Variant report

Variant	esv3350194
Chromosome Location	chr22:29468252-29470350
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr22:29468477-29468734	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr22:29470226-29470418	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr22:29468536-29468887	K562	blood:	n/a	n/a
4	BHLHE40	chr22:29468567-29468814	GM12878	blood:	n/a	n/a
5	BRCA1	chr22:29470118-29470255	HepG2	liver:	n/a	n/a
6	BRCA1	chr22:29470117-29470230	GM12878	blood:	n/a	n/a
7	CBX3	chr22:29468342-29468790	K562	blood:	n/a	n/a
8	CCNT2	chr22:29468640-29469201	K562	blood:	n/a	chr22:29468759-29468768
9	CEBPD	chr22:29468766-29469244	HepG2	liver:	n/a	n/a
10	CHD1	chr22:29470288-29470451	H1-hESC	embryonic stem cell:	n/a	n/a
11	CHD2	chr22:29470013-29470275	H1-hESC	embryonic stem cell:	n/a	chr22:29470050-29470060
12	CHD2	chr22:29470055-29470282	GM12878	blood:	n/a	n/a
13	CHD2	chr22:29469861-29470313	HepG2	liver:	n/a	chr22:29469995-29470005 chr22:29470050-29470060
14	CHD2	chr22:29468784-29469016	Hela-S3	cervix:	n/a	n/a
15	CHD2	chr22:29468809-29468811	GM12878	blood:	n/a	n/a
16	CREB1	chr22:29468433-29469126	HepG2	liver:	n/a	n/a
17	CTBP2	chr22:29469949-29470393	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr22:29469740-29469890	Caco-2	colon:	n/a	n/a
19	CTCF	chr22:29470072-29470184	GM12878	blood:	n/a	n/a
20	CTCF	chr22:29468795-29468910	Spleen_OC	spleen:	n/a	n/a
21	CTCF	chr22:29470060-29470210	AG10803	skin:	n/a	n/a
22	CTCF	chr22:29469980-29470130	Caco-2	colon:	n/a	n/a
23	CTCF	chr22:29470040-29470190	BJ	skin:	n/a	n/a
24	CTCF	chr22:29470080-29470230	NHEK	skin:	n/a	n/a
25	CTCF	chr22:29470060-29470210	AoAF	blood vessel:	n/a	n/a
26	CTCF	chr22:29468784-29468789	Spleen_OC	spleen:	n/a	n/a
27	CTCF	chr22:29469300-29469450	Caco-2	colon:	n/a	n/a
28	CTCF	chr22:29470059-29470179	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr22:29470020-29470170	HCM	heart:	n/a	n/a
30	CTCF	chr22:29470080-29470230	HEEpiC	esophagus:	n/a	n/a
31	CTCF	chr22:29470300-29470450	HepG2	liver:	n/a	n/a
32	CTCF	chr22:29470060-29470210	HMF	breast:	n/a	n/a
33	CTCF	chr22:29470020-29470170	HPF	lung:	n/a	n/a
34	CTCF	chr22:29469980-29470130	HCPEpiC	choroid plexus:	n/a	n/a
35	CTCF	chr22:29470060-29470210	HRPEpiC	eye:	n/a	n/a
36	CTCF	chr22:29470025-29470225	Kidney_OC	kidney:	n/a	n/a
37	CTCF	chr22:29470063-29470115	Lung_OC	lung:	n/a	n/a
38	CTCF	chr22:29469940-29470090	NHDF-neo	bronchial:	n/a	n/a
39	CTCF	chr22:29470040-29470190	AG10803	skin:	n/a	n/a
40	CTCF	chr22:29470140-29470290	NHDF-neo	bronchial:	n/a	n/a
41	CTCF	chr22:29470020-29470170	HMF	breast:	n/a	n/a
42	CTCF	chr22:29470040-29470190	AG04449	skin:	n/a	n/a
43	CTCF	chr22:29470020-29470170	BJ	skin:	n/a	n/a
44	CTCF	chr22:29469240-29469390	GM12874	blood:	n/a	n/a
45	CTCF	chr22:29470340-29470490	NHDF-neo	bronchial:	n/a	n/a
46	E2F4	chr22:29468585-29468958	MCF10A-Er-Src	breast:	n/a	n/a
47	EBF1	chr22:29469651-29469672	GM12878	blood:	n/a	n/a
48	EGR1	chr22:29468775-29469147	K562	blood:	n/a	chr22:29468894-29468903 chr22:29469054-29469064 chr22:29469050-29469063
49	EGR1	chr22:29469695-29470325	HCT-116	colon:	n/a	chr22:29469971-29469984 chr22:29469972-29469983 chr22:29469972-29469981 chr22:29469971-29469984 chr22:29469968-29469982 chr22:29469997-29470011 chr22:29469972-29469982 chr22:29469971-29469984 chr22:29469970-29469984 chr22:29469972-29469982
50	EGR1	chr22:29469895-29470089	GM12878	blood:	n/a	chr22:29469971-29469984 chr22:29469972-29469983 chr22:29469972-29469981 chr22:29469971-29469984 chr22:29469968-29469982 chr22:29469997-29470011 chr22:29469972-29469982 chr22:29469971-29469984 chr22:29469970-29469984 chr22:29469972-29469982

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:29470232-29470282	MCF-7	breast:	n/a
2	chr22:29470232-29470282	MCF-7	breast:	n/a
3	chr22:29469035-29469085	HUVEC	blood vessel:	n/a
4	chr22:29470264-29470314	AG04450	lung:	fetal
5	chr22:29469461-29469511	GM12891	blood:	n/a
6	chr22:29469461-29469511	LNCaP	prostate:	n/a
7	chr22:29468997-29469047	SK-N-MC	brain:	n/a
