Variant report

Variant	nsv482272
Chromosome Location	chr20:29884928-30043331
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:858)
CpG islands
(count:2078)
Chromatin interactive
region (count:35)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:858 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:30001402-30001664	HepG2	liver:	n/a	n/a
2	ARID3A	chr20:29901133-29901495	HepG2	liver:	n/a	n/a
3	ARID3A	chr20:30033920-30034156	HepG2	liver:	n/a	n/a
4	ARID3A	chr20:30037622-30037661	HepG2	liver:	n/a	n/a
5	ATF1	chr20:29901261-29901460	K562	blood:	n/a	n/a
6	CEBPB	chr20:29901178-29901527	HepG2	liver:	n/a	n/a
7	CEBPB	chr20:29886470-29886721	A549	lung:	n/a	chr20:29886585-29886596
8	CEBPB	chr20:29891290-29891604	HepG2	liver:	n/a	chr20:29891449-29891460
9	CEBPB	chr20:30042832-30043031	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr20:30021121-30021265	HepG2	liver:	n/a	n/a
11	CEBPB	chr20:29891404-29891489	IMR90	lung:	n/a	chr20:29891449-29891460
12	CEBPB	chr20:29886588-29886598	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr20:30043057-30043355	MCF-7	breast:	n/a	chr20:30043163-30043174
14	CEBPB	chr20:30043140-30043294	HepG2	liver:	n/a	chr20:30043163-30043174
15	CEBPB	chr20:29929046-29929296	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr20:30023127-30023161	HepG2	liver:	n/a	chr20:30023145-30023156
17	CEBPB	chr20:29901179-29901489	IMR90	lung:	n/a	n/a
18	CEBPB	chr20:30016863-30016945	HepG2	liver:	n/a	chr20:30016923-30016934
19	CEBPB	chr20:30043112-30043298	A549	lung:	n/a	chr20:30043163-30043174
20	CEBPB	chr20:29930995-29931186	HepG2	liver:	n/a	chr20:29931087-29931098
21	CEBPB	chr20:30034509-30034535	HepG2	liver:	n/a	n/a
22	CEBPB	chr20:29939648-29939720	HepG2	liver:	n/a	chr20:29939667-29939678
23	CEBPB	chr20:29970579-29970843	HepG2	liver:	n/a	chr20:29970692-29970701 chr20:29970692-29970703
24	CEBPB	chr20:30013786-30013875	HepG2	liver:	n/a	chr20:30013846-30013859 chr20:30013846-30013857
25	CEBPB	chr20:30043004-30043199	IMR90	lung:	n/a	chr20:30043163-30043174
26	CEBPB	chr20:29901113-29901610	MCF-7	breast:	n/a	n/a
27	CEBPB	chr20:29929475-29929483	K562	blood:	n/a	n/a
28	CEBPB	chr20:29886446-29886770	HepG2	liver:	n/a	chr20:29886585-29886596
29	CEBPB	chr20:29970567-29970830	A549	lung:	n/a	chr20:29970692-29970701 chr20:29970692-29970703
30	CEBPB	chr20:29926865-29926997	HepG2	liver:	n/a	n/a
31	CHD2	chr20:30041847-30041872	K562	blood:	n/a	n/a
32	CHD2	chr20:29952144-29952438	HepG2	liver:	n/a	n/a
33	CHD2	chr20:29952083-29952448	K562	blood:	n/a	n/a
34	CTCF	chr20:30028039-30028381	K562	blood:	n/a	chr20:30028233-30028254 chr20:30028239-30028255 chr20:30028238-30028256 chr20:30028240-30028253 chr20:30028240-30028253
35	CTCF	chr20:29901260-29901410	BJ	skin:	n/a	chr20:29901352-29901373 chr20:29901332-29901353 chr20:29901350-29901368
36	CTCF	chr20:30001540-30001690	GM12865	blood:	n/a	n/a
37	CTCF	chr20:30001480-30001630	HEK293	kidney:	n/a	n/a
38	CTCF	chr20:30001480-30001630	GM12866	blood:	n/a	n/a
39	CTCF	chr20:29901268-29901458	A549	lung:	n/a	chr20:29901352-29901373 chr20:29901332-29901353 chr20:29901350-29901368
40	CTCF	chr20:30028120-30028270	MCF-7	breast:	n/a	chr20:30028233-30028254 chr20:30028239-30028255 chr20:30028238-30028256 chr20:30028240-30028253 chr20:30028240-30028253
41	CTCF	chr20:30001431-30001639	Spleen_OC	spleen:	n/a	n/a
42	CTCF	chr20:30028193-30028344	MCF-7	breast:	n/a	chr20:30028233-30028254 chr20:30028239-30028255 chr20:30028238-30028256 chr20:30028240-30028253 chr20:30028240-30028253
43	CTCF	chr20:30028161-30028389	MCF-7	breast:	n/a	chr20:30028233-30028254 chr20:30028239-30028255 chr20:30028238-30028256 chr20:30028240-30028253 chr20:30028240-30028253
44	CTCF	chr20:29901231-29901467	LNCaP	prostate:	n/a	chr20:29901352-29901373 chr20:29901332-29901353 chr20:29901350-29901368
45	CTCF	chr20:29935260-29935410	Caco-2	colon:	n/a	chr20:29935293-29935311
46	CTCF	chr20:29901260-29901410	AG09309	skin:	n/a	chr20:29901352-29901373 chr20:29901332-29901353 chr20:29901350-29901368
47	CTCF	chr20:29901300-29901450	HL-60	blood:	n/a	chr20:29901352-29901373 chr20:29901332-29901353 chr20:29901350-29901368
