Variant report

Variant	nsv884716
Chromosome Location	chr6:32223258-32278670
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:393)
CpG islands
(count:1465)
Chromatin interactive
region (count:16)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:393 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:32266393-32267029	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:32223063-32223297	K562	blood:	n/a	n/a
3	ARID3A	chr6:32255974-32256593	K562	blood:	n/a	n/a
4	ATF1	chr6:32256293-32256538	K562	blood:	n/a	n/a
5	ATF2	chr6:32222882-32223504	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr6:32222903-32223396	K562	blood:	n/a	chr6:32223031-32223040
7	BACH1	chr6:32271978-32272098	K562	blood:	n/a	n/a
8	BACH1	chr6:32222680-32223331	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr6:32222956-32223318	GM12878	blood:	n/a	chr6:32223142-32223153 chr6:32223143-32223153
10	BCL3	chr6:32266417-32267156	A549	lung:	n/a	n/a
11	BRCA1	chr6:32222989-32223296	Hela-S3	cervix:	n/a	n/a
12	CBX3	chr6:32222859-32223833	K562	blood:	n/a	n/a
13	CBX3	chr6:32256247-32256605	K562	blood:	n/a	n/a
14	CCNT2	chr6:32256257-32256567	K562	blood:	n/a	n/a
15	CEBPB	chr6:32222869-32223431	A549	lung:	n/a	n/a
16	CEBPB	chr6:32222989-32223307	A549	lung:	n/a	n/a
17	CEBPB	chr6:32222939-32223352	MCF-7	breast:	n/a	n/a
18	CEBPB	chr6:32222804-32223535	HCT-116	colon:	n/a	n/a
19	CEBPB	chr6:32222955-32223320	A549	lung:	n/a	n/a
20	CEBPB	chr6:32223025-32223328	ECC-1	luminal epithelium:	n/a	n/a
21	CEBPB	chr6:32266776-32267032	HepG2	liver:	n/a	n/a
22	CEBPB	chr6:32222975-32223376	K562	blood:	n/a	n/a
23	CEBPB	chr6:32222945-32223319	IMR90	lung:	n/a	n/a
24	CEBPB	chr6:32266321-32266946	A549	lung:	n/a	chr6:32266507-32266519
25	CEBPB	chr6:32222929-32223377	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr6:32222898-32223290	K562	blood:	n/a	n/a
27	CEBPB	chr6:32266452-32266855	A549	lung:	n/a	chr6:32266507-32266519
28	CEBPD	chr6:32256147-32256663	K562	blood:	n/a	n/a
29	CEBPD	chr6:32256246-32256683	K562	blood:	n/a	n/a
30	CHD2	chr6:32223185-32223372	GM12878	blood:	n/a	n/a
31	CHD2	chr6:32222916-32223457	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr6:32223169-32223315	K562	blood:	n/a	n/a
33	CHD2	chr6:32222965-32223431	Hela-S3	cervix:	n/a	n/a
34	CTCF	chr6:32222761-32223487	A549	lung:	n/a	chr6:32223073-32223091 chr6:32223022-32223035 chr6:32223048-32223066 chr6:32223049-32223065
35	CTCF	chr6:32238356-32238384	Kidney_OC	kidney:	n/a	n/a
36	CTCF	chr6:32264940-32265090	NHDF-neo	bronchial:	n/a	n/a
37	CTCF	chr6:32222876-32223301	K562	blood:	n/a	chr6:32223073-32223091 chr6:32223022-32223035 chr6:32223048-32223066 chr6:32223049-32223065
38	CTCF	chr6:32222529-32223526	SK-N-SH	brain:	n/a	chr6:32223073-32223091 chr6:32223022-32223035 chr6:32223048-32223066 chr6:32223049-32223065
39	CTCF	chr6:32223369-32223425	Medullo	brain:	n/a	n/a
40	CTCF	chr6:32241667-32241719	Spleen_OC	spleen:	n/a	n/a
41	CTCF	chr6:32223160-32223310	AG04450	lung:	n/a	n/a
42	CTCF	chr6:32222878-32223318	MCF-7	breast:	n/a	chr6:32223073-32223091 chr6:32223022-32223035 chr6:32223048-32223066 chr6:32223049-32223065
43	CTCF	chr6:32265000-32265150	HMF	breast:	n/a	n/a
44	CTCF	chr6:32223237-32223365	Lung_OC	lung:	n/a	n/a
45	CTCF	chr6:32222883-32223260	GM12878	blood:	n/a	chr6:32223073-32223091 chr6:32223022-32223035 chr6:32223048-32223066 chr6:32223049-32223065
46	CTCF	chr6:32239296-32239350	Spleen_OC	spleen:	n/a	n/a
47	CTCF	chr6:32223280-32223430	GM12874	blood:	n/a	n/a
48	CTCF	chr6:32259484-32259585	Spleen_OC	spleen:	n/a	n/a
49	CTCF	chr6:32237465-32237509	Lung_OC	lung:	n/a	n/a
50	CTCF	chr6:32264920-32265070	HPAF	blood vessel:	n/a	n/a