8	chr22:29468762-29468812	BE2_C	brain:	n/a
9	chr22:29469719-29469769	PANC-1	pancreas:	n/a
10	chr22:29469014-29469064	Caco-2	colon:	n/a
11	chr22:29470264-29470314	BE2_C	brain:	n/a
12	chr22:29468762-29468812	Hepatocyte	liver:	n/a
13	chr22:29470264-29470314	HEK293	kidney:	embryo
14	chr22:29469461-29469511	PANC-1	pancreas:	n/a
15	chr22:29470232-29470282	Hepatocyte	liver:	n/a
16	chr22:29468762-29468812	HCF	heart:	n/a
17	chr22:29468762-29468812	PrEC	prostate:	n/a
18	chr22:29469033-29469083	HUVEC	blood vessel:	n/a
19	chr22:29469033-29469083	HCT-116	colon:	n/a
20	chr22:29468588-29468638	Hela-S3	cervix:	n/a
21	chr22:29468762-29468812	HCPEpiC	choroid plexus:	n/a
22	chr22:29469035-29469085	NHBE	bronchial:	n/a
23	chr22:29469035-29469085	BE2_C	brain:	n/a
24	chr22:29469719-29469769	HRCEpiC	kidney:	n/a
25	chr22:29470232-29470282	GM12891	blood:	n/a
26	chr22:29469033-29469083	HRCEpiC	kidney:	n/a
27	chr22:29468588-29468638	HepG2	liver:	n/a
28	chr22:29470232-29470282	Jurkat	blood:	n/a
29	chr22:29469490-29469540	SK-N-SH_RA	brain:	n/a
30	chr22:29469014-29469064	NT2-D1	testis:	n/a
31	chr22:29470264-29470314	Caco-2	colon:	n/a
32	chr22:29468892-29468942	SK-N-MC	brain:	n/a
33	chr22:29468588-29468638	GM19239	blood:	n/a
34	chr22:29470232-29470282	H1-hESC	embryonic stem cell:	embryo
35	chr22:29469014-29469064	Hela-S3	cervix:	n/a
36	chr22:29469014-29469064	T-47D	breast:	n/a
37	chr22:29469035-29469085	SK-N-MC	brain:	n/a
38	chr22:29468892-29468942	GM12891	blood:	n/a
39	chr22:29469490-29469540	Hepatocyte	liver:	n/a
40	chr22:29468762-29468812	SKMC	muscle:	n/a
41	chr22:29469490-29469540	Hela-S3	cervix:	n/a
42	chr22:29469461-29469511	Hela-S3	cervix:	n/a
43	chr22:29469014-29469064	MCF-7	breast:	n/a
44	chr22:29469461-29469511	NHDF-neo	bronchial:	n/a
45	chr22:29468892-29468942	SK-N-SH_RA	brain:	n/a
46	chr22:29469014-29469064	Jurkat	blood:	n/a
47	chr22:29468997-29469047	ovcar-3	ovarian:	n/a
48	chr22:29468997-29469047	MCF-7	breast:	n/a
49	chr22:29468762-29468812	SAEC	small airway:	n/a
50	chr22:29468892-29468942	NHDF-neo	bronchial:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr22:29296014..29298873-chr22:29469784..29471423,2	K562	blood:
2	chr22:29279568..29281765-chr22:29467462..29470387,2	K562	blood:

Variant related genes	Relation type
KREMEN1	TF binding region
KREMEN1	CpG island
ENSG00000183579	chromatin interactions

Extended variants
information (count: 60 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:60 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571744632	chr22:29468320-29468321	Bivalent/Poised TSS Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs539260465	chr22:29468331-29468332	Bivalent/Poised TSS Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs186358882	chr22:29468352-29468353	Bivalent/Poised TSS Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs142668842	chr22:29468394-29468395	Bivalent/Poised TSS Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs189292175	chr22:29468441-29468442	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs543363096	chr22:29468444-29468445	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs554967181	chr22:29468450-29468451	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs134594	chr22:29468456-29468457	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs543527206	chr22:29468500-29468501	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs140636784	chr22:29468524-29468525	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs147820205	chr22:29468546-29468547	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs201014305	chr22:29468550-29468551	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs34967120	chr22:29468721-29468722	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs541174709	chr22:29468734-29468735	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs559146158	chr22:29468764-29468765	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs529905292	chr22:29468776-29468777	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs548113783	