Variant report

Variant	nsv891230
Chromosome Location	chr8:102569309-102604306
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:397)
CpG islands
(count:366)
Chromatin interactive
region (count:73)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:397 , 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	chr8:102587713-102587898	K562	blood:	n/a	n/a
2	ATF1	chr8:102599575-102599670	K562	blood:	n/a	n/a
3	CCNT2	chr8:102599475-102599707	K562	blood:	n/a	n/a
4	CEBPB	chr8:102593859-102594303	MCF-7	breast:	n/a	chr8:102594127-102594138
5	CEBPB	chr8:102598814-102599115	A549	lung:	n/a	chr8:102598944-102598955
6	CEBPB	chr8:102593990-102594297	K562	blood:	n/a	chr8:102594127-102594138
7	CEBPB	chr8:102577777-102577988	K562	blood:	n/a	n/a
8	CEBPB	chr8:102598791-102599110	HepG2	liver:	n/a	chr8:102598944-102598955
9	CEBPB	chr8:102593973-102594293	HepG2	liver:	n/a	chr8:102594127-102594138
10	CEBPB	chr8:102585590-102585910	HepG2	liver:	n/a	chr8:102585633-102585646
11	CEBPB	chr8:102593969-102594245	IMR90	lung:	n/a	chr8:102594127-102594138
12	CEBPB	chr8:102575946-102576501	A549	lung:	n/a	n/a
13	CEBPB	chr8:102598846-102599085	K562	blood:	n/a	chr8:102598944-102598955
14	CEBPB	chr8:102577651-102578150	MCF-7	breast:	n/a	chr8:102578052-102578069
15	CEBPB	chr8:102593953-102594239	A549	lung:	n/a	chr8:102594127-102594138
16	CEBPB	chr8:102577789-102578018	A549	lung:	n/a	n/a
17	CEBPB	chr8:102598727-102599108	MCF-7	breast:	n/a	chr8:102598944-102598955
18	CEBPB	chr8:102598887-102599054	Hela-S3	cervix:	n/a	chr8:102598944-102598955
19	CTCF	chr8:102577810-102578042	K562	blood:	n/a	n/a
20	CTCF	chr8:102586780-102586930	SAEC	small airway:	n/a	n/a
21	CTCF	chr8:102586460-102586610	HRPEpiC	eye:	n/a	chr8:102586533-102586542
22	CTCF	chr8:102569614-102569672	GM20000	blood:	n/a	n/a
23	CTCF	chr8:102586810-102586923	Medullo	brain:	n/a	n/a
24	CTCF	chr8:102586820-102586970	SAEC	small airway:	n/a	n/a
25	CTCF	chr8:102577860-102578010	HRE	kidney:	n/a	n/a
26	CTCF	chr8:102594740-102594890	RPTEC	kidney:	n/a	n/a
27	CTCF	chr8:102590460-102590610	WERI-Rb-1	eye:	n/a	n/a
28	CTCF	chr8:102586480-102586630	Hela-S3	cervix:	n/a	chr8:102586533-102586542
29	CTCF	chr8:102586810-102586901	Pancreas_OC	pancreas:	n/a	n/a
30	CTCF	chr8:102594780-102594930	HBMEC	blood vessel:	n/a	n/a
31	CTCF	chr8:102586831-102586908	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr8:102594800-102594950	MCF-7	breast:	n/a	n/a
33	CTCF	chr8:102577837-102577930	Hela-S3	cervix:	n/a	n/a
34	CTCF	chr8:102577819-102577942	MCF-7	breast:	n/a	n/a
35	CTCF	chr8:102577820-102577944	K562	blood:	n/a	n/a
36	CTCF	chr8:102598040-102598190	BE2_C	brain:	n/a	n/a
37	CTCF	chr8:102577812-102577966	MCF-7	breast:	n/a	n/a
38	CTCF	chr8:102586835-102586843	GM12892	blood:	n/a	n/a
39	CTCF	chr8:102586480-102586630	HPAF	blood vessel:	n/a	chr8:102586533-102586542
40	CTCF	chr8:102600680-102600830	GM12869	blood:	n/a	n/a
41	CTCF	chr8:102594780-102594930	HCT-116	colon:	n/a	n/a
42	CTCF	chr8:102577800-102577950	BE2_C	brain:	n/a	n/a
43	CTCF	chr8:102594800-102594950	HEK293	kidney:	n/a	n/a
44	CTCF	chr8:102586813-102586936	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr8:102577819-102577948	GM12878	blood:	n/a	n/a
46	CTCF	chr8:102586560-102586710	HRE	kidney:	n/a	n/a
47	CTCF	chr8:102594760-102594910	Caco-2	colon:	n/a	n/a
48	CTCF	chr8:102586480-102586630	HCPEpiC	choroid plexus:	n/a	chr8:102586533-102586542
49	CTCF	chr8:102594860-102595010	MCF-7	breast:	n/a	n/a
50	CTCF	chr8:102586460-102586610	HCM	heart:	n/a	chr8:102586533-102586542

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:102570487-102570537	HCF	heart:	n/a
2	chr8:102570909-102570959	A549	lung:	n/a
3	chr8:102570888-102570938	ECC-1	luminal epithelium:	n/a
4	chr8:102570487-102570537	HIPEpiC	eye:	n/a
5	chr8:102570909-102570959	HCT-116	colon:	n/a
6	chr8:102570768-102570818	HCPEpiC	choroid plexus:	n/a
7	chr8:102570503-102570553	HPAEpiC	pulmonary alveolar:	n/a
