Variant report

Variant	nsv1032736
Chromosome Location	chr8:11727357-11762693
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1355)
CpG islands
(count:793)
Chromatin interactive
region (count:53)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1355 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:11743681-11743940	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:11754879-11755097	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:11758928-11760170	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:11746984-11747236	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:11736830-11737436	K562	blood:	n/a	n/a
6	ARID3A	chr8:11741338-11742065	K562	blood:	n/a	n/a
7	ATF1	chr8:11736841-11737531	K562	blood:	n/a	n/a
8	ATF2	chr8:11739306-11739735	GM12878	blood:	n/a	n/a
9	ATF2	chr8:11739202-11739721	GM12878	blood:	n/a	n/a
10	ATF2	chr8:11735207-11736519	GM12878	blood:	n/a	n/a
11	ATF2	chr8:11754354-11755726	GM12878	blood:	n/a	n/a
12	ATF2	chr8:11759720-11760180	GM12878	blood:	n/a	n/a
13	ATF2	chr8:11754279-11755628	GM12878	blood:	n/a	n/a
14	ATF3	chr8:11759787-11760027	K562	blood:	n/a	n/a
15	BACH1	chr8:11759765-11760312	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr8:11729699-11729701	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr8:11741878-11742461	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr8:11741689-11742495	K562	blood:	n/a	n/a
19	BACH1	chr8:11743792-11743922	K562	blood:	n/a	n/a
20	BATF	chr8:11739125-11739726	GM12878	blood:	n/a	n/a
21	BATF	chr8:11754746-11755153	GM12878	blood:	n/a	n/a
22	BATF	chr8:11739242-11739663	GM12878	blood:	n/a	n/a
23	BATF	chr8:11754598-11755318	GM12878	blood:	n/a	n/a
24	BCL11A	chr8:11754571-11755235	GM12878	blood:	n/a	chr8:11754779-11754792 chr8:11754784-11754793 chr8:11754786-11754799
25	BCL11A	chr8:11754614-11755041	GM12878	blood:	n/a	chr8:11754779-11754792 chr8:11754784-11754793 chr8:11754786-11754799
26	BCL3	chr8:11754724-11755297	GM12878	blood:	n/a	chr8:11754779-11754792 chr8:11754784-11754793 chr8:11754786-11754799
27	BCLAF1	chr8:11754337-11755211	GM12878	blood:	n/a	chr8:11754779-11754792 chr8:11754784-11754793 chr8:11754786-11754799
28	BCLAF1	chr8:11754389-11755233	GM12878	blood:	n/a	chr8:11754779-11754792 chr8:11754784-11754793 chr8:11754786-11754799
29	BCLAF1	chr8:11739227-11739626	GM12878	blood:	n/a	n/a
30	BHLHE40	chr8:11748511-11748817	K562	blood:	n/a	n/a
31	BHLHE40	chr8:11743736-11743936	K562	blood:	n/a	n/a
32	BHLHE40	chr8:11759739-11760276	K562	blood:	n/a	chr8:11759889-11759905 chr8:11759886-11759902
33	BHLHE40	chr8:11732430-11732634	GM12878	blood:	n/a	n/a
34	BHLHE40	chr8:11728451-11728697	HepG2	liver:	n/a	n/a
35	BHLHE40	chr8:11754544-11755330	K562	blood:	n/a	chr8:11754786-11754802
36	BHLHE40	chr8:11754438-11755412	GM12878	blood:	n/a	chr8:11754786-11754802
37	BHLHE40	chr8:11735169-11735606	K562	blood:	n/a	n/a
38	BHLHE40	chr8:11739351-11739624	GM12878	blood:	n/a	n/a
39	BHLHE40	chr8:11736840-11737595	K562	blood:	n/a	chr8:11737004-11737020
40	BHLHE40	chr8:11759743-11760084	GM12878	blood:	n/a	chr8:11759889-11759905 chr8:11759886-11759902
41	BHLHE40	chr8:11735995-11736016	K562	blood:	n/a	n/a
42	BHLHE40	chr8:11759086-11760250	HepG2	liver:	n/a	chr8:11759889-11759905 chr8:11759886-11759902
43	BHLHE40	chr8:11754703-11755212	HepG2	liver:	n/a	chr8:11754786-11754802
44	BHLHE40	chr8:11743236-11743356	HepG2	liver:	n/a	n/a
45	BRCA1	chr8:11759696-11760000	H1-hESC	embryonic stem cell:	n/a	n/a
46	BRCA1	chr8:11759733-11760090	HepG2	liver:	n/a	n/a
47	BRCA1	chr8:11759673-11760101	Hela-S3	cervix:	n/a	n/a
48	BRCA1	chr8:11759068-11759443	HepG2	liver:	n/a	n/a
49	CBX3	chr8:11736732-11737531	K562	blood:	n/a	n/a
50	CBX3	chr8:11735099-11735805	K562	blood:	n/a	n/a

