Variant report

Variant	nsv428326
Chromosome Location	chr16:34357763-34769642
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1748)
CpG islands
(count:4582)
Chromatin interactive
region (count:7)
LncRNA
region (count:73)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1748 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr16:34643912-34644196	K562	blood:	n/a	n/a
2	ATF1	chr16:34589373-34589390	K562	blood:	n/a	n/a
3	ATF1	chr16:34573796-34574082	K562	blood:	n/a	n/a
4	ATF1	chr16:34715569-34715609	K562	blood:	n/a	n/a
5	ATF1	chr16:34625774-34626005	K562	blood:	n/a	n/a
6	ATF1	chr16:34486728-34487212	K562	blood:	n/a	n/a
7	ATF1	chr16:34574452-34574460	K562	blood:	n/a	n/a
8	ATF1	chr16:34765990-34765998	K562	blood:	n/a	n/a
9	ATF1	chr16:34768061-34768441	K562	blood:	n/a	n/a
10	BATF	chr16:34539865-34540180	GM12878	blood:	n/a	chr16:34540044-34540055
11	BATF	chr16:34539887-34540221	GM12878	blood:	n/a	chr16:34540044-34540055
12	BATF	chr16:34731803-34731989	GM12878	blood:	n/a	chr16:34731883-34731894 chr16:34731915-34731926
13	BATF	chr16:34731793-34732055	GM12878	blood:	n/a	chr16:34731883-34731894 chr16:34731915-34731926
14	BATF	chr16:34536693-34536965	GM12878	blood:	n/a	chr16:34536834-34536845
15	BHLHE40	chr16:34732021-34732023	GM12878	blood:	n/a	n/a
16	BHLHE40	chr16:34647001-34647022	GM12878	blood:	n/a	n/a
17	BHLHE40	chr16:34740335-34740524	K562	blood:	n/a	n/a
18	BHLHE40	chr16:34741044-34741235	K562	blood:	n/a	n/a
19	BHLHE40	chr16:34625806-34626006	GM12878	blood:	n/a	n/a
20	BHLHE40	chr16:34429795-34429892	K562	blood:	n/a	chr16:34429875-34429891
21	BHLHE40	chr16:34745103-34745432	GM12878	blood:	n/a	chr16:34745242-34745251
22	BHLHE40	chr16:34726730-34726951	K562	blood:	n/a	chr16:34726896-34726912
23	BHLHE40	chr16:34598011-34598017	K562	blood:	n/a	n/a
24	BHLHE40	chr16:34721874-34721912	GM12878	blood:	n/a	n/a
25	BHLHE40	chr16:34625401-34626021	K562	blood:	n/a	n/a
26	BHLHE40	chr16:34745112-34745352	K562	blood:	n/a	chr16:34745242-34745251
27	BRCA1	chr16:34666402-34666616	H1-hESC	embryonic stem cell:	n/a	n/a
28	BRCA1	chr16:34666658-34666728	GM12878	blood:	n/a	n/a
29	CBX3	chr16:34625799-34625988	K562	blood:	n/a	n/a
30	CEBPB	chr16:34539085-34539474	HepG2	liver:	n/a	n/a
31	CEBPB	chr16:34598745-34598792	K562	blood:	n/a	n/a
32	CEBPB	chr16:34637648-34637812	K562	blood:	n/a	chr16:34637709-34637720
33	CEBPB	chr16:34600051-34600514	ECC-1	luminal epithelium:	n/a	chr16:34600335-34600346
34	CEBPB	chr16:34486734-34487193	K562	blood:	n/a	n/a
35	CEBPB	chr16:34542362-34542582	HepG2	liver:	n/a	n/a
36	CEBPB	chr16:34449667-34450116	A549	lung:	n/a	n/a
37	CEBPB	chr16:34767993-34768467	HepG2	liver:	n/a	n/a
38	CEBPB	chr16:34368818-34369342	ECC-1	luminal epithelium:	n/a	chr16:34369018-34369029
39	CEBPB	chr16:34685080-34685431	HepG2	liver:	n/a	n/a
40	CEBPB	chr16:34599864-34600530	HepG2	liver:	n/a	chr16:34600335-34600346
41	CEBPB	chr16:34597947-34598296	A549	lung:	n/a	n/a
42	CEBPB	chr16:34597882-34598141	IMR90	lung:	n/a	n/a
43	CEBPB	chr16:34369435-34369709	HepG2	liver:	n/a	chr16:34369584-34369595
44	CEBPB	chr16:34536217-34536514	HepG2	liver:	n/a	n/a
45	CEBPB	chr16:34685136-34685387	IMR90	lung:	n/a	n/a
46	CEBPB	chr16:34483631-34483649	K562	blood:	n/a	n/a
47	CEBPB	chr16:34599887-34600514	A549	lung:	n/a	chr16:34600335-34600346
48	CEBPB	chr16:34411891-34412110	IMR90	lung:	n/a	n/a
49	CEBPB	chr16:34598601-34599065	A549	lung:	n/a	n/a
50	CEBPB	chr16:34632715-34632941	HepG2	liver:	n/a	n/a

