Variant report

Variant	esv12676
Chromosome Location	chr4:57772270-57775584
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:744)
CpG islands
(count:977)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:744 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:57773599-57773917	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF3	chr4:57774758-57775163	K562	blood:	n/a	chr4:57775039-57775048 chr4:57774857-57774865
3	BACH1	chr4:57775378-57775589	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr4:57774775-57774975	GM12878	blood:	n/a	chr4:57774864-57774875
5	BCL11A	chr4:57773599-57773878	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL11A	chr4:57773622-57773841	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL3	chr4:57774654-57775204	GM12878	blood:	n/a	chr4:57774933-57774946 chr4:57774937-57774950 chr4:57774979-57774992
8	BCLAF1	chr4:57774682-57775296	K562	blood:	n/a	chr4:57774933-57774946 chr4:57774937-57774950 chr4:57774979-57774992
9	BCLAF1	chr4:57774722-57775828	GM12878	blood:	n/a	chr4:57774933-57774946 chr4:57774937-57774950 chr4:57775290-57775298 chr4:57774979-57774992
10	BHLHE40	chr4:57775318-57775591	K562	blood:	n/a	n/a
11	BHLHE40	chr4:57774804-57775591	GM12878	blood:	n/a	n/a
12	BHLHE40	chr4:57774383-57775008	K562	blood:	n/a	chr4:57774426-57774442 chr4:57774470-57774486 chr4:57774572-57774588
13	BHLHE40	chr4:57773816-57774431	GM12878	blood:	n/a	chr4:57774120-57774136 chr4:57774166-57774182 chr4:57774164-57774180
14	BHLHE40	chr4:57775334-57775534	HepG2	liver:	n/a	n/a
15	BRCA1	chr4:57775259-57776137	Hela-S3	cervix:	n/a	n/a
16	CCNT2	chr4:57773807-57775656	K562	blood:	n/a	chr4:57774981-57774990 chr4:57773943-57773952 chr4:57775240-57775249 chr4:57774585-57774594 chr4:57775309-57775318 chr4:57774805-57774814
17	CEBPB	chr4:57772879-57773119	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr4:57774741-57774941	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr4:57775488-57775761	IMR90	lung:	n/a	n/a
20	CEBPB	chr4:57772889-57773155	HepG2	liver:	n/a	n/a
21	CEBPB	chr4:57775509-57775838	K562	blood:	n/a	n/a
22	CEBPB	chr4:57775425-57775831	ECC-1	luminal epithelium:	n/a	n/a
23	CEBPB	chr4:57775490-57775811	K562	blood:	n/a	n/a
24	CEBPB	chr4:57772842-57773384	K562	blood:	n/a	n/a
25	CEBPB	chr4:57772840-57773146	K562	blood:	n/a	n/a
26	CEBPB	chr4:57775505-57775833	HepG2	liver:	n/a	n/a
27	CEBPB	chr4:57772923-57773298	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr4:57775386-57775888	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr4:57773819-57774266	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr4:57775560-57775967	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPD	chr4:57774118-57774384	HepG2	liver:	n/a	n/a
32	CEBPD	chr4:57774901-57775192	HepG2	liver:	n/a	n/a
33	CHD1	chr4:57774719-57776234	GM12878	blood:	n/a	n/a
34	CHD1	chr4:57774494-57776306	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr4:57773352-57773355	GM12878	blood:	n/a	n/a
36	CHD2	chr4:57774598-57775544	K562	blood:	n/a	n/a
37	CHD2	chr4:57775253-57775639	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD2	chr4:57774206-57774339	K562	blood:	n/a	n/a
39	CHD2	chr4:57773765-57773965	GM12878	blood:	n/a	chr4:57773944-57773954
40	CHD2	chr4:57773952-57775683	Hela-S3	cervix:	n/a	n/a
41	CHD2	chr4:57774378-57774385	HepG2	liver:	n/a	n/a
42	CHD2	chr4:57774972-57775229	HepG2	liver:	n/a	n/a
43	CHD2	chr4:57774201-57775632	GM12878	blood:	n/a	n/a
44	CHD2	chr4:57774511-57774526	H1-hESC	embryonic stem cell:	n/a	n/a
45	CREB1	chr4:57774341-57774886	H1-hESC	embryonic stem cell:	n/a	n/a
46	CREB1	chr4:57773496-57774172	H1-hESC	embryonic stem cell:	n/a	n/a
47	CREB1	chr4:57773837-57774154	A549	lung:	n/a	n/a
48	CREB1	chr4:57773724-57774283	H1-hESC	embryonic stem cell:	n/a	n/a
49	CREB1	chr4:57773690-57775254	GM12878	blood:	n/a	n/a
50	CREB1	chr4:57774829-57775084	A549	lung:	n/a	n/a

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:57773300-57773350	Hela-S3	cervix:	n/a
2	chr4:57773300-57773350	Hela-S3	cervix:	n/a
3	chr4:57773149-57773199	IMR90	lung:	fetal
4	chr4:57773955-57774005	HIPEpiC	eye:	n/a
5	chr4:57773300-57773350	Hepatocyte	liver:	n/a
6	chr4:57774202-57774252	ECC-1	luminal epithelium:	n/a