8	chr8:102570503-102570553	HCPEpiC	choroid plexus:	n/a
9	chr8:102570888-102570938	AG09309	skin:	n/a
10	chr8:102570487-102570537	GM12892	blood:	n/a
11	chr8:102570888-102570938	GM19239	blood:	n/a
12	chr8:102570768-102570818	BJ	skin:	n/a
13	chr8:102570454-102570504	AG10803	skin:	n/a
14	chr8:102570768-102570818	HAEpiC	amniotic membrane:	n/a
15	chr8:102570888-102570938	PrEC	prostate:	n/a
16	chr8:102570454-102570504	MCF-7	breast:	n/a
17	chr8:102570503-102570553	SK-N-MC	brain:	n/a
18	chr8:102570768-102570818	HRE	kidney:	n/a
19	chr8:102570454-102570504	SK-N-SH	brain:	n/a
20	chr8:102570503-102570553	H1-hESC	embryonic stem cell:	embryo
21	chr8:102570454-102570504	AG09309	skin:	n/a
22	chr8:102570768-102570818	GM12878	blood:	n/a
23	chr8:102570503-102570553	HRCEpiC	kidney:	n/a
24	chr8:102570503-102570553	AG09319	gingival:	n/a
25	chr8:102570454-102570504	HNPCEpiC	eye:	n/a
26	chr8:102570503-102570553	MCF10A-Er-Src	breast:	n/a
27	chr8:102570909-102570959	ECC-1	luminal epithelium:	n/a
28	chr8:102570454-102570504	GM12892	blood:	n/a
29	chr8:102570503-102570553	CMK	blood:	n/a
30	chr8:102570454-102570504	HAEpiC	amniotic membrane:	n/a
31	chr8:102570503-102570553	HepG2	liver:	n/a
32	chr8:102570503-102570553	BE2_C	brain:	n/a
33	chr8:102570768-102570818	AG04450	lung:	fetal
34	chr8:102570487-102570537	K562	blood:	n/a
35	chr8:102570487-102570537	NT2-D1	testis:	n/a
36	chr8:102570487-102570537	AG09319	gingival:	n/a
37	chr8:102570909-102570959	GM19239	blood:	n/a
38	chr8:102570888-102570938	SK-N-SH	brain:	n/a
39	chr8:102570454-102570504	HCPEpiC	choroid plexus:	n/a
40	chr8:102570487-102570537	GM06990	blood:	n/a
41	chr8:102570503-102570553	SKMC	muscle:	n/a
42	chr8:102570888-102570938	PANC-1	pancreas:	n/a
43	chr8:102570503-102570553	GM06990	blood:	n/a
44	chr8:102570768-102570818	PANC-1	pancreas:	n/a
45	chr8:102570909-102570959	HCPEpiC	choroid plexus:	n/a
46	chr8:102570768-102570818	AoSMC	blood vessel:	n/a
47	chr8:102570487-102570537	NH-A	brain:	n/a
48	chr8:102570768-102570818	GM12892	blood:	n/a
49	chr8:102570503-102570553	T-47D	breast:	n/a
50	chr8:102570768-102570818	AG04449	skin:	fetal

(count:73 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:102574719..102576400-chr8:102576482..102578890,2	MCF-7	breast:
2	chr8:102504953..102507256-chr8:102590036..102592865,2	MCF-7	breast:
3	chr8:102593460..102597757-chr8:102598202..102602881,7	MCF-7	breast:
4	chr8:102575422..102576923-chr8:102579897..102582847,2	MCF-7	breast:
5	chr8:102525583..102527812-chr8:102595474..102597221,3	MCF-7	breast:
6	chr8:102577206..102577740-chr8:102644735..102645456,2	MCF-7	breast:
7	chr8:102375493..102378356-chr8:102595970..102598513,2	MCF-7	breast:
8	chr8:102503060..102507030-chr8:102601716..102605768,5	MCF-7	breast:
9	chr8:102598688..102600794-chr8:102642302..102645052,2	MCF-7	breast:
10	chr8:102599405..102601179-chr8:102618530..102620423,2	MCF-7	breast:
11	chr8:102567759..102570730-chr8:102585094..102586847,2	MCF-7	breast:
12	chr8:102576519..102579331-chr8:102581793..102585306,3	MCF-7	breast:
13	chr8:102524517..102526581-chr8:102582052..102584606,2	MCF-7	breast:
14	chr8:102585772..102587387-chr8:102587401..102588904,2	MCF-7	breast:
15	chr8:102590095..102591654-chr8:102593333..102595255,2	MCF-7	breast:
16	chr8:102578394..102580436-chr8:102646392..102647892,2	MCF-7	breast:
17	chr8:102535633..102538629-chr8:102574811..102576314,2	MCF-7	breast:
18	chr8:102599624..102601949-chr8:102615535..102617652,3	MCF-7	breast:
19	chr8:102584672..102587092-chr8:102594880..102596520,2	MCF-7	breast:
20	chr8:102579728..102581419-chr8:102594217..102596451,2	MCF-7	breast:
21	chr8:102588119..102597900-chr8:102614552..102624670,18	MCF-7	breast:
22	chr8:102511469..102513508-chr8:102595474..102597315,2	MCF-7	breast:
23	chr8:102586663..102588864-chr8:102589452..102591832,2	MCF-7	breast:
24	chr8:102594059..102599317-chr8:102614223..102621570,11	MCF-7	breast:
25	chr8:102504396..102506932-chr8:102582821..102584601,2	MCF-7	breast:
26	chr8:102591202..102591897-chr8:102618452..102619177,2	MCF-7	breast:
27	chr8:102504593..102507266-chr8:102598553..102601179,3	MCF-7	breast:
28	chr8:102584397..102586462-chr8:102595922..102598854,2	MCF-7	breast:
29	chr8:102577611..102578416-chr8:102644647..102645261,2	MCF-7	breast:
30	chr8:102593559..102596370-chr8:102642553..102644659,2	MCF-7	breast:
31	chr8:102595468..102600144-chr8:102610576..102613880,7	MCF-7	breast:
32	chr8:102576342..102577944-chr8:102615348..102618284,2	MCF-7	breast:
33	chr8:102582322..102584576-chr8:102588630..102591641,3	MCF-7	breast:
34	chr8:102569718..102571436-chr8:102646624..102648953,2	MCF-7	breast:
35	chr8:102585772..102587387-chr8:102587401..102588904,2	MCF-7	breast:
36	chr8:102568954..102571543-chr8:102577396..102579070,2	MCF-7	breast:
37	chr8:102574170..102577190-chr8:102593117..102596726,4	MCF-7	breast:
38	chr8:102551350..102553008-chr8:102581604..102583551,2	MCF-7	breast:
39	chr8:102570719..102573453-chr8:102576572..102578084,2	MCF-7	breast:
40	chr8:102568954..102571543-chr8:102577396..102579070,2	MCF-7	breast:
41	chr8:102576519..102579331-chr8:102581793..102585306,3	MCF-7	breast:
42	chr14:81656858..81657712-chr8:102572368..102573072,2	MCF-7	breast:
43	chr8:102584672..102587092-chr8:102594880..102596520,2	MCF-7	breast:
44	chr8:102595035..102599988-chr8:102610070..102614354,7	MCF-7	breast:
45	chr8:102579728..102581419-chr8:102594217..102596451,2	MCF-7	breast:
46	chr8:102592230..102595916-chr8:103666218..103670162,3	MCF-7	breast:
47	chr8:102589864..102591664-chr8:102607587..102610544,2	MCF-7	breast:
48	chr8:102584389..102586925-chr8:102611656..102613755,2	MCF-7	breast:
49	chr8:102575422..102576923-chr8:102579897..102582847,2	MCF-7	breast:
50	chr8:102515552..102517978-chr8:102590842..102593312,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NCALD-2	chr8:102574236-102574716	NONHSAT128064

No data

Variant related genes	Relation type
ENSG00000253153	TF binding region
ENSG00000253153	CpG island
ENSG00000254024	chromatin interactions
ENSG00000253153	chromatin interactions
ENSG00000083307	chromatin interactions
ENSG00000155090	chromatin interactions

Extended variants
information (count: 1295 )
Associated
traits (count: 113 )

Variant overlapped rSNPs/rCNVs (count:1295 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs510426	chr8:102569309-102569310	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs533343168	chr8:102569331-102569332	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs191562523	chr8:102569340-102569341	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs371583369	chr8:102569344-102569345	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs569738311	chr8:102569397-102569398	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs34785282	chr8:102569452-102569453	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs531063828	chr8:102569453-102569454	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs562198804	chr8:102569478-102569479	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs2096554	chr8:102569504-102569505	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs543616891	chr8:102569521-102569522	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs563591818	chr8:102569522-102569523	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs547448807	chr8:102569577-102569578	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs565673931	chr8:102569597-102569598	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs140900051	chr8:102569603-102569604	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs201274407	chr8:102569626-102569627	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs111954140	chr8:102569635-102569636	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs375324966	chr8:102569640-102569641	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs537330351	chr8:102569695-102569696	