48	CTCF	chr20:29901303-29901426	GM10248	blood:	n/a	chr20:29901352-29901373 chr20:29901332-29901353 chr20:29901350-29901368
49	CTCF	chr20:29900640-29900790	GM12872	blood:	n/a	n/a
50	CTCF	chr20:30001457-30001614	Medullo	brain:	n/a	n/a

(count:2078 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:30012193-30012243	HepG2	liver:	n/a
2	chr20:30027638-30027688	ovcar-3	ovarian:	n/a
3	chr20:29960982-29961032	HCM	heart:	n/a
4	chr20:29994089-29994139	HAEpiC	amniotic membrane:	n/a
5	chr20:30012193-30012243	HepG2	liver:	n/a
6	chr20:30027638-30027688	ovcar-3	ovarian:	n/a
7	chr20:29960982-29961032	HCM	heart:	n/a
8	chr20:29994089-29994139	HAEpiC	amniotic membrane:	n/a
9	chr20:30028241-30028291	SK-N-SH_RA	brain:	n/a
10	chr20:29994192-29994242	PrEC	prostate:	n/a
11	chr20:30028206-30028256	HAEpiC	amniotic membrane:	n/a
12	chr20:30008986-30009036	GM12878	blood:	n/a
13	chr20:30028241-30028291	HepG2	liver:	n/a
14	chr20:29994173-29994223	AG09309	skin:	n/a
15	chr20:29956330-29956380	HCF	heart:	n/a
16	chr20:29896456-29896506	PFSK-1	brain:	n/a
17	chr20:29994192-29994242	HCF	heart:	n/a
18	chr20:29956330-29956380	NHBE	bronchial:	n/a
19	chr20:29956330-29956380	PrEC	prostate:	n/a
20	chr20:30028292-30028342	GM12892	blood:	n/a
21	chr20:30008986-30009036	Caco-2	colon:	n/a
22	chr20:30028292-30028342	HCF	heart:	n/a
23	chr20:29955259-29955309	AG09309	skin:	n/a
24	chr20:29892486-29892536	HCT-116	colon:	n/a
25	chr20:29956028-29956078	IMR90	lung:	fetal
26	chr20:29978114-29978164	H1-hESC	embryonic stem cell:	embryo
27	chr20:30028223-30028273	HRPEpiC	eye:	n/a
28	chr20:30028241-30028291	AG10803	skin:	n/a
29	chr20:29896456-29896506	H1-hESC	embryonic stem cell:	embryo
30	chr20:29896928-29896978	CMK	blood:	n/a
31	chr20:29892486-29892536	IMR90	lung:	fetal
32	chr20:30028241-30028291	HPAEpiC	pulmonary alveolar:	n/a
33	chr20:29956062-29956112	K562	blood:	n/a
34	chr20:29978114-29978164	NT2-D1	testis:	n/a
35	chr20:29994173-29994223	SK-N-SH	brain:	n/a
36	chr20:29993663-29993713	AG04449	skin:	fetal
37	chr20:30028418-30028468	MCF-7	breast:	n/a
38	chr20:30008986-30009036	HCT-116	colon:	n/a
39	chr20:29965177-29965227	IMR90	lung:	fetal
40	chr20:29994173-29994223	H1-hESC	embryonic stem cell:	embryo
41	chr20:29960982-29961032	SAEC	small airway:	n/a
42	chr20:29978176-29978226	HNPCEpiC	eye:	n/a
43	chr20:30028229-30028279	SK-N-MC	brain:	n/a
44	chr20:30028062-30028112	A549	lung:	n/a
45	chr20:30012193-30012243	Hepatocyte	liver:	n/a
46	chr20:29960982-29961032	U87	brain:	n/a
47	chr20:30027638-30027688	SK-N-MC	brain:	n/a
48	chr20:29993663-29993713	MCF-7	breast:	n/a
49	chr20:30028062-30028112	GM12891	blood:	n/a
50	chr20:30028893-30028943	NB4	blood:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr20:30023186..30025887-chr20:30031461..30033796,2	K562	blood:
2	chr20:30034296..30036142-chr20:30059251..30061850,2	K562	blood:
3	chr20:29905971..29908391-chr20:29910613..29913391,2	K562	blood:
4	chr20:29940769..29942399-chr20:29945457..29948097,2	MCF-7	breast:
5	chr20:30001098..30001991-chr20:30090702..30091623,2	MCF-7	breast:
6	chr20:30006873..30009795-chr20:30012384..30014922,2	MCF-7	breast:
7	chr20:30043021..30045109-chr20:30047141..30048737,2	K562	blood:
8	chr20:29905971..29908391-chr20:29910613..29913391,2	K562	blood:
9	chr20:30027160..30029164-chr20:30031582..30034603,3	K562	blood:
10	chr20:30031405..30034135-chr20:30036580..30038805,2	K562	blood:
11	chr20:29976860..29979727-chr20:29989751..29991908,2	MCF-7	breast:
12	chr20:30001102..30001956-chr20:30200407..30201209,2	MCF-7	breast:
13	chr20:30042574..30044997-chr20:30046543..30048384,2	MCF-7	breast:
14	chr20:29984307..29986959-chr20:29988552..29991737,3	K562	blood:
15	chr20:29955069..29955719-chr20:29963915..29964847,2	MCF-7	breast:
16	chr20:30027160..30029656-chr20:30030161..30033253,3	K562	blood:
17	chr20:29900827..29901742-chr20:30090593..30091579,4	MCF-7	breast:
18	chr20:29933564..29935935-chr20:29935958..29938008,2	MCF-7	breast:
19	chr20:29900644..29901274-chr20:30041865..30042847,4	MCF-7	breast:
20	chr20:30001111..30001772-chr20:30200396..30200937,2	MCF-7	breast:
21	chr20:29900754..29901422-chr20:30042008..30042651,2	MCF-7	breast:
22	chr20:30023186..30025887-chr20:30031461..30033796,2	K562	blood:
23	chr20:29900754..29901422-chr20:30042008..30042651,2	MCF-7	breast:
24	chr20:29960399..29962900-chr20:29964371..29965877,2	MCF-7	breast:
25	chr20:29933564..29935935-chr20:29935958..29938008,2	MCF-7	breast:
26	chr20:29992014..29994023-chr20:30071484..30073415,2	K562	blood:
27	chr20:30006873..30009795-chr20:30012384..30014922,2	MCF-7	breast:
28	chr20:29874751..29877240-chr20:29903779..29906129,2	K562	blood:
29	chr20:29984307..29986959-chr20:29988552..29991737,3	K562	blood:
30	chr20:29960399..29962900-chr20:29964371..29965877,2	MCF-7	breast:
31	chr20:29940769..29942399-chr20:29945457..29948097,2	MCF-7	breast:
32	chr20:29962541..29965456-chr20:29970473..29972766,2	K562	blood:
33	chr20:30001115..30001627-chr20:30090661..30091593,2	MCF-7	breast:
34	chr20:30031405..30034135-chr20:30036580..30038805,2	K562	blood:
35	chr20:29900644..29901274-chr20:30041865..30042847,4	MCF-7	breast:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DEFB119-2	chr20:29930249-29931017	NONHSAT079285
2	lnc-DEFB119-1	chr20:29966155-29966194	NONHSAT079289
3	lnc-DEFB119-1	chr20:29978226-29978452	NR_073153
4	lnc-DEFB119-1	chr20:29978226-29978452	NONHSAT079289
5	lnc-DEFB116-4	chr20:29899106-29899362	NONHSAT079284
6	lnc-DEFB119-1	chr20:29976126-29976162	NONHSAT079289
7	lnc-DEFB119-2	chr20:29929174-29929962	NONHSAT079285
8	lnc-DEFB119-1	chr20:29966155-29966194	NR_073153
9	lnc-DEFB119-1	chr20:29964966-29965242	NR_073153
10	lnc-DEFB116-4	chr20:29899691-29899765	NONHSAT079284
11	lnc-DEFB119-1	chr20:29978226-29978452	NONHSAT079290
12	lnc-DEFB119-1	chr20:29964966-29965165	NONHSAT079290
13	lnc-DEFB119-1	chr20:29964966-29965242	NONHSAT079289
14	lnc-DEFB119-2	chr20:29931511-29932274	NONHSAT079285
15	lnc-DEFB119-1	chr20:29976126-29976162	NONHSAT079290
16	lnc-DEFB119-2	chr20:29931121-29931202	NONHSAT079285
17	lnc-DEFB121-1	chr20:30011613-30011670	NONHSAT079292
18	lnc-DEFB121-1	chr20:30009242-30009481	NONHSAT079292

No data

Variant related genes	Relation type
RPL31P3	TF binding region
ENSG00000212134	TF binding region
DEFB118	TF binding region
RNA5SP480	TF binding region
DEFB117	TF binding region
HAUS6P2	TF binding region
DEFB119	TF binding region
DEFB116	TF binding region
DEFB122	TF binding region
DEFB123	TF binding region
DEFB121	TF binding region
RPL31P3	CpG island
ENSG00000212134	CpG island
DEFB118	CpG island
RNA5SP480	CpG island
DEFB117	CpG island
HAUS6P2	CpG island
DEFB119	CpG island
DEFB116	CpG island
DEFB122	CpG island
DEFB123	CpG island
DEFB121	CpG island
ENSG00000180383	chromatin interactions
ENSG00000212134	chromatin interactions
ENSG00000180483	chromatin interactions
ENSG00000180424	chromatin interactions

Extended variants
information (count: 1726 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:1726 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567040481	chr20:29896479-29896480	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
2	rs114153561	chr20:29896480-29896481	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
3	rs552662348	chr20:29896507-29896508	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
4	rs145509874	chr20:29896511-29896512	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
5	rs572248634	chr20:29897203-29897204	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs367847596	chr20:29897217-29897218	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs376217953	chr20:29897236-29897237	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs553795153	chr20:29899076-29899077	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs556897603	chr20:29899118-29899119	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs376149753	chr20:29899129-29899130	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
11	rs544394686	chr20:29899137-29899138	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
12	rs570265462	chr20:29899150-29899151	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
