Variant report

Variant	nsv539482
Chromosome Location	chr8:11754663-11849955
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2388)
CpG islands
(count:3052)
Chromatin interactive
region (count:57)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2388 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:11801213-11801488	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:11754879-11755097	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:11769447-11769628	K562	blood:	n/a	n/a
4	ARID3A	chr8:11767366-11767469	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:11813783-11814113	HepG2	liver:	n/a	n/a
6	ARID3A	chr8:11758928-11760170	HepG2	liver:	n/a	n/a
7	ARID3A	chr8:11799803-11800003	K562	blood:	n/a	n/a
8	ATF1	chr8:11793688-11793744	K562	blood:	n/a	n/a
9	ATF1	chr8:11799573-11800081	K562	blood:	n/a	n/a
10	ATF1	chr8:11807083-11807365	K562	blood:	n/a	n/a
11	ATF2	chr8:11754279-11755628	GM12878	blood:	n/a	n/a
12	ATF2	chr8:11754354-11755726	GM12878	blood:	n/a	n/a
13	ATF2	chr8:11759720-11760180	GM12878	blood:	n/a	n/a
14	ATF3	chr8:11759787-11760027	K562	blood:	n/a	n/a
15	ATF3	chr8:11801205-11801445	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF3	chr8:11801205-11801436	K562	blood:	n/a	n/a
17	BACH1	chr8:11766653-11766839	K562	blood:	n/a	n/a
18	BACH1	chr8:11816433-11816692	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr8:11759765-11760312	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr8:11815300-11815374	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr8:11791553-11791787	K562	blood:	n/a	n/a
22	BATF	chr8:11754746-11755153	GM12878	blood:	n/a	n/a
23	BATF	chr8:11764476-11764781	GM12878	blood:	n/a	n/a
24	BATF	chr8:11754598-11755318	GM12878	blood:	n/a	n/a
25	BATF	chr8:11768607-11768792	GM12878	blood:	n/a	n/a
26	BCL11A	chr8:11754571-11755235	GM12878	blood:	n/a	chr8:11754779-11754792 chr8:11754784-11754793 chr8:11754786-11754799
27	BCL11A	chr8:11754614-11755041	GM12878	blood:	n/a	chr8:11754779-11754792 chr8:11754784-11754793 chr8:11754786-11754799
28	BCL11A	chr8:11783650-11783829	GM12878	blood:	n/a	n/a
29	BCL3	chr8:11822405-11822652	GM12878	blood:	n/a	n/a
30	BCL3	chr8:11754724-11755297	GM12878	blood:	n/a	chr8:11754779-11754792 chr8:11754784-11754793 chr8:11754786-11754799
31	BCLAF1	chr8:11754337-11755211	GM12878	blood:	n/a	chr8:11754779-11754792 chr8:11754784-11754793 chr8:11754786-11754799
32	BCLAF1	chr8:11754389-11755233	GM12878	blood:	n/a	chr8:11754779-11754792 chr8:11754784-11754793 chr8:11754786-11754799
33	BHLHE40	chr8:11793297-11793881	K562	blood:	n/a	n/a
34	BHLHE40	chr8:11815181-11815494	K562	blood:	n/a	n/a
35	BHLHE40	chr8:11769211-11769482	K562	blood:	n/a	n/a
36	BHLHE40	chr8:11799584-11800147	K562	blood:	n/a	n/a
37	BHLHE40	chr8:11801130-11801571	K562	blood:	n/a	chr8:11801359-11801372
38	BHLHE40	chr8:11801183-11801540	HepG2	liver:	n/a	chr8:11801359-11801372
39	BHLHE40	chr8:11759739-11760276	K562	blood:	n/a	chr8:11759889-11759905 chr8:11759886-11759902
40	BHLHE40	chr8:11801171-11801545	GM12878	blood:	n/a	chr8:11801359-11801372
41	BHLHE40	chr8:11812950-11813081	K562	blood:	n/a	n/a
42	BHLHE40	chr8:11815192-11815513	HepG2	liver:	n/a	n/a
43	BHLHE40	chr8:11754703-11755212	HepG2	liver:	n/a	chr8:11754786-11754802
44	BHLHE40	chr8:11754438-11755412	GM12878	blood:	n/a	chr8:11754786-11754802
45	BHLHE40	chr8:11806929-11807352	K562	blood:	n/a	n/a
46	BHLHE40	chr8:11816398-11816683	K562	blood:	n/a	n/a
47	BHLHE40	chr8:11754544-11755330	K562	blood:	n/a	chr8:11754786-11754802
48	BHLHE40	chr8:11759743-11760084	GM12878	blood:	n/a	chr8:11759889-11759905 chr8:11759886-11759902
49	BHLHE40	chr8:11759086-11760250	HepG2	liver:	n/a	chr8:11759889-11759905 chr8:11759886-11759902
50	BHLHE40	chr8:11801158-11801425	A549	lung:	n/a	chr8:11801359-11801372

