Variant report

Variant	nsv1059993
Chromosome Location	chr16:34527249-34781252
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1213)
CpG islands
(count:2137)
Chromatin interactive
region (count:5)
LncRNA
region (count:56)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1213 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr16:34574452-34574460	K562	blood:	n/a	n/a
2	ATF1	chr16:34589373-34589390	K562	blood:	n/a	n/a
3	ATF1	chr16:34715569-34715609	K562	blood:	n/a	n/a
4	ATF1	chr16:34573796-34574082	K562	blood:	n/a	n/a
5	ATF1	chr16:34625774-34626005	K562	blood:	n/a	n/a
6	ATF1	chr16:34643912-34644196	K562	blood:	n/a	n/a
7	ATF1	chr16:34768061-34768441	K562	blood:	n/a	n/a
8	ATF1	chr16:34765990-34765998	K562	blood:	n/a	n/a
9	BATF	chr16:34731793-34732055	GM12878	blood:	n/a	chr16:34731883-34731894 chr16:34731915-34731926
10	BATF	chr16:34539887-34540221	GM12878	blood:	n/a	chr16:34540044-34540055
11	BATF	chr16:34539865-34540180	GM12878	blood:	n/a	chr16:34540044-34540055
12	BATF	chr16:34731803-34731989	GM12878	blood:	n/a	chr16:34731883-34731894 chr16:34731915-34731926
13	BATF	chr16:34536693-34536965	GM12878	blood:	n/a	chr16:34536834-34536845
14	BHLHE40	chr16:34726730-34726951	K562	blood:	n/a	chr16:34726896-34726912
15	BHLHE40	chr16:34745103-34745432	GM12878	blood:	n/a	chr16:34745242-34745251
16	BHLHE40	chr16:34732021-34732023	GM12878	blood:	n/a	n/a
17	BHLHE40	chr16:34741044-34741235	K562	blood:	n/a	n/a
18	BHLHE40	chr16:34647001-34647022	GM12878	blood:	n/a	n/a
19	BHLHE40	chr16:34625401-34626021	K562	blood:	n/a	n/a
20	BHLHE40	chr16:34740335-34740524	K562	blood:	n/a	n/a
21	BHLHE40	chr16:34625806-34626006	GM12878	blood:	n/a	n/a
22	BHLHE40	chr16:34721874-34721912	GM12878	blood:	n/a	n/a
23	BHLHE40	chr16:34598011-34598017	K562	blood:	n/a	n/a
24	BHLHE40	chr16:34745112-34745352	K562	blood:	n/a	chr16:34745242-34745251
25	BRCA1	chr16:34666658-34666728	GM12878	blood:	n/a	n/a
26	BRCA1	chr16:34666402-34666616	H1-hESC	embryonic stem cell:	n/a	n/a
27	CBX3	chr16:34625799-34625988	K562	blood:	n/a	n/a
28	CEBPB	chr16:34573711-34574084	HepG2	liver:	n/a	chr16:34573875-34573886
29	CEBPB	chr16:34759219-34759383	MCF-7	breast:	n/a	n/a
30	CEBPB	chr16:34540548-34540632	IMR90	lung:	n/a	n/a
31	CEBPB	chr16:34535207-34535347	HepG2	liver:	n/a	n/a
32	CEBPB	chr16:34598601-34599065	A549	lung:	n/a	n/a
33	CEBPB	chr16:34768061-34768461	IMR90	lung:	n/a	n/a
34	CEBPB	chr16:34539206-34539440	A549	lung:	n/a	n/a
35	CEBPB	chr16:34621172-34621181	HepG2	liver:	n/a	n/a
36	CEBPB	chr16:34602083-34602267	A549	lung:	n/a	n/a
37	CEBPB	chr16:34573756-34574077	A549	lung:	n/a	chr16:34573875-34573886
38	CEBPB	chr16:34603901-34604333	A549	lung:	n/a	n/a
39	CEBPB	chr16:34597883-34598280	HepG2	liver:	n/a	n/a
40	CEBPB	chr16:34715384-34715712	HepG2	liver:	n/a	n/a
41	CEBPB	chr16:34536217-34536514	HepG2	liver:	n/a	n/a
42	CEBPB	chr16:34768026-34768406	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr16:34600160-34600470	ECC-1	luminal epithelium:	n/a	chr16:34600335-34600346
44	CEBPB	chr16:34532887-34533747	HepG2	liver:	n/a	chr16:34533406-34533417
45	CEBPB	chr16:34768107-34768405	K562	blood:	n/a	n/a
46	CEBPB	chr16:34573755-34574035	K562	blood:	n/a	chr16:34573875-34573886
47	CEBPB	chr16:34611205-34611346	A549	lung:	n/a	chr16:34611274-34611285
48	CEBPB	chr16:34542362-34542582	HepG2	liver:	n/a	n/a
49	CEBPB	chr16:34597882-34598141	IMR90	lung:	n/a	n/a
50	CEBPB	chr16:34530917-34531822	A549	lung:	n/a	n/a

