Variant report

Variant	nsv833196
Chromosome Location	chr16:31897381-32068953
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1214)
CpG islands
(count:427)
Chromatin interactive
region (count:26)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1214 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr16:31921392-31921528	K562	blood:	n/a	n/a
2	BATF	chr16:32059238-32059578	GM12878	blood:	n/a	n/a
3	BATF	chr16:32059227-32059446	GM12878	blood:	n/a	n/a
4	BATF	chr16:31967621-31968011	GM12878	blood:	n/a	n/a
5	BATF	chr16:32001426-32001621	GM12878	blood:	n/a	n/a
6	BATF	chr16:32050371-32050791	GM12878	blood:	n/a	n/a
7	BATF	chr16:32007628-32007992	GM12878	blood:	n/a	n/a
8	BCL11A	chr16:32001120-32001954	GM12878	blood:	n/a	n/a
9	BCL11A	chr16:31967573-31967758	GM12878	blood:	n/a	n/a
10	BCL11A	chr16:32001344-32001697	GM12878	blood:	n/a	n/a
11	BCL11A	chr16:32059954-32060170	GM12878	blood:	n/a	n/a
12	BCL3	chr16:31930017-31930282	GM12878	blood:	n/a	n/a
13	BCLAF1	chr16:31931788-31931977	GM12878	blood:	n/a	n/a
14	BCLAF1	chr16:31930908-31931183	GM12878	blood:	n/a	n/a
15	BHLHE40	chr16:31985679-31985857	HepG2	liver:	n/a	chr16:31985733-31985749
16	CBX3	chr16:32050646-32050949	K562	blood:	n/a	n/a
17	CBX3	chr16:31926914-31927807	K562	blood:	n/a	n/a
18	CBX3	chr16:32050399-32050591	K562	blood:	n/a	n/a
19	CBX3	chr16:31967467-31967998	K562	blood:	n/a	n/a
20	CBX3	chr16:32007689-32008189	K562	blood:	n/a	n/a
21	CBX3	chr16:31967501-31967949	K562	blood:	n/a	n/a
22	CBX3	chr16:31927092-31927896	K562	blood:	n/a	n/a
23	CBX3	chr16:31903333-31903820	K562	blood:	n/a	n/a
24	CEBPB	chr16:31939618-31939872	HepG2	liver:	n/a	n/a
25	CEBPB	chr16:31992336-31992524	K562	blood:	n/a	chr16:31992407-31992418
26	CEBPB	chr16:31992228-31992528	HepG2	liver:	n/a	chr16:31992407-31992418
27	CEBPB	chr16:31897426-31897569	K562	blood:	n/a	n/a
28	CEBPB	chr16:31897387-31897628	HepG2	liver:	n/a	n/a
29	CEBPB	chr16:31992231-31992592	K562	blood:	n/a	chr16:31992407-31992418
30	CEBPB	chr16:31927886-31927943	HepG2	liver:	n/a	n/a
31	CEBPB	chr16:31992189-31992618	K562	blood:	n/a	chr16:31992407-31992418
32	CHD2	chr16:32051321-32051488	HepG2	liver:	n/a	n/a
33	CTCF	chr16:31985670-31985828	GM12878	blood:	n/a	chr16:31985751-31985764 chr16:31985749-31985765 chr16:31985748-31985766 chr16:31985753-31985763
34	CTCF	chr16:31967592-31967918	Spleen_OC	spleen:	n/a	n/a
35	CTCF	chr16:32000820-32000970	WI-38	lung:	n/a	n/a
36	CTCF	chr16:32050085-32051257	A549	lung:	n/a	chr16:32050439-32050448
37	CTCF	chr16:32050540-32050690	HL-60	blood:	n/a	n/a
38	CTCF	chr16:31967477-31968073	A549	lung:	n/a	chr16:31967478-31967487
39	CTCF	chr16:31967620-31967770	GM12874	blood:	n/a	n/a
40	CTCF	chr16:32050180-32050330	HRPEpiC	eye:	n/a	n/a
41	CTCF	chr16:31967600-31967959	Medullo	brain:	n/a	n/a
42	CTCF	chr16:32000660-32000810	SK-N-SH_RA	brain:	n/a	chr16:32000681-32000702 chr16:32000686-32000704 chr16:32000688-32000701 chr16:32000692-32000701
43	CTCF	chr16:31985640-31985790	HCPEpiC	choroid plexus:	n/a	chr16:31985751-31985764 chr16:31985749-31985765 chr16:31985748-31985766 chr16:31985753-31985763
44	CTCF	chr16:32049926-32051512	K562	blood:	n/a	chr16:32051440-32051456 chr16:32050439-32050448 chr16:32051444-32051454
45	CTCF	chr16:32050540-32050690	BE2_C	brain:	n/a	n/a
46	CTCF	chr16:32050280-32050430	HCFaa	heart:	n/a	n/a
47	CTCF	chr16:32050260-32050410	GM12868	blood:	n/a	n/a
48	CTCF	chr16:32050547-32050759	HepG2	liver:	n/a	n/a
49	CTCF	chr16:32051360-32051510	GM12874	blood:	n/a	chr16:32051440-32051456 chr16:32051444-32051454
50	CTCF	chr16:32007705-32007944	MCF-7	breast:	n/a	chr16:32007831-32007849 chr16:32007834-32007847 chr16:32007833-32007854 chr16:32007888-32007901

