Variant report

Variant	esv2751594
Chromosome Location	chr16:34467499-34790371
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1397)
CpG islands
(count:2563)
Chromatin interactive
region (count:6)
LncRNA
region (count:68)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1397 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr16:34768061-34768441	K562	blood:	n/a	n/a
2	ATF1	chr16:34643912-34644196	K562	blood:	n/a	n/a
3	ATF1	chr16:34787094-34787358	K562	blood:	n/a	n/a
4	ATF1	chr16:34486728-34487212	K562	blood:	n/a	n/a
5	ATF1	chr16:34573796-34574082	K562	blood:	n/a	n/a
6	ATF1	chr16:34589373-34589390	K562	blood:	n/a	n/a
7	ATF1	chr16:34625774-34626005	K562	blood:	n/a	n/a
8	ATF1	chr16:34765990-34765998	K562	blood:	n/a	n/a
9	ATF1	chr16:34574452-34574460	K562	blood:	n/a	n/a
10	ATF1	chr16:34715569-34715609	K562	blood:	n/a	n/a
11	BATF	chr16:34536693-34536965	GM12878	blood:	n/a	chr16:34536834-34536845
12	BATF	chr16:34539865-34540180	GM12878	blood:	n/a	chr16:34540044-34540055
13	BATF	chr16:34731803-34731989	GM12878	blood:	n/a	chr16:34731883-34731894 chr16:34731915-34731926
14	BATF	chr16:34731793-34732055	GM12878	blood:	n/a	chr16:34731883-34731894 chr16:34731915-34731926
15	BATF	chr16:34539887-34540221	GM12878	blood:	n/a	chr16:34540044-34540055
16	BHLHE40	chr16:34745103-34745432	GM12878	blood:	n/a	chr16:34745242-34745251
17	BHLHE40	chr16:34741044-34741235	K562	blood:	n/a	n/a
18	BHLHE40	chr16:34721874-34721912	GM12878	blood:	n/a	n/a
19	BHLHE40	chr16:34625401-34626021	K562	blood:	n/a	n/a
20	BHLHE40	chr16:34647001-34647022	GM12878	blood:	n/a	n/a
21	BHLHE40	chr16:34740335-34740524	K562	blood:	n/a	n/a
22	BHLHE40	chr16:34732021-34732023	GM12878	blood:	n/a	n/a
23	BHLHE40	chr16:34745112-34745352	K562	blood:	n/a	chr16:34745242-34745251
24	BHLHE40	chr16:34726730-34726951	K562	blood:	n/a	chr16:34726896-34726912
25	BHLHE40	chr16:34598011-34598017	K562	blood:	n/a	n/a
26	BHLHE40	chr16:34625806-34626006	GM12878	blood:	n/a	n/a
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	chr16:34532926-34533600	ECC-1	luminal epithelium:	n/a	chr16:34533406-34533417
31	CEBPB	chr16:34573739-34574089	IMR90	lung:	n/a	chr16:34573875-34573886
32	CEBPB	chr16:34539206-34539440	A549	lung:	n/a	n/a
33	CEBPB	chr16:34767984-34768445	A549	lung:	n/a	n/a
34	CEBPB	chr16:34602083-34602267	A549	lung:	n/a	n/a
35	CEBPB	chr16:34637662-34637759	A549	lung:	n/a	chr16:34637709-34637720
36	CEBPB	chr16:34730704-34731069	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr16:34790349-34790522	HepG2	liver:	n/a	n/a
38	CEBPB	chr16:34729400-34729667	A549	lung:	n/a	n/a
39	CEBPB	chr16:34532914-34533612	ECC-1	luminal epithelium:	n/a	chr16:34533406-34533417
40	CEBPB	chr16:34730735-34731108	IMR90	lung:	n/a	n/a
41	CEBPB	chr16:34767993-34768467	HepG2	liver:	n/a	n/a
42	CEBPB	chr16:34715406-34715705	A549	lung:	n/a	n/a
43	CEBPB	chr16:34730661-34731121	HepG2	liver:	n/a	n/a
44	CEBPB	chr16:34486708-34487148	A549	lung:	n/a	chr16:34486713-34486730
45	CEBPB	chr16:34483511-34483748	HepG2	liver:	n/a	n/a
46	CEBPB	chr16:34540533-34540804	A549	lung:	n/a	n/a
47	CEBPB	chr16:34685018-34685433	A549	lung:	n/a	n/a
48	CEBPB	chr16:34530956-34532127	HepG2	liver:	n/a	n/a
49	CEBPB	chr16:34531259-34531620	ECC-1	luminal epithelium:	n/a	n/a
50	CEBPB	chr16:34530917-34531822	A549	lung:	n/a	n/a

