Variant report

Variant	nsv977958
Chromosome Location	chr16:30547064-30550984
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:482)
CpG islands
(count:61)
Chromatin interactive
region (count:29)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:482 , 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	chr16:30547103-30547385	K562	blood:	n/a	n/a
2	ARID3A	chr16:30547104-30547218	HepG2	liver:	n/a	n/a
3	ATF1	chr16:30547015-30547445	K562	blood:	n/a	n/a
4	ATF2	chr16:30546791-30547675	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr16:30547057-30547483	GM12878	blood:	n/a	n/a
6	ATF2	chr16:30546979-30547452	GM12878	blood:	n/a	n/a
7	ATF3	chr16:30547032-30547497	K562	blood:	n/a	n/a
8	BACH1	chr16:30546935-30547089	K562	blood:	n/a	n/a
9	BACH1	chr16:30550975-30551229	K562	blood:	n/a	n/a
10	BCLAF1	chr16:30545872-30547492	GM12878	blood:	n/a	chr16:30546242-30546255
11	BCLAF1	chr16:30545860-30547508	GM12878	blood:	n/a	chr16:30546242-30546255
12	BHLHE40	chr16:30545994-30547528	K562	blood:	n/a	n/a
13	BHLHE40	chr16:30550827-30550933	K562	blood:	n/a	n/a
14	BHLHE40	chr16:30547020-30547518	GM12878	blood:	n/a	n/a
15	BRCA1	chr16:30546940-30547290	Hela-S3	cervix:	n/a	n/a
16	CBX3	chr16:30545392-30547589	K562	blood:	n/a	n/a
17	CCNT2	chr16:30547097-30547295	K562	blood:	n/a	n/a
18	CEBPB	chr16:30546067-30547094	GM12878	blood:	n/a	n/a
19	CHD1	chr16:30545964-30547410	GM12878	blood:	n/a	chr16:30546240-30546250
20	CHD1	chr16:30546094-30547184	H1-hESC	embryonic stem cell:	n/a	chr16:30546240-30546250
21	CHD2	chr16:30547086-30547200	Hela-S3	cervix:	n/a	n/a
22	CHD2	chr16:30547142-30547360	K562	blood:	n/a	n/a
23	CHD2	chr16:30547189-30547295	HepG2	liver:	n/a	n/a
24	CHD2	chr16:30547050-30547258	GM12878	blood:	n/a	n/a
25	CREB1	chr16:30545693-30547547	HepG2	liver:	n/a	n/a
26	CTCF	chr16:30547010-30547364	K562	blood:	n/a	n/a
27	CTCF	chr16:30547100-30547250	AG10803	skin:	n/a	n/a
28	CTCF	chr16:30547096-30547288	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr16:30547120-30547270	HepG2	liver:	n/a	n/a
30	CTCF	chr16:30547120-30547270	AG09319	gingival:	n/a	n/a
31	CTCF	chr16:30547085-30547294	HUVEC	blood vessel:	n/a	n/a
32	CTCF	chr16:30547100-30547250	HPF	lung:	n/a	n/a
33	CTCF	chr16:30547120-30547270	HCT-116	colon:	n/a	n/a
34	CTCF	chr16:30547100-30547250	HCM	heart:	n/a	n/a
35	CTCF	chr16:30547062-30547343	GM12892	blood:	n/a	n/a
36	CTCF	chr16:30546984-30547318	T-47D	breast:	n/a	n/a
37	CTCF	chr16:30547140-30547290	HAc	cerebellar:	n/a	n/a
38	CTCF	chr16:30547120-30547270	HCFaa	heart:	n/a	n/a
39	CTCF	chr16:30547100-30547250	BJ	skin:	n/a	n/a
40	CTCF	chr16:30547106-30547275	A549	lung:	n/a	n/a
41	CTCF	chr16:30547100-30547250	GM12869	blood:	n/a	n/a
42	CTCF	chr16:30547160-30547310	HFF-Myc	foreskin:	n/a	n/a
43	CTCF	chr16:30547180-30547330	HL-60	blood:	n/a	n/a
44	CTCF	chr16:30547140-30547290	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr16:30547100-30547250	AG04450	lung:	n/a	n/a
46	CTCF	chr16:30547140-30547290	GM12871	blood:	n/a	n/a
47	CTCF	chr16:30547120-30547270	HBMEC	blood vessel:	n/a	n/a
48	CTCF	chr16:30547098-30547291	GM10248	blood:	n/a	n/a
49	CTCF	chr16:30547120-30547270	AoAF	blood vessel:	n/a	n/a
50	CTCF	chr16:30547100-30547250	HMF	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:30550239-30550289	Hepatocyte	liver:	n/a
2	chr16:30550239-30550289	HEEpiC	esophagus:	n/a
3	chr16:30550239-30550289	Jurkat	blood:	n/a
4	chr16:30550239-30550289	HepG2	liver:	n/a
5	chr16:30550239-30550289	PrEC	prostate:	n/a
6	chr16:30550239-30550289	U87	brain:	n/a
7	chr16:30550239-30550289	HMEC	breast:	n/a
8	chr16:30550239-30550289	NHBE	bronchial:	n/a
9	chr16:30550239-30550289	NHDF-neo	bronchial:	n/a
10	chr16:30550239-30550289	HCF	heart:	n/a
11	chr16:30550239-30550289	HEK293	kidney:	embryo
12	chr16:30550239-30550289	MCF10A-Er-Src	breast:	n/a
13	chr16:30550239-30550289	PFSK-1	brain:	n/a
14	chr16:30550239-30550289	SK-N-MC	brain:	n/a
15	chr16:30550239-30550289	PANC-1	pancreas:	n/a
16	chr16:30550239-30550289	SAEC	small airway:	n/a
17	chr16:30550239-30550289	A549	lung:	n/a
18	chr16:30550239-30550289	HCPEpiC	choroid plexus:	n/a
19	chr16:30550239-30550289	IMR90	lung:	fetal
