Variant report

Variant	nsv1010802
Chromosome Location	chr3:329018-611720
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1502)
CpG islands
(count:1159)
Chromatin interactive
region (count:43)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:1502 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:418748-419094	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:534692-534822	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:455772-456068	HepG2	liver:	n/a	chr3:455850-455866
4	ATF2	chr3:331761-332103	GM12878	blood:	n/a	n/a
5	BACH1	chr3:541423-541496	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr3:577662-577951	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr3:516562-516874	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr3:462357-462600	GM12878	blood:	n/a	chr3:462485-462494
9	BATF	chr3:462277-462661	GM12878	blood:	n/a	chr3:462485-462494
10	BATF	chr3:341729-341996	GM12878	blood:	n/a	n/a
11	BATF	chr3:599789-600089	GM12878	blood:	n/a	chr3:599953-599962
12	BATF	chr3:505464-505768	GM12878	blood:	n/a	n/a
13	BATF	chr3:599827-600084	GM12878	blood:	n/a	chr3:599953-599962
14	BATF	chr3:515030-515408	GM12878	blood:	n/a	chr3:515252-515263
15	BATF	chr3:515014-515376	GM12878	blood:	n/a	chr3:515252-515263
16	BCLAF1	chr3:599656-600200	GM12878	blood:	n/a	chr3:599779-599788 chr3:599826-599835
17	BHLHE40	chr3:462348-462658	GM12878	blood:	n/a	n/a
18	BHLHE40	chr3:342270-342502	GM12878	blood:	n/a	n/a
19	BHLHE40	chr3:394710-394716	GM12878	blood:	n/a	n/a
20	BHLHE40	chr3:543200-543216	GM12878	blood:	n/a	n/a
21	BHLHE40	chr3:401416-401710	GM12878	blood:	n/a	n/a
22	BRCA1	chr3:467465-468300	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr3:463605-463647	Hela-S3	cervix:	n/a	n/a
24	CBX3	chr3:396059-396404	K562	blood:	n/a	n/a
25	CEBPB	chr3:560575-560880	HepG2	liver:	n/a	chr3:560731-560742
26	CEBPB	chr3:468928-469135	H1-hESC	embryonic stem cell:	n/a	chr3:468996-469009 chr3:469100-469117 chr3:468998-469009
27	CEBPB	chr3:544957-545231	H1-hESC	embryonic stem cell:	n/a	chr3:545063-545076 chr3:545064-545075
28	CEBPB	chr3:534600-534964	HepG2	liver:	n/a	chr3:534767-534778
29	CEBPB	chr3:591255-591764	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr3:466898-468265	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr3:438085-438248	K562	blood:	n/a	chr3:438182-438195 chr3:438184-438193
32	CEBPB	chr3:438001-438370	HepG2	liver:	n/a	chr3:438182-438195 chr3:438184-438193
33	CEBPB	chr3:452366-452605	IMR90	lung:	n/a	chr3:452447-452458
34	CEBPB	chr3:438012-438371	IMR90	lung:	n/a	chr3:438182-438195 chr3:438184-438193
35	CEBPB	chr3:459160-459210	K562	blood:	n/a	chr3:459185-459196
36	CEBPB	chr3:494829-495089	A549	lung:	n/a	n/a
37	CEBPB	chr3:560581-560882	A549	lung:	n/a	chr3:560731-560742
38	CEBPB	chr3:450769-450941	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr3:406009-406340	HepG2	liver:	n/a	chr3:406169-406180 chr3:406169-406182 chr3:406171-406182
40	CEBPB	chr3:450708-451032	IMR90	lung:	n/a	n/a
41	CEBPB	chr3:458278-458461	A549	lung:	n/a	chr3:458369-458380 chr3:458369-458380 chr3:458369-458382 chr3:458369-458382
42	CEBPB	chr3:473256-473490	A549	lung:	n/a	chr3:473347-473358
43	CEBPB	chr3:406067-406268	H1-hESC	embryonic stem cell:	n/a	chr3:406169-406180 chr3:406169-406182 chr3:406171-406182
44	CEBPB	chr3:397430-397763	IMR90	lung:	n/a	n/a
45	CEBPB	chr3:452335-452549	HepG2	liver:	n/a	chr3:452447-452458
46	CEBPB	chr3:544911-545212	IMR90	lung:	n/a	chr3:545063-545076 chr3:545064-545075
47	CEBPB	chr3:450741-451052	HepG2	liver:	n/a	n/a
48	CEBPB	chr3:544919-545200	A549	lung:	n/a	chr3:545063-545076 chr3:545064-545075
49	CEBPB	chr3:544910-545217	Hela-S3	cervix:	n/a	chr3:545063-545076 chr3:545064-545075
50	CEBPB	chr3:438003-438367	A549	lung:	n/a	chr3:438182-438195 chr3:438184-438193