(count:3052 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:11839764-11839814	HepG2	liver:	n/a
2	chr8:11813211-11813261	HRCEpiC	kidney:	n/a
3	chr8:11839764-11839814	HepG2	liver:	n/a
4	chr8:11813211-11813261	HRCEpiC	kidney:	n/a
5	chr8:11759863-11759913	HCM	heart:	n/a
6	chr8:11843816-11843866	SK-N-MC	brain:	n/a
7	chr8:11772734-11772784	HNPCEpiC	eye:	n/a
8	chr8:11833039-11833089	Jurkat	blood:	n/a
9	chr8:11831823-11831873	ECC-1	luminal epithelium:	n/a
10	chr8:11801365-11801415	NT2-D1	testis:	n/a
11	chr8:11832762-11832812	SKMC	muscle:	n/a
12	chr8:11801365-11801415	HNPCEpiC	eye:	n/a
13	chr8:11770970-11771020	GM12891	blood:	n/a
14	chr8:11838532-11838582	LNCaP	prostate:	n/a
15	chr8:11772734-11772784	LNCaP	prostate:	n/a
16	chr8:11770970-11771020	GM06990	blood:	n/a
17	chr8:11772215-11772265	K562	blood:	n/a
18	chr8:11831823-11831873	HPAEpiC	pulmonary alveolar:	n/a
19	chr8:11832565-11832615	GM19239	blood:	n/a
20	chr8:11760342-11760392	HCM	heart:	n/a
21	chr8:11759663-11759713	PANC-1	pancreas:	n/a
22	chr8:11838843-11838893	AG09309	skin:	n/a
23	chr8:11843971-11844021	HPAEpiC	pulmonary alveolar:	n/a
24	chr8:11794950-11795000	NHDF-neo	bronchial:	n/a
25	chr8:11838532-11838582	SK-N-SH_RA	brain:	n/a
26	chr8:11835607-11835657	MCF10A-Er-Src	breast:	n/a
27	chr8:11771244-11771294	PANC-1	pancreas:	n/a
28	chr8:11790559-11790609	BE2_C	brain:	n/a
29	chr8:11832762-11832812	HEK293	kidney:	embryo
30	chr8:11774497-11774547	BE2_C	brain:	n/a
31	chr8:11843971-11844021	HEK293	kidney:	embryo
32	chr8:11772568-11772618	SKMC	muscle:	n/a
33	chr8:11772119-11772169	GM12892	blood:	n/a
34	chr8:11774336-11774386	HCF	heart:	n/a
35	chr8:11772568-11772618	HCT-116	colon:	n/a
36	chr8:11763828-11763878	Jurkat	blood:	n/a
37	chr8:11839138-11839188	Hela-S3	cervix:	n/a
38	chr8:11774497-11774547	PrEC	prostate:	n/a
39	chr8:11801320-11801370	HMEC	breast:	n/a
40	chr8:11771345-11771395	ProgFib	skin:	n/a
41	chr8:11839780-11839830	GM06990	blood:	n/a
42	chr8:11832039-11832089	K562	blood:	n/a
43	chr8:11772119-11772169	T-47D	breast:	n/a
44	chr8:11838532-11838582	AG10803	skin:	n/a
45	chr8:11790559-11790609	U87	brain:	n/a
46	chr8:11833191-11833241	HCM	heart:	n/a
47	chr8:11838532-11838582	PANC-1	pancreas:	n/a
48	chr8:11759863-11759913	HRPEpiC	eye:	n/a
49	chr8:11833039-11833089	HEK293	kidney:	embryo
50	chr8:11772568-11772618	SK-N-SH_RA	brain:	n/a

