Variant report

Variant	nsv482371
Chromosome Location	chr3:84880813-85031486
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:890)
CpG islands
(count:1526)
Chromatin interactive
region (count:8)
LncRNA
region (count:47)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:890 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr3:84886062-84886466	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF3	chr3:85014321-85014662	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF3	chr3:85014281-85014577	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr3:85008844-85009156	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr3:85007700-85007990	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr3:85011727-85011885	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr3:84954233-84954576	HepG2	liver:	n/a	n/a
8	BRCA1	chr3:85007545-85007619	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr3:84886005-84886347	MCF-7	breast:	n/a	n/a
10	CEBPB	chr3:85016947-85017327	H1-hESC	embryonic stem cell:	n/a	chr3:85017262-85017273
11	CEBPB	chr3:85014296-85014633	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr3:84886127-84886390	ECC-1	luminal epithelium:	n/a	n/a
13	CEBPB	chr3:84930983-84931198	A549	lung:	n/a	n/a
14	CEBPB	chr3:84992560-84992803	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr3:84930981-84931137	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr3:85014267-85014637	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr3:84886016-84886489	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr3:85016899-85017319	Hela-S3	cervix:	n/a	chr3:85017262-85017273
19	CEBPB	chr3:84958813-84959139	HepG2	liver:	n/a	chr3:84958954-84958965
20	CEBPB	chr3:85010675-85010724	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr3:84958863-84959065	A549	lung:	n/a	chr3:84958954-84958965
22	CEBPB	chr3:84886070-84886388	HepG2	liver:	n/a	n/a
23	CHD1	chr3:85016866-85017054	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD1	chr3:85009160-85009452	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD1	chr3:85007333-85007372	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD1	chr3:85008169-85008877	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD1	chr3:85007777-85007910	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr3:84886026-84886697	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr3:85007616-85008518	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr3:85007816-85008169	HepG2	liver:	n/a	n/a
31	CHD2	chr3:85007823-85008268	GM12878	blood:	n/a	n/a
32	CHD2	chr3:85007701-85008149	K562	blood:	n/a	n/a
33	CHD2	chr3:85008771-85009363	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr3:85007748-85008250	Hela-S3	cervix:	n/a	n/a
35	CREB1	chr3:85014249-85014675	H1-hESC	embryonic stem cell:	n/a	n/a
36	CREB1	chr3:85014243-85014716	H1-hESC	embryonic stem cell:	n/a	n/a
37	CREB1	chr3:85007924-85008243	A549	lung:	n/a	n/a
38	CTBP2	chr3:85008265-85009372	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr3:85007720-85007870	AoAF	blood vessel:	n/a	chr3:85007805-85007821 chr3:85007804-85007822 chr3:85007806-85007819
40	CTCF	chr3:84992580-84992730	GM12866	blood:	n/a	chr3:84992712-84992725 chr3:84992709-84992727 chr3:84992712-84992721
41	CTCF	chr3:85012360-85012510	WERI-Rb-1	eye:	n/a	n/a
42	CTCF	chr3:85014380-85014530	HMEC	breast:	n/a	n/a
43	CTCF	chr3:85014380-85014530	HPF	lung:	n/a	n/a
44	CTCF	chr3:85007969-85007973	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr3:85023640-85023790	MCF-7	breast:	n/a	n/a
46	CTCF	chr3:85023540-85023690	MCF-7	breast:	n/a	n/a
47	CTCF	chr3:85014340-85014490	A549	lung:	n/a	n/a
48	CTCF	chr3:84992600-84992750	WERI-Rb-1	eye:	n/a	chr3:84992712-84992725 chr3:84992711-84992732 chr3:84992709-84992727 chr3:84992712-84992721
49	CTCF	chr3:85014322-85014463	K562	blood:	n/a	n/a
50	CTCF	chr3:85007740-85007890	HEEpiC	esophagus:	n/a	chr3:85007805-85007821 chr3:85007804-85007822 chr3:85007806-85007819

