Variant report

Variant	nsv572537
Chromosome Location	chr16:47411203-47599502
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2091)
CpG islands
(count:1099)
Chromatin interactive
region (count:144)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:2091 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:47428252-47428453	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:47494825-47496228	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:47507313-47507485	HepG2	liver:	n/a	n/a
4	ARID3A	chr16:47507738-47508382	HepG2	liver:	n/a	n/a
5	ARID3A	chr16:47499795-47500033	K562	blood:	n/a	n/a
6	ARID3A	chr16:47421094-47421294	HepG2	liver:	n/a	n/a
7	ARID3A	chr16:47526802-47527555	K562	blood:	n/a	n/a
8	ARID3A	chr16:47500293-47502483	K562	blood:	n/a	n/a
9	ARID3A	chr16:47556945-47557537	HepG2	liver:	n/a	n/a
10	ARID3A	chr16:47498536-47498645	K562	blood:	n/a	n/a
11	ARID3A	chr16:47426038-47426363	K562	blood:	n/a	n/a
12	ARID3A	chr16:47484519-47484647	HepG2	liver:	n/a	n/a
13	ARID3A	chr16:47509336-47510111	HepG2	liver:	n/a	n/a
14	ARID3A	chr16:47554148-47554743	K562	blood:	n/a	n/a
15	ARID3A	chr16:47572269-47572803	HepG2	liver:	n/a	n/a
16	ARID3A	chr16:47538556-47538932	K562	blood:	n/a	n/a
17	ARID3A	chr16:47495283-47496261	K562	blood:	n/a	n/a
18	ARID3A	chr16:47526816-47527197	HepG2	liver:	n/a	n/a
19	ARID3A	chr16:47482890-47483076	K562	blood:	n/a	n/a
20	ARID3A	chr16:47533067-47533932	HepG2	liver:	n/a	n/a
21	ARID3A	chr16:47519386-47519410	HepG2	liver:	n/a	n/a
22	ARID3A	chr16:47431618-47431623	HepG2	liver:	n/a	n/a
23	ARID3A	chr16:47524403-47524722	K562	blood:	n/a	n/a
24	ATF1	chr16:47495611-47496214	K562	blood:	n/a	n/a
25	ATF1	chr16:47422668-47422993	K562	blood:	n/a	n/a
26	ATF1	chr16:47554214-47554593	K562	blood:	n/a	n/a
27	ATF1	chr16:47599472-47599607	K562	blood:	n/a	n/a
28	ATF1	chr16:47526819-47527180	K562	blood:	n/a	n/a
29	ATF1	chr16:47501985-47502361	K562	blood:	n/a	n/a
30	ATF1	chr16:47427309-47427338	K562	blood:	n/a	n/a
31	ATF1	chr16:47426003-47426482	K562	blood:	n/a	n/a
32	ATF2	chr16:47557169-47557724	GM12878	blood:	n/a	n/a
33	ATF2	chr16:47526273-47527368	GM12878	blood:	n/a	n/a
34	ATF3	chr16:47494801-47495349	K562	blood:	n/a	n/a
35	ATF3	chr16:47501997-47502334	K562	blood:	n/a	n/a
36	ATF3	chr16:47494617-47495423	HepG2	liver:	n/a	n/a
37	ATF3	chr16:47494735-47495286	K562	blood:	n/a	n/a
38	ATF3	chr16:47494770-47495381	GM12878	blood:	n/a	n/a
39	ATF3	chr16:47494755-47495369	HepG2	liver:	n/a	n/a
40	ATF3	chr16:47494783-47495259	H1-hESC	embryonic stem cell:	n/a	n/a
41	ATF3	chr16:47494797-47495311	H1-hESC	embryonic stem cell:	n/a	n/a
42	ATF3	chr16:47494883-47495224	GM12878	blood:	n/a	n/a
43	BACH1	chr16:47495280-47495285	K562	blood:	n/a	n/a
44	BACH1	chr16:47502056-47502356	H1-hESC	embryonic stem cell:	n/a	n/a
45	BACH1	chr16:47502025-47502424	K562	blood:	n/a	n/a
46	BACH1	chr16:47538552-47539389	K562	blood:	n/a	n/a
47	BACH1	chr16:47495724-47496205	K562	blood:	n/a	n/a
48	BACH1	chr16:47495881-47496208	H1-hESC	embryonic stem cell:	n/a	n/a
49	BATF	chr16:47426120-47426365	GM12878	blood:	n/a	n/a
50	BATF	chr16:47578156-47578439	GM12878	blood:	n/a	chr16:47578328-47578339

