Variant report

Variant	esv1803802
Chromosome Location	chr16:47115776-47367144
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2520)
CpG islands
(count:1466)
Chromatin interactive
region (count:98)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:5)

(count:2520 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:47176783-47176815	K562	blood:	n/a	n/a
2	ARID3A	chr16:47175602-47176202	K562	blood:	n/a	n/a
3	ARID3A	chr16:47178303-47178477	HepG2	liver:	n/a	n/a
4	ARID3A	chr16:47196782-47196800	HepG2	liver:	n/a	n/a
5	ARID3A	chr16:47169900-47170121	K562	blood:	n/a	n/a
6	ARID3A	chr16:47357253-47357463	HepG2	liver:	n/a	n/a
7	ARID3A	chr16:47180937-47181312	K562	blood:	n/a	n/a
8	ARID3A	chr16:47166225-47166502	K562	blood:	n/a	n/a
9	ARID3A	chr16:47216266-47216628	HepG2	liver:	n/a	n/a
10	ARID3A	chr16:47175635-47176566	HepG2	liver:	n/a	n/a
11	ARID3A	chr16:47171892-47172010	K562	blood:	n/a	n/a
12	ARID3A	chr16:47177441-47177480	K562	blood:	n/a	n/a
13	ARID3A	chr16:47177086-47177176	HepG2	liver:	n/a	n/a
14	ATF1	chr16:47170098-47170312	K562	blood:	n/a	n/a
15	ATF1	chr16:47175658-47176054	K562	blood:	n/a	n/a
16	ATF1	chr16:47197545-47197587	K562	blood:	n/a	n/a
17	ATF2	chr16:47351722-47352080	GM12878	blood:	n/a	n/a
18	ATF2	chr16:47344576-47345243	GM12878	blood:	n/a	n/a
19	ATF2	chr16:47176142-47176695	GM12878	blood:	n/a	n/a
20	ATF2	chr16:47175571-47176087	GM12878	blood:	n/a	n/a
21	ATF2	chr16:47176226-47176738	GM12878	blood:	n/a	n/a
22	ATF2	chr16:47175531-47176062	GM12878	blood:	n/a	n/a
23	ATF3	chr16:47171874-47172117	K562	blood:	n/a	n/a
24	ATF3	chr16:47177260-47177528	K562	blood:	n/a	n/a
25	BACH1	chr16:47176731-47177908	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr16:47175631-47176087	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr16:47152449-47152458	K562	blood:	n/a	n/a
28	BACH1	chr16:47178178-47178180	H1-hESC	embryonic stem cell:	n/a	n/a
29	BATF	chr16:47364473-47364700	GM12878	blood:	n/a	n/a
30	BATF	chr16:47147784-47148314	GM12878	blood:	n/a	n/a
31	BATF	chr16:47364453-47364807	GM12878	blood:	n/a	n/a
32	BATF	chr16:47175661-47175976	GM12878	blood:	n/a	n/a
33	BATF	chr16:47176399-47176669	GM12878	blood:	n/a	n/a
34	BATF	chr16:47365904-47366048	GM12878	blood:	n/a	n/a
35	BATF	chr16:47176365-47176663	GM12878	blood:	n/a	n/a
36	BATF	chr16:47344674-47344855	GM12878	blood:	n/a	n/a
37	BCL11A	chr16:47176367-47176707	GM12878	blood:	n/a	n/a
38	BCL11A	chr16:47345681-47345863	H1-hESC	embryonic stem cell:	n/a	n/a
39	BCL11A	chr16:47344674-47344906	GM12878	blood:	n/a	n/a
40	BCL3	chr16:47351809-47352137	GM12878	blood:	n/a	n/a
41	BCLAF1	chr16:47177145-47177707	GM12878	blood:	n/a	chr16:47177425-47177438 chr16:47177593-47177602 chr16:47177563-47177572
42	BCLAF1	chr16:47177271-47177669	GM12878	blood:	n/a	chr16:47177425-47177438 chr16:47177593-47177602 chr16:47177563-47177572
43	BCLAF1	chr16:47175544-47176047	GM12878	blood:	n/a	n/a
44	BCLAF1	chr16:47175480-47176190	GM12878	blood:	n/a	n/a
45	BCLAF1	chr16:47176319-47176951	GM12878	blood:	n/a	n/a
46	BHLHE40	chr16:47351717-47352098	GM12878	blood:	n/a	n/a
47	BHLHE40	chr16:47177335-47177732	HepG2	liver:	n/a	chr16:47177449-47177465
48	BHLHE40	chr16:47177272-47178380	K562	blood:	n/a	chr16:47178152-47178168 chr16:47177449-47177465 chr16:47178004-47178020 chr16:47178144-47178160
49	BHLHE40	chr16:47175636-47176200	K562	blood:	n/a	n/a
50	BHLHE40	chr16:47175534-47176602	GM12878	blood:	n/a	n/a

