Variant report

Variant	nsv1035015
Chromosome Location	chr7:16144928-16273061
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:467)
CpG islands
(count:123)
Chromatin interactive
region (count:58)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:467 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:16249884-16249963	K562	blood:	n/a	n/a
2	ARID3A	chr7:16154325-16154591	K562	blood:	n/a	n/a
3	ARID3A	chr7:16169136-16169227	K562	blood:	n/a	n/a
4	ARID3A	chr7:16252388-16252536	K562	blood:	n/a	n/a
5	ATF1	chr7:16266719-16266733	K562	blood:	n/a	n/a
6	ATF1	chr7:16230945-16230986	K562	blood:	n/a	n/a
7	BACH1	chr7:16190493-16190510	K562	blood:	n/a	n/a
8	BACH1	chr7:16243269-16243380	K562	blood:	n/a	n/a
9	BHLHE40	chr7:16242216-16242218	K562	blood:	n/a	n/a
10	CBX3	chr7:16152690-16153053	K562	blood:	n/a	n/a
11	CBX3	chr7:16269828-16270194	K562	blood:	n/a	n/a
12	CBX3	chr7:16168849-16169768	HCT-116	colon:	n/a	n/a
13	CBX3	chr7:16240929-16241356	K562	blood:	n/a	n/a
14	CBX3	chr7:16146844-16147145	K562	blood:	n/a	n/a
15	CBX3	chr7:16184160-16184557	K562	blood:	n/a	n/a
16	CBX3	chr7:16146409-16147202	K562	blood:	n/a	n/a
17	CBX3	chr7:16146437-16146839	K562	blood:	n/a	n/a
18	CBX3	chr7:16146547-16146856	HCT-116	colon:	n/a	n/a
19	CBX3	chr7:16271850-16272277	K562	blood:	n/a	n/a
20	CBX3	chr7:16269898-16270150	K562	blood:	n/a	n/a
21	CCNT2	chr7:16254761-16254970	K562	blood:	n/a	n/a
22	CEBPB	chr7:16221312-16221339	K562	blood:	n/a	n/a
23	CEBPB	chr7:16246794-16247066	K562	blood:	n/a	n/a
24	CEBPB	chr7:16169034-16169377	IMR90	lung:	n/a	n/a
25	CEBPB	chr7:16229080-16229110	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr7:16220104-16220262	IMR90	lung:	n/a	n/a
27	CEBPB	chr7:16169142-16169366	A549	lung:	n/a	n/a
28	CEBPB	chr7:16246860-16247062	A549	lung:	n/a	n/a
29	CEBPB	chr7:16240258-16240479	IMR90	lung:	n/a	chr7:16240358-16240369 chr7:16240357-16240370
30	CEBPB	chr7:16216852-16216879	K562	blood:	n/a	n/a
31	CEBPB	chr7:16251244-16251545	K562	blood:	n/a	n/a
32	CEBPB	chr7:16234605-16234660	K562	blood:	n/a	chr7:16234630-16234641
33	CEBPB	chr7:16228989-16229268	IMR90	lung:	n/a	chr7:16229185-16229197
34	CEBPB	chr7:16216843-16216912	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr7:16251340-16251603	HepG2	liver:	n/a	n/a
36	CEBPB	chr7:16251298-16251575	K562	blood:	n/a	n/a
37	CEBPB	chr7:16169033-16169381	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr7:16234545-16234739	HepG2	liver:	n/a	chr7:16234630-16234641
39	CEBPB	chr7:16234751-16234761	IMR90	lung:	n/a	n/a
40	CEBPB	chr7:16240297-16240490	A549	lung:	n/a	chr7:16240358-16240369 chr7:16240357-16240370
41	CEBPB	chr7:16240270-16240516	HepG2	liver:	n/a	chr7:16240358-16240369 chr7:16240357-16240370
42	CEBPZ	chr7:16247712-16247786	HepG2	liver:	n/a	n/a
43	CTCF	chr7:16154340-16154490	HPAF	blood vessel:	n/a	n/a
44	CTCF	chr7:16154143-16154791	HCT-116	colon:	n/a	n/a
45	CTCF	chr7:16154286-16154581	ECC-1	luminal epithelium:	n/a	n/a
46	CTCF	chr7:16154360-16154510	AG04449	skin:	n/a	n/a
47	CTCF	chr7:16154420-16154570	NHDF-neo	bronchial:	n/a	n/a
48	CTCF	chr7:16154380-16154530	BE2_C	brain:	n/a	n/a
49	CTCF	chr7:16154332-16154515	MCF-7	breast:	n/a	n/a
50	CTCF	chr7:16154460-16154610	MCF-7	breast:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:16223374-16223424	PFSK-1	brain:	n/a
2	chr7:16223374-16223424	PFSK-1	brain:	n/a
3	chr7:16223374-16223424	HEK293	kidney:	embryo
4	chr7:16223374-16223424	HEEpiC	esophagus:	n/a
5	chr7:16254882-16254932	AG04449	skin:	fetal
6	chr7:16223374-16223424	NT2-D1	testis:	n/a
7	chr7:16254882-16254932	HNPCEpiC	eye:	n/a
8	chr7:16254882-16254932	HCF	heart:	n/a
9	chr7:16254882-16254932	CMK	blood:	n/a
10	chr7:16254882-16254932	LNCaP	prostate:	n/a
11	chr7:16223374-16223424	AG09309	skin:	n/a
12	chr7:16223374-16223424	HNPCEpiC	eye:	n/a
