Variant report

Variant	nsv1011107
Chromosome Location	chr4:10290726-10324361
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	BACH1	chr4:10291449-10291596	K562	blood:	n/a	n/a
2	BACH1	chr4:10296613-10296622	K562	blood:	n/a	n/a
3	BACH1	chr4:10306752-10306755	K562	blood:	n/a	n/a
4	CCNT2	chr4:10323672-10323734	K562	blood:	n/a	n/a
5	CEBPB	chr4:10311017-10311187	HepG2	liver:	n/a	chr4:10311067-10311078
6	CEBPB	chr4:10310964-10311220	K562	blood:	n/a	chr4:10311067-10311078
7	CEBPB	chr4:10302967-10303233	K562	blood:	n/a	n/a
8	CEBPB	chr4:10304348-10304548	K562	blood:	n/a	n/a
9	CTCF	chr4:10321860-10322010	Caco-2	colon:	n/a	chr4:10321896-10321917 chr4:10321901-10321919
10	CTCF	chr4:10323660-10323810	WERI-Rb-1	eye:	n/a	n/a
11	CTCF	chr4:10321860-10322010	HepG2	liver:	n/a	chr4:10321896-10321917 chr4:10321901-10321919
12	CTCF	chr4:10314423-10314451	Lung_OC	lung:	n/a	n/a
13	CTCF	chr4:10321837-10322004	HepG2	liver:	n/a	chr4:10321896-10321917 chr4:10321901-10321919
14	CTCF	chr4:10303720-10303870	HMEC	breast:	n/a	n/a
15	CTCF	chr4:10318700-10318850	GM06990	blood:	n/a	n/a
16	CTCF	chr4:10321840-10321990	HepG2	liver:	n/a	chr4:10321896-10321917 chr4:10321901-10321919
17	CTCF	chr4:10323611-10323811	K562	blood:	n/a	n/a
18	CTCF	chr4:10319540-10319690	GM06990	blood:	n/a	n/a
19	CTCF	chr4:10299053-10299135	GM13976	blood:	n/a	n/a
20	CTCF	chr4:10321791-10322026	HepG2	liver:	n/a	chr4:10321896-10321917 chr4:10321901-10321919
21	CTCF	chr4:10323677-10323783	NHEK	skin:	n/a	n/a
22	CTCF	chr4:10323640-10323790	WERI-Rb-1	eye:	n/a	n/a
23	CTCF	chr4:10321780-10321930	Caco-2	colon:	n/a	chr4:10321896-10321917 chr4:10321901-10321919
24	CTCF	chr4:10320760-10320910	GM12872	blood:	n/a	n/a
25	CTCF	chr4:10321840-10321990	GM12872	blood:	n/a	chr4:10321896-10321917 chr4:10321901-10321919
26	E2F4	chr4:10295657-10295659	MCF10A-Er-Src	breast:	n/a	n/a
27	ELF1	chr4:10291215-10291515	K562	blood:	n/a	chr4:10291316-10291329
28	EP300	chr4:10323706-10323891	K562	blood:	n/a	n/a
29	EP300	chr4:10321951-10322148	HepG2	liver:	n/a	n/a
30	EP300	chr4:10319177-10319351	K562	blood:	n/a	n/a
31	EP300	chr4:10306114-10306189	K562	blood:	n/a	n/a
32	FOS	chr4:10301280-10301608	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr4:10303929-10303965	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr4:10290460-10290959	HUVEC	blood vessel:	n/a	chr4:10290705-10290715 chr4:10290706-10290714 chr4:10290705-10290715 chr4:10290706-10290713 chr4:10290705-10290715 chr4:10290705-10290715 chr4:10290706-10290714
35	FOS	chr4:10290551-10290812	MCF10A-Er-Src	breast:	n/a	chr4:10290705-10290715 chr4:10290706-10290714 chr4:10290705-10290715 chr4:10290706-10290713 chr4:10290705-10290715 chr4:10290705-10290715 chr4:10290706-10290714
36	FOS	chr4:10290533-10290891	MCF10A-Er-Src	breast:	n/a	chr4:10290705-10290715 chr4:10290706-10290714 chr4:10290705-10290715 chr4:10290706-10290713 chr4:10290705-10290715 chr4:10290705-10290715 chr4:10290706-10290714
37	FOS	chr4:10290533-10290862	MCF10A-Er-Src	breast:	n/a	chr4:10290705-10290715 chr4:10290706-10290714 chr4:10290705-10290715 chr4:10290706-10290713 chr4:10290705-10290715 chr4:10290705-10290715 chr4:10290706-10290714
38	FOS	chr4:10301338-10301508	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr4:10290503-10291242	MCF10A-Er-Src	breast:	n/a	chr4:10290705-10290715 chr4:10290706-10290714 chr4:10290705-10290715 chr4:10290706-10290713 chr4:10290705-10290715 chr4:10290705-10290715 chr4:10290706-10290714
40	FOS	chr4:10301304-10301511	MCF10A-Er-Src	breast:	n/a	n/a
