Variant report

Variant	nsv428747
Chromosome Location	chr3:162883968-163033938
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:231)
CpG islands
(count:61)
Chromatin interactive
region (count:10)
LncRNA
region (count:65)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:231 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:163005669-163005678	K562	blood:	n/a	n/a
2	CBX3	chr3:163024140-163024571	HCT-116	colon:	n/a	n/a
3	CEBPB	chr3:162932427-162932441	A549	lung:	n/a	n/a
4	CEBPB	chr3:163004712-163004916	K562	blood:	n/a	chr3:163004841-163004852 chr3:163004841-163004850 chr3:163004841-163004850 chr3:163004839-163004852 chr3:163004841-163004850 chr3:163004841-163004850 chr3:163004839-163004852 chr3:163004839-163004852 chr3:163004839-163004850
5	CEBPB	chr3:163004791-163004858	H1-hESC	embryonic stem cell:	n/a	chr3:163004841-163004852 chr3:163004841-163004850 chr3:163004841-163004850 chr3:163004839-163004852 chr3:163004841-163004850 chr3:163004841-163004850 chr3:163004839-163004852 chr3:163004839-163004852 chr3:163004839-163004850
6	CEBPB	chr3:162929432-162929720	Hela-S3	cervix:	n/a	chr3:162929588-162929605 chr3:162929590-162929601 chr3:162929560-162929571 chr3:162929562-162929573
7	CEBPB	chr3:162932325-162932463	IMR90	lung:	n/a	n/a
8	CEBPB	chr3:162932353-162932482	K562	blood:	n/a	n/a
9	CEBPB	chr3:162897199-162897419	A549	lung:	n/a	n/a
10	CEBPB	chr3:163004717-163004994	IMR90	lung:	n/a	chr3:163004841-163004852 chr3:163004841-163004850 chr3:163004841-163004850 chr3:163004839-163004852 chr3:163004841-163004850 chr3:163004841-163004850 chr3:163004839-163004852 chr3:163004839-163004852 chr3:163004839-163004850
11	CEBPB	chr3:162929413-162929748	A549	lung:	n/a	chr3:162929588-162929605 chr3:162929590-162929601 chr3:162929560-162929571 chr3:162929562-162929573
12	CEBPB	chr3:163016685-163016894	A549	lung:	n/a	n/a
13	CEBPB	chr3:162929418-162929759	HepG2	liver:	n/a	chr3:162929588-162929605 chr3:162929590-162929601 chr3:162929560-162929571 chr3:162929562-162929573
14	CEBPB	chr3:162929409-162929718	IMR90	lung:	n/a	chr3:162929588-162929605 chr3:162929590-162929601 chr3:162929560-162929571 chr3:162929562-162929573
15	CEBPB	chr3:162929417-162929749	K562	blood:	n/a	chr3:162929588-162929605 chr3:162929590-162929601 chr3:162929560-162929571 chr3:162929562-162929573
16	CEBPB	chr3:162978995-162979027	K562	blood:	n/a	n/a
17	CEBPB	chr3:162995031-162995257	A549	lung:	n/a	chr3:162995163-162995176
18	CEBPB	chr3:163004771-163005007	HepG2	liver:	n/a	chr3:163004841-163004852 chr3:163004841-163004850 chr3:163004841-163004850 chr3:163004839-163004852 chr3:163004841-163004850 chr3:163004841-163004850 chr3:163004839-163004852 chr3:163004839-163004852 chr3:163004839-163004850
19	CEBPB	chr3:162893798-162893837	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr3:162984654-162984921	GM12878	blood:	n/a	n/a
21	CHD2	chr3:162976142-162976148	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD2	chr3:162900110-162900118	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr3:162991580-162991730	HEEpiC	esophagus:	n/a	n/a
24	CTCF	chr3:162991540-162991690	Caco-2	colon:	n/a	n/a
25	CTCF	chr3:162968471-162968556	GM20000	blood:	n/a	n/a
26	CTCF	chr3:162991580-162991730	A549	lung:	n/a	n/a
27	CTCF	chr3:162991580-162991730	BE2_C	brain:	n/a	n/a
28	CTCF	chr3:162991675-162991692	HepG2	liver:	n/a	n/a
29	CTCF	chr3:162888037-162888039	GM13976	blood:	n/a	n/a
30	CTCF	chr3:162991625-162991739	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr3:162917440-162917590	AG09319	gingival:	n/a	n/a
32	CTCF	chr3:162953064-162953107	Spleen_OC	spleen:	n/a	n/a
33	CTCF	chr3:162991660-162991810	HA-sp	spinal cord:	n/a	n/a
34	CTCF	chr3:162991640-162991790	WERI-Rb-1	eye:	n/a	n/a
35	CTCF	chr3:162991616-162991751	LNCaP	prostate:	n/a	n/a
36	CTCF	chr3:162991541-162991829	GM12878	blood:	n/a	n/a
37	CTCF	chr3:162991600-162991750	MCF-7	breast:	n/a	n/a
38	CTCF	chr3:162884766-162884837	Lung_OC	lung:	n/a	n/a
39	CTCF	chr3:162946522-162946561	GM20000	blood:	n/a	n/a
40	CTCF	chr3:162991404-162991910	MCF-7	breast:	n/a	n/a
41	CTCF	chr3:163002704-163002730	GM20000	blood:	n/a	n/a
42	CTCF	chr3:162887978-162888033	GM13976	blood:	n/a	n/a
43	CTCF	chr3:162991630-162991752	LNCaP	prostate:	n/a	n/a
44	CTCF	chr3:162973547-162973685	Medullo	brain:	n/a	chr3:162973613-162973621 chr3:162973609-162973625 chr3:162973610-162973631
