Variant report

Variant	nsv516623
Chromosome Location	chr3:46680063-46852679
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2347)
CpG islands
(count:4647)
Chromatin interactive
region (count:181)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2347 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr3:46684585-46684909	K562	blood:	n/a	n/a
2	ATF2	chr3:46759302-46759627	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr3:46755533-46755773	GM12878	blood:	n/a	n/a
4	ATF2	chr3:46746461-46746813	GM12878	blood:	n/a	n/a
5	ATF2	chr3:46755483-46755920	GM12878	blood:	n/a	n/a
6	ATF3	chr3:46792267-46792609	K562	blood:	n/a	n/a
7	ATF3	chr3:46759265-46759598	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr3:46759282-46759598	K562	blood:	n/a	n/a
9	ATF3	chr3:46759331-46759550	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chr3:46792308-46792631	K562	blood:	n/a	n/a
11	BACH1	chr3:46735430-46735744	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr3:46746558-46746758	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr3:46734048-46734515	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr3:46759334-46759543	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr3:46834950-46835224	GM12878	blood:	n/a	n/a
16	BATF	chr3:46755501-46755889	GM12878	blood:	n/a	n/a
17	BATF	chr3:46773261-46773680	GM12878	blood:	n/a	n/a
18	BATF	chr3:46720130-46720422	GM12878	blood:	n/a	n/a
19	BATF	chr3:46773278-46773701	GM12878	blood:	n/a	n/a
20	BATF	chr3:46720127-46720375	GM12878	blood:	n/a	n/a
21	BATF	chr3:46834909-46835249	GM12878	blood:	n/a	n/a
22	BATF	chr3:46755589-46755797	GM12878	blood:	n/a	n/a
23	BCL11A	chr3:46834834-46835220	GM12878	blood:	n/a	n/a
24	BCL11A	chr3:46755551-46755755	GM12878	blood:	n/a	chr3:46755588-46755601
25	BCL11A	chr3:46755446-46755860	GM12878	blood:	n/a	chr3:46755588-46755601
26	BCL3	chr3:46755447-46755829	GM12878	blood:	n/a	chr3:46755588-46755601
27	BCLAF1	chr3:46759179-46759647	K562	blood:	n/a	n/a
28	BHLHE40	chr3:46759435-46759439	K562	blood:	n/a	n/a
29	BHLHE40	chr3:46735446-46735593	K562	blood:	n/a	n/a
30	BHLHE40	chr3:46736984-46737365	GM12878	blood:	n/a	n/a
31	BHLHE40	chr3:46792161-46792741	K562	blood:	n/a	chr3:46792470-46792479 chr3:46792470-46792479
32	BHLHE40	chr3:46734263-46734269	A549	lung:	n/a	n/a
33	BHLHE40	chr3:46798309-46798511	K562	blood:	n/a	n/a
34	BHLHE40	chr3:46734493-46734748	K562	blood:	n/a	n/a
35	BHLHE40	chr3:46755577-46755866	GM12878	blood:	n/a	n/a
36	BHLHE40	chr3:46746528-46746852	K562	blood:	n/a	n/a
37	BHLHE40	chr3:46773339-46773653	GM12878	blood:	n/a	n/a
38	BHLHE40	chr3:46736761-46737392	K562	blood:	n/a	n/a
39	BRCA1	chr3:46746485-46746854	Hela-S3	cervix:	n/a	n/a
40	BRCA1	chr3:46746586-46746696	HepG2	liver:	n/a	n/a
41	BRCA1	chr3:46755567-46755723	GM12878	blood:	n/a	n/a
42	BRCA1	chr3:46708976-46709045	Hela-S3	cervix:	n/a	n/a
43	BRCA1	chr3:46759337-46759615	H1-hESC	embryonic stem cell:	n/a	n/a
44	BRCA1	chr3:46700658-46700720	H1-hESC	embryonic stem cell:	n/a	n/a
45	BRCA1	chr3:46734876-46735076	Hela-S3	cervix:	n/a	n/a
46	BRCA1	chr3:46746601-46746847	H1-hESC	embryonic stem cell:	n/a	n/a
47	CBX3	chr3:46693497-46693764	K562	blood:	n/a	n/a
48	CBX3	chr3:46798157-46798548	K562	blood:	n/a	n/a
49	CBX3	chr3:46759328-46759544	K562	blood:	n/a	n/a
50	CBX3	chr3:46792069-46792673	K562	blood:	n/a	n/a

