Variant report

Variant	esv3326059
Chromosome Location	chr8:63950223-63952971
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	ARID3A	chr8:63951168-63951603	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:63951817-63952680	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:63951206-63951633	K562	blood:	n/a	n/a
4	ATF3	chr8:63951345-63951646	K562	blood:	n/a	chr8:63951467-63951476
5	BACH1	chr8:63952024-63952135	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr8:63951504-63951573	K562	blood:	n/a	n/a
7	BACH1	chr8:63951010-63951810	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL3	chr8:63951579-63952167	A549	lung:	n/a	n/a
9	BCLAF1	chr8:63951145-63951650	GM12878	blood:	n/a	chr8:63951371-63951384 chr8:63951146-63951155 chr8:63951148-63951161 chr8:63951488-63951497 chr8:63951483-63951496 chr8:63951337-63951350
10	BHLHE40	chr8:63951150-63952171	GM12878	blood:	n/a	chr8:63951191-63951207 chr8:63951365-63951381 chr8:63951368-63951384 chr8:63951513-63951529 chr8:63951371-63951387 chr8:63951183-63951199
11	BHLHE40	chr8:63950992-63952486	K562	blood:	n/a	chr8:63951191-63951207 chr8:63951365-63951381 chr8:63951368-63951384 chr8:63951513-63951529 chr8:63951371-63951387 chr8:63951183-63951199
12	BHLHE40	chr8:63951150-63952557	HepG2	liver:	n/a	chr8:63951191-63951207 chr8:63951365-63951381 chr8:63951368-63951384 chr8:63951513-63951529 chr8:63951371-63951387 chr8:63951183-63951199
13	BRCA1	chr8:63950960-63951611	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr8:63951862-63952155	H1-hESC	embryonic stem cell:	n/a	n/a
15	BRCA1	chr8:63951964-63952107	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr8:63951151-63952071	HepG2	liver:	n/a	n/a
17	BRCA1	chr8:63951115-63951918	GM12878	blood:	n/a	n/a
18	BRCA1	chr8:63951115-63951555	H1-hESC	embryonic stem cell:	n/a	n/a
19	CBX3	chr8:63951654-63952228	K562	blood:	n/a	n/a
20	CCNT2	chr8:63951054-63952252	K562	blood:	n/a	chr8:63951575-63951584
21	CEBPB	chr8:63951865-63952600	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr8:63952361-63952542	HepG2	liver:	n/a	n/a
23	CEBPB	chr8:63951176-63951783	A549	lung:	n/a	n/a
24	CEBPB	chr8:63952262-63952676	HepG2	liver:	n/a	n/a
25	CEBPB	chr8:63952286-63952631	K562	blood:	n/a	n/a
26	CEBPB	chr8:63951074-63952629	HepG2	liver:	n/a	n/a
27	CEBPB	chr8:63951601-63951843	HepG2	liver:	n/a	n/a
28	CEBPB	chr8:63951018-63951657	Hela-S3	cervix:	n/a	n/a
29	CEBPD	chr8:63951169-63951488	HepG2	liver:	n/a	n/a
30	CHD1	chr8:63951623-63951751	GM12878	blood:	n/a	n/a
31	CHD1	chr8:63951244-63951375	GM12878	blood:	n/a	chr8:63951337-63951347
32	CHD2	chr8:63950954-63952293	Hela-S3	cervix:	n/a	chr8:63951151-63951161 chr8:63951337-63951347
33	CHD2	chr8:63951020-63952197	GM12878	blood:	n/a	chr8:63951151-63951161 chr8:63951337-63951347
34	CHD2	chr8:63950911-63951760	H1-hESC	embryonic stem cell:	n/a	chr8:63951151-63951161 chr8:63951337-63951347
35	CHD2	chr8:63951144-63951996	HepG2	liver:	n/a	chr8:63951151-63951161 chr8:63951337-63951347
36	CHD2	chr8:63951041-63952174	K562	blood:	n/a	chr8:63951151-63951161 chr8:63951337-63951347
37	CHD2	chr8:63952016-63952092	H1-hESC	embryonic stem cell:	n/a	n/a
38	CREB1	chr8:63951800-63952313	ECC-1	luminal epithelium:	n/a	n/a
39	CREB1	chr8:63951087-63952280	A549	lung:	n/a	n/a
40	CREB1	chr8:63951599-63952274	H1-hESC	embryonic stem cell:	n/a	n/a
41	CREB1	chr8:63951122-63952346	H1-hESC	embryonic stem cell:	n/a	n/a
42	CREB1	chr8:63951017-63952294	K562	blood:	n/a	n/a
43	CREB1	chr8:63951020-63952321	HepG2	liver:	n/a	n/a
44	CREB1	chr8:63951316-63951450	A549	lung:	n/a	n/a
45	CREB1	chr8:63951110-63952211	GM12878	blood:	n/a	n/a
46	CTBP2	chr8:63951072-63952201	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr8:63951400-63951550	GM12873	blood:	n/a	n/a
48	CTCF	chr8:63951160-63951310	AG04449	skin:	n/a	n/a
49	CTCF	chr8:63951842-63951896	GM12891	blood:	n/a	n/a
50	CTCF	chr8:63952001-63952202	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:63951642-63951692	HMEC	breast:	n/a
2	chr8:63951642-63951692	HMEC	breast:	n/a
3	chr8:63951797-63951847	ProgFib	skin:	n/a
4	chr8:63951123-63951173	PFSK-1	brain:	n/a
5	chr8:63951879-63951929	HUVEC	blood vessel:	n/a
