Variant report

Variant	esv1847175
Chromosome Location	chr7:16155335-16272661
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:305)
CpG islands
(count:122)
Chromatin interactive
region (count:53)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

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	chr7:16252388-16252536	K562	blood:	n/a	n/a
3	ARID3A	chr7:16169136-16169227	K562	blood:	n/a	n/a
4	ATF1	chr7:16230945-16230986	K562	blood:	n/a	n/a
5	ATF1	chr7:16266719-16266733	K562	blood:	n/a	n/a
6	BACH1	chr7:16243269-16243380	K562	blood:	n/a	n/a
7	BACH1	chr7:16190493-16190510	K562	blood:	n/a	n/a
8	BHLHE40	chr7:16242216-16242218	K562	blood:	n/a	n/a
9	CBX3	chr7:16269898-16270150	K562	blood:	n/a	n/a
10	CBX3	chr7:16271850-16272277	K562	blood:	n/a	n/a
11	CBX3	chr7:16184160-16184557	K562	blood:	n/a	n/a
12	CBX3	chr7:16269828-16270194	K562	blood:	n/a	n/a
13	CBX3	chr7:16168849-16169768	HCT-116	colon:	n/a	n/a
14	CBX3	chr7:16240929-16241356	K562	blood:	n/a	n/a
15	CCNT2	chr7:16254761-16254970	K562	blood:	n/a	n/a
16	CEBPB	chr7:16228989-16229268	IMR90	lung:	n/a	chr7:16229185-16229197
17	CEBPB	chr7:16251340-16251603	HepG2	liver:	n/a	n/a
18	CEBPB	chr7:16251298-16251575	K562	blood:	n/a	n/a
19	CEBPB	chr7:16240258-16240479	IMR90	lung:	n/a	chr7:16240358-16240369 chr7:16240357-16240370
20	CEBPB	chr7:16221312-16221339	K562	blood:	n/a	n/a
21	CEBPB	chr7:16216843-16216912	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr7:16246794-16247066	K562	blood:	n/a	n/a
23	CEBPB	chr7:16229080-16229110	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr7:16169034-16169377	IMR90	lung:	n/a	n/a
25	CEBPB	chr7:16169142-16169366	A549	lung:	n/a	n/a
26	CEBPB	chr7:16246860-16247062	A549	lung:	n/a	n/a
27	CEBPB	chr7:16240297-16240490	A549	lung:	n/a	chr7:16240358-16240369 chr7:16240357-16240370
28	CEBPB	chr7:16234545-16234739	HepG2	liver:	n/a	chr7:16234630-16234641
29	CEBPB	chr7:16216852-16216879	K562	blood:	n/a	n/a
30	CEBPB	chr7:16240270-16240516	HepG2	liver:	n/a	chr7:16240358-16240369 chr7:16240357-16240370
31	CEBPB	chr7:16234605-16234660	K562	blood:	n/a	chr7:16234630-16234641
32	CEBPB	chr7:16251244-16251545	K562	blood:	n/a	n/a
33	CEBPB	chr7:16234751-16234761	IMR90	lung:	n/a	n/a
34	CEBPB	chr7:16169033-16169381	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr7:16220104-16220262	IMR90	lung:	n/a	n/a
36	CEBPZ	chr7:16247712-16247786	HepG2	liver:	n/a	n/a
37	CTCF	chr7:16204300-16204450	BE2_C	brain:	n/a	n/a
38	CTCF	chr7:16178080-16178230	GM06990	blood:	n/a	n/a
39	CTCF	chr7:16206936-16206994	GM13976	blood:	n/a	n/a
40	CTCF	chr7:16181540-16181690	HAc	cerebellar:	n/a	n/a
41	CTCF	chr7:16237499-16237527	GM13977	blood:	n/a	n/a
42	CTCF	chr7:16180009-16180085	GM13977	blood:	n/a	n/a
43	CTCF	chr7:16175400-16175550	AG10803	skin:	n/a	n/a
44	E2F4	chr7:16214093-16214275	MCF10A-Er-Src	breast:	n/a	n/a
45	E2F4	chr7:16169221-16169421	MCF10A-Er-Src	breast:	n/a	n/a
46	EGR1	chr7:16249834-16250068	K562	blood:	n/a	n/a
47	EGR1	chr7:16249857-16250173	K562	blood:	n/a	n/a
48	ELF1	chr7:16168967-16170461	SK-N-SH	brain:	n/a	n/a
49	ELF1	chr7:16169314-16169768	SK-N-SH	brain:	n/a	n/a
50	EP300	chr7:16170080-16170347	SK-N-SH_RA	brain:	n/a	chr7:16170244-16170258

