Variant report

Variant	nsv3966
Chromosome Location	chr1:192976457-193004886
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	ARID3A	chr1:192976723-192977711	HepG2	liver:	n/a	n/a
2	BACH1	chr1:192999214-192999317	K562	blood:	n/a	n/a
3	BCL3	chr1:192978340-192978899	A549	lung:	n/a	n/a
4	BCL3	chr1:192976889-192977423	A549	lung:	n/a	n/a
5	CBX3	chr1:192988503-192988967	HCT-116	colon:	n/a	n/a
6	CCNT2	chr1:192980322-192980539	K562	blood:	n/a	n/a
7	CEBPB	chr1:192976910-192977353	HepG2	liver:	n/a	n/a
8	CEBPB	chr1:192980594-192980864	IMR90	lung:	n/a	chr1:192980715-192980728 chr1:192980717-192980726 chr1:192980717-192980726 chr1:192980715-192980728 chr1:192980715-192980726 chr1:192980717-192980728 chr1:192980717-192980726 chr1:192980717-192980726
9	CEBPB	chr1:192982217-192982528	IMR90	lung:	n/a	n/a
10	CEBPB	chr1:193004683-193004692	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr1:192980568-192980846	Hela-S3	cervix:	n/a	chr1:192980715-192980728 chr1:192980717-192980726 chr1:192980717-192980726 chr1:192980715-192980728 chr1:192980715-192980726 chr1:192980717-192980728 chr1:192980717-192980726 chr1:192980717-192980726
12	CEBPB	chr1:192980540-192980898	K562	blood:	n/a	chr1:192980715-192980728 chr1:192980717-192980726 chr1:192980717-192980726 chr1:192980715-192980728 chr1:192980715-192980726 chr1:192980717-192980728 chr1:192980717-192980726 chr1:192980717-192980726
13	CEBPB	chr1:192980548-192980815	A549	lung:	n/a	chr1:192980715-192980728 chr1:192980717-192980726 chr1:192980717-192980726 chr1:192980715-192980728 chr1:192980715-192980726 chr1:192980717-192980728 chr1:192980717-192980726 chr1:192980717-192980726
14	CEBPB	chr1:192980618-192980834	HepG2	liver:	n/a	chr1:192980715-192980728 chr1:192980717-192980726 chr1:192980717-192980726 chr1:192980715-192980728 chr1:192980715-192980726 chr1:192980717-192980728 chr1:192980717-192980726 chr1:192980717-192980726
15	CEBPZ	chr1:192977513-192977736	HepG2	liver:	n/a	n/a
16	CTCF	chr1:193000640-193000790	AG04449	skin:	n/a	chr1:193000715-193000733 chr1:193000710-193000731 chr1:193000716-193000732
17	CTCF	chr1:193000580-193000730	GM06990	blood:	n/a	n/a
18	CTCF	chr1:193000680-193000830	GM12873	blood:	n/a	chr1:193000715-193000733 chr1:193000710-193000731 chr1:193000716-193000732
19	CTCF	chr1:193000620-193000770	AoAF	blood vessel:	n/a	chr1:193000715-193000733 chr1:193000710-193000731 chr1:193000716-193000732
20	CTCF	chr1:193000600-193000750	HEEpiC	esophagus:	n/a	chr1:193000715-193000733 chr1:193000710-193000731 chr1:193000716-193000732
21	CTCF	chr1:192988700-192988850	AoAF	blood vessel:	n/a	chr1:192988762-192988780 chr1:192988757-192988778
22	CTCF	chr1:192988640-192988790	HRPEpiC	eye:	n/a	chr1:192988762-192988780 chr1:192988757-192988778
23	CTCF	chr1:192988591-192988922	A549	lung:	n/a	chr1:192988762-192988780 chr1:192988757-192988778
24	CTCF	chr1:192988652-192988815	SK-N-SH_RA	brain:	n/a	chr1:192988762-192988780 chr1:192988757-192988778
25	CTCF	chr1:193000600-193000750	AG09309	skin:	n/a	chr1:193000715-193000733 chr1:193000710-193000731 chr1:193000716-193000732
26	CTCF	chr1:193000540-193000690	HCM	heart:	n/a	n/a
27	CTCF	chr1:192988660-192988810	HMEC	breast:	n/a	chr1:192988762-192988780 chr1:192988757-192988778
28	CTCF	chr1:193000640-193000790	NHDF-neo	bronchial:	n/a	chr1:193000715-193000733 chr1:193000710-193000731 chr1:193000716-193000732
29	CTCF	chr1:193000436-193001025	HCT-116	colon:	n/a	chr1:193000715-193000733 chr1:193000710-193000731 chr1:193000716-193000732
30	CTCF	chr1:193000600-193000750	HMEC	breast:	n/a	chr1:193000715-193000733 chr1:193000710-193000731 chr1:193000716-193000732
31	CTCF	chr1:192988660-192988810	AG04449	skin:	n/a	chr1:192988762-192988780 chr1:192988757-192988778
32	CTCF	chr1:193000640-193000790	HRE	kidney:	n/a	chr1:193000715-193000733 chr1:193000710-193000731 chr1:193000716-193000732
33	CTCF	chr1:192988620-192988770	NHDF-neo	bronchial:	n/a	n/a
34	CTCF	chr1:192988545-192988976	IMR90	lung:	n/a	chr1:192988762-192988780 chr1:192988757-192988778
35	CTCF	chr1:193000660-193000810	AG04450	lung:	n/a	chr1:193000715-193000733 chr1:193000710-193000731 chr1:193000716-193000732