6	chr8:63952060-63952110	AG09309	skin:	n/a
7	chr8:63951642-63951692	GM12891	blood:	n/a
8	chr8:63951797-63951847	HRPEpiC	eye:	n/a
9	chr8:63951123-63951173	AG09319	gingival:	n/a
10	chr8:63952060-63952110	H1-hESC	embryonic stem cell:	embryo
11	chr8:63952370-63952420	HRCEpiC	kidney:	n/a
12	chr8:63951123-63951173	HEK293	kidney:	embryo
13	chr8:63951076-63951126	HCPEpiC	choroid plexus:	n/a
14	chr8:63951797-63951847	HPAEpiC	pulmonary alveolar:	n/a
15	chr8:63951123-63951173	SK-N-SH	brain:	n/a
16	chr8:63951076-63951126	A549	lung:	n/a
17	chr8:63951797-63951847	NH-A	brain:	n/a
18	chr8:63951669-63951719	PANC-1	pancreas:	n/a
19	chr8:63951797-63951847	HCT-116	colon:	n/a
20	chr8:63951076-63951126	BE2_C	brain:	n/a
21	chr8:63951472-63951522	NH-A	brain:	n/a
22	chr8:63951642-63951692	A549	lung:	n/a
23	chr8:63951123-63951173	ECC-1	luminal epithelium:	n/a
24	chr8:63951669-63951719	SK-N-SH_RA	brain:	n/a
25	chr8:63951797-63951847	HCPEpiC	choroid plexus:	n/a
26	chr8:63951812-63951862	AG04450	lung:	fetal
27	chr8:63951669-63951719	Jurkat	blood:	n/a
28	chr8:63951879-63951929	MCF-7	breast:	n/a
29	chr8:63951812-63951862	PrEC	prostate:	n/a
30	chr8:63951797-63951847	GM12878	blood:	n/a
31	chr8:63951879-63951929	A549	lung:	n/a
32	chr8:63951472-63951522	GM12878	blood:	n/a
33	chr8:63951812-63951862	HAEpiC	amniotic membrane:	n/a
34	chr8:63952370-63952420	SKMC	muscle:	n/a
35	chr8:63951644-63951694	HEK293	kidney:	embryo
36	chr8:63951797-63951847	SK-N-MC	brain:	n/a
37	chr8:63952060-63952110	ECC-1	luminal epithelium:	n/a
38	chr8:63951797-63951847	HUVEC	blood vessel:	n/a
39	chr8:63951644-63951694	BJ	skin:	n/a
40	chr8:63951472-63951522	SK-N-SH_RA	brain:	n/a
41	chr8:63951868-63951918	MCF10A-Er-Src	breast:	n/a
42	chr8:63951472-63951522	LNCaP	prostate:	n/a
43	chr8:63951123-63951173	MCF-7	breast:	n/a
44	chr8:63951472-63951522	HPAEpiC	pulmonary alveolar:	n/a
45	chr8:63951879-63951929	RPTEC	kidney:	n/a
46	chr8:63951642-63951692	MCF10A-Er-Src	breast:	n/a
47	chr8:63951868-63951918	AG04449	skin:	fetal
48	chr8:63951879-63951929	IMR90	lung:	fetal
49	chr8:63951123-63951173	HCPEpiC	choroid plexus:	n/a
50	chr8:63951076-63951126	AoSMC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:63925789..63928059-chr8:63949158..63951177,2	MCF-7	breast:
2	chr8:63950192..63952306-chr8:64079468..64082451,3	K562	blood:
3	chr8:63952036..63954071-chr8:63997414..63999820,2	MCF-7	breast:
4	chr8:63937516..63940331-chr8:63949992..63952545,2	K562	blood:
5	chr8:63951570..63952420-chr9:131419013..131419573,2	NB4	blood:
6	chr8:62675951..62679045-chr8:63950013..63952575,3	K562	blood:
7	chr8:63932840..63934408-chr8:63951913..63953581,2	K562	blood:
8	chr8:63949699..63952423-chr8:63997523..63999992,2	K562	blood:
9	chr8:63940680..63942601-chr8:63949219..63951590,2	MCF-7	breast:
10	chr8:62626734..62628934-chr8:63949908..63951935,2	K562	blood:
11	chr8:62625715..62628343-chr8:63949746..63952148,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TTPA-3	chr8:63951219-63951361	NONHSAT126916
2	lnc-NKAIN3-9	chr8:63951612-63954212	NONHSAT126917

Variant related genes	Relation type
GGH	TF binding region
GGH	CpG island
ENSG00000185728	chromatin interactions
ENSG00000137561	chromatin interactions
ENSG00000270673	chromatin interactions
ENSG00000198363	chromatin interactions
ENSG00000264408	chromatin interactions
ENSG00000251127	chromatin interactions
ENSG00000119333	chromatin interactions
ENSG00000137563	chromatin interactions
GNA13	miRNA target sites

Extended variants
information (count: 104 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:104 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566816275	chr8:63950228-63950229	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
