Variant report

Variant	nsv548576
Chromosome Location	chr1:190963860-191349614
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1061)
CpG islands
(count:184)
Chromatin interactive
region (count:62)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1061 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

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	ARID3A	chr1:191035067-191035242	K562	blood:	n/a	n/a
3	ATF1	chr1:191159156-191159163	K562	blood:	n/a	n/a
4	ATF1	chr1:191122236-191122374	K562	blood:	n/a	n/a
5	ATF1	chr1:191338119-191338421	K562	blood:	n/a	n/a
6	ATF1	chr1:191297314-191297326	K562	blood:	n/a	n/a
7	ATF1	chr1:191034981-191035158	K562	blood:	n/a	n/a
8	ATF2	chr1:191143328-191144013	GM12878	blood:	n/a	n/a
9	BACH1	chr1:191253401-191253595	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr1:191274761-191274805	K562	blood:	n/a	n/a
11	BATF	chr1:191143439-191143828	GM12878	blood:	n/a	n/a
12	BATF	chr1:191143451-191143751	GM12878	blood:	n/a	n/a
13	BCL11A	chr1:191143469-191143830	GM12878	blood:	n/a	n/a
14	BCLAF1	chr1:191143259-191143906	GM12878	blood:	n/a	n/a
15	BHLHE40	chr1:191259569-191259784	K562	blood:	n/a	n/a
16	BHLHE40	chr1:191338189-191338354	K562	blood:	n/a	n/a
17	BHLHE40	chr1:191143231-191143785	GM12878	blood:	n/a	n/a
18	BRCA1	chr1:190964984-190965019	Hela-S3	cervix:	n/a	n/a
19	CBX3	chr1:191253318-191253712	K562	blood:	n/a	n/a
20	CBX3	chr1:191186779-191187146	K562	blood:	n/a	n/a
21	CBX3	chr1:191275577-191275852	K562	blood:	n/a	n/a
22	CBX3	chr1:191297007-191297287	K562	blood:	n/a	n/a
23	CBX3	chr1:191126404-191126763	K562	blood:	n/a	n/a
24	CBX3	chr1:191120966-191121245	K562	blood:	n/a	n/a
25	CBX3	chr1:191253357-191253679	K562	blood:	n/a	n/a
26	CEBPB	chr1:191128031-191128288	K562	blood:	n/a	chr1:191128163-191128174
27	CEBPB	chr1:191226072-191226414	IMR90	lung:	n/a	chr1:191226236-191226247
28	CEBPB	chr1:191334355-191334735	K562	blood:	n/a	chr1:191334417-191334428 chr1:191334711-191334722
29	CEBPB	chr1:191248507-191248874	K562	blood:	n/a	chr1:191248692-191248703
30	CEBPB	chr1:191128063-191128248	HepG2	liver:	n/a	chr1:191128163-191128174
31	CEBPB	chr1:190973765-190974042	A549	lung:	n/a	chr1:190973884-190973895
32	CEBPB	chr1:191044439-191044785	K562	blood:	n/a	chr1:191044564-191044575 chr1:191044606-191044617
33	CEBPB	chr1:191338151-191338521	K562	blood:	n/a	n/a
34	CEBPB	chr1:191128034-191128422	IMR90	lung:	n/a	chr1:191128163-191128174
35	CEBPB	chr1:191274538-191274856	H1-hESC	embryonic stem cell:	n/a	chr1:191274702-191274713
36	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
37	CEBPB	chr1:190997021-190997221	A549	lung:	n/a	n/a
38	CEBPB	chr1:191024457-191024633	H1-hESC	embryonic stem cell:	n/a	chr1:191024518-191024535
39	CEBPB	chr1:191043512-191043648	K562	blood:	n/a	chr1:191043541-191043552 chr1:191043540-191043551
40	CEBPB	chr1:191248512-191248886	HepG2	liver:	n/a	chr1:191248692-191248703
41	CEBPB	chr1:191044575-191044647	H1-hESC	embryonic stem cell:	n/a	chr1:191044606-191044617
42	CEBPB	chr1:191334326-191334597	HepG2	liver:	n/a	chr1:191334417-191334428
43	CEBPB	chr1:191109191-191109512	IMR90	lung:	n/a	chr1:191109350-191109361
44	CEBPB	chr1:191248505-191248873	H1-hESC	embryonic stem cell:	n/a	chr1:191248692-191248703
45	CEBPB	chr1:190970672-190970955	HepG2	liver:	n/a	chr1:190970828-190970839 chr1:190970828-190970841 chr1:190970828-190970841 chr1:190970830-190970841 chr1:190970830-190970839
46	CEBPB	chr1:191204015-191204017	K562	blood:	n/a	n/a
47	CEBPB	chr1:191248490-191249000	MCF-7	breast:	n/a	chr1:191248692-191248703
48	CEBPB	chr1:190966874-190967137	HepG2	liver:	n/a	chr1:190967033-190967046 chr1:190967033-190967046 chr1:190967033-190967044 chr1:190967033-190967046 chr1:190967034-190967045 chr1:190967023-190967036
49	CEBPB	chr1:191050206-191050422	HepG2	liver:	n/a	chr1:191050334-191050347
