Variant report

Variant	nsv890631
Chromosome Location	chr8:19712564-19756813
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr8:19752064-19752243	K562	blood:	n/a	n/a
2	ATF1	chr8:19748706-19748730	K562	blood:	n/a	n/a
3	ATF2	chr8:19717761-19718202	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr8:19719257-19719669	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL11A	chr8:19717799-19718118	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL11A	chr8:19717930-19718078	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr8:19727841-19728121	GM12878	blood:	n/a	n/a
8	BHLHE40	chr8:19727856-19728054	K562	blood:	n/a	n/a
9	BRCA1	chr8:19732279-19732313	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr8:19719276-19719590	A549	lung:	n/a	n/a
11	CEBPB	chr8:19719250-19719589	HepG2	liver:	n/a	n/a
12	CEBPB	chr8:19719289-19719482	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr8:19717402-19717496	HepG2	liver:	n/a	chr8:19717430-19717441
14	CEBPB	chr8:19719271-19719591	IMR90	lung:	n/a	n/a
15	CEBPB	chr8:19719325-19719549	K562	blood:	n/a	n/a
16	CEBPB	chr8:19749024-19749191	A549	lung:	n/a	n/a
17	CEBPB	chr8:19719244-19719638	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr8:19732364-19732392	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr8:19727795-19728220	GM12878	blood:	n/a	chr8:19727986-19728004 chr8:19727989-19728002 chr8:19727987-19728003 chr8:19727988-19728009 chr8:19727989-19727997
20	CTCF	chr8:19727560-19727710	AG04450	lung:	n/a	n/a
21	CTCF	chr8:19727860-19728010	NHDF-neo	bronchial:	n/a	chr8:19727986-19728004 chr8:19727989-19728002 chr8:19727987-19728003 chr8:19727988-19728009 chr8:19727989-19727997
22	CTCF	chr8:19728180-19728330	SK-N-SH_RA	brain:	n/a	n/a
23	CTCF	chr8:19727900-19728050	GM12875	blood:	n/a	chr8:19727986-19728004 chr8:19727989-19728002 chr8:19727987-19728003 chr8:19727988-19728009 chr8:19727989-19727997
24	CTCF	chr8:19727880-19728030	GM12872	blood:	n/a	chr8:19727986-19728004 chr8:19727989-19728002 chr8:19727987-19728003 chr8:19727988-19728009 chr8:19727989-19727997
25	CTCF	chr8:19727900-19728050	HPAF	blood vessel:	n/a	chr8:19727986-19728004 chr8:19727989-19728002 chr8:19727987-19728003 chr8:19727988-19728009 chr8:19727989-19727997
26	CTCF	chr8:19728700-19728850	GM12873	blood:	n/a	n/a
27	CTCF	chr8:19727976-19728062	MCF-7	breast:	n/a	chr8:19727986-19728004 chr8:19727989-19728002 chr8:19727987-19728003 chr8:19727988-19728009 chr8:19727989-19727997
28	CTCF	chr8:19727920-19728070	AG09319	gingival:	n/a	chr8:19727986-19728004 chr8:19727989-19728002 chr8:19727987-19728003 chr8:19727988-19728009 chr8:19727989-19727997
29	CTCF	chr8:19727641-19727788	Medullo	brain:	n/a	n/a
30	CTCF	chr8:19727940-19728090	GM12866	blood:	n/a	chr8:19727986-19728004 chr8:19727989-19728002 chr8:19727987-19728003 chr8:19727988-19728009 chr8:19727989-19727997
31	CTCF	chr8:19727940-19728090	HEK293	kidney:	n/a	chr8:19727986-19728004 chr8:19727989-19728002 chr8:19727987-19728003 chr8:19727988-19728009 chr8:19727989-19727997
32	CTCF	chr8:19727880-19728030	HRPEpiC	eye:	n/a	chr8:19727986-19728004 chr8:19727989-19728002 chr8:19727987-19728003 chr8:19727988-19728009 chr8:19727989-19727997
33	CTCF	chr8:19727860-19728010	WI-38	lung:	n/a	chr8:19727986-19728004 chr8:19727989-19728002 chr8:19727987-19728003 chr8:19727988-19728009 chr8:19727989-19727997
34	CTCF	chr8:19732935-19732993	GM10248	blood:	n/a	n/a
35	CTCF	chr8:19727940-19728090	HRE	kidney:	n/a	chr8:19727986-19728004 chr8:19727989-19728002 chr8:19727987-19728003 chr8:19727988-19728009 chr8:19727989-19727997
36	CTCF	chr8:19727880-19728030	HUVEC	blood vessel:	n/a	chr8:19727986-19728004 chr8:19727989-19728002 chr8:19727987-19728003 chr8:19727988-19728009 chr8:19727989-19727997
37	CTCF	chr8:19727900-19728050	HEEpiC	esophagus:	n/a	chr8:19727986-19728004 chr8:19727989-19728002 chr8:19727987-19728003 chr8:19727988-19728009 chr8:19727989-19727997
38	CTCF	chr8:19727860-19728010	GM12868	blood:	n/a	chr8:19727986-19728004 chr8:19727989-19728002 chr8:19727987-19728003 chr8:19727988-19728009 chr8:19727989-19727997
39	CTCF	chr8:19727770-19728133	HCT-116	colon:	n/a	chr8:19727986-19728004 chr8:19727989-19728002 chr8:19727987-19728003 chr8:19727988-19728009 chr8:19727989-19727997
40	CTCF	chr8:19727920-19728070	HCM	heart:	n/a	chr8:19727986-19728004 chr8:19727989-19728002 chr8:19727987-19728003 chr8:19727988-19728009 chr8:19727989-19727997
41	CTCF	chr8:19727900-19728050	NHLF	lung:	n/a	chr8:19727986-19728004 chr8:19727989-19728002 chr8:19727987-19728003 chr8:19727988-19728009 chr8:19727989-19727997
42	CTCF	chr8:19727900-19728050	HFF	foreskin:	n/a	chr8:19727986-19728004 chr8:19727989-19728002 chr8:19727987-19728003 chr8:19727988-19728009 chr8:19727989-19727997
43	CTCF	chr8:19727960-19728110	GM12870	blood:	n/a	chr8:19727986-19728004 chr8:19727989-19728002 chr8:19727987-19728003 chr8:19727988-19728009 chr8:19727989-19727997
44	CTCF	chr8:19727980-19728130	NHEK	skin:	n/a	chr8:19727986-19728004 chr8:19727989-19728002 chr8:19727987-19728003 chr8:19727988-19728009 chr8:19727989-19727997
45	CTCF	chr8:19727905-19728106	A549	lung:	n/a	chr8:19727986-19728004 chr8:19727989-19728002 chr8:19727987-19728003 chr8:19727988-19728009 chr8:19727989-19727997
46	CTCF	chr8:19728300-19728450	GM12874	blood:	n/a	n/a
47	CTCF	chr8:19727860-19728010	MCF-7	breast:	n/a	chr8:19727986-19728004 chr8:19727989-19728002 chr8:19727987-19728003 chr8:19727988-19728009 chr8:19727989-19727997
48	CTCF	chr8:19728000-19728150	HFF-Myc	foreskin:	n/a	n/a
49	CTCF	chr8:19727982-19728058	NHEK	skin:	n/a	chr8:19727986-19728004 chr8:19727989-19728002 chr8:19727987-19728003 chr8:19727988-19728009 chr8:19727989-19727997
50	CTCF	chr8:19727940-19728090	GM12869	blood:	n/a	chr8:19727986-19728004 chr8:19727989-19728002 chr8:19727987-19728003 chr8:19727988-19728009 chr8:19727989-19727997

