Variant report

Variant	nsv1002730
Chromosome Location	chr1:92302541-92565229
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3208)
CpG islands
(count:4031)
Chromatin interactive
region (count:74)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3208 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:92545681-92545684	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:92463047-92463494	K562	blood:	n/a	n/a
3	ARID3A	chr1:92392911-92393150	K562	blood:	n/a	n/a
4	ARID3A	chr1:92424619-92424819	HepG2	liver:	n/a	n/a
5	ARID3A	chr1:92545717-92545724	K562	blood:	n/a	n/a
6	ARID3A	chr1:92463265-92463529	HepG2	liver:	n/a	n/a
7	ARID3A	chr1:92392821-92393186	HepG2	liver:	n/a	n/a
8	ARID3A	chr1:92348921-92349309	HepG2	liver:	n/a	n/a
9	ARID3A	chr1:92317145-92317468	HepG2	liver:	n/a	n/a
10	ARID3A	chr1:92504254-92504757	HepG2	liver:	n/a	n/a
11	ARID3A	chr1:92310527-92311162	HepG2	liver:	n/a	n/a
12	ARID3A	chr1:92348918-92349315	K562	blood:	n/a	n/a
13	ARID3A	chr1:92344000-92344448	HepG2	liver:	n/a	n/a
14	ARID3A	chr1:92351519-92352531	HepG2	liver:	n/a	n/a
15	ARID3A	chr1:92351242-92351293	HepG2	liver:	n/a	n/a
16	ATF1	chr1:92360017-92360202	K562	blood:	n/a	n/a
17	ATF1	chr1:92530637-92530857	K562	blood:	n/a	n/a
18	ATF2	chr1:92338095-92338511	GM12878	blood:	n/a	n/a
19	ATF2	chr1:92343078-92343855	GM12878	blood:	n/a	n/a
20	ATF2	chr1:92341664-92342230	GM12878	blood:	n/a	n/a
21	ATF2	chr1:92343239-92343765	GM12878	blood:	n/a	n/a
22	ATF2	chr1:92338008-92338650	GM12878	blood:	n/a	n/a
23	ATF3	chr1:92414808-92414936	K562	blood:	n/a	chr1:92414878-92414887 chr1:92414867-92414887
24	ATF3	chr1:92351477-92351827	A549	lung:	n/a	n/a
25	BACH1	chr1:92352167-92352293	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr1:92494875-92495995	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr1:92331752-92331754	K562	blood:	n/a	n/a
28	BACH1	chr1:92458760-92458932	K562	blood:	n/a	n/a
29	BACH1	chr1:92351076-92351915	H1-hESC	embryonic stem cell:	n/a	n/a
30	BATF	chr1:92338142-92338596	GM12878	blood:	n/a	n/a
31	BATF	chr1:92343331-92343754	GM12878	blood:	n/a	chr1:92343581-92343591 chr1:92343580-92343591
32	BATF	chr1:92341701-92342110	GM12878	blood:	n/a	n/a
33	BATF	chr1:92341639-92342169	GM12878	blood:	n/a	n/a
34	BATF	chr1:92343339-92343755	GM12878	blood:	n/a	chr1:92343581-92343591 chr1:92343580-92343591
35	BATF	chr1:92338200-92338562	GM12878	blood:	n/a	n/a
36	BATF	chr1:92324984-92325220	GM12878	blood:	n/a	n/a
37	BCL11A	chr1:92338227-92338457	GM12878	blood:	n/a	n/a
38	BCL11A	chr1:92343450-92343624	GM12878	blood:	n/a	n/a
39	BCL11A	chr1:92343351-92343764	GM12878	blood:	n/a	n/a
40	BCL11A	chr1:92338171-92338574	GM12878	blood:	n/a	n/a
41	BCL3	chr1:92365986-92366640	A549	lung:	n/a	n/a
42	BCL3	chr1:92351428-92352124	A549	lung:	n/a	chr1:92351982-92351995
43	BCL3	chr1:92310304-92310983	A549	lung:	n/a	chr1:92310955-92310963
44	BCL3	chr1:92343289-92343788	GM12878	blood:	n/a	n/a
45	BCL3	chr1:92338173-92338456	GM12878	blood:	n/a	n/a
46	BCL3	chr1:92366001-92366544	A549	lung:	n/a	n/a
47	BCL3	chr1:92343437-92343812	GM12878	blood:	n/a	n/a
48	BCLAF1	chr1:92351455-92352057	GM12878	blood:	n/a	chr1:92351982-92351995
49	BCLAF1	chr1:92341662-92342157	GM12878	blood:	n/a	n/a
50	BCLAF1	chr1:92343347-92343682	GM12878	blood:	n/a	n/a

(count:4031 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:92350786-92350836	NH-A	brain:	n/a
2	chr1:92546447-92546497	IMR90	lung:	fetal
3	chr1:92495004-92495054	HPAEpiC	pulmonary alveolar:	n/a
4	chr1:92352481-92352531	K562	blood:	n/a
5	chr1:92495342-92495392	AG09319	gingival:	n/a
6	chr1:92350786-92350836	NH-A	brain:	n/a
7	chr1:92546447-92546497	IMR90	lung:	fetal
8	chr1:92495004-92495054	HPAEpiC	pulmonary alveolar:	n/a
9	chr1:92352481-92352531	K562	blood:	n/a
10	chr1:92495342-92495392	AG09319	gingival:	n/a
11	chr1:92415048-92415098	GM12891	blood:	n/a
12	chr1:92414344-92414394	CMK	blood:	n/a
13	chr1:92351547-92351597	HRCEpiC	kidney:	n/a
14	chr1:92545768-92545818	HL-60	blood:	n/a
15	chr1:92546447-92546497	SK-N-SH_RA	brain:	n/a
16	chr1:92414985-92415035	SK-N-SH_RA	brain:	n/a
17	chr1:92414782-92414832	HRPEpiC	eye:	n/a
18	chr1:92414737-92414787	NH-A	brain:	n/a
19	chr1:92351487-92351537	HL-60	blood:	n/a
20	chr1:92352481-92352531	NHDF-neo	bronchial:	n/a
21	chr1:92417998-92418048	NT2-D1	testis:	n/a
