Variant report

Variant	nsv1030738
Chromosome Location	chr8:19989194-20022150
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	CEBPB	chr8:20002799-20003239	Hela-S3	cervix:	n/a	n/a
2	CEBPB	chr8:20002798-20003127	IMR90	lung:	n/a	n/a
3	CEBPB	chr8:19994678-19994913	HepG2	liver:	n/a	chr8:19994762-19994773
4	CEBPB	chr8:19999638-19999919	Hela-S3	cervix:	n/a	n/a
5	CTCF	chr8:19990940-19991090	AoAF	blood vessel:	n/a	n/a
6	CTCF	chr8:19991720-19991870	BJ	skin:	n/a	n/a
7	CTCF	chr8:19991340-19991490	GM12869	blood:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
8	CTCF	chr8:19991283-19991442	GM12892	blood:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
9	CTCF	chr8:19991300-19991450	HPAF	blood vessel:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
10	CTCF	chr8:20013196-20013266	Lung_OC	lung:	n/a	n/a
11	CTCF	chr8:19991047-19991704	HCT-116	colon:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
12	CTCF	chr8:19991280-19991430	GM12873	blood:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
13	CTCF	chr8:19991300-19991450	HPF	lung:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
14	CTCF	chr8:19991205-19991478	SK-N-SH_RA	brain:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
15	CTCF	chr8:19990984-19991650	SK-N-SH	brain:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
16	CTCF	chr8:19991280-19991430	BJ	skin:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
17	CTCF	chr8:19990835-19990845	Medullo	brain:	n/a	n/a
18	CTCF	chr8:19991320-19991470	NHLF	lung:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
19	CTCF	chr8:19991262-19991453	A549	lung:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
20	CTCF	chr8:19991180-19991574	HepG2	liver:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
21	CTCF	chr8:19991278-19991453	GM19240	blood:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
22	CTCF	chr8:19991265-19991506	Pancreas_OC	pancreas:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
23	CTCF	chr8:19991260-19991410	HCM	heart:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
24	CTCF	chr8:19991162-19991540	A549	lung:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
25	CTCF	chr8:19991660-19991810	HRE	kidney:	n/a	n/a
26	CTCF	chr8:19991340-19991490	HVMF	connective:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
27	CTCF	chr8:19991260-19991410	SAEC	small airway:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
28	CTCF	chr8:19991320-19991470	GM12872	blood:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
29	CTCF	chr8:19991300-19991450	GM12868	blood:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
30	CTCF	chr8:20008100-20008250	HEEpiC	esophagus:	n/a	n/a
31	CTCF	chr8:19991252-19991502	GM10248	blood:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
32	CTCF	chr8:19991300-19991450	HCM	heart:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
33	CTCF	chr8:19991251-19991500	HepG2	liver:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
34	CTCF	chr8:19991300-19991450	GM12873	blood:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
35	CTCF	chr8:19991269-19991486	ProgFib	skin:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
36	CTCF	chr8:19991300-19991450	HCPEpiC	choroid plexus:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
37	CTCF	chr8:19991125-19991551	MCF-7	breast:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
38	CTCF	chr8:19991300-19991450	HMF	breast:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
39	CTCF	chr8:19991260-19991410	GM12870	blood:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
40	CTCF	chr8:19991280-19991430	HRE	kidney:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
41	CTCF	chr8:19991160-19991310	A549	lung:	n/a	n/a
