Variant report

Variant	nsv889734
Chromosome Location	chr8:1870992-1906630
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:308)
CpG islands
(count:4029)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:308 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr8:1905426-1905729	K562	blood:	n/a	n/a
2	BHLHE40	chr8:1883927-1884121	K562	blood:	n/a	chr8:1884045-1884054
3	BHLHE40	chr8:1872763-1873004	K562	blood:	n/a	n/a
4	BHLHE40	chr8:1900444-1900619	K562	blood:	n/a	chr8:1900518-1900531
5	BHLHE40	chr8:1878968-1878979	K562	blood:	n/a	n/a
6	BHLHE40	chr8:1898324-1898578	K562	blood:	n/a	n/a
7	BHLHE40	chr8:1906190-1906595	K562	blood:	n/a	n/a
8	BHLHE40	chr8:1904989-1905720	K562	blood:	n/a	n/a
9	BHLHE40	chr8:1904080-1904391	K562	blood:	n/a	n/a
10	BHLHE40	chr8:1880551-1880723	K562	blood:	n/a	n/a
11	CEBPB	chr8:1897489-1897740	K562	blood:	n/a	n/a
12	CEBPB	chr8:1905506-1905747	K562	blood:	n/a	n/a
13	CEBPB	chr8:1901757-1901948	K562	blood:	n/a	chr8:1901763-1901774
14	CEBPB	chr8:1888262-1888338	HepG2	liver:	n/a	chr8:1888289-1888300
15	CEBPB	chr8:1905512-1905727	K562	blood:	n/a	n/a
16	CEBPB	chr8:1905439-1905837	IMR90	lung:	n/a	n/a
17	CEBPB	chr8:1897522-1897802	K562	blood:	n/a	n/a
18	CEBPB	chr8:1901636-1901913	HepG2	liver:	n/a	chr8:1901763-1901774
19	CEBPB	chr8:1870616-1871016	K562	blood:	n/a	n/a
20	CTCF	chr8:1878940-1879090	WERI-Rb-1	eye:	n/a	chr8:1878992-1879008
21	CTCF	chr8:1878940-1879090	HCPEpiC	choroid plexus:	n/a	chr8:1878992-1879008
22	CTCF	chr8:1878920-1879070	RPTEC	kidney:	n/a	chr8:1878992-1879008
23	CTCF	chr8:1878940-1879090	SAEC	small airway:	n/a	chr8:1878992-1879008
24	CTCF	chr8:1875060-1875210	HA-sp	spinal cord:	n/a	n/a
25	CTCF	chr8:1878880-1879030	K562	blood:	n/a	chr8:1878992-1879008
26	CTCF	chr8:1880424-1880686	GM19239	blood:	n/a	n/a
27	CTCF	chr8:1878020-1878170	AG04449	skin:	n/a	n/a
28	CTCF	chr8:1905000-1905150	WERI-Rb-1	eye:	n/a	n/a
29	CTCF	chr8:1880545-1880667	MCF-7	breast:	n/a	n/a
30	CTCF	chr8:1878869-1879137	Pancreas_OC	pancreas:	n/a	chr8:1878992-1879008
31	CTCF	chr8:1875100-1875250	HCPEpiC	choroid plexus:	n/a	n/a
32	CTCF	chr8:1875060-1875210	HBMEC	blood vessel:	n/a	n/a
33	CTCF	chr8:1875120-1875270	HCPEpiC	choroid plexus:	n/a	n/a
34	CTCF	chr8:1878960-1879110	HepG2	liver:	n/a	chr8:1878992-1879008
35	CTCF	chr8:1871940-1872090	HCPEpiC	choroid plexus:	n/a	n/a
36	CTCF	chr8:1878920-1879070	SAEC	small airway:	n/a	chr8:1878992-1879008
37	CTCF	chr8:1880537-1880593	MCF-7	breast:	n/a	n/a
38	CTCF	chr8:1878881-1879145	K562	blood:	n/a	chr8:1878992-1879008
39	CTCF	chr8:1895277-1895357	LNCaP	prostate:	n/a	n/a
40	CTCF	chr8:1878907-1879071	Kidney_OC	kidney:	n/a	chr8:1878992-1879008
41	CTCF	chr8:1880576-1880627	GM12891	blood:	n/a	n/a
42	CTCF	chr8:1886600-1886750	HMEC	breast:	n/a	n/a
43	CTCF	chr8:1878920-1879070	Caco-2	colon:	n/a	chr8:1878992-1879008
44	CTCF	chr8:1895267-1895271	LNCaP	prostate:	n/a	n/a
45	CTCF	chr8:1878906-1879099	K562	blood:	n/a	chr8:1878992-1879008
46	CTCF	chr8:1880590-1880664	MCF-7	breast:	n/a	n/a
47	CTCF	chr8:1878880-1879030	HEEpiC	esophagus:	n/a	chr8:1878992-1879008
48	CTCF	chr8:1889359-1889380	GM20000	blood:	n/a	n/a
49	CTCF	chr8:1878920-1879070	WERI-Rb-1	eye:	n/a	chr8:1878992-1879008
50	CTCF	chr8:1870952-1871043	K562	blood:	n/a	n/a

