Variant report

Variant	nsv886769
Chromosome Location	chr6:150346037-150364009
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:174)
CpG islands
(count:1221)
Chromatin interactive
region (count:9)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:174 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr6:150346621-150346888	GM12878	blood:	n/a	chr6:150346723-150346734 chr6:150346728-150346738 chr6:150346724-150346734
2	CEBPB	chr6:150349144-150349326	HepG2	liver:	n/a	n/a
3	CEBPB	chr6:150353985-150354064	HepG2	liver:	n/a	n/a
4	CEBPB	chr6:150346556-150346899	Hela-S3	cervix:	n/a	n/a
5	CHD2	chr6:150346552-150346904	Hela-S3	cervix:	n/a	n/a
6	CTCF	chr6:150359484-150359715	A549	lung:	n/a	n/a
7	CTCF	chr6:150359560-150359710	SAEC	small airway:	n/a	n/a
8	CTCF	chr6:150359537-150359747	MCF-7	breast:	n/a	n/a
9	CTCF	chr6:150359580-150359730	HEEpiC	esophagus:	n/a	n/a
10	CTCF	chr6:150359560-150359710	HEEpiC	esophagus:	n/a	n/a
11	CTCF	chr6:150351936-150351995	GM13977	blood:	n/a	n/a
12	CTCF	chr6:150359560-150359710	HEK293	kidney:	n/a	n/a
13	CTCF	chr6:150361681-150361729	Medullo	brain:	n/a	n/a
14	CTCF	chr6:150347740-150347890	HEK293	kidney:	n/a	n/a
15	CTCF	chr6:150359606-150359665	Spleen_OC	spleen:	n/a	n/a
16	CTCF	chr6:150359519-150359751	Fibrobl	skin:	n/a	n/a
17	CTCF	chr6:150346500-150346650	HCPEpiC	choroid plexus:	n/a	n/a
18	CTCF	chr6:150350200-150350350	GM12866	blood:	n/a	n/a
19	CTCF	chr6:150359515-150359753	MCF-7	breast:	n/a	n/a
20	CTCF	chr6:150359580-150359730	NHEK	skin:	n/a	n/a
21	CTCF	chr6:150359529-150359665	A549	lung:	n/a	n/a
22	CTCF	chr6:150359587-150359677	Pancreas_OC	pancreas:	n/a	n/a
23	CTCF	chr6:150359560-150359710	HRE	kidney:	n/a	n/a
24	CTCF	chr6:150359508-150359813	K562	blood:	n/a	n/a
25	CTCF	chr6:150359544-150359746	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr6:150359523-150359749	K562	blood:	n/a	n/a
27	CTCF	chr6:150359580-150359730	SAEC	small airway:	n/a	n/a
28	CTCF	chr6:150359545-150359689	GM19239	blood:	n/a	n/a
29	CTCF	chr6:150359513-150359751	Gliobla	brain:	n/a	n/a
30	CTCF	chr6:150359528-150359745	MCF-7	breast:	n/a	n/a
31	CTCF	chr6:150359521-150359738	MCF-7	breast:	n/a	n/a
32	CTCF	chr6:150359532-150359729	HUVEC	blood vessel:	n/a	n/a
33	CTCF	chr6:150359560-150359710	AG04449	skin:	n/a	n/a
34	CTCF	chr6:150359526-150359711	GM12892	blood:	n/a	n/a
35	CTCF	chr6:150359526-150359748	GM12878	blood:	n/a	n/a
36	CTCF	chr6:150359574-150359739	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr6:150359541-150359719	HepG2	liver:	n/a	n/a
38	CTCF	chr6:150359600-150359750	NHEK	skin:	n/a	n/a
39	CTCF	chr6:150359528-150359736	ProgFib	skin:	n/a	n/a
40	CTCF	chr6:150359600-150359750	HMEC	breast:	n/a	n/a
41	CTCF	chr6:150359571-150359716	GM19240	blood:	n/a	n/a
42	CTCF	chr6:150359524-150359750	A549	lung:	n/a	n/a
43	CTCF	chr6:150359566-150359568	GM19240	blood:	n/a	n/a
44	CTCF	chr6:150359500-150359650	HPAF	blood vessel:	n/a	n/a
45	CTCF	chr6:150347680-150347830	HRE	kidney:	n/a	n/a
46	CTCF	chr6:150359533-150359722	GM19238	blood:	n/a	n/a
47	CTCF	chr6:150359509-150359772	K562	blood:	n/a	n/a
48	CTCF	chr6:150359524-150359720	GM12891	blood:	n/a	n/a
49	CTCF	chr6:150359514-150359748	MCF-7	breast:	n/a	n/a
50	CTCF	chr6:150359506-150359763	NHEK	skin:	n/a	n/a

(count:1221 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:150359130-150359180	ovcar-3	ovarian:	n/a
2	chr6:150359130-150359180	ovcar-3	ovarian:	n/a
3	chr6:150359383-150359433	HRPEpiC	eye:	n/a
4	chr6:150346721-150346771	HL-60	blood:	n/a
5	chr6:150346787-150346837	NHDF-neo	bronchial:	n/a
6	chr6:150346863-150346913	K562	blood:	n/a
7	chr6:150362502-150362552	HEK293	kidney:	embryo
8	chr6:150346800-150346850	AG09319	gingival:	n/a
9	chr6:150359130-150359180	PrEC	prostate:	n/a
10	chr6:150347012-150347062	LNCaP	prostate:	n/a
11	chr6:150346816-150346866	U87	brain:	n/a
12	chr6:150362502-150362552	HRPEpiC	eye:	n/a
13	chr6:150347012-150347062	H1-hESC	embryonic stem cell:	embryo
14	chr6:150362502-150362552	HNPCEpiC	eye:	n/a
15	chr6:150356698-150356748	SK-N-SH_RA	brain:	n/a
16	chr6:150346886-150346936	HRCEpiC	kidney:	n/a
