Variant report

Variant	nsv870667
Chromosome Location	chr1:92697188-92813741
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1289)
CpG islands
(count:916)
Chromatin interactive
region (count:54)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:1289 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

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	chr1:92766611-92766631	K562	blood:	n/a	n/a
3	ARID3A	chr1:92783280-92783972	K562	blood:	n/a	n/a
4	ARID3A	chr1:92763503-92763504	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	chr1:92799529-92799536	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr1:92766645-92766648	K562	blood:	n/a	n/a
10	BACH1	chr1:92764301-92764587	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	chr1:92764027-92764709	GM12878	blood:	n/a	n/a
14	BHLHE40	chr1:92756997-92757267	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	chr1:92771826-92771859	A549	lung:	n/a	n/a
24	CEBPB	chr1:92808725-92808920	K562	blood:	n/a	n/a
25	CEBPB	chr1:92813356-92813609	HepG2	liver:	n/a	chr1:92813453-92813464 chr1:92813454-92813465
26	CEBPB	chr1:92783071-92783306	IMR90	lung:	n/a	n/a
27	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
28	CEBPB	chr1:92808642-92808982	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr1:92808709-92808944	A549	lung:	n/a	n/a
30	CEBPB	chr1:92742694-92743206	IMR90	lung:	n/a	n/a
31	CEBPB	chr1:92808638-92809009	K562	blood:	n/a	n/a
32	CEBPB	chr1:92808669-92808973	K562	blood:	n/a	n/a
33	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
34	CEBPB	chr1:92808676-92808981	MCF-7	breast:	n/a	n/a
35	CEBPB	chr1:92808672-92809031	ECC-1	luminal epithelium:	n/a	n/a
36	CEBPB	chr1:92813357-92813557	A549	lung:	n/a	chr1:92813453-92813464 chr1:92813454-92813465
37	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
38	CEBPB	chr1:92717841-92718018	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr1:92783037-92783606	K562	blood:	n/a	chr1:92783382-92783395
40	CEBPB	chr1:92764006-92764665	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr1:92808642-92809002	HepG2	liver:	n/a	n/a
42	CEBPB	chr1:92808717-92808941	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr1:92808645-92808986	A549	lung:	n/a	n/a
44	CEBPB	chr1:92790412-92790461	A549	lung:	n/a	n/a
45	CEBPB	chr1:92709968-92710275	IMR90	lung:	n/a	n/a
46	CEBPB	chr1:92808641-92809003	IMR90	lung:	n/a	n/a
47	CEBPB	chr1:92771822-92771931	K562	blood:	n/a	n/a
48	CEBPB	chr1:92764454-92764538	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPD	chr1:92764388-92764748	HepG2	liver:	n/a	n/a
50	CEBPD	chr1:92764083-92764697	K562	blood:	n/a	n/a

