Variant report

Variant	nsv1056021
Chromosome Location	chr16:75955522-76729765
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2778)
CpG islands
(count:1772)
Chromatin interactive
region (count:78)
LncRNA
region (count:20)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2778 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:76256042-76256283	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:76684292-76684820	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	chr16:76668888-76668938	K562	blood:	n/a	n/a
6	ARID3A	chr16:76566183-76566513	HepG2	liver:	n/a	n/a
7	ARID3A	chr16:76687350-76687721	HepG2	liver:	n/a	n/a
8	ATF1	chr16:76489943-76489993	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	ATF1	chr16:76614425-76614592	K562	blood:	n/a	n/a
13	ATF1	chr16:76549644-76549672	K562	blood:	n/a	n/a
14	ATF2	chr16:76198817-76199366	GM12878	blood:	n/a	n/a
15	ATF2	chr16:76209888-76210374	GM12878	blood:	n/a	n/a
16	ATF2	chr16:76209899-76210415	GM12878	blood:	n/a	n/a
17	ATF3	chr16:76687346-76687640	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF3	chr16:76668818-76669064	K562	blood:	n/a	n/a
19	BACH1	chr16:76345213-76345518	H1-hESC	embryonic stem cell:	n/a	chr16:76345351-76345365
20	BACH1	chr16:76703299-76703491	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr16:76345268-76345454	K562	blood:	n/a	chr16:76345351-76345365
22	BACH1	chr16:76228619-76228977	H1-hESC	embryonic stem cell:	n/a	n/a
23	BATF	chr16:76610960-76611272	GM12878	blood:	n/a	n/a
24	BATF	chr16:76210041-76210280	GM12878	blood:	n/a	n/a
25	BATF	chr16:76610931-76611290	GM12878	blood:	n/a	n/a
26	BATF	chr16:76337571-76337856	GM12878	blood:	n/a	n/a
27	BATF	chr16:76617883-76618255	GM12878	blood:	n/a	chr16:76618063-76618074
28	BATF	chr16:76332579-76332876	GM12878	blood:	n/a	n/a
29	BATF	chr16:76617930-76618131	GM12878	blood:	n/a	chr16:76618063-76618074
30	BATF	chr16:76332607-76332868	GM12878	blood:	n/a	n/a
31	BATF	chr16:76337590-76337814	GM12878	blood:	n/a	n/a
32	BCL11A	chr16:76332629-76332848	GM12878	blood:	n/a	n/a
33	BCL3	chr16:76504679-76505105	GM12878	blood:	n/a	n/a
34	BHLHE40	chr16:76209948-76210288	GM12878	blood:	n/a	n/a
35	BHLHE40	chr16:76199039-76199164	GM12878	blood:	n/a	n/a
36	BHLHE40	chr16:76556000-76556061	K562	blood:	n/a	n/a
37	BHLHE40	chr16:76704362-76704737	K562	blood:	n/a	chr16:76704597-76704606
38	BHLHE40	chr16:76327637-76327903	GM12878	blood:	n/a	n/a
39	BHLHE40	chr16:76329070-76329115	GM12878	blood:	n/a	n/a
40	BHLHE40	chr16:76610846-76611310	GM12878	blood:	n/a	n/a
41	BHLHE40	chr16:76668642-76669184	K562	blood:	n/a	n/a
42	BHLHE40	chr16:76608424-76608923	HepG2	liver:	n/a	n/a
43	BRCA1	chr16:76328051-76328056	GM12878	blood:	n/a	n/a
44	BRCA1	chr16:76355174-76355243	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chr16:76536310-76536336	H1-hESC	embryonic stem cell:	n/a	n/a
46	CBX3	chr16:76371448-76371774	K562	blood:	n/a	n/a
47	CBX3	chr16:76668556-76669332	K562	blood:	n/a	n/a
48	CBX3	chr16:76668672-76669213	K562	blood:	n/a	n/a
49	CCNT2	chr16:76027103-76027303	K562	blood:	n/a	n/a
50	CCNT2	chr16:76668739-76669178	K562	blood:	n/a	n/a

