Variant report

Variant	nsv481709
Chromosome Location	chr6:162611340-163119381
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1565)
CpG islands
(count:795)
Chromatin interactive
region (count:41)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1565 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:163102512-163102850	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:162910482-162910786	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:162794306-162794665	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:162671087-162671724	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:162857639-162857816	HepG2	liver:	n/a	n/a
6	ATF1	chr6:163037119-163037243	K562	blood:	n/a	n/a
7	ATF1	chr6:162782228-162782581	K562	blood:	n/a	n/a
8	ATF1	chr6:162812215-162812339	K562	blood:	n/a	n/a
9	ATF1	chr6:162784797-162785113	K562	blood:	n/a	n/a
10	ATF1	chr6:162812647-162812847	K562	blood:	n/a	n/a
11	ATF2	chr6:163042363-163042635	GM12878	blood:	n/a	n/a
12	ATF3	chr6:163042298-163042684	HCT-116	colon:	n/a	n/a
13	ATF3	chr6:162784742-162785052	K562	blood:	n/a	n/a
14	BACH1	chr6:162975725-162976098	K562	blood:	n/a	n/a
15	BATF	chr6:163042398-163042636	GM12878	blood:	n/a	chr6:163042519-163042530
16	BATF	chr6:163042347-163042655	GM12878	blood:	n/a	chr6:163042519-163042530
17	BHLHE40	chr6:163042376-163042676	GM12878	blood:	n/a	n/a
18	BHLHE40	chr6:163102590-163102846	HepG2	liver:	n/a	n/a
19	BHLHE40	chr6:162899266-162899534	GM12878	blood:	n/a	n/a
20	BRCA1	chr6:162658617-162658742	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr6:162871740-162871751	H1-hESC	embryonic stem cell:	n/a	n/a
22	CBX3	chr6:162784775-162785143	K562	blood:	n/a	n/a
23	CBX3	chr6:162785538-162785848	K562	blood:	n/a	n/a
24	CCNT2	chr6:163001825-163002025	K562	blood:	n/a	n/a
25	CEBPB	chr6:162910493-162910789	HepG2	liver:	n/a	n/a
26	CEBPB	chr6:162857234-162857635	HepG2	liver:	n/a	chr6:162857420-162857431
27	CEBPB	chr6:162794250-162794499	HepG2	liver:	n/a	chr6:162794312-162794323
28	CEBPB	chr6:162670249-162670473	HepG2	liver:	n/a	chr6:162670378-162670389
29	CEBPB	chr6:163106060-163106305	HepG2	liver:	n/a	n/a
30	CEBPB	chr6:162745722-162745922	HepG2	liver:	n/a	chr6:162745751-162745762
31	CEBPB	chr6:162871405-162871712	H1-hESC	embryonic stem cell:	n/a	chr6:162871605-162871616
32	CEBPB	chr6:163036084-163036403	A549	lung:	n/a	chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036235-163036248 chr6:163036235-163036248 chr6:163036237-163036246 chr6:163036116-163036129 chr6:163036236-163036247
33	CEBPB	chr6:162857280-162857594	HepG2	liver:	n/a	chr6:162857420-162857431
34	CEBPB	chr6:162861366-162861450	H1-hESC	embryonic stem cell:	n/a	chr6:162861390-162861403
35	CEBPB	chr6:162634276-162634544	A549	lung:	n/a	chr6:162634418-162634429
36	CEBPB	chr6:162656289-162656489	A549	lung:	n/a	n/a
37	CEBPB	chr6:162672448-162672478	HepG2	liver:	n/a	n/a
38	CEBPB	chr6:163042252-163042579	MCF-7	breast:	n/a	n/a
39	CEBPB	chr6:163036070-163036411	IMR90	lung:	n/a	chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036235-163036248 chr6:163036235-163036248 chr6:163036237-163036246 chr6:163036116-163036129 chr6:163036236-163036247
40	CEBPB	chr6:163067647-163067800	HepG