Variant report

Variant	nsv21
Chromosome Location	chr8:6814803-6859626
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr8:6829807-6830004	K562	blood:	n/a	n/a
2	BACH1	chr8:6829927-6829940	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr8:6815704-6815918	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr8:6815759-6815899	K562	blood:	n/a	chr8:6815801-6815817
5	BHLHE40	chr8:6825706-6825903	K562	blood:	n/a	chr8:6825850-6825859 chr8:6825848-6825857 chr8:6825847-6825860 chr8:6825849-6825858 chr8:6825843-6825864 chr8:6825849-6825858
6	BRCA1	chr8:6815742-6815942	H1-hESC	embryonic stem cell:	n/a	n/a
7	CHD2	chr8:6815705-6815992	H1-hESC	embryonic stem cell:	n/a	n/a
8	CTCF	chr8:6815740-6815890	HA-sp	spinal cord:	n/a	chr8:6815799-6815820 chr8:6815800-6815813 chr8:6815802-6815812 chr8:6815785-6815798 chr8:6815797-6815815 chr8:6815798-6815814
9	CTCF	chr8:6814900-6815050	HFF-Myc	foreskin:	n/a	n/a
10	CTCF	chr8:6815661-6815905	GM20000	blood:	n/a	chr8:6815799-6815820 chr8:6815800-6815813 chr8:6815802-6815812 chr8:6815785-6815798 chr8:6815797-6815815 chr8:6815798-6815814
11	CTCF	chr8:6815740-6815890	HBMEC	blood vessel:	n/a	chr8:6815799-6815820 chr8:6815800-6815813 chr8:6815802-6815812 chr8:6815785-6815798 chr8:6815797-6815815 chr8:6815798-6815814
12	CTCF	chr8:6815740-6815890	GM12864	blood:	n/a	chr8:6815799-6815820 chr8:6815800-6815813 chr8:6815802-6815812 chr8:6815785-6815798 chr8:6815797-6815815 chr8:6815798-6815814
13	CTCF	chr8:6815631-6815936	ProgFib	skin:	n/a	chr8:6815799-6815820 chr8:6815800-6815813 chr8:6815802-6815812 chr8:6815785-6815798 chr8:6815797-6815815 chr8:6815798-6815814
14	CTCF	chr8:6815637-6815945	A549	lung:	n/a	chr8:6815799-6815820 chr8:6815800-6815813 chr8:6815802-6815812 chr8:6815785-6815798 chr8:6815797-6815815 chr8:6815798-6815814
15	CTCF	chr8:6815660-6815810	GM12868	blood:	n/a	chr8:6815785-6815798
16	CTCF	chr8:6815720-6815870	GM12865	blood:	n/a	chr8:6815799-6815820 chr8:6815800-6815813 chr8:6815802-6815812 chr8:6815785-6815798 chr8:6815797-6815815 chr8:6815798-6815814
17	CTCF	chr8:6815573-6815974	GM19238	blood:	n/a	chr8:6815799-6815820 chr8:6815800-6815813 chr8:6815802-6815812 chr8:6815785-6815798 chr8:6815797-6815815 chr8:6815798-6815814
18	CTCF	chr8:6815612-6816004	MCF-7	breast:	n/a	chr8:6815799-6815820 chr8:6815800-6815813 chr8:6815802-6815812 chr8:6815785-6815798 chr8:6815797-6815815 chr8:6815798-6815814
19	CTCF	chr8:6815760-6815910	GM12875	blood:	n/a	chr8:6815799-6815820 chr8:6815800-6815813 chr8:6815802-6815812 chr8:6815785-6815798 chr8:6815797-6815815 chr8:6815798-6815814
20	CTCF	chr8:6815720-6815870	BJ	skin:	n/a	chr8:6815799-6815820 chr8:6815800-6815813 chr8:6815802-6815812 chr8:6815785-6815798 chr8:6815797-6815815 chr8:6815798-6815814
21	CTCF	chr8:6815510-6815966	GM12891	blood:	n/a	chr8:6815799-6815820 chr8:6815800-6815813 chr8:6815802-6815812 chr8:6815785-6815798 chr8:6815797-6815815 chr8:6815798-6815814
22	CTCF	chr8:6815586-6816036	H1-hESC	embryonic stem cell:	n/a	chr8:6815799-6815820 chr8:6815800-6815813 chr8:6815802-6815812 chr8:6815785-6815798 chr8:6815797-6815815 chr8:6815798-6815814
23	CTCF	chr8:6829420-6829509	LNCaP	prostate:	n/a	n/a
24	CTCF	chr8:6815641-6815944	MCF-7	breast:	n/a	chr8:6815799-6815820 chr8:6815800-6815813 chr8:6815802-6815812 chr8:6815785-6815798 chr8:6815797-6815815 chr8:6815798-6815814
25	CTCF	chr8:6815660-6815810	GM12874	blood:	n/a	chr8:6815785-6815798
26	CTCF	chr8:6815660-6815810	GM12875	blood:	n/a	chr8:6815785-6815798
27	CTCF	chr8:6815700-6815850	HCT-116	colon:	n/a	chr8:6815799-6815820 chr8:6815800-6815813 chr8:6815802-6815812 chr8:6815785-6815798 chr8:6815797-6815815 chr8:6815798-6815814
28	CTCF	chr8:6827960-6828110	K562	blood:	n/a	n/a
29	CTCF	chr8:6815880-6816030	HFF-Myc	foreskin:	n/a	n/a
