Variant report

Variant	esv3357318
Chromosome Location	chr5:43042995-43045168
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:558)
CpG islands
(count:427)
Chromatin interactive
region (count:17)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:558 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:43043206-43043650	K562	blood:	n/a	n/a
2	ATF2	chr5:43042371-43043414	GM12878	blood:	n/a	n/a
3	ATF2	chr5:43041815-43043562	GM12878	blood:	n/a	n/a
4	BACH1	chr5:43040915-43043581	K562	blood:	n/a	n/a
5	BACH1	chr5:43041519-43043395	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr5:43044381-43044691	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr5:43043154-43043460	GM12878	blood:	n/a	n/a
8	BCL11A	chr5:43043084-43043455	GM12878	blood:	n/a	n/a
9	BCL3	chr5:43043182-43043566	GM12878	blood:	n/a	n/a
10	BCL3	chr5:43042378-43043480	A549	lung:	n/a	n/a
11	BCLAF1	chr5:43042405-43043689	K562	blood:	n/a	n/a
12	BCLAF1	chr5:43041490-43043660	GM12878	blood:	n/a	n/a
13	BCLAF1	chr5:43041592-43043675	GM12878	blood:	n/a	n/a
14	BHLHE40	chr5:43039461-43043625	K562	blood:	n/a	n/a
15	BHLHE40	chr5:43041716-43043591	GM12878	blood:	n/a	n/a
16	BRCA1	chr5:43043269-43043445	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr5:43040381-43043069	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr5:43043403-43043506	GM12878	blood:	n/a	n/a
19	CBX3	chr5:43041623-43043702	K562	blood:	n/a	n/a
20	CBX3	chr5:43042181-43043733	K562	blood:	n/a	n/a
21	CCNT2	chr5:43041844-43043620	K562	blood:	n/a	n/a
22	CEBPB	chr5:43043267-43043417	HepG2	liver:	n/a	chr5:43043277-43043288
23	CEBPB	chr5:43043062-43043598	MCF-7	breast:	n/a	chr5:43043277-43043288
24	CEBPB	chr5:43043030-43043381	H1-hESC	embryonic stem cell:	n/a	chr5:43043277-43043288
25	CEBPB	chr5:43042517-43043530	K562	blood:	n/a	chr5:43043277-43043288
26	CEBPB	chr5:43043133-43043536	A549	lung:	n/a	chr5:43043277-43043288
27	CEBPB	chr5:43042337-43043610	A549	lung:	n/a	chr5:43043277-43043288
28	CEBPB	chr5:43043123-43043550	A549	lung:	n/a	chr5:43043277-43043288
29	CEBPB	chr5:43042418-43043563	K562	blood:	n/a	chr5:43043277-43043288
30	CEBPB	chr5:43042308-43043185	GM12878	blood:	n/a	n/a
31	CEBPB	chr5:43043140-43043485	K562	blood:	n/a	chr5:43043277-43043288
32	CEBPB	chr5:43042443-43043519	IMR90	lung:	n/a	chr5:43043277-43043288
33	CEBPB	chr5:43043112-43043564	Hela-S3	cervix:	n/a	chr5:43043277-43043288
34	CEBPB	chr5:43043172-43043423	HepG2	liver:	n/a	chr5:43043277-43043288
35	CEBPD	chr5:43043036-43043663	K562	blood:	n/a	n/a
36	CEBPD	chr5:43042575-43043725	K562	blood:	n/a	n/a
37	CHD1	chr5:43041913-43043636	GM12878	blood:	n/a	n/a
38	CHD2	chr5:43041422-43043623	GM12878	blood:	n/a	n/a
39	CHD2	chr5:43043244-43043613	Hela-S3	cervix:	n/a	n/a
40	CHD2	chr5:43042559-43043138	HepG2	liver:	n/a	n/a
41	CHD2	chr5:43041402-43043565	K562	blood:	n/a	n/a
42	CREB1	chr5:43041765-43043676	GM12878	blood:	n/a	n/a
43	CREB1	chr5:43042779-43043626	A549	lung:	n/a	n/a
44	CREB1	chr5:43042812-43043692	K562	blood:	n/a	n/a
45	CTBP2	chr5:43041835-43043551	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr5:43043520-43043670	HUVEC	blood vessel:	n/a	n/a
47	CTCF	chr5:43042940-43043090	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr5:43043040-43043190	HUVEC	blood vessel:	n/a	n/a
49	CTCF	chr5:43043360-43043510	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr5:43043266-43043500	MCF-7	breast:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:43044640-43044690	AG09319	gingival:	n/a
2	chr5:43044573-43044623	SK-N-SH_RA	brain:	n/a
3	chr5:43044703-43044753	HMEC	breast:	n/a
4	chr5:43044703-43044753	GM12878	blood:	n/a
5	chr5:43044640-43044690	GM12892	blood:	n/a
6	chr5:43044640-43044690	K562	blood:	n/a
7	chr5:43044675-43044725	HRPEpiC	eye:	n/a
8	chr5:43044640-43044690	CMK	blood:	n/a
9	chr5:43043140-43043190	AG10803	skin:	n/a
10	chr5:43044703-43044753	K562	blood:	n/a
11	chr5:43044675-43044725	SAEC	small airway:	n/a
12	chr5:43044675-43044725	Caco-2	colon:	n/a
13	chr5:43043360-43043410	HNPCEpiC	eye:	n/a
14	chr5:43044640-43044690	T-47D	breast:	n/a
15	chr5:43043140-43043190	GM19239	blood:	n/a
16	chr5:43044640-43044690	HNPCEpiC	eye:	n/a
17	chr5:43044573-43044623	RPTEC	kidney:	n/a
