Variant report

Variant	nsv6071
Chromosome Location	chr8:8269444-8304320
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:366)
CpG islands
(count:61)
Chromatin interactive
region (count:25)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:8285133-8285725	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:8283141-8283395	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:8286275-8287368	HepG2	liver:	n/a	n/a
4	ATF2	chr8:8293199-8293483	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr8:8286690-8287352	A549	lung:	n/a	n/a
6	ATF3	chr8:8286695-8287347	A549	lung:	n/a	n/a
7	BCL3	chr8:8286658-8287363	A549	lung:	n/a	n/a
8	BCL3	chr8:8286570-8287287	A549	lung:	n/a	n/a
9	BHLHE40	chr8:8285152-8285676	HepG2	liver:	n/a	chr8:8285292-8285305 chr8:8285288-8285309
10	BHLHE40	chr8:8286354-8287280	HepG2	liver:	n/a	n/a
11	BHLHE40	chr8:8284870-8286026	HepG2	liver:	n/a	chr8:8285292-8285305 chr8:8285288-8285309
12	BHLHE40	chr8:8285206-8285429	K562	blood:	n/a	chr8:8285292-8285305 chr8:8285288-8285309
13	BHLHE40	chr8:8285203-8285486	HepG2	liver:	n/a	chr8:8285292-8285305 chr8:8285288-8285309
14	BRCA1	chr8:8283400-8283413	HepG2	liver:	n/a	n/a
15	BRCA1	chr8:8274625-8275040	Hela-S3	cervix:	n/a	n/a
16	CBX3	chr8:8293081-8293537	HCT-116	colon:	n/a	n/a
17	CBX3	chr8:8293104-8293495	K562	blood:	n/a	n/a
18	CBX3	chr8:8298711-8299537	HCT-116	colon:	n/a	n/a
19	CBX3	chr8:8293131-8293493	K562	blood:	n/a	n/a
20	CBX3	chr8:8298667-8299528	HCT-116	colon:	n/a	n/a
21	CBX3	chr8:8293023-8293525	HCT-116	colon:	n/a	n/a
22	CEBPB	chr8:8269262-8269549	IMR90	lung:	n/a	chr8:8269392-8269403
23	CEBPB	chr8:8286862-8287314	HepG2	liver:	n/a	n/a
24	CEBPB	chr8:8286731-8287340	A549	lung:	n/a	n/a
25	CEBPB	chr8:8269248-8269592	A549	lung:	n/a	chr8:8269392-8269403
26	CEBPB	chr8:8285267-8285739	HepG2	liver:	n/a	n/a
27	CEBPB	chr8:8286874-8287324	HepG2	liver:	n/a	n/a
28	CEBPB	chr8:8288159-8288360	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr8:8269235-8269561	A549	lung:	n/a	chr8:8269392-8269403
30	CEBPB	chr8:8286630-8287443	A549	lung:	n/a	n/a
31	CEBPB	chr8:8286904-8287289	IMR90	lung:	n/a	n/a
32	CEBPB	chr8:8269054-8269616	Hela-S3	cervix:	n/a	chr8:8269392-8269403
33	CEBPB	chr8:8269098-8269622	A549	lung:	n/a	chr8:8269392-8269403
34	CEBPB	chr8:8269236-8269536	HepG2	liver:	n/a	chr8:8269392-8269403
35	CEBPB	chr8:8277590-8277799	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr8:8274608-8275045	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr8:8269265-8269520	K562	blood:	n/a	chr8:8269392-8269403
38	CEBPB	chr8:8286926-8287259	A549	lung:	n/a	n/a
39	CEBPB	chr8:8286999-8287221	HepG2	liver:	n/a	n/a
40	CEBPB	chr8:8269090-8269623	MCF-7	breast:	n/a	chr8:8269392-8269403
41	CEBPB	chr8:8269188-8269552	MCF-7	breast:	n/a	chr8:8269392-8269403
42	CEBPB	chr8:8286803-8287335	HepG2	liver:	n/a	n/a
43	CEBPD	chr8:8286992-8287221	HepG2	liver:	n/a	n/a
44	CEBPD	chr8:8286964-8287209	HepG2	liver:	n/a	n/a
45	CHD2	chr8:8286860-8287226	HepG2	liver:	n/a	n/a
46	CREB1	chr8:8286512-8287343	HepG2	liver:	n/a	n/a
47	CTCF	chr8:8281200-8281350	MCF-7	breast:	n/a	n/a
48	CTCF	chr8:8280783-8280875	K562	blood:	n/a	n/a
49	CTCF	chr8:8300220-8300370	SAEC	small airway:	n/a	n/a
50	CTCF	chr8:8281280-8281430	NHEK	skin:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:8283032-8283082	SAEC	small airway:	n/a
2	chr8:8283032-8283082	SK-N-SH_RA	brain:	n/a
3	chr8:8283032-8283082	NHDF-neo	bronchial:	n/a
4	chr8:8283032-8283082	NB4	blood:	n/a
5	chr8:8283032-8283082	MCF-7	breast:	n/a
6	chr8:8283032-8283082	ProgFib	skin:	n/a
7	chr8:8283032-8283082	HNPCEpiC	eye:	n/a
8	chr8:8283032-8283082	AG04450	lung:	fetal
9	chr8:8283032-8283082	HCF	heart:	n/a