30	CTCF	chr8:6827929-6828105	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr8:6816340-6816490	GM12873	blood:	n/a	n/a
32	CTCF	chr8:6829826-6829954	LNCaP	prostate:	n/a	n/a
33	CTCF	chr8:6815658-6815931	GM13977	blood:	n/a	chr8:6815799-6815820 chr8:6815800-6815813 chr8:6815802-6815812 chr8:6815785-6815798 chr8:6815797-6815815 chr8:6815798-6815814
34	CTCF	chr8:6815680-6815830	GM12865	blood:	n/a	chr8:6815799-6815820 chr8:6815800-6815813 chr8:6815802-6815812 chr8:6815785-6815798 chr8:6815797-6815815 chr8:6815798-6815814
35	CTCF	chr8:6815720-6815870	GM12872	blood:	n/a	chr8:6815799-6815820 chr8:6815800-6815813 chr8:6815802-6815812 chr8:6815785-6815798 chr8:6815797-6815815 chr8:6815798-6815814
36	CTCF	chr8:6815672-6815940	Medullo	brain:	n/a	chr8:6815799-6815820 chr8:6815800-6815813 chr8:6815802-6815812 chr8:6815785-6815798 chr8:6815797-6815815 chr8:6815798-6815814
37	CTCF	chr8:6815631-6815973	IMR90	lung:	n/a	chr8:6815799-6815820 chr8:6815800-6815813 chr8:6815802-6815812 chr8:6815785-6815798 chr8:6815797-6815815 chr8:6815798-6815814
38	CTCF	chr8:6815760-6815910	K562	blood:	n/a	chr8:6815799-6815820 chr8:6815800-6815813 chr8:6815802-6815812 chr8:6815785-6815798 chr8:6815797-6815815 chr8:6815798-6815814
39	CTCF	chr8:6815376-6816197	A549	lung:	n/a	chr8:6815799-6815820 chr8:6815800-6815813 chr8:6815802-6815812 chr8:6815785-6815798 chr8:6815797-6815815 chr8:6815798-6815814
40	CTCF	chr8:6815634-6815947	MCF-7	breast:	n/a	chr8:6815799-6815820 chr8:6815800-6815813 chr8:6815802-6815812 chr8:6815785-6815798 chr8:6815797-6815815 chr8:6815798-6815814
41	CTCF	chr8:6815660-6815810	NHEK	skin:	n/a	chr8:6815785-6815798
42	CTCF	chr8:6815720-6815870	HUVEC	blood vessel:	n/a	chr8:6815799-6815820 chr8:6815800-6815813 chr8:6815802-6815812 chr8:6815785-6815798 chr8:6815797-6815815 chr8:6815798-6815814
43	CTCF	chr8:6815705-6815877	A549	lung:	n/a	chr8:6815799-6815820 chr8:6815800-6815813 chr8:6815802-6815812 chr8:6815785-6815798 chr8:6815797-6815815 chr8:6815798-6815814
44	CTCF	chr8:6815680-6815830	GM12866	blood:	n/a	chr8:6815799-6815820 chr8:6815800-6815813 chr8:6815802-6815812 chr8:6815785-6815798 chr8:6815797-6815815 chr8:6815798-6815814
45	CTCF	chr8:6815560-6815810	HAc	cerebellar:	n/a	chr8:6815785-6815798
46	CTCF	chr8:6815700-6815850	RPTEC	kidney:	n/a	chr8:6815799-6815820 chr8:6815800-6815813 chr8:6815802-6815812 chr8:6815785-6815798 chr8:6815797-6815815 chr8:6815798-6815814
47	CTCF	chr8:6815660-6815810	AG04449	skin:	n/a	chr8:6815785-6815798
48	CTCF	chr8:6815760-6815910	HPF	lung:	n/a	chr8:6815799-6815820 chr8:6815800-6815813 chr8:6815802-6815812 chr8:6815785-6815798 chr8:6815797-6815815 chr8:6815798-6815814
49	CTCF	chr8:6815650-6815932	MCF-7	breast:	n/a	chr8:6815799-6815820 chr8:6815800-6815813 chr8:6815802-6815812 chr8:6815785-6815798 chr8:6815797-6815815 chr8:6815798-6815814
50	CTCF	chr8:6815635-6815939	MCF-7	breast:	n/a	chr8:6815799-6815820 chr8:6815800-6815813 chr8:6815802-6815812 chr8:6815785-6815798 chr8:6815797-6815815 chr8:6815798-6815814

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:6828103-6828153	ovcar-3	ovarian:	n/a
2	chr8:6828103-6828153	ovcar-3	ovarian:	n/a
3	chr8:6827800-6827850	GM12878	blood:	n/a
4	chr8:6837932-6837982	AG09319	gingival:	n/a
5	chr8:6826392-6826442	HCF	heart:	n/a
6	chr8:6838024-6838074	PANC-1	pancreas:	n/a
7	chr8:6828103-6828153	HAEpiC	amniotic membrane:	n/a
8	chr8:6827800-6827850	AoSMC	blood vessel:	n/a
9	chr8:6827814-6827864	NT2-D1	testis:	n/a
10	chr8:6827800-6827850	HAEpiC	amniotic membrane:	n/a
11	chr8:6837932-6837982	NHDF-neo	bronchial:	n/a
12	chr8:6838024-6838074	AG10803	skin:	n/a
13	chr8:6828103-6828153	Caco-2	colon:	n/a
14	chr8:6827814-6827864	GM06990	blood:	n/a
15	chr8:6838024-6838074	AG09309	skin:	n/a
16	chr8:6828103-6828153	HCT-116	colon:	n/a