20	chr16:30550239-30550289	HRPEpiC	eye:	n/a
21	chr16:30550239-30550289	HIPEpiC	eye:	n/a
22	chr16:30550239-30550289	LNCaP	prostate:	n/a
23	chr16:30550239-30550289	HL-60	blood:	n/a
24	chr16:30550239-30550289	GM06990	blood:	n/a
25	chr16:30550239-30550289	HUVEC	blood vessel:	n/a
26	chr16:30550239-30550289	AG10803	skin:	n/a
27	chr16:30550239-30550289	Caco-2	colon:	n/a
28	chr16:30550239-30550289	ProgFib	skin:	n/a
29	chr16:30550239-30550289	HCM	heart:	n/a
30	chr16:30550239-30550289	CMK	blood:	n/a
31	chr16:30550239-30550289	HAEpiC	amniotic membrane:	n/a
32	chr16:30550239-30550289	NB4	blood:	n/a
33	chr16:30550239-30550289	ovcar-3	ovarian:	n/a
34	chr16:30550239-30550289	SK-N-SH_RA	brain:	n/a
35	chr16:30550239-30550289	BE2_C	brain:	n/a
36	chr16:30550239-30550289	GM12878	blood:	n/a
37	chr16:30550239-30550289	HRE	kidney:	n/a
38	chr16:30550239-30550289	K562	blood:	n/a
39	chr16:30550239-30550289	GM12892	blood:	n/a
40	chr16:30550239-30550289	AG09319	gingival:	n/a
41	chr16:30550239-30550289	ECC-1	luminal epithelium:	n/a
42	chr16:30550239-30550289	HPAEpiC	pulmonary alveolar:	n/a
43	chr16:30550239-30550289	AoSMC	blood vessel:	n/a
44	chr16:30550239-30550289	AG04449	skin:	fetal
45	chr16:30550239-30550289	HNPCEpiC	eye:	n/a
46	chr16:30550239-30550289	NH-A	brain:	n/a
47	chr16:30550239-30550289	AG09309	skin:	n/a
48	chr16:30550239-30550289	HRCEpiC	kidney:	n/a
49	chr16:30550239-30550289	MCF-7	breast:	n/a
50	chr16:30550239-30550289	SK-N-SH	brain:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:30543696..30550338-chr16:30595198..30599305,8	MCF-7	breast:
2	chr16:30545950..30548016-chr16:30593866..30595434,2	MCF-7	breast:
3	chr16:30541129..30548783-chr16:30576543..30583587,16	MCF-7	breast:
4	chr16:30533019..30535927-chr16:30549702..30551377,2	MCF-7	breast:
5	chr16:30545719..30548048-chr16:30583510..30586476,3	MCF-7	breast:
6	chr16:30541481..30548892-chr16:30595486..30600580,13	MCF-7	breast:
7	chr16:30454856..30459511-chr16:30543910..30548861,10	K562	blood:
8	chr16:30005844..30008552-chr16:30546352..30548283,2	K562	blood:
9	chr16:30545798..30549380-chr16:30578344..30585176,6	K562	blood:
10	chr16:30545394..30548849-chr16:30597035..30599710,5	K562	blood:
11	chr16:30534557..30548684-chr16:30561877..30572653,49	MCF-7	breast:
12	chr16:30545465..30548885-chr16:30620195..30623109,3	MCF-7	breast:
13	chr16:30544371..30547496-chr16:30661598..30664666,3	K562	blood:
14	chr16:30440316..30443197-chr16:30545164..30548518,4	MCF-7	breast:
15	chr16:30544664..30548849-chr16:30597277..30601099,4	K562	blood:
16	chr15:74987753..74988712-chr16:30546350..30547141,2	Hela-S3	cervix:
17	chr16:30545157..30547413-chr16:30708234..30710909,2	K562	blood:
18	chr16:30544993..30547961-chr16:30709430..30711142,2	MCF-7	breast:
19	chr16:30544819..30547359-chr16:30669370..30671346,2	MCF-7	breast:
20	chr16:30460806..30461674-chr16:30546744..30547629,4	MCF-7	breast:
21	chr16:30545917..30548270-chr16:30592742..30594990,2	K562	blood:
22	chr16:30454223..30458795-chr16:30544992..30549263,8	K562	blood:
23	chr16:30439809..30443048-chr16:30544747..30548003,3	K562	blood:
24	chr16:30455846..30458629-chr16:30545743..30547752,2	MCF-7	breast:
25	chr16:30545977..30548808-chr16:30568240..30572636,5	K562	blood:
26	chr16:30453263..30460635-chr16:30534974..30549190,40	MCF-7	breast:
27	chr16:30545944..30548930-chr16:30568116..30571083,5	K562	blood:
28	chr16:30439652..30442096-chr16:30544594..30547144,2	MCF-7	breast:
29	chr16:30544644..30549200-chr16:30579756..30585399,7	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF747-1	chr16:30548523-30548773	NONHSAT141765
2	lnc-ITGAL-2	chr16:30547750-30548465	ENSG00000235560.3
3	lnc-ITGAL-2	chr16:30547139-30547520	ENSG00000235560.3
4	lnc-ITGAL-2	chr16:30547750-30548465	ENSG00000235560
5	lnc-ZNF747-1	chr16:30549081-30549552	NONHSAT141765

No data

Variant related genes	Relation type
ENSG00000261459	TF binding region
ENSG00000260494	TF binding region
ZNF747	TF binding region
ENSG00000261459	CpG island
ENSG00000260494	CpG island
ZNF747	CpG island
ENSG00000080603	chromatin interactions
ENSG00000179958	chromatin interactions
