Variant report

Variant	nsv1059842
Chromosome Location	chr16:32033374-32634752
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3968)
CpG islands
(count:3972)
Chromatin interactive
region (count:1)
LncRNA
region (count:36)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3968 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:32590243-32590613	K562	blood:	n/a	n/a
2	ARID3A	chr16:32131861-32132041	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:32547652-32548159	K562	blood:	n/a	n/a
4	ARID3A	chr16:32295698-32295892	HepG2	liver:	n/a	n/a
5	ARID3A	chr16:32345726-32345816	HepG2	liver:	n/a	n/a
6	ATF1	chr16:32526924-32527721	K562	blood:	n/a	n/a
7	ATF1	chr16:32549843-32550009	K562	blood:	n/a	n/a
8	ATF1	chr16:32558594-32558903	K562	blood:	n/a	n/a
9	ATF1	chr16:32583782-32583972	K562	blood:	n/a	n/a
10	ATF1	chr16:32559923-32560294	K562	blood:	n/a	n/a
11	ATF1	chr16:32515726-32516011	K562	blood:	n/a	n/a
12	ATF1	chr16:32568174-32568349	K562	blood:	n/a	n/a
13	ATF1	chr16:32521319-32521519	K562	blood:	n/a	n/a
14	ATF1	chr16:32194699-32194908	K562	blood:	n/a	n/a
15	ATF1	chr16:32363593-32363793	K562	blood:	n/a	n/a
16	ATF1	chr16:32547497-32547620	K562	blood:	n/a	n/a
17	ATF1	chr16:32550785-32551178	K562	blood:	n/a	n/a
18	BACH1	chr16:32553830-32554374	K562	blood:	n/a	n/a
19	BACH1	chr16:32531668-32531907	K562	blood:	n/a	n/a
20	BACH1	chr16:32590237-32590618	K562	blood:	n/a	n/a
21	BATF	chr16:32435147-32435451	GM12878	blood:	n/a	n/a
22	BATF	chr16:32150053-32150293	GM12878	blood:	n/a	n/a
23	BATF	chr16:32059238-32059578	GM12878	blood:	n/a	n/a
24	BATF	chr16:32101215-32101624	GM12878	blood:	n/a	chr16:32101437-32101448
25	BATF	chr16:32108354-32108543	GM12878	blood:	n/a	n/a
26	BATF	chr16:32099142-32100510	GM12878	blood:	n/a	n/a
27	BATF	chr16:32333643-32333817	GM12878	blood:	n/a	n/a
28	BATF	chr16:32099023-32099501	GM12878	blood:	n/a	n/a
29	BATF	chr16:32094016-32094261	GM12878	blood:	n/a	chr16:32094090-32094099
30	BATF	chr16:32368458-32368823	GM12878	blood:	n/a	n/a
31	BATF	chr16:32451259-32451478	GM12878	blood:	n/a	n/a
32	BATF	chr16:32144456-32144674	GM12878	blood:	n/a	n/a
33	BATF	chr16:32148154-32148425	GM12878	blood:	n/a	n/a
34	BATF	chr16:32139079-32139319	GM12878	blood:	n/a	n/a
35	BATF	chr16:32059227-32059446	GM12878	blood:	n/a	n/a
36	BATF	chr16:32102770-32103216	GM12878	blood:	n/a	n/a
37	BATF	chr16:32335047-32335307	GM12878	blood:	n/a	n/a
38	BATF	chr16:32102790-32103063	GM12878	blood:	n/a	n/a
39	BATF	chr16:32100565-32100763	GM12878	blood:	n/a	n/a
40	BATF	chr16:32366962-32367454	GM12878	blood:	n/a	chr16:32367243-32367254
41	BATF	chr16:32144482-32144672	GM12878	blood:	n/a	n/a
42	BATF	chr16:32140974-32141195	GM12878	blood:	n/a	n/a
43	BATF	chr16:32361068-32361342	GM12878	blood:	n/a	n/a
44	BATF	chr16:32099644-32100206	GM12878	blood:	n/a	n/a
45	BATF	chr16:32133941-32134130	GM12878	blood:	n/a	n/a
46	BATF	chr16:32133244-32133444	GM12878	blood:	n/a	n/a
47	BATF	chr16:32101090-32101595	GM12878	blood:	n/a	chr16:32101437-32101448
48	BATF	chr16:32335083-32335294	GM12878	blood:	n/a	n/a
49	BATF	chr16:32050371-32050791	GM12878	blood:	n/a	n/a
50	BATF	chr16:32098574-32098849	GM12878	blood:	n/a	n/a

