Variant report

Variant	nsv830592
Chromosome Location	chr1:92669282-92805629
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1323)
CpG islands
(count:1471)
Chromatin interactive
region (count:56)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:1323 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:92764599-92764839	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:92783280-92783972	K562	blood:	n/a	n/a
3	ARID3A	chr1:92763503-92763504	K562	blood:	n/a	n/a
4	ARID3A	chr1:92766611-92766631	K562	blood:	n/a	n/a
5	ARID3A	chr1:92715276-92715280	K562	blood:	n/a	n/a
6	ATF1	chr1:92783398-92784024	K562	blood:	n/a	n/a
7	ATF2	chr1:92764096-92764644	GM12878	blood:	n/a	n/a
8	BACH1	chr1:92766645-92766648	K562	blood:	n/a	n/a
9	BACH1	chr1:92764301-92764587	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr1:92799529-92799536	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCLAF1	chr1:92764045-92764833	GM12878	blood:	n/a	chr1:92764418-92764427
12	BCLAF1	chr1:92764017-92765143	GM12878	blood:	n/a	chr1:92764418-92764427
13	BHLHE40	chr1:92756997-92757267	GM12878	blood:	n/a	n/a
14	BHLHE40	chr1:92764027-92764709	GM12878	blood:	n/a	n/a
15	BHLHE40	chr1:92764095-92764711	K562	blood:	n/a	n/a
16	BRCA1	chr1:92763513-92764724	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr1:92764324-92764518	H1-hESC	embryonic stem cell:	n/a	n/a
18	CBX3	chr1:92764060-92764743	K562	blood:	n/a	n/a
19	CBX3	chr1:92793362-92793654	K562	blood:	n/a	n/a
20	CBX3	chr1:92793313-92793793	K562	blood:	n/a	n/a
21	CCNT2	chr1:92783392-92783684	K562	blood:	n/a	n/a
22	CCNT2	chr1:92764104-92764787	K562	blood:	n/a	n/a
23	CEBPB	chr1:92742694-92743206	IMR90	lung:	n/a	n/a
24	CEBPB	chr1:92726346-92726574	IMR90	lung:	n/a	chr1:92726435-92726448 chr1:92726435-92726446 chr1:92726437-92726446 chr1:92726435-92726448 chr1:92726437-92726446 chr1:92726437-92726446 chr1:92726437-92726446 chr1:92726437-92726448
25	CEBPB	chr1:92709968-92710275	IMR90	lung:	n/a	n/a
26	CEBPB	chr1:92771822-92771931	K562	blood:	n/a	n/a
27	CEBPB	chr1:92764454-92764538	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr1:92696987-92696998	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr1:92726352-92726563	HepG2	liver:	n/a	chr1:92726435-92726448 chr1:92726435-92726446 chr1:92726437-92726446 chr1:92726435-92726448 chr1:92726437-92726446 chr1:92726437-92726446 chr1:92726437-92726446 chr1:92726437-92726448
30	CEBPB	chr1:92676282-92677116	IMR90	lung:	n/a	n/a
31	CEBPB	chr1:92783037-92783606	K562	blood:	n/a	chr1:92783382-92783395
32	CEBPB	chr1:92764006-92764665	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr1:92717841-92718018	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr1:92771826-92771859	A549	lung:	n/a	n/a
35	CEBPB	chr1:92790412-92790461	A549	lung:	n/a	n/a
36	CEBPB	chr1:92726400-92726574	K562	blood:	n/a	chr1:92726435-92726448 chr1:92726435-92726446 chr1:92726437-92726446 chr1:92726435-92726448 chr1:92726437-92726446 chr1:92726437-92726446 chr1:92726437-92726446 chr1:92726437-92726448
37	CEBPB	chr1:92783071-92783306	IMR90	lung:	n/a	n/a
