Variant report

Variant	nsv878592
Chromosome Location	chr4:8105399-8163560
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:795)
CpG islands
(count:3725)
Chromatin interactive
region (count:43)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:8115011-8115374	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:8160518-8160811	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:8146857-8146914	HepG2	liver:	n/a	n/a
4	ATF1	chr4:8147937-8148244	K562	blood:	n/a	n/a
5	ATF1	chr4:8122382-8122602	K562	blood:	n/a	n/a
6	ATF1	chr4:8129887-8130059	K562	blood:	n/a	n/a
7	ATF2	chr4:8111959-8112520	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr4:8129807-8130459	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr4:8160572-8160865	K562	blood:	n/a	n/a
10	ATF3	chr4:8160566-8160839	HepG2	liver:	n/a	n/a
11	BACH1	chr4:8118943-8119235	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr4:8125113-8125263	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr4:8160434-8161068	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr4:8113954-8113964	H1-hESC	embryonic stem cell:	n/a	n/a
15	BCL3	chr4:8108204-8108381	GM12878	blood:	n/a	n/a
16	BHLHE40	chr4:8119078-8119200	K562	blood:	n/a	n/a
17	BHLHE40	chr4:8134822-8134988	K562	blood:	n/a	n/a
18	BHLHE40	chr4:8160437-8160887	GM12878	blood:	n/a	n/a
19	BHLHE40	chr4:8112457-8112602	K562	blood:	n/a	n/a
20	BHLHE40	chr4:8107498-8107697	K562	blood:	n/a	chr4:8107654-8107667 chr4:8107650-8107671
21	BHLHE40	chr4:8160344-8161077	K562	blood:	n/a	n/a
22	BRCA1	chr4:8111993-8112692	H1-hESC	embryonic stem cell:	n/a	chr4:8112518-8112527
23	BRCA1	chr4:8108394-8108406	GM12878	blood:	n/a	n/a
24	BRCA1	chr4:8151083-8151149	H1-hESC	embryonic stem cell:	n/a	n/a
25	CCNT2	chr4:8160162-8160844	K562	blood:	n/a	n/a
26	CCNT2	chr4:8144371-8144570	K562	blood:	n/a	n/a
27	CEBPB	chr4:8160444-8161220	ECC-1	luminal epithelium:	n/a	n/a
28	CEBPB	chr4:8160504-8161209	K562	blood:	n/a	n/a
29	CEBPB	chr4:8160491-8161101	K562	blood:	n/a	n/a
30	CEBPB	chr4:8160435-8161166	MCF-7	breast:	n/a	n/a
31	CEBPB	chr4:8160620-8160903	HepG2	liver:	n/a	n/a
32	CEBPB	chr4:8160446-8161178	MCF-7	breast:	n/a	n/a
33	CEBPB	chr4:8160370-8161059	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr4:8160618-8161004	K562	blood:	n/a	n/a
35	CEBPB	chr4:8160624-8161081	A549	lung:	n/a	n/a
36	CEBPB	chr4:8160527-8161087	GM12878	blood:	n/a	n/a
37	CEBPB	chr4:8147586-8147802	HepG2	liver:	n/a	n/a
38	CEBPB	chr4:8160328-8161337	HCT-116	colon:	n/a	n/a
39	CEBPB	chr4:8112104-8112611	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr4:8160608-8160979	HepG2	liver:	n/a	n/a
41	CEBPB	chr4:8160576-8161015	A549	lung:	n/a	n/a
42	CEBPB	chr4:8160585-8161038	HepG2	liver:	n/a	n/a
43	CEBPB	chr4:8160542-8161183	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr4:8160447-8160988	HepG2	liver:	n/a	n/a
45	CEBPB	chr4:8160501-8161324	IMR90	lung:	n/a	n/a
46	CEBPB	chr4:8160423-8161226	HCT-116	colon:	n/a	n/a
47	CEBPB	chr4:8160424-8161196	A549	lung:	n/a	n/a
48	CEBPB	chr4:8160662-8160841	GM12878	blood:	n/a	n/a
49	CEBPB	chr4:8160556-8161062	ECC-1	luminal epithelium:	n/a	n/a
50	CEBPD	chr4:8160679-8160930	HepG2	liver:	n/a	n/a