50	CEBPB	chr1:191274527-191274827	A549	lung:	n/a	chr1:191274702-191274713

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:191120792-191120842	SAEC	small airway:	n/a
2	chr1:191120792-191120842	SAEC	small airway:	n/a
3	chr1:191120792-191120842	AG09309	skin:	n/a
4	chr1:191120792-191120842	GM06990	blood:	n/a
5	chr1:190995429-190995479	HEK293	kidney:	embryo
6	chr1:191120792-191120842	Jurkat	blood:	n/a
7	chr1:191120792-191120842	U87	brain:	n/a
8	chr1:191120792-191120842	AG10803	skin:	n/a
9	chr1:191120830-191120880	NHDF-neo	bronchial:	n/a
10	chr1:191120830-191120880	AG10803	skin:	n/a
11	chr1:191120792-191120842	HIPEpiC	eye:	n/a
12	chr1:191120792-191120842	HEEpiC	esophagus:	n/a
13	chr1:191120830-191120880	LNCaP	prostate:	n/a
14	chr1:191120792-191120842	HNPCEpiC	eye:	n/a
15	chr1:191120792-191120842	HMEC	breast:	n/a
16	chr1:191120792-191120842	CMK	blood:	n/a
17	chr1:190995429-190995479	SKMC	muscle:	n/a
18	chr1:190995429-190995479	A549	lung:	n/a
19	chr1:190995429-190995479	NHDF-neo	bronchial:	n/a
20	chr1:191120792-191120842	HCF	heart:	n/a
21	chr1:191120792-191120842	MCF-7	breast:	n/a
22	chr1:191120792-191120842	HCM	heart:	n/a
23	chr1:191120792-191120842	SK-N-SH_RA	brain:	n/a
24	chr1:191120830-191120880	ovcar-3	ovarian:	n/a
25	chr1:190995429-190995479	AG09319	gingival:	n/a
26	chr1:191120830-191120880	IMR90	lung:	fetal
27	chr1:191120792-191120842	HL-60	blood:	n/a
28	chr1:191120792-191120842	GM12878	blood:	n/a
29	chr1:191120830-191120880	HIPEpiC	eye:	n/a
30	chr1:191120830-191120880	NHBE	bronchial:	n/a
31	chr1:191120830-191120880	HRE	kidney:	n/a
32	chr1:191120792-191120842	A549	lung:	n/a
33	chr1:191120792-191120842	HRPEpiC	eye:	n/a
34	chr1:190995429-190995479	ovcar-3	ovarian:	n/a
35	chr1:191120830-191120880	NH-A	brain:	n/a
36	chr1:191120830-191120880	HMEC	breast:	n/a
37	chr1:191120830-191120880	GM12891	blood:	n/a
38	chr1:191120830-191120880	GM19239	blood:	n/a
39	chr1:191120792-191120842	MCF10A-Er-Src	breast:	n/a
40	chr1:191120830-191120880	BJ	skin:	n/a
41	chr1:191120830-191120880	HRPEpiC	eye:	n/a
42	chr1:191120830-191120880	AoSMC	blood vessel:	n/a
43	chr1:191120792-191120842	HAEpiC	amniotic membrane:	n/a
44	chr1:191120792-191120842	SKMC	muscle:	n/a
45	chr1:191120830-191120880	Caco-2	colon:	n/a
46	chr1:191120830-191120880	AG04449	skin:	fetal
47	chr1:191120830-191120880	GM12892	blood:	n/a
48	chr1:190995429-190995479	HIPEpiC	eye:	n/a
49	chr1:191120830-191120880	NB4	blood:	n/a
50	chr1:191120830-191120880	Hela-S3	cervix:	n/a

(count:62 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:191006072..191007919-chr7:61967833..61970042,2	MCF-7	breast:
2	chr1:191251451..191253394-chr1:191255335..191256855,2	K562	blood:
3	chr1:191123228..191125504-chr1:191129557..191132140,2	K562	blood:
4	chr1:191262328..191265076-chr1:191299134..191300928,2	K562	blood:
5	chr1:191117376..191119882-chr1:191120970..191122736,2	MCF-7	breast:
6	chr1:191212442..191214167-chr1:191217333..191219833,2	MCF-7	breast:
7	chr1:191139593..191142388-chr1:191149120..191151841,2	MCF-7	breast:
8	chr1:191154442..191156572-chr1:191159468..191162029,2	K562	blood:
9	chr1:191071401..191072988-chr1:191075213..191077807,2	MCF-7	breast:
10	chr1:191285545..191288478-chr1:191311947..191313590,2	MCF-7	breast:
11	chr1:191332317..191334180-chr1:191337399..191339945,2	K562	blood:
12	chr1:191334925..191337085-chr1:191337771..191340212,3	K562	blood:
13	chr1:191056730..191058944-chr1:191065674..191068306,2	K562	blood:
14	chr1:191078284..191080144-chr1:191088639..191091448,2	K562	blood:
15	chr1:191235053..191236832-chr1:191299467..191301857,2	MCF-7	breast:
16	chr1:191088572..191091264-chr1:191094632..191096483,2	MCF-7	breast:
17	chr1:191311585..191313743-chr1:191315163..191316847,2	K562	blood:
18	chr1:191015853..191018214-chr1:191018760..191021606,2	MCF-7	breast:
19	chr1:190987156..190989063-chr1:190989667..190991830,2	K562	blood:
20	chr1:191015853..191018214-chr1:191018760..191021606,2	MCF-7	breast:
21	chr1:191332317..191334180-chr1:191337399..191339945,2	K562	blood:
22	chr1:191157793..191160088-chr1:191162179..191165102,2	K562	blood:
23	chr1:191277227..191279088-chr1:191280511..191283131,2	K562	blood:
24	chr1:190978633..190980595-chr1:190983607..190985514,2	K562	blood:
25	chr1:191150998..191152501-chr1:191156325..191158082,2	K562	blood:
26	chr1:191287950..191289463-chr1:191291967..191294234,2	K562	blood:
27	chr1:191311585..191313743-chr1:191315163..191316847,2	K562	blood:
28	chr1:191285545..191288478-chr1:191311947..191313590,2	MCF-7	breast:
29	chr1:191154442..191156572-chr1:191159468..191162029,2	K562	blood:
30	chr1:190987156..190989063-chr1:190989667..190991830,2	K562	blood:
31	chr1:191277227..191279088-chr1:191280511..191283131,2	K562	blood:
32	chr1:191150998..191152501-chr1:191156325..191158082,2	K562	blood:
33	chr1:191071401..191072988-chr1:191075213..191077807,2	MCF-7	breast:
34	chr1:191157793..191160088-chr1:191162179..191165102,2	K562	blood:
35	chr1:191160823..191162731-chr1:191477898..191480311,2	K562	blood:
36	chr1:191191547..191193153-chr1:191196709..191199112,2	K562	blood:
37	chr1:190907314..190910311-chr1:190988688..190990783,2	K562	blood:
38	chr1:191287950..191289463-chr1:191291967..191294234,2	K562	blood:
39	chr1:191235053..191236832-chr1:191299467..191301857,2	MCF-7	breast:
40	chr1:191010882..191013695-chr1:191014255..191017163,2	K562	blood:
41	chr1:191262328..191265076-chr1:191299134..191300928,2	K562	blood:
42	chr1:191088572..191091264-chr1:191094632..191096483,2	MCF-7	breast:
43	chr1:191245868..191248178-chr1:191250282..191252170,2	K562	blood:
44	chr1:191123228..191125504-chr1:191129557..191132140,2	K562	blood:
45	chr1:190978633..190980595-chr1:190983607..190985514,2	K562	blood:
46	chr1:191102072..191104300-chr1:191107376..191108877,2	K562	blood:
47	chr1:191121690..191123350-chr1:191124411..191127560,3	K562	blood:
48	chr1:191251451..191253394-chr1:191255335..191256855,2	K562	blood:
49	chr1:191013676..191015855-chr1:191017030..191019137,2	K562	blood:
50	chr1:191013676..191015855-chr1:191017030..191019137,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM5C-8	chr1:191000528-191000708	l_159_chr1:191000527-191001930_76bGuttman_hLF
2	lnc-RGS18-2	chr1:191190289-191190442	XLOC_000506
3	lnc-FAM5C-9	chr1:191115155-191116091	NONHSAT008514
4	lnc-FAM5C-11	chr1:191183856-191184010	NONHSAT008517
5	lnc-FAM5C-11	chr1:191173053-191173173	NONHSAT008517
6	lnc-RGS18-2	chr1:191197453-191197597	XLOC_000506
7	lnc-FAM5C-10	chr1:191148651-191148869	NONHSAT008516
8	lnc-FAM5C-12	chr1:191190289-191190442	ENSG00000233882.2
9	lnc-FAM5C-8	chr1:191001792-191001930	l_159_chr1:191000527-191001930_76bGuttman_hLF
10	lnc-FAM5C-12	chr1:191197453-191197597	ENSG00000233882.2

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
BCOR	miRNA target sites
GSK3B	miRNA target sites

Extended variants
information (count: 2285 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:2285 , 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	rs567454529	chr1:190990433-190990434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs536194748	chr1:190990442-190990443	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs182824735	chr1:190990448-190990449	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs546464942	chr1:190990471-190990472	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs553216846	chr1:190990505-190990506	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs572502431	chr1:190990514-190990515	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs368114580	chr1:190990515-190990516	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs541410089	