38	CEBPD	chr1:92764083-92764697	K562	blood:	n/a	n/a
39	CEBPD	chr1:92764388-92764748	HepG2	liver:	n/a	n/a
40	CEBPD	chr1:92783298-92783907	K562	blood:	n/a	n/a
41	CEBPD	chr1:92783312-92783988	K562	blood:	n/a	n/a
42	CEBPD	chr1:92764215-92764762	HepG2	liver:	n/a	n/a
43	CHD1	chr1:92763931-92765499	GM12878	blood:	n/a	n/a
44	CHD1	chr1:92764651-92765033	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD1	chr1:92763593-92764440	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD2	chr1:92764068-92764890	GM12878	blood:	n/a	n/a
47	CHD2	chr1:92764260-92764530	HepG2	liver:	n/a	n/a
48	CHD2	chr1:92764830-92764837	HepG2	liver:	n/a	n/a
49	CHD2	chr1:92764087-92765032	Hela-S3	cervix:	n/a	n/a
50	CHD2	chr1:92764188-92764682	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1471 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:92764833-92764883	BJ	skin:	n/a
2	chr1:92764777-92764827	SAEC	small airway:	n/a
3	chr1:92764770-92764820	ovcar-3	ovarian:	n/a
4	chr1:92762956-92763006	HCPEpiC	choroid plexus:	n/a
5	chr1:92683554-92683604	PrEC	prostate:	n/a
6	chr1:92687615-92687665	AG04450	lung:	fetal
7	chr1:92705964-92706014	A549	lung:	n/a
8	chr1:92764833-92764883	BJ	skin:	n/a
9	chr1:92764777-92764827	SAEC	small airway:	n/a
10	chr1:92764770-92764820	ovcar-3	ovarian:	n/a
11	chr1:92762956-92763006	HCPEpiC	choroid plexus:	n/a
12	chr1:92683554-92683604	PrEC	prostate:	n/a
13	chr1:92687615-92687665	AG04450	lung:	fetal
14	chr1:92705964-92706014	A549	lung:	n/a
15	chr1:92683530-92683580	T-47D	breast:	n/a
16	chr1:92682514-92682564	SK-N-MC	brain:	n/a
17	chr1:92683403-92683453	HL-60	blood:	n/a
18	chr1:92764419-92764469	NT2-D1	testis:	n/a
19	chr1:92764574-92764624	GM19239	blood:	n/a
20	chr1:92764833-92764883	SK-N-SH	brain:	n/a
21	chr1:92683675-92683725	HUVEC	blood vessel:	n/a
22	chr1:92764422-92764472	K562	blood:	n/a
23	chr1:92764349-92764399	HPAEpiC	pulmonary alveolar:	n/a
24	chr1:92764422-92764472	HCM	heart:	n/a
25	chr1:92683514-92683564	NH-A	brain:	n/a
26	chr1:92764574-92764624	Caco-2	colon:	n/a
27	chr1:92683514-92683564	BJ	skin:	n/a
28	chr1:92683530-92683580	HRCEpiC	kidney:	n/a
29	chr1:92764536-92764586	GM19239	blood:	n/a
30	chr1:92764349-92764399	T-47D	breast:	n/a
31	chr1:92683675-92683725	SK-N-SH_RA	brain:	n/a
32	chr1:92683530-92683580	PANC-1	pancreas:	n/a
33	chr1:92683403-92683453	HCT-116	colon:	n/a
34	chr1:92764770-92764820	NB4	blood:	n/a
35	chr1:92764419-92764469	Jurkat	blood:	n/a
36	chr1:92764574-92764624	Hepatocyte	liver:	n/a
37	chr1:92764349-92764399	Hela-S3	cervix:	n/a
38	chr1:92764188-92764238	AG04449	skin:	fetal
39	chr1:92683554-92683604	GM12892	blood:	n/a
40	chr1:92764833-92764883	AG10803	skin:	n/a
41	chr1:92764419-92764469	SK-N-SH	brain:	n/a
42	chr1:92764188-92764238	HMEC	breast:	n/a
43	chr1:92683454-92683504	PrEC	prostate:	n/a
44	chr1:92764431-92764481	IMR90	lung:	fetal
45	chr1:92760687-92760737	Hela-S3	cervix:	n/a
46	chr1:92687615-92687665	ovcar-3	ovarian:	n/a
47	chr1:92764349-92764399	NHBE	bronchial:	n/a
48	chr1:92683514-92683564	SK-N-MC	brain:	n/a
49	chr1:92683403-92683453	PFSK-1	brain:	n/a
50	chr1:92705964-92706014	HIPEpiC	eye:	n/a

