Variant report

Variant	nsv1023866
Chromosome Location	chr8:96273255-96306378
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:885)
CpG islands
(count:1039)
Chromatin interactive
region (count:50)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:885 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:96280441-96280462	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:96281168-96282588	HepG2	liver:	n/a	chr8:96282168-96282184
3	ARID3A	chr8:96281485-96282681	K562	blood:	n/a	chr8:96282168-96282184
4	ATF2	chr8:96281611-96282284	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr8:96281365-96282264	GM12878	blood:	n/a	n/a
6	ATF2	chr8:96281357-96282339	GM12878	blood:	n/a	n/a
7	ATF2	chr8:96281369-96282292	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr8:96281297-96282354	K562	blood:	n/a	chr8:96281543-96281551
9	ATF3	chr8:96281209-96282457	A549	lung:	n/a	chr8:96281543-96281551
10	ATF3	chr8:96281055-96282486	A549	lung:	n/a	chr8:96281543-96281551
11	BACH1	chr8:96281405-96282038	K562	blood:	n/a	n/a
12	BACH1	chr8:96281401-96282442	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr8:96282858-96283039	K562	blood:	n/a	n/a
14	BATF	chr8:96281465-96282110	GM12878	blood:	n/a	n/a
15	BATF	chr8:96281564-96282116	GM12878	blood:	n/a	n/a
16	BCL11A	chr8:96281588-96282111	GM12878	blood:	n/a	n/a
17	BCL3	chr8:96281255-96282440	A549	lung:	n/a	n/a
18	BCL3	chr8:96281272-96282318	A549	lung:	n/a	n/a
19	BCLAF1	chr8:96281032-96282306	GM12878	blood:	n/a	chr8:96281109-96281118 chr8:96281191-96281200
20	BCLAF1	chr8:96281041-96282287	GM12878	blood:	n/a	chr8:96281109-96281118 chr8:96281191-96281200
21	BDP1	chr8:96281773-96282617	K562	blood:	n/a	n/a
22	BDP1	chr8:96281681-96282236	Hela-S3	cervix:	n/a	n/a
23	BHLHE40	chr8:96280800-96282656	GM12878	blood:	n/a	n/a
24	BHLHE40	chr8:96280360-96282828	K562	blood:	n/a	n/a
25	BHLHE40	chr8:96281817-96282298	A549	lung:	n/a	n/a
26	BHLHE40	chr8:96280372-96282584	HepG2	liver:	n/a	n/a
27	BRCA1	chr8:96281274-96282736	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr8:96281386-96282036	GM12878	blood:	n/a	n/a
29	BRCA1	chr8:96281230-96282244	HepG2	liver:	n/a	n/a
30	BRF1	chr8:96281816-96282187	Hela-S3	cervix:	n/a	n/a
31	BRF1	chr8:96281799-96282183	K562	blood:	n/a	n/a
32	CBX3	chr8:96281550-96282342	K562	blood:	n/a	n/a
33	CBX3	chr8:96293355-96293570	HCT-116	colon:	n/a	n/a
34	CBX3	chr8:96281004-96282208	K562	blood:	n/a	n/a
35	CCNT2	chr8:96280801-96282061	K562	blood:	n/a	n/a
36	CEBPB	chr8:96290207-96290533	K562	blood:	n/a	n/a
37	CEBPB	chr8:96281551-96282587	A549	lung:	n/a	chr8:96282246-96282257 chr8:96282248-96282259
38	CEBPB	chr8:96281566-96282583	IMR90	lung:	n/a	chr8:96282246-96282257 chr8:96282248-96282259
39	CEBPB	chr8:96290192-96290564	K562	blood:	n/a	n/a
40	CEBPB	chr8:96281035-96282612	MCF-7	breast:	n/a	chr8:96282246-96282257 chr8:96282248-96282259
41	CEBPB	chr8:96290219-96290503	K562	blood:	n/a	n/a
42	CEBPB	chr8:96281478-96282446	K562	blood:	n/a	chr8:96282246-96282257 chr8:96282248-96282259
43	CEBPB	chr8:96280417-96282718	Hela-S3	cervix:	n/a	chr8:96282246-96282257 chr8:96282248-96282259
44	CEBPB	chr8:96281806-96282480	ECC-1	luminal epithelium:	n/a	chr8:96282246-96282257 chr8:96282248-96282259
45	CEBPB	chr8:96281873-96282093	HepG2	liver:	n/a	n/a
46	CEBPB	chr8:96281905-96282407	K562	blood:	n/a	chr8:96282246-96282257 chr8:96282248-96282259
47	CEBPB	chr8:96281688-96282432	A549	lung:	n/a	chr8:96282246-96282257 chr8:96282248-96282259
48	CEBPB	chr8:96280405-96280793	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr8:96281531-96282453	H1-hESC	embryonic stem cell:	n/a	chr8:96282246-96282257 chr8:96282248-96282259
50	CEBPB	chr8:96280425-96280775	K562	blood:	n/a	n/a

(count:1039 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:96282015-96282065	HCF	heart:	n/a
2	chr8:96281600-96281650	BE2_C	brain:	n/a
3	chr8:96282015-96282065	HCF	heart:	n/a
4	chr8:96281600-96281650	BE2_C	brain:	n/a
5	chr8:96278372-96278422	SKMC	muscle:	n/a
