Variant report

Variant	nsv1044547
Chromosome Location	chr11:32435753-32465233
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:849)
CpG islands
(count:4271)
Chromatin interactive
region (count:24)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:849 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:32442369-32442946	K562	blood:	n/a	n/a
2	ARID3A	chr11:32454692-32454702	K562	blood:	n/a	n/a
3	ARID3A	chr11:32448538-32448699	K562	blood:	n/a	n/a
4	ARID3A	chr11:32443218-32443546	K562	blood:	n/a	n/a
5	ARID3A	chr11:32445718-32445872	K562	blood:	n/a	n/a
6	ARID3A	chr11:32454165-32454216	K562	blood:	n/a	n/a
7	ATF1	chr11:32442306-32443006	K562	blood:	n/a	n/a
8	ATF1	chr11:32448358-32448788	K562	blood:	n/a	chr11:32448533-32448547
9	ATF1	chr11:32445649-32445939	K562	blood:	n/a	n/a
10	ATF2	chr11:32448367-32448863	H1-hESC	embryonic stem cell:	n/a	chr11:32448533-32448547
11	ATF2	chr11:32456014-32456333	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr11:32448401-32448772	H1-hESC	embryonic stem cell:	n/a	chr11:32448533-32448547
13	BACH1	chr11:32455973-32456381	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr11:32460301-32460326	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr11:32452728-32452950	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr11:32455379-32455942	K562	blood:	n/a	n/a
17	BACH1	chr11:32448333-32448772	H1-hESC	embryonic stem cell:	n/a	n/a
18	BHLHE40	chr11:32448367-32448924	K562	blood:	n/a	n/a
19	BHLHE40	chr11:32456917-32457665	K562	blood:	n/a	n/a
20	BHLHE40	chr11:32455078-32456429	K562	blood:	n/a	n/a
21	BHLHE40	chr11:32454126-32454775	K562	blood:	n/a	n/a
22	BHLHE40	chr11:32442252-32443024	K562	blood:	n/a	n/a
23	CBX3	chr11:32448657-32449024	K562	blood:	n/a	n/a
24	CBX3	chr11:32442259-32443020	K562	blood:	n/a	n/a
25	CBX3	chr11:32452392-32452763	K562	blood:	n/a	n/a
26	CBX3	chr11:32457000-32457776	K562	blood:	n/a	n/a
27	CBX3	chr11:32455237-32455642	K562	blood:	n/a	n/a
28	CBX3	chr11:32457827-32458191	K562	blood:	n/a	n/a
29	CBX3	chr11:32456002-32456405	K562	blood:	n/a	n/a
30	CBX3	chr11:32455679-32456442	K562	blood:	n/a	n/a
31	CCNT2	chr11:32455203-32455550	K562	blood:	n/a	n/a
32	CCNT2	chr11:32442431-32442884	K562	blood:	n/a	n/a
33	CCNT2	chr11:32455902-32457475	K562	blood:	n/a	n/a
34	CCNT2	chr11:32448312-32449106	K562	blood:	n/a	chr11:32448688-32448697
35	CCNT2	chr11:32449444-32449576	K562	blood:	n/a	n/a
36	CEBPB	chr11:32456123-32456324	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr11:32445547-32445872	K562	blood:	n/a	n/a
38	CEBPB	chr11:32442618-32443020	K562	blood:	n/a	n/a
39	CEBPB	chr11:32445588-32445886	K562	blood:	n/a	n/a
40	CEBPB	chr11:32456077-32456412	K562	blood:	n/a	n/a
41	CEBPB	chr11:32456117-32456437	K562	blood:	n/a	n/a
42	CEBPB	chr11:32445605-32445839	K562	blood:	n/a	n/a
43	CEBPB	chr11:32442484-32443041	K562	blood:	n/a	n/a
44	CEBPB	chr11:32457256-32457412	K562	blood:	n/a	n/a
45	CEBPD	chr11:32442308-32443149	K562	blood:	n/a	n/a
46	CHD1	chr11:32457830-32458091	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD1	chr11:32448122-32448128	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr11:32442529-32442724	GM12878	blood:	n/a	n/a
49	CHD2	chr11:32448495-32448686	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD2	chr11:32447740-32447846	K562	blood:	n/a	n/a

