Variant report

Variant	nsv974848
Chromosome Location	chr16:12005053-12020022
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:12009658-12010951	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:12008585-12008859	K562	blood:	n/a	n/a
3	ARID3A	chr16:12009977-12010322	K562	blood:	n/a	n/a
4	ATF1	chr16:12009714-12010168	K562	blood:	n/a	n/a
5	ATF2	chr16:12009771-12010305	GM12878	blood:	n/a	n/a
6	ATF2	chr16:12009671-12010205	GM12878	blood:	n/a	n/a
7	ATF3	chr16:12009662-12010144	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr16:12009828-12010230	HepG2	liver:	n/a	n/a
9	ATF3	chr16:12009819-12010191	K562	blood:	n/a	n/a
10	ATF3	chr16:12009886-12010165	GM12878	blood:	n/a	n/a
11	ATF3	chr16:12009863-12010791	A549	lung:	n/a	n/a
12	ATF3	chr16:12009602-12010039	A549	lung:	n/a	n/a
13	BACH1	chr16:12010242-12010754	H1-hESC	embryonic stem cell:	n/a	chr16:12010574-12010588
14	BACH1	chr16:12009695-12009830	K562	blood:	n/a	n/a
15	BACH1	chr16:12009120-12009416	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr16:12010279-12010878	K562	blood:	n/a	chr16:12010574-12010588
17	BACH1	chr16:12009639-12010027	H1-hESC	embryonic stem cell:	n/a	n/a
18	BCL3	chr16:12009698-12010335	A549	lung:	n/a	chr16:12009769-12009782 chr16:12009719-12009732 chr16:12010050-12010059 chr16:12009770-12009779 chr16:12009773-12009782 chr16:12009772-12009785
19	BCL3	chr16:12009498-12010377	A549	lung:	n/a	chr16:12009769-12009782 chr16:12009667-12009680 chr16:12009719-12009732 chr16:12010050-12010059 chr16:12009770-12009779 chr16:12009773-12009782 chr16:12009772-12009785
20	BCLAF1	chr16:12009551-12010336	GM12878	blood:	n/a	chr16:12009769-12009782 chr16:12009667-12009680 chr16:12009719-12009732 chr16:12010050-12010059 chr16:12009770-12009779 chr16:12009773-12009782 chr16:12009772-12009785
21	BCLAF1	chr16:12009547-12010311	GM12878	blood:	n/a	chr16:12009769-12009782 chr16:12009667-12009680 chr16:12009719-12009732 chr16:12010050-12010059 chr16:12009770-12009779 chr16:12009773-12009782 chr16:12009772-12009785
22	BCLAF1	chr16:12009482-12010321	K562	blood:	n/a	chr16:12009769-12009782 chr16:12009667-12009680 chr16:12009719-12009732 chr16:12010050-12010059 chr16:12009770-12009779 chr16:12009773-12009782 chr16:12009772-12009785
23	BCLAF1	chr16:12009704-12010225	K562	blood:	n/a	chr16:12009769-12009782 chr16:12009719-12009732 chr16:12010050-12010059 chr16:12009770-12009779 chr16:12009773-12009782 chr16:12009772-12009785
24	BCLAF1	chr16:12008629-12009154	GM12878	blood:	n/a	chr16:12008962-12008975 chr16:12008898-12008907 chr16:12008972-12008981
25	BHLHE40	chr16:12008235-12009393	K562	blood:	n/a	n/a
26	BHLHE40	chr16:12007501-12009376	GM12878	blood:	n/a	n/a
27	BHLHE40	chr16:12009616-12010643	HepG2	liver:	n/a	chr16:12009769-12009785 chr16:12009772-12009788 chr16:12009719-12009735
28	BHLHE40	chr16:12009628-12010657	K562	blood:	n/a	chr16:12009769-12009785 chr16:12009772-12009788 chr16:12009719-12009735
29	BHLHE40	chr16:12008926-12009352	HepG2	liver:	n/a	n/a
30	BHLHE40	chr16:12009619-12010324	GM12878	blood:	n/a	chr16:12009769-12009785 chr16:12009772-12009788 chr16:12009719-12009735
31	BRCA1	chr16:12009695-12010539	HepG2	liver:	n/a	n/a
32	BRCA1	chr16:12009741-12010897	Hela-S3	cervix:	n/a	n/a
33	CBX3	chr16:12009614-12010892	K562	blood:	n/a	n/a
34	CCNT2	chr16:12008509-12010285	K562	blood:	n/a	chr16:12009857-12009866
35	CEBPB	chr16:12009911-12010228	HepG2	liver:	n/a	n/a
36	CEBPB	chr16:12005065-12005248	A549	lung:	n/a	chr16:12005197-12005208
37	CEBPB	chr16:12014945-12015096	A549	lung:	n/a	chr16:12014987-12014998
38	CEBPB	chr16:12009656-12010954	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr16:12009861-12010072	K562	blood:	n/a	n/a
40	CEBPB	chr16:12014960-12015012	HepG2	liver:	n/a	chr16:12014987-12014998
41	CEBPB	chr16:12009979-12010282	HepG2	liver:	n/a	n/a
42	CEBPB	chr16:12009680-12010283	HepG2	liver:	n/a	n/a
43	CEBPB	chr16:12009742-12010110	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr16:12005093-12005275	HepG2	liver:	n/a	chr16:12005197-12005208
