Variant report

Variant	nsv523952
Chromosome Location	chr11:45983385-46028281
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1053)
CpG islands
(count:184)
Chromatin interactive
region (count:62)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1053 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:46004417-46005159	K562	blood:	n/a	n/a
2	ARID3A	chr11:46028063-46028286	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:46007587-46007691	K562	blood:	n/a	chr11:46007590-46007606 chr11:46007591-46007607
4	ARID3A	chr11:46027925-46028306	K562	blood:	n/a	n/a
5	ARID3A	chr11:46013641-46013653	K562	blood:	n/a	n/a
6	ARID3A	chr11:46017777-46018374	K562	blood:	n/a	n/a
7	ARID3A	chr11:46016855-46017444	K562	blood:	n/a	n/a
8	ARID3A	chr11:46025963-46026014	K562	blood:	n/a	n/a
9	ARID3A	chr11:45986381-45986828	K562	blood:	n/a	n/a
10	ARID3A	chr11:46015297-46016584	K562	blood:	n/a	n/a
11	ARID3A	chr11:46019084-46019651	K562	blood:	n/a	n/a
12	ATF1	chr11:46027984-46028254	K562	blood:	n/a	n/a
13	ATF1	chr11:46015869-46016403	K562	blood:	n/a	n/a
14	ATF1	chr11:46004503-46005404	K562	blood:	n/a	n/a
15	ATF1	chr11:46016925-46017332	K562	blood:	n/a	n/a
16	ATF2	chr11:46022819-46023576	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr11:46022548-46023422	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF3	chr11:46004444-46005057	K562	blood:	n/a	n/a
19	ATF3	chr11:46015863-46016498	K562	blood:	n/a	n/a
20	BACH1	chr11:46015955-46016597	K562	blood:	n/a	n/a
21	BACH1	chr11:46016807-46017312	K562	blood:	n/a	n/a
22	BATF	chr11:46004578-46004802	GM12878	blood:	n/a	n/a
23	BHLHE40	chr11:45983427-45983640	K562	blood:	n/a	chr11:45983548-45983561
24	BHLHE40	chr11:46015232-46015653	K562	blood:	n/a	chr11:46015385-46015401
25	BHLHE40	chr11:46016736-46017359	K562	blood:	n/a	n/a
26	BHLHE40	chr11:46028016-46028284	K562	blood:	n/a	n/a
27	BHLHE40	chr11:46004602-46004865	K562	blood:	n/a	n/a
28	BHLHE40	chr11:45986479-45986876	K562	blood:	n/a	n/a
29	BHLHE40	chr11:46015922-46016454	K562	blood:	n/a	n/a
30	BRCA1	chr11:46028006-46028319	Hela-S3	cervix:	n/a	n/a
31	BRCA1	chr11:45986363-45986783	Hela-S3	cervix:	n/a	n/a
32	CBX3	chr11:46004431-46005153	K562	blood:	n/a	n/a
33	CBX3	chr11:46015798-46016543	K562	blood:	n/a	n/a
34	CBX3	chr11:45986340-45987007	K562	blood:	n/a	n/a
35	CCNT2	chr11:46015951-46016343	K562	blood:	n/a	n/a
36	CCNT2	chr11:46004587-46005252	K562	blood:	n/a	chr11:46004787-46004796
37	CCNT2	chr11:46017063-46017325	K562	blood:	n/a	chr11:46017191-46017211
38	CEBPB	chr11:46025255-46025577	K562	blood:	n/a	n/a
39	CEBPB	chr11:46016923-46017416	K562	blood:	n/a	n/a
40	CEBPB	chr11:46004640-46004962	K562	blood:	n/a	n/a
41	CEBPB	chr11:46015752-46016819	K562	blood:	n/a	chr11:46016227-46016238
42	CEBPB	chr11:45986436-45986789	K562	blood:	n/a	n/a
43	CEBPB	chr11:45986432-45986814	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr11:46016084-46016378	K562	blood:	n/a	chr11:46016227-46016238
45	CEBPB	chr11:46025225-46025557	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr11:46015983-46016396	H1-hESC	embryonic stem cell:	n/a	chr11:46016227-46016238
47	CEBPB	chr11:46025255-46025542	K562	blood:	n/a	n/a
48	CEBPB	chr11:46015915-46016539	K562	blood:	n/a	chr11:46016227-46016238
49	CEBPB	chr11:46004704-46005005	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr11:46016130-46016391	HepG2	liver:	n/a	chr11:46016227-46016238