ENSG00000156858	chromatin interactions
ENSG00000149929	chromatin interactions
ENSG00000261840	chromatin interactions
ENSG00000197162	chromatin interactions
ENSG00000260869	chromatin interactions
ENSG00000239791	chromatin interactions
ENSG00000260167	chromatin interactions
ENSG00000179918	chromatin interactions
ENSG00000169951	chromatin interactions
ENSG00000169592	chromatin interactions
ENSG00000156853	chromatin interactions
ENSG00000179151	chromatin interactions
ENSG00000229809	chromatin interactions
ENSG00000261588	chromatin interactions
ENSG00000156860	chromatin interactions
ZMYM2	miRNA target sites

Extended variants
information (count: 137 )
Associated
traits (count: 118 )

Variant overlapped rSNPs/rCNVs (count:137 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562722857	chr16:30547086-30547087	Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
2	rs529813812	chr16:30547093-30547094	Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
3	rs371063022	chr16:30547102-30547103	Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
4	rs548670091	chr16:30547127-30547128	Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
5	rs566577462	chr16:30547130-30547131	Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
6	rs527775248	chr16:30547150-30547151	Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	18 gene(s)	Overlapped CNVs	n/a
7	rs552192168	chr16:30547219-30547220	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	18 gene(s)	Overlapped CNVs	n/a
8	rs576130741	chr16:30547284-30547285	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	18 gene(s)	Overlapped CNVs	n/a
9	rs185146702	chr16:30547322-30547323	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	18 gene(s)	Overlapped CNVs	n/a
10	rs144151548	chr16:30547388-30547389	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	17 gene(s)	Overlapped CNVs	n/a
11	rs189031935	chr16:30547444-30547445	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	17 gene(s)	Overlapped CNVs	n/a
12	rs535634868	chr16:30547458-30547459	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	17 gene(s)	Overlapped CNVs	n/a
13	rs554708981	chr16:30547513-30547514	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	16 gene(s)	Overlapped CNVs	n/a
14	rs28563803	chr16:30547593-30547594	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
15	rs573023281	chr16:30547600-30547601	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
16	rs181739756	chr16:30547639-30547640	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
17	rs374444160	chr16:30547645-30547646	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
18	rs558623944	chr16:30547649-30547650	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
19	rs576889184	chr16:30547703-30547704	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
20	rs200580274	chr16:30547732-30547733	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
21	rs547200590	chr16:30547766-30547767	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	16 gene(s)	Overlapped CNVs	n/a
22	rs56404031	chr16:30547787-30547788	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	16 gene(s)	Overlapped CNVs	n/a
23	rs368805646	chr16:30547799-30547800	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	16 gene(s)	Overlapped CNVs	n/a
24	rs145046829	chr16:30547800-30547801	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	16 gene(s)	Overlapped CNVs	n/a
25	rs536735654	chr16:30547811-30547812	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	16 gene(s)	Overlapped CNVs	n/a
26	rs111235386	chr16:30547822-30547823	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	16 gene(s)	Overlapped CNVs	n/a
27	rs541703386	chr16:30547859-30547860	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	16 gene(s)	Overlapped CNVs	n/a
28	rs559904908	chr16:30547886-30547887	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	16 gene(s)	Overlapped CNVs	n/a
29	rs184747586	chr16:30547887-30547888	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	16 gene(s)	Overlapped CNVs	n/a
30	rs552230920	chr16:30547900-30547901	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	16 gene(s)	Overlapped CNVs	n/a