(count:1465 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:32264336-32264386	MCF10A-Er-Src	breast:	n/a
2	chr6:32264336-32264386	MCF10A-Er-Src	breast:	n/a
3	chr6:32273375-32273425	SK-N-SH_RA	brain:	n/a
4	chr6:32223208-32223258	RPTEC	kidney:	n/a
5	chr6:32261558-32261608	BJ	skin:	n/a
6	chr6:32223236-32223286	Caco-2	colon:	n/a
7	chr6:32223430-32223480	HRE	kidney:	n/a
8	chr6:32268374-32268424	BE2_C	brain:	n/a
9	chr6:32264336-32264386	HUVEC	blood vessel:	n/a
10	chr6:32223430-32223480	Hepatocyte	liver:	n/a
11	chr6:32223226-32223276	AoSMC	blood vessel:	n/a
12	chr6:32269215-32269265	AG09309	skin:	n/a
13	chr6:32223430-32223480	AG10803	skin:	n/a
14	chr6:32268055-32268105	K562	blood:	n/a
15	chr6:32272050-32272100	T-47D	breast:	n/a
16	chr6:32227480-32227530	HRPEpiC	eye:	n/a
17	chr6:32272050-32272100	HRCEpiC	kidney:	n/a
18	chr6:32269111-32269161	HRCEpiC	kidney:	n/a
19	chr6:32223208-32223258	NT2-D1	testis:	n/a
20	chr6:32223208-32223258	HRCEpiC	kidney:	n/a
21	chr6:32223236-32223286	NH-A	brain:	n/a
22	chr6:32223430-32223480	MCF-7	breast:	n/a
23	chr6:32267874-32267924	AG09309	skin:	n/a
24	chr6:32223336-32223386	HUVEC	blood vessel:	n/a
25	chr6:32223208-32223258	T-47D	breast:	n/a
26	chr6:32223336-32223386	HCF	heart:	n/a
27	chr6:32223226-32223276	HRCEpiC	kidney:	n/a
28	chr6:32272050-32272100	NT2-D1	testis:	n/a
29	chr6:32268374-32268424	GM19239	blood:	n/a
30	chr6:32223226-32223276	NB4	blood:	n/a
31	chr6:32223430-32223480	ovcar-3	ovarian:	n/a
32	chr6:32263335-32263385	ovcar-3	ovarian:	n/a
33	chr6:32274241-32274291	SK-N-SH_RA	brain:	n/a
34	chr6:32223236-32223286	Hela-S3	cervix:	n/a
35	chr6:32223226-32223276	MCF-7	breast:	n/a
36	chr6:32260812-32260862	AG04450	lung:	fetal
37	chr6:32268374-32268424	HEEpiC	esophagus:	n/a
38	chr6:32273375-32273425	HRE	kidney:	n/a
39	chr6:32223336-32223386	HIPEpiC	eye:	n/a
40	chr6:32273347-32273397	PFSK-1	brain:	n/a
41	chr6:32273375-32273425	HCPEpiC	choroid plexus:	n/a
42	chr6:32268055-32268105	CMK	blood:	n/a
43	chr6:32278653-32278703	HUVEC	blood vessel:	n/a
44	chr6:32269478-32269528	U87	brain:	n/a
45	chr6:32223236-32223286	PFSK-1	brain:	n/a
46	chr6:32261558-32261608	RPTEC	kidney:	n/a
47	chr6:32268374-32268424	SAEC	small airway:	n/a
48	chr6:32269111-32269161	HCPEpiC	choroid plexus:	n/a
49	chr6:32263335-32263385	NHDF-neo	bronchial:	n/a
50	chr6:32269478-32269528	Hepatocyte	liver:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:32259346..32261422-chr6:32263927..32266328,2	MCF-7	breast:
2	chr6:32084866..32087270-chr6:32222075..32224600,2	K562	blood:
3	chr6:32221059..32223929-chr6:32261762..32264103,2	MCF-7	breast:
4	chr6:32260150..32262258-chr6:32267045..32269420,2	MCF-7	breast:
5	chr6:32266172..32268310-chr6:32269017..32271310,2	MCF-7	breast:
6	chr6:32260223..32261904-chr6:32262964..32264831,2	K562	blood:
7	chr6:32222652..32223330-chr6:32667895..32668502,2	K562	blood:
8	chr6:32251349..32253695-chr6:32277418..32279197,2	MCF-7	breast:
9	chr6:32260150..32262258-chr6:32267045..32269420,2	MCF-7	breast:
10	chr6:32259346..32261422-chr6:32263927..32266328,2	MCF-7	breast:
11	chr6:32251349..32253695-chr6:32277418..32279197,2	MCF-7	breast:
12	chr6:32086335..32087255-chr6:32222559..32223401,4	K562	blood:
13	chr6:32260223..32261904-chr6:32262964..32264831,2	K562	blood:
14	chr6:32264476..32267942-chr6:32268038..32271496,3	K562	blood:
15	chr6:32264476..32267942-chr6:32268038..32271496,3	K562	blood:
16	chr6:32266172..32268310-chr6:32269017..32271310,2	MCF-7	breast:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RNF5-1	chr6:32230389-32233615	ENSG00000225914.1
2	lnc-RNF5-1	chr6:32223488-32223718	ENSG00000225914.1