41	HNF4A	chr4:10321773-10322156	HepG2	liver:	n/a	chr4:10321962-10321974 chr4:10321961-10321975 chr4:10321960-10321975 chr4:10321962-10321975 chr4:10321959-10321977 chr4:10321962-10321974 chr4:10321962-10321974 chr4:10321961-10321975 chr4:10321962-10321974 chr4:10321960-10321975 chr4:10321961-10321974 chr4:10321965-10321977 chr4:10321960-10321975
42	HNF4A	chr4:10321766-10322131	HepG2	liver:	n/a	chr4:10321962-10321974 chr4:10321961-10321975 chr4:10321960-10321975 chr4:10321962-10321975 chr4:10321959-10321977 chr4:10321962-10321974 chr4:10321962-10321974 chr4:10321961-10321975 chr4:10321962-10321974 chr4:10321960-10321975 chr4:10321961-10321974 chr4:10321965-10321977 chr4:10321960-10321975
43	HNF4G	chr4:10321742-10322147	HepG2	liver:	n/a	chr4:10321962-10321974 chr4:10321961-10321975 chr4:10321961-10321976 chr4:10321960-10321975 chr4:10321962-10321975 chr4:10321959-10321977 chr4:10321962-10321974 chr4:10321962-10321974 chr4:10321961-10321975 chr4:10321962-10321974 chr4:10321961-10321974 chr4:10321965-10321977 chr4:10321960-10321975
44	IRF1	chr4:10297604-10297616	K562	blood:	n/a	n/a
45	IRF1	chr4:10303422-10303744	K562	blood:	n/a	n/a
46	IRF1	chr4:10303281-10303687	K562	blood:	n/a	n/a
47	JUN	chr4:10321803-10322068	HepG2	liver:	n/a	chr4:10321931-10321944
48	JUND	chr4:10291145-10291499	K562	blood:	n/a	n/a
49	JUND	chr4:10321779-10322118	HepG2	liver:	n/a	n/a
50	MAFF	chr4:10320615-10320793	K562	blood:	n/a	chr4:10320647-10320661

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:10299145-10299195	HL-60	blood:	n/a
2	chr4:10299145-10299195	SK-N-MC	brain:	n/a
3	chr4:10299145-10299195	SK-N-SH_RA	brain:	n/a
4	chr4:10299145-10299195	AoSMC	blood vessel:	n/a
5	chr4:10299145-10299195	HCM	heart:	n/a
6	chr4:10299145-10299195	PANC-1	pancreas:	n/a
7	chr4:10299145-10299195	Hela-S3	cervix:	n/a
8	chr4:10299145-10299195	HPAEpiC	pulmonary alveolar:	n/a
9	chr4:10299145-10299195	HRPEpiC	eye:	n/a
10	chr4:10299145-10299195	H1-hESC	embryonic stem cell:	embryo
11	chr4:10299145-10299195	U87	brain:	n/a
12	chr4:10299145-10299195	AG04450	lung:	fetal
13	chr4:10299145-10299195	NHDF-neo	bronchial:	n/a
14	chr4:10299145-10299195	Caco-2	colon:	n/a
15	chr4:10299145-10299195	SAEC	small airway:	n/a
16	chr4:10299145-10299195	HMEC	breast:	n/a
17	chr4:10299145-10299195	GM12891	blood:	n/a
18	chr4:10299145-10299195	PFSK-1	brain:	n/a
19	chr4:10299145-10299195	HRE	kidney:	n/a
20	chr4:10299145-10299195	AG09319	gingival:	n/a
21	chr4:10299145-10299195	NT2-D1	testis:	n/a
22	chr4:10299145-10299195	HCPEpiC	choroid plexus:	n/a
23	chr4:10299145-10299195	GM12878	blood:	n/a
24	chr4:10299145-10299195	LNCaP	prostate:	n/a
25	chr4:10299145-10299195	T-47D	breast:	n/a
26	chr4:10299145-10299195	Hepatocyte	liver:	n/a
27	chr4:10299145-10299195	Jurkat	blood:	n/a
28	chr4:10299145-10299195	K562	blood:	n/a
29	chr4:10299145-10299195	A549	lung:	n/a
30	chr4:10299145-10299195	CMK	blood:	n/a
31	chr4:10299145-10299195	GM19239	blood:	n/a
32	chr4:10299145-10299195	IMR90	lung:	fetal
33	chr4:10299145-10299195	ovcar-3	ovarian:	n/a
34	chr4:10299145-10299195	HIPEpiC	eye:	n/a
35	chr4:10299145-10299195	NH-A	brain:	n/a
36	chr4:10299145-10299195	HCF	heart:	n/a
37	chr4:10299145-10299195	NB4	blood:	n/a
38	chr4:10299145-10299195	GM06990	blood:	n/a
39	chr4:10299145-10299195	MCF-7	breast:	n/a
40	chr4:10299145-10299195	HRCEpiC	kidney:	n/a
41	chr4:10299145-10299195	HepG2	liver:	n/a
42	chr4:10299145-10299195	GM12892	blood:	n/a
43	chr4:10299145-10299195	HEEpiC	esophagus:	n/a
44	chr4:10299145-10299195	HNPCEpiC	eye:	n/a
45	chr4:10299145-10299195	SK-N-SH	brain:	n/a
46	chr4:10299145-10299195	HCT-116	colon:	n/a
47	chr4:10299145-10299195	SKMC	muscle:	n/a
48	chr4:10299145-10299195	ProgFib	skin:	n/a
49	chr4:10299145-10299195	NHBE	bronchial:	n/a
50	chr4:10299145-10299195	AG04449	skin:	fetal

