Variant report

Variant	nsv1004879
Chromosome Location	chr1:196738611-196916787
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:774)
CpG islands
(count:794)
Chromatin interactive
region (count:21)
LncRNA
region (count:21)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:774 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:196856986-196857227	HepG2	liver:	n/a	n/a
2	BACH1	chr1:196866267-196866431	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr1:196857035-196857206	GM12878	blood:	n/a	n/a
4	BATF	chr1:196743800-196744098	GM12878	blood:	n/a	chr1:196743977-196743985
5	BATF	chr1:196856972-196857380	GM12878	blood:	n/a	chr1:196857241-196857249
6	BCL11A	chr1:196856976-196857372	GM12878	blood:	n/a	n/a
7	BHLHE40	chr1:196902803-196903015	K562	blood:	n/a	n/a
8	CBX3	chr1:196855726-196856081	K562	blood:	n/a	n/a
9	CBX3	chr1:196855776-196855984	K562	blood:	n/a	n/a
10	CBX3	chr1:196902544-196903655	K562	blood:	n/a	n/a
11	CBX3	chr1:196902699-196903046	K562	blood:	n/a	n/a
12	CCNT2	chr1:196902726-196903313	K562	blood:	n/a	n/a
13	CEBPB	chr1:196825838-196826029	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr1:196910745-196910996	HepG2	liver:	n/a	n/a
15	CEBPB	chr1:196910800-196910933	K562	blood:	n/a	n/a
16	CEBPB	chr1:196868749-196868968	IMR90	lung:	n/a	n/a
17	CEBPB	chr1:196916588-196916860	HepG2	liver:	n/a	chr1:196916715-196916728 chr1:196916716-196916727 chr1:196916717-196916726 chr1:196916715-196916726
18	CEBPB	chr1:196848074-196848355	IMR90	lung:	n/a	chr1:196848177-196848188
19	CEBPB	chr1:196825893-196826006	K562	blood:	n/a	n/a
20	CEBPB	chr1:196856906-196857273	HepG2	liver:	n/a	chr1:196857077-196857088 chr1:196857110-196857123 chr1:196857112-196857123
21	CEBPB	chr1:196868787-196869010	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr1:196848041-196848299	Hela-S3	cervix:	n/a	chr1:196848177-196848188
23	CEBPB	chr1:196848022-196848331	HepG2	liver:	n/a	chr1:196848177-196848188
24	CEBPB	chr1:196868753-196869031	A549	lung:	n/a	n/a
25	CEBPB	chr1:196792559-196792845	IMR90	lung:	n/a	chr1:196792695-196792706 chr1:196792696-196792707 chr1:196792695-196792708 chr1:196792826-196792839 chr1:196792697-196792706
26	CEBPB	chr1:196792658-196792868	A549	lung:	n/a	chr1:196792695-196792706 chr1:196792696-196792707 chr1:196792695-196792708 chr1:196792826-196792839 chr1:196792697-196792706
27	CEBPB	chr1:196910739-196910903	HepG2	liver:	n/a	n/a
28	CEBPB	chr1:196792584-196792829	HepG2	liver:	n/a	chr1:196792695-196792706 chr1:196792696-196792707 chr1:196792695-196792708 chr1:196792697-196792706
29	CEBPB	chr1:196910749-196910930	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr1:196745101-196745132	IMR90	lung:	n/a	n/a
31	CEBPB	chr1:196916608-196916825	K562	blood:	n/a	chr1:196916715-196916728 chr1:196916716-196916727 chr1:196916717-196916726 chr1:196916715-196916726
32	CEBPB	chr1:196916630-196916864	H1-hESC	embryonic stem cell:	n/a	chr1:196916715-196916728 chr1:196916716-196916727 chr1:196916717-196916726 chr1:196916715-196916726
33	CEBPB	chr1:196916603-196916881	A549	lung:	n/a	chr1:196916715-196916728 chr1:196916716-196916727 chr1:196916717-196916726 chr1:196916715-196916726
34	CEBPB	chr1:196916577-196916873	IMR90	lung:	n/a	chr1:196916715-196916728 chr1:196916716-196916727 chr1:196916717-196916726 chr1:196916715-196916726
35	CEBPD	chr1:196910706-196910978	HepG2	liver:	n/a	n/a
36	CTCF	chr1:196903080-196903230	MCF-7	breast:	n/a	n/a
37	CTCF	chr1:196808521-196808574	GM20000	blood:	n/a	n/a
38	CTCF	chr1:196879420-196879570	HCPEpiC	choroid plexus:	n/a	n/a
39	CTCF	chr1:196866260-196866410	HRE	kidney:	n/a	n/a
40	CTCF	chr1:196866280-196866430	HCFaa	heart:	n/a	n/a
41	CTCF	chr1:196871740-196871890	A549	lung:	n/a	n/a
42	CTCF	chr1:196859973-196860151	GM12878	blood:	n/a	n/a
43	CTCF	chr1:196748380-196748530	GM12872	blood:	n/a	n/a