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:16254882-16254932	NT2-D1	testis:	n/a
2	chr7:16254882-16254932	HCM	heart:	n/a
3	chr7:16223374-16223424	HNPCEpiC	eye:	n/a
4	chr7:16254882-16254932	AoSMC	blood vessel:	n/a
5	chr7:16223374-16223424	GM12878	blood:	n/a
6	chr7:16254882-16254932	K562	blood:	n/a
7	chr7:16223374-16223424	HCPEpiC	choroid plexus:	n/a
8	chr7:16223374-16223424	SK-N-SH_RA	brain:	n/a
9	chr7:16223374-16223424	HRCEpiC	kidney:	n/a
10	chr7:16254882-16254932	IMR90	lung:	fetal
11	chr7:16223374-16223424	BJ	skin:	n/a
12	chr7:16254882-16254932	PrEC	prostate:	n/a
13	chr7:16254882-16254932	AG09319	gingival:	n/a
14	chr7:16223374-16223424	Caco-2	colon:	n/a
15	chr7:16254882-16254932	HCT-116	colon:	n/a
16	chr7:16223374-16223424	GM19239	blood:	n/a
17	chr7:16254882-16254932	RPTEC	kidney:	n/a
18	chr7:16223374-16223424	A549	lung:	n/a
19	chr7:16223374-16223424	RPTEC	kidney:	n/a
20	chr7:16254882-16254932	HRPEpiC	eye:	n/a
21	chr7:16254882-16254932	HepG2	liver:	n/a
22	chr7:16223374-16223424	Hepatocyte	liver:	n/a
23	chr7:16223374-16223424	HPAEpiC	pulmonary alveolar:	n/a
24	chr7:16223374-16223424	K562	blood:	n/a
25	chr7:16254882-16254932	NHBE	bronchial:	n/a
26	chr7:16223374-16223424	Hela-S3	cervix:	n/a
27	chr7:16223374-16223424	ECC-1	luminal epithelium:	n/a
28	chr7:16223374-16223424	HRE	kidney:	n/a
29	chr7:16254882-16254932	HRE	kidney:	n/a
30	chr7:16223374-16223424	HRPEpiC	eye:	n/a
31	chr7:16223374-16223424	AoSMC	blood vessel:	n/a
32	chr7:16254882-16254932	ProgFib	skin:	n/a
33	chr7:16223374-16223424	NHBE	bronchial:	n/a
34	chr7:16254882-16254932	SK-N-SH	brain:	n/a
35	chr7:16254882-16254932	HEEpiC	esophagus:	n/a
36	chr7:16223374-16223424	PrEC	prostate:	n/a
37	chr7:16254882-16254932	SK-N-MC	brain:	n/a
38	chr7:16254882-16254932	Hela-S3	cervix:	n/a
39	chr7:16254882-16254932	PFSK-1	brain:	n/a
40	chr7:16223374-16223424	U87	brain:	n/a
41	chr7:16254882-16254932	HRCEpiC	kidney:	n/a
42	chr7:16223374-16223424	AG09309	skin:	n/a
43	chr7:16254882-16254932	HL-60	blood:	n/a
44	chr7:16254882-16254932	AG09309	skin:	n/a
45	chr7:16254882-16254932	HMEC	breast:	n/a
46	chr7:16223374-16223424	ProgFib	skin:	n/a
47	chr7:16254882-16254932	HCF	heart:	n/a
48	chr7:16223374-16223424	IMR90	lung:	fetal
49	chr7:16254882-16254932	MCF-7	breast:	n/a
50	chr7:16223374-16223424	LNCaP	prostate:	n/a