(count:4271 , 50 per page) page: 1 2 3 4 5 6 7 ... 86

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:32457386-32457436	H1-hESC	embryonic stem cell:	embryo
2	chr11:32457386-32457436	H1-hESC	embryonic stem cell:	embryo
3	chr11:32455444-32455494	ovcar-3	ovarian:	n/a
4	chr11:32460656-32460706	NT2-D1	testis:	n/a
5	chr11:32457727-32457777	HUVEC	blood vessel:	n/a
6	chr11:32461240-32461290	Jurkat	blood:	n/a
7	chr11:32454216-32454266	CMK	blood:	n/a
8	chr11:32460980-32461030	BJ	skin:	n/a
9	chr11:32455735-32455785	PANC-1	pancreas:	n/a
10	chr11:32449638-32449688	HepG2	liver:	n/a
11	chr11:32455642-32455692	AG09319	gingival:	n/a
12	chr11:32457386-32457436	AoSMC	blood vessel:	n/a
13	chr11:32450244-32450294	CMK	blood:	n/a
14	chr11:32449163-32449213	HL-60	blood:	n/a
15	chr11:32448067-32448117	HNPCEpiC	eye:	n/a
16	chr11:32452771-32452821	A549	lung:	n/a
17	chr11:32448769-32448819	HUVEC	blood vessel:	n/a
18	chr11:32454975-32455025	HMEC	breast:	n/a
19	chr11:32454718-32454768	GM12891	blood:	n/a
20	chr11:32458656-32458706	RPTEC	kidney:	n/a
21	chr11:32460799-32460849	SKMC	muscle:	n/a
22	chr11:32456340-32456390	HCT-116	colon:	n/a
23	chr11:32448293-32448343	NH-A	brain:	n/a
24	chr11:32456912-32456962	BE2_C	brain:	n/a
25	chr11:32454748-32454798	H1-hESC	embryonic stem cell:	embryo
26	chr11:32455192-32455242	SK-N-MC	brain:	n/a
27	chr11:32452187-32452237	AoSMC	blood vessel:	n/a
28	chr11:32450104-32450154	HEEpiC	esophagus:	n/a
29	chr11:32449254-32449304	HepG2	liver:	n/a
30	chr11:32455192-32455242	Hepatocyte	liver:	n/a
31	chr11:32455192-32455242	HRE	kidney:	n/a
32	chr11:32458966-32459016	Caco-2	colon:	n/a
33	chr11:32455735-32455785	SAEC	small airway:	n/a
34	chr11:32450692-32450742	Caco-2	colon:	n/a
35	chr11:32457727-32457777	Hela-S3	cervix:	n/a
36	chr11:32454768-32454818	AG04450	lung:	fetal
37	chr11:32456912-32456962	SK-N-SH_RA	brain:	n/a
38	chr11:32455362-32455412	GM19239	blood:	n/a
39	chr11:32454840-32454890	NH-A	brain:	n/a
40	chr11:32448067-32448117	PrEC	prostate:	n/a
41	chr11:32457727-32457777	BJ	skin:	n/a
42	chr11:32449450-32449500	U87	brain:	n/a
43	chr11:32459057-32459107	SAEC	small airway:	n/a
44	chr11:32447944-32447994	T-47D	breast:	n/a
45	chr11:32455025-32455075	NH-A	brain:	n/a
46	chr11:32451461-32451511	GM12878	blood:	n/a
47	chr11:32461212-32461262	SK-N-MC	brain:	n/a
48	chr11:32449163-32449213	HCT-116	colon:	n/a
49	chr11:32456912-32456962	ProgFib	skin:	n/a
50	chr11:32451461-32451511	HRPEpiC	eye:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:32426521..32428841-chr11:32446378..32448492,2	K562	blood:
2	chr11:32420914..32422943-chr11:32448387..32450097,2	K562	blood:
3	chr11:32455544..32456179-chr21:40555264..40555769,2	NB4	blood:
4	chr11:32455134..32458517-chr11:32603988..32607695,5	K562	blood:
5	chr11:32413367..32415903-chr11:32442457..32444810,2	K562	blood:
6	chr11:32431798..32437144-chr11:32439795..32446613,10	K562	blood:
7	chr11:32431798..32437144-chr11:32439795..32446613,10	K562	blood:
8	chr11:32437656..32439428-chr11:32440957..32443152,2	K562	blood:
9	chr11:32399722..32401595-chr11:32443789..32446145,2	K562	blood:
10	chr11:32447031..32449133-chr11:32603580..32605616,2	K562	blood:
11	chr11:32440943..32443516-chr11:32607260..32609866,2	K562	blood:
12	chr11:32413863..32417759-chr11:32446575..32449998,5	K562	blood:
13	chr11:32455462..32457058-chr11:32608687..32611459,2	K562	blood:
14	chr11:32441708..32444112-chr11:32605234..32608760,5	K562	blood:
15	chr11:32431985..32434925-chr11:32436480..32438156,2	K562	blood:
16	chr11:32455369..32457971-chr11:32914210..32916339,2	K562	blood:
17	chr11:32465131..32467084-chr11:32469130..32471983,4	K562	blood:
18	chr11:32453512..32456485-chr11:32618384..32621260,2	K562	blood:
19	chr11:32455883..32456817-chr20:34329968..34330790,2	NB4	blood:
20	chr11:32455134..32460391-chr11:32603988..32611641,10	K562	blood:
21	chr11:32404442..32407230-chr11:32442115..32444001,2	K562	blood:
22	chr11:32460248..32463699-chr11:32486018..32490383,4	K562	blood:
23	chr11:32397666..32400035-chr11:32435330..32437389,2	K562	blood:
24	chr11:32445943..32448522-chr11:32612638..32615463,2	K562	blood:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EIF3M-2	chr11:32459391-32461618	NONHSAT018663
2	lnc-EIF3M-2	chr11:32460418-32460678	ENSG00000183242
3	lnc-EIF3M-2	chr11:32459391-32461620	NR_023920
4	lnc-EIF3M-2	chr11:32458341-32458597	ENSG00000183242
5	lnc-EIF3M-2	chr11:32457064-32457392	ENSG00000183242
6	lnc-EIF3M-2	chr11:32460325-32460505	NONHSAT018664
7	lnc-EIF3M-2	chr11:32459475-32461618	ENSG00000183242
8	lnc-EIF3M-2	chr11:32457285-32457392	NR_023920
9	lnc-EIF3M-2	chr11:32459916-32460136	ENSG00000183242
10	lnc-EIF3M-2	chr11:32457125-32457392	ENSG00000183242
11	lnc-EIF3M-2	chr11:32457347-32457392	ENSG00000183242
12	lnc-EIF3M-2	chr11:32457585-32460136	NONHSAT018664
13	lnc-EIF3M-2	chr11:32459391-32462950	ENSG00000183242
14	lnc-EIF3M-2	chr11:32459169-32459247	ENSG00000183242
15	lnc-EIF3M-2	chr11:32457322-32457392	ENSG00000183242
16	lnc-EIF3M-2	chr11:32459391-32460253	ENSG00000183242
17	lnc-EIF3M-2	chr11:32457585-32458383	NONHSAT018663
18	lnc-EIF3M-2	chr11:32459391-32459872	ENSG00000183242
19	lnc-EIF3M-2	chr11:32458616-32458743	ENSG00000183242

