Variant report

Variant	nsv917579
Chromosome Location	chr16:34427599-34727491
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1290)
CpG islands
(count:2748)
Chromatin interactive
region (count:3)
LncRNA
region (count:55)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1290 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr16:34625774-34626005	K562	blood:	n/a	n/a
2	ATF1	chr16:34573796-34574082	K562	blood:	n/a	n/a
3	ATF1	chr16:34715569-34715609	K562	blood:	n/a	n/a
4	ATF1	chr16:34486728-34487212	K562	blood:	n/a	n/a
5	ATF1	chr16:34643912-34644196	K562	blood:	n/a	n/a
6	ATF1	chr16:34574452-34574460	K562	blood:	n/a	n/a
7	ATF1	chr16:34589373-34589390	K562	blood:	n/a	n/a
8	BATF	chr16:34539887-34540221	GM12878	blood:	n/a	chr16:34540044-34540055
9	BATF	chr16:34539865-34540180	GM12878	blood:	n/a	chr16:34540044-34540055
10	BATF	chr16:34536693-34536965	GM12878	blood:	n/a	chr16:34536834-34536845
11	BHLHE40	chr16:34721874-34721912	GM12878	blood:	n/a	n/a
12	BHLHE40	chr16:34625401-34626021	K562	blood:	n/a	n/a
13	BHLHE40	chr16:34647001-34647022	GM12878	blood:	n/a	n/a
14	BHLHE40	chr16:34726730-34726951	K562	blood:	n/a	chr16:34726896-34726912
15	BHLHE40	chr16:34429795-34429892	K562	blood:	n/a	chr16:34429875-34429891
16	BHLHE40	chr16:34598011-34598017	K562	blood:	n/a	n/a
17	BHLHE40	chr16:34625806-34626006	GM12878	blood:	n/a	n/a
18	BRCA1	chr16:34666402-34666616	H1-hESC	embryonic stem cell:	n/a	n/a
19	BRCA1	chr16:34666658-34666728	GM12878	blood:	n/a	n/a
20	CBX3	chr16:34625799-34625988	K562	blood:	n/a	n/a
21	CEBPB	chr16:34539206-34539440	A549	lung:	n/a	n/a
22	CEBPB	chr16:34486702-34487146	IMR90	lung:	n/a	chr16:34486713-34486730
23	CEBPB	chr16:34637662-34637759	A549	lung:	n/a	chr16:34637709-34637720
24	CEBPB	chr16:34600114-34600449	MCF-7	breast:	n/a	chr16:34600335-34600346
25	CEBPB	chr16:34643905-34644193	A549	lung:	n/a	n/a
26	CEBPB	chr16:34605882-34606100	HepG2	liver:	n/a	n/a
27	CEBPB	chr16:34540547-34540747	K562	blood:	n/a	n/a
28	CEBPB	chr16:34535207-34535347	HepG2	liver:	n/a	n/a
29	CEBPB	chr16:34486708-34487148	A549	lung:	n/a	chr16:34486713-34486730
30	CEBPB	chr16:34542362-34542582	HepG2	liver:	n/a	n/a
31	CEBPB	chr16:34486734-34487193	K562	blood:	n/a	n/a
32	CEBPB	chr16:34599907-34600526	IMR90	lung:	n/a	chr16:34600335-34600346
33	CEBPB	chr16:34715384-34715712	HepG2	liver:	n/a	n/a
34	CEBPB	chr16:34603901-34604333	A549	lung:	n/a	n/a
35	CEBPB	chr16:34540417-34540828	HepG2	liver:	n/a	n/a
36	CEBPB	chr16:34632715-34632941	HepG2	liver:	n/a	n/a
37	CEBPB	chr16:34598584-34598949	HepG2	liver:	n/a	n/a
38	CEBPB	chr16:34449685-34450030	K562	blood:	n/a	n/a
39	CEBPB	chr16:34532887-34533747	HepG2	liver:	n/a	chr16:34533406-34533417
40	CEBPB	chr16:34611205-34611346	A549	lung:	n/a	chr16:34611274-34611285
41	CEBPB	chr16:34603883-34604326	HepG2	liver:	n/a	n/a
42	CEBPB	chr16:34536231-34536434	A549	lung:	n/a	n/a
43	CEBPB	chr16:34598745-34598792	K562	blood:	n/a	n/a
44	CEBPB	chr16:34514068-34514216	HepG2	liver:	n/a	n/a
45	CEBPB	chr16:34533242-34533527	Hela-S3	cervix:	n/a	chr16:34533406-34533417
46	CEBPB	chr16:34662346-34662546	IMR90	lung:	n/a	n/a
47	CEBPB	chr16:34683500-34683711	A549	lung:	n/a	chr16:34683618-34683629
48	CEBPB	chr16:34643966-34644271	IMR90	lung:	n/a	n/a
49	CEBPB	chr16:34600193-34600428	K562	blood:	n/a	chr16:34600335-34600346
50	CEBPB	chr16:34643934-34644258	K562	blood:	n/a	n/a

(count:2748 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:34712713-34712763	ECC-1	luminal epithelium:	n/a
2	chr16:34579002-34579052	NHDF-neo	bronchial:	n/a
3	chr16:34716002-34716052	CMK	blood:	n/a
4	chr16:34712713-34712763	ECC-1	luminal epithelium:	n/a
5	chr16:34579002-34579052	NHDF-neo	bronchial:	n/a
6	chr16:34716002-34716052	CMK	blood:	n/a
7	chr16:34648842-34648892	GM12892	blood:	n/a
8	chr16:34648842-34648892	Hela-S3	cervix:	n/a
9	chr16:34726856-34726906	NB4	blood:	n/a
10	chr16:34490033-34490083	BJ	skin:	n/a
11	chr16:34429930-34429980	HIPEpiC	eye:	n/a
