Variant report

Variant	esv2755743
Chromosome Location	chr1:191113343-191376343
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:703)
CpG islands
(count:122)
Chromatin interactive
region (count:47)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:703 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:191338195-191338459	K562	blood:	n/a	n/a
2	ATF1	chr1:191297314-191297326	K562	blood:	n/a	n/a
3	ATF1	chr1:191338119-191338421	K562	blood:	n/a	n/a
4	ATF1	chr1:191159156-191159163	K562	blood:	n/a	n/a
5	ATF1	chr1:191122236-191122374	K562	blood:	n/a	n/a
6	ATF2	chr1:191143328-191144013	GM12878	blood:	n/a	n/a
7	ATF3	chr1:191373403-191373752	K562	blood:	n/a	n/a
8	BACH1	chr1:191274761-191274805	K562	blood:	n/a	n/a
9	BACH1	chr1:191253401-191253595	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr1:191143451-191143751	GM12878	blood:	n/a	n/a
11	BATF	chr1:191143439-191143828	GM12878	blood:	n/a	n/a
12	BCL11A	chr1:191143469-191143830	GM12878	blood:	n/a	n/a
13	BCLAF1	chr1:191143259-191143906	GM12878	blood:	n/a	n/a
14	BHLHE40	chr1:191338189-191338354	K562	blood:	n/a	n/a
15	BHLHE40	chr1:191143231-191143785	GM12878	blood:	n/a	n/a
16	BHLHE40	chr1:191259569-191259784	K562	blood:	n/a	n/a
17	BRCA1	chr1:191370538-191370577	Hela-S3	cervix:	n/a	n/a
18	CBX3	chr1:191373433-191373795	K562	blood:	n/a	n/a
19	CBX3	chr1:191253357-191253679	K562	blood:	n/a	n/a
20	CBX3	chr1:191275577-191275852	K562	blood:	n/a	n/a
21	CBX3	chr1:191367627-191368055	K562	blood:	n/a	n/a
22	CBX3	chr1:191365747-191366197	K562	blood:	n/a	n/a
23	CBX3	chr1:191357458-191357801	K562	blood:	n/a	n/a
24	CBX3	chr1:191120966-191121245	K562	blood:	n/a	n/a
25	CBX3	chr1:191126404-191126763	K562	blood:	n/a	n/a
26	CBX3	chr1:191253318-191253712	K562	blood:	n/a	n/a
27	CBX3	chr1:191365898-191366123	K562	blood:	n/a	n/a
28	CBX3	chr1:191186779-191187146	K562	blood:	n/a	n/a
29	CBX3	chr1:191297007-191297287	K562	blood:	n/a	n/a
30	CBX3	chr1:191357460-191357656	K562	blood:	n/a	n/a
31	CCNT2	chr1:191353485-191353497	K562	blood:	n/a	n/a
32	CEBPB	chr1:191354616-191354924	K562	blood:	n/a	chr1:191354766-191354775 chr1:191354766-191354775 chr1:191354764-191354775 chr1:191354766-191354775 chr1:191354766-191354775
33	CEBPB	chr1:191299249-191299565	HepG2	liver:	n/a	chr1:191299415-191299424 chr1:191299413-191299426 chr1:191299413-191299426 chr1:191299415-191299424 chr1:191299413-191299424 chr1:191299415-191299424 chr1:191299415-191299426 chr1:191299415-191299424
34	CEBPB	chr1:191204015-191204017	K562	blood:	n/a	n/a
35	CEBPB	chr1:191134053-191134241	MCF-7	breast:	n/a	n/a
36	CEBPB	chr1:191218998-191219203	A549	lung:	n/a	chr1:191219071-191219082
37	CEBPB	chr1:191338151-191338521	K562	blood:	n/a	n/a
38	CEBPB	chr1:191299244-191299565	K562	blood:	n/a	chr1:191299415-191299424 chr1:191299413-191299426 chr1:191299413-191299426 chr1:191299415-191299424 chr1:191299413-191299424 chr1:191299415-191299424 chr1:191299415-191299426 chr1:191299415-191299424
39	CEBPB	chr1:191226100-191226380	A549	lung:	n/a	chr1:191226236-191226247
40	CEBPB	chr1:191211379-191211586	K562	blood:	n/a	n/a
41	CEBPB	chr1:191274516-191274867	IMR90	lung:	n/a	chr1:191274702-191274713
42	CEBPB	chr1:191248382-191248980	MCF-7	breast:	n/a	chr1:191248692-191248703
43	CEBPB	chr1:191248508-191248878	A549	lung:	n/a	chr1:191248692-191248703
44	CEBPB	chr1:191128063-191128248	HepG2	liver:	n/a	chr1:191128163-191128174
45	CEBPB	chr1:191299311-191299468	H1-hESC	embryonic stem cell:	n/a	chr1:191299415-191299424 chr1:191299413-191299426 chr1:191299413-191299426 chr1:191299415-191299424 chr1:191299413-191299424 chr1:191299415-191299424 chr1:191299415-191299426 chr1:191299415-191299424
46	CEBPB	chr1:191128031-191128288	K562	blood:	n/a	chr1:191128163-191128174
47	CEBPB	chr1:191334350-191334667	A549	lung:	n/a	chr1:191334417-191334428
48	CEBPB	chr1:191274526-191274855	HepG2	liver:	n/a	chr1:191274702-191274713
49	CEBPB	chr1:191248482-191248877	HCT-116	colon:	n/a	chr1:191248692-191248703
