Variant report

Variant	nsv906943
Chromosome Location	chr16:76413757-76768178
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1508)
CpG islands
(count:428)
Chromatin interactive
region (count:46)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1508 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:76566183-76566513	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:76673948-76674099	K562	blood:	n/a	n/a
3	ARID3A	chr16:76608141-76609300	HepG2	liver:	n/a	n/a
4	ARID3A	chr16:76668888-76668938	K562	blood:	n/a	n/a
5	ARID3A	chr16:76684292-76684820	HepG2	liver:	n/a	n/a
6	ARID3A	chr16:76687350-76687721	HepG2	liver:	n/a	n/a
7	ATF1	chr16:76668805-76669470	K562	blood:	n/a	n/a
8	ATF1	chr16:76489943-76489993	K562	blood:	n/a	n/a
9	ATF1	chr16:76614425-76614592	K562	blood:	n/a	n/a
10	ATF1	chr16:76687134-76687664	K562	blood:	n/a	n/a
11	ATF1	chr16:76581402-76581528	K562	blood:	n/a	n/a
12	ATF1	chr16:76549644-76549672	K562	blood:	n/a	n/a
13	ATF3	chr16:76668818-76669064	K562	blood:	n/a	n/a
14	ATF3	chr16:76687346-76687640	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr16:76703299-76703491	H1-hESC	embryonic stem cell:	n/a	n/a
16	BATF	chr16:76610931-76611290	GM12878	blood:	n/a	n/a
17	BATF	chr16:76610960-76611272	GM12878	blood:	n/a	n/a
18	BATF	chr16:76617883-76618255	GM12878	blood:	n/a	chr16:76618063-76618074
19	BATF	chr16:76617930-76618131	GM12878	blood:	n/a	chr16:76618063-76618074
20	BCL3	chr16:76504679-76505105	GM12878	blood:	n/a	n/a
21	BHLHE40	chr16:76668642-76669184	K562	blood:	n/a	n/a
22	BHLHE40	chr16:76608424-76608923	HepG2	liver:	n/a	n/a
23	BHLHE40	chr16:76556000-76556061	K562	blood:	n/a	n/a
24	BHLHE40	chr16:76704362-76704737	K562	blood:	n/a	chr16:76704597-76704606
25	BHLHE40	chr16:76610846-76611310	GM12878	blood:	n/a	n/a
26	BRCA1	chr16:76536310-76536336	H1-hESC	embryonic stem cell:	n/a	n/a
27	CBX3	chr16:76668672-76669213	K562	blood:	n/a	n/a
28	CBX3	chr16:76668556-76669332	K562	blood:	n/a	n/a
29	CCNT2	chr16:76668739-76669178	K562	blood:	n/a	n/a
30	CEBPB	chr16:76420802-76420826	K562	blood:	n/a	chr16:76420812-76420823
31	CEBPB	chr16:76737550-76737552	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr16:76420686-76420983	HepG2	liver:	n/a	chr16:76420812-76420823
33	CEBPB	chr16:76640194-76640523	K562	blood:	n/a	chr16:76640353-76640364
34	CEBPB	chr16:76673910-76674162	K562	blood:	n/a	n/a
35	CEBPB	chr16:76608534-76608982	HepG2	liver:	n/a	n/a
36	CEBPB	chr16:76626164-76626375	A549	lung:	n/a	chr16:76626265-76626276
37	CEBPB	chr16:76687291-76687702	HepG2	liver:	n/a	n/a
38	CEBPB	chr16:76710451-76710670	HepG2	liver:	n/a	n/a
39	CEBPB	chr16:76551481-76551748	A549	lung:	n/a	n/a
40	CEBPB	chr16:76687301-76687681	IMR90	lung:	n/a	n/a
41	CEBPB	chr16:76756359-76756661	HepG2	liver:	n/a	chr16:76756489-76756502 chr16:76756490-76756501 chr16:76756620-76756631
42	CEBPB	chr16:76551445-76551764	HepG2	liver:	n/a	n/a