No data

Variant related genes	Relation type
ENSG00000225914	TF binding region
ENSG00000225914	CpG island
ENSG00000213676	chromatin interactions
ENSG00000225914	chromatin interactions

Extended variants
information (count: 1587 )
Associated
traits (count: 133 )

Variant overlapped rSNPs/rCNVs (count:1587 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3130320	chr6:32223258-32223259	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
2	rs558806722	chr6:32223265-32223266	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs570750422	chr6:32223285-32223286	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs372574388	chr6:32223397-32223398	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs3130321	chr6:32223418-32223419	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs6902431	chr6:32223430-32223431	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs572068752	chr6:32223497-32223498	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs145005807	chr6:32223510-32223511	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
9	rs6925278	chr6:32223516-32223517	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs9268000	chr6:32223531-32223532	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs543775049	chr6:32223539-32223540	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
12	rs559867183	chr6:32223542-32223543	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
13	rs530339465	chr6:32223587-32223588	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs6925474	chr6:32223615-32223616	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs11450850	chr6:32223626-32223627	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
16	rs377544174	chr6:32223627-32223628	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
17	rs3132966	chr6:32223632-32223633	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs7741477	chr6:32223637-32223638	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs559607706	chr6:32223656-32223657	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
20	rs142231891	chr6:32223695-32223696	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
21	rs116539104	chr6:32223715-32223716	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
22	rs151212619	chr6:32223767-32223768	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs6457513	chr6:32223770-32223771	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs6457514	chr6:32223775-32223776	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs6457515	chr6:32223785-32223786	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs6457516	chr6:32223830-32223831	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs547139853	chr6:32223875-32223876	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs3130322	chr6:32223925-32223926	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs2510070	chr6:32223943-32223944	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs3132967	chr6:32223947-32223948	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs141580215	chr6:32223962-32223963	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs557686992	chr6:32223999-32224000	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs3115569	chr6:32224139-32224140	Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs190394688	chr6:32224226-32224227	Enhancers Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs3115568	chr6:32224319-32224320	Enhancers Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs181596043	chr6:32224341-32224342	Enhancers Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs28895018	chr6:32224378-32224379	Enhancers Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs574528771	chr6:32224379-32224380	Enhancers Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs186984777	chr6:32224387-32224388	Enhancers Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs9268005	chr6:32224388-32224389	Enhancers Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs573942542	chr6:32224423-32224424	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs192270475	chr6:32224433-32224434	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs6908903	chr6:32224439-32224440	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs6908464	chr6:32224445-32224446	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs184048983	chr6:32224449-32224450	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs546957361	chr6:32224456-32224457	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs568672155	chr6:32224457-32224458	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs6931322	chr6:32224463-32224464	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs6908927	chr6:32224489-32224490	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs569725267	chr6:32224491-32224492	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:133)

