Variant report

Variant	nsv4687
Chromosome Location	chr1:223565080-223610362
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:268)
CpG islands
(count:1040)
Chromatin interactive
region (count:35)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:268 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:223575820-223576201	K562	blood:	n/a	n/a
2	ARID3A	chr1:223590836-223591158	HepG2	liver:	n/a	n/a
3	ATF1	chr1:223575824-223576299	K562	blood:	n/a	n/a
4	ATF1	chr1:223591787-223591811	K562	blood:	n/a	n/a
5	BACH1	chr1:223575778-223576211	K562	blood:	n/a	n/a
6	BACH1	chr1:223575942-223576127	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr1:223576484-223576849	K562	blood:	n/a	n/a
8	BHLHE40	chr1:223568349-223568477	K562	blood:	n/a	n/a
9	CBX3	chr1:223575786-223576251	HCT-116	colon:	n/a	n/a
10	CCNT2	chr1:223576227-223576453	K562	blood:	n/a	n/a
11	CCNT2	chr1:223575788-223575995	K562	blood:	n/a	n/a
12	CEBPB	chr1:223576940-223577037	HepG2	liver:	n/a	chr1:223576977-223576994 chr1:223576979-223576990
13	CEBPB	chr1:223576793-223577154	Hela-S3	cervix:	n/a	chr1:223576977-223576994 chr1:223576979-223576990
14	CEBPB	chr1:223582381-223582578	A549	lung:	n/a	n/a
15	CEBPB	chr1:223591410-223591576	H1-hESC	embryonic stem cell:	n/a	chr1:223591521-223591532
16	CEBPB	chr1:223591396-223591593	IMR90	lung:	n/a	chr1:223591521-223591532
17	CEBPB	chr1:223594972-223595328	MCF-7	breast:	n/a	n/a
18	CEBPB	chr1:223608721-223608787	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr1:223583533-223583548	K562	blood:	n/a	n/a
20	CEBPB	chr1:223591488-223591545	A549	lung:	n/a	chr1:223591521-223591532
21	CEBPB	chr1:223591367-223591641	HepG2	liver:	n/a	chr1:223591521-223591532
22	CEBPB	chr1:223601000-223601170	A549	lung:	n/a	n/a
23	CEBPB	chr1:223582375-223582612	IMR90	lung:	n/a	n/a
24	CEBPB	chr1:223600982-223601148	K562	blood:	n/a	n/a
25	CEBPB	chr1:223583399-223583752	IMR90	lung:	n/a	n/a
26	CEBPB	chr1:223582425-223582499	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr1:223576843-223577132	IMR90	lung:	n/a	chr1:223576977-223576994 chr1:223576979-223576990
28	CEBPB	chr1:223575754-223576141	Hela-S3	cervix:	n/a	n/a
29	CTCF	chr1:223602860-223603010	NHEK	skin:	n/a	n/a
30	CTCF	chr1:223602758-223602998	Fibrobl	skin:	n/a	n/a
31	CTCF	chr1:223602960-223603110	AG09309	skin:	n/a	n/a
32	CTCF	chr1:223602741-223603042	NHEK	skin:	n/a	n/a
33	CTCF	chr1:223602740-223602890	AoAF	blood vessel:	n/a	n/a
34	CTCF	chr1:223577600-223577750	HepG2	liver:	n/a	n/a
35	CTCF	chr1:223591363-223591412	Kidney_OC	kidney:	n/a	n/a
36	CTCF	chr1:223602805-223602989	ProgFib	skin:	n/a	n/a
37	CTCF	chr1:223568260-223568410	GM12865	blood:	n/a	n/a
38	CTCF	chr1:223602832-223603008	Gliobla	brain:	n/a	n/a
39	CTCF	chr1:223602958-223603012	LNCaP	prostate:	n/a	n/a
40	CTCF	chr1:223602760-223602910	HMEC	breast:	n/a	n/a
41	CTCF	chr1:223602900-223603050	HEEpiC	esophagus:	n/a	n/a
42	CTCF	chr1:223602860-223603010	HMEC	breast:	n/a	n/a
43	CTCF	chr1:223602880-223603030	RPTEC	kidney:	n/a	n/a
44	CTCF	chr1:223575953-223576183	K562	blood:	n/a	n/a
45	CTCF	chr1:223602937-223602962	Kidney_OC	kidney:	n/a	n/a
46	CTCF	chr1:223577640-223577790	HEK293	kidney:	n/a	n/a
47	CTCF	chr1:223602860-223603010	AG09319	gingival:	n/a	n/a
48	CTCF	chr1:223602888-223602955	Pancreas_OC	pancreas:	n/a	n/a
49	CTCF	chr1:223595672-223595712	LNCaP	prostate:	n/a	n/a
50	CTCF	chr1:223602820-223602970	AG10803	skin:	n/a	n/a