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:31993231-31993281	Hepatocyte	liver:	n/a
2	chr16:31995423-31995473	Jurkat	blood:	n/a
3	chr16:32037687-32037737	T-47D	breast:	n/a
4	chr16:31993479-31993529	GM19239	blood:	n/a
5	chr16:32037687-32037737	HUVEC	blood vessel:	n/a
6	chr16:32049224-32049274	HCT-116	colon:	n/a
7	chr16:32049224-32049274	SKMC	muscle:	n/a
8	chr16:31990956-31991006	AG09309	skin:	n/a
9	chr16:31995423-31995473	HRCEpiC	kidney:	n/a
10	chr16:31995423-31995473	PrEC	prostate:	n/a
11	chr16:32049224-32049274	HIPEpiC	eye:	n/a
12	chr16:31993231-31993281	HPAEpiC	pulmonary alveolar:	n/a
13	chr16:31997067-31997117	Jurkat	blood:	n/a
14	chr16:31995423-31995473	HCM	heart:	n/a
15	chr16:31995423-31995473	GM12878	blood:	n/a
16	chr16:31993231-31993281	MCF-7	breast:	n/a
17	chr16:31993231-31993281	Caco-2	colon:	n/a
18	chr16:31990956-31991006	SKMC	muscle:	n/a
19	chr16:31995423-31995473	BJ	skin:	n/a
20	chr16:31995423-31995473	HAEpiC	amniotic membrane:	n/a
21	chr16:32049224-32049274	AG09319	gingival:	n/a
22	chr16:32049224-32049274	HPAEpiC	pulmonary alveolar:	n/a
23	chr16:32049224-32049274	Caco-2	colon:	n/a
24	chr16:31993231-31993281	HCPEpiC	choroid plexus:	n/a
25	chr16:31997067-31997117	HRE	kidney:	n/a
26	chr16:31990956-31991006	H1-hESC	embryonic stem cell:	embryo
27	chr16:32037687-32037737	NHBE	bronchial:	n/a
28	chr16:31993479-31993529	AG04449	skin:	fetal
29	chr16:31993479-31993529	NH-A	brain:	n/a
30	chr16:32037687-32037737	MCF-7	breast:	n/a
31	chr16:31993479-31993529	SKMC	muscle:	n/a
32	chr16:32049224-32049274	HRCEpiC	kidney:	n/a
33	chr16:31993231-31993281	GM12891	blood:	n/a
34	chr16:32049224-32049274	ProgFib	skin:	n/a
35	chr16:31997067-31997117	AG09309	skin:	n/a
36	chr16:31995423-31995473	HL-60	blood:	n/a
37	chr16:31995423-31995473	PFSK-1	brain:	n/a
38	chr16:31995423-31995473	GM19239	blood:	n/a
39	chr16:32049224-32049274	HRE	kidney:	n/a
40	chr16:31993479-31993529	NHBE	bronchial:	n/a
41	chr16:31990956-31991006	GM19239	blood:	n/a
42	chr16:32037687-32037737	HCM	heart:	n/a
43	chr16:32037687-32037737	BJ	skin:	n/a
44	chr16:31993231-31993281	HCT-116	colon:	n/a
45	chr16:32049224-32049274	MCF-7	breast:	n/a
46	chr16:31993231-31993281	SK-N-MC	brain:	n/a
47	chr16:32049224-32049274	HCPEpiC	choroid plexus:	n/a
48	chr16:31993231-31993281	K562	blood:	n/a
49	chr16:32049224-32049274	IMR90	lung:	fetal
50	chr16:32049224-32049274	SAEC	small airway:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:31893208..31894819-chr16:31924723..31927123,2	K562	blood:
2	chr16:31897518..31899829-chr16:31901532..31903567,2	K562	blood:
3	chr16:31926933..31929361-chr16:31930312..31932712,3	K562	blood:
4	chr16:31932903..31935520-chr16:31946813..31948460,2	K562	blood:
5	chr16:31926461..31927983-chr16:31935855..31938647,2	K562	blood:
6	chr16:31930170..31932707-chr16:31934024..31936447,2	K562	blood:
7	chr14:106598214..106598843-chr16:32050606..32051126,2	MCF-7	breast:
8	chr16:31884754..31886636-chr16:31917954..31920190,2	MCF-7	breast:
9	chr16:31932491..31936311-chr16:31936605..31941493,6	K562	blood:
10	chr16:31897518..31899829-chr16:31901532..31903567,2	K562	blood:
11	chr16:31908381..31911064-chr16:31928039..31930191,2	K562	blood:
12	chr16:31900905..31903577-chr16:31904504..31907027,3	K562	blood:
13	chr16:31931465..31935999-chr16:31936605..31940603,7	K562	blood:
14	chr16:31926461..31927983-chr16:31935855..31938647,2	K562	blood:
15	chr16:31908381..31911064-chr16:31928039..31930191,2	K562	blood:
16	chr16:31929792..31932707-chr16:31934299..31936447,2	K562	blood:
17	chr16:31930170..31932707-chr16:31934024..31936447,2	K562	blood:
18	chr16:31932491..31936311-chr16:31936605..31941493,6	K562	blood:
19	chr16:31896123..31898130-chr16:31922083..31923795,2	MCF-7	breast:
20	chr16:31929792..31932707-chr16:31934299..31936447,2	K562	blood:
21	chr16:31929972..31932646-chr16:31933691..31936236,4	MCF-7	breast:
22	chr16:31926933..31929361-chr16:31930312..31932712,3	K562	blood:
23	chr16:31900859..31903730-chr16:31904016..31907027,3	K562	blood:
24	chr16:31929972..31932646-chr16:31933691..31936236,4	MCF-7	breast:
25	chr16:31931465..31935999-chr16:31936605..31940603,7	K562	blood:
26	chr16:31932903..31935520-chr16:31946813..31948460,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF267-4	chr16:31973257-31973743	NONHSAT141979
2	lnc-ZNF720-2	chr16:31925797-31928629	NR_049749
3	lnc-ZNF720-2	chr16:31923175-31928172	ENSG00000262657.1
4	lnc-ZNF720-2	chr16:31901528-31901571	NR_049749
5	lnc-ZNF267-4	chr16:31975124-31975400	NONHSAT141983
6	lnc-ZNF267-3	chr16:31963481-31963794	NONHSAT141978
7	lnc-ZNF267-4	chr16:31972893-31972899	NONHSAT141979