(count:56 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:92763854..92764472-chr6:86388159..86388864,2	Hela-S3	cervix:
2	chr1:92398059..92398985-chr1:92756667..92757204,2	MCF-7	breast:
3	chr1:92764662..92766279-chr1:92768201..92769903,2	MCF-7	breast:
4	chr1:92724491..92726278-chr1:92728631..92730987,2	K562	blood:
5	chr1:92726438..92729412-chr1:92763997..92765974,2	K562	blood:
6	chr1:92724491..92726278-chr1:92728631..92730987,2	K562	blood:
7	chr1:92775257..92776314-chr1:93064696..93065442,3	MCF-7	breast:
8	chr1:92770418..92773011-chr1:92773916..92776545,2	K562	blood:
9	chr1:92706202..92709030-chr1:92713250..92715808,3	K562	blood:
10	chr1:92751701..92754444-chr1:92763776..92766491,2	MCF-7	breast:
11	chr1:92775543..92777429-chr1:92779885..92782284,2	K562	blood:
12	chr1:92775543..92777429-chr1:92779885..92782284,2	K562	blood:
13	chr1:92764662..92766279-chr1:92768201..92769903,2	MCF-7	breast:
14	chr1:92494741..92496705-chr1:92764193..92766152,2	MCF-7	breast:
15	chr1:92763702..92766598-chr1:92771008..92773495,2	MCF-7	breast:
16	chr1:92763773..92764454-chr6:30711937..30712495,2	Hela-S3	cervix:
17	chr1:92739930..92741567-chr1:92757034..92759673,2	K562	blood:
18	chr1:92751701..92754444-chr1:92763776..92766491,2	MCF-7	breast:
19	chr1:92751144..92752872-chr1:92762540..92765121,2	K562	blood:
20	chr1:92764332..92765052-chr7:105924734..105925596,2	Hela-S3	cervix:
21	chr1:92734882..92736683-chr1:92742818..92746079,3	K562	blood:
22	chr1:92681548..92684394-chr1:92687363..92690320,2	K562	blood:
23	chr1:92798322..92801081-chr1:92801191..92803127,2	K562	blood:
24	chr1:92768070..92770349-chr1:92773069..92775193,2	K562	blood:
25	chr1:92734882..92736683-chr1:92742818..92746079,3	K562	blood:
26	chr1:92762794..92765730-chr1:93295925..93298205,3	K562	blood:
27	chr1:92763308..92766374-chr1:92766490..92770872,7	K562	blood:
28	chr1:92674870..92677201-chr1:92679894..92682491,3	MCF-7	breast:
29	chr1:92762166..92764342-chr1:93135404..93137126,2	K562	blood:
30	chr1:92763878..92764562-chr7:107220034..107220754,2	Hela-S3	cervix:
31	chr1:92764074..92765656-chr1:93296705..93299037,2	K562	blood:
32	chr1:92801067..92802871-chr1:92812427..92814790,2	MCF-7	breast:
33	chr1:92764055..92764636-chr11:62608722..62609700,2	HCT-116	colon:
34	chr1:92676560..92677060-chr7:88229821..88230322,2	Hela-S3	cervix:
35	chr1:92781038..92783482-chr1:92784277..92786700,2	K562	blood:
36	chr1:92768070..92770349-chr1:92773069..92775193,2	K562	blood:
37	chr1:92763867..92766149-chr1:92769063..92771043,2	K562	blood:
38	chr1:92763470..92767298-chr1:92785657..92788225,3	K562	blood:
39	chr1:92774363..92776060-chr1:92906114..92908200,2	MCF-7	breast:
40	chr1:92753480..92757055-chr1:92763323..92765725,4	K562	blood:
41	chr1:92751144..92752872-chr1:92762540..92765121,2	K562	blood:
42	chr1:92790206..92790996-chr2:74694205..74695187,2	NB4	blood:
43	chr1:92763984..92764912-chr17:17184143..17184722,2	Hela-S3	cervix:
44	chr1:92463193..92463783-chr1:92756674..92757244,2	MCF-7	breast:
45	chr1:92674870..92677201-chr1:92679894..92682491,3	MCF-7	breast:
46	chr1:92764606..92767220-chr1:92781297..92784112,2	K562	blood:
47	chr1:92781038..92783482-chr1:92784277..92786700,2	K562	blood:
48	chr1:92704937..92705925-chr1:92715140..92715847,2	K562	blood:
49	chr1:92756651..92759126-chr1:92759145..92761543,4	K562	blood:
50	chr1:92704937..92705925-chr1:92715140..92715847,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GLMN-1	chr1:92763078-92763586	NONHSAT004453
2	lnc-GLMN-1	chr1:92764482-92764544	NONHSAT004453
3	lnc-C1orf146-1	chr1:92668705-92669548	NONHSAT004450