50	CEBPB	chr1:191334326-191334597	HepG2	liver:	n/a	chr1:191334417-191334428

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:191120792-191120842	MCF-7	breast:	n/a
2	chr1:191120830-191120880	AG04450	lung:	fetal
3	chr1:191120792-191120842	BJ	skin:	n/a
4	chr1:191120830-191120880	AG09309	skin:	n/a
5	chr1:191120830-191120880	ECC-1	luminal epithelium:	n/a
6	chr1:191120830-191120880	PrEC	prostate:	n/a
7	chr1:191120792-191120842	ovcar-3	ovarian:	n/a
8	chr1:191120792-191120842	HepG2	liver:	n/a
9	chr1:191120830-191120880	LNCaP	prostate:	n/a
10	chr1:191120792-191120842	HEEpiC	esophagus:	n/a
11	chr1:191120830-191120880	SK-N-SH_RA	brain:	n/a
12	chr1:191120792-191120842	AG09309	skin:	n/a
13	chr1:191120830-191120880	HCPEpiC	choroid plexus:	n/a
14	chr1:191120830-191120880	HCM	heart:	n/a
15	chr1:191120830-191120880	Jurkat	blood:	n/a
16	chr1:191120792-191120842	HUVEC	blood vessel:	n/a
17	chr1:191120792-191120842	PANC-1	pancreas:	n/a
18	chr1:191120792-191120842	HCT-116	colon:	n/a
19	chr1:191120830-191120880	HCF	heart:	n/a
20	chr1:191120792-191120842	AoSMC	blood vessel:	n/a
21	chr1:191120792-191120842	T-47D	breast:	n/a
22	chr1:191120830-191120880	IMR90	lung:	fetal
23	chr1:191120792-191120842	NB4	blood:	n/a
24	chr1:191120830-191120880	GM06990	blood:	n/a
25	chr1:191120792-191120842	HCM	heart:	n/a
26	chr1:191120830-191120880	NB4	blood:	n/a
27	chr1:191120792-191120842	ECC-1	luminal epithelium:	n/a
28	chr1:191120830-191120880	NHDF-neo	bronchial:	n/a
29	chr1:191120792-191120842	AG10803	skin:	n/a
30	chr1:191120830-191120880	GM19239	blood:	n/a
31	chr1:191120792-191120842	SK-N-SH	brain:	n/a
32	chr1:191120792-191120842	Hela-S3	cervix:	n/a
33	chr1:191120792-191120842	SK-N-SH_RA	brain:	n/a
34	chr1:191120792-191120842	NH-A	brain:	n/a
35	chr1:191120830-191120880	T-47D	breast:	n/a
36	chr1:191120792-191120842	AG04449	skin:	fetal
37	chr1:191120830-191120880	HRPEpiC	eye:	n/a
38	chr1:191120830-191120880	AoSMC	blood vessel:	n/a
39	chr1:191120792-191120842	MCF10A-Er-Src	breast:	n/a
40	chr1:191120792-191120842	NT2-D1	testis:	n/a
41	chr1:191120830-191120880	Hepatocyte	liver:	n/a
42	chr1:191120830-191120880	HCT-116	colon:	n/a
43	chr1:191120792-191120842	Jurkat	blood:	n/a
44	chr1:191120830-191120880	ProgFib	skin:	n/a
45	chr1:191120792-191120842	AG09319	gingival:	n/a
46	chr1:191120792-191120842	GM12892	blood:	n/a
47	chr1:191120830-191120880	HEEpiC	esophagus:	n/a
48	chr1:191120830-191120880	SAEC	small airway:	n/a
49	chr1:191120792-191120842	Hepatocyte	liver:	n/a
50	chr1:191120830-191120880	NHBE	bronchial:	n/a

(count:47 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:191367727..191369748-chr1:191373061..191374879,2	K562	blood:
2	chr1:191368248..191370695-chr1:191372787..191374561,2	K562	blood:
3	chr1:191251451..191253394-chr1:191255335..191256855,2	K562	blood:
4	chr1:191245868..191248178-chr1:191250282..191252170,2	K562	blood:
5	chr1:191334925..191337085-chr1:191337771..191340212,3	K562	blood:
6	chr1:191287950..191289463-chr1:191291967..191294234,2	K562	blood:
7	chr1:191334925..191337085-chr1:191337771..191340212,3	K562	blood:
8	chr1:191357719..191359865-chr1:191368131..191370717,2	K562	blood:
9	chr1:191332317..191334180-chr1:191337399..191339945,2	K562	blood:
10	chr1:191368248..191370695-chr1:191372787..191374561,2	K562	blood:
11	chr1:191150998..191152501-chr1:191156325..191158082,2	K562	blood:
12	chr1:191235053..191236832-chr1:191299467..191301857,2	MCF-7	breast:
13	chr1:191212442..191214167-chr1:191217333..191219833,2	MCF-7	breast:
14	chr1:191117376..191119882-chr1:191120970..191122736,2	MCF-7	breast:
15	chr1:191154442..191156572-chr1:191159468..191162029,2	K562	blood:
16	chr1:191287950..191289463-chr1:191291967..191294234,2	K562	blood:
17	chr1:191285545..191288478-chr1:191311947..191313590,2	MCF-7	breast:
18	chr1:191235053..191236832-chr1:191299467..191301857,2	MCF-7	breast:
19	chr1:191139593..191142388-chr1:191149120..191151841,2	MCF-7	breast:
20	chr1:191262328..191265076-chr1:191299134..191300928,2	K562	blood:
21	chr1:191191547..191193153-chr1:191196709..191199112,2	K562	blood:
22	chr1:191251451..191253394-chr1:191255335..191256855,2	K562	blood:
23	chr1:191150998..191152501-chr1:191156325..191158082,2	K562	blood:
24	chr1:191212442..191214167-chr1:191217333..191219833,2	MCF-7	breast:
25	chr1:191367727..191369748-chr1:191373061..191374879,2	K562	blood:
26	chr1:191123228..191125504-chr1:191129557..191132140,2	K562	blood:
27	chr1:191117376..191119882-chr1:191120970..191122736,2	MCF-7	breast:
28	chr1:191311585..191313743-chr1:191315163..191316847,2	K562	blood:
29	chr1:191285545..191288478-chr1:191311947..191313590,2	MCF-7	breast:
30	chr1:191332317..191334180-chr1:191337399..191339945,2	K562	blood:
31	chr1:191245868..191248178-chr1:191250282..191252170,2	K562	blood:
32	chr1:191250975..191253394-chr1:191254576..191256855,3	K562	blood:
33	chr1:191121690..191123350-chr1:191124411..191127560,3	K562	blood:
34	chr1:191160823..191162731-chr1:191477898..191480311,2	K562	blood:
35	chr1:191139593..191142388-chr1:191149120..191151841,2	MCF-7	breast:
36	chr1:191123228..191125504-chr1:191129557..191132140,2	K562	blood:
37	chr1:191371943..191373778-chr1:191427254..191429182,2	K562	blood:
38	chr1:191277227..191279088-chr1:191280511..191283131,2	K562	blood:
39	chr1:191157793..191160088-chr1:191162179..191165102,2	K562	blood:
40	chr1:191157793..191160088-chr1:191162179..191165102,2	K562	blood:
41	chr1:191311585..191313743-chr1:191315163..191316847,2	K562	blood:
42	chr1:191277227..191279088-chr1:191280511..191283131,2	K562	blood:
43	chr1:191250975..191253394-chr1:191254576..191256855,3	K562	blood:
44	chr1:191357719..191359865-chr1:191368131..191370717,2	K562	blood:
45	chr1:191154442..191156572-chr1:191159468..191162029,2	K562	blood:
46	chr1:191262328..191265076-chr1:191299134..191300928,2	K562	blood:
47	chr1:191121690..191123350-chr1:191124411..191127560,3	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM5C-12	chr1:191197453-191197597	ENSG00000233882.2
2	lnc-FAM5C-10	chr1:191148651-191148869	NONHSAT008516
3	lnc-FAM5C-11	chr1:191183856-191184010	NONHSAT008517
4	lnc-FAM5C-12	chr1:191190289-191190442	ENSG00000233882.2
5	lnc-RGS18-2	chr1:191190289-191190442	XLOC_000506
6	lnc-FAM5C-9	chr1:191115155-191116091	NONHSAT008514
7	lnc-FAM5C-11	chr1:191173053-191173173	NONHSAT008517
8	lnc-RGS18-2	chr1:191197453-191197597	XLOC_000506

No data

Variant related genes	Relation type
ENSG00000261642	TF binding region
HNRNPA1P46	TF binding region
ENSG00000233882	TF binding region
ENSG00000271187	TF binding region
ENSG00000261642	CpG island
HNRNPA1P46	CpG island
ENSG00000233882	CpG island
ENSG00000271187	CpG island
ENSG00000233882	chromatin interactions
GSK3B	miRNA target sites
BCOR	miRNA target sites

Extended variants
information (count: 2280 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:2280 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192229103	chr1:191115156-191115157	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs56180053	chr1:191115178-191115179	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs111581521	chr1:191115192-191115193	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs570171169	chr1:191115194-191115195	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs536082648	chr1:191115247-191115248	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs186648177	chr1:191115279-191115280	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs566412318	chr1:191115286-191115287	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs367764017	chr1:191115331-191115332	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs145040198	chr1:191115355-191115356	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs74129887	chr1:191115362-191115363	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs570861333	chr1:191115400-191115401	