(count:4647 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:46776775-46776825	SK-N-MC	brain:	n/a
2	chr3:46735009-46735059	Caco-2	colon:	n/a
3	chr3:46759588-46759638	ovcar-3	ovarian:	n/a
4	chr3:46850588-46850638	HPAEpiC	pulmonary alveolar:	n/a
5	chr3:46733475-46733525	Caco-2	colon:	n/a
6	chr3:46734393-46734443	HUVEC	blood vessel:	n/a
7	chr3:46719834-46719884	SK-N-SH	brain:	n/a
8	chr3:46718990-46719040	H1-hESC	embryonic stem cell:	embryo
9	chr3:46735782-46735832	SK-N-MC	brain:	n/a
10	chr3:46850588-46850638	LNCaP	prostate:	n/a
11	chr3:46790182-46790232	NB4	blood:	n/a
12	chr3:46776775-46776825	SK-N-MC	brain:	n/a
13	chr3:46735009-46735059	Caco-2	colon:	n/a
14	chr3:46759588-46759638	ovcar-3	ovarian:	n/a
15	chr3:46850588-46850638	HPAEpiC	pulmonary alveolar:	n/a
16	chr3:46733475-46733525	Caco-2	colon:	n/a
17	chr3:46734393-46734443	HUVEC	blood vessel:	n/a
18	chr3:46719834-46719884	SK-N-SH	brain:	n/a
19	chr3:46718990-46719040	H1-hESC	embryonic stem cell:	embryo
20	chr3:46735782-46735832	SK-N-MC	brain:	n/a
21	chr3:46850588-46850638	LNCaP	prostate:	n/a
22	chr3:46790182-46790232	NB4	blood:	n/a
23	chr3:46742898-46742948	NH-A	brain:	n/a
24	chr3:46735801-46735851	HEK293	kidney:	embryo
25	chr3:46735335-46735385	Caco-2	colon:	n/a
26	chr3:46741492-46741542	HCPEpiC	choroid plexus:	n/a
27	chr3:46785957-46786007	U87	brain:	n/a
28	chr3:46719086-46719136	SKMC	muscle:	n/a
29	chr3:46768322-46768372	U87	brain:	n/a
30	chr3:46792462-46792512	SK-N-SH	brain:	n/a
31	chr3:46755916-46755966	PrEC	prostate:	n/a
32	chr3:46789735-46789785	AG04449	skin:	fetal
33	chr3:46792462-46792512	HepG2	liver:	n/a
34	chr3:46792192-46792242	SK-N-MC	brain:	n/a
35	chr3:46798240-46798290	SK-N-SH_RA	brain:	n/a
36	chr3:46746779-46746829	BJ	skin:	n/a
37	chr3:46787073-46787123	GM06990	blood:	n/a
38	chr3:46735338-46735388	HAEpiC	amniotic membrane:	n/a
39	chr3:46776775-46776825	CMK	blood:	n/a
40	chr3:46775899-46775949	PANC-1	pancreas:	n/a
41	chr3:46719834-46719884	NB4	blood:	n/a
42	chr3:46792192-46792242	HRCEpiC	kidney:	n/a
43	chr3:46741803-46741853	HepG2	liver:	n/a
44	chr3:46741492-46741542	SK-N-SH_RA	brain:	n/a
45	chr3:46730941-46730991	SK-N-SH_RA	brain:	n/a
46	chr3:46734393-46734443	AG09319	gingival:	n/a
47	chr3:46787073-46787123	AoSMC	blood vessel:	n/a
48	chr3:46735319-46735369	GM12891	blood:	n/a
49	chr3:46798240-46798290	Caco-2	colon:	n/a
50	chr3:46759438-46759488	HCT-116	colon:	n/a

