Variant report

Variant	nsv906944
Chromosome Location	chr16:76521236-76768178
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1266)
CpG islands
(count:366)
Chromatin interactive
region (count:42)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1266 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:76673948-76674099	K562	blood:	n/a	n/a
2	ARID3A	chr16:76684292-76684820	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:76668888-76668938	K562	blood:	n/a	n/a
4	ARID3A	chr16:76687350-76687721	HepG2	liver:	n/a	n/a
5	ARID3A	chr16:76608141-76609300	HepG2	liver:	n/a	n/a
6	ARID3A	chr16:76566183-76566513	HepG2	liver:	n/a	n/a
7	ATF1	chr16:76549644-76549672	K562	blood:	n/a	n/a
8	ATF1	chr16:76614425-76614592	K562	blood:	n/a	n/a
9	ATF1	chr16:76581402-76581528	K562	blood:	n/a	n/a
10	ATF1	chr16:76668805-76669470	K562	blood:	n/a	n/a
11	ATF1	chr16:76687134-76687664	K562	blood:	n/a	n/a
12	ATF3	chr16:76668818-76669064	K562	blood:	n/a	n/a
13	ATF3	chr16:76687346-76687640	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr16:76703299-76703491	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr16:76617930-76618131	GM12878	blood:	n/a	chr16:76618063-76618074
16	BATF	chr16:76610960-76611272	GM12878	blood:	n/a	n/a
17	BATF	chr16:76610931-76611290	GM12878	blood:	n/a	n/a
18	BATF	chr16:76617883-76618255	GM12878	blood:	n/a	chr16:76618063-76618074
19	BHLHE40	chr16:76704362-76704737	K562	blood:	n/a	chr16:76704597-76704606
20	BHLHE40	chr16:76608424-76608923	HepG2	liver:	n/a	n/a
21	BHLHE40	chr16:76610846-76611310	GM12878	blood:	n/a	n/a
22	BHLHE40	chr16:76556000-76556061	K562	blood:	n/a	n/a
23	BHLHE40	chr16:76668642-76669184	K562	blood:	n/a	n/a
24	BRCA1	chr16:76536310-76536336	H1-hESC	embryonic stem cell:	n/a	n/a
25	CBX3	chr16:76668672-76669213	K562	blood:	n/a	n/a
26	CBX3	chr16:76668556-76669332	K562	blood:	n/a	n/a
27	CCNT2	chr16:76668739-76669178	K562	blood:	n/a	n/a
28	CEBPB	chr16:76589711-76590032	HepG2	liver:	n/a	chr16:76589843-76589855 chr16:76589975-76589987
29	CEBPB	chr16:76551445-76551764	HepG2	liver:	n/a	n/a
30	CEBPB	chr16:76552574-76552900	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr16:76687293-76687724	K562	blood:	n/a	n/a
32	CEBPB	chr16:76608672-76608920	A549	lung:	n/a	n/a
33	CEBPB	chr16:76687286-76687682	HepG2	liver:	n/a	n/a
34	CEBPB	chr16:76687239-76687712	MCF-7	breast:	n/a	n/a
35	CEBPB	chr16:76734138-76734455	HepG2	liver:	n/a	n/a
36	CEBPB	chr16:76687258-76687706	A549	lung:	n/a	n/a
37	CEBPB	chr16:76734183-76734406	K562	blood:	n/a	n/a
38	CEBPB	chr16:76710226-76710819	MCF-7	breast:	n/a	n/a
39	CEBPB	chr16:76687308-76687632	K562	blood:	n/a	n/a
40	CEBPB	chr16:76668375-76668595	HepG2	liver:	n/a	chr16:76668457-76668468
41	CEBPB	chr16:76698299-76698542	HepG2	liver:	n/a	n/a
42	CEBPB	chr16:76710097-76710858	MCF-7	breast:	n/a	n/a
43	CEBPB	chr16:76640219-76640497	Hela-S3	cervix:	n/a	chr16:76640353-76640364
44	CEBPB	chr16:76591052-76591187	HepG2	liver:	n/a	n/a
45	CEBPB	chr16:76669262-76669518	HepG2	liver:	n/a	chr16:76669437-76669448
46	CEBPB	chr16:76700933-76701106	HepG2	liver:	n/a	chr16:76700935-76700946 chr16:76701040-76701051 chr16:76700935-76700946
47	CEBPB	chr16:76756458-76756533	K562	blood:	n/a	chr16:76756489-76756502 chr16:76756490-76756501
48	CEBPB	chr16:76687366-76687695	HepG2	liver:	n/a	n/a
49	CEBPB	chr16:76626178-76626377	H1-hESC	embryonic stem cell:	n/a	chr16:76626265-76626276
50	CEBPB	chr16:76640302-76640497	H1-hESC	embryonic stem cell:	n/a	chr16:76640353-76640364

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:76708064-76708114	AG04449	skin:	fetal
2	chr16:76708064-76708114	LNCaP	prostate:	n/a
3	chr16:76665665-76665715	NHDF-neo	bronchial:	n/a
4	chr16:76669151-76669201	BE2_C	brain:	n/a
5	chr16:76708064-76708114	MCF-7	breast:	n/a
6	chr16:76666860-76666910	Hepatocyte	liver:	n/a
7	chr16:76668836-76668886	SK-N-SH_RA	brain:	n/a
