Variant report

Variant	nsv431488
Chromosome Location	chr16:34467540-35139485
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2271)
CpG islands
(count:4028)
Chromatin interactive
region (count:13)
LncRNA
region (count:74)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2271 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr16:34486728-34487212	K562	blood:	n/a	n/a
2	ATF1	chr16:34625774-34626005	K562	blood:	n/a	n/a
3	ATF1	chr16:34768061-34768441	K562	blood:	n/a	n/a
4	ATF1	chr16:34589373-34589390	K562	blood:	n/a	n/a
5	ATF1	chr16:34787094-34787358	K562	blood:	n/a	n/a
6	ATF1	chr16:34765990-34765998	K562	blood:	n/a	n/a
7	ATF1	chr16:34643912-34644196	K562	blood:	n/a	n/a
8	ATF1	chr16:34715569-34715609	K562	blood:	n/a	n/a
9	ATF1	chr16:34574452-34574460	K562	blood:	n/a	n/a
10	ATF1	chr16:34573796-34574082	K562	blood:	n/a	n/a
11	ATF2	chr16:34833744-34834198	GM12878	blood:	n/a	n/a
12	BATF	chr16:34894940-34895190	GM12878	blood:	n/a	chr16:34895069-34895080
13	BATF	chr16:34731793-34732055	GM12878	blood:	n/a	chr16:34731883-34731894 chr16:34731915-34731926
14	BATF	chr16:34539887-34540221	GM12878	blood:	n/a	chr16:34540044-34540055
15	BATF	chr16:34894892-34895125	GM12878	blood:	n/a	chr16:34895069-34895080
16	BATF	chr16:34795349-34795509	GM12878	blood:	n/a	chr16:34795453-34795464
17	BATF	chr16:34795249-34795638	GM12878	blood:	n/a	chr16:34795453-34795464
18	BATF	chr16:34854854-34855022	GM12878	blood:	n/a	n/a
19	BATF	chr16:34539865-34540180	GM12878	blood:	n/a	chr16:34540044-34540055
20	BATF	chr16:34792970-34793204	GM12878	blood:	n/a	chr16:34793057-34793068 chr16:34793089-34793100
21	BATF	chr16:34536693-34536965	GM12878	blood:	n/a	chr16:34536834-34536845
22	BATF	chr16:34731803-34731989	GM12878	blood:	n/a	chr16:34731883-34731894 chr16:34731915-34731926
23	BATF	chr16:34796038-34796270	GM12878	blood:	n/a	chr16:34796152-34796163
24	BATF	chr16:34796836-34797144	GM12878	blood:	n/a	chr16:34797014-34797025
25	BCL11A	chr16:34833758-34834113	GM12878	blood:	n/a	n/a
26	BCL3	chr16:34894998-34895220	GM12878	blood:	n/a	n/a
27	BCL3	chr16:34833700-34834141	GM12878	blood:	n/a	n/a
28	BHLHE40	chr16:34647001-34647022	GM12878	blood:	n/a	n/a
29	BHLHE40	chr16:34745103-34745432	GM12878	blood:	n/a	chr16:34745242-34745251
30	BHLHE40	chr16:34740335-34740524	K562	blood:	n/a	n/a
31	BHLHE40	chr16:34741044-34741235	K562	blood:	n/a	n/a
32	BHLHE40	chr16:34836978-34836992	GM12878	blood:	n/a	n/a
33	BHLHE40	chr16:34796951-34797111	GM12878	blood:	n/a	n/a
34	BHLHE40	chr16:34745112-34745352	K562	blood:	n/a	chr16:34745242-34745251
35	BHLHE40	chr16:34833735-34834061	GM12878	blood:	n/a	n/a
36	BHLHE40	chr16:34726730-34726951	K562	blood:	n/a	chr16:34726896-34726912
37	BHLHE40	chr16:34721874-34721912	GM12878	blood:	n/a	n/a
38	BHLHE40	chr16:34732021-34732023	GM12878	blood:	n/a	n/a
39	BHLHE40	chr16:34625401-34626021	K562	blood:	n/a	n/a
40	BHLHE40	chr16:34795575-34795581	GM12878	blood:	n/a	n/a
41	BHLHE40	chr16:34598011-34598017	K562	blood:	n/a	n/a
42	BHLHE40	chr16:34625806-34626006	GM12878	blood:	n/a	n/a
43	BRCA1	chr16:34666658-34666728	GM12878	blood:	n/a	n/a
44	BRCA1	chr16:34666402-34666616	H1-hESC	embryonic stem cell:	n/a	n/a
45	CBX3	chr16:34849319-34849535	K562	blood:	n/a	n/a
46	CBX3	chr16:34825393-34825600	K562	blood:	n/a	n/a
47	CBX3	chr16:34625799-34625988	K562	blood:	n/a	n/a
48	CEBPB	chr16:34643898-34644263	HepG2	liver:	n/a	n/a
49	CEBPB	chr16:34805162-34805662	HepG2	liver:	n/a	n/a
50	CEBPB	chr16:34611205-34611346	A549	lung:	n/a	chr16:34611274-34611285

(count:4028 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:34979671-34979721	K562	blood:	n/a
2	chr16:34778087-34778137	HMEC	breast:	n/a
