Variant report

Variant	nsv1010042
Chromosome Location	chr1:74798856-75001977
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:956)
CpG islands
(count:489)
Chromatin interactive
region (count:22)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:956 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:74943746-74943751	K562	blood:	n/a	n/a
2	ARID3A	chr1:74822262-74822579	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:74934711-74935007	HepG2	liver:	n/a	n/a
4	ATF2	chr1:74929255-74929663	GM12878	blood:	n/a	n/a
5	BACH1	chr1:74952507-74952628	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr1:75000150-75000202	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr1:74865039-74865204	GM12878	blood:	n/a	chr1:74865097-74865108
8	BATF	chr1:74929254-74929656	GM12878	blood:	n/a	chr1:74929478-74929489
9	BATF	chr1:74862633-74862912	GM12878	blood:	n/a	n/a
10	BATF	chr1:74864921-74865285	GM12878	blood:	n/a	chr1:74865097-74865108
11	BATF	chr1:74929264-74929606	GM12878	blood:	n/a	chr1:74929478-74929489
12	BCL11A	chr1:74929322-74929595	GM12878	blood:	n/a	n/a
13	BCL11A	chr1:74864896-74865230	GM12878	blood:	n/a	n/a
14	BCL11A	chr1:74929185-74929684	GM12878	blood:	n/a	n/a
15	BCL3	chr1:74822171-74822614	A549	lung:	n/a	n/a
16	BHLHE40	chr1:74969836-74970190	GM12878	blood:	n/a	n/a
17	BHLHE40	chr1:74969965-74970040	K562	blood:	n/a	n/a
18	BHLHE40	chr1:74929307-74929660	GM12878	blood:	n/a	n/a
19	CEBPB	chr1:74808826-74809251	IMR90	lung:	n/a	chr1:74808957-74808968
20	CEBPB	chr1:74889142-74889769	IMR90	lung:	n/a	chr1:74889354-74889367
21	CEBPB	chr1:74808794-74809117	H1-hESC	embryonic stem cell:	n/a	chr1:74808957-74808968
22	CEBPB	chr1:74969867-74970067	HepG2	liver:	n/a	chr1:74970021-74970032
23	CEBPB	chr1:74822165-74822718	A549	lung:	n/a	chr1:74822623-74822634
24	CEBPB	chr1:74863899-74864221	IMR90	lung:	n/a	chr1:74864058-74864069
25	CEBPB	chr1:74863934-74864174	A549	lung:	n/a	chr1:74864058-74864069
26	CEBPB	chr1:74933490-74933834	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr1:74822142-74822758	IMR90	lung:	n/a	chr1:74822623-74822634
28	CEBPB	chr1:74933510-74933831	HepG2	liver:	n/a	n/a
29	CEBPB	chr1:74929812-74930102	A549	lung:	n/a	chr1:74929930-74929941 chr1:74929928-74929941 chr1:74929928-74929941 chr1:74929930-74929939 chr1:74929928-74929939
30	CEBPB	chr1:74929299-74930127	IMR90	lung:	n/a	chr1:74929930-74929941 chr1:74929928-74929941 chr1:74929928-74929941 chr1:74929930-74929939 chr1:74929928-74929939
31	CEBPB	chr1:74872122-74872453	IMR90	lung:	n/a	chr1:74872295-74872306
32	CEBPB	chr1:74933543-74933820	ECC-1	luminal epithelium:	n/a	n/a
33	CEBPB	chr1:74859847-74860070	IMR90	lung:	n/a	chr1:74859944-74859957
34	CEBPB	chr1:74929751-74930102	HepG2	liver:	n/a	chr1:74929930-74929941 chr1:74929928-74929941 chr1:74929928-74929941 chr1:74929930-74929939 chr1:74929928-74929939
35	CEBPB	chr1:74808794-74809122	HepG2	liver:	n/a	chr1:74808957-74808968
36	CEBPB	chr1:74933478-74933842	ECC-1	luminal epithelium:	n/a	n/a
37	CEBPB	chr1:74933511-74933815	IMR90	lung:	n/a	n/a
38	CEBPB	chr1:74933587-74933713	HepG2	liver:	n/a	n/a
39	CEBPB	chr1:74822239-74822574	HepG2	liver:	n/a	n/a
