Variant report

Variant	esv3344080
Chromosome Location	chr4:7043676-7046224
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:624)
CpG islands
(count:1039)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:624 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:7044760-7044954	K562	blood:	n/a	n/a
2	ARID3A	chr4:7044722-7044922	HepG2	liver:	n/a	n/a
3	BACH1	chr4:7044082-7044194	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr4:7044587-7045024	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr4:7044640-7044927	K562	blood:	n/a	chr4:7044684-7044700
6	BHLHE40	chr4:7045671-7046237	GM12878	blood:	n/a	n/a
7	BHLHE40	chr4:7045972-7046032	K562	blood:	n/a	n/a
8	BHLHE40	chr4:7044618-7045423	GM12878	blood:	n/a	chr4:7044926-7044942 chr4:7044684-7044700
9	BHLHE40	chr4:7045367-7045662	K562	blood:	n/a	n/a
10	BHLHE40	chr4:7044156-7044392	K562	blood:	n/a	n/a
11	BRCA1	chr4:7044749-7044921	Hela-S3	cervix:	n/a	n/a
12	CBX3	chr4:7044684-7044922	K562	blood:	n/a	n/a
13	CCNT2	chr4:7044207-7046106	K562	blood:	n/a	n/a
14	CEBPB	chr4:7045752-7045963	IMR90	lung:	n/a	n/a
15	CEBPB	chr4:7045725-7046023	A549	lung:	n/a	n/a
16	CEBPB	chr4:7045713-7046083	K562	blood:	n/a	n/a
17	CEBPB	chr4:7045729-7046021	HepG2	liver:	n/a	n/a
18	CEBPB	chr4:7045622-7045965	Hela-S3	cervix:	n/a	n/a
19	CEBPD	chr4:7044885-7045231	HepG2	liver:	n/a	n/a
20	CHD1	chr4:7045256-7046943	IMR90	lung:	n/a	n/a
21	CHD1	chr4:7045356-7045857	GM12878	blood:	n/a	n/a
22	CHD2	chr4:7045639-7045945	Hela-S3	cervix:	n/a	n/a
23	CHD2	chr4:7045316-7045828	GM12878	blood:	n/a	n/a
24	CHD2	chr4:7045380-7045488	HepG2	liver:	n/a	n/a
25	CHD2	chr4:7044478-7044859	HepG2	liver:	n/a	n/a
26	CHD2	chr4:7044505-7045125	Hela-S3	cervix:	n/a	chr4:7044936-7044946
27	CHD2	chr4:7044618-7044979	H1-hESC	embryonic stem cell:	n/a	chr4:7044936-7044946
28	CHD2	chr4:7044591-7045017	K562	blood:	n/a	chr4:7044936-7044946
29	CHD2	chr4:7044120-7044260	K562	blood:	n/a	n/a
30	CHD2	chr4:7044530-7045008	GM12878	blood:	n/a	chr4:7044936-7044946
31	CHD2	chr4:7043836-7043853	H1-hESC	embryonic stem cell:	n/a	n/a
32	CREB1	chr4:7044536-7045007	HepG2	liver:	n/a	n/a
33	CREB1	chr4:7044497-7045106	H1-hESC	embryonic stem cell:	n/a	n/a
34	CREB1	chr4:7044100-7046023	HepG2	liver:	n/a	n/a
35	CREB1	chr4:7044570-7045005	ECC-1	luminal epithelium:	n/a	n/a
36	CREB1	chr4:7044477-7045156	GM12878	blood:	n/a	n/a
37	CREB1	chr4:7044526-7045083	H1-hESC	embryonic stem cell:	n/a	n/a
38	CREB1	chr4:7044532-7045192	A549	lung:	n/a	n/a
39	CTCF	chr4:7044751-7045117	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr4:7044900-7045050	AG09309	skin:	n/a	n/a
41	CTCF	chr4:7044881-7045169	MCF-7	breast:	n/a	n/a
42	CTCF	chr4:7044860-7045010	HVMF	connective:	n/a	n/a
43	CTCF	chr4:7043920-7044070	HCPEpiC	choroid plexus:	n/a	n/a
44	CTCF	chr4:7044900-7045050	GM12874	blood:	n/a	n/a
45	CTCF	chr4:7044940-7045090	GM12873	blood:	n/a	n/a
46	CTCF	chr4:7044891-7045145	Gliobla	brain:	n/a	n/a
47	CTCF	chr4:7044900-7045050	AG04449	skin:	n/a	n/a
48	CTCF	chr4:7045720-7045870	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr4:7044915-7045130	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr4:7044900-7045050	HCPEpiC	choroid plexus:	n/a	n/a