chr1:190990574-190990575	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs558298900	chr1:190990658-190990659	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs578113777	chr1:190990679-190990680	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs543997922	chr1:190990713-190990714	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs560314386	chr1:190990721-190990722	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs563776029	chr1:190990744-190990745	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs145980717	chr1:190990772-190990773	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs12080081	chr1:190990792-190990793	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs373566835	chr1:190990802-190990803	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs559594172	chr1:190990839-190990840	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs187829003	chr1:190990870-190990871	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs533677830	chr1:190990965-190990966	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs550923096	chr1:190990998-190990999	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs139803964	chr1:190991006-190991007	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs571014831	chr1:190991009-190991010	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs77412739	chr1:190991035-190991036	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs397781959	chr1:190991044-190991045	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs563321505	chr1:190991046-190991047	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs191891334	chr1:190991081-190991082	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs550643879	chr1:190991099-190991100	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs78885033	chr1:190991155-190991156	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs536427077	chr1:190991164-190991165	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs546938317	chr1:190991255-190991256	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs566738147	chr1:190991292-190991293	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs535024969	chr1:190991310-190991311	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs558137443	chr1:190991390-190991391	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs183322634	chr1:190991398-190991399	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs575200997	chr1:190991401-190991402	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs555436406	chr1:190991437-190991438	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs557409302	chr1:190991459-190991460	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs543711374	chr1:190991510-190991511	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs574177666	chr1:190991517-190991518	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs564986826	chr1:190991540-190991541	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs143193286	chr1:190991599-190991600	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs147466422	chr1:190991620-190991621	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs74129829	chr1:190991621-190991622	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs374402259	chr1:190991642-190991643	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs573155979	chr1:190991649-190991650	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs192643047	chr1:190991651-190991652	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs564581372	chr1:190991665-190991666	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs377040811	chr1:190991764-190991765	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs184623029	chr1:190991771-190991772	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs111586801	chr1:190991791-190991792	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