13	chr7:16254882-16254932	SK-N-SH	brain:	n/a
14	chr7:16254882-16254932	RPTEC	kidney:	n/a
15	chr7:16254882-16254932	ovcar-3	ovarian:	n/a
16	chr7:16254882-16254932	HRE	kidney:	n/a
17	chr7:16223374-16223424	Caco-2	colon:	n/a
18	chr7:16223374-16223424	HRCEpiC	kidney:	n/a
19	chr7:16254882-16254932	SKMC	muscle:	n/a
20	chr7:16223374-16223424	Hepatocyte	liver:	n/a
21	chr7:16254882-16254932	NHBE	bronchial:	n/a
22	chr7:16223374-16223424	HL-60	blood:	n/a
23	chr7:16254882-16254932	HIPEpiC	eye:	n/a
24	chr7:16223374-16223424	GM19239	blood:	n/a
25	chr7:16223374-16223424	T-47D	breast:	n/a
26	chr7:16223374-16223424	U87	brain:	n/a
27	chr7:16223374-16223424	PrEC	prostate:	n/a
28	chr7:16254882-16254932	Caco-2	colon:	n/a
29	chr7:16254882-16254932	HCPEpiC	choroid plexus:	n/a
30	chr7:16254882-16254932	GM06990	blood:	n/a
31	chr7:16223374-16223424	SAEC	small airway:	n/a
32	chr7:16223374-16223424	Hela-S3	cervix:	n/a
33	chr7:16254882-16254932	H1-hESC	embryonic stem cell:	embryo
34	chr7:16223374-16223424	SK-N-MC	brain:	n/a
35	chr7:16254882-16254932	HEK293	kidney:	embryo
36	chr7:16223374-16223424	SK-N-SH	brain:	n/a
37	chr7:16223374-16223424	MCF10A-Er-Src	breast:	n/a
38	chr7:16223374-16223424	HMEC	breast:	n/a
39	chr7:16223374-16223424	H1-hESC	embryonic stem cell:	embryo
40	chr7:16254882-16254932	T-47D	breast:	n/a
41	chr7:16223374-16223424	HRE	kidney:	n/a
42	chr7:16254882-16254932	HCT-116	colon:	n/a
43	chr7:16254882-16254932	Hepatocyte	liver:	n/a
44	chr7:16223374-16223424	AG10803	skin:	n/a
45	chr7:16254882-16254932	HEEpiC	esophagus:	n/a
46	chr7:16223374-16223424	HUVEC	blood vessel:	n/a
47	chr7:16254882-16254932	AG09309	skin:	n/a
48	chr7:16254882-16254932	Jurkat	blood:	n/a
49	chr7:16223374-16223424	ECC-1	luminal epithelium:	n/a
50	chr7:16223374-16223424	AG04449	skin:	fetal

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

No.	Distal block	Cell Line	Cell type
1	chr7:16226388..16229084-chr7:16230552..16232417,2	K562	blood:
2	chr7:16211386..16214233-chr7:16216618..16219049,2	MCF-7	breast:
3	chr7:16153945..16154474-chr7:16460404..16460914,2	MCF-7	breast:
4	chr7:16262958..16265861-chr7:16270760..16273242,2	K562	blood:
5	chr7:16174593..16177204-chr7:16180297..16182169,2	K562	blood:
6	chr7:16160260..16161964-chr7:16601044..16602872,2	K562	blood:
7	chr7:16195841..16198251-chr7:16237665..16240574,2	K562	blood:
8	chr7:16155299..16158240-chr7:16469053..16471948,2	MCF-7	breast:
9	chr7:16262958..16265861-chr7:16270760..16273242,2	K562	blood:
10	chr7:16237727..16240035-chr7:16245292..16248267,2	K562	blood:
11	chr7:16182339..16184575-chr7:16186755..16189879,4	K562	blood:
12	chr7:16175890..16178369-chr7:16460107..16461891,2	K562	blood:
13	chr7:16179426..16181583-chr7:16183166..16185185,2	K562	blood:
14	chr7:16237727..16240035-chr7:16245292..16248267,2	K562	blood:
15	chr7:16272248..16274869-chr7:16305157..16307096,2	K562	blood:
16	chr7:16163332..16166682-chr7:16168579..16171460,3	K562	blood:
17	chr7:16150627..16153575-chr7:16159253..16161215,2	MCF-7	breast:
18	chr7:16161067..16163627-chr7:16461364..16462917,2	K562	blood:
19	chr7:16271837..16274588-chr7:16275186..16279473,3	K562	blood:
20	chr7:16225600..16227633-chr7:16239698..16241301,2	K562	blood:
21	chr7:16263097..16266771-chr7:16270720..16274586,3	K562	blood:
22	chr7:16271772..16276074-chr7:16279630..16282231,4	K562	blood:
23	chr5:118549863..118550376-chr7:16168238..16169156,2	MCF-7	breast:
24	chr7:16175890..16178369-chr7:16460107..16462203,3	K562	blood:
25	chr7:16216050..16218726-chr7:16604270..16606079,2	K562	blood:
26	chr7:16165242..16168046-chr7:16300329..16302056,2	K562	blood:
27	chr7:16174593..16177204-chr7:16180297..16182169,2	K562	blood:
28	chr7:16195841..16198251-chr7:16237665..16240574,2	K562	blood:
29	chr7:16211386..16214233-chr7:16216618..16219049,2	MCF-7	breast:
30	chr7:16263097..16266771-chr7:16270720..16274586,3	K562	blood:
31	chr7:16247118..16249897-chr7:16251885..16253666,2	K562	blood:
32	chr7:16154506..16156134-chr7:16470584..16472097,2	MCF-7	breast:
33	chr7:16150627..16153575-chr7:16159253..16161215,2	MCF-7	breast:
34	chr7:16226388..16229084-chr7:16230552..16232417,2	K562	blood:
35	chr7:16272248..16275452-chr7:16305157..16308165,4	K562	blood:
36	chr7:16242380..16245309-chr7:16338722..16341323,2	K562	blood:
37	chr7:16155027..16159755-chr7:16165295..16168369,4	K562	blood:
38	chr7:16217013..16219760-chr7:16220726..16222323,2	K562	blood:
39	chr7:16207885..16209563-chr7:16230892..16233884,2	K562	blood:
40	chr7:16153998..16154693-chr7:16604258..16605163,3	K562	blood:
41	chr7:16225600..16227633-chr7:16239698..16241301,2	K562	blood:
42	chr7:16217459..16219153-chr7:16224658..16227242,2	K562	blood:
43	chr7:16217013..16219760-chr7:16220726..16222323,2	K562	blood:
44	chr7:16221967..16224628-chr7:16306153..16308389,2	K562	blood:
45	chr7:16192281..16194569-chr7:16210731..16212589,2	K562	blood:
46	chr7:16242935..16245142-chr7:16460996..16462500,2	MCF-7	breast:
47	chr7:16153898..16154837-chr7:16604199..16605221,3	MCF-7	breast:
48	chr7:16179426..16181583-chr7:16183166..16185185,2	K562	blood:
49	chr7:16207885..16209563-chr7:16230892..16233884,2	K562	blood:
50	chr7:16232287..16234085-chr7:16683259..16685789,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC006035.2-1	chr7:16250111-16250228	NONHSAT119293
2	lnc-AC006035.2-1	chr7:16250132-16250228	ENSG00000229688.3
3	lnc-AC006035.2-1	chr7:16250113-16250228	ENSG00000229688
4	lnc-AC006035.2-1	chr7:16250130-16250228	NONHSAT119296
5	lnc-AC006035.2-1	chr7:16256009-16256194	ENSG00000229688.3
6	lnc-AC006035.2-1	chr7:16268049-16268246	ucscGeneNc_uc003stf_2
7	lnc-AC006035.2-1	chr7:16250111-16250228	NONHSAT119292
8	lnc-AC006035.2-6	chr7:16248570-16248890	NONHSAT119291
9	lnc-AC006035.2-1	chr7:16216643-16216753	ucscGeneNc_uc003stf_2
10	lnc-AC006035.2-1	chr7:16243459-16243563	ucscGeneNc_uc003stf_2
11	lnc-AC006035.2-1	chr7:16250130-16250228	NONHSAT119295
12	lnc-AC006035.2-1	chr7:16272377-16272461	ucscGeneNc_uc003stf_2
13	lnc-AC006035.2-1	chr7:16250118-16250228	NONHSAT119294
14	lnc-AC006035.2-1	chr7:16250167-16250228	ENSG00000229688.3
15	lnc-AC006035.2-1	chr7:16255958-16256194	ENSG00000229688.3
16	lnc-AC006035.2-1	chr7:16250169-16250228	ENSG00000229688

No data

Variant related genes	Relation type
RPL36AP29	TF binding region
ISPD-AS1	TF binding region
RPL36AP29	CpG island
ISPD-AS1	CpG island
ENSG00000214960	chromatin interactions
ENSG00000224683	chromatin interactions
ENSG00000136261	chromatin interactions
ENSG00000273477	chromatin interactions
ENSG00000106524	chromatin interactions
ERCC4	miRNA target sites
RANBP9	miRNA target sites

Extended variants
information (count: 3227 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:3227 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs527254547	chr7:16144930-16144931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs116773289	chr7:16144970-16144971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs138929230	chr7:16144979-16144980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs74816913	chr7:16144994-16144995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs549663555	chr7:16145080-16145081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs143002547	chr7:16145121-16145122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs538724306	chr7:16145126-16145127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs554264202	chr7:16145145-16145146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs77234223	chr7:16145152-16145153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs192406179	