Variant report

Variant	nsv1035133
Chromosome Location	chr6:141156919-141650334
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2272)
CpG islands
(count:610)
Chromatin interactive
region (count:75)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2272 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:141233801-141234207	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:141647618-141647926	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:141347701-141348052	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:141219654-141219754	K562	blood:	n/a	n/a
5	ARID3A	chr6:141263537-141263547	K562	blood:	n/a	n/a
6	ARID3A	chr6:141219526-141219833	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:141586969-141587287	HepG2	liver:	n/a	n/a
8	ATF1	chr6:141236361-141236561	K562	blood:	n/a	n/a
9	ATF1	chr6:141178980-141179277	K562	blood:	n/a	n/a
10	ATF1	chr6:141242769-141243022	K562	blood:	n/a	n/a
11	ATF1	chr6:141218607-141218807	K562	blood:	n/a	n/a
12	ATF1	chr6:141612636-141612753	K562	blood:	n/a	n/a
13	ATF2	chr6:141426579-141427068	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr6:141474627-141475071	GM12878	blood:	n/a	n/a
15	ATF2	chr6:141426574-141427030	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF3	chr6:141647541-141647917	A549	lung:	n/a	n/a
17	BACH1	chr6:141586960-141586966	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr6:141441909-141442156	H1-hESC	embryonic stem cell:	n/a	n/a
19	BATF	chr6:141647651-141647932	GM12878	blood:	n/a	chr6:141647803-141647814
20	BATF	chr6:141474651-141475037	GM12878	blood:	n/a	n/a
21	BATF	chr6:141428710-141429022	GM12878	blood:	n/a	chr6:141428864-141428875
22	BATF	chr6:141625060-141625335	GM12878	blood:	n/a	n/a
23	BATF	chr6:141179510-141179919	GM12878	blood:	n/a	n/a
24	BCL11A	chr6:141426702-141426936	H1-hESC	embryonic stem cell:	n/a	n/a
25	BCL11A	chr6:141474759-141475057	GM12878	blood:	n/a	n/a
26	BCL11A	chr6:141474772-141475048	H1-hESC	embryonic stem cell:	n/a	n/a
27	BCL11A	chr6:141474827-141475050	H1-hESC	embryonic stem cell:	n/a	n/a
28	BCL3	chr6:141647588-141647832	GM12878	blood:	n/a	n/a
29	BCL3	chr6:141647553-141647910	GM12878	blood:	n/a	n/a
30	BHLHE40	chr6:141178965-141179291	K562	blood:	n/a	n/a
31	BHLHE40	chr6:141233841-141234246	HepG2	liver:	n/a	n/a
32	BHLHE40	chr6:141179621-141179991	K562	blood:	n/a	n/a
33	BHLHE40	chr6:141218694-141218754	K562	blood:	n/a	n/a
34	BHLHE40	chr6:141219396-141219402	K562	blood:	n/a	n/a
35	BHLHE40	chr6:141347764-141348000	HepG2	liver:	n/a	n/a
36	BRCA1	chr6:141647463-141648010	Hela-S3	cervix:	n/a	n/a
37	BRCA1	chr6:141630527-141630762	H1-hESC	embryonic stem cell:	n/a	n/a
38	BRCA1	chr6:141236422-141236424	HepG2	liver:	n/a	n/a
39	BRCA1	chr6:141516590-141516647	HepG2	liver:	n/a	n/a
40	CBX3	chr6:141265879-141266203	K562	blood:	n/a	n/a
41	CBX3	chr6:141265947-141266292	HCT-116	colon:	n/a	n/a
42	CBX3	chr6:141398720-141399284	HCT-116	colon:	n/a	n/a