36	CTCF	chr1:192988680-192988830	AG09319	gingival:	n/a	chr1:192988762-192988780 chr1:192988757-192988778
37	CTCF	chr1:192988680-192988830	GM12878	blood:	n/a	chr1:192988762-192988780 chr1:192988757-192988778
38	CTCF	chr1:192988522-192989046	HCT-116	colon:	n/a	chr1:192988762-192988780 chr1:192988757-192988778
39	CTCF	chr1:193000580-193000730	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr1:193000680-193000830	GM12801	blood:	n/a	chr1:193000715-193000733 chr1:193000710-193000731 chr1:193000716-193000732
41	CTCF	chr1:192988670-192988847	MCF-7	breast:	n/a	chr1:192988762-192988780 chr1:192988757-192988778
42	CTCF	chr1:193000640-193000790	HCPEpiC	choroid plexus:	n/a	chr1:193000715-193000733 chr1:193000710-193000731 chr1:193000716-193000732
43	CTCF	chr1:193000640-193000790	HPAF	blood vessel:	n/a	chr1:193000715-193000733 chr1:193000710-193000731 chr1:193000716-193000732
44	CTCF	chr1:192988262-192989077	SK-N-SH	brain:	n/a	chr1:192988762-192988780 chr1:192988757-192988778
45	CTCF	chr1:193000740-193000890	Hela-S3	cervix:	n/a	n/a
46	CTCF	chr1:192988739-192988794	MCF-7	breast:	n/a	chr1:192988762-192988780 chr1:192988757-192988778
47	CTCF	chr1:193000580-193000825	A549	lung:	n/a	chr1:193000715-193000733 chr1:193000710-193000731 chr1:193000716-193000732
48	CTCF	chr1:192993369-192993375	GM10248	blood:	n/a	n/a
49	CTCF	chr1:192988720-192988870	GM12873	blood:	n/a	chr1:192988762-192988780 chr1:192988757-192988778
50	CTCF	chr1:192988680-192988830	HCPEpiC	choroid plexus:	n/a	chr1:192988762-192988780 chr1:192988757-192988778

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:192983012-192983062	NB4	blood:	n/a
2	chr1:192983012-192983062	PFSK-1	brain:	n/a
3	chr1:192983012-192983062	MCF10A-Er-Src	breast:	n/a
4	chr1:192983012-192983062	RPTEC	kidney:	n/a
5	chr1:192983012-192983062	Hela-S3	cervix:	n/a
6	chr1:192983012-192983062	GM12892	blood:	n/a
7	chr1:192983012-192983062	AoSMC	blood vessel:	n/a
8	chr1:192983012-192983062	SK-N-SH_RA	brain:	n/a
9	chr1:192983012-192983062	HMEC	breast:	n/a
10	chr1:192983012-192983062	SAEC	small airway:	n/a
11	chr1:192983012-192983062	NT2-D1	testis:	n/a
12	chr1:192983012-192983062	CMK	blood:	n/a
13	chr1:192983012-192983062	HNPCEpiC	eye:	n/a
14	chr1:192983012-192983062	HCPEpiC	choroid plexus:	n/a
15	chr1:192983012-192983062	U87	brain:	n/a
16	chr1:192983012-192983062	NHBE	bronchial:	n/a
17	chr1:192983012-192983062	LNCaP	prostate:	n/a
18	chr1:192983012-192983062	BJ	skin:	n/a
19	chr1:192983012-192983062	HL-60	blood:	n/a
20	chr1:192983012-192983062	HCM	heart:	n/a
21	chr1:192983012-192983062	GM19239	blood:	n/a
22	chr1:192983012-192983062	NH-A	brain:	n/a
23	chr1:192983012-192983062	SKMC	muscle:	n/a
24	chr1:192983012-192983062	HCF	heart:	n/a
25	chr1:192983012-192983062	AG09319	gingival:	n/a
26	chr1:192983012-192983062	PANC-1	pancreas:	n/a
27	chr1:192983012-192983062	H1-hESC	embryonic stem cell:	embryo
28	chr1:192983012-192983062	GM12878	blood:	n/a
29	chr1:192983012-192983062	HIPEpiC	eye:	n/a
30	chr1:192983012-192983062	Jurkat	blood:	n/a
31	chr1:192983012-192983062	AG04450	lung:	fetal
32	chr1:192983012-192983062	HEEpiC	esophagus:	n/a
33	chr1:192983012-192983062	NHDF-neo	bronchial:	n/a
34	chr1:192983012-192983062	HRCEpiC	kidney:	n/a
35	chr1:192983012-192983062	HPAEpiC	pulmonary alveolar:	n/a
36	chr1:192983012-192983062	GM12891	blood:	n/a
37	chr1:192983012-192983062	Caco-2	colon:	n/a
38	chr1:192983012-192983062	GM06990	blood:	n/a
39	chr1:192983012-192983062	HepG2	liver:	n/a
40	chr1:192983012-192983062	PrEC	prostate:	n/a
41	chr1:192983012-192983062	MCF-7	breast:	n/a
42	chr1:192983012-192983062	T-47D	breast:	n/a
43	chr1:192983012-192983062	AG10803	skin:	n/a
44	chr1:192983012-192983062	SK-N-SH	brain:	n/a
45	chr1:192983012-192983062	SK-N-MC	brain:	n/a
46	chr1:192983012-192983062	K562	blood:	n/a
47	chr1:192983012-192983062	BE2_C	brain:	n/a
48	chr1:192983012-192983062	AG09309	skin:	n/a
49	chr1:192983012-192983062	IMR90	lung:	fetal
50	chr1:192983012-192983062	ECC-1	luminal epithelium:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:193001316..193003311-chr1:193006679..193008894,2	K562	blood:
2	chr1:192995040..192997652-chr1:192998864..193001424,2	MCF-7	breast:
3	chr1:193004621..193006727-chr1:193089404..193092194,2	K562	blood:
4	chr1:192995946..192996514-chr15:83878116..83878651,2	MCF-7	breast:
5	chr1:192978102..192980139-chr1:193100169..193103053,2	K562	blood:
6	chr1:192992147..192995725-chr1:192998536..193000592,4	K562	blood:
7	chr1:192973548..192977447-chr1:192979869..192983384,3	K562	blood:
8	chr1:192964363..192967314-chr1:192975848..192978969,3	K562	blood:
9	chr1:192981169..192983545-chr1:192999201..193001195,2	K562	blood:
10	chr1:192995490..192998261-chr1:193001490..193003087,2	K562	blood:
11	chr1:192980684..192984723-chr1:192984841..192989093,4	K562	blood:
12	chr1:192971893..192973529-chr1:192975096..192977591,2	K562	blood:
13	chr1:193000934..193002560-chr1:193027136..193029192,2	MCF-7	breast:
14	chr1:192774616..192775596-chr1:192988271..192989252,4	K562	blood:
15	chr1:192993820..193002591-chr1:193021038..193030016,12	K562	blood:
16	chr1:192777515..192779632-chr1:192993913..192995891,2	MCF-7	breast:
17	chr1:192995746..192997937-chr1:192999203..193000719,2	K562	blood:
18	chr1:192980684..192984723-chr1:192984841..192989093,4	K562	blood:
19	chr1:192984947..192986543-chr1:193027186..193029315,2	K562	blood:
20	chr1:193003748..193005424-chr1:193026753..193029243,2	MCF-7	breast:
21	chr1:192995746..192997937-chr1:192999203..193000719,2	K562	blood:
22	chr1:192995490..192998261-chr1:193001490..193003087,2	K562	blood:
23	chr1:192446513..192447432-chr1:192988667..192989486,2	K562	blood:
24	chr1:192775702..192778041-chr1:192986871..192988604,2	MCF-7	breast:
25	chr1:192976396..192978239-chr1:192979297..192981493,2	MCF-7	breast:
26	chr1:192992147..192995725-chr1:192998536..193000592,4	K562	blood:
27	chr1:192973548..192977447-chr1:192979869..192983384,3	K562	blood:
28	chr1:192996006..192999093-chr1:193026171..193028166,3	K562	blood:
29	chr1:192979947..192982887-chr1:192983438..192986734,3	K562	blood:
30	chr1:192993626..192995725-chr1:192998924..193000592,2	K562	blood:
31	chr1:192998924..193001741-chr1:193027494..193030058,4	MCF-7	breast:
32	chr1:192446612..192447642-chr1:192988286..192989297,3	MCF-7	breast:
33	chr1:192981169..192983545-chr1:192999201..193001195,2	K562	blood:
34	chr1:192773819..192775227-chr1:192988234..192989224,6	MCF-7	breast:
35	chr1:192979947..192982887-chr1:192983438..192986734,3	K562	blood:
36	chr1:193004279..193005988-chr1:193007207..193008711,2	K562	blood:
37	chr1:192998541..193001288-chr1:193004559..193007081,2	MCF-7	breast:
38	chr1:192993626..192995725-chr1:192998924..193000592,2	K562	blood:
39	chr1:192957649..192960395-chr1:192982012..192983675,2	K562	blood:
40	chr1:192976057..192978615-chr1:193027631..193029509,2	MCF-7	breast:
41	chr1:192976396..192978239-chr1:192979297..192981493,2	MCF-7	breast:
42	chr1:192996026..192997937-chr1:192998425..193000719,2	K562	blood:
43	chr1:192995040..192997652-chr1:192998864..193001424,2	MCF-7	breast:
44	chr1:192442920..192443850-chr1:192988643..192989239,2	K562	blood:
45	chr1:193003150..193004895-chr1:193006252..193008709,2	MCF-7	breast:
46	chr1:193002497..193005080-chr1:193010739..193013056,2	K562	blood:
47	chr1:192762496..192765465-chr1:192982382..192985012,2	K562	blood:
48	chr1:192774668..192775652-chr1:192988368..192989269,6	MCF-7	breast:

Variant related genes	Relation type
UCHL5	TF binding region
UCHL5	CpG island
ENSG00000134371	chromatin interactions
ENSG00000116747	chromatin interactions
ENSG00000238754	chromatin interactions
ENSG00000116741	chromatin interactions
ENSG00000116750	chromatin interactions

Extended variants
