Variant report

Variant	esv1823679
Chromosome Location	chr16:47089357-47194051
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1931)
CpG islands
(count:1162)
Chromatin interactive
region (count:58)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:5)

(count:1931 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:47178303-47178477	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:47175602-47176202	K562	blood:	n/a	n/a
3	ARID3A	chr16:47171892-47172010	K562	blood:	n/a	n/a
4	ARID3A	chr16:47169900-47170121	K562	blood:	n/a	n/a
5	ARID3A	chr16:47166225-47166502	K562	blood:	n/a	n/a
6	ARID3A	chr16:47175635-47176566	HepG2	liver:	n/a	n/a
7	ARID3A	chr16:47177086-47177176	HepG2	liver:	n/a	n/a
8	ARID3A	chr16:47176783-47176815	K562	blood:	n/a	n/a
9	ARID3A	chr16:47177441-47177480	K562	blood:	n/a	n/a
10	ARID3A	chr16:47092472-47093002	HepG2	liver:	n/a	n/a
11	ARID3A	chr16:47180937-47181312	K562	blood:	n/a	n/a
12	ATF1	chr16:47170098-47170312	K562	blood:	n/a	n/a
13	ATF1	chr16:47175658-47176054	K562	blood:	n/a	n/a
14	ATF2	chr16:47175571-47176087	GM12878	blood:	n/a	n/a
15	ATF2	chr16:47176226-47176738	GM12878	blood:	n/a	n/a
16	ATF2	chr16:47176142-47176695	GM12878	blood:	n/a	n/a
17	ATF2	chr16:47175531-47176062	GM12878	blood:	n/a	n/a
18	ATF3	chr16:47171874-47172117	K562	blood:	n/a	n/a
19	ATF3	chr16:47177260-47177528	K562	blood:	n/a	n/a
20	BACH1	chr16:47175631-47176087	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr16:47152449-47152458	K562	blood:	n/a	n/a
22	BACH1	chr16:47178178-47178180	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr16:47176731-47177908	H1-hESC	embryonic stem cell:	n/a	n/a
24	BATF	chr16:47175661-47175976	GM12878	blood:	n/a	n/a
25	BATF	chr16:47147784-47148314	GM12878	blood:	n/a	n/a
26	BATF	chr16:47176365-47176663	GM12878	blood:	n/a	n/a
27	BATF	chr16:47176399-47176669	GM12878	blood:	n/a	n/a
28	BCL11A	chr16:47176367-47176707	GM12878	blood:	n/a	n/a
29	BCLAF1	chr16:47175480-47176190	GM12878	blood:	n/a	n/a
30	BCLAF1	chr16:47175544-47176047	GM12878	blood:	n/a	n/a
31	BCLAF1	chr16:47177145-47177707	GM12878	blood:	n/a	chr16:47177425-47177438 chr16:47177593-47177602 chr16:47177563-47177572
32	BCLAF1	chr16:47176319-47176951	GM12878	blood:	n/a	n/a
33	BCLAF1	chr16:47177271-47177669	GM12878	blood:	n/a	chr16:47177425-47177438 chr16:47177593-47177602 chr16:47177563-47177572
34	BHLHE40	chr16:47175534-47176602	GM12878	blood:	n/a	n/a
35	BHLHE40	chr16:47177272-47178380	K562	blood:	n/a	chr16:47178152-47178168 chr16:47177449-47177465 chr16:47178004-47178020 chr16:47178144-47178160
36	BHLHE40	chr16:47177335-47177732	HepG2	liver:	n/a	chr16:47177449-47177465
37	BHLHE40	chr16:47176815-47178581	GM12878	blood:	n/a	chr16:47178152-47178168 chr16:47176993-47177009 chr16:47176944-47176960 chr16:47177449-47177465 chr16:47178004-47178020 chr16:47178144-47178160
38	BHLHE40	chr16:47175636-47176200	K562	blood:	n/a	n/a
39	BRCA1	chr16:47176374-47176777	Hela-S3	cervix:	n/a	n/a
40	BRCA1	chr16:47164027-47164063	GM12878	blood:	n/a	n/a
41	BRCA1	chr16:47175537-47175997	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr16:47178424-47178462	GM12878	blood:	n/a	n/a
43	BRCA1	chr16:47178549-47178596	HepG2	liver:	n/a	n/a
44	CBX3	chr16:47178273-47178641	K562	blood:	n/a	n/a
45	CBX3	chr16:47177298-47177690	K562	blood:	n/a	n/a
46	CBX3	chr16:47186439-47186720	K562	blood:	n/a	n/a
47	CCNT2	chr16:47173695-47173896	K562	blood:	n/a	n/a
48	CCNT2	chr16:47176712-47178516	K562	blood:	n/a	chr16:47177471-47177480
49	CEBPB	chr16:47121303-47121604	HepG2	liver:	n/a	chr16:47121439-47121450
50	CEBPB	chr16:47121303-47121536	A549	lung:	n/a	chr16:47121439-47121450

