Variant report

Variant	nsv871387
Chromosome Location	chr1:92765102-92813741
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:92783280-92783972	K562	blood:	n/a	n/a
2	ARID3A	chr1:92766611-92766631	K562	blood:	n/a	n/a
3	ATF1	chr1:92783398-92784024	K562	blood:	n/a	n/a
4	BACH1	chr1:92799529-92799536	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr1:92766645-92766648	K562	blood:	n/a	n/a
6	BCLAF1	chr1:92764017-92765143	GM12878	blood:	n/a	chr1:92764418-92764427
7	CBX3	chr1:92793313-92793793	K562	blood:	n/a	n/a
8	CBX3	chr1:92793362-92793654	K562	blood:	n/a	n/a
9	CCNT2	chr1:92783392-92783684	K562	blood:	n/a	n/a
10	CEBPB	chr1:92790412-92790461	A549	lung:	n/a	n/a
11	CEBPB	chr1:92808638-92809009	K562	blood:	n/a	n/a
12	CEBPB	chr1:92808669-92808973	K562	blood:	n/a	n/a
13	CEBPB	chr1:92808709-92808944	A549	lung:	n/a	n/a
14	CEBPB	chr1:92808676-92808981	MCF-7	breast:	n/a	n/a
15	CEBPB	chr1:92808642-92808982	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr1:92808645-92808986	A549	lung:	n/a	n/a
17	CEBPB	chr1:92808642-92809002	HepG2	liver:	n/a	n/a
18	CEBPB	chr1:92813357-92813557	A549	lung:	n/a	chr1:92813453-92813464 chr1:92813454-92813465
19	CEBPB	chr1:92808672-92809031	ECC-1	luminal epithelium:	n/a	n/a
20	CEBPB	chr1:92808641-92809003	IMR90	lung:	n/a	n/a
21	CEBPB	chr1:92783071-92783306	IMR90	lung:	n/a	n/a
22	CEBPB	chr1:92808717-92808941	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr1:92771822-92771931	K562	blood:	n/a	n/a
24	CEBPB	chr1:92771826-92771859	A549	lung:	n/a	n/a
25	CEBPB	chr1:92813356-92813609	HepG2	liver:	n/a	chr1:92813453-92813464 chr1:92813454-92813465
26	CEBPB	chr1:92808725-92808920	K562	blood:	n/a	n/a
27	CEBPB	chr1:92783037-92783606	K562	blood:	n/a	chr1:92783382-92783395
28	CEBPD	chr1:92783298-92783907	K562	blood:	n/a	n/a
29	CEBPD	chr1:92783312-92783988	K562	blood:	n/a	n/a
30	CHD1	chr1:92763931-92765499	GM12878	blood:	n/a	n/a
31	CREB1	chr1:92764028-92765116	HepG2	liver:	n/a	n/a
32	CTCF	chr1:92775740-92775890	GM06990	blood:	n/a	chr1:92775835-92775851 chr1:92775836-92775857 chr1:92775834-92775852
33	CTCF	chr1:92775800-92775950	Hela-S3	cervix:	n/a	chr1:92775835-92775851 chr1:92775836-92775857 chr1:92775834-92775852
34	CTCF	chr1:92775648-92775932	A549	lung:	n/a	chr1:92775835-92775851 chr1:92775836-92775857 chr1:92775834-92775852
35	CTCF	chr1:92775760-92775910	GM12864	blood:	n/a	chr1:92775835-92775851 chr1:92775836-92775857 chr1:92775834-92775852
36	CTCF	chr1:92775739-92775926	Pancreas_OC	pancreas:	n/a	chr1:92775835-92775851 chr1:92775836-92775857 chr1:92775834-92775852
37	CTCF	chr1:92775760-92775910	HRPEpiC	eye:	n/a	chr1:92775835-92775851 chr1:92775836-92775857 chr1:92775834-92775852
38	CTCF	chr1:92775780-92775930	AG10803	skin:	n/a	chr1:92775835-92775851 chr1:92775836-92775857 chr1:92775834-92775852
39	CTCF	chr1:92795120-92795270	SAEC	small airway:	n/a	n/a
40	CTCF	chr1:92775760-92775910	BE2_C	brain:	n/a	chr1:92775835-92775851 chr1:92775836-92775857 chr1:92775834-92775852
41	CTCF	chr1:92775665-92775935	ECC-1	luminal epithelium:	n/a	chr1:92775835-92775851 chr1:92775836-92775857 chr1:92775834-92775852
42	CTCF	chr1:92775820-92775970	K562	blood:	n/a	chr1:92775835-92775851 chr1:92775836-92775857 chr1:92775834-92775852
43	CTCF	chr1:92775760-92775910	HBMEC	blood vessel:	n/a	chr1:92775835-92775851 chr1:92775836-92775857 chr1:92775834-92775852
44	CTCF	chr1:92775720-92775870	BJ	skin:	n/a	chr1:92775835-92775851 chr1:92775836-92775857 chr1:92775834-92775852
45	CTCF	chr1:92775420-92775570	HRPEpiC	eye:	n/a	n/a
46	CTCF	chr1:92795100-92795250	HCPEpiC	choroid plexus:	n/a	n/a
47	CTCF	chr1:92775740-92775890	HA-sp	spinal cord:	n/a	chr1:92775835-92775851 chr1:92775836-92775857 chr1:92775834-92775852
48	CTCF	chr1:92775780-92775930	SK-N-SH_RA	brain:	n/a	chr1:92775835-92775851 chr1:92775836-92775857 chr1:92775834-92775852
49	CTCF	chr1:92775760-92775910	HepG2	liver:	n/a	chr1:92775835-92775851 chr1:92775836-92775857 chr1:92775834-92775852
50	CTCF	chr1:92775434-92776130	SK-N-SH	brain:	n/a	chr1:92775835-92775851 chr1:92775836-92775857 chr1:92775834-92775852

