Variant report

Variant	nsv1030116
Chromosome Location	chr6:163273707-163525678
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:949)
CpG islands
(count:1531)
Chromatin interactive
region (count:20)
LncRNA
region (count:22)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:949 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:163304083-163304357	HepG2	liver:	n/a	n/a
2	ATF2	chr6:163422341-163422769	GM12878	blood:	n/a	n/a
3	ATF3	chr6:163303817-163304198	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF3	chr6:163303885-163304152	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr6:163277893-163278240	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr6:163523786-163523817	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr6:163422365-163422747	GM12878	blood:	n/a	chr6:163422593-163422603
8	BATF	chr6:163422337-163422713	GM12878	blood:	n/a	chr6:163422593-163422603
9	BCL11A	chr6:163422413-163422668	GM12878	blood:	n/a	n/a
10	BCL11A	chr6:163422425-163422741	GM12878	blood:	n/a	n/a
11	BCL3	chr6:163476202-163476485	GM12878	blood:	n/a	n/a
12	BCL3	chr6:163479255-163479599	GM12878	blood:	n/a	n/a
13	BCL3	chr6:163295916-163296614	GM12878	blood:	n/a	n/a
14	BCL3	chr6:163476237-163476563	GM12878	blood:	n/a	n/a
15	BCL3	chr6:163295660-163296500	GM12878	blood:	n/a	n/a
16	BCL3	chr6:163479336-163479590	GM12878	blood:	n/a	n/a
17	BHLHE40	chr6:163304111-163304430	HepG2	liver:	n/a	n/a
18	CBX3	chr6:163385583-163386388	HCT-116	colon:	n/a	n/a
19	CBX3	chr6:163453013-163453248	K562	blood:	n/a	n/a
20	CBX3	chr6:163385655-163386353	HCT-116	colon:	n/a	n/a
21	CCNT2	chr6:163484404-163484537	K562	blood:	n/a	n/a
22	CCNT2	chr6:163315115-163315237	K562	blood:	n/a	n/a
23	CCNT2	chr6:163334181-163334374	K562	blood:	n/a	n/a
24	CCNT2	chr6:163293683-163293879	K562	blood:	n/a	n/a
25	CEBPB	chr6:163478428-163478563	HepG2	liver:	n/a	chr6:163478503-163478514
26	CEBPB	chr6:163303926-163304412	A549	lung:	n/a	chr6:163304059-163304070
27	CEBPB	chr6:163478305-163478612	K562	blood:	n/a	chr6:163478503-163478514
28	CEBPB	chr6:163301784-163302058	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr6:163478322-163478698	H1-hESC	embryonic stem cell:	n/a	chr6:163478503-163478514
30	CEBPB	chr6:163478412-163478549	K562	blood:	n/a	chr6:163478503-163478514
31	CEBPB	chr6:163303990-163304154	K562	blood:	n/a	chr6:163304059-163304070
32	CEBPB	chr6:163303993-163304101	HepG2	liver:	n/a	chr6:163304059-163304070
33	CEBPB	chr6:163289803-163289880	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr6:163325129-163325412	IMR90	lung:	n/a	chr6:163325287-163325298
35	CEBPB	chr6:163303909-163304113	IMR90	lung:	n/a	chr6:163304059-163304070
36	CEBPB	chr6:163462678-163462805	HepG2	liver:	n/a	chr6:163462716-163462727 chr6:163462715-163462728 chr6:163462715-163462726 chr6:163462717-163462726 chr6:163462717-163462726 chr6:163462717-163462726 chr6:163462717-163462726
37	CEBPB	chr6:163478331-163478677	MCF-7	breast:	n/a	chr6:163478503-163478514
38	CEBPB	chr6:163325122-163325456	HepG2	liver:	n/a	chr6:163325287-163325298
39	CEBPB	chr6:163520664-163521093	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr6:163325142-163325406	H1-hESC	embryonic stem cell:	n/a	chr6:163325287-163325298
41	CEBPB	chr6:163325154-163325392	K562	blood:	n/a	chr6:163325287-163325298
42	CEBPB	chr6:163442138-163442402	A549	lung:	n/a	chr6:163442250-163442261
43	CEBPB	chr6:163384837-163385142	IMR90	lung:	n/a	n/a
44	CEBPB	chr6:163303869-163304224	HepG2	liver:	n/a	chr6:163304059-163304070
45	CEBPB	chr6:163289641-163289999	HepG2	liver:	n/a	n/a
46	CEBPB	chr6:163442088-163442410	HepG2	liver:	n/a	chr6:163442250-163442261
47	CEBPB	chr6:163478376-163478685	ECC-1	luminal epithelium:	n/a	chr6:163478503-163478514
48	CEBPB	chr6:163478322-163478694	A549	lung:	n/a	chr6:163478503-163478514
49	CEBPB	chr6:163385746-163386445	HCT-116	colon:	n/a	n/a
50	CEBPB	chr6:163325809-163326020	HepG2	liver:	n/a	chr6:163325933-163325944