(count:2137 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:34741304-34741354	MCF-7	breast:	n/a
2	chr16:34649152-34649202	PANC-1	pancreas:	n/a
3	chr16:34741304-34741354	MCF-7	breast:	n/a
4	chr16:34649152-34649202	PANC-1	pancreas:	n/a
5	chr16:34760531-34760581	ovcar-3	ovarian:	n/a
6	chr16:34777963-34778013	AG10803	skin:	n/a
7	chr16:34726734-34726784	Caco-2	colon:	n/a
8	chr16:34741304-34741354	MCF10A-Er-Src	breast:	n/a
9	chr16:34716002-34716052	HEEpiC	esophagus:	n/a
10	chr16:34737523-34737573	RPTEC	kidney:	n/a
11	chr16:34587307-34587357	SKMC	muscle:	n/a
12	chr16:34587307-34587357	SK-N-SH_RA	brain:	n/a
13	chr16:34660044-34660094	SKMC	muscle:	n/a
14	chr16:34741304-34741354	SK-N-SH_RA	brain:	n/a
15	chr16:34778087-34778137	SK-N-SH_RA	brain:	n/a
16	chr16:34740585-34740635	AG04449	skin:	fetal
17	chr16:34659771-34659821	HAEpiC	amniotic membrane:	n/a
18	chr16:34648842-34648892	GM19239	blood:	n/a
19	chr16:34648955-34649005	HepG2	liver:	n/a
20	chr16:34659771-34659821	NHBE	bronchial:	n/a
21	chr16:34760531-34760581	LNCaP	prostate:	n/a
22	chr16:34777963-34778013	NH-A	brain:	n/a
23	chr16:34663929-34663979	NHDF-neo	bronchial:	n/a
24	chr16:34659771-34659821	PFSK-1	brain:	n/a
25	chr16:34737523-34737573	A549	lung:	n/a
26	chr16:34760531-34760581	SK-N-SH_RA	brain:	n/a
27	chr16:34648842-34648892	PANC-1	pancreas:	n/a
28	chr16:34726856-34726906	MCF-7	breast:	n/a
29	chr16:34596941-34596991	GM19239	blood:	n/a
30	chr16:34648842-34648892	SK-N-SH_RA	brain:	n/a
31	chr16:34659771-34659821	AoSMC	blood vessel:	n/a
32	chr16:34712713-34712763	AG09319	gingival:	n/a
33	chr16:34712713-34712763	GM12878	blood:	n/a
34	chr16:34663929-34663979	BJ	skin:	n/a
35	chr16:34625446-34625496	NH-A	brain:	n/a
36	chr16:34587120-34587170	HIPEpiC	eye:	n/a
37	chr16:34663929-34663979	SKMC	muscle:	n/a
38	chr16:34726734-34726784	AG04450	lung:	fetal
39	chr16:34741493-34741543	NH-A	brain:	n/a
40	chr16:34596941-34596991	HIPEpiC	eye:	n/a
41	chr16:34777963-34778013	MCF-7	breast:	n/a
42	chr16:34660044-34660094	HRE	kidney:	n/a
43	chr16:34737523-34737573	GM12892	blood:	n/a
44	chr16:34578819-34578869	MCF-7	breast:	n/a
45	chr16:34740520-34740570	HIPEpiC	eye:	n/a
46	chr16:34587307-34587357	SK-N-MC	brain:	n/a
47	chr16:34583045-34583095	NH-A	brain:	n/a
48	chr16:34648842-34648892	IMR90	lung:	fetal
49	chr16:34659664-34659714	HCPEpiC	choroid plexus:	n/a
50	chr16:34598029-34598079	AG09319	gingival:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:34726782..34727382-chr16:34760283..34761051,3	MCF-7	breast:
2	chr15:57024256..57026523-chr16:34752267..34754460,2	MCF-7	breast:
3	chr16:34726782..34727382-chr16:34760283..34761051,3	MCF-7	breast:
4	chr16:34422640..34423667-chr16:34625487..34626782,3	MCF-7	breast:
5	chr15:56788863..56789371-chr16:34759996..34760825,2	MCF-7	breast:

(count:56 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LINC00273-28	chr16:34740963-34741308	NONHSAT142204
2	lnc-LINC00273-25	chr16:34712988-34713065	NONHSAT142191
3	lnc-LINC00273-27	chr16:34739459-34739785	NONHSAT142198
4	lnc-CTD-2144E22.5.1-6	chr16:34610877-34611020	ENSG00000259841.2
5	lnc-CTD-2144E22.5.1-6	chr16:34620250-34620420	NONHSAT142183
6	lnc-CTD-2144E22.5.1-31	chr16:34743025-34743136	NONHSAT142207
7	lnc-LINC00273-24	chr16:34641253-34641302	NONHSAT142186
8	lnc-CTD-2144E22.5.1-6	chr16:34615965-34616632	ENSG00000259841.2
9	lnc-LINC00273-25	chr16:34713636-34713735	NONHSAT142191
10	lnc-CTD-2144E22.5.1-31	chr16:34751386-34751515	NONHSAT142207
11	lnc-LINC00273-7	chr16:34729913-34729959	ENSG00000261445.1
12	lnc-CTD-2144E22.5.1-6	chr16:34614340-34614458	ENSG00000259841.2
13	lnc-LINC00273-22	chr16:34571082-34571260	NONHSAT142179
14	lnc-LINC00273-7	chr16:34728125-34728568	ENSG00000261445.1
15	lnc-LINC00273-22	chr16:34569648-34570147	NONHSAT142179
16	lnc-CTD-2144E22.5.1-6	chr16:34612943-34613184	ENSG00000259841.2
17	lnc-CTD-2144E22.5.1-31	chr16:34756490-34756676	NONHSAT142207
18	lnc-LINC00273-22	chr16:34570437-34570514	NONHSAT142179
19	lnc-LINC00273-22	chr16:34570743-34570817	NONHSAT142179
20	lnc-LINC00273-25	chr16:34713636-34713810	NONHSAT142192
21	lnc-LINC00273-27	chr16:34739464-34739785	ENSG00000260857.2
22	lnc-LINC00273-25	chr16:34713293-34713362	NONHSAT142192
23	lnc-LINC00273-25	chr16:34712988-34713065	NONHSAT142192
24	lnc-LINC00273-25	chr16:34714529-34714852	NONHSAT142191
25	lnc-CTD-2144E22.5.1-6	chr16:34616840-34616969	ENSG00000259841.2
26	lnc-CTD-2144E22.5.1-6	chr16:34612943-34613184	NONHSAT142183
27	lnc-CTD-2144E22.5.1-6	chr16:34624074-34624955	ENSG00000259841.2
28	lnc-LINC00273-27	chr16:34740697-34740833	ENSG00000260857.2
29	lnc-CTD-2144E22.5.1-6	chr16:34597783-34597899	ENSG00000259841.2
30	lnc-LINC00273-27	chr16:34740697-34740840	NONHSAT142198
31	lnc-CTD-2144E22.5.1-29	chr16:34723608-34724583	NONHSAT142194
32	lnc-LINC00273-23	chr16:34618515-34618930	NONHSAT142185
33	lnc-CTD-2144E22.5.1-6	chr16:34620250-34620420	ENSG00000259841.2
34	lnc-CTD-2144E22.5.1-6	chr16:34610877-34611020	NONHSAT142183
35	lnc-LINC00273-24	chr16:34640930-34641001	NONHSAT142186
36	lnc-LINC00273-8	chr16:34766012-34766124	XLOC_011927
37	lnc-CTD-2144E22.5.1-6	chr16:34597787-34597899	NONHSAT142183
38	lnc-LINC00273-24	chr16:34641562-34641720	NONHSAT142186
39	lnc-LINC00273-23	chr16:34619259-34619457	NONHSAT142185
40	lnc-CTD-2144E22.5.1-6	chr16:34616795-34616837	ENSG00000259841.2
41	lnc-CTD-2144E22.5.1-6	chr16:34612943-34613184	ENSG00000259841.2
42	lnc-LINC00273-25	chr16:34712350-34712699	NONHSAT142191
43	lnc-CTD-2144E22.5.1-6	chr16:34614340-34614458	NONHSAT142183
44	lnc-CTD-2144E22.5.1-6	chr16:34616795-34616969	NONHSAT142183
45	lnc-LINC00273-8	chr16:34765218-34765705	XLOC_011927
46	lnc-CTD-2144E22.5.1-24	chr16:34581756-34582668	NONHSAT142180
47	lnc-LINC00273-24	chr16:34640118-34640617	NONHSAT142186
48	lnc-LINC00273-7	chr16:34730748-34730828	ENSG00000261445.1
49	lnc-CTD-2144E22.5.1-6	chr16:34614340-34614458	ENSG00000259841.2
50	lnc-CTD-2144E22.5.1-31	chr16:34758333-34758358	NONHSAT142207