45	CEBPB	chr16:12005040-12005314	K562	blood:	n/a	chr16:12005197-12005208
46	CEBPB	chr16:12005042-12005303	IMR90	lung:	n/a	chr16:12005197-12005208
47	CEBPB	chr16:12014912-12015127	K562	blood:	n/a	chr16:12014987-12014998
48	CEBPB	chr16:12010512-12010824	MCF-7	breast:	n/a	n/a
49	CEBPB	chr16:12014976-12015000	IMR90	lung:	n/a	chr16:12014987-12014998
50	CEBPD	chr16:12009444-12010289	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:12009989-12010039	MCF10A-Er-Src	breast:	n/a
2	chr16:12010052-12010102	HEEpiC	esophagus:	n/a
3	chr16:12005841-12005891	GM06990	blood:	n/a
4	chr16:12010698-12010748	HCPEpiC	choroid plexus:	n/a
5	chr16:12009839-12009889	SK-N-MC	brain:	n/a
6	chr16:12005841-12005891	LNCaP	prostate:	n/a
7	chr16:12005841-12005891	AG09309	skin:	n/a
8	chr16:12009983-12010033	NB4	blood:	n/a
9	chr16:12009405-12009455	AoSMC	blood vessel:	n/a
10	chr16:12012117-12012167	HRCEpiC	kidney:	n/a
11	chr16:12009378-12009428	NHBE	bronchial:	n/a
12	chr16:12009839-12009889	HAEpiC	amniotic membrane:	n/a
13	chr16:12010179-12010229	SKMC	muscle:	n/a
14	chr16:12009839-12009889	GM12891	blood:	n/a
15	chr16:12010179-12010229	GM12878	blood:	n/a
16	chr16:12010179-12010229	HCF	heart:	n/a
17	chr16:12011342-12011392	SKMC	muscle:	n/a
18	chr16:12009378-12009428	SK-N-MC	brain:	n/a
19	chr16:12009842-12009892	HIPEpiC	eye:	n/a
20	chr16:12009989-12010039	SK-N-SH	brain:	n/a
21	chr16:12005841-12005891	HMEC	breast:	n/a
22	chr16:12011342-12011392	HRCEpiC	kidney:	n/a
23	chr16:12009842-12009892	HCT-116	colon:	n/a
24	chr16:12009700-12009750	HL-60	blood:	n/a
25	chr16:12010698-12010748	HepG2	liver:	n/a
26	chr16:12009839-12009889	LNCaP	prostate:	n/a
27	chr16:12010698-12010748	NB4	blood:	n/a
28	chr16:12012117-12012167	AG09319	gingival:	n/a
29	chr16:12009989-12010039	HCM	heart:	n/a
30	chr16:12011342-12011392	AG04449	skin:	fetal
31	chr16:12010052-12010102	RPTEC	kidney:	n/a
32	chr16:12009842-12009892	U87	brain:	n/a
33	chr16:12010052-12010102	HRE	kidney:	n/a
34	chr16:12009378-12009428	Hela-S3	cervix:	n/a
35	chr16:12009842-12009892	HCM	heart:	n/a
36	chr16:12009700-12009750	HepG2	liver:	n/a
37	chr16:12009842-12009892	GM19239	blood:	n/a
38	chr16:12009700-12009750	BJ	skin:	n/a
39	chr16:12009378-12009428	ovcar-3	ovarian:	n/a
40	chr16:12009839-12009889	HNPCEpiC	eye:	n/a
41	chr16:12009700-12009750	AG09309	skin:	n/a
42	chr16:12011342-12011392	GM06990	blood:	n/a
43	chr16:12012117-12012167	HEEpiC	esophagus:	n/a
44	chr16:12009839-12009889	HepG2	liver:	n/a
45	chr16:12012117-12012167	A549	lung:	n/a
46	chr16:12009842-12009892	NT2-D1	testis:	n/a
47	chr16:12009842-12009892	MCF-7	breast:	n/a
48	chr16:12010179-12010229	K562	blood:	n/a
49	chr16:12012117-12012167	SK-N-SH_RA	brain:	n/a
50	chr16:12012117-12012167	HepG2	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr16:12008410..12010246-chr16:15742278..15744306,2	MCF-7	breast:
2	chr16:11835219..11836957-chr16:12010044..12011553,2	MCF-7	breast:
3	chr16:12007765..12009301-chr16:12009316..12010905,2	MCF-7	breast:
4	chr16:11889469..11891900-chr16:12008639..12011975,4	MCF-7	breast:
5	chr16:12007765..12009301-chr16:12009316..12010905,2	MCF-7	breast:
6	chr16:10710065..10712953-chr16:12010240..12012086,2	MCF-7	breast:
7	chr16:11836330..11838361-chr16:12008535..12010129,2	MCF-7	breast:
8	chr16:11988100..11996073-chr16:12007143..12011577,10	MCF-7	breast:
9	chr10:101379675..101380180-chr16:12009652..12010648,2	Hela-S3	cervix:
10	chr16:12009392..12009947-chr19:48866680..48867321,2	NB4	blood:
11	chr16:12010326..12012796-chr16:12069017..12071833,3	MCF-7	breast:
12	chr16:11943912..11945965-chr16:12008319..12011491,4	MCF-7	breast:
13	chr16:12008162..12010269-chr16:12142729..12146819,3	K562	blood:
14	chr16:12010691..12013114-chr16:12155698..12158691,2	MCF-7	breast:
15	chr16:12007951..12010484-chr17:59476175..59479111,2	MCF-7	breast:
16	chr16:11835593..11837984-chr16:12009045..12011349,2	K562	blood:
17	chr16:12007711..12010113-chr16:12069770..12071913,2	MCF-7	breast:
18	chr16:12008899..12009895-chr19:48825023..48825708,2	Hela-S3	cervix:
19	chr16:11831944..11836692-chr16:12007199..12011492,4	K562	blood:
20	chr16:12012124..12014555-chr16:12045355..12047902,2	K562	blood:
21	chr16:11886565..11889362-chr16:12006902..12008695,2	K562	blood:
22	chr16:12006809..12011472-chr16:12069677..12072698,7	MCF-7	breast:
23	chr16:12009346..12010195-chr2:201676259..201676837,2	Hela-S3	cervix:
24	chr16:12008780..12010777-chr16:12013125..12015097,2	MCF-7	breast:
25	chr16:11941713..11946689-chr16:12006948..12011249,6	MCF-7	breast:
26	chr16:12008911..12011067-chr16:12016765..12018435,3	MCF-7	breast:
27	chr16:12010494..12013016-chr16:12016316..12019639,3	MCF-7	breast:
28	chr16:11942158..11945019-chr16:12007276..12009748,2	K562	blood:
29	chr16:12006532..12011371-chr16:12068460..12073371,6	K562	blood:
30	chr16:12008413..12010461-chr16:12056035..12059014,2	MCF-7	breast:
31	chr16:11439089..11440838-chr16:12008767..12010529,2	K562	blood:
32	chr16:11944315..11946480-chr16:12008232..12011350,3	K562	blood:
33	chr10:124133719..124134527-chr16:12008397..12008926,2	Hela-S3	cervix:
34	chr16:11988764..11995180-chr16:12006980..12012068,9	MCF-7	breast:
35	chr16:12010494..12013016-chr16:12016316..12019639,3	MCF-7	breast:
36	chr16:11982694..11985676-chr16:12003356..12006033,2	MCF-7	breast:

Variant related genes	Relation type
GSPT1	TF binding region
ENSG00000266163	TF binding region
GSPT1	CpG island
ENSG00000266163	CpG island
ENSG00000260488	chromatin interactions
ENSG00000263307	chromatin interactions
ENSG00000234719	chromatin interactions
ENSG00000262420	chromatin interactions
ENSG00000048471	chromatin interactions
ENSG00000121068	chromatin interactions
ENSG00000103342	chromatin interactions
ENSG00000267131	chromatin interactions
ENSG00000082153	chromatin interactions
ENSG00000153066	chromatin interactions
ENSG00000175643	chromatin interactions
ENSG00000155287	chromatin interactions
ENSG00000105479	chromatin interactions
ENSG00000266163	chromatin interactions
ENSG00000171490	chromatin interactions
ENSG00000161558	chromatin interactions
ENSG00000122299	chromatin interactions
ENSG00000072864	chromatin interactions
ENSG00000267280	chromatin interactions
ENSG00000048462	chromatin interactions
ENSG00000107679	chromatin interactions

Extended variants
information (count: 601 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:601 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs74784226	chr16:12005075-12005076	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs77754836	chr16:12005192-12005193	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs560348197	chr16:12005241-12005242	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs182518183	chr16:12005267-12005268	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs539188613	chr16:12005272-12005273	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs73511694	chr16:12005287-12005288	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs386789057	chr16:12005305-12005306	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs75017203	chr16:12005306-12005307	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs548587387	chr16:12005359-12005360	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs367982197	chr16:12005363-12005364	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs13337465	chr16:12005364-12005365	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs151143658	chr16:12005408-12005409	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs540446851	chr16:12005409-12005410	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs78514565	chr16:12005410-12005411	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs533527587	chr16:12005463-12005464	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs559186323	chr16:12005479-12005480	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs553745672	chr16:12005515-12005516	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs187112157	chr16:12005524-12005525	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs371113649	