No data

Variant related genes	Relation type
ENSG00000261289	TF binding region
ENSG00000223931	TF binding region
ENSG00000260628	TF binding region
ZNF267	TF binding region
ENSG00000197476	TF binding region
IGHV1OR16-1	TF binding region
ENSG00000260218	TF binding region
ENSG00000259950	TF binding region
IGHV1OR16-3	TF binding region
ENSG00000261289	CpG island
ENSG00000223931	CpG island
ENSG00000260628	CpG island
ZNF267	CpG island
ENSG00000197476	CpG island
IGHV1OR16-1	CpG island
ENSG00000260218	CpG island
ENSG00000259950	CpG island
IGHV1OR16-3	CpG island
ENSG00000259950	chromatin interactions
ENSG00000185947	chromatin interactions

Extended variants
information (count: 1920 )
Associated
traits (count: 126 )

Variant overlapped rSNPs/rCNVs (count:1920 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs187012718	chr16:31897394-31897395	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs554305940	chr16:31897576-31897577	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs573463207	chr16:31897597-31897598	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs540595833	chr16:31897602-31897603	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs558688163	chr16:31897626-31897627	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs564544995	chr16:31897632-31897633	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs577029444	chr16:31897633-31897634	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs544249841	chr16:31897637-31897638	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs577303145	chr16:31897643-31897644	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs562637592	chr16:31897684-31897685	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs376213958	chr16:31897690-31897691	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs530174249	chr16:31897698-31897699	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs369488186	chr16:31897720-31897721	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs192264304	chr16:31897768-31897769	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs182491942	chr16:31897837-31897838	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs186717802	chr16:31897880-31897881	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs549733582	chr16:31897885-31897886	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs571420322	chr16:31897886-31897887	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs113966892	chr16:31897904-31897905	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs532344466	chr16:31897947-31897948	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs561893790	chr16:31898016-31898017	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs550835703	chr16:31898027-31898028	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs145122721	chr16:31898064-31898065	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs535993939	chr16:31898122-31898123	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs576732182	chr16:31898151-31898152	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs554523920	chr16:31898176-31898177	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs116163484	chr16:31898182-31898183	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs149029153	chr16:31898226-31898227	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs542076125	chr16:31898238-31898239	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs558824992	chr16:31898253-31898254	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs577163092	chr16:31898258-31898259	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs544390650	chr16:31898270-31898271	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs145785745	chr16:31898330-31898331	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs190375630	chr16:31898458-31898459	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs372771733	chr16:31898516-31898517	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs541981154	chr16:31898529-31898530	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs78360529	chr16:31898573-31898574	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs79040275	chr16:31898587-31898588	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs75820426	chr16:31898588-31898589	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs182543420	chr16:31898643-31898644	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs147791139	chr16:31898660-31898661	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs546268014	chr16:31898666-31898667	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs540809172	chr16:31898682-31898683	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs565169920	chr16:31898698-31898699	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs532484591	chr16:31898699-31898700	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs377138028	chr16:31898713-31898714	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs77065823	chr16:31898724-31898725	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs376853699	chr16:31898772-31898773	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs568981303	chr16:31898796-31898797	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs188737770	chr16:31898807-31898808	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:126)