8	chr16:76708064-76708114	HCPEpiC	choroid plexus:	n/a
9	chr16:76669151-76669201	HRPEpiC	eye:	n/a
10	chr16:76666860-76666910	K562	blood:	n/a
11	chr16:76670197-76670247	AG09309	skin:	n/a
12	chr16:76666860-76666910	HNPCEpiC	eye:	n/a
13	chr16:76665665-76665715	SK-N-MC	brain:	n/a
14	chr16:76665665-76665715	NT2-D1	testis:	n/a
15	chr16:76669151-76669201	SK-N-MC	brain:	n/a
16	chr16:76708064-76708114	HMEC	breast:	n/a
17	chr16:76708064-76708114	HEEpiC	esophagus:	n/a
18	chr16:76669151-76669201	HCF	heart:	n/a
19	chr16:76666860-76666910	ECC-1	luminal epithelium:	n/a
20	chr16:76668836-76668886	PrEC	prostate:	n/a
21	chr16:76668836-76668886	A549	lung:	n/a
22	chr16:76669151-76669201	GM19239	blood:	n/a
23	chr16:76665665-76665715	SK-N-SH_RA	brain:	n/a
24	chr16:76669151-76669201	ProgFib	skin:	n/a
25	chr16:76669151-76669201	SK-N-SH_RA	brain:	n/a
26	chr16:76670197-76670247	HepG2	liver:	n/a
27	chr16:76666860-76666910	AG04450	lung:	fetal
28	chr16:76670197-76670247	HPAEpiC	pulmonary alveolar:	n/a
29	chr16:76666860-76666910	NB4	blood:	n/a
30	chr16:76666860-76666910	SK-N-MC	brain:	n/a
31	chr16:76668836-76668886	HPAEpiC	pulmonary alveolar:	n/a
32	chr16:76669151-76669201	HCPEpiC	choroid plexus:	n/a
33	chr16:76669151-76669201	HepG2	liver:	n/a
34	chr16:76665665-76665715	MCF-7	breast:	n/a
35	chr16:76670197-76670247	Hepatocyte	liver:	n/a
36	chr16:76665665-76665715	HCT-116	colon:	n/a
37	chr16:76665665-76665715	GM06990	blood:	n/a
38	chr16:76670197-76670247	NT2-D1	testis:	n/a
39	chr16:76668836-76668886	NB4	blood:	n/a
40	chr16:76665665-76665715	HRCEpiC	kidney:	n/a
41	chr16:76670197-76670247	HCPEpiC	choroid plexus:	n/a
42	chr16:76670197-76670247	K562	blood:	n/a
43	chr16:76708064-76708114	GM12892	blood:	n/a
44	chr16:76670197-76670247	AG09319	gingival:	n/a
45	chr16:76669151-76669201	LNCaP	prostate:	n/a
46	chr16:76668836-76668886	HUVEC	blood vessel:	n/a
47	chr16:76666860-76666910	GM06990	blood:	n/a
48	chr16:76708064-76708114	HEK293	kidney:	embryo
49	chr16:76670197-76670247	GM19239	blood:	n/a
50	chr16:76666860-76666910	HIPEpiC	eye:	n/a

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:76703589..76705752-chr16:76708591..76711050,2	MCF-7	breast:
2	chr16:76701550..76704283-chr16:76707898..76709517,2	K562	blood:
3	chr16:76747877..76750802-chr16:76754682..76756382,2	K562	blood:
4	chr16:76607256..76609840-chr16:76614807..76617382,2	K562	blood:
5	chr16:76312365..76313607-chr16:76673596..76674287,4	MCF-7	breast:
6	chr16:76669652..76671358-chr16:76701917..76703611,2	K562	blood:
7	chr16:76687235..76688893-chr16:76692839..76694713,2	K562	blood:
8	chr16:76747877..76750802-chr16:76754682..76756382,2	K562	blood:
9	chr16:76699506..76700441-chr16:77205329..77206242,3	MCF-7	breast:
10	chr16:76687235..76688893-chr16:76692839..76694713,2	K562	blood:
11	chr16:76607256..76609840-chr16:76614807..76617382,2	K562	blood:
12	chr16:76756661..76759781-chr16:76761311..76764642,3	K562	blood:
13	chr16:76756661..76759781-chr16:76761311..76764642,3	K562	blood:
14	chr16:76687186..76688106-chr16:76857078..76857671,2	MCF-7	breast:
15	chr16:76519348..76521301-chr16:76524212..76526573,2	K562	blood:
16	chr16:76636023..76638622-chr16:76652291..76654068,2	K562	blood:
17	chr16:76534271..76535887-chr16:76537682..76540215,2	MCF-7	breast:
18	chr16:76741499..76743675-chr16:76746368..76748815,2	K562	blood:
19	chr16:76741499..76743675-chr16:76746368..76748815,2	K562	blood:
20	chr16:76560975..76563666-chr16:76569503..76571277,2	K562	blood:
21	chr16:76679307..76681357-chr16:76683795..76685911,2	MCF-7	breast:
22	chr16:76741969..76744727-chr16:76747101..76748627,2	K562	blood:
23	chr16:76669652..76671358-chr16:76701917..76703611,2	K562	blood:
24	chr16:76527293..76528859-chr16:76529180..76530762,2	MCF-7	breast:
25	chr16:76312246..76313469-chr16:76687103..76688657,6	MCF-7	breast:
26	chr16:76741969..76744727-chr16:76747101..76748627,2	K562	blood:
27	chr16:76319924..76320753-chr16:76686923..76687617,2	MCF-7	breast:
28	chr16:76534271..76535887-chr16:76537682..76540215,2	MCF-7	breast:
29	chr16:76519348..76521301-chr16:76524212..76526573,2	K562	blood:
30	chr16:76699516..76700310-chr16:77203606..77204151,2	MCF-7	breast:
31	chr16:76665227..76667688-chr16:76668445..76671290,2	K562	blood:
32	chr16:76701550..76704283-chr16:76707898..76709517,2	K562	blood:
33	chr16:76542177..76544098-chr6:26155995..26158781,2	MCF-7	breast:
34	chr16:76527293..76528859-chr16:76529180..76530762,2	MCF-7	breast:
35	chr16:76679307..76681357-chr16:76683795..76685911,2	MCF-7	breast:
36	chr16:76699528..76700343-chr16:77076632..77077627,2	MCF-7	breast:
37	chr16:76584372..76585914-chr16:76586080..76587632,2	MCF-7	breast:
38	chr16:76636023..76638622-chr16:76652291..76654068,2	K562	blood:
39	chr16:75835108..75835786-chr16:76687075..76687822,2	MCF-7	breast:
40	chr16:76703589..76705752-chr16:76708591..76711050,2	MCF-7	breast:
41	chr16:75834944..75835823-chr16:76687371..76688062,3	MCF-7	breast:
42	chr16:76560975..76563666-chr16:76569503..76571277,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-58C22.1.1-2	chr16:76737141-76737172	XLOC_011792
2	lnc-RP11-58C22.1.1-1	chr16:76669394-76669520	ENSG00000250514
3	lnc-RP11-58C22.1.1-1	chr16:76668895-76669046	ENSG00000250514
4	lnc-RP11-58C22.1.1-1	chr16:76690565-76692375	ENSG00000250514
5	lnc-RP11-58C22.1.1-1	chr16:76689454-76689561	ENSG00000250514
6	lnc-RP11-58C22.1.1-2	chr16:76733678-76734033	XLOC_011792

No data

Variant related genes	Relation type
ENSG00000261833	TF binding region
ENSG00000259995	TF binding region
ENSG00000250514	TF binding region
ENSG00000261833	CpG island
ENSG00000259995	CpG island
ENSG00000250514	CpG island
ENSG00000158373	chromatin interactions
ENSG00000168298	chromatin interactions
ENSG00000261833	chromatin interactions
ENSG00000250514	chromatin interactions
DDX3Y	miRNA target sites
SPRYD3	miRNA target sites
CDV3	miRNA target sites
CDKN1A	miRNA target sites

Extended variants
information (count: 6740 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:6740 , 50 per page) page: 1 2 3 4 5 6 7 ... 135

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4423447	chr16:76521236-76521237	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs532673544	chr16:76521241-76521242	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs541869504	chr16:76521292-76521293	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs555296959	chr16:76521318-76521319	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs555622881	chr16:76521344-76521345	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs574402336	chr16:76521377-76521378	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs181900831	chr16:76521393-76521394	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs186592227	chr16:76521433-76521434	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs139177642	chr16:76521475-76521476	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs545962904	chr16:76521513-76521514	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs9923842	chr16:76521527-76521528	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs12926636	chr16:76521528-76521529	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs76290350	chr16:76521542-76521543	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs568016521	chr16:76521548-76521549	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs566948038	chr16:76521608-76521609	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs528005311	chr16:76521655-76521656	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs548078711	chr16:76521691-76521692	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs571111970	chr16:76521699-76521700	