No.	Distal block	Cell Line	Cell type
1	chr1:92781038..92783482-chr1:92784277..92786700,2	K562	blood:
2	chr1:92751701..92754444-chr1:92763776..92766491,2	MCF-7	breast:
3	chr1:92781038..92783482-chr1:92784277..92786700,2	K562	blood:
4	chr1:92768070..92770349-chr1:92773069..92775193,2	K562	blood:
5	chr1:92764662..92766279-chr1:92768201..92769903,2	MCF-7	breast:
6	chr1:92494741..92496705-chr1:92764193..92766152,2	MCF-7	breast:
7	chr1:92801067..92802871-chr1:92812427..92814790,2	MCF-7	breast:
8	chr1:92764606..92767220-chr1:92781297..92784112,2	K562	blood:
9	chr1:92763702..92766598-chr1:92771008..92773495,2	MCF-7	breast:
10	chr1:92770418..92773011-chr1:92773916..92776545,2	K562	blood:
11	chr1:92790206..92790996-chr2:74694205..74695187,2	NB4	blood:
12	chr1:92763470..92767298-chr1:92785657..92788225,3	K562	blood:
13	chr1:92775543..92777429-chr1:92779885..92782284,2	K562	blood:
14	chr1:92751144..92752872-chr1:92762540..92765121,2	K562	blood:
15	chr1:92770418..92773011-chr1:92773916..92776545,2	K562	blood:
16	chr1:92801067..92802871-chr1:92812427..92814790,2	MCF-7	breast:
17	chr1:92764074..92765656-chr1:93296705..93299037,2	K562	blood:
18	chr1:92764662..92766279-chr1:92768201..92769903,2	MCF-7	breast:
19	chr1:92798322..92801081-chr1:92801191..92803127,2	K562	blood:
20	chr1:92763867..92766149-chr1:92769063..92771043,2	K562	blood:
21	chr1:92811074..92812742-chr1:92812855..92814750,2	K562	blood:
22	chr1:92768070..92770349-chr1:92773069..92775193,2	K562	blood:
23	chr1:92774363..92776060-chr1:92906114..92908200,2	MCF-7	breast:
24	chr1:92811074..92812742-chr1:92812855..92814750,2	K562	blood:
25	chr1:92775257..92776314-chr1:93064696..93065442,3	MCF-7	breast:
26	chr1:92775543..92777429-chr1:92779885..92782284,2	K562	blood:
27	chr1:92763308..92766374-chr1:92766490..92770872,7	K562	blood:
28	chr1:92762794..92765730-chr1:93295925..93298205,3	K562	blood:

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

Variant related genes	Relation type
RPAP2	TF binding region
GLMN	TF binding region
ENSG00000174842	chromatin interactions
ENSG00000172031	chromatin interactions
ENSG00000122484	chromatin interactions
ENSG00000122406	chromatin interactions