31	rs142163571	chr16:30547929-30547930	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	16 gene(s)	Overlapped CNVs	n/a
32	rs531573224	chr16:30547940-30547941	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	16 gene(s)	Overlapped CNVs	n/a
33	rs368632775	chr16:30547961-30547962	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	16 gene(s)	Overlapped CNVs	n/a
34	rs151281055	chr16:30547964-30547965	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	14 gene(s)	Overlapped CNVs	n/a
35	rs141635519	chr16:30547978-30547979	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	14 gene(s)	Overlapped CNVs	n/a
36	rs371916669	chr16:30547986-30547987	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	14 gene(s)	Overlapped CNVs	n/a
37	rs147053918	chr16:30548006-30548007	Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	14 gene(s)	Overlapped CNVs	n/a
38	rs564586304	chr16:30548060-30548061	Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	14 gene(s)	Overlapped CNVs	n/a
39	rs376400311	chr16:30548123-30548124	Weak transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a
40	rs548052564	chr16:30548135-30548136	Weak transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a
41	rs138319935	chr16:30548149-30548150	Weak transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a
42	rs533905475	chr16:30548207-30548208	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a
43	rs369670945	chr16:30548220-30548221	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a
44	rs576779060	chr16:30548221-30548222	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a
45	rs142319603	chr16:30548319-30548320	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	10 gene(s)	Overlapped CNVs	n/a
46	rs72793342	chr16:30548352-30548353	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs371946369	chr16:30548362-30548363	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	10 gene(s)	Overlapped CNVs	n/a
48	rs188126241	chr16:30548384-30548385	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a
49	rs114401126	chr16:30548447-30548448	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a
50	rs559943542	chr16:30548489-30548490	Weak transcription Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:118)

Disease	PMID	Source
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	17603634	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
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
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Mental retardation	19951919	CNVD
Colorectal cancer	16272173	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Bladder cancer	21909424	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21990379	CNVD
Astrocytoma	22246337	CNVD
Myelofibrosis	22110671	CNVD
Epilepsy	22499536	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Austim spectrum disorder	21302340	CNVD
Autism	22513405	CNVD
Autism	22958593	CNVD
Autism	18184952	CNVD
Autism	19966786	CNVD
Autism	21394203	CNVD
Autism	21969575	CNVD
Autism	22241247	CNVD
Autism	20970697	CNVD
Autism	20942916	CNVD
Epilepsy	20970697	CNVD
Intellectual disability	22045946	CNVD
Mental retardation	19966786	CNVD
Developmental delay	20808231	CNVD
Obesity	20808231	CNVD
Autism	18923514	CNVD
Obesity	21881559	CNVD
Obesity	21956041	CNVD
Autism	20659124	CNVD
Mental retardation	21062444	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	22885689	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	20970697	CNVD
Schizophrenia	20433910	CNVD
Schizophrenia	22241247	CNVD
Autism	19242545	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Intracranial ependymoma	16609018	CNVD
Schizophrenia	21399695	CNVD
Autism	21956041	CNVD
Disorders of sex development	21048976	CNVD
Autism	22067053	CNVD
Autism	18156158	CNVD
Mental retardation	20152051	CNVD
Autism	19218893	CNVD
Autism	21289514	CNVD
Schizophrenia	19855392	CNVD
neurodevelopmental Syndrome	20503337	CNVD
Benign familial neonatal-infantile seizures	21060786	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Cancer	21183584	CNVD
Low-grade fibromyxoid sarcoma	21536545	CNVD