18	chr5:43044675-43044725	GM06990	blood:	n/a
19	chr5:43044703-43044753	AG10803	skin:	n/a
20	chr5:43044573-43044623	HEK293	kidney:	embryo
21	chr5:43044640-43044690	PANC-1	pancreas:	n/a
22	chr5:43044703-43044753	SAEC	small airway:	n/a
23	chr5:43044703-43044753	RPTEC	kidney:	n/a
24	chr5:43043360-43043410	GM12878	blood:	n/a
25	chr5:43044703-43044753	HRCEpiC	kidney:	n/a
26	chr5:43043360-43043410	Caco-2	colon:	n/a
27	chr5:43043140-43043190	GM12891	blood:	n/a
28	chr5:43045001-43045051	HepG2	liver:	n/a
29	chr5:43043360-43043410	PFSK-1	brain:	n/a
30	chr5:43044640-43044690	Jurkat	blood:	n/a
31	chr5:43044703-43044753	Hepatocyte	liver:	n/a
32	chr5:43044703-43044753	NH-A	brain:	n/a
33	chr5:43043360-43043410	HRCEpiC	kidney:	n/a
34	chr5:43044675-43044725	K562	blood:	n/a
35	chr5:43044703-43044753	HUVEC	blood vessel:	n/a
36	chr5:43043140-43043190	LNCaP	prostate:	n/a
37	chr5:43044573-43044623	AoSMC	blood vessel:	n/a
38	chr5:43043140-43043190	HPAEpiC	pulmonary alveolar:	n/a
39	chr5:43044675-43044725	HCF	heart:	n/a
40	chr5:43044675-43044725	SK-N-SH	brain:	n/a
41	chr5:43044573-43044623	SK-N-SH	brain:	n/a
42	chr5:43045001-43045051	HMEC	breast:	n/a
43	chr5:43044675-43044725	SK-N-SH_RA	brain:	n/a
44	chr5:43044573-43044623	HCF	heart:	n/a
45	chr5:43044675-43044725	Jurkat	blood:	n/a
46	chr5:43043360-43043410	CMK	blood:	n/a
47	chr5:43045001-43045051	K562	blood:	n/a
48	chr5:43045001-43045051	GM12891	blood:	n/a
49	chr5:43044573-43044623	GM19239	blood:	n/a
50	chr5:43044573-43044623	HMEC	breast:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:43040708..43045055-chr5:43119670..43122847,6	K562	blood:
2	chr5:43044445..43046601-chr5:43140326..43141953,2	MCF-7	breast:
3	chr5:43038662..43048059-chr5:43059399..43070773,40	MCF-7	breast:
4	chr5:43005322..43013124-chr5:43037748..43043287,15	K562	blood:
5	chr5:43037720..43044659-chr5:43062293..43069444,31	K562	blood:
6	chr5:43036901..43050217-chr5:43060442..43069391,53	MCF-7	breast:
7	chr5:43007547..43009866-chr5:43041551..43043821,3	MCF-7	breast:
8	chr5:43016691..43021968-chr5:43036071..43044426,17	MCF-7	breast:
9	chr5:43041481..43043742-chr5:43120386..43122867,3	MCF-7	breast:
10	chr1:145438010..145439003-chr5:43043227..43043821,2	NB4	blood:
11	chr5:43040123..43044169-chr5:43120216..43122879,6	K562	blood:
12	chr5:43005892..43011349-chr5:43037590..43043804,20	K562	blood:
13	chr5:43041320..43043003-chr5:43064736..43065650,5	MCF-7	breast:
14	chr5:43014739..43026335-chr5:43034830..43045515,33	MCF-7	breast:
15	chr5:43007330..43009530-chr5:43039640..43043303,5	MCF-7	breast:
16	chr5:43034726..43053192-chr5:43061725..43074206,66	K562	blood:
17	chr5:43041491..43043698-chr5:43120008..43122438,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF131-1	chr5:43044801-43044988	ENSG00000215068
2	lnc-ZNF131-1	chr5:43043574-43043669	ENSG00000215068

No data

Variant related genes	Relation type
ANXA2R	TF binding region
ANXA2R	CpG island
ENSG00000177738	chromatin interactions
ENSG00000117289	chromatin interactions
ENSG00000172262	chromatin interactions
ENSG00000272144	chromatin interactions
ENSG00000251131	chromatin interactions
ENSG00000271788	chromatin interactions

Extended variants
information (count: 101 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:101 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567198318	chr5:43043051-43043052	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs534492461	chr5:43043060-43043061	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs559233345	chr5:43043079-43043080	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs112383398	chr5:43043099-43043100	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs370267377	chr5:43043112-43043113	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs143202736	chr5:43043138-43043139	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs554508416	chr5:43043180-43043181	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs369509168	chr5:43043182-43043183	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs192616896	chr5:43043200-43043201	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs541857429	chr5:43043206-43043207	