(count:3725 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:8160892-8160942	SK-N-MC	brain:	n/a
2	chr4:8108207-8108257	Caco-2	colon:	n/a
3	chr4:8160566-8160616	BJ	skin:	n/a
4	chr4:8108443-8108493	HCPEpiC	choroid plexus:	n/a
5	chr4:8160892-8160942	SK-N-MC	brain:	n/a
6	chr4:8108207-8108257	Caco-2	colon:	n/a
7	chr4:8160566-8160616	BJ	skin:	n/a
8	chr4:8108443-8108493	HCPEpiC	choroid plexus:	n/a
9	chr4:8137064-8137114	H1-hESC	embryonic stem cell:	embryo
10	chr4:8160569-8160619	NB4	blood:	n/a
11	chr4:8130202-8130252	HCF	heart:	n/a
12	chr4:8154317-8154367	ECC-1	luminal epithelium:	n/a
13	chr4:8160295-8160345	HRE	kidney:	n/a
14	chr4:8154405-8154455	RPTEC	kidney:	n/a
15	chr4:8126658-8126708	HUVEC	blood vessel:	n/a
16	chr4:8126658-8126708	U87	brain:	n/a
17	chr4:8145692-8145742	SAEC	small airway:	n/a
18	chr4:8113095-8113145	NHBE	bronchial:	n/a
19	chr4:8161776-8161826	AG04450	lung:	fetal
20	chr4:8154317-8154367	HCPEpiC	choroid plexus:	n/a
21	chr4:8160584-8160634	GM12891	blood:	n/a
22	chr4:8137465-8137515	PrEC	prostate:	n/a
23	chr4:8137121-8137171	ECC-1	luminal epithelium:	n/a
24	chr4:8107846-8107896	IMR90	lung:	fetal
25	chr4:8136996-8137046	HNPCEpiC	eye:	n/a
26	chr4:8154208-8154258	BJ	skin:	n/a
27	chr4:8135668-8135718	NT2-D1	testis:	n/a
28	chr4:8108443-8108493	IMR90	lung:	fetal
29	chr4:8153305-8153355	HCF	heart:	n/a
30	chr4:8113095-8113145	HEEpiC	esophagus:	n/a
31	chr4:8108433-8108483	LNCaP	prostate:	n/a
32	chr4:8108433-8108483	Hela-S3	cervix:	n/a
33	chr4:8145692-8145742	SKMC	muscle:	n/a
34	chr4:8122559-8122609	Caco-2	colon:	n/a
35	chr4:8157616-8157666	Caco-2	colon:	n/a
36	chr4:8161093-8161143	HUVEC	blood vessel:	n/a
37	chr4:8126305-8126355	HPAEpiC	pulmonary alveolar:	n/a
38	chr4:8135668-8135718	GM12892	blood:	n/a
39	chr4:8106273-8106323	GM19239	blood:	n/a
40	chr4:8107258-8107308	LNCaP	prostate:	n/a
41	chr4:8160591-8160641	NT2-D1	testis:	n/a
42	chr4:8137121-8137171	HRPEpiC	eye:	n/a
43	chr4:8107392-8107442	SK-N-SH_RA	brain:	n/a
44	chr4:8109411-8109461	AG09319	gingival:	n/a
45	chr4:8110246-8110296	SK-N-SH	brain:	n/a
46	chr4:8137121-8137171	ovcar-3	ovarian:	n/a
47	chr4:8107118-8107168	MCF-7	breast:	n/a
48	chr4:8108443-8108493	AG04450	lung:	fetal
49	chr4:8137155-8137205	GM12891	blood:	n/a
50	chr4:8107258-8107308	AG04449	skin:	fetal