45	CTCF	chr3:162884697-162884750	GM20000	blood:	n/a	n/a
46	CTCF	chr3:163018869-163018905	GM20000	blood:	n/a	n/a
47	CTCF	chr3:162987299-162987376	Lung_OC	lung:	n/a	n/a
48	CTCF	chr3:162991580-162991730	MCF-7	breast:	n/a	n/a
49	CTCF	chr3:163009617-163009656	GM10248	blood:	n/a	n/a
50	CTCF	chr3:162991447-162991896	MCF-7	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:163021378-163021428	HUVEC	blood vessel:	n/a
2	chr3:163021378-163021428	Caco-2	colon:	n/a
3	chr3:163021378-163021428	SKMC	muscle:	n/a
4	chr3:163021378-163021428	SK-N-MC	brain:	n/a
5	chr3:163021378-163021428	Hepatocyte	liver:	n/a
6	chr3:163021378-163021428	T-47D	breast:	n/a
7	chr3:163021378-163021428	ECC-1	luminal epithelium:	n/a
8	chr3:163021378-163021428	HEK293	kidney:	embryo
9	chr3:163021378-163021428	NT2-D1	testis:	n/a
10	chr3:163021378-163021428	GM12891	blood:	n/a
11	chr3:163021378-163021428	HCM	heart:	n/a
12	chr3:163021378-163021428	CMK	blood:	n/a
13	chr3:163021378-163021428	ovcar-3	ovarian:	n/a
14	chr3:163021378-163021428	Hela-S3	cervix:	n/a
15	chr3:163021378-163021428	NHBE	bronchial:	n/a
16	chr3:163021378-163021428	HRE	kidney:	n/a
17	chr3:163021378-163021428	HAEpiC	amniotic membrane:	n/a
18	chr3:163021378-163021428	BE2_C	brain:	n/a
19	chr3:163021378-163021428	HEEpiC	esophagus:	n/a
20	chr3:163021378-163021428	GM06990	blood:	n/a
21	chr3:163021378-163021428	GM19239	blood:	n/a
22	chr3:163021378-163021428	AG10803	skin:	n/a
23	chr3:163021378-163021428	SK-N-SH	brain:	n/a
24	chr3:163021378-163021428	IMR90	lung:	fetal
25	chr3:163021378-163021428	AG09319	gingival:	n/a
26	chr3:163021378-163021428	HepG2	liver:	n/a
27	chr3:163021378-163021428	HCF	heart:	n/a
28	chr3:163021378-163021428	MCF-7	breast:	n/a
29	chr3:163021378-163021428	NH-A	brain:	n/a
30	chr3:163021378-163021428	K562	blood:	n/a
31	chr3:163021378-163021428	AoSMC	blood vessel:	n/a
32	chr3:163021378-163021428	AG04450	lung:	fetal
33	chr3:163021378-163021428	AG04449	skin:	fetal
34	chr3:163021378-163021428	HIPEpiC	eye:	n/a
35	chr3:163021378-163021428	Jurkat	blood:	n/a
36	chr3:163021378-163021428	SAEC	small airway:	n/a
37	chr3:163021378-163021428	HCPEpiC	choroid plexus:	n/a
38	chr3:163021378-163021428	GM12892	blood:	n/a
39	chr3:163021378-163021428	HRPEpiC	eye:	n/a
40	chr3:163021378-163021428	U87	brain:	n/a
41	chr3:163021378-163021428	BJ	skin:	n/a
42	chr3:163021378-163021428	HNPCEpiC	eye:	n/a
43	chr3:163021378-163021428	SK-N-SH_RA	brain:	n/a
44	chr3:163021378-163021428	PrEC	prostate:	n/a
45	chr3:163021378-163021428	RPTEC	kidney:	n/a
46	chr3:163021378-163021428	PFSK-1	brain:	n/a
47	chr3:163021378-163021428	NHDF-neo	bronchial:	n/a
48	chr3:163021378-163021428	MCF10A-Er-Src	breast:	n/a
49	chr3:163021378-163021428	HPAEpiC	pulmonary alveolar:	n/a
50	chr3:163021378-163021428	LNCaP	prostate:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:162924888..162927929-chr3:162929573..162933579,3	K562	blood:
2	chr3:162965564..162967593-chr3:162971986..162973917,2	K562	blood:
3	chr3:162973215..162973789-chr3:163207913..163208691,2	MCF-7	breast:
4	chr3:162924888..162927929-chr3:162929573..162933579,3	K562	blood:
5	chr3:162965564..162967593-chr3:162971986..162973917,2	K562	blood:
6	chr3:163029844..163032021-chr3:163043055..163045557,2	K562	blood:
7	chr10:69265595..69266499-chr3:162973315..162973821,2	MCF-7	breast:
8	chr3:162774576..162775267-chr3:162991199..162992106,3	MCF-7	breast:
9	chr3:163011480..163014323-chr3:163020834..163023758,2	MCF-7	breast:
10	chr3:162468849..162471720-chr3:162897232..162899564,2	K562	blood:

(count:65 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SI-4	chr3:162917365-162917542	ENSG00000241369
2	lnc-SI-4	chr3:163021026-163021110	ENSG00000241369
3	lnc-SI-4	chr3:163021026-163021105	ENSG00000241369
4	lnc-SI-4	chr3:162996298-162996391	ENSG00000241369
5	lnc-SI-4	chr3:162919326-162919405	ENSG00000241369
6	lnc-SI-4	chr3:162937889-162937975	ENSG00000241369
7	lnc-OTOL1-2	chr3:162948497-162949934	NONHSAT093026
8	lnc-SI-4	chr3:162895689-162895889	ENSG00000241369
9	lnc-SI-4	chr3:162919870-162920037	ENSG00000241369
10	lnc-SI-4	chr3:162900619-162900698	ENSG00000241369
11	lnc-SI-4	chr3:162996298-162996391	ENSG00000241369
12	lnc-SI-4	chr3:162919871-162920037	NONHSAT093037