(count:1159 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:427757-427807	HCM	heart:	n/a
2	chr3:353166-353216	A549	lung:	n/a
3	chr3:351003-351053	HEK293	kidney:	embryo
4	chr3:447414-447464	PANC-1	pancreas:	n/a
5	chr3:350503-350553	HRCEpiC	kidney:	n/a
6	chr3:353166-353216	HEEpiC	esophagus:	n/a
7	chr3:577821-577871	GM06990	blood:	n/a
8	chr3:350602-350652	HUVEC	blood vessel:	n/a
9	chr3:427757-427807	HMEC	breast:	n/a
10	chr3:350503-350553	RPTEC	kidney:	n/a
11	chr3:577964-578014	GM19239	blood:	n/a
12	chr3:577964-578014	HepG2	liver:	n/a
13	chr3:577964-578014	HL-60	blood:	n/a
14	chr3:350789-350839	ProgFib	skin:	n/a
15	chr3:390449-390499	SK-N-SH_RA	brain:	n/a
16	chr3:350789-350839	CMK	blood:	n/a
17	chr3:350503-350553	HCT-116	colon:	n/a
18	chr3:501673-501723	Hela-S3	cervix:	n/a
19	chr3:491979-492029	HMEC	breast:	n/a
20	chr3:353166-353216	SAEC	small airway:	n/a
21	chr3:523375-523425	HMEC	breast:	n/a
22	chr3:577964-578014	MCF-7	breast:	n/a
23	chr3:347869-347919	HCM	heart:	n/a
24	chr3:577821-577871	HEEpiC	esophagus:	n/a
25	chr3:577964-578014	GM12892	blood:	n/a
26	chr3:447414-447464	ovcar-3	ovarian:	n/a
27	chr3:351003-351053	HMEC	breast:	n/a
28	chr3:577629-577679	SAEC	small airway:	n/a
29	chr3:523012-523062	HAEpiC	amniotic membrane:	n/a
30	chr3:523012-523062	NHBE	bronchial:	n/a
31	chr3:577821-577871	HRPEpiC	eye:	n/a
32	chr3:350789-350839	GM06990	blood:	n/a
33	chr3:350789-350839	BE2_C	brain:	n/a
34	chr3:350892-350942	H1-hESC	embryonic stem cell:	embryo
35	chr3:523375-523425	AG04450	lung:	fetal
36	chr3:350503-350553	GM12891	blood:	n/a
37	chr3:350602-350652	NT2-D1	testis:	n/a
38	chr3:347869-347919	HCF	heart:	n/a
39	chr3:577821-577871	U87	brain:	n/a
40	chr3:350789-350839	HCPEpiC	choroid plexus:	n/a
41	chr3:350789-350839	SK-N-SH	brain:	n/a
42	chr3:351003-351053	RPTEC	kidney:	n/a
43	chr3:350682-350732	PANC-1	pancreas:	n/a
44	chr3:427558-427608	Hepatocyte	liver:	n/a
45	chr3:447414-447464	HPAEpiC	pulmonary alveolar:	n/a
46	chr3:577964-578014	PANC-1	pancreas:	n/a
47	chr3:350602-350652	PFSK-1	brain:	n/a
48	chr3:347869-347919	BE2_C	brain:	n/a
49	chr3:353166-353216	AG04450	lung:	fetal
50	chr3:523012-523062	GM12892	blood:	n/a

