Variant report

Variant	nsv949449
Chromosome Location	chr1:92211020-92585831
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4787)
CpG islands
(count:4708)
Chromatin interactive
region (count:140)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:4787 , 50 per page) page: 1 2 3 4 5 6 7 ... 96

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:92424619-92424819	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:92282827-92282923	K562	blood:	n/a	n/a
3	ARID3A	chr1:92463047-92463494	K562	blood:	n/a	n/a
4	ARID3A	chr1:92292432-92293961	HepG2	liver:	n/a	n/a
5	ARID3A	chr1:92296732-92297514	HepG2	liver:	n/a	chr1:92297485-92297501
6	ARID3A	chr1:92348921-92349309	HepG2	liver:	n/a	n/a
7	ARID3A	chr1:92256925-92256931	K562	blood:	n/a	n/a
8	ARID3A	chr1:92545717-92545724	K562	blood:	n/a	n/a
9	ARID3A	chr1:92281548-92281943	HepG2	liver:	n/a	n/a
10	ARID3A	chr1:92504254-92504757	HepG2	liver:	n/a	n/a
11	ARID3A	chr1:92351242-92351293	HepG2	liver:	n/a	n/a
12	ARID3A	chr1:92344000-92344448	HepG2	liver:	n/a	n/a
13	ARID3A	chr1:92392911-92393150	K562	blood:	n/a	n/a
14	ARID3A	chr1:92351519-92352531	HepG2	liver:	n/a	n/a
15	ARID3A	chr1:92348918-92349315	K562	blood:	n/a	n/a
16	ARID3A	chr1:92392821-92393186	HepG2	liver:	n/a	n/a
17	ARID3A	chr1:92545681-92545684	HepG2	liver:	n/a	n/a
18	ARID3A	chr1:92228764-92229274	K562	blood:	n/a	n/a
19	ARID3A	chr1:92463265-92463529	HepG2	liver:	n/a	n/a
20	ARID3A	chr1:92283136-92283452	HepG2	liver:	n/a	n/a
21	ARID3A	chr1:92310527-92311162	HepG2	liver:	n/a	n/a
22	ARID3A	chr1:92300668-92300994	HepG2	liver:	n/a	n/a
23	ARID3A	chr1:92295888-92296212	HepG2	liver:	n/a	n/a
24	ARID3A	chr1:92258609-92258748	K562	blood:	n/a	n/a
25	ARID3A	chr1:92235102-92235184	K562	blood:	n/a	n/a
26	ARID3A	chr1:92317145-92317468	HepG2	liver:	n/a	n/a
27	ARID3A	chr1:92272469-92272669	HepG2	liver:	n/a	n/a
28	ARID3A	chr1:92285078-92285270	HepG2	liver:	n/a	n/a
29	ARID3A	chr1:92210546-92211835	HepG2	liver:	n/a	n/a
30	ATF1	chr1:92231509-92231735	K562	blood:	n/a	n/a
31	ATF1	chr1:92270129-92270816	K562	blood:	n/a	n/a
32	ATF1	chr1:92530637-92530857	K562	blood:	n/a	n/a
33	ATF1	chr1:92228791-92229259	K562	blood:	n/a	n/a
34	ATF1	chr1:92360017-92360202	K562	blood:	n/a	n/a
35	ATF2	chr1:92217758-92218330	GM12878	blood:	n/a	n/a
36	ATF2	chr1:92269217-92270649	GM12878	blood:	n/a	n/a
37	ATF2	chr1:92217766-92218281	GM12878	blood:	n/a	n/a
38	ATF2	chr1:92338008-92338650	GM12878	blood:	n/a	n/a
39	ATF2	chr1:92343078-92343855	GM12878	blood:	n/a	n/a
40	ATF2	chr1:92341664-92342230	GM12878	blood:	n/a	n/a
41	ATF2	chr1:92269352-92269901	GM12878	blood:	n/a	n/a
42	ATF2	chr1:92343239-92343765	GM12878	blood:	n/a	n/a
43	ATF2	chr1:92270002-92270575	GM12878	blood:	n/a	n/a
44	ATF2	chr1:92338095-92338511	GM12878	blood:	n/a	n/a
45	ATF3	chr1:92351477-92351827	A549	lung:	n/a	n/a
46	ATF3	chr1:92414808-92414936	K562	blood:	n/a	chr1:92414878-92414887 chr1:92414867-92414887
47	ATF3	chr1:92270157-92270708	K562	blood:	n/a	n/a
48	BACH1	chr1:92228760-92228893	K562	blood:	n/a	n/a
49	BACH1	chr1:92351076-92351915	H1-hESC	embryonic stem cell:	n/a	n/a
50	BACH1	chr1:92352167-92352293	H1-hESC	embryonic stem cell:	n/a	n/a

