Variant report

Variant	nsv886312
Chromosome Location	chr6:81166178-81309481
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1117)
CpG islands
(count:244)
Chromatin interactive
region (count:21)
LncRNA
region (count:30)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1117 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:81218332-81219179	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:81233387-81233833	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:81213448-81213851	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:81236915-81238174	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:81178014-81178558	HepG2	liver:	n/a	n/a
6	BACH1	chr6:81233340-81233540	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr6:81197933-81198186	GM12878	blood:	n/a	n/a
8	BATF	chr6:81250971-81251188	GM12878	blood:	n/a	n/a
9	BCL3	chr6:81253516-81253752	GM12878	blood:	n/a	n/a
10	BHLHE40	chr6:81218529-81218978	HepG2	liver:	n/a	n/a
11	BHLHE40	chr6:81236966-81237738	HepG2	liver:	n/a	n/a
12	BHLHE40	chr6:81213410-81213759	HepG2	liver:	n/a	n/a
13	BRCA1	chr6:81259042-81259178	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr6:81250843-81251214	Hela-S3	cervix:	n/a	n/a
15	CBX3	chr6:81245604-81246020	HCT-116	colon:	n/a	n/a
16	CBX3	chr6:81250692-81251437	HCT-116	colon:	n/a	n/a
17	CBX3	chr6:81233225-81233635	HCT-116	colon:	n/a	n/a
18	CEBPB	chr6:81237197-81237687	A549	lung:	n/a	chr6:81237484-81237495 chr6:81237484-81237497
19	CEBPB	chr6:81218525-81218986	HepG2	liver:	n/a	chr6:81218792-81218801 chr6:81218790-81218801 chr6:81218792-81218803
20	CEBPB	chr6:81218601-81218983	HepG2	liver:	n/a	chr6:81218792-81218801 chr6:81218790-81218801 chr6:81218792-81218803
21	CEBPB	chr6:81250908-81251217	IMR90	lung:	n/a	n/a
22	CEBPB	chr6:81237147-81237743	HepG2	liver:	n/a	chr6:81237484-81237495 chr6:81237484-81237497
23	CEBPB	chr6:81218608-81218987	IMR90	lung:	n/a	chr6:81218792-81218801 chr6:81218790-81218801 chr6:81218792-81218803
24	CEBPB	chr6:81250767-81251382	HCT-116	colon:	n/a	n/a
25	CEBPB	chr6:81218665-81218957	K562	blood:	n/a	chr6:81218792-81218801 chr6:81218790-81218801 chr6:81218792-81218803
26	CEBPB	chr6:81258155-81258675	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr6:81218637-81218947	H1-hESC	embryonic stem cell:	n/a	chr6:81218792-81218801 chr6:81218790-81218801 chr6:81218792-81218803
28	CEBPB	chr6:81244256-81244456	HepG2	liver:	n/a	chr6:81244327-81244338
29	CEBPB	chr6:81189440-81189640	A549	lung:	n/a	n/a
30	CEBPB	chr6:81213464-81213792	HepG2	liver:	n/a	n/a
31	CEBPB	chr6:81237124-81237773	MCF-7	breast:	n/a	chr6:81237484-81237495 chr6:81237484-81237497
32	CEBPB	chr6:81239940-81240112	A549	lung:	n/a	chr6:81240005-81240017 chr6:81240074-81240086
33	CEBPB	chr6:81212628-81212986	ECC-1	luminal epithelium:	n/a	n/a
34	CEBPB	chr6:81218608-81218976	Hela-S3	cervix:	n/a	chr6:81218792-81218801 chr6:81218790-81218801 chr6:81218792-81218803
35	CEBPB	chr6:81258297-81258625	IMR90	lung:	n/a	n/a
36	CEBPB	chr6:81237325-81237627	HepG2	liver:	n/a	chr6:81237484-81237495 chr6:81237484-81237497
37	CEBPB	chr6:81186095-81186341	HepG2	liver:	n/a	chr6:81186178-81186189
38	CEBPB	chr6:81241001-81241238	HepG2	liver:	n/a	chr6:81241131-81241144 chr6:81241131-81241142 chr6:81241133-81241144 chr6:81241131-81241144 chr6:81241168-81241179
39	CEBPB	chr6:81233344-81233544	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr6:81230052-81230378	IMR90	lung:	n/a	chr6:81230255-81230266
41	CEBPB	chr6:81167034-81167365	MCF-7	breast:	n/a	chr6:81167259-81167267
42	CEBPB	chr6:81169728-81170059	HepG2	liver:	n/a	chr6:81169948-81169965 chr6:81169951-81169962 chr6:81169953-81169964 chr6:81169951-81169964
43	CEBPB	chr6:81237374-81237607	A549	lung:	n/a	chr6:81237484-81237495 chr6:81237484-81237497
44	CEBPB	chr6:81169761-81170098	IMR90	lung:	n/a	chr6:81169948-81169965 chr6:81169951-81169962 chr6:81169953-81169964 chr6:81169951-81169964
