Variant report

Variant	nsv573047
Chromosome Location	chr16:76540798-76881625
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1578)
CpG islands
(count:366)
Chromatin interactive
region (count:49)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1578 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:76687350-76687721	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:76566183-76566513	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:76608141-76609300	HepG2	liver:	n/a	n/a
4	ARID3A	chr16:76673948-76674099	K562	blood:	n/a	n/a
5	ARID3A	chr16:76684292-76684820	HepG2	liver:	n/a	n/a
6	ARID3A	chr16:76668888-76668938	K562	blood:	n/a	n/a
7	ATF1	chr16:76789952-76789998	K562	blood:	n/a	n/a
8	ATF1	chr16:76549644-76549672	K562	blood:	n/a	n/a
9	ATF1	chr16:76581402-76581528	K562	blood:	n/a	n/a
10	ATF1	chr16:76614425-76614592	K562	blood:	n/a	n/a
11	ATF1	chr16:76687134-76687664	K562	blood:	n/a	n/a
12	ATF1	chr16:76668805-76669470	K562	blood:	n/a	n/a
13	ATF2	chr16:76839037-76839302	GM12878	blood:	n/a	n/a
14	ATF3	chr16:76687346-76687640	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF3	chr16:76668818-76669064	K562	blood:	n/a	n/a
16	BACH1	chr16:76703299-76703491	H1-hESC	embryonic stem cell:	n/a	n/a
17	BATF	chr16:76856327-76856649	GM12878	blood:	n/a	n/a
18	BATF	chr16:76617930-76618131	GM12878	blood:	n/a	chr16:76618063-76618074
19	BATF	chr16:76856386-76856604	GM12878	blood:	n/a	n/a
20	BATF	chr16:76610931-76611290	GM12878	blood:	n/a	n/a
21	BATF	chr16:76850471-76850665	GM12878	blood:	n/a	chr16:76850562-76850573
22	BATF	chr16:76617883-76618255	GM12878	blood:	n/a	chr16:76618063-76618074
23	BATF	chr16:76838952-76839361	GM12878	blood:	n/a	n/a
24	BATF	chr16:76850433-76850727	GM12878	blood:	n/a	chr16:76850562-76850573
25	BATF	chr16:76610960-76611272	GM12878	blood:	n/a	n/a
26	BATF	chr16:76838975-76839411	GM12878	blood:	n/a	n/a
27	BCL11A	chr16:76839015-76839347	GM12878	blood:	n/a	chr16:76839215-76839224 chr16:76839226-76839235
28	BCL11A	chr16:76839121-76839299	GM12878	blood:	n/a	chr16:76839215-76839224 chr16:76839226-76839235
29	BHLHE40	chr16:76704362-76704737	K562	blood:	n/a	chr16:76704597-76704606
30	BHLHE40	chr16:76668642-76669184	K562	blood:	n/a	n/a
31	BHLHE40	chr16:76608424-76608923	HepG2	liver:	n/a	n/a
32	BHLHE40	chr16:76610846-76611310	GM12878	blood:	n/a	n/a
33	BHLHE40	chr16:76556000-76556061	K562	blood:	n/a	n/a
34	CBX3	chr16:76668556-76669332	K562	blood:	n/a	n/a
35	CBX3	chr16:76668672-76669213	K562	blood:	n/a	n/a
36	CCNT2	chr16:76668739-76669178	K562	blood:	n/a	n/a
37	CEBPB	chr16:76756458-76756533	K562	blood:	n/a	chr16:76756489-76756502 chr16:76756490-76756501
38	CEBPB	chr16:76687301-76687681	IMR90	lung:	n/a	n/a
39	CEBPB	chr16:76804175-76804292	HepG2	liver:	n/a	chr16:76804250-76804261
40	CEBPB	chr16:76687286-76687682	HepG2	liver:	n/a	n/a
41	CEBPB	chr16:76700933-76701106	HepG2	liver:	n/a	chr16:76700935-76700946 chr16:76701040-76701051 chr16:76700935-76700946
42	CEBPB	chr16:76640219-76640497	Hela-S3	cervix:	n/a	chr16:76640353-76640364
43	CEBPB	chr16:76702300-76702493	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr16:76857050-76857179	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr16:76734183-76734406	K562	blood:	n/a	n/a
46	CEBPB	chr16:76811841-76811942	HepG2	liver:	n/a	n/a
47	CEBPB	chr16:76821360-76821589	A549	lung:	n/a	chr16:76821486-76821497
48	CEBPB	chr16:76673910-76674162	K562	blood:	n/a	n/a
49	CEBPB	chr16:76687295-76687707	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr16:76687171-76687709	MCF-7	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:76670197-76670247	IMR90	lung:	fetal
2	chr16:76668836-76668886	GM12878	blood:	n/a
3	chr16:76668836-76668886	T-47D	breast:	n/a
4	chr16:76669151-76669201	NHBE	bronchial:	n/a
5	chr16:76669151-76669201	H1-hESC	embryonic stem cell:	embryo
6	chr16:76668836-76668886	U87	brain:	n/a
7	chr16:76665665-76665715	BJ	skin:	n/a
8	chr16:76665665-76665715	LNCaP	prostate:	n/a
9	chr16:76708064-76708114	T-47D	breast:	n/a
10	chr16:76668836-76668886	MCF-7	breast:	n/a
11	chr16:76669151-76669201	SK-N-MC	brain:	n/a
12	chr16:76665665-76665715	SK-N-SH	brain:	n/a
13	chr16:76665665-76665715	RPTEC	kidney:	n/a
14	chr16:76666860-76666910	SK-N-MC	brain:	n/a
15	chr16:76666860-76666910	MCF-7	breast:	n/a
16	chr16:76665665-76665715	U87	brain:	n/a
17	chr16:76670197-76670247	BJ	skin:	n/a
18	chr16:76668836-76668886	IMR90	lung:	fetal
19	chr16:76670197-76670247	K562	blood:	n/a
20	chr16:76666860-76666910	AG04450	lung:	fetal
21	chr16:76668836-76668886	HCT-116	colon:	n/a
22	chr16:76666860-76666910	SK-N-SH	brain:	n/a
23	chr16:76666860-76666910	Jurkat	blood:	n/a
