Variant report

Variant	esv2755670
Chromosome Location	chr6:15624762-15736008
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1617)
CpG islands
(count:1589)
Chromatin interactive
region (count:168)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1617 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:15691499-15691880	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:15735943-15736361	K562	blood:	n/a	n/a
3	ARID3A	chr6:15638702-15639076	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:15629087-15629381	K562	blood:	n/a	n/a
5	ARID3A	chr6:15683822-15683870	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:15691365-15691874	K562	blood:	n/a	n/a
7	ARID3A	chr6:15698603-15699017	K562	blood:	n/a	n/a
8	ARID3A	chr6:15631591-15631961	HepG2	liver:	n/a	n/a
9	ARID3A	chr6:15730625-15730942	K562	blood:	n/a	n/a
10	ARID3A	chr6:15683225-15683480	K562	blood:	n/a	n/a
11	ARID3A	chr6:15651167-15651439	HepG2	liver:	n/a	n/a
12	ARID3A	chr6:15631526-15631532	K562	blood:	n/a	n/a
13	ARID3A	chr6:15662901-15662999	HepG2	liver:	n/a	n/a
14	ARID3A	chr6:15643829-15644082	HepG2	liver:	n/a	n/a
15	ATF1	chr6:15629022-15629311	K562	blood:	n/a	n/a
16	ATF1	chr6:15735885-15736519	K562	blood:	n/a	n/a
17	ATF1	chr6:15730512-15730980	K562	blood:	n/a	n/a
18	ATF1	chr6:15734430-15734669	K562	blood:	n/a	n/a
19	ATF2	chr6:15658511-15659115	GM12878	blood:	n/a	n/a
20	ATF2	chr6:15691375-15691973	GM12878	blood:	n/a	n/a
21	ATF2	chr6:15735859-15736416	GM12878	blood:	n/a	n/a
22	ATF2	chr6:15691400-15691898	GM12878	blood:	n/a	n/a
23	ATF2	chr6:15691380-15691878	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF2	chr6:15735906-15736314	GM12878	blood:	n/a	n/a
25	ATF2	chr6:15658392-15659089	GM12878	blood:	n/a	n/a
26	ATF2	chr6:15662399-15662941	GM12878	blood:	n/a	n/a
27	ATF3	chr6:15735984-15736442	K562	blood:	n/a	n/a
28	ATF3	chr6:15662486-15662859	HepG2	liver:	n/a	chr6:15662824-15662838
29	ATF3	chr6:15662588-15662866	K562	blood:	n/a	chr6:15662824-15662838
30	ATF3	chr6:15662955-15663393	K562	blood:	n/a	n/a
31	ATF3	chr6:15691420-15691769	GM12878	blood:	n/a	chr6:15691501-15691511
32	ATF3	chr6:15691538-15691799	GM12878	blood:	n/a	n/a
33	ATF3	chr6:15698676-15699089	K562	blood:	n/a	n/a
34	BACH1	chr6:15663025-15663406	H1-hESC	embryonic stem cell:	n/a	n/a
35	BACH1	chr6:15642576-15642857	H1-hESC	embryonic stem cell:	n/a	n/a
36	BATF	chr6:15691483-15691834	GM12878	blood:	n/a	n/a
37	BATF	chr6:15658488-15658997	GM12878	blood:	n/a	n/a
38	BATF	chr6:15678015-15678371	GM12878	blood:	n/a	n/a
39	BCL11A	chr6:15658542-15658979	GM12878	blood:	n/a	chr6:15658848-15658857
40	BCL11A	chr6:15658556-15658979	GM12878	blood:	n/a	chr6:15658848-15658857
41	BCL11A	chr6:15629101-15629280	GM12878	blood:	n/a	n/a
42	BCL3	chr6:15658456-15658948	GM12878	blood:	n/a	chr6:15658848-15658857
43	BCL3	chr6:15735884-15736310	GM12878	blood:	n/a	n/a
44	BCLAF1	chr6:15662327-15662890	GM12878	blood:	n/a	n/a
45	BCLAF1	chr6:15658528-15659076	GM12878	blood:	n/a	chr6:15658848-15658857
46	BCLAF1	chr6:15691317-15691909	GM12878	blood:	n/a	chr6:15691691-15691700
47	BCLAF1	chr6:15691403-15691896	GM12878	blood:	n/a	chr6:15691691-15691700
48	BCLAF1	chr6:15653780-15654252	GM12878	blood:	n/a	chr6:15653990-15653999
49	BHLHE40	chr6:15683772-15684015	GM12878	blood:	n/a	n/a
50	BHLHE40	chr6:15658618-15658950	GM12878	blood:	n/a	n/a