13	rs370088618	chr20:29899158-29899159	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs571966124	chr20:29899163-29899164	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
15	rs555684127	chr20:29899189-29899190	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
16	rs4911555	chr20:29899208-29899209	Inactive region	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs117394984	chr20:29899223-29899224	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs557876204	chr20:29899235-29899236	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs373371852	chr20:29899319-29899320	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs543486392	chr20:29899341-29899342	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs576173305	chr20:29899344-29899345	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs576921002	chr20:29899717-29899718	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs148614732	chr20:29899718-29899719	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs186872895	chr20:29899729-29899730	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs557915052	chr20:29899730-29899731	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs6061207	chr20:29899742-29899743	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs140395026	chr20:29900620-29900621	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
28	rs374946428	chr20:29900663-29900664	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
29	rs531161722	chr20:29900693-29900694	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
30	rs560447555	chr20:29900695-29900696	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
31	rs573877321	chr20:29900703-29900704	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
32	rs534157897	chr20:29900762-29900763	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
33	rs71336537	chr20:29900796-29900797	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
34	rs536210451	chr20:29900803-29900804	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
35	rs536700819	chr20:29900865-29900866	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
36	rs553428286	chr20:29900900-29900901	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
37	rs11700052	chr20:29900925-29900926	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
38	rs566840422	chr20:29900929-29900930	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
39	rs539021182	chr20:29900932-29900933	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
40	rs144115480	chr20:29900943-29900944	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
41	rs367704152	chr20:29901029-29901030	Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
42	rs112499575	chr20:29901037-29901038	Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
43	rs36000803	chr20:29901074-29901075	Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
44	rs575446482	chr20:29901087-29901088	Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
45	rs397779197	chr20:29901090-29901091	Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
46	rs116758474	chr20:29901091-29901092	Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
47	rs28448310	chr20:29901120-29901121	Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
48	rs57214825	chr20:29901125-29901126	Active TSS	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs74183446	chr20:29901127-29901128	Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
50	rs146480535	chr20:29901128-29901129	Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Colorectal cancer	21645411	CNVD
Autism	22495311	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Chordoma	18071362	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21806811	CNVD
Melanoma	21693616	CNVD
Astrocytoma	17387387	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
colon cancer	17210682	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	22028636	CNVD
Breast cancer	21264507	CNVD
Thyroid cancer	19087340	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Soft tissue tumor	16732325	CNVD
Colorectal cancer	19359472	CNVD
Gastric cancer	17167181	CNVD