chr7:16145159-16145160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs182141550	chr7:16145172-16145173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs576327418	chr7:16145198-16145199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs531466331	chr7:16145423-16145424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs73681736	chr7:16145506-16145507	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs144657072	chr7:16145507-16145508	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs76847026	chr7:16145514-16145515	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs112368216	chr7:16145516-16145517	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs565827936	chr7:16145532-16145533	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs536397269	chr7:16145544-16145545	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs148117970	chr7:16145567-16145568	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs569727985	chr7:16145578-16145579	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs141878369	chr7:16145582-16145583	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs185220698	chr7:16145584-16145585	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs555014136	chr7:16145598-16145599	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs150636642	chr7:16145634-16145635	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs577499523	chr7:16145735-16145736	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs79183323	chr7:16145787-16145788	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs574879349	chr7:16145790-16145791	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs571739884	chr7:16145825-16145826	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs190081468	chr7:16145826-16145827	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs539239111	chr7:16145858-16145859	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs542753514	chr7:16145887-16145888	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs111932714	chr7:16145905-16145906	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs560834088	chr7:16145924-16145925	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs544178008	chr7:16145984-16145985	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs182401533	chr7:16146016-16146017	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs565172059	chr7:16146023-16146024	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs549986379	chr7:16146053-16146054	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs532346351	chr7:16146066-16146067	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs547188123	chr7:16146074-16146075	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs140150446	chr7:16146107-16146108	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs530096713	chr7:16146121-16146122	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs188333022	chr7:16146128-16146129	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs76573402	chr7:16146144-16146145	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs370709893	chr7:16146149-16146150	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs374121321	chr7:16146157-16146158	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs532628808	chr7:16146200-16146201	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs558721054	chr7:16146206-16146207	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs571119714	chr7:16146210-16146211	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs367869362	chr7:16146239-16146240	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Rubinstein-Taybi syndrome	22470819	CNVD
Alzheimer''s disease	22166940	CNVD
Abnormal phenotypes	18644119	CNVD
Non-syndromic sensorineural hearing loss	22570644	CNVD