(count:181 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr3:46707530..46709982-chr3:46711149..46714588,3	K562	blood:
2	chr3:46751695..46753830-chr3:46756302..46759551,4	K562	blood:
3	chr3:46787160..46789838-chr3:46792836..46795181,2	K562	blood:
4	chr3:46679942..46681539-chr3:46683800..46686351,2	K562	blood:
5	chr3:46703743..46706705-chr3:46719567..46721829,2	K562	blood:
6	chr3:46727228..46728966-chr3:46733953..46736309,2	MCF-7	breast:
7	chr3:46746189..46747162-chr3:46936459..46937309,7	MCF-7	breast:
8	chr3:46703608..46706840-chr3:46708905..46711367,3	K562	blood:
9	chr3:46724809..46726431-chr3:46731600..46733617,2	K562	blood:
10	chr3:46774758..46775741-chr3:46797694..46798443,2	K562	blood:
11	chr3:46707530..46709982-chr3:46711149..46714588,3	K562	blood:
12	chr3:46764632..46767218-chr3:46782393..46785331,2	K562	blood:
13	chr3:46724809..46726431-chr3:46731600..46733617,2	K562	blood:
14	chr3:46679942..46681539-chr3:46683800..46686351,2	K562	blood:
15	chr3:46529944..46530794-chr3:46705110..46706015,2	K562	blood:
16	chr3:46746227..46747136-chr3:46797879..46798830,2	K562	blood:
17	chr3:46733801..46735413-chr3:46924430..46926212,2	MCF-7	breast:
18	chr3:46745401..46748199-chr3:46947346..46950114,2	K562	blood:
19	chr3:46671153..46671844-chr3:46736764..46737267,2	MCF-7	breast:
20	chr3:46733050..46735013-chr3:46736523..46739104,3	K562	blood:
21	chr3:46787160..46789838-chr3:46792836..46795181,2	K562	blood:
22	chr3:46650273..46651172-chr3:46707945..46708857,6	MCF-7	breast:
23	chr3:46780631..46782178-chr3:46786371..46787877,2	K562	blood:
24	chr3:46745129..46746095-chr3:46936433..46937176,2	MCF-7	breast:
25	chr3:46700787..46702922-chr3:46710281..46712322,2	K562	blood:
26	chr3:46739910..46741419-chr3:46753549..46755761,2	MCF-7	breast:
27	chr3:46739910..46741419-chr3:46753549..46755761,2	MCF-7	breast:
28	chr3:46788120..46791042-chr3:46798895..46800766,2	K562	blood:
29	chr3:46738781..46740669-chr3:46750489..46752316,2	K562	blood:
30	chr3:46733050..46735013-chr3:46736523..46739104,3	K562	blood:
31	chr3:46743022..46745285-chr3:46747232..46748921,2	MCF-7	breast:
32	chr3:46720300..46721832-chr3:46725360..46727686,2	K562	blood:
33	chr3:46761792..46767256-chr3:46770894..46774909,6	K562	blood:
34	chr3:46764632..46767218-chr3:46782393..46785331,2	K562	blood:
35	chr3:46770529..46772210-chr3:46784902..46786498,2	K562	blood:
36	chr3:46751695..46753844-chr3:46756302..46759946,5	K562	blood:
37	chr3:46720266..46726397-chr3:46730234..46736031,11	MCF-7	breast:
38	chr3:46707418..46709371-chr3:46712225..46713806,2	K562	blood:
39	chr3:46698830..46701329-chr3:46704770..46706744,2	K562	blood:
40	chr3:46776204..46778019-chr3:46778181..46780158,2	K562	blood:
41	chr3:46746540..46747094-chr3:46948369..46948995,2	K562	blood:
42	chr3:46720178..46722487-chr3:46787613..46789601,2	K562	blood:
43	chr3:46707418..46709371-chr3:46712225..46713806,2	K562	blood:
44	chr3:46670110..46673240-chr3:46702336..46706371,4	MCF-7	breast:
45	chr3:46707887..46708803-chr3:46920018..46920840,3	MCF-7	breast:
46	chr3:46796204..46798578-chr3:46800470..46803401,3	K562	blood:
47	chr3:46730164..46732483-chr3:46734488..46736983,2	MCF-7	breast:
48	chr3:46789741..46793223-chr3:46794604..46798425,5	K562	blood:
49	chr3:46796974..46798578-chr3:46800470..46803376,2	K562	blood:
50	chr3:46698830..46701329-chr3:46704770..46706744,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRSS50-1	chr3:46797532-46798119	NONHSAT089457
2	lnc-PTH1R-2	chr3:46839613-46839880	NONHSAT089458
3	lnc-PRSS50-1	chr3:46795974-46796138	NONHSAT089457