3	chr16:34979671-34979721	K562	blood:	n/a
4	chr16:34778087-34778137	HMEC	breast:	n/a
5	chr16:34740585-34740635	CMK	blood:	n/a
6	chr16:34726734-34726784	HCPEpiC	choroid plexus:	n/a
7	chr16:34659771-34659821	U87	brain:	n/a
8	chr16:34760531-34760581	HEK293	kidney:	embryo
9	chr16:35029997-35030047	NH-A	brain:	n/a
10	chr16:34726734-34726784	SKMC	muscle:	n/a
11	chr16:34659664-34659714	HL-60	blood:	n/a
12	chr16:34579002-34579052	HCM	heart:	n/a
13	chr16:34812259-34812309	HRPEpiC	eye:	n/a
14	chr16:34649152-34649202	AoSMC	blood vessel:	n/a
15	chr16:34809256-34809306	Caco-2	colon:	n/a
16	chr16:34777682-34777732	MCF-7	breast:	n/a
17	chr16:34777963-34778013	NB4	blood:	n/a
18	chr16:34806416-34806466	NHBE	bronchial:	n/a
19	chr16:34659771-34659821	GM12892	blood:	n/a
20	chr16:34586894-34586944	ovcar-3	ovarian:	n/a
21	chr16:34787392-34787442	HepG2	liver:	n/a
22	chr16:34741251-34741301	HAEpiC	amniotic membrane:	n/a
23	chr16:34741304-34741354	MCF-7	breast:	n/a
24	chr16:34741251-34741301	Jurkat	blood:	n/a
25	chr16:34983384-34983434	SK-N-SH	brain:	n/a
26	chr16:34848776-34848826	HNPCEpiC	eye:	n/a
27	chr16:34807860-34807910	HL-60	blood:	n/a
28	chr16:34583045-34583095	BE2_C	brain:	n/a
29	chr16:34786998-34787048	HCPEpiC	choroid plexus:	n/a
30	chr16:34489904-34489954	T-47D	breast:	n/a
31	chr16:34808939-34808989	HepG2	liver:	n/a
32	chr16:34808939-34808989	AG09309	skin:	n/a
33	chr16:35026985-35027035	MCF10A-Er-Src	breast:	n/a
34	chr16:34781451-34781501	HCT-116	colon:	n/a
35	chr16:34791202-34791252	SK-N-SH	brain:	n/a
36	chr16:34659771-34659821	Hepatocyte	liver:	n/a
37	chr16:34716002-34716052	HCT-116	colon:	n/a
38	chr16:34660044-34660094	H1-hESC	embryonic stem cell:	embryo
39	chr16:34740585-34740635	HepG2	liver:	n/a
40	chr16:34587120-34587170	AG09319	gingival:	n/a
41	chr16:34579002-34579052	HepG2	liver:	n/a
42	chr16:34979671-34979721	GM12892	blood:	n/a
43	chr16:35029890-35029940	SK-N-MC	brain:	n/a
44	chr16:35029997-35030047	SK-N-MC	brain:	n/a
45	chr16:34659664-34659714	NH-A	brain:	n/a
46	chr16:34583045-34583095	AG09309	skin:	n/a
47	chr16:34660044-34660094	BJ	skin:	n/a
48	chr16:34809256-34809306	HRE	kidney:	n/a
49	chr16:35029890-35029940	IMR90	lung:	fetal
50	chr16:34808479-34808529	NB4	blood:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:57024256..57026523-chr16:34752267..34754460,2	MCF-7	breast:
2	chr16:34815137..34816427-chr16:34875759..34876664,4	MCF-7	breast:
3	chr16:34815137..34816427-chr16:34875759..34876664,4	MCF-7	breast:
4	chr16:35133889..35136586-chr16:35136893..35138863,2	MCF-7	breast:
5	chr16:34799028..34799683-chr16:34875753..34876623,3	MCF-7	breast:
6	chr16:34815853..34816462-chr16:34876054..34876591,2	MCF-7	breast:
7	chr16:34815853..34816462-chr16:34876054..34876591,2	MCF-7	breast:
8	chr16:34799028..34799683-chr16:34875753..34876623,3	MCF-7	breast:
9	chr16:34726782..34727382-chr16:34760283..34761051,3	MCF-7	breast:
10	chr16:34422640..34423667-chr16:34625487..34626782,3	MCF-7	breast:
11	chr16:34726782..34727382-chr16:34760283..34761051,3	MCF-7	breast:
12	chr16:34429328..34431681-chr16:34466203..34469132,2	K562	blood:
13	chr15:56788863..56789371-chr16:34759996..34760825,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LINC00273-22	chr16:34570743-34570817	NONHSAT142179
2	lnc-LINC00273-8	chr16:34765218-34765705	XLOC_011927
3	lnc-LINC00273-27	chr16:34740697-34740840	NONHSAT142198
4	lnc-CTD-2144E22.5.1-4	chr16:34477709-34479085	NONHSAT142171
5	lnc-CTD-2144E22.5.1-5	chr16:34487252-34487506	ENSG00000260958.2
6	lnc-CTD-2144E22.5.1-6	chr16:34617082-34617226	ENSG00000259841.2
7	lnc-LINC00273-25	chr16:34712988-34713065	NONHSAT142192
