Variant report

Variant	nsv522967
Chromosome Location	chr1:113384015-113400990
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:207)
CpG islands
(count:612)
Chromatin interactive
region (count:6)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:207 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr1:113391962-113392548	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr1:113387894-113388170	GM12878	blood:	n/a	chr1:113388042-113388053
3	CEBPB	chr1:113397800-113398144	IMR90	lung:	n/a	chr1:113397958-113397969
4	CEBPB	chr1:113386872-113387013	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr1:113394351-113394537	A549	lung:	n/a	n/a
6	CEBPB	chr1:113383779-113384209	MCF-7	breast:	n/a	n/a
7	CEBPB	chr1:113394303-113394797	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr1:113399996-113400299	K562	blood:	n/a	n/a
9	CEBPB	chr1:113394323-113394637	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr1:113386765-113387060	A549	lung:	n/a	n/a
11	CEBPB	chr1:113386774-113387098	IMR90	lung:	n/a	n/a
12	CEBPB	chr1:113394309-113394671	IMR90	lung:	n/a	n/a
13	CEBPB	chr1:113383834-113384109	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr1:113399987-113400263	K562	blood:	n/a	n/a
15	CEBPB	chr1:113397795-113398109	HepG2	liver:	n/a	chr1:113397958-113397969
16	CEBPB	chr1:113383814-113384195	MCF-7	breast:	n/a	n/a
17	CEBPB	chr1:113394312-113394617	K562	blood:	n/a	n/a
18	CEBPB	chr1:113386784-113387058	K562	blood:	n/a	n/a
19	CEBPB	chr1:113397822-113398064	K562	blood:	n/a	chr1:113397958-113397969
20	CEBPB	chr1:113394315-113394515	HepG2	liver:	n/a	n/a
21	CEBPB	chr1:113394293-113394634	K562	blood:	n/a	n/a
22	CEBPB	chr1:113386785-113387076	HepG2	liver:	n/a	n/a
23	CEBPB	chr1:113397788-113398124	A549	lung:	n/a	chr1:113397958-113397969
24	CEBPB	chr1:113386881-113387074	Hela-S3	cervix:	n/a	n/a
25	CHD2	chr1:113392081-113392251	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr1:113392180-113392330	SK-N-SH_RA	brain:	n/a	n/a
27	CTCF	chr1:113393341-113393404	GM10248	blood:	n/a	n/a
28	CTCF	chr1:113392300-113392450	HUVEC	blood vessel:	n/a	n/a
29	CTCF	chr1:113385600-113385750	GM12867	blood:	n/a	n/a
30	CTCF	chr1:113392360-113392510	SK-N-SH_RA	brain:	n/a	n/a
31	CTCF	chr1:113392420-113392570	HCPEpiC	choroid plexus:	n/a	n/a
32	E2F4	chr1:113392947-113393147	MCF10A-Er-Src	breast:	n/a	n/a
33	E2F4	chr1:113394388-113394639	MCF10A-Er-Src	breast:	n/a	n/a
34	E2F4	chr1:113392230-113392617	MCF10A-Er-Src	breast:	n/a	n/a
35	E2F6	chr1:113398207-113398417	K562	blood:	n/a	n/a
36	E2F6	chr1:113398170-113398427	K562	blood:	n/a	n/a
37	E2F6	chr1:113392117-113392650	A549	lung:	n/a	n/a
38	E2F6	chr1:113391912-113392829	H1-hESC	embryonic stem cell:	n/a	n/a
39	E2F6	chr1:113391825-113392891	H1-hESC	embryonic stem cell:	n/a	n/a
40	EP300	chr1:113395570-113395575	K562	blood:	n/a	n/a
41	FOS	chr1:113394379-113394613	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr1:113387983-113388176	HUVEC	blood vessel:	n/a	chr1:113388044-113388055
43	FOS	chr1:113387872-113388323	MCF10A-Er-Src	breast:	n/a	chr1:113388044-113388055
44	FOS	chr1:113398119-113398319	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr1:113394381-113394615	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr1:113394362-113394587	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr1:113387990-113388169	MCF10A-Er-Src	breast:	n/a	chr1:113388044-113388055
48	FOS	chr1:113393407-113393535	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr1:113394354-113394640	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr1:113385879-113385970	MCF10A-Er-Src	breast:	n/a	n/a

(count:612 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:113390019-113390069	HRCEpiC	kidney:	n/a
2	chr1:113392116-113392166	AG10803	skin:	n/a
3	chr1:113390019-113390069	HRCEpiC	kidney:	n/a
4	chr1:113392116-113392166	AG10803	skin:	n/a
5	chr1:113390019-113390069	AG04450	lung:	fetal
6	chr1:113393322-113393372	A549	lung:	n/a
7	chr1:113393322-113393372	AoSMC	blood vessel:	n/a
8	chr1:113392781-113392831	GM12891	blood:	n/a
9	chr1:113392781-113392831	SK-N-SH	brain:	n/a
10	chr1:113393176-113393226	HL-60	blood:	n/a
11	chr1:113392617-113392667	HCPEpiC	choroid plexus:	n/a
12	chr1:113393322-113393372	Jurkat	blood:	n/a
