Variant report

Variant	nsv431454
Chromosome Location	chr16:34321463-34790434
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1953)
CpG islands
(count:5129)
Chromatin interactive
region (count:7)
LncRNA
region (count:74)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1953 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr16:34765990-34765998	K562	blood:	n/a	n/a
2	ATF1	chr16:34787094-34787358	K562	blood:	n/a	n/a
3	ATF1	chr16:34573796-34574082	K562	blood:	n/a	n/a
4	ATF1	chr16:34768061-34768441	K562	blood:	n/a	n/a
5	ATF1	chr16:34574452-34574460	K562	blood:	n/a	n/a
6	ATF1	chr16:34589373-34589390	K562	blood:	n/a	n/a
7	ATF1	chr16:34486728-34487212	K562	blood:	n/a	n/a
8	ATF1	chr16:34643912-34644196	K562	blood:	n/a	n/a
9	ATF1	chr16:34715569-34715609	K562	blood:	n/a	n/a
10	ATF1	chr16:34625774-34626005	K562	blood:	n/a	n/a
11	BATF	chr16:34536693-34536965	GM12878	blood:	n/a	chr16:34536834-34536845
12	BATF	chr16:34731793-34732055	GM12878	blood:	n/a	chr16:34731883-34731894 chr16:34731915-34731926
13	BATF	chr16:34539865-34540180	GM12878	blood:	n/a	chr16:34540044-34540055
14	BATF	chr16:34731803-34731989	GM12878	blood:	n/a	chr16:34731883-34731894 chr16:34731915-34731926
15	BATF	chr16:34539887-34540221	GM12878	blood:	n/a	chr16:34540044-34540055
16	BHLHE40	chr16:34726730-34726951	K562	blood:	n/a	chr16:34726896-34726912
17	BHLHE40	chr16:34625401-34626021	K562	blood:	n/a	n/a
18	BHLHE40	chr16:34647001-34647022	GM12878	blood:	n/a	n/a
19	BHLHE40	chr16:34745103-34745432	GM12878	blood:	n/a	chr16:34745242-34745251
20	BHLHE40	chr16:34598011-34598017	K562	blood:	n/a	n/a
21	BHLHE40	chr16:34429795-34429892	K562	blood:	n/a	chr16:34429875-34429891
22	BHLHE40	chr16:34625806-34626006	GM12878	blood:	n/a	n/a
23	BHLHE40	chr16:34741044-34741235	K562	blood:	n/a	n/a
24	BHLHE40	chr16:34745112-34745352	K562	blood:	n/a	chr16:34745242-34745251
25	BHLHE40	chr16:34740335-34740524	K562	blood:	n/a	n/a
26	BHLHE40	chr16:34732021-34732023	GM12878	blood:	n/a	n/a
27	BHLHE40	chr16:34721874-34721912	GM12878	blood:	n/a	n/a
28	BRCA1	chr16:34666402-34666616	H1-hESC	embryonic stem cell:	n/a	n/a
29	BRCA1	chr16:34666658-34666728	GM12878	blood:	n/a	n/a
30	CBX3	chr16:34625799-34625988	K562	blood:	n/a	n/a
31	CEBPB	chr16:34715384-34715712	HepG2	liver:	n/a	n/a
32	CEBPB	chr16:34536217-34536514	HepG2	liver:	n/a	n/a
33	CEBPB	chr16:34600160-34600470	ECC-1	luminal epithelium:	n/a	chr16:34600335-34600346
34	CEBPB	chr16:34662346-34662546	IMR90	lung:	n/a	n/a
35	CEBPB	chr16:34532926-34533600	ECC-1	luminal epithelium:	n/a	chr16:34533406-34533417
36	CEBPB	chr16:34532934-34533739	IMR90	lung:	n/a	chr16:34533406-34533417
37	CEBPB	chr16:34533242-34533527	Hela-S3	cervix:	n/a	chr16:34533406-34533417
38	CEBPB	chr16:34637662-34637759	A549	lung:	n/a	chr16:34637709-34637720
39	CEBPB	chr16:34730704-34731069	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr16:34662373-34662658	HepG2	liver:	n/a	n/a
41	CEBPB	chr16:34369463-34369642	A549	lung:	n/a	chr16:34369584-34369595
42	CEBPB	chr16:34369427-34369724	ECC-1	luminal epithelium:	n/a	chr16:34369584-34369595
43	CEBPB	chr16:34537182-34537560	K562	blood:	n/a	n/a
44	CEBPB	chr16:34790370-34790445	IMR90	lung:	n/a	n/a
45	CEBPB	chr16:34573739-34574089	IMR90	lung:	n/a	chr16:34573875-34573886
46	CEBPB	chr16:34539206-34539440	A549	lung:	n/a	n/a
47	CEBPB	chr16:34730731-34731119	A549	lung:	n/a	n/a
48	CEBPB	chr16:34790349-34790522	HepG2	liver:	n/a	n/a
49	CEBPB	chr16:34539085-34539474	HepG2	liver:	n/a	n/a
50	CEBPB	chr16:34759185-34759725	HepG2	liver:	n/a	chr16:34759593-34759604 chr16:34759630-34759641 chr16:34759565-34759576