43	CBX3	chr6:141647419-141648088	HCT-116	colon:	n/a	n/a
44	CBX3	chr6:141647435-141648087	HCT-116	colon:	n/a	n/a
45	CBX3	chr6:141428603-141429239	HCT-116	colon:	n/a	n/a
46	CCNT2	chr6:141281282-141281459	K562	blood:	n/a	n/a
47	CCNT2	chr6:141546232-141546292	K562	blood:	n/a	n/a
48	CCNT2	chr6:141438727-141438866	K562	blood:	n/a	n/a
49	CEBPB	chr6:141416518-141416875	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr6:141489010-141489161	HepG2	liver:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:141643325-141643375	HIPEpiC	eye:	n/a
2	chr6:141167819-141167869	BE2_C	brain:	n/a
3	chr6:141167819-141167869	HNPCEpiC	eye:	n/a
4	chr6:141520754-141520804	NHDF-neo	bronchial:	n/a
5	chr6:141473527-141473577	PANC-1	pancreas:	n/a
6	chr6:141486137-141486187	GM06990	blood:	n/a
7	chr6:141335463-141335513	ovcar-3	ovarian:	n/a
8	chr6:141301409-141301459	HRPEpiC	eye:	n/a
9	chr6:141473527-141473577	NH-A	brain:	n/a
10	chr6:141167819-141167869	AoSMC	blood vessel:	n/a
11	chr6:141301409-141301459	HNPCEpiC	eye:	n/a
12	chr6:141603542-141603592	HPAEpiC	pulmonary alveolar:	n/a
13	chr6:141603542-141603592	SK-N-MC	brain:	n/a
14	chr6:141486137-141486187	Hela-S3	cervix:	n/a
15	chr6:141473527-141473577	ProgFib	skin:	n/a
16	chr6:141643325-141643375	GM12878	blood:	n/a
17	chr6:141335831-141335881	GM12878	blood:	n/a
18	chr6:141167819-141167869	H1-hESC	embryonic stem cell:	embryo
19	chr6:141427033-141427083	HMEC	breast:	n/a
20	chr6:141167819-141167869	ProgFib	skin:	n/a
21	chr6:141427033-141427083	SK-N-SH_RA	brain:	n/a
22	chr6:141335463-141335513	Jurkat	blood:	n/a
23	chr6:141643325-141643375	GM19239	blood:	n/a
24	chr6:141520754-141520804	Hela-S3	cervix:	n/a
25	chr6:141520754-141520804	A549	lung:	n/a
26	chr6:141520754-141520804	Hepatocyte	liver:	n/a
27	chr6:141520754-141520804	HepG2	liver:	n/a
28	chr6:141473527-141473577	HCM	heart:	n/a
29	chr6:141335463-141335513	A549	lung:	n/a
30	chr6:141520754-141520804	GM12878	blood:	n/a
31	chr6:141473527-141473577	ovcar-3	ovarian:	n/a
32	chr6:141335463-141335513	K562	blood:	n/a
33	chr6:141335463-141335513	MCF10A-Er-Src	breast:	n/a
34	chr6:141603542-141603592	GM06990	blood:	n/a
35	chr6:141427033-141427083	HCPEpiC	choroid plexus:	n/a
36	chr6:141427033-141427083	MCF10A-Er-Src	breast:	n/a
37	chr6:141335463-141335513	HEEpiC	esophagus:	n/a
38	chr6:141335831-141335881	U87	brain:	n/a
39	chr6:141335463-141335513	HNPCEpiC	eye:	n/a
40	chr6:141603542-141603592	AG09319	gingival:	n/a
41	chr6:141335463-141335513	NHDF-neo	bronchial:	n/a
42	chr6:141486137-141486187	HPAEpiC	pulmonary alveolar:	n/a
43	chr6:141643325-141643375	HRCEpiC	kidney:	n/a
44	chr6:141520754-141520804	HL-60	blood:	n/a
45	chr6:141520754-141520804	HRPEpiC	eye:	n/a
46	chr6:141167819-141167869	HRE	kidney:	n/a
47	chr6:141335831-141335881	GM12892	blood:	n/a
48	chr6:141473527-141473577	HRCEpiC	kidney:	n/a
49	chr6:141486137-141486187	HEEpiC	esophagus:	n/a
50	chr6:141473527-141473577	HEK293	kidney:	embryo