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:457571..459756-chr3:462210..465015,2	K562	blood:
2	chr3:379607..381981-chr3:384960..386643,2	K562	blood:
3	chr3:84468..85168-chr3:395782..396503,2	MCF-7	breast:
4	chr3:380749..382647-chr3:383286..385545,2	MCF-7	breast:
5	chr3:423895..425881-chr3:427804..430449,2	K562	blood:
6	chr3:426526..428688-chr3:432686..435480,2	K562	blood:
7	chr3:571404..573075-chr3:573790..576325,2	MCF-7	breast:
8	chr3:453296..456199-chr3:456966..458950,2	K562	blood:
9	chr3:323232..326179-chr3:404720..407065,2	K562	blood:
10	chr3:395767..396427-chr3:418920..419430,2	MCF-7	breast:
11	chr3:457571..459756-chr3:462210..465015,2	K562	blood:
12	chr3:84540..85233-chr3:395143..396665,5	MCF-7	breast:
13	chr3:556350..557928-chr3:558208..559835,2	MCF-7	breast:
14	chr3:554700..557337-chr3:557649..560284,2	K562	blood:
15	chr3:565796..568589-chr3:571178..572728,2	K562	blood:
16	chr3:84682..85249-chr3:418773..419384,2	MCF-7	breast:
17	chr3:389768..391549-chr3:394844..396538,2	MCF-7	breast:
18	chr3:389768..391549-chr3:394844..396538,2	MCF-7	breast:
19	chr3:512741..514299-chr3:528430..530623,2	K562	blood:
20	chr3:571404..573075-chr3:573790..576325,2	MCF-7	breast:
21	chr3:188824..190368-chr3:386265..388997,2	MCF-7	breast:
22	chr3:565796..568589-chr3:571178..572728,2	K562	blood:
23	chr3:554700..557337-chr3:557649..560284,2	K562	blood:
24	chr3:556350..557928-chr3:558208..559835,2	MCF-7	breast:
25	chr3:453296..456199-chr3:456966..458950,2	K562	blood:
26	chr3:383287..386050-chr3:389112..391059,2	MCF-7	breast:
27	chr3:379607..381981-chr3:384960..386643,2	K562	blood:
28	chr2:137975660..137976445-chr3:388390..389053,2	MCF-7	breast:
29	chr3:333238..334968-chr3:337821..339342,2	MCF-7	breast:
30	chr3:383287..386050-chr3:389112..391059,2	MCF-7	breast:
31	chr3:333238..334968-chr3:337821..339342,2	MCF-7	breast:
32	chr3:423895..425881-chr3:427804..430449,2	K562	blood:
33	chr3:369627..372241-chr3:375088..376630,2	K562	blood:
34	chr3:512741..514299-chr3:528430..530623,2	K562	blood:
35	chr3:380749..382647-chr3:383286..385545,2	MCF-7	breast:
36	chr3:395767..396427-chr3:418920..419430,2	MCF-7	breast:
37	chr3:86365..87356-chr3:395941..396726,2	MCF-7	breast:
38	chr3:522873..523625-chr3:674344..674995,2	MCF-7	breast:
39	chr3:321596..323780-chr3:337949..340526,2	MCF-7	breast:
40	chr3:369627..372241-chr3:375088..376630,2	K562	blood:
41	chr3:496434..499262-chr3:500586..502601,2	K562	blood:
42	chr3:455533..456082-chr3:893341..894026,2	MCF-7	breast:
43	chr3:496434..499262-chr3:500586..502601,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHL1-3	chr3:577941-579275	NONHSAT087570
2	lnc-CHL1-3	chr3:577936-578010	ENSG00000224957
3	lnc-IL5RA-5	chr3:427386-427478	ENSG00000234661.1
4	lnc-IL5RA-5	chr3:424250-424415	ENSG00000234661.1
5	lnc-CHL1-6	chr3:552914-553010	ucscGeneNc_uc003boy_1
6	lnc-IL5RA-15	chr3:350397-351005	NONHSAT087564
7	lnc-CHL1-6	chr3:608788-608866	ucscGeneNc_uc003boy_1
8	lnc-IL5RA-5	chr3:405518-405706	ENSG00000234661.2
9	lnc-IL5RA-5	chr3:405053-405706	ENSG00000234661.1
10	lnc-IL5RA-5	chr3:415500-415735	ENSG00000234661.2

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	CHL1	hsa-miR-181a-5p	chr3:448562-448584
2	CHL1	hsa-miR-10a-5p	chr3:450171-450192
3	CHL1	hsa-miR-10a-5p	chr3:450185-450191

Variant related genes	Relation type
RNU6-1194P	TF binding region
RPS8P6	TF binding region
CHL1-AS1	TF binding region
ENSG00000224957	TF binding region
CHL1	TF binding region
RNU6-1194P	CpG island
RPS8P6	CpG island
CHL1-AS1	CpG island
ENSG00000224957	CpG island
CHL1	CpG island
ENSG00000234661	chromatin interactions
ENSG00000252017	chromatin interactions
DCBLD2	miRNA target sites

Extended variants
information (count: 10946 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:10946 , 50 per page) page: 1 2 3 4 5 6 7 ... 219