2	rs185850266	chr8:63950290-63950291	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs188653399	chr8:63950358-63950359	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs549499356	chr8:63950399-63950400	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs115588447	chr8:63950405-63950406	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs67742771	chr8:63950420-63950421	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs201776459	chr8:63950476-63950477	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs181077289	chr8:63950484-63950485	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs141696738	chr8:63950538-63950539	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs62510072	chr8:63950581-63950582	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs186128463	chr8:63950620-63950621	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs191693437	chr8:63950703-63950704	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs572054320	chr8:63950753-63950754	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs542237357	chr8:63950755-63950756	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs150505118	chr8:63950792-63950793	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs140338692	chr8:63950838-63950839	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs183965531	chr8:63950863-63950864	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs187276102	chr8:63950891-63950892	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
19	rs532455556	chr8:63950926-63950927	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
20	rs547752026	chr8:63950938-63950939	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs559381767	chr8:63950954-63950955	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
22	rs143312763	chr8:63950956-63950957	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
23	rs78367902	chr8:63951026-63951027	Active TSS Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs567771154	chr8:63951114-63951115	Active TSS Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs190945668	chr8:63951116-63951117	Active TSS Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs549972560	chr8:63951138-63951139	Active TSS Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs571549892	chr8:63951142-63951143	Active TSS Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs147536505	chr8:63951156-63951157	Active TSS Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs546095627	chr8:63951165-63951166	Active TSS Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
30	rs563081883	chr8:63951173-63951174	Active TSS Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs369584231	chr8:63951207-63951208	Active TSS Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs531939120	chr8:63951220-63951221	Active TSS Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
33	rs11545077	chr8:63951237-63951238	Active TSS Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region lncRNA	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs201836906	chr8:63951283-63951284	Active TSS Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
35	rs1800909	chr8:63951312-63951313	Active TSS Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region lncRNA	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs376225287	chr8:63951322-63951323	Active TSS Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
37	rs554238614	chr8:63951358-63951359	Active TSS Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
38	rs576207255	chr8:63951365-63951366	Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
39	rs201285211	chr8:63951370-63951371	Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs558675099	chr8:63951383-63951384	Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
41	rs182198219	chr8:63951394-63951395	Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
42	rs2736678	chr8:63951401-63951402	Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
43	rs547764450	chr8:63951419-63951420	Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs559618319	chr8:63951421-63951422	Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
45	rs140038759	chr8:63951423-63951424	Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
46	rs546748531	chr8:63951424-63951425	Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
47	rs561087716	chr8:63951430-63951431	Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
48	rs11545076	chr8:63951451-63951452	Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs4590435	chr8:63951483-63951484	Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