(count:2563 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:34740520-34740570	Jurkat	blood:	n/a
2	chr16:34740520-34740570	Jurkat	blood:	n/a
3	chr16:34579002-34579052	MCF-7	breast:	n/a
4	chr16:34737523-34737573	LNCaP	prostate:	n/a
5	chr16:34586894-34586944	AG09309	skin:	n/a
6	chr16:34583045-34583095	SKMC	muscle:	n/a
7	chr16:34587307-34587357	Caco-2	colon:	n/a
8	chr16:34489904-34489954	GM19239	blood:	n/a
9	chr16:34587307-34587357	Hela-S3	cervix:	n/a
10	chr16:34716002-34716052	IMR90	lung:	fetal
11	chr16:34659664-34659714	SK-N-MC	brain:	n/a
12	chr16:34726856-34726906	HRE	kidney:	n/a
13	chr16:34712713-34712763	Hela-S3	cervix:	n/a
14	chr16:34740520-34740570	RPTEC	kidney:	n/a
15	chr16:34741966-34742016	T-47D	breast:	n/a
16	chr16:34741493-34741543	HIPEpiC	eye:	n/a
17	chr16:34726856-34726906	Hepatocyte	liver:	n/a
18	chr16:34659664-34659714	HEEpiC	esophagus:	n/a
19	chr16:34741304-34741354	AG04450	lung:	fetal
20	chr16:34583045-34583095	BJ	skin:	n/a
21	chr16:34741493-34741543	SK-N-SH	brain:	n/a
22	chr16:34587120-34587170	BJ	skin:	n/a
23	chr16:34778087-34778137	PrEC	prostate:	n/a
24	chr16:34490033-34490083	AG09319	gingival:	n/a
25	chr16:34787597-34787647	HL-60	blood:	n/a
26	chr16:34490033-34490083	HPAEpiC	pulmonary alveolar:	n/a
27	chr16:34596941-34596991	NH-A	brain:	n/a
28	chr16:34648955-34649005	HRCEpiC	kidney:	n/a
29	chr16:34741966-34742016	AG04450	lung:	fetal
30	chr16:34787597-34787647	AG09319	gingival:	n/a
31	chr16:34625446-34625496	HRCEpiC	kidney:	n/a
32	chr16:34787392-34787442	AG09319	gingival:	n/a
33	chr16:34777963-34778013	HRE	kidney:	n/a
34	chr16:34648955-34649005	Hela-S3	cervix:	n/a
35	chr16:34579002-34579052	GM12892	blood:	n/a
36	chr16:34659771-34659821	Hepatocyte	liver:	n/a
37	chr16:34778087-34778137	HepG2	liver:	n/a
38	chr16:34786998-34787048	IMR90	lung:	fetal
39	chr16:34489904-34489954	K562	blood:	n/a
40	chr16:34787199-34787249	GM19239	blood:	n/a
41	chr16:34740585-34740635	HCPEpiC	choroid plexus:	n/a
42	chr16:34741493-34741543	H1-hESC	embryonic stem cell:	embryo
43	chr16:34660044-34660094	ProgFib	skin:	n/a
44	chr16:34587120-34587170	MCF10A-Er-Src	breast:	n/a
45	chr16:34778087-34778137	AG04450	lung:	fetal
46	chr16:34741304-34741354	HRPEpiC	eye:	n/a
47	chr16:34586837-34586887	HMEC	breast:	n/a
48	chr16:34579002-34579052	ProgFib	skin:	n/a
49	chr16:34663929-34663979	NB4	blood:	n/a
50	chr16:34716002-34716052	U87	brain:	n/a