45	CEBPB	chr6:81166932-81167493	IMR90	lung:	n/a	chr6:81167259-81167267
46	CEBPB	chr6:81218543-81219039	MCF-7	breast:	n/a	chr6:81218792-81218801 chr6:81218790-81218801 chr6:81218792-81218803
47	CEBPB	chr6:81218495-81219018	MCF-7	breast:	n/a	chr6:81218792-81218801 chr6:81218790-81218801 chr6:81218792-81218803
48	CEBPB	chr6:81283814-81284092	HepG2	liver:	n/a	n/a
49	CEBPB	chr6:81237352-81237661	HepG2	liver:	n/a	chr6:81237484-81237495 chr6:81237484-81237497
50	CEBPB	chr6:81237204-81237773	MCF-7	breast:	n/a	chr6:81237484-81237495 chr6:81237484-81237497

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:81233028-81233078	IMR90	lung:	fetal
2	chr6:81233028-81233078	HRPEpiC	eye:	n/a
3	chr6:81233028-81233078	H1-hESC	embryonic stem cell:	embryo
4	chr6:81259014-81259064	HepG2	liver:	n/a
5	chr6:81283368-81283418	ECC-1	luminal epithelium:	n/a
6	chr6:81259014-81259064	HEK293	kidney:	embryo
7	chr6:81252663-81252713	ECC-1	luminal epithelium:	n/a
8	chr6:81283368-81283418	NB4	blood:	n/a
9	chr6:81252663-81252713	AG04450	lung:	fetal
10	chr6:81233028-81233078	HCM	heart:	n/a
11	chr6:81252663-81252713	NT2-D1	testis:	n/a
12	chr6:81233028-81233078	K562	blood:	n/a
13	chr6:81259014-81259064	HPAEpiC	pulmonary alveolar:	n/a
14	chr6:81259014-81259064	SK-N-SH	brain:	n/a
15	chr6:81233028-81233078	AG04449	skin:	fetal
16	chr6:81283368-81283418	HCT-116	colon:	n/a
17	chr6:81233028-81233078	HRCEpiC	kidney:	n/a
18	chr6:81283368-81283418	PANC-1	pancreas:	n/a
19	chr6:81259014-81259064	NH-A	brain:	n/a
20	chr6:81259014-81259064	RPTEC	kidney:	n/a
21	chr6:81252663-81252713	ProgFib	skin:	n/a
22	chr6:81252663-81252713	GM06990	blood:	n/a
23	chr6:81259014-81259064	NB4	blood:	n/a
24	chr6:81283368-81283418	MCF10A-Er-Src	breast:	n/a
25	chr6:81252663-81252713	SK-N-SH_RA	brain:	n/a
26	chr6:81259014-81259064	BJ	skin:	n/a
27	chr6:81283368-81283418	PFSK-1	brain:	n/a
28	chr6:81233028-81233078	SK-N-SH	brain:	n/a
29	chr6:81252663-81252713	HAEpiC	amniotic membrane:	n/a
30	chr6:81283368-81283418	T-47D	breast:	n/a
31	chr6:81233028-81233078	AG10803	skin:	n/a
32	chr6:81252663-81252713	PFSK-1	brain:	n/a
33	chr6:81233028-81233078	AG04450	lung:	fetal
34	chr6:81233028-81233078	AG09319	gingival:	n/a
35	chr6:81283368-81283418	Jurkat	blood:	n/a
36	chr6:81233028-81233078	HUVEC	blood vessel:	n/a
37	chr6:81259014-81259064	SAEC	small airway:	n/a
38	chr6:81283368-81283418	AoSMC	blood vessel:	n/a
39	chr6:81233028-81233078	SAEC	small airway:	n/a
40	chr6:81283368-81283418	BJ	skin:	n/a
41	chr6:81259014-81259064	HRPEpiC	eye:	n/a
42	chr6:81252663-81252713	PrEC	prostate:	n/a
43	chr6:81259014-81259064	HRE	kidney:	n/a
44	chr6:81259014-81259064	MCF-7	breast:	n/a
45	chr6:81259014-81259064	MCF10A-Er-Src	breast:	n/a
46	chr6:81283368-81283418	RPTEC	kidney:	n/a
47	chr6:81233028-81233078	HEEpiC	esophagus:	n/a
48	chr6:81283368-81283418	K562	blood:	n/a
49	chr6:81233028-81233078	GM12878	blood:	n/a
50	chr6:81252663-81252713	HNPCEpiC	eye:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:81244830..81247376-chr6:81252160..81253797,2	MCF-7	breast:
2	chr6:81168885..81171049-chr6:81175786..81177907,2	MCF-7	breast:
3	chr6:81213174..81214838-chr6:81216651..81219122,2	MCF-7	breast:
4	chr6:81260471..81262004-chr6:81266433..81268034,2	MCF-7	breast:
5	chr6:81047988..81048553-chr6:81186140..81186935,2	MCF-7	breast:
6	chr16:28172997..28173848-chr6:81237133..81237839,2	MCF-7	breast:
7	chr6:81254930..81257563-chr6:81262833..81265650,2	K562	blood:
8	chr6:81249220..81251616-chr6:81254290..81256470,2	MCF-7	breast:
9	chr6:80924251..80924826-chr6:81185969..81186765,2	MCF-7	breast:
10	chr6:81266263..81267805-chr6:81274227..81276426,2	MCF-7	breast:
11	chr6:81264062..81265646-chr6:81268549..81270670,2	MCF-7	breast:
12	chr6:81298968..81300811-chr6:81302050..81303773,2	MCF-7	breast:
13	chr6:81264062..81265646-chr6:81268549..81270670,2	MCF-7	breast:
14	chr6:81159444..81161746-chr6:81166176..81167812,2	MCF-7	breast:
15	chr6:81244830..81247376-chr6:81252160..81253797,2	MCF-7	breast:
16	chr6:81298968..81300811-chr6:81302050..81303773,2	MCF-7	breast:
17	chr6:81213174..81214838-chr6:81216651..81219122,2	MCF-7	breast:
18	chr6:80843054..80844740-chr6:81198148..81200503,2	MCF-7	breast:
19	chr6:81249220..81251616-chr6:81254290..81256470,2	MCF-7	breast:
20	chr6:81047651..81048631-chr6:81237581..81238534,2	MCF-7	breast:
21	chr6:81254930..81257563-chr6:81262833..81265650,2	K562	blood:

(count:30 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ELOVL4-3	chr6:81179788-81180145	NONHSAT113735
2	lnc-BCKDHB-7	chr6:81219593-81219697	NONHSAT113737
3	lnc-BCKDHB-7	chr6:81232183-81232291	NONHSAT113738
4	lnc-BCKDHB-7	chr6:81219570-81219697	NONHSAT113738
5	lnc-BCKDHB-7	chr6:81220546-81220756	NONHSAT113738
6	lnc-BCKDHB-1	chr6:81172589-81172770	ENSG00000233967.2
7	lnc-BCKDHB-7	chr6:81220546-81220756	NONHSAT113739
8	lnc-BCKDHB-1	chr6:81172589-81172871	NONHSAT113727
9	lnc-BCKDHB-1	chr6:81172589-81172789	XLOC_005365
10	lnc-BCKDHB-1	chr6:81172589-81172878	XLOC_005365
11	lnc-BCKDHB-1	chr6:81172589-81172789	XLOC_005365
12	lnc-BCKDHB-7	chr6:81209780-81209974	NONHSAT113737
13	lnc-BCKDHB-7	chr6:81229308-81229643	NONHSAT113739
14	lnc-BCKDHB-1	chr6:81175464-81175644	XLOC_005365
15	lnc-BCKDHB-1	chr6:81172589-81172632	XLOC_005365
16	lnc-BCKDHB-7	chr6:81229427-81229502	l_3211_chr6:81209944-81229502_76bGuttman_hES
17	lnc-BCKDHB-7	chr6:81209892-81209974	NONHSAT113739
18	lnc-BCKDHB-2	chr6:81176675-81178797	ENSG00000260645.1
19	lnc-BCKDHB-7	chr6:81232183-81232363	NONHSAT113737
20	lnc-BCKDHB-7	chr6:81220546-81220626	l_3211_chr6:81209944-81229502_76bGuttman_hES
21	lnc-BCKDHB-7	chr6:81209892-81209974	NONHSAT113738
22	lnc-BCKDHB-7	chr6:81229308-81229508	NONHSAT113737
23	lnc-BCKDHB-1	chr6:81172589-81172924	ENSG00000233967.2
24	lnc-BCKDHB-1	chr6:81172589-81172913	XLOC_005365
25	lnc-BCKDHB-1	chr6:81175464-81175572	XLOC_005365
26	lnc-BCKDHB-7	chr6:81219593-81219697	l_3211_chr6:81209944-81229502_76bGuttman_hES
27	lnc-BCKDHB-7	chr6:81209945-81209974	l_3211_chr6:81209944-81229502_76bGuttman_hES
28	lnc-BCKDHB-1	chr6:81172589-81172924	XLOC_005365
29	lnc-BCKDHB-7	chr6:81219570-81219697	NONHSAT113739
30	lnc-BCKDHB-7	chr6:81229308-81229508	NONHSAT113738

No data

Variant related genes	Relation type
ENSG00000216352	TF binding region
ENSG00000260645	TF binding region
ENSG00000219361	TF binding region
ENSG00000181705	TF binding region
ENSG00000216352	CpG island
ENSG00000260645	CpG island
ENSG00000219361	CpG island
ENSG00000181705	CpG island
ENSG00000260645	chromatin interactions
ENSG00000216352	chromatin interactions
RABEP1	miRNA target sites
DNAJA1	miRNA target sites
CTDSPL	miRNA target sites

Extended variants
information (count: 4765 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:4765 , 50 per page) page: 1 2 3 4 5 6 7 ... 96

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13199780	chr6:81166178-81166179	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs559448575	chr6:81166198-81166199	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs73751649	chr6:81166238-81166239	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs188031740	chr6:81166263-81166264	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs565452451	chr6:81166267-81166268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs74692350	chr6:81166321-81166322	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs531219327	chr6:81166377-81166378	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs550920489	chr6:81166418-81166419	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs567516398	chr6:81166424-81166425	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs12660954	chr6:81166435-81166436	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs543370800	chr6:81166504-81166505	