(count:4708 , 50 per page) page: 1 2 3 4 5 6 7 ... 95

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:92352084-92352134	IMR90	lung:	fetal
2	chr1:92415524-92415574	HRCEpiC	kidney:	n/a
3	chr1:92247732-92247782	PrEC	prostate:	n/a
4	chr1:92351686-92351736	Hela-S3	cervix:	n/a
5	chr1:92416320-92416370	K562	blood:	n/a
6	chr1:92351695-92351745	GM12878	blood:	n/a
7	chr1:92491486-92491536	AG09309	skin:	n/a
8	chr1:92414344-92414394	MCF-7	breast:	n/a
9	chr1:92350430-92350480	RPTEC	kidney:	n/a
10	chr1:92351547-92351597	PrEC	prostate:	n/a
11	chr1:92234946-92234996	SK-N-MC	brain:	n/a
12	chr1:92352084-92352134	IMR90	lung:	fetal
13	chr1:92415524-92415574	HRCEpiC	kidney:	n/a
14	chr1:92247732-92247782	PrEC	prostate:	n/a
15	chr1:92351686-92351736	Hela-S3	cervix:	n/a
16	chr1:92416320-92416370	K562	blood:	n/a
17	chr1:92351695-92351745	GM12878	blood:	n/a
18	chr1:92491486-92491536	AG09309	skin:	n/a
19	chr1:92414344-92414394	MCF-7	breast:	n/a
20	chr1:92350430-92350480	RPTEC	kidney:	n/a
21	chr1:92351547-92351597	PrEC	prostate:	n/a
22	chr1:92234946-92234996	SK-N-MC	brain:	n/a
23	chr1:92545662-92545712	HMEC	breast:	n/a
24	chr1:92414295-92414345	ECC-1	luminal epithelium:	n/a
25	chr1:92350133-92350183	HRCEpiC	kidney:	n/a
26	chr1:92351047-92351097	GM12891	blood:	n/a
27	chr1:92414737-92414787	NT2-D1	testis:	n/a
28	chr1:92351047-92351097	NHDF-neo	bronchial:	n/a
29	chr1:92414221-92414271	HRPEpiC	eye:	n/a
30	chr1:92223917-92223967	HMEC	breast:	n/a
31	chr1:92545580-92545630	NHBE	bronchial:	n/a
32	chr1:92495342-92495392	CMK	blood:	n/a
33	chr1:92352084-92352134	AoSMC	blood vessel:	n/a
34	chr1:92494898-92494948	NHBE	bronchial:	n/a
35	chr1:92263858-92263908	HEK293	kidney:	embryo
36	chr1:92416676-92416726	HAEpiC	amniotic membrane:	n/a
37	chr1:92542467-92542517	LNCaP	prostate:	n/a
38	chr1:92351047-92351097	HRE	kidney:	n/a
39	chr1:92352407-92352457	HIPEpiC	eye:	n/a
40	chr1:92549234-92549284	RPTEC	kidney:	n/a
41	chr1:92350786-92350836	GM12891	blood:	n/a
42	chr1:92495720-92495770	ProgFib	skin:	n/a
43	chr1:92347850-92347900	PANC-1	pancreas:	n/a
44	chr1:92545188-92545238	HRE	kidney:	n/a
45	chr1:92494997-92495047	Caco-2	colon:	n/a
46	chr1:92415145-92415195	AG10803	skin:	n/a
47	chr1:92350568-92350618	Jurkat	blood:	n/a
48	chr1:92417998-92418048	HRPEpiC	eye:	n/a
49	chr1:92352293-92352343	ECC-1	luminal epithelium:	n/a
50	chr1:92417998-92418048	IMR90	lung:	fetal