(count:1466 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:47178359-47178409	SK-N-MC	brain:	n/a
2	chr16:47173093-47173143	BE2_C	brain:	n/a
3	chr16:47178359-47178409	SK-N-MC	brain:	n/a
4	chr16:47173093-47173143	BE2_C	brain:	n/a
5	chr16:47178070-47178120	A549	lung:	n/a
6	chr16:47338451-47338501	HepG2	liver:	n/a
7	chr16:47178078-47178128	NT2-D1	testis:	n/a
8	chr16:47176710-47176760	AoSMC	blood vessel:	n/a
9	chr16:47178250-47178300	T-47D	breast:	n/a
10	chr16:47178250-47178300	GM19239	blood:	n/a
11	chr16:47178723-47178773	NB4	blood:	n/a
12	chr16:47344826-47344876	LNCaP	prostate:	n/a
13	chr16:47164168-47164218	AG09309	skin:	n/a
14	chr16:47178070-47178120	HCF	heart:	n/a
15	chr16:47177603-47177653	ECC-1	luminal epithelium:	n/a
16	chr16:47178723-47178773	SKMC	muscle:	n/a
17	chr16:47175936-47175986	CMK	blood:	n/a
18	chr16:47117092-47117142	Jurkat	blood:	n/a
19	chr16:47362879-47362929	A549	lung:	n/a
20	chr16:47178357-47178407	ProgFib	skin:	n/a
21	chr16:47178208-47178258	NHDF-neo	bronchial:	n/a
22	chr16:47178070-47178120	GM19239	blood:	n/a
23	chr16:47216988-47217038	H1-hESC	embryonic stem cell:	embryo
24	chr16:47175936-47175986	HMEC	breast:	n/a
25	chr16:47175842-47175892	RPTEC	kidney:	n/a
26	chr16:47178357-47178407	SKMC	muscle:	n/a
27	chr16:47177603-47177653	NHBE	bronchial:	n/a
28	chr16:47177480-47177530	HNPCEpiC	eye:	n/a
29	chr16:47177603-47177653	HCT-116	colon:	n/a
30	chr16:47178078-47178128	A549	lung:	n/a
31	chr16:47175936-47175986	AG04450	lung:	fetal
32	chr16:47175912-47175962	H1-hESC	embryonic stem cell:	embryo
33	chr16:47176710-47176760	HEK293	kidney:	embryo
34	chr16:47338451-47338501	SK-N-SH_RA	brain:	n/a
35	chr16:47178208-47178258	HMEC	breast:	n/a
36	chr16:47178067-47178117	HCT-116	colon:	n/a
37	chr16:47177603-47177653	BJ	skin:	n/a
38	chr16:47177175-47177225	ovcar-3	ovarian:	n/a
39	chr16:47178357-47178407	ovcar-3	ovarian:	n/a
40	chr16:47178208-47178258	GM19239	blood:	n/a
41	chr16:47214942-47214992	HCF	heart:	n/a
42	chr16:47164168-47164218	HRPEpiC	eye:	n/a
43	chr16:47178208-47178258	Caco-2	colon:	n/a
44	chr16:47178359-47178409	GM12892	blood:	n/a
45	chr16:47117092-47117142	PrEC	prostate:	n/a
46	chr16:47175842-47175892	SK-N-SH	brain:	n/a
47	chr16:47362879-47362929	HepG2	liver:	n/a
48	chr16:47181961-47182011	Hepatocyte	liver:	n/a
49	chr16:47117092-47117142	HEEpiC	esophagus:	n/a
50	chr16:47117092-47117142	HCT-116	colon:	n/a