8	lnc-LINC00273-22	chr16:34571082-34571260	NONHSAT142179
9	lnc-LINC00273-25	chr16:34713636-34713810	NONHSAT142192
10	lnc-CTD-2144E22.5.1-6	chr16:34612943-34613184	ENSG00000259841.2
11	lnc-LINC00273-30	chr16:34956639-34956900	NONHSAT142221
12	lnc-CTD-2144E22.5.1-6	chr16:34614340-34614458	NONHSAT142183
13	lnc-CTD-2144E22.5.1-6	chr16:34614340-34614458	ENSG00000259841.2
14	lnc-LINC00273-33	chr16:35113407-35113869	NONHSAT142247
15	lnc-CTD-2144E22.5.1-6	chr16:34612943-34613184	ENSG00000259841.2
16	lnc-LINC00273-25	chr16:34714529-34714852	NONHSAT142191
17	lnc-CTD-2144E22.5.1-6	chr16:34616840-34616969	ENSG00000259841.2
18	lnc-LINC00273-22	chr16:34570437-34570514	NONHSAT142179
19	lnc-CTD-2144E22.5.1-4	chr16:34478641-34479038	XLOC_011699
20	lnc-LINC00273-25	chr16:34712988-34713065	NONHSAT142191
21	lnc-CTD-2144E22.5.1-5	chr16:34487252-34487411	NONHSAT142170
22	lnc-LINC00273-7	chr16:34728125-34728568	ENSG00000261445.1
23	lnc-CTD-2144E22.5.1-18	chr16:34493001-34494000	NONHSAT142176
24	lnc-CTD-2144E22.5.1-6	chr16:34620250-34620420	NONHSAT142183
25	lnc-CTD-2144E22.5.1-6	chr16:34612943-34613184	NONHSAT142183
26	lnc-CTD-2144E22.5.1-6	chr16:34616795-34616969	NONHSAT142183
27	lnc-CTD-2144E22.5.1-24	chr16:34581756-34582668	NONHSAT142180
28	lnc-LINC00273-25	chr16:34712350-34712699	NONHSAT142191
29	lnc-CTD-2144E22.5.1-5	chr16:34518127-34518517	ENSG00000260958.2
30	lnc-LINC00273-7	chr16:34729913-34729959	ENSG00000261445.1
31	lnc-LINC00273-28	chr16:34740963-34741308	NONHSAT142204
32	lnc-LINC00273-7	chr16:34730748-34730828	ENSG00000261445.1
33	lnc-CTD-2144E22.5.1-6	chr16:34625678-34626084	NONHSAT142183
34	lnc-CTD-2144E22.5.1-6	chr16:34610877-34611020	ENSG00000259841.2
35	lnc-LINC00273-27	chr16:34740133-34740549	NONHSAT142200
36	lnc-LINC00273-31	chr16:35036459-35037041	NONHSAT142244
37	lnc-LINC00273-25	chr16:34713636-34713735	NONHSAT142191
38	lnc-CTD-2144E22.5.1-4	chr16:34477761-34477848	XLOC_011699
39	lnc-LINC00273-24	chr16:34640930-34641001	NONHSAT142186
40	lnc-LINC00273-24	chr16:34640118-34640617	NONHSAT142186
41	lnc-CTD-2144E22.5.1-32	chr16:34782288-34783200	NONHSAT142214
42	lnc-CTD-2144E22.5.1-31	chr16:34743025-34743136	NONHSAT142207
43	lnc-CTD-2144E22.5.1-6	chr16:34616795-34616837	ENSG00000259841.2
44	lnc-CTD-2144E22.5.1-29	chr16:34723608-34724583	NONHSAT142194
45	lnc-LINC00273-9	chr16:35019940-35021258	ENSG00000260611.1
46	lnc-CTD-2144E22.5.1-35	chr16:35071257-35072103	NONHSAT142246
47	lnc-LINC00273-27	chr16:34739464-34739785	ENSG00000260857.2
48	lnc-CTD-2144E22.5.1-6	chr16:34597783-34597899	ENSG00000259841.2
49	lnc-LINC00273-27	chr16:34739459-34739785	NONHSAT142198
50	lnc-CTD-2144E22.5.1-31	chr16:34756490-34756676	NONHSAT142207

No data

Variant related genes	Relation type
ENSG00000260134	TF binding region
VN1R70P	TF binding region
RARRES2P9	TF binding region
RNA5SP417	TF binding region
ENSG00000259836	TF binding region
ENSG00000260611	TF binding region
ENSG00000259897	TF binding region
ENSG00000261046	TF binding region
ENSG00000221532	TF binding region
ENSG00000261122	TF binding region
ENSG00000261752	TF binding region
ENSG00000269622	TF binding region
ENSG00000260427	TF binding region
ENSG00000221580	TF binding region
ENSG00000260341	TF binding region
RNA5SP409	TF binding region
ENSG00000260291	TF binding region
ENSG00000260746	TF binding region
RNA5SP419	TF binding region
RNA5SP407	TF binding region
ENSG00000261299	TF binding region
ENSG00000260994	TF binding region
ENSG00000260598	TF binding region
RNA5SP421	TF binding region
ENSG00000261733	TF binding region
ENSG00000260857	TF binding region
ENSG00000261445	TF binding region
