Variant report

Variant	nsv872584
Chromosome Location	chr1:184678290-184716457
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:196)
CpG islands
(count:61)
Chromatin interactive
region (count:57)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:196 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:184714297-184714467	K562	blood:	n/a	n/a
2	ARID3A	chr1:184708580-184708874	K562	blood:	n/a	n/a
3	ARID3A	chr1:184712126-184712865	K562	blood:	n/a	n/a
4	ATF2	chr1:184712054-184712786	GM12878	blood:	n/a	n/a
5	ATF2	chr1:184712195-184712647	GM12878	blood:	n/a	n/a
6	ATF2	chr1:184716336-184716838	GM12878	blood:	n/a	n/a
7	BACH1	chr1:184711303-184711349	K562	blood:	n/a	n/a
8	BATF	chr1:184712268-184712529	GM12878	blood:	n/a	chr1:184712498-184712508 chr1:184712502-184712512
9	BCL11A	chr1:184712274-184712562	GM12878	blood:	n/a	n/a
10	BCLAF1	chr1:184712079-184712626	GM12878	blood:	n/a	n/a
11	BCLAF1	chr1:184716228-184716855	GM12878	blood:	n/a	n/a
12	BHLHE40	chr1:184712199-184712666	GM12878	blood:	n/a	n/a
13	BHLHE40	chr1:184715032-184715232	GM12878	blood:	n/a	n/a
14	CCNT2	chr1:184689528-184689641	K562	blood:	n/a	n/a
15	CEBPB	chr1:184682673-184682743	HepG2	liver:	n/a	chr1:184682712-184682723 chr1:184682710-184682721 chr1:184682712-184682721
16	CEBPB	chr1:184682667-184682867	K562	blood:	n/a	chr1:184682712-184682723 chr1:184682710-184682721 chr1:184682712-184682721
17	CEBPB	chr1:184694957-184695192	A549	lung:	n/a	chr1:184695075-184695092
18	CEBPB	chr1:184713880-184714181	K562	blood:	n/a	n/a
19	CEBPB	chr1:184709806-184710093	A549	lung:	n/a	n/a
20	CEBPB	chr1:184686380-184686637	K562	blood:	n/a	n/a
21	CEBPB	chr1:184694981-184695231	HepG2	liver:	n/a	chr1:184695075-184695092
22	CEBPB	chr1:184682682-184682779	A549	lung:	n/a	chr1:184682712-184682723 chr1:184682710-184682721 chr1:184682712-184682721
23	CHD1	chr1:184700047-184700209	GM12878	blood:	n/a	n/a
24	CHD2	chr1:184715062-184715329	GM12878	blood:	n/a	n/a
25	CHD2	chr1:184712260-184712757	GM12878	blood:	n/a	n/a
26	CTCF	chr1:184711080-184711230	MCF-7	breast:	n/a	n/a
27	CTCF	chr1:184694200-184694350	MCF-7	breast:	n/a	n/a
28	CTCF	chr1:184711120-184711270	HPAF	blood vessel:	n/a	n/a
29	CTCF	chr1:184702750-184702841	Pancreas_OC	pancreas:	n/a	n/a
30	CTCF	chr1:184699386-184699448	GM20000	blood:	n/a	n/a
31	CUX1	chr1:184686796-184686992	K562	blood:	n/a	n/a
32	CUX1	chr1:184707676-184707853	GM12878	blood:	n/a	n/a
33	CUX1	chr1:184715004-184716022	K562	blood:	n/a	n/a
34	E2F4	chr1:184699985-184700149	MCF10A-Er-Src	breast:	n/a	n/a
35	E2F4	chr1:184701691-184701937	MCF10A-Er-Src	breast:	n/a	n/a
36	E2F4	chr1:184685252-184685416	MCF10A-Er-Src	breast:	n/a	n/a
37	E2F4	chr1:184694019-184694093	MCF10A-Er-Src	breast:	n/a	n/a
38	EBF1	chr1:184716454-184716942	GM12878	blood:	n/a	n/a
39	EBF1	chr1:184712195-184712736	GM12878	blood:	n/a	n/a
40	EBF1	chr1:184715037-184715415	GM12878	blood:	n/a	n/a
41	EP300	chr1:184714916-184715653	K562	blood:	n/a	n/a
42	EP300	chr1:184713909-184714146	K562	blood:	n/a	n/a
43	EP300	chr1:184712105-184712610	GM12878	blood:	n/a	chr1:184712501-184712510
44	EP300	chr1:184716353-184716765	GM12878	blood:	n/a	chr1:184716601-184716615 chr1:184716576-184716583 chr1:184716602-184716611
45	EP300	chr1:184712824-184712981	GM12878	blood:	n/a	n/a
46	EP300	chr1:184712159-184712830	GM12878	blood:	n/a	chr1:184712501-184712510
47	EP300	chr1:184715023-184715390	GM12878	blood:	n/a	n/a
48	EP300	chr1:184709463-184709851	HepG2	liver:	n/a	n/a
49	EP300	chr1:184712199-184712612	GM12878	blood:	n/a	chr1:184712501-184712510
50	EP300	chr1:184714959-184715463	GM12878	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:184715203-184715253	ECC-1	luminal epithelium:	n/a
2	chr1:184715203-184715253	MCF-7	breast:	n/a
3	chr1:184715203-184715253	T-47D	breast:	n/a
4	chr1:184715203-184715253	Caco-2	colon:	n/a
5	chr1:184715203-184715253	HAEpiC	amniotic membrane:	n/a
6	chr1:184715203-184715253	HepG2	liver:	n/a
7	chr1:184715203-184715253	A549	lung:	n/a
8	chr1:184715203-184715253	HRPEpiC	eye:	n/a
9	chr1:184715203-184715253	HUVEC	blood vessel:	n/a
10	chr1:184715203-184715253	AG09309	skin:	n/a
11	chr1:184715203-184715253	HRCEpiC	kidney:	n/a
12	chr1:184715203-184715253	BJ	skin:	n/a
13	chr1:184715203-184715253	GM06990	blood:	n/a
14	chr1:184715203-184715253	SK-N-SH_RA	brain:	n/a
15	chr1:184715203-184715253	PANC-1	pancreas:	n/a
16	chr1:184715203-184715253	AoSMC	blood vessel:	n/a
17	chr1:184715203-184715253	Jurkat	blood:	n/a
18	chr1:184715203-184715253	K562	blood:	n/a
19	chr1:184715203-184715253	Hepatocyte	liver:	n/a
20	chr1:184715203-184715253	HEK293	kidney:	embryo
21	chr1:184715203-184715253	RPTEC	kidney:	n/a
22	chr1:184715203-184715253	Hela-S3	cervix:	n/a
23	chr1:184715203-184715253	HL-60	blood:	n/a
24	chr1:184715203-184715253	PFSK-1	brain:	n/a