Bladder cancer	21909424	CNVD
Cancer	21183584	CNVD
Autism	19492091	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	19805367	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Autism	20808228	CNVD

Chromatin state (count:287 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:16135800-16145200	Weak transcription	Left Ventricle	heart
2	chr7:16145400-16145800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr7:16145800-16146000	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr7:16146000-16148600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr7:16146800-16147800	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr7:16155600-16158600	Weak transcription	Fetal Stomach	stomach
7	chr7:16155800-16158600	Weak transcription	Ovary	ovary
8	chr7:16156200-16160200	Weak transcription	Primary hematopoietic stem cells	blood
9	chr7:16156800-16157800	Weak transcription	Pancreas	Pancrea
10	chr7:16156800-16164200	Weak transcription	Stomach Smooth Muscle	stomach
11	chr7:16157200-16160800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr7:16157800-16158200	Enhancers	Cortex derived primary cultured neurospheres	brain
13	chr7:16157800-16158400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr7:16157800-16158400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr7:16158000-16158200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr7:16158000-16158400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr7:16158200-16170400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr7:16158600-16159000	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
19	chr7:16159600-16159800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr7:16160000-16163200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr7:16160200-16160400	Active TSS	Primary hematopoietic stem cells	blood
22	chr7:16163200-16163400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr7:16163400-16169000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr7:16165000-16169800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr7:16167600-16167800	ZNF genes & repeats	Left Ventricle	heart
26	chr7:16167800-16170400	Weak transcription	Left Ventricle	heart
27	chr7:16168200-16168400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr7:16168200-16168600	Enhancers	Muscle Satellite Cultured Cells	--
29	chr7:16168200-16169000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr7:16168200-16170800	Enhancers	HSMM	muscle
31	chr7:16168400-16168800	Enhancers	Osteobl	bone
32	chr7:16168400-16169000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr7:16168400-16170200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr7:16168600-16168800	Enhancers	HSMMtube	muscle
35	chr7:16168600-16168800	Enhancers	NH-A	brain
36	chr7:16168600-16168800	Enhancers	NHDF-Ad	bronchial
37	chr7:16168600-16169000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr7:16168600-16169000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr7:16168600-16169600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr7:16168600-16170000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
41	chr7:16168600-16170600	Enhancers	HMEC	breast
42	chr7:16168600-16171000	Enhancers	HUVEC	blood vessel
43	chr7:16168800-16169000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr7:16168800-16169200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr7:16168800-16169200	Flanking Active TSS	NH-A	brain
46	chr7:16168800-16169600	Flanking Active TSS	NHDF-Ad	bronchial
47	chr7:16168800-16169800	Flanking Active TSS	HSMMtube	muscle
48	chr7:16168800-16169800	Enhancers	NHEK	skin
49	chr7:16168800-16170000	Flanking Active TSS	Osteobl	bone
50	chr7:16168800-16170600	Enhancers	NHLF	lung

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