43	CEBPB	chr16:76702300-76702493	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr16:76687308-76687632	K562	blood:	n/a	n/a
45	CEBPB	chr16:76714462-76714734	HepG2	liver:	n/a	chr16:76714617-76714628 chr16:76714616-76714629
46	CEBPB	chr16:76489932-76490163	HepG2	liver:	n/a	chr16:76490083-76490094
47	CEBPB	chr16:76687359-76687568	HepG2	liver:	n/a	n/a
48	CEBPB	chr16:76430878-76431056	HepG2	liver:	n/a	n/a
49	CEBPB	chr16:76551464-76551752	IMR90	lung:	n/a	n/a
50	CEBPB	chr16:76687392-76687580	K562	blood:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:76669151-76669201	GM19239	blood:	n/a
2	chr16:76669151-76669201	GM19239	blood:	n/a
3	chr16:76521159-76521209	Hela-S3	cervix:	n/a
4	chr16:76669151-76669201	BE2_C	brain:	n/a
5	chr16:76708064-76708114	MCF-7	breast:	n/a
6	chr16:76668836-76668886	Caco-2	colon:	n/a
7	chr16:76668836-76668886	K562	blood:	n/a
8	chr16:76670197-76670247	Hepatocyte	liver:	n/a
9	chr16:76669151-76669201	HAEpiC	amniotic membrane:	n/a
10	chr16:76666860-76666910	PANC-1	pancreas:	n/a
11	chr16:76670197-76670247	T-47D	breast:	n/a
12	chr16:76670197-76670247	U87	brain:	n/a
13	chr16:76670197-76670247	NT2-D1	testis:	n/a
14	chr16:76670197-76670247	HCF	heart:	n/a
15	chr16:76521159-76521209	HCM	heart:	n/a
16	chr16:76666860-76666910	SKMC	muscle:	n/a
17	chr16:76670197-76670247	Caco-2	colon:	n/a
18	chr16:76670197-76670247	CMK	blood:	n/a
19	chr16:76665665-76665715	HRE	kidney:	n/a
20	chr16:76665665-76665715	HAEpiC	amniotic membrane:	n/a
21	chr16:76665665-76665715	HUVEC	blood vessel:	n/a
22	chr16:76665665-76665715	NHBE	bronchial:	n/a
23	chr16:76665665-76665715	AG09319	gingival:	n/a
24	chr16:76521159-76521209	HCT-116	colon:	n/a
25	chr16:76665665-76665715	K562	blood:	n/a
26	chr16:76708064-76708114	HRPEpiC	eye:	n/a
27	chr16:76669151-76669201	ProgFib	skin:	n/a
28	chr16:76665665-76665715	HPAEpiC	pulmonary alveolar:	n/a
29	chr16:76666860-76666910	NHBE	bronchial:	n/a
30	chr16:76665665-76665715	A549	lung:	n/a
31	chr16:76669151-76669201	GM12878	blood:	n/a
32	chr16:76670197-76670247	ProgFib	skin:	n/a
33	chr16:76666860-76666910	HRE	kidney:	n/a
34	chr16:76666860-76666910	NB4	blood:	n/a
35	chr16:76665665-76665715	AG04450	lung:	fetal
36	chr16:76665665-76665715	RPTEC	kidney:	n/a
37	chr16:76670197-76670247	HCPEpiC	choroid plexus:	n/a
38	chr16:76521159-76521209	LNCaP	prostate:	n/a
39	chr16:76670197-76670247	SKMC	muscle:	n/a
40	chr16:76670197-76670247	Jurkat	blood:	n/a
41	chr16:76669151-76669201	K562	blood:	n/a
42	chr16:76521159-76521209	K562	blood:	n/a
43	chr16:76670197-76670247	AG10803	skin:	n/a
44	chr16:76668836-76668886	HCPEpiC	choroid plexus:	n/a
45	chr16:76668836-76668886	HPAEpiC	pulmonary alveolar:	n/a
46	chr16:76668836-76668886	SKMC	muscle:	n/a
47	chr16:76670197-76670247	HNPCEpiC	eye:	n/a
48	chr16:76668836-76668886	AG09309	skin:	n/a
49	chr16:76669151-76669201	Hepatocyte	liver:	n/a
50	chr16:76666860-76666910	HEK293	kidney:	embryo

