Variant report

Variant	nsv1033562
Chromosome Location	chr5:36927652-36994811
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	chr5:36929569-36929706	K562	blood:	n/a	n/a
2	ARID3A	chr5:36944696-36945107	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:36962968-36963071	K562	blood:	n/a	n/a
4	ARID3A	chr5:36944203-36945211	K562	blood:	n/a	n/a
5	ARID3A	chr5:36929086-36929329	K562	blood:	n/a	n/a
6	BHLHE40	chr5:36955382-36955388	GM12878	blood:	n/a	n/a
7	BRCA1	chr5:36951118-36951430	Hela-S3	cervix:	n/a	n/a
8	CCNT2	chr5:36954726-36954853	K562	blood:	n/a	n/a
9	CCNT2	chr5:36980063-36980115	K562	blood:	n/a	n/a
10	CCNT2	chr5:36946283-36946471	K562	blood:	n/a	n/a
11	CCNT2	chr5:36982251-36982514	K562	blood:	n/a	n/a
12	CEBPB	chr5:36936502-36936838	HepG2	liver:	n/a	chr5:36936639-36936650
13	CEBPB	chr5:36962325-36962389	A549	lung:	n/a	n/a
14	CEBPB	chr5:36934087-36934337	A549	lung:	n/a	n/a
15	CEBPB	chr5:36952876-36953114	HepG2	liver:	n/a	chr5:36953005-36953016 chr5:36953006-36953017
16	CEBPB	chr5:36929052-36929726	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr5:36934890-36935226	IMR90	lung:	n/a	chr5:36935065-36935076
18	CEBPB	chr5:36993961-36994063	HepG2	liver:	n/a	chr5:36993984-36993997 chr5:36993985-36993996 chr5:36993984-36993995
19	CEBPB	chr5:36934936-36935214	A549	lung:	n/a	chr5:36935065-36935076
20	CEBPB	chr5:36952917-36953126	Hela-S3	cervix:	n/a	chr5:36953005-36953016 chr5:36953006-36953017
21	CEBPB	chr5:36934167-36934308	K562	blood:	n/a	n/a
22	CEBPB	chr5:36934902-36935214	HepG2	liver:	n/a	chr5:36935065-36935076
23	CEBPB	chr5:36934880-36935229	K562	blood:	n/a	chr5:36935065-36935076
24	CEBPB	chr5:36934973-36935215	Hela-S3	cervix:	n/a	chr5:36935065-36935076
25	CEBPB	chr5:36982317-36982544	Hela-S3	cervix:	n/a	n/a
26	CTCF	chr5:36944840-36944990	HRE	kidney:	n/a	chr5:36944892-36944913 chr5:36944898-36944914 chr5:36944897-36944915 chr5:36944899-36944912
27	CTCF	chr5:36959224-36959265	Fibrobl	skin:	n/a	n/a
28	CTCF	chr5:36944860-36945010	HAc	cerebellar:	n/a	chr5:36944892-36944913 chr5:36944898-36944914 chr5:36944897-36944915 chr5:36944899-36944912
29	CTCF	chr5:36944880-36945030	GM12872	blood:	n/a	chr5:36944892-36944913 chr5:36944898-36944914 chr5:36944897-36944915 chr5:36944899-36944912
30	CTCF	chr5:36944840-36944990	WI-38	lung:	n/a	chr5:36944892-36944913 chr5:36944898-36944914 chr5:36944897-36944915 chr5:36944899-36944912
31	CTCF	chr5:36944840-36944990	AG04450	lung:	n/a	chr5:36944892-36944913 chr5:36944898-36944914 chr5:36944897-36944915 chr5:36944899-36944912
32	CTCF	chr5:36944760-36944910	RPTEC	kidney:	n/a	n/a
33	CTCF	chr5:36944901-36944939	GM13976	blood:	n/a	n/a
34	CTCF	chr5:36944800-36944950	GM12874	blood:	n/a	chr5:36944892-36944913 chr5:36944898-36944914 chr5:36944897-36944915 chr5:36944899-36944912
35	CTCF	chr5:36944840-36944982	GM10248	blood:	n/a	chr5:36944892-36944913 chr5:36944898-36944914 chr5:36944897-36944915 chr5:36944899-36944912
36	CTCF	chr5:36983776-36983812	LNCaP	prostate:	n/a	n/a
37	CTCF	chr5:36944900-36945050	GM06990	blood:	n/a	n/a
38	CTCF	chr5:36944710-36945011	MCF-7	breast:	n/a	chr5:36944892-36944913 chr5:36944898-36944914 chr5:36944897-36944915 chr5:36944899-36944912
39	CTCF	chr5:36944780-36944930	HEK293	kidney:	n/a	chr5:36944892-36944913 chr5:36944898-36944914 chr5:36944897-36944915 chr5:36944899-36944912
40	CTCF	chr5:36983780-36983930	HPAF	blood vessel:	n/a	n/a
41	CTCF	chr5:36953300-36953450	Caco-2	colon:	n/a	n/a
42	CTCF	chr5:36944784-36945049	HUVEC	blood vessel:	n/a	chr5:36944892-36944913 chr5:36944898-36944914 chr5:36944897-36944915 chr5:36944899-36944912
43	CTCF	chr5:36944800-36944950	GM12801	blood:	n/a	chr5:36944892-36944913 chr5:36944898-36944914 chr5:36944897-36944915 chr5:36944899-36944912
44	CTCF	chr5:36944860-36945010	GM12871	blood:	n/a	chr5:36944892-36944913 chr5:36944898-36944914 chr5:36944897-36944915 chr5:36944899-36944912
45	CTCF	chr5:36944800-36944950	GM12872	blood:	n/a	chr5:36944892-36944913 chr5:36944898-36944914 chr5:36944897-36944915 chr5:36944899-36944912