(count:98 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr16:47247078..47250065-chr16:47259080..47261996,2	K562	blood:
2	chr16:47288247..47290542-chr16:47297549..47300017,2	K562	blood:
3	chr16:47288247..47290542-chr16:47297549..47300017,2	K562	blood:
4	chr16:47201430..47205164-chr16:47207074..47210552,4	K562	blood:
5	chr16:47298562..47302472-chr16:47302634..47305844,3	K562	blood:
6	chr16:47282712..47286365-chr16:47287931..47291615,3	K562	blood:
7	chr16:47009479..47012393-chr16:47173213..47175154,2	K562	blood:
8	chr16:47136112..47138156-chr16:47139156..47141395,2	K562	blood:
9	chr16:47079162..47080799-chr16:47167858..47170799,2	MCF-7	breast:
10	chr16:47352976..47355256-chr16:47362064..47365437,3	K562	blood:
11	chr16:47233614..47236128-chr16:47259100..47261091,2	K562	blood:
12	chr16:47257065..47259254-chr16:47293834..47296356,2	K562	blood:
13	chr16:47203225..47205164-chr16:47207074..47209665,2	K562	blood:
14	chr16:47284043..47286034-chr16:47297265..47300260,2	K562	blood:
15	chr16:47174837..47177337-chr16:47189035..47191316,2	K562	blood:
16	chr16:47259812..47262289-chr16:47267299..47269084,2	K562	blood:
17	chr16:47151336..47152923-chr16:48188531..48190153,2	K562	blood:
18	chr16:47174790..47177797-chr16:47493413..47496816,5	K562	blood:
19	chr16:47233470..47235990-chr16:47244208..47246996,2	K562	blood:
20	chr16:47177383..47180950-chr16:47184423..47188537,5	K562	blood:
21	chr16:47177500..47180441-chr16:47180510..47182693,2	K562	blood:
22	chr16:47071376..47072506-chr16:47175620..47176296,3	K562	blood:
23	chr16:47233614..47236128-chr16:47259100..47261091,2	K562	blood:
24	chr16:47144717..47146770-chr16:47176377..47178573,2	K562	blood:
25	chr16:47142677..47145551-chr16:47151565..47154001,2	K562	blood:
26	chr16:47167732..47169803-chr16:47176534..47179100,2	MCF-7	breast:
27	chr16:47290686..47293346-chr16:47302878..47305751,2	K562	blood:
28	chr16:47114863..47118029-chr16:47121766..47124133,3	K562	blood:
29	chr16:47269900..47272616-chr16:47277828..47281996,3	K562	blood:
30	chr16:47180495..47185251-chr16:47187387..47190587,4	K562	blood:
31	chr16:47281267..47281944-chr3:111725286..111725871,2	MCF-7	breast:
32	chr16:47141593..47145551-chr16:47150754..47154001,3	K562	blood:
33	chr16:47189136..47190025-chr20:45802278..45803128,2	MCF-7	breast:
34	chr16:47239252..47239752-chr3:67770876..67771427,2	Hela-S3	cervix:
35	chr16:47005815..47008447-chr16:47177298..47179122,2	K562	blood:
36	chr16:47178986..47180526-chr16:47182698..47184295,2	K562	blood:
37	chr16:47245162..47247780-chr16:47248160..47249782,2	K562	blood:
38	chr16:47282712..47286365-chr16:47287931..47291615,3	K562	blood:
39	chr16:47177997..47179501-chr16:47190203..47192834,2	K562	blood:
40	chr16:47246745..47249247-chr16:47253084..47254713,2	K562	blood:
41	chr16:47352976..47355256-chr16:47362064..47365437,3	K562	blood:
42	chr16:47178385..47180317-chr16:47705518..47707688,2	K562	blood:
43	chr16:47165353..47167030-chr16:47501273..47503652,2	K562	blood:
44	chr16:47189381..47191014-chr16:47191815..47193762,2	K562	blood:
45	chr16:47310628..47312888-chr16:47313901..47316020,2	K562	blood:
46	chr16:47257065..47259254-chr16:47293834..47296356,2	K562	blood:
47	chr16:47263413..47265450-chr16:47271876..47274264,2	K562	blood:
48	chr16:47189381..47191014-chr16:47191815..47193762,2	K562	blood:
49	chr16:47173268..47175899-chr16:48024944..48027276,2	K562	blood:
50	chr16:47149178..47150875-chr16:47154165..47156077,2	K562	blood:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PHKB-3	chr16:47235986-47236340	ENSG00000260744.1
2	lnc-NETO2-3	chr16:47310408-47311851	NONHSAT142289
3	lnc-PHKB-3	chr16:47230222-47230630	ENSG00000260744.1
4	lnc-PHKB-1	chr16:47351460-47351725	ENSG00000261369.1
5	lnc-GPT2-11	chr16:47211652-47211793	l_1316_chr16:47211651-47213507_testes
6	lnc-PHKB-1	chr16:47346550-47346651	ENSG00000261369.1
7	lnc-GPT2-10	chr16:47185464-47185705	NONHSAT142284
8	lnc-PHKB-1	chr16:47333358-47333859	ENSG00000261369.1
9	lnc-NETO2-2	chr16:47296678-47296925	NONHSAT142288
10	lnc-GPT2-11	chr16:47213203-47213513	l_1316_chr16:47211651-47213507_testes
11	lnc-GPT2-3	chr16:47177999-47178405	NONHSAT142282
12	lnc-NETO2-2	chr16:47294571-47294606	NONHSAT142288
13	lnc-GPT2-3	chr16:47195460-47195501	NONHSAT142282
14	lnc-GPT2-3	chr16:47216667-47217006	NONHSAT142282
15	lnc-GPT2-3	chr16:47191466-47191515	NONHSAT142282
16	lnc-GPT2-3	chr16:47187543-47187707	NONHSAT142282