42	CTCF	chr8:19991329-19991398	MCF-7	breast:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
43	CTCF	chr8:19991300-19991450	AG04450	lung:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
44	CTCF	chr8:19991100-19991564	A549	lung:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
45	CTCF	chr8:19991300-19991450	HBMEC	blood vessel:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
46	CTCF	chr8:19991300-19991450	GM12875	blood:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
47	CTCF	chr8:19990900-19991050	AG04450	lung:	n/a	n/a
48	CTCF	chr8:19991280-19991430	AG04450	lung:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
49	CTCF	chr8:19991660-19991810	BE2_C	brain:	n/a	n/a
50	CTCF	chr8:19991280-19991430	HCFaa	heart:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:20010728-20010778	H1-hESC	embryonic stem cell:	embryo
2	chr8:20002826-20002876	HepG2	liver:	n/a
3	chr8:20010728-20010778	SKMC	muscle:	n/a
4	chr8:20010728-20010778	ECC-1	luminal epithelium:	n/a
5	chr8:20010728-20010778	HRPEpiC	eye:	n/a
6	chr8:20010728-20010778	HepG2	liver:	n/a
7	chr8:20002826-20002876	HRPEpiC	eye:	n/a
8	chr8:20002826-20002876	AG09309	skin:	n/a
9	chr8:20002826-20002876	A549	lung:	n/a
10	chr8:20002826-20002876	BJ	skin:	n/a
11	chr8:20010728-20010778	SK-N-SH_RA	brain:	n/a
12	chr8:20002826-20002876	NT2-D1	testis:	n/a
13	chr8:20002826-20002876	Caco-2	colon:	n/a
14	chr8:20002826-20002876	AG10803	skin:	n/a
15	chr8:20010728-20010778	HRE	kidney:	n/a
16	chr8:20002826-20002876	SK-N-MC	brain:	n/a
17	chr8:20002826-20002876	Hepatocyte	liver:	n/a
18	chr8:20010728-20010778	IMR90	lung:	fetal
19	chr8:20010728-20010778	HCT-116	colon:	n/a
20	chr8:20002826-20002876	NHDF-neo	bronchial:	n/a
21	chr8:20002826-20002876	HEEpiC	esophagus:	n/a
22	chr8:20002826-20002876	IMR90	lung:	fetal
23	chr8:20002826-20002876	HCM	heart:	n/a
24	chr8:20002826-20002876	Jurkat	blood:	n/a
25	chr8:20010728-20010778	HCPEpiC	choroid plexus:	n/a
26	chr8:20010728-20010778	HAEpiC	amniotic membrane:	n/a
27	chr8:20010728-20010778	NT2-D1	testis:	n/a
28	chr8:20010728-20010778	HMEC	breast:	n/a
29	chr8:20010728-20010778	RPTEC	kidney:	n/a
30	chr8:20002826-20002876	BE2_C	brain:	n/a
31	chr8:20002826-20002876	H1-hESC	embryonic stem cell:	embryo
32	chr8:20010728-20010778	Caco-2	colon:	n/a
33	chr8:20010728-20010778	AG04449	skin:	fetal
34	chr8:20010728-20010778	BE2_C	brain:	n/a
35	chr8:20010728-20010778	AG10803	skin:	n/a
36	chr8:20002826-20002876	AoSMC	blood vessel:	n/a
37	chr8:20010728-20010778	PFSK-1	brain:	n/a
38	chr8:20002826-20002876	ECC-1	luminal epithelium:	n/a
39	chr8:20002826-20002876	HUVEC	blood vessel:	n/a
40	chr8:20002826-20002876	K562	blood:	n/a
41	chr8:20010728-20010778	MCF-7	breast:	n/a
42	chr8:20010728-20010778	LNCaP	prostate:	n/a
43	chr8:20010728-20010778	U87	brain:	n/a
44	chr8:20002826-20002876	LNCaP	prostate:	n/a
45	chr8:20010728-20010778	MCF10A-Er-Src	breast:	n/a
46	chr8:20002826-20002876	MCF10A-Er-Src	breast:	n/a
47	chr8:20002826-20002876	ovcar-3	ovarian:	n/a
48	chr8:20002826-20002876	Hela-S3	cervix:	n/a
49	chr8:20010728-20010778	AG04450	lung:	fetal
50	chr8:20010728-20010778	HIPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:19727572..19728249-chr8:19990904..19991781,3	K562	blood:
2	chr8:20007650..20009745-chr8:20016355..20018698,2	K562	blood:
3	chr8:19674771..19677183-chr8:19988400..19991254,2	K562	blood:
4	chr8:19670534..19671042-chr8:19990928..19991891,2	MCF-7	breast:
5	chr8:20020373..20021951-chr8:20028843..20031840,2	MCF-7	breast:
6	chr8:19229314..19230191-chr8:19990957..19991686,3	K562	blood:
7	chr8:19614946..19615490-chr8:19990822..19991486,2	MCF-7	breast:
8	chr8:19991226..19991903-chr8:20233790..20234437,2	MCF-7	breast:
9	chr8:20007650..20009376-chr8:20017198..20019566,2	K562	blood:

Variant related genes	Relation type
SLC18A1	TF binding region
SLC18A1	CpG island
ENSG00000147408	chromatin interactions
ENSG00000104613	chromatin interactions
ENSG00000036565	chromatin interactions

Extended variants
information (count: 1777 )
Associated
traits (count: 116 )

Variant overlapped rSNPs/rCNVs (count:1777 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11783715	chr8:19989194-19989195	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs529019845	chr8:19989199-19989200	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs547192557	chr8:19989213-19989214	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs77553668	chr8:19989216-19989217	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs113925346	chr8:19989259-19989260	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs542936295	chr8:19989260-19989261	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs557864228	chr8:19989269-19989270	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs539261959	chr8:19989272-19989273	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs369844324	chr8:19989285-19989286	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs386412253	chr8:19989286-19989287	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs145114660	chr8:19989291-19989292	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs555623810	chr8:19989298-19989299	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs569658661	chr8:19989302-19989303	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs573882618	chr8:19989316-19989317	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs555366720	chr8:19989319-19989320	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs534810567	chr8:19989321-19989322	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs574033219	chr8:19989322-19989323	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs185172693	chr8:19989342-19989343	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs553245052	chr8:19989344-19989345	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs149119936	chr8:19989357-19989358	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs189962352	chr8:19989358-19989359	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs578087478	chr8:19989384-19989385	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs545626070	chr8:19989394-19989395	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs577923097	chr8:19989432-19989433	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs563962123	chr8:19989438-19989439	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs200294877	chr8:19989446-19989447	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs531260031	chr8:19989490-19989491	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs13439592	chr8:19989544-19989545	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs543426676	chr8:19989567-19989568	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs182547467	chr8:19989584-19989585	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs185675060	chr8:19989599-19989600	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs547424489	chr8:19989604-19989605	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs13439593	chr8:19989637-19989638	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs565649878	chr8:19989641-19989642	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs532955357	chr8:19989644-19989645	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs575560475	chr8:19989719-19989720	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs551211644	chr8:19989728-19989729	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs143512056	chr8:19989753-19989754	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs542689752	chr8:19989769-19989770	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs569590090	chr8:19989832-19989833	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs542999422	chr8:19989861-19989862	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs549020949	chr8:19989884-19989885	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs567622183	chr8:19989885-19989886	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs564668230	chr8:19989909-19989910	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs553390454	chr8:19989952-19989953	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs578066702	chr8:19990023-19990024	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs150953016	chr8:19990025-19990026	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs73669720	chr8:19990033-19990034	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs575926636	chr8:19990053-19990054	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs367994547	chr8:19990098-19990099	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	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
Prostate cancer	22341455	CNVD

Chromatin state (count:202 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:19978000-19993600	Weak transcription	Right Ventricle	heart
2	chr8:19987000-19992400	Weak transcription	Esophagus	oesophagus
3	chr8:19987200-19992600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr8:19987200-19992600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr8:19987200-19995000	Weak transcription	HMEC	breast
6	chr8:19987400-19992200	Weak transcription	NHEK	skin
7	chr8:19987600-19992400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr8:19988000-19992800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr8:19990000-19990200	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr8:19992200-19993600	Enhancers	NHEK	skin
11	chr8:19992400-19993000	Enhancers	Esophagus	oesophagus
12	chr8:19992400-19993600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr8:19992600-19993200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr8:19992600-19993200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr8:19992800-19993000	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr8:19992800-19993000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr8:19992800-19993000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr8:19992800-19993200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr8:19992800-19993200	Enhancers	Fetal Intestine Large	intestine
20	chr8:19993000-19993200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr8:19993000-19993400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr8:19993000-19993800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr8:19993000-19995000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr8:19993000-19999400	Weak transcription	Esophagus	oesophagus
25	chr8:19993200-19993600	Weak transcription	Fetal Intestine Large	intestine
26	chr8:19993200-19995000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr8:19993200-19995400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr8:19993200-19998400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr8:19993200-20000400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr8:19993400-19994200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr8:19993600-19993800	Enhancers	Right Ventricle	heart
32	chr8:19993600-19994200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr8:19993600-19994200	Enhancers	Fetal Intestine Large	intestine
34	chr8:19993600-19995000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr8:19993600-19995000	Weak transcription	NHEK	skin
36	chr8:19993800-19994000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr8:19993800-19994000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr8:19993800-19994200	Enhancers	H9 Cell Line	embryonic stem cell
39	chr8:19993800-19994200	Enhancers	Fetal Intestine Small	intestine
40	chr8:19993800-19994200	Enhancers	Fetal Kidney	kidney
41	chr8:19994000-19994200	Enhancers	H1 Cell Line	embryonic stem cell
42	chr8:19994000-19994200	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr8:19994000-19994400	Enhancers	Fetal Muscle Trunk	muscle
44	chr8:19994000-19994800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr8:19994000-19995000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr8:19994200-19994800	Weak transcription	H1 Cell Line	embryonic stem cell
47	chr8:19994200-19995000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr8:19994200-19995200	Weak transcription	Fetal Intestine Small	intestine
49	chr8:19994200-19995200	Weak transcription	Fetal Kidney	kidney
50	chr8:19994200-19995400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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