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:92764419-92764469	GM12892	blood:	n/a
2	chr1:92764419-92764469	GM12892	blood:	n/a
3	chr1:92764422-92764472	PrEC	prostate:	n/a
4	chr1:92762956-92763006	GM12892	blood:	n/a
5	chr1:92764536-92764586	AG04449	skin:	fetal
6	chr1:92764419-92764469	HEK293	kidney:	embryo
7	chr1:92764349-92764399	ProgFib	skin:	n/a
8	chr1:92764770-92764820	HIPEpiC	eye:	n/a
9	chr1:92764770-92764820	CMK	blood:	n/a
10	chr1:92764775-92764825	GM12891	blood:	n/a
11	chr1:92764174-92764224	SK-N-MC	brain:	n/a
12	chr1:92764833-92764883	GM12878	blood:	n/a
13	chr1:92764775-92764825	RPTEC	kidney:	n/a
14	chr1:92764777-92764827	K562	blood:	n/a
15	chr1:92764770-92764820	Hepatocyte	liver:	n/a
16	chr1:92762956-92763006	CMK	blood:	n/a
17	chr1:92764174-92764224	Hela-S3	cervix:	n/a
18	chr1:92764775-92764825	CMK	blood:	n/a
19	chr1:92764188-92764238	H1-hESC	embryonic stem cell:	embryo
20	chr1:92764174-92764224	H1-hESC	embryonic stem cell:	embryo
21	chr1:92764536-92764586	HCPEpiC	choroid plexus:	n/a
22	chr1:92764174-92764224	HCT-116	colon:	n/a
23	chr1:92764536-92764586	PrEC	prostate:	n/a
24	chr1:92764419-92764469	LNCaP	prostate:	n/a
25	chr1:92764349-92764399	AG09309	skin:	n/a
26	chr1:92764431-92764481	T-47D	breast:	n/a
27	chr1:92764431-92764481	NHBE	bronchial:	n/a
28	chr1:92764188-92764238	NHBE	bronchial:	n/a
29	chr1:92764174-92764224	HEK293	kidney:	embryo
30	chr1:92764775-92764825	SK-N-SH_RA	brain:	n/a
31	chr1:92764174-92764224	MCF-7	breast:	n/a
32	chr1:92764777-92764827	BE2_C	brain:	n/a
33	chr1:92764188-92764238	HEK293	kidney:	embryo
34	chr1:92764777-92764827	HPAEpiC	pulmonary alveolar:	n/a
35	chr1:92764419-92764469	PANC-1	pancreas:	n/a
36	chr1:92764574-92764624	MCF-7	breast:	n/a
37	chr1:92760687-92760737	H1-hESC	embryonic stem cell:	embryo
38	chr1:92764536-92764586	T-47D	breast:	n/a
39	chr1:92764574-92764624	HCT-116	colon:	n/a
40	chr1:92764419-92764469	CMK	blood:	n/a
41	chr1:92764833-92764883	SK-N-SH_RA	brain:	n/a
42	chr1:92764833-92764883	CMK	blood:	n/a
43	chr1:92764422-92764472	SAEC	small airway:	n/a
44	chr1:92764574-92764624	HEK293	kidney:	embryo
45	chr1:92764536-92764586	NH-A	brain:	n/a
46	chr1:92764770-92764820	SK-N-SH_RA	brain:	n/a
47	chr1:92764833-92764883	LNCaP	prostate:	n/a
48	chr1:92764349-92764399	HEEpiC	esophagus:	n/a
49	chr1:92762956-92763006	NT2-D1	testis:	n/a
50	chr1:92762956-92763006	BE2_C	brain:	n/a

