Variant report

Variant	esv1795199
Chromosome Location	chr16:47111119-47732476
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:5575)
CpG islands
(count:2747)
Chromatin interactive
region (count:303)
LncRNA
region (count:26)
Mature miRNA
region (count: 0)
miRNA target
sites (count:6)

(count:5575 , 50 per page) page: 1 2 3 4 5 6 7 ... 112

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:47482890-47483076	K562	blood:	n/a	n/a
2	ARID3A	chr16:47484519-47484647	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:47538556-47538932	K562	blood:	n/a	n/a
4	ARID3A	chr16:47196782-47196800	HepG2	liver:	n/a	n/a
5	ARID3A	chr16:47507738-47508382	HepG2	liver:	n/a	n/a
6	ARID3A	chr16:47177441-47177480	K562	blood:	n/a	n/a
7	ARID3A	chr16:47428252-47428453	HepG2	liver:	n/a	n/a
8	ARID3A	chr16:47426038-47426363	K562	blood:	n/a	n/a
9	ARID3A	chr16:47421094-47421294	HepG2	liver:	n/a	n/a
10	ARID3A	chr16:47431618-47431623	HepG2	liver:	n/a	n/a
11	ARID3A	chr16:47526816-47527197	HepG2	liver:	n/a	n/a
12	ARID3A	chr16:47698347-47698941	HepG2	liver:	n/a	chr16:47698627-47698643
13	ARID3A	chr16:47556945-47557537	HepG2	liver:	n/a	n/a
14	ARID3A	chr16:47216266-47216628	HepG2	liver:	n/a	n/a
15	ARID3A	chr16:47690725-47691453	HepG2	liver:	n/a	n/a
16	ARID3A	chr16:47554148-47554743	K562	blood:	n/a	n/a
17	ARID3A	chr16:47572269-47572803	HepG2	liver:	n/a	n/a
18	ARID3A	chr16:47177086-47177176	HepG2	liver:	n/a	n/a
19	ARID3A	chr16:47524403-47524722	K562	blood:	n/a	n/a
20	ARID3A	chr16:47176783-47176815	K562	blood:	n/a	n/a
21	ARID3A	chr16:47526802-47527555	K562	blood:	n/a	n/a
22	ARID3A	chr16:47612461-47612663	K562	blood:	n/a	n/a
23	ARID3A	chr16:47166225-47166502	K562	blood:	n/a	n/a
24	ARID3A	chr16:47533067-47533932	HepG2	liver:	n/a	n/a
25	ARID3A	chr16:47658634-47659953	K562	blood:	n/a	n/a
26	ARID3A	chr16:47178303-47178477	HepG2	liver:	n/a	n/a
27	ARID3A	chr16:47180937-47181312	K562	blood:	n/a	n/a
28	ARID3A	chr16:47509336-47510111	HepG2	liver:	n/a	n/a
29	ARID3A	chr16:47175635-47176566	HepG2	liver:	n/a	n/a
30	ARID3A	chr16:47495283-47496261	K562	blood:	n/a	n/a
31	ARID3A	chr16:47615141-47615378	HepG2	liver:	n/a	n/a
32	ARID3A	chr16:47507313-47507485	HepG2	liver:	n/a	n/a
33	ARID3A	chr16:47171892-47172010	K562	blood:	n/a	n/a
34	ARID3A	chr16:47500293-47502483	K562	blood:	n/a	n/a
35	ARID3A	chr16:47169900-47170121	K562	blood:	n/a	n/a
36	ARID3A	chr16:47494825-47496228	HepG2	liver:	n/a	n/a
37	ARID3A	chr16:47498536-47498645	K562	blood:	n/a	n/a
38	ARID3A	chr16:47703753-47704095	HepG2	liver:	n/a	n/a
39	ARID3A	chr16:47499795-47500033	K562	blood:	n/a	n/a
40	ARID3A	chr16:47667679-47668530	HepG2	liver:	n/a	n/a
41	ARID3A	chr16:47357253-47357463	HepG2	liver:	n/a	n/a
42	ARID3A	chr16:47519386-47519410	HepG2	liver:	n/a	n/a
43	ARID3A	chr16:47175602-47176202	K562	blood:	n/a	n/a
44	ATF1	chr16:47426003-47426482	K562	blood:	n/a	n/a
45	ATF1	chr16:47526819-47527180	K562	blood:	n/a	n/a
46	ATF1	chr16:47599472-47599607	K562	blood:	n/a	n/a
47	ATF1	chr16:47427309-47427338	K562	blood:	n/a	n/a
48	ATF1	chr16:47422668-47422993	K562	blood:	n/a	n/a
49	ATF1	chr16:47626832-47626837	K562	blood:	n/a	n/a
50	ATF1	chr16:47197545-47197587	K562	blood:	n/a	n/a