17	chr6:150358873-150358923	NT2-D1	testis:	n/a
18	chr6:150360829-150360879	Hepatocyte	liver:	n/a
19	chr6:150346816-150346866	ProgFib	skin:	n/a
20	chr6:150347053-150347103	SK-N-SH	brain:	n/a
21	chr6:150359383-150359433	LNCaP	prostate:	n/a
22	chr6:150359130-150359180	RPTEC	kidney:	n/a
23	chr6:150346497-150346547	HCF	heart:	n/a
24	chr6:150362502-150362552	SAEC	small airway:	n/a
25	chr6:150362502-150362552	Hepatocyte	liver:	n/a
26	chr6:150358873-150358923	SK-N-SH_RA	brain:	n/a
27	chr6:150346863-150346913	MCF10A-Er-Src	breast:	n/a
28	chr6:150346721-150346771	HRPEpiC	eye:	n/a
29	chr6:150358985-150359035	AG09319	gingival:	n/a
30	chr6:150346886-150346936	HCM	heart:	n/a
31	chr6:150346863-150346913	GM12891	blood:	n/a
32	chr6:150346816-150346866	AG04449	skin:	fetal
33	chr6:150358873-150358923	SKMC	muscle:	n/a
34	chr6:150347053-150347103	H1-hESC	embryonic stem cell:	embryo
35	chr6:150358873-150358923	Hepatocyte	liver:	n/a
36	chr6:150346800-150346850	Hela-S3	cervix:	n/a
37	chr6:150346721-150346771	SK-N-SH_RA	brain:	n/a
38	chr6:150347012-150347062	HCF	heart:	n/a
39	chr6:150346800-150346850	HCF	heart:	n/a
40	chr6:150346921-150346971	MCF10A-Er-Src	breast:	n/a
41	chr6:150360829-150360879	AG04450	lung:	fetal
42	chr6:150347053-150347103	GM12891	blood:	n/a
43	chr6:150360829-150360879	AG04449	skin:	fetal
44	chr6:150358873-150358923	HCT-116	colon:	n/a
45	chr6:150346800-150346850	PrEC	prostate:	n/a
46	chr6:150358985-150359035	H1-hESC	embryonic stem cell:	embryo
47	chr6:150360829-150360879	H1-hESC	embryonic stem cell:	embryo
48	chr6:150346497-150346547	LNCaP	prostate:	n/a
49	chr6:150346721-150346771	SAEC	small airway:	n/a
50	chr6:150346886-150346936	HCT-116	colon:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:150354931..150357925-chr6:150386556..150388661,2	K562	blood:
2	chr6:150351052..150353254-chr6:150355645..150357982,2	K562	blood:
3	chr6:150155381..150157771-chr6:150346025..150347800,2	MCF-7	breast:
4	chr6:150351052..150353254-chr6:150355645..150357982,2	K562	blood:
5	chr6:150261749..150263311-chr6:150348518..150350047,2	MCF-7	breast:
6	chr6:150350371..150352271-chr6:150387708..150390265,2	MCF-7	breast:
7	chr6:150355810..150358323-chr6:150360175..150362251,2	K562	blood:
8	chr6:150354901..150357527-chr6:150362159..150364156,2	MCF-7	breast:
9	chr6:150355810..150358323-chr6:150360175..150362251,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ULBP1-2	chr6:150354375-150354702	NONHSAT115530
2	lnc-RAET1L-1	chr6:150361683-150362309	XLOC_005876
3	lnc-ULBP1-2	chr6:150353905-150354172	NONHSAT115530
4	lnc-RAET1L-1	chr6:150362917-150363169	XLOC_005876

No data

Variant related genes	Relation type
PHBP1	TF binding region
RAET1L	TF binding region
RAET1M	TF binding region
ENSG00000235972	TF binding region
PHBP1	CpG island
RAET1L	CpG island
RAET1M	CpG island
ENSG00000235972	CpG island
ENSG00000131015	chromatin interactions
ENSG00000131019	chromatin interactions
ENSG00000120256	chromatin interactions
ENSG00000213091	chromatin interactions
ENSG00000235972	chromatin interactions
WDR11	miRNA target sites
INTS6	miRNA target sites

Extended variants
information (count: 739 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:739 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6907188	chr6:150346037-150346038	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs189185720	chr6:150346066-150346067	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs530471559	chr6:150346075-150346076	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs550740015	chr6:150346086-150346087	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs564064107	chr6:150346088-150346089	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs565397835	chr6:150346190-150346191	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs532968589	chr6:150346194-150346195	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs371682659	chr6:150346196-150346197	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs371691600	chr6:150346197-150346198	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs56761194	chr6:150346211-150346212	