6	chr8:96281113-96281163	HIPEpiC	eye:	n/a
7	chr8:96283750-96283800	BJ	skin:	n/a
8	chr8:96281478-96281528	PFSK-1	brain:	n/a
9	chr8:96281885-96281935	MCF-7	breast:	n/a
10	chr8:96281700-96281750	HIPEpiC	eye:	n/a
11	chr8:96281769-96281819	HIPEpiC	eye:	n/a
12	chr8:96281113-96281163	NT2-D1	testis:	n/a
13	chr8:96281491-96281541	GM12891	blood:	n/a
14	chr8:96281195-96281245	MCF10A-Er-Src	breast:	n/a
15	chr8:96281478-96281528	T-47D	breast:	n/a
16	chr8:96283750-96283800	RPTEC	kidney:	n/a
17	chr8:96281600-96281650	HNPCEpiC	eye:	n/a
18	chr8:96281769-96281819	GM06990	blood:	n/a
19	chr8:96281478-96281528	HepG2	liver:	n/a
20	chr8:96282015-96282065	Hela-S3	cervix:	n/a
21	chr8:96281195-96281245	HCPEpiC	choroid plexus:	n/a
22	chr8:96281700-96281750	HCPEpiC	choroid plexus:	n/a
23	chr8:96281600-96281650	GM06990	blood:	n/a
24	chr8:96281619-96281669	GM12892	blood:	n/a
25	chr8:96278372-96278422	Hepatocyte	liver:	n/a
26	chr8:96281600-96281650	HRCEpiC	kidney:	n/a
27	chr8:96281491-96281541	SK-N-SH_RA	brain:	n/a
28	chr8:96281960-96282010	AoSMC	blood vessel:	n/a
29	chr8:96281619-96281669	NT2-D1	testis:	n/a
30	chr8:96281960-96282010	HCT-116	colon:	n/a
31	chr8:96281491-96281541	HCT-116	colon:	n/a
32	chr8:96281600-96281650	T-47D	breast:	n/a
33	chr8:96281885-96281935	AG09309	skin:	n/a
34	chr8:96279250-96279300	NHDF-neo	bronchial:	n/a
35	chr8:96281491-96281541	GM19239	blood:	n/a
36	chr8:96281619-96281669	GM12878	blood:	n/a
37	chr8:96281399-96281449	LNCaP	prostate:	n/a
38	chr8:96279250-96279300	IMR90	lung:	fetal
39	chr8:96280555-96280605	HIPEpiC	eye:	n/a
40	chr8:96279250-96279300	H1-hESC	embryonic stem cell:	embryo
41	chr8:96281491-96281541	HNPCEpiC	eye:	n/a
42	chr8:96283750-96283800	HRE	kidney:	n/a
43	chr8:96280555-96280605	GM12892	blood:	n/a
44	chr8:96278372-96278422	A549	lung:	n/a
45	chr8:96281504-96281554	HUVEC	blood vessel:	n/a
46	chr8:96281478-96281528	AG09309	skin:	n/a
47	chr8:96281960-96282010	NHDF-neo	bronchial:	n/a
48	chr8:96281600-96281650	HUVEC	blood vessel:	n/a
49	chr8:96282015-96282065	HUVEC	blood vessel:	n/a
50	chr8:96281399-96281449	SAEC	small airway:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr8:96280503..96282050-chr8:96293644..96295501,2	K562	blood:
2	chr8:96266342..96268440-chr8:96282035..96284401,2	K562	blood:
3	chr8:96143208..96147491-chr8:96279441..96282856,8	MCF-7	breast:
4	chr17:54909734..54911738-chr8:96280729..96282427,2	MCF-7	breast:
5	chr8:96280353..96283480-chr8:96283563..96287896,7	K562	blood:
6	chr8:96072969..96074984-chr8:96296064..96297996,2	K562	blood:
7	chr8:96282451..96284903-chr8:96296240..96298528,2	K562	blood:
8	chr8:96280318..96283415-chr8:96287906..96290439,4	K562	blood:
9	chr2:97521965..97524958-chr8:96280956..96282974,2	MCF-7	breast:
10	chr8:96303570..96306835-chr8:96307527..96312633,4	K562	blood:
11	chr8:96291447..96293219-chr8:96295566..96298347,2	K562	blood:
12	chr8:96271978..96274186-chr8:96280108..96281656,2	MCF-7	breast:
13	chr8:96267529..96269819-chr8:96274003..96276020,2	MCF-7	breast:
14	chr14:70232370..70233879-chr8:96280749..96282540,2	MCF-7	breast:
15	chr20:3776660..3777368-chr8:96281076..96281913,2	HCT-116	colon:
16	chr8:96260878..96262975-chr8:96277953..96279731,2	K562	blood:
17	chr8:96285143..96287149-chr8:96306307..96308487,2	K562	blood:
18	chr8:96262492..96264147-chr8:96281511..96283438,2	MCF-7	breast:
19	chr8:96044471..96047276-chr8:96280162..96282608,2	MCF-7	breast:
20	chr8:96291447..96293219-chr8:96295566..96298347,2	K562	blood:
21	chr16:2033986..2034667-chr8:96282041..96282606,2	Hela-S3	cervix:
22	chr8:96264938..96266728-chr8:96285414..96287456,2	K562	blood:
23	chr8:96306052..96307788-chr8:96313764..96316362,2	K562	blood:
24	chr8:95835507..95837268-chr8:96280531..96283343,2	MCF-7	breast:
25	chr3:126816678..126819092-chr8:96304711..96306843,2	MCF-7	breast:
26	chr8:95651016..95653604-chr8:96280429..96282986,2	MCF-7	breast:
27	chr12:92538830..92539812-chr8:96281362..96282131,2	Hela-S3	cervix:
28	chr8:96267958..96270319-chr8:96278452..96280953,2	K562	blood:
29	chr8:96275452..96279040-chr8:96279400..96281500,3	MCF-7	breast:
30	chr8:96142341..96149648-chr8:96278644..96282772,12	MCF-7	breast:
31	chr8:96082478..96088281-chr8:96279501..96283230,8	MCF-7	breast:
32	chr8:95907501..95911346-chr8:96279945..96283030,5	MCF-7	breast:
33	chr8:96115025..96117970-chr8:96278759..96280968,3	MCF-7	breast:
34	chr8:96111950..96115004-chr8:96279819..96283605,3	MCF-7	breast:
35	chr2:61244154..61244948-chr8:96281339..96281903,2	Hela-S3	cervix:
36	chr8:96285088..96287347-chr8:96288286..96290521,2	K562	blood:
37	chr8:96098333..96100158-chr8:96278509..96280957,2	MCF-7	breast:
38	chr8:96285088..96287347-chr8:96288286..96290521,2	K562	blood:
39	chr8:96140207..96143129-chr8:96281545..96283235,2	MCF-7	breast:
40	chr8:96282451..96284903-chr8:96296240..96298528,2	K562	blood:
41	chr8:96280901..96282887-chr8:96293101..96295575,3	MCF-7	breast:
42	chr8:96144909..96147734-chr8:96280323..96283069,4	K562	blood:
43	chr8:95907099..95910081-chr8:96279389..96285203,6	K562	blood:
44	chr8:96285143..96287149-chr8:96306307..96308487,2	K562	blood:
45	chr8:95906455..95910081-chr8:96279389..96281894,5	K562	blood:
46	chr8:96145606..96147268-chr8:96277073..96279637,2	K562	blood:
47	chr8:96279721..96282098-chr8:97246962..97249259,2	MCF-7	breast:
48	chr8:96097741..96100033-chr8:96272742..96274690,2	MCF-7	breast:
49	chr8:95834579..95836869-chr8:96281817..96284598,2	K562	blood:
50	chr8:95960086..95962162-chr8:96280907..96282894,2	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PLEKHF2-2	chr8:96281064-96281118	NONHSAT127837
2	lnc-PLEKHF2-2	chr8:96281064-96281118	NONHSAT127833
3	lnc-PLEKHF2-2	chr8:96281064-96281118	NONHSAT127832
4	lnc-PLEKHF2-2	chr8:96281064-96281118	NONHSAT127830
5	lnc-PLEKHF2-2	chr8:96281064-96281118	NONHSAT127829
6	lnc-PLEKHF2-2	chr8:96281064-96281118	NONHSAT127838
7	lnc-PLEKHF2-2	chr8:96281064-96281118	NONHSAT127831
8	lnc-PLEKHF2-2	chr8:96281064-96281118	ENSG00000253773.1
9	lnc-PLEKHF2-2	chr8:96281064-96281118	NONHSAT127834
10	lnc-PLEKHF2-2	chr8:96281064-96281118	NONHSAT127835

No data

Variant related genes	Relation type
ENSG00000253773	TF binding region
C8orf37	TF binding region
ENSG00000253773	CpG island
C8orf37	CpG island
ENSG00000156170	chromatin interactions
ENSG00000153933	chromatin interactions
ENSG00000164941	chromatin interactions
ENSG00000254248	chromatin interactions
ENSG00000162928	chromatin interactions
ENSG00000196408	chromatin interactions
ENSG00000214226	chromatin interactions
ENSG00000162927	chromatin interactions
ENSG00000245080	chromatin interactions
ENSG00000245904	chromatin interactions
ENSG00000175895	chromatin interactions
ENSG00000127554	chromatin interactions
ENSG00000133639	chromatin interactions
ENSG00000261437	chromatin interactions
ENSG00000175305	chromatin interactions
ENSG00000104413	chromatin interactions
ENSG00000163126	chromatin interactions
ENSG00000253773	chromatin interactions
ENSG00000156467	chromatin interactions
ENSG00000100650	chromatin interactions
ENSG00000254224	chromatin interactions
ENSG00000213337	chromatin interactions
ENSG00000156172	chromatin interactions
ENSG00000164938	chromatin interactions
ENSG00000101224	chromatin interactions

Extended variants
information (count: 820 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:820 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13270004	chr8:96273255-96273256	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs141972201	chr8:96273264-96273265	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs575639359	chr8:96273307-96273308	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs184259980	chr8:96273347-96273348	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs556830814	chr8:96273358-96273359	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs576975181	chr8:96273384-96273385	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs545656013	chr8:96273412-96273413	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs79492338	