Variant report

Variant	nsv538718
Chromosome Location	chr7:6572916-6604115
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:6598567-6598706	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:6583036-6583373	HepG2	liver:	n/a	n/a
3	ATF2	chr7:6593208-6593692	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr7:6593225-6593689	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr7:6586728-6586798	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr7:6598618-6598770	K562	blood:	n/a	n/a
7	BHLHE40	chr7:6585459-6585787	GM12878	blood:	n/a	chr7:6585463-6585479
8	BHLHE40	chr7:6581206-6581323	K562	blood:	n/a	n/a
9	BRCA1	chr7:6598589-6598725	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr7:6598548-6598800	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr7:6583005-6583423	HepG2	liver:	n/a	n/a
12	CEBPB	chr7:6583034-6583411	MCF-7	breast:	n/a	n/a
13	CEBPB	chr7:6583075-6583352	HepG2	liver:	n/a	n/a
14	CEBPB	chr7:6583124-6583352	IMR90	lung:	n/a	n/a
15	CEBPB	chr7:6583047-6583368	K562	blood:	n/a	n/a
16	CEBPB	chr7:6583013-6583424	HepG2	liver:	n/a	n/a
17	CEBPB	chr7:6583083-6583351	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr7:6583018-6583366	HepG2	liver:	n/a	n/a
19	CEBPB	chr7:6583040-6583323	Hela-S3	cervix:	n/a	n/a
20	CEBPD	chr7:6583033-6583328	HepG2	liver:	n/a	n/a
21	CHD2	chr7:6586524-6586735	H1-hESC	embryonic stem cell:	n/a	n/a
22	CREB1	chr7:6574023-6574241	A549	lung:	n/a	n/a
23	CREB1	chr7:6593239-6593690	H1-hESC	embryonic stem cell:	n/a	n/a
24	CREB1	chr7:6593377-6593677	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr7:6593180-6593330	BE2_C	brain:	n/a	chr7:6593276-6593285
26	CTCF	chr7:6593128-6593453	K562	blood:	n/a	chr7:6593276-6593285
27	CTCF	chr7:6593179-6593337	MCF-7	breast:	n/a	chr7:6593276-6593285
28	CTCF	chr7:6595946-6596040	Lung_OC	lung:	n/a	chr7:6596030-6596039
29	CTCF	chr7:6595936-6596158	GM12891	blood:	n/a	chr7:6596061-6596068 chr7:6596030-6596043 chr7:6596029-6596050 chr7:6596027-6596045 chr7:6596030-6596039
30	CTCF	chr7:6595920-6596070	SK-N-SH_RA	brain:	n/a	chr7:6596061-6596068 chr7:6596030-6596043 chr7:6596029-6596050 chr7:6596027-6596045 chr7:6596030-6596039
31	CTCF	chr7:6598600-6598750	NB4	blood:	n/a	n/a
32	CTCF	chr7:6593160-6593310	AG04449	skin:	n/a	chr7:6593276-6593285
33	CTCF	chr7:6595722-6596180	A549	lung:	n/a	chr7:6595839-6595852 chr7:6596061-6596068 chr7:6596030-6596043 chr7:6596029-6596050 chr7:6596027-6596045 chr7:6596030-6596039
34	CTCF	chr7:6593018-6593046	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr7:6595960-6596110	NHEK	skin:	n/a	chr7:6596061-6596068 chr7:6596030-6596043 chr7:6596029-6596050 chr7:6596027-6596045 chr7:6596030-6596039
36	CTCF	chr7:6598460-6598610	HFF-Myc	foreskin:	n/a	n/a
37	CTCF	chr7:6598600-6598750	GM12873	blood:	n/a	n/a
38	CTCF	chr7:6598440-6598967	MCF-7	breast:	n/a	n/a
39	CTCF	chr7:6595957-6596122	A549	lung:	n/a	chr7:6596061-6596068 chr7:6596030-6596043 chr7:6596029-6596050 chr7:6596027-6596045 chr7:6596030-6596039
40	CTCF	chr7:6598600-6598750	HBMEC	blood vessel:	n/a	n/a
41	CTCF	chr7:6595960-6596110	SAEC	small airway:	n/a	chr7:6596061-6596068 chr7:6596030-6596043 chr7:6596029-6596050 chr7:6596027-6596045 chr7:6596030-6596039
42	CTCF	chr7:6598580-6598730	GM12864	blood:	n/a	n/a
43	CTCF	chr7:6598572-6598791	GM12878	blood:	n/a	n/a
44	CTCF	chr7:6575760-6575910	WERI-Rb-1	eye:	n/a	n/a
45	CTCF	chr7:6595940-6596090	GM12870	blood:	n/a	chr7:6596061-6596068 chr7:6596030-6596043 chr7:6596029-6596050 chr7:6596027-6596045 chr7:6596030-6596039
46	CTCF	chr7:6601680-6601830	AoAF	blood vessel:	n/a	n/a
47	CTCF	chr7:6598520-6598670	HFF-Myc	foreskin:	n/a	n/a
48	CTCF	chr7:6595920-6596070	GM12878	blood:	n/a	chr7:6596061-6596068 chr7:6596030-6596043 chr7:6596029-6596050 chr7:6596027-6596045 chr7:6596030-6596039
49	CTCF	chr7:6595920-6596070	HCPEpiC	choroid plexus:	n/a	chr7:6596061-6596068 chr7:6596030-6596043 chr7:6596029-6596050 chr7:6596027-6596045 chr7:6596030-6596039
50	CTCF	chr7:6601700-6601850	A549	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:6592322-6592372	GM19239	blood:	n/a