(count:1526 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:85007992-85008042	LNCaP	prostate:	n/a
2	chr3:85007992-85008042	LNCaP	prostate:	n/a
3	chr3:85008828-85008878	IMR90	lung:	fetal
4	chr3:85010606-85010656	HEEpiC	esophagus:	n/a
5	chr3:85007959-85008009	PrEC	prostate:	n/a
6	chr3:84909261-84909311	RPTEC	kidney:	n/a
7	chr3:85007894-85007944	GM06990	blood:	n/a
8	chr3:85008061-85008111	HIPEpiC	eye:	n/a
9	chr3:85017543-85017593	SK-N-MC	brain:	n/a
10	chr3:85008105-85008155	NH-A	brain:	n/a
11	chr3:84919226-84919276	AG04450	lung:	fetal
12	chr3:85007817-85007867	AG09309	skin:	n/a
13	chr3:85010677-85010727	HCF	heart:	n/a
14	chr3:84909261-84909311	HEK293	kidney:	embryo
15	chr3:85006115-85006165	T-47D	breast:	n/a
16	chr3:85011052-85011102	PANC-1	pancreas:	n/a
17	chr3:85008061-85008111	U87	brain:	n/a
18	chr3:85005177-85005227	NB4	blood:	n/a
19	chr3:85008156-85008206	HCPEpiC	choroid plexus:	n/a
20	chr3:85010677-85010727	HCPEpiC	choroid plexus:	n/a
21	chr3:85008105-85008155	AG10803	skin:	n/a
22	chr3:84919438-84919488	NT2-D1	testis:	n/a
23	chr3:85008828-85008878	SK-N-SH_RA	brain:	n/a
24	chr3:84919438-84919488	SKMC	muscle:	n/a
25	chr3:85008156-85008206	GM12891	blood:	n/a
26	chr3:85010677-85010727	AG09319	gingival:	n/a
27	chr3:84919226-84919276	NT2-D1	testis:	n/a
28	chr3:84909261-84909311	IMR90	lung:	fetal
29	chr3:85011052-85011102	HCF	heart:	n/a
30	chr3:85007817-85007867	U87	brain:	n/a
31	chr3:85007894-85007944	HL-60	blood:	n/a
32	chr3:85007894-85007944	BJ	skin:	n/a
33	chr3:85007992-85008042	A549	lung:	n/a
34	chr3:85011052-85011102	SK-N-SH	brain:	n/a
35	chr3:85008156-85008206	K562	blood:	n/a
36	chr3:85007959-85008009	PFSK-1	brain:	n/a
37	chr3:84909261-84909311	AG04450	lung:	fetal
38	chr3:85006115-85006165	NHBE	bronchial:	n/a
39	chr3:85007894-85007944	AG10803	skin:	n/a
40	chr3:85008786-85008836	HPAEpiC	pulmonary alveolar:	n/a
41	chr3:84885990-84886040	HAEpiC	amniotic membrane:	n/a
42	chr3:85010606-85010656	HUVEC	blood vessel:	n/a
43	chr3:85008828-85008878	U87	brain:	n/a
44	chr3:85007992-85008042	HAEpiC	amniotic membrane:	n/a
45	chr3:85007959-85008009	LNCaP	prostate:	n/a
46	chr3:84919438-84919488	GM12891	blood:	n/a
47	chr3:85008156-85008206	HCT-116	colon:	n/a
48	chr3:84885990-84886040	HCF	heart:	n/a
49	chr3:85008828-85008878	SAEC	small airway:	n/a
50	chr3:85007817-85007867	AG10803	skin:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:85011548..85014009-chr3:85014905..85018347,3	MCF-7	breast:
2	chr3:84992684..84993232-chr3:85391799..85392321,2	MCF-7	breast:
3	chr3:85029590..85031359-chr3:85035312..85037118,2	K562	blood:
4	chr3:84994697..84996927-chr3:85551100..85552839,2	K562	blood:
5	chr3:85011548..85014009-chr3:85014905..85018347,3	MCF-7	breast:
6	chr3:84968846..84970373-chr6:74221820..74224403,2	K562	blood:
7	chr3:85023240..85023756-chr3:85409642..85410352,2	MCF-7	breast:
8	chr3:84967378..84970376-chr6:74219853..74222987,3	MCF-7	breast:

(count:47 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-VGLL3-9	chr3:85001119-85001416	ucscGeneNc_uc003dqi_2
2	lnc-VGLL3-6	chr3:84912857-84913156	ENSG00000242641.1
3	lnc-VGLL3-6	chr3:84918429-84918637	NONHSAT090652
4	lnc-VGLL3-6	chr3:84912367-84912587	ENSG00000242641.1
5	lnc-VGLL3-9	chr3:84994564-84994662	ucscGeneNc_uc003dqi_2
6	lnc-VGLL3-6	chr3:84903093-84903166	ENSG00000242641.1
7	lnc-VGLL3-6	chr3:84911874-84911972	NONHSAT090649
8	lnc-CHMP2B-6	chr3:85009248-85009589	NONHSAT090658
9	lnc-CHMP2B-6	chr3:85008741-85008787	NONHSAT090657
10	lnc-VGLL3-6	chr3:84908966-84909074	ENSG00000242641.1
11	lnc-VGLL3-6	chr3:84911874-84911972	ENSG00000242641.1
12	lnc-CADM2-1	chr3:84942082-84942116	NONHSAT090654
13	lnc-VGLL3-9	chr3:84985783-84985856	ucscGeneNc_uc003dqi_2
14	lnc-VGLL3-9	chr3:85000744-85000865	ucscGeneNc_uc003dqi_2
15	lnc-CADM2-1	chr3:84934086-84934274	NONHSAT090654
16	lnc-CHMP2B-6	chr3:85008140-85008643	NONHSAT090657
17	lnc-VGLL3-6	chr3:84930640-84930830	ENSG00000242641.1
18	lnc-VGLL3-6	chr3:84917749-84917819	NONHSAT090652
19	lnc-VGLL3-9	chr3:84921479-84921613	ucscGeneNc_uc003dqi_2
20	lnc-VGLL3-6	chr3:84918054-84918175	NONHSAT090649
21	lnc-VGLL3-6	chr3:84917279-84917406	ENSG00000242641.1
22	lnc-VGLL3-9	chr3:85000439-85000509	ucscGeneNc_uc003dqi_2
23	lnc-VGLL3-6	chr3:84912367-84912587	NONHSAT090649
24	lnc-CADM2-1	chr3:84934087-84934274	XLOC_002723
25	lnc-VGLL3-6	chr3:84917749-84917819	NONHSAT090649
26	lnc-VGLL3-9	chr3:84924009-84924132	ucscGeneNc_uc003dqi_2
27	lnc-VGLL3-6	chr3:84903093-84903166	NONHSAT090649
28	lnc-VGLL3-6	chr3:84917933-84917994	ENSG00000242641.1
29	lnc-CADM2-1	chr3:84942083-84942116	XLOC_002723
30	lnc-CADM2-1	chr3:84942392-84942530	NONHSAT090654
31	lnc-VGLL3-6	chr3:84917749-84917819	ENSG00000242641.1
32	lnc-VGLL3-6	chr3:84917749-84917819	ENSG00000242641.1
33	lnc-VGLL3-9	chr3:84995547-84995846	ucscGeneNc_uc003dqi_2
34	lnc-VGLL3-6	chr3:84918054-84918175	ENSG00000242641.1
35	lnc-VGLL3-6	chr3:84918054-84918175	NONHSAT090652
36	lnc-VGLL3-9	chr3:84991656-84991764	ucscGeneNc_uc003dqi_2
37	lnc-VGLL3-9	chr3:84995057-84995277	ucscGeneNc_uc003dqi_2
38	lnc-VGLL3-6	chr3:84918429-84918726	NONHSAT090649
39	lnc-VGLL3-6	chr3:84917749-84917819	ENSG00000242641.1
40	lnc-VGLL3-6	chr3:84918054-84918175	ENSG00000242641.1
41	lnc-CHMP2B-6	chr3:85008156-85008819	NONHSAT090658
42	lnc-VGLL3-6	chr3:84918429-84918726	ENSG00000242641.1
43	lnc-VGLL3-6	chr3:84918742-84918779	ENSG00000242641.1
44	lnc-VGLL3-6	chr3:84912387-84912587	NONHSAT090652
45	lnc-VGLL3-6	chr3:84908966-84909074	NONHSAT090649
46	lnc-VGLL3-6	chr3:84912857-84913156	NONHSAT090649
47	lnc-CADM2-1	chr3:84942393-84942530	XLOC_002723

No data

Variant related genes	Relation type
ENSG00000266025	TF binding region
CADM2	TF binding region
ENSG00000242339	TF binding region
LINC00971	TF binding region
ENSG00000266025	CpG island
CADM2	CpG island
ENSG00000242339	CpG island
LINC00971	CpG island
THAP6	miRNA target sites
TCEAL1	miRNA target sites
YES1	miRNA target sites