44	CTCF	chr1:196879420-196879570	AG09319	gingival:	n/a	n/a
45	CTCF	chr1:196748280-196748430	HEEpiC	esophagus:	n/a	n/a
46	CTCF	chr1:196797060-196797210	HEEpiC	esophagus:	n/a	chr1:196797163-196797184 chr1:196797161-196797179 chr1:196797165-196797172 chr1:196797162-196797178
47	CTCF	chr1:196797044-196797302	Hela-S3	cervix:	n/a	chr1:196797163-196797184 chr1:196797161-196797179 chr1:196797165-196797172 chr1:196797162-196797178
48	CTCF	chr1:196847222-196847423	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr1:196847160-196847310	HRPEpiC	eye:	n/a	n/a
50	CTCF	chr1:196847074-196847537	H1-hESC	embryonic stem cell:	n/a	n/a

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:196787850-196787900	HCPEpiC	choroid plexus:	n/a
2	chr1:196787850-196787900	HCPEpiC	choroid plexus:	n/a
3	chr1:196844364-196844414	AG04450	lung:	fetal
4	chr1:196847182-196847232	HUVEC	blood vessel:	n/a
5	chr1:196847182-196847232	GM12878	blood:	n/a
6	chr1:196743672-196743722	BJ	skin:	n/a
7	chr1:196855851-196855901	NT2-D1	testis:	n/a
8	chr1:196787850-196787900	SK-N-SH	brain:	n/a
9	chr1:196866322-196866372	K562	blood:	n/a
10	chr1:196847859-196847909	HL-60	blood:	n/a
11	chr1:196865686-196865736	HL-60	blood:	n/a
12	chr1:196911888-196911938	SK-N-SH_RA	brain:	n/a
13	chr1:196847859-196847909	AoSMC	blood vessel:	n/a
14	chr1:196902941-196902991	ovcar-3	ovarian:	n/a
15	chr1:196865686-196865736	ProgFib	skin:	n/a
16	chr1:196902941-196902991	PFSK-1	brain:	n/a
17	chr1:196787850-196787900	MCF-7	breast:	n/a
18	chr1:196795943-196795993	Hela-S3	cervix:	n/a
19	chr1:196787850-196787900	GM06990	blood:	n/a
20	chr1:196865686-196865736	HCF	heart:	n/a
21	chr1:196847182-196847232	AG10803	skin:	n/a
22	chr1:196847182-196847232	HRPEpiC	eye:	n/a
23	chr1:196787850-196787900	K562	blood:	n/a
24	chr1:196902941-196902991	HCT-116	colon:	n/a
25	chr1:196902941-196902991	SAEC	small airway:	n/a
26	chr1:196847859-196847909	HCPEpiC	choroid plexus:	n/a
27	chr1:196866322-196866372	PrEC	prostate:	n/a
28	chr1:196902941-196902991	SK-N-SH	brain:	n/a
29	chr1:196855851-196855901	GM12878	blood:	n/a
30	chr1:196902941-196902991	HEK293	kidney:	embryo
31	chr1:196743672-196743722	T-47D	breast:	n/a
32	chr1:196743672-196743722	MCF-7	breast:	n/a
33	chr1:196902941-196902991	HEEpiC	esophagus:	n/a
34	chr1:196795943-196795993	ECC-1	luminal epithelium:	n/a
35	chr1:196844364-196844414	HEK293	kidney:	embryo
36	chr1:196855851-196855901	CMK	blood:	n/a
37	chr1:196743672-196743722	Jurkat	blood:	n/a
38	chr1:196844364-196844414	HIPEpiC	eye:	n/a
39	chr1:196847182-196847232	A549	lung:	n/a
40	chr1:196787850-196787900	HEK293	kidney:	embryo
41	chr1:196746875-196746925	NHBE	bronchial:	n/a
42	chr1:196844364-196844414	HNPCEpiC	eye:	n/a
43	chr1:196787850-196787900	AoSMC	blood vessel:	n/a
44	chr1:196746875-196746925	HIPEpiC	eye:	n/a
45	chr1:196902941-196902991	HIPEpiC	eye:	n/a
46	chr1:196855851-196855901	SAEC	small airway:	n/a
47	chr1:196743672-196743722	GM12892	blood:	n/a
48	chr1:196902941-196902991	HNPCEpiC	eye:	n/a
49	chr1:196743672-196743722	HL-60	blood:	n/a
50	chr1:196743672-196743722	IMR90	lung:	fetal

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:196734362..196735975-chr1:196744220..196746531,2	MCF-7	breast:
2	chr1:196712168..196712942-chr1:196796703..196797590,3	MCF-7	breast:
3	chr1:196866686..196869291-chr1:196870395..196872004,2	K562	blood:
4	chr1:196738269..196739930-chr1:196742962..196745311,2	MCF-7	breast:
5	chr1:196821183..196821683-chr13:114578689..114579580,2	NB4	blood:
6	chr1:196874466..196877134-chr1:196878401..196880151,2	MCF-7	breast:
7	chr1:196833036..196835508-chr1:196837217..196839600,2	K562	blood:
8	chr1:196286813..196287729-chr1:196859599..196860261,2	MCF-7	breast:
9	chr1:196833036..196835508-chr1:196837217..196839600,2	K562	blood:
10	chr1:196796721..196797658-chr1:196859492..196860452,2	MCF-7	breast:
11	chr1:196692236..196693111-chr1:196859470..196860182,3	MCF-7	breast:
12	chr1:196711011..196712654-chr1:196796494..196798129,2	MCF-7	breast:
13	chr1:196866686..196869291-chr1:196870395..196872004,2	K562	blood:
14	chr1:196870703..196871324-chr2:207697433..207698180,2	MCF-7	breast:
15	chr1:196796721..196797658-chr1:196859492..196860452,2	MCF-7	breast:
16	chr1:196863909..196866784-chr1:196987706..196990469,2	K562	blood:
17	chr1:196700723..196702673-chr1:196877017..196878794,2	K562	blood:
18	chr1:196874466..196877134-chr1:196878401..196880151,2	MCF-7	breast:
19	chr1:196711931..196712944-chr1:196796605..196797511,4	MCF-7	breast:
20	chr1:196852522..196854884-chr1:197003323..197006250,2	K562	blood:
21	chr1:196902868..196904408-chr1:196927162..196928980,2	K562	blood:

(count:21 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CFHR2-1	chr1:196788893-196789032	NONHSAT008600
2	lnc-CFHR5-1	chr1:196912957-196913068	NONHSAT008608
3	lnc-CFHR5-1	chr1:196912902-196913068	NONHSAT008606
4	lnc-CFHR1-1	chr1:196762447-196762763	NONHSAT008599
5	lnc-CFHR2-1	chr1:196788952-196789032	NONHSAT008601
6	lnc-CFHR2-1	chr1:196794354-196794801	NONHSAT008603
7	lnc-CFHR2-1	chr1:196797280-196797376	NONHSAT008600
8	lnc-CFHR2-1	chr1:196795959-196796135	NONHSAT008600
9	lnc-CFHR2-1	chr1:196794607-196795156	NONHSAT008602
10	lnc-CFHR5-1	chr1:196912902-196913068	NONHSAT008605
11	lnc-CFHR5-1	chr1:196912947-196913068	NONHSAT008607
12	lnc-CFHR1-1	chr1:196758890-196759357	NONHSAT008599
13	lnc-CFHR2-1	chr1:196797200-196797225	NONHSAT008600
14	lnc-CFHR2-1	chr1:196788995-196789032	NONHSAT008602
15	lnc-CFHR2-1	chr1:196794607-196794801	NONHSAT008600
16	lnc-CFHR5-1	chr1:196912988-196913068	NONHSAT008609
17	lnc-F13B-1	chr1:196833477-196833736	NONHSAT008604
18	lnc-CFHR2-1	chr1:196795959-196796135	NONHSAT008603
19	lnc-CFHR2-1	chr1:196797200-196797297	NONHSAT008603
20	lnc-CFHR2-1	chr1:196790015-196790332	NONHSAT008601
21	lnc-F13B-1	chr1:196834519-196834621	NONHSAT008604

No data

Variant related genes	Relation type
CFHR4	TF binding region
CFHR2	TF binding region
CFHR1	TF binding region
CFHR3	TF binding region
CFHR4	CpG island
CFHR2	CpG island
CFHR1	CpG island
CFHR3	CpG island
ENSG00000116785	chromatin interactions

Extended variants
information (count: 3944 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:3944 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs117601282	chr1:196738625-196738626	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs574020026	chr1:196738676-196738677	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs555502407	chr1:196738715-196738716	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs184240720	chr1:196738728-196738729	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs12039050	chr1:196738732-196738733	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs538991558	chr1:196738760-196738761	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs12046285	chr1:196738770-196738771	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs566729916	chr1:196738810-196738811	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs534120251	chr1:196738829-196738830	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs555595972	chr1:196738833-196738834	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs34130738	chr1:196738850-196738851	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs573909036	chr1:196738855-196738856	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs537526623	chr1:196738950-196738951	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs369816	chr1:196738955-196738956	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs139415460	chr1:196738961-196738962	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs577687424	chr1:196738970-196738971	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs370081811	