Variant report

Variant	nsv1023384
Chromosome Location	chr6:121235867-121683448
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2182)
CpG islands
(count:854)
Chromatin interactive
region (count:89)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2182 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:121315738-121316078	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:121376734-121377082	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:121655370-121656425	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:121655316-121656248	K562	blood:	n/a	n/a
5	ARID3A	chr6:121543876-121544076	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:121364821-121365152	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:121599133-121599134	K562	blood:	n/a	n/a
8	ARID3A	chr6:121654343-121654797	K562	blood:	n/a	n/a
9	ARID3A	chr6:121675962-121676151	HepG2	liver:	n/a	n/a
10	ATF1	chr6:121655564-121656189	K562	blood:	n/a	chr6:121655914-121655928
11	ATF2	chr6:121655547-121656303	GM12878	blood:	n/a	chr6:121655914-121655928 chr6:121655916-121655927
12	ATF2	chr6:121655444-121656250	H1-hESC	embryonic stem cell:	n/a	chr6:121655914-121655928 chr6:121655916-121655927
13	ATF2	chr6:121655449-121656378	GM12878	blood:	n/a	chr6:121655914-121655928 chr6:121655916-121655927
14	ATF2	chr6:121655484-121656264	H1-hESC	embryonic stem cell:	n/a	chr6:121655914-121655928 chr6:121655916-121655927
15	ATF2	chr6:121286942-121287261	GM12878	blood:	n/a	n/a
16	ATF3	chr6:121655676-121656024	A549	lung:	n/a	chr6:121655916-121655927 chr6:121655916-121655927 chr6:121655917-121655928 chr6:121655916-121655929 chr6:121655917-121655925 chr6:121655918-121655925 chr6:121655915-121655928 chr6:121655915-121655928 chr6:121655918-121655928
17	ATF3	chr6:121655514-121656080	K562	blood:	n/a	chr6:121655916-121655927 chr6:121655916-121655927 chr6:121655917-121655928 chr6:121655916-121655929 chr6:121655917-121655925 chr6:121655918-121655925 chr6:121655915-121655928 chr6:121655915-121655928 chr6:121655918-121655928
18	BACH1	chr6:121655464-121656094	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr6:121478005-121478021	K562	blood:	n/a	n/a
20	BACH1	chr6:121654518-121654622	K562	blood:	n/a	n/a
21	BATF	chr6:121287068-121287331	GM12878	blood:	n/a	chr6:121287131-121287142 chr6:121287180-121287191
22	BATF	chr6:121287512-121287843	GM12878	blood:	n/a	n/a
23	BATF	chr6:121286998-121287351	GM12878	blood:	n/a	chr6:121287131-121287142 chr6:121287180-121287191
24	BATF	chr6:121642420-121642768	GM12878	blood:	n/a	n/a
25	BATF	chr6:121655588-121656239	GM12878	blood:	n/a	n/a
26	BATF	chr6:121651818-121652073	GM12878	blood:	n/a	n/a
27	BATF	chr6:121329823-121330072	GM12878	blood:	n/a	chr6:121329971-121329982
28	BATF	chr6:121281970-121282363	GM12878	blood:	n/a	chr6:121282272-121282282 chr6:121282183-121282194
29	BCL11A	chr6:121282026-121282355	GM12878	blood:	n/a	chr6:121282271-121282280
30	BCL11A	chr6:121252692-121252841	H1-hESC	embryonic stem cell:	n/a	n/a
31	BCLAF1	chr6:121655626-121656284	GM12878	blood:	n/a	chr6:121656086-121656095
32	BHLHE40	chr6:121655429-121656124	K562	blood:	n/a	n/a
33	BHLHE40	chr6:121655416-121656356	GM12878	blood:	n/a	n/a
34	BHLHE40	chr6:121259917-121260313	GM12878	blood:	n/a	n/a
35	BHLHE40	chr6:121287045-121287056	GM12878	blood:	n/a	n/a
36	BHLHE40	chr6:121376842-121377070	GM12878	blood:	n/a	n/a
37	BRCA1	chr6:121656836-121656893	GM12878	blood:	n/a	n/a
38	BRCA1	chr6:121281657-121281728	Hela-S3	cervix:	n/a	n/a
39	BRCA1	chr6:121655532-121656152	Hela-S3	cervix:	n/a	n/a
40	BRCA1	chr6:121270387-121270388	GM12878	blood:	n/a	n/a
41	BRCA1	chr6:121655445-121655948	HepG2	liver:	n/a	n/a
42	CBX3	chr6:121445754-121446131	HCT-116	colon:	n/a	n/a
43	CBX3	chr6:121655364-121656249	K562	blood:	n/a	n/a
44	CBX3	chr6:121445743-121446140	K562	blood:	n/a	n/a
45	CBX3	chr6:121445765-121446095	K562	blood:	n/a	n/a
46	CCNT2	chr6:121655494-121656016	K562	blood:	n/a	n/a
47	CEBPB	chr6:121355598-121355799	HepG2	liver:	n/a	chr6:121355645-121355656
48	CEBPB	chr6:121299329-121299529	HepG2	liver:	n/a	chr6:121299405-121299416
49	CEBPB	chr6:121620344-121620684	HepG2	liver:	n/a	chr6:121620474-121620485 chr6:121620528-121620539 chr6:121620482-121620495 chr6:121620556-121620567
50	CEBPB	chr6:121318517-121318659	H1-hESC	embryonic stem cell:	n/a	chr6:121318605-121318616