24	chr16:76708064-76708114	GM12892	blood:	n/a
25	chr16:76665665-76665715	GM12878	blood:	n/a
26	chr16:76670197-76670247	GM06990	blood:	n/a
27	chr16:76669151-76669201	BJ	skin:	n/a
28	chr16:76670197-76670247	GM12892	blood:	n/a
29	chr16:76669151-76669201	GM06990	blood:	n/a
30	chr16:76666860-76666910	Hepatocyte	liver:	n/a
31	chr16:76668836-76668886	HNPCEpiC	eye:	n/a
32	chr16:76665665-76665715	HMEC	breast:	n/a
33	chr16:76670197-76670247	HRPEpiC	eye:	n/a
34	chr16:76666860-76666910	HNPCEpiC	eye:	n/a
35	chr16:76666860-76666910	HMEC	breast:	n/a
36	chr16:76665665-76665715	GM06990	blood:	n/a
37	chr16:76665665-76665715	HUVEC	blood vessel:	n/a
38	chr16:76665665-76665715	Hela-S3	cervix:	n/a
39	chr16:76666860-76666910	HCPEpiC	choroid plexus:	n/a
40	chr16:76665665-76665715	HCPEpiC	choroid plexus:	n/a
41	chr16:76665665-76665715	K562	blood:	n/a
42	chr16:76668836-76668886	GM12892	blood:	n/a
43	chr16:76665665-76665715	SK-N-SH_RA	brain:	n/a
44	chr16:76668836-76668886	AoSMC	blood vessel:	n/a
45	chr16:76669151-76669201	AG04450	lung:	fetal
46	chr16:76668836-76668886	PFSK-1	brain:	n/a
47	chr16:76708064-76708114	A549	lung:	n/a
48	chr16:76669151-76669201	Caco-2	colon:	n/a
49	chr16:76665665-76665715	HAEpiC	amniotic membrane:	n/a
50	chr16:76668836-76668886	HCM	heart:	n/a

(count:49 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:76312365..76313607-chr16:76673596..76674287,4	MCF-7	breast:
2	chr16:76687186..76688106-chr16:76857078..76857671,2	MCF-7	breast:
3	chr16:76669652..76671358-chr16:76701917..76703611,2	K562	blood:
4	chr16:76699516..76700310-chr16:77203606..77204151,2	MCF-7	breast:
5	chr16:76844876..76847420-chr19:45599129..45600971,2	MCF-7	breast:
6	chr16:76747877..76750802-chr16:76754682..76756382,2	K562	blood:
7	chr16:76687235..76688893-chr16:76692839..76694713,2	K562	blood:
8	chr16:76741969..76744727-chr16:76747101..76748627,2	K562	blood:
9	chr16:76687235..76688893-chr16:76692839..76694713,2	K562	blood:
10	chr16:76741499..76743675-chr16:76746368..76748815,2	K562	blood:
11	chr16:76784883..76787638-chr16:76787899..76789936,2	MCF-7	breast:
12	chr16:76846196..76848121-chr16:76848521..76851117,2	MCF-7	breast:
13	chr16:75834944..75835823-chr16:76687371..76688062,3	MCF-7	breast:
14	chr16:76607256..76609840-chr16:76614807..76617382,2	K562	blood:
15	chr16:76701550..76704283-chr16:76707898..76709517,2	K562	blood:
16	chr16:76703589..76705752-chr16:76708591..76711050,2	MCF-7	breast:
17	chr16:76846196..76848121-chr16:76848521..76851117,2	MCF-7	breast:
18	chr16:76319924..76320753-chr16:76686923..76687617,2	MCF-7	breast:
19	chr16:76856883..76857419-chr16:77076804..77077643,2	MCF-7	breast:
20	chr16:76773881..76775450-chr16:76881262..76882791,2	MCF-7	breast:
21	chr16:76636023..76638622-chr16:76652291..76654068,2	K562	blood:
22	chr16:76756661..76759781-chr16:76761311..76764642,3	K562	blood:
23	chr16:76607256..76609840-chr16:76614807..76617382,2	K562	blood:
24	chr16:76741969..76744727-chr16:76747101..76748627,2	K562	blood:
25	chr16:75835108..75835786-chr16:76687075..76687822,2	MCF-7	breast:
26	chr16:76878928..76880909-chr16:76882753..76884640,2	K562	blood:
27	chr16:76817240..76820216-chr16:76820936..76823507,2	K562	blood:
28	chr16:76665227..76667688-chr16:76668445..76671290,2	K562	blood:
29	chr16:76773881..76775450-chr16:76881262..76882791,2	MCF-7	breast:
30	chr16:76560975..76563666-chr16:76569503..76571277,2	K562	blood:
31	chr16:76312246..76313469-chr16:76687103..76688657,6	MCF-7	breast:
32	chr16:76699506..76700441-chr16:77205329..77206242,3	MCF-7	breast:
33	chr16:76679307..76681357-chr16:76683795..76685911,2	MCF-7	breast:
34	chr16:76560975..76563666-chr16:76569503..76571277,2	K562	blood:
35	chr16:76741499..76743675-chr16:76746368..76748815,2	K562	blood:
36	chr16:76636023..76638622-chr16:76652291..76654068,2	K562	blood:
37	chr16:76699528..76700343-chr16:77076632..77077627,2	MCF-7	breast:
38	chr16:76703589..76705752-chr16:76708591..76711050,2	MCF-7	breast:
39	chr16:76687186..76688106-chr16:76857078..76857671,2	MCF-7	breast:
40	chr16:76584372..76585914-chr16:76586080..76587632,2	MCF-7	breast:
41	chr16:76747877..76750802-chr16:76754682..76756382,2	K562	blood:
42	chr16:76784883..76787638-chr16:76787899..76789936,2	MCF-7	breast:
43	chr16:76756661..76759781-chr16:76761311..76764642,3	K562	blood:
44	chr16:76881611..76883954-chr16:76887729..76889678,2	MCF-7	breast:
45	chr16:76701550..76704283-chr16:76707898..76709517,2	K562	blood:
46	chr16:76669652..76671358-chr16:76701917..76703611,2	K562	blood:
47	chr16:76542177..76544098-chr6:26155995..26158781,2	MCF-7	breast:
48	chr16:76679307..76681357-chr16:76683795..76685911,2	MCF-7	breast:
49	chr16:76817240..76820216-chr16:76820936..76823507,2	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-58C22.1.1-4	chr16:76770239-76770376	ENSG00000259995.1
2	lnc-RP11-58C22.1.1-3	chr16:76806570-76806959	XLOC_011793
3	lnc-RP11-58C22.1.1-1	chr16:76668895-76669046	ENSG00000250514
4	lnc-RP11-58C22.1.1-2	chr16:76733678-76734033	XLOC_011792
5	lnc-RP11-58C22.1.1-1	chr16:76689454-76689561	ENSG00000250514
6	lnc-RP11-58C22.1.1-3	chr16:76803213-76803278	XLOC_011793
7	lnc-RP11-58C22.1.1-1	chr16:76690565-76692375	ENSG00000250514
8	lnc-RP11-58C22.1.1-2	chr16:76737141-76737172	XLOC_011792
9	lnc-RP11-58C22.1.1-1	chr16:76669394-76669520	ENSG00000250514

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
ENSG00000168298	chromatin interactions
ENSG00000250514	chromatin interactions
ENSG00000261833	chromatin interactions
ENSG00000158373	chromatin interactions
DDX3Y	miRNA target sites
SPRYD3	miRNA target sites
CDKN1A	miRNA target sites
CDV3	miRNA target sites

Extended variants
information (count: 9069 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:9069 , 50 per page) page: 1 2 3 4 5 6 7 ... 182

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs369931691	chr16:76540803-76540804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs533899456	chr16:76540874-76540875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs553819016	chr16:76540898-76540899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs576807091	chr16:76540920-76540921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs11149910	chr16:76540931-76540932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs556584233	chr16:76540953-76540954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs9937287	chr16:76540989-76540990	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs9927954	chr16:76541012-76541013	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs558953204	chr16:76541067-76541068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs555513940	chr16:76541073-76541074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs572284107	chr16:76541082-76541083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs565284082	chr16:76541090-76541091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs541208024	chr16:76541117-76541118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs115912337	chr16:76541154-76541155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs533174956	chr16:76541260-76541261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs112812676	chr16:76541272-76541273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs371034987	chr16:76541278-76541279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs56824172	chr16:76541280-76541281	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs117392677	chr16:76541326-76541327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs188529469	chr16:76541346-76541347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs150243969	chr16:76541377-76541378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs57541769	chr16:76541404-76541405	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs370221741	chr16:76541415-76541416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs60866391	chr16:76541449-76541450	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs570482807	chr16:76541507-76541508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs191841651	chr16:76541530-76541531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs73618196	chr16:76541542-76541543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs141429848	chr16:76541545-76541546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs60485810	chr16:76541558-76541559	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs4422007	chr16:76541644-76541645	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs572351104	chr16:76541646-76541647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs541565842	chr16:76541647-76541648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs557978415	chr16:76541653-76541654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs73619803	chr16:76541656-76541657	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs550963654	chr16:76541675-76541676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs61047558	chr16:76541689-76541690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs541058586	chr16:76541841-76541842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs549389351	chr16:76541842-76541843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs563698731	chr16:76541873-76541874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs529287922	