information (count: 861 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:861 , 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	rs567780835	chr1:192976458-192976459	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs73052226	chr1:192976503-192976504	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs553100856	chr1:192976514-192976515	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs540561742	chr1:192976518-192976519	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs144189116	chr1:192976533-192976534	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs539308172	chr1:192976534-192976535	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs558713259	chr1:192976611-192976612	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs151038083	chr1:192976632-192976633	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs371680598	chr1:192976634-192976635	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs538216035	chr1:192976678-192976679	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs555118362	chr1:192976712-192976713	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs567934866	chr1:192976719-192976720	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs140387109	chr1:192976858-192976859	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs540430701	chr1:192976868-192976869	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs535446564	chr1:192976879-192976880	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs181716969	chr1:192976882-192976883	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs546055196	chr1:192976947-192976948	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs562611555	chr1:192976970-192976971	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs148752515	chr1:192976977-192976978	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs376305818	chr1:192976979-192976980	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs531353370	chr1:192976982-192976983	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs34238022	chr1:192976983-192976984	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs74130910	chr1:192976984-192976985	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs376303321	chr1:192976986-192976987	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs541914147	chr1:192977022-192977023	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs146447417	chr1:192977024-192977025	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs56055595	chr1:192977026-192977027	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs561448317	chr1:192977054-192977055	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs527379602	chr1:192977078-192977079	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs12132305	chr1:192977081-192977082	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs376974452	chr1:192977151-192977152	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs568959931	chr1:192977170-192977171	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs186507087	chr1:192977205-192977206	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs538993994	chr1:192977226-192977227	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs12129832	chr1:192977251-192977252	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs191329707	chr1:192977337-192977338	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs6699666	chr1:192977420-192977421	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs180814523	chr1:192977528-192977529	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs116424920	chr1:192977544-192977545	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs113664616	chr1:192977641-192977642	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs142202518	chr1:192977698-192977699	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs186009401	chr1:192977801-192977802	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs577048322	chr1:192977813-192977814	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs190863659	chr1:192977839-192977840	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs11383017	chr1:192977840-192977841	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs537476520	chr1:192977841-192977842	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs397822993	chr1:192977855-192977856	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs568942060	chr1:192977889-192977890	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs183371655	chr1:192977907-192977908	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs541247956	chr1:192977925-192977926	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	20688739	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21611746	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	19010865	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Trisomy 5 syndrome	21098271	CNVD