(count:1589 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:15629162-15629212	HRE	kidney:	n/a
2	chr6:15727374-15727424	SKMC	muscle:	n/a
3	chr6:15663360-15663410	AG09319	gingival:	n/a
4	chr6:15629162-15629212	HRE	kidney:	n/a
5	chr6:15727374-15727424	SKMC	muscle:	n/a
6	chr6:15663360-15663410	AG09319	gingival:	n/a
7	chr6:15691258-15691308	U87	brain:	n/a
8	chr6:15675176-15675226	Hepatocyte	liver:	n/a
9	chr6:15727374-15727424	HEK293	kidney:	embryo
10	chr6:15691258-15691308	T-47D	breast:	n/a
11	chr6:15664231-15664281	HRPEpiC	eye:	n/a
12	chr6:15675176-15675226	H1-hESC	embryonic stem cell:	embryo
13	chr6:15691717-15691767	U87	brain:	n/a
14	chr6:15663468-15663518	HEK293	kidney:	embryo
15	chr6:15663344-15663394	SK-N-SH_RA	brain:	n/a
16	chr6:15663024-15663074	HUVEC	blood vessel:	n/a
17	chr6:15691800-15691850	K562	blood:	n/a
18	chr6:15663024-15663074	ovcar-3	ovarian:	n/a
19	chr6:15691800-15691850	HUVEC	blood vessel:	n/a
20	chr6:15663448-15663498	GM19239	blood:	n/a
21	chr6:15664231-15664281	NT2-D1	testis:	n/a
22	chr6:15663344-15663394	U87	brain:	n/a
23	chr6:15663170-15663220	MCF-7	breast:	n/a
24	chr6:15727374-15727424	MCF10A-Er-Src	breast:	n/a
25	chr6:15666243-15666293	GM12878	blood:	n/a
26	chr6:15663134-15663184	NH-A	brain:	n/a
27	chr6:15663501-15663551	HAEpiC	amniotic membrane:	n/a
28	chr6:15663134-15663184	HCPEpiC	choroid plexus:	n/a
29	chr6:15663356-15663406	SAEC	small airway:	n/a
30	chr6:15727374-15727424	NH-A	brain:	n/a
31	chr6:15663344-15663394	MCF-7	breast:	n/a
32	chr6:15662707-15662757	AG09309	skin:	n/a
33	chr6:15629162-15629212	U87	brain:	n/a
34	chr6:15663448-15663498	HNPCEpiC	eye:	n/a
35	chr6:15691258-15691308	SK-N-MC	brain:	n/a
36	chr6:15727374-15727424	AG04450	lung:	fetal
37	chr6:15727374-15727424	HCT-116	colon:	n/a
38	chr6:15691258-15691308	Jurkat	blood:	n/a
39	chr6:15663134-15663184	PrEC	prostate:	n/a
40	chr6:15675176-15675226	U87	brain:	n/a
41	chr6:15663360-15663410	BJ	skin:	n/a
42	chr6:15663468-15663518	Caco-2	colon:	n/a
43	chr6:15691705-15691755	HEEpiC	esophagus:	n/a
44	chr6:15675176-15675226	NH-A	brain:	n/a
45	chr6:15691800-15691850	GM19239	blood:	n/a
46	chr6:15691800-15691850	PrEC	prostate:	n/a
47	chr6:15663442-15663492	BJ	skin:	n/a
48	chr6:15663501-15663551	IMR90	lung:	fetal
49	chr6:15663134-15663184	AG10803	skin:	n/a
50	chr6:15663442-15663492	Jurkat	blood:	n/a