Disease	PMID	Source
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
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Lung cancer	18438408	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ovarian cancer	21781307	CNVD
Ependymoma	19289631	CNVD
Breast cancer	22844521	CNVD
Gestational infection	22844521	CNVD
HIV/AIDS	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	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
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
abnormal development	18461090	CNVD
Melanoma	17363583	CNVD
Breast cancer	16397240	CNVD
Retinoblastoma	22278416	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Systemic lupus erythematosus	20877625	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Systemic lupus erythematosus	19279649	CNVD
Retinoblastoma	16790693	CNVD
Acute myocardial infarction	18032375	CNVD
Renal cell carcinoma	19150565	CNVD
Systemic lupus erythematosus	19591781	CNVD
Attention deficit hyperactivity disorder	19287146	CNVD
Autism	19287146	CNVD
Erythema nodosum in leprosy	19287146	CNVD
Henoch-schoenlein purpura	19287146	CNVD
Liver cirrhosis	19287146	CNVD
Systemic lupus erythematosus	19287146	CNVD
Autoimmune disease	19135723	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	CNVD
Osteosarcoma	16790693	CNVD
Acute lymphoblastic leukemia	22237106	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
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Myelofibrosis	22110671	CNVD
Incontinentia Pigmenti	22033527	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Encephalopathy	20692195	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Immune disease	17576883	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:313 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:32222200-32223400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr6:32222200-32223400	Active TSS	Breast Myoepithelial Primary Cells	Breast
3	chr6:32222200-32223400	Active TSS	Brain Inferior Temporal Lobe	brain
4	chr6:32222200-32223400	Active TSS	Fetal Lung	lung
5	chr6:32222200-32223600	Active TSS	Brain Angular Gyrus	brain
6	chr6:32222200-32224200	Active TSS	ES-I3 Cell Line	embryonic stem cell
7	chr6:32222200-32224200	Active TSS	Brain Germinal Matrix	brain
8	chr6:32222200-32224400	Active TSS	Fetal Kidney	kidney
9	chr6:32222200-32224800	Active TSS	Fetal Brain Female	brain
10	chr6:32222400-32223400	Active TSS	Aorta	Aorta
11	chr6:32222400-32223800	Flanking Active TSS	Fetal Muscle Leg	muscle
12	chr6:32222400-32224000	Flanking Active TSS	Fetal Brain Male	brain
13	chr6:32222600-32223400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr6:32222600-32223400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
15	chr6:32222600-32223400	Active TSS	Colonic Mucosa	Colon
16	chr6:32222600-32223400	Active TSS	Colon Smooth Muscle	Colon
17	chr6:32222600-32223400	Active TSS	Ovary	ovary
18	chr6:32222600-32223400	Active TSS	Thymus	Thymus
19	chr6:32222600-32223600	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr6:32222600-32223600	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr6:32222600-32223600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr6:32222600-32223600	Enhancers	Placenta	Placenta
23	chr6:32222600-32223600	Enhancers	Lung	lung
24	chr6:32222600-32223600	Active TSS	Psoas Muscle	Psoas
25	chr6:32222600-32223800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr6:32222600-32223800	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
27	chr6:32222600-32223800	Flanking Active TSS	Fetal Thymus	thymus
28	chr6:32222600-32223800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
29	chr6:32222800-32223400	Active TSS	Placenta Amnion	Placenta Amnion
30	chr6:32222800-32223600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
31	chr6:32222800-32223600	Flanking Active TSS	Primary hematopoietic stem cells	blood
32	chr6:32222800-32223600	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
33	chr6:32222800-32223600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
34	chr6:32222800-32223600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
35	chr6:32222800-32223600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr6:32222800-32223600	Transcr. at gene 5' and 3'	Right Atrium	heart
37	chr6:32222800-32223800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr6:32222800-32223800	Flanking Active TSS	Primary B cells from peripheral blood	blood
39	chr6:32223000-32223400	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
40	chr6:32223000-32223400	Flanking Active TSS	Primary T cells fromperipheralblood	blood
41	chr6:32223000-32223400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
42	chr6:32223000-32223400	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
43	chr6:32223000-32223400	Flanking Active TSS	Sigmoid Colon	Sigmoid Colon
44	chr6:32223000-32223400	Active TSS	Small Intestine	intestine
45	chr6:32223000-32223600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr6:32223000-32223600	Flanking Bivalent TSS/Enh	Primary T regulatory cells fromperipheralblood	blood
47	chr6:32223000-32223600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr6:32223000-32223800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
49	chr6:32223000-32223800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr6:32223200-32223400	Flanking Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell

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