40	CEBPB	chr1:75000289-75000474	IMR90	lung:	n/a	n/a
41	CEBPB	chr1:74944840-74944920	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr1:74864001-74864166	H1-hESC	embryonic stem cell:	n/a	chr1:74864058-74864069
43	CEBPB	chr1:74929306-74930122	Hela-S3	cervix:	n/a	chr1:74929930-74929941 chr1:74929928-74929941 chr1:74929928-74929941 chr1:74929930-74929939 chr1:74929928-74929939
44	CEBPB	chr1:74933483-74933825	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr1:74863892-74864211	HepG2	liver:	n/a	chr1:74864058-74864069
46	CEBPB	chr1:74832214-74832457	HepG2	liver:	n/a	n/a
47	CEBPB	chr1:74872165-74872467	A549	lung:	n/a	chr1:74872295-74872306
48	CEBPB	chr1:74872136-74872456	HepG2	liver:	n/a	chr1:74872295-74872306
49	CHD2	chr1:74987849-74988223	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD2	chr1:74993857-74993943	HepG2	liver:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:74941958-74942008	GM06990	blood:	n/a
2	chr1:74941958-74942008	GM06990	blood:	n/a
3	chr1:74888995-74889045	GM19239	blood:	n/a
4	chr1:74988194-74988244	RPTEC	kidney:	n/a
5	chr1:74832752-74832802	BJ	skin:	n/a
6	chr1:74933557-74933607	HEEpiC	esophagus:	n/a
7	chr1:74891564-74891614	HEK293	kidney:	embryo
8	chr1:74941958-74942008	ProgFib	skin:	n/a
9	chr1:74970626-74970676	SK-N-MC	brain:	n/a
10	chr1:74988194-74988244	T-47D	breast:	n/a
11	chr1:74945347-74945397	PFSK-1	brain:	n/a
12	chr1:74945347-74945397	RPTEC	kidney:	n/a
13	chr1:74933557-74933607	BE2_C	brain:	n/a
14	chr1:74941958-74942008	HL-60	blood:	n/a
15	chr1:74941958-74942008	GM19239	blood:	n/a
16	chr1:74888995-74889045	HepG2	liver:	n/a
17	chr1:74891564-74891614	MCF-7	breast:	n/a
18	chr1:74832752-74832802	GM12891	blood:	n/a
19	chr1:74941958-74942008	AG04450	lung:	fetal
20	chr1:74970626-74970676	NH-A	brain:	n/a
21	chr1:74832752-74832802	CMK	blood:	n/a
22	chr1:74941958-74942008	HCT-116	colon:	n/a
23	chr1:74933557-74933607	Hela-S3	cervix:	n/a
24	chr1:74945347-74945397	MCF10A-Er-Src	breast:	n/a
25	chr1:74970626-74970676	HNPCEpiC	eye:	n/a
26	chr1:74941958-74942008	AG09309	skin:	n/a
27	chr1:74891564-74891614	HRPEpiC	eye:	n/a
28	chr1:74941958-74942008	MCF-7	breast:	n/a
29	chr1:74832752-74832802	AG04449	skin:	fetal
30	chr1:74888995-74889045	Jurkat	blood:	n/a
31	chr1:74888995-74889045	SK-N-SH_RA	brain:	n/a
32	chr1:74970626-74970676	HepG2	liver:	n/a
33	chr1:74988194-74988244	HCM	heart:	n/a
34	chr1:74832752-74832802	T-47D	breast:	n/a
35	chr1:74888995-74889045	K562	blood:	n/a
36	chr1:74941958-74942008	SK-N-SH	brain:	n/a
37	chr1:74970626-74970676	Jurkat	blood:	n/a
38	chr1:74832752-74832802	HCT-116	colon:	n/a
39	chr1:74933557-74933607	GM06990	blood:	n/a
40	chr1:74832752-74832802	ProgFib	skin:	n/a
41	chr1:74832752-74832802	AG04450	lung:	fetal
42	chr1:74891564-74891614	T-47D	breast:	n/a
43	chr1:74941958-74942008	AG04449	skin:	fetal
44	chr1:74941958-74942008	SAEC	small airway:	n/a
45	chr1:74933557-74933607	GM12891	blood:	n/a
46	chr1:74970626-74970676	T-47D	breast:	n/a
47	chr1:74988194-74988244	HCF	heart:	n/a
48	chr1:74933557-74933607	HCF	heart:	n/a
49	chr1:74941958-74942008	HepG2	liver:	n/a
50	chr1:74933557-74933607	AG04449	skin:	fetal