No data

Variant related genes	Relation type
ENSG00000238013	TF binding region
ALS2CL	TF binding region
ENSG00000251967	TF binding region
PRSS45	TF binding region
PRSS46	TF binding region
TMIE	TF binding region
PRSS50	TF binding region
ENSG00000238013	CpG island
ALS2CL	CpG island
ENSG00000251967	CpG island
PRSS45	CpG island
PRSS46	CpG island
TMIE	CpG island
PRSS50	CpG island
ENSG00000229320	chromatin interactions
ENSG00000270006	chromatin interactions
ENSG00000206549	chromatin interactions
ENSG00000178038	chromatin interactions
ENSG00000264306	chromatin interactions
ENSG00000160799	chromatin interactions
ENSG00000113558	chromatin interactions
ENSG00000188086	chromatin interactions
ENSG00000201558	chromatin interactions
ENSG00000160796	chromatin interactions
ENSG00000006062	chromatin interactions
ENSG00000181585	chromatin interactions
ENSG00000101558	chromatin interactions
ENSG00000186432	chromatin interactions
ENSG00000160801	chromatin interactions
ENSG00000260456	chromatin interactions
ENSG00000261603	chromatin interactions

Extended variants
information (count: 5353 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:5353 , 50 per page) page: 1 2 3 4 5 6 7 ... 108

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11709020	chr3:46680063-46680064	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs180779934	chr3:46680077-46680078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs2385859	chr3:46680132-46680133	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs570123061	chr3:46680145-46680146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs537661311	chr3:46680205-46680206	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs183507271	chr3:46680220-46680221	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs188234663	chr3:46680241-46680242	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs181727503	chr3:46680248-46680249	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs534992100	chr3:46680253-46680254	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs553436468	chr3:46680260-46680261	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs574788326	chr3:46680275-46680276	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs140799466	chr3:46680314-46680315	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs575117697	chr3:46680406-46680407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs557433916	chr3:46680417-46680418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs187209095	chr3:46680425-46680426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs11709936	chr3:46680483-46680484	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs564836227	chr3:46680485-46680486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs191795215	chr3:46680518-46680519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs553725723	chr3:46680522-46680523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs181894570	chr3:46680531-46680532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs559052720	chr3:46680538-46680539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs529714989	chr3:46680564-46680565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs547935211	chr3:46680665-46680666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs186418247	chr3:46680729-46680730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs370478154	chr3:46680743-46680744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs191329847	chr3:46680756-46680757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs531008004	chr3:46680777-46680778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs552831814	chr3:46680815-46680816	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs571142049	chr3:46680836-46680837	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs535298728	chr3:46680864-46680865	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs547335769	chr3:46680880-46680881	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs374121151	chr3:46680883-46680884	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs76149802	chr3:46680896-46680897	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs34891848	chr3:46680952-46680953	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs573105616	chr3:46680984-46680985	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs182735944	chr3:46680995-46680996	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs185213683	chr3:46681092-46681093	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs573430032	chr3:46681097-46681098	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs189868917	chr3:46681204-46681205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs536830177	chr3:46681236-46681237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs80266446	chr3:46681353-46681354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs13083665	chr3:46681373-46681374	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs576644458	chr3:46681430-46681431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs115888033	chr3:46681460-46681461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs73077579	chr3:46681461-46681462	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs11715108	chr3:46681505-46681506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs183249739	chr3:46681541-46681542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs574340638	chr3:46681565-46681566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs542454309	chr3:46681584-46681585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs541855822	chr3:46681670-46681671	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