(count:5129 , 50 per page) page: 1 2 3 4 5 6 7 ... 103

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:34579002-34579052	HCM	heart:	n/a
2	chr16:34659771-34659821	PFSK-1	brain:	n/a
3	chr16:34586894-34586944	Caco-2	colon:	n/a
4	chr16:34456419-34456469	LNCaP	prostate:	n/a
5	chr16:34429930-34429980	HRCEpiC	kidney:	n/a
6	chr16:34579002-34579052	HCM	heart:	n/a
7	chr16:34659771-34659821	PFSK-1	brain:	n/a
8	chr16:34586894-34586944	Caco-2	colon:	n/a
9	chr16:34456419-34456469	LNCaP	prostate:	n/a
10	chr16:34429930-34429980	HRCEpiC	kidney:	n/a
11	chr16:34430905-34430955	MCF10A-Er-Src	breast:	n/a
12	chr16:34428061-34428111	SK-N-SH_RA	brain:	n/a
13	chr16:34408014-34408064	HPAEpiC	pulmonary alveolar:	n/a
14	chr16:34659664-34659714	SK-N-MC	brain:	n/a
15	chr16:34716002-34716052	AoSMC	blood vessel:	n/a
16	chr16:34405690-34405740	NHDF-neo	bronchial:	n/a
17	chr16:34586894-34586944	HCT-116	colon:	n/a
18	chr16:34378069-34378119	NT2-D1	testis:	n/a
19	chr16:34408014-34408064	HCT-116	colon:	n/a
20	chr16:34649152-34649202	RPTEC	kidney:	n/a
21	chr16:34375039-34375089	NT2-D1	testis:	n/a
22	chr16:34405690-34405740	PrEC	prostate:	n/a
23	chr16:34740520-34740570	H1-hESC	embryonic stem cell:	embryo
24	chr16:34405690-34405740	HepG2	liver:	n/a
25	chr16:34741251-34741301	HEEpiC	esophagus:	n/a
26	chr16:34777963-34778013	PFSK-1	brain:	n/a
27	chr16:34456429-34456479	HIPEpiC	eye:	n/a
28	chr16:34407918-34407968	GM12892	blood:	n/a
29	chr16:34578819-34578869	SK-N-SH	brain:	n/a
30	chr16:34737523-34737573	T-47D	breast:	n/a
31	chr16:34586837-34586887	Jurkat	blood:	n/a
32	chr16:34375039-34375089	PANC-1	pancreas:	n/a
33	chr16:34445785-34445835	Hepatocyte	liver:	n/a
34	chr16:34741966-34742016	K562	blood:	n/a
35	chr16:34578819-34578869	Caco-2	colon:	n/a
36	chr16:34443120-34443170	NH-A	brain:	n/a
37	chr16:34442373-34442423	AG09319	gingival:	n/a
38	chr16:34579002-34579052	HAEpiC	amniotic membrane:	n/a
39	chr16:34442373-34442423	MCF10A-Er-Src	breast:	n/a
40	chr16:34407918-34407968	PANC-1	pancreas:	n/a
41	chr16:34430078-34430128	AG04450	lung:	fetal
42	chr16:34659771-34659821	NT2-D1	testis:	n/a
43	chr16:34380215-34380265	MCF-7	breast:	n/a
44	chr16:34432979-34433029	Hepatocyte	liver:	n/a
45	chr16:34378069-34378119	HCPEpiC	choroid plexus:	n/a
46	chr16:34660044-34660094	BE2_C	brain:	n/a
47	chr16:34741251-34741301	NH-A	brain:	n/a
48	chr16:34578819-34578869	GM12878	blood:	n/a
49	chr16:34429609-34429659	SAEC	small airway:	n/a
50	chr16:34405690-34405740	ECC-1	luminal epithelium:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:34726782..34727382-chr16:34760283..34761051,3	MCF-7	breast:
2	chr16:34422640..34423667-chr16:34625487..34626782,3	MCF-7	breast:
3	chr15:57024256..57026523-chr16:34752267..34754460,2	MCF-7	breast:
4	chr16:34726782..34727382-chr16:34760283..34761051,3	MCF-7	breast:
5	chr15:56788863..56789371-chr16:34759996..34760825,2	MCF-7	breast:
6	chr16:34422640..34423667-chr16:34625487..34626782,3	MCF-7	breast:
7	chr16:34429328..34431681-chr16:34466203..34469132,2	K562	blood:

(count:74 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LINC00273-24	chr16:34641562-34641720	NONHSAT142186
2	lnc-CTD-2144E22.5.1-4	chr16:34478641-34479038	XLOC_011699
3	lnc-LINC00273-7	chr16:34730748-34730828	ENSG00000261445.1
4	lnc-LINC00273-22	chr16:34571082-34571260	NONHSAT142179
5	lnc-CTD-2144E22.5.1-6	chr16:34614340-34614458	NONHSAT142183
6	lnc-LINC00273-27	chr16:34740697-34740833	ENSG00000260857.2
7	lnc-CTD-2144E22.5.1-6	chr16:34614340-34614458	ENSG00000259841.2
8	lnc-LINC00273-25	chr16:34714529-34714852	NONHSAT142191
9	lnc-CTD-2144E22.5.1-32	chr16:34782288-34783200	NONHSAT142214
10	lnc-LINC00273-25	chr16:34713636-34713735	NONHSAT142191
11	lnc-LINC00273-25	chr16:34712350-34712699	NONHSAT142191
12	lnc-LINC00273-27	chr16:34739464-34739785	ENSG00000260857.2
13	lnc-LINC00273-7	chr16:34728125-34728568	ENSG00000261445.1
14	lnc-LINC00273-7	chr16:34729913-34729959	ENSG00000261445.1
15	lnc-CTD-2144E22.5.1-5	chr16:34482858-34483251	NONHSAT142170
16	lnc-LINC00273-8	chr16:34765218-34765705	XLOC_011927
17	lnc-CTD-2144E22.5.1-6	chr16:34612943-34613184	NONHSAT142183
18	lnc-CTD-2144E22.5.1-6	chr16:34612943-34613184	ENSG00000259841.2
19	lnc-CTD-2144E22.5.1-17	chr16:34427706-34428105	NONHSAT142163
20	lnc-LINC00273-22	chr16:34570437-34570514	NONHSAT142179
21	lnc-CTD-2144E22.5.1-6	chr16:34610877-34611020	NONHSAT142183
22	lnc-CTD-2144E22.5.1-5	chr16:34487609-34488020	ENSG00000260958.2
23	lnc-CTD-2144E22.5.1-6	chr16:34597783-34597899	ENSG00000259841.2
24	lnc-CTD-2144E22.5.1-5	chr16:34442330-34442392	ENSG00000260958.2
25	lnc-LINC00273-8	chr16:34766012-34766124	XLOC_011927
26	lnc-CTD-2144E22.5.1-6	chr16:34620250-34620420	NONHSAT142183
27	lnc-CTD-2144E22.5.1-6	chr16:34615965-34616632	ENSG00000259841.2
28	lnc-CTD-2144E22.5.1-31	chr16:34756490-34756676	NONHSAT142207
29	lnc-LINC00273-28	chr16:34740963-34741308	NONHSAT142204
30	lnc-LINC00273-25	chr16:34712988-34713065	NONHSAT142192
31	lnc-CTD-2144E22.5.1-5	chr16:34487252-34487411	NONHSAT142170
32	lnc-CTD-2144E22.5.1-6	chr16:34610877-34611020	ENSG00000259841.2
33	lnc-CTD-2144E22.5.1-6	chr16:34616795-34616837	ENSG00000259841.2
34	lnc-CTD-2144E22.5.1-5	chr16:34483054-34483172	ENSG00000260958.2
35	lnc-CTD-2144E22.5.1-6	chr16:34625678-34626084	NONHSAT142183
36	lnc-CTD-2144E22.5.1-5	chr16:34487252-34487506	ENSG00000260958.2
37	lnc-LINC00273-24	chr16:34640118-34640617	NONHSAT142186
38	lnc-CTD-2144E22.5.1-31	chr16:34743025-34743136	NONHSAT142207
39	lnc-CTD-2144E22.5.1-6	chr16:34617082-34617226	ENSG00000259841.2
40	lnc-LINC00273-18	chr16:34455954-34456419	NONHSAT142168
41	lnc-CTD-2144E22.5.1-31	chr16:34758333-34758358	NONHSAT142207
42	lnc-LINC00273-24	chr16:34640930-34641001	NONHSAT142186
43	lnc-LINC00273-22	chr16:34570743-34570817	NONHSAT142179
44	lnc-LINC00273-23	chr16:34619259-34619457	NONHSAT142185
45	lnc-LINC00273-25	chr16:34713636-34713810	NONHSAT142192
46	lnc-LINC00273-25	chr16:34713293-34713362	NONHSAT142192
47	lnc-LINC00273-27	chr16:34739472-34739785	NONHSAT142200
48	lnc-LINC00273-15	chr16:34383828-34384161	NONHSAT142158
49	lnc-CTD-2144E22.5.1-18	chr16:34493001-34494000	NONHSAT142176
50	lnc-CTD-2144E22.5.1-6	chr16:34616840-34616969	ENSG00000259841.2