No data

Variant related genes	Relation type
RARRES2P9	TF binding region
ENSG00000259836	TF binding region
ENSG00000269622	TF binding region
ENSG00000260427	TF binding region
ENSG00000260341	TF binding region
ENSG00000260291	TF binding region
ENSG00000261299	TF binding region
ENSG00000260994	TF binding region
ENSG00000260598	TF binding region
ENSG00000261733	TF binding region
ENSG00000260857	TF binding region
ENSG00000261445	TF binding region
AGGF1P4	TF binding region
ENSG00000261350	TF binding region
ENSG00000260153	TF binding region
ENSG00000214581	TF binding region
ENSG00000259841	TF binding region
RARRES2P8	TF binding region
ENSG00000261711	TF binding region
RARRES2P7	TF binding region
ENSG00000260480	TF binding region
ENSG00000260680	TF binding region
ENSG00000260846	TF binding region
RARRES2P9	CpG island
ENSG00000259836	CpG island
ENSG00000269622	CpG island
ENSG00000260427	CpG island
ENSG00000260341	CpG island
ENSG00000260291	CpG island
ENSG00000261299	CpG island
ENSG00000260994	CpG island
ENSG00000260598	CpG island
ENSG00000261733	CpG island
ENSG00000260857	CpG island
ENSG00000261445	CpG island
AGGF1P4	CpG island
ENSG00000261350	CpG island
ENSG00000260153	CpG island
ENSG00000214581	CpG island
ENSG00000259841	CpG island
RARRES2P8	CpG island
ENSG00000261711	CpG island
RARRES2P7	CpG island
ENSG00000260480	CpG island
ENSG00000260680	CpG island
ENSG00000260846	CpG island
ENSG00000137871	chromatin interactions
ZNF451	miRNA target sites
ZNF407	miRNA target sites

Extended variants
information (count: 5072 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:5072 , 50 per page) page: 1 2 3 4 5 6 7 ... 102

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs375198579	chr16:34531217-34531218	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs539498779	chr16:34531252-34531253	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs34624501	chr16:34531264-34531265	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs545460567	chr16:34531298-34531299	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs557722773	chr16:34531352-34531353	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs140733809	chr16:34531360-34531361	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs187741701	chr16:34531371-34531372	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs568293150	chr16:34531403-34531404	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs555559826	chr16:34531425-34531426	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs372541992	chr16:34531454-34531455	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs528203221	chr16:34531567-34531568	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs78288843	chr16:34531592-34531593	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs552819127	chr16:34531602-34531603	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs577663863	chr16:34531607-34531608	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs190971085	chr16:34531629-34531630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs563233922	chr16:34531635-34531636	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs530828011	chr16:34531699-34531700	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs542908986	chr16:34531737-34531738	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs561150704	chr16:34531760-34531761	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs528305256	chr16:34531766-34531767	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs183125772	chr16:34531791-34531792	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs565237741	chr16:34531792-34531793	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs117286591	chr16:34531810-34531811	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs140397649	chr16:34531811-34531812	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs188361730	chr16:34531913-34531914	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs71378663	chr16:34532030-34532031	Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs369355067	chr16:34532112-34532113	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs569689374	chr16:34532148-34532149	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs529588842	chr16:34532149-34532150	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs147020496	chr16:34532183-34532184	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs192589416	chr16:34532186-34532187	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs184579254	chr16:34532259-34532260	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs114542560	chr16:34532270-34532271	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs113825754	chr16:34532274-34532275	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs569433145	chr16:34532309-34532310	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs187350765	chr16:34532322-34532323	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs577673344	chr16:34532344-34532345	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs142198673	chr16:34532398-34532399	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs557012035	chr16:34532438-34532439	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs575346225	chr16:34532473-34532474	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs145855857	chr16:34532555-34532556	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs113828332	chr16:34532576-34532577	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs561076743	chr16:34532586-34532587	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs372873300	chr16:34532601-34532602	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs573085430	chr16:34532648-34532649	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs540064764	chr16:34532658-34532659	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs138739445	chr16:34532669-34532670	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs112333067	chr16:34532723-34532724	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs551424340	chr16:34532768-34532769	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs563423742	chr16:34532795-34532796	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Autism	22566537	CNVD
Intellectual disability	22566537	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	22958593	CNVD
Ductal carcinoma	22052326	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	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 lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Benign familial neonatal-infantile seizures	21060786	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Cancer	21183584	CNVD
Disorders of sex development	21048976	CNVD
Low-grade fibromyxoid sarcoma	21536545	CNVD
Breast cancer	21045282	CNVD
Neuroblastoma	20406844	CNVD
Autism	19050728	CNVD
Epilepsy	20923578	CNVD
Psychiatric disorder	19050728	CNVD
Schizophrenia	19348701	CNVD
Attention deficit hyperactivity disorder	19097825	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	19571808	CNVD
Breast cancer	20409316	CNVD
Severe combined immunodeficiency	19097825	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Autism	18522746	CNVD
Wilms tumour	21544195	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	21364760	CNVD
Renal cell carcinoma	18194544	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21509527	CNVD
Schizophrenia	20967226	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD
Bipolar disorder	19214233	CNVD
early-passage human iPS cells	21368824	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Rett syndrome	21593744	CNVD
Myelofibrosis	22110671	CNVD
Autism	19287141	CNVD
Prostate cancer	18632612	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Autism	18414403	CNVD

