr17:16946247-16946297	GM06990	blood:	n/a
15	chr17:16934655-16934705	HCM	heart:	n/a
16	chr17:16945301-16945351	GM06990	blood:	n/a
17	chr17:16941778-16941828	Hepatocyte	liver:	n/a
18	chr17:16947406-16947456	NH-A	brain:	n/a
19	chr17:16946247-16946297	GM12891	blood:	n/a
20	chr17:16945603-16945653	AG09319	gingival:	n/a
21	chr17:16948762-16948812	CMK	blood:	n/a
22	chr17:16947406-16947456	Hepatocyte	liver:	n/a
23	chr17:16945298-16945348	HCF	heart:	n/a
24	chr17:16945603-16945653	AoSMC	blood vessel:	n/a
25	chr17:16945385-16945435	MCF-7	breast:	n/a
26	chr17:16946995-16947045	ovcar-3	ovarian:	n/a
27	chr17:16946995-16947045	HepG2	liver:	n/a
28	chr17:16946995-16947045	GM12878	blood:	n/a
29	chr17:16945298-16945348	GM12891	blood:	n/a
30	chr17:16931836-16931886	GM12878	blood:	n/a
31	chr17:16945301-16945351	LNCaP	prostate:	n/a
32	chr17:16946995-16947045	GM06990	blood:	n/a
33	chr17:16945385-16945435	HMEC	breast:	n/a
34	chr17:16934655-16934705	HAEpiC	amniotic membrane:	n/a
35	chr17:16941778-16941828	AG09319	gingival:	n/a
36	chr17:16946247-16946297	RPTEC	kidney:	n/a
37	chr17:16948762-16948812	HCT-116	colon:	n/a
38	chr17:16945298-16945348	HCPEpiC	choroid plexus:	n/a
39	chr17:16941778-16941828	AoSMC	blood vessel:	n/a
40	chr17:16945298-16945348	IMR90	lung:	fetal
41	chr17:16945298-16945348	HEEpiC	esophagus:	n/a
42	chr17:16948762-16948812	ProgFib	skin:	n/a
43	chr17:16931836-16931886	NHDF-neo	bronchial:	n/a
44	chr17:16945301-16945351	CMK	blood:	n/a
45	chr17:16945298-16945348	LNCaP	prostate:	n/a
46	chr17:16945596-16945646	BJ	skin:	n/a
47	chr17:16945385-16945435	HPAEpiC	pulmonary alveolar:	n/a
48	chr17:16934655-16934705	HMEC	breast:	n/a
49	chr17:16941778-16941828	HAEpiC	amniotic membrane:	n/a
50	chr17:16948762-16948812	K562	blood:	n/a

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:16947403..16948944-chr17:16950340..16952252,2	MCF-7	breast:
2	chr17:16941343..16943728-chr17:16947873..16949492,2	MCF-7	breast:
3	chr17:16930112..16931615-chr17:16942008..16944719,2	K562	blood:
4	chr17:16932063..16934977-chr17:16936868..16939174,3	K562	blood:
5	chr17:16922760..16925384-chr17:16927836..16930121,3	K562	blood:
6	chr17:16922760..16926151-chr17:16927403..16930298,5	K562	blood:
7	chr17:16922009..16924326-chr17:16949178..16951661,2	MCF-7	breast:
8	chr17:16920777..16926602-chr17:16943525..16948995,8	MCF-7	breast:
9	chr17:16931173..16933175-chr17:17108970..17110599,2	K562	blood:
10	chr17:16947403..16948944-chr17:16950340..16952252,2	MCF-7	breast:
11	chr17:16947719..16948219-chr17:17109224..17109847,2	NB4	blood:
12	chr17:16904092..16907044-chr17:16930901..16933093,2	MCF-7	breast:
13	chr17:16924719..16926363-chr17:16928237..16932446,3	MCF-7	breast:
14	chr17:16938674..16940195-chr17:16944421..16946987,2	K562	blood:
15	chr17:16948833..16952528-chr17:16954016..16957501,7	K562	blood:
16	chr17:16945686..16947847-chr3:44621097..44624084,2	MCF-7	breast:
17	chr17:16931293..16933179-chr17:16934223..16937186,2	MCF-7	breast:
18	chr17:16924719..16926363-chr17:16928237..16932446,3	MCF-7	breast:
19	chr17:16944536..16947207-chr17:17109103..17111480,2	MCF-7	breast:
20	chr17:16913150..16913949-chr17:16935742..16936397,2	MCF-7	breast:
21	chr17:16943909..16948439-chr17:16949478..16955691,9	K562	blood:
22	chr17:16931573..16934044-chr17:16934220..16938314,3	MCF-7	breast:
23	chr17:16941343..16943728-chr17:16947873..16949492,2	MCF-7	breast:
24	chr17:16944952..16946961-chr17:17072835..17074607,2	K562	blood:
25	chr17:16944416..16947050-chr17:16979219..16983384,3	MCF-7	breast:
26	chr17:16931573..16934044-chr17:16934220..16938314,3	MCF-7	breast:
27	chr17:16905205..16905735-chr17:16935481..16936004,2	MCF-7	breast:
28	chr17:16932063..16934977-chr17:16936868..16939174,3	K562	blood:
29	chr17:16930112..16931615-chr17:16942008..16944719,2	K562	blood:
30	chr17:16923260..16925095-chr17:16929732..16931336,2	MCF-7	breast:
31	chr17:16943176..16945630-chr17:17102978..17105800,2	K562	blood:
32	chr17:16917707..16920531-chr17:16944662..16947361,2	MCF-7	breast:
33	chr17:16931293..16933179-chr17:16934223..16937186,2	MCF-7	breast:
34	chr17:16931372..16933195-chr17:16979927..16982548,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TNFRSF13B-3	chr17:16944523-16944627	XLOC_012406
2	lnc-MPRIP-1	chr17:16926501-16926546	XLOC_012127