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs139718262	chr6:81166529-81166530	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs546785722	chr6:81166588-81166589	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs111901057	chr6:81166600-81166601	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs566579632	chr6:81166601-81166602	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs146185410	chr6:81166704-81166705	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs116491005	chr6:81166712-81166713	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs192129095	chr6:81166732-81166733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs144367066	chr6:81166794-81166795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs184720664	chr6:81166803-81166804	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs528533481	chr6:81166804-81166805	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs35413145	chr6:81166898-81166899	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs555833512	chr6:81166921-81166922	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs372169044	chr6:81166940-81166941	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs681085	chr6:81166952-81166953	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs542794562	chr6:81166957-81166958	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs146639171	chr6:81167063-81167064	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs572937798	chr6:81167081-81167082	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs541234603	chr6:81167141-81167142	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs188498874	chr6:81167243-81167244	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs531155229	chr6:81167244-81167245	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs559316833	chr6:81167368-81167369	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs148785279	chr6:81167404-81167405	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs561206839	chr6:81167415-81167416	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs191822320	chr6:81167445-81167446	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs115495612	chr6:81167457-81167458	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs369404287	chr6:81167475-81167476	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs117084041	chr6:81167485-81167486	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs505678	chr6:81167494-81167495	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs117642408	chr6:81167503-81167504	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs569233621	chr6:81167532-81167533	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs536987989	chr6:81167588-81167589	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs557294074	chr6:81167660-81167661	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs567537305	chr6:81167669-81167670	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs536463940	chr6:81167710-81167711	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs553187819	chr6:81167711-81167712	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs549658475	chr6:81167717-81167718	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs572880274	chr6:81167732-81167733	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs530530763	chr6:81167811-81167812	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs538722785	chr6:81167817-81167818	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:107)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	22495311	CNVD
Gastric cancer	17908304	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Follicular lymphoma	17699855	CNVD
Breast cancer	17133270	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Developmental delay	21147756	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Salivary gland tumor	18059337	CNVD
Lung cancer	16773561	CNVD