(count:46 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:76584372..76585914-chr16:76586080..76587632,2	MCF-7	breast:
2	chr16:76636023..76638622-chr16:76652291..76654068,2	K562	blood:
3	chr16:76527293..76528859-chr16:76529180..76530762,2	MCF-7	breast:
4	chr16:76319924..76320753-chr16:76686923..76687617,2	MCF-7	breast:
5	chr16:76312365..76313607-chr16:76673596..76674287,4	MCF-7	breast:
6	chr16:76669652..76671358-chr16:76701917..76703611,2	K562	blood:
7	chr16:76519348..76521301-chr16:76524212..76526573,2	K562	blood:
8	chr16:76636023..76638622-chr16:76652291..76654068,2	K562	blood:
9	chr16:76741499..76743675-chr16:76746368..76748815,2	K562	blood:
10	chr16:76741499..76743675-chr16:76746368..76748815,2	K562	blood:
11	chr16:76472874..76474659-chr16:76475007..76477052,2	K562	blood:
12	chr16:76703589..76705752-chr16:76708591..76711050,2	MCF-7	breast:
13	chr16:76747877..76750802-chr16:76754682..76756382,2	K562	blood:
14	chr16:76472874..76474659-chr16:76475007..76477052,2	K562	blood:
15	chr16:76560975..76563666-chr16:76569503..76571277,2	K562	blood:
16	chr16:76421818..76424813-chr16:76424956..76427110,2	MCF-7	breast:
17	chr16:76703589..76705752-chr16:76708591..76711050,2	MCF-7	breast:
18	chr16:76679307..76681357-chr16:76683795..76685911,2	MCF-7	breast:
19	chr16:76534271..76535887-chr16:76537682..76540215,2	MCF-7	breast:
20	chr16:76312246..76313469-chr16:76687103..76688657,6	MCF-7	breast:
21	chr16:76701550..76704283-chr16:76707898..76709517,2	K562	blood:
22	chr16:76607256..76609840-chr16:76614807..76617382,2	K562	blood:
23	chr16:76527293..76528859-chr16:76529180..76530762,2	MCF-7	breast:
24	chr16:76542177..76544098-chr6:26155995..26158781,2	MCF-7	breast:
25	chr16:76669652..76671358-chr16:76701917..76703611,2	K562	blood:
26	chr16:76665227..76667688-chr16:76668445..76671290,2	K562	blood:
27	chr16:76741969..76744727-chr16:76747101..76748627,2	K562	blood:
28	chr16:76701550..76704283-chr16:76707898..76709517,2	K562	blood:
29	chr16:76756661..76759781-chr16:76761311..76764642,3	K562	blood:
30	chr16:76699506..76700441-chr16:77205329..77206242,3	MCF-7	breast:
31	chr16:76687235..76688893-chr16:76692839..76694713,2	K562	blood:
32	chr16:76741969..76744727-chr16:76747101..76748627,2	K562	blood:
33	chr16:75835108..75835786-chr16:76687075..76687822,2	MCF-7	breast:
34	chr16:76699528..76700343-chr16:77076632..77077627,2	MCF-7	breast:
35	chr16:76699516..76700310-chr16:77203606..77204151,2	MCF-7	breast:
36	chr16:76534271..76535887-chr16:76537682..76540215,2	MCF-7	breast:
37	chr16:76607256..76609840-chr16:76614807..76617382,2	K562	blood:
38	chr16:76519348..76521301-chr16:76524212..76526573,2	K562	blood:
39	chr16:76679307..76681357-chr16:76683795..76685911,2	MCF-7	breast:
40	chr16:76756661..76759781-chr16:76761311..76764642,3	K562	blood:
41	chr16:76747877..76750802-chr16:76754682..76756382,2	K562	blood:
42	chr16:76687186..76688106-chr16:76857078..76857671,2	MCF-7	breast:
43	chr16:76687235..76688893-chr16:76692839..76694713,2	K562	blood:
44	chr16:76421818..76424813-chr16:76424956..76427110,2	MCF-7	breast:
45	chr16:76560975..76563666-chr16:76569503..76571277,2	K562	blood:
46	chr16:75834944..75835823-chr16:76687371..76688062,3	MCF-7	breast:

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

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

No data

Variant related genes	Relation type
ENSG00000264645	TF binding region
ENSG00000261833	TF binding region
ENSG00000252022	TF binding region
ENSG00000250514	TF binding region
ENSG00000259995	TF binding region
ENSG00000264645	CpG island
ENSG00000261833	CpG island
ENSG00000252022	CpG island
ENSG00000250514	CpG island
ENSG00000259995	CpG island
ENSG00000250514	chromatin interactions
ENSG00000168298	chromatin interactions
ENSG00000158373	chromatin interactions
ENSG00000261833	chromatin interactions
CDKN1A	miRNA target sites
DDX3Y	miRNA target sites
CDV3	miRNA target sites
SPRYD3	miRNA target sites

Extended variants
information (count: 10695 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:10695 , 50 per page) page: 1 2 3 4 5 6 7 ... 214

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9937490	chr16:76413757-76413758	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs184910422	chr16:76413796-76413797	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs189811022	chr16:76413803-76413804	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs538814835	chr16:76413856-76413857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs182459297	chr16:76413864-76413865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs188408928	chr16:76413883-76413884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs192886721	chr16:76413900-76413901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs183852910	chr16:76413989-76413990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs7200808	chr16:76413993-76413994	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs574797234	chr16:76414015-76414016	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs530424708	chr16:76414028-76414029	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs540573291	chr16:76414039-76414040	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs560406653	chr16:76414050-76414051	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs532631027	chr16:76414087-76414088	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs150956961	chr16:76414105-76414106	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs567047399	chr16:76414114-76414115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs374155722	chr16:76414124-76414125	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs562863618	chr16:76414143-76414144	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs531798624	chr16:76414168-76414169	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs548609789	chr16:76414194-76414195	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs530448921	chr16:76414254-76414255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs527682646	chr16:76414262-76414263	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs74026756	chr16:76414279-76414280	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs16944328	chr16:76414308-76414309	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs188389975	chr16:76414313-76414314	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs142017555	chr16:76414315-76414316	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs542497581	chr16:76414401-76414402	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs369616133	chr16:76414402-76414403	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs537902844	chr16:76414410-76414411	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs568864739	chr16:76414436-76414437	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs6564325	chr16:76414463-76414464	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs558580055	chr16:76414468-76414469	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs145884338	chr16:76414476-76414477	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs193214021	chr16:76414567-76414568	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs577439585	chr16:76414587-76414588	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs558223119	chr16:76414616-76414617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs546097562	chr16:76414621-76414622	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs563056244	chr16:76414638-76414639	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs531714017	chr16:76414666-76414667	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs542389090	chr16:76414674-76414675	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs8057832	chr16:76414692-76414693	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs527719126	chr16:76414709-76414710	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs547787985	chr16:76414763-76414764	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs566673365	chr16:76414769-76414770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs532400084	chr16:76414794-76414795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs147763240	chr16:76414796-76414797	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs16944329	chr16:76414801-76414802	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs8059439	chr16:76414819-76414820	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs554974900	chr16:76414837-76414838	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs8059490	chr16:76414884-76414885	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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:445 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:76395400-76421800	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr16:76410000-76422000	Weak transcription	Brain Hippocampus Middle	brain
3	chr16:76410000-76427400	Weak transcription	Brain Cingulate Gyrus	brain
4	chr16:76414000-76415600	Enhancers	Fetal Brain Male	brain
5	chr16:76416600-76417200	Enhancers	Brain Substantia Nigra	brain
6	chr16:76417200-76422000	Weak transcription	Brain Substantia Nigra	brain
7	chr16:76419600-76420000	Enhancers	Placenta Amnion	Placenta Amnion
8	chr16:76420000-76420400	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr16:76420400-76420600	Enhancers	Placenta Amnion	Placenta Amnion
10	chr16:76420400-76422200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr16:76420600-76424000	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr16:76421000-76421200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr16:76421600-76422200	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr16:76421800-76422200	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr16:76421800-76422200	Enhancers	Brain Inferior Temporal Lobe	brain
16	chr16:76422000-76422400	Enhancers	Brain Hippocampus Middle	brain
17	chr16:76422000-76423200	Enhancers	Brain Substantia Nigra	brain
18	chr16:76422200-76426600	Weak transcription	HUES48 Cell Line	embryonic stem cell
19	chr16:76422200-76432200	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr16:76422400-76432000	Weak transcription	Brain Hippocampus Middle	brain
21	chr16:76422600-76424600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr16:76423000-76423600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr16:76423200-76427000	Weak transcription	Brain Substantia Nigra	brain
24	chr16:76423400-76424200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr16:76424000-76424400	Enhancers	Placenta Amnion	Placenta Amnion
26	chr16:76424400-76425600	Weak transcription	Placenta Amnion	Placenta Amnion
27	chr16:76425600-76425800	Enhancers	Placenta Amnion	Placenta Amnion
28	chr16:76426600-76427200	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr16:76426600-76427400	Enhancers	H9 Cell Line	embryonic stem cell
30	chr16:76426800-76427200	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr16:76427000-76427600	Enhancers	Brain Substantia Nigra	brain
32	chr16:76427800-76428200	Enhancers	Fetal Lung	lung
33	chr16:76428800-76429000	Enhancers	HepG2	liver
34	chr16:76429200-76430200	Weak transcription	HepG2	liver
35	chr16:76430200-76431600	Enhancers	HepG2	liver
36	chr16:76430800-76431200	Enhancers	Liver	Liver
37	chr16:76432200-76432400	ZNF genes & repeats	Brain Inferior Temporal Lobe	brain
38	chr16:76432200-76432400	Enhancers	Skeletal Muscle Female	skeletal muscle
39	chr16:76442600-76444600	Enhancers	Fetal Lung	lung
40	chr16:76452800-76453600	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr16:76452800-76453800	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr16:76453000-76475000	Weak transcription	Brain Cingulate Gyrus	brain
43	chr16:76455200-76456800	Weak transcription	Brain Angular Gyrus	brain
44	chr16:76455400-76455800	Enhancers	Fetal Lung	lung
45	chr16:76456800-76457000	Enhancers	Brain Angular Gyrus	brain
46	chr16:76458800-76459400	Enhancers	Brain Hippocampus Middle	brain
47	chr16:76459400-76466600	Weak transcription	Brain Hippocampus Middle	brain
48	chr16:76460400-76461400	Enhancers	Brain Substantia Nigra	brain
49	chr16:76461000-76461400	Enhancers	Brain Inferior Temporal Lobe	brain
50	chr16:76461400-76464000	Weak transcription	Brain Inferior Temporal Lobe	brain

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