3	lnc-TNFRSF13B-3	chr17:16936688-16937346	XLOC_012406
4	lnc-MPRIP-1	chr17:16926378-16926772	NONHSAT146035

No data

Variant related genes	Relation type
MPRIP	TF binding region
MPRIP	CpG island
ENSG00000225442	chromatin interactions
ENSG00000133030	chromatin interactions
ENSG00000214820	chromatin interactions
ENSG00000179598	chromatin interactions
ENSG00000206859	chromatin interactions
ENSG00000260328	chromatin interactions
CCND1	miRNA target sites

Extended variants
information (count: 878 )
Associated
traits (count: 161 )

Variant overlapped rSNPs/rCNVs (count:878 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs575181111	chr17:16926257-16926258	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs148494387	chr17:16926303-16926304	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs557339316	chr17:16926342-16926343	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs376872396	chr17:16926353-16926354	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs35005794	chr17:16926358-16926359	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs537046962	chr17:16926427-16926428	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs74619256	chr17:16926440-16926441	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs556957219	chr17:16926473-16926474	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
9	rs112716957	chr17:16926486-16926487	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs546308265	chr17:16926502-16926503	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
11	rs559679212	chr17:16926549-16926550	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
12	rs528726240	chr17:16926556-16926557	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
13	rs4267379	chr17:16926566-16926567	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs188297429	chr17:16926595-16926596	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
15	rs559366703	chr17:16926623-16926624	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
16	rs193058040	chr17:16926637-16926638	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
17	rs550561953	chr17:16926651-16926652	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
18	rs570454346	chr17:16926679-16926680	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
19	rs555541577	chr17:16926694-16926695	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
20	rs573030368	chr17:16926714-16926715	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
21	rs184398814	chr17:16926728-16926729	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
22	rs546714931	chr17:16926773-16926774	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs139930078	chr17:16926778-16926779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs535223744	chr17:16926792-16926793	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs186870268	chr17:16926800-16926801	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs202173882	chr17:16926845-16926846	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs58702370	chr17:16926854-16926855	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs575838998	chr17:16926856-16926857	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs374249082	chr17:16926857-16926858	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs200297587	chr17:16926858-16926859	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs537769558	chr17:16926860-16926861	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs557057635	chr17:16926917-16926918	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs373658633	chr17:16926961-16926962	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs577205076	chr17:16926967-16926968	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs191694714	chr17:16926969-16926970	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs76730052	chr17:16926984-16926985	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs542401618	chr17:16926995-16926996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs117201734	chr17:16927007-16927008	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs146826363	chr17:16927018-16927019	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs544953951	chr17:16927083-16927084	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs183613953	