Extended variants
information (count: 1546 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:1546 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10875349	chr1:92765102-92765103	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs545054169	chr1:92765111-92765112	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs146530793	chr1:92765112-92765113	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs572125219	chr1:92765162-92765163	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs540422796	chr1:92765196-92765197	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs141103779	chr1:92765197-92765198	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs529485927	chr1:92765217-92765218	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs150411457	chr1:92765241-92765242	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs562870857	chr1:92765256-92765257	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs371501026	chr1:92765282-92765283	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs533123675	chr1:92765307-92765308	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs551383344	chr1:92765336-92765337	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs200808917	chr1:92765414-92765415	Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs566806611	chr1:92765499-92765500	Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs185193905	chr1:92765503-92765504	Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs549253556	chr1:92765544-92765545	Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs567452869	chr1:92765612-92765613	Flanking Active TSS Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs538069416	chr1:92765637-92765638	Flanking Active TSS Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs371737280	chr1:92765691-92765692	Flanking Active TSS Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs138131683	chr1:92765699-92765700	Flanking Active TSS Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs538606469	chr1:92765702-92765703	Flanking Active TSS Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs200138332	chr1:92765707-92765708	Flanking Active TSS Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs139939334	chr1:92765756-92765757	Flanking Active TSS Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs149555004	chr1:92765759-92765760	Flanking Active TSS Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs72958781	chr1:92765761-92765762	Flanking Active TSS Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs374443226	chr1:92765791-92765792	Flanking Active TSS Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs377748337	chr1:92765811-92765812	Flanking Active TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs542697396	chr1:92765840-92765841	Flanking Active TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs1542685	chr1:92765848-92765849	Flanking Active TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs565648906	chr1:92765881-92765882	Flanking Active TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs386633448	chr1:92765890-92765891	Flanking Active TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs78799891	chr1:92765891-92765892	Flanking Active TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs562815021	chr1:92765892-92765893	Flanking Active TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs533449197	chr1:92765894-92765895	Flanking Active TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs143294814	chr1:92765905-92765906	Flanking Active TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs560532178	chr1:92765929-92765930	Flanking Active TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs527734257	chr1:92765932-92765933	Flanking Active TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs75968796	chr1:92765960-92765961	Flanking Active TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs186384767	chr1:92765973-92765974	Flanking Active TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs531498486	chr1:92765977-92765978	Flanking Active TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs567094156	chr1:92766013-92766014	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs372082758	chr1:92766052-92766053	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs17578954	chr1:92766065-92766066	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	mRNA abundance
44	rs571516846	chr1:92766140-92766141	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs139093592	chr1:92766143-92766144	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs144767171	chr1:92766199-92766200	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs553822077	chr1:92766237-92766238	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs35258040	chr1:92766297-92766298	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs535895954	chr1:92766307-92766308	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs75508716	chr1:92766316-92766317	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	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
Lung adenocarcinoma	21935476	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1843 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:92762800-92767200	Active TSS	GM12878-XiMat	blood
2	chr1:92763200-92765400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr1:92763200-92765400	Active TSS	HUES6 Cell Line	embryonic stem cell
4	chr1:92763200-92765400	Active TSS	HMEC	breast
5	chr1:92763200-92765800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr1:92763200-92765800	Active TSS	A549	lung
7	chr1:92763200-92766200	Active TSS	iPS-20b Cell Line	embryonic stem cell
8	chr1:92763200-92766800	Active TSS	HUES64 Cell Line	embryonic stem cell
9	chr1:92763400-92765200	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr1:92763400-92765200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr1:92763400-92765200	Active TSS	Brain Angular Gyrus	brain
12	chr1:92763400-92765200	Active TSS	NHEK	skin
13	chr1:92763400-92765400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr1:92763400-92765400	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr1:92763400-92765400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr1:92763400-92765400	Active TSS	K562	blood
17	chr1:92763400-92765800	Active TSS	H1 Cell Line	embryonic stem cell
18	chr1:92763400-92765800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr1:92763400-92765800	Active TSS	HepG2	liver
20	chr1:92763400-92766000	Active TSS	iPS-18 Cell Line	embryonic stem cell
21	chr1:92763600-92765200	Active TSS	HUES48 Cell Line	embryonic stem cell
22	chr1:92763600-92765200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr1:92763600-92765200	Active TSS	Muscle Satellite Cultured Cells	--
24	chr1:92763600-92765200	Active TSS	Colon Smooth Muscle	Colon
25	chr1:92763600-92765200	Active TSS	Duodenum Mucosa	Duodenum
26	chr1:92763600-92765200	Active TSS	Duodenum Smooth Muscle	Duodenum
27	chr1:92763600-92765200	Active TSS	Fetal Heart	heart
28	chr1:92763600-92765200	Active TSS	Fetal Kidney	kidney
29	chr1:92763600-92765200	Active TSS	Pancreatic Islets	Pancreatic Islet
30	chr1:92763600-92765200	Active TSS	Rectal Mucosa Donor 29	rectum
31	chr1:92763600-92765200	Active TSS	Hela-S3	cervix
32	chr1:92763600-92765200	Active TSS	NH-A	brain
33	chr1:92763600-92765200	Active TSS	NHLF	lung
34	chr1:92763600-92765200	Active TSS	Osteobl	bone
35	chr1:92763600-92765400	Active TSS	Breast Myoepithelial Primary Cells	Breast
36	chr1:92763600-92765400	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
37	chr1:92763600-92765400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr1:92763600-92765400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr1:92763600-92765400	Active TSS	Fetal Brain Female	brain
40	chr1:92763600-92765400	Active TSS	Stomach Smooth Muscle	stomach
41	chr1:92763600-92765400	Active TSS	NHDF-Ad	bronchial
42	chr1:92763600-92765800	Active TSS	Fetal Intestine Large	intestine
43	chr1:92763800-92765200	Active TSS	iPS-15b Cell Line	embryonic stem cell
44	chr1:92763800-92765200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr1:92763800-92765200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr1:92763800-92765200	Active TSS	Primary hematopoietic stem cells short term culture	blood
47	chr1:92763800-92765200	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
48	chr1:92763800-92765200	Active TSS	Primary T helper naive cells from peripheral blood	blood
49	chr1:92763800-92765200	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
50	chr1:92763800-92765200	Active TSS	Primary T killer memory cells from peripheral blood	blood

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