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs555744898	chr8:102569709-102569710	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs531207408	chr8:102569732-102569733	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs573757834	chr8:102569778-102569779	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs6994300	chr8:102569817-102569818	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs73279169	chr8:102569850-102569851	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs188776143	chr8:102569963-102569964	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs73279172	chr8:102569980-102569981	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs368213866	chr8:102570033-102570034	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs563303166	chr8:102570096-102570097	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs77910219	chr8:102570110-102570111	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs549265183	chr8:102570172-102570173	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs551006665	chr8:102570229-102570230	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs532409615	chr8:102570231-102570232	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs528671013	chr8:102570241-102570242	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs369866588	chr8:102570260-102570261	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs142730078	chr8:102570337-102570338	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs59905624	chr8:102570339-102570340	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs571813376	chr8:102570358-102570359	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs539495597	chr8:102570382-102570383	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs551538658	chr8:102570394-102570395	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs79138916	chr8:102570399-102570400	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs6981104	chr8:102570479-102570480	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs555619746	chr8:102570481-102570482	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs146958485	chr8:102570488-102570489	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs185667428	chr8:102570523-102570524	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs138060738	chr8:102570570-102570571	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs189324398	chr8:102570599-102570600	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs371351441	chr8:102570619-102570620	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs559133364	chr8:102570628-102570629	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs545089001	chr8:102570632-102570633	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs200781848	chr8:102570633-102570634	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs575214822	chr8:102570657-102570658	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:113)

Disease	PMID	Source
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
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	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
abnormal development	18461090	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
Cancer	16751803	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
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	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
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16461302	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
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	17260012	CNVD
Sezary syndrome	18413736	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Cancer	20164920	CNVD
Urothelial cell carcinoma	18451213	CNVD
Colorectal cancer	21645411	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	16912164	CNVD
Breast cancer	20409316	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Breast cancer	21611746	CNVD