(count:6 , 50 per page) page: 1

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

(count:68 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTD-2144E22.5.1-24	chr16:34581756-34582668	NONHSAT142180
2	lnc-LINC00273-22	chr16:34569648-34570147	NONHSAT142179
3	lnc-LINC00273-8	chr16:34766012-34766124	XLOC_011927
4	lnc-LINC00273-23	chr16:34618515-34618930	NONHSAT142185
5	lnc-LINC00273-27	chr16:34740133-34740549	NONHSAT142200
6	lnc-LINC00273-25	chr16:34712988-34713065	NONHSAT142192
7	lnc-LINC00273-22	chr16:34571082-34571260	NONHSAT142179
8	lnc-LINC00273-7	chr16:34730748-34730828	ENSG00000261445.1
9	lnc-CTD-2144E22.5.1-31	chr16:34743025-34743136	NONHSAT142207
10	lnc-LINC00273-27	chr16:34740697-34740840	NONHSAT142198
11	lnc-CTD-2144E22.5.1-31	chr16:34756490-34756676	NONHSAT142207
12	lnc-CTD-2144E22.5.1-5	chr16:34483054-34483172	ENSG00000260958.2
13	lnc-CTD-2144E22.5.1-6	chr16:34614340-34614458	ENSG00000259841.2
14	lnc-CTD-2144E22.5.1-6	chr16:34610877-34611020	ENSG00000259841.2
15	lnc-CTD-2144E22.5.1-31	chr16:34751386-34751515	NONHSAT142207
16	lnc-CTD-2144E22.5.1-5	chr16:34487252-34487411	NONHSAT142170
17	lnc-LINC00273-23	chr16:34619259-34619457	NONHSAT142185
18	lnc-CTD-2144E22.5.1-5	chr16:34487609-34488020	ENSG00000260958.2
19	lnc-LINC00273-25	chr16:34714529-34714852	NONHSAT142191
20	lnc-CTD-2144E22.5.1-6	chr16:34610877-34611020	NONHSAT142183
21	lnc-LINC00273-25	chr16:34713636-34713735	NONHSAT142191
22	lnc-CTD-2144E22.5.1-6	chr16:34614340-34614458	NONHSAT142183
23	lnc-CTD-2144E22.5.1-6	chr16:34597783-34597899	ENSG00000259841.2
24	lnc-CTD-2144E22.5.1-6	chr16:34624074-34624955	ENSG00000259841.2
25	lnc-CTD-2144E22.5.1-6	chr16:34615965-34616632	ENSG00000259841.2
26	lnc-CTD-2144E22.5.1-5	chr16:34487252-34487506	ENSG00000260958.2
27	lnc-CTD-2144E22.5.1-31	chr16:34758333-34758358	NONHSAT142207
28	lnc-LINC00273-25	chr16:34712988-34713065	NONHSAT142191
29	lnc-LINC00273-25	chr16:34713636-34713810	NONHSAT142192
30	lnc-LINC00273-24	chr16:34640930-34641001	NONHSAT142186
31	lnc-CTD-2144E22.5.1-4	chr16:34478641-34479038	XLOC_011699
32	lnc-CTD-2144E22.5.1-6	chr16:34597902-34598201	ENSG00000259841.2
33	lnc-LINC00273-25	chr16:34712350-34712699	NONHSAT142191
34	lnc-LINC00273-8	chr16:34765218-34765705	XLOC_011927
35	lnc-CTD-2144E22.5.1-6	chr16:34612943-34613184	ENSG00000259841.2
36	lnc-LINC00273-7	chr16:34728125-34728568	ENSG00000261445.1
37	lnc-CTD-2144E22.5.1-5	chr16:34471671-34474425	NONHSAT142170
38	lnc-CTD-2144E22.5.1-29	chr16:34723608-34724583	NONHSAT142194
39	lnc-LINC00273-7	chr16:34729913-34729959	ENSG00000261445.1
40	lnc-CTD-2144E22.5.1-4	chr16:34477709-34479085	NONHSAT142171
41	lnc-CTD-2144E22.5.1-6	chr16:34612943-34613184	ENSG00000259841.2
42	lnc-CTD-2144E22.5.1-6	chr16:34610877-34611020	ENSG00000259841.2
43	lnc-CTD-2144E22.5.1-5	chr16:34482858-34483251	NONHSAT142170
44	lnc-LINC00273-27	chr16:34739472-34739785	NONHSAT142200
45	lnc-LINC00273-22	chr16:34570437-34570514	NONHSAT142179
46	lnc-CTD-2144E22.5.1-6	chr16:34617082-34617226	ENSG00000259841.2
47	lnc-CTD-2144E22.5.1-4	chr16:34477761-34477848	XLOC_011699
48	lnc-CTD-2144E22.5.1-6	chr16:34616795-34616837	ENSG00000259841.2
49	lnc-LINC00273-24	chr16:34641562-34641720	NONHSAT142186
50	lnc-CTD-2144E22.5.1-6	chr16:34612943-34613184	NONHSAT142183