Disease	PMID	Source
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
Glioblastoma multiforme	21080181	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
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Kartagener syndrome	16639409	CNVD
Biliary cancer	19435499	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Breast cancer	21509527	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22032731	CNVD
Non-small cell lung cancer	20864512	CNVD
Colorectal cancer	16912164	CNVD
Non-small cell lung cancer	19010865	CNVD
Colorectal cancer	16272173	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute myeloid leukemia	17268525	CNVD
Salivary gland tumor	18059337	CNVD
Gastric cancer	16891809	CNVD
Night blindness	17160897	CNVD
Cancer	17160897	CNVD
Breast cancer	20409316	CNVD
Lung cancer	17297452	CNVD
Multiple myeloma	16616336	CNVD
Effusion lymphoma	18079361	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Urothelial cell carcinoma	18451213	CNVD
Neuroblastoma	17327916	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Melanoma	17363583	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Adrenocortical carcinoma	18281524	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian cancer	21781307	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Recurrent pregnancy loss	19789632	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:2168 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:46672000-46681600	Weak transcription	Left Ventricle	heart
2	chr3:46675600-46688000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr3:46680200-46680400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr3:46680400-46680800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr3:46680800-46681200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr3:46681600-46681800	ZNF genes & repeats	Left Ventricle	heart
7	chr3:46682400-46683000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr3:46683200-46683600	Enhancers	Fetal Heart	heart
9	chr3:46684800-46685200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr3:46684800-46685400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr3:46684800-46685400	Enhancers	Dnd41	blood
12	chr3:46687800-46688800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr3:46687800-46688800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr3:46687800-46688800	Enhancers	NHLF	lung
15	chr3:46687800-46689200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr3:46687800-46689200	Enhancers	NHDF-Ad	bronchial
17	chr3:46688000-46688400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr3:46688000-46688400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr3:46688000-46688800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr3:46688000-46688800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr3:46688000-46688800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr3:46688000-46688800	Enhancers	Left Ventricle	heart
23	chr3:46688000-46688800	Enhancers	HMEC	breast
24	chr3:46688200-46688600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr3:46688200-46688600	Enhancers	HSMM	muscle
26	chr3:46688200-46688800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr3:46688400-46688600	Enhancers	Skeletal Muscle Male	skeletal muscle
28	chr3:46688400-46688600	Enhancers	NHEK	skin
29	chr3:46688400-46700800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr3:46688800-46690800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr3:46689200-46691000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr3:46691000-46691200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr3:46691000-46691200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr3:46691000-46691200	Enhancers	HMEC	breast
35	chr3:46693400-46701800	Weak transcription	Right Atrium	heart
36	chr3:46695800-46696000	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr3:46695800-46696200	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr3:46696000-46696200	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr3:46696200-46696400	Enhancers	H1 Cell Line	embryonic stem cell
40	chr3:46696200-46697800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
41	chr3:46696400-46698000	Weak transcription	HUES64 Cell Line	embryonic stem cell
42	chr3:46696600-46696800	Enhancers	NHDF-Ad	bronchial
43	chr3:46696600-46698000	Weak transcription	H1 Cell Line	embryonic stem cell
44	chr3:46696600-46698000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
45	chr3:46696800-46697400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr3:46696800-46698000	Weak transcription	NHDF-Ad	bronchial
47	chr3:46697400-46697800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr3:46697800-46698800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr3:46697800-46699000	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr3:46698000-46699000	Enhancers	H1 Cell Line	embryonic stem cell

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