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:74868917..74870654-chr1:74871411..74874146,2	K562	blood:
2	chr1:74847175..74848707-chr1:74848769..74850609,2	MCF-7	breast:
3	chr1:74835693..74838448-chr1:74838770..74840795,2	K562	blood:
4	chr1:74969628..74970367-chr1:75199475..75200023,2	MCF-7	breast:
5	chr1:74949493..74951450-chr1:74951854..74954172,2	MCF-7	breast:
6	chr1:74641537..74643099-chr1:74809509..74811733,2	K562	blood:
7	chr1:74971580..74976038-chr1:74977181..74980046,4	K562	blood:
8	chr1:74949493..74951450-chr1:74951854..74954172,2	MCF-7	breast:
9	chr1:74921227..74923766-chr1:74925738..74927601,2	K562	blood:
10	chr1:74921227..74923766-chr1:74925738..74927601,2	K562	blood:
11	chr1:74789903..74792042-chr1:74796412..74799113,2	MCF-7	breast:
12	chr1:74934779..74936281-chr1:74938303..74940454,2	K562	blood:
13	chr1:74835693..74838448-chr1:74838770..74840795,2	K562	blood:
14	chr1:74868917..74870654-chr1:74871411..74874146,2	K562	blood:
15	chr1:74847175..74848707-chr1:74848769..74850609,2	MCF-7	breast:
16	chr1:74799781..74801961-chr1:74805527..74808251,2	MCF-7	breast:
17	chr1:74977554..74979985-chr1:75198825..75201036,2	K562	blood:
18	chr1:74990321..74992157-chr1:75009741..75011754,2	K562	blood:
19	chr1:74934779..74936281-chr1:74938303..74940454,2	K562	blood:
20	chr1:74835693..74838448-chr1:74838770..74840805,3	K562	blood:
21	chr1:74867146..74867864-chr13:25216133..25216958,2	MCF-7	breast:
22	chr1:74835693..74838448-chr1:74838770..74840805,3	K562	blood:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FPGT-1	chr1:74949131-74949200	NONHSAT003963
2	lnc-FPGT-1	chr1:74933443-74934233	NONHSAT003961
3	lnc-FPGT-1	chr1:74933443-74934233	NONHSAT003960
4	lnc-LRRC53-1	chr1:74807263-74807671	ENSG00000237324.2
5	lnc-LRRC53-1	chr1:74832267-74832410	ENSG00000237324.2
6	lnc-FPGT-7	chr1:74853478-74853568	ucscGeneNc_uc001dgh_2
7	lnc-FPGT-1	chr1:74933443-74934233	NONHSAT003963
8	lnc-FPGT-1	chr1:74941196-74941236	NONHSAT003961
9	lnc-FPGT-1	chr1:74934667-74934715	NONHSAT003962
10	lnc-LRRC53-1	chr1:74844380-74844486	ENSG00000237324.2
11	lnc-FPGT-1	chr1:74933879-74934233	ENSG00000233894.1
12	lnc-FPGT-7	chr1:74815702-74815781	ucscGeneNc_uc001dgh_2
13	lnc-FPGT-1	chr1:74934820-74934979	NONHSAT003960
14	lnc-FPGT-1	chr1:74934820-74935227	ENSG00000233894.1
15	lnc-LRRC53-1	chr1:74834673-74834803	ENSG00000237324.2
16	lnc-FPGT-1	chr1:74934197-74934233	ENSG00000233894.1
17	lnc-FPGT-1	chr1:74933443-74934233	NONHSAT003962
18	lnc-FPGT-1	chr1:74934667-74934808	ENSG00000233894.1
19	lnc-FPGT-7	chr1:74859668-74864369	ucscGeneNc_uc001dgh_2