(count:140 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr1:92351741..92353429-chr1:92365967..92368466,2	K562	blood:
2	chr1:92359348..92361445-chr1:92361640..92364597,2	K562	blood:
3	chr1:92316915..92318823-chr1:92321459..92323103,2	K562	blood:
4	chr1:91964010..91966765-chr1:92464590..92467417,2	K562	blood:
5	chr1:92097267..92098889-chr1:92337688..92339607,2	K562	blood:
6	chr1:92221438..92225438-chr1:92226162..92228913,3	K562	blood:
7	chr1:92329344..92331517-chr1:92335405..92337042,2	K562	blood:
8	chr1:92195746..92200158-chr1:92212228..92214643,4	K562	blood:
9	chr1:92494787..92497358-chr1:92544717..92548251,3	MCF-7	breast:
10	chr1:92222836..92226137-chr1:92226478..92228913,3	K562	blood:
11	chr1:92398059..92398985-chr1:92756667..92757204,2	MCF-7	breast:
12	chr1:91994551..91996997-chr1:92385610..92388191,2	K562	blood:
13	chr1:92411395..92413821-chr1:92420439..92422796,2	K562	blood:
14	chr1:92085074..92086910-chr1:92278209..92279900,2	K562	blood:
15	chr1:92288953..92291560-chr1:92301020..92303109,2	K562	blood:
16	chr1:92411395..92413821-chr1:92420439..92422796,2	K562	blood:
17	chr1:92329344..92331517-chr1:92335405..92337042,2	K562	blood:
18	chr1:92529291..92531947-chr1:92544374..92546080,2	K562	blood:
19	chr1:92202754..92203402-chr1:92392489..92393086,2	MCF-7	breast:
20	chr1:92418160..92421480-chr1:92423319..92426988,3	K562	blood:
21	chr1:92545812..92549091-chr1:92549918..92553923,4	K562	blood:
22	chr1:92252697..92255267-chr1:92255906..92257431,2	K562	blood:
23	chr1:92274050..92276390-chr1:92277677..92279989,2	K562	blood:
24	chr1:92082754..92083639-chr1:92392516..92393512,4	MCF-7	breast:
25	chr1:92274046..92275550-chr1:92277677..92280459,2	K562	blood:
26	chr1:92415221..92417669-chr1:92420291..92422618,2	K562	blood:
27	chr1:92542913..92545844-chr1:92825979..92827706,2	K562	blood:
28	chr1:92519730..92522449-chr1:92522597..92525189,3	K562	blood:
29	chr1:92208195..92211012-chr1:92213162..92216237,4	K562	blood:
30	chr1:92271912..92274176-chr1:92284969..92287951,2	K562	blood:
31	chr1:92211221..92213860-chr1:92214321..92216295,2	K562	blood:
32	chr1:92076490..92078813-chr1:92209944..92211883,2	K562	blood:
33	chr1:92506546..92509433-chr1:92514602..92517083,2	K562	blood:
34	chr1:92556197..92558083-chr1:92563000..92565811,2	MCF-7	breast:
35	chr1:92088173..92091117-chr1:92308700..92311610,2	MCF-7	breast:
36	chr1:92535153..92538093-chr1:92546590..92548474,2	K562	blood:
37	chr1:91978918..91979433-chr1:92392533..92393092,2	K562	blood:
38	chr1:91869631..91870341-chr1:92392565..92393108,2	K562	blood:
39	chr1:92271912..92274176-chr1:92284969..92287951,2	K562	blood:
40	chr1:91995716..91996502-chr1:92392369..92393018,2	MCF-7	breast:
41	chr1:92218784..92221286-chr1:92225561..92227867,2	K562	blood:
42	chr1:92493964..92495908-chr1:92496400..92499100,2	K562	blood:
43	chr1:92226019..92229425-chr1:92229716..92232598,3	K562	blood:
44	chr1:92243502..92246899-chr1:92255853..92258486,3	K562	blood:
45	chr1:92258357..92261493-chr1:92263209..92266078,3	K562	blood:
46	chr1:92082816..92083446-chr1:92348571..92349551,5	MCF-7	breast:
47	chr1:92288953..92291560-chr1:92301020..92303109,3	K562	blood:
48	chr1:92194536..92198402-chr1:92243329..92245903,3	K562	blood:
49	chr1:91976686..91977638-chr1:92392584..92393518,2	K562	blood:
50	chr1:92359622..92362110-chr1:92365556..92367175,2	K562	blood:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EPHX4-2	chr1:92414955-92415045	NONHSAT004445
2	lnc-EPHX4-2	chr1:92415195-92415239	NONHSAT004444
3	lnc-EPHX4-2	chr1:92415195-92415239	NONHSAT004446
4	lnc-HFM1-3	chr1:92329396-92329836	NONHSAT004441
5	lnc-EPHX4-2	chr1:92415457-92415856	NONHSAT004444
6	lnc-EPHX4-2	chr1:92415447-92415869	NONHSAT004446
7	lnc-EPHX4-2	chr1:92415457-92415859	NONHSAT004443
8	lnc-BRDT-1	chr1:92404826-92405131	NONHSAT004442
9	lnc-GLMN-2	chr1:92295333-92295631	NONHSAT004440
10	lnc-EPHX4-2	chr1:92414960-92415076	NONHSAT004446
11	lnc-EPHX4-2	chr1:92414955-92415076	NONHSAT004444
12	lnc-EPHX4-2	chr1:92415447-92415889	NONHSAT004445
13	lnc-EPHX4-2	chr1:92415195-92415239	NONHSAT004445
14	lnc-EPHX4-2	chr1:92414955-92415045	NONHSAT004443
15	lnc-HFM1-3	chr1:92351587-92351708	NONHSAT004441
16	lnc-EPHX4-2	chr1:92415195-92415239	NONHSAT004443