(count:3972 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:32326062-32326112	HRE	kidney:	n/a
2	chr16:32265747-32265797	RPTEC	kidney:	n/a
3	chr16:32489820-32489870	T-47D	breast:	n/a
4	chr16:32599417-32599467	HMEC	breast:	n/a
5	chr16:32360428-32360478	GM12892	blood:	n/a
6	chr16:32096623-32096673	HCF	heart:	n/a
7	chr16:32096623-32096673	Jurkat	blood:	n/a
8	chr16:32326062-32326112	HRE	kidney:	n/a
9	chr16:32265747-32265797	RPTEC	kidney:	n/a
10	chr16:32489820-32489870	T-47D	breast:	n/a
11	chr16:32599417-32599467	HMEC	breast:	n/a
12	chr16:32360428-32360478	GM12892	blood:	n/a
13	chr16:32096623-32096673	HCF	heart:	n/a
14	chr16:32096623-32096673	Jurkat	blood:	n/a
15	chr16:32486117-32486167	IMR90	lung:	fetal
16	chr16:32095405-32095455	HCPEpiC	choroid plexus:	n/a
17	chr16:32214185-32214235	T-47D	breast:	n/a
18	chr16:32049224-32049274	HPAEpiC	pulmonary alveolar:	n/a
19	chr16:32300250-32300300	AG04449	skin:	fetal
20	chr16:32264389-32264439	ovcar-3	ovarian:	n/a
21	chr16:32037687-32037737	CMK	blood:	n/a
22	chr16:32214185-32214235	HRE	kidney:	n/a
23	chr16:32201912-32201962	K562	blood:	n/a
24	chr16:32288799-32288849	HMEC	breast:	n/a
25	chr16:32359536-32359586	LNCaP	prostate:	n/a
26	chr16:32599417-32599467	HUVEC	blood vessel:	n/a
27	chr16:32452725-32452775	HCPEpiC	choroid plexus:	n/a
28	chr16:32127313-32127363	HPAEpiC	pulmonary alveolar:	n/a
29	chr16:32321943-32321993	NT2-D1	testis:	n/a
30	chr16:32276952-32277002	IMR90	lung:	fetal
31	chr16:32127659-32127709	RPTEC	kidney:	n/a
32	chr16:32213913-32213963	HCT-116	colon:	n/a
33	chr16:32486117-32486167	AG04450	lung:	fetal
34	chr16:32123983-32124033	SK-N-SH_RA	brain:	n/a
35	chr16:32486334-32486384	AoSMC	blood vessel:	n/a
36	chr16:32252787-32252837	CMK	blood:	n/a
37	chr16:32485636-32485686	PANC-1	pancreas:	n/a
38	chr16:32360428-32360478	H1-hESC	embryonic stem cell:	embryo
39	chr16:32127656-32127706	Hepatocyte	liver:	n/a
40	chr16:32360338-32360388	H1-hESC	embryonic stem cell:	embryo
41	chr16:32214185-32214235	Hela-S3	cervix:	n/a
42	chr16:32096623-32096673	RPTEC	kidney:	n/a
43	chr16:32276952-32277002	MCF10A-Er-Src	breast:	n/a
44	chr16:32127659-32127709	HCM	heart:	n/a
45	chr16:32214185-32214235	Caco-2	colon:	n/a
46	chr16:32452502-32452552	A549	lung:	n/a
47	chr16:32452502-32452552	AG09319	gingival:	n/a
48	chr16:32290371-32290421	HUVEC	blood vessel:	n/a
49	chr16:32127313-32127363	HNPCEpiC	eye:	n/a
50	chr16:32305114-32305164	HCPEpiC	choroid plexus:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:106598214..106598843-chr16:32050606..32051126,2	MCF-7	breast:

(count:36 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC133485.1.1-2	chr16:32619515-32619545	NONHSAT142022
2	lnc-AC133485.1.1-2	chr16:32626742-32626807	NONHSAT142022
3	lnc-AC133485.1.1-2	chr16:32626742-32626953	XLOC_011694
4	lnc-AC133485.1.1-2	chr16:32616957-32617035	NONHSAT142021
5	lnc-TP53TG3-3	chr16:32334099-32334218	XLOC_011921
6	lnc-AC133485.1.1-2	chr16:32616227-32616285	NONHSAT142022
7	lnc-AC133485.1.1-2	chr16:32611620-32611754	NONHSAT142021
8	lnc-AC133485.1.1-8	chr16:32438035-32438184	NONHSAT142015
9	lnc-AC133485.1.1-2	chr16:32619006-32619076	NONHSAT142022
10	lnc-AC133485.1.1-2	chr16:32619515-32619547	NONHSAT142021
11	lnc-AC133485.1.1-8	chr16:32447309-32447521	NONHSAT142015
12	lnc-AC133485.1.1-8	chr16:32437097-32437203	NONHSAT142015
13	lnc-TP53TG3-4	chr16:32274229-32274612	ENSG00000260402.1
14	lnc-TP53TG3-4	chr16:32275068-32275108	ENSG00000260402.1
15	lnc-AC133485.1.1-1	chr16:32204071-32204851	ENSG00000260847.1
16	lnc-AC133485.1.1-8	chr16:32403379-32403556	NONHSAT142015
17	lnc-TP53TG3-7	chr16:32261941-32262132	ENSG00000260575.1
18	lnc-AC133485.1.1-8	chr16:32442004-32442108	NONHSAT142015
19	lnc-AC133485.1.1-8	chr16:32416298-32416473	NONHSAT142015
20	lnc-TP53TG3-16	chr16:32450390-32451887	NONHSAT142016
21	lnc-TP53TG3-2	chr16:32465933-32470079	ENSG00000261541.1
22	lnc-AC133485.1.1-2	chr16:32618849-32619005	NONHSAT142021
23	lnc-AC133485.1.1-7	chr16:32200583-32200802	NONHSAT141994
24	lnc-AC133485.1.1-2	chr16:32626287-32626324	NONHSAT142022
25	lnc-AC133485.1.1-2	chr16:32626903-32626960	NONHSAT142022
26	lnc-AC133485.1.1-2	chr16:32613896-32614018	NONHSAT142022
27	lnc-AC133485.1.1-8	chr16:32399456-32399634	NONHSAT142015
28	lnc-AC133485.1.1-2	chr16:32626088-32626324	XLOC_011694
29	lnc-TP53TG3-7	chr16:32265674-32265743	ENSG00000260575.1
30	lnc-AC133485.1.1-8	chr16:32402131-32402273	NONHSAT142015
31	lnc-AC133485.1.1-1	chr16:32199654-32199738	ENSG00000260847.1
32	lnc-AC133485.1.1-2	chr16:32616227-32616285	NONHSAT142021
33	lnc-AC133485.1.1-8	chr16:32443002-32443139	NONHSAT142015
34	lnc-TP53TG3-16	chr16:32452294-32452480	NONHSAT142016
35	lnc-TP53TG3-3	chr16:32335100-32335382	XLOC_011921
36	lnc-AC133485.1.1-2	chr16:32613844-32613953	NONHSAT142021