10	chr8:8283032-8283082	HRCEpiC	kidney:	n/a
11	chr8:8283032-8283082	SK-N-MC	brain:	n/a
12	chr8:8283032-8283082	SK-N-SH	brain:	n/a
13	chr8:8283032-8283082	ECC-1	luminal epithelium:	n/a
14	chr8:8283032-8283082	Jurkat	blood:	n/a
15	chr8:8283032-8283082	MCF10A-Er-Src	breast:	n/a
16	chr8:8283032-8283082	AG09309	skin:	n/a
17	chr8:8283032-8283082	HPAEpiC	pulmonary alveolar:	n/a
18	chr8:8283032-8283082	PrEC	prostate:	n/a
19	chr8:8283032-8283082	HRPEpiC	eye:	n/a
20	chr8:8283032-8283082	GM12878	blood:	n/a
21	chr8:8283032-8283082	BJ	skin:	n/a
22	chr8:8283032-8283082	PANC-1	pancreas:	n/a
23	chr8:8283032-8283082	A549	lung:	n/a
24	chr8:8283032-8283082	HAEpiC	amniotic membrane:	n/a
25	chr8:8283032-8283082	IMR90	lung:	fetal
26	chr8:8283032-8283082	ovcar-3	ovarian:	n/a
27	chr8:8283032-8283082	K562	blood:	n/a
28	chr8:8283032-8283082	GM12892	blood:	n/a
29	chr8:8283032-8283082	T-47D	breast:	n/a
30	chr8:8283032-8283082	GM12891	blood:	n/a
31	chr8:8283032-8283082	GM19239	blood:	n/a
32	chr8:8283032-8283082	H1-hESC	embryonic stem cell:	embryo
33	chr8:8283032-8283082	HIPEpiC	eye:	n/a
34	chr8:8283032-8283082	NT2-D1	testis:	n/a
35	chr8:8283032-8283082	HCT-116	colon:	n/a
36	chr8:8283032-8283082	AoSMC	blood vessel:	n/a
37	chr8:8283032-8283082	HL-60	blood:	n/a
38	chr8:8283032-8283082	HCPEpiC	choroid plexus:	n/a
39	chr8:8283032-8283082	LNCaP	prostate:	n/a
40	chr8:8283032-8283082	HUVEC	blood vessel:	n/a
41	chr8:8283032-8283082	RPTEC	kidney:	n/a
42	chr8:8283032-8283082	Hela-S3	cervix:	n/a
43	chr8:8283032-8283082	NH-A	brain:	n/a
44	chr8:8283032-8283082	HEEpiC	esophagus:	n/a
45	chr8:8283032-8283082	Caco-2	colon:	n/a
46	chr8:8283032-8283082	HCM	heart:	n/a
47	chr8:8283032-8283082	NHBE	bronchial:	n/a
48	chr8:8283032-8283082	CMK	blood:	n/a
49	chr8:8283032-8283082	HMEC	breast:	n/a
50	chr8:8283032-8283082	SKMC	muscle:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:8301355..8304096-chr8:8318371..8320187,2	MCF-7	breast:
2	chr8:8285563..8288242-chr8:8289388..8292203,2	K562	blood:
3	chr8:8242907..8245706-chr8:8295976..8300172,6	MCF-7	breast:
4	chr8:8299483..8301064-chr8:8302628..8304305,2	K562	blood:
5	chr8:8296841..8301166-chr8:8305645..8310086,5	MCF-7	breast:
6	chr8:8243706..8245938-chr8:8270141..8271973,2	MCF-7	breast:
7	chr8:8286859..8289510-chr8:8290140..8291896,2	MCF-7	breast:
8	chr8:8276737..8279265-chr8:8282228..8283969,2	K562	blood:
9	chr8:8278185..8279913-chr8:8280272..8281825,2	MCF-7	breast:
10	chr8:8269803..8273225-chr8:8273897..8276218,3	K562	blood:
11	chr8:8295699..8297664-chr8:8297694..8299367,2	MCF-7	breast:
12	chr8:8281489..8283205-chr8:8283537..8285806,2	MCF-7	breast:
13	chr8:8298645..8300548-chr8:8312022..8313794,2	MCF-7	breast:
14	chr8:8242445..8245313-chr8:8297878..8301672,4	MCF-7	breast:
15	chr8:8237781..8239370-chr8:8268947..8270951,2	MCF-7	breast:
16	chr8:8239788..8242444-chr8:8287010..8288532,2	MCF-7	breast:
17	chr8:8299483..8301064-chr8:8302628..8304305,2	K562	blood:
18	chr8:8269803..8273225-chr8:8273897..8276218,3	K562	blood:
19	chr8:8278185..8279913-chr8:8280272..8281825,2	MCF-7	breast:
20	chr8:8295699..8297664-chr8:8297694..8299367,2	MCF-7	breast:
21	chr8:8276737..8279265-chr8:8282228..8283969,2	K562	blood:
22	chr8:8285563..8288242-chr8:8289388..8292203,2	K562	blood:
23	chr8:8299017..8300539-chr8:8317523..8321166,3	MCF-7	breast:
24	chr8:8297402..8302075-chr8:8309900..8314859,7	MCF-7	breast:
25	chr8:8286859..8289510-chr8:8290140..8291896,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRAGMIN.1-1	chr8:8272200-8272611	ENSG00000253505
2	lnc-PRAGMIN.1-1	chr8:8279934-8280523	ENSG00000253505
3	lnc-PRAGMIN.1-1	chr8:8281998-8282142	ENSG00000253505
4	lnc-PRAGMIN.1-1	chr8:8281998-8282088	ENSG00000253505