chr16:76541907-76541908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs7203626	chr16:76541913-76541914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs561962742	chr16:76541934-76541935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs138513925	chr16:76541960-76541961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs547531000	chr16:76541970-76541971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs570469765	chr16:76542024-76542025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs4384621	chr16:76542071-76542072	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs141862190	chr16:76542117-76542118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs146259125	chr16:76542138-76542139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs10660069	chr16:76542155-76542156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs67944576	chr16:76542156-76542157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

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
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:378 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:76525200-76554000	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr16:76547000-76548200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr16:76548000-76548600	Enhancers	Brain Germinal Matrix	brain
4	chr16:76548200-76553000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr16:76551400-76551600	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr16:76551400-76551600	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr16:76551600-76552200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr16:76551800-76553000	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr16:76552200-76554400	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr16:76552400-76552800	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr16:76552400-76553000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr16:76552400-76554200	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr16:76552600-76553000	Enhancers	H1 Cell Line	embryonic stem cell
14	chr16:76552600-76553000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr16:76552600-76554000	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr16:76552600-76554400	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr16:76552800-76553200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr16:76552800-76553800	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr16:76552800-76554600	Enhancers	Brain Cingulate Gyrus	brain
20	chr16:76553000-76553800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr16:76553000-76554400	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr16:76553200-76554000	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr16:76553400-76553600	Enhancers	Liver	Liver
24	chr16:76553600-76562200	Weak transcription	Liver	Liver
25	chr16:76553800-76554200	Enhancers	Brain Angular Gyrus	brain
26	chr16:76554000-76554600	Enhancers	Brain Hippocampus Middle	brain
27	chr16:76554000-76554600	Enhancers	Brain Inferior Temporal Lobe	brain
28	chr16:76554000-76554600	Enhancers	Fetal Lung	lung
29	chr16:76554200-76569400	Weak transcription	Brain Angular Gyrus	brain
30	chr16:76554400-76556000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
31	chr16:76554600-76555600	Weak transcription	Fetal Lung	lung
32	chr16:76554600-76587200	Weak transcription	Brain Cingulate Gyrus	brain
33	chr16:76554600-76587200	Weak transcription	Brain Hippocampus Middle	brain
34	chr16:76554600-76599400	Weak transcription	Brain Inferior Temporal Lobe	brain
35	chr16:76555600-76555800	Enhancers	Fetal Lung	lung
36	chr16:76555800-76556200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr16:76555800-76556200	Active TSS	Brain Substantia Nigra	brain
38	chr16:76555800-76558200	Weak transcription	Fetal Lung	lung
39	chr16:76556000-76556200	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr16:76556200-76581800	Weak transcription	Brain Substantia Nigra	brain
41	chr16:76558400-76558600	Enhancers	Fetal Lung	lung
42	chr16:76558600-76559000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr16:76562200-76562800	Enhancers	Liver	Liver
44	chr16:76562800-76563400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr16:76562800-76563400	Flanking Active TSS	Liver	Liver
46	chr16:76563000-76564000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr16:76563400-76563600	Active TSS	Liver	Liver
48	chr16:76563600-76563800	Flanking Active TSS	Liver	Liver
49	chr16:76563800-76566600	Active TSS	Liver	Liver
50	chr16:76564000-76564400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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