No data

Variant related genes	Relation type
RARRES2P9	TF binding region
ENSG00000259836	TF binding region
ENSG00000259897	TF binding region
ENSG00000261046	TF binding region
ENSG00000221532	TF binding region
ENSG00000261752	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
RARRES2P6	TF binding region
ENSG00000260480	TF binding region
FGFR3P5	TF binding region
ENSG00000260680	TF binding region
ENSG00000260846	TF binding region
RARRES2P9	CpG island
ENSG00000259836	CpG island
ENSG00000259897	CpG island
ENSG00000261046	CpG island
ENSG00000221532	CpG island
ENSG00000261752	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
RARRES2P6	CpG island
ENSG00000260480	CpG island
FGFR3P5	CpG island
ENSG00000260680	CpG island
ENSG00000260846	CpG island
ENSG00000261398	chromatin interactions
ENSG00000137871	chromatin interactions
ENSG00000260073	chromatin interactions
ZNF451	miRNA target sites
ZNF407	miRNA target sites

Extended variants
information (count: 5968 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:5968 , 50 per page) page: 1 2 3 4 5 6 7 ... 120

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8046955	chr16:34467504-34467505	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs7499910	chr16:34467540-34467541	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs539049908	chr16:34467583-34467584	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs557043805	chr16:34467621-34467622	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs148369538	chr16:34467646-34467647	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs188201774	chr16:34467654-34467655	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs555232290	chr16:34467682-34467683	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs573145788	chr16:34467713-34467714	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs540413279	chr16:34467720-34467721	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs191707007	chr16:34467725-34467726	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs576504222	chr16:34467741-34467742	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs76455224	chr16:34467743-34467744	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs562304475	chr16:34467779-34467780	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs529684260	chr16:34467797-34467798	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs576222719	chr16:34467799-34467800	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs7500004	chr16:34467802-34467803	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs183761808	chr16:34467817-34467818	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs527515845	chr16:34467822-34467823	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs552366408	chr16:34467847-34467848	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs543576883	chr16:34467854-34467855	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs571790147	chr16:34467865-34467866	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs539086830	chr16:34467872-34467873	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs564876695	chr16:34467916-34467917	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs34120368	chr16:34467974-34467975	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs544993688	chr16:34467975-34467976	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs373217970	chr16:34467993-34467994	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs188233683	chr16:34468003-34468004	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs570684483	chr16:34468004-34468005	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs141577903	chr16:34468007-34468008	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs201338865	chr16:34468033-34468034	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs117564699	chr16:34468068-34468069	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs537815818	chr16:34468076-34468077	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs12928771	chr16:34468077-34468078	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs114189348	chr16:34468127-34468128	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs558681791	chr16:34468179-34468180	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs116413530	chr16:34468180-34468181	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs544017068	chr16:34468225-34468226	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs59211504	chr16:34468263-34468264	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs559806254	chr16:34468282-34468283	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs574377930	chr16:34468313-34468314	