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:46016312-46016362	Hela-S3	cervix:	n/a
2	chr11:46016312-46016362	Hela-S3	cervix:	n/a
3	chr11:46021979-46022029	GM19239	blood:	n/a
4	chr11:46005268-46005318	Hepatocyte	liver:	n/a
5	chr11:46021979-46022029	HIPEpiC	eye:	n/a
6	chr11:46005268-46005318	AG04450	lung:	fetal
7	chr11:46016312-46016362	NH-A	brain:	n/a
8	chr11:46005268-46005318	HepG2	liver:	n/a
9	chr11:46005268-46005318	NHBE	bronchial:	n/a
10	chr11:46021979-46022029	U87	brain:	n/a
11	chr11:46021979-46022029	SAEC	small airway:	n/a
12	chr11:46016312-46016362	SK-N-SH_RA	brain:	n/a
13	chr11:46016312-46016362	NHBE	bronchial:	n/a
14	chr11:46005268-46005318	HIPEpiC	eye:	n/a
15	chr11:46016312-46016362	HCF	heart:	n/a
16	chr11:46016312-46016362	BJ	skin:	n/a
17	chr11:46005268-46005318	LNCaP	prostate:	n/a
18	chr11:46021979-46022029	GM06990	blood:	n/a
19	chr11:46021979-46022029	Jurkat	blood:	n/a
20	chr11:46005268-46005318	GM12891	blood:	n/a
21	chr11:46005268-46005318	T-47D	breast:	n/a
22	chr11:46005268-46005318	BJ	skin:	n/a
23	chr11:46005268-46005318	MCF-7	breast:	n/a
24	chr11:46005268-46005318	AG04449	skin:	fetal
25	chr11:46005268-46005318	HAEpiC	amniotic membrane:	n/a
26	chr11:46005268-46005318	Jurkat	blood:	n/a
27	chr11:46005268-46005318	PrEC	prostate:	n/a
28	chr11:46021979-46022029	PFSK-1	brain:	n/a
29	chr11:46005268-46005318	PFSK-1	brain:	n/a
30	chr11:46016312-46016362	A549	lung:	n/a
31	chr11:46021979-46022029	CMK	blood:	n/a
32	chr11:46005268-46005318	HPAEpiC	pulmonary alveolar:	n/a
33	chr11:46016312-46016362	Jurkat	blood:	n/a
34	chr11:46021979-46022029	HEEpiC	esophagus:	n/a
35	chr11:46016312-46016362	Caco-2	colon:	n/a
36	chr11:46005268-46005318	CMK	blood:	n/a
37	chr11:46016312-46016362	HCM	heart:	n/a
38	chr11:46005268-46005318	AG09319	gingival:	n/a
39	chr11:46021979-46022029	HNPCEpiC	eye:	n/a
40	chr11:46021979-46022029	K562	blood:	n/a
41	chr11:46016312-46016362	HEEpiC	esophagus:	n/a
42	chr11:46021979-46022029	HMEC	breast:	n/a
43	chr11:46016312-46016362	AG09319	gingival:	n/a
44	chr11:46005268-46005318	SAEC	small airway:	n/a
45	chr11:46021979-46022029	MCF10A-Er-Src	breast:	n/a
46	chr11:46016312-46016362	AG09309	skin:	n/a
47	chr11:46016312-46016362	GM12892	blood:	n/a
48	chr11:46005268-46005318	IMR90	lung:	fetal
49	chr11:46016312-46016362	U87	brain:	n/a
50	chr11:46016312-46016362	CMK	blood:	n/a