46	CTCF	chr5:36944867-36944981	LNCaP	prostate:	n/a	chr5:36944892-36944913 chr5:36944898-36944914 chr5:36944897-36944915 chr5:36944899-36944912
47	CTCF	chr5:36944900-36945050	GM12875	blood:	n/a	n/a
48	CTCF	chr5:36944860-36945010	HCM	heart:	n/a	chr5:36944892-36944913 chr5:36944898-36944914 chr5:36944897-36944915 chr5:36944899-36944912
49	CTCF	chr5:36944820-36944970	HPF	lung:	n/a	chr5:36944892-36944913 chr5:36944898-36944914 chr5:36944897-36944915 chr5:36944899-36944912
50	CTCF	chr5:36944840-36944990	SK-N-SH_RA	brain:	n/a	chr5:36944892-36944913 chr5:36944898-36944914 chr5:36944897-36944915 chr5:36944899-36944912

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:36986137-36986187	HNPCEpiC	eye:	n/a
2	chr5:36986137-36986187	GM12878	blood:	n/a
3	chr5:36985656-36985706	HAEpiC	amniotic membrane:	n/a
4	chr5:36986137-36986187	HEK293	kidney:	embryo
5	chr5:36985656-36985706	LNCaP	prostate:	n/a
6	chr5:36986137-36986187	BJ	skin:	n/a
7	chr5:36985656-36985706	T-47D	breast:	n/a
8	chr5:36985656-36985706	SK-N-SH_RA	brain:	n/a
9	chr5:36986137-36986187	GM12891	blood:	n/a
10	chr5:36985656-36985706	HL-60	blood:	n/a
11	chr5:36986137-36986187	AG09309	skin:	n/a
12	chr5:36985656-36985706	GM12878	blood:	n/a
13	chr5:36985656-36985706	Caco-2	colon:	n/a
14	chr5:36986137-36986187	Hela-S3	cervix:	n/a
15	chr5:36986137-36986187	PrEC	prostate:	n/a
16	chr5:36986137-36986187	HRPEpiC	eye:	n/a
17	chr5:36985656-36985706	CMK	blood:	n/a
18	chr5:36985656-36985706	ECC-1	luminal epithelium:	n/a
19	chr5:36985656-36985706	SK-N-SH	brain:	n/a
20	chr5:36986137-36986187	HAEpiC	amniotic membrane:	n/a
21	chr5:36985656-36985706	PFSK-1	brain:	n/a
22	chr5:36985656-36985706	HRE	kidney:	n/a
23	chr5:36986137-36986187	SK-N-SH_RA	brain:	n/a
24	chr5:36986137-36986187	NB4	blood:	n/a
25	chr5:36986137-36986187	ovcar-3	ovarian:	n/a
26	chr5:36985656-36985706	GM12892	blood:	n/a
27	chr5:36986137-36986187	NH-A	brain:	n/a
28	chr5:36985656-36985706	MCF10A-Er-Src	breast:	n/a
29	chr5:36985656-36985706	PrEC	prostate:	n/a
30	chr5:36986137-36986187	PANC-1	pancreas:	n/a
31	chr5:36985656-36985706	NH-A	brain:	n/a
32	chr5:36985656-36985706	ovcar-3	ovarian:	n/a
33	chr5:36985656-36985706	Jurkat	blood:	n/a
34	chr5:36986137-36986187	HRE	kidney:	n/a
35	chr5:36986137-36986187	A549	lung:	n/a
36	chr5:36986137-36986187	HCF	heart:	n/a
37	chr5:36985656-36985706	PANC-1	pancreas:	n/a
38	chr5:36986137-36986187	LNCaP	prostate:	n/a
39	chr5:36985656-36985706	AG04449	skin:	fetal
40	chr5:36986137-36986187	ProgFib	skin:	n/a
41	chr5:36985656-36985706	AG09319	gingival:	n/a
42	chr5:36986137-36986187	AG04449	skin:	fetal
43	chr5:36985656-36985706	HRPEpiC	eye:	n/a
44	chr5:36985656-36985706	HPAEpiC	pulmonary alveolar:	n/a
45	chr5:36985656-36985706	HUVEC	blood vessel:	n/a
46	chr5:36986137-36986187	NHBE	bronchial:	n/a
47	chr5:36985656-36985706	HCM	heart:	n/a
48	chr5:36986137-36986187	HMEC	breast:	n/a
49	chr5:36986137-36986187	HCM	heart:	n/a
50	chr5:36986137-36986187	K562	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:36875507..36877384-chr5:36931274..36933956,2	MCF-7	breast:
2	chr5:36932364..36935161-chr5:36941200..36944542,3	K562	blood:
3	chr5:36875852..36878173-chr5:36948175..36949997,2	MCF-7	breast:
4	chr5:36945026..36947869-chr5:36950785..36953502,2	K562	blood:
5	chr5:36874711..36878038-chr5:36947695..36950933,3	K562	blood:
6	chr5:36739462..36740370-chr5:36944609..36945180,2	K562	blood:
7	chr5:36989118..36992920-chr5:36994202..36998219,3	K562	blood:
8	chr5:36926669..36929078-chr5:36937999..36941125,3	MCF-7	breast:
9	chr5:36870534..36872265-chr5:36955998..36958154,2	K562	blood:
10	chr5:36932364..36935161-chr5:36941200..36944542,3	K562	blood:
11	chr5:36935171..36938055-chr5:36942349..36945199,2	MCF-7	breast:
12	chr5:36951924..36954172-chr5:36959176..36961699,2	K562	blood:
13	chr5:36874429..36878345-chr5:36984473..36987380,3	MCF-7	breast:
14	chr5:36959262..36961457-chr5:36965516..36967978,2	K562	blood:
15	chr5:36979639..36981390-chr5:36990947..36992768,2	K562	blood:
16	chr5:36926669..36929078-chr5:36937999..36941125,3	MCF-7	breast:
17	chr5:36875293..36878744-chr5:36944693..36947433,6	MCF-7	breast:
18	chr5:36966039..36969773-chr5:36970364..36974397,4	K562	blood:
19	chr5:36980854..36983652-chr5:37007051..37009220,2	K562	blood:
20	chr5:36876634..36880507-chr5:36935586..36937738,3	MCF-7	breast:
21	chr5:36979639..36981390-chr5:36990947..36992768,2	K562	blood:
22	chr5:36987049..36989193-chr5:36992034..36994434,2	MCF-7	breast:
23	chr5:36971660..36974021-chr5:36977884..36980284,2	K562	blood:
24	chr5:36876643..36878544-chr5:36988862..36990983,2	MCF-7	breast:
25	chr5:36984839..36987108-chr5:36990813..36992695,2	MCF-7	breast:
26	chr5:36876484..36879168-chr5:36940218..36943816,3	MCF-7	breast:
27	chr5:36906209..36908902-chr5:36936450..36938338,2	K562	blood:
28	chr5:36980489..36983193-chr5:36983998..36987194,3	K562	blood:
29	chr5:36973522..36975991-chr5:36979839..36981489,2	MCF-7	breast:
30	chr5:36979203..36982071-chr5:36982407..36984591,2	MCF-7	breast:
31	chr5:36935171..36938055-chr5:36942349..36945199,2	MCF-7	breast:
32	chr5:36971660..36974021-chr5:36977884..36980284,2	K562	blood:
33	chr5:36743938..36745907-chr5:36986468..36988860,2	MCF-7	breast:
34	chr5:36952816..36955037-chr5:36959684..36961296,2	K562	blood:
35	chr5:36975370..36977212-chr5:36981265..36983072,2	MCF-7	breast:
36	chr5:36937263..36939579-chr5:36939659..36941382,2	MCF-7	breast:
37	chr5:36927710..36929639-chr5:36961627..36963604,2	MCF-7	breast:
38	chr5:36975370..36977212-chr5:36981265..36983072,2	MCF-7	breast:
39	chr5:36959037..36960971-chr5:36969014..36971044,2	K562	blood:
40	chr5:36937606..36940951-chr5:36941936..36944746,3	K562	blood:
41	chr5:36945602..36948266-chr5:36961950..36964005,2	K562	blood:
42	chr5:36937263..36939579-chr5:36939659..36941382,2	MCF-7	breast:
43	chr5:36931581..36933729-chr5:36940700..36943226,2	MCF-7	breast:
44	chr3:109682867..109683387-chr5:36941291..36942072,2	MCF-7	breast:
45	chr5:36874857..36877485-chr5:36989379..36990958,2	MCF-7	breast:
46	chr5:36875559..36878395-chr5:36942609..36944650,2	MCF-7	breast:
47	chr5:36875672..36878039-chr5:36951739..36953901,2	MCF-7	breast:
48	chr5:36984035..36986257-chr5:36992707..36994891,2	K562	blood:
49	chr5:36943349..36945887-chr5:36955686..36957216,2	K562	blood:
50	chr5:36920129..36922816-chr5:36925625..36927920,2	MCF-7	breast:

Variant related genes	Relation type
NIPBL	TF binding region
NIPBL	CpG island
ENSG00000164190	chromatin interactions

Extended variants
information (count: 2256 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:2256 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6868571	chr5:36927652-36927653	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs546651278	chr5:36927821-36927822	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs371927454	chr5:36927859-36927860	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs374905671	chr5:36927895-36927896	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs371422927	chr5:36927914-36927915	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs186738729	chr5:36927939-36927940	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs114480894	chr5:36927943-36927944	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs377448575	chr5:36927977-36927978	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs7729475	chr5:36927981-36927982	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs7709810	chr5:36927985-36927986	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs536425557	chr5:36927990-36927991	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs554778693	chr5:36928045-36928046	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs191541777	chr5:36928070-36928071	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs140684447	chr5:36928080-36928081	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs537495289	chr5:36928102-36928103	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs199679798	chr5:36928103-36928104	