25	chr1:184715203-184715253	NHBE	bronchial:	n/a
26	chr1:184715203-184715253	AG04449	skin:	fetal
27	chr1:184715203-184715253	ovcar-3	ovarian:	n/a
28	chr1:184715203-184715253	BE2_C	brain:	n/a
29	chr1:184715203-184715253	U87	brain:	n/a
30	chr1:184715203-184715253	HCM	heart:	n/a
31	chr1:184715203-184715253	GM12892	blood:	n/a
32	chr1:184715203-184715253	NB4	blood:	n/a
33	chr1:184715203-184715253	CMK	blood:	n/a
34	chr1:184715203-184715253	GM12891	blood:	n/a
35	chr1:184715203-184715253	HMEC	breast:	n/a
36	chr1:184715203-184715253	NH-A	brain:	n/a
37	chr1:184715203-184715253	LNCaP	prostate:	n/a
38	chr1:184715203-184715253	SKMC	muscle:	n/a
39	chr1:184715203-184715253	SAEC	small airway:	n/a
40	chr1:184715203-184715253	HIPEpiC	eye:	n/a
41	chr1:184715203-184715253	GM12878	blood:	n/a
42	chr1:184715203-184715253	IMR90	lung:	fetal
43	chr1:184715203-184715253	HCPEpiC	choroid plexus:	n/a
44	chr1:184715203-184715253	HPAEpiC	pulmonary alveolar:	n/a
45	chr1:184715203-184715253	HCT-116	colon:	n/a
46	chr1:184715203-184715253	NHDF-neo	bronchial:	n/a
47	chr1:184715203-184715253	AG09319	gingival:	n/a
48	chr1:184715203-184715253	HCF	heart:	n/a
49	chr1:184715203-184715253	AG10803	skin:	n/a
50	chr1:184715203-184715253	PrEC	prostate:	n/a

(count:57 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:184691316..184693435-chr1:184696792..184698671,2	K562	blood:
2	chr1:184708169..184713415-chr1:184713456..184716461,4	MCF-7	breast:
3	chr1:184708496..184710858-chr1:184733789..184736072,2	K562	blood:
4	chr1:184684929..184687575-chr1:184691047..184694725,3	K562	blood:
5	chr1:184681652..184683327-chr1:184949938..184952588,2	K562	blood:
6	chr1:184697119..184698633-chr1:184706582..184709227,2	MCF-7	breast:
7	chr1:184682030..184684517-chr1:184685764..184688834,3	K562	blood:
8	chr1:184692283..184693990-chr1:184704527..184706346,2	K562	blood:
9	chr1:184691631..184695143-chr1:184721197..184724514,4	K562	blood:
10	chr1:184709738..184712321-chr1:184713250..184716697,3	K562	blood:
11	chr1:184684929..184687575-chr1:184691047..184694725,3	K562	blood:
12	chr1:184694527..184697597-chr1:184706651..184709728,3	K562	blood:
13	chr1:184689208..184691791-chr1:184942117..184944886,2	K562	blood:
14	chr1:184687867..184690558-chr1:184692162..184694552,2	MCF-7	breast:
15	chr1:184691316..184693435-chr1:184696792..184698671,2	K562	blood:
16	chr1:184697668..184700399-chr1:184702400..184704230,2	K562	blood:
17	chr1:184692283..184693990-chr1:184704527..184706346,2	K562	blood:
18	chr1:184692034..184695028-chr1:184695067..184697135,2	K562	blood:
19	chr1:184684929..184687575-chr1:184691047..184693770,2	K562	blood:
20	chr1:184703854..184706366-chr1:184709752..184714206,4	K562	blood:
21	chr1:184687987..184690948-chr1:184692371..184695173,3	K562	blood:
22	chr1:184669558..184672098-chr1:184694218..184695882,2	K562	blood:
23	chr1:184700886..184703045-chr1:184708042..184709740,3	K562	blood:
24	chr1:184715138..184717798-chr17:57916015..57918507,3	MCF-7	breast:
25	chr1:184687896..184689795-chr1:184715143..184716835,2	MCF-7	breast:
26	chr1:184688642..184690448-chr1:184695282..184698252,2	K562	blood:
27	chr1:184687896..184689795-chr1:184715143..184716835,2	MCF-7	breast:
28	chr1:184708584..184710764-chr1:184716187..184718399,2	MCF-7	breast:
29	chr1:184705153..184707744-chr1:184942725..184944472,2	K562	blood:
30	chr1:184707417..184709159-chr1:184712217..184714987,3	MCF-7	breast:
31	chr1:184708584..184710764-chr1:184716187..184718399,2	MCF-7	breast:
32	chr1:184679455..184682205-chr1:184682828..184685276,2	MCF-7	breast:
33	chr1:184683246..184684894-chr1:185126908..185129341,2	K562	blood:
34	chr1:184673163..184675215-chr1:184695509..184697119,2	K562	blood:
35	chr1:184697668..184700399-chr1:184702400..184704230,2	K562	blood:
36	chr1:184700886..184703045-chr1:184708042..184709740,3	K562	blood:
37	chr1:184707417..184709159-chr1:184712217..184714987,3	MCF-7	breast:
38	chr1:184698326..184700782-chr1:184705878..184708037,2	K562	blood:
39	chr1:184688642..184690448-chr1:184695282..184698252,2	K562	blood:
40	chr1:184706332..184708758-chr1:184714030..184715698,2	K562	blood:
41	chr1:184682030..184684517-chr1:184685764..184688834,3	K562	blood:
42	chr1:184702362..184703932-chr1:184704085..184706758,2	K562	blood:
43	chr1:184702362..184703932-chr1:184704085..184706758,2	K562	blood:
44	chr1:184683195..184685107-chr1:184721891..184724158,3	K562	blood:
45	chr1:184703854..184706366-chr1:184709752..184714206,4	K562	blood:
46	chr1:184687987..184690948-chr1:184692371..184695173,3	K562	blood:
47	chr1:184692034..184695028-chr1:184695067..184697135,2	K562	blood:
48	chr1:184684929..184687575-chr1:184691047..184693770,2	K562	blood:
49	chr1:184694488..184696027-chr1:184706651..184709157,2	K562	blood:
50	chr1:184698428..184700782-chr1:184704829..184707378,2	K562	blood:

No data

Variant related genes	Relation type
EDEM3	TF binding region
EDEM3	CpG island
ENSG00000116406	chromatin interactions
ENSG00000135842	chromatin interactions

Extended variants
information (count: 1355 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:1355 , 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	rs12567226	chr1:184678290-184678291	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs560514092	chr1:184678313-184678314	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs527784224	chr1:184678329-184678330	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs557641100	chr1:184678361-184678362	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs559504542	chr1:184678369-184678370	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs143240975	chr1:184678371-184678372	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs545314663	chr1:184678396-184678397	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs533761280	chr1:184678402-184678403	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs184685636	chr1:184678411-184678412	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs563603507	chr1:184678451-184678452	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs147087024	chr1:184678493-184678494	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs138763354	chr1:184678527-184678528	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs543061238	chr1:184678539-184678540	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs560860272	chr1:184678548-184678549	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs528175493	chr1:184678552-184678553	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs188702964	chr1:184678593-184678594	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs115580620	chr1:184678623-184678624	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs538804772	chr1:184678677-184678678	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs35420457	chr1:184678696-184678697	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs573738710	chr1:184678744-184678745	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs180845437	chr1:184678770-184678771	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs569084725	chr1:184678795-184678796	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs544372450	chr1:184678820-184678821	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs142755304	chr1:184678911-184678912	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs4469687	chr1:184679019-184679020	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs150731902	chr1:184679024-184679025	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs535096141	chr1:184679073-184679074	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs12093441	chr1:184679116-184679117	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs116357269	chr1:184679202-184679203	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs2224092	chr1:184679234-184679235	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs199692067	chr1:184679255-184679256	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs139049818	chr1:184679283-184679284	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs113037404	chr1:184679337-184679338	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs371906776	chr1:184679349-184679350	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs575886074	chr1:184679389-184679390	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs116206389	chr1:184679421-184679422	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs560920396	chr1:184679424-184679425	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs528049707	chr1:184679474-184679475	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs201539914	chr1:184679487-184679488	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs200409619	chr1:184679498-184679499	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs114636195	chr1:184679512-184679513	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs367888852	chr1:184679513-184679514	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs183961574	chr1:184679517-184679518	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs371763731	chr1:184679535-184679536	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs199800822	chr1:184679576-184679577	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs140549505	chr1:184679637-184679638	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs569095375	chr1:184679651-184679652	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs140264427	chr1:184679653-184679654	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs376219287	chr1:184679693-184679694	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs368902257	chr1:184679706-184679707	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