(count:4029 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:1872335-1872385	ProgFib	skin:	n/a
2	chr8:1905131-1905181	PrEC	prostate:	n/a
3	chr8:1885575-1885625	K562	blood:	n/a
4	chr8:1872335-1872385	ProgFib	skin:	n/a
5	chr8:1905131-1905181	PrEC	prostate:	n/a
6	chr8:1885575-1885625	K562	blood:	n/a
7	chr8:1885244-1885294	GM12878	blood:	n/a
8	chr8:1876686-1876736	HRPEpiC	eye:	n/a
9	chr8:1900191-1900241	AG09319	gingival:	n/a
10	chr8:1885886-1885936	BE2_C	brain:	n/a
11	chr8:1899231-1899281	U87	brain:	n/a
12	chr8:1892416-1892466	Hela-S3	cervix:	n/a
13	chr8:1894604-1894654	SK-N-SH	brain:	n/a
14	chr8:1891006-1891056	NH-A	brain:	n/a
15	chr8:1897020-1897070	HUVEC	blood vessel:	n/a
16	chr8:1885575-1885625	HCF	heart:	n/a
17	chr8:1906498-1906548	AG10803	skin:	n/a
18	chr8:1905131-1905181	AoSMC	blood vessel:	n/a
19	chr8:1900524-1900574	AG09319	gingival:	n/a
20	chr8:1896553-1896603	BE2_C	brain:	n/a
21	chr8:1900089-1900139	IMR90	lung:	fetal
22	chr8:1900778-1900828	NHDF-neo	bronchial:	n/a
23	chr8:1889949-1889999	HepG2	liver:	n/a
24	chr8:1885083-1885133	ProgFib	skin:	n/a
25	chr8:1892956-1893006	HCF	heart:	n/a
26	chr8:1905280-1905330	HNPCEpiC	eye:	n/a
27	chr8:1905343-1905393	MCF10A-Er-Src	breast:	n/a
28	chr8:1906498-1906548	RPTEC	kidney:	n/a
29	chr8:1894814-1894864	AG10803	skin:	n/a
30	chr8:1898270-1898320	AG04449	skin:	fetal
31	chr8:1898270-1898320	HCPEpiC	choroid plexus:	n/a
32	chr8:1885458-1885508	GM12891	blood:	n/a
33	chr8:1885083-1885133	NHBE	bronchial:	n/a
34	chr8:1879551-1879601	Caco-2	colon:	n/a
35	chr8:1896437-1896487	U87	brain:	n/a
36	chr8:1885244-1885294	AG09319	gingival:	n/a
37	chr8:1897035-1897085	HNPCEpiC	eye:	n/a
38	chr8:1893793-1893843	SK-N-SH_RA	brain:	n/a
39	chr8:1897020-1897070	T-47D	breast:	n/a
40	chr8:1894814-1894864	PFSK-1	brain:	n/a
41	chr8:1897020-1897070	HL-60	blood:	n/a
42	chr8:1899538-1899588	NHDF-neo	bronchial:	n/a
43	chr8:1897035-1897085	T-47D	breast:	n/a
44	chr8:1879091-1879141	HPAEpiC	pulmonary alveolar:	n/a
45	chr8:1906338-1906388	NB4	blood:	n/a
46	chr8:1877888-1877938	MCF10A-Er-Src	breast:	n/a
47	chr8:1889949-1889999	ProgFib	skin:	n/a
48	chr8:1885575-1885625	IMR90	lung:	fetal
49	chr8:1885458-1885508	U87	brain:	n/a
50	chr8:1885458-1885508	GM06990	blood:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:1905928..1907788-chr8:1909949..1911807,2	MCF-7	breast:
2	chr8:1888469..1891151-chr8:1893688..1896485,2	K562	blood:
3	chr8:1876158..1879042-chr8:1903928..1907345,3	K562	blood:
4	chr8:1902551..1904412-chr8:1906073..1908055,2	K562	blood:
5	chr8:1877543..1880354-chr8:1915068..1917833,2	K562	blood:
6	chr8:1900404..1902135-chr8:1904270..1906707,2	K562	blood:
7	chr8:1904438..1906943-chr8:1908364..1910920,2	K562	blood:
8	chr8:1880957..1882903-chr8:1922237..1924079,2	MCF-7	breast:
9	chr8:1876812..1880065-chr8:1886346..1889205,3	K562	blood:
10	chr8:1815516..1817789-chr8:1884960..1887477,2	K562	blood:
11	chr8:1887349..1889723-chr8:1904508..1906219,2	K562	blood:
12	chr8:1888469..1891151-chr8:1893688..1896485,2	K562	blood:
13	chr8:1876158..1879042-chr8:1903928..1907345,3	K562	blood:
14	chr8:1887349..1889723-chr8:1904508..1906219,2	K562	blood:
15	chr8:1869392..1872141-chr8:1901807..1903545,2	K562	blood:
16	chr8:1876812..1880065-chr8:1886346..1889205,3	K562	blood:
17	chr8:1900404..1902135-chr8:1904270..1906707,2	K562	blood:
18	chr8:1902551..1904412-chr8:1906073..1908055,2	K562	blood:

No data

Variant related genes	Relation type
ARHGEF10	TF binding region
ARHGEF10	CpG island
ENSG00000253764	chromatin interactions
ENSG00000104728	chromatin interactions
ENSG00000270988	chromatin interactions

Extended variants
information (count: 2071 )
Associated
traits (count: 119 )

Variant overlapped rSNPs/rCNVs (count:2071 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17830000	chr8:1870992-1870993	Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs374560702	chr8:1871026-1871027	Strong transcription Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs558402154	chr8:1871039-1871040	Strong transcription Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs572023294	chr8:1871053-1871054	Strong transcription Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs534468893	chr8:1871062-1871063	Strong transcription Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs578174141	chr8:1871076-1871077	Strong transcription Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs554345759	chr8:1871083-1871084	Strong transcription Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs574076802	chr8:1871089-1871090	Strong transcription Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs373239929	chr8:1871110-1871111	Strong transcription Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs112914148	chr8:1871114-1871115	Strong transcription Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs367690979	chr8:1871165-1871166	Strong transcription Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs200619686	chr8:1871171-1871172	Strong transcription Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs146291427	chr8:1871182-1871183	Strong transcription Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs147531758	chr8:1871183-1871184	Strong transcription Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs371736644	chr8:1871184-1871185	Strong transcription Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs374906068	chr8:1871227-1871228	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs267601843	chr8:1871239-1871240	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs369600980	chr8:1871254-1871255	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs368429109	chr8:1871260-1871261	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs184465243	chr8:1871261-1871262	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs371896350	chr8:1871277-1871278	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs376759458	chr8:1871293-1871294	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs140218511	chr8:1871328-1871329	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs528003119	chr8:1871342-1871343	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs189443862	chr8:1871376-1871377	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs561503665	chr8:1871380-1871381	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs377198250	chr8:1871386-1871387	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs373466107	chr8:1871449-1871450	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs377296459	chr8:1871456-1871457	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs549637129	chr8:1871478-1871479	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs569753210	chr8:1871479-1871480	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs531976242	chr8:1871488-1871489	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs541482295	chr8:1871490-1871491	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs551764103	chr8:1871533-1871534	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs565590832	chr8:1871545-1871546	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs534647105	chr8:1871548-1871549	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs561630766	chr8:1871561-1871562	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs369766051	chr8:1871612-1871613	Strong transcription Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs373909732	chr8:1871615-1871616	Strong transcription Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs377464971	chr8:1871645-1871646	Strong transcription Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs370752117	chr8:1871666-1871667	Strong transcription Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs557345250	chr8:1871669-1871670	Strong transcription Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs368756089	chr8:1871681-1871682	Strong transcription Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs143459815	chr8:1871716-1871717	Strong transcription Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs146766107	chr8:1871748-1871749	Strong transcription Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs34036746	chr8:1871759-1871760	Strong transcription Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs371243281	chr8:1871764-1871765	Strong transcription Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs374161442	chr8:1871788-1871789	Strong transcription Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs181442826	chr8:1871801-1871802	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs2272614	chr8:1871896-1871897	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:119)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Cancer	18840272	CNVD