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:11756069-11756119	RPTEC	kidney:	n/a
2	chr8:11742488-11742538	HRE	kidney:	n/a
3	chr8:11760061-11760111	ECC-1	luminal epithelium:	n/a
4	chr8:11735419-11735469	RPTEC	kidney:	n/a
5	chr8:11760061-11760111	Caco-2	colon:	n/a
6	chr8:11759665-11759715	ovcar-3	ovarian:	n/a
7	chr8:11760061-11760111	HEK293	kidney:	embryo
8	chr8:11756069-11756119	LNCaP	prostate:	n/a
9	chr8:11759663-11759713	IMR90	lung:	fetal
10	chr8:11759665-11759715	U87	brain:	n/a
11	chr8:11735419-11735469	GM12878	blood:	n/a
12	chr8:11742488-11742538	IMR90	lung:	fetal
13	chr8:11728558-11728608	GM06990	blood:	n/a
14	chr8:11759930-11759980	SAEC	small airway:	n/a
15	chr8:11760342-11760392	GM19239	blood:	n/a
16	chr8:11755993-11756043	MCF10A-Er-Src	breast:	n/a
17	chr8:11760061-11760111	AG04450	lung:	fetal
18	chr8:11759863-11759913	MCF-7	breast:	n/a
19	chr8:11760342-11760392	PANC-1	pancreas:	n/a
20	chr8:11755993-11756043	A549	lung:	n/a
21	chr8:11760342-11760392	HepG2	liver:	n/a
22	chr8:11756069-11756119	HMEC	breast:	n/a
23	chr8:11756069-11756119	NHBE	bronchial:	n/a
24	chr8:11759663-11759713	Hela-S3	cervix:	n/a
25	chr8:11760136-11760186	Hepatocyte	liver:	n/a
26	chr8:11760061-11760111	ovcar-3	ovarian:	n/a
27	chr8:11735419-11735469	HNPCEpiC	eye:	n/a
28	chr8:11728558-11728608	HMEC	breast:	n/a
29	chr8:11760136-11760186	HMEC	breast:	n/a
30	chr8:11755993-11756043	HRE	kidney:	n/a
31	chr8:11756069-11756119	Hepatocyte	liver:	n/a
32	chr8:11760061-11760111	GM12891	blood:	n/a
33	chr8:11728558-11728608	NHDF-neo	bronchial:	n/a
34	chr8:11742488-11742538	AG09309	skin:	n/a
35	chr8:11735419-11735469	AoSMC	blood vessel:	n/a
36	chr8:11735419-11735469	HIPEpiC	eye:	n/a
37	chr8:11728558-11728608	Hepatocyte	liver:	n/a
38	chr8:11759665-11759715	SK-N-MC	brain:	n/a
39	chr8:11760136-11760186	NT2-D1	testis:	n/a
40	chr8:11759665-11759715	HCF	heart:	n/a
41	chr8:11728558-11728608	AG09309	skin:	n/a
42	chr8:11760061-11760111	MCF-7	breast:	n/a
43	chr8:11760342-11760392	MCF10A-Er-Src	breast:	n/a
44	chr8:11759863-11759913	HNPCEpiC	eye:	n/a
45	chr8:11759863-11759913	K562	blood:	n/a
46	chr8:11759930-11759980	PANC-1	pancreas:	n/a
47	chr8:11760061-11760111	LNCaP	prostate:	n/a
48	chr8:11760136-11760186	NB4	blood:	n/a
49	chr8:11760136-11760186	SK-N-MC	brain:	n/a
50	chr8:11759665-11759715	GM19239	blood:	n/a