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
Breast cancer	22522925	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

Chromatin state (count:1146 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:31886800-31897600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
2	chr16:31886800-31898200	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr16:31886800-31901000	Weak transcription	Fetal Brain Male	brain
4	chr16:31887000-31901600	Weak transcription	Fetal Brain Female	brain
5	chr16:31887000-31902200	ZNF genes & repeats	A549	lung
6	chr16:31887200-31900800	Weak transcription	Brain Germinal Matrix	brain
7	chr16:31887400-31900800	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr16:31887800-31907400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr16:31889400-31911600	ZNF genes & repeats	Primary B cells from cord blood	blood
10	chr16:31889600-31897600	Weak transcription	Brain Cingulate Gyrus	brain
11	chr16:31890000-31897600	Strong transcription	Fetal Intestine Large	intestine
12	chr16:31890200-31897600	Weak transcription	Fetal Muscle Trunk	muscle
13	chr16:31890200-31905800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr16:31891800-31901800	Weak transcription	Brain Inferior Temporal Lobe	brain
15	chr16:31892000-31900800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr16:31892000-31905000	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr16:31892000-31910400	ZNF genes & repeats	GM12878-XiMat	blood
18	chr16:31892200-31898800	Strong transcription	Dnd41	blood
19	chr16:31892200-31900800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr16:31892200-31901600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr16:31892200-31905000	Weak transcription	Fetal Heart	heart
22	chr16:31892400-31897400	Weak transcription	Rectal Smooth Muscle	rectum
23	chr16:31892400-31899600	Genic enhancers	Primary T helper cells PMA-I stimulated	--
24	chr16:31892400-31903400	Weak transcription	Skeletal Muscle Male	skeletal muscle
25	chr16:31892400-31904200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr16:31892400-31905000	Weak transcription	Brain Substantia Nigra	brain
27	chr16:31892400-31905800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
28	chr16:31892800-31898000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr16:31892800-31899000	Strong transcription	Duodenum Mucosa	Duodenum
30	chr16:31892800-31899200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr16:31892800-31900800	Weak transcription	Ovary	ovary
32	chr16:31892800-31901600	Weak transcription	Brain Anterior Caudate	brain
33	chr16:31892800-31902600	Weak transcription	Pancreas	Pancrea
34	chr16:31892800-31905200	Weak transcription	Right Ventricle	heart
35	chr16:31892800-31906000	Weak transcription	Psoas Muscle	Psoas
36	chr16:31893000-31897400	Weak transcription	Cortex derived primary cultured neurospheres	brain
37	chr16:31893000-31897600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr16:31893000-31899400	Strong transcription	Osteobl	bone
39	chr16:31893000-31900800	Strong transcription	Primary B cells from peripheral blood	blood
40	chr16:31893000-31913200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr16:31893200-31911800	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr16:31893400-31897600	Strong transcription	Primary monocytes fromperipheralblood	blood
43	chr16:31893400-31902800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
44	chr16:31893400-31911400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr16:31893400-31911800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr16:31893400-31912000	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
47	chr16:31893600-31917800	Weak transcription	Colon Smooth Muscle	Colon
48	chr16:31893800-31903400	Strong transcription	HSMM	muscle
49	chr16:31894000-31903000	Weak transcription	Stomach Mucosa	stomach
50	chr16:31894200-31897800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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