(count:1039 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:7043935-7043985	HUVEC	blood vessel:	n/a
2	chr4:7043935-7043985	AoSMC	blood vessel:	n/a
3	chr4:7043935-7043985	HUVEC	blood vessel:	n/a
4	chr4:7043935-7043985	AoSMC	blood vessel:	n/a
5	chr4:7044595-7044645	HRE	kidney:	n/a
6	chr4:7046066-7046116	AG04450	lung:	fetal
7	chr4:7044595-7044645	NHDF-neo	bronchial:	n/a
8	chr4:7044863-7044913	GM12891	blood:	n/a
9	chr4:7045168-7045218	HIPEpiC	eye:	n/a
10	chr4:7045183-7045233	AG09309	skin:	n/a
11	chr4:7044978-7045028	SK-N-MC	brain:	n/a
12	chr4:7044981-7045031	MCF-7	breast:	n/a
13	chr4:7044981-7045031	ovcar-3	ovarian:	n/a
14	chr4:7044863-7044913	HCT-116	colon:	n/a
15	chr4:7043935-7043985	RPTEC	kidney:	n/a
16	chr4:7044983-7045033	AG09309	skin:	n/a
17	chr4:7043935-7043985	SAEC	small airway:	n/a
18	chr4:7046094-7046144	HUVEC	blood vessel:	n/a
19	chr4:7044990-7045040	ovcar-3	ovarian:	n/a
20	chr4:7046094-7046144	GM12891	blood:	n/a
21	chr4:7044863-7044913	T-47D	breast:	n/a
22	chr4:7044595-7044645	HIPEpiC	eye:	n/a
23	chr4:7044863-7044913	GM12892	blood:	n/a
24	chr4:7045720-7045770	BE2_C	brain:	n/a
25	chr4:7046094-7046144	HRE	kidney:	n/a
26	chr4:7045183-7045233	NT2-D1	testis:	n/a
27	chr4:7044735-7044785	NH-A	brain:	n/a
28	chr4:7045168-7045218	HMEC	breast:	n/a
29	chr4:7044859-7044909	HCF	heart:	n/a
30	chr4:7044990-7045040	AG09319	gingival:	n/a
31	chr4:7044735-7044785	AG10803	skin:	n/a
32	chr4:7044735-7044785	AoSMC	blood vessel:	n/a
33	chr4:7044737-7044787	Caco-2	colon:	n/a
34	chr4:7045183-7045233	HCM	heart:	n/a
35	chr4:7044873-7044923	ovcar-3	ovarian:	n/a
36	chr4:7044978-7045028	LNCaP	prostate:	n/a
37	chr4:7046094-7046144	HRPEpiC	eye:	n/a
38	chr4:7044735-7044785	ECC-1	luminal epithelium:	n/a
39	chr4:7044595-7044645	MCF-7	breast:	n/a
40	chr4:7044863-7044913	SK-N-MC	brain:	n/a
41	chr4:7044735-7044785	SK-N-SH	brain:	n/a
42	chr4:7046094-7046144	NT2-D1	testis:	n/a
43	chr4:7044863-7044913	HRCEpiC	kidney:	n/a
44	chr4:7045168-7045218	AG09319	gingival:	n/a
45	chr4:7044735-7044785	HCF	heart:	n/a
46	chr4:7044873-7044923	HMEC	breast:	n/a
47	chr4:7044968-7045018	HAEpiC	amniotic membrane:	n/a
48	chr4:7044735-7044785	HNPCEpiC	eye:	n/a
49	chr4:7044990-7045040	PFSK-1	brain:	n/a
50	chr4:7044737-7044787	BJ	skin:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:79691250..79693205-chr4:7045398..7046907,2	MCF-7	breast:
2	chr4:6711584..6713629-chr4:7043225..7044994,2	MCF-7	breast:
3	chr4:7044811..7045632-chr4:7069385..7070353,2	NB4	blood:
4	chr4:6987653..6990708-chr4:7043238..7045970,4	MCF-7	breast:
5	chr4:6999677..7002587-chr4:7042055..7044238,2	K562	blood:
6	chr4:6674690..6677394-chr4:7044280..7046366,2	K562	blood:
7	chr11:58345437..58346957-chr4:7043706..7045674,2	K562	blood:
8	chr4:7031028..7032644-chr4:7045295..7046851,2	MCF-7	breast:
9	chr4:6909981..6913772-chr4:7044379..7047071,5	MCF-7	breast:
10	chr4:7042421..7051559-chr4:7062214..7072674,24	MCF-7	breast:
11	chr4:7043790..7046279-chr4:7102506..7105292,2	K562	blood:
12	chr4:7041999..7051916-chr4:7066728..7075643,37	MCF-7	breast:
13	chr4:6999660..7002155-chr4:7043088..7045317,3	MCF-7	breast:
14	chr4:6909683..6913053-chr4:7043553..7046923,6	MCF-7	breast:
15	chr4:7000132..7002859-chr4:7044384..7046741,2	MCF-7	breast:

No data

Variant related genes	Relation type
TADA2B	TF binding region
CCDC96	TF binding region
TADA2B	CpG island
CCDC96	CpG island
ENSG00000109519	chromatin interactions
ENSG00000170846	chromatin interactions
ENSG00000255073	chromatin interactions
ENSG00000110031	chromatin interactions
ENSG00000245468	chromatin interactions
ENSG00000178988	chromatin interactions
ENSG00000251580	chromatin interactions
ENSG00000132405	chromatin interactions
ENSG00000186660	chromatin interactions

Extended variants
information (count: 98 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:98 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372041606	chr4:7043683-7043684	Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs141992507	chr4:7043700-7043701	Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs200146451	chr4:7043726-7043727	Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs199844890	chr4:7043771-7043772	Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs59204906	chr4:7043778-7043779	Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Active TSS	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs114895671	chr4:7043795-7043796	Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
7	rs201971169	chr4:7043823-7043824	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
8	rs142049391	chr4:7043830-7043831	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
9	rs200732240	chr4:7043843-7043844	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
10	rs377461773	chr4:7043864-7043865	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
11	rs561818755	chr4:7043865-7043866	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
12	rs370637587	chr4:7043886-7043887	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
13	rs375345995	chr4:7043900-7043901	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
14	rs376178176	chr4:7043904-7043905	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
15	rs146317749	chr4:7043916-7043917	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
16	rs139316839	chr4:7043925-7043926	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
17	rs543659626	chr4:7043940-7043941	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
18	rs550858107	chr4:7043941-7043942	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
19	rs181515863	chr4:7043945-7043946	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
20	rs375336133	chr4:7043952-7043953	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
21	rs369759265	chr4:7043953-7043954	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
22	rs533110978	chr4:7043969-7043970	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
23	rs374259671	chr4:7043973-7043974	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
24	rs139612326	chr4:7043981-7043982	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
25	rs371063673	chr4:7043994-7043995	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
26	rs75719146	chr4:7044006-7044007	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
27	rs141859161	chr4:7044021-7044022	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
28	rs374287436	chr4:7044026-7044027	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
29	rs368710664	chr4:7044043-7044044	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
30	rs370554794	chr4:7044074-7044075	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
31	rs534252962	chr4:7044093-7044094	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
32	rs549220952	chr4:7044117-7044118	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
33	rs567489271	chr4:7044126-7044127	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs147077157	chr4:7044165-7044166	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs372351063	chr4:7044168-7044169	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs577899866	chr4:7044188-7044189	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
37	rs201135458	chr4:7044189-7044190	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs571129315	chr4:7044228-7044229	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
39	rs202179693	chr4:7044241-7044242	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs377654678	chr4:7044242-7044243	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
41	rs200887088	chr4:7044250-7044251	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
42	rs148696572	chr4:7044267-7044268	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
43	rs367797996	chr4:7044291-7044292	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
44	rs371584162	chr4:7044296-7044297	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
45	rs871133	chr4:7044357-7044358	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs555516788	chr4:7044366-7044367	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
47	rs573851271	chr4:7044377-7044378	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
48	rs871134	chr4:7044380-7044381	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs112443376	chr4:7044441-7044442	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
50	rs562714159	chr4:7044444-7044445	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:53)