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs541792487	chr16:34468368-34468369	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs560469215	chr16:34468370-34468371	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs192530465	chr16:34468419-34468420	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs549586412	chr16:34468428-34468429	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs369682311	chr16:34468471-34468472	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs138269803	chr16:34468477-34468478	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs531520840	chr16:34468538-34468539	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs530187220	chr16:34468543-34468544	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs184526788	chr16:34468585-34468586	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs561497842	chr16:34468604-34468605	ZNF genes & repeats	Chromatin interactive region	2 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:175 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:34466600-34472200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
2	chr16:34466800-34469400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr16:34467000-34468200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
4	chr16:34467000-34470200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr16:34468200-34469400	ZNF genes & repeats	Brain Germinal Matrix	brain
6	chr16:34474800-34476000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr16:34478600-34479000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
8	chr16:34480400-34481000	Enhancers	Adipose Nuclei	Adipose
9	chr16:34489600-34490400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
10	chr16:34489600-34490800	Active TSS	ES-I3 Cell Line	embryonic stem cell
11	chr16:34489800-34490200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
12	chr16:34492800-34493400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
13	chr16:34505000-34507800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
14	chr16:34517800-34518400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
15	chr16:34531200-34534000	Enhancers	HMEC	breast
16	chr16:34531400-34534200	Enhancers	NHEK	skin
17	chr16:34531800-34532400	Active TSS	Fetal Heart	heart
18	chr16:34533800-34534000	Enhancers	Esophagus	oesophagus
19	chr16:34534200-34538800	Weak transcription	NHEK	skin
20	chr16:34535000-34537200	Weak transcription	Esophagus	oesophagus
21	chr16:34537000-34537400	ZNF genes & repeats	Fetal Heart	heart
22	chr16:34537200-34537400	Enhancers	Esophagus	oesophagus
23	chr16:34537400-34542200	Weak transcription	Esophagus	oesophagus
24	chr16:34538000-34538800	Active TSS	Fetal Heart	heart
25	chr16:34538600-34544000	Enhancers	HMEC	breast
26	chr16:34538800-34539600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
27	chr16:34538800-34543800	Enhancers	NHEK	skin
28	chr16:34539400-34539800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr16:34539800-34540200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr16:34540200-34540400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr16:34540400-34542800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr16:34542200-34543000	Enhancers	Esophagus	oesophagus
33	chr16:34542200-34546800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
34	chr16:34542800-34543000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr16:34542800-34543600	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr16:34543000-34543400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr16:34543200-34544000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr16:34543400-34543800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr16:34543600-34543800	Enhancers	Esophagus	oesophagus
40	chr16:34545200-34552000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
41	chr16:34545400-34546800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr16:34545400-34552000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
43	chr16:34546200-34546400	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
44	chr16:34549000-34549200	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
45	chr16:34550000-34550200	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
46	chr16:34553800-34554800	Enhancers	Brain Hippocampus Middle	brain
47	chr16:34554200-34554600	Enhancers	Brain Angular Gyrus	brain
48	chr16:34554200-34554600	Enhancers	Brain Cingulate Gyrus	brain
49	chr16:34554200-34554600	Enhancers	Brain Substantia Nigra	brain
50	chr16:34562400-34562800	Active TSS	Fetal Heart	heart

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