No data

Variant related genes	Relation type
WT1-AS	TF binding region
WT1	TF binding region
WT1-AS	CpG island
WT1	CpG island
ENSG00000149100	chromatin interactions
ENSG00000060749	chromatin interactions
ENSG00000183527	chromatin interactions
ENSG00000184937	chromatin interactions
ENSG00000131051	chromatin interactions
ENSG00000270903	chromatin interactions

Extended variants
information (count: 1240 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:1240 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541548795	chr11:32435776-32435777	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs111667510	chr11:32435791-32435792	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs544541683	chr11:32435812-32435813	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs190593544	chr11:32435853-32435854	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs34558926	chr11:32435861-32435862	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs540646541	chr11:32435871-32435872	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs149718206	chr11:32435895-32435896	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs529741511	chr11:32435905-32435906	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs79141954	chr11:32436000-32436001	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs182891635	chr11:32436023-32436024	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs557538383	chr11:32436050-32436051	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs113510018	chr11:32436065-32436066	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs187912152	chr11:32436101-32436102	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs552473576	chr11:32436103-32436104	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs565959899	chr11:32436144-32436145	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs72909441	chr11:32436145-32436146	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs115733467	chr11:32436148-32436149	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs568488328	chr11:32436198-32436199	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs537103265	chr11:32436199-32436200	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs557043974	chr11:32436240-32436241	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs193226516	chr11:32436270-32436271	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs7116462	chr11:32436414-32436415	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs111624321	chr11:32436415-32436416	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs573439271	chr11:32436419-32436420	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs374164197	chr11:32436481-32436482	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs542547772	chr11:32436501-32436502	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs560676930	chr11:32436566-32436567	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs574384968	chr11:32436596-32436597	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs543119528	chr11:32436610-32436611	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs563396864	chr11:32436617-32436618	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs527523230	chr11:32436627-32436628	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs527277671	chr11:32436629-32436630	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs552385003	chr11:32436683-32436684	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs559627975	chr11:32436702-32436703	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs551935008	chr11:32436806-32436807	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs370627165	chr11:32436833-32436834	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs548467418	chr11:32436868-32436869	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs5030224	chr11:32436892-32436893	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs5030223	chr11:32436927-32436928	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs372938696	chr11:32436929-32436930	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs537467935	chr11:32436932-32436933	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs550632461	chr11:32436943-32436944	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs570586802	chr11:32436955-32436956	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs539576871	chr11:32436963-32436964	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs553139649	chr11:32436972-32436973	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs573428404	chr11:32436984-32436985	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs5030222	chr11:32436985-32436986	Strong transcription Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs556042092	chr11:32437003-32437004	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs575612883	chr11:32437046-32437047	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs543422163	chr11:32437050-32437051	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

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
Acute myeloid leukemia	21518781	CNVD
Breast cancer	16620391	CNVD

Chromatin state (count:1145 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:32433400-32437200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
2	chr11:32434000-32442400	Weak transcription	Right Ventricle	heart
3	chr11:32434200-32438000	Weak transcription	Ovary	ovary
4	chr11:32435400-32437800	Weak transcription	K562	blood
5	chr11:32435600-32438000	Weak transcription	Fetal Kidney	kidney
6	chr11:32436400-32441800	Enhancers	Dnd41	blood
7	chr11:32436600-32442200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr11:32436600-32442200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr11:32436800-32438200	Weak transcription	Left Ventricle	heart
10	chr11:32437200-32438800	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr11:32437600-32437800	Enhancers	Primary hematopoietic stem cells	blood
12	chr11:32437600-32438000	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr11:32437800-32438000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
14	chr11:32437800-32439200	Enhancers	Fetal Thymus	thymus
15	chr11:32437800-32440200	Strong transcription	K562	blood
16	chr11:32437800-32440800	Weak transcription	Primary hematopoietic stem cells	blood
17	chr11:32438000-32438200	Strong transcription	Ovary	ovary
18	chr11:32438000-32438400	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
19	chr11:32438000-32438800	Strong transcription	Fetal Kidney	kidney
20	chr11:32438200-32438400	Enhancers	Left Ventricle	heart
21	chr11:32438200-32438400	Genic enhancers	Ovary	ovary
22	chr11:32438400-32438800	Strong transcription	Ovary	ovary
23	chr11:32438400-32442200	Weak transcription	Left Ventricle	heart
24	chr11:32438800-32439600	Genic enhancers	Fetal Kidney	kidney
25	chr11:32438800-32442200	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr11:32438800-32447800	Weak transcription	Ovary	ovary
27	chr11:32439200-32440200	Weak transcription	Fetal Thymus	thymus
28	chr11:32439600-32440200	Enhancers	Fetal Kidney	kidney
29	chr11:32439800-32440200	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
30	chr11:32439800-32441000	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr11:32440000-32440200	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr11:32440000-32440400	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr11:32440000-32440600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr11:32440000-32440600	Enhancers	Fetal Heart	heart
35	chr11:32440000-32440800	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr11:32440000-32440800	Enhancers	Thymus	Thymus
37	chr11:32440000-32441000	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr11:32440000-32444400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr11:32440200-32440400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr11:32440200-32440400	Flanking Active TSS	Fetal Kidney	kidney
41	chr11:32440200-32440600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
42	chr11:32440200-32440600	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr11:32440200-32440800	Enhancers	H9 Cell Line	embryonic stem cell
44	chr11:32440200-32440800	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr11:32440200-32440800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
46	chr11:32440200-32441800	Weak transcription	K562	blood
47	chr11:32440200-32442400	Enhancers	Fetal Thymus	thymus
48	chr11:32440400-32440600	Enhancers	H1 Cell Line	embryonic stem cell
49	chr11:32440400-32440600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
50	chr11:32440400-32440800	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell

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