17	chr8:6828103-6828153	HCM	heart:	n/a
18	chr8:6827800-6827850	ovcar-3	ovarian:	n/a
19	chr8:6826392-6826442	AG04450	lung:	fetal
20	chr8:6838024-6838074	GM12891	blood:	n/a
21	chr8:6827814-6827864	HCT-116	colon:	n/a
22	chr8:6827814-6827864	SKMC	muscle:	n/a
23	chr8:6828103-6828153	H1-hESC	embryonic stem cell:	embryo
24	chr8:6837932-6837982	HAEpiC	amniotic membrane:	n/a
25	chr8:6826392-6826442	SAEC	small airway:	n/a
26	chr8:6837932-6837982	AG09309	skin:	n/a
27	chr8:6826392-6826442	PrEC	prostate:	n/a
28	chr8:6827800-6827850	NHDF-neo	bronchial:	n/a
29	chr8:6826392-6826442	T-47D	breast:	n/a
30	chr8:6838024-6838074	Jurkat	blood:	n/a
31	chr8:6827800-6827850	GM19239	blood:	n/a
32	chr8:6827800-6827850	SK-N-MC	brain:	n/a
33	chr8:6827800-6827850	PrEC	prostate:	n/a
34	chr8:6827800-6827850	Hepatocyte	liver:	n/a
35	chr8:6826392-6826442	LNCaP	prostate:	n/a
36	chr8:6828103-6828153	U87	brain:	n/a
37	chr8:6826392-6826442	A549	lung:	n/a
38	chr8:6838024-6838074	HPAEpiC	pulmonary alveolar:	n/a
39	chr8:6826392-6826442	GM19239	blood:	n/a
40	chr8:6827800-6827850	NHBE	bronchial:	n/a
41	chr8:6827814-6827864	AG04450	lung:	fetal
42	chr8:6838024-6838074	H1-hESC	embryonic stem cell:	embryo
43	chr8:6828103-6828153	NHDF-neo	bronchial:	n/a
44	chr8:6838024-6838074	GM19239	blood:	n/a
45	chr8:6826392-6826442	BJ	skin:	n/a
46	chr8:6838024-6838074	BJ	skin:	n/a
47	chr8:6827814-6827864	ECC-1	luminal epithelium:	n/a
48	chr8:6827814-6827864	RPTEC	kidney:	n/a
49	chr8:6827800-6827850	HRCEpiC	kidney:	n/a
50	chr8:6827800-6827850	SKMC	muscle:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:6813895..6816114-chr8:6818168..6820677,2	MCF-7	breast:
2	chr8:6813895..6816114-chr8:6818168..6820677,2	MCF-7	breast:
3	chr8:6810171..6811870-chr8:6814020..6816721,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DEFA1-1	chr8:6825663-6825769	NONHSAT124802
2	lnc-DEFA1-1	chr8:6825663-6825775	NONHSAT124803
3	lnc-DEFA1B-1	chr8:6844700-6844945	NONHSAT124804
4	lnc-DEFA1-2	chr8:6816811-6816923	NONHSAT124801
5	lnc-DEFA1B-1	chr8:6847181-6847243	NONHSAT124804
6	lnc-DEFA1-1	chr8:6826461-6826635	NONHSAT124803
7	lnc-DEFA1-2	chr8:6817512-6817683	NONHSAT124801
8	lnc-DEFA1-1	chr8:6826452-6826635	NONHSAT124802
9	lnc-DEFA1B-1	chr8:6845622-6845808	NONHSAT124804

Variant related genes	Relation type
DEFA1B	TF binding region
DEFA9P	TF binding region
DEFA10P	TF binding region
DEFA1	TF binding region
DEFT1P	TF binding region
DEFA1B	CpG island
DEFA9P	CpG island
DEFA10P	CpG island
DEFA1	CpG island
DEFT1P	CpG island

Extended variants
information (count: 1413 )
Associated
traits (count: 141 )

Variant overlapped rSNPs/rCNVs (count:1413 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573756193	chr8:6814822-6814823	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs542864991	chr8:6814843-6814844	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs559377707	chr8:6814853-6814854	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs148798476	chr8:6814862-6814863	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs76333965	chr8:6814872-6814873	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs564889562	chr8:6814883-6814884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs373070505	chr8:6814887-6814888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs530593361	chr8:6814896-6814897	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs201502434	chr8:6814902-6814903	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs183799617	chr8:6814904-6814905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs567808025	chr8:6814926-6814927	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs77491803	chr8:6814944-6814945	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs189277470	chr8:6814945-6814946	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs199830503	