chr8:96273456-96273457	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs572838607	chr8:96273495-96273496	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs541416932	chr8:96273551-96273552	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs149932306	chr8:96273566-96273567	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs188494561	chr8:96273570-96273571	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs530477477	chr8:96273583-96273584	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs34079000	chr8:96273590-96273591	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs563753425	chr8:96273626-96273627	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs533595493	chr8:96273697-96273698	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs150243561	chr8:96273721-96273722	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs537778613	chr8:96273723-96273724	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs536193413	chr8:96273724-96273725	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs180894830	chr8:96273753-96273754	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs569235708	chr8:96273787-96273788	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs537910157	chr8:96273813-96273814	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs558245368	chr8:96273840-96273841	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs201405968	chr8:96273843-96273844	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs74854379	chr8:96273844-96273845	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs570523656	chr8:96273852-96273853	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs539236766	chr8:96273906-96273907	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs116457398	chr8:96273914-96273915	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs112481770	chr8:96273975-96273976	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs77671549	chr8:96273994-96273995	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs186244474	chr8:96274018-96274019	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs189155643	chr8:96274019-96274020	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs532698394	chr8:96274055-96274056	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs538635079	chr8:96274059-96274060	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs4560758	chr8:96274198-96274199	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs548256233	chr8:96274218-96274219	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs564187340	chr8:96274263-96274264	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs533094187	chr8:96274321-96274322	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs7814173	chr8:96274331-96274332	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs138871529	chr8:96274351-96274352	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs149436139	chr8:96274352-96274353	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs549707000	chr8:96274365-96274366	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs146383166	chr8:96274385-96274386	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs139829883	chr8:96274391-96274392	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs551509217	chr8:96274394-96274395	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs112957139	chr8:96274491-96274492	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs534076473	chr8:96274497-96274498	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs552704355	chr8:96274528-96274529	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs566341019	chr8:96274547-96274548	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs374985166	chr8:96274599-96274600	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:110)

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
Epilepsy	20502679	CNVD
Acute myeloid leukemia	19651601	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Mental retardation	17847001	CNVD