No.	Distal block	Cell Line	Cell type
1	chr4:10300976..10303713-chr4:10304138..10305960,3	K562	blood:
2	chr4:10278587..10280479-chr4:10297418..10299087,2	K562	blood:
3	chr4:10116497..10118720-chr4:10304788..10307219,2	K562	blood:
4	chr4:10290044..10292857-chr4:10295207..10297834,2	K562	blood:
5	chr4:10118597..10121491-chr4:10308024..10311461,4	K562	blood:
6	chr4:10306958..10308632-chr4:10319609..10321643,2	K562	blood:
7	chr4:10226621..10229156-chr4:10309809..10312332,2	K562	blood:
8	chr4:10298581..10300458-chr4:10305111..10307586,2	K562	blood:
9	chr4:10306958..10308632-chr4:10319609..10321643,2	K562	blood:
10	chr4:10321044..10322655-chr4:10326498..10328725,2	K562	blood:
11	chr4:10119416..10121932-chr4:10294541..10296176,2	K562	blood:
12	chr4:10283364..10286619-chr4:10288507..10291288,3	K562	blood:
13	chr4:10181898..10186356-chr4:10317430..10320755,4	K562	blood:
14	chr4:10312898..10315516-chr4:10318323..10320073,4	K562	blood:
15	chr4:10186571..10188279-chr4:10316070..10319056,2	K562	blood:
16	chr4:10120346..10122319-chr4:10312436..10314039,2	K562	blood:
17	chr4:10289644..10291282-chr4:10323806..10326517,2	K562	blood:
18	chr4:10289644..10291282-chr4:10323806..10326517,2	K562	blood:
19	chr4:10293712..10297687-chr4:10307102..10309576,3	K562	blood:
20	chr4:10119318..10121113-chr4:10298083..10300540,2	K562	blood:
21	chr4:10303834..10305662-chr4:10370006..10372655,2	K562	blood:
22	chr4:10305228..10307997-chr4:10310331..10312718,2	K562	blood:
23	chr4:10301025..10303713-chr4:10304138..10305960,2	K562	blood:
24	chr4:10322922..10325786-chr4:10326394..10328675,2	K562	blood:
25	chr19:17416908..17417590-chr4:10322243..10323174,2	Hela-S3	cervix:
26	chr4:10312898..10315516-chr4:10318323..10320073,4	K562	blood:
27	chr4:10301025..10303713-chr4:10304138..10305960,2	K562	blood:
28	chr4:10298581..10300458-chr4:10305111..10307586,2	K562	blood:
29	chr4:10300976..10303713-chr4:10304138..10305960,3	K562	blood:
30	chr4:10305228..10307997-chr4:10310331..10312718,2	K562	blood:
31	chr4:10288926..10293598-chr4:10293770..10299284,5	K562	blood:
32	chr4:10320256..10323019-chr4:10334627..10337093,2	K562	blood:
33	chr4:10119978..10123045-chr4:10320529..10323793,3	K562	blood:
34	chr4:10313155..10314762-chr4:10457693..10459658,2	K562	blood:
35	chr4:10118483..10121328-chr4:10309961..10311571,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF518B-2	chr4:10293819-10294332	NONHSAT095494

Variant related genes	Relation type
ENSG00000251338	TF binding region
ENSG00000251278	TF binding region
ENSG00000250505	TF binding region
ENSG00000251338	CpG island
ENSG00000251278	CpG island
ENSG00000250505	CpG island
ENSG00000071127	chromatin interactions
ENSG00000251338	chromatin interactions
ENSG00000251278	chromatin interactions
ENSG00000178163	chromatin interactions
ENSG00000223086	chromatin interactions

Extended variants
information (count: 2242 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:2242 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7692559	chr4:10290726-10290727	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs185832580	chr4:10290743-10290744	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs188765966	chr4:10290750-10290751	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs181158153	chr4:10290755-10290756	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs528660837	chr4:10290770-10290771	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs559941661	chr4:10290776-10290777	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs546379546	chr4:10290783-10290784	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs186126615	chr4:10290787-10290788	