chr8:6814955-6814956	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs553267072	chr8:6814956-6814957	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs567029052	chr8:6814973-6814974	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs377349770	chr8:6814989-6814990	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs555611324	chr8:6815011-6815012	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs142382938	chr8:6815025-6815026	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs17078409	chr8:6815031-6815032	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs572956867	chr8:6815035-6815036	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs537903707	chr8:6815054-6815055	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs554775994	chr8:6815057-6815058	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs573198071	chr8:6815086-6815087	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs535690755	chr8:6815094-6815095	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs181316048	chr8:6815099-6815100	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs542455869	chr8:6815112-6815113	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs151310958	chr8:6815154-6815155	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs370849108	chr8:6815160-6815161	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs573159041	chr8:6815161-6815162	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs545343778	chr8:6815170-6815171	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs139304963	chr8:6815194-6815195	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs186370299	chr8:6815205-6815206	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs190076437	chr8:6815222-6815223	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs560815696	chr8:6815284-6815285	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs529822944	chr8:6815287-6815288	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs144327241	chr8:6815305-6815306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs563760921	chr8:6815325-6815326	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs2738082	chr8:6815328-6815329	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs79516655	chr8:6815334-6815335	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs181707734	chr8:6815340-6815341	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs577885492	chr8:6815359-6815360	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs186055456	chr8:6815371-6815372	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs56961747	chr8:6815399-6815400	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs28622941	chr8:6815413-6815414	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs35182259	chr8:6815430-6815431	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs67759749	chr8:6815444-6815445	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs534336460	chr8:6815448-6815449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs552864128	chr8:6815449-6815450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs201541802	chr8:6815456-6815457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:141)

Disease	PMID	Source
Ovarian clear cell carcinoma	21343371	CNVD
abnormal development	18461090	CNVD
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Epilepsy	22083797	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16774939	CNVD
Breast cancer	21364760	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Cancer	20164919	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Bladder cancer	21909424	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Cognitive impairment	21505072	CNVD
Breast cancer	17142309	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Breast cancer	22522925	CNVD