12	chr16:34587307-34587357	BE2_C	brain:	n/a
13	chr16:34431003-34431053	ProgFib	skin:	n/a
14	chr16:34596941-34596991	SAEC	small airway:	n/a
15	chr16:34445785-34445835	BJ	skin:	n/a
16	chr16:34578819-34578869	HepG2	liver:	n/a
17	chr16:34586837-34586887	ProgFib	skin:	n/a
18	chr16:34429609-34429659	K562	blood:	n/a
19	chr16:34716002-34716052	PrEC	prostate:	n/a
20	chr16:34441787-34441837	PANC-1	pancreas:	n/a
21	chr16:34442090-34442140	HPAEpiC	pulmonary alveolar:	n/a
22	chr16:34442602-34442652	HUVEC	blood vessel:	n/a
23	chr16:34456419-34456469	Hepatocyte	liver:	n/a
24	chr16:34663929-34663979	HNPCEpiC	eye:	n/a
25	chr16:34586837-34586887	HEEpiC	esophagus:	n/a
26	chr16:34648842-34648892	PANC-1	pancreas:	n/a
27	chr16:34586837-34586887	HCM	heart:	n/a
28	chr16:34578819-34578869	HUVEC	blood vessel:	n/a
29	chr16:34596583-34596633	HEEpiC	esophagus:	n/a
30	chr16:34583045-34583095	NB4	blood:	n/a
31	chr16:34596583-34596633	IMR90	lung:	fetal
32	chr16:34489904-34489954	HRE	kidney:	n/a
33	chr16:34648955-34649005	SAEC	small airway:	n/a
34	chr16:34726856-34726906	NHBE	bronchial:	n/a
35	chr16:34659664-34659714	HNPCEpiC	eye:	n/a
36	chr16:34490033-34490083	A549	lung:	n/a
37	chr16:34430905-34430955	HMEC	breast:	n/a
38	chr16:34726856-34726906	SKMC	muscle:	n/a
39	chr16:34445785-34445835	Hepatocyte	liver:	n/a
40	chr16:34442602-34442652	NHDF-neo	bronchial:	n/a
41	chr16:34726856-34726906	SK-N-SH_RA	brain:	n/a
42	chr16:34442090-34442140	HCM	heart:	n/a
43	chr16:34596941-34596991	BJ	skin:	n/a
44	chr16:34442090-34442140	AG04449	skin:	fetal
45	chr16:34583045-34583095	HUVEC	blood vessel:	n/a
46	chr16:34579002-34579052	HMEC	breast:	n/a
47	chr16:34428061-34428111	LNCaP	prostate:	n/a
48	chr16:34431003-34431053	H1-hESC	embryonic stem cell:	embryo
49	chr16:34430078-34430128	A549	lung:	n/a
50	chr16:34439811-34439861	HCM	heart:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:34422640..34423667-chr16:34625487..34626782,3	MCF-7	breast:
2	chr16:34726782..34727382-chr16:34760283..34761051,3	MCF-7	breast:
3	chr16:34429328..34431681-chr16:34466203..34469132,2	K562	blood:

(count:55 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTD-2144E22.5.1-6	chr16:34597902-34598201	ENSG00000259841.2
2	lnc-CTD-2144E22.5.1-6	chr16:34612943-34613184	ENSG00000259841.2
3	lnc-LINC00273-25	chr16:34713293-34713362	NONHSAT142192
4	lnc-CTD-2144E22.5.1-5	chr16:34518127-34518517	ENSG00000260958.2
5	lnc-LINC00273-24	chr16:34640930-34641001	NONHSAT142186
6	lnc-CTD-2144E22.5.1-5	chr16:34487252-34487411	NONHSAT142170
7	lnc-CTD-2144E22.5.1-5	chr16:34487609-34488020	ENSG00000260958.2
8	lnc-LINC00273-24	chr16:34641562-34641720	NONHSAT142186
9	lnc-CTD-2144E22.5.1-6	chr16:34620250-34620420	ENSG00000259841.2
10	lnc-CTD-2144E22.5.1-6	chr16:34616795-34616969	NONHSAT142183
11	lnc-CTD-2144E22.5.1-6	chr16:34625678-34626084	NONHSAT142183
12	lnc-CTD-2144E22.5.1-6	chr16:34616840-34616969	ENSG00000259841.2
13	lnc-CTD-2144E22.5.1-6	chr16:34597783-34597899	ENSG00000259841.2
14	lnc-CTD-2144E22.5.1-5	chr16:34482858-34483251	NONHSAT142170
15	lnc-CTD-2144E22.5.1-6	chr16:34624074-34624955	ENSG00000259841.2
16	lnc-LINC00273-22	chr16:34571082-34571260	NONHSAT142179
17	lnc-LINC00273-25	chr16:34713636-34713810	NONHSAT142192
18	lnc-CTD-2144E22.5.1-5	chr16:34483054-34483172	ENSG00000260958.2
19	lnc-CTD-2144E22.5.1-6	chr16:34620250-34620420	NONHSAT142183
20	lnc-CTD-2144E22.5.1-18	chr16:34493001-34494000	NONHSAT142176
21	lnc-CTD-2144E22.5.1-4	chr16:34477709-34479085	NONHSAT142171
22	lnc-LINC00273-25	chr16:34713636-34713735	NONHSAT142191
23	lnc-LINC00273-18	chr16:34455954-34456419	NONHSAT142168
24	lnc-CTD-2144E22.5.1-6	chr16:34612943-34613184	NONHSAT142183
25	lnc-LINC00273-22	chr16:34569648-34570147	NONHSAT142179
26	lnc-CTD-2144E22.5.1-6	chr16:34615965-34616632	ENSG00000259841.2
27	lnc-CTD-2144E22.5.1-6	chr16:34614340-34614458	NONHSAT142183
28	lnc-LINC00273-24	chr16:34641253-34641302	NONHSAT142186