(count:1040 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:223566761-223566811	T-47D	breast:	n/a
2	chr1:223566669-223566719	IMR90	lung:	fetal
3	chr1:223565773-223565823	Caco-2	colon:	n/a
4	chr1:223566761-223566811	T-47D	breast:	n/a
5	chr1:223566669-223566719	IMR90	lung:	fetal
6	chr1:223565773-223565823	Caco-2	colon:	n/a
7	chr1:223566646-223566696	HCPEpiC	choroid plexus:	n/a
8	chr1:223566669-223566719	Hepatocyte	liver:	n/a
9	chr1:223566278-223566328	HEK293	kidney:	embryo
10	chr1:223568700-223568750	HL-60	blood:	n/a
11	chr1:223566278-223566328	MCF10A-Er-Src	breast:	n/a
12	chr1:223566646-223566696	NHBE	bronchial:	n/a
13	chr1:223566794-223566844	AoSMC	blood vessel:	n/a
14	chr1:223567949-223567999	NHDF-neo	bronchial:	n/a
15	chr1:223567173-223567223	SK-N-SH	brain:	n/a
16	chr1:223566643-223566693	AG09319	gingival:	n/a
17	chr1:223565773-223565823	SK-N-SH_RA	brain:	n/a
18	chr1:223566709-223566759	GM12878	blood:	n/a
19	chr1:223575793-223575843	BJ	skin:	n/a
20	chr1:223565773-223565823	GM12878	blood:	n/a
21	chr1:223566646-223566696	GM12891	blood:	n/a
22	chr1:223567173-223567223	HRE	kidney:	n/a
23	chr1:223568700-223568750	HRE	kidney:	n/a
24	chr1:223566127-223566177	HCF	heart:	n/a
25	chr1:223566447-223566497	AG10803	skin:	n/a
26	chr1:223568700-223568750	AG09319	gingival:	n/a
27	chr1:223567949-223567999	NHBE	bronchial:	n/a
28	chr1:223565102-223565152	ProgFib	skin:	n/a
29	chr1:223567949-223567999	HCM	heart:	n/a
30	chr1:223567949-223567999	BJ	skin:	n/a
31	chr1:223566127-223566177	HCT-116	colon:	n/a
32	chr1:223567173-223567223	HMEC	breast:	n/a
33	chr1:223565102-223565152	IMR90	lung:	fetal
34	chr1:223566669-223566719	CMK	blood:	n/a
35	chr1:223566709-223566759	AG04450	lung:	fetal
36	chr1:223565773-223565823	HRE	kidney:	n/a
37	chr1:223567173-223567223	PrEC	prostate:	n/a
38	chr1:223566127-223566177	ovcar-3	ovarian:	n/a
39	chr1:223565773-223565823	ovcar-3	ovarian:	n/a
40	chr1:223565102-223565152	U87	brain:	n/a
41	chr1:223567955-223568005	HAEpiC	amniotic membrane:	n/a
42	chr1:223567955-223568005	MCF10A-Er-Src	breast:	n/a
43	chr1:223568700-223568750	HEEpiC	esophagus:	n/a
44	chr1:223567955-223568005	PrEC	prostate:	n/a
45	chr1:223567173-223567223	SK-N-SH_RA	brain:	n/a
46	chr1:223566794-223566844	RPTEC	kidney:	n/a
47	chr1:223567173-223567223	GM12878	blood:	n/a
48	chr1:223565773-223565823	AG10803	skin:	n/a
49	chr1:223566447-223566497	BJ	skin:	n/a
50	chr1:223575793-223575843	HUVEC	blood vessel:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:223604902..223607898-chr1:223616304..223618206,2	MCF-7	breast:
2	chr1:223607026..223608626-chr1:223610171..223611706,2	K562	blood:
3	chr1:223566045..223568415-chr1:223593690..223595373,2	MCF-7	breast:
4	chr1:223596035..223598867-chr1:223600908..223603274,2	K562	blood:
5	chr1:223585376..223587984-chr1:223593733..223596236,2	MCF-7	breast:
6	chr1:223595218..223598867-chr1:223599008..223602408,5	K562	blood:
7	chr1:223599220..223603471-chr1:223604968..223609274,4	MCF-7	breast:
8	chr1:223536303..223538270-chr1:223574488..223576964,2	K562	blood:
9	chr1:223605027..223607773-chr1:223615819..223618091,2	MCF-7	breast:
10	chr1:223534957..223537393-chr1:223566287..223567830,2	MCF-7	breast:
11	chr1:223595218..223598867-chr1:223599008..223602408,5	K562	blood:
12	chr1:223592334..223594672-chr1:223600258..223603185,3	K562	blood:
13	chr1:223589830..223593487-chr1:223595187..223598316,3	K562	blood:
14	chr1:223585376..223587984-chr1:223593733..223596236,2	MCF-7	breast:
15	chr1:223575927..223578563-chr1:223880828..223883618,2	K562	blood:
16	chr1:223607026..223608626-chr1:223610171..223611706,2	K562	blood:
17	chr1:223586120..223587741-chr1:223590261..223592377,2	K562	blood:
18	chr1:223597589..223600437-chr1:223603071..223605858,2	K562	blood:
19	chr1:223575712..223579320-chr1:223583036..223585021,3	MCF-7	breast:
20	chr1:223574260..223577674-chr1:223613937..223618124,4	MCF-7	breast:
21	chr1:223608260..223610550-chr1:223616264..223617958,2	MCF-7	breast:
22	chr1:223596035..223598867-chr1:223600908..223603274,2	K562	blood:
23	chr1:223563307..223565736-chr1:223565983..223568885,3	MCF-7	breast:
24	chr1:223589830..223593487-chr1:223595187..223598316,3	K562	blood:
25	chr1:223599220..223603471-chr1:223604968..223609274,4	MCF-7	breast:
26	chr1:223566366..223568039-chr1:223593781..223595649,2	MCF-7	breast:
27	chr1:223597589..223600437-chr1:223603071..223605858,2	K562	blood:
28	chr1:223575712..223579320-chr1:223583036..223585021,3	MCF-7	breast:
29	chr1:223594003..223597385-chr1:223616098..223619072,3	MCF-7	breast:
30	chr1:223586120..223587741-chr1:223590261..223592377,2	K562	blood:
31	chr1:223322245..223323048-chr1:223608788..223609563,2	MCF-7	breast:
32	chr1:223306620..223308748-chr1:223595185..223597717,2	MCF-7	breast:
33	chr1:223598585..223601286-chr1:223707386..223708910,2	MCF-7	breast:
34	chr1:223592334..223594672-chr1:223600258..223603185,3	K562	blood:
35	chr1:223536493..223539077-chr1:223583884..223586551,3	MCF-7	breast:

No data

Variant related genes	Relation type
C1orf65	TF binding region
C1orf65	CpG island
ENSG00000143502	chromatin interactions
ENSG00000187554	chromatin interactions
ENSG00000178395	chromatin interactions

Extended variants
information (count: 1572 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:1572 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190004318	chr1:223565104-223565105	Weak transcription	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs575662091	chr1:223565180-223565181	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs551715957	chr1:223565186-223565187	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs75547790	chr1:223565191-223565192	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs564239798	chr1:223565195-223565196	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs532218490	chr1:223565302-223565303	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs540789246	chr1:223565320-223565321	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs116741615	chr1:223565323-223565324	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs529972596	chr1:223565324-223565325	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs529271686	chr1:223565357-223565358	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs547894193	chr1:223565364-223565365	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs569668090	chr1:223565378-223565379	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs149091195	chr1:223565422-223565423	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs571955216	chr1:223565425-223565426	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs574757734	chr1:223565448-223565449	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs542011035	chr1:223565489-223565490	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs374217514	chr1:223565490-223565491	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs534514128	chr1:223565567-223565568	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs570552899	chr1:223565601-223565602	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs78180684	chr1:223565623-223565624	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs6701453	chr1:223565676-223565677	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs143271494	chr1:223565773-223565774	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
23	rs536109699	chr1:223565774-223565775	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
24	rs557354087	chr1:223565813-223565814	Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
25	rs575642695	chr1:223565815-223565816	Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
26	rs186197273	chr1:223565857-223565858	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs545784911	chr1:223565884-223565885	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs76716587	chr1:223565997-223565998	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs190728688	chr1:223566017-223566018	Weak transcription Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs558618569	chr1:223566058-223566059	Weak transcription Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs74835296	chr1:223566072-223566073	Weak transcription Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs181496859	chr1:223566092-223566093	Weak transcription Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs148327270	chr1:223566111-223566112	Weak transcription Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs141492179	chr1:223566121-223566122	Weak transcription Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs186469141	chr1:223566169-223566170	Weak transcription Bivalent/Poised TSS Bivalent Enhancer	CpG island	1 gene(s)	Overlapped CNVs	n/a
36	rs191801977	chr1:223566183-223566184	Weak transcription Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs147034681	chr1:223566205-223566206	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
38	rs563431443	chr1:223566290-223566291	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs530560752	chr1:223566303-223566304	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs183052453	chr1:223566352-223566353	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs570563035	chr1:223566370-223566371	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs369483663	chr1:223566379-223566380	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs528163297	chr1:223566380-223566381	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs371333255	chr1:223566468-223566469	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs115995867	chr1:223566494-223566495	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs2678371	chr1:223566508-223566509	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs576874104	chr1:223566535-223566536	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs535670835	chr1:223566661-223566662	Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs557678563	chr1:223566670-223566671	Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs569169878	chr1:223566690-223566691	Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Acute myeloid leukemia	17268525	CNVD
Lung cancer	16740712	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17053054	CNVD
Developmental delay	21147756	CNVD
Autism	14699429	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	20808228	CNVD
Fumarase deficiency	21572526	CNVD
Autism	17483303	CNVD
Kartagener syndrome	16639409	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Leukoplakia	24403051	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Glioblastoma multiforme	21138945	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Ovarian clear cell carcinoma	21343371	CNVD