Myeloproliferative neoplasm	19047681	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	22860045	CNVD
Ovarian cancer	20844748	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	17603634	CNVD
Melanoma	18172304	CNVD
Breast cancer	16608533	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
early-passage human iPS cells	21368824	CNVD
Lung cancer	18438408	CNVD
Gastric cancer	16891809	CNVD
Prostate cancer	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Oral cancer	21386901	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21509527	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Amyotrophic lateral sclerosis	20688871	CNVD
Gastric cancer	22014070	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Melanoma	20877625	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:29901000-29901400	Active TSS	A549	lung
2	chr20:29901000-29901600	Active TSS	ES-I3 Cell Line	embryonic stem cell
3	chr20:29901200-29901400	Enhancers	Hela-S3	cervix
4	chr20:29901800-29902200	Active TSS	Fetal Heart	heart
5	chr20:29912400-29912800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr20:29918400-29919800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
7	chr20:29935800-29937200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
8	chr20:29956200-29956800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr20:29976800-29978400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
10	chr20:29982200-29983400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
11	chr20:29983200-29983400	Enhancers	Spleen	Spleen
12	chr20:29987000-29987600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
13	chr20:30001400-30001600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr20:30002200-30002800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr20:30006200-30006600	Active TSS	K562	blood
16	chr20:30012800-30013600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr20:30013000-30013600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr20:30018200-30019000	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr20:30024800-30025000	Enhancers	Spleen	Spleen
20	chr20:30025000-30028400	Weak transcription	Spleen	Spleen
21	chr20:30027800-30028800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
22	chr20:30028000-30028600	Enhancers	K562	blood
23	chr20:30028000-30028800	Active TSS	ES-I3 Cell Line	embryonic stem cell
24	chr20:30028000-30029800	Bivalent Enhancer	HepG2	liver
25	chr20:30028200-30028800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr20:30028200-30029400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
27	chr20:30028400-30028800	Enhancers	Spleen	Spleen
28	chr20:30028600-30029400	Weak transcription	K562	blood
29	chr20:30028800-30029200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
30	chr20:30029200-30030000	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr20:30029400-30029600	Enhancers	K562	blood
32	chr20:30029600-30033800	Weak transcription	K562	blood
33	chr20:30029800-30030400	Enhancers	HepG2	liver
34	chr20:30030000-30034000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr20:30030400-30030800	Weak transcription	HepG2	liver
36	chr20:30030800-30031000	Enhancers	HepG2	liver
37	chr20:30031000-30033600	Weak transcription	HepG2	liver
38	chr20:30033600-30034200	Enhancers	HepG2	liver
39	chr20:30033600-30034600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr20:30033600-30034600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr20:30033800-30034400	Enhancers	K562	blood
42	chr20:30034000-30034600	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr20:30034200-30034600	Flanking Active TSS	HepG2	liver
44	chr20:30034400-30034600	Flanking Active TSS	K562	blood
45	chr20:30034600-30034800	Active TSS	K562	blood
46	chr20:30034600-30037200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr20:30034600-30037800	Enhancers	HepG2	liver
48	chr20:30037000-30037400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr20:30037200-30037600	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr20:30037800-30038000	Flanking Active TSS	HepG2	liver

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