(count:1531 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:163517573-163517623	HCT-116	colon:	n/a
2	chr6:163321157-163321207	ovcar-3	ovarian:	n/a
3	chr6:163506790-163506840	PrEC	prostate:	n/a
4	chr6:163278126-163278176	HepG2	liver:	n/a
5	chr6:163521522-163521572	HCM	heart:	n/a
6	chr6:163475324-163475374	PrEC	prostate:	n/a
7	chr6:163517573-163517623	HCT-116	colon:	n/a
8	chr6:163321157-163321207	ovcar-3	ovarian:	n/a
9	chr6:163506790-163506840	PrEC	prostate:	n/a
10	chr6:163278126-163278176	HepG2	liver:	n/a
11	chr6:163521522-163521572	HCM	heart:	n/a
12	chr6:163475324-163475374	PrEC	prostate:	n/a
13	chr6:163321435-163321485	K562	blood:	n/a
14	chr6:163506790-163506840	Jurkat	blood:	n/a
15	chr6:163525424-163525474	MCF-7	breast:	n/a
16	chr6:163321157-163321207	HCPEpiC	choroid plexus:	n/a
17	chr6:163321157-163321207	Hela-S3	cervix:	n/a
18	chr6:163362155-163362205	MCF10A-Er-Src	breast:	n/a
19	chr6:163521522-163521572	HMEC	breast:	n/a
20	chr6:163517573-163517623	HUVEC	blood vessel:	n/a
21	chr6:163517573-163517623	MCF-7	breast:	n/a
22	chr6:163521371-163521421	HUVEC	blood vessel:	n/a
23	chr6:163275980-163276030	AG04449	skin:	fetal
24	chr6:163475252-163475302	ECC-1	luminal epithelium:	n/a
25	chr6:163362155-163362205	AoSMC	blood vessel:	n/a
26	chr6:163475333-163475383	LNCaP	prostate:	n/a
27	chr6:163289631-163289681	GM12878	blood:	n/a
28	chr6:163521167-163521217	BJ	skin:	n/a
29	chr6:163275952-163276002	A549	lung:	n/a
30	chr6:163475333-163475383	H1-hESC	embryonic stem cell:	embryo
31	chr6:163276038-163276088	IMR90	lung:	fetal
32	chr6:163289514-163289564	HEK293	kidney:	embryo
33	chr6:163475718-163475768	MCF-7	breast:	n/a
34	chr6:163517573-163517623	HMEC	breast:	n/a
35	chr6:163321305-163321355	SK-N-SH	brain:	n/a
36	chr6:163276038-163276088	NHDF-neo	bronchial:	n/a
37	chr6:163521167-163521217	HAEpiC	amniotic membrane:	n/a
38	chr6:163289702-163289752	AG09319	gingival:	n/a
39	chr6:163514605-163514655	LNCaP	prostate:	n/a
40	chr6:163321305-163321355	Hepatocyte	liver:	n/a
41	chr6:163517573-163517623	HL-60	blood:	n/a
42	chr6:163475333-163475383	HCPEpiC	choroid plexus:	n/a
43	chr6:163275980-163276030	NH-A	brain:	n/a
44	chr6:163475324-163475374	LNCaP	prostate:	n/a
45	chr6:163514605-163514655	K562	blood:	n/a
46	chr6:163275952-163276002	HL-60	blood:	n/a
47	chr6:163475718-163475768	HAEpiC	amniotic membrane:	n/a
48	chr6:163321435-163321485	GM12892	blood:	n/a
49	chr6:163362155-163362205	HPAEpiC	pulmonary alveolar:	n/a
50	chr6:163520766-163520816	HEEpiC	esophagus:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:163312379..163314050-chr6:163315693..163317902,2	K562	blood:
2	chr6:163458107..163459739-chr6:163463183..163466142,2	K562	blood:
3	chr6:163509761..163512247-chr6:163514199..163516689,2	K562	blood:
4	chr6:163458107..163459739-chr6:163463183..163466142,2	K562	blood:
5	chr6:163426091..163427659-chr6:163429418..163431049,2	K562	blood:
6	chr6:163332495..163335026-chr6:163337698..163339412,2	K562	blood:
7	chr6:163312379..163314050-chr6:163315693..163317902,2	K562	blood:
8	chr6:163383289..163384996-chr6:163389712..163391752,2	MCF-7	breast:
9	chr6:163426091..163427659-chr6:163429418..163431049,2	K562	blood:
10	chr12:104252627..104253426-chr6:163440642..163441162,2	MCF-7	breast:
11	chr6:163429068..163430008-chrX:51497389..51498171,2	MCF-7	breast:
12	chr6:163509761..163512247-chr6:163514199..163516689,2	K562	blood:
13	chr6:163321321..163323965-chr6:163834423..163836018,2	MCF-7	breast:
14	chr6:163467143..163469243-chr6:163471356..163474324,2	K562	blood:
15	chr6:163467143..163469243-chr6:163471356..163474324,2	K562	blood:
16	chr6:163320477..163321997-chr6:163470936..163472773,2	K562	blood:
17	chr6:163316641..163319996-chr6:163320032..163324686,4	K562	blood:
18	chr6:163332495..163335026-chr6:163337698..163339412,2	K562	blood:
19	chr6:163383289..163384996-chr6:163389712..163391752,2	MCF-7	breast:
20	chr6:163316641..163319996-chr6:163320032..163324686,4	K562	blood:

(count:22 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL078585.1-1	chr6:163471578-163473064	NONHSAT115951
2	lnc-AL078585.1-1	chr6:163474957-163475193	ENSG00000225437.1
3	lnc-AL078585.1-13	chr6:163392282-163393054	ucscGeneNc_uc003qud_1
4	lnc-AL078585.1-9	chr6:163523625-163524579	ucscGeneNc_uc010kkf_1
5	lnc-AL078585.1-1	chr6:163474957-163475173	NONHSAT115951
6	lnc-AL078585.1-14	chr6:163378290-163378580	NONHSAT115947
7	lnc-AL078585.1-13	chr6:163384002-163384191	ucscGeneNc_uc003qud_1
8	lnc-AL078585.1-13	chr6:163387606-163387705	ucscGeneNc_uc003qud_1
9	lnc-QKI-10	chr6:163307016-163311030	NONHSAT115946
10	lnc-AL078585.1-1	chr6:163472292-163473064	ENSG00000225437.1
11	lnc-AL078585.1-13	chr6:163394947-163395183	ucscGeneNc_uc003qud_1
12	lnc-AL078585.1-1	chr6:163467616-163467717	ENSG00000225437.1
13	lnc-AL078585.1-1	chr6:163467616-163467715	ENSG00000225437.1
14	lnc-AL078585.1-1	chr6:163463589-163463729	ENSG00000225437.1
15	lnc-AL078585.1-1	chr6:163465681-163465778	ENSG00000225437.1
16	lnc-AL078585.1-1	chr6:163467647-163467715	NONHSAT115951
17	lnc-AL078585.1-1	chr6:163464086-163464201	ENSG00000225437.1
18	lnc-AL078585.1-1	chr6:163464012-163464201	ENSG00000225437.1
19	lnc-AL078585.1-1	chr6:163472292-163472446	ENSG00000225437.1
20	lnc-AL078585.1-1	chr6:163464011-163464201	ENSG00000225437.1
21	lnc-AL078585.1-1	chr6:163465681-163465778	ENSG00000225437.1
22	lnc-AL078585.1-1	chr6:163467616-163467715	ENSG00000225437.1

No data

Variant related genes	Relation type
ENSG00000225437	TF binding region
PACRG	TF binding region
ENSG00000217557	TF binding region
ENSG00000225437	CpG island
PACRG	CpG island
ENSG00000217557	CpG island
ENSG00000270419	chromatin interactions
ENSG00000112531	chromatin interactions
ENSG00000225437	chromatin interactions

Extended variants
information (count: 6424 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:6424 , 50 per page) page: 1 2 3 4 5 6 7 ... 129

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545748203	chr6:163273722-163273723	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs73603881	chr6:163273735-163273736	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs532001772	chr6:163273761-163273762	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs531910597	chr6:163273827-163273828	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs568622803	chr6:163273854-163273855	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs185605648	chr6:163273885-163273886	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs79780861	chr6:163273890-163273891	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs570601445	chr6:163273897-163273898	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs76115844	chr6:163273912-163273913	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs568553553	chr6:163273981-163273982	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs536541310	chr6:163273984-163273985	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs556167834	chr6:163273985-163273986	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs116178493	chr6:163273986-163273987	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs535726492	chr6:163274025-163274026	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs112419082	chr6:163274049-163274050	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs12527753	chr6:163274054-163274055	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs78071473	chr6:163274111-163274112	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs540911365	chr6:163274124-163274125	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs117050298	chr6:163274126-163274127	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs146152878	chr6:163274208-163274209	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs529651163	chr6:163274249-163274250	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs373402847	chr6:163274285-163274286	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs190748474	chr6:163274288-163274289	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs12665063	chr6:163274306-163274307	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	mRNA abundance
25	rs183366523	chr6:163274337-163274338	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs140046356	chr6:163274339-163274340	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs189224914	chr6:163274340-163274341	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs34753567	chr6:163274390-163274391	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs60835899	chr6:163274393-163274394	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs141936244	chr6:163274411-163274412	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs193095479	chr6:163274412-163274413	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs564693032	chr6:163274421-163274422	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs34443744	chr6:163274428-163274429	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs183864216	chr6:163274529-163274530	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs55709292	chr6:163274540-163274541	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs12660616	chr6:163274561-163274562	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs535154379	chr6:163274602-163274603	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs139635101	chr6:163274621-163274622	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs570753270	chr6:163274673-163274674	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs142852527	chr6:163274688-163274689	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs538180480	chr6:163274715-163274716	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs557500208	chr6:163274744-163274745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs112613716	chr6:163274752-163274753	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs13216389	chr6:163274757-163274758	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs559508735	chr6:163274774-163274775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs557438082	chr6:163274778-163274779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs186685348	chr6:163274818-163274819	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs35314719	chr6:163274868-163274869	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs576380101	chr6:163274899-163274900	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs541897715	chr6:163274970-163274971	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