Breast cancer	21045282	CNVD
Neuroblastoma	20406844	CNVD
Autism	19050728	CNVD
Epilepsy	20923578	CNVD
Psychiatric disorder	19050728	CNVD
Schizophrenia	19348701	CNVD
Attention deficit hyperactivity disorder	19097825	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	19571808	CNVD
Breast cancer	20409316	CNVD
Severe combined immunodeficiency	19097825	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Autism	18522746	CNVD
Urothelial carcinoma	21177765	CNVD
Chronic myeloid leukemia	21384125	CNVD
Prostate cancer	18632612	CNVD

Chromatin state (count:360 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:30544600-30547200	Active TSS	HUES48 Cell Line	embryonic stem cell
2	chr16:30544600-30547200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr16:30544600-30547600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr16:30544800-30547400	Active TSS	Pancreatic Islets	Pancreatic Islet
5	chr16:30544800-30547400	Active TSS	Gastric	stomach
6	chr16:30544800-30547600	Active TSS	H9 Cell Line	embryonic stem cell
7	chr16:30544800-30547600	Active TSS	Fetal Kidney	kidney
8	chr16:30544800-30547800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr16:30544800-30547800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr16:30545000-30547200	Active TSS	HUES64 Cell Line	embryonic stem cell
11	chr16:30545000-30547200	Active TSS	iPS-15b Cell Line	embryonic stem cell
12	chr16:30545000-30547200	Active TSS	Pancreas	Pancrea
13	chr16:30545000-30547200	Active TSS	GM12878-XiMat	blood
14	chr16:30545000-30547200	Active TSS	Hela-S3	cervix
15	chr16:30545000-30547400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
16	chr16:30545200-30547200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
17	chr16:30545200-30547200	Active TSS	H1 Cell Line	embryonic stem cell
18	chr16:30545200-30547200	Active TSS	Aorta	Aorta
19	chr16:30545200-30547200	Active TSS	Ovary	ovary
20	chr16:30545200-30547400	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
21	chr16:30545200-30547400	Active TSS	Fetal Brain Female	brain
22	chr16:30545200-30547400	Active TSS	Psoas Muscle	Psoas
23	chr16:30545200-30547400	Active TSS	Small Intestine	intestine
24	chr16:30545200-30547400	Active TSS	HSMMtube	muscle
25	chr16:30545200-30547400	Flanking Active TSS	HUVEC	blood vessel
26	chr16:30545200-30547600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr16:30545200-30547600	Flanking Active TSS	Primary hematopoietic stem cells	blood
28	chr16:30545200-30547600	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
29	chr16:30545200-30547800	Active TSS	ES-I3 Cell Line	embryonic stem cell
30	chr16:30545200-30547800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr16:30545200-30547800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr16:30545400-30547200	Active TSS	iPS-20b Cell Line	embryonic stem cell
33	chr16:30545400-30547200	Active TSS	Primary T helper cells PMA-I stimulated	--
34	chr16:30545400-30547200	Active TSS	Fetal Stomach	stomach
35	chr16:30545400-30547200	Active TSS	Left Ventricle	heart
36	chr16:30545400-30547200	Active TSS	Sigmoid Colon	Sigmoid Colon
37	chr16:30545400-30547400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr16:30545400-30547600	Active TSS	Esophagus	oesophagus
39	chr16:30545600-30547200	Active TSS	Lung	lung
40	chr16:30545600-30547400	Active TSS	Thymus	Thymus
41	chr16:30545800-30547200	Active TSS	Brain Germinal Matrix	brain
42	chr16:30545800-30547200	Active TSS	Fetal Brain Male	brain
43	chr16:30545800-30547600	Flanking Active TSS	K562	blood
44	chr16:30546000-30547200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr16:30546400-30547400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr16:30546400-30547400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
47	chr16:30546400-30547400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
48	chr16:30546400-30547400	Flanking Active TSS	Adipose Nuclei	Adipose
49	chr16:30546400-30547600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr16:30546400-30547600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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