13	chr1:113393322-113393372	H1-hESC	embryonic stem cell:	embryo
14	chr1:113392116-113392166	AoSMC	blood vessel:	n/a
15	chr1:113393179-113393229	SK-N-SH	brain:	n/a
16	chr1:113393179-113393229	SK-N-SH_RA	brain:	n/a
17	chr1:113390019-113390069	HCT-116	colon:	n/a
18	chr1:113392116-113392166	BE2_C	brain:	n/a
19	chr1:113394877-113394927	HIPEpiC	eye:	n/a
20	chr1:113394877-113394927	Jurkat	blood:	n/a
21	chr1:113394877-113394927	AG09319	gingival:	n/a
22	chr1:113394877-113394927	HCPEpiC	choroid plexus:	n/a
23	chr1:113392617-113392667	SK-N-SH	brain:	n/a
24	chr1:113392116-113392166	PFSK-1	brain:	n/a
25	chr1:113393176-113393226	GM12892	blood:	n/a
26	chr1:113394877-113394927	U87	brain:	n/a
27	chr1:113392388-113392438	HEEpiC	esophagus:	n/a
28	chr1:113392781-113392831	Caco-2	colon:	n/a
29	chr1:113392781-113392831	ovcar-3	ovarian:	n/a
30	chr1:113393179-113393229	HEEpiC	esophagus:	n/a
31	chr1:113392116-113392166	GM19239	blood:	n/a
32	chr1:113392617-113392667	BE2_C	brain:	n/a
33	chr1:113393179-113393229	HUVEC	blood vessel:	n/a
34	chr1:113393322-113393372	HAEpiC	amniotic membrane:	n/a
35	chr1:113392116-113392166	U87	brain:	n/a
36	chr1:113393176-113393226	ECC-1	luminal epithelium:	n/a
37	chr1:113390019-113390069	MCF-7	breast:	n/a
38	chr1:113392617-113392667	K562	blood:	n/a
39	chr1:113392781-113392831	RPTEC	kidney:	n/a
40	chr1:113392781-113392831	ProgFib	skin:	n/a
41	chr1:113394877-113394927	Caco-2	colon:	n/a
42	chr1:113392781-113392831	HAEpiC	amniotic membrane:	n/a
43	chr1:113393179-113393229	U87	brain:	n/a
44	chr1:113392162-113392212	PFSK-1	brain:	n/a
45	chr1:113392617-113392667	BJ	skin:	n/a
46	chr1:113393179-113393229	PFSK-1	brain:	n/a
47	chr1:113393322-113393372	HEK293	kidney:	embryo
48	chr1:113394877-113394927	HRPEpiC	eye:	n/a
49	chr1:113392116-113392166	K562	blood:	n/a
50	chr1:113392162-113392212	HCM	heart:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:113346242..113347922-chr1:113394008..113395856,2	MCF-7	breast:
2	chr1:113393846..113396397-chr1:113410611..113412289,2	K562	blood:
3	chr1:113383663..113385223-chr1:113386866..113389078,2	MCF-7	breast:
4	chr1:113383663..113385223-chr1:113386866..113389078,2	MCF-7	breast:
5	chr1:113382661..113385204-chr1:113393197..113394858,2	MCF-7	breast:
6	chr1:113379016..113381976-chr1:113384140..113386902,2	MCF-7	breast:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC16A1-1	chr1:113391576-113391672	NONHSAT005284
2	lnc-FAM19A3-7	chr1:113399850-113401156	NONHSAT005291
3	lnc-FAM19A3-6	chr1:113390931-113391200	NONHSAT005288
4	lnc-SLC16A1-1	chr1:113392302-113392399	ENSG00000215866.3
5	lnc-SLC16A1-1	chr1:113392302-113392437	XLOC_000966
6	lnc-SLC16A1-1	chr1:113392302-113393265	XLOC_000966
7	lnc-FAM19A3-7	chr1:113400759-113400763	NONHSAT005292
8	lnc-FAM19A3-2	chr1:113392698-113393049	XLOC_000348
9	lnc-SLC16A1-1	chr1:113392568-113392706	ucscGeneNc_uc001ede_1
10	lnc-FAM19A3-7	chr1:113400131-113400686	NONHSAT005292
11	lnc-SLC16A1-1	chr1:113392302-113392401	XLOC_000966
12	lnc-SLC16A1-1	chr1:113392302-113393265	NONHSAT005284
13	lnc-SLC16A1-1	chr1:113391576-113391672	XLOC_000966
14	lnc-FAM19A3-6	chr1:113390931-113391200	NONHSAT005281
15	lnc-FAM19A3-2	chr1:113392392-113393049	NONHSAT005289
16	lnc-FAM19A3-2	chr1:113392650-113393049	XLOC_000348

No data

Variant related genes	Relation type
ENSG00000215866	TF binding region
ENSG00000224167	TF binding region
ENSG00000215866	CpG island
ENSG00000224167	CpG island
ENSG00000215866	chromatin interactions
NCOR2	miRNA target sites
CREB5	miRNA target sites
HAUS6	miRNA target sites
CTDSPL	miRNA target sites
CDH12	miRNA target sites

Extended variants