(count:75 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:141607703..141609358-chr6:141615352..141617178,2	K562	blood:
2	chr6:141563813..141566176-chr6:141569270..141571804,2	K562	blood:
3	chr6:141457381..141459115-chr6:141461082..141463007,2	MCF-7	breast:
4	chr6:141201313..141204931-chr6:141205813..141208687,3	K562	blood:
5	chr6:141356659..141359545-chr6:141368726..141370733,2	K562	blood:
6	chr10:79621997..79624207-chr6:141528494..141531301,2	MCF-7	breast:
7	chr6:141535806..141537434-chr6:141539065..141540907,2	K562	blood:
8	chr6:141368847..141371211-chr6:141441776..141443428,2	K562	blood:
9	chr6:141210884..141213823-chr6:141384643..141387034,2	K562	blood:
10	chr6:141209671..141212646-chr6:141217346..141220652,3	K562	blood:
11	chr6:141565815..141567855-chr6:141569717..141571593,2	MCF-7	breast:
12	chr6:141328979..141331399-chr6:141334184..141335963,2	K562	blood:
13	chr6:141466947..141468620-chr6:141486006..141488236,2	K562	blood:
14	chr6:141450586..141452410-chr6:141456165..141457885,2	K562	blood:
15	chr6:141212782..141215020-chr6:141216248..141219853,3	K562	blood:
16	chr6:141245976..141248049-chr6:141253125..141254687,2	MCF-7	breast:
17	chr6:141557548..141559369-chr6:141561478..141563521,2	K562	blood:
18	chr6:141602459..141604737-chr6:141622065..141624728,2	K562	blood:
19	chr6:141314907..141317721-chr6:141319915..141321447,2	K562	blood:
20	chr6:141225214..141229759-chr6:141230098..141233300,4	K562	blood:
21	chr6:141201035..141203602-chr6:141204106..141206324,2	MCF-7	breast:
22	chr6:141204507..141206612-chr6:141209189..141212114,2	K562	blood:
23	chr6:141212244..141214629-chr6:141219189..141220964,2	MCF-7	breast:
24	chr6:141194790..141196921-chr6:141201066..141202633,2	K562	blood:
25	chr6:140202949..140203456-chr6:141242488..141243293,2	MCF-7	breast:
26	chr6:141201035..141203602-chr6:141204106..141206324,2	MCF-7	breast:
27	chr6:141204507..141206612-chr6:141209189..141212114,2	K562	blood:
28	chr6:141210884..141213823-chr6:141384643..141387034,2	K562	blood:
29	chr6:141209671..141212646-chr6:141217346..141220652,3	K562	blood:
30	chr6:141557220..141559048-chr6:141561478..141563410,2	K562	blood:
31	chr6:141569154..141570819-chr6:141571531..141574122,2	K562	blood:
32	chr6:141368847..141371211-chr6:141441776..141443428,2	K562	blood:
33	chr6:141630179..141631093-chr6:141883723..141884605,3	MCF-7	breast:
34	chr6:141194790..141196921-chr6:141201066..141202633,2	K562	blood:
35	chr6:141314907..141317721-chr6:141319915..141321447,2	K562	blood:
36	chr6:141203363..141207943-chr6:141209189..141214513,5	K562	blood:
37	chr6:141557548..141559369-chr6:141561478..141563521,2	K562	blood:
38	chr5:98131550..98132070-chr6:141289515..141290035,2	MCF-7	breast:
39	chr6:141194692..141196921-chr6:141200242..141202633,2	K562	blood:
40	chr6:141630271..141631033-chr6:141883682..141884206,2	MCF-7	breast:
41	chr6:141474693..141476532-chr6:141479215..141481575,2	MCF-7	breast:
42	chr6:141186030..141188645-chr6:141209021..141211970,2	K562	blood:
43	chr6:141569154..141570819-chr6:141571531..141574122,2	K562	blood:
44	chr6:141535806..141537434-chr6:141539065..141540907,2	K562	blood:
45	chr6:141201313..141204931-chr6:141205813..141208687,3	K562	blood:
46	chr6:141324954..141326818-chr6:141329009..141331828,2	K562	blood:
47	chr6:141606885..141609429-chr6:141611912..141614017,2	MCF-7	breast:
48	chr6:141324954..141326818-chr6:141329009..141331828,2	K562	blood:
49	chr6:141194692..141196921-chr6:141200242..141202633,2	K562	blood:
50	chr6:141565815..141567855-chr6:141569717..141571593,2	MCF-7	breast:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NMBR-2	chr6:141173956-141174059	NONHSAT115288
2	lnc-NMBR-2	chr6:141173956-141174061	ENSG00000234147
3	lnc-NMBR-2	chr6:141184950-141184976	NONHSAT115288
4	lnc-NMBR-2	chr6:141167095-141167471	NONHSAT115288
5	lnc-NMBR-8	chr6:141215649-141215754	NONHSAT115290
6	lnc-NMBR-8	chr6:141208788-141209134	NONHSAT115290
7	lnc-NMBR-2	chr6:141185039-141185580	NONHSAT115288
8	lnc-NMBR-2	chr6:141167095-141167441	ENSG00000234147
9	lnc-NMBR-2	chr6:141184986-141185033	NONHSAT115288
10	lnc-NMBR-2	chr6:141216940-141217067	NONHSAT115288
11	lnc-NMBR-2	chr6:141219325-141219567	NONHSAT115288