(count:1162 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:47178357-47178407	HCPEpiC	choroid plexus:	n/a
2	chr16:47177480-47177530	U87	brain:	n/a
3	chr16:47177603-47177653	BJ	skin:	n/a
4	chr16:47178357-47178407	HCPEpiC	choroid plexus:	n/a
5	chr16:47177480-47177530	U87	brain:	n/a
6	chr16:47177603-47177653	BJ	skin:	n/a
7	chr16:47177175-47177225	SK-N-SH_RA	brain:	n/a
8	chr16:47175842-47175892	HMEC	breast:	n/a
9	chr16:47175936-47175986	BE2_C	brain:	n/a
10	chr16:47173093-47173143	AG04450	lung:	fetal
11	chr16:47176710-47176760	ovcar-3	ovarian:	n/a
12	chr16:47178078-47178128	HMEC	breast:	n/a
13	chr16:47178067-47178117	K562	blood:	n/a
14	chr16:47178357-47178407	BE2_C	brain:	n/a
15	chr16:47178357-47178407	SK-N-SH	brain:	n/a
16	chr16:47178250-47178300	SK-N-MC	brain:	n/a
17	chr16:47178723-47178773	BE2_C	brain:	n/a
18	chr16:47178067-47178117	HCPEpiC	choroid plexus:	n/a
19	chr16:47175936-47175986	K562	blood:	n/a
20	chr16:47178078-47178128	HL-60	blood:	n/a
21	chr16:47178067-47178117	HCT-116	colon:	n/a
22	chr16:47173093-47173143	GM06990	blood:	n/a
23	chr16:47178357-47178407	AG10803	skin:	n/a
24	chr16:47164168-47164218	AG09309	skin:	n/a
25	chr16:47177175-47177225	HPAEpiC	pulmonary alveolar:	n/a
26	chr16:47164168-47164218	PFSK-1	brain:	n/a
27	chr16:47177175-47177225	PrEC	prostate:	n/a
28	chr16:47173093-47173143	SK-N-MC	brain:	n/a
29	chr16:47181961-47182011	NHBE	bronchial:	n/a
30	chr16:47178723-47178773	AG04449	skin:	fetal
31	chr16:47178723-47178773	PFSK-1	brain:	n/a
32	chr16:47164168-47164218	HCM	heart:	n/a
33	chr16:47178208-47178258	Jurkat	blood:	n/a
34	chr16:47178070-47178120	HRCEpiC	kidney:	n/a
35	chr16:47175912-47175962	PrEC	prostate:	n/a
36	chr16:47117092-47117142	HCT-116	colon:	n/a
37	chr16:47177603-47177653	NT2-D1	testis:	n/a
38	chr16:47177603-47177653	GM12891	blood:	n/a
39	chr16:47178208-47178258	CMK	blood:	n/a
40	chr16:47164168-47164218	HCF	heart:	n/a
41	chr16:47175936-47175986	GM06990	blood:	n/a
42	chr16:47177480-47177530	HL-60	blood:	n/a
43	chr16:47181961-47182011	HIPEpiC	eye:	n/a
44	chr16:47177175-47177225	H1-hESC	embryonic stem cell:	embryo
45	chr16:47176710-47176760	SK-N-SH_RA	brain:	n/a
46	chr16:47176710-47176760	U87	brain:	n/a
47	chr16:47181961-47182011	SAEC	small airway:	n/a
48	chr16:47175912-47175962	T-47D	breast:	n/a
49	chr16:47175842-47175892	HRE	kidney:	n/a
50	chr16:47177603-47177653	HUVEC	blood vessel:	n/a