29	lnc-CTD-2144E22.5.1-6	chr16:34614340-34614458	ENSG00000259841.2
30	lnc-CTD-2144E22.5.1-6	chr16:34617082-34617226	ENSG00000259841.2
31	lnc-CTD-2144E22.5.1-5	chr16:34442330-34442392	ENSG00000260958.2
32	lnc-CTD-2144E22.5.1-5	chr16:34487252-34487506	ENSG00000260958.2
33	lnc-CTD-2144E22.5.1-6	chr16:34612943-34613184	ENSG00000259841.2
34	lnc-CTD-2144E22.5.1-6	chr16:34610877-34611020	ENSG00000259841.2
35	lnc-LINC00273-23	chr16:34619259-34619457	NONHSAT142185
36	lnc-LINC00273-22	chr16:34570743-34570817	NONHSAT142179
37	lnc-CTD-2144E22.5.1-4	chr16:34477761-34477848	XLOC_011699
38	lnc-LINC00273-22	chr16:34570437-34570514	NONHSAT142179
39	lnc-CTD-2144E22.5.1-24	chr16:34581756-34582668	NONHSAT142180
40	lnc-CTD-2144E22.5.1-6	chr16:34616795-34616837	ENSG00000259841.2
41	lnc-CTD-2144E22.5.1-4	chr16:34478641-34479038	XLOC_011699
42	lnc-CTD-2144E22.5.1-5	chr16:34471671-34474425	NONHSAT142170
43	lnc-LINC00273-24	chr16:34640118-34640617	NONHSAT142186
44	lnc-LINC00273-25	chr16:34712988-34713065	NONHSAT142191
45	lnc-CTD-2144E22.5.1-17	chr16:34427706-34428105	NONHSAT142163
46	lnc-CTD-2144E22.5.1-6	chr16:34610877-34611020	ENSG00000259841.2
47	lnc-LINC00273-23	chr16:34618515-34618930	NONHSAT142185
48	lnc-LINC00273-25	chr16:34714529-34714852	NONHSAT142191
49	lnc-LINC00273-25	chr16:34712988-34713065	NONHSAT142192
50	lnc-CTD-2144E22.5.1-6	chr16:34610877-34611020	NONHSAT142183

No data

Variant related genes	Relation type
ENSG00000260073	TF binding region
RARRES2P9	TF binding region
ENSG00000259836	TF binding region
ENSG00000259897	TF binding region
ENSG00000221532	TF binding region
ENSG00000261752	TF binding region
ENSG00000264479	TF binding region
ENSG00000260427	TF binding region
ENSG00000260341	TF binding region
ENSG00000261398	TF binding region
ENSG00000260291	TF binding region
ENSG00000261299	TF binding region
ENSG00000260598	TF binding region
AGGF1P4	TF binding region
ENSG00000260958	TF binding region
ENSG00000261350	TF binding region
ENSG00000260153	TF binding region
ENSG00000214581	TF binding region
RARRES2P5	TF binding region
ENSG00000260590	TF binding region
ENSG00000261274	TF binding region
ENSG00000259841	TF binding region
ENSG00000261711	TF binding region
RARRES2P7	TF binding region
RARRES2P6	TF binding region
ENSG00000260480	TF binding region
FGFR3P5	TF binding region
ENSG00000260680	TF binding region
ENSG00000260846	TF binding region
ENSG00000260073	CpG island
RARRES2P9	CpG island
ENSG00000259836	CpG island
ENSG00000259897	CpG island
ENSG00000221532	CpG island
ENSG00000261752	CpG island
ENSG00000264479	CpG island
ENSG00000260427	CpG island
ENSG00000260341	CpG island
ENSG00000261398	CpG island
ENSG00000260291	CpG island
ENSG00000261299	CpG island
ENSG00000260598	CpG island
AGGF1P4	CpG island
ENSG00000260958	CpG island
ENSG00000261350	CpG island
ENSG00000260153	CpG island
ENSG00000214581	CpG island
RARRES2P5	CpG island
ENSG00000260590	CpG island
ENSG00000261274	CpG island
ENSG00000259841	CpG island
ENSG00000261711	CpG island
RARRES2P7	CpG island
RARRES2P6	CpG island
ENSG00000260480	CpG island
FGFR3P5	CpG island
ENSG00000260680	CpG island
ENSG00000260846	CpG island
ENSG00000260073	chromatin interactions
ENSG00000261398	chromatin interactions

Extended variants
information (count: 5255 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:5255 , 50 per page) page: 1 2 3 4 5 6 7 ... 106

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs35261086	chr16:34427712-34427713	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs575761107	chr16:34427731-34427732	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs542753604	chr16:34427788-34427789	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs560919812	chr16:34427792-34427793	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs528193317	chr16:34427805-34427806	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs189662031	chr16:34427813-34427814	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs564883064	chr16:34427849-34427850	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs143454295	chr16:34427891-34427892	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs550821761	chr16:34427893-34427894	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs375580376	chr16:34427910-34427911	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs207475859	chr16:34427996-34427997	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