(count:1099 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:47495768-47495818	HRE	kidney:	n/a
2	chr16:47495768-47495818	HRE	kidney:	n/a
3	chr16:47495110-47495160	MCF10A-Er-Src	breast:	n/a
4	chr16:47495113-47495163	HCF	heart:	n/a
5	chr16:47495113-47495163	RPTEC	kidney:	n/a
6	chr16:47494824-47494874	AG04450	lung:	fetal
7	chr16:47494735-47494785	U87	brain:	n/a
8	chr16:47495113-47495163	GM19239	blood:	n/a
9	chr16:47588660-47588710	MCF-7	breast:	n/a
10	chr16:47494824-47494874	HL-60	blood:	n/a
11	chr16:47497822-47497872	PANC-1	pancreas:	n/a
12	chr16:47494735-47494785	A549	lung:	n/a
13	chr16:47495113-47495163	AG04450	lung:	fetal
14	chr16:47527034-47527084	HEEpiC	esophagus:	n/a
15	chr16:47539137-47539187	NT2-D1	testis:	n/a
16	chr16:47495768-47495818	LNCaP	prostate:	n/a
17	chr16:47497822-47497872	HCM	heart:	n/a
18	chr16:47495445-47495495	HRCEpiC	kidney:	n/a
19	chr16:47494711-47494761	AG09309	skin:	n/a
20	chr16:47420506-47420556	AG10803	skin:	n/a
21	chr16:47588660-47588710	NHBE	bronchial:	n/a
22	chr16:47494711-47494761	ProgFib	skin:	n/a
23	chr16:47527034-47527084	SK-N-MC	brain:	n/a
24	chr16:47494735-47494785	HCT-116	colon:	n/a
25	chr16:47588660-47588710	GM19239	blood:	n/a
26	chr16:47495113-47495163	HUVEC	blood vessel:	n/a
27	chr16:47495746-47495796	K562	blood:	n/a
28	chr16:47495541-47495591	A549	lung:	n/a
29	chr16:47494824-47494874	AoSMC	blood vessel:	n/a
30	chr16:47539137-47539187	HCPEpiC	choroid plexus:	n/a
31	chr16:47495445-47495495	PrEC	prostate:	n/a
32	chr16:47495541-47495591	GM12892	blood:	n/a
33	chr16:47539203-47539253	MCF10A-Er-Src	breast:	n/a
34	chr16:47527034-47527084	PrEC	prostate:	n/a
35	chr16:47539166-47539216	NHDF-neo	bronchial:	n/a
36	chr16:47494824-47494874	PANC-1	pancreas:	n/a
37	chr16:47494258-47494308	HAEpiC	amniotic membrane:	n/a
38	chr16:47539203-47539253	MCF-7	breast:	n/a
39	chr16:47494735-47494785	AG04450	lung:	fetal
40	chr16:47497822-47497872	AG09319	gingival:	n/a
41	chr16:47539137-47539187	SAEC	small airway:	n/a
42	chr16:47494711-47494761	HCF	heart:	n/a
43	chr16:47495113-47495163	HAEpiC	amniotic membrane:	n/a
44	chr16:47494824-47494874	Caco-2	colon:	n/a
45	chr16:47494711-47494761	SK-N-SH_RA	brain:	n/a
46	chr16:47539137-47539187	HIPEpiC	eye:	n/a
47	chr16:47494711-47494761	HepG2	liver:	n/a
48	chr16:47495768-47495818	AG09319	gingival:	n/a
49	chr16:47495768-47495818	GM12891	blood:	n/a
50	chr16:47494735-47494785	ovcar-3	ovarian:	n/a