No data

Variant related genes	Relation type
ENSG00000261510	TF binding region
UBE2MP1	TF binding region
ENSG00000260073	TF binding region
ENSG00000259836	TF binding region
ENSG00000259897	TF binding region
ENSG00000221532	TF binding region
ENSG00000260449	TF binding region
ENSG00000261752	TF binding region
ENSG00000261398	TF binding region
ENSG00000260291	TF binding region
ENSG00000261299	TF binding region
ENSG00000261733	TF binding region
ENSG00000260857	TF binding region
ENSG00000261445	TF binding region
AGGF1P4	TF binding region
ENSG00000261350	TF binding region
ENSG00000214581	TF binding region
RARRES2P5	TF binding region
ENSG00000260590	TF binding region
ENSG00000261274	TF binding region
RARRES2P7	TF binding region
RARRES2P6	TF binding region
ENSG00000260480	TF binding region
FGFR3P5	TF binding region
ENSG00000261836	TF binding region
SLC25A1P4	TF binding region
RARRES2P9	TF binding region
ENSG00000261046	TF binding region
ENSG00000264479	TF binding region
ENSG00000269622	TF binding region
ENSG00000260427	TF binding region
ENSG00000260341	TF binding region
ENSG00000260994	TF binding region
ENSG00000260598	TF binding region
ENSG00000260809	TF binding region
ENSG00000260958	TF binding region
ENSG00000260153	TF binding region
VN1R69P	TF binding region
VN1R68P	TF binding region
ENSG00000259841	TF binding region
RARRES2P8	TF binding region
ENSG00000261711	TF binding region
ENSG00000261800	TF binding region
ENSG00000260680	TF binding region
ENSG00000260846	TF binding region
ENSG00000261510	CpG island
UBE2MP1	CpG island
ENSG00000260073	CpG island
ENSG00000259836	CpG island
ENSG00000259897	CpG island
ENSG00000221532	CpG island
ENSG00000260449	CpG island
ENSG00000261752	CpG island
ENSG00000261398	CpG island
ENSG00000260291	CpG island
ENSG00000261299	CpG island
ENSG00000261733	CpG island
ENSG00000260857	CpG island
ENSG00000261445	CpG island
AGGF1P4	CpG island
ENSG00000261350	CpG island
ENSG00000214581	CpG island
RARRES2P5	CpG island
ENSG00000260590	CpG island
ENSG00000261274	CpG island
RARRES2P7	CpG island
RARRES2P6	CpG island
ENSG00000260480	CpG island
FGFR3P5	CpG island
ENSG00000261836	CpG island
SLC25A1P4	CpG island
RARRES2P9	CpG island
ENSG00000261046	CpG island
ENSG00000264479	CpG island
ENSG00000269622	CpG island
ENSG00000260427	CpG island
ENSG00000260341	CpG island
ENSG00000260994	CpG island
ENSG00000260598	CpG island
ENSG00000260809	CpG island
ENSG00000260958	CpG island
ENSG00000260153	CpG island
VN1R69P	CpG island
VN1R68P	CpG island
ENSG00000259841	CpG island
RARRES2P8	CpG island
ENSG00000261711	CpG island
ENSG00000261800	CpG island
ENSG00000260680	CpG island
ENSG00000260846	CpG island
ENSG00000260073	chromatin interactions
ENSG00000137871	chromatin interactions
ENSG00000261398	chromatin interactions
ZNF451	miRNA target sites
ZNF407	miRNA target sites