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:8110955..8113093-chr4:8123812..8126057,2	MCF-7	breast:
2	chr4:8127943..8130325-chr4:8131891..8134790,3	K562	blood:
3	chr4:8127943..8130325-chr4:8131891..8134790,3	K562	blood:
4	chr4:8112046..8112998-chr4:8194067..8194612,3	K562	blood:
5	chr4:8137600..8139609-chr4:8142915..8145694,2	MCF-7	breast:
6	chr4:8119371..8122507-chr4:8131514..8133327,3	K562	blood:
7	chr4:8158369..8164233-chr4:8200767..8204083,4	MCF-7	breast:
8	chr4:8110955..8113093-chr4:8123812..8126057,2	MCF-7	breast:
9	chr4:8133809..8136137-chr4:8137763..8139798,2	K562	blood:
10	chr4:8101919..8103661-chr4:8104511..8106585,2	K562	blood:
11	chr4:8137600..8139609-chr4:8142915..8145694,2	MCF-7	breast:
12	chr4:8117714..8119692-chr4:8121281..8123487,2	MCF-7	breast:
13	chr4:8121607..8124062-chr4:8128700..8130723,2	K562	blood:
14	chr4:8117484..8120480-chr4:8150571..8152947,2	MCF-7	breast:
15	chr4:8113926..8116157-chr4:8119118..8122388,3	MCF-7	breast:
16	chr4:8159576..8163492-chr4:8163504..8167545,5	MCF-7	breast:
17	chr4:8104135..8106823-chr4:8110568..8113011,2	MCF-7	breast:
18	chr4:8125674..8128386-chr4:8156706..8158737,2	MCF-7	breast:
19	chr4:8138114..8139768-chr4:8143187..8145337,2	MCF-7	breast:
20	chr4:8122047..8124105-chr4:8136576..8138325,2	K562	blood:
21	chr4:8119371..8122507-chr4:8131514..8133327,3	K562	blood:
22	chr4:8102999..8104721-chr4:8104874..8107526,2	MCF-7	breast:
23	chr4:8102885..8104984-chr4:8106744..8108953,3	K562	blood:
24	chr4:8138114..8139768-chr4:8143187..8145337,2	MCF-7	breast:
25	chr22:43008550..43011275-chr4:8161727..8163687,2	MCF-7	breast:
26	chr4:8098463..8100832-chr4:8106304..8108910,3	MCF-7	breast:
27	chr4:8117484..8120480-chr4:8150571..8152947,2	MCF-7	breast:
28	chr4:8117714..8119692-chr4:8121281..8123487,2	MCF-7	breast:
29	chr4:8136885..8140079-chr4:8151401..8153857,3	MCF-7	breast:
30	chr4:8160114..8162361-chr4:8163405..8165822,2	K562	blood:
31	chr4:8153109..8155276-chr4:8158816..8161389,2	K562	blood:
32	chr4:8136885..8140079-chr4:8151401..8153857,3	MCF-7	breast:
33	chr4:8121607..8124062-chr4:8128700..8130723,2	K562	blood:
34	chr4:8097226..8098995-chr4:8106673..8109329,2	K562	blood:
35	chr4:8147667..8148302-chrX:5458311..5459167,2	MCF-7	breast:
36	chr4:8104135..8106823-chr4:8110568..8113011,2	MCF-7	breast:
37	chr4:8113926..8116157-chr4:8119118..8122388,3	MCF-7	breast:
38	chr4:8122047..8124105-chr4:8136576..8138325,2	K562	blood:
39	chr4:8125329..8127502-chr4:8128258..8131209,2	MCF-7	breast:
40	chr4:8125329..8127502-chr4:8128258..8131209,2	MCF-7	breast:
41	chr4:8154984..8157975-chr4:8158726..8162007,4	MCF-7	breast:
42	chr4:8133809..8136137-chr4:8137763..8139798,2	K562	blood:
43	chr4:8125674..8128386-chr4:8156706..8158737,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ABLIM2-1	chr4:8160852-8162635	XLOC_003874

No data

Variant related genes	Relation type
ABLIM2	TF binding region
ABLIM2	CpG island
ENSG00000125089	chromatin interactions
ENSG00000163995	chromatin interactions
ENSG00000100227	chromatin interactions
ENSG00000270022	chromatin interactions

