Variant report

Variant	nsv1038188
Chromosome Location	chr11:32410305-32449799
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:452)
CpG islands
(count:978)
Chromatin interactive
region (count:42)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:452 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:32445718-32445872	K562	blood:	n/a	n/a
2	ARID3A	chr11:32443218-32443546	K562	blood:	n/a	n/a
3	ARID3A	chr11:32448538-32448699	K562	blood:	n/a	n/a
4	ARID3A	chr11:32442369-32442946	K562	blood:	n/a	n/a
5	ATF1	chr11:32421863-32422205	K562	blood:	n/a	n/a
6	ATF1	chr11:32442306-32443006	K562	blood:	n/a	n/a
7	ATF1	chr11:32448358-32448788	K562	blood:	n/a	chr11:32448533-32448547
8	ATF1	chr11:32445649-32445939	K562	blood:	n/a	n/a
9	ATF2	chr11:32448367-32448863	H1-hESC	embryonic stem cell:	n/a	chr11:32448533-32448547
10	ATF2	chr11:32448401-32448772	H1-hESC	embryonic stem cell:	n/a	chr11:32448533-32448547
11	ATF3	chr11:32421810-32422213	K562	blood:	n/a	n/a
12	BACH1	chr11:32448333-32448772	H1-hESC	embryonic stem cell:	n/a	n/a
13	BHLHE40	chr11:32417811-32418240	GM12878	blood:	n/a	n/a
14	BHLHE40	chr11:32427375-32427398	K562	blood:	n/a	n/a
15	BHLHE40	chr11:32421957-32422102	K562	blood:	n/a	n/a
16	BHLHE40	chr11:32442252-32443024	K562	blood:	n/a	n/a
17	BHLHE40	chr11:32448367-32448924	K562	blood:	n/a	n/a
18	CBX3	chr11:32442259-32443020	K562	blood:	n/a	n/a
19	CBX3	chr11:32448657-32449024	K562	blood:	n/a	n/a
20	CCNT2	chr11:32449444-32449576	K562	blood:	n/a	n/a
21	CCNT2	chr11:32442431-32442884	K562	blood:	n/a	n/a
22	CCNT2	chr11:32448312-32449106	K562	blood:	n/a	chr11:32448688-32448697
23	CEBPB	chr11:32442484-32443041	K562	blood:	n/a	n/a
24	CEBPB	chr11:32413090-32413352	K562	blood:	n/a	chr11:32413226-32413237
25	CEBPB	chr11:32421868-32422219	HepG2	liver:	n/a	n/a
26	CEBPB	chr11:32421858-32422192	K562	blood:	n/a	n/a
27	CEBPB	chr11:32427121-32427409	K562	blood:	n/a	n/a
28	CEBPB	chr11:32421853-32422195	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr11:32445605-32445839	K562	blood:	n/a	n/a
30	CEBPB	chr11:32427131-32427331	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr11:32413105-32413263	HepG2	liver:	n/a	chr11:32413226-32413237
32	CEBPB	chr11:32421852-32422214	MCF-7	breast:	n/a	n/a
33	CEBPB	chr11:32421862-32422223	K562	blood:	n/a	n/a
34	CEBPB	chr11:32445588-32445886	K562	blood:	n/a	n/a
35	CEBPB	chr11:32421954-32422117	K562	blood:	n/a	n/a
36	CEBPB	chr11:32421861-32422193	IMR90	lung:	n/a	n/a
37	CEBPB	chr11:32442618-32443020	K562	blood:	n/a	n/a
38	CEBPB	chr11:32435422-32435548	HepG2	liver:	n/a	n/a
39	CEBPB	chr11:32421872-32422407	A549	lung:	n/a	n/a
40	CEBPB	chr11:32445547-32445872	K562	blood:	n/a	n/a
41	CEBPB	chr11:32421910-32422189	Hela-S3	cervix:	n/a	n/a
42	CEBPD	chr11:32442308-32443149	K562	blood:	n/a	n/a
43	CHD1	chr11:32418134-32418135	GM12878	blood:	n/a	n/a
44	CHD1	chr11:32448122-32448128	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD2	chr11:32447984-32448040	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD2	chr11:32442529-32442724	GM12878	blood:	n/a	n/a
47	CHD2	chr11:32448356-32448700	K562	blood:	n/a	n/a
48	CHD2	chr11:32442262-32442724	K562	blood:	n/a	n/a
49	CHD2	chr11:32447740-32447846	K562	blood:	n/a	n/a
50	CHD2	chr11:32448495-32448686	H1-hESC	embryonic stem cell:	n/a	n/a