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:121655706-121655756	AG09309	skin:	n/a
2	chr6:121658870-121658920	GM12878	blood:	n/a
3	chr6:121655792-121655842	AG04449	skin:	fetal
4	chr6:121655383-121655433	MCF10A-Er-Src	breast:	n/a
5	chr6:121656329-121656379	ovcar-3	ovarian:	n/a
6	chr6:121655782-121655832	HEEpiC	esophagus:	n/a
7	chr6:121655383-121655433	HRE	kidney:	n/a
8	chr6:121655792-121655842	H1-hESC	embryonic stem cell:	embryo
9	chr6:121655706-121655756	HIPEpiC	eye:	n/a
10	chr6:121658870-121658920	H1-hESC	embryonic stem cell:	embryo
11	chr6:121656105-121656155	ProgFib	skin:	n/a
12	chr6:121658870-121658920	U87	brain:	n/a
13	chr6:121618081-121618131	H1-hESC	embryonic stem cell:	embryo
14	chr6:121655782-121655832	AoSMC	blood vessel:	n/a
15	chr6:121655784-121655834	ovcar-3	ovarian:	n/a
16	chr6:121655792-121655842	HRCEpiC	kidney:	n/a
17	chr6:121655706-121655756	PANC-1	pancreas:	n/a
18	chr6:121658870-121658920	PFSK-1	brain:	n/a
19	chr6:121658870-121658920	GM12891	blood:	n/a
20	chr6:121656329-121656379	HIPEpiC	eye:	n/a
21	chr6:121655784-121655834	HIPEpiC	eye:	n/a
22	chr6:121655792-121655842	SK-N-MC	brain:	n/a
23	chr6:121525721-121525771	IMR90	lung:	fetal
24	chr6:121656542-121656592	AG09309	skin:	n/a
25	chr6:121274369-121274419	AG10803	skin:	n/a
26	chr6:121274369-121274419	HEK293	kidney:	embryo
27	chr6:121525721-121525771	HRCEpiC	kidney:	n/a
28	chr6:121655896-121655946	ECC-1	luminal epithelium:	n/a
29	chr6:121525721-121525771	NHBE	bronchial:	n/a
30	chr6:121618081-121618131	HCPEpiC	choroid plexus:	n/a
31	chr6:121655896-121655946	ProgFib	skin:	n/a
32	chr6:121656105-121656155	HCPEpiC	choroid plexus:	n/a
33	chr6:121655896-121655946	Caco-2	colon:	n/a
34	chr6:121426802-121426852	GM12892	blood:	n/a
35	chr6:121655383-121655433	ovcar-3	ovarian:	n/a
36	chr6:121656329-121656379	BE2_C	brain:	n/a
37	chr6:121274369-121274419	HCT-116	colon:	n/a
38	chr6:121655383-121655433	NT2-D1	testis:	n/a
39	chr6:121655383-121655433	NHDF-neo	bronchial:	n/a
40	chr6:121525721-121525771	K562	blood:	n/a
41	chr6:121655782-121655832	BE2_C	brain:	n/a
42	chr6:121655896-121655946	HCT-116	colon:	n/a
43	chr6:121655784-121655834	IMR90	lung:	fetal
44	chr6:121655784-121655834	AG09319	gingival:	n/a
45	chr6:121525721-121525771	MCF10A-Er-Src	breast:	n/a
46	chr6:121658870-121658920	K562	blood:	n/a
47	chr6:121658870-121658920	HRPEpiC	eye:	n/a
48	chr6:121658870-121658920	HCT-116	colon:	n/a
49	chr6:121655782-121655832	HMEC	breast:	n/a
50	chr6:121274369-121274419	MCF10A-Er-Src	breast:	n/a