chr22:29468838-29468839	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs569289019	chr22:29468921-29468922	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs530575130	chr22:29469033-29469034	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs112588138	chr22:29469083-29469084	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs7292708	chr22:29469130-29469131	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs570486799	chr22:29469195-29469196	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs534421912	chr22:29469227-29469228	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs139628031	chr22:29469262-29469263	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs566290944	chr22:29469278-29469279	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs536928026	chr22:29469282-29469283	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs370513107	chr22:29469326-29469327	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs555326716	chr22:29469402-29469403	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs145154292	chr22:29469424-29469425	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs543762134	chr22:29469435-29469436	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs558686777	chr22:29469482-29469483	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs134595	chr22:29469526-29469527	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs373032553	chr22:29469529-29469530	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs577242355	chr22:29469541-29469542	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs541183302	chr22:29469544-29469545	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs559107686	chr22:29469576-29469577	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs111529360	chr22:29469589-29469590	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs371284853	chr22:29469657-29469658	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs147576042	chr22:29469675-29469676	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs542664354	chr22:29469716-29469717	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs117554223	chr22:29469750-29469751	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs114780941	chr22:29469792-29469793	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs185185563	chr22:29469837-29469838	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs75292652	chr22:29469873-29469874	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs528151810	chr22:29469890-29469891	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs546750105	chr22:29469901-29469902	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs531341967	chr22:29469905-29469906	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs566252295	chr22:29469906-29469907	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs576052074	chr22:29469917-29469918	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs73154219	chr22:29469938-29469939	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Velocardiofacial syndrome	20111667	CNVD
Medulloblastoma	21979893	CNVD
sporadic solitary meningiomas	19589153	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Congenital heart defect	22511896	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Seminomas	18059402	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Metachromatic leukodystrophy	18421352	CNVD
Basal cell lymphoma	17170743	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Breast cancer	21858162	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	22174824	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Wilms tumour	21544195	CNVD
Acute myeloid leukemia	21251322	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Lung cancer	18438408	CNVD
Pancreatic endocrine tumor	17639061	CNVD
abnormal development	18461090	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
small cell lung cancer	20016488	CNVD
Cancer	21183584	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Cat eye syndrome	16708226	CNVD