13	lnc-SI-4	chr3:162919326-162919405	ENSG00000241369
14	lnc-SI-4	chr3:162919326-162919405	ENSG00000241369
15	lnc-SI-4	chr3:162905018-162905052	NONHSAT093031
16	lnc-SI-4	chr3:162996298-162996391	ENSG00000241369
17	lnc-SI-4	chr3:162917363-162917542	ENSG00000241369
18	lnc-SI-4	chr3:162900619-162900716	ENSG00000241369
19	lnc-SI-4	chr3:162937889-162937975	ENSG00000241369
20	lnc-OTOL1-2	chr3:162946486-162946540	ENSG00000241168.1
21	lnc-SI-4	chr3:162992984-162993107	ENSG00000241369
22	lnc-SI-4	chr3:162917416-162917542	ENSG00000241369
23	lnc-SI-4	chr3:162919326-162919405	ENSG00000241369
24	lnc-SI-4	chr3:162917662-162917739	ENSG00000241369
25	lnc-SI-4	chr3:162921206-162921303	ENSG00000241369
26	lnc-SI-4	chr3:162921206-162921298	NONHSAT093037
27	lnc-OTOL1-10	chr3:163021583-163022065	NONHSAT093040
28	lnc-OTOL1-10	chr3:163031456-163031501	NONHSAT093040
29	lnc-SI-4	chr3:162917662-162917719	NONHSAT093031
30	lnc-SI-4	chr3:162992984-162993107	ENSG00000241369
31	lnc-OTOL1-2	chr3:162925763-162925882	NONHSAT093026
32	lnc-SI-4	chr3:162937889-162937975	ENSG00000241369
33	lnc-SI-4	chr3:162919326-162919405	ENSG00000241369
34	lnc-OTOL1-2	chr3:162937866-162937980	ENSG00000241168.1
35	lnc-SI-4	chr3:162936848-162936965	ENSG00000241369
36	lnc-SI-4	chr3:162967053-162967162	ENSG00000241369
37	lnc-OTOL1-2	chr3:162937866-162937980	NONHSAT093026
38	lnc-SI-4	chr3:162917366-162917542	ENSG00000241369
39	lnc-SI-4	chr3:162937889-162937975	ENSG00000241369
40	lnc-SI-4	chr3:163020984-163021076	ENSG00000241369
41	lnc-SI-4	chr3:162917416-162917542	NONHSAT093031
42	lnc-SI-4	chr3:162925431-162925545	ENSG00000241369
43	lnc-SI-4	chr3:162992984-162993107	ENSG00000241369
44	lnc-SI-4	chr3:162917363-162917542	ENSG00000241369
45	lnc-SI-4	chr3:162996298-162996391	ENSG00000241369
46	lnc-SI-4	chr3:162992984-162993107	ENSG00000241369
47	lnc-SI-4	chr3:162996298-162996391	ENSG00000241369
48	lnc-SI-4	chr3:162904856-162905052	ENSG00000241369
49	lnc-SI-4	chr3:162937704-162937975	ENSG00000241369
50	lnc-SI-4	chr3:162996298-162996391	ENSG00000241369

No data

Variant related genes	Relation type
CT64	TF binding region
ENSG00000238398	TF binding region
CT64	CpG island
ENSG00000238398	CpG island
ENSG00000241369	chromatin interactions

Extended variants
information (count: 1293 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:1293 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs552778678	chr3:162889816-162889817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs370782256	chr3:162889847-162889848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs370227461	chr3:162889856-162889857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs373720986	chr3:162889943-162889944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs183502845	chr3:162890011-162890012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs138695682	chr3:162890041-162890042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs149355205	chr3:162890042-162890043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs188573706	chr3:162890048-162890049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs578036786	chr3:162890057-162890058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs544891398	chr3:162890058-162890059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs147473388	chr3:162890066-162890067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs376084011	chr3:162890074-162890075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs181036846	chr3:162890092-162890093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs529929288	chr3:162890114-162890115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs139985324	chr3:162890160-162890161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs563466873	chr3:162890171-162890172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs532385536	chr3:162890175-162890176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs552258387	chr3:162890190-162890191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs565805573	chr3:162890232-162890233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs186331895	chr3:162890255-162890256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs547863489	chr3:162890284-162890285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs143992280	