Glioblastoma multiforme	22286061	CNVD
Urothelial carcinoma	21177765	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Mental retardation	21062444	CNVD
Liver carcinoma	19366792	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:547 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:192953600-192982400	Weak transcription	HSMMtube	muscle
2	chr1:192954200-192991200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
3	chr1:192954800-192978800	Weak transcription	Right Ventricle	heart
4	chr1:192955800-192990600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
5	chr1:192956200-192988400	Weak transcription	Brain Hippocampus Middle	brain
6	chr1:192961200-192983600	Weak transcription	Hela-S3	cervix
7	chr1:192962600-192986400	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr1:192963000-192982000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr1:192963600-192983000	Weak transcription	Primary T helper cells fromperipheralblood	blood
10	chr1:192963800-192981400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr1:192963800-192981600	Weak transcription	NHLF	lung
12	chr1:192963800-192982000	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr1:192963800-192982200	Weak transcription	Aorta	Aorta
14	chr1:192963800-192983000	Weak transcription	NH-A	brain
15	chr1:192963800-192990000	Weak transcription	HMEC	breast
16	chr1:192963800-192994400	Weak transcription	Primary hematopoietic stem cells	blood
17	chr1:192963800-192996200	Weak transcription	Fetal Lung	lung
18	chr1:192963800-193012400	Weak transcription	NHEK	skin
19	chr1:192963800-193019600	Weak transcription	Ovary	ovary
20	chr1:192964000-192977200	Weak transcription	Cortex derived primary cultured neurospheres	brain
21	chr1:192964000-192981000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr1:192964000-192981800	Weak transcription	HSMM	muscle
23	chr1:192964000-192983000	Weak transcription	Fetal Thymus	thymus
24	chr1:192964000-192984600	Weak transcription	Primary B cells from cord blood	blood
25	chr1:192964000-192990400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr1:192964000-192994400	Weak transcription	Left Ventricle	heart
27	chr1:192965000-192990800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr1:192966200-192994200	Weak transcription	Primary T cells from cord blood	blood
29	chr1:192966400-192976800	Weak transcription	A549	lung
30	chr1:192966400-192985200	Weak transcription	Primary T cells fromperipheralblood	blood
31	chr1:192967200-192983600	Weak transcription	HUVEC	blood vessel
32	chr1:192967600-192982800	Weak transcription	Skeletal Muscle Female	skeletal muscle
33	chr1:192967600-192993000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr1:192968000-192978000	Weak transcription	Rectal Mucosa Donor 29	rectum
35	chr1:192968000-192981600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr1:192968000-192984600	Weak transcription	Primary T helper cells PMA-I stimulated	--
37	chr1:192968000-192992000	Weak transcription	Placenta	Placenta
38	chr1:192968000-193009400	Weak transcription	HUES6 Cell Line	embryonic stem cell
39	chr1:192968000-193012400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr1:192968000-193019400	Weak transcription	Skeletal Muscle Male	skeletal muscle
41	chr1:192972400-192982000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr1:192972800-192981800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
43	chr1:192972800-192983200	Weak transcription	K562	blood
44	chr1:192972800-192991200	Weak transcription	Primary B cells from peripheral blood	blood
45	chr1:192972800-192991200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
46	chr1:192973200-192992800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr1:192975200-192981600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr1:192975200-192985000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr1:192975400-192982800	Weak transcription	Psoas Muscle	Psoas
50	chr1:192975400-192991200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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