12	rs568970991	chr16:34428028-34428029	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
13	rs148159706	chr16:34428059-34428060	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs142011298	chr16:34428062-34428063	Inactive region	CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
15	rs573450133	chr16:34428986-34428987	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
16	rs147476900	chr16:34428993-34428994	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
17	rs11149539	chr16:34429019-34429020	Inactive region	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs541699603	chr16:34429204-34429205	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs377751808	chr16:34429222-34429223	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs375285658	chr16:34429247-34429248	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs559937266	chr16:34429325-34429326	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs527441300	chr16:34429342-34429343	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs546783652	chr16:34429348-34429349	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs34283732	chr16:34429361-34429362	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs571760487	chr16:34429362-34429363	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs186827107	chr16:34429391-34429392	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs550989327	chr16:34429401-34429402	Bivalent/Poised TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs140012627	chr16:34429412-34429413	Bivalent/Poised TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs77881843	chr16:34429448-34429449	Bivalent/Poised TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs531762845	chr16:34429493-34429494	Bivalent/Poised TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs544175731	chr16:34429494-34429495	Bivalent/Poised TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs149553025	chr16:34429504-34429505	Bivalent/Poised TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs144244345	chr16:34429521-34429522	Bivalent/Poised TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs567077057	chr16:34429560-34429561	Bivalent/Poised TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs371879683	chr16:34429625-34429626	ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
36	rs558878844	chr16:34429652-34429653	ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
37	rs192700563	chr16:34429693-34429694	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs115423614	chr16:34429703-34429704	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs555768615	chr16:34429711-34429712	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs574065743	chr16:34429712-34429713	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs562484632	chr16:34429729-34429730	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs559969862	chr16:34429737-34429738	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs532923346	chr16:34429738-34429739	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs370938240	chr16:34429753-34429754	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs184921768	chr16:34429754-34429755	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs370931054	chr16:34429789-34429790	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs564112406	chr16:34429924-34429925	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs62059544	chr16:34429998-34429999	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs532669245	chr16:34430002-34430003	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs551070297	chr16:34430029-34430030	ZNF genes & repeats	TF binding region	1 gene(s)	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:155 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:34429200-34433000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