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:19719149-19719199	PANC-1	pancreas:	n/a
2	chr8:19719149-19719199	HIPEpiC	eye:	n/a
3	chr8:19719149-19719199	HCF	heart:	n/a
4	chr8:19719149-19719199	A549	lung:	n/a
5	chr8:19719149-19719199	BE2_C	brain:	n/a
6	chr8:19719149-19719199	AG04449	skin:	fetal
7	chr8:19719149-19719199	AG04450	lung:	fetal
8	chr8:19719149-19719199	ovcar-3	ovarian:	n/a
9	chr8:19719149-19719199	K562	blood:	n/a
10	chr8:19719149-19719199	HRE	kidney:	n/a
11	chr8:19719149-19719199	AG09309	skin:	n/a
12	chr8:19719149-19719199	MCF-7	breast:	n/a
13	chr8:19719149-19719199	HEK293	kidney:	embryo
14	chr8:19719149-19719199	PrEC	prostate:	n/a
15	chr8:19719149-19719199	AG09319	gingival:	n/a
16	chr8:19719149-19719199	AoSMC	blood vessel:	n/a
17	chr8:19719149-19719199	HL-60	blood:	n/a
18	chr8:19719149-19719199	NB4	blood:	n/a
19	chr8:19719149-19719199	GM06990	blood:	n/a
20	chr8:19719149-19719199	MCF10A-Er-Src	breast:	n/a
21	chr8:19719149-19719199	HEEpiC	esophagus:	n/a
22	chr8:19719149-19719199	NH-A	brain:	n/a
23	chr8:19719149-19719199	BJ	skin:	n/a
24	chr8:19719149-19719199	SK-N-MC	brain:	n/a
25	chr8:19719149-19719199	H1-hESC	embryonic stem cell:	embryo
26	chr8:19719149-19719199	HCPEpiC	choroid plexus:	n/a
27	chr8:19719149-19719199	Caco-2	colon:	n/a
28	chr8:19719149-19719199	HepG2	liver:	n/a
29	chr8:19719149-19719199	HPAEpiC	pulmonary alveolar:	n/a
30	chr8:19719149-19719199	NHBE	bronchial:	n/a
31	chr8:19719149-19719199	IMR90	lung:	fetal
32	chr8:19719149-19719199	HMEC	breast:	n/a
33	chr8:19719149-19719199	HRCEpiC	kidney:	n/a
34	chr8:19719149-19719199	GM12878	blood:	n/a
35	chr8:19719149-19719199	LNCaP	prostate:	n/a
36	chr8:19719149-19719199	HRPEpiC	eye:	n/a
37	chr8:19719149-19719199	SK-N-SH	brain:	n/a
38	chr8:19719149-19719199	HCM	heart:	n/a
39	chr8:19719149-19719199	AG10803	skin:	n/a
40	chr8:19719149-19719199	HAEpiC	amniotic membrane:	n/a
41	chr8:19719149-19719199	Jurkat	blood:	n/a
42	chr8:19719149-19719199	RPTEC	kidney:	n/a
43	chr8:19719149-19719199	HUVEC	blood vessel:	n/a
44	chr8:19719149-19719199	PFSK-1	brain:	n/a
45	chr8:19719149-19719199	NT2-D1	testis:	n/a
46	chr8:19719149-19719199	HNPCEpiC	eye:	n/a
47	chr8:19719149-19719199	U87	brain:	n/a
48	chr8:19719149-19719199	SAEC	small airway:	n/a
49	chr8:19719149-19719199	GM19239	blood:	n/a
50	chr8:19719149-19719199	Hepatocyte	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:19727136..19729555-chr8:19732389..19735213,2	K562	blood:
2	chr8:19737734..19739441-chr8:19740524..19742384,2	K562	blood:
3	chr8:19726580..19729500-chr8:19735751..19737530,2	K562	blood:
4	chr8:19737734..19739441-chr8:19740524..19742384,2	K562	blood:
5	chr8:19709783..19712662-chr8:19713981..19716108,2	K562	blood:
6	chr8:19727405..19728444-chr8:19980912..19981476,3	MCF-7	breast:
7	chr8:19747137..19751203-chr8:19751679..19754086,4	K562	blood:
8	chr8:19727939..19728690-chr8:19971015..19972062,3	MCF-7	breast:
9	chr8:19726580..19729500-chr8:19735751..19737530,2	K562	blood:
10	chr8:19747137..19751203-chr8:19751679..19754086,4	K562	blood:
11	chr8:19727572..19728249-chr8:19990904..19991781,3	K562	blood:
12	chr8:19727136..19729555-chr8:19732389..19735213,2	K562	blood:
13	chr8:19709783..19712662-chr8:19713981..19716108,2	K562	blood:
14	chr8:19727581..19728428-chr8:19971178..19971906,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LPL-1	chr8:19750703-19750937	expReg_chr8_827_+