(count:57 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:11710424..11713168-chr8:11798660..11801424,2	K562	blood:
2	chr8:11838617..11840884-chr8:11844089..11846019,2	K562	blood:
3	chr8:11759679..11760322-chr8:11800851..11801844,2	K562	blood:
4	chr8:11816060..11816951-chr8:11827752..11828579,2	MCF-7	breast:
5	chr8:11746436..11748896-chr8:11754900..11757322,2	K562	blood:
6	chr8:11424253..11424822-chr8:11800849..11801372,2	K562	blood:
7	chr8:11702751..11703651-chr8:11759392..11760311,3	MCF-7	breast:
8	chr8:11702698..11703665-chr8:11759456..11760160,2	MCF-7	breast:
9	chr8:11819737..11820672-chr8:11872272..11872975,3	MCF-7	breast:
10	chr8:11816060..11816951-chr8:11827752..11828579,2	MCF-7	breast:
11	chr8:11816131..11817071-chr8:11827985..11828641,3	K562	blood:
12	chr8:11835676..11837241-chr8:11840654..11843342,2	K562	blood:
13	chr8:11835676..11837241-chr8:11840654..11843342,2	K562	blood:
14	chr8:11603020..11605526-chr8:11757590..11759777,2	K562	blood:
15	chr8:11711030..11711819-chr8:11759482..11760312,2	MCF-7	breast:
16	chr8:11658805..11661004-chr8:11802756..11805427,2	K562	blood:
17	chr8:11622750..11623420-chr8:11815244..11815854,2	MCF-7	breast:
18	chr8:11612285..11613206-chr8:11801217..11801735,2	MCF-7	breast:
19	chr8:11723911..11726339-chr8:11798413..11801274,2	K562	blood:
20	chr8:11836841..11840054-chr8:11842955..11845395,3	MCF-7	breast:
21	chr8:11699877..11702780-chr8:11758303..11760780,3	K562	blood:
22	chr8:11835676..11838476-chr8:11840654..11843385,2	K562	blood:
23	chr8:11835676..11838476-chr8:11840654..11843385,2	K562	blood:
24	chr8:11768991..11769997-chr8:11800815..11801744,4	MCF-7	breast:
25	chr8:11759912..11760480-chr8:11816112..11816711,2	K562	blood:
26	chr8:11833455..11835537-chr8:11843531..11845955,2	K562	blood:
27	chr8:11801089..11802817-chr8:11804319..11806900,3	K562	blood:
28	chr8:11724192..11726313-chr8:11753136..11754724,2	MCF-7	breast:
29	chr8:11724862..11726557-chr8:11758521..11760693,2	MCF-7	breast:
30	chr8:11622669..11623564-chr8:11800869..11801753,3	K562	blood:
31	chr8:11744571..11746987-chr8:11757045..11759456,2	MCF-7	breast:
32	chr8:11759679..11760322-chr8:11800851..11801844,2	K562	blood:
33	chr8:11718467..11721222-chr8:11754378..11756104,3	K562	blood:
34	chr8:11622903..11623629-chr8:11815893..11817036,5	K562	blood:
35	chr8:11827300..11830194-chr8:11832454..11834607,2	K562	blood:
36	chr8:11830756..11832686-chr8:11834027..11835713,2	K562	blood:
37	chr8:11768991..11769997-chr8:11800815..11801744,4	MCF-7	breast:
38	chr8:11833455..11835537-chr8:11843531..11845955,2	K562	blood:
39	chr8:11820183..11822422-chr8:11827376..11829261,2	K562	blood:
40	chr8:11421685..11422256-chr8:11800840..11801381,2	K562	blood:
41	chr8:11718857..11721432-chr8:11753489..11755957,2	K562	blood:
42	chr8:11798435..11800299-chr8:11803537..11805187,2	K562	blood:
43	chr8:11622652..11623752-chr8:11800899..11801806,5	MCF-7	breast:
44	chr8:11622902..11623629-chr8:11759456..11760412,3	MCF-7	breast:
45	chr8:11424139..11425217-chr8:11815416..11817027,6	K562	blood:
46	chr8:11816131..11817071-chr8:11827985..11828641,3	K562	blood:
47	chr8:11827300..11830194-chr8:11832454..11834607,2	K562	blood:
48	chr8:11820183..11822422-chr8:11827376..11829261,2	K562	blood:
49	chr8:11798435..11800299-chr8:11803537..11805187,2	K562	blood:
50	chr8:11724650..11727565-chr8:11758155..11761309,4	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTSB-2	chr8:11777409-11778318	NONHSAT125102