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs545066028	chr5:36928118-36928119	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs529010228	chr5:36928126-36928127	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs184905818	chr5:36928157-36928158	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs200960966	chr5:36928234-36928235	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs190548650	chr5:36928235-36928236	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs193029003	chr5:36928256-36928257	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs568695255	chr5:36928316-36928317	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs185179956	chr5:36928319-36928320	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs189730277	chr5:36928356-36928357	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs565224227	chr5:36928407-36928408	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs532367077	chr5:36928449-36928450	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs181245042	chr5:36928469-36928470	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs143710045	chr5:36928473-36928474	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs530100837	chr5:36928483-36928484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs548299243	chr5:36928509-36928510	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs566905391	chr5:36928564-36928565	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs112615240	chr5:36928569-36928570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs36035695	chr5:36928572-36928573	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs558979918	chr5:36928656-36928657	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs571173028	chr5:36928673-36928674	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs567517451	chr5:36928689-36928690	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs372397221	chr5:36928705-36928706	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs185600584	chr5:36928707-36928708	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs556961110	chr5:36928743-36928744	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs551026591	chr5:36928749-36928750	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs575331771	chr5:36928761-36928762	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs536303272	chr5:36928835-36928836	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs188057361	chr5:36928860-36928861	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs554654895	chr5:36928934-36928935	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs570803781	chr5:36928948-36928949	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs181010020	chr5:36928969-36928970	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs539496881	chr5:36929002-36929003	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs565010893	chr5:36929115-36929116	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs578197136	chr5:36929118-36929119	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:99)

Disease	PMID	Source
Myofibroblastic sarcoma	19369631	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Non-small cell lung cancer	20864512	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Breast cancer	21858162	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Cancer	16751803	CNVD
Breast cancer	16608533	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Non-small cell lung cancer	19010865	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	21720365	CNVD
Lung cancer	18438408	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Prostate cancer	18632612	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	19553991	CNVD
Lung cancer	19553991	CNVD
Melanoma	19553991	CNVD
Ovarian cancer	19553991	CNVD
Prostate cancer	19553991	CNVD
Non-small cell lung cancer	17156491	CNVD
Breast cancer	17133270	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Breast cancer	17393978	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Lung cancer	19153074	CNVD