(count:1772 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:76668836-76668886	GM12892	blood:	n/a
2	chr16:76349255-76349305	GM06990	blood:	n/a
3	chr16:76269043-76269093	NHBE	bronchial:	n/a
4	chr16:76668836-76668886	GM12892	blood:	n/a
5	chr16:76349255-76349305	GM06990	blood:	n/a
6	chr16:76269043-76269093	NHBE	bronchial:	n/a
7	chr16:76521159-76521209	Hepatocyte	liver:	n/a
8	chr16:76665665-76665715	HRCEpiC	kidney:	n/a
9	chr16:76343663-76343713	ProgFib	skin:	n/a
10	chr16:76228294-76228344	HepG2	liver:	n/a
11	chr16:76342620-76342670	PANC-1	pancreas:	n/a
12	chr16:76311266-76311316	NT2-D1	testis:	n/a
13	chr16:76256948-76256998	Jurkat	blood:	n/a
14	chr16:76521159-76521209	HEEpiC	esophagus:	n/a
15	chr16:76228294-76228344	HPAEpiC	pulmonary alveolar:	n/a
16	chr16:76521159-76521209	SAEC	small airway:	n/a
17	chr16:76670197-76670247	PFSK-1	brain:	n/a
18	chr16:76256948-76256998	Hepatocyte	liver:	n/a
19	chr16:76343663-76343713	AG10803	skin:	n/a
20	chr16:76311050-76311100	GM12878	blood:	n/a
21	chr16:76309968-76310018	SAEC	small airway:	n/a
22	chr16:76343663-76343713	NHBE	bronchial:	n/a
23	chr16:76342377-76342427	LNCaP	prostate:	n/a
24	chr16:76272351-76272401	HNPCEpiC	eye:	n/a
25	chr16:76343868-76343918	LNCaP	prostate:	n/a
26	chr16:76269184-76269234	GM06990	blood:	n/a
27	chr16:76272351-76272401	ECC-1	luminal epithelium:	n/a
28	chr16:76668836-76668886	PFSK-1	brain:	n/a
29	chr16:76268785-76268835	T-47D	breast:	n/a
30	chr16:76665665-76665715	NT2-D1	testis:	n/a
31	chr16:76309968-76310018	SK-N-MC	brain:	n/a
32	chr16:76521159-76521209	MCF10A-Er-Src	breast:	n/a
33	chr16:76665665-76665715	HIPEpiC	eye:	n/a
34	chr16:76521159-76521209	HAEpiC	amniotic membrane:	n/a
35	chr16:76311050-76311100	IMR90	lung:	fetal
36	chr16:76269043-76269093	HCPEpiC	choroid plexus:	n/a
37	chr16:76665665-76665715	HCPEpiC	choroid plexus:	n/a
38	chr16:76311266-76311316	HL-60	blood:	n/a
39	chr16:76269192-76269242	PrEC	prostate:	n/a
40	chr16:76228294-76228344	H1-hESC	embryonic stem cell:	embryo
41	chr16:76666860-76666910	HCPEpiC	choroid plexus:	n/a
42	chr16:76269192-76269242	ovcar-3	ovarian:	n/a
43	chr16:76349255-76349305	HCT-116	colon:	n/a
44	chr16:76670197-76670247	HEEpiC	esophagus:	n/a
45	chr16:76343663-76343713	HRCEpiC	kidney:	n/a
46	chr16:76269043-76269093	SKMC	muscle:	n/a
47	chr16:76269409-76269459	HEK293	kidney:	embryo
48	chr16:76665665-76665715	ECC-1	luminal epithelium:	n/a
49	chr16:76228294-76228344	AG09309	skin:	n/a
50	chr16:76256948-76256998	HCT-116	colon:	n/a