(count:54 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:92768070..92770349-chr1:92773069..92775193,2	K562	blood:
2	chr1:92801067..92802871-chr1:92812427..92814790,2	MCF-7	breast:
3	chr1:92764606..92767220-chr1:92781297..92784112,2	K562	blood:
4	chr1:92781038..92783482-chr1:92784277..92786700,2	K562	blood:
5	chr1:92734882..92736683-chr1:92742818..92746079,3	K562	blood:
6	chr1:92763867..92766149-chr1:92769063..92771043,2	K562	blood:
7	chr1:92704937..92705925-chr1:92715140..92715847,2	K562	blood:
8	chr1:92764332..92765052-chr7:105924734..105925596,2	Hela-S3	cervix:
9	chr1:92494741..92496705-chr1:92764193..92766152,2	MCF-7	breast:
10	chr1:92756651..92759126-chr1:92759145..92761543,4	K562	blood:
11	chr1:92764662..92766279-chr1:92768201..92769903,2	MCF-7	breast:
12	chr1:92751701..92754444-chr1:92763776..92766491,2	MCF-7	breast:
13	chr1:92811074..92812742-chr1:92812855..92814750,2	K562	blood:
14	chr1:92463193..92463783-chr1:92756674..92757244,2	MCF-7	breast:
15	chr1:92770418..92773011-chr1:92773916..92776545,2	K562	blood:
16	chr1:92801067..92802871-chr1:92812427..92814790,2	MCF-7	breast:
17	chr1:92753480..92757055-chr1:92763323..92765725,4	K562	blood:
18	chr1:92790206..92790996-chr2:74694205..74695187,2	NB4	blood:
19	chr1:92762794..92765730-chr1:93295925..93298205,3	K562	blood:
20	chr1:92763773..92764454-chr6:30711937..30712495,2	Hela-S3	cervix:
21	chr1:92726438..92729412-chr1:92763997..92765974,2	K562	blood:
22	chr1:92751144..92752872-chr1:92762540..92765121,2	K562	blood:
23	chr1:92706202..92709030-chr1:92713250..92715808,3	K562	blood:
24	chr1:92763470..92767298-chr1:92785657..92788225,3	K562	blood:
25	chr1:92764074..92765656-chr1:93296705..93299037,2	K562	blood:
26	chr1:92775257..92776314-chr1:93064696..93065442,3	MCF-7	breast:
27	chr1:92763854..92764472-chr6:86388159..86388864,2	Hela-S3	cervix:
28	chr1:92764662..92766279-chr1:92768201..92769903,2	MCF-7	breast:
29	chr1:92774363..92776060-chr1:92906114..92908200,2	MCF-7	breast:
30	chr1:92775543..92777429-chr1:92779885..92782284,2	K562	blood:
31	chr1:92768070..92770349-chr1:92773069..92775193,2	K562	blood:
32	chr1:92724491..92726278-chr1:92728631..92730987,2	K562	blood:
33	chr1:92763308..92766374-chr1:92766490..92770872,7	K562	blood:
34	chr1:92724491..92726278-chr1:92728631..92730987,2	K562	blood:
35	chr1:92763984..92764912-chr17:17184143..17184722,2	Hela-S3	cervix:
36	chr1:92763702..92766598-chr1:92771008..92773495,2	MCF-7	breast:
37	chr1:92707530..92709675-chr1:92712279..92714750,2	K562	blood:
38	chr1:92762166..92764342-chr1:93135404..93137126,2	K562	blood:
39	chr1:92763878..92764562-chr7:107220034..107220754,2	Hela-S3	cervix:
40	chr1:92811074..92812742-chr1:92812855..92814750,2	K562	blood:
41	chr1:92764062..92764602-chr19:36390162..36391104,2	Hela-S3	cervix:
42	chr1:92751701..92754444-chr1:92763776..92766491,2	MCF-7	breast:
43	chr1:92751144..92752872-chr1:92762540..92765121,2	K562	blood:
44	chr1:92781038..92783482-chr1:92784277..92786700,2	K562	blood:
45	chr1:92798322..92801081-chr1:92801191..92803127,2	K562	blood:
46	chr1:92704937..92705925-chr1:92715140..92715847,2	K562	blood:
47	chr1:92756651..92759126-chr1:92759145..92761543,4	K562	blood:
48	chr1:92739930..92741567-chr1:92757034..92759673,2	K562	blood:
49	chr1:92770418..92773011-chr1:92773916..92776545,2	K562	blood:
50	chr1:92398059..92398985-chr1:92756667..92757204,2	MCF-7	breast:

(count:2 , 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

No data

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

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

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

Extended variants
information (count: 3747 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:3747 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567034638	chr1:92697481-92697482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs535998488	chr1:92697564-92697565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs150264840	chr1:92697637-92697638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs377358468	chr1:92697640-92697641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs577505099	chr1:92697675-92697676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs539729641	chr1:92697704-92697705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs34203450	chr1:92697708-92697709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs397769793	chr1:92697710-92697711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs558515663	chr1:92697713-92697714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs3103170	chr1:92697733-92697734	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs558376825	chr1:92697773-92697774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs80094393	chr1:92697786-92697787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs77976714	chr1:92697788-92697789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs74468357	chr1:92697790-92697791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs79678056	chr1:92697791-92697792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs534199409	chr1:92697794-92697795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs555854880	chr1:92697798-92697799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs559758564	chr1:92704260-92704261	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs527371765	chr1:92704271-92704272	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs182222428	chr1:92704286-92704287	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs114900375	chr1:92704295-92704296	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs534210554	chr1:92704362-92704363	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs562163274	chr1:92704425-92704426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs529508387	chr1:92704439-92704440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs550955051	chr1:92704458-92704459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs547629074	chr1:92704465-92704466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs569575545	chr1:92704470-92704471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs540184659	chr1:92704472-92704473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs558172325	chr1:92704512-92704513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs186234812	chr1:92704625-92704626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs534011907	chr1:92704626-92704627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs189863929	chr1:92704720-92704721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs6679259	chr1:92704761-92704762	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs182224202	chr1:92704778-92704779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs555991538	chr1:92704779-92704780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs184981407	chr1:92704836-92704837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs544937085	chr1:92704844-92704845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs559697410	chr1:92704892-92704893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs3131825	chr1:92704927-92704928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs2046617	chr1:92704950-92704951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs118064404	chr1:92705033-92705034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs542325533	chr1:92705044-92705045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs561051694	chr1:92705053-92705054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs529421643	chr1:92705067-92705068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs146249570	chr1:92705074-92705075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs141855426	chr1:92705208-92705209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs3103173	chr1:92705224-92705225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs200547494	chr1:92705227-92705228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs533650035	chr1:92705230-92705231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs552127959	chr1:92705238-92705239	Weak transcription	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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Lung adenocarcinoma	21935476	CNVD

Chromatin state (count:3398 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:92697400-92697800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr1:92704200-92704400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr1:92704400-92705400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr1:92705400-92705600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr1:92705400-92705800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr1:92705600-92705800	Enhancers	Brain Inferior Temporal Lobe	brain
7	chr1:92705600-92726800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr1:92705800-92711400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr1:92705800-92729200	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr1:92707200-92764000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr1:92708200-92741200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr1:92708400-92708600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr1:92708400-92708600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr1:92708400-92708600	Enhancers	Osteobl	bone
15	chr1:92708600-92711400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
16	chr1:92708600-92712000	Weak transcription	Osteobl	bone
17	chr1:92708800-92710000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr1:92708800-92710400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr1:92708800-92710600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr1:92708800-92711000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr1:92708800-92712200	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr1:92709000-92711200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr1:92709000-92711600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
24	chr1:92709000-92711600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr1:92709000-92711600	Weak transcription	HUVEC	blood vessel
26	chr1:92709000-92712000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
27	chr1:92709000-92712200	Weak transcription	Fetal Lung	lung
28	chr1:92709000-92712200	Weak transcription	Fetal Stomach	stomach
29	chr1:92709000-92717400	Weak transcription	Primary T cells fromperipheralblood	blood
30	chr1:92709000-92718800	Weak transcription	Lung	lung
31	chr1:92709000-92737200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr1:92709000-92762800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
33	chr1:92709200-92710800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr1:92709200-92710800	Weak transcription	Monocytes-CD14+_RO01746	blood
35	chr1:92709200-92711000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
36	chr1:92709200-92712200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
37	chr1:92709200-92718800	Weak transcription	Pancreas	Pancrea
38	chr1:92709400-92711000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr1:92709400-92711000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr1:92709400-92711000	Weak transcription	Primary B cells from peripheral blood	blood
41	chr1:92709400-92711000	Weak transcription	Dnd41	blood
42	chr1:92709400-92711200	Weak transcription	HUES48 Cell Line	embryonic stem cell
43	chr1:92709400-92711400	Weak transcription	Fetal Intestine Large	intestine
44	chr1:92709400-92712200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr1:92709400-92712200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
46	chr1:92709400-92712400	Weak transcription	Primary T helper cells fromperipheralblood	blood
47	chr1:92709400-92735800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
48	chr1:92709600-92711400	Weak transcription	HUES64 Cell Line	embryonic stem cell
49	chr1:92709600-92730800	Weak transcription	Hela-S3	cervix
50	chr1:92709800-92710600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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