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs11949983	chr5:43043388-43043389	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs566753439	chr5:43043449-43043450	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs527628386	chr5:43043456-43043457	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs545684569	chr5:43043477-43043478	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs183611774	chr5:43043486-43043487	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs531537418	chr5:43043487-43043488	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs549682111	chr5:43043520-43043521	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs188308316	chr5:43043602-43043603	Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
19	rs533869677	chr5:43043631-43043632	Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
20	rs528974884	chr5:43043651-43043652	Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
21	rs576195594	chr5:43043767-43043768	Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
22	rs113616074	chr5:43043822-43043823	Active TSS Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs12697441	chr5:43043839-43043840	Active TSS Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs565333886	chr5:43043856-43043857	Active TSS Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs565669198	chr5:43043857-43043858	Active TSS Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs372917064	chr5:43043866-43043867	Active TSS Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs539397335	chr5:43043867-43043868	Active TSS Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs12697442	chr5:43043874-43043875	Active TSS Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs13359736	chr5:43043884-43043885	Active TSS Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs13360191	chr5:43043899-43043900	Active TSS Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs13358136	chr5:43043916-43043917	Active TSS Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs28550786	chr5:43043923-43043924	Active TSS Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs369528429	chr5:43043924-43043925	Active TSS Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs34545519	chr5:43043930-43043931	Active TSS Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs376206210	chr5:43043933-43043934	Active TSS Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs374026284	chr5:43043934-43043935	Active TSS Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs370884182	chr5:43043963-43043964	Active TSS Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs374444023	chr5:43043984-43043985	Active TSS Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs111217568	chr5:43043995-43043996	Active TSS Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs376939418	chr5:43043997-43043998	Active TSS Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs189662999	chr5:43044013-43044014	Bivalent Enhancer Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs181644702	chr5:43044044-43044045	Bivalent Enhancer Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs547759313	chr5:43044052-43044053	Bivalent Enhancer Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs559204915	chr5:43044058-43044059	Bivalent Enhancer Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs186906378	chr5:43044081-43044082	Bivalent Enhancer Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs571025797	chr5:43044089-43044090	Bivalent Enhancer Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs376986516	chr5:43044094-43044095	Bivalent Enhancer Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs70991469	chr5:43044098-43044099	Bivalent Enhancer Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs538445795	chr5:43044114-43044115	Bivalent Enhancer Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs556467731	chr5:43044115-43044116	Bivalent Enhancer Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Cancer	16751803	CNVD
Breast cancer	16608533	CNVD
Autism	22495311	CNVD
Intellectual disability	22102821	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	21720365	CNVD