(count:58 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr16:47189381..47191014-chr16:47191815..47193762,2	K562	blood:
2	chr16:47116484..47118029-chr16:47121766..47123830,2	K562	blood:
3	chr16:47178986..47180526-chr16:47182698..47184295,2	K562	blood:
4	chr16:47102804..47105348-chr16:47108276..47109997,2	K562	blood:
5	chr16:47171642..47174584-chr16:47493767..47496687,2	K562	blood:
6	chr16:47136112..47138156-chr16:47139156..47141395,2	K562	blood:
7	chr16:47109054..47112111-chr16:47113966..47116275,3	K562	blood:
8	chr16:47174837..47177337-chr16:47189035..47191316,2	K562	blood:
9	chr16:47176885..47177462-chr16:47479483..47480444,2	K562	blood:
10	chr16:47109054..47112111-chr16:47113966..47116275,3	K562	blood:
11	chr16:47177383..47180950-chr16:47184423..47188537,5	K562	blood:
12	chr16:47151336..47152923-chr16:48188531..48190153,2	K562	blood:
13	chr16:47142677..47145551-chr16:47151565..47154001,2	K562	blood:
14	chr16:47184664..47186977-chr16:47194583..47196786,2	K562	blood:
15	chr16:47094426..47096201-chr16:47098961..47101014,2	K562	blood:
16	chr16:47167732..47169803-chr16:47176534..47179100,2	MCF-7	breast:
17	chr16:47175627..47176240-chr16:48199483..48200032,2	MCF-7	breast:
18	chr16:47173268..47175899-chr16:48024944..48027276,2	K562	blood:
19	chr16:47158314..47161055-chr16:47162074..47164177,2	K562	blood:
20	chr16:47158720..47160557-chr16:47177080..47179479,2	K562	blood:
21	chr16:47102804..47105348-chr16:47108276..47109997,2	K562	blood:
22	chr16:47009479..47012393-chr16:47173213..47175154,2	K562	blood:
23	chr16:47116484..47118029-chr16:47121766..47123830,2	K562	blood:
24	chr16:47006401..47008071-chr16:47164549..47167547,2	K562	blood:
25	chr16:47114863..47118029-chr16:47121766..47124133,3	K562	blood:
26	chr16:47094426..47096201-chr16:47098961..47101014,2	K562	blood:
27	chr16:47174005..47175581-chr16:47176201..47178952,2	MCF-7	breast:
28	chr16:47071376..47072506-chr16:47175620..47176296,3	K562	blood:
29	chr16:47155510..47158192-chr16:47174850..47176528,2	K562	blood:
30	chr16:47174837..47177337-chr16:47189035..47191316,2	K562	blood:
31	chr16:47180495..47185251-chr16:47187387..47190587,4	K562	blood:
32	chr16:47178385..47180317-chr16:47705518..47707688,2	K562	blood:
33	chr16:47141593..47145551-chr16:47150754..47154001,3	K562	blood:
34	chr16:47177997..47179501-chr16:47190203..47192834,2	K562	blood:
35	chr16:47189381..47191014-chr16:47191815..47193762,2	K562	blood:
36	chr16:47005665..47009288-chr16:47176479..47179650,5	K562	blood:
37	chr16:47149538..47152356-chr16:47176160..47177758,2	MCF-7	breast:
38	chr16:47093709..47095926-chr16:47097350..47100461,3	K562	blood:
39	chr16:47079162..47080799-chr16:47167858..47170799,2	MCF-7	breast:
40	chr16:47136112..47138156-chr16:47139156..47141395,2	K562	blood:
41	chr16:47175524..47179141-chr16:47493736..47496005,3	MCF-7	breast:
42	chr16:47006185..47008137-chr16:47174529..47176605,2	K562	blood:
43	chr16:47189136..47190025-chr20:45802278..45803128,2	MCF-7	breast:
44	chr16:47093709..47095926-chr16:47097350..47100461,3	K562	blood:
45	chr16:47178986..47180526-chr16:47182698..47184295,2	K562	blood:
46	chr16:47175322..47176299-chr16:48190360..48191104,3	K562	blood:
47	chr16:47174790..47177797-chr16:47493413..47496816,5	K562	blood:
48	chr16:47175994..47177897-chr16:48278487..48280949,2	MCF-7	breast:
49	chr16:47165353..47167030-chr16:47501273..47503652,2	K562	blood:
50	chr16:47071055..47073725-chr16:47087478..47089914,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPT2-10	chr16:47185464-47185705	NONHSAT142284
2	lnc-GPT2-3	chr16:47177999-47178405	NONHSAT142282
3	lnc-GPT2-3	chr16:47191466-47191515	NONHSAT142282
4	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-20a-5p	chr16:47116042-47116066
2	NETO2	hsa-miR-20a-5p	chr16:47116059-47116081
3	ITFG1	hsa-miR-23b-3p	chr16:47189629-47189649
4	NETO2	hsa-miR-21-5p	chr16:47115813-47115831
5	NETO2	hsa-miR-1	chr16:47116733-47116754