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
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Lung adenocarcinoma	21935476	CNVD

Chromatin state (count:171 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:190990400-190993200	Enhancers	HUVEC	blood vessel
2	chr1:190991600-190992800	Enhancers	NH-A	brain
3	chr1:190991800-190992200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr1:190992200-190995200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr1:190995200-190995600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr1:190995200-190995600	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr1:191034400-191035200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr1:191034600-191035200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr1:191043600-191044800	Enhancers	Dnd41	blood
10	chr1:191044800-191045800	Weak transcription	Dnd41	blood
11	chr1:191046000-191046200	Enhancers	Dnd41	blood
12	chr1:191095200-191095600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr1:191095200-191096000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr1:191096200-191096400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr1:191103400-191104000	Enhancers	HUVEC	blood vessel
16	chr1:191103800-191104000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr1:191103800-191104400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr1:191103800-191104400	Active TSS	Stomach Smooth Muscle	stomach
19	chr1:191104000-191104400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr1:191104000-191104400	Flanking Active TSS	HUVEC	blood vessel
21	chr1:191104200-191104600	Enhancers	Colon Smooth Muscle	Colon
22	chr1:191104400-191105000	Enhancers	HUVEC	blood vessel
23	chr1:191120400-191120800	Enhancers	Placenta	Placenta
24	chr1:191121800-191122400	Enhancers	GM12878-XiMat	blood
25	chr1:191123600-191124600	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr1:191123800-191124800	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr1:191124000-191124600	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr1:191124000-191124600	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr1:191124200-191124600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
30	chr1:191124200-191124600	Active TSS	K562	blood
31	chr1:191128400-191130200	Weak transcription	Fetal Kidney	kidney
32	chr1:191129200-191129600	Enhancers	Placenta	Placenta
33	chr1:191129600-191129800	Active TSS	HSMM	muscle
34	chr1:191129800-191130000	Flanking Active TSS	HSMM	muscle
35	chr1:191130200-191130600	ZNF genes & repeats	Fetal Kidney	kidney
36	chr1:191140800-191141000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr1:191141600-191141800	Enhancers	Primary monocytes fromperipheralblood	blood
38	chr1:191141800-191142800	Weak transcription	Primary monocytes fromperipheralblood	blood
39	chr1:191142600-191143000	Enhancers	Dnd41	blood
40	chr1:191142600-191144000	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr1:191142800-191143800	Enhancers	Primary monocytes fromperipheralblood	blood
42	chr1:191142800-191144000	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr1:191142800-191144400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr1:191143000-191143400	Enhancers	GM12878-XiMat	blood
45	chr1:191143000-191143600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr1:191143000-191143800	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr1:191143000-191144000	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr1:191143000-191144000	Flanking Active TSS	Dnd41	blood
49	chr1:191143200-191143400	Active TSS	Colon Smooth Muscle	Colon
50	chr1:191143200-191143600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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