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs539688360	chr16:76521701-76521702	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs556715618	chr16:76521807-76521808	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs77184690	chr16:76521817-76521818	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs191052528	chr16:76521818-76521819	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs571682096	chr16:76521871-76521872	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs149371461	chr16:76521916-76521917	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs555358108	chr16:76521942-76521943	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs572550185	chr16:76521993-76521994	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs144328593	chr16:76522008-76522009	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs182400068	chr16:76522118-76522119	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs553976467	chr16:76522141-76522142	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs77210724	chr16:76522145-76522146	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs374841263	chr16:76522202-76522203	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs368915727	chr16:76522231-76522232	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs553814338	chr16:76522245-76522246	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs187938219	chr16:76522268-76522269	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs78239834	chr16:76522341-76522342	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs530076675	chr16:76522355-76522356	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs191077028	chr16:76522409-76522410	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs7193963	chr16:76522419-76522420	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs541909462	chr16:76522425-76522426	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs561685248	chr16:76522478-76522479	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs80251396	chr16:76522534-76522535	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs148499296	chr16:76522542-76522543	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs183393410	chr16:76522552-76522553	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs188303530	chr16:76522569-76522570	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs16944468	chr16:76522590-76522591	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs550118458	chr16:76522613-76522614	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs35320538	chr16:76522662-76522663	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs570199102	chr16:76522679-76522680	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs535575643	chr16:76522710-76522711	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs555469332	chr16:76522752-76522753	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16702952	CNVD
Medulloblastoma	16968546	CNVD
Prostate cancer	19242612	CNVD
Cancer	22429812	CNVD
Ewing''s sarcoma	21437220	CNVD
Ewing''s sarcoma	22429812	CNVD
Melanoma	18172304	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Multiple myeloma	21628407	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17603634	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	17245344	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Melanoma	22183965	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Poland''s syndrome	22110015	CNVD
Neuroblastoma	21899760	CNVD
Liver carcinoma	19366792	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	19156837	CNVD
Acute myeloid leukemia	17377590	CNVD
Breast cancer	20409316	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	21509527	CNVD
Schizophrenia	23813976	CNVD
Lung cancer	24585490	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Neuroblastoma	18923524	CNVD
Cancer	20164920	CNVD
Cancer	20581869	CNVD