(count:78 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr16:76337650..76339476-chr16:76348712..76351275,2	MCF-7	breast:
2	chr16:75963255..75965166-chr16:75978260..75980431,2	K562	blood:
3	chr16:76373071..76375700-chr16:76381006..76383022,2	MCF-7	breast:
4	chr16:76703589..76705752-chr16:76708591..76711050,2	MCF-7	breast:
5	chr16:76701550..76704283-chr16:76707898..76709517,2	K562	blood:
6	chr16:76264260..76266317-chr16:76268267..76270250,2	MCF-7	breast:
7	chr16:76319924..76320753-chr16:76686923..76687617,2	MCF-7	breast:
8	chr16:76679307..76681357-chr16:76683795..76685911,2	MCF-7	breast:
9	chr16:76607256..76609840-chr16:76614807..76617382,2	K562	blood:
10	chr16:76312786..76313346-chr16:77205382..77206025,2	MCF-7	breast:
11	chr16:76699516..76700310-chr16:77203606..77204151,2	MCF-7	breast:
12	chr16:76560975..76563666-chr16:76569503..76571277,2	K562	blood:
13	chr16:76109470..76111074-chr16:76115250..76116774,2	MCF-7	breast:
14	chr16:75977745..75979693-chr16:75980372..75982208,2	MCF-7	breast:
15	chr16:75834944..75835823-chr16:76687371..76688062,3	MCF-7	breast:
16	chr16:76665227..76667688-chr16:76668445..76671290,2	K562	blood:
17	chr16:76703589..76705752-chr16:76708591..76711050,2	MCF-7	breast:
18	chr16:76687235..76688893-chr16:76692839..76694713,2	K562	blood:
19	chr16:76150031..76151626-chr16:76156509..76159199,2	MCF-7	breast:
20	chr16:76534271..76535887-chr16:76537682..76540215,2	MCF-7	breast:
21	chr16:76527293..76528859-chr16:76529180..76530762,2	MCF-7	breast:
22	chr16:76472874..76474659-chr16:76475007..76477052,2	K562	blood:
23	chr16:76636023..76638622-chr16:76652291..76654068,2	K562	blood:
24	chr16:76679307..76681357-chr16:76683795..76685911,2	MCF-7	breast:
25	chr16:76312365..76313607-chr16:76673596..76674287,4	MCF-7	breast:
26	chr16:76272213..76274617-chr16:76275881..76278722,3	MCF-7	breast:
27	chr16:75963255..75965166-chr16:75978260..75980431,2	K562	blood:
28	chr16:76421818..76424813-chr16:76424956..76427110,2	MCF-7	breast:
29	chr16:76312246..76313469-chr16:76687103..76688657,6	MCF-7	breast:
30	chr16:75962160..75963903-chr16:75968199..75970527,2	K562	blood:
31	chr16:76152673..76155052-chr16:76163507..76166139,2	K562	blood:
32	chr16:76150031..76151626-chr16:76156509..76159199,2	MCF-7	breast:
33	chr16:76699506..76700441-chr16:77205329..77206242,3	MCF-7	breast:
34	chr16:76230231..76230851-chr2:70141294..70141952,2	Hela-S3	cervix:
35	chr16:76584372..76585914-chr16:76586080..76587632,2	MCF-7	breast:
36	chr16:76527293..76528859-chr16:76529180..76530762,2	MCF-7	breast:
37	chr16:76607256..76609840-chr16:76614807..76617382,2	K562	blood:
38	chr10:3005128..3007874-chr16:76409893..76412241,2	MCF-7	breast:
39	chr16:76687235..76688893-chr16:76692839..76694713,2	K562	blood:
40	chr16:75967179..75969484-chr17:4845937..4847850,2	MCF-7	breast:
41	chr16:76519348..76521301-chr16:76524212..76526573,2	K562	blood:
42	chr16:76560975..76563666-chr16:76569503..76571277,2	K562	blood:
43	chr16:76109470..76111074-chr16:76115250..76116774,2	MCF-7	breast:
44	chr16:76319924..76320753-chr16:76686923..76687617,2	MCF-7	breast:
45	chr16:76377031..76378891-chr17:57920053..57922098,2	MCF-7	breast:
46	chr16:76472874..76474659-chr16:76475007..76477052,2	K562	blood:
47	chr16:76167106..76169562-chr16:76172402..76175397,2	MCF-7	breast:
48	chr16:75977745..75979693-chr16:75980372..75982208,2	MCF-7	breast:
49	chr16:76312246..76313469-chr16:76687103..76688657,6	MCF-7	breast:
50	chr16:76076451..76078848-chr2:55275762..55278542,2	MCF-7	breast:

(count:20 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC025287.1-2	chr16:76141181-76141401	ENSG00000260223.1
2	lnc-RP11-58C22.1.1-1	chr16:76669394-76669520	ENSG00000250514
3	lnc-AC025287.1-3	chr16:76296129-76296234	NONHSAT143776
4	lnc-RP11-58C22.1.1-1	chr16:76690565-76692375	ENSG00000250514
5	lnc-AC025287.1-3	chr16:76262283-76262757	ENSG00000260983.1
6	lnc-RP11-58C22.1.1-1	chr16:76689454-76689561	ENSG00000250514
7	lnc-AC025287.1-2	chr16:76181458-76181704	ENSG00000260223.1
8	lnc-AC025287.1-3	chr16:76296129-76296263	ENSG00000260983.1
9	lnc-AC025287.1-2	chr16:76170020-76170263	ENSG00000260223.1
10	lnc-RP11-58C22.1.1-1	chr16:76668895-76669046	ENSG00000250514
11	lnc-AC025287.1-3	chr16:76268585-76269326	NONHSAT143776
12	lnc-AC025287.1-3	chr16:76265215-76265343	ENSG00000260983.1
13	lnc-AC025287.1-2	chr16:76142134-76142240	ENSG00000260223.1
14	lnc-AC025287.1-2	chr16:76181453-76181621	NONHSAT143772
15	lnc-AC025287.1-2	chr16:76181454-76181621	XLOC_012013
16	lnc-AC025287.1-2	chr16:76169537-76169877	NONHSAT143772
17	lnc-AC025287.1-3	chr16:76268953-76269521	NONHSAT143777
18	lnc-AC025287.1-2	chr16:76181458-76181677	ENSG00000260223.1
19	lnc-AC025287.1-2	chr16:76174260-76174301	ENSG00000260223.1
20	lnc-AC025287.1-2	chr16:76169538-76169877	XLOC_012013

No data

Variant related genes	Relation type
ENSG00000260223	TF binding region
ENSG00000260983	TF binding region
ENSG00000264645	TF binding region
ENSG00000261833	TF binding region
ENSG00000252022	TF binding region
RPL18P13	TF binding region
ENSG00000250514	TF binding region
CNTNAP4	TF binding region
RN7SKP233	TF binding region
ENSG00000260223	CpG island
ENSG00000260983	CpG island
ENSG00000264645	CpG island
ENSG00000261833	CpG island
ENSG00000252022	CpG island
RPL18P13	CpG island
ENSG00000250514	CpG island
CNTNAP4	CpG island
RN7SKP233	CpG island
ENSG00000152910	chromatin interactions
ENSG00000264645	chromatin interactions
ENSG00000108523	chromatin interactions
ENSG00000261833	chromatin interactions
ENSG00000260983	chromatin interactions
ENSG00000158373	chromatin interactions
ENSG00000115310	chromatin interactions
ENSG00000168298	chromatin interactions
ENSG00000250514	chromatin interactions
ENSG00000244485	chromatin interactions
CDV3	miRNA target sites
DDX3Y	miRNA target sites
SPRYD3	miRNA target sites

Extended variants
information (count: 28227 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:28227 , 50 per page) page: 1 2 3 4 5 6 7 ... 565