No data

Variant related genes	Relation type
ENSG00000223931	TF binding region
ENSG00000259966	TF binding region
ENSG00000260540	TF binding region
ENSG00000260344	TF binding region
TP53TG3D	TF binding region
ENSG00000260584	TF binding region
ENSG00000261541	TF binding region
ENSG00000260402	TF binding region
ENSG00000261127	TF binding region
IGHV1OR16-1	TF binding region
ENSG00000260649	TF binding region
IGHV3OR16-9	TF binding region
ACTR3BP3	TF binding region
ENSG00000260662	TF binding region
ENSG00000260575	TF binding region
ENSG00000259822	TF binding region
HERC2P4	TF binding region
ENSG00000260847	TF binding region
ENSG00000262187	TF binding region
ENSG00000261727	TF binding region
ENSG00000260866	TF binding region
IGHV1OR16-3	TF binding region
ABCD1P3	TF binding region
PABPC1P13	TF binding region
ENSG00000260516	TF binding region
ENSG00000223931	CpG island
ENSG00000259966	CpG island
ENSG00000260540	CpG island
ENSG00000260344	CpG island
TP53TG3D	CpG island
ENSG00000260584	CpG island
ENSG00000261541	CpG island
ENSG00000260402	CpG island
ENSG00000261127	CpG island
IGHV1OR16-1	CpG island
ENSG00000260649	CpG island
IGHV3OR16-9	CpG island
ACTR3BP3	CpG island
ENSG00000260662	CpG island
ENSG00000260575	CpG island
ENSG00000259822	CpG island
HERC2P4	CpG island
ENSG00000260847	CpG island
ENSG00000262187	CpG island
ENSG00000261727	CpG island
ENSG00000260866	CpG island
IGHV1OR16-3	CpG island
ABCD1P3	CpG island
PABPC1P13	CpG island
ENSG00000260516	CpG island
LBR	miRNA target sites

Extended variants
information (count: 14456 )
Associated
traits (count: 139 )

Variant overlapped rSNPs/rCNVs (count:14456 , 50 per page) page: 1 2 3 4 5 6 7 ... 290

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs374621972	chr16:32041277-32041278	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs554216038	chr16:32041293-32041294	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs549639226	chr16:32043308-32043309	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs374793907	chr16:32043576-32043577	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs62052060	chr16:32044022-32044023	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs573823538	chr16:32051203-32051204	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs540758058	chr16:32051236-32051237	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs574541773	chr16:32051240-32051241	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs532907939	chr16:32051304-32051305	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs188681550	chr16:32051312-32051313	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs143757583	chr16:32051319-32051320	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs148152079	chr16:32051333-32051334	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs549677262	chr16:32051356-32051357	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs377754252	chr16:32051360-32051361	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs28660045	chr16:32051370-32051371	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs546649757	chr16:32051371-32051372	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs571414226	chr16:32051373-32051374	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs538623887	chr16:32051378-32051379	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs556954074	chr16:32051396-32051397	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs575630441	chr16:32051404-32051405	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs147335069	chr16:32051434-32051435	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs191538664	chr16:32051439-32051440	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs573711752	chr16:32051450-32051451	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs541222318	chr16:32051453-32051454	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs559462573	chr16:32051454-32051455	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs577828885	chr16:32051466-32051467	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs113971092	chr16:32051468-32051469	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs563251256	chr16:32051483-32051484	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs530575389	chr16:32051484-32051485	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs111324647	chr16:32051501-32051502	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs549404447	chr16:32051504-32051505	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs117429084	chr16:32051522-32051523	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs112866414	chr16:32051549-32051550	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs528631124	chr16:32051556-32051557	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs546814951	chr16:32051568-32051569	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs546319081	chr16:32058660-32058661	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs551814989	chr16:32059209-32059210	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs570457121	chr16:32059210-32059211	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs531309151	chr16:32059264-32059265	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs549526887	chr16:32059417-32059418	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs568084109	chr16:32059431-32059432	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs536135465	chr16:32059469-32059470	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs554554866	chr16:32059521-32059522	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs566270669	chr16:32059586-32059587	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs540050697	chr16:32059587-32059588	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs558252279	chr16:32059619-32059620	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs113469618	chr16:32059959-32059960	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs574023865	chr16:32060122-32060123	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs377053334	chr16:32062924-32062925	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs532997278	chr16:32062943-32062944	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:139)