Chromatin state (count:307 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:76516800-76523800	Weak transcription	Brain Angular Gyrus	brain
2	chr16:76517400-76522600	Enhancers	Liver	Liver
3	chr16:76518600-76523600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr16:76518600-76526800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr16:76518800-76523600	Weak transcription	Brain Anterior Caudate	brain
6	chr16:76518800-76523800	Weak transcription	Brain Cingulate Gyrus	brain
7	chr16:76519600-76522200	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr16:76519600-76522800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr16:76520200-76522400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr16:76520400-76522200	Enhancers	Brain Substantia Nigra	brain
11	chr16:76520600-76521400	Enhancers	Brain Hippocampus Middle	brain
12	chr16:76520600-76523600	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr16:76521400-76521600	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
14	chr16:76521400-76521800	Enhancers	Placenta Amnion	Placenta Amnion
15	chr16:76521400-76522200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
16	chr16:76521400-76523600	Weak transcription	Brain Hippocampus Middle	brain
17	chr16:76521800-76522000	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr16:76522200-76522400	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr16:76522200-76523600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr16:76522200-76523600	Weak transcription	Brain Substantia Nigra	brain
21	chr16:76523600-76524000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr16:76523600-76524000	Genic enhancers	Brain Substantia Nigra	brain
23	chr16:76523600-76524000	Active TSS	Left Ventricle	heart
24	chr16:76523600-76524400	Enhancers	Breast Myoepithelial Primary Cells	Breast
25	chr16:76523600-76524400	Enhancers	Brain Anterior Caudate	brain
26	chr16:76523600-76524600	Enhancers	Fetal Lung	lung
27	chr16:76523600-76524800	Enhancers	Cortex derived primary cultured neurospheres	brain
28	chr16:76523600-76524800	Genic enhancers	Brain Hippocampus Middle	brain
29	chr16:76523600-76525200	Enhancers	Brain Inferior Temporal Lobe	brain
30	chr16:76523800-76524600	Enhancers	Brain Angular Gyrus	brain
31	chr16:76523800-76524600	Genic enhancers	Brain Cingulate Gyrus	brain
32	chr16:76524000-76524400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr16:76524000-76537000	Weak transcription	Brain Substantia Nigra	brain
34	chr16:76524400-76525600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr16:76524400-76537000	Weak transcription	Brain Anterior Caudate	brain
36	chr16:76524600-76526400	Weak transcription	Brain Angular Gyrus	brain
37	chr16:76524600-76537200	Weak transcription	Brain Cingulate Gyrus	brain
38	chr16:76524800-76525600	Strong transcription	Brain Hippocampus Middle	brain
39	chr16:76525200-76554000	Weak transcription	Brain Inferior Temporal Lobe	brain
40	chr16:76525600-76535600	Weak transcription	Brain Hippocampus Middle	brain
41	chr16:76547000-76548200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr16:76548000-76548600	Enhancers	Brain Germinal Matrix	brain
43	chr16:76548200-76553000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr16:76551400-76551600	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr16:76551400-76551600	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr16:76551600-76552200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
47	chr16:76551800-76553000	Weak transcription	HUES48 Cell Line	embryonic stem cell
48	chr16:76552200-76554400	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr16:76552400-76552800	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr16:76552400-76553000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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