7	chr4:57773953-57774003	PFSK-1	brain:	n/a
8	chr4:57773948-57773998	GM06990	blood:	n/a
9	chr4:57773149-57773199	GM12891	blood:	n/a
10	chr4:57773955-57774005	HCM	heart:	n/a
11	chr4:57773948-57773998	SK-N-MC	brain:	n/a
12	chr4:57773948-57773998	MCF-7	breast:	n/a
13	chr4:57775294-57775344	ovcar-3	ovarian:	n/a
14	chr4:57773955-57774005	HRCEpiC	kidney:	n/a
15	chr4:57773398-57773448	Hela-S3	cervix:	n/a
16	chr4:57775294-57775344	AG04450	lung:	fetal
17	chr4:57774717-57774767	SK-N-SH_RA	brain:	n/a
18	chr4:57773868-57773918	HMEC	breast:	n/a
19	chr4:57773300-57773350	NT2-D1	testis:	n/a
20	chr4:57774717-57774767	AoSMC	blood vessel:	n/a
21	chr4:57773308-57773358	Hepatocyte	liver:	n/a
22	chr4:57774717-57774767	HepG2	liver:	n/a
23	chr4:57774406-57774456	A549	lung:	n/a
24	chr4:57773962-57774012	GM19239	blood:	n/a
25	chr4:57773436-57773486	HepG2	liver:	n/a
26	chr4:57773883-57773933	GM19239	blood:	n/a
27	chr4:57773883-57773933	HCM	heart:	n/a
28	chr4:57773398-57773448	BE2_C	brain:	n/a
29	chr4:57773149-57773199	AG10803	skin:	n/a
30	chr4:57773308-57773358	HUVEC	blood vessel:	n/a
31	chr4:57773768-57773818	U87	brain:	n/a
32	chr4:57773953-57774003	HRCEpiC	kidney:	n/a
33	chr4:57773883-57773933	BJ	skin:	n/a
34	chr4:57773768-57773818	SK-N-MC	brain:	n/a
35	chr4:57775294-57775344	NHDF-neo	bronchial:	n/a
36	chr4:57775294-57775344	AG04449	skin:	fetal
37	chr4:57775294-57775344	HIPEpiC	eye:	n/a
38	chr4:57773436-57773486	AG10803	skin:	n/a
39	chr4:57775294-57775344	GM06990	blood:	n/a
40	chr4:57773768-57773818	HCM	heart:	n/a
41	chr4:57774202-57774252	NB4	blood:	n/a
42	chr4:57775294-57775344	HCPEpiC	choroid plexus:	n/a
43	chr4:57773948-57773998	GM12878	blood:	n/a
44	chr4:57773149-57773199	AG09319	gingival:	n/a
45	chr4:57773868-57773918	HCM	heart:	n/a
46	chr4:57773953-57774003	HL-60	blood:	n/a
47	chr4:57773948-57773998	HepG2	liver:	n/a
48	chr4:57773308-57773358	CMK	blood:	n/a
49	chr4:57773308-57773358	AG09309	skin:	n/a
50	chr4:57773948-57773998	K562	blood:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:57766086..57769107-chr4:57769697..57772712,3	K562	blood:
2	chr4:57772988..57775343-chr4:57776220..57778579,3	MCF-7	breast:
3	chr4:57773933..57775544-chr4:57843880..57845543,2	MCF-7	breast:
4	chr4:57771524..57779492-chr4:57841270..57849741,26	K562	blood:
5	chr4:57772839..57777394-chr4:57841397..57848240,17	K562	blood:
6	chr4:57299951..57301849-chr4:57773604..57776000,3	K562	blood:
7	chr4:57301355..57303854-chr4:57773620..57776020,4	MCF-7	breast:
8	chr4:57773986..57774521-chr9:139685816..139686316,2	Hela-S3	cervix:
9	chr4:57774412..57776864-chr4:57776976..57782053,6	K562	blood:
10	chr4:57771688..57776264-chr4:57841866..57845328,7	MCF-7	breast:
11	chr19:1248083..1248884-chr4:57773766..57774545,2	Hela-S3	cervix:
12	chr4:57302175..57303989-chr4:57773484..57775623,2	MCF-7	breast:

No data

Variant related genes	Relation type
REST	TF binding region
REST	CpG island
ENSG00000128059	chromatin interactions
ENSG00000084093	chromatin interactions
ENSG00000244187	chromatin interactions
ENSG00000128050	chromatin interactions
ENSG00000047315	chromatin interactions
ENSG00000272896	chromatin interactions
ENSG00000167470	chromatin interactions
ENSG00000084092	chromatin interactions

Extended variants
information (count: 100 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:100 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs77991152	chr4:57772328-57772329	Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs556457564	chr4:57772348-57772349	Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs143268205	chr4:57772378-57772379	Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs542151328	chr4:57772439-57772440	Enhancers Bivalent Enhancer Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs376432849	chr4:57772456-57772457	Enhancers Bivalent Enhancer Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs572780803	chr4:57772458-57772459	Enhancers Bivalent Enhancer Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs577017758	chr4:57772460-57772461	Enhancers Bivalent Enhancer Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs541399633	chr4:57772471-57772472	Enhancers Bivalent Enhancer Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs550036915	