(count:89 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:121634384..121637118-chr6:121723532..121726369,2	MCF-7	breast:
2	chr6:121477367..121479870-chr6:121507284..121508935,2	MCF-7	breast:
3	chr6:121639940..121640818-chr6:121721671..121722649,4	MCF-7	breast:
4	chr6:121452531..121454187-chr6:121456361..121459088,2	K562	blood:
5	chr6:121559791..121562429-chr6:121562632..121564241,2	K562	blood:
6	chr6:121645992..121651624-chr6:121651961..121657811,7	K562	blood:
7	chr6:121635999..121638850-chr6:121643981..121646181,2	K562	blood:
8	chr6:121376783..121377622-chr6:121626950..121627772,3	MCF-7	breast:
9	chr6:121376879..121377380-chr6:121543841..121544431,2	K562	blood:
10	chr6:121370528..121372083-chr6:121382046..121383647,2	K562	blood:
11	chr6:121635999..121638850-chr6:121643981..121646181,2	K562	blood:
12	chr6:121630562..121632167-chr6:121640292..121642248,2	K562	blood:
13	chr6:121648529..121650157-chr6:121661271..121663004,2	MCF-7	breast:
14	chr6:121377193..121378906-chr6:121509031..121511609,2	MCF-7	breast:
15	chr6:121376435..121377426-chr6:121544734..121545558,2	MCF-7	breast:
16	chr6:121634382..121637140-chr6:121639253..121640761,2	K562	blood:
17	chr6:121377193..121378906-chr6:121509031..121511609,2	MCF-7	breast:
18	chr6:121495458..121497370-chr6:121499505..121502108,2	MCF-7	breast:
19	chr6:121490346..121493740-chr6:121494679..121497011,3	K562	blood:
20	chr6:121490346..121492777-chr6:121495275..121497722,2	K562	blood:
21	chr6:121622881..121625518-chr6:121651420..121653237,2	MCF-7	breast:
22	chr6:121630562..121632167-chr6:121640292..121642248,2	K562	blood:
23	chr6:121295924..121297821-chr6:121298707..121301135,2	K562	blood:
24	chr6:121560929..121562459-chr6:121562741..121565281,2	K562	blood:
25	chr6:121394181..121397153-chr6:121399643..121401552,2	K562	blood:
26	chr6:121648529..121650157-chr6:121661271..121663004,2	MCF-7	breast:
27	chr6:121400057..121403003-chr6:121403745..121405643,2	K562	blood:
28	chr6:121412403..121414647-chr6:121418696..121420931,2	K562	blood:
29	chr6:121394181..121397153-chr6:121399643..121401552,2	K562	blood:
30	chr6:121376879..121377380-chr6:121543841..121544431,2	K562	blood:
31	chr6:121376484..121377440-chr6:121626832..121627562,3	MCF-7	breast:
32	chr6:121577028..121580353-chr6:121583189..121585636,3	K562	blood:
33	chr6:121577643..121580353-chr6:121583189..121585636,2	K562	blood:
34	chr6:121376496..121377369-chr6:121557870..121558396,2	MCF-7	breast:
35	chr6:121559791..121562429-chr6:121562632..121564241,2	K562	blood:
36	chr6:121447900..121449925-chr6:121452116..121453757,2	K562	blood:
37	chr6:121490346..121492777-chr6:121495275..121497722,2	K562	blood:
38	chr6:121411153..121412968-chr6:121418070..121419760,2	MCF-7	breast:
39	chr6:121295924..121297821-chr6:121298707..121301135,2	K562	blood:
40	chr6:119886303..119888450-chr6:121450603..121452607,2	K562	blood:
41	chr6:121653058..121658241-chr6:121659261..121663570,7	MCF-7	breast:
42	chr6:121447900..121449925-chr6:121452116..121453757,2	K562	blood:
43	chr6:121495458..121497370-chr6:121499505..121502108,2	MCF-7	breast:
44	chr6:121376109..121377626-chr6:121543516..121544370,7	MCF-7	breast:
45	chr6:121508220..121509830-chr6:121510757..121512526,2	MCF-7	breast:
46	chr6:121490346..121493740-chr6:121494679..121497011,3	K562	blood:
47	chr6:121432266..121434727-chr6:121435842..121438416,2	K562	blood:
48	chr6:121393095..121394934-chr6:121401987..121403872,2	MCF-7	breast:
49	chr6:121376484..121377440-chr6:121626832..121627562,3	MCF-7	breast:
50	chr6:121654494..121658196-chr6:121658584..121663246,8	K562	blood:

No data

Variant related genes	Relation type
RNU6-1286P	TF binding region
TBC1D32	TF binding region
RNU6-1286P	CpG island
TBC1D32	CpG island
ENSG00000134905	chromatin interactions
ENSG00000169851	chromatin interactions
ENSG00000146350	chromatin interactions
ENSG00000153487	chromatin interactions

Extended variants
information (count: 13451 )
Associated
traits (count: 118 )

Variant overlapped rSNPs/rCNVs (count:13451 , 50 per page) page: 1 2 3 4 5 6 7 ... 270

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568360704	chr6:121243020-121243021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs537124964	chr6:121243025-121243026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs557066743	chr6:121243051-121243052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs141822162	chr6:121243072-121243073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs540965568	chr6:121243098-121243099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs570797542	chr6:121243112-121243113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs539453870	chr6:121243137-121243138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs371871257	chr6:121243141-121243142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs572242381	chr6:121243175-121243176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs372062343	chr6:121243187-121243188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs541385621	chr6:121243195-121243196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs192107056	chr6:121243210-121243211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs574723610	chr6:121243221-121243222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs182615317	chr6:121243281-121243282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs187744040	chr6:121243310-121243311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs143422949	chr6:121243312-121243313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs545489774	chr6:121243313-121243314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs559339496	chr6:121243368-121243369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs539266114	chr6:121243369-121243370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs548499527	chr6:121243372-121243373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs568299524	chr6:121243402-121243403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs538839052	chr6:121243417-121243418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs9482097	chr6:121243438-121243439	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs550614344	chr6:121243443-121243444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs570868002	chr6:121243467-121243468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs146755987	chr6:121243588-121243589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs191773217	chr6:121243643-121243644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs566888547	chr6:121243657-121243658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs113736537	chr6:121243660-121243661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs183902965	chr6:121243702-121243703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs73766620	chr6:121243709-121243710	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs544677264	chr6:121243712-121243713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs537244231	chr6:121243716-121243717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs78075157	chr6:121243749-121243750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs576853273	chr6:121243803-121243804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs77034398	chr6:121243878-121243879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs143437997	chr6:121243891-121243892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs562857166	chr6:121243909-121243910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs187511385	chr6:121243968-121243969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs562047398	chr6:121244006-121244007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs147972135	chr6:121244012-121244013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs533329777	chr6:121244020-121244021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs112435559	chr6:121244022-121244023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs550885773	chr6:121244072-121244073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs6569166	chr6:121244081-121244082	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs79436670	chr6:121244140-121244141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs541404978	chr6:121244155-121244156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs547107458	chr6:121244165-121244166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs566840591	chr6:121244181-121244182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs115747057	chr6:121244186-121244187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:118)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Gastric cancer	17908304	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