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576044187	chr16:75955528-75955529	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs537247374	chr16:75955580-75955581	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs544900880	chr16:75955660-75955661	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs561538081	chr16:75955685-75955686	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs545892153	chr16:75955699-75955700	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs115389771	chr16:75955701-75955702	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs145227065	chr16:75955710-75955711	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs560639017	chr16:75955730-75955731	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs532497163	chr16:75955745-75955746	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs551586326	chr16:75955803-75955804	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs147604273	chr16:75955911-75955912	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs372511222	chr16:75955923-75955924	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs13334488	chr16:75955974-75955975	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs550475351	chr16:75955995-75955996	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs567181269	chr16:75955997-75955998	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs536245081	chr16:75956007-75956008	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs142172093	chr16:75956049-75956050	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs76037439	chr16:75956054-75956055	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs59445759	chr16:75956055-75956056	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs114588976	chr16:75956119-75956120	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs559225153	chr16:75956120-75956121	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs13334859	chr16:75956128-75956129	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs544784572	chr16:75956188-75956189	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs191286304	chr16:75956199-75956200	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs372836835	chr16:75956233-75956234	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs536272883	chr16:75956249-75956250	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs57961261	chr16:75956285-75956286	Bivalent Enhancer Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs540670514	chr16:75956381-75956382	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs545257189	chr16:75956387-75956388	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs375011700	chr16:75956452-75956453	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs150211775	chr16:75956501-75956502	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs367673818	chr16:75956557-75956558	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs368897818	chr16:75956558-75956559	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs183826162	chr16:75956569-75956570	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs138819638	chr16:75956602-75956603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs562607560	chr16:75956626-75956627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs527713273	chr16:75956660-75956661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs550313065	chr16:75956779-75956780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs567267328	chr16:75956829-75956830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs529933774	chr16:75956836-75956837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs550411521	chr16:75956885-75956886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs117485032	chr16:75956911-75956912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs566324959	chr16:75956916-75956917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs538602709	chr16:75956918-75956919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs372422792	chr16:75956959-75956960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs17608180	chr16:75956973-75956974	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs148924691	chr16:75956983-75956984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs538444900	chr16:75956998-75956999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs555198130	chr16:75957020-75957021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs575118152	chr16:75957044-75957045	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
Breast cancer	21364760	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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	23813976	CNVD
Lung cancer	24585490	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	20164919	CNVD
Neuroblastoma	18923524	CNVD
Cancer	20164920	CNVD
Cancer	20581869	CNVD

Chromatin state (count:1316 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:75954400-75955600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
2	chr16:75954400-75958400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr16:75955000-75955800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
4	chr16:75955000-75956200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr16:75955200-75955600	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
6	chr16:75955400-75955600	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr16:75955400-75955600	Enhancers	Ovary	ovary
8	chr16:75955400-75956000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
9	chr16:75955600-75955800	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
10	chr16:75955600-75956600	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
11	chr16:75955800-75956200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
12	chr16:75956200-75956400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
13	chr16:75956200-75956400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
14	chr16:75958400-75958800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr16:75958800-75961400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr16:75961400-75961600	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
17	chr16:75961400-75961600	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
18	chr16:75961400-75961800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
19	chr16:75961400-75962000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr16:75961400-75963200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr16:75961600-75961800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
22	chr16:75961600-75961800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
23	chr16:75961600-75961800	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
24	chr16:75961800-75963200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr16:75962000-75962200	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr16:75962000-75962200	Enhancers	HMEC	breast
27	chr16:75962200-75964400	Weak transcription	HMEC	breast
28	chr16:75963000-75963200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr16:75963200-75964200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr16:75963200-75964400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr16:75963200-75964400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr16:75964200-75964600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
33	chr16:75964200-75965600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr16:75964400-75965600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr16:75964400-75965600	Enhancers	HMEC	breast
36	chr16:75964400-75965800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr16:75965200-75965400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr16:75972000-75973600	Enhancers	HMEC	breast
39	chr16:75972400-75972800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr16:75972600-75973200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr16:75972800-75973200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr16:75972800-75973400	Enhancers	Brain Cingulate Gyrus	brain
43	chr16:75972800-75973600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr16:75973000-75973200	Enhancers	Brain Inferior Temporal Lobe	brain
45	chr16:75973200-75978800	Weak transcription	Brain Inferior Temporal Lobe	brain
46	chr16:75973200-75991800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr16:75973400-75975000	Weak transcription	Brain Cingulate Gyrus	brain
48	chr16:75974400-75974600	Enhancers	Fetal Intestine Large	intestine
49	chr16:75974800-75975800	Weak transcription	Fetal Intestine Large	intestine
50	chr16:75975000-75975600	Enhancers	Brain Anterior Caudate	brain

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