Breast cancer	21364760	CNVD
Cornelia de Lange syndrome	21085971	CNVD
Autism	21701786	CNVD
Cervical cancer	16585170	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1711 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:36895800-36928600	Weak transcription	HSMM	muscle
2	chr5:36905200-36927800	Weak transcription	Psoas Muscle	Psoas
3	chr5:36907400-36928600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr5:36907400-36938200	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr5:36910200-36928000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
6	chr5:36911200-36928600	Weak transcription	A549	lung
7	chr5:36911600-36928600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr5:36913800-36931400	Weak transcription	Primary T cells fromperipheralblood	blood
9	chr5:36919600-36928000	Weak transcription	Ovary	ovary
10	chr5:36919600-36928000	Weak transcription	Small Intestine	intestine
11	chr5:36919600-36931400	Weak transcription	Left Ventricle	heart
12	chr5:36919600-36938200	Weak transcription	Pancreas	Pancrea
13	chr5:36919800-36953000	Weak transcription	Primary B cells from peripheral blood	blood
14	chr5:36919800-36961600	Weak transcription	K562	blood
15	chr5:36920000-36928200	Weak transcription	Duodenum Smooth Muscle	Duodenum
16	chr5:36920000-36928600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
17	chr5:36920400-36951400	Weak transcription	Primary hematopoietic stem cells	blood
18	chr5:36921600-36929200	Weak transcription	Skeletal Muscle Male	skeletal muscle
19	chr5:36921600-36931600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr5:36923400-36931400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr5:36923600-36943600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
22	chr5:36924600-36943600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr5:36924800-36931000	Weak transcription	Skeletal Muscle Female	skeletal muscle
24	chr5:36924800-36933000	Weak transcription	Aorta	Aorta
25	chr5:36924800-36939000	Weak transcription	Fetal Thymus	thymus
26	chr5:36924800-36955200	Weak transcription	Dnd41	blood
27	chr5:36925000-36929000	Weak transcription	Pancreatic Islets	Pancreatic Islet
28	chr5:36925200-36929200	Weak transcription	Fetal Heart	heart
29	chr5:36925400-36933800	Enhancers	Primary T helper cells fromperipheralblood	blood
30	chr5:36925600-36935200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
31	chr5:36926000-36936800	Enhancers	Primary T helper cells PMA-I stimulated	--
32	chr5:36926400-36928000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
33	chr5:36926600-36927800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr5:36926600-36928200	Weak transcription	Hela-S3	cervix
35	chr5:36926600-36928800	Weak transcription	Primary T cells from cord blood	blood
36	chr5:36926600-36931600	Weak transcription	GM12878-XiMat	blood
37	chr5:36926600-36939400	Weak transcription	Fetal Intestine Small	intestine
38	chr5:36926800-36928200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
39	chr5:36926800-36934200	Weak transcription	Colon Smooth Muscle	Colon
40	chr5:36927200-36928200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
41	chr5:36927600-36929000	Enhancers	Primary T helper naive cells from peripheral blood	blood
42	chr5:36927600-36929000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
43	chr5:36927600-36929800	Enhancers	NHDF-Ad	bronchial
44	chr5:36927600-36961600	Weak transcription	Cortex derived primary cultured neurospheres	brain
45	chr5:36927800-36928000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr5:36927800-36928200	Enhancers	Psoas Muscle	Psoas
47	chr5:36928000-36928200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
48	chr5:36928000-36928400	Enhancers	Ovary	ovary
49	chr5:36928000-36928600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr5:36928000-36928600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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