(count:144 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr16:47500342..47506721-chr16:47514207..47520673,8	K562	blood:
2	chr16:47414999..47416779-chr16:47426275..47428924,2	MCF-7	breast:
3	chr16:47505221..47508195-chr16:47519032..47520673,2	K562	blood:
4	chr16:47500040..47503767-chr16:47514818..47518136,4	K562	blood:
5	chr16:47514982..47517180-chr16:47517561..47520425,2	MCF-7	breast:
6	chr16:47541164..47545156-chr16:47546024..47549793,5	K562	blood:
7	chr16:47548754..47550733-chr16:47554531..47556036,2	MCF-7	breast:
8	chr16:47484770..47486422-chr16:47488487..47490664,2	K562	blood:
9	chr16:47431082..47433440-chr16:47448856..47451690,2	K562	blood:
10	chr16:47502099..47504584-chr16:47526951..47528627,3	K562	blood:
11	chr16:47439487..47441195-chr16:47493204..47494931,2	K562	blood:
12	chr1:192021477..192022058-chr16:47435294..47435896,2	MCF-7	breast:
13	chr16:47485624..47489187-chr16:47492609..47496944,6	K562	blood:
14	chr16:47481523..47483741-chr16:47529384..47531603,2	K562	blood:
15	chr16:47484770..47486422-chr16:47488487..47490664,2	K562	blood:
16	chr16:47431082..47433440-chr16:47448856..47451690,2	K562	blood:
17	chr16:47493905..47495976-chr16:47496733..47498612,2	MCF-7	breast:
18	chr16:47165353..47167030-chr16:47501273..47503652,2	K562	blood:
19	chr16:47494278..47496656-chr16:47499941..47502861,2	MCF-7	breast:
20	chr16:47486141..47491798-chr16:47493044..47496709,8	MCF-7	breast:
21	chr16:47500719..47503610-chr16:47510639..47513571,4	K562	blood:
22	chr16:47517170..47520211-chr16:47526974..47528925,3	K562	blood:
23	chr16:47506877..47508386-chr16:47511006..47513909,2	K562	blood:
24	chr16:47493908..47496119-chr16:47525530..47527640,2	K562	blood:
25	chr16:47495762..47498105-chr16:47514546..47516108,2	K562	blood:
26	chr1:155214276..155214874-chr16:47494461..47494978,2	Hela-S3	cervix:
27	chr16:47410478..47412557-chr16:47418181..47419832,2	K562	blood:
28	chr16:47432128..47434331-chr16:47440523..47442173,2	K562	blood:
29	chr16:47512020..47514843-chr16:47517675..47520024,2	K562	blood:
30	chr16:47426138..47427741-chr16:47428449..47430981,2	K562	blood:
31	chr16:47547375..47549482-chr16:47556202..47558891,2	K562	blood:
32	chr16:47493905..47495976-chr16:47496733..47498612,2	MCF-7	breast:
33	chr16:47538624..47539255-chr19:24184251..24185320,3	MCF-7	breast:
34	chr16:47538608..47539209-chr19:24184105..24184774,2	MCF-7	breast:
35	chr16:47516457..47520432-chr16:47524851..47526977,4	K562	blood:
36	chr16:47521997..47524877-chr16:47525537..47527944,2	K562	blood:
37	chr16:47503725..47506287-chr16:47510577..47512512,2	K562	blood:
38	chr16:47547375..47549482-chr16:47556202..47558891,2	K562	blood:
39	chr16:47506877..47508389-chr16:47511649..47513909,2	K562	blood:
40	chr16:47530496..47533304-chr16:47537314..47539255,2	K562	blood:
41	chr16:47410478..47412557-chr16:47418181..47419832,2	K562	blood:
42	chr16:47493122..47496299-chr16:47497105..47499562,3	MCF-7	breast:
43	chr16:47497354..47500127-chr16:47526363..47529187,2	K562	blood:
44	chr16:47493122..47496299-chr16:47497105..47499562,3	MCF-7	breast:
45	chr16:47530496..47533304-chr16:47537314..47539255,2	K562	blood:
46	chr16:47315203..47316940-chr16:47529898..47531487,2	K562	blood:
47	chr16:47404244..47406062-chr16:47411179..47413433,2	K562	blood:
48	chr16:47504741..47507121-chr16:47699160..47701122,2	K562	blood:
49	chr16:47494533..47496670-chr16:47528896..47531498,2	MCF-7	breast:
50	chr16:47502629..47504464-chr16:47550187..47553009,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPT2-12	chr16:47495240-47495337	NONHSAT142295
2	lnc-GPT2-4	chr16:47563387-47563827	ENSG00000262038.1
3	lnc-GPT2-12	chr16:47497009-47497433	NONHSAT142295
4	lnc-GPT2-4	chr16:47563386-47563827	NONHSAT142298
5	lnc-GPT2-4	chr16:47563101-47563152	ENSG00000262038.1
6	lnc-GPT2-4	chr16:47563101-47563152	NONHSAT142298
7	lnc-ITFG1-1	chr16:47595218-47596391	NONHSAT142300