(count:62 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:46014298..46016604-chr11:46031314..46033806,2	K562	blood:
2	chr11:45937806..45941201-chr11:46015490..46019535,4	K562	blood:
3	chr11:45967819..45970756-chr11:46009123..46011676,2	K562	blood:
4	chr11:45867572..45870391-chr11:46015670..46018079,2	K562	blood:
5	chr11:45938159..45940217-chr11:46005267..46008166,2	MCF-7	breast:
6	chr11:45963701..45965937-chr11:46018859..46021293,2	K562	blood:
7	chr11:46027780..46028615-chr11:46097223..46097734,2	MCF-7	breast:
8	chr11:45943006..45945483-chr11:46015565..46017353,3	K562	blood:
9	chr11:46021583..46025208-chr11:46025456..46028440,3	K562	blood:
10	chr11:45986022..45987159-chr11:46027654..46029158,13	K562	blood:
11	chr11:45966883..45969814-chr11:46013235..46015702,2	K562	blood:
12	chr11:45926761..45929094-chr11:46013316..46015853,2	MCF-7	breast:
13	chr11:45990331..45993127-chr11:46002263..46005168,2	K562	blood:
14	chr11:45998746..46001549-chr11:46002921..46008009,7	K562	blood:
15	chr11:45986047..45986874-chr11:46097120..46098139,3	MCF-7	breast:
16	chr11:45987934..45989618-chr11:46004381..46006271,2	K562	blood:
17	chr11:45945921..45947947-chr11:46005632..46007133,2	K562	blood:
18	chr11:45919268..45921220-chr11:46000248..46001826,2	MCF-7	breast:
19	chr11:46022169..46024500-chr11:46257893..46260465,2	K562	blood:
20	chr11:45986214..45986722-chr11:46139048..46139638,2	MCF-7	breast:
21	chr11:46002933..46004911-chr11:46139730..46142231,2	K562	blood:
22	chr11:45894297..45894854-chr11:45986083..45986742,2	MCF-7	breast:
23	chr11:45986178..45987053-chr11:46027578..46028603,4	MCF-7	breast:
24	chr11:45937806..45940023-chr11:46017253..46018800,2	K562	blood:
25	chr11:45988485..45990717-chr11:46014188..46017080,2	K562	blood:
26	chr11:45893895..45894589-chr11:46027736..46028724,3	MCF-7	breast:
27	chr11:45927204..45929356-chr11:46025400..46027265,2	K562	blood:
28	chr11:45899726..45902315-chr11:45996941..45999150,2	MCF-7	breast:
29	chr11:45949887..45952560-chr11:46020571..46022730,2	K562	blood:
30	chr11:45957153..45959424-chr11:45981539..45983603,2	K562	blood:
31	chr11:45985864..45988587-chr11:45989343..45991964,3	K562	blood:
32	chr11:46028036..46029889-chr11:46143429..46146254,2	K562	blood:
33	chr11:45997750..46001916-chr11:46003160..46008009,7	K562	blood:
34	chr11:45869552..45871506-chr11:46003139..46005373,2	K562	blood:
35	chr11:45998746..46001549-chr11:46002921..46008009,7	K562	blood:
36	chr11:45942896..45944721-chr11:46003049..46005001,2	K562	blood:
37	chr11:45864388..45864916-chr11:46027549..46028549,2	K562	blood:
38	chr11:45994869..45996498-chr11:46000981..46003078,2	K562	blood:
39	chr11:46002612..46004470-chr11:46141856..46143588,2	MCF-7	breast:
40	chr11:45981105..45984613-chr11:45985057..45988704,3	K562	blood:
41	chr11:45988485..45990717-chr11:46014188..46017080,2	K562	blood:
42	chr11:46019054..46021565-chr11:46025255..46027912,2	K562	blood:
43	chr11:45997750..46001916-chr11:46003160..46008009,7	K562	blood:
44	chr11:46013966..46016594-chr11:46138214..46140856,2	K562	blood:
45	chr11:46000949..46006706-chr11:46011674..46018213,17	K562	blood:
46	chr11:45994869..45996498-chr11:46000981..46003078,2	K562	blood:
47	chr11:45894042..45894935-chr11:46027854..46028664,3	MCF-7	breast:
48	chr11:46024538..46028805-chr11:46032055..46036011,4	K562	blood:
49	chr11:45986502..45989270-chr11:45998897..46001765,2	K562	blood:
50	chr11:45905426..45907240-chr11:46014639..46017352,2	MCF-7	breast:

No data

Variant related genes	Relation type
PHF21A	TF binding region
PHF21A	CpG island
ENSG00000255498	chromatin interactions
ENSG00000121653	chromatin interactions
ENSG00000254639	chromatin interactions
ENSG00000165905	chromatin interactions
ENSG00000121671	chromatin interactions
ENSG00000135365	chromatin interactions
ENSG00000121680	chromatin interactions
ENSG00000234776	chromatin interactions