AGGF1P4	TF binding region
RNA5SP406	TF binding region
ENSG00000261350	TF binding region
ENSG00000259791	TF binding region
RNA5SP408	TF binding region
ENSG00000260153	TF binding region
ENSG00000214581	TF binding region
RNA5SP416	TF binding region
RNA5SP410	TF binding region
RNA5SP413	TF binding region
ENSG00000259841	TF binding region
ENSG00000261782	TF binding region
ENSG00000260522	TF binding region
RNA5SP420	TF binding region
RNA5SP423	TF binding region
RNA5SP415	TF binding region
RNA5SP418	TF binding region
RNA5SP422	TF binding region
RARRES2P8	TF binding region
ENSG00000261711	TF binding region
RARRES2P7	TF binding region
RARRES2P6	TF binding region
HMGN2P41	TF binding region
ENSG00000260480	TF binding region
FGFR3P5	TF binding region
ENSG00000260680	TF binding region
ENSG00000260846	TF binding region
ENSG00000260134	CpG island
VN1R70P	CpG island
RARRES2P9	CpG island
RNA5SP417	CpG island
ENSG00000259836	CpG island
ENSG00000260611	CpG island
ENSG00000259897	CpG island
ENSG00000261046	CpG island
ENSG00000221532	CpG island
ENSG00000261122	CpG island
ENSG00000261752	CpG island
ENSG00000269622	CpG island
ENSG00000260427	CpG island
ENSG00000221580	CpG island
ENSG00000260341	CpG island
RNA5SP409	CpG island
ENSG00000260291	CpG island
ENSG00000260746	CpG island
RNA5SP419	CpG island
RNA5SP407	CpG island
ENSG00000261299	CpG island
ENSG00000260994	CpG island
ENSG00000260598	CpG island
RNA5SP421	CpG island
ENSG00000261733	CpG island
ENSG00000260857	CpG island
ENSG00000261445	CpG island
AGGF1P4	CpG island
RNA5SP406	CpG island
ENSG00000261350	CpG island
ENSG00000259791	CpG island
RNA5SP408	CpG island
ENSG00000260153	CpG island
ENSG00000214581	CpG island
RNA5SP416	CpG island
RNA5SP410	CpG island
RNA5SP413	CpG island
ENSG00000259841	CpG island
ENSG00000261782	CpG island
ENSG00000260522	CpG island
RNA5SP420	CpG island
RNA5SP423	CpG island
RNA5SP415	CpG island
RNA5SP418	CpG island
RNA5SP422	CpG island
RARRES2P8	CpG island
ENSG00000261711	CpG island
RARRES2P7	CpG island
RARRES2P6	CpG island
HMGN2P41	CpG island
ENSG00000260480	CpG island
FGFR3P5	CpG island
ENSG00000260680	CpG island
ENSG00000260846	CpG island
ENSG00000221580	chromatin interactions
ENSG00000260073	chromatin interactions
ENSG00000137871	chromatin interactions
ENSG00000261398	chromatin interactions
ZNF407	miRNA target sites
ZNF451	miRNA target sites

Extended variants
information (count: 12940 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:12940 , 50 per page) page: 1 2 3 4 5 6 7 ... 259

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7499910	chr16:34467540-34467541	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs539049908	chr16:34467583-34467584	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs557043805	chr16:34467621-34467622	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs148369538	chr16:34467646-34467647	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs188201774	chr16:34467654-34467655	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs555232290	chr16:34467682-34467683	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs573145788	chr16:34467713-34467714	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs540413279	chr16:34467720-34467721	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs191707007	chr16:34467725-34467726	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs576504222	chr16:34467741-34467742	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs76455224	chr16:34467743-34467744	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs562304475	chr16:34467779-34467780	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs529684260	