Variant report

Variant	nsv876625
Chromosome Location	chr3:23390301-23509597
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:552)
CpG islands
(count:307)
Chromatin interactive
region (count:36)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:552 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr3:23472393-23472877	GM12878	blood:	n/a	n/a
2	BATF	chr3:23436607-23436931	GM12878	blood:	n/a	chr3:23436755-23436764
3	BATF	chr3:23463964-23464237	GM12878	blood:	n/a	n/a
4	BATF	chr3:23480171-23480448	GM12878	blood:	n/a	n/a
5	BATF	chr3:23480155-23480444	GM12878	blood:	n/a	n/a
6	BCLAF1	chr3:23463910-23464435	GM12878	blood:	n/a	n/a
7	BHLHE40	chr3:23429181-23429214	GM12878	blood:	n/a	n/a
8	BHLHE40	chr3:23446575-23446933	GM12878	blood:	n/a	n/a
9	BRCA1	chr3:23445745-23446118	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr3:23404642-23405196	A549	lung:	n/a	chr3:23404763-23404774
11	CEBPB	chr3:23445735-23446103	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr3:23397720-23397889	Hela-S3	cervix:	n/a	chr3:23397809-23397820
13	CEBPB	chr3:23474391-23474588	HepG2	liver:	n/a	chr3:23474444-23474455
14	CEBPB	chr3:23496565-23496985	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr3:23466068-23466225	A549	lung:	n/a	n/a
16	CEBPB	chr3:23497489-23497638	HepG2	liver:	n/a	chr3:23497512-23497523
17	CEBPB	chr3:23496588-23496982	IMR90	lung:	n/a	n/a
18	CEBPB	chr3:23497275-23497697	A549	lung:	n/a	chr3:23497512-23497523
19	CEBPB	chr3:23497254-23497800	A549	lung:	n/a	chr3:23497512-23497523
20	CEBPB	chr3:23496509-23497059	A549	lung:	n/a	n/a
21	CEBPB	chr3:23466027-23466260	HepG2	liver:	n/a	n/a
22	CEBPB	chr3:23490711-23490952	IMR90	lung:	n/a	n/a
23	CEBPB	chr3:23438328-23438606	Hela-S3	cervix:	n/a	chr3:23438451-23438464 chr3:23438451-23438464 chr3:23438451-23438462
24	CEBPB	chr3:23425510-23425634	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr3:23397764-23397950	HepG2	liver:	n/a	chr3:23397809-23397820
26	CEBPB	chr3:23404659-23405168	HepG2	liver:	n/a	chr3:23404763-23404774
27	CEBPB	chr3:23496572-23497013	MCF-7	breast:	n/a	n/a
28	CEBPB	chr3:23497222-23497725	Hela-S3	cervix:	n/a	chr3:23497512-23497523
29	CEBPB	chr3:23404653-23405172	IMR90	lung:	n/a	chr3:23404763-23404774
30	CEBPB	chr3:23496598-23496966	A549	lung:	n/a	n/a
31	CEBPB	chr3:23466021-23466291	IMR90	lung:	n/a	n/a
32	CEBPB	chr3:23496592-23497016	A549	lung:	n/a	n/a
33	CEBPB	chr3:23490735-23491001	A549	lung:	n/a	n/a
34	CEBPB	chr3:23438342-23438564	A549	lung:	n/a	chr3:23438451-23438464 chr3:23438451-23438464 chr3:23438451-23438462
35	CEBPB	chr3:23490782-23490938	K562	blood:	n/a	n/a
36	CEBPB	chr3:23497196-23497786	IMR90	lung:	n/a	chr3:23497512-23497523
37	CEBPB	chr3:23404746-23404806	Hela-S3	cervix:	n/a	chr3:23404763-23404774
38	CEBPB	chr3:23490748-23491018	HepG2	liver:	n/a	n/a
39	CEBPB	chr3:23454462-23454480	HepG2	liver:	n/a	n/a
40	CEBPB	chr3:23438341-23438541	HepG2	liver:	n/a	chr3:23438451-23438464 chr3:23438451-23438464 chr3:23438451-23438462
41	CEBPB	chr3:23490807-23490949	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr3:23474439-23474469	K562	blood:	n/a	chr3:23474444-23474455
43	CHD1	chr3:23446784-23446957	GM12878	blood:	n/a	n/a
44	CHD2	chr3:23429199-23429204	GM12878	blood:	n/a	n/a
45	CHD2	chr3:23472562-23472714	GM12878	blood:	n/a	n/a
46	CTCF	chr3:23413880-23414030	NHLF	lung:	n/a	n/a
47	CTCF	chr3:23412100-23412250	WERI-Rb-1	eye:	n/a	n/a
48	CTCF	chr3:23413880-23414030	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr3:23486200-23486350	MCF-7	breast:	n/a	n/a
50	CTCF	chr3:23413860-23414010	HPAF	blood vessel:	n/a	n/a

