Variant report

Variant	nsv824563
Chromosome Location	chr8:19984763-20026090
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	chr8:20002798-20003127	IMR90	lung:	n/a	n/a
2	CEBPB	chr8:20002799-20003239	Hela-S3	cervix:	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	chr8:19991136-19991591	K562	blood:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
6	CTCF	chr8:19991640-19991790	GM12868	blood:	n/a	n/a
7	CTCF	chr8:19991320-19991470	HMEC	breast:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
8	CTCF	chr8:19997741-19997821	Lung_OC	lung:	n/a	n/a
9	CTCF	chr8:19991320-19991470	GM12873	blood:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
10	CTCF	chr8:19991302-19991523	GM20000	blood:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
11	CTCF	chr8:19991300-19991450	HVMF	connective:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
12	CTCF	chr8:19991260-19991410	HUVEC	blood vessel:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
13	CTCF	chr8:19991300-19991450	Hela-S3	cervix:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
14	CTCF	chr8:19991212-19991516	GM12878	blood:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
15	CTCF	chr8:20022359-20022412	GM19239	blood:	n/a	n/a
16	CTCF	chr8:19991280-19991430	GM12872	blood:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
17	CTCF	chr8:19991300-19991450	GM12874	blood:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
18	CTCF	chr8:20022355-20022397	A549	lung:	n/a	n/a
19	CTCF	chr8:19991131-19991568	H1-hESC	embryonic stem cell:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
20	CTCF	chr8:19991249-19991515	GM13977	blood:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
21	CTCF	chr8:19991269-19991486	ProgFib	skin:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
22	CTCF	chr8:19991280-19991430	NHDF-neo	bronchial:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
23	CTCF	chr8:19991283-19991442	GM12892	blood:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
24	CTCF	chr8:19991260-19991410	GM12865	blood:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
25	CTCF	chr8:20022316-20022421	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr8:19991260-19991410	GM12867	blood:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
27	CTCF	chr8:19991320-19991470	HAc	cerebellar:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
28	CTCF	chr8:20014613-20014695	Kidney_OC	kidney:	n/a	n/a
29	CTCF	chr8:19991300-19991450	NB4	blood:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
30	CTCF	chr8:19991205-19991478	SK-N-SH_RA	brain:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
31	CTCF	chr8:20022340-20022490	HepG2	liver:	n/a	n/a
32	CTCF	chr8:19991700-19991850	GM12864	blood:	n/a	n/a
33	CTCF	chr8:19991280-19991430	GM12866	blood:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
34	CTCF	chr8:19991320-19991470	NHEK	skin:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
35	CTCF	chr8:20022240-20022390	SK-N-SH_RA	brain:	n/a	n/a
36	CTCF	chr8:19991245-19991511	Gliobla	brain:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
37	CTCF	chr8:19990803-19990822	Medullo	brain:	n/a	n/a
38	CTCF	chr8:19991241-19991532	K562	blood:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
39	CTCF	chr8:19991197-19991534	HUVEC	blood vessel:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
40	CTCF	chr8:19991320-19991470	HPF	lung:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
41	CTCF	chr8:19991280-19991430	BE2_C	brain:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
42	CTCF	chr8:19991300-19991450	HPF	lung:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
43	CTCF	chr8:20008100-20008250	HEEpiC	esophagus:	n/a	n/a
44	CTCF	chr8:19992000-19992150	HUVEC	blood vessel:	n/a	n/a
45	CTCF	chr8:19991300-19991450	HRPEpiC	eye:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
46	CTCF	chr8:20022260-20022410	WERI-Rb-1	eye:	n/a	n/a
47	CTCF	chr8:19991320-19991470	BJ	skin:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
48	CTCF	chr8:19991320-19991470	NHLF	lung:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
49	CTCF	chr8:19991320-19991470	WI-38	lung:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387
50	CTCF	chr8:19991280-19991430	HL-60	blood:	n/a	chr8:19991372-19991390 chr8:19991367-19991388 chr8:19991373-19991389 chr8:19991374-19991387