(count:978 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:32449638-32449688	HepG2	liver:	n/a
2	chr11:32444987-32445037	GM19239	blood:	n/a
3	chr11:32449638-32449688	HepG2	liver:	n/a
4	chr11:32444987-32445037	GM19239	blood:	n/a
5	chr11:32447944-32447994	HRCEpiC	kidney:	n/a
6	chr11:32448293-32448343	ECC-1	luminal epithelium:	n/a
7	chr11:32444987-32445037	HRE	kidney:	n/a
8	chr11:32421752-32421802	T-47D	breast:	n/a
9	chr11:32448067-32448117	HCT-116	colon:	n/a
10	chr11:32448678-32448728	SKMC	muscle:	n/a
11	chr11:32421845-32421895	SK-N-SH	brain:	n/a
12	chr11:32421514-32421564	GM12892	blood:	n/a
13	chr11:32449163-32449213	ECC-1	luminal epithelium:	n/a
14	chr11:32449638-32449688	ProgFib	skin:	n/a
15	chr11:32449254-32449304	AG09309	skin:	n/a
16	chr11:32421635-32421685	MCF10A-Er-Src	breast:	n/a
17	chr11:32421752-32421802	BJ	skin:	n/a
18	chr11:32448067-32448117	CMK	blood:	n/a
19	chr11:32449638-32449688	GM12892	blood:	n/a
20	chr11:32421845-32421895	HEEpiC	esophagus:	n/a
21	chr11:32421808-32421858	HL-60	blood:	n/a
22	chr11:32448067-32448117	SAEC	small airway:	n/a
23	chr11:32449450-32449500	ECC-1	luminal epithelium:	n/a
24	chr11:32448293-32448343	Hela-S3	cervix:	n/a
25	chr11:32421808-32421858	HIPEpiC	eye:	n/a
26	chr11:32449163-32449213	Caco-2	colon:	n/a
27	chr11:32448293-32448343	AG04450	lung:	fetal
28	chr11:32448067-32448117	HCF	heart:	n/a
29	chr11:32449254-32449304	HCT-116	colon:	n/a
30	chr11:32421808-32421858	T-47D	breast:	n/a
31	chr11:32448678-32448728	AG04450	lung:	fetal
32	chr11:32447944-32447994	HIPEpiC	eye:	n/a
33	chr11:32444987-32445037	IMR90	lung:	fetal
34	chr11:32448067-32448117	Hela-S3	cervix:	n/a
35	chr11:32447944-32447994	BE2_C	brain:	n/a
36	chr11:32448293-32448343	AoSMC	blood vessel:	n/a
37	chr11:32448293-32448343	AG04449	skin:	fetal
38	chr11:32421518-32421568	HCF	heart:	n/a
39	chr11:32421518-32421568	MCF10A-Er-Src	breast:	n/a
40	chr11:32449638-32449688	SK-N-SH	brain:	n/a
41	chr11:32421635-32421685	GM06990	blood:	n/a
42	chr11:32449638-32449688	NT2-D1	testis:	n/a
43	chr11:32421845-32421895	MCF10A-Er-Src	breast:	n/a
44	chr11:32448769-32448819	IMR90	lung:	fetal
45	chr11:32444987-32445037	GM12892	blood:	n/a
46	chr11:32448067-32448117	SKMC	muscle:	n/a
47	chr11:32421514-32421564	HCF	heart:	n/a
48	chr11:32448293-32448343	SK-N-MC	brain:	n/a
49	chr11:32421514-32421564	GM19239	blood:	n/a
50	chr11:32421752-32421802	HPAEpiC	pulmonary alveolar:	n/a