No data

Variant related genes	Relation type
DEFB136	TF binding region
OR7E161P	TF binding region
DEFB135	TF binding region
OR7E158P	TF binding region
ENSG00000255144	TF binding region
DEFB136	CpG island
OR7E161P	CpG island
DEFB135	CpG island
OR7E158P	CpG island
ENSG00000255144	CpG island
ENSG00000079459	chromatin interactions
ENSG00000205883	chromatin interactions
ENSG00000205884	chromatin interactions
ENSG00000164733	chromatin interactions
ENSG00000255046	chromatin interactions
ENSG00000255144	chromatin interactions

Extended variants
information (count: 5494 )
Associated
traits (count: 141 )

Variant overlapped rSNPs/rCNVs (count:5494 , 50 per page) page: 1 2 3 4 5 6 7 ... 110

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138563841	chr8:11754664-11754665	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs527618284	chr8:11754667-11754668	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs140178724	chr8:11754668-11754669	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs541951731	chr8:11754707-11754708	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs1874543	chr8:11754759-11754760	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs531414420	chr8:11754761-11754762	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs549520203	chr8:11754768-11754769	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs571012848	chr8:11754789-11754790	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs115680348	chr8:11754796-11754797	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs4451265	chr8:11754800-11754801	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs567522028	chr8:11754826-11754827	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs536169785	chr8:11754827-11754828	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs566086748	chr8:11754828-11754829	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs527251453	chr8:11754859-11754860	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs555252432	chr8:11754866-11754867	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs547387714	chr8:11754872-11754873	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs570314796	chr8:11754947-11754948	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs537690347	chr8:11754959-11754960	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs376375793	chr8:11754977-11754978	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs559188119	chr8:11754991-11754992	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs116142644	chr8:11755004-11755005	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs545066943	chr8:11755025-11755026	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs553561487	chr8:11755036-11755037	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs1908814	chr8:11755055-11755056	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs542219212	chr8:11755072-11755073	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs138032743	chr8:11755129-11755130	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs78750629	chr8:11755135-11755136	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs543246437	chr8:11755153-11755154	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs149546518	chr8:11755178-11755179	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs147207442	chr8:11755183-11755184	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs73546792	chr8:11755190-11755191	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs565999460	chr8:11755192-11755193	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs115004008	chr8:11755193-11755194	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs139035798	chr8:11755204-11755205	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs142967184	chr8:11755219-11755220	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs561108590	chr8:11755231-11755232	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs552832081	chr8:11755298-11755299	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs571078719	chr8:11755316-11755317	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs534874696	chr8:11755321-11755322	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs553843793	chr8:11755364-11755365	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs117474952	chr8:11755368-11755369	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs147453742	chr8:11755393-11755394	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs148541811	chr8:11755411-11755412	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs543332000	chr8:11755416-11755417	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs374158377	chr8:11755429-11755430	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs576977165	chr8:11755442-11755443	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs181984996	chr8:11755448-11755449	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs142871027	chr8:11755497-11755498	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs9644757	chr8:11755513-11755514	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs548599000	chr8:11755521-11755522	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:141)