(count:53 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:16207885..16209563-chr7:16230892..16233884,2	K562	blood:
2	chr7:16271837..16274588-chr7:16275186..16279473,3	K562	blood:
3	chr7:16182339..16184575-chr7:16186755..16189879,4	K562	blood:
4	chr7:16211386..16214233-chr7:16216618..16219049,2	MCF-7	breast:
5	chr7:16262958..16265861-chr7:16270760..16273242,2	K562	blood:
6	chr7:16226388..16229084-chr7:16230552..16232417,2	K562	blood:
7	chr7:16237727..16240035-chr7:16245292..16248267,2	K562	blood:
8	chr7:16192281..16194569-chr7:16210731..16212589,2	K562	blood:
9	chr7:16226388..16229084-chr7:16230552..16232417,2	K562	blood:
10	chr7:16155027..16159755-chr7:16165295..16168369,4	K562	blood:
11	chr7:16272248..16274869-chr7:16305157..16307096,2	K562	blood:
12	chr7:16216050..16218726-chr7:16604270..16606079,2	K562	blood:
13	chr7:16175890..16178369-chr7:16460107..16461891,2	K562	blood:
14	chr7:16262958..16265861-chr7:16270760..16273242,2	K562	blood:
15	chr7:16263097..16266771-chr7:16270720..16274586,3	K562	blood:
16	chr7:16211386..16214233-chr7:16216618..16219049,2	MCF-7	breast:
17	chr7:16179426..16181583-chr7:16183166..16185185,2	K562	blood:
18	chr7:16207885..16209563-chr7:16230892..16233884,2	K562	blood:
19	chr7:16174593..16177204-chr7:16180297..16182169,2	K562	blood:
20	chr7:16225600..16227633-chr7:16239698..16241301,2	K562	blood:
21	chr7:16217013..16219760-chr7:16220726..16222323,2	K562	blood:
22	chr7:16150627..16153575-chr7:16159253..16161215,2	MCF-7	breast:
23	chr7:16163332..16166682-chr7:16168579..16171460,3	K562	blood:
24	chr7:16165242..16168046-chr7:16300329..16302056,2	K562	blood:
25	chr7:16174593..16177204-chr7:16180297..16182169,2	K562	blood:
26	chr7:16155299..16158240-chr7:16469053..16471948,2	MCF-7	breast:
27	chr7:16263097..16266771-chr7:16270720..16274586,3	K562	blood:
28	chr7:16237727..16240035-chr7:16245292..16248267,2	K562	blood:
29	chr7:16221967..16224628-chr7:16306153..16308389,2	K562	blood:
30	chr7:16213039..16215303-chr7:16232402..16234352,2	K562	blood:
31	chr7:16217459..16219153-chr7:16224658..16227242,2	K562	blood:
32	chr7:16179426..16181583-chr7:16183166..16185185,2	K562	blood:
33	chr7:16154506..16156134-chr7:16470584..16472097,2	MCF-7	breast:
34	chr7:16242380..16245309-chr7:16338722..16341323,2	K562	blood:
35	chr7:16247118..16249897-chr7:16251885..16253666,2	K562	blood:
36	chr7:16213039..16215303-chr7:16232402..16234352,2	K562	blood:
37	chr7:16163332..16166682-chr7:16168579..16171460,3	K562	blood:
38	chr7:16217013..16219760-chr7:16220726..16222323,2	K562	blood:
39	chr7:16232287..16234085-chr7:16683259..16685789,2	K562	blood:
40	chr7:16217459..16219153-chr7:16224658..16227242,2	K562	blood:
41	chr7:16195841..16198251-chr7:16237665..16240574,2	K562	blood:
42	chr7:16195841..16198251-chr7:16237665..16240574,2	K562	blood:
43	chr7:16242935..16245142-chr7:16460996..16462500,2	MCF-7	breast:
44	chr7:16161067..16163627-chr7:16461364..16462917,2	K562	blood:
45	chr7:16192281..16194569-chr7:16210731..16212589,2	K562	blood:
46	chr7:16272248..16275452-chr7:16305157..16308165,4	K562	blood:
47	chr5:118549863..118550376-chr7:16168238..16169156,2	MCF-7	breast:
48	chr7:16155027..16159755-chr7:16165295..16168369,4	K562	blood:
49	chr7:16175890..16178369-chr7:16460107..16462203,3	K562	blood:
50	chr7:16160260..16161964-chr7:16601044..16602872,2	K562	blood:

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

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

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
ENSG00000106524	chromatin interactions
ENSG00000136261	chromatin interactions
RANBP9	miRNA target sites
ERCC4	miRNA target sites