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs558423387	chr4:10290798-10290799	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs190605174	chr4:10290813-10290814	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs564519446	chr4:10290833-10290834	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs375651165	chr4:10290839-10290840	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs547236384	chr4:10290847-10290848	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs184243695	chr4:10290849-10290850	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs140324611	chr4:10290857-10290858	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs186230680	chr4:10290866-10290867	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs80220164	chr4:10290876-10290877	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs531939981	chr4:10290892-10290893	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs551032532	chr4:10290901-10290902	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs370713885	chr4:10290909-10290910	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs550438480	chr4:10290913-10290914	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs571957189	chr4:10290933-10290934	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs532887160	chr4:10290940-10290941	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs190644383	chr4:10290957-10290958	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs200473001	chr4:10290962-10290963	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs182798634	chr4:10290984-10290985	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs569231657	chr4:10291024-10291025	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs536707933	chr4:10291031-10291032	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs187267721	chr4:10291053-10291054	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs192939763	chr4:10291062-10291063	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs6449438	chr4:10291063-10291064	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs558364819	chr4:10291074-10291075	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs576704011	chr4:10291104-10291105	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs534633104	chr4:10291132-10291133	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs552897945	chr4:10291136-10291137	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs115797876	chr4:10291178-10291179	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs541857759	chr4:10291214-10291215	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs563364001	chr4:10291220-10291221	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs575445830	chr4:10291248-10291249	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs566642207	chr4:10291264-10291265	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs115792397	chr4:10291272-10291273	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs533713148	chr4:10291281-10291282	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs371692252	chr4:10291293-10291294	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs182799821	chr4:10291297-10291298	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs187875223	chr4:10291299-10291300	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs375824398	chr4:10291310-10291311	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs192297798	chr4:10291321-10291322	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs555124605	chr4:10291322-10291323	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs56133633	chr4:10291351-10291352	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs115465984	chr4:10291353-10291354	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:175 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:10284800-10291200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr4:10289200-10292400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr4:10289200-10293200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr4:10289400-10292800	Enhancers	NHEK	skin