Variant related genes	Relation type
LPL	TF binding region
LPL	CpG island
ENSG00000242709	chromatin interactions

Extended variants
information (count: 1885 )
Associated
traits (count: 116 )

Variant overlapped rSNPs/rCNVs (count:1885 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6998248	chr8:19712564-19712565	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs17091565	chr8:19712579-19712580	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs563469565	chr8:19712601-19712602	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs532468037	chr8:19712602-19712603	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs552212521	chr8:19712656-19712657	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs559324399	chr8:19712663-19712664	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs569003087	chr8:19712709-19712710	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs548201962	chr8:19712754-19712755	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs568327371	chr8:19712794-19712795	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs113113783	chr8:19712806-19712807	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs111586031	chr8:19712919-19712920	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs536874141	chr8:19712924-19712925	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs550789143	chr8:19712963-19712964	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs570603655	chr8:19712964-19712965	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs34291424	chr8:19712982-19712983	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs78713594	chr8:19712988-19712989	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs553058889	chr8:19713006-19713007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs190312663	chr8:19713044-19713045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs181994410	chr8:19713060-19713061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs371942317	chr8:19713070-19713071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs57060363	chr8:19713153-19713154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs114152768	chr8:19713191-19713192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs563548270	chr8:19713360-19713361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs186376017	chr8:19713364-19713365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs545913908	chr8:19713365-19713366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs559386387	chr8:19713438-19713439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs528509121	chr8:19713465-19713466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs571017021	chr8:19713478-19713479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs7832264	chr8:19713500-19713501	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs191178056	chr8:19713529-19713530	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs180838562	chr8:19713547-19713548	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs530822502	chr8:19713629-19713630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs550855984	chr8:19713646-19713647	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs570666442	chr8:19713680-19713681	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs117130611	chr8:19713718-19713719	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs77775840	chr8:19713728-19713729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs374768862	chr8:19713748-19713749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs546735656	chr8:19713814-19713815	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs539607453	chr8:19713861-19713862	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs142557613	chr8:19713884-19713885	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs555340233	chr8:19713912-19713913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs146620476	chr8:19713916-19713917	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs368061647	chr8:19713927-19713928	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs7837466	chr8:19713994-19713995	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs577037915	chr8:19714031-19714032	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs540229125	chr8:19714032-19714033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs141338568	chr8:19714057-19714058	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs558945514	chr8:19714100-19714101	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs6586871	chr8:19714106-19714107	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs557950212	chr8:19714126-19714127	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:116)