(count:4582 , 50 per page) page: 1 2 3 4 5 6 7 ... 92

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:34659664-34659714	HNPCEpiC	eye:	n/a
2	chr16:34442283-34442333	Hepatocyte	liver:	n/a
3	chr16:34407715-34407765	SK-N-SH	brain:	n/a
4	chr16:34442373-34442423	Hela-S3	cervix:	n/a
5	chr16:34375039-34375089	CMK	blood:	n/a
6	chr16:34378804-34378854	HCPEpiC	choroid plexus:	n/a
7	chr16:34659664-34659714	SK-N-SH	brain:	n/a
8	chr16:34659664-34659714	HNPCEpiC	eye:	n/a
9	chr16:34442283-34442333	Hepatocyte	liver:	n/a
10	chr16:34407715-34407765	SK-N-SH	brain:	n/a
11	chr16:34442373-34442423	Hela-S3	cervix:	n/a
12	chr16:34375039-34375089	CMK	blood:	n/a
13	chr16:34378804-34378854	HCPEpiC	choroid plexus:	n/a
14	chr16:34659664-34659714	SK-N-SH	brain:	n/a
15	chr16:34407715-34407765	PANC-1	pancreas:	n/a
16	chr16:34659664-34659714	HL-60	blood:	n/a
17	chr16:34404673-34404723	RPTEC	kidney:	n/a
18	chr16:34407760-34407810	HPAEpiC	pulmonary alveolar:	n/a
19	chr16:34430837-34430887	HCM	heart:	n/a
20	chr16:34378497-34378547	MCF10A-Er-Src	breast:	n/a
21	chr16:34408014-34408064	GM12892	blood:	n/a
22	chr16:34430382-34430432	HRCEpiC	kidney:	n/a
23	chr16:34712713-34712763	SK-N-SH_RA	brain:	n/a
24	chr16:34439811-34439861	NH-A	brain:	n/a
25	chr16:34741304-34741354	HEEpiC	esophagus:	n/a
26	chr16:34648955-34649005	GM12878	blood:	n/a
27	chr16:34741304-34741354	SK-N-SH	brain:	n/a
28	chr16:34428061-34428111	HMEC	breast:	n/a
29	chr16:34429930-34429980	HRCEpiC	kidney:	n/a
30	chr16:34378069-34378119	ovcar-3	ovarian:	n/a
31	chr16:34741251-34741301	ProgFib	skin:	n/a
32	chr16:34441787-34441837	AoSMC	blood vessel:	n/a
33	chr16:34712713-34712763	HRPEpiC	eye:	n/a
34	chr16:34441787-34441837	HIPEpiC	eye:	n/a
35	chr16:34429930-34429980	HIPEpiC	eye:	n/a
36	chr16:34443120-34443170	HepG2	liver:	n/a
37	chr16:34430905-34430955	HCM	heart:	n/a
38	chr16:34375039-34375089	HMEC	breast:	n/a
39	chr16:34428061-34428111	ECC-1	luminal epithelium:	n/a
40	chr16:34439811-34439861	PrEC	prostate:	n/a
41	chr16:34625446-34625496	HCT-116	colon:	n/a
42	chr16:34741251-34741301	AG09309	skin:	n/a
43	chr16:34587307-34587357	IMR90	lung:	fetal
44	chr16:34430905-34430955	HEK293	kidney:	embryo
45	chr16:34404772-34404822	HCF	heart:	n/a
46	chr16:34648955-34649005	HUVEC	blood vessel:	n/a
47	chr16:34378497-34378547	HRPEpiC	eye:	n/a
48	chr16:34741966-34742016	HNPCEpiC	eye:	n/a
49	chr16:34404774-34404824	LNCaP	prostate:	n/a
50	chr16:34442373-34442423	HMEC	breast:	n/a