Bladder cancer	19088036	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
Urothelial carcinoma	21177765	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
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Hepatocellular carcinoma	16750200	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Glioblastoma multiforme	17369134	CNVD
Cancer	17440070	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Metanephric adenoma	20802469	CNVD
Renal cell carcinoma	18765545	CNVD
Nephroblastoma	17189400	CNVD
Melanoma	20688739	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21611746	CNVD
Myelofibrosis	22110671	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	17393978	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:924 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:184653200-184705000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr1:184654000-184710800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr1:184654200-184701200	Weak transcription	Stomach Mucosa	stomach
4	chr1:184654200-184710000	Weak transcription	Esophagus	oesophagus
5	chr1:184656600-184684000	Weak transcription	Fetal Heart	heart
6	chr1:184658400-184706800	Strong transcription	Primary neutrophils fromperipheralblood	blood
7	chr1:184659200-184707000	Strong transcription	Monocytes-CD14+_RO01746	blood
8	chr1:184660000-184704200	Strong transcription	Primary monocytes fromperipheralblood	blood
9	chr1:184660800-184680400	Weak transcription	Right Ventricle	heart
10	chr1:184661000-184678600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
11	chr1:184661000-184705600	Strong transcription	Rectal Mucosa Donor 29	rectum
12	chr1:184661200-184690400	Strong transcription	Primary T cells fromperipheralblood	blood
13	chr1:184661200-184707800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr1:184661400-184678600	Strong transcription	Liver	Liver
15	chr1:184661400-184690400	Strong transcription	Duodenum Mucosa	Duodenum
16	chr1:184661600-184693200	Strong transcription	Dnd41	blood
17	chr1:184662000-184698000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr1:184662200-184706600	Strong transcription	Primary T helper cells fromperipheralblood	blood
19	chr1:184662600-184699400	Weak transcription	Psoas Muscle	Psoas
20	chr1:184663600-184679400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr1:184665200-184683800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr1:184665200-184706800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
23	chr1:184665600-184687600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr1:184665600-184700400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr1:184666000-184678400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr1:184666000-184691400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr1:184666200-184704600	Weak transcription	HUES6 Cell Line	embryonic stem cell
28	chr1:184667000-184681000	Strong transcription	Primary hematopoietic stem cells	blood
29	chr1:184668400-184686000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
30	chr1:184668400-184690400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr1:184668400-184690600	Strong transcription	Fetal Thymus	thymus
32	chr1:184668400-184707000	Strong transcription	Rectal Mucosa Donor 31	rectum
33	chr1:184668600-184693000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr1:184669200-184688800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr1:184669200-184707000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr1:184669400-184687400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr1:184669400-184692600	Strong transcription	Osteobl	bone
38	chr1:184669400-184707000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr1:184669600-184690400	Strong transcription	Primary T helper cells PMA-I stimulated	--
40	chr1:184669800-184692600	Strong transcription	Placenta	Placenta
41	chr1:184670600-184681600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr1:184670800-184690200	Strong transcription	Fetal Intestine Large	intestine
43	chr1:184670800-184690400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr1:184671000-184680600	Weak transcription	Placenta Amnion	Placenta Amnion
45	chr1:184671000-184686200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
46	chr1:184671200-184678400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr1:184671200-184686200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr1:184671200-184687000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
49	chr1:184671200-184690200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr1:184671200-184707400	Weak transcription	Pancreatic Islets	Pancreatic Islet

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