No data

Variant related genes	Relation type
LPCAT2BP	TF binding region
GAPDHP46	TF binding region
RN7SL653P	TF binding region
TGFBR3	TF binding region
BTBD8	TF binding region
SETSIP	TF binding region
BRDT	TF binding region
EPHX4	TF binding region
RN7SL235P	TF binding region
LPCAT2BP	CpG island
GAPDHP46	CpG island
RN7SL653P	CpG island
TGFBR3	CpG island
BTBD8	CpG island
SETSIP	CpG island
BRDT	CpG island
EPHX4	CpG island
RN7SL235P	CpG island
ENSG00000116830	chromatin interactions
ENSG00000069702	chromatin interactions
ENSG00000174842	chromatin interactions
ENSG00000122484	chromatin interactions
ENSG00000172031	chromatin interactions
ENSG00000097046	chromatin interactions
ENSG00000189195	chromatin interactions
ENSG00000233228	chromatin interactions
ENSG00000162669	chromatin interactions
ENSG00000239794	chromatin interactions

Extended variants
information (count: 11351 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:11351 , 50 per page) page: 1 2 3 4 5 6 7 ... 228

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17131547	chr1:92211020-92211021	Weak transcription Flanking Active TSS Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	disease
2	rs375407196	chr1:92211029-92211030	Weak transcription Flanking Active TSS Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs539873170	chr1:92211055-92211056	Weak transcription Flanking Active TSS Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs72965101	chr1:92211126-92211127	Weak transcription Flanking Active TSS Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs114833945	chr1:92211163-92211164	Weak transcription Flanking Active TSS Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs141828680	chr1:92211167-92211168	Weak transcription Flanking Active TSS Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs368611940	chr1:92211205-92211206	Weak transcription Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs560857171	chr1:92211208-92211209	Weak transcription Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs189118274	chr1:92211213-92211214	Weak transcription Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs574196128	chr1:92211214-92211215	Weak transcription Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs532558914	chr1:92211222-92211223	Weak transcription Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs537147338	chr1:92211252-92211253	Weak transcription Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs543943764	chr1:92211283-92211284	Weak transcription Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs556253403	chr1:92211289-92211290	Weak transcription Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs577204411	chr1:92211297-92211298	Weak transcription Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs368716930	chr1:92211317-92211318	Weak transcription Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs529996951	chr1:92211370-92211371	Weak transcription Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs556768095	chr1:92211397-92211398	Weak transcription Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs529437569	chr1:92211426-92211427	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs372345520	chr1:92211450-92211451	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs192384811	chr1:92211629-92211630	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs559720034	chr1:92211640-92211641	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs549582930	chr1:92211674-92211675	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs546614037	chr1:92211675-92211676	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs542526525	chr1:92211701-92211702	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs113588428	chr1:92211724-92211725	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs377124440	chr1:92211734-92211735	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs375843209	chr1:92211736-92211737	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs568598052	chr1:92211776-92211777	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs531561210	chr1:92211789-92211790	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs183788519	chr1:92211814-92211815	Weak transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs569373543	chr1:92211985-92211986	Weak transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs188277811	chr1:92212015-92212016	Weak transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs551755086	chr1:92212018-92212019	Weak transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs566883178	chr1:92212021-92212022	Weak transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs181382572	chr1:92212025-92212026	Weak transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs550959888	chr1:92212028-92212029	Weak transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs556048439	chr1:92212068-92212069	Weak transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs200584691	chr1:92212070-92212071	Weak transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs72714497	chr1:92212102-92212103	Weak transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs150653284	chr1:92212121-92212122	Weak transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs555978268	chr1:92212140-92212141	Weak transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs577366106	chr1:92212170-92212171	Weak transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs201890091	chr1:92212171-92212172	Weak transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs376564433	chr1:92212183-92212184	Weak transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs80336614	chr1:92212184-92212185	Weak transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs78198515	chr1:92212185-92212186	Weak transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs114708262	chr1:92212208-92212209	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs553315364	chr1:92212280-92212281	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs202175740	chr1:92212295-92212296	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Medulloblastoma	21979893	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
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
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	22429812	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17133270	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	16397240	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Prostate cancer	19156837	CNVD
Autism	17483303	CNVD
Malignant melanoma	17260012	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:6748 , 50 per page) page: 1 2 3 4 5 6 7 ... 135