Extended variants
information (count: 7821 )
Associated
traits (count: 132 )

Variant overlapped rSNPs/rCNVs (count:7821 , 50 per page) page: 1 2 3 4 5 6 7 ... 157

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs186465342	chr16:34322812-34322813	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs554312382	chr16:34322859-34322860	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs112199501	chr16:34322863-34322864	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs113475216	chr16:34322870-34322871	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs558815713	chr16:34322876-34322877	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs576596367	chr16:34322968-34322969	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs191846125	chr16:34322971-34322972	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs369203506	chr16:34323083-34323084	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs576199655	chr16:34323085-34323086	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs575384182	chr16:34323119-34323120	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs542999573	chr16:34323139-34323140	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs182927905	chr16:34323159-34323160	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs528490892	chr16:34323222-34323223	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs546951338	chr16:34323272-34323273	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs527490178	chr16:34323294-34323295	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs538146945	chr16:34323311-34323312	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs146943612	chr16:34323333-34323334	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs370636494	chr16:34323338-34323339	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs35551339	chr16:34353009-34353010	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs201174557	chr16:34353015-34353016	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs567271385	chr16:34353016-34353017	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs542583217	chr16:34353025-34353026	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs116354745	chr16:34353026-34353027	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs180681273	chr16:34353052-34353053	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs551842065	chr16:34353070-34353071	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs570011733	chr16:34353082-34353083	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs61747984	chr16:34353091-34353092	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs555447837	chr16:34353094-34353095	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs186594784	chr16:34353103-34353104	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs567679667	chr16:34353117-34353118	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs9930859	chr16:34353179-34353180	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs572494965	chr16:34354338-34354339	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs183540578	chr16:34355287-34355288	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs385974	chr16:34355350-34355351	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs113172203	chr16:34355363-34355364	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs186437730	chr16:34355389-34355390	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs540763193	chr16:34355409-34355410	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs565254504	chr16:34355441-34355442	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs189871045	chr16:34355467-34355468	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs139245886	chr16:34355577-34355578	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs409110	chr16:34357402-34357403	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs72810736	chr16:34357416-34357417	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs565932711	chr16:34357420-34357421	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs375327534	chr16:34357477-34357478	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs116448873	chr16:34357494-34357495	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs575318278	chr16:34357495-34357496	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs576192024	chr16:34357552-34357553	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs139384000	chr16:34357559-34357560	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs191337025	chr16:34357575-34357576	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs115263205	chr16:34357593-34357594	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:132)