(count:307 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:23504894-23504944	HIPEpiC	eye:	n/a
2	chr3:23415040-23415090	SK-N-SH	brain:	n/a
3	chr3:23504894-23504944	HIPEpiC	eye:	n/a
4	chr3:23415040-23415090	SK-N-SH	brain:	n/a
5	chr3:23478304-23478354	HRE	kidney:	n/a
6	chr3:23496403-23496453	AG04449	skin:	fetal
7	chr3:23478304-23478354	PrEC	prostate:	n/a
8	chr3:23504894-23504944	ovcar-3	ovarian:	n/a
9	chr3:23448023-23448073	HUVEC	blood vessel:	n/a
10	chr3:23496403-23496453	SAEC	small airway:	n/a
11	chr3:23496403-23496453	U87	brain:	n/a
12	chr3:23496403-23496453	NT2-D1	testis:	n/a
13	chr3:23504894-23504944	BE2_C	brain:	n/a
14	chr3:23504894-23504944	AG04450	lung:	fetal
15	chr3:23415040-23415090	ovcar-3	ovarian:	n/a
16	chr3:23496403-23496453	Jurkat	blood:	n/a
17	chr3:23478304-23478354	SK-N-MC	brain:	n/a
18	chr3:23448023-23448073	AG10803	skin:	n/a
19	chr3:23496403-23496453	Hepatocyte	liver:	n/a
20	chr3:23496403-23496453	MCF-7	breast:	n/a
21	chr3:23478304-23478354	AG09309	skin:	n/a
22	chr3:23478304-23478354	HRPEpiC	eye:	n/a
23	chr3:23415040-23415090	U87	brain:	n/a
24	chr3:23478304-23478354	BJ	skin:	n/a
25	chr3:23415040-23415090	GM19239	blood:	n/a
26	chr3:23504894-23504944	HCF	heart:	n/a
27	chr3:23478304-23478354	GM06990	blood:	n/a
28	chr3:23496403-23496453	SK-N-MC	brain:	n/a
29	chr3:23496403-23496453	HEEpiC	esophagus:	n/a
30	chr3:23478304-23478354	GM12878	blood:	n/a
31	chr3:23496403-23496453	Hela-S3	cervix:	n/a
32	chr3:23504894-23504944	RPTEC	kidney:	n/a
33	chr3:23504894-23504944	HMEC	breast:	n/a
34	chr3:23415040-23415090	NHBE	bronchial:	n/a
35	chr3:23478304-23478354	HepG2	liver:	n/a
36	chr3:23496403-23496453	HCF	heart:	n/a
37	chr3:23448023-23448073	HL-60	blood:	n/a
38	chr3:23448023-23448073	HMEC	breast:	n/a
39	chr3:23496403-23496453	AG09319	gingival:	n/a
40	chr3:23496403-23496453	MCF10A-Er-Src	breast:	n/a
41	chr3:23496403-23496453	AG09309	skin:	n/a
42	chr3:23448023-23448073	PrEC	prostate:	n/a
43	chr3:23415040-23415090	HCPEpiC	choroid plexus:	n/a
44	chr3:23504894-23504944	AG04449	skin:	fetal
45	chr3:23448023-23448073	BJ	skin:	n/a
46	chr3:23478304-23478354	HMEC	breast:	n/a
47	chr3:23478304-23478354	HNPCEpiC	eye:	n/a
48	chr3:23496403-23496453	HRCEpiC	kidney:	n/a
49	chr3:23496403-23496453	AG04450	lung:	fetal
50	chr3:23496403-23496453	H1-hESC	embryonic stem cell:	embryo