Olfactory neuroblastoma	18408657	CNVD
Renal cell carcinoma	18765545	CNVD
Schizophrenia	19521646	CNVD
Schizophrenia	18990708	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Hepatocellular carcinoma	16750200	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	21829676	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:463 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:29463800-29468400	Weak transcription	Dnd41	blood
2	chr22:29465800-29468400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr22:29466800-29468600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr22:29467000-29468800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr22:29467000-29470400	Enhancers	Fetal Heart	heart
6	chr22:29467200-29468400	Bivalent/Poised TSS	Brain Germinal Matrix	brain
7	chr22:29467200-29468400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
8	chr22:29467200-29468400	Weak transcription	K562	blood
9	chr22:29467200-29468600	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
10	chr22:29467200-29468600	Weak transcription	Gastric	stomach
11	chr22:29467200-29468600	Enhancers	Left Ventricle	heart
12	chr22:29467200-29468800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr22:29467200-29468800	Flanking Active TSS	Stomach Smooth Muscle	stomach
14	chr22:29467200-29469000	Bivalent Enhancer	Fetal Brain Male	brain
15	chr22:29467200-29470200	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
16	chr22:29467200-29470400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
17	chr22:29467200-29470400	Active TSS	Pancreatic Islets	Pancreatic Islet
18	chr22:29467200-29470600	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
19	chr22:29467200-29471200	Active TSS	Ovary	ovary
20	chr22:29467400-29468400	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
21	chr22:29467400-29468800	Flanking Bivalent TSS/Enh	Primary T helper cells PMA-I stimulated	--
22	chr22:29467400-29468800	Flanking Active TSS	Brain Hippocampus Middle	brain
23	chr22:29467400-29468800	Flanking Bivalent TSS/Enh	Fetal Thymus	thymus
24	chr22:29467400-29468800	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
25	chr22:29467400-29469600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr22:29467400-29469600	Active TSS	Right Ventricle	heart
27	chr22:29467400-29470000	Active TSS	Aorta	Aorta
28	chr22:29467400-29470200	Active TSS	Psoas Muscle	Psoas
29	chr22:29467400-29470200	Active TSS	Right Atrium	heart
30	chr22:29467600-29468800	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
31	chr22:29467600-29468800	Flanking Active TSS	Liver	Liver
32	chr22:29467600-29468800	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
33	chr22:29467600-29468800	Flanking Bivalent TSS/Enh	Thymus	Thymus
34	chr22:29467600-29470400	Active TSS	HSMM	muscle
35	chr22:29467800-29468400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr22:29467800-29468400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr22:29467800-29468400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr22:29467800-29468400	Enhancers	Placenta Amnion	Placenta Amnion
39	chr22:29467800-29468600	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr22:29467800-29468600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
41	chr22:29467800-29468600	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
42	chr22:29467800-29468600	Flanking Bivalent TSS/Enh	Duodenum Smooth Muscle	Duodenum
43	chr22:29467800-29468600	Enhancers	Pancreas	Pancrea
44	chr22:29467800-29468600	Flanking Active TSS	Stomach Mucosa	stomach
45	chr22:29467800-29468600	Enhancers	Spleen	Spleen
46	chr22:29467800-29468600	Active TSS	GM12878-XiMat	blood
47	chr22:29467800-29468800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr22:29467800-29468800	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
49	chr22:29467800-29468800	Flanking Bivalent TSS/Enh	Primary B cells from cord blood	blood
50	chr22:29467800-29468800	Flanking Bivalent TSS/Enh	Primary T cells from cord blood	blood

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