Extended variants
information (count: 2884 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:2884 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17795569	chr4:8105399-8105400	Bivalent Enhancer Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs569983887	chr4:8105409-8105410	Bivalent Enhancer Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs182646148	chr4:8105412-8105413	Bivalent Enhancer Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs555029852	chr4:8105442-8105443	Bivalent Enhancer Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs73796883	chr4:8105488-8105489	Bivalent Enhancer Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs190650152	chr4:8105489-8105490	Bivalent Enhancer Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs570940887	chr4:8105491-8105492	Bivalent Enhancer Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs535149853	chr4:8105512-8105513	Bivalent Enhancer Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs553982983	chr4:8105518-8105519	Bivalent Enhancer Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs572286823	chr4:8105535-8105536	Bivalent Enhancer Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs78432613	chr4:8105572-8105573	Bivalent Enhancer Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs573685275	chr4:8105598-8105599	Bivalent Enhancer Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs182888599	chr4:8105603-8105604	Bivalent Enhancer Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs576335028	chr4:8105636-8105637	Bivalent Enhancer Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs543045112	chr4:8105640-8105641	Bivalent Enhancer Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs537847671	chr4:8105675-8105676	Bivalent Enhancer Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs564931412	chr4:8105722-8105723	Bivalent Enhancer Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs555929269	chr4:8105738-8105739	Bivalent Enhancer Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs115871863	chr4:8105742-8105743	Bivalent Enhancer Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs372965779	chr4:8105754-8105755	Bivalent Enhancer Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs559478079	chr4:8105787-8105788	Bivalent Enhancer Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs567421483	chr4:8105833-8105834	Bivalent Enhancer Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs61286102	chr4:8105841-8105842	Bivalent Enhancer Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs188842096	chr4:8105849-8105850	Bivalent Enhancer Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs570242857	chr4:8105856-8105857	Bivalent Enhancer Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs531270606	chr4:8105885-8105886	Bivalent Enhancer Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs55750784	chr4:8105953-8105954	Bivalent Enhancer Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs570879491	chr4:8105968-8105969	Bivalent Enhancer Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs373642020	chr4:8106001-8106002	Bivalent Enhancer Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs193227039	chr4:8106002-8106003	Bivalent Enhancer Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs553514289	chr4:8106010-8106011	Bivalent Enhancer Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs565834138	chr4:8106018-8106019	Bivalent Enhancer Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs57553754	chr4:8106078-8106079	Bivalent Enhancer Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs528404903	chr4:8106088-8106089	Bivalent Enhancer Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs576244500	chr4:8106102-8106103	Bivalent Enhancer Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs73796888	chr4:8106109-8106110	Bivalent Enhancer Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs558241117	chr4:8106110-8106111	Bivalent Enhancer Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs572252118	chr4:8106150-8106151	Bivalent Enhancer Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs540676166	chr4:8106153-8106154	Bivalent Enhancer Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs542869787	chr4:8106161-8106162	Bivalent Enhancer Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs559017990	chr4:8106165-8106166	Bivalent Enhancer Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs562160591	chr4:8106171-8106172	Bivalent Enhancer Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs546636426	chr4:8106211-8106212	Bivalent Enhancer Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs150140179	chr4:8106235-8106236	Bivalent Enhancer Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs138866919	chr4:8106237-8106238	Bivalent Enhancer Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs4696758	chr4:8106249-8106250	Bivalent Enhancer Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs114806939	chr4:8106276-8106277	Bivalent Enhancer Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs552851274	chr4:8106299-8106300	Bivalent Enhancer Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs184470087	chr4:8106305-8106306	Bivalent Enhancer Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs528497658	chr4:8106308-8106309	Bivalent Enhancer Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:1456 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:8081600-8114400	Weak transcription	Gastric	stomach
2	chr4:8085800-8112000	Weak transcription	Brain Angular Gyrus	brain
3	chr4:8096800-8111600	Weak transcription	Brain Hippocampus Middle	brain
4	chr4:8098400-8109600	Weak transcription	Stomach Smooth Muscle	stomach
5	chr4:8098400-8110200	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr4:8102800-8105400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
7	chr4:8103400-8105400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr4:8103400-8105800	Weak transcription	Lung	lung
9	chr4:8103800-8105400	Genic enhancers	Skeletal Muscle Male	skeletal muscle
10	chr4:8104000-8106800	Weak transcription	Esophagus	oesophagus
11	chr4:8104000-8109000	Weak transcription	HMEC	breast
12	chr4:8104000-8110800	Weak transcription	Psoas Muscle	Psoas
13	chr4:8104200-8106600	Weak transcription	Fetal Brain Female	brain
14	chr4:8104400-8114400	Genic enhancers	Skeletal Muscle Female	skeletal muscle
15	chr4:8104600-8106400	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr4:8104600-8108800	Strong transcription	Aorta	Aorta
17	chr4:8104600-8109400	Strong transcription	Spleen	Spleen
18	chr4:8104600-8119400	Weak transcription	Hela-S3	cervix
19	chr4:8104800-8109600	Weak transcription	Pancreas	Pancrea
20	chr4:8104800-8114600	Weak transcription	Right Ventricle	heart
21	chr4:8105000-8107200	Enhancers	H1 Cell Line	embryonic stem cell
22	chr4:8105000-8107400	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
23	chr4:8105000-8107400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr4:8105200-8105400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
25	chr4:8105200-8106000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr4:8105200-8106200	Enhancers	H9 Cell Line	embryonic stem cell
27	chr4:8105200-8106400	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr4:8105200-8106600	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr4:8105200-8107200	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr4:8105200-8107200	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr4:8105200-8107400	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr4:8105400-8105600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr4:8105400-8106200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
34	chr4:8105400-8106200	Enhancers	Brain Germinal Matrix	brain
35	chr4:8105400-8107000	Strong transcription	Skeletal Muscle Male	skeletal muscle
36	chr4:8105400-8107400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr4:8105600-8106200	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr4:8105600-8106600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr4:8105600-8107200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr4:8105800-8106000	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
41	chr4:8106000-8111600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr4:8106200-8107400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
43	chr4:8106200-8111800	Weak transcription	HUES64 Cell Line	embryonic stem cell
44	chr4:8106400-8107000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
45	chr4:8106400-8107400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr4:8106600-8106800	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
47	chr4:8106600-8107400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr4:8106600-8111800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
49	chr4:8106800-8108200	Enhancers	Cortex derived primary cultured neurospheres	brain
50	chr4:8106800-8108600	Strong transcription	Esophagus	oesophagus

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