50	rs549910927	chr8:63951552-63951553	Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:97)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	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
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Salivary gland tumor	18059337	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Melanoma	22183965	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Sezary syndrome	18413736	CNVD
Colorectal cancer	21645411	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:345 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:63922800-63950800	Weak transcription	Fetal Muscle Leg	muscle
2	chr8:63923800-63950600	Weak transcription	Fetal Kidney	kidney
3	chr8:63938200-63950600	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr8:63945800-63950600	Weak transcription	Fetal Intestine Small	intestine
5	chr8:63945800-63950800	Weak transcription	Primary neutrophils fromperipheralblood	blood
6	chr8:63946000-63950600	Weak transcription	Monocytes-CD14+_RO01746	blood
7	chr8:63946000-63950800	Weak transcription	Primary monocytes fromperipheralblood	blood
8	chr8:63948600-63950600	Enhancers	Cortex derived primary cultured neurospheres	brain
9	chr8:63949000-63950400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr8:63949000-63950400	Flanking Active TSS	Brain Germinal Matrix	brain
11	chr8:63949000-63950400	Flanking Active TSS	HepG2	liver
12	chr8:63949200-63950400	Enhancers	Fetal Brain Male	brain
13	chr8:63949200-63950600	Enhancers	NHEK	skin
14	chr8:63949400-63950400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr8:63949400-63950600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr8:63949400-63951000	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr8:63949600-63950400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr8:63949600-63950400	Flanking Active TSS	GM12878-XiMat	blood
19	chr8:63949600-63950800	Weak transcription	Brain Angular Gyrus	brain
20	chr8:63949800-63950400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr8:63949800-63950400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr8:63949800-63950400	Flanking Active TSS	Fetal Brain Female	brain
23	chr8:63949800-63950800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr8:63949800-63952600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr8:63950000-63950400	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
26	chr8:63950000-63950400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr8:63950000-63950400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr8:63950000-63950400	Enhancers	Liver	Liver
29	chr8:63950000-63950400	Enhancers	Fetal Heart	heart
30	chr8:63950000-63950400	Weak transcription	Fetal Intestine Large	intestine
31	chr8:63950000-63950600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr8:63950000-63950600	Enhancers	Fetal Lung	lung
33	chr8:63950000-63950600	Flanking Active TSS	A549	lung
34	chr8:63950000-63950800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr8:63950000-63950800	Flanking Active TSS	Hela-S3	cervix
36	chr8:63950000-63951000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr8:63950000-63951000	Weak transcription	Esophagus	oesophagus
38	chr8:63950000-63952000	Active TSS	Rectal Mucosa Donor 29	rectum
39	chr8:63950000-63952200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr8:63950000-63952400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
41	chr8:63950000-63952600	Active TSS	NHLF	lung
42	chr8:63950200-63950400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr8:63950200-63950400	Active TSS	Muscle Satellite Cultured Cells	--
44	chr8:63950200-63950400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr8:63950200-63950600	Weak transcription	H9 Cell Line	embryonic stem cell
46	chr8:63950200-63950600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr8:63950200-63950600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr8:63950200-63950600	Weak transcription	Rectal Mucosa Donor 31	rectum
49	chr8:63950200-63950600	Active TSS	NH-A	brain
50	chr8:63950200-63950800	Flanking Active TSS	HUVEC	blood vessel

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