chr1:196738971-196738972	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs35191813	chr1:196738974-196738975	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs544942653	chr1:196738996-196738997	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs562316400	chr1:196739003-196739004	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs144093111	chr1:196739004-196739005	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs572397950	chr1:196739019-196739020	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs542962686	chr1:196739087-196739088	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs561126778	chr1:196739122-196739123	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs189465628	chr1:196739127-196739128	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs116430402	chr1:196739185-196739186	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs565330201	chr1:196739192-196739193	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs532505519	chr1:196739215-196739216	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs547801930	chr1:196739233-196739234	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs192575700	chr1:196739245-196739246	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs510755	chr1:196739246-196739247	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs184608369	chr1:196739319-196739320	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs366162	chr1:196739331-196739332	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs538015700	chr1:196739343-196739344	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs188953416	chr1:196739370-196739371	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs181501911	chr1:196739372-196739373	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs538388153	chr1:196739380-196739381	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs372952977	chr1:196739420-196739421	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs373665490	chr1:196739423-196739424	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs2878713	chr1:196739431-196739432	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs554811447	chr1:196739434-196739435	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs375144761	chr1:196739444-196739445	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs76908711	chr1:196739459-196739460	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs366818	chr1:196739463-196739464	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs113952284	chr1:196739467-196739468	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs529344639	chr1:196739470-196739471	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs112988959	chr1:196739492-196739493	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs551034048	chr1:196739555-196739556	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs532634215	chr1:196739556-196739557	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs185050261	chr1:196739557-196739558	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Carcinoma ex pleomorphic adenoma	18828159	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
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
Neuroblastoma	21899760	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	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
Hepatocellular carcinoma	18803288	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
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21611746	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	19010865	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Trisomy 5 syndrome	21098271	CNVD
Glioblastoma multiforme	22286061	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Mental retardation	21062444	CNVD
Liver carcinoma	19366792	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