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

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

(count:73 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LINC00273-25	chr16:34712988-34713065	NONHSAT142191
2	lnc-CTD-2144E22.5.1-6	chr16:34620250-34620420	NONHSAT142183
3	lnc-CTD-2144E22.5.1-6	chr16:34615965-34616632	ENSG00000259841.2
4	lnc-LINC00273-25	chr16:34713636-34713735	NONHSAT142191
5	lnc-CTD-2144E22.5.1-6	chr16:34610877-34611020	ENSG00000259841.2
6	lnc-LINC00273-27	chr16:34740697-34740840	NONHSAT142198
7	lnc-LINC00273-25	chr16:34713293-34713362	NONHSAT142192
8	lnc-CTD-2144E22.5.1-17	chr16:34427706-34428105	NONHSAT142163
9	lnc-CTD-2144E22.5.1-31	chr16:34751386-34751515	NONHSAT142207
10	lnc-CTD-2144E22.5.1-5	chr16:34487252-34487506	ENSG00000260958.2
11	lnc-CTD-2144E22.5.1-31	chr16:34756490-34756676	NONHSAT142207
12	lnc-CTD-2144E22.5.1-6	chr16:34624074-34624955	ENSG00000259841.2
13	lnc-LINC00273-25	chr16:34712350-34712699	NONHSAT142191
14	lnc-CTD-2144E22.5.1-5	chr16:34518127-34518517	ENSG00000260958.2
15	lnc-LINC00273-24	chr16:34641253-34641302	NONHSAT142186
16	lnc-CTD-2144E22.5.1-5	chr16:34442308-34442392	ENSG00000260958.2
17	lnc-LINC00273-24	chr16:34640930-34641001	NONHSAT142186
18	lnc-CTD-2144E22.5.1-31	chr16:34758333-34758358	NONHSAT142207
19	lnc-CTD-2144E22.5.1-5	chr16:34471671-34474425	NONHSAT142170
20	lnc-CTD-2144E22.5.1-5	chr16:34482858-34483251	NONHSAT142170
21	lnc-CTD-2144E22.5.1-6	chr16:34616840-34616969	ENSG00000259841.2
22	lnc-CTD-2144E22.5.1-6	chr16:34597783-34597899	ENSG00000259841.2
23	lnc-CTD-2144E22.5.1-6	chr16:34610877-34611020	NONHSAT142183
24	lnc-CTD-2144E22.5.1-6	chr16:34617082-34617226	ENSG00000259841.2
25	lnc-CTD-2144E22.5.1-29	chr16:34723608-34724583	NONHSAT142194
26	lnc-CTD-2144E22.5.1-6	chr16:34625678-34626084	NONHSAT142183
27	lnc-CTD-2144E22.5.1-6	chr16:34597787-34597899	NONHSAT142183
28	lnc-CTD-2144E22.5.1-6	chr16:34597902-34598201	ENSG00000259841.2
29	lnc-LINC00273-22	chr16:34570437-34570514	NONHSAT142179
30	lnc-CTD-2144E22.5.1-5	chr16:34442330-34442392	ENSG00000260958.2
31	lnc-LINC00273-22	chr16:34570743-34570817	NONHSAT142179
32	lnc-LINC00273-18	chr16:34455954-34456419	NONHSAT142168
33	lnc-LINC00273-24	chr16:34640118-34640617	NONHSAT142186
34	lnc-CTD-2144E22.5.1-6	chr16:34620250-34620420	ENSG00000259841.2
35	lnc-CTD-2144E22.5.1-4	chr16:34477709-34479085	NONHSAT142171
36	lnc-LINC00273-27	chr16:34740133-34740549	NONHSAT142200
37	lnc-CTD-2144E22.5.1-4	chr16:34478641-34479038	XLOC_011699
38	lnc-CTD-2144E22.5.1-14	chr16:34368885-34369446	NONHSAT142152
39	lnc-CTD-2144E22.5.1-6	chr16:34614340-34614458	ENSG00000259841.2
40	lnc-LINC00273-27	chr16:34739459-34739785	NONHSAT142198
41	lnc-LINC00273-7	chr16:34729913-34729959	ENSG00000261445.1
42	lnc-LINC00273-25	chr16:34714529-34714852	NONHSAT142191
43	lnc-LINC00273-8	chr16:34765218-34765705	XLOC_011927
44	lnc-LINC00273-7	chr16:34730748-34730828	ENSG00000261445.1
45	lnc-LINC00273-25	chr16:34712988-34713065	NONHSAT142192
46	lnc-LINC00273-28	chr16:34740963-34741308	NONHSAT142204
47	lnc-LINC00273-15	chr16:34383828-34384161	NONHSAT142158
48	lnc-CTD-2144E22.5.1-4	chr16:34477761-34477848	XLOC_011699
49	lnc-CTD-2144E22.5.1-24	chr16:34581756-34582668	NONHSAT142180
50	lnc-LINC00273-27	chr16:34739464-34739785	ENSG00000260857.2

No data

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

Extended variants
information (count: 7437 )
Associated
traits (count: 131 )

Variant overlapped rSNPs/rCNVs (count:7437 , 50 per page) page: 1 2 3 4 5 6 7 ... 149