(count:2747 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:47495746-47495796	SK-N-SH_RA	brain:	n/a
2	chr16:47677874-47677924	MCF-7	breast:	n/a
3	chr16:47495746-47495796	SK-N-SH_RA	brain:	n/a
4	chr16:47677874-47677924	MCF-7	breast:	n/a
5	chr16:47495113-47495163	U87	brain:	n/a
6	chr16:47175842-47175892	LNCaP	prostate:	n/a
7	chr16:47409367-47409417	ProgFib	skin:	n/a
8	chr16:47338451-47338501	HUVEC	blood vessel:	n/a
9	chr16:47420506-47420556	H1-hESC	embryonic stem cell:	embryo
10	chr16:47164168-47164218	GM19239	blood:	n/a
11	chr16:47618685-47618735	NHBE	bronchial:	n/a
12	chr16:47494824-47494874	NT2-D1	testis:	n/a
13	chr16:47494735-47494785	CMK	blood:	n/a
14	chr16:47494735-47494785	HEEpiC	esophagus:	n/a
15	chr16:47495110-47495160	HRCEpiC	kidney:	n/a
16	chr16:47178359-47178409	Jurkat	blood:	n/a
17	chr16:47175936-47175986	H1-hESC	embryonic stem cell:	embryo
18	chr16:47177480-47177530	HPAEpiC	pulmonary alveolar:	n/a
19	chr16:47494735-47494785	GM12892	blood:	n/a
20	chr16:47181961-47182011	HRPEpiC	eye:	n/a
21	chr16:47178067-47178117	HEK293	kidney:	embryo
22	chr16:47539203-47539253	AG10803	skin:	n/a
23	chr16:47494711-47494761	HRE	kidney:	n/a
24	chr16:47178078-47178128	GM12892	blood:	n/a
25	chr16:47177175-47177225	HAEpiC	amniotic membrane:	n/a
26	chr16:47409367-47409417	AG09319	gingival:	n/a
27	chr16:47175842-47175892	PANC-1	pancreas:	n/a
28	chr16:47178357-47178407	HRCEpiC	kidney:	n/a
29	chr16:47178078-47178128	NT2-D1	testis:	n/a
30	chr16:47338451-47338501	T-47D	breast:	n/a
31	chr16:47338451-47338501	IMR90	lung:	fetal
32	chr16:47527034-47527084	HNPCEpiC	eye:	n/a
33	chr16:47178357-47178407	U87	brain:	n/a
34	chr16:47539137-47539187	MCF-7	breast:	n/a
35	chr16:47539166-47539216	RPTEC	kidney:	n/a
36	chr16:47409367-47409417	HRPEpiC	eye:	n/a
37	chr16:47178723-47178773	IMR90	lung:	fetal
38	chr16:47177480-47177530	NHBE	bronchial:	n/a
39	chr16:47176710-47176760	AG09309	skin:	n/a
40	chr16:47164168-47164218	ECC-1	luminal epithelium:	n/a
41	chr16:47344826-47344876	H1-hESC	embryonic stem cell:	embryo
42	chr16:47178067-47178117	HIPEpiC	eye:	n/a
43	chr16:47495445-47495495	HCM	heart:	n/a
44	chr16:47175936-47175986	PrEC	prostate:	n/a
45	chr16:47178357-47178407	GM19239	blood:	n/a
46	chr16:47177603-47177653	BJ	skin:	n/a
47	chr16:47178067-47178117	HRPEpiC	eye:	n/a
48	chr16:47495768-47495818	AG04450	lung:	fetal
49	chr16:47117092-47117142	NT2-D1	testis:	n/a
50	chr16:47494711-47494761	A549	lung:	n/a