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs79206040	chr6:150346234-150346235	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs139206728	chr6:150346288-150346289	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs549145819	chr6:150346316-150346317	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs568987037	chr6:150346323-150346324	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs537147147	chr6:150346327-150346328	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs557044046	chr6:150346334-150346335	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs149528530	chr6:150346335-150346336	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs539468950	chr6:150346408-150346409	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs114811584	chr6:150346424-150346425	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs117522681	chr6:150346440-150346441	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs116975750	chr6:150346446-150346447	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs181884687	chr6:150346460-150346461	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs144066641	chr6:150346472-150346473	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs544284619	chr6:150346492-150346493	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs564174948	chr6:150346497-150346498	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs201140566	chr6:150346504-150346505	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs546637938	chr6:150346511-150346512	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs142930646	chr6:150346524-150346525	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs377737907	chr6:150346525-150346526	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs117766916	chr6:150346529-150346530	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs1543547	chr6:150346532-150346533	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs200401216	chr6:150346542-150346543	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs199585067	chr6:150346545-150346546	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs537650384	chr6:150346547-150346548	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs199713884	chr6:150346553-150346554	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs202054834	chr6:150346560-150346561	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs200535107	chr6:150346566-150346567	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs376111192	chr6:150346596-150346597	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs141551402	chr6:150346607-150346608	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs377165514	chr6:150346639-150346640	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs374975536	chr6:150346644-150346645	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs553308843	chr6:150346659-150346660	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs1544123	chr6:150346740-150346741	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs536136417	chr6:150346787-150346788	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs555796647	chr6:150346808-150346809	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs140497742	chr6:150346825-150346826	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs369726715	chr6:150346826-150346827	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs144356849	chr6:150346843-150346844	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs564135884	chr6:150346863-150346864	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs114722136	chr6:150346881-150346882	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
Autism	22495311	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
Melanoma	18172304	CNVD
Cancer	21637783	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
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	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
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Soft tissue tumor	16732325	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
Cancer	17160897	CNVD