Extended variants
information (count: 2077 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:2077 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576937981	chr3:84882080-84882081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs544170324	chr3:84882097-84882098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs78976348	chr3:84882098-84882099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs193029240	chr3:84882116-84882117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs450335	chr3:84882132-84882133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs608760	chr3:84882133-84882134	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs542156941	chr3:84882156-84882157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs184574617	chr3:84882172-84882173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs370192785	chr3:84882191-84882192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs546362912	chr3:84882198-84882199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs571287259	chr3:84882219-84882220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs374205909	chr3:84882246-84882247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs532266784	chr3:84882294-84882295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs187446721	chr3:84882358-84882359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs191824077	chr3:84882388-84882389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs560833243	chr3:84882389-84882390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs529903392	chr3:84882413-84882414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs554897691	chr3:84882477-84882478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs9838751	chr3:84882491-84882492	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs184324127	chr3:84882498-84882499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs558491933	chr3:84882534-84882535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs76590373	chr3:84882538-84882539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs188665369	chr3:84882561-84882562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs556129695	chr3:84882631-84882632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs4380419	chr3:84882758-84882759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs539136202	chr3:84882804-84882805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs546418773	chr3:84882819-84882820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs138604478	chr3:84882874-84882875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs181693267	chr3:84882880-84882881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs1248842	chr3:84882896-84882897	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs546350939	chr3:84882924-84882925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs564672957	chr3:84882953-84882954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs532207662	chr3:84882997-84882998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs548147578	chr3:84883046-84883047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs372892644	chr3:84883076-84883077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs201674764	chr3:84883080-84883081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs148356362	chr3:84883081-84883082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs141694177	chr3:84883109-84883110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs185112204	chr3:84883124-84883125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs569872630	chr3:84883137-84883138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs532118984	chr3:84883141-84883142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs533846090	chr3:84883205-84883206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs552305671	chr3:84883231-84883232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs76997666	chr3:84883260-84883261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs115535119	chr3:84883276-84883277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs556265048	chr3:84883307-84883308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs190720052	chr3:84883323-84883324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs574478332	chr3:84883347-84883348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs147033271	chr3:84883391-84883392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs553900957	chr3:84883395-84883396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Melanoma	18172304	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Acute myeloid leukemia	20729466	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Metanephric adenoma	20802469	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Wilms tumour	21544195	CNVD
Colorectal cancer	16272173	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Soft tissue tumor	16732325	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Neurodevelopmental disorder	22521361	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Mental retardation	17124404	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
craniofacial dysmorphism	21918468	CNVD
Schizophrenia	23813976	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Autism	22102821	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:887 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:84882000-84884800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr3:84883200-84887200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr3:84883400-84884000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
4	chr3:84883400-84884200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
5	chr3:84884000-84885800	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr3:84884200-84884600	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr3:84884600-84885200	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr3:84884600-84885400	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr3:84884600-84886800	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr3:84884600-84886800	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr3:84884600-84886800	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr3:84884600-84887200	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr3:84884800-84886800	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr3:84885200-84885600	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr3:84885400-84885800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
16	chr3:84885600-84886800	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr3:84885800-84886000	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr3:84885800-84886200	Enhancers	H9 Cell Line	embryonic stem cell
19	chr3:84885800-84886200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr3:84885800-84886800	Enhancers	H1 Cell Line	embryonic stem cell
21	chr3:84886000-84886200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
22	chr3:84886000-84886800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr3:84886200-84886400	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr3:84886200-84886600	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr3:84886200-84886600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr3:84886200-84890600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr3:84886400-84886800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
28	chr3:84886600-84886800	Enhancers	H9 Cell Line	embryonic stem cell
29	chr3:84886800-84889000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
30	chr3:84886800-84890600	Weak transcription	HUES48 Cell Line	embryonic stem cell
31	chr3:84886800-84890600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
32	chr3:84886800-84891000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
33	chr3:84886800-84891000	Weak transcription	H9 Cell Line	embryonic stem cell
34	chr3:84886800-84891000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
35	chr3:84886800-84891200	Weak transcription	H1 Cell Line	embryonic stem cell
36	chr3:84887200-84890400	Weak transcription	HUES64 Cell Line	embryonic stem cell
37	chr3:84887400-84887600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr3:84889000-84889200	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr3:84889200-84889600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
40	chr3:84889600-84889800	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr3:84889800-84890800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
42	chr3:84890400-84891200	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr3:84890600-84891400	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr3:84890600-84891400	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr3:84890600-84892200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr3:84890800-84891400	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr3:84891000-84891200	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr3:84891000-84891400	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr3:84891000-84891400	Enhancers	H9 Cell Line	embryonic stem cell
50	chr3:84891200-84891600	Enhancers	H1 Cell Line	embryonic stem cell

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