chr17:16927089-16927090	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs189622233	chr17:16927149-16927150	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs546281138	chr17:16927150-16927151	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs368172460	chr17:16927156-16927157	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs566518868	chr17:16927220-16927221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs528968730	chr17:16927248-16927249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs182039810	chr17:16927267-16927268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs568737473	chr17:16927269-16927270	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs537734884	chr17:16927277-16927278	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs79735463	chr17:16927289-16927290	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:161)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Esophageal adenocarcinoma	18519675	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16608533	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Chordoma	21602918	CNVD
Miller-Dieker syndrome	22283845	CNVD
Non-syndromic sensorineural hearing loss	17457615	CNVD
Cancer	22429812	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Ewing''s sarcoma	21437220	CNVD
Follicular lymphoma	19010834	CNVD
Colorectal cancer	20709793	CNVD
Acute myeloid leukemia	16864856	CNVD
Endometrial cancer	22040021	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Breast cancer	22028636	CNVD
Breast cancer	20837533	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
colon cancer	17210682	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Chronic lymphocytic leukemia	17971485	CNVD
Basal cell lymphoma	17170743	CNVD
Breast cancer	16461572	CNVD
Colorectal cancer	16272173	CNVD
Follicular lymphoma	17170743	CNVD
Human rectal carcinomas	16397240	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Moyamoya disease	22323933	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelodysplastic syndrome	21251322	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20724749	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Acute myeloid leukemia	17237825	CNVD
Colorectal cancer	21645411	CNVD
HIV/AIDS	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
HIV/AIDS	17953491	CNVD
HIV/AIDS	20877625	CNVD
Immune disease	21076436	CNVD
Rheumatoid arthritis	17953491	CNVD
Type 1 diabetes	17953491	CNVD
HIV/AIDS	15637236	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21781307	CNVD
Autism	22495311	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Neurofibromatosis	18196300	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Colorectal cancer	16774939	CNVD
Pancreatic cancer	21811587	CNVD
Breast cancer	17001317	CNVD
Rhabdomyosarcoma	16790082	CNVD
Charcot-marie-tooth disease	16463004	CNVD
Osteosarcoma	22292074	CNVD
Breast cancer	17603634	CNVD
Charcot	16760730	CNVD
Mental retardation	17901693	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
ovarian endometriomas	16273235	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Gastric cancer	18160780	CNVD
Smith-Magenis syndrome	18923513	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Austim spectrum disorder	21302340	CNVD
Autism	22492990	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	18414209	CNVD
Developmental delay	21549014	CNVD
Epilepsy	20970697	CNVD
Mental retardation	18414209	CNVD
Mental retardation	21549014	CNVD
Smith-Magenis syndrome	21981782	CNVD
Smith-Magenis syndrome	20188345	CNVD
Smith-Magenis syndrome	16775514	CNVD
Smith-Magenis syndrome	22585170	CNVD
Smith-Magenis syndrome	22241247	CNVD
Autism	20970697	CNVD
Mental retardation	19951919	CNVD
Potocki-Lupski syndrome	21271655	CNVD
Potocki-lupski syndrome	17357070	CNVD
Potocki-lupski syndrome	20110824	CNVD
Potocki-lupski syndrome	18923514	CNVD
Potocki-lupski syndrome	22241247	CNVD
Potocki-lupski syndrome	20188345	CNVD
Schizophrenia	21399695	CNVD
Mental retardation	16773131	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Charcot-marie-tooth disease	22470819	CNVD
Neurofibromatosis	22470819	CNVD
Neuropathy	22470819	CNVD
Smith-Magenis syndrome	18301319	CNVD
Smith-Magenis syndrome	17357070	CNVD
Smith-Magenis syndrome	18469339	CNVD
Smith-Magenis syndrome	22241097	CNVD