chr4:57772503-57772504	Enhancers Bivalent Enhancer Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs112936783	chr4:57772514-57772515	Enhancers Bivalent Enhancer Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs564490870	chr4:57772556-57772557	Enhancers Bivalent Enhancer Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs533242204	chr4:57772562-57772563	Enhancers Bivalent Enhancer Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs183736000	chr4:57772606-57772607	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs550278995	chr4:57772612-57772613	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs544870607	chr4:57772621-57772622	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs563326509	chr4:57772656-57772657	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs1002285	chr4:57772712-57772713	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs562779383	chr4:57772734-57772735	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs548766563	chr4:57772747-57772748	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs374230867	chr4:57772758-57772759	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs562481715	chr4:57772777-57772778	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs151275104	chr4:57772911-57772912	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs140431654	chr4:57773041-57773042	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs550933278	chr4:57773126-57773127	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs570937316	chr4:57773176-57773177	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs59929817	chr4:57773203-57773204	Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs377199432	chr4:57773236-57773237	Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs185356430	chr4:57773260-57773261	Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs3806746	chr4:57773330-57773331	Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs190121728	chr4:57773347-57773348	Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs549265716	chr4:57773383-57773384	Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs3806745	chr4:57773388-57773389	Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs2458552	chr4:57773442-57773443	Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs1713993	chr4:57773477-57773478	Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs138330497	chr4:57773486-57773487	Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs143709867	chr4:57773490-57773491	Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs372772661	chr4:57773491-57773492	Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs182076259	chr4:57773492-57773493	Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs802920	chr4:57773498-57773499	Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs186804668	chr4:57773499-57773500	Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs202055906	chr4:57773568-57773569	Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs1623306	chr4:57773595-57773596	Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs71601658	chr4:57773601-57773602	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs550546870	chr4:57773673-57773674	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs542379239	chr4:57773785-57773786	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs559144231	chr4:57773818-57773819	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs528346795	chr4:57773831-57773832	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs66790703	chr4:57773908-57773909	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs571146930	chr4:57773994-57773995	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
50	rs556350912	chr4:57774041-57774042	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	19435819	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian neoplasms	16753589	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Glioblastoma	17504929	CNVD
Glioblastoma	16823502	CNVD
Melanoma	16908931	CNVD
Glioblastoma	20031968	CNVD
Medulloblastoma	19270706	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Olfactory neuroblastoma	18408657	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Rhabdomyosarcoma	16790082	CNVD