No data

(count:5 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	NETO2	hsa-miR-1	chr16:47116733-47116754
2	NETO2	hsa-miR-20a-5p	chr16:47116042-47116066
3	NETO2	hsa-miR-21-5p	chr16:47115813-47115831
4	NETO2	hsa-miR-20a-5p	chr16:47116059-47116081
5	ITFG1	hsa-miR-23b-3p	chr16:47189629-47189649

Variant related genes	Relation type
ENSG00000261369	TF binding region
ENSG00000260281	TF binding region
NETO2	TF binding region
ENSG00000238834	TF binding region
ENSG00000222767	TF binding region
RPL23AP72	TF binding region
ITFG1	TF binding region
ENSG00000260012	TF binding region
ENSG00000260744	TF binding region
ENSG00000261369	CpG island
ENSG00000260281	CpG island
NETO2	CpG island
ENSG00000238834	CpG island
ENSG00000222767	CpG island
RPL23AP72	CpG island
ITFG1	CpG island
ENSG00000260012	CpG island
ENSG00000260744	CpG island
ENSG00000121270	chromatin interactions
ENSG00000129636	chromatin interactions
ENSG00000074800	chromatin interactions
ENSG00000260281	chromatin interactions
ENSG00000140798	chromatin interactions
ENSG00000239840	chromatin interactions
ENSG00000261173	chromatin interactions
ENSG00000230679	chromatin interactions
ENSG00000102893	chromatin interactions
ENSG00000238834	chromatin interactions
ENSG00000069345	chromatin interactions
ENSG00000171208	chromatin interactions

Extended variants
information (count: 7894 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:7894 , 50 per page) page: 1 2 3 4 5 6 7 ... 158