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:20002826-20002876	SK-N-SH_RA	brain:	n/a
2	chr8:20002826-20002876	SK-N-SH_RA	brain:	n/a
3	chr8:20010728-20010778	AG04450	lung:	fetal
4	chr8:20002826-20002876	H1-hESC	embryonic stem cell:	embryo
5	chr8:20010728-20010778	GM12891	blood:	n/a
6	chr8:20010728-20010778	LNCaP	prostate:	n/a
7	chr8:20002826-20002876	PFSK-1	brain:	n/a
8	chr8:20002826-20002876	AG04449	skin:	fetal
9	chr8:20010728-20010778	HIPEpiC	eye:	n/a
10	chr8:20002826-20002876	NHDF-neo	bronchial:	n/a
11	chr8:20010728-20010778	HPAEpiC	pulmonary alveolar:	n/a
12	chr8:20002826-20002876	NT2-D1	testis:	n/a
13	chr8:20010728-20010778	MCF-7	breast:	n/a
14	chr8:20002826-20002876	T-47D	breast:	n/a
15	chr8:20002826-20002876	HEK293	kidney:	embryo
16	chr8:20010728-20010778	Jurkat	blood:	n/a
17	chr8:20002826-20002876	BE2_C	brain:	n/a
18	chr8:20010728-20010778	GM06990	blood:	n/a
19	chr8:20010728-20010778	IMR90	lung:	fetal
20	chr8:20002826-20002876	ECC-1	luminal epithelium:	n/a
21	chr8:20010728-20010778	NHBE	bronchial:	n/a
22	chr8:20002826-20002876	AG09319	gingival:	n/a
23	chr8:20002826-20002876	HCM	heart:	n/a
24	chr8:20002826-20002876	HRCEpiC	kidney:	n/a
25	chr8:20002826-20002876	NHBE	bronchial:	n/a
26	chr8:20010728-20010778	NT2-D1	testis:	n/a
27	chr8:20002826-20002876	MCF10A-Er-Src	breast:	n/a
28	chr8:20010728-20010778	ProgFib	skin:	n/a
29	chr8:20010728-20010778	ovcar-3	ovarian:	n/a
30	chr8:20002826-20002876	HMEC	breast:	n/a
31	chr8:20010728-20010778	GM12892	blood:	n/a
32	chr8:20010728-20010778	AG10803	skin:	n/a
33	chr8:20002826-20002876	PrEC	prostate:	n/a
34	chr8:20010728-20010778	GM12878	blood:	n/a
35	chr8:20010728-20010778	HNPCEpiC	eye:	n/a
36	chr8:20010728-20010778	RPTEC	kidney:	n/a
37	chr8:20002826-20002876	Caco-2	colon:	n/a
38	chr8:20002826-20002876	PANC-1	pancreas:	n/a
39	chr8:20002826-20002876	SK-N-SH	brain:	n/a
40	chr8:20010728-20010778	HAEpiC	amniotic membrane:	n/a
41	chr8:20002826-20002876	HCPEpiC	choroid plexus:	n/a
42	chr8:20010728-20010778	HRPEpiC	eye:	n/a
43	chr8:20010728-20010778	HUVEC	blood vessel:	n/a
44	chr8:20010728-20010778	Hepatocyte	liver:	n/a
45	chr8:20010728-20010778	NH-A	brain:	n/a
46	chr8:20010728-20010778	Hela-S3	cervix:	n/a
47	chr8:20010728-20010778	ECC-1	luminal epithelium:	n/a
48	chr8:20002826-20002876	AG04450	lung:	fetal
49	chr8:20010728-20010778	SKMC	muscle:	n/a
50	chr8:20010728-20010778	GM19239	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:19670534..19671042-chr8:19990928..19991891,2	MCF-7	breast:
2	chr8:19991226..19991903-chr8:20233790..20234437,2	MCF-7	breast:
3	chr8:20007650..20009745-chr8:20016355..20018698,2	K562	blood:
4	chr8:20007650..20009376-chr8:20017198..20019566,2	K562	blood:
5	chr8:19727572..19728249-chr8:19990904..19991781,3	K562	blood:
6	chr8:20020373..20021951-chr8:20028843..20031840,2	MCF-7	breast:
7	chr8:19229314..19230191-chr8:19990957..19991686,3	K562	blood:
8	chr8:19674771..19677183-chr8:19988400..19991254,2	K562	blood:
9	chr8:19614946..19615490-chr8:19990822..19991486,2	MCF-7	breast:
10	chr8:19980514..19983511-chr8:19986584..19989159,2	K562	blood:

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

Extended variants
information (count: 2240 )
Associated
traits (count: 117 )