2	chr16:34429400-34429600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
3	chr16:34429400-34430400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr16:34432200-34433400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr16:34437400-34438400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr16:34438400-34441200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr16:34441200-34442800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr16:34441400-34442600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
9	chr16:34442000-34443200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
10	chr16:34442200-34443000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
11	chr16:34442200-34443000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr16:34442600-34442800	Active TSS	ES-I3 Cell Line	embryonic stem cell
13	chr16:34456000-34456800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr16:34456200-34456400	ZNF genes & repeats	Gastric	stomach
15	chr16:34456200-34456600	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr16:34465600-34466200	Active TSS	ES-I3 Cell Line	embryonic stem cell
17	chr16:34465600-34466200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
18	chr16:34466600-34472200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
19	chr16:34466800-34467000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr16:34466800-34469400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr16:34467000-34468200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
22	chr16:34467000-34470200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr16:34468200-34469400	ZNF genes & repeats	Brain Germinal Matrix	brain
24	chr16:34474800-34476000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr16:34478600-34479000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
26	chr16:34480400-34481000	Enhancers	Adipose Nuclei	Adipose
27	chr16:34489600-34490400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
28	chr16:34489600-34490800	Active TSS	ES-I3 Cell Line	embryonic stem cell
29	chr16:34489800-34490200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
30	chr16:34492800-34493400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
31	chr16:34505000-34507800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
32	chr16:34517800-34518400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
33	chr16:34531200-34534000	Enhancers	HMEC	breast
34	chr16:34531400-34534200	Enhancers	NHEK	skin
35	chr16:34531800-34532400	Active TSS	Fetal Heart	heart
36	chr16:34533800-34534000	Enhancers	Esophagus	oesophagus
37	chr16:34534200-34538800	Weak transcription	NHEK	skin
38	chr16:34535000-34537200	Weak transcription	Esophagus	oesophagus
39	chr16:34537000-34537400	ZNF genes & repeats	Fetal Heart	heart
40	chr16:34537200-34537400	Enhancers	Esophagus	oesophagus
41	chr16:34537400-34542200	Weak transcription	Esophagus	oesophagus
42	chr16:34538000-34538800	Active TSS	Fetal Heart	heart
43	chr16:34538600-34544000	Enhancers	HMEC	breast
44	chr16:34538800-34539600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
45	chr16:34538800-34543800	Enhancers	NHEK	skin
46	chr16:34539400-34539800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr16:34539800-34540200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr16:34540200-34540400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr16:34540400-34542800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr16:34542200-34543000	Enhancers	Esophagus	oesophagus

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