information (count: 730 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:730 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7539948	chr1:113384015-113384016	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs566347658	chr1:113384117-113384118	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs538698187	chr1:113384138-113384139	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs563381959	chr1:113384149-113384150	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs558383670	chr1:113384161-113384162	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs187754501	chr1:113384196-113384197	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs190926137	chr1:113384197-113384198	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs182754571	chr1:113384207-113384208	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs188170611	chr1:113384208-113384209	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs367925774	chr1:113384229-113384230	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs192891318	chr1:113384234-113384235	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs184577443	chr1:113384235-113384236	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs553662074	chr1:113384279-113384280	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs187366278	chr1:113384290-113384291	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs12081613	chr1:113384300-113384301	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs376616165	chr1:113384323-113384324	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs191958268	chr1:113384375-113384376	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs531071092	chr1:113384401-113384402	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs368725241	chr1:113384422-113384423	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs184761433	chr1:113384427-113384428	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs6674386	chr1:113384466-113384467	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs6687054	chr1:113384500-113384501	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs546599654	chr1:113384506-113384507	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs369722091	chr1:113384509-113384510	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs531996559	chr1:113384536-113384537	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs6698018	chr1:113384542-113384543	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs72996317	chr1:113384565-113384566	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs78907641	chr1:113384566-113384567	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs537590569	chr1:113384568-113384569	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs141742899	chr1:113384570-113384571	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs557093290	chr1:113384637-113384638	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs567524761	chr1:113384651-113384652	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs373143094	chr1:113384660-113384661	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs536523213	chr1:113384735-113384736	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs533333927	chr1:113384742-113384743	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs112441581	chr1:113384743-113384744	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs10687618	chr1:113384744-113384745	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs553408491	chr1:113384766-113384767	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs189261684	chr1:113384788-113384789	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs6677225	chr1:113384799-113384800	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs6677237	chr1:113384830-113384831	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs575766533	chr1:113384831-113384832	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs142987652	chr1:113384919-113384920	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs6692406	chr1:113384920-113384921	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs180981506	chr1:113384952-113384953	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs184455681	chr1:113384972-113384973	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs560165506	chr1:113384976-113384977	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs532485246	chr1:113384992-113384993	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs551876932	chr1:113385031-113385032	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs375693165	chr1:113385032-113385033	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21720365	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	17550852	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Asthma	20841430	CNVD