Prostate cancer	22341455	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:599 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:102551400-102577400	Weak transcription	Fetal Stomach	stomach
2	chr8:102552200-102620600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr8:102553000-102573600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr8:102554200-102570600	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr8:102554400-102570400	Weak transcription	Duodenum Mucosa	Duodenum
6	chr8:102557200-102570600	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr8:102557400-102577400	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr8:102557600-102570600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
9	chr8:102560800-102569400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr8:102564800-102570400	Weak transcription	Gastric	stomach
11	chr8:102565600-102582800	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr8:102566000-102582800	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr8:102566200-102572600	Weak transcription	Fetal Intestine Large	intestine
14	chr8:102566600-102569600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr8:102566600-102570200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr8:102566600-102570200	Weak transcription	Fetal Intestine Small	intestine
17	chr8:102566600-102570400	Weak transcription	Placenta	Placenta
18	chr8:102566600-102570400	Weak transcription	NHEK	skin
19	chr8:102566600-102585600	Weak transcription	Pancreas	Pancrea
20	chr8:102566800-102570400	Weak transcription	H1 Cell Line	embryonic stem cell
21	chr8:102567400-102575600	Weak transcription	HMEC	breast
22	chr8:102567800-102571800	Weak transcription	Placenta Amnion	Placenta Amnion
23	chr8:102568200-102569600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr8:102568200-102570000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
25	chr8:102568600-102570200	Weak transcription	Esophagus	oesophagus
26	chr8:102569000-102570400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr8:102569200-102570400	Weak transcription	HUES48 Cell Line	embryonic stem cell
28	chr8:102569200-102570600	Weak transcription	HUES64 Cell Line	embryonic stem cell
29	chr8:102569200-102582800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
30	chr8:102569400-102569800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr8:102569600-102572600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr8:102569600-102574800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr8:102569800-102570600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr8:102570000-102573000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
35	chr8:102570200-102571200	Strong transcription	Esophagus	oesophagus
36	chr8:102570200-102572600	Strong transcription	Fetal Intestine Small	intestine
37	chr8:102570200-102573000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr8:102570400-102571000	Strong transcription	Gastric	stomach
39	chr8:102570400-102571200	Strong transcription	Duodenum Mucosa	Duodenum
40	chr8:102570400-102571200	Strong transcription	NHEK	skin
41	chr8:102570400-102571400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr8:102570400-102572200	Strong transcription	H1 Cell Line	embryonic stem cell
43	chr8:102570400-102572400	Strong transcription	Placenta	Placenta
44	chr8:102570400-102573200	Strong transcription	HUES48 Cell Line	embryonic stem cell
45	chr8:102570600-102571000	Strong transcription	HUES6 Cell Line	embryonic stem cell
46	chr8:102570600-102571000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr8:102570600-102571000	Strong transcription	Rectal Mucosa Donor 31	rectum
48	chr8:102570600-102572200	Strong transcription	HUES64 Cell Line	embryonic stem cell
49	chr8:102570600-102573000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
50	chr8:102571000-102572000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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