chr16:34467797-34467798	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs576222719	chr16:34467799-34467800	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs7500004	chr16:34467802-34467803	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs183761808	chr16:34467817-34467818	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs527515845	chr16:34467822-34467823	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs552366408	chr16:34467847-34467848	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs543576883	chr16:34467854-34467855	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs571790147	chr16:34467865-34467866	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs539086830	chr16:34467872-34467873	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs564876695	chr16:34467916-34467917	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs34120368	chr16:34467974-34467975	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs544993688	chr16:34467975-34467976	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs373217970	chr16:34467993-34467994	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs188233683	chr16:34468003-34468004	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs570684483	chr16:34468004-34468005	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs141577903	chr16:34468007-34468008	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs201338865	chr16:34468033-34468034	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs117564699	chr16:34468068-34468069	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs537815818	chr16:34468076-34468077	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs12928771	chr16:34468077-34468078	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs114189348	chr16:34468127-34468128	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs558681791	chr16:34468179-34468180	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs116413530	chr16:34468180-34468181	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs544017068	chr16:34468225-34468226	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs59211504	chr16:34468263-34468264	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs559806254	chr16:34468282-34468283	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs574377930	chr16:34468313-34468314	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs541792487	chr16:34468368-34468369	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs560469215	chr16:34468370-34468371	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs192530465	chr16:34468419-34468420	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs549586412	chr16:34468428-34468429	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs369682311	chr16:34468471-34468472	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs138269803	chr16:34468477-34468478	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs531520840	chr16:34468538-34468539	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs530187220	chr16:34468543-34468544	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs184526788	chr16:34468585-34468586	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs561497842	chr16:34468604-34468605	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs115613102	chr16:34468606-34468607	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
Lung adenocarcinoma	21935476	CNVD
Medulloblastoma	21163964	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:339 , 50 per page) page: 1 2 3 4 5 6 7

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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