No data

Variant related genes	Relation type
LRRC53	TF binding region
ENSG00000237324	TF binding region
TNNI3K	TF binding region
ENSG00000233894	TF binding region
LRRC53	CpG island
ENSG00000237324	CpG island
TNNI3K	CpG island
ENSG00000233894	CpG island
ENSG00000116791	chromatin interactions
ENSG00000116783	chromatin interactions
ENSG00000162623	chromatin interactions
ENSG00000162621	chromatin interactions
IP6K2	miRNA target sites
TARBP2	miRNA target sites

Extended variants
information (count: 7877 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:7877 , 50 per page) page: 1 2 3 4 5 6 7 ... 158

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs45457895	chr1:74798856-74798857	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs186105899	chr1:74798930-74798931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs549120484	chr1:74798939-74798940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs147472132	chr1:74798996-74798997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs528806802	chr1:74799002-74799003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs547349772	chr1:74799005-74799006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs75858284	chr1:74799026-74799027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs45612831	chr1:74799041-74799042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs489990	chr1:74799045-74799046	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs569659324	chr1:74799119-74799120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs537004677	chr1:74799126-74799127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs189313073	chr1:74799132-74799133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs573846092	chr1:74799176-74799177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs534589898	chr1:74799198-74799199	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs181973933	chr1:74799227-74799228	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs577413843	chr1:74799231-74799232	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs512920	chr1:74799268-74799269	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs185988282	chr1:74799360-74799361	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs536999226	chr1:74799380-74799381	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs554844498	chr1:74799460-74799461	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs575653880	chr1:74799535-74799536	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs569972641	chr1:74799600-74799601	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs141830542	chr1:74799614-74799615	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs528511992	chr1:74799650-74799651	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs547307134	chr1:74799667-74799668	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs537261364	chr1:74799673-74799674	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs45587138	chr1:74799678-74799679	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs532710715	chr1:74799679-74799680	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs150624615	chr1:74799685-74799686	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs377133338	chr1:74799762-74799763	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs45627538	chr1:74799801-74799802	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs536762537	chr1:74799816-74799817	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs549096337	chr1:74799827-74799828	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs35937147	chr1:74799863-74799864	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
35	rs139978616	chr1:74799946-74799947	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs557552962	chr1:74799963-74799964	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs552840612	chr1:74799972-74799973	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs544090449	chr1:74799990-74799991	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs577528061	chr1:74799991-74799992	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs538402118	chr1:74800052-74800053	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs556902415	chr1:74800065-74800066	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs17095150	chr1:74800085-74800086	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs77581462	chr1:74800138-74800139	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs149864783	chr1:74800149-74800150	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs573144968	chr1:74800167-74800168	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs190750462	chr1:74800174-74800175	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs146879975	chr1:74800175-74800176	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs78211006	chr1:74800181-74800182	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs182619876	chr1:74800192-74800193	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs562923827	chr1:74800199-74800200	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:106)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ewing''s sarcoma	17952124	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:899 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:74785600-74808800	Weak transcription	Left Ventricle	heart
2	chr1:74790400-74814200	Weak transcription	Aorta	Aorta
3	chr1:74791200-74807400	Weak transcription	Fetal Heart	heart
4	chr1:74797000-74809000	Weak transcription	Ovary	ovary
5	chr1:74799600-74800200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr1:74799600-74800400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr1:74801200-74808800	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr1:74804200-74805200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr1:74804200-74809400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr1:74804200-74809600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr1:74804400-74805200	Enhancers	Muscle Satellite Cultured Cells	--
12	chr1:74804400-74805200	Enhancers	HSMM	muscle
13	chr1:74804600-74804800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr1:74804600-74804800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr1:74804800-74805800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr1:74804800-74808800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr1:74805200-74806200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr1:74805600-74807400	Weak transcription	Brain Angular Gyrus	brain
19	chr1:74805800-74807800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr1:74806200-74806400	Enhancers	Brain Germinal Matrix	brain
21	chr1:74806200-74806400	Enhancers	Right Ventricle	heart
22	chr1:74806200-74806800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr1:74806200-74807400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr1:74806400-74806600	Enhancers	Brain Anterior Caudate	brain
25	chr1:74806400-74806600	Enhancers	Fetal Brain Female	brain
26	chr1:74806400-74807400	Weak transcription	Brain Germinal Matrix	brain
27	chr1:74806400-74807400	Weak transcription	Right Ventricle	heart
28	chr1:74806400-74807600	Enhancers	Brain Substantia Nigra	brain
29	chr1:74806400-74808000	Enhancers	Brain Cingulate Gyrus	brain
30	chr1:74806400-74809200	Enhancers	Brain Inferior Temporal Lobe	brain
31	chr1:74806600-74806800	Enhancers	Cortex derived primary cultured neurospheres	brain
32	chr1:74806600-74807400	Weak transcription	Brain Anterior Caudate	brain
33	chr1:74806600-74807600	Weak transcription	Fetal Brain Female	brain
34	chr1:74807400-74807600	Enhancers	Brain Angular Gyrus	brain
35	chr1:74807400-74807600	Enhancers	Brain Anterior Caudate	brain
36	chr1:74807400-74807600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
37	chr1:74807400-74807600	ZNF genes & repeats	Pancreas	Pancrea
38	chr1:74807400-74808000	Enhancers	Brain Hippocampus Middle	brain
39	chr1:74807400-74808200	Enhancers	Fetal Muscle Leg	muscle
40	chr1:74807400-74808400	Enhancers	Fetal Heart	heart
41	chr1:74807400-74809400	Enhancers	Right Ventricle	heart
42	chr1:74807400-74809600	Enhancers	Brain Germinal Matrix	brain
43	chr1:74807400-74810000	Weak transcription	Gastric	stomach
44	chr1:74807600-74808000	Enhancers	Fetal Brain Female	brain
45	chr1:74807600-74808600	Weak transcription	Brain Anterior Caudate	brain
46	chr1:74807600-74808600	Weak transcription	Brain Substantia Nigra	brain
47	chr1:74807600-74808800	Weak transcription	Brain Angular Gyrus	brain
48	chr1:74807600-74808800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
49	chr1:74807600-74809200	Weak transcription	Pancreas	Pancrea
50	chr1:74808000-74808400	Weak transcription	Brain Cingulate Gyrus	brain

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