chr16:12005541-12005542	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs189666374	chr16:12005554-12005555	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs555881034	chr16:12005555-12005556	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs575815390	chr16:12005606-12005607	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs73511695	chr16:12005610-12005611	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs200206036	chr16:12005611-12005612	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs182102247	chr16:12005618-12005619	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs561267677	chr16:12005642-12005643	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs143463069	chr16:12005652-12005653	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs540219405	chr16:12005660-12005661	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs575957089	chr16:12005684-12005685	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs190461	chr16:12005745-12005746	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs150512749	chr16:12005794-12005795	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs546313160	chr16:12005816-12005817	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs62038799	chr16:12005901-12005902	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs371293585	chr16:12005903-12005904	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs566455379	chr16:12005904-12005905	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs377722411	chr16:12005931-12005932	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs373159176	chr16:12005933-12005934	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs371482669	chr16:12005934-12005935	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs138357316	chr16:12005943-12005944	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs531921435	chr16:12005949-12005950	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs33624	chr16:12005971-12005972	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs144583034	chr16:12006024-12006025	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs376746079	chr16:12006025-12006026	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs552069132	chr16:12006040-12006041	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs368356748	chr16:12006053-12006054	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs527998192	chr16:12006064-12006065	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs139342312	chr16:12006066-12006067	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs574291480	chr16:12006098-12006099	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs60307457	chr16:12006104-12006105	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs539080389	chr16:12006151-12006152	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	17603634	CNVD
Hodgkin''s lymphoma	20651079	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	16608533	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Autism	22566537	CNVD
Intellectual disability	22566537	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
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
Lung cancer	18438408	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21858162	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22102821	CNVD
Autism	22495311	CNVD
idiopathic generalized epilepsy	19843651	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Intellectual disability	22102821	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Myelofibrosis	22110671	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Prostate cancer	18632612	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Lujan-Fryns syndrom	21521776	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	20553308	CNVD
Autism	19786961	CNVD
Mental retardation	19786961	CNVD
Schizophrenia	19786961	CNVD
Mental retardation	19951919	CNVD
Autism	18791038	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Malignant germ cell tumour	17285132	CNVD