No data

Variant related genes	Relation type
ENSG00000253505	TF binding region
ENSG00000253505	CpG island
ENSG00000253505	chromatin interactions
ENSG00000254153	chromatin interactions
ENSG00000182319	chromatin interactions

Extended variants
information (count: 1950 )
Associated
traits (count: 140 )

Variant overlapped rSNPs/rCNVs (count:1950 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2979137	chr8:8269468-8269469	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs557387518	chr8:8269472-8269473	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs577665068	chr8:8269494-8269495	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs182603666	chr8:8269509-8269510	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs146863350	chr8:8269533-8269534	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs371031338	chr8:8269543-8269544	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs59586214	chr8:8269574-8269575	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs188576866	chr8:8269575-8269576	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs193090891	chr8:8269618-8269619	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs528736697	chr8:8269639-8269640	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs115619806	chr8:8269643-8269644	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs565352626	chr8:8269651-8269652	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs538982156	chr8:8269671-8269672	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs185012718	chr8:8269675-8269676	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs2945865	chr8:8269691-8269692	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs567583899	chr8:8269698-8269699	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs139234029	chr8:8269711-8269712	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs548909504	chr8:8269755-8269756	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs570303595	chr8:8269763-8269764	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs565643448	chr8:8269788-8269789	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs2979136	chr8:8269789-8269790	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs564521041	chr8:8269826-8269827	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs557688287	chr8:8269841-8269842	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs189071976	chr8:8269851-8269852	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs193048011	chr8:8269861-8269862	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs568149171	chr8:8269881-8269882	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs536705204	chr8:8269882-8269883	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs183739583	chr8:8269885-8269886	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs573725654	chr8:8269889-8269890	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs543333195	chr8:8269910-8269911	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs553656215	chr8:8269937-8269938	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs556954806	chr8:8269952-8269953	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs35860560	chr8:8269970-8269971	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs573601248	chr8:8270038-8270039	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs188061634	chr8:8270055-8270056	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs565374071	chr8:8270063-8270064	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs552619821	chr8:8270074-8270075	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs531015090	chr8:8270075-8270076	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs141656396	chr8:8270090-8270091	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs561328767	chr8:8270100-8270101	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs6601696	chr8:8270118-8270119	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs181350936	chr8:8270134-8270135	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs565608790	chr8:8270151-8270152	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs528383685	chr8:8270161-8270162	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs551536152	chr8:8270176-8270177	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs571379676	chr8:8270177-8270178	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs183951538	chr8:8270228-8270229	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs189398047	chr8:8270232-8270233	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs567377792	chr8:8270247-8270248	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs138160423	chr8:8270248-8270249	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:140)