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs536769503	chr1:191115407-191115408	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs112313404	chr1:191115428-191115429	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs573636973	chr1:191115504-191115505	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs542834240	chr1:191115564-191115565	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs375842807	chr1:191115574-191115575	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs552888617	chr1:191115575-191115576	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs10753974	chr1:191115638-191115639	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs545277651	chr1:191115639-191115640	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs564494959	chr1:191115642-191115643	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs191855592	chr1:191115677-191115678	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs138878921	chr1:191115689-191115690	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs569376741	chr1:191115696-191115697	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs563835271	chr1:191115767-191115768	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs56145453	chr1:191115800-191115801	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs529367530	chr1:191115803-191115804	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs141393909	chr1:191115813-191115814	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs558345850	chr1:191115876-191115877	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
29	rs566104005	chr1:191115893-191115894	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
30	rs528760312	chr1:191115908-191115909	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
31	rs551627158	chr1:191115964-191115965	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
32	rs377249329	chr1:191116005-191116006	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
33	rs368662629	chr1:191116006-191116007	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
34	rs536681570	chr1:191116023-191116024	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
35	rs556659525	chr1:191116067-191116068	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs370661692	chr1:191116072-191116073	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
37	rs112184765	chr1:191117026-191117027	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
38	rs1463340	chr1:191117027-191117028	Inactive region	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs77931829	chr1:191119452-191119453	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
40	rs527584539	chr1:191119490-191119491	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
41	rs11805775	chr1:191119503-191119504	Inactive region	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs372926286	chr1:191120413-191120414	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs539393796	chr1:191120426-191120427	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs537973303	chr1:191120465-191120466	Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
45	rs375668768	chr1:191120467-191120468	Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
46	rs548627332	chr1:191120488-191120489	Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
47	rs557421928	chr1:191120496-191120497	Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
48	rs557608211	chr1:191120519-191120520	Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
49	rs569147158	chr1:191120537-191120538	Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
50	rs577654367	chr1:191120569-191120570	Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	20688739	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21611746	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	19010865	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Trisomy 5 syndrome	21098271	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Lung adenocarcinoma	17086460	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	17086460	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Lung adenocarcinoma	21935476	CNVD