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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:453 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:7013200-7044400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr4:7032800-7044000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
3	chr4:7033800-7043800	Weak transcription	Small Intestine	intestine
4	chr4:7034400-7043800	Weak transcription	Dnd41	blood
5	chr4:7034400-7044000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
6	chr4:7034400-7044000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr4:7034600-7043800	Weak transcription	Primary T helper cells PMA-I stimulated	--
8	chr4:7035000-7043800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
9	chr4:7037000-7043800	Weak transcription	NHEK	skin
10	chr4:7040000-7044000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
11	chr4:7040200-7043800	Weak transcription	K562	blood
12	chr4:7042600-7044200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
13	chr4:7043000-7043800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
14	chr4:7043000-7043800	Enhancers	Breast Myoepithelial Primary Cells	Breast
15	chr4:7043000-7043800	Enhancers	Placenta	Placenta
16	chr4:7043000-7043800	Enhancers	Lung	lung
17	chr4:7043000-7043800	Enhancers	Pancreas	Pancrea
18	chr4:7043000-7043800	Enhancers	Sigmoid Colon	Sigmoid Colon
19	chr4:7043000-7043800	Enhancers	Stomach Mucosa	stomach
20	chr4:7043000-7043800	Enhancers	Spleen	Spleen
21	chr4:7043000-7044000	Enhancers	Primary T cells fromperipheralblood	blood
22	chr4:7043000-7044000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
23	chr4:7043200-7043800	Bivalent Enhancer	Primary hematopoietic stem cells	blood
24	chr4:7043200-7043800	Enhancers	Fetal Heart	heart
25	chr4:7043200-7043800	Enhancers	Placenta Amnion	Placenta Amnion
26	chr4:7043200-7044000	Flanking Active TSS	Brain Anterior Caudate	brain
27	chr4:7043200-7044200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr4:7043200-7044200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr4:7043200-7044200	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
30	chr4:7043200-7044200	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
31	chr4:7043200-7044600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
32	chr4:7043200-7044600	Flanking Active TSS	Stomach Smooth Muscle	stomach
33	chr4:7043400-7043800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
34	chr4:7043400-7043800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr4:7043400-7043800	Active TSS	Brain Substantia Nigra	brain
36	chr4:7043400-7043800	Flanking Active TSS	Colon Smooth Muscle	Colon
37	chr4:7043400-7043800	Bivalent Enhancer	Fetal Brain Female	brain
38	chr4:7043400-7043800	Enhancers	Ovary	ovary
39	chr4:7043400-7043800	Flanking Bivalent TSS/Enh	HepG2	liver
40	chr4:7043400-7044000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr4:7043400-7044000	Flanking Active TSS	Brain Angular Gyrus	brain
42	chr4:7043400-7044200	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr4:7043400-7044200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr4:7043400-7044200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
45	chr4:7043400-7044200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr4:7043400-7044200	Flanking Active TSS	Colonic Mucosa	Colon
47	chr4:7043400-7044200	Flanking Active TSS	Duodenum Mucosa	Duodenum
48	chr4:7043400-7044200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
49	chr4:7043400-7044400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr4:7043400-7044400	Flanking Active TSS	Brain Hippocampus Middle	brain

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