(count:168 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr6:15691141..15692187-chr6:16128576..16130145,22	MCF-7	breast:
2	chr6:15648890..15651570-chr6:15661615..15664723,3	K562	blood:
3	chr6:15678420..15680634-chr6:15684808..15686738,2	K562	blood:
4	chr6:15657500..15659223-chr6:15666722..15668599,2	K562	blood:
5	chr6:15676701..15679445-chr6:16128067..16130744,3	K562	blood:
6	chr6:15655170..15659272-chr6:15659508..15662983,5	MCF-7	breast:
7	chr6:15720658..15723365-chr6:15731775..15733502,2	K562	blood:
8	chr6:15652481..15654857-chr6:15657741..15659899,3	K562	blood:
9	chr6:15625351..15627546-chr6:16128970..16130700,2	K562	blood:
10	chr6:15676839..15679833-chr6:16153654..16155926,2	K562	blood:
11	chr6:15732987..15734688-chr6:16162557..16165293,2	K562	blood:
12	chr6:15668138..15670397-chr6:15673156..15674994,2	K562	blood:
13	chr6:15642319..15645214-chr6:15647219..15649863,3	K562	blood:
14	chr6:15729983..15731869-chr6:16128035..16130955,3	K562	blood:
15	chr6:15690815..15692594-chr6:16152230..16153735,2	K562	blood:
16	chr6:15704434..15705965-chr6:16129192..16132083,2	K562	blood:
17	chr6:15698629..15701193-chr6:15707870..15711464,3	K562	blood:
18	chr6:15682633..15685781-chr6:15685826..15688802,3	K562	blood:
19	chr6:15704050..15705965-chr6:16130583..16132835,2	K562	blood:
20	chr6:15660394..15662870-chr6:15679792..15681475,2	K562	blood:
21	chr6:15696979..15700313-chr6:15702500..15706211,4	K562	blood:
22	chr6:15631159..15634142-chr6:15637366..15640748,3	K562	blood:
23	chr6:15678420..15680634-chr6:15684808..15686738,2	K562	blood:
24	chr6:15688875..15695962-chr6:16127988..16134034,16	MCF-7	breast:
25	chr6:15628080..15630749-chr6:15690393..15693220,2	K562	blood:
26	chr6:15696754..15698975-chr6:15892314..15894571,2	K562	blood:
27	chr6:15667725..15669780-chr6:16137146..16139008,2	K562	blood:
28	chr6:15714362..15716528-chr6:15718042..15720964,2	MCF-7	breast:
29	chr6:15551863..15553566-chr6:15629613..15631115,2	K562	blood:
30	chr6:15689774..15693088-chr6:16205829..16209132,3	K562	blood:
31	chr6:15691584..15692147-chr6:16171307..16172061,2	MCF-7	breast:
32	chr6:15661124..15663645-chr6:15690658..15693451,3	K562	blood:
33	chr6:15701703..15703207-chr6:16129315..16131066,2	K562	blood:
34	chr6:15690946..15692172-chr6:16206408..16207438,18	K562	blood:
35	chr6:15699837..15703207-chr6:16128795..16131066,3	K562	blood:
36	chr6:15710538..15713074-chr6:16127901..16130794,2	MCF-7	breast:
37	chr6:15661311..15664347-chr6:16127901..16131243,6	K562	blood:
38	chr6:15642319..15645214-chr6:15647219..15649442,2	K562	blood:
39	chr6:15631602..15633808-chr6:16128378..16130825,3	K562	blood:
40	chr6:15686242..15688880-chr6:15691006..15692946,2	K562	blood:
41	chr6:15733392..15737807-chr6:16127623..16131334,6	K562	blood:
42	chr6:15676527..15678703-chr6:16128031..16129735,2	MCF-7	breast:
43	chr6:15244609..15248031-chr6:15625118..15627694,4	K562	blood:
44	chr6:15649452..15651058-chr6:15652747..15654421,2	K562	blood:
45	chr6:15646355..15648529-chr6:15650273..15652824,2	K562	blood:
46	chr6:15657500..15659223-chr6:15666722..15668599,2	K562	blood:
47	chr6:15682033..15684824-chr6:15685357..15687470,3	MCF-7	breast:
48	chr6:15689750..15690620-chr6:16183530..16184123,2	MCF-7	breast:
49	chr6:15681922..15683868-chr6:16145722..16147306,2	K562	blood:
50	chr6:15692594..15695303-chr6:15695960..15699366,3	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DTNBP1-1	chr6:15682235-15682336	XLOC_005620
2	lnc-DTNBP1-1	chr6:15674470-15675115	XLOC_005620
3	lnc-DTNBP1-2	chr6:15730473-15730763	XLOC_005621
4	lnc-DTNBP1-7	chr6:15708809-15709169	NONHSAT107877
5	lnc-DTNBP1-2	chr6:15730384-15730763	XLOC_005621
6	lnc-DTNBP1-7	chr6:15708733-15708781	NONHSAT107877
7	lnc-DTNBP1-2	chr6:15695349-15695670	XLOC_005621
8	lnc-DTNBP1-7	chr6:15725264-15726229	NONHSAT107877