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

Extended variants
information (count: 3188 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:3188 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4625742	chr16:47089357-47089358	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs376609750	chr16:47089365-47089366	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs117264359	chr16:47089433-47089434	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs570594501	chr16:47089435-47089436	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs542773617	chr16:47089474-47089475	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs192539627	chr16:47089494-47089495	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs184873748	chr16:47089514-47089515	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs574887808	chr16:47089516-47089517	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs535094670	chr16:47089540-47089541	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs553445029	chr16:47089622-47089623	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs11247543	chr16:47089627-47089628	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs540614218	chr16:47089675-47089676	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs565559488	chr16:47089683-47089684	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs375343451	chr16:47089723-47089724	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs577542699	chr16:47089744-47089745	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs544791906	chr16:47089756-47089757	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs562987992	chr16:47089757-47089758	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs147166800	chr16:47089782-47089783	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs535819380	chr16:47089789-47089790	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs369422652	chr16:47089872-47089873	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs189760053	chr16:47089927-47089928	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs560329932	chr16:47089989-47089990	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs373284176	chr16:47090079-47090080	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs180835808	chr16:47090087-47090088	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs552222400	chr16:47090095-47090096	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs140447357	chr16:47090097-47090098	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs564916057	chr16:47090098-47090099	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs533093343	chr16:47090114-47090115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs551227889	chr16:47090135-47090136	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs537668604	chr16:47090136-47090137	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs150623571	chr16:47090137-47090138	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs549528492	chr16:47090159-47090160	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs567821859	chr16:47090170-47090171	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs369937471	chr16:47090182-47090183	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs185160903	chr16:47090204-47090205	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs566571904	chr16:47090234-47090235	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs189187132	chr16:47090235-47090236	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs571983246	chr16:47090278-47090279	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs144293830	chr16:47090279-47090280	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs113235670	chr16:47090337-47090338	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs112812811	chr16:47090362-47090363	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs539306509	chr16:47090380-47090381	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs548816689	chr16:47090397-47090398	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs368450095	chr16:47090404-47090405	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs71134533	chr16:47090432-47090433	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs372223922	chr16:47090433-47090434	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs376374661	chr16:47090461-47090462	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs559009785	chr16:47090492-47090493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs370000105	chr16:47090495-47090496	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs567397380	chr16:47090498-47090499	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

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
Breast cancer	22522925	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:1631 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:47072400-47096800	Weak transcription	Right Atrium	heart
2	chr16:47082800-47093800	Weak transcription	Spleen	Spleen
3	chr16:47087000-47093200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr16:47088200-47091400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
5	chr16:47089000-47091400	Enhancers	HepG2	liver
6	chr16:47089400-47089800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr16:47089800-47091000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr16:47090800-47091000	Enhancers	Brain Germinal Matrix	brain
9	chr16:47091000-47091200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr16:47091000-47091400	Active TSS	Breast Myoepithelial Primary Cells	Breast
11	chr16:47091000-47091400	Enhancers	Pancreas	Pancrea
12	chr16:47091000-47092000	Weak transcription	Brain Germinal Matrix	brain
13	chr16:47091200-47091400	Bivalent Enhancer	NHLF	lung
14	chr16:47091200-47091600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr16:47091400-47091800	Flanking Active TSS	HepG2	liver
16	chr16:47091400-47093400	Enhancers	Rectal Mucosa Donor 29	rectum
17	chr16:47091400-47093600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
18	chr16:47091600-47091800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr16:47091800-47092400	Enhancers	HepG2	liver
20	chr16:47091800-47093400	Enhancers	Colonic Mucosa	Colon
21	chr16:47092000-47092200	Enhancers	Brain Germinal Matrix	brain
22	chr16:47092200-47092600	Enhancers	Duodenum Mucosa	Duodenum
23	chr16:47092200-47092800	Weak transcription	Brain Germinal Matrix	brain
24	chr16:47092400-47093200	Flanking Active TSS	HepG2	liver
25	chr16:47092600-47093400	Enhancers	Rectal Mucosa Donor 31	rectum
26	chr16:47092800-47093000	Enhancers	Brain Germinal Matrix	brain
27	chr16:47092800-47093600	Enhancers	HMEC	breast
28	chr16:47092800-47093600	Enhancers	NHEK	skin
29	chr16:47093200-47093400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr16:47093200-47093800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr16:47093200-47096000	Enhancers	HepG2	liver
32	chr16:47093400-47094600	Weak transcription	Rectal Mucosa Donor 31	rectum
33	chr16:47093800-47094400	Enhancers	Spleen	Spleen
34	chr16:47094400-47095200	Weak transcription	Spleen	Spleen
35	chr16:47094600-47094800	Enhancers	Rectal Mucosa Donor 31	rectum
36	chr16:47095200-47095400	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
37	chr16:47095200-47095600	Active TSS	Spleen	Spleen
38	chr16:47095400-47095600	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
39	chr16:47095600-47095800	Enhancers	Spleen	Spleen
40	chr16:47097200-47097400	Bivalent Enhancer	HepG2	liver
41	chr16:47097400-47097600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
42	chr16:47099600-47100000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
43	chr16:47099600-47100200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr16:47099600-47100400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr16:47099800-47100200	Enhancers	H1 Cell Line	embryonic stem cell
46	chr16:47099800-47100200	Enhancers	Cortex derived primary cultured neurospheres	brain
47	chr16:47099800-47100200	Enhancers	Brain Germinal Matrix	brain
48	chr16:47099800-47100200	Bivalent Enhancer	HepG2	liver
49	chr16:47099800-47100400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr16:47100200-47100400	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived

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