Gastrointestinal stromal cancer	17438095	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	19208797	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	21138945	CNVD
Cancer	22183965	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:391 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:57761600-57773000	Weak transcription	Right Atrium	heart
2	chr4:57771800-57773200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr4:57772000-57772400	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
4	chr4:57772000-57772400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
5	chr4:57772000-57772600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
6	chr4:57772000-57772800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr4:57772000-57772800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
8	chr4:57772000-57773000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
9	chr4:57772000-57773400	Enhancers	Cortex derived primary cultured neurospheres	brain
10	chr4:57772200-57772400	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
11	chr4:57772200-57772400	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
12	chr4:57772200-57772400	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
13	chr4:57772200-57772600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr4:57772200-57773000	Enhancers	Primary T cells from cord blood	blood
15	chr4:57772200-57773200	Enhancers	Primary B cells from cord blood	blood
16	chr4:57772400-57772600	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr4:57772400-57772600	Active TSS	HUES6 Cell Line	embryonic stem cell
18	chr4:57772400-57772600	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
19	chr4:57772400-57772600	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
20	chr4:57772400-57772600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr4:57772400-57772800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
22	chr4:57772600-57772800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
23	chr4:57772600-57772800	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
24	chr4:57772600-57772800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr4:57772600-57772800	Enhancers	Fetal Kidney	kidney
26	chr4:57772600-57772800	Enhancers	Monocytes-CD14+_RO01746	blood
27	chr4:57772600-57773000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr4:57772600-57773000	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
29	chr4:57772600-57773000	Enhancers	Primary hematopoietic stem cells short term culture	blood
30	chr4:57772600-57773000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
31	chr4:57772600-57773000	Enhancers	Primary T helper cells PMA-I stimulated	--
32	chr4:57772600-57773000	Enhancers	Primary T helper cells fromperipheralblood	blood
33	chr4:57772600-57773000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
34	chr4:57772600-57773200	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
35	chr4:57772600-57773200	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
36	chr4:57772600-57773200	Enhancers	Primary monocytes fromperipheralblood	blood
37	chr4:57772600-57773200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
38	chr4:57772600-57773200	Enhancers	Adipose Nuclei	Adipose
39	chr4:57772600-57773200	Enhancers	Brain Hippocampus Middle	brain
40	chr4:57772600-57773200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
41	chr4:57772600-57773200	Enhancers	Fetal Thymus	thymus
42	chr4:57772600-57773200	Enhancers	Stomach Mucosa	stomach
43	chr4:57772600-57773200	Enhancers	Dnd41	blood
44	chr4:57772600-57773200	Bivalent Enhancer	K562	blood
45	chr4:57772600-57773400	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
46	chr4:57772600-57773600	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
47	chr4:57772800-57773000	Enhancers	Primary neutrophils fromperipheralblood	blood
48	chr4:57772800-57773000	Enhancers	Primary hematopoietic stem cells	blood
49	chr4:57772800-57773000	Enhancers	Primary T killer memory cells from peripheral blood	blood
50	chr4:57772800-57773000	Enhancers	Brain Anterior Caudate	brain

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