small cell lung cancer	20016488	CNVD
Neuroblastoma	20406844	CNVD
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:256 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:196735000-196743200	Weak transcription	Liver	Liver
2	chr1:196743200-196743600	Flanking Active TSS	Liver	Liver
3	chr1:196743600-196748600	Active TSS	Liver	Liver
4	chr1:196748600-196749000	Weak transcription	Liver	Liver
5	chr1:196749000-196749200	ZNF genes & repeats	Pancreas	Pancrea
6	chr1:196749000-196749800	ZNF genes & repeats	Liver	Liver
7	chr1:196749800-196755800	Weak transcription	Liver	Liver
8	chr1:196755000-196756200	Active TSS	ES-I3 Cell Line	embryonic stem cell
9	chr1:196755200-196755800	Active TSS	HUES64 Cell Line	embryonic stem cell
10	chr1:196755200-196756400	Active TSS	HUES48 Cell Line	embryonic stem cell
11	chr1:196755200-196756400	Active TSS	HUES6 Cell Line	embryonic stem cell
12	chr1:196755400-196755600	Enhancers	H1 Cell Line	embryonic stem cell
13	chr1:196755600-196755800	Flanking Active TSS	H1 Cell Line	embryonic stem cell
14	chr1:196755600-196756000	Active TSS	iPS-20b Cell Line	embryonic stem cell
15	chr1:196755600-196756000	Active TSS	Placenta	Placenta
16	chr1:196755600-196756200	Active TSS	H9 Cell Line	embryonic stem cell
17	chr1:196755600-196756200	Active TSS	iPS-15b Cell Line	embryonic stem cell
18	chr1:196755600-196756400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
19	chr1:196755800-196756000	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
20	chr1:196755800-196756000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr1:196755800-196756400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr1:196755800-196756400	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
23	chr1:196755800-196756400	ZNF genes & repeats	Liver	Liver
24	chr1:196755800-196756400	Active TSS	A549	lung
25	chr1:196756000-196756200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr1:196756000-196756400	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr1:196756000-196756400	Active TSS	K562	blood
28	chr1:196756200-196756400	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
29	chr1:196756200-196756400	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
30	chr1:196756400-196756600	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr1:196756400-196756600	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr1:196756400-196756800	Weak transcription	HUES48 Cell Line	embryonic stem cell
33	chr1:196756400-196757800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr1:196756400-196758200	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr1:196756400-196764800	Weak transcription	Liver	Liver
36	chr1:196756600-196757000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
37	chr1:196756600-196757000	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr1:196756800-196757000	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr1:196757000-196758200	Weak transcription	HUES48 Cell Line	embryonic stem cell
40	chr1:196757200-196757400	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr1:196757800-196758200	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr1:196758200-196758400	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr1:196770800-196771200	Enhancers	Muscle Satellite Cultured Cells	--
44	chr1:196778000-196778400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr1:196778400-196778800	Active TSS	Spleen	Spleen
46	chr1:196778400-196779600	Enhancers	Primary hematopoietic stem cells short term culture	blood
47	chr1:196778800-196779200	Enhancers	Spleen	Spleen
48	chr1:196786400-196786600	Active TSS	Liver	Liver
49	chr1:196786600-196786800	Flanking Active TSS	Liver	Liver
50	chr1:196786600-196787000	Enhancers	HUES6 Cell Line	embryonic stem cell

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