Lung cancer	18438408	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Breast cancer	17393978	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Hirschsprung''s Disease	21712996	CNVD
Breast cancer	21364760	CNVD
Intellectual disability	21811512	CNVD
Lung adenocarcinoma	21935476	CNVD
Myelofibrosis	22110671	CNVD
Intracranial aneurysm	16715129	CNVD
Multiple myeloma	16616336	CNVD
Cancer	21359685	CNVD
adenomatous polyposis	22470819	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Lung cancer	21569311	CNVD
Autism	20531469	CNVD

Chromatin state (count:474 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:43036800-43043800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr5:43037400-43043000	Active TSS	HSMM	muscle
3	chr5:43037400-43045000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr5:43037800-43043400	Active TSS	Right Atrium	heart
5	chr5:43038000-43043600	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
6	chr5:43038800-43043600	Active TSS	A549	lung
7	chr5:43039000-43043600	Active TSS	Psoas Muscle	Psoas
8	chr5:43039000-43043800	Active TSS	Thymus	Thymus
9	chr5:43039000-43043800	Active TSS	NHDF-Ad	bronchial
10	chr5:43039400-43043000	Active TSS	HSMMtube	muscle
11	chr5:43039400-43043600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
12	chr5:43039400-43043600	Bivalent/Poised TSS	Pancreatic Islets	Pancreatic Islet
13	chr5:43039400-43043800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr5:43039400-43044800	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr5:43039600-43043400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
16	chr5:43039600-43043400	Bivalent/Poised TSS	Brain Angular Gyrus	brain
17	chr5:43039600-43043600	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
18	chr5:43039600-43043600	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
19	chr5:43039600-43043800	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
20	chr5:43039800-43043600	Active TSS	Brain Substantia Nigra	brain
21	chr5:43039800-43043800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
22	chr5:43039800-43044400	Active TSS	NHLF	lung
23	chr5:43039800-43044800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr5:43040000-43043400	Active TSS	Esophagus	oesophagus
25	chr5:43040000-43043600	Active TSS	Aorta	Aorta
26	chr5:43040000-43045000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr5:43040200-43043200	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr5:43040200-43043200	Active TSS	Small Intestine	intestine
29	chr5:43040200-43043400	Active TSS	Lung	lung
30	chr5:43040200-43043600	Active TSS	Brain Hippocampus Middle	brain
31	chr5:43040400-43043800	Active TSS	Rectal Mucosa Donor 31	rectum
32	chr5:43040400-43045000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr5:43040600-43043600	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr5:43040800-43043600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
35	chr5:43040800-43043600	Flanking Bivalent TSS/Enh	Fetal Intestine Small	intestine
36	chr5:43040800-43043600	Active TSS	Ovary	ovary
37	chr5:43040800-43043800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr5:43041000-43043600	Active TSS	Brain Cingulate Gyrus	brain
39	chr5:43041000-43043800	Active TSS	Breast Myoepithelial Primary Cells	Breast
40	chr5:43041400-43043600	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
41	chr5:43041400-43043800	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
42	chr5:43041600-43043400	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr5:43041600-43043600	Bivalent/Poised TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr5:43041600-43043600	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
45	chr5:43041600-43043600	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain
46	chr5:43041600-43043600	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr5:43041600-43043600	Flanking Bivalent TSS/Enh	Fetal Intestine Large	intestine
48	chr5:43041600-43043600	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
49	chr5:43041600-43043600	Flanking Active TSS	HUVEC	blood vessel
50	chr5:43041600-43043800	Flanking Active TSS	Primary T cells fromperipheralblood	blood

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