No data

(count:4 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	RPAP2	hsa-miR-215-5p	chr1:92789423-92789444
2	RPAP2	hsa-miR-215-5p	chr1:92789508-92789528
3	RPAP2	hsa-miR-192-5p	chr1:92789423-92789444
4	RPAP2	hsa-miR-192-5p	chr1:92789508-92789528

Variant related genes	Relation type
ACTBP12	TF binding region
RPAP2	TF binding region
ENSG00000265543	TF binding region
C1orf146	TF binding region
GLMN	TF binding region
ACTBP12	CpG island
RPAP2	CpG island
ENSG00000265543	CpG island
C1orf146	CpG island
GLMN	CpG island
ENSG00000172031	chromatin interactions
ENSG00000075790	chromatin interactions
ENSG00000122406	chromatin interactions
ENSG00000203910	chromatin interactions
ENSG00000137331	chromatin interactions
ENSG00000174842	chromatin interactions
ENSG00000122484	chromatin interactions
ENSG00000233125	chromatin interactions
ENSG00000265543	chromatin interactions
ENSG00000167604	chromatin interactions
ENSG00000272854	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000203875	chromatin interactions
ENSG00000105835	chromatin interactions
ENSG00000141030	chromatin interactions

Extended variants
information (count: 3876 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:3876 , 50 per page) page: 1 2 3 4 5 6 7 ... 78