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
Breast cancer	21509527	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
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Mental retardation	19951919	CNVD
Colorectal cancer	16272173	CNVD
Bladder cancer	21909424	CNVD
small cell lung cancer	20016488	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
Sezary syndrome	18413736	CNVD
Wilms tumour	21544195	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164920	CNVD
Autism	19287141	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	20967226	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Melanoma	20877625	CNVD
Breast cancer	17142309	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22297974	CNVD
Recurrent pregnancy loss	19789632	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioma	20126413	CNVD
Osteosarcoma	21215367	CNVD
Autism	21865298	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD

Chromatin state (count:568 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:32051200-32051600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
2	chr16:32051400-32051600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr16:32051400-32051600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr16:32077600-32078000	Enhancers	Dnd41	blood
5	chr16:32095200-32095400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
6	chr16:32095400-32096400	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
7	chr16:32096000-32096200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
8	chr16:32096000-32096200	Active TSS	Primary T regulatory cells fromperipheralblood	blood
9	chr16:32096200-32096400	Flanking Bivalent TSS/Enh	Primary B cells from peripheral blood	blood
10	chr16:32096200-32096400	Flanking Bivalent TSS/Enh	Primary T regulatory cells fromperipheralblood	blood
11	chr16:32096200-32096400	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
12	chr16:32096200-32096600	Flanking Bivalent TSS/Enh	Placenta	Placenta
13	chr16:32096200-32096800	Active TSS	Primary T helper cells fromperipheralblood	blood
14	chr16:32096200-32096800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr16:32096200-32097000	Bivalent/Poised TSS	Primary T helper cells PMA-I stimulated	--
16	chr16:32096200-32097200	Active TSS	Primary T cells from cord blood	blood
17	chr16:32096200-32097200	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
18	chr16:32096200-32097200	Active TSS	Primary T helper naive cells fromperipheralblood	blood
19	chr16:32096200-32097200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr16:32096200-32097200	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
21	chr16:32096200-32097400	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr16:32096200-32097400	Active TSS	Right Atrium	heart
23	chr16:32096200-32097400	Bivalent/Poised TSS	A549	lung
24	chr16:32096200-32097400	Active TSS	Osteobl	bone
25	chr16:32096400-32096600	Flanking Bivalent TSS/Enh	Primary monocytes fromperipheralblood	blood
26	chr16:32096400-32096600	Flanking Bivalent TSS/Enh	Primary Natural Killer cells fromperipheralblood	blood
27	chr16:32096400-32096600	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
28	chr16:32096400-32096800	Bivalent/Poised TSS	Primary B cells from peripheral blood	blood
29	chr16:32096400-32096800	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
30	chr16:32096400-32096800	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr16:32096400-32096800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
32	chr16:32096400-32096800	ZNF genes & repeats	Right Ventricle	heart
33	chr16:32096400-32096800	Active TSS	HSMM	muscle
34	chr16:32096400-32097000	Bivalent Enhancer	Fetal Muscle Leg	muscle
35	chr16:32096400-32097200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr16:32096400-32097200	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr16:32096400-32097200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr16:32096400-32097200	Active TSS	Rectal Smooth Muscle	rectum
39	chr16:32096400-32097400	Bivalent/Poised TSS	Primary T regulatory cells fromperipheralblood	blood
40	chr16:32096400-32097600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr16:32096600-32096800	Bivalent Enhancer	Placenta	Placenta
42	chr16:32096600-32097000	Bivalent/Poised TSS	Primary monocytes fromperipheralblood	blood
43	chr16:32096600-32097000	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
44	chr16:32096600-32097200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr16:32096800-32097000	Flanking Bivalent TSS/Enh	Primary T helper cells fromperipheralblood	blood
46	chr16:32096800-32097000	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr16:32096800-32097000	Bivalent Enhancer	Dnd41	blood
48	chr16:32096800-32097200	Flanking Bivalent TSS/Enh	Primary B cells from peripheral blood	blood
49	chr16:32096800-32097200	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr16:32096800-32097200	Bivalent/Poised TSS	Cortex derived primary cultured neurospheres	brain

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