(count:303 , 50 per page) page: 1 2 3 4 5 6 7

No.	Distal block	Cell Line	Cell type
1	chr16:47594118..47597140-chr16:47598345..47602068,5	K562	blood:
2	chr16:47646276..47649578-chr16:47653598..47656458,3	K562	blood:
3	chr16:47247078..47250065-chr16:47259080..47261996,2	K562	blood:
4	chr16:47352976..47355256-chr16:47362064..47365437,3	K562	blood:
5	chr16:47201430..47205164-chr16:47207074..47210552,4	K562	blood:
6	chr16:47493252..47495240-chr16:47633671..47635380,2	K562	blood:
7	chr16:47495155..47497057-chr16:47571448..47573039,2	K562	blood:
8	chr16:47006185..47008137-chr16:47174529..47176605,2	K562	blood:
9	chr16:47165353..47167030-chr16:47501273..47503652,2	K562	blood:
10	chr16:47480415..47483126-chr16:47520058..47521883,2	K562	blood:
11	chr16:47500040..47503767-chr16:47514818..47518136,4	K562	blood:
12	chr16:47477872..47480473-chr16:47495017..47496798,2	MCF-7	breast:
13	chr16:47538608..47539204-chr19:24184110..24185018,4	MCF-7	breast:
14	chr16:47269900..47272616-chr16:47277828..47281996,3	K562	blood:
15	chr16:47177492..47179325-chr16:47500185..47502883,2	K562	blood:
16	chr16:47607769..47610118-chr16:47633916..47636393,2	K562	blood:
17	chr16:47652198..47653880-chr16:47657938..47660462,2	K562	blood:
18	chr16:47158720..47160557-chr16:47177080..47179479,2	K562	blood:
19	chr16:47495762..47498105-chr16:47514546..47516108,2	K562	blood:
20	chr16:47404244..47406062-chr16:47411179..47413433,2	K562	blood:
21	chr16:47482556..47484709-chr16:47493898..47495616,2	MCF-7	breast:
22	chr16:47311388..47314338-chr16:47314364..47316020,2	K562	blood:
23	chr16:47496037..47497585-chr16:47610458..47612436,2	K562	blood:
24	chr16:47687860..47689573-chr16:47695289..47697558,2	K562	blood:
25	chr16:47503725..47506287-chr16:47510577..47512512,2	K562	blood:
26	chr16:47006401..47008071-chr16:47164549..47167547,2	K562	blood:
27	chr16:47673393..47675073-chr16:47721240..47723950,2	K562	blood:
28	chr16:47538686..47539206-chr5:50081215..50081735,2	MCF-7	breast:
29	chr16:47407846..47410097-chr16:47493720..47495618,2	MCF-7	breast:
30	chr16:47175524..47179141-chr16:47493736..47496005,3	MCF-7	breast:
31	chr16:47176370..47177924-chr16:47205584..47208161,2	MCF-7	breast:
32	chr16:47548754..47550733-chr16:47554531..47556036,2	MCF-7	breast:
33	chr16:47505221..47508195-chr16:47519032..47520673,2	K562	blood:
34	chr16:47189381..47191014-chr16:47191815..47193762,2	K562	blood:
35	chr16:47479859..47483126-chr16:47518741..47522601,4	K562	blood:
36	chr1:155214276..155214874-chr16:47494461..47494978,2	Hela-S3	cervix:
37	chr16:47538608..47539209-chr19:24184105..24184774,2	MCF-7	breast:
38	chr16:47311388..47314338-chr16:47314364..47316020,2	K562	blood:
39	chr16:47189381..47191014-chr16:47191815..47193762,2	K562	blood:
40	chr16:47521997..47524877-chr16:47525537..47527944,2	K562	blood:
41	chr16:47689743..47692961-chr16:47700339..47703493,3	K562	blood:
42	chr16:47416227..47418087-chr16:47500282..47502102,2	K562	blood:
43	chr16:47481523..47483741-chr16:47529384..47531603,2	K562	blood:
44	chr16:47538608..47539232-chr19:24184323..24185236,2	MCF-7	breast:
45	chr16:47352976..47355256-chr16:47362064..47365437,3	K562	blood:
46	chr16:47284043..47286034-chr16:47297265..47300260,2	K562	blood:
47	chr16:47001442..47003182-chr16:47662025..47664778,2	K562	blood:
48	chr16:47620363..47622593-chr16:47623592..47625913,2	K562	blood:
49	chr16:47174790..47177797-chr16:47493413..47496816,5	K562	blood:
50	chr16:47497354..47500127-chr16:47526363..47529187,2	K562	blood:

(count:26 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ITFG1-1	chr16:47595218-47596391	NONHSAT142300
2	lnc-GPT2-3	chr16:47177999-47178405	NONHSAT142282
3	lnc-GPT2-11	chr16:47213203-47213513	l_1316_chr16:47211651-47213507_testes
4	lnc-GPT2-3	chr16:47195460-47195501	NONHSAT142282
5	lnc-GPT2-3	chr16:47191466-47191515	NONHSAT142282
6	lnc-PHKB-3	chr16:47235986-47236340	ENSG00000260744.1
7	lnc-GPT2-3	chr16:47216667-47217006	NONHSAT142282
8	lnc-GPT2-3	chr16:47187543-47187707	NONHSAT142282
9	lnc-PHKB-1	chr16:47333358-47333859	ENSG00000261369.1
10	lnc-GPT2-10	chr16:47185464-47185705	NONHSAT142284
11	lnc-GPT2-4	chr16:47563101-47563152	NONHSAT142298
12	lnc-GPT2-4	chr16:47563387-47563827	ENSG00000262038.1
13	lnc-GPT2-12	chr16:47495240-47495337	NONHSAT142295
14	lnc-LONP2-12	chr16:47652232-47652439	uc_396_+
15	lnc-NETO2-2	chr16:47296678-47296925	NONHSAT142288
16	lnc-ITFG1-3	chr16:47652232-47652439	uc_396_-
17	lnc-NETO2-2	chr16:47294571-47294606	NONHSAT142288
18	lnc-GPT2-12	chr16:47497009-47497433	NONHSAT142295
19	lnc-PHKB-3	chr16:47230222-47230630	ENSG00000260744.1
20	lnc-PHKB-1	chr16:47351460-47351725	ENSG00000261369.1
21	lnc-NETO2-3	chr16:47310408-47311851	NONHSAT142289
22	lnc-GPT2-4	chr16:47563101-47563152	ENSG00000262038.1
23	lnc-GPT2-11	chr16:47211652-47211793	l_1316_chr16:47211651-47213507_testes
24	lnc-PHKB-1	chr16:47346550-47346651	ENSG00000261369.1
25	lnc-ITFG1-2	chr16:47632565-47632907	NONHSAT142302
26	lnc-GPT2-4	chr16:47563386-47563827	NONHSAT142298

No data

(count:6 , 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	ITFG1	hsa-miR-23b-3p	chr16:47189629-47189649
4	ITFG1	hsa-miR-23b-3p	chr16:47484216-47484236
5	NETO2	hsa-miR-20a-5p	chr16:47116059-47116081
6	NETO2	hsa-miR-21-5p	chr16:47115813-47115831

Variant related genes	Relation type
NETO2	TF binding region
EIF4BP5	TF binding region
RNA5SP424	TF binding region
RPL23AP72	TF binding region
ITFG1	TF binding region
ENSG00000262038	TF binding region
ENSG00000261369	TF binding region
ENSG00000260281	TF binding region
NDUFA5P11	TF binding region
ENSG00000259866	TF binding region
ENSG00000238834	TF binding region
ENSG00000222767	TF binding region
PHKB	TF binding region
ENSG00000260012	TF binding region
RNA5SP425	TF binding region
ENSG00000260744	TF binding region
NETO2	CpG island
EIF4BP5	CpG island
RNA5SP424	CpG island
RPL23AP72	CpG island
ITFG1	CpG island
ENSG00000262038	CpG island
ENSG00000261369	CpG island
ENSG00000260281	CpG island
NDUFA5P11	CpG island
ENSG00000259866	CpG island
ENSG00000238834	CpG island
ENSG00000222767	CpG island
PHKB	CpG island
ENSG00000260012	CpG island
RNA5SP425	CpG island
ENSG00000260744	CpG island
ENSG00000261336	chromatin interactions
ENSG00000102893	chromatin interactions
ENSG00000129636	chromatin interactions
ENSG00000222268	chromatin interactions
ENSG00000261173	chromatin interactions
ENSG00000121270	chromatin interactions
ENSG00000238834	chromatin interactions
ENSG00000260281	chromatin interactions
ENSG00000140798	chromatin interactions
ENSG00000104613	chromatin interactions
ENSG00000162664	chromatin interactions
ENSG00000239840	chromatin interactions
ENSG00000230679	chromatin interactions
ENSG00000177628	chromatin interactions
ENSG00000074800	chromatin interactions
ENSG00000212290	chromatin interactions
ENSG00000115875	chromatin interactions
ENSG00000069345	chromatin interactions
ENSG00000133703	chromatin interactions
ENSG00000152147	chromatin interactions
ENSG00000259866	chromatin interactions
ENSG00000259918	chromatin interactions
ENSG00000171208	chromatin interactions

Extended variants
information (count: 19849 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:19849 , 50 per page) page: 1 2 3 4 5 6 7 ... 397