Smith-Magenis syndrome	22470819	CNVD
Tourette syndrome	18923514	CNVD
Type 1 diabetes	22470819	CNVD
Potocki-lupski syndrome	18469339	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Neuropathy	17597781	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	17015230	CNVD
Smith-Magenis syndrome	17597781	CNVD
Potocki-lupski syndrome	18059269	CNVD
Potocki-lupski syndrome	17597781	CNVD
Mental retardation	17847001	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	20409316	CNVD
Breast cancer	21509527	CNVD
Ductal carcinoma	22052326	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	22522925	CNVD
Lung adenocarcinoma	21935476	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1643 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:16918800-16930800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr17:16922400-16928000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr17:16922800-16928800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr17:16923600-16926800	Enhancers	Brain Anterior Caudate	brain
5	chr17:16923800-16928200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr17:16923800-16929000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr17:16923800-16929000	Weak transcription	NHEK	skin
8	chr17:16924000-16926600	Enhancers	Placenta Amnion	Placenta Amnion
9	chr17:16924200-16926400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr17:16924200-16926600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr17:16924200-16926600	Enhancers	Brain Angular Gyrus	brain
12	chr17:16924200-16926800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr17:16924200-16926800	Enhancers	Brain Cingulate Gyrus	brain
14	chr17:16924200-16926800	Enhancers	Brain Hippocampus Middle	brain
15	chr17:16924200-16926800	Enhancers	Brain Substantia Nigra	brain
16	chr17:16924200-16929000	Weak transcription	Lung	lung
17	chr17:16924400-16926600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr17:16924800-16926600	Enhancers	Brain Inferior Temporal Lobe	brain
19	chr17:16924800-16927400	Enhancers	Fetal Intestine Large	intestine
20	chr17:16925000-16930800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr17:16925200-16930600	Weak transcription	Rectal Mucosa Donor 29	rectum
22	chr17:16925200-16931000	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr17:16925400-16928000	Weak transcription	Adipose Nuclei	Adipose
24	chr17:16925400-16928400	Weak transcription	Fetal Lung	lung
25	chr17:16925400-16929000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr17:16925400-16930800	Weak transcription	NH-A	brain
27	chr17:16925400-16931000	Enhancers	A549	lung
28	chr17:16925600-16928200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr17:16925600-16930800	Weak transcription	Rectal Mucosa Donor 31	rectum
30	chr17:16925600-16930800	Weak transcription	Sigmoid Colon	Sigmoid Colon
31	chr17:16925600-16931800	Weak transcription	Osteobl	bone
32	chr17:16925800-16926600	Enhancers	HSMMtube	muscle
33	chr17:16925800-16929400	Enhancers	Fetal Intestine Small	intestine
34	chr17:16925800-16930600	Weak transcription	Muscle Satellite Cultured Cells	--
35	chr17:16925800-16930800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr17:16926000-16927400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
37	chr17:16926000-16927800	Weak transcription	Fetal Heart	heart
38	chr17:16926000-16928000	Weak transcription	Fetal Stomach	stomach
39	chr17:16926000-16928000	Weak transcription	Right Ventricle	heart
40	chr17:16926000-16928200	Weak transcription	Right Atrium	heart
41	chr17:16926000-16928600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr17:16926000-16928600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr17:16926000-16930600	Weak transcription	Esophagus	oesophagus
44	chr17:16926000-16930600	Weak transcription	HMEC	breast
45	chr17:16926000-16930800	Weak transcription	Colonic Mucosa	Colon
46	chr17:16926000-16930800	Weak transcription	Spleen	Spleen
47	chr17:16926000-16931400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr17:16926200-16927400	Enhancers	Hela-S3	cervix
49	chr17:16926200-16928000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr17:16926200-16928000	Weak transcription	Fetal Muscle Leg	muscle

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