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:32418279..32421670-chr11:32424343..32426756,3	K562	blood:
2	chr11:32397666..32400035-chr11:32435330..32437389,2	K562	blood:
3	chr11:32407611..32410379-chr11:32410899..32412970,3	K562	blood:
4	chr11:32414284..32417176-chr11:32418319..32421153,2	K562	blood:
5	chr11:32413863..32417759-chr11:32446575..32449998,5	K562	blood:
6	chr11:32431985..32434925-chr11:32436480..32438156,2	K562	blood:
7	chr11:32426521..32428841-chr11:32446378..32448492,2	K562	blood:
8	chr11:32413863..32417759-chr11:32446575..32449998,5	K562	blood:
9	chr11:32417288..32419262-chr11:32603773..32605536,2	K562	blood:
10	chr11:32399722..32401595-chr11:32443789..32446145,2	K562	blood:
11	chr11:32414284..32415861-chr11:32418319..32421122,2	K562	blood:
12	chr11:32409338..32411295-chr11:32455558..32457233,2	K562	blood:
13	chr11:32422364..32424970-chr11:32429339..32430871,2	K562	blood:
14	chr11:32431798..32437144-chr11:32439795..32446613,10	K562	blood:
15	chr11:32402052..32403912-chr11:32416610..32418334,2	K562	blood:
16	chr11:32426055..32429120-chr11:32454398..32457565,3	K562	blood:
17	chr11:32431985..32434925-chr11:32436480..32438156,2	K562	blood:
18	chr11:32413367..32415903-chr11:32442457..32444810,2	K562	blood:
19	chr11:32441708..32444112-chr11:32605234..32608760,5	K562	blood:
20	chr11:32413367..32415903-chr11:32442457..32444810,2	K562	blood:
21	chr11:32426521..32428841-chr11:32446378..32448492,2	K562	blood:
22	chr11:32366531..32369221-chr11:32412798..32414828,2	K562	blood:
23	chr11:32420914..32422943-chr11:32448387..32450097,2	K562	blood:
24	chr11:32445943..32448522-chr11:32612638..32615463,2	K562	blood:
25	chr11:32418279..32421670-chr11:32423686..32426756,5	K562	blood:
26	chr11:32422364..32424970-chr11:32429339..32430871,2	K562	blood:
27	chr11:32447031..32449133-chr11:32603580..32605616,2	K562	blood:
28	chr11:32408220..32412580-chr11:32413005..32416101,5	K562	blood:
29	chr11:32407611..32410379-chr11:32410899..32412970,3	K562	blood:
30	chr11:32407039..32411612-chr11:32452457..32458118,5	K562	blood:
31	chr11:32440943..32443516-chr11:32607260..32609866,2	K562	blood:
32	chr11:32408220..32412580-chr11:32413005..32416101,5	K562	blood:
33	chr11:32437656..32439428-chr11:32440957..32443152,2	K562	blood:
34	chr11:32418279..32421670-chr11:32424343..32426756,3	K562	blood:
35	chr11:32404442..32407230-chr11:32442115..32444001,2	K562	blood:
36	chr11:32396138..32399032-chr11:32408436..32411201,2	K562	blood:
37	chr11:32414284..32417176-chr11:32418319..32421153,2	K562	blood:
38	chr11:32431798..32437144-chr11:32439795..32446613,10	K562	blood:
39	chr11:32414284..32415861-chr11:32418319..32421122,2	K562	blood:
40	chr11:32418279..32421670-chr11:32423686..32426756,5	K562	blood:
41	chr11:32407201..32409874-chr11:32413838..32416426,2	K562	blood:
42	chr11:32404951..32407417-chr11:32425366..32427411,2	K562	blood:

No data

Variant related genes	Relation type
WT1	TF binding region
WT1	CpG island
ENSG00000270903	chromatin interactions
ENSG00000149100	chromatin interactions
ENSG00000183242	chromatin interactions
ENSG00000184937	chromatin interactions