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
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:1318 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11738000-11755800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr8:11745800-11759600	Weak transcription	Right Atrium	heart
3	chr8:11748000-11755400	Weak transcription	Spleen	Spleen
4	chr8:11749200-11754800	Weak transcription	NHLF	lung
5	chr8:11749800-11759400	Weak transcription	NHEK	skin
6	chr8:11750000-11754800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr8:11752400-11755000	Weak transcription	HMEC	breast
8	chr8:11753400-11756400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
9	chr8:11753600-11756800	Enhancers	Primary B cells from cord blood	blood
10	chr8:11754000-11756200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr8:11754200-11755000	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
12	chr8:11754200-11755400	Flanking Active TSS	HepG2	liver
13	chr8:11754200-11755600	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr8:11754200-11755800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr8:11754200-11756200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr8:11754200-11756200	Flanking Active TSS	GM12878-XiMat	blood
17	chr8:11754400-11754800	Flanking Active TSS	Fetal Intestine Large	intestine
18	chr8:11754400-11754800	Flanking Active TSS	Fetal Intestine Small	intestine
19	chr8:11754400-11754800	Enhancers	Rectal Mucosa Donor 31	rectum
20	chr8:11754400-11755000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr8:11754400-11755000	Flanking Active TSS	Primary B cells from peripheral blood	blood
22	chr8:11754400-11755000	Active TSS	Liver	Liver
23	chr8:11754400-11755000	Enhancers	Esophagus	oesophagus
24	chr8:11754400-11755000	Enhancers	Pancreas	Pancrea
25	chr8:11754400-11755000	Flanking Active TSS	K562	blood
26	chr8:11754400-11755000	Flanking Active TSS	Osteobl	bone
27	chr8:11754400-11755200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr8:11754400-11755200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr8:11754400-11755200	Flanking Active TSS	Duodenum Mucosa	Duodenum
30	chr8:11754400-11755200	Enhancers	Stomach Mucosa	stomach
31	chr8:11754400-11755200	Enhancers	A549	lung
32	chr8:11754400-11755600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr8:11754400-11755600	Enhancers	NH-A	brain
34	chr8:11754400-11755800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
35	chr8:11754400-11756000	Enhancers	Muscle Satellite Cultured Cells	--
36	chr8:11754400-11756000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr8:11754400-11756000	Enhancers	NHDF-Ad	bronchial
38	chr8:11754400-11756200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr8:11754400-11756600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
40	chr8:11754600-11754800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr8:11754600-11754800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr8:11754600-11755000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr8:11754600-11755000	Enhancers	Ovary	ovary
44	chr8:11754600-11755200	Flanking Active TSS	Adipose Nuclei	Adipose
45	chr8:11754600-11755200	Enhancers	Left Ventricle	heart
46	chr8:11754600-11755400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr8:11754600-11755400	Enhancers	Fetal Thymus	thymus
48	chr8:11754600-11755600	Enhancers	Fetal Kidney	kidney
49	chr8:11754600-11755800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
50	chr8:11754600-11756000	Enhancers	Placenta	Placenta

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