Chromatin state (count:442 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:223563800-223566200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr1:223565800-223566000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
3	chr1:223566000-223566200	Bivalent Enhancer	Fetal Lung	lung
4	chr1:223566000-223566200	Bivalent Enhancer	Stomach Mucosa	stomach
5	chr1:223566000-223567000	Bivalent/Poised TSS	Primary T cells from cord blood	blood
6	chr1:223566200-223566400	Flanking Bivalent TSS/Enh	Primary T helper naive cells fromperipheralblood	blood
7	chr1:223566200-223566400	Enhancers	Esophagus	oesophagus
8	chr1:223566200-223566600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr1:223566200-223566600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr1:223566200-223566600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
11	chr1:223566200-223566600	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
12	chr1:223566200-223566600	Bivalent Enhancer	Stomach Smooth Muscle	stomach
13	chr1:223566200-223566800	Active TSS	Breast Myoepithelial Primary Cells	Breast
14	chr1:223566200-223566800	Bivalent Enhancer	Fetal Intestine Small	intestine
15	chr1:223566200-223567000	Bivalent Enhancer	Fetal Brain Male	brain
16	chr1:223566200-223567000	Bivalent Enhancer	Rectal Mucosa Donor 31	rectum
17	chr1:223566200-223567200	Active TSS	Brain Anterior Caudate	brain
18	chr1:223566200-223567200	Bivalent/Poised TSS	Colon Smooth Muscle	Colon
19	chr1:223566200-223567200	Bivalent/Poised TSS	NHEK	skin
20	chr1:223566400-223566600	Bivalent Enhancer	Esophagus	oesophagus
21	chr1:223566400-223566800	Active TSS	Primary T helper naive cells fromperipheralblood	blood
22	chr1:223566400-223567000	Active TSS	Right Ventricle	heart
23	chr1:223566400-223567200	Active TSS	Ovary	ovary
24	chr1:223566600-223566800	Flanking Bivalent TSS/Enh	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr1:223566600-223566800	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr1:223566600-223566800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
27	chr1:223566600-223566800	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
28	chr1:223566600-223566800	Bivalent/Poised TSS	Primary T helper cells fromperipheralblood	blood
29	chr1:223566600-223566800	Bivalent/Poised TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr1:223566600-223566800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr1:223566600-223566800	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr1:223566600-223566800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
33	chr1:223566600-223566800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
34	chr1:223566600-223566800	Flanking Bivalent TSS/Enh	Left Ventricle	heart
35	chr1:223566600-223566800	ZNF genes & repeats	Lung	lung
36	chr1:223566600-223566800	Active TSS	Pancreas	Pancrea
37	chr1:223566600-223566800	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
38	chr1:223566600-223567000	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
39	chr1:223566600-223567000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr1:223566600-223567000	Bivalent/Poised TSS	Primary T helper cells PMA-I stimulated	--
41	chr1:223566600-223567000	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr1:223566600-223567000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr1:223566600-223567000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr1:223566600-223567000	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
45	chr1:223566600-223567000	Active TSS	Gastric	stomach
46	chr1:223566600-223567000	Bivalent/Poised TSS	Sigmoid Colon	Sigmoid Colon
47	chr1:223566600-223567000	Bivalent Enhancer	Thymus	Thymus
48	chr1:223566600-223567000	Bivalent/Poised TSS	NH-A	brain
49	chr1:223566600-223567200	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr1:223566600-223567200	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin02	Skin

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