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs76152911	chr3:329030-329031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs145400796	chr3:329033-329034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs531495235	chr3:329039-329040	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs550107598	chr3:329040-329041	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs188688119	chr3:329063-329064	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs17274959	chr3:329106-329107	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs193045166	chr3:329169-329170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs35410090	chr3:329185-329186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs565619912	chr3:329196-329197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs377750785	chr3:329210-329211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs73815830	chr3:329260-329261	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs149207332	chr3:329262-329263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs570638682	chr3:329288-329289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs185175206	chr3:329290-329291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs370251229	chr3:329306-329307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs567858910	chr3:329321-329322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs538103611	chr3:329338-329339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs556460389	chr3:329346-329347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs143395053	chr3:329347-329348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs538631811	chr3:329414-329415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs554162170	chr3:329420-329421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs3933036	chr3:329422-329423	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs191362	chr3:329445-329446	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs331877	chr3:329485-329486	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs568054279	chr3:329511-329512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs576328226	chr3:329525-329526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs331878	chr3:329529-329530	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs373565455	chr3:329530-329531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs565162090	chr3:329539-329540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs147058459	chr3:329542-329543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs547416725	chr3:329551-329552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs368332979	chr3:329552-329553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs559343545	chr3:329554-329555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs138419770	chr3:329560-329561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs548271486	chr3:329574-329575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs577318028	chr3:329593-329594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs538062249	chr3:329594-329595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs549994672	chr3:329597-329598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs35113233	chr3:329614-329615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs376946795	chr3:329645-329646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs533584359	chr3:329659-329660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs571584923	chr3:329663-329664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs190462214	chr3:329673-329674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs182049297	chr3:329679-329680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs572412136	chr3:329685-329686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs557071350	chr3:329699-329700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs141838394	chr3:329716-329717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs150625797	chr3:329731-329732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs78254141	chr3:329741-329742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs186576423	chr3:329748-329749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Cancer	20164920	CNVD
Lung cancer	16618734	CNVD
Autism	18349135	CNVD
Breast cancer	20409316	CNVD
Myelofibrosis	22110671	CNVD
Autism	22241247	CNVD
Intellectual disability	22045946	CNVD
Squamous cell cancer	19607727	CNVD
Gastric adenocarcinoma	19115996	CNVD
sporadic birth defects	19047251	CNVD
Mental retardation	17124404	CNVD
abnormal development	18461090	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Sudden cardiac death	19188705	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	21720365	CNVD
Neuroblastoma	18923191	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	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
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
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	20967226	CNVD
Autism	22543975	CNVD
Attention deficit hyperactivity disorder	19546859	CNVD
lymphocytic leukemia	21291569	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Tetralogy of Fallot	22912587	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	20685689	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:815 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:326400-331600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr3:326600-336200	Weak transcription	Fetal Brain Female	brain
3	chr3:330000-334400	Weak transcription	Esophagus	oesophagus
4	chr3:330200-330400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr3:330200-330400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr3:330200-330400	Enhancers	Primary B cells from peripheral blood	blood
7	chr3:330200-330400	Enhancers	Fetal Brain Male	brain
8	chr3:330400-331000	Weak transcription	Primary B cells from peripheral blood	blood
9	chr3:330400-331600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr3:330600-331800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr3:331000-331800	Enhancers	Primary B cells from cord blood	blood
12	chr3:331000-334000	Enhancers	Primary B cells from peripheral blood	blood
13	chr3:331400-331600	Enhancers	GM12878-XiMat	blood
14	chr3:331600-331800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr3:331600-332200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr3:331600-332400	Flanking Active TSS	GM12878-XiMat	blood
17	chr3:331800-332200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr3:331800-332400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr3:331800-332400	Flanking Active TSS	Primary B cells from cord blood	blood
20	chr3:332200-332400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr3:332400-332600	Enhancers	Small Intestine	intestine
22	chr3:332400-333000	Enhancers	GM12878-XiMat	blood
23	chr3:332400-333400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr3:332400-333600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr3:332400-333800	Enhancers	Primary B cells from cord blood	blood
26	chr3:333200-334000	Enhancers	Pancreatic Islets	Pancreatic Islet
27	chr3:333400-334000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr3:333400-334000	Enhancers	Colon Smooth Muscle	Colon
29	chr3:333400-334400	Enhancers	Fetal Lung	lung
30	chr3:333800-334000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr3:333800-338800	Weak transcription	Primary B cells from cord blood	blood
32	chr3:334000-338200	Weak transcription	Primary B cells from peripheral blood	blood
33	chr3:334200-334400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr3:334400-334600	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr3:334400-335800	Enhancers	Esophagus	oesophagus
36	chr3:334600-336400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr3:335800-337000	Enhancers	NHEK	skin
38	chr3:336200-336800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr3:336400-337600	Enhancers	Cortex derived primary cultured neurospheres	brain
40	chr3:336400-337800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr3:336800-337400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr3:338200-340600	Enhancers	Primary B cells from peripheral blood	blood
43	chr3:338800-340400	Enhancers	Primary B cells from cord blood	blood
44	chr3:339400-339800	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr3:340600-341000	Weak transcription	Primary B cells from peripheral blood	blood
46	chr3:341000-341200	Enhancers	Primary B cells from peripheral blood	blood
47	chr3:341200-343000	Weak transcription	Primary B cells from peripheral blood	blood
48	chr3:343000-343200	Enhancers	Primary B cells from peripheral blood	blood
49	chr3:343000-343200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
50	chr3:343200-343600	Weak transcription	Primary B cells from peripheral blood	blood

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