Autism	21865298	CNVD
Pancreatic cancer	17952125	CNVD
Behcet''s disease	22219625	CNVD

Chromatin state (count:50 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:6794600-6829200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr8:6811000-6818000	Enhancers	Dnd41	blood
3	chr8:6813800-6815000	Weak transcription	Thymus	Thymus
4	chr8:6814400-6816200	Enhancers	Primary neutrophils fromperipheralblood	blood
5	chr8:6814600-6817000	Enhancers	Fetal Thymus	thymus
6	chr8:6815000-6815800	Enhancers	Thymus	Thymus
7	chr8:6816200-6817400	Weak transcription	Primary neutrophils fromperipheralblood	blood
8	chr8:6817000-6817600	Weak transcription	Fetal Thymus	thymus
9	chr8:6817400-6818800	Enhancers	Primary neutrophils fromperipheralblood	blood
10	chr8:6817600-6817800	Enhancers	Fetal Thymus	thymus
11	chr8:6817600-6817800	Flanking Active TSS	Lung	lung
12	chr8:6817800-6820600	Weak transcription	Fetal Thymus	thymus
13	chr8:6818000-6820400	Weak transcription	Dnd41	blood
14	chr8:6818800-6822800	Weak transcription	Primary neutrophils fromperipheralblood	blood
15	chr8:6820400-6821800	Enhancers	Dnd41	blood
16	chr8:6820600-6821600	Enhancers	Fetal Thymus	thymus
17	chr8:6821400-6821800	Enhancers	Thymus	Thymus
18	chr8:6822800-6830000	Enhancers	Primary neutrophils fromperipheralblood	blood
19	chr8:6824000-6824800	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
20	chr8:6824200-6824600	Enhancers	H1 Cell Line	embryonic stem cell
21	chr8:6824400-6824800	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
22	chr8:6824600-6824800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr8:6824600-6828200	Weak transcription	H1 Cell Line	embryonic stem cell
24	chr8:6824800-6829200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr8:6826400-6826600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr8:6826400-6826800	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
27	chr8:6826400-6826800	Enhancers	Primary T cells fromperipheralblood	blood
28	chr8:6826400-6826800	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
29	chr8:6826400-6826800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr8:6826400-6827000	Bivalent Enhancer	Primary B cells from peripheral blood	blood
31	chr8:6826600-6826800	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
32	chr8:6828200-6828600	Enhancers	H1 Cell Line	embryonic stem cell
33	chr8:6828200-6828600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr8:6828400-6828600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr8:6828600-6829600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr8:6829200-6829400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr8:6829200-6829400	Enhancers	Right Ventricle	heart
38	chr8:6829200-6830200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr8:6829600-6830000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr8:6829600-6830000	Enhancers	Fetal Brain Male	brain
41	chr8:6829600-6830200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr8:6829800-6830000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr8:6830000-6833000	Weak transcription	Primary neutrophils fromperipheralblood	blood
44	chr8:6831000-6831200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
45	chr8:6833000-6833600	Enhancers	Primary neutrophils fromperipheralblood	blood
46	chr8:6833600-6837800	Weak transcription	Primary neutrophils fromperipheralblood	blood
47	chr8:6837800-6838200	Enhancers	Primary neutrophils fromperipheralblood	blood
48	chr8:6838200-6840600	Weak transcription	Primary neutrophils fromperipheralblood	blood
49	chr8:6840600-6841800	Enhancers	Primary neutrophils fromperipheralblood	blood
50	chr8:6856800-6857400	Enhancers	Primary neutrophils fromperipheralblood	blood

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