T-cell lymphomas	19863542	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	19242612	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Burkitt''s lymphoma	18698080	CNVD
Ovarian cancer	21720365	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Cancer	20164920	CNVD
Breast cancer	21364760	CNVD
Chordoma	21602918	CNVD
Kartagener syndrome	16639409	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	CNVD
Mental retardation	17621639	CNVD
Hypoplastic	20877625	CNVD
Hypotonia	20877625	CNVD
Mental retardation	20877625	CNVD
Microcephaly	20877625	CNVD
brachycephaly	20877625	CNVD
epicanthic folds	20877625	CNVD
micrognathia	20877625	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Metastatic melanoma	18483359	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	18698023	CNVD
Mental retardation	18854857	CNVD
Leukemia	18688285	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Liver carcinoma	19366792	CNVD
Breast cancer	21611746	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Ependymoma	18628472	CNVD
Ewing''s sarcoma	18628472	CNVD
Leukemia	18628472	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:2275 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:121243000-121252000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr6:121246600-121247000	Active TSS	H9 Cell Line	embryonic stem cell
3	chr6:121250800-121251000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr6:121251200-121252200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr6:121251400-121252000	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr6:121251800-121252000	Active TSS	ES-I3 Cell Line	embryonic stem cell
7	chr6:121251800-121252000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr6:121251800-121252000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
9	chr6:121251800-121252200	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr6:121251800-121252400	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr6:121252000-121252200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
12	chr6:121252000-121252400	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
13	chr6:121252000-121252400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr6:121252000-121252400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
15	chr6:121252000-121252600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
16	chr6:121252000-121252600	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
17	chr6:121252000-121252600	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
18	chr6:121252000-121253000	Enhancers	H1 Cell Line	embryonic stem cell
19	chr6:121252000-121253000	Enhancers	Stomach Mucosa	stomach
20	chr6:121252200-121252400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
21	chr6:121252200-121252800	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
22	chr6:121252200-121253200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr6:121252400-121252600	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
24	chr6:121252400-121252600	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
25	chr6:121252400-121252600	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
26	chr6:121252400-121253200	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
27	chr6:121252400-121253400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr6:121252600-121252800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
29	chr6:121252600-121253000	Active TSS	iPS-15b Cell Line	embryonic stem cell
30	chr6:121252600-121253000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
31	chr6:121252600-121253200	Active TSS	ES-I3 Cell Line	embryonic stem cell
32	chr6:121252600-121253200	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
33	chr6:121252600-121253600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
34	chr6:121252800-121253400	Active TSS	iPS-20b Cell Line	embryonic stem cell
35	chr6:121252800-121253600	Active TSS	HUES64 Cell Line	embryonic stem cell
36	chr6:121253000-121253400	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr6:121253000-121256200	Weak transcription	H1 Cell Line	embryonic stem cell
38	chr6:121253200-121253800	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr6:121253200-121255600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
40	chr6:121253200-121260800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr6:121253400-121253600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr6:121253400-121253600	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
43	chr6:121253400-121254000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
44	chr6:121253600-121253800	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
45	chr6:121253600-121254000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr6:121253600-121254200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
47	chr6:121253600-121254200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
48	chr6:121253600-121254400	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
49	chr6:121253800-121254400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
50	chr6:121253800-121254400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell

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