22	chr1:92352481-92352531	HNPCEpiC	eye:	n/a
23	chr1:92351047-92351097	NH-A	brain:	n/a
24	chr1:92494997-92495047	BE2_C	brain:	n/a
25	chr1:92545224-92545274	HL-60	blood:	n/a
26	chr1:92414985-92415035	PFSK-1	brain:	n/a
27	chr1:92352084-92352134	SK-N-SH	brain:	n/a
28	chr1:92350112-92350162	ECC-1	luminal epithelium:	n/a
29	chr1:92351487-92351537	AG09309	skin:	n/a
30	chr1:92351641-92351691	GM12891	blood:	n/a
31	chr1:92347850-92347900	U87	brain:	n/a
32	chr1:92545888-92545938	Hepatocyte	liver:	n/a
33	chr1:92546135-92546185	CMK	blood:	n/a
34	chr1:92416676-92416726	AG04450	lung:	fetal
35	chr1:92414520-92414570	AoSMC	blood vessel:	n/a
36	chr1:92415145-92415195	RPTEC	kidney:	n/a
37	chr1:92414344-92414394	Jurkat	blood:	n/a
38	chr1:92494997-92495047	HepG2	liver:	n/a
39	chr1:92545888-92545938	GM12892	blood:	n/a
40	chr1:92351487-92351537	U87	brain:	n/a
41	chr1:92495342-92495392	NB4	blood:	n/a
42	chr1:92416320-92416370	IMR90	lung:	fetal
43	chr1:92414985-92415035	LNCaP	prostate:	n/a
44	chr1:92350133-92350183	HL-60	blood:	n/a
45	chr1:92545580-92545630	NB4	blood:	n/a
46	chr1:92352404-92352454	HRCEpiC	kidney:	n/a
47	chr1:92494898-92494948	HepG2	liver:	n/a
48	chr1:92495729-92495779	IMR90	lung:	fetal
49	chr1:92351956-92352006	GM12878	blood:	n/a
50	chr1:92495083-92495133	K562	blood:	n/a

(count:74 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:92354436..92357349-chr1:92361835..92364580,4	K562	blood:
2	chr1:92359622..92362110-chr1:92365556..92367175,2	K562	blood:
3	chr1:92531679..92534472-chr1:92536505..92538325,2	K562	blood:
4	chr1:92535153..92538093-chr1:92546590..92548474,2	K562	blood:
5	chr1:92500741..92502488-chr1:92762793..92765174,2	MCF-7	breast:
6	chr1:92542913..92545844-chr1:92825979..92827706,2	K562	blood:
7	chr1:92463193..92463783-chr1:92756674..92757244,2	MCF-7	breast:
8	chr1:92519730..92522449-chr1:92522597..92525189,3	K562	blood:
9	chr1:92418160..92421480-chr1:92423319..92426988,3	K562	blood:
10	chr1:92341690..92345444-chr1:92349151..92352209,5	K562	blood:
11	chr1:92529291..92531947-chr1:92544374..92546080,2	K562	blood:
12	chr1:92415221..92417669-chr1:92420291..92422618,2	K562	blood:
13	chr1:92556197..92558083-chr1:92563000..92565811,2	MCF-7	breast:
14	chr1:92545812..92549091-chr1:92549918..92553923,4	K562	blood:
15	chr1:92493964..92495908-chr1:92496400..92499100,2	K562	blood:
16	chr1:92494787..92497358-chr1:92544717..92548251,3	MCF-7	breast:
17	chr1:92494787..92497358-chr1:92544717..92548251,3	MCF-7	breast:
18	chr1:91869631..91870341-chr1:92392565..92393108,2	K562	blood:
19	chr1:92329344..92331517-chr1:92335405..92337042,2	K562	blood:
20	chr1:92288953..92291560-chr1:92301020..92303109,3	K562	blood:
21	chr1:92316915..92318823-chr1:92321459..92323103,2	K562	blood:
22	chr1:92346372..92348538-chr1:92370919..92373851,2	K562	blood:
23	chr1:92359622..92362110-chr1:92365556..92367175,2	K562	blood:
24	chr1:92306378..92308491-chr1:92309526..92312029,2	K562	blood:
25	chr1:91966132..91968252-chr1:92404869..92406833,2	K562	blood:
26	chr1:91976686..91977638-chr1:92392584..92393518,2	K562	blood:
27	chr1:92544652..92546280-chr1:92558053..92559585,2	K562	blood:
28	chr1:92351002..92351971-chr1:117602866..117603496,2	Hela-S3	cervix:
29	chr1:92529291..92531947-chr1:92544374..92546080,2	K562	blood:
30	chr1:92357381..92360848-chr1:92361441..92364289,5	K562	blood:
31	chr1:92506546..92509433-chr1:92514602..92517083,2	K562	blood:
32	chr1:92493964..92495908-chr1:92496400..92499100,2	K562	blood:
33	chr1:92398059..92398985-chr1:92756667..92757204,2	MCF-7	breast:
34	chr1:92309780..92313855-chr1:92314421..92317529,4	K562	blood:
35	chr1:92309780..92313855-chr1:92314421..92317529,4	K562	blood:
36	chr1:92490161..92492607-chr1:92493368..92497617,3	K562	blood:
37	chr1:92354436..92357349-chr1:92361835..92364580,4	K562	blood:
38	chr1:91994551..91996997-chr1:92385610..92388191,2	K562	blood:
39	chr1:92329344..92331517-chr1:92335405..92337042,2	K562	blood:
40	chr1:92532650..92534894-chr1:92538818..92540475,2	K562	blood:
41	chr1:92418160..92421480-chr1:92423319..92426988,3	K562	blood:
42	chr1:92351741..92353429-chr1:92365967..92368466,2	K562	blood:
43	chr1:92202754..92203402-chr1:92392489..92393086,2	MCF-7	breast:
44	chr1:92357381..92360848-chr1:92361441..92364289,5	K562	blood:
45	chr1:92359348..92361445-chr1:92361640..92364597,2	K562	blood:
46	chr1:92350409..92353610-chr1:92359343..92362400,3	K562	blood:
47	chr1:91976702..91977558-chr1:92348916..92349656,2	MCF-7	breast:
48	chr1:92415221..92417669-chr1:92420291..92422618,2	K562	blood:
49	chr1:92535153..92538093-chr1:92546590..92548474,2	K562	blood:
50	chr1:91995716..91996502-chr1:92392369..92393018,2	MCF-7	breast:

(count:15 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 7336 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:7336 , 50 per page) page: 1 2 3 4 5 6 7 ... 147

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11165595	chr1:92302541-92302542	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs148154011	chr1:92302567-92302568	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs180842536	chr1:92302607-92302608	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs185059631	chr1:92302695-92302696	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs551874402	chr1:92302704-92302705	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs374151453	chr1:92302721-92302722	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs570412887	chr1:92302742-92302743	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs531271957	chr1:92302778-92302779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs139255891	chr1:92302779-92302780	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs386367648	chr1:92302786-92302787	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs200230027	chr1:92302802-92302803	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs3039475	chr1:92302809-92302810	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs536428969	chr1:92302832-92302833	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs142360375	chr1:92302851-92302852	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs567969930	chr1:92302893-92302894	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs2996482	chr1:92302901-92302902	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs556858229	chr1:92302960-92302961	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs139876499	chr1:92302991-92302992	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs35216083	chr1:92303002-92303003	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs556363530	chr1:92303005-92303006	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs535785872	chr1:92303018-92303019	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs557259486	chr1:92303086-92303087	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs575534469	chr1:92303090-92303091	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs141665520	chr1:92303128-92303129	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs573036784	chr1:92303152-92303153	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs559018390	chr1:92303200-92303201	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs577304659	chr1:92303288-92303289	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs140443290	chr1:92303364-92303365	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs66990307	chr1:92303368-92303369	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs190262347	chr1:92303403-92303404	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs376836706	chr1:92303408-92303409	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs545627129	chr1:92303453-92303454	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs559515386	chr1:92303474-92303475	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs182917482	chr1:92303499-92303500	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs542131258	chr1:92303556-92303557	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs563609699	chr1:92303601-92303602	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs531020716	chr1:92303644-92303645	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs558618516	chr1:92303687-92303688	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs187081332	chr1:92303699-92303700	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs564700240	chr1:92303707-92303708	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs528202406	chr1:92303812-92303813	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs191674625	chr1:92303823-92303824	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs567982144	