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs189373044	chr16:34357764-34357765	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs72810738	chr16:34363936-34363937	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs537487736	chr16:34363963-34363964	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs373308229	chr16:34363976-34363977	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs191879914	chr16:34363984-34363985	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs568330893	chr16:34363987-34363988	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs79983807	chr16:34363998-34363999	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs373395798	chr16:34364015-34364016	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs553989491	chr16:34364025-34364026	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs140621377	chr16:34366293-34366294	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs183498108	chr16:34366310-34366311	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs375605560	chr16:34366384-34366385	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs538365477	chr16:34368629-34368630	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs556513875	chr16:34368782-34368783	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs35341995	chr16:34368786-34368787	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs574936526	chr16:34368797-34368798	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs193286490	chr16:34368806-34368807	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs554398558	chr16:34368866-34368867	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs573065618	chr16:34368928-34368929	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
20	rs558622640	chr16:34368942-34368943	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
21	rs540389585	chr16:34368946-34368947	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
22	rs184674492	chr16:34368978-34368979	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
23	rs188342702	chr16:34369123-34369124	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
24	rs533445395	chr16:34369126-34369127	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
25	rs367743175	chr16:34369154-34369155	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
26	rs180682492	chr16:34369192-34369193	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
27	rs545561589	chr16:34369251-34369252	Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
28	rs563663981	chr16:34369262-34369263	Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
29	rs530972655	chr16:34369278-34369279	Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
30	rs138740236	chr16:34369300-34369301	Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
31	rs576853777	chr16:34369352-34369353	Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
32	rs564234198	chr16:34369354-34369355	Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
33	rs567906014	chr16:34369355-34369356	Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
34	rs528796442	chr16:34369440-34369441	Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
35	rs114610950	chr16:34369446-34369447	Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
36	rs185512521	chr16:34369468-34369469	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs117710026	chr16:34369483-34369484	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs141371225	chr16:34369491-34369492	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs375754831	chr16:34369549-34369550	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs550311163	chr16:34369564-34369565	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs546614571	chr16:34369573-34369574	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs370415098	chr16:34369577-34369578	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs568615841	chr16:34369584-34369585	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs535807500	chr16:34369609-34369610	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs554285601	chr16:34369699-34369700	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs548387080	chr16:34369732-34369733	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs189718955	chr16:34369733-34369734	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs533871289	chr16:34369754-34369755	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs558702310	chr16:34369755-34369756	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs562002520	chr16:34369918-34369919	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:131)

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
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:227 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:34368800-34369200	Enhancers	NHEK	skin
2	chr16:34369200-34369400	Enhancers	HMEC	breast
3	chr16:34369200-34369400	Flanking Active TSS	NHEK	skin
4	chr16:34369200-34370600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr16:34369400-34369600	Enhancers	NHEK	skin
6	chr16:34369400-34369800	Flanking Active TSS	HMEC	breast
7	chr16:34369600-34369800	Flanking Active TSS	NHEK	skin
8	chr16:34369800-34370600	Enhancers	HMEC	breast
9	chr16:34369800-34370600	Enhancers	NHEK	skin
10	chr16:34370600-34371600	Weak transcription	NHEK	skin
11	chr16:34370600-34371800	Weak transcription	HMEC	breast
12	chr16:34371600-34372400	Enhancers	NHEK	skin
13	chr16:34371800-34372200	Enhancers	HMEC	breast
14	chr16:34374000-34387000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
15	chr16:34374200-34376800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr16:34374600-34374800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr16:34379000-34384200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr16:34380400-34385200	ZNF genes & repeats	Fetal Brain Female	brain
19	chr16:34380800-34383200	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
20	chr16:34381000-34382400	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr16:34382600-34382800	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr16:34385200-34385800	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr16:34386000-34386200	ZNF genes & repeats	Fetal Stomach	stomach
24	chr16:34407600-34409200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr16:34408200-34409000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr16:34408400-34409000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr16:34409000-34410800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr16:34409200-34410600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr16:34410600-34411600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr16:34410800-34411600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr16:34411200-34411400	Enhancers	Right Atrium	heart
32	chr16:34415000-34419400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
33	chr16:34416200-34416400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr16:34416200-34417400	ZNF genes & repeats	Fetal Muscle Trunk	muscle
35	chr16:34418800-34419400	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
36	chr16:34419600-34422800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
37	chr16:34420000-34422200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr16:34420400-34420800	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
39	chr16:34421000-34421200	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr16:34423000-34423200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr16:34429200-34433000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
42	chr16:34429400-34429600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
43	chr16:34429400-34430400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr16:34432200-34433400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr16:34437400-34438400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr16:34438400-34441200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr16:34441200-34442800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr16:34441400-34442600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
49	chr16:34442000-34443200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
50	chr16:34442200-34443000	Active TSS	ES-WA7 Cell Line	embryonic stem cell

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