Disease	PMID	Source
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Epilepsy	22083797	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	17603634	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	17550852	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21364760	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cancer	18840272	CNVD
Breast cancer	19602461	CNVD
Osteosarcoma	19286668	CNVD
Prostate cancer	19242612	CNVD
Prostate cancer	19258508	CNVD
small cell lung cancer	20016488	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Gastric adenocarcinoma	19115996	CNVD
Colorectal cancer	19455253	CNVD
Melanoma	20688739	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:397 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:19700000-19714000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr8:19701800-19719400	Weak transcription	Fetal Heart	heart
3	chr8:19702800-19713600	Weak transcription	Small Intestine	intestine
4	chr8:19703200-19713400	Weak transcription	Fetal Lung	lung
5	chr8:19703400-19713800	Weak transcription	Fetal Kidney	kidney
6	chr8:19705600-19713200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
7	chr8:19705600-19713400	Weak transcription	Psoas Muscle	Psoas
8	chr8:19705600-19714200	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr8:19706000-19714800	Weak transcription	HMEC	breast
10	chr8:19706200-19713400	Weak transcription	Skeletal Muscle Female	skeletal muscle
11	chr8:19706600-19714400	Weak transcription	HUVEC	blood vessel
12	chr8:19706600-19715000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr8:19706800-19713200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
14	chr8:19706800-19713400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr8:19706800-19715400	Weak transcription	HepG2	liver
16	chr8:19707000-19713400	Weak transcription	Primary B cells from cord blood	blood
17	chr8:19707000-19714200	Weak transcription	NHDF-Ad	bronchial
18	chr8:19707800-19712600	Weak transcription	Primary T helper cells fromperipheralblood	blood
19	chr8:19707800-19713000	Weak transcription	Osteobl	bone
20	chr8:19708400-19712800	Weak transcription	Primary T cells fromperipheralblood	blood
21	chr8:19709200-19712600	Weak transcription	Right Ventricle	heart
22	chr8:19709200-19712800	Weak transcription	Esophagus	oesophagus
23	chr8:19709400-19713000	Weak transcription	Placenta Amnion	Placenta Amnion
24	chr8:19709400-19714800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr8:19709400-19715200	Weak transcription	Sigmoid Colon	Sigmoid Colon
26	chr8:19709600-19714200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr8:19710200-19713600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr8:19710200-19714600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
29	chr8:19710400-19712600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr8:19710400-19712600	Weak transcription	Liver	Liver
31	chr8:19710400-19712600	Weak transcription	Gastric	stomach
32	chr8:19710400-19712600	Weak transcription	Spleen	Spleen
33	chr8:19710400-19713000	Weak transcription	Placenta	Placenta
34	chr8:19710400-19713000	Weak transcription	GM12878-XiMat	blood
35	chr8:19710400-19713200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr8:19710400-19713200	Weak transcription	Aorta	Aorta
37	chr8:19710400-19713200	Weak transcription	Duodenum Mucosa	Duodenum
38	chr8:19710400-19713400	Weak transcription	Rectal Mucosa Donor 29	rectum
39	chr8:19710400-19713400	Weak transcription	Skeletal Muscle Male	skeletal muscle
40	chr8:19710400-19713600	Weak transcription	Primary monocytes fromperipheralblood	blood
41	chr8:19710400-19713800	Weak transcription	Fetal Muscle Leg	muscle
42	chr8:19710400-19714000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr8:19710400-19714200	Weak transcription	Fetal Intestine Small	intestine
44	chr8:19710400-19715000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr8:19710400-19715000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr8:19710400-19715000	Weak transcription	Fetal Thymus	thymus
47	chr8:19710400-19715400	Weak transcription	Pancreas	Pancrea
48	chr8:19710400-19719600	Weak transcription	Adipose Nuclei	Adipose
49	chr8:19710600-19712600	Weak transcription	Stomach Smooth Muscle	stomach
50	chr8:19710600-19713000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood

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