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9646368	chr16:47111119-47111120	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs78330341	chr16:47111143-47111144	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs76481020	chr16:47111144-47111145	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs543132952	chr16:47111156-47111157	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs561299597	chr16:47111199-47111200	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs192589672	chr16:47111200-47111201	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs372965887	chr16:47111237-47111238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs75720109	chr16:47111256-47111257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs62059137	chr16:47111258-47111259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs546599644	chr16:47111273-47111274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs571484400	chr16:47111282-47111283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs570990566	chr16:47111318-47111319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs532216168	chr16:47111394-47111395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs368971201	chr16:47111406-47111407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs373168259	chr16:47111410-47111411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs376428223	chr16:47111411-47111412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs370814631	chr16:47111417-47111418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs184405376	chr16:47111421-47111422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs374184838	chr16:47111423-47111424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs376239676	chr16:47111425-47111426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs370887958	chr16:47111428-47111429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs535975179	chr16:47111432-47111433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs374522341	chr16:47111433-47111434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs368945473	chr16:47111434-47111435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs189078065	chr16:47111523-47111524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs114320949	chr16:47111525-47111526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs561964919	chr16:47111552-47111553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs111449096	chr16:47111597-47111598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs144686620	chr16:47111601-47111602	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs207475879	chr16:47111604-47111605	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs533508518	chr16:47111638-47111639	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs11247545	chr16:47111692-47111693	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs149969146	chr16:47111731-47111732	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs138557181	chr16:47111788-47111789	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs569491246	chr16:47111794-47111795	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs545377452	chr16:47111801-47111802	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs530393676	chr16:47111804-47111805	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs141630418	chr16:47111815-47111816	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs557574738	chr16:47111855-47111856	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs575892984	chr16:47111909-47111910	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs184707482	chr16:47111911-47111912	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs564581947	chr16:47111929-47111930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs561341943	chr16:47111931-47111932	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs528770931	chr16:47111940-47111941	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs540580463	chr16:47111950-47111951	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs377626816	chr16:47111985-47111986	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs565037482	chr16:47112016-47112017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs189981679	chr16:47112042-47112043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs180773789	chr16:47112052-47112053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs568616570	chr16:47112117-47112118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:11457 , 50 per page) page: 1 2 3 4 5 6 7 ... 230

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	chr16:47108200-47113800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr16:47108200-47114000	Weak transcription	Fetal Brain Female	brain
6	chr16:47108200-47116600	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr16:47108200-47116800	Weak transcription	GM12878-XiMat	blood
8	chr16:47108200-47130000	Weak transcription	Brain Germinal Matrix	brain
9	chr16:47108600-47112400	Weak transcription	Fetal Brain Male	brain
10	chr16:47110400-47111200	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr16:47110800-47111600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr16:47110800-47113600	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr16:47110800-47122200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr16:47110800-47158000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr16:47111000-47113600	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr16:47111000-47131000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr16:47111200-47113600	Weak transcription	HUES64 Cell Line	embryonic stem cell
18	chr16:47111200-47113600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chr16:47111600-47111800	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr16:47111600-47111800	Enhancers	Primary hematopoietic stem cells	blood
21	chr16:47111800-47112000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr16:47111800-47112000	Enhancers	Esophagus	oesophagus
23	chr16:47111800-47112000	Enhancers	Spleen	Spleen
24	chr16:47111800-47113600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr16:47112000-47132000	Weak transcription	Esophagus	oesophagus
26	chr16:47112000-47144800	Weak transcription	Spleen	Spleen
27	chr16:47112400-47113200	Enhancers	Fetal Brain Male	brain
28	chr16:47112600-47114600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr16:47112600-47116600	Weak transcription	Monocytes-CD14+_RO01746	blood
30	chr16:47112800-47115000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr16:47112800-47115400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr16:47113200-47113600	Weak transcription	Fetal Brain Male	brain
33	chr16:47113200-47115600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr16:47113200-47142200	Weak transcription	Hela-S3	cervix
35	chr16:47113400-47141000	Weak transcription	NH-A	brain
36	chr16:47113600-47113800	Enhancers	H1 Cell Line	embryonic stem cell
37	chr16:47113600-47113800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
38	chr16:47113600-47114000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
39	chr16:47113600-47114000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
40	chr16:47113600-47114200	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr16:47113600-47114800	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr16:47113600-47114800	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr16:47113600-47115000	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr16:47113600-47115000	Enhancers	Fetal Brain Male	brain
45	chr16:47113600-47116800	Weak transcription	NHEK	skin
46	chr16:47113600-47116800	Weak transcription	NHLF	lung
47	chr16:47113800-47114000	Active TSS	iPS-20b Cell Line	embryonic stem cell
48	chr16:47113800-47114200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr16:47113800-47114400	Weak transcription	H1 Cell Line	embryonic stem cell
50	chr16:47114000-47114400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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