(count:53 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:11746436..11748896-chr8:11754900..11757322,2	K562	blood:
2	chr8:11731939..11733861-chr8:11735868..11738030,2	K562	blood:
3	chr8:11718467..11721222-chr8:11754378..11756104,3	K562	blood:
4	chr8:11727352..11730707-chr8:11734493..11737265,3	K562	blood:
5	chr8:11724862..11726557-chr8:11758521..11760693,2	MCF-7	breast:
6	chr8:11728396..11730707-chr8:11735513..11737265,2	K562	blood:
7	chr8:11702751..11703651-chr8:11759392..11760311,3	MCF-7	breast:
8	chr8:11658066..11660009-chr8:11744623..11746128,2	K562	blood:
9	chr8:11723128..11726794-chr8:11729764..11731890,4	MCF-7	breast:
10	chr8:11724101..11727184-chr8:11750037..11752895,4	K562	blood:
11	chr8:11746436..11748896-chr8:11754900..11757322,2	K562	blood:
12	chr8:11734290..11736871-chr8:11743194..11744743,2	K562	blood:
13	chr8:11752267..11756149-chr8:11756562..11759200,3	MCF-7	breast:
14	chr8:11702698..11703665-chr8:11759456..11760160,2	MCF-7	breast:
15	chr8:11718857..11721432-chr8:11753489..11755957,2	K562	blood:
16	chr8:11724372..11727512-chr8:11735176..11737878,3	MCF-7	breast:
17	chr8:11724112..11726454-chr8:11732632..11735297,3	K562	blood:
18	chr8:11722381..11725684-chr8:11738607..11743840,4	K562	blood:
19	chr8:11622902..11623629-chr8:11759456..11760412,3	MCF-7	breast:
20	chr8:11626549..11628051-chr8:11739939..11742141,2	K562	blood:
21	chr8:11711601..11714581-chr8:11730061..11732215,2	K562	blood:
22	chr8:11728396..11730707-chr8:11735513..11737265,2	K562	blood:
23	chr8:11724109..11726850-chr8:11734821..11736918,2	MCF-7	breast:
24	chr8:11759912..11760480-chr8:11816112..11816711,2	K562	blood:
25	chr8:11717376..11719253-chr8:11741735..11744320,2	K562	blood:
26	chr8:11732515..11734330-chr8:11735926..11737604,2	K562	blood:
27	chr8:11710084..11711593-chr8:11733792..11735545,2	K562	blood:
28	chr8:11720357..11728660-chr8:11741310..11749437,9	K562	blood:
29	chr8:11724192..11726313-chr8:11753136..11754724,2	MCF-7	breast:
30	chr8:11724650..11727565-chr8:11758155..11761309,4	MCF-7	breast:
31	chr8:11717778..11719934-chr8:11735920..11738113,2	MCF-7	breast:
32	chr8:11732515..11734330-chr8:11735926..11737604,2	K562	blood:
33	chr8:11729883..11732100-chr8:11739868..11741394,2	K562	blood:
34	chr8:11742257..11745256-chr8:11747591..11749952,2	K562	blood:
35	chr8:11625866..11628884-chr8:11724599..11727626,3	MCF-7	breast:
36	chr8:11699877..11702780-chr8:11758303..11760780,3	K562	blood:
37	chr8:11734290..11736871-chr8:11743194..11744743,2	K562	blood:
38	chr8:11718826..11720544-chr8:11749993..11751511,2	MCF-7	breast:
39	chr8:11200722..11203684-chr8:11734586..11737466,2	K562	blood:
40	chr8:11729883..11732100-chr8:11739868..11741394,2	K562	blood:
41	chr8:11603020..11605526-chr8:11757590..11759777,2	K562	blood:
42	chr8:11711030..11711819-chr8:11759482..11760312,2	MCF-7	breast:
43	chr8:11727352..11730707-chr8:11734493..11737265,3	K562	blood:
44	chr8:11724798..11726931-chr8:11734409..11737375,2	K562	blood:
45	chr8:11725495..11727126-chr8:11727465..11729533,2	MCF-7	breast:
46	chr8:11731939..11733861-chr8:11735868..11738030,2	K562	blood:
47	chr8:11742257..11745256-chr8:11747591..11749952,2	K562	blood:
48	chr8:11744571..11746987-chr8:11757045..11759456,2	MCF-7	breast:
49	chr8:11724948..11727474-chr8:11747087..11750082,2	MCF-7	breast:
50	chr8:11740192..11742116-chr8:11742160..11745016,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTSB-1	chr8:11754271-11754379	NONHSAT125100
2	lnc-CTSB-1	chr8:11753359-11753626	NONHSAT125100

No data

Variant related genes	Relation type
CTSB	TF binding region
ENSG00000255144	TF binding region
CTSB	CpG island
ENSG00000255144	CpG island
ENSG00000164733	chromatin interactions
ENSG00000255144	chromatin interactions
ENSG00000079459	chromatin interactions
ENSG00000154328	chromatin interactions

Extended variants
information (count: 1877 )
Associated
traits (count: 140 )