Chromatin state (count:159 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:34531200-34534000	Enhancers	HMEC	breast
2	chr16:34531400-34534200	Enhancers	NHEK	skin
3	chr16:34531800-34532400	Active TSS	Fetal Heart	heart
4	chr16:34533800-34534000	Enhancers	Esophagus	oesophagus
5	chr16:34534200-34538800	Weak transcription	NHEK	skin
6	chr16:34535000-34537200	Weak transcription	Esophagus	oesophagus
7	chr16:34537000-34537400	ZNF genes & repeats	Fetal Heart	heart
8	chr16:34537200-34537400	Enhancers	Esophagus	oesophagus
9	chr16:34537400-34542200	Weak transcription	Esophagus	oesophagus
10	chr16:34538000-34538800	Active TSS	Fetal Heart	heart
11	chr16:34538600-34544000	Enhancers	HMEC	breast
12	chr16:34538800-34539600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
13	chr16:34538800-34543800	Enhancers	NHEK	skin
14	chr16:34539400-34539800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr16:34539800-34540200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr16:34540200-34540400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr16:34540400-34542800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr16:34542200-34543000	Enhancers	Esophagus	oesophagus
19	chr16:34542200-34546800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
20	chr16:34542800-34543000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr16:34542800-34543600	Enhancers	Breast Myoepithelial Primary Cells	Breast
22	chr16:34543000-34543400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr16:34543200-34544000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr16:34543400-34543800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr16:34543600-34543800	Enhancers	Esophagus	oesophagus
26	chr16:34545200-34552000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
27	chr16:34545400-34546800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr16:34545400-34552000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
29	chr16:34546200-34546400	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
30	chr16:34549000-34549200	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
31	chr16:34550000-34550200	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
32	chr16:34553800-34554800	Enhancers	Brain Hippocampus Middle	brain
33	chr16:34554200-34554600	Enhancers	Brain Angular Gyrus	brain
34	chr16:34554200-34554600	Enhancers	Brain Cingulate Gyrus	brain
35	chr16:34554200-34554600	Enhancers	Brain Substantia Nigra	brain
36	chr16:34562400-34562800	Active TSS	Fetal Heart	heart
37	chr16:34571600-34577800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
38	chr16:34578400-34579200	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr16:34578600-34579000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
40	chr16:34578800-34579000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr16:34578800-34579200	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr16:34586600-34587000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
43	chr16:34586600-34587000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr16:34586600-34587200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
45	chr16:34586600-34587200	Active TSS	Brain Cingulate Gyrus	brain
46	chr16:34586600-34587400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
47	chr16:34586800-34587000	ZNF genes & repeats	Pancreas	Pancrea
48	chr16:34586800-34587200	Active TSS	Brain Substantia Nigra	brain
49	chr16:34586800-34587200	ZNF genes & repeats	Esophagus	oesophagus
50	chr16:34587000-34587200	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived

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