2	chr7:6592322-6592372	GM19239	blood:	n/a
3	chr7:6584987-6585037	GM19239	blood:	n/a
4	chr7:6576353-6576403	AG09319	gingival:	n/a
5	chr7:6576529-6576579	HEK293	kidney:	embryo
6	chr7:6591968-6592018	PFSK-1	brain:	n/a
7	chr7:6590564-6590614	AG10803	skin:	n/a
8	chr7:6576529-6576579	HRPEpiC	eye:	n/a
9	chr7:6575581-6575631	SK-N-MC	brain:	n/a
10	chr7:6576152-6576202	NHBE	bronchial:	n/a
11	chr7:6575581-6575631	ProgFib	skin:	n/a
12	chr7:6594886-6594936	Hepatocyte	liver:	n/a
13	chr7:6590947-6590997	HL-60	blood:	n/a
14	chr7:6576152-6576202	AoSMC	blood vessel:	n/a
15	chr7:6591968-6592018	HIPEpiC	eye:	n/a
16	chr7:6575581-6575631	HCPEpiC	choroid plexus:	n/a
17	chr7:6576529-6576579	Hepatocyte	liver:	n/a
18	chr7:6579213-6579263	GM12891	blood:	n/a
19	chr7:6591968-6592018	AG09309	skin:	n/a
20	chr7:6576353-6576403	IMR90	lung:	fetal
21	chr7:6576152-6576202	BE2_C	brain:	n/a
22	chr7:6579213-6579263	HIPEpiC	eye:	n/a
23	chr7:6594886-6594936	AG09319	gingival:	n/a
24	chr7:6575581-6575631	NH-A	brain:	n/a
25	chr7:6575968-6576018	HAEpiC	amniotic membrane:	n/a
26	chr7:6576152-6576202	H1-hESC	embryonic stem cell:	embryo
27	chr7:6579213-6579263	U87	brain:	n/a
28	chr7:6590947-6590997	GM12891	blood:	n/a
29	chr7:6590947-6590997	AoSMC	blood vessel:	n/a
30	chr7:6591968-6592018	BE2_C	brain:	n/a
31	chr7:6592322-6592372	Caco-2	colon:	n/a
32	chr7:6573259-6573309	MCF-7	breast:	n/a
33	chr7:6586786-6586836	SK-N-SH_RA	brain:	n/a
34	chr7:6594886-6594936	HMEC	breast:	n/a
35	chr7:6586786-6586836	GM19239	blood:	n/a
36	chr7:6576152-6576202	IMR90	lung:	fetal
37	chr7:6575968-6576018	ovcar-3	ovarian:	n/a
38	chr7:6573259-6573309	NHDF-neo	bronchial:	n/a
39	chr7:6575968-6576018	Hela-S3	cervix:	n/a
40	chr7:6586786-6586836	NHDF-neo	bronchial:	n/a
41	chr7:6592322-6592372	HRE	kidney:	n/a
42	chr7:6575581-6575631	HIPEpiC	eye:	n/a
43	chr7:6576353-6576403	GM19239	blood:	n/a
44	chr7:6589601-6589651	HMEC	breast:	n/a
45	chr7:6576152-6576202	HAEpiC	amniotic membrane:	n/a
46	chr7:6589601-6589651	RPTEC	kidney:	n/a
47	chr7:6584987-6585037	PFSK-1	brain:	n/a
48	chr7:6591968-6592018	AG04449	skin:	fetal
49	chr7:6584987-6585037	AG09319	gingival:	n/a
50	chr7:6589601-6589651	U87	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:6555645..6556331-chr7:6598481..6599481,2	MCF-7	breast:
2	chr7:6569353..6570981-chr7:6572499..6575185,2	MCF-7	breast:
3	chr7:6570876..6573831-chr7:6581104..6583743,3	MCF-7	breast:
4	chr7:6567226..6571093-chr7:6573864..6577446,5	K562	blood:
5	chr7:6599967..6601686-chr7:6615495..6617237,2	K562	blood:
6	chr7:6595453..6597411-chr7:6675882..6677849,2	MCF-7	breast:
7	chr7:6567990..6570069-chr7:6570914..6573457,2	K562	blood:
8	chr7:6582625..6584643-chr7:6586210..6588627,2	K562	blood:
9	chr7:6541570..6543326-chr7:6585489..6588258,2	MCF-7	breast:
10	chr7:6588615..6590348-chr7:6593540..6596272,2	K562	blood:
11	chr7:6595343..6598208-chr7:6598737..6601436,2	K562	blood:
12	chr7:6588615..6590348-chr7:6593540..6596272,2	K562	blood:
13	chr7:6597937..6600168-chr7:6615971..6618581,2	MCF-7	breast:
14	chr7:6572401..6574115-chr7:6615696..6617407,2	MCF-7	breast:
15	chr7:6570876..6573831-chr7:6581104..6583743,3	MCF-7	breast:
16	chr7:6582625..6584643-chr7:6586210..6588627,2	K562	blood:
17	chr7:6572621..6574294-chr7:6616211..6618140,2	K562	blood:
18	chr7:6599534..6602029-chr7:6628855..6631430,2	K562	blood:
19	chr7:6594435..6597385-chr7:6628015..6630445,4	MCF-7	breast:
20	chr7:6595343..6598208-chr7:6598737..6601436,2	K562	blood:

Variant related genes	Relation type
GRID2IP	TF binding region
GRID2IP	CpG island
ENSG00000215045	chromatin interactions
ENSG00000146576	chromatin interactions
ENSG00000136247	chromatin interactions
ENSG00000205903	chromatin interactions
ENSG00000232581	chromatin interactions

Extended variants