Variant overlapped rSNPs/rCNVs (count:1877 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192586438	chr8:11727392-11727393	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs80057996	chr8:11727419-11727420	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs138039469	chr8:11727425-11727426	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs114466412	chr8:11727475-11727476	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs374533923	chr8:11727489-11727490	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs538640574	chr8:11727531-11727532	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs386722333	chr8:11727566-11727567	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs75561686	chr8:11727568-11727569	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs184778090	chr8:11727599-11727600	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs554750199	chr8:11727620-11727621	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs372614277	chr8:11727631-11727632	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs563926784	chr8:11727635-11727636	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs149497430	chr8:11727712-11727713	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs576844547	chr8:11727732-11727733	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs144164814	chr8:11727740-11727741	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs372809421	chr8:11727751-11727752	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs538175600	chr8:11727761-11727762	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs148680916	chr8:11727762-11727763	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs375399734	chr8:11727767-11727768	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs544702991	chr8:11727773-11727774	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs560061711	chr8:11727776-11727777	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs572381451	chr8:11727793-11727794	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs189209810	chr8:11727815-11727816	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs561115529	chr8:11727882-11727883	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs192864361	chr8:11727899-11727900	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs1965989	chr8:11727918-11727919	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs550283167	chr8:11727944-11727945	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs559384881	chr8:11727979-11727980	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs185079849	chr8:11727982-11727983	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs532610452	chr8:11727986-11727987	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs547488604	chr8:11728019-11728020	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs189544307	chr8:11728028-11728029	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs536549840	chr8:11728031-11728032	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs548467808	chr8:11728048-11728049	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs569952569	chr8:11728062-11728063	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs1297511	chr8:11728069-11728070	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs559082003	chr8:11728116-11728117	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs374141117	chr8:11728146-11728147	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs548211591	chr8:11728151-11728152	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs147470230	chr8:11728157-11728158	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs572067695	chr8:11728222-11728223	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs542984578	chr8:11728232-11728233	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs181134002	chr8:11728233-11728234	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs73663036	chr8:11728249-11728250	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs139864936	chr8:11728295-11728296	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs368660063	chr8:11728357-11728358	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs532507008	chr8:11728366-11728367	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs547821545	chr8:11728406-11728407	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs7845259	chr8:11728426-11728427	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs185080111	chr8:11728469-11728470	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:140)

Disease	PMID	Source
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
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
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
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
abnormal development	18461090	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Gastric cancer	21811585	CNVD
Colorectal cancer	16774939	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cancer	20164919	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1129 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11724000-11727400	Active TSS	Rectal Smooth Muscle	rectum
2	chr8:11725600-11734600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr8:11726200-11731600	Weak transcription	Dnd41	blood
4	chr8:11726400-11727400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr8:11726400-11727400	Weak transcription	Adipose Nuclei	Adipose
6	chr8:11726400-11727600	Enhancers	Fetal Intestine Small	intestine
7	chr8:11726400-11729400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr8:11726400-11729600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr8:11726400-11729600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr8:11726400-11729600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr8:11726400-11729600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr8:11726400-11729600	Weak transcription	Brain Cingulate Gyrus	brain
13	chr8:11726400-11729600	Weak transcription	NHDF-Ad	bronchial
14	chr8:11726400-11729600	Weak transcription	Osteobl	bone
15	chr8:11726400-11729800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr8:11726400-11730200	Weak transcription	Fetal Muscle Leg	muscle
17	chr8:11726400-11731200	Weak transcription	HMEC	breast
18	chr8:11726400-11731200	Weak transcription	NHEK	skin
19	chr8:11726400-11731800	Weak transcription	Primary B cells from peripheral blood	blood
20	chr8:11726400-11731800	Weak transcription	Skeletal Muscle Male	skeletal muscle
21	chr8:11726400-11731800	Weak transcription	GM12878-XiMat	blood
22	chr8:11726400-11731800	Weak transcription	NH-A	brain
23	chr8:11726400-11732000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr8:11726400-11732000	Weak transcription	HSMM	muscle
25	chr8:11726400-11732600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr8:11726400-11734600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr8:11726400-11734800	Weak transcription	Esophagus	oesophagus
28	chr8:11726400-11735200	Weak transcription	Cortex derived primary cultured neurospheres	brain
29	chr8:11726400-11735200	Weak transcription	Right Ventricle	heart
30	chr8:11726600-11727400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chr8:11726600-11727400	Enhancers	A549	lung
32	chr8:11726600-11729400	Weak transcription	Primary monocytes fromperipheralblood	blood
33	chr8:11726600-11729600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
34	chr8:11726600-11729600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr8:11726600-11729600	Weak transcription	Monocytes-CD14+_RO01746	blood
36	chr8:11726600-11729800	Weak transcription	Fetal Intestine Large	intestine
37	chr8:11726600-11731200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr8:11726600-11731800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr8:11726600-11731800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr8:11726600-11731800	Weak transcription	HUVEC	blood vessel
41	chr8:11726600-11732000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr8:11726600-11732000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr8:11726600-11732000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr8:11726600-11732000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr8:11726600-11734200	Weak transcription	Lung	lung
46	chr8:11726600-11736400	Weak transcription	Spleen	Spleen
47	chr8:11726800-11727400	Enhancers	Placenta	Placenta
48	chr8:11726800-11727400	Enhancers	Rectal Mucosa Donor 31	rectum
49	chr8:11726800-11731800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr8:11726800-11732000	Weak transcription	K562	blood

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