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16952122	chr16:47115776-47115777	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs572201348	chr16:47115784-47115785	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs35433537	chr16:47115790-47115791	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs562159058	chr16:47115794-47115795	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs546075654	chr16:47115805-47115806	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs151000137	chr16:47115820-47115821	Weak transcription Strong transcription Enhancers	miRNA target site	1 gene(s)	Overlapped CNVs	n/a
7	rs576163813	chr16:47115845-47115846	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs543564430	chr16:47115856-47115857	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs372142096	chr16:47115857-47115858	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs140832312	chr16:47115874-47115875	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs551105087	chr16:47115900-47115901	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs540977902	chr16:47115927-47115928	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs183481091	chr16:47115963-47115964	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs563012418	chr16:47115975-47115976	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs375197707	chr16:47115994-47115995	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs533464366	chr16:47116010-47116011	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs528013185	chr16:47116055-47116056	Weak transcription Strong transcription Enhancers	miRNA target site	1 gene(s)	Overlapped CNVs	n/a
18	rs72812490	chr16:47116066-47116067	Weak transcription Strong transcription Enhancers	miRNA target site	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs540243330	chr16:47116142-47116143	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs16952126	chr16:47116184-47116185	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs144830689	chr16:47116215-47116216	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs549880308	chr16:47116226-47116227	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs534630998	chr16:47116262-47116263	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs74560591	chr16:47116302-47116303	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs77120094	chr16:47116318-47116319	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs547521788	chr16:47116334-47116335	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs566056107	chr16:47116390-47116391	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs181023842	chr16:47116433-47116434	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs184680586	chr16:47116464-47116465	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs557061100	chr16:47116521-47116522	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs577409719	chr16:47116624-47116625	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs576319518	chr16:47116643-47116644	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs567915512	chr16:47116667-47116668	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs16952129	chr16:47116679-47116680	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs555502569	chr16:47116686-47116687	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs190784016	chr16:47116688-47116689	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs117916748	chr16:47116712-47116713	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs28584709	chr16:47116770-47116771	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs112455767	chr16:47116835-47116836	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs530685652	chr16:47116837-47116838	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs74724581	chr16:47116839-47116840	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs11554121	chr16:47116846-47116847	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs11554120	chr16:47116848-47116849	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs140306182	chr16:47116859-47116860	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs145321104	chr16:47116862-47116863	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs35313755	chr16:47116877-47116878	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs137924889	chr16:47116909-47116910	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs11554122	chr16:47116930-47116931	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs114112349	chr16:47116932-47116933	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs112354967	chr16:47117030-47117031	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
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
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Wilms tumour	21544195	CNVD
Cancer	20164920	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	21339820	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
Renal cell carcinoma	18765545	CNVD
Sudden cardiac death	19188705	CNVD
Multiple myeloma	16616336	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	21364760	CNVD
Ewing''s sarcoma	17952124	CNVD
Myelofibrosis	22110671	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Colorectal cancer	19359472	CNVD
Olfactory neuroblastoma	18408657	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	22341455	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:3031 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:47103800-47116800	Weak transcription	Primary monocytes fromperipheralblood	blood
2	chr16:47107400-47138400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr16:47108000-47145600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr16:47108200-47116600	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr16:47108200-47116800	Weak transcription	GM12878-XiMat	blood
6	chr16:47108200-47130000	Weak transcription	Brain Germinal Matrix	brain
7	chr16:47110800-47122200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr16:47110800-47158000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr16:47111000-47131000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr16:47112000-47132000	Weak transcription	Esophagus	oesophagus
11	chr16:47112000-47144800	Weak transcription	Spleen	Spleen
12	chr16:47112600-47116600	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr16:47113200-47142200	Weak transcription	Hela-S3	cervix
14	chr16:47113400-47141000	Weak transcription	NH-A	brain
15	chr16:47113600-47116800	Weak transcription	NHEK	skin
16	chr16:47113600-47116800	Weak transcription	NHLF	lung
17	chr16:47114000-47141000	Weak transcription	HSMM	muscle
18	chr16:47114200-47116800	Weak transcription	HUES6 Cell Line	embryonic stem cell
19	chr16:47114200-47116800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr16:47114200-47116800	Weak transcription	A549	lung
21	chr16:47114200-47126600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr16:47114200-47127200	Weak transcription	K562	blood
23	chr16:47114400-47116800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr16:47114400-47130800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr16:47114400-47139800	Weak transcription	Muscle Satellite Cultured Cells	--
26	chr16:47114600-47120200	Weak transcription	H1 Cell Line	embryonic stem cell
27	chr16:47114600-47138600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr16:47114600-47140800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
29	chr16:47114600-47147000	Weak transcription	Brain Anterior Caudate	brain
30	chr16:47114800-47116200	Weak transcription	Fetal Brain Female	brain
31	chr16:47114800-47116400	Weak transcription	HMEC	breast
32	chr16:47114800-47116600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr16:47114800-47118000	Weak transcription	HUVEC	blood vessel
34	chr16:47114800-47120600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
35	chr16:47114800-47132000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr16:47115000-47116200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr16:47115000-47116200	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr16:47115200-47118200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr16:47115400-47116200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr16:47115400-47116200	Enhancers	Fetal Brain Male	brain
41	chr16:47115400-47163400	Weak transcription	HUES48 Cell Line	embryonic stem cell
42	chr16:47115600-47119800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr16:47115600-47123000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
44	chr16:47115600-47131000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr16:47115800-47117400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr16:47115800-47130600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr16:47116200-47116600	Weak transcription	Fetal Brain Male	brain
48	chr16:47116200-47116800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
49	chr16:47116200-47117400	Enhancers	Fetal Brain Female	brain
50	chr16:47116200-47119400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood

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