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:23478332..23479926-chr3:23487725..23489400,2	MCF-7	breast:
2	chr3:23477379..23479456-chr3:23479836..23482736,2	MCF-7	breast:
3	chr3:23442881..23445228-chr3:23445484..23447259,2	K562	blood:
4	chr3:23489870..23492697-chr3:23493234..23495139,2	MCF-7	breast:
5	chr3:23483538..23485535-chr3:23501695..23503485,2	K562	blood:
6	chr3:23429124..23431176-chr3:23435283..23438143,3	MCF-7	breast:
7	chr3:23398268..23400293-chr3:23402710..23405112,2	MCF-7	breast:
8	chr3:23489870..23492697-chr3:23493234..23495139,2	MCF-7	breast:
9	chr3:23436371..23438292-chr3:23438375..23440407,2	MCF-7	breast:
10	chr3:23443862..23447627-chr3:23449749..23452969,4	MCF-7	breast:
11	chr3:23506645..23508747-chr3:23509649..23511446,2	MCF-7	breast:
12	chr3:23466052..23468838-chr3:23474911..23476655,2	MCF-7	breast:
13	chr3:23489983..23492292-chr3:23500438..23503341,2	MCF-7	breast:
14	chr3:23442881..23445378-chr3:23445759..23448586,2	K562	blood:
15	chr3:23505766..23508563-chr3:23511877..23514869,2	K562	blood:
16	chr3:23442881..23445228-chr3:23445484..23447259,2	K562	blood:
17	chr3:23477632..23480027-chr3:23493781..23495810,2	MCF-7	breast:
18	chr3:23483538..23485535-chr3:23501695..23503485,2	K562	blood:
19	chr3:23442881..23445378-chr3:23445759..23448586,2	K562	blood:
20	chr3:23436579..23438931-chr3:23441202..23443899,2	K562	blood:
21	chr3:23429124..23431176-chr3:23435283..23438143,3	MCF-7	breast:
22	chr3:23466052..23468838-chr3:23474911..23476655,2	MCF-7	breast:
23	chr3:23436579..23438931-chr3:23441202..23443899,2	K562	blood:
24	chr3:23413992..23416641-chr3:23420982..23423774,2	MCF-7	breast:
25	chr3:23478332..23479926-chr3:23487725..23489400,2	MCF-7	breast:
26	chr3:23447289..23448831-chr3:23450533..23452284,2	K562	blood:
27	chr3:23398268..23400293-chr3:23402710..23405112,2	MCF-7	breast:
28	chr3:23477379..23479456-chr3:23479836..23482736,2	MCF-7	breast:
29	chr3:23482059..23483566-chr3:23484032..23486053,2	MCF-7	breast:
30	chr3:23443862..23447627-chr3:23449749..23452969,4	MCF-7	breast:
31	chr3:23436371..23438292-chr3:23438375..23440407,2	MCF-7	breast:
32	chr3:23447289..23448831-chr3:23450533..23452284,2	K562	blood:
33	chr3:23489983..23492292-chr3:23500438..23503341,2	MCF-7	breast:
34	chr3:23413992..23416641-chr3:23420982..23423774,2	MCF-7	breast:
35	chr3:23482059..23483566-chr3:23484032..23486053,2	MCF-7	breast:
36	chr3:23477632..23480027-chr3:23493781..23495810,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NKIRAS1-5	chr3:23431152-23431400	NONHSAT088668

No data

Variant related genes	Relation type
ENSG00000221506	TF binding region
ENSG00000228171	TF binding region
ENSG00000221506	CpG island
ENSG00000228171	CpG island

Extended variants
information (count: 4746 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:4746 , 50 per page) page: 1 2 3 4 5 6 7 ... 95