Glioblastoma multiforme	21510904	CNVD
Intellectual disability	21811512	CNVD
Parathyroid adenoma	20824076	CNVD

Chromatin state (count:159 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:191120400-191120800	Enhancers	Placenta	Placenta
2	chr1:191121800-191122400	Enhancers	GM12878-XiMat	blood
3	chr1:191123600-191124600	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr1:191123800-191124800	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr1:191124000-191124600	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr1:191124000-191124600	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr1:191124200-191124600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
8	chr1:191124200-191124600	Active TSS	K562	blood
9	chr1:191128400-191130200	Weak transcription	Fetal Kidney	kidney
10	chr1:191129200-191129600	Enhancers	Placenta	Placenta
11	chr1:191129600-191129800	Active TSS	HSMM	muscle
12	chr1:191129800-191130000	Flanking Active TSS	HSMM	muscle
13	chr1:191130200-191130600	ZNF genes & repeats	Fetal Kidney	kidney
14	chr1:191140800-191141000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr1:191141600-191141800	Enhancers	Primary monocytes fromperipheralblood	blood
16	chr1:191141800-191142800	Weak transcription	Primary monocytes fromperipheralblood	blood
17	chr1:191142600-191143000	Enhancers	Dnd41	blood
18	chr1:191142600-191144000	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr1:191142800-191143800	Enhancers	Primary monocytes fromperipheralblood	blood
20	chr1:191142800-191144000	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr1:191142800-191144400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr1:191143000-191143400	Enhancers	GM12878-XiMat	blood
23	chr1:191143000-191143600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr1:191143000-191143800	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr1:191143000-191144000	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr1:191143000-191144000	Flanking Active TSS	Dnd41	blood
27	chr1:191143200-191143400	Active TSS	Colon Smooth Muscle	Colon
28	chr1:191143200-191143600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr1:191143200-191143600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr1:191143200-191144000	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr1:191143200-191144200	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr1:191143400-191143600	Flanking Active TSS	Colon Smooth Muscle	Colon
33	chr1:191143400-191143600	Enhancers	Monocytes-CD14+_RO01746	blood
34	chr1:191143400-191143800	Enhancers	H9 Cell Line	embryonic stem cell
35	chr1:191143400-191144000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr1:191143400-191144200	Flanking Active TSS	GM12878-XiMat	blood
37	chr1:191143400-191144400	Enhancers	Primary B cells from peripheral blood	blood
38	chr1:191143400-191145400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr1:191143600-191144000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr1:191143800-191144400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr1:191144000-191144600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
42	chr1:191144000-191144800	Enhancers	Dnd41	blood
43	chr1:191144200-191145400	Enhancers	GM12878-XiMat	blood
44	chr1:191144800-191150000	Weak transcription	Dnd41	blood
45	chr1:191150000-191150400	Enhancers	Dnd41	blood
46	chr1:191162800-191163400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr1:191167600-191168200	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr1:191167800-191168200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr1:191168200-191168800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr1:191175000-191176400	Enhancers	Dnd41	blood

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