Neuropsychiatric disorder	20069037	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Colorectal cancer	21645411	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Breast cancer	21611746	CNVD
Breast cancer	17142309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Malignant melanoma	17260012	CNVD

Chromatin state (count:522 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:96242200-96280600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:96243800-96280400	Weak transcription	Primary hematopoietic stem cells	blood
3	chr8:96245600-96280400	Weak transcription	Fetal Stomach	stomach
4	chr8:96245600-96280400	Weak transcription	Pancreas	Pancrea
5	chr8:96249000-96280800	Weak transcription	Gastric	stomach
6	chr8:96250600-96280400	Weak transcription	Left Ventricle	heart
7	chr8:96251200-96280400	Weak transcription	Psoas Muscle	Psoas
8	chr8:96253400-96280400	Weak transcription	Esophagus	oesophagus
9	chr8:96255200-96280400	Weak transcription	Fetal Brain Male	brain
10	chr8:96256800-96280400	Weak transcription	Lung	lung
11	chr8:96257000-96280400	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr8:96257400-96280400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr8:96257800-96280400	Weak transcription	Fetal Kidney	kidney
14	chr8:96258000-96280400	Weak transcription	Duodenum Smooth Muscle	Duodenum
15	chr8:96258200-96280400	Weak transcription	Colon Smooth Muscle	Colon
16	chr8:96258400-96280400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr8:96260000-96280400	Weak transcription	Fetal Lung	lung
18	chr8:96260400-96280400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
19	chr8:96260800-96280400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
20	chr8:96261000-96280400	Weak transcription	Fetal Heart	heart
21	chr8:96261200-96280400	Weak transcription	Primary T helper cells fromperipheralblood	blood
22	chr8:96261400-96280000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr8:96261800-96280400	Weak transcription	Brain Hippocampus Middle	brain
24	chr8:96262000-96280400	Weak transcription	Rectal Smooth Muscle	rectum
25	chr8:96262200-96280400	Weak transcription	Adipose Nuclei	Adipose
26	chr8:96262200-96280400	Weak transcription	Fetal Thymus	thymus
27	chr8:96262600-96280400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr8:96263200-96280400	Weak transcription	Placenta	Placenta
29	chr8:96264200-96276800	Weak transcription	Primary T cells from cord blood	blood
30	chr8:96264200-96280400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr8:96264200-96280400	Weak transcription	Liver	Liver
32	chr8:96264200-96280400	Weak transcription	Brain Inferior Temporal Lobe	brain
33	chr8:96264200-96280400	Weak transcription	Brain Substantia Nigra	brain
34	chr8:96264400-96280000	Weak transcription	Brain Angular Gyrus	brain
35	chr8:96266000-96280400	Weak transcription	Fetal Intestine Small	intestine
36	chr8:96267000-96280400	Weak transcription	Primary T helper cells PMA-I stimulated	--
37	chr8:96268800-96276200	Weak transcription	Pancreatic Islets	Pancreatic Islet
38	chr8:96268800-96280400	Weak transcription	Thymus	Thymus
39	chr8:96269200-96280400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr8:96269400-96280600	Weak transcription	HSMMtube	muscle
41	chr8:96269600-96280400	Weak transcription	GM12878-XiMat	blood
42	chr8:96270800-96275400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
43	chr8:96271000-96280400	Weak transcription	Fetal Muscle Leg	muscle
44	chr8:96271800-96280400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr8:96271800-96280400	Weak transcription	Brain Cingulate Gyrus	brain
46	chr8:96271800-96280400	Weak transcription	Fetal Muscle Trunk	muscle
47	chr8:96272000-96280200	Weak transcription	A549	lung
48	chr8:96272000-96280400	Weak transcription	Fetal Brain Female	brain
49	chr8:96272000-96280600	Weak transcription	Aorta	Aorta
50	chr8:96272000-96280600	Weak transcription	Ovary	ovary

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