Extended variants
information (count: 1585 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:1585 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs181881769	chr11:32410324-32410325	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs5030317	chr11:32410337-32410338	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs5030316	chr11:32410380-32410381	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs560907250	chr11:32410396-32410397	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs111351882	chr11:32410466-32410467	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs5030315	chr11:32410516-32410517	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs563643335	chr11:32410523-32410524	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs376972948	chr11:32410569-32410570	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs2234594	chr11:32410588-32410589	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs77462662	chr11:32410592-32410593	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs148856160	chr11:32410605-32410606	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs202118284	chr11:32410610-32410611	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs267602848	chr11:32410619-32410620	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs528613270	chr11:32410626-32410627	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs369940913	chr11:32410646-32410647	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs139893274	chr11:32410704-32410705	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs267602849	chr11:32410710-32410711	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs185744719	chr11:32410735-32410736	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs1799937	chr11:32410774-32410775	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs145414435	chr11:32410887-32410888	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs190941620	chr11:32410929-32410930	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs5030312	chr11:32410954-32410955	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs372695151	chr11:32410988-32410989	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs558144125	chr11:32411013-32411014	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs571741446	chr11:32411027-32411028	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs534395243	chr11:32411041-32411042	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs554693611	chr11:32411052-32411053	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs533175047	chr11:32411062-32411063	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs5030311	chr11:32411100-32411101	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs543616358	chr11:32411163-32411164	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs201605903	chr11:32411164-32411165	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs75848325	chr11:32411203-32411204	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs577232828	chr11:32411207-32411208	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs563678708	chr11:32411234-32411235	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs5030310	chr11:32411240-32411241	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs559768580	chr11:32411258-32411259	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs147696325	chr11:32411270-32411271	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs79147948	chr11:32411275-32411276	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs570075227	chr11:32411291-32411292	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs530959175	chr11:32411330-32411331	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs551175807	chr11:32411339-32411340	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs570772861	chr11:32411341-32411342	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs539726520	chr11:32411352-32411353	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs5030309	chr11:32411372-32411373	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs5030308	chr11:32411420-32411421	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs534658026	chr11:32411444-32411445	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs554330657	chr11:32411448-32411449	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs574479630	chr11:32411507-32411508	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs536820150	chr11:32411543-32411544	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs528648019	chr11:32411568-32411569	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	16783165	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21364760	CNVD
Glioblastoma multiforme	22286061	CNVD
Aniridia syndrome	21572526	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Retinoblastoma	22278416	CNVD
Denys-drash syndrome	21085971	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
WAGR syndrome	16773131	CNVD
Disorders of sex development	22290220	CNVD
Aniridia syndrome	17204608	CNVD
Mental retardation	17204608	CNVD
WAGR syndrome	19617690	CNVD
genitourinary abnormalities	17204608	CNVD
Breast cancer	16397240	CNVD
Mental retardation	16773131	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Cancer	21183584	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
WAGR syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Denys-drash syndrome	19566914	CNVD
Familial wilms tumor	19566914	CNVD
Frasier syndrome	19566914	CNVD
Non-small cell lung cancer	21829676	CNVD
WAGR syndrome	20603712	CNVD
Autism	17322880	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21858162	CNVD
Cancer	20164920	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Wilms tumour	17204608	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute myeloid leukemia	21518781	CNVD
Ependymoma	20639864	CNVD
Breast cancer	16620391	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:478 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:32403200-32411800	Weak transcription	Spleen	Spleen
2	chr11:32404000-32411800	Weak transcription	Right Ventricle	heart
3	chr11:32406000-32412800	Genic enhancers	Dnd41	blood
4	chr11:32406600-32411400	Weak transcription	Ovary	ovary
5	chr11:32408400-32413000	Enhancers	Fetal Heart	heart
6	chr11:32408600-32413600	Weak transcription	NH-A	brain
7	chr11:32408600-32421600	Weak transcription	Left Ventricle	heart
8	chr11:32408800-32410600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr11:32409200-32410400	Genic enhancers	K562	blood
10	chr11:32409400-32413400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr11:32409400-32422000	Weak transcription	Fetal Kidney	kidney
12	chr11:32409600-32413600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
13	chr11:32409600-32413800	Weak transcription	Primary hematopoietic stem cells	blood
14	chr11:32410200-32410800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr11:32410200-32413600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr11:32410400-32410600	Enhancers	GM12878-XiMat	blood
17	chr11:32410400-32410800	Strong transcription	K562	blood
18	chr11:32410600-32411000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr11:32410600-32413600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr11:32410800-32412000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr11:32410800-32412600	Weak transcription	K562	blood
22	chr11:32411400-32412400	Strong transcription	Ovary	ovary
23	chr11:32411800-32412000	Enhancers	Right Ventricle	heart
24	chr11:32411800-32412200	Enhancers	Spleen	Spleen
25	chr11:32412000-32412400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr11:32412000-32417800	Weak transcription	Right Ventricle	heart
27	chr11:32412200-32418000	Weak transcription	Spleen	Spleen
28	chr11:32412400-32413600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr11:32412400-32417600	Weak transcription	Ovary	ovary
30	chr11:32412600-32412800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr11:32412600-32421800	Strong transcription	K562	blood
32	chr11:32412800-32413200	Transcr. at gene 5' and 3'	Dnd41	blood
33	chr11:32413000-32416200	Weak transcription	Fetal Heart	heart
34	chr11:32413200-32413600	Genic enhancers	Dnd41	blood
35	chr11:32413400-32414400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr11:32413600-32414000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr11:32413600-32414000	Enhancers	GM12878-XiMat	blood
38	chr11:32413600-32414200	Enhancers	NH-A	brain
39	chr11:32413600-32414600	Enhancers	Fetal Thymus	thymus
40	chr11:32413600-32414800	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
41	chr11:32413600-32415200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr11:32413600-32415400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr11:32413600-32415400	Transcr. at gene 5' and 3'	Dnd41	blood
44	chr11:32413800-32414200	Enhancers	Thymus	Thymus
45	chr11:32413800-32414400	Enhancers	Primary hematopoietic stem cells	blood
46	chr11:32414000-32415000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr11:32414400-32415000	Enhancers	Rectal Mucosa Donor 29	rectum
48	chr11:32414400-32418200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr11:32414800-32415200	Enhancers	Sigmoid Colon	Sigmoid Colon
50	chr11:32414800-32424200	Strong transcription	Primary hematopoietic stem cells short term culture	blood

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