No data

Variant related genes	Relation type
ENSG00000234147	TF binding region
ENSG00000216548	TF binding region
ENSG00000234147	CpG island
ENSG00000216548	CpG island

Extended variants
information (count: 11700 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:11700 , 50 per page) page: 1 2 3 4 5 6 7 ... 234

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561107870	chr6:141156980-141156981	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs73581268	chr6:141156992-141156993	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs150455271	chr6:141157018-141157019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs192944275	chr6:141157022-141157023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs558991047	chr6:141157049-141157050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs572486837	chr6:141157086-141157087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs138295323	chr6:141157096-141157097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs578232605	chr6:141157118-141157119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs141386240	chr6:141157121-141157122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs560586735	chr6:141157127-141157128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs528008591	chr6:141157142-141157143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs549059047	chr6:141157160-141157161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs561342724	chr6:141157186-141157187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs183512945	chr6:141157247-141157248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs371607735	chr6:141157297-141157298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs549909055	chr6:141157338-141157339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs568688455	chr6:141157398-141157399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs539214090	chr6:141157438-141157439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs145173457	chr6:141157465-141157466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs563588422	chr6:141157537-141157538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs566604334	chr6:141157557-141157558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs534103858	chr6:141157576-141157577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs631153	chr6:141157634-141157635	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs554548063	chr6:141157717-141157718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs631576	chr6:141157732-141157733	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs537920957	chr6:141157758-141157759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs631659	chr6:141157797-141157798	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs545587129	chr6:141157815-141157816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs138793842	chr6:141157823-141157824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs572608173	chr6:141157853-141157854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs543344871	chr6:141157867-141157868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs188811139	chr6:141157875-141157876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs632083	chr6:141157881-141157882	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs543495374	chr6:141157974-141157975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs565010271	chr6:141157989-141157990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs193206524	chr6:141158063-141158064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs374353781	chr6:141158076-141158077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs76938182	chr6:141158078-141158079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs643558	chr6:141158127-141158128	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs527590046	chr6:141158138-141158139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs112457927	chr6:141158204-141158205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs372099029	chr6:141158313-141158314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs644443	chr6:141158321-141158322	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs537805238	chr6:141158328-141158329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs556214551	chr6:141158331-141158332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs144693367	chr6:141158333-141158334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs546115812	chr6:141158344-141158345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs148112110	chr6:141158362-141158363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs554062804	chr6:141158462-141158463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs584727	chr6:141158509-141158510	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:87)

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
Autism	22495311	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
Gastric cancer	17908304	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
Colorectal cancer	16272173	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
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Follicular lymphoma	18703704	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Breast cancer	21364760	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute monocytic leukemia	16498392	CNVD
Endocrine pancreatic tumor	17914106	CNVD
Soft tissue tumor	16732325	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
craniofacial dysmorphism	21918468	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Medulloblastoma	21163964	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD

Chromatin state (count:1463 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:141152800-141171600	Weak transcription	Aorta	Aorta
2	chr6:141156600-141157000	Enhancers	Left Ventricle	heart
3	chr6:141156600-141157000	Enhancers	Ovary	ovary
4	chr6:141164600-141164800	ZNF genes & repeats	NHLF	lung
5	chr6:141164800-141166200	Weak transcription	NHLF	lung
6	chr6:141165000-141188400	Weak transcription	HepG2	liver
7	chr6:141166200-141166400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr6:141166200-141167000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr6:141166200-141167400	Enhancers	Muscle Satellite Cultured Cells	--
10	chr6:141166200-141167800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr6:141166200-141168200	Enhancers	NHLF	lung
12	chr6:141166400-141167000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr6:141166600-141167000	Enhancers	Fetal Heart	heart
14	chr6:141166600-141167600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr6:141166600-141169200	Enhancers	Osteobl	bone
16	chr6:141166600-141169800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr6:141166600-141172400	Enhancers	NHDF-Ad	bronchial
18	chr6:141166800-141168200	Enhancers	NH-A	brain
19	chr6:141166800-141169200	Enhancers	Hela-S3	cervix
20	chr6:141166800-141172600	Enhancers	HUVEC	blood vessel
21	chr6:141166800-141173600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr6:141167000-141170000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr6:141167200-141167400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr6:141167200-141168000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr6:141167200-141169800	Enhancers	HSMM	muscle
26	chr6:141167400-141167800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
27	chr6:141167400-141167800	Enhancers	HSMMtube	muscle
28	chr6:141167400-141168000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr6:141167600-141168000	Enhancers	Adipose Nuclei	Adipose
30	chr6:141167600-141168000	Enhancers	A549	lung
31	chr6:141167600-141168200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr6:141167600-141183000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr6:141167800-141170400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr6:141167800-141170800	Weak transcription	HSMMtube	muscle
35	chr6:141167800-141172600	Enhancers	Muscle Satellite Cultured Cells	--
36	chr6:141168000-141168600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr6:141168000-141168800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr6:141168200-141168800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr6:141168200-141169000	Weak transcription	NHLF	lung
40	chr6:141168200-141171400	Weak transcription	NH-A	brain
41	chr6:141168600-141169200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr6:141168800-141169000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr6:141168800-141169000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr6:141169000-141169200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr6:141169000-141169200	Enhancers	NHLF	lung
46	chr6:141169000-141169600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr6:141169200-141169400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr6:141169200-141169800	Weak transcription	NHLF	lung
49	chr6:141169200-141170400	Weak transcription	Osteobl	bone
50	chr6:141169200-141171400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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