chr1:92303824-92303825	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs528868219	chr1:92303851-92303852	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs183540214	chr1:92303880-92303881	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs370944852	chr1:92303940-92303941	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs72969176	chr1:92303943-92303944	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs12134904	chr1:92303960-92303961	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs539093148	chr1:92304016-92304017	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs538781382	chr1:92304027-92304028	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:3593 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:92294800-92311600	Weak transcription	Gastric	stomach
2	chr1:92296400-92335800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr1:92296800-92307400	Weak transcription	Lung	lung
4	chr1:92296800-92307800	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr1:92296800-92309400	Weak transcription	Left Ventricle	heart
6	chr1:92296800-92311400	Weak transcription	Stomach Mucosa	stomach
7	chr1:92297000-92308000	Weak transcription	Primary T cells fromperipheralblood	blood
8	chr1:92297000-92310400	Weak transcription	Pancreas	Pancrea
9	chr1:92297000-92311000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr1:92297200-92306600	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr1:92297200-92308200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr1:92297200-92311800	Weak transcription	Fetal Intestine Large	intestine
13	chr1:92297200-92313600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
14	chr1:92297400-92304600	Weak transcription	NHDF-Ad	bronchial
15	chr1:92297800-92310400	Weak transcription	Duodenum Smooth Muscle	Duodenum
16	chr1:92298200-92306600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr1:92298200-92314600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
18	chr1:92298800-92306400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
19	chr1:92299800-92302600	Enhancers	Stomach Smooth Muscle	stomach
20	chr1:92300000-92306200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr1:92300000-92310200	Weak transcription	Fetal Lung	lung
22	chr1:92300800-92305200	Weak transcription	Placenta	Placenta
23	chr1:92300800-92309600	Weak transcription	Fetal Muscle Trunk	muscle
24	chr1:92300800-92329600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr1:92301000-92303000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr1:92301000-92303400	Weak transcription	A549	lung
27	chr1:92301000-92306600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr1:92301000-92306600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr1:92301000-92307000	Weak transcription	Ovary	ovary
30	chr1:92301000-92309400	Weak transcription	Fetal Stomach	stomach
31	chr1:92301000-92311000	Weak transcription	Rectal Smooth Muscle	rectum
32	chr1:92301200-92306600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr1:92301200-92306800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr1:92301200-92307800	Weak transcription	Rectal Mucosa Donor 29	rectum
35	chr1:92301200-92309200	Weak transcription	Fetal Muscle Leg	muscle
36	chr1:92301800-92302800	Enhancers	Colon Smooth Muscle	Colon
37	chr1:92302000-92302600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr1:92302200-92302600	Enhancers	Fetal Heart	heart
39	chr1:92302400-92309200	Enhancers	HepG2	liver
40	chr1:92302600-92303200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr1:92302600-92309200	Weak transcription	Right Ventricle	heart
42	chr1:92302600-92310000	Weak transcription	Fetal Heart	heart
43	chr1:92302600-92310800	Weak transcription	Stomach Smooth Muscle	stomach
44	chr1:92302800-92303600	Enhancers	Psoas Muscle	Psoas
45	chr1:92302800-92306600	Weak transcription	Colon Smooth Muscle	Colon
46	chr1:92303000-92304000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
47	chr1:92303200-92303800	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr1:92303400-92303800	Enhancers	A549	lung
49	chr1:92303800-92304600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr1:92303800-92307800	Weak transcription	A549	lung

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