No data

Variant related genes	Relation type
DTNBP1	TF binding region
DTNBP1	CpG island
ENSG00000047579	chromatin interactions
ENSG00000271888	chromatin interactions
ENSG00000008083	chromatin interactions
ENSG00000217078	chromatin interactions
ENSG00000007944	chromatin interactions
ENSG00000216364	chromatin interactions
ENSG00000263712	chromatin interactions
KPNA1	miRNA target sites

Extended variants
information (count: 3863 )
Associated
traits (count: 113 )

Variant overlapped rSNPs/rCNVs (count:3863 , 50 per page) page: 1 2 3 4 5 6 7 ... 78

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2743870	chr6:15624762-15624763	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs147791224	chr6:15624765-15624766	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs572689617	chr6:15624902-15624903	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs541609468	chr6:15624914-15624915	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs185521173	chr6:15624933-15624934	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs574707562	chr6:15624980-15624981	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs113725588	chr6:15625045-15625046	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs16876732	chr6:15625084-15625085	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs141246809	chr6:15625172-15625173	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs146927102	chr6:15625203-15625204	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs180812926	chr6:15625377-15625378	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs184915735	chr6:15625380-15625381	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs188510380	chr6:15625395-15625396	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs548471709	chr6:15625417-15625418	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs533166434	chr6:15625441-15625442	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs2743869	chr6:15625484-15625485	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs9396595	chr6:15625499-15625500	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs550275467	chr6:15625540-15625541	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs570196640	chr6:15625581-15625582	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs566765046	chr6:15625586-15625587	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs547802554	chr6:15625611-15625612	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs539025264	chr6:15625653-15625654	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs181718175	chr6:15625725-15625726	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs527634006	chr6:15625801-15625802	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs2743868	chr6:15625808-15625809	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs534973351	chr6:15625858-15625859	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs555266819	chr6:15625880-15625881	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs2743867	chr6:15625886-15625887	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs140882166	chr6:15625901-15625902	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs574371707	chr6:15625941-15625942	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs556630996	chr6:15625946-15625947	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs576579683	chr6:15625994-15625995	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs538307170	chr6:15625995-15625996	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs545889768	chr6:15626011-15626012	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs371183953	chr6:15626013-15626014	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs559043251	chr6:15626016-15626017	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs572808590	chr6:15626040-15626041	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs138645265	chr6:15626044-15626045	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs561988694	chr6:15626055-15626056	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs530707369	chr6:15626087-15626088	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs550833514	chr6:15626134-15626135	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs71533648	chr6:15626181-15626182	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs532452928	chr6:15626193-15626194	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs185889269	chr6:15626212-15626213	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs2743866	chr6:15626215-15626216	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs535048054	chr6:15626256-15626257	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs190348362	chr6:15626266-15626267	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs113568420	chr6:15626301-15626302	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs2743865	chr6:15626303-15626304	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs11962577	chr6:15626326-15626327	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:113)