Pilocytic astrocytoma	18622384	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
abnormal development	18461090	CNVD
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	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
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	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
Cancer	20164919	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	20729466	CNVD
Ductal carcinoma	22052326	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Epilepsy	22083797	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Breast cancer	20932292	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Ependymoma	20639864	CNVD
Ovarian cancer	22355333	CNVD
Tetralogy of Fallot	22912587	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Lung adenocarcinoma	21935476	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1366 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:1841000-1877600	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr8:1845400-1879600	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr8:1845400-1908000	Weak transcription	Right Atrium	heart
4	chr8:1854200-1872000	Weak transcription	Primary hematopoietic stem cells	blood
5	chr8:1857000-1890600	Weak transcription	Psoas Muscle	Psoas
6	chr8:1858200-1872000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr8:1858400-1872800	Weak transcription	Colon Smooth Muscle	Colon
8	chr8:1858400-1873200	Weak transcription	Duodenum Smooth Muscle	Duodenum
9	chr8:1859800-1871800	Weak transcription	Osteobl	bone
10	chr8:1860400-1876400	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr8:1860600-1878000	Weak transcription	Rectal Smooth Muscle	rectum
12	chr8:1860800-1871800	Weak transcription	Aorta	Aorta
13	chr8:1860800-1872400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr8:1862200-1880400	Weak transcription	Fetal Heart	heart
15	chr8:1862600-1872200	Weak transcription	Left Ventricle	heart
16	chr8:1862600-1873400	Weak transcription	Ovary	ovary
17	chr8:1863200-1871800	Weak transcription	Right Ventricle	heart
18	chr8:1863400-1872000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr8:1863800-1871800	Weak transcription	HSMMtube	muscle
20	chr8:1864400-1871800	Weak transcription	Gastric	stomach
21	chr8:1864400-1872000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr8:1864400-1872200	Weak transcription	Stomach Smooth Muscle	stomach
23	chr8:1864400-1873400	Weak transcription	Pancreas	Pancrea
24	chr8:1865800-1871600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
25	chr8:1865800-1872000	Weak transcription	Fetal Brain Male	brain
26	chr8:1865800-1872000	Weak transcription	Fetal Muscle Trunk	muscle
27	chr8:1866000-1871600	Weak transcription	Brain Hippocampus Middle	brain
28	chr8:1866400-1871600	Weak transcription	Cortex derived primary cultured neurospheres	brain
29	chr8:1866400-1871600	Weak transcription	Brain Anterior Caudate	brain
30	chr8:1866400-1871800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr8:1866600-1871200	Weak transcription	NHEK	skin
32	chr8:1867000-1883600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
33	chr8:1867400-1871800	Weak transcription	Spleen	Spleen
34	chr8:1867400-1873400	Weak transcription	NHDF-Ad	bronchial
35	chr8:1867400-1883400	Weak transcription	Hela-S3	cervix
36	chr8:1867800-1871800	Weak transcription	H1 Cell Line	embryonic stem cell
37	chr8:1867800-1871800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr8:1867800-1871800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr8:1867800-1871800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr8:1867800-1871800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr8:1867800-1871800	Weak transcription	Adipose Nuclei	Adipose
42	chr8:1867800-1871800	Weak transcription	HUVEC	blood vessel
43	chr8:1867800-1872000	Weak transcription	Lung	lung
44	chr8:1868000-1871200	Weak transcription	HSMM	muscle
45	chr8:1868000-1871600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr8:1868000-1871600	Weak transcription	Fetal Lung	lung
47	chr8:1868000-1871800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr8:1868000-1871800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr8:1868000-1871800	Weak transcription	Fetal Intestine Small	intestine
50	chr8:1868000-1872000	Weak transcription	Fetal Muscle Leg	muscle

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