Aetanephric adenomas	20802469	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Systemic lupus erythematosus	21956041	CNVD
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	16573809	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Breast cancer	17899364	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Melanoma	19671679	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	23813976	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:573 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:113364200-113392000	Weak transcription	Right Atrium	heart
2	chr1:113369200-113392000	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr1:113382600-113384200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
4	chr1:113382600-113384200	Enhancers	HUVEC	blood vessel
5	chr1:113382600-113384400	Enhancers	Dnd41	blood
6	chr1:113382600-113385000	Enhancers	Primary hematopoietic stem cells short term culture	blood
7	chr1:113382800-113384200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
8	chr1:113382800-113384200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
9	chr1:113382800-113384200	Enhancers	NHEK	skin
10	chr1:113382800-113384800	Enhancers	Primary T helper cells fromperipheralblood	blood
11	chr1:113382800-113384800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr1:113382800-113384800	Enhancers	Hela-S3	cervix
13	chr1:113382800-113385000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr1:113382800-113385800	Enhancers	Primary monocytes fromperipheralblood	blood
15	chr1:113383000-113384200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
16	chr1:113383000-113384200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr1:113383000-113384200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
18	chr1:113383000-113384800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr1:113383000-113384800	Enhancers	Primary hematopoietic stem cells	blood
20	chr1:113383000-113384800	Enhancers	Primary T helper cells PMA-I stimulated	--
21	chr1:113383000-113385600	Enhancers	Primary B cells from cord blood	blood
22	chr1:113383000-113386200	Enhancers	Primary B cells from peripheral blood	blood
23	chr1:113383200-113384200	Enhancers	Primary T killer memory cells from peripheral blood	blood
24	chr1:113383200-113384200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr1:113383200-113384200	Enhancers	Stomach Mucosa	stomach
26	chr1:113383200-113384800	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr1:113383400-113384200	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr1:113383400-113384200	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr1:113383400-113384200	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr1:113383400-113384200	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr1:113383400-113384200	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr1:113383400-113389600	Weak transcription	Right Ventricle	heart
33	chr1:113383600-113384200	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr1:113383600-113384200	Enhancers	Duodenum Mucosa	Duodenum
35	chr1:113383600-113384200	Enhancers	Rectal Mucosa Donor 29	rectum
36	chr1:113383600-113384200	Enhancers	Rectal Mucosa Donor 31	rectum
37	chr1:113383600-113384200	Enhancers	A549	lung
38	chr1:113383600-113384800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
39	chr1:113383800-113384200	Enhancers	H1 Cell Line	embryonic stem cell
40	chr1:113383800-113384200	Enhancers	HepG2	liver
41	chr1:113383800-113385000	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
42	chr1:113383800-113392000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr1:113384000-113384600	Enhancers	Primary T cells from cord blood	blood
44	chr1:113384000-113384800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr1:113384000-113386000	Enhancers	GM12878-XiMat	blood
46	chr1:113384000-113387400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr1:113384000-113387800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr1:113384000-113387800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr1:113384000-113387800	Weak transcription	HMEC	breast
50	chr1:113384000-113388200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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