Disease	PMID	Source
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
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
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
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
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16774939	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Bladder cancer	21909424	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Developmental disorder	20461109	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:452 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:8265400-8270400	Weak transcription	Rectal Mucosa Donor 29	rectum
2	chr8:8266600-8274000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr8:8269000-8269600	Enhancers	A549	lung
4	chr8:8269000-8269800	Enhancers	Primary neutrophils fromperipheralblood	blood
5	chr8:8269000-8269800	Enhancers	Placenta	Placenta
6	chr8:8269000-8269800	Enhancers	Hela-S3	cervix
7	chr8:8269000-8269800	Enhancers	NHEK	skin
8	chr8:8269000-8270000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr8:8269000-8270000	Enhancers	Fetal Intestine Large	intestine
10	chr8:8269000-8270800	Enhancers	Fetal Intestine Small	intestine
11	chr8:8269000-8271400	Enhancers	Rectal Mucosa Donor 31	rectum
12	chr8:8269200-8269800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr8:8269400-8269800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr8:8269400-8269800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr8:8269400-8269800	Enhancers	Placenta Amnion	Placenta Amnion
16	chr8:8269400-8270800	Enhancers	Duodenum Mucosa	Duodenum
17	chr8:8269600-8273800	Weak transcription	A549	lung
18	chr8:8269800-8272200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr8:8269800-8273800	Weak transcription	Hela-S3	cervix
20	chr8:8269800-8274000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr8:8269800-8274400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr8:8269800-8274600	Weak transcription	NHEK	skin
23	chr8:8270000-8274200	Weak transcription	Fetal Intestine Large	intestine
24	chr8:8270000-8284200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr8:8270400-8271400	Enhancers	Rectal Mucosa Donor 29	rectum
26	chr8:8270800-8274000	Weak transcription	Fetal Intestine Small	intestine
27	chr8:8270800-8274800	Weak transcription	Duodenum Mucosa	Duodenum
28	chr8:8271200-8271400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr8:8271400-8274800	Weak transcription	Rectal Mucosa Donor 31	rectum
30	chr8:8272200-8272600	Enhancers	Brain Cingulate Gyrus	brain
31	chr8:8272200-8272600	Enhancers	Brain Hippocampus Middle	brain
32	chr8:8272200-8273200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr8:8272400-8272600	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr8:8272400-8272600	Enhancers	Brain Inferior Temporal Lobe	brain
35	chr8:8272400-8272800	Enhancers	Cortex derived primary cultured neurospheres	brain
36	chr8:8272400-8275000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr8:8272600-8276200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
38	chr8:8272600-8276400	Weak transcription	Brain Hippocampus Middle	brain
39	chr8:8272800-8274800	Weak transcription	Cortex derived primary cultured neurospheres	brain
40	chr8:8273200-8289400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr8:8273600-8277200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr8:8273600-8281000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr8:8273800-8274000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr8:8273800-8274800	Enhancers	A549	lung
45	chr8:8273800-8275400	Enhancers	Hela-S3	cervix
46	chr8:8274000-8274400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr8:8274000-8276200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr8:8274000-8278200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr8:8274000-8282400	Enhancers	Fetal Intestine Small	intestine
50	chr8:8274200-8274800	Enhancers	Fetal Intestine Large	intestine

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