Autism	17480035	CNVD
Schizophrenia	19955444	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Melanoma	20877625	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:791 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:11966200-12006200	Weak transcription	Fetal Heart	heart
2	chr16:11977000-12007200	Weak transcription	Colonic Mucosa	Colon
3	chr16:11982000-12007400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr16:11984600-12006800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr16:11985000-12007000	Weak transcription	Primary neutrophils fromperipheralblood	blood
6	chr16:11987800-12007600	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr16:11987800-12008400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr16:11989800-12007200	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr16:11989800-12007400	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr16:11990000-12007400	Weak transcription	Lung	lung
11	chr16:11990600-12006600	Weak transcription	Brain Germinal Matrix	brain
12	chr16:11990800-12007000	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr16:11991000-12006800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr16:11991000-12007400	Weak transcription	Placenta	Placenta
15	chr16:11991400-12007000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr16:11991600-12006200	Weak transcription	Primary hematopoietic stem cells	blood
17	chr16:11992000-12007000	Weak transcription	Primary B cells from cord blood	blood
18	chr16:11992200-12007000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chr16:11996000-12006800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr16:11997200-12006800	Weak transcription	Spleen	Spleen
21	chr16:11997400-12006600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr16:11999800-12008000	Weak transcription	Fetal Muscle Trunk	muscle
23	chr16:12000000-12007400	Weak transcription	HSMMtube	muscle
24	chr16:12000400-12007400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr16:12000600-12006800	Weak transcription	Fetal Stomach	stomach
26	chr16:12000600-12007000	Weak transcription	HUES6 Cell Line	embryonic stem cell
27	chr16:12001400-12006600	Weak transcription	Monocytes-CD14+_RO01746	blood
28	chr16:12001600-12006200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr16:12001600-12006800	Weak transcription	HUES64 Cell Line	embryonic stem cell
30	chr16:12001800-12006200	Weak transcription	Thymus	Thymus
31	chr16:12001800-12007200	Weak transcription	Fetal Muscle Leg	muscle
32	chr16:12002000-12008200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr16:12002800-12005200	Enhancers	Adipose Nuclei	Adipose
34	chr16:12002800-12005400	Enhancers	Rectal Smooth Muscle	rectum
35	chr16:12002800-12007200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
36	chr16:12003000-12005200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
37	chr16:12003000-12007000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
38	chr16:12003000-12007200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
39	chr16:12003000-12007200	Enhancers	Primary T killer memory cells from peripheral blood	blood
40	chr16:12003200-12005200	Enhancers	Skeletal Muscle Male	skeletal muscle
41	chr16:12003200-12005200	Genic enhancers	Hela-S3	cervix
42	chr16:12003200-12005200	Genic enhancers	HepG2	liver
43	chr16:12003200-12006200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr16:12003200-12007200	Enhancers	Primary T helper naive cells from peripheral blood	blood
45	chr16:12003400-12006400	Enhancers	Primary T helper cells fromperipheralblood	blood
46	chr16:12003400-12006600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr16:12003800-12005200	Enhancers	Muscle Satellite Cultured Cells	--
48	chr16:12003800-12005400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr16:12003800-12005400	Enhancers	Stomach Smooth Muscle	stomach
50	chr16:12003800-12005600	Enhancers	Primary T cells from cord blood	blood

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