Extended variants
information (count: 1443 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:1443 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10769176	chr11:45983385-45983386	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs567643583	chr11:45983397-45983398	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs536284187	chr11:45983418-45983419	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs112674014	chr11:45983466-45983467	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs143980683	chr11:45983477-45983478	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs568835928	chr11:45983478-45983479	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs545536170	chr11:45983529-45983530	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs558734020	chr11:45983538-45983539	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs575476209	chr11:45983541-45983542	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs531445088	chr11:45983554-45983555	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs75985978	chr11:45983629-45983630	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs537417935	chr11:45983657-45983658	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs563075263	chr11:45983663-45983664	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs528869395	chr11:45983680-45983681	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs542274248	chr11:45983730-45983731	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs201494316	chr11:45983783-45983784	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs559569995	chr11:45983830-45983831	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs528380918	chr11:45983841-45983842	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs551562703	chr11:45983849-45983850	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs192750358	chr11:45983858-45983859	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs185094810	chr11:45983859-45983860	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs33984397	chr11:45983860-45983861	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs397718456	chr11:45983861-45983862	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs77580310	chr11:45983862-45983863	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs554180139	chr11:45983883-45983884	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs367666888	chr11:45983925-45983926	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs2959087	chr11:45983969-45983970	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs530753109	chr11:45983975-45983976	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs551078832	chr11:45983997-45983998	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs189763825	chr11:45984062-45984063	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs140876547	chr11:45984068-45984069	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs201221455	chr11:45984085-45984086	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs150457423	chr11:45984107-45984108	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs145306787	chr11:45984150-45984151	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs12224582	chr11:45984208-45984209	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs12221890	chr11:45984209-45984210	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs12796678	chr11:45984217-45984218	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs143014906	chr11:45984220-45984221	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	mRNA abundance
39	rs556606093	chr11:45984223-45984224	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs67513675	chr11:45984225-45984226	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs201978704	chr11:45984237-45984238	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs66486473	chr11:45984240-45984241	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs11038727	chr11:45984248-45984249	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs11038728	chr11:45984255-45984256	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs113642312	chr11:45984300-45984301	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs573677029	chr11:45984376-45984377	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs10769177	chr11:45984400-45984401	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs559096012	chr11:45984435-45984436	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs572841291	chr11:45984559-45984560	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs545300363	chr11:45984561-45984562	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Parathyroid adenoma	22454399	CNVD
Medulloblastoma	21979893	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
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	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
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21364760	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Myelofibrosis	22110671	CNVD
Melanoma	18172304	CNVD
Intracranial ependymoma	16609018	CNVD
Myxofibrosarcoma	16751306	CNVD
Potocki-Shaffer syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	16608533	CNVD
Hirschsprung''s Disease	21712996	CNVD
Follicular lymphoma	20505157	CNVD
Colorectal cancer	21128281	CNVD
Breast cancer	20409316	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Mantle cell lymphoma	19029149	CNVD
Glioblastoma multiforme	21138945	CNVD
Prostate cancer	18632612	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1483 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:45952400-45996200	Weak transcription	Stomach Mucosa	stomach
2	chr11:45953000-45988600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr11:45957200-46004400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr11:45957200-46004400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr11:45957600-45986400	Weak transcription	HMEC	breast
6	chr11:45957800-45986400	Weak transcription	NHEK	skin
7	chr11:45960400-45986600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr11:45967600-46004600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr11:45968000-45985800	Weak transcription	K562	blood
10	chr11:45969800-45983400	Weak transcription	Fetal Heart	heart
11	chr11:45970400-45985200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr11:45970600-45983400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr11:45970600-45986200	Weak transcription	NHLF	lung
14	chr11:45970600-45986600	Weak transcription	Pancreas	Pancrea
15	chr11:45970600-45986800	Weak transcription	HepG2	liver
16	chr11:45970800-45989200	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr11:45970800-45990400	Weak transcription	NHDF-Ad	bronchial
18	chr11:45971000-45983400	Weak transcription	Right Ventricle	heart
19	chr11:45971000-45985800	Weak transcription	Rectal Smooth Muscle	rectum
20	chr11:45971000-45986800	Weak transcription	Gastric	stomach
21	chr11:45971000-45990000	Weak transcription	Colonic Mucosa	Colon
22	chr11:45971000-45990600	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr11:45971000-45992400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr11:45971200-45985200	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr11:45971200-45986600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr11:45971200-45989600	Weak transcription	HUES6 Cell Line	embryonic stem cell
27	chr11:45971200-45992400	Weak transcription	Small Intestine	intestine
28	chr11:45971400-45990800	Weak transcription	HUVEC	blood vessel
29	chr11:45971600-45986600	Weak transcription	Fetal Brain Male	brain
30	chr11:45971800-45991400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
31	chr11:45972000-45986600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr11:45972000-45986800	Weak transcription	Aorta	Aorta
33	chr11:45972000-45989000	Weak transcription	Brain Cingulate Gyrus	brain
34	chr11:45972200-45992400	Weak transcription	Psoas Muscle	Psoas
35	chr11:45972400-45983400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
36	chr11:45972600-45986600	Weak transcription	Skeletal Muscle Male	skeletal muscle
37	chr11:45972800-45986000	Weak transcription	HUES48 Cell Line	embryonic stem cell
38	chr11:45972800-45988600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
39	chr11:45974000-45986600	Weak transcription	Sigmoid Colon	Sigmoid Colon
40	chr11:45974200-45986000	Weak transcription	Colon Smooth Muscle	Colon
41	chr11:45975000-45983600	Weak transcription	NH-A	brain
42	chr11:45975000-45985400	Weak transcription	Duodenum Mucosa	Duodenum
43	chr11:45975000-45986800	Weak transcription	Brain Inferior Temporal Lobe	brain
44	chr11:45975000-45989000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
45	chr11:45975200-45985800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr11:45975200-45985800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr11:45975200-45986400	Weak transcription	Muscle Satellite Cultured Cells	--
48	chr11:45975200-45986400	Weak transcription	Stomach Smooth Muscle	stomach
49	chr11:45975200-45988600	Weak transcription	Brain Substantia Nigra	brain
50	chr11:45975200-45991600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood

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