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs189286378	chr1:92669299-92669300	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs143248427	chr1:92669300-92669301	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs369767312	chr1:92669358-92669359	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs572451731	chr1:92669393-92669394	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs368277226	chr1:92669406-92669407	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs543379420	chr1:92669459-92669460	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs180835709	chr1:92669464-92669465	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs114322663	chr1:92669534-92669535	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs543999075	chr1:92669543-92669544	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs114782634	chr1:92674681-92674682	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs556412978	chr1:92674685-92674686	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs139825514	chr1:92674704-92674705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs538451327	chr1:92674723-92674724	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs553511508	chr1:92674729-92674730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs529918731	chr1:92674731-92674732	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs35886968	chr1:92674882-92674883	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs543601451	chr1:92674922-92674923	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs143131669	chr1:92675028-92675029	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs561970664	chr1:92675058-92675059	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs573965784	chr1:92675066-92675067	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs146698491	chr1:92675075-92675076	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs563195951	chr1:92675093-92675094	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs374391645	chr1:92675100-92675101	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs552017470	chr1:92675150-92675151	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs531881568	chr1:92675217-92675218	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs1384613	chr1:92675361-92675362	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs3131817	chr1:92675386-92675387	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs192301552	chr1:92675403-92675404	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs57994453	chr1:92675434-92675435	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs377487918	chr1:92675536-92675537	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs1384612	chr1:92675563-92675564	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs547387472	chr1:92675576-92675577	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs549463500	chr1:92675581-92675582	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs371342447	chr1:92675585-92675586	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs549473393	chr1:92675594-92675595	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs538512299	chr1:92675600-92675601	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs553573047	chr1:92675632-92675633	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs375102366	chr1:92675635-92675636	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs183091043	chr1:92675650-92675651	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs547707820	chr1:92675657-92675658	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs185227142	chr1:92675677-92675678	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs189698862	chr1:92675686-92675687	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs555822899	chr1:92675720-92675721	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs149943548	chr1:92675761-92675762	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs144996470	chr1:92675825-92675826	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs562835663	chr1:92675868-92675869	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs578254837	chr1:92675889-92675890	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs545693097	chr1:92675908-92675909	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs200470944	chr1:92675973-92675974	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs35815669	chr1:92675983-92675984	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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Lung adenocarcinoma	21935476	CNVD

Chromatin state (count:3269 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:92674600-92674800	Enhancers	Sigmoid Colon	Sigmoid Colon
2	chr1:92674800-92676800	Enhancers	Primary T cells from cord blood	blood
3	chr1:92675000-92675200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
4	chr1:92675200-92677000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
5	chr1:92675400-92676800	Enhancers	Primary T helper naive cells from peripheral blood	blood
6	chr1:92675400-92676800	Enhancers	Primary T helper cells fromperipheralblood	blood
7	chr1:92675600-92677000	Enhancers	Primary T helper cells PMA-I stimulated	--
8	chr1:92676000-92676200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr1:92676000-92676200	Enhancers	Muscle Satellite Cultured Cells	--
10	chr1:92676000-92676200	Enhancers	Osteobl	bone
11	chr1:92676000-92676600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr1:92676000-92676600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr1:92676000-92676800	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr1:92676000-92676800	Enhancers	Dnd41	blood
15	chr1:92676200-92676400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr1:92676200-92676600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
17	chr1:92676200-92676600	Enhancers	Aorta	Aorta
18	chr1:92676200-92676600	Enhancers	Thymus	Thymus
19	chr1:92676200-92676600	Enhancers	HMEC	breast
20	chr1:92676200-92676600	Enhancers	NH-A	brain
21	chr1:92676200-92676800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr1:92676200-92676800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr1:92676200-92676800	Enhancers	Primary T killer memory cells from peripheral blood	blood
24	chr1:92676200-92676800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
25	chr1:92676200-92676800	Flanking Active TSS	Osteobl	bone
26	chr1:92676200-92677000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr1:92676200-92677000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
28	chr1:92676200-92677000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr1:92676400-92676800	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr1:92676400-92676800	Enhancers	HSMM	muscle
31	chr1:92676400-92676800	Enhancers	HSMMtube	muscle
32	chr1:92676400-92677000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
33	chr1:92676400-92677200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr1:92676800-92677000	Enhancers	Osteobl	bone
35	chr1:92676800-92677200	Enhancers	Muscle Satellite Cultured Cells	--
36	chr1:92676800-92677400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr1:92676800-92677800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr1:92676800-92677800	Weak transcription	HSMMtube	muscle
39	chr1:92677400-92677800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr1:92677800-92678600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr1:92678000-92678200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr1:92678000-92678200	Enhancers	HSMMtube	muscle
43	chr1:92684200-92684400	Enhancers	HepG2	liver
44	chr1:92694400-92694800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
45	chr1:92694600-92694800	Enhancers	Pancreas	Pancrea
46	chr1:92695000-92695400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr1:92697400-92697800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr1:92704200-92704400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr1:92704400-92705400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr1:92705400-92705600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin

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