chr3:162890338-162890339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs190399778	chr3:162890368-162890369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs557272863	chr3:162890394-162890395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs181674604	chr3:162890412-162890413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs13094605	chr3:162890453-162890454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs539647304	chr3:162890483-162890484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs553021141	chr3:162890496-162890497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs187566627	chr3:162890498-162890499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs542343098	chr3:162890512-162890513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs555451871	chr3:162890523-162890524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs190898288	chr3:162890529-162890530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs571700303	chr3:162890532-162890533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs543341516	chr3:162890546-162890547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs540676045	chr3:162890558-162890559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs542900684	chr3:162890584-162890585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs147309187	chr3:162890618-162890619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs577085727	chr3:162890622-162890623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs546038185	chr3:162890626-162890627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs182336101	chr3:162890627-162890628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs185131252	chr3:162890651-162890652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs189844111	chr3:162890721-162890722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs56691025	chr3:162890743-162890744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs530538559	chr3:162890870-162890871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs12636618	chr3:162890878-162890879	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs142471187	chr3:162890956-162890957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs532208950	chr3:162890969-162890970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs368556283	chr3:162890979-162890980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs183434757	chr3:162891025-162891026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs150910261	chr3:162891042-162891043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	16608533	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-small cell lung cancer	19010865	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16547154	CNVD
Breast cancer	21364760	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	21785460	CNVD
Sudden cardiac death	19188705	CNVD
Mantle cell lymphoma	19029149	CNVD
Malformation	19546859	CNVD
Schizophrenia	19546859	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
epilepsy	18472482	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Myxofibrosarcoma	16751306	CNVD
Parkinson disease	21907011	CNVD
Bladder cancer	21909424	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:162889800-162894200	Weak transcription	Fetal Heart	heart
2	chr3:162892200-162892400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr3:162892200-162892800	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr3:162892200-162892800	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr3:162892800-162893800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr3:162893800-162894000	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr3:162894200-162895200	Enhancers	Fetal Heart	heart
8	chr3:162904600-162905000	ZNF genes & repeats	Dnd41	blood
9	chr3:162914400-162915000	Enhancers	Dnd41	blood
10	chr3:162936400-162950200	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr3:162947400-162954200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr3:162953800-162954800	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr3:162954200-162954800	Active TSS	ES-I3 Cell Line	embryonic stem cell
14	chr3:162954200-162954800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
15	chr3:162975800-162976200	Enhancers	ES-I3 Cell Line	embryonic stem cell

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