Extended variants
information (count: 3057 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:3057 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555798473	chr7:16155606-16155607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs146794782	chr7:16155652-16155653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs34612021	chr7:16155673-16155674	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs183108931	chr7:16155675-16155676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs577908262	chr7:16155698-16155699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs530613766	chr7:16155703-16155704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs140492345	chr7:16155721-16155722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs538110809	chr7:16155800-16155801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs145733594	chr7:16155811-16155812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs148113250	chr7:16155814-16155815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs187803693	chr7:16155841-16155842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs561781604	chr7:16155854-16155855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs528983528	chr7:16156011-16156012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs141047143	chr7:16156012-16156013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs562506145	chr7:16156016-16156017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs533247213	chr7:16156115-16156116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs370258275	chr7:16156120-16156121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs35271539	chr7:16156123-16156124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs150235493	chr7:16156144-16156145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs527443775	chr7:16156156-16156157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs548910643	chr7:16156167-16156168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs567748264	chr7:16156173-16156174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs537995485	chr7:16156174-16156175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs533955816	chr7:16156233-16156234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs191167334	chr7:16156240-16156241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs533431263	chr7:16156245-16156246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs182528055	chr7:16156253-16156254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs375708010	chr7:16156285-16156286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs112867393	chr7:16156300-16156301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs36019928	chr7:16156301-16156302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs538670780	chr7:16156312-16156313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs554008386	chr7:16156314-16156315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs367563106	chr7:16156319-16156320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs371414116	chr7:16156327-16156328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs375192080	chr7:16156331-16156332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs369507766	chr7:16156334-16156335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs369987186	chr7:16156339-16156340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs373039113	chr7:16156340-16156341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs572657941	chr7:16156446-16156447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs536805934	chr7:16156452-16156453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs554910841	chr7:16156465-16156466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs1405591	chr7:16156475-16156476	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs528348171	chr7:16156526-16156527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs544355415	chr7:16156620-16156621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs562443506	chr7:16156674-16156675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs577679038	chr7:16156678-16156679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs7803005	chr7:16156706-16156707	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs138954067	chr7:16156736-16156737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs188045946	chr7:16156742-16156743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs370829526	chr7:16156743-16156744	Weak transcription	n/a	n/a	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:280 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:16155600-16158600	Weak transcription	Fetal Stomach	stomach
2	chr7:16155800-16158600	Weak transcription	Ovary	ovary
3	chr7:16156200-16160200	Weak transcription	Primary hematopoietic stem cells	blood
4	chr7:16156800-16157800	Weak transcription	Pancreas	Pancrea
5	chr7:16156800-16164200	Weak transcription	Stomach Smooth Muscle	stomach
6	chr7:16157200-16160800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr7:16157800-16158200	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr7:16157800-16158400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr7:16157800-16158400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr7:16158000-16158200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr7:16158000-16158400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr7:16158200-16170400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr7:16158600-16159000	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
14	chr7:16159600-16159800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr7:16160000-16163200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr7:16160200-16160400	Active TSS	Primary hematopoietic stem cells	blood
17	chr7:16163200-16163400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr7:16163400-16169000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr7:16165000-16169800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr7:16167600-16167800	ZNF genes & repeats	Left Ventricle	heart
21	chr7:16167800-16170400	Weak transcription	Left Ventricle	heart
22	chr7:16168200-16168400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr7:16168200-16168600	Enhancers	Muscle Satellite Cultured Cells	--
24	chr7:16168200-16169000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr7:16168200-16170800	Enhancers	HSMM	muscle
26	chr7:16168400-16168800	Enhancers	Osteobl	bone
27	chr7:16168400-16169000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr7:16168400-16170200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr7:16168600-16168800	Enhancers	HSMMtube	muscle
30	chr7:16168600-16168800	Enhancers	NH-A	brain
31	chr7:16168600-16168800	Enhancers	NHDF-Ad	bronchial
32	chr7:16168600-16169000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr7:16168600-16169000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr7:16168600-16169600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr7:16168600-16170000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
36	chr7:16168600-16170600	Enhancers	HMEC	breast
37	chr7:16168600-16171000	Enhancers	HUVEC	blood vessel
38	chr7:16168800-16169000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr7:16168800-16169200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr7:16168800-16169200	Flanking Active TSS	NH-A	brain
41	chr7:16168800-16169600	Flanking Active TSS	NHDF-Ad	bronchial
42	chr7:16168800-16169800	Flanking Active TSS	HSMMtube	muscle
43	chr7:16168800-16169800	Enhancers	NHEK	skin
44	chr7:16168800-16170000	Flanking Active TSS	Osteobl	bone
45	chr7:16168800-16170600	Enhancers	NHLF	lung
46	chr7:16168800-16170800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr7:16169000-16169200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr7:16169000-16169200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr7:16169000-16169200	Enhancers	Psoas Muscle	Psoas
50	chr7:16169000-16169400	Enhancers	Skeletal Muscle Male	skeletal muscle

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