information (count: 1354 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:1354 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562418672	chr7:6572939-6572940	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs77398712	chr7:6572967-6572968	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs372139436	chr7:6572978-6572979	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs547946145	chr7:6572987-6572988	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs567078535	chr7:6572994-6572995	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs544933964	chr7:6572995-6572996	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs113268191	chr7:6573071-6573072	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs527861502	chr7:6573086-6573087	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs7783799	chr7:6573087-6573088	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs183934608	chr7:6573138-6573139	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs530489841	chr7:6573153-6573154	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs542659333	chr7:6573164-6573165	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs376980802	chr7:6573186-6573187	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs556142213	chr7:6573187-6573188	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs560950768	chr7:6573195-6573196	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs568079579	chr7:6573202-6573203	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs143319844	chr7:6573212-6573213	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs553952118	chr7:6573214-6573215	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs528224235	chr7:6573248-6573249	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs573026263	chr7:6573262-6573263	Weak transcription Enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs540042383	chr7:6573307-6573308	Weak transcription Enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs386709833	chr7:6573448-6573449	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs181508670	chr7:6573450-6573451	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs371030264	chr7:6573453-6573454	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs544481094	chr7:6573482-6573483	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs377397166	chr7:6573507-6573508	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs547966933	chr7:6573582-6573583	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs369013136	chr7:6573606-6573607	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs562485798	chr7:6573621-6573622	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs529632008	chr7:6573639-6573640	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs186686314	chr7:6573689-6573690	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs145508365	chr7:6573701-6573702	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs559737067	chr7:6573726-6573727	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs73674129	chr7:6573731-6573732	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs570664015	chr7:6573805-6573806	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs148779728	chr7:6573857-6573858	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs34009907	chr7:6573882-6573883	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs142392461	chr7:6573906-6573907	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs550033043	chr7:6573914-6573915	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs151331581	chr7:6573917-6573918	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs141820272	chr7:6573946-6573947	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs551742635	chr7:6573978-6573979	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs554280534	chr7:6573989-6573990	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs570036981	chr7:6573991-6573992	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs566034888	chr7:6574012-6574013	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs539872095	chr7:6574057-6574058	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs558792239	chr7:6574083-6574084	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs575926152	chr7:6574093-6574094	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs577081329	chr7:6574094-6574095	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs147038324	chr7:6574167-6574168	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21045282	CNVD