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ITFG1	hsa-miR-23b-3p	chr16:47484216-47484236

Variant related genes	Relation type
RNA5SP424	TF binding region
ITFG1	TF binding region
ENSG00000262038	TF binding region
ENSG00000259866	TF binding region
PHKB	TF binding region
RNA5SP425	TF binding region
RNA5SP424	CpG island
ITFG1	CpG island
ENSG00000262038	CpG island
ENSG00000259866	CpG island
PHKB	CpG island
RNA5SP425	CpG island
ENSG00000260281	chromatin interactions
ENSG00000171208	chromatin interactions
ENSG00000133703	chromatin interactions
ENSG00000261336	chromatin interactions
ENSG00000222268	chromatin interactions
ENSG00000259918	chromatin interactions
ENSG00000102893	chromatin interactions
ENSG00000162664	chromatin interactions
ENSG00000177628	chromatin interactions
ENSG00000212290	chromatin interactions
ENSG00000259866	chromatin interactions
ENSG00000104613	chromatin interactions
ENSG00000129636	chromatin interactions

Extended variants
information (count: 6192 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:6192 , 50 per page) page: 1 2 3 4 5 6 7 ... 124

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13332786	chr16:47411203-47411204	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs547269436	chr16:47411204-47411205	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs190857273	chr16:47411242-47411243	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs149092627	chr16:47411261-47411262	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs182618733	chr16:47411279-47411280	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs375842225	chr16:47411280-47411281	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs186803388	chr16:47411319-47411320	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs369778253	chr16:47411330-47411331	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs75512431	chr16:47411334-47411335	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs374001148	chr16:47411350-47411351	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs566499720	chr16:47411395-47411396	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs143121951	chr16:47411403-47411404	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs190884170	chr16:47411417-47411418	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs577008250	chr16:47411464-47411465	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs183388573	chr16:47411476-47411477	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs556249435	chr16:47411556-47411557	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs148223654	chr16:47411583-47411584	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs187315000	chr16:47411607-47411608	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs560195040	chr16:47411719-47411720	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs141180109	chr16:47411737-47411738	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs115476985	chr16:47411747-47411748	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs569569848	chr16:47411760-47411761	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs112063065	chr16:47411833-47411834	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs147355553	chr16:47411856-47411857	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs74764402	chr16:47411875-47411876	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs564608328	chr16:47411900-47411901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs550881263	chr16:47411949-47411950	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs563066041	chr16:47412022-47412023	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs530158114	chr16:47412083-47412084	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs114505327	chr16:47412097-47412098	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs558430404	chr16:47412172-47412173	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs79932354	chr16:47412187-47412188	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs192934079	chr16:47412207-47412208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs552097962	chr16:47412228-47412229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs184693002	chr16:47412255-47412256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs538077298	chr16:47412285-47412286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs574946517	chr16:47412353-47412354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs113296823	chr16:47412355-47412356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs188014410	chr16:47412364-47412365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs74016205	chr16:47412392-47412393	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs192990676	chr16:47412418-47412419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs572120661	chr16:47412428-47412429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs137950203	chr16:47412448-47412449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs565606390	chr16:47412464-47412465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs376455189	chr16:47412477-47412478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs143417762	chr16:47412483-47412484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs544862468	chr16:47412559-47412560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs562942207	chr16:47412560-47412561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs147333676	chr16:47412581-47412582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs576950916	chr16:47412670-47412671	Weak transcription	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
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:4958 , 50 per page) page: 1 2 3 4 5 6 7 ... 100