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:92197000-92215200	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr1:92197200-92215400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr1:92197600-92230000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr1:92198200-92224400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr1:92199200-92218600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr1:92199400-92219000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
7	chr1:92201200-92219000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr1:92201400-92217600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
9	chr1:92203200-92212800	Weak transcription	Spleen	Spleen
10	chr1:92204800-92247000	Weak transcription	Primary T helper cells fromperipheralblood	blood
11	chr1:92205000-92212400	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr1:92206200-92212000	Enhancers	Colon Smooth Muscle	Colon
13	chr1:92206200-92212400	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr1:92206200-92213600	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
15	chr1:92207600-92211400	Enhancers	Skeletal Muscle Male	skeletal muscle
16	chr1:92207800-92211200	Weak transcription	A549	lung
17	chr1:92208400-92235800	Weak transcription	Rectal Mucosa Donor 29	rectum
18	chr1:92208800-92212600	Weak transcription	Lung	lung
19	chr1:92208800-92214800	Weak transcription	Brain Substantia Nigra	brain
20	chr1:92209000-92212400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr1:92209000-92212400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr1:92209000-92212400	Weak transcription	Fetal Muscle Trunk	muscle
23	chr1:92209200-92212400	Weak transcription	Muscle Satellite Cultured Cells	--
24	chr1:92209200-92212600	Weak transcription	NHLF	lung
25	chr1:92209200-92215600	Weak transcription	Osteobl	bone
26	chr1:92209200-92217000	Weak transcription	Primary T cells fromperipheralblood	blood
27	chr1:92209400-92212600	Weak transcription	Left Ventricle	heart
28	chr1:92209400-92213400	Weak transcription	Psoas Muscle	Psoas
29	chr1:92209600-92212200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr1:92209600-92212400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
31	chr1:92209800-92211800	Enhancers	Fetal Muscle Leg	muscle
32	chr1:92210000-92211400	Enhancers	Skeletal Muscle Female	skeletal muscle
33	chr1:92210000-92211800	Enhancers	Fetal Kidney	kidney
34	chr1:92210000-92212000	Enhancers	Adipose Nuclei	Adipose
35	chr1:92210200-92211200	Enhancers	Ovary	ovary
36	chr1:92210200-92211600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
37	chr1:92210200-92211800	Enhancers	Brain Anterior Caudate	brain
38	chr1:92210200-92212200	Enhancers	NHEK	skin
39	chr1:92210400-92211200	Enhancers	Fetal Brain Male	brain
40	chr1:92210400-92211200	Enhancers	Stomach Mucosa	stomach
41	chr1:92210400-92211200	Enhancers	Stomach Smooth Muscle	stomach
42	chr1:92210400-92211400	Flanking Active TSS	Liver	Liver
43	chr1:92210400-92211400	Enhancers	Brain Angular Gyrus	brain
44	chr1:92210400-92211400	Enhancers	Fetal Heart	heart
45	chr1:92210400-92211800	Enhancers	Pancreas	Pancrea
46	chr1:92210400-92212000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr1:92210400-92212000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr1:92210400-92212000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr1:92210400-92212000	Enhancers	Right Atrium	heart
50	chr1:92210400-92212200	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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