Variant overlapped rSNPs/rCNVs (count:2240 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs78736967	chr8:19984790-19984791	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs568054647	chr8:19984804-19984805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs367952914	chr8:19984827-19984828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs78546497	chr8:19984842-19984843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs538482547	chr8:19984844-19984845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs553921838	chr8:19984867-19984868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs147635226	chr8:19984875-19984876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs539623341	chr8:19984913-19984914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs142007431	chr8:19984919-19984920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs576328914	chr8:19984922-19984923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs373149543	chr8:19984970-19984971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs181087166	chr8:19984985-19984986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs561776211	chr8:19985003-19985004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs117448061	chr8:19985025-19985026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs553900629	chr8:19985068-19985069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs559817663	chr8:19985073-19985074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs185067971	chr8:19985075-19985076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs377353685	chr8:19985119-19985120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs571679618	chr8:19985134-19985135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs563818307	chr8:19985174-19985175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs531278807	chr8:19985190-19985191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs545409838	chr8:19985244-19985245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs549788055	chr8:19985305-19985306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs568026626	chr8:19985310-19985311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs370352577	chr8:19985317-19985318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs572262815	chr8:19985323-19985324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs565780023	chr8:19985352-19985353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs10503670	chr8:19985382-19985383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs557981238	chr8:19985384-19985385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs60486223	chr8:19985390-19985391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs536982008	chr8:19985404-19985405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs555255800	chr8:19985411-19985412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs573667503	chr8:19985429-19985430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs533521207	chr8:19985437-19985438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs541028144	chr8:19985486-19985487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs559546672	chr8:19985490-19985491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs578078279	chr8:19985491-19985492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs545267996	chr8:19985503-19985504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs189029408	chr8:19985513-19985514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs113357559	chr8:19985595-19985596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs531144693	chr8:19985616-19985617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs543316618	chr8:19985631-19985632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs561571105	chr8:19985645-19985646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs528853516	chr8:19985650-19985651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs547412350	chr8:19985665-19985666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs73669717	chr8:19985687-19985688	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs533078136	chr8:19985689-19985690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs551273822	chr8:19985765-19985766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs569475336	chr8:19985802-19985803	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs536867625	chr8:19985858-19985859	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:117)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:228 , 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	chr8:19978200-19987000	Weak transcription	Left Ventricle	heart
3	chr8:19980200-19986000	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr8:19980800-19986000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr8:19981200-19985800	Weak transcription	HMEC	breast
6	chr8:19982800-19984800	Bivalent Enhancer	Placenta	Placenta
7	chr8:19984200-19985800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr8:19984600-19984800	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr8:19985800-19987200	Enhancers	HMEC	breast
10	chr8:19985800-19987600	Enhancers	Placenta	Placenta
11	chr8:19985800-19988000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr8:19986000-19986400	Enhancers	Esophagus	oesophagus
13	chr8:19986000-19987200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr8:19986000-19987200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr8:19986000-19987400	Enhancers	NHEK	skin
16	chr8:19986000-19987600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr8:19986000-19988000	Enhancers	Placenta Amnion	Placenta Amnion
18	chr8:19986400-19986800	Weak transcription	Esophagus	oesophagus
19	chr8:19986600-19987200	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr8:19986600-19987400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr8:19986800-19987000	Enhancers	Esophagus	oesophagus
22	chr8:19987000-19987800	Enhancers	Left Ventricle	heart
23	chr8:19987000-19992400	Weak transcription	Esophagus	oesophagus
24	chr8:19987200-19992600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr8:19987200-19992600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr8:19987200-19995000	Weak transcription	HMEC	breast
27	chr8:19987400-19992200	Weak transcription	NHEK	skin
28	chr8:19987600-19988000	Bivalent Enhancer	Placenta	Placenta
29	chr8:19987600-19992400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr8:19988000-19992800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr8:19990000-19990200	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr8:19992200-19993600	Enhancers	NHEK	skin
33	chr8:19992400-19993000	Enhancers	Esophagus	oesophagus
34	chr8:19992400-19993600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr8:19992600-19993200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr8:19992600-19993200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr8:19992800-19993000	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr8:19992800-19993000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr8:19992800-19993000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr8:19992800-19993200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr8:19992800-19993200	Enhancers	Fetal Intestine Large	intestine
42	chr8:19993000-19993200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr8:19993000-19993400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr8:19993000-19993800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr8:19993000-19995000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr8:19993000-19999400	Weak transcription	Esophagus	oesophagus
47	chr8:19993200-19993600	Weak transcription	Fetal Intestine Large	intestine
48	chr8:19993200-19995000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr8:19993200-19995400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr8:19993200-19998400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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