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:47372000-47426200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr16:47379600-47432000	Weak transcription	Fetal Lung	lung
3	chr16:47382000-47426000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr16:47387800-47429800	Weak transcription	Right Ventricle	heart
5	chr16:47388600-47414800	Weak transcription	Brain Angular Gyrus	brain
6	chr16:47388600-47445000	Weak transcription	NHEK	skin
7	chr16:47388800-47429800	Weak transcription	Duodenum Mucosa	Duodenum
8	chr16:47389400-47425600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr16:47390000-47430000	Weak transcription	HSMMtube	muscle
10	chr16:47393000-47458200	Weak transcription	Pancreas	Pancrea
11	chr16:47393000-47459000	Weak transcription	NHDF-Ad	bronchial
12	chr16:47396200-47411400	Weak transcription	A549	lung
13	chr16:47396200-47414200	Weak transcription	Psoas Muscle	Psoas
14	chr16:47396200-47425800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
15	chr16:47397800-47458800	Weak transcription	Colonic Mucosa	Colon
16	chr16:47399000-47414800	Weak transcription	Spleen	Spleen
17	chr16:47399200-47420200	Weak transcription	Left Ventricle	heart
18	chr16:47399200-47421400	Weak transcription	K562	blood
19	chr16:47399200-47430000	Weak transcription	Rectal Mucosa Donor 31	rectum
20	chr16:47401000-47411400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
21	chr16:47404000-47432600	Weak transcription	Fetal Kidney	kidney
22	chr16:47404400-47458800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr16:47404600-47414400	Weak transcription	Esophagus	oesophagus
24	chr16:47404600-47428200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr16:47404800-47414400	Weak transcription	Brain Germinal Matrix	brain
26	chr16:47404800-47414400	Weak transcription	Fetal Stomach	stomach
27	chr16:47404800-47416400	Weak transcription	Gastric	stomach
28	chr16:47404800-47419600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr16:47404800-47420200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr16:47404800-47425800	Weak transcription	Primary hematopoietic stem cells	blood
31	chr16:47404800-47426000	Weak transcription	Placenta	Placenta
32	chr16:47404800-47426000	Weak transcription	Sigmoid Colon	Sigmoid Colon
33	chr16:47404800-47426000	Weak transcription	Thymus	Thymus
34	chr16:47404800-47444400	Weak transcription	Lung	lung
35	chr16:47404800-47444800	Weak transcription	Fetal Intestine Small	intestine
36	chr16:47404800-47458600	Weak transcription	Aorta	Aorta
37	chr16:47405000-47414400	Weak transcription	Fetal Brain Female	brain
38	chr16:47405000-47425600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
39	chr16:47405400-47413200	Weak transcription	Primary neutrophils fromperipheralblood	blood
40	chr16:47405400-47426200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
41	chr16:47405600-47413800	Weak transcription	Colon Smooth Muscle	Colon
42	chr16:47405600-47414200	Weak transcription	Liver	Liver
43	chr16:47405600-47458200	Weak transcription	Brain Anterior Caudate	brain
44	chr16:47405800-47420200	Weak transcription	Fetal Muscle Leg	muscle
45	chr16:47405800-47425600	Weak transcription	GM12878-XiMat	blood
46	chr16:47405800-47454000	Weak transcription	Rectal Mucosa Donor 29	rectum
47	chr16:47406200-47425600	Weak transcription	Stomach Mucosa	stomach
48	chr16:47407600-47411600	Strong transcription	Primary B cells from cord blood	blood
49	chr16:47407800-47429800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr16:47408000-47411600	Enhancers	Cortex derived primary cultured neurospheres	brain

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