Breast cancer	17417639	CNVD
Breast cancer	17850661	CNVD
Renal cell carcinoma	18765545	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Ovarian neoplasms	16753589	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20556506	CNVD
Hirschsprung''s Disease	21712996	CNVD
Testicular germ cell tumor	18059402	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:471 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:150345800-150346200	Enhancers	HMEC	breast
2	chr6:150345800-150346400	Enhancers	Hela-S3	cervix
3	chr6:150345800-150346600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr6:150345800-150346800	Enhancers	Lung	lung
5	chr6:150345800-150347000	Enhancers	Gastric	stomach
6	chr6:150345800-150347000	Bivalent Enhancer	Stomach Mucosa	stomach
7	chr6:150345800-150347200	Flanking Active TSS	Esophagus	oesophagus
8	chr6:150345800-150347400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
9	chr6:150346000-150346200	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
10	chr6:150346000-150346200	Enhancers	NHEK	skin
11	chr6:150346000-150346400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr6:150346000-150346400	Bivalent Enhancer	Colonic Mucosa	Colon
13	chr6:150346000-150346400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
14	chr6:150346000-150346600	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
15	chr6:150346000-150346800	Bivalent Enhancer	Fetal Stomach	stomach
16	chr6:150346000-150347000	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr6:150346000-150347400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr6:150346000-150348200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr6:150346200-150346400	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr6:150346200-150346400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr6:150346200-150346400	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
22	chr6:150346200-150346400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr6:150346200-150346400	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
24	chr6:150346200-150346400	Bivalent Enhancer	Adipose Nuclei	Adipose
25	chr6:150346200-150346400	Bivalent Enhancer	Brain Hippocampus Middle	brain
26	chr6:150346200-150346400	Flanking Bivalent TSS/Enh	Colon Smooth Muscle	Colon
27	chr6:150346200-150346400	Bivalent Enhancer	Fetal Thymus	thymus
28	chr6:150346200-150346400	Bivalent Enhancer	Right Ventricle	heart
29	chr6:150346200-150346400	Enhancers	NH-A	brain
30	chr6:150346200-150346400	Bivalent Enhancer	Osteobl	bone
31	chr6:150346200-150346600	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr6:150346200-150346600	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr6:150346200-150346600	Bivalent Enhancer	Rectal Mucosa Donor 29	rectum
34	chr6:150346200-150346800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
35	chr6:150346200-150346800	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
36	chr6:150346200-150346800	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
37	chr6:150346200-150346800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr6:150346200-150346800	Bivalent Enhancer	Brain Germinal Matrix	brain
39	chr6:150346200-150346800	Bivalent Enhancer	Fetal Muscle Leg	muscle
40	chr6:150346200-150346800	Enhancers	Ovary	ovary
41	chr6:150346200-150346800	Bivalent Enhancer	Spleen	Spleen
42	chr6:150346200-150347000	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
43	chr6:150346200-150347000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
44	chr6:150346200-150347000	Bivalent Enhancer	Placenta	Placenta
45	chr6:150346200-150347000	Enhancers	Placenta Amnion	Placenta Amnion
46	chr6:150346200-150347200	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
47	chr6:150346200-150347200	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
48	chr6:150346200-150347200	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
49	chr6:150346200-150347200	Flanking Active TSS	HMEC	breast
50	chr6:150346200-150347400	Bivalent Enhancer	Primary B cells from peripheral blood	blood

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