5	chr4:10289600-10292800	Enhancers	HMEC	breast
6	chr4:10289800-10293200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr4:10290000-10291000	Weak transcription	K562	blood
8	chr4:10291000-10291800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr4:10291000-10292800	Enhancers	K562	blood
10	chr4:10291200-10291600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr4:10291600-10296800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr4:10292600-10292800	Enhancers	Cortex derived primary cultured neurospheres	brain
13	chr4:10292800-10297000	Weak transcription	HMEC	breast
14	chr4:10293200-10296800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr4:10293200-10298000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr4:10294200-10294800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr4:10294800-10297200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr4:10295200-10296400	Enhancers	Thymus	Thymus
19	chr4:10296600-10298600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr4:10296800-10297400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr4:10296800-10298400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr4:10297000-10297200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr4:10297000-10298000	Enhancers	Brain Substantia Nigra	brain
24	chr4:10297000-10299000	Enhancers	HMEC	breast
25	chr4:10297200-10298200	Enhancers	Brain Hippocampus Middle	brain
26	chr4:10297200-10298800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr4:10297200-10299600	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr4:10297200-10299800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr4:10297400-10298000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr4:10297400-10298200	Enhancers	Brain Anterior Caudate	brain
31	chr4:10297400-10300000	Enhancers	Cortex derived primary cultured neurospheres	brain
32	chr4:10297600-10298200	Enhancers	Brain Cingulate Gyrus	brain
33	chr4:10297600-10298200	Enhancers	Brain Inferior Temporal Lobe	brain
34	chr4:10297600-10298400	Enhancers	Fetal Brain Male	brain
35	chr4:10297800-10298000	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr4:10297800-10298600	Enhancers	Brain Angular Gyrus	brain
37	chr4:10298000-10298200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr4:10298000-10298400	Flanking Active TSS	Brain Substantia Nigra	brain
39	chr4:10298000-10298800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr4:10298000-10299000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr4:10298000-10299000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr4:10298000-10299000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr4:10298000-10299000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr4:10298000-10299000	Enhancers	NHEK	skin
45	chr4:10298000-10299200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr4:10298200-10298600	Flanking Active TSS	Brain Anterior Caudate	brain
47	chr4:10298200-10298600	Flanking Active TSS	Brain Cingulate Gyrus	brain
48	chr4:10298200-10298600	Enhancers	Brain Germinal Matrix	brain
49	chr4:10298200-10298600	Flanking Active TSS	Brain Hippocampus Middle	brain
50	chr4:10298200-10298600	Flanking Active TSS	Brain Inferior Temporal Lobe	brain

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