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1353322	chr3:23390301-23390302	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs185413549	chr3:23390308-23390309	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs560853159	chr3:23390313-23390314	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs5847229	chr3:23390319-23390320	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs189772515	chr3:23390343-23390344	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs143765379	chr3:23390386-23390387	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs528270875	chr3:23390387-23390388	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs183428734	chr3:23390397-23390398	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs372826542	chr3:23390399-23390400	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs75622117	chr3:23390425-23390426	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs549846665	chr3:23390429-23390430	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs147213586	chr3:23390431-23390432	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs17013099	chr3:23390432-23390433	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs74419190	chr3:23390452-23390453	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs373987407	chr3:23390456-23390457	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs12630883	chr3:23390488-23390489	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs536125754	chr3:23390499-23390500	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs12633613	chr3:23390507-23390508	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs186335241	chr3:23390575-23390576	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs140762617	chr3:23390583-23390584	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs13073761	chr3:23390594-23390595	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs191235812	chr3:23390630-23390631	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs545404931	chr3:23390646-23390647	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs376290833	chr3:23390674-23390675	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs560268870	chr3:23390721-23390722	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs183467861	chr3:23390782-23390783	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs528028579	chr3:23390788-23390789	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs187261821	chr3:23390835-23390836	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs369391903	chr3:23390864-23390865	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs192598028	chr3:23390887-23390888	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs552786674	chr3:23390892-23390893	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs367936676	chr3:23390899-23390900	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs535679194	chr3:23390900-23390901	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs550067039	chr3:23390906-23390907	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs183165855	chr3:23390907-23390908	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs571334998	chr3:23390933-23390934	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs555503997	chr3:23390943-23390944	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs547403957	chr3:23390967-23390968	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs565327248	chr3:23390988-23390989	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs536191772	chr3:23390990-23390991	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs372993736	chr3:23390991-23390992	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs186775109	chr3:23390995-23390996	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs12715046	chr3:23391005-23391006	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs151276869	chr3:23391012-23391013	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs544481632	chr3:23391026-23391027	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs545159710	chr3:23391029-23391030	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs554182276	chr3:23391040-23391041	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs572470286	chr3:23391053-23391054	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs542998701	chr3:23391054-23391055	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs561579062	chr3:23391057-23391058	ZNF genes & repeats Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	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
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
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Esophageal cancer	20955586	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Squamous cell cancer	20885788	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:999 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:23367400-23391400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr3:23368000-23391000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr3:23384400-23391800	Weak transcription	Primary B cells from cord blood	blood
4	chr3:23384600-23390600	Weak transcription	Primary B cells from peripheral blood	blood
5	chr3:23386600-23403800	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr3:23388800-23390600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr3:23389400-23391000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
8	chr3:23390000-23390800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
9	chr3:23390200-23390600	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr3:23390200-23391200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
11	chr3:23390400-23390800	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
12	chr3:23390400-23391000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
13	chr3:23390400-23391200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
14	chr3:23390400-23391200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr3:23390600-23391200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr3:23390600-23391200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr3:23390600-23391200	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
18	chr3:23390600-23391200	Enhancers	Primary B cells from peripheral blood	blood
19	chr3:23390800-23391200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr3:23391200-23395000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr3:23397400-23398400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr3:23397600-23398000	Enhancers	Primary neutrophils fromperipheralblood	blood
23	chr3:23397600-23398000	Enhancers	Liver	Liver
24	chr3:23398200-23398600	Enhancers	Adipose Nuclei	Adipose
25	chr3:23398400-23398600	Enhancers	Psoas Muscle	Psoas
26	chr3:23398400-23413000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr3:23398600-23414600	Weak transcription	Psoas Muscle	Psoas
28	chr3:23399600-23399800	Enhancers	Brain Cingulate Gyrus	brain
29	chr3:23399800-23400800	Weak transcription	Brain Cingulate Gyrus	brain
30	chr3:23400200-23401600	Enhancers	Brain Substantia Nigra	brain
31	chr3:23400800-23401800	Enhancers	Brain Cingulate Gyrus	brain
32	chr3:23403800-23404200	Enhancers	Gastric	stomach
33	chr3:23403800-23404200	Enhancers	Skeletal Muscle Male	skeletal muscle
34	chr3:23403800-23404400	Enhancers	Skeletal Muscle Female	skeletal muscle
35	chr3:23404000-23404400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr3:23404200-23418000	Weak transcription	Skeletal Muscle Male	skeletal muscle
37	chr3:23404400-23418000	Weak transcription	Skeletal Muscle Female	skeletal muscle
38	chr3:23406000-23407200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr3:23406200-23406600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr3:23406400-23407200	Enhancers	HUVEC	blood vessel
41	chr3:23406600-23407000	Enhancers	Primary B cells from peripheral blood	blood
42	chr3:23407000-23411000	Weak transcription	Primary B cells from peripheral blood	blood
43	chr3:23408800-23409600	Enhancers	GM12878-XiMat	blood
44	chr3:23409000-23409200	ZNF genes & repeats	Aorta	Aorta
45	chr3:23409000-23409400	Enhancers	Spleen	Spleen
46	chr3:23409200-23431800	Weak transcription	Aorta	Aorta
47	chr3:23409600-23411400	Weak transcription	GM12878-XiMat	blood
48	chr3:23410600-23410800	Enhancers	Brain Cingulate Gyrus	brain
49	chr3:23410800-23426800	Weak transcription	Brain Cingulate Gyrus	brain
50	chr3:23411000-23411200	Enhancers	Primary B cells from peripheral blood	blood

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