Disease	PMID	Source
Cancer	20164920	CNVD
Colorectal cancer	21297112	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
small cell lung cancer	20016488	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Osteosarcoma	16790693	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17133270	CNVD
Autism	22495311	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Bladder cancer	21909424	CNVD
Burkitt''s lymphoma	19759907	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	17606441	CNVD
abnormal development	18461090	CNVD
Cancer	16790693	CNVD
Breast cancer	22032731	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21785460	CNVD
Bladder cancer	16790693	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Retinoblastoma	16790693	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17142309	CNVD
Digeorge syndrome	20186050	CNVD
velo-cardio-facial conotruncal-face syndrome	20186050	CNVD
Pancreatic cancer	17952125	CNVD
Urothelial cell carcinoma	18451213	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Ovarian cancer	20844748	CNVD
Developmental delay	19490664	CNVD
T-cell lymphomas	19863542	CNVD
Urothelial carcinoma	18382360	CNVD
Schizophrenia	22423091	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1679 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:15594000-15626600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr6:15597000-15641600	Weak transcription	Spleen	Spleen
3	chr6:15600000-15660400	Weak transcription	Hela-S3	cervix
4	chr6:15609000-15628200	Weak transcription	HSMM	muscle
5	chr6:15609600-15627400	Weak transcription	HUVEC	blood vessel
6	chr6:15610400-15626000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
7	chr6:15610600-15640200	Weak transcription	Aorta	Aorta
8	chr6:15611800-15641800	Weak transcription	Fetal Muscle Trunk	muscle
9	chr6:15614800-15641600	Weak transcription	Lung	lung
10	chr6:15615000-15652600	Weak transcription	Colonic Mucosa	Colon
11	chr6:15615200-15626000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr6:15615200-15626000	Weak transcription	Rectal Mucosa Donor 29	rectum
13	chr6:15615200-15641000	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr6:15615200-15642200	Weak transcription	Thymus	Thymus
15	chr6:15615200-15662200	Weak transcription	Gastric	stomach
16	chr6:15615400-15628800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
17	chr6:15615400-15643000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
18	chr6:15615600-15626600	Weak transcription	Primary T helper cells fromperipheralblood	blood
19	chr6:15615600-15639000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
20	chr6:15616800-15630200	Weak transcription	HepG2	liver
21	chr6:15616800-15631800	Weak transcription	Sigmoid Colon	Sigmoid Colon
22	chr6:15616800-15632000	Weak transcription	Esophagus	oesophagus
23	chr6:15616800-15638600	Weak transcription	Psoas Muscle	Psoas
24	chr6:15616800-15662000	Weak transcription	Placenta	Placenta
25	chr6:15616800-15662200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr6:15617000-15626000	Weak transcription	Duodenum Mucosa	Duodenum
27	chr6:15617000-15631400	Weak transcription	Fetal Intestine Large	intestine
28	chr6:15618800-15626200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
29	chr6:15621000-15627800	Weak transcription	Fetal Brain Female	brain
30	chr6:15621800-15662200	Weak transcription	Pancreas	Pancrea
31	chr6:15622000-15626000	Enhancers	Pancreatic Islets	Pancreatic Islet
32	chr6:15622000-15628800	Weak transcription	Fetal Stomach	stomach
33	chr6:15622200-15625200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr6:15622200-15625600	Weak transcription	Primary B cells from peripheral blood	blood
35	chr6:15622200-15626200	Weak transcription	Fetal Thymus	thymus
36	chr6:15622200-15627000	Weak transcription	Ovary	ovary
37	chr6:15622200-15627600	Weak transcription	Cortex derived primary cultured neurospheres	brain
38	chr6:15622200-15628200	Weak transcription	NHLF	lung
39	chr6:15622200-15632000	Weak transcription	Fetal Intestine Small	intestine
40	chr6:15622200-15637800	Weak transcription	Small Intestine	intestine
41	chr6:15622200-15638800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
42	chr6:15622200-15641000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr6:15622200-15641600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr6:15622200-15641800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr6:15622200-15643600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
46	chr6:15622200-15649200	Weak transcription	Skeletal Muscle Female	skeletal muscle
47	chr6:15622400-15625400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chr6:15622400-15627200	Weak transcription	Osteobl	bone
49	chr6:15622400-15627400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr6:15622800-15627400	Weak transcription	Muscle Satellite Cultured Cells	--

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