Disorders of sex development	21048976	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	21525872	CNVD
Autism	20685689	CNVD
Intracranial arachnoid cysts	20187927	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:326 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:6570800-6573400	Weak transcription	Gastric	stomach
2	chr7:6571000-6576000	Weak transcription	Right Atrium	heart
3	chr7:6571200-6573800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr7:6571400-6573400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
5	chr7:6571400-6573600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
6	chr7:6571400-6575800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr7:6571600-6573400	Weak transcription	Primary hematopoietic stem cells	blood
8	chr7:6571600-6576000	Weak transcription	Primary B cells from cord blood	blood
9	chr7:6572800-6573200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr7:6573200-6573600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr7:6573400-6573600	Enhancers	GM12878-XiMat	blood
12	chr7:6573400-6574400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
13	chr7:6573400-6574600	Enhancers	Primary hematopoietic stem cells	blood
14	chr7:6573600-6574200	Flanking Active TSS	GM12878-XiMat	blood
15	chr7:6573600-6574400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr7:6573800-6574000	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
17	chr7:6573800-6574000	Bivalent Enhancer	K562	blood
18	chr7:6573800-6574200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
19	chr7:6573800-6574200	Bivalent Enhancer	HepG2	liver
20	chr7:6573800-6574400	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr7:6573800-6574400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
22	chr7:6574000-6574200	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr7:6574000-6574200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
24	chr7:6574000-6574200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
25	chr7:6574000-6574200	Flanking Bivalent TSS/Enh	Duodenum Mucosa	Duodenum
26	chr7:6574000-6574200	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
27	chr7:6574000-6574600	Bivalent Enhancer	Fetal Muscle Leg	muscle
28	chr7:6574200-6574400	Enhancers	GM12878-XiMat	blood
29	chr7:6574400-6575400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr7:6574600-6575600	Weak transcription	Primary hematopoietic stem cells	blood
31	chr7:6575400-6575600	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
32	chr7:6575400-6575600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
33	chr7:6575400-6575600	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr7:6575400-6575600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr7:6575400-6575600	Bivalent Enhancer	Esophagus	oesophagus
36	chr7:6575400-6575600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
37	chr7:6575400-6575600	Bivalent/Poised TSS	Rectal Mucosa Donor 29	rectum
38	chr7:6575400-6575800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
39	chr7:6575400-6575800	Bivalent Enhancer	Fetal Muscle Leg	muscle
40	chr7:6575400-6577000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr7:6575600-6575800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
42	chr7:6575600-6575800	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr7:6575600-6575800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
44	chr7:6575600-6575800	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr7:6575600-6575800	Enhancers	Primary hematopoietic stem cells	blood
46	chr7:6575600-6575800	Flanking Bivalent TSS/Enh	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr7:6575600-6575800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr7:6575600-6575800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr7:6575600-6575800	Flanking Bivalent TSS/Enh	Brain Anterior Caudate	brain
50	chr7:6575600-6575800	Bivalent/Poised TSS	Brain Hippocampus Middle	brain

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