Glioblastoma multiforme	22286061	CNVD
Urothelial cell carcinoma	18451213	CNVD
Prostate cancer	16461572	CNVD
Mental retardation	21045960	CNVD
Obesity	21045960	CNVD
learning difficulties	21045960	CNVD
Prostate cancer	17245344	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Cancer	20164920	CNVD
Burkitt''s lymphoma	20823134	CNVD
Ductal carcinoma	22052326	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Tetralogy of Fallot	22912587	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:81156400-81166800	Weak transcription	Aorta	Aorta
2	chr6:81156400-81167000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr6:81156400-81167000	Weak transcription	Pancreas	Pancrea
4	chr6:81158000-81166400	Weak transcription	Liver	Liver
5	chr6:81162800-81166200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
6	chr6:81162800-81168400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr6:81162800-81168400	Enhancers	HMEC	breast
8	chr6:81163000-81179800	Weak transcription	Right Ventricle	heart
9	chr6:81163200-81166800	Weak transcription	Brain Hippocampus Middle	brain
10	chr6:81163200-81168200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr6:81163200-81169800	Weak transcription	Fetal Heart	heart
12	chr6:81163400-81166800	Weak transcription	Brain Angular Gyrus	brain
13	chr6:81163400-81167200	Weak transcription	Brain Cingulate Gyrus	brain
14	chr6:81163400-81168400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr6:81164200-81166200	Weak transcription	Duodenum Smooth Muscle	Duodenum
16	chr6:81164400-81166800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr6:81164400-81167000	Weak transcription	Ovary	ovary
18	chr6:81164600-81166800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr6:81164600-81166800	Weak transcription	Fetal Muscle Leg	muscle
20	chr6:81164600-81166800	Weak transcription	HSMMtube	muscle
21	chr6:81164600-81167000	Weak transcription	Duodenum Mucosa	Duodenum
22	chr6:81165000-81166400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr6:81165000-81166800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr6:81165000-81166800	Weak transcription	Stomach Mucosa	stomach
25	chr6:81165000-81166800	Weak transcription	HSMM	muscle
26	chr6:81165200-81166600	Weak transcription	Fetal Stomach	stomach
27	chr6:81165200-81166600	Weak transcription	Osteobl	bone
28	chr6:81165200-81166800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr6:81165200-81166800	Weak transcription	NH-A	brain
30	chr6:81165200-81167000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
31	chr6:81165200-81167200	Enhancers	HUVEC	blood vessel
32	chr6:81165400-81166400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr6:81165400-81166400	Weak transcription	NHDF-Ad	bronchial
34	chr6:81165400-81166600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr6:81165400-81166800	Weak transcription	Muscle Satellite Cultured Cells	--
36	chr6:81165600-81166800	Weak transcription	Placenta Amnion	Placenta Amnion
37	chr6:81165600-81166800	Weak transcription	Hela-S3	cervix
38	chr6:81165800-81166200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr6:81165800-81166200	Weak transcription	NHEK	skin
40	chr6:81165800-81166200	Weak transcription	NHLF	lung
41	chr6:81166200-81167400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr6:81166200-81168200	Enhancers	Duodenum Smooth Muscle	Duodenum
43	chr6:81166200-81168400	Enhancers	NHEK	skin
44	chr6:81166200-81168400	Enhancers	NHLF	lung
45	chr6:81166400-81166600	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
46	chr6:81166400-81167600	Enhancers	Stomach Smooth Muscle	stomach
47	chr6:81166400-81167800	Enhancers	Liver	Liver
48	chr6:81166400-81168200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr6:81166400-81168400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr6:81166400-81168400	Enhancers	NHDF-Ad	bronchial

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