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
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
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
Gastric cancer	17908304	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
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	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
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Testicular germ cell tumor	18059402	CNVD
Developmental delay	21147756	CNVD
Chordoma	18071362	CNVD
Myelofibrosis	22110671	CNVD
Autism	22241247	CNVD
Breast cancer	16397240	CNVD
Atherosclerosis	21956041	CNVD
Maculopathy	20981449	CNVD
Retinoblastoma	22278416	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian cancer	20844748	CNVD
Uveal melanoma	20484589	CNVD
Glioblastoma multiforme	19435819	CNVD
Astrocytoma	16205629	CNVD
Parkinson disease	17160897	CNVD
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian cancer	22355333	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
abnormal development	18461090	CNVD
Cancer	20164919	CNVD

Chromatin state (count:969 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:163267400-163275800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr6:163270400-163274000	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr6:163270400-163275800	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr6:163270400-163275800	Weak transcription	Fetal Brain Male	brain
5	chr6:163270400-163277800	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr6:163270600-163274000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr6:163270600-163274200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr6:163270600-163275600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr6:163270600-163275600	Weak transcription	Fetal Heart	heart
10	chr6:163270600-163275800	Weak transcription	Left Ventricle	heart
11	chr6:163271800-163277600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
12	chr6:163272200-163277400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr6:163272400-163273800	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr6:163272400-163274000	Weak transcription	Brain Angular Gyrus	brain
15	chr6:163272400-163274600	Enhancers	Brain Inferior Temporal Lobe	brain
16	chr6:163272400-163277800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr6:163273200-163273800	Enhancers	Brain Substantia Nigra	brain
18	chr6:163273200-163274000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
19	chr6:163273200-163274200	Enhancers	Brain Anterior Caudate	brain
20	chr6:163273200-163274600	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr6:163273200-163275800	Enhancers	Brain Hippocampus Middle	brain
22	chr6:163273200-163276400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr6:163273200-163278200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr6:163273400-163273800	Enhancers	Brain Cingulate Gyrus	brain
25	chr6:163273400-163274000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr6:163273400-163274200	Enhancers	Brain Germinal Matrix	brain
27	chr6:163273400-163274600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr6:163273600-163275000	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr6:163273600-163275800	Weak transcription	Pancreas	Pancrea
30	chr6:163273800-163274000	Flanking Active TSS	Brain Substantia Nigra	brain
31	chr6:163273800-163274200	Enhancers	H1 Cell Line	embryonic stem cell
32	chr6:163273800-163274200	Enhancers	HUES6 Cell Line	embryonic stem cell
33	chr6:163273800-163274200	Flanking Active TSS	Brain Cingulate Gyrus	brain
34	chr6:163273800-163276200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr6:163274000-163274200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr6:163274000-163274400	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr6:163274000-163274400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
38	chr6:163274000-163274400	Active TSS	Brain Substantia Nigra	brain
39	chr6:163274000-163274600	Enhancers	Brain Angular Gyrus	brain
40	chr6:163274000-163276200	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr6:163274200-163274600	Flanking Active TSS	Brain Anterior Caudate	brain
42	chr6:163274200-163275600	Weak transcription	Brain Germinal Matrix	brain
43	chr6:163274200-163275800	Weak transcription	H1 Cell Line	embryonic stem cell
44	chr6:163274200-163275800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr6:163274200-163275800	Enhancers	Brain Cingulate Gyrus	brain
46	chr6:163274200-163277600	Weak transcription	HUES6 Cell Line	embryonic stem cell
47	chr6:163274200-163277800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr6:163274400-163274600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
49	chr6:163274400-163274600	Flanking Active TSS	Brain Substantia Nigra	brain
50	chr6:163274400-163277400	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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