Disease	PMID	Source
Hodgkin''s lymphoma	20651079	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	16608533	CNVD
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
Mental retardation	19951919	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21990379	CNVD
Astrocytoma	22246337	CNVD
Myelofibrosis	22110671	CNVD
Epilepsy	22499536	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Austim spectrum disorder	21302340	CNVD
Autism	22513405	CNVD
Autism	22958593	CNVD
Autism	18184952	CNVD
Autism	19966786	CNVD
Autism	21394203	CNVD
Autism	21969575	CNVD
Autism	22241247	CNVD
Autism	20970697	CNVD
Autism	20942916	CNVD
Epilepsy	20970697	CNVD
Intellectual disability	22045946	CNVD
Mental retardation	19966786	CNVD
Developmental delay	20808231	CNVD
Obesity	20808231	CNVD
Autism	18923514	CNVD
Obesity	21881559	CNVD
Obesity	21956041	CNVD
Autism	20659124	CNVD
Mental retardation	21062444	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	22885689	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	20970697	CNVD
Schizophrenia	20433910	CNVD
Schizophrenia	22241247	CNVD
Autism	19242545	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Intracranial ependymoma	16609018	CNVD
Schizophrenia	21399695	CNVD
Autism	21956041	CNVD
Disorders of sex development	21048976	CNVD
Autism	22067053	CNVD
Autism	18156158	CNVD
Mental retardation	20152051	CNVD
Autism	19218893	CNVD
Autism	21289514	CNVD
Schizophrenia	19855392	CNVD
neurodevelopmental Syndrome	20503337	CNVD
Benign familial neonatal-infantile seizures	21060786	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Cancer	21183584	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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Schizophrenia	23813976	CNVD
Bipolar disorder	19214233	CNVD
early-passage human iPS cells	21368824	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22522925	CNVD
Rett syndrome	21593744	CNVD
Autism	19287141	CNVD
Prostate cancer	18632612	CNVD
Cancer	20164919	CNVD
Autism	18414403	CNVD

Chromatin state (count:235 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:34353000-34353200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr16:34368800-34369200	Enhancers	NHEK	skin
3	chr16:34369200-34369400	Enhancers	HMEC	breast
4	chr16:34369200-34369400	Flanking Active TSS	NHEK	skin
5	chr16:34369200-34370600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr16:34369400-34369600	Enhancers	NHEK	skin
7	chr16:34369400-34369800	Flanking Active TSS	HMEC	breast
8	chr16:34369600-34369800	Flanking Active TSS	NHEK	skin
9	chr16:34369800-34370600	Enhancers	HMEC	breast
10	chr16:34369800-34370600	Enhancers	NHEK	skin
11	chr16:34370600-34371600	Weak transcription	NHEK	skin
12	chr16:34370600-34371800	Weak transcription	HMEC	breast
13	chr16:34371600-34372400	Enhancers	NHEK	skin
14	chr16:34371800-34372200	Enhancers	HMEC	breast
15	chr16:34374000-34387000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
16	chr16:34374200-34376800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr16:34374600-34374800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr16:34379000-34384200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr16:34380400-34385200	ZNF genes & repeats	Fetal Brain Female	brain
20	chr16:34380800-34383200	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
21	chr16:34381000-34382400	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr16:34382600-34382800	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr16:34385200-34385800	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr16:34386000-34386200	ZNF genes & repeats	Fetal Stomach	stomach
25	chr16:34407600-34409200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr16:34408200-34409000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr16:34408400-34409000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr16:34409000-34410800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr16:34409200-34410600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr16:34410600-34411600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr16:34410800-34411600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr16:34411200-34411400	Enhancers	Right Atrium	heart
33	chr16:34415000-34419400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
34	chr16:34416200-34416400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr16:34416200-34417400	ZNF genes & repeats	Fetal Muscle Trunk	muscle
36	chr16:34418800-34419400	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
37	chr16:34419600-34422800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
38	chr16:34420000-34422200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr16:34420400-34420800	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
40	chr16:34421000-34421200	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr16:34423000-34423200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr16:34429200-34433000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
43	chr16:34429400-34429600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
44	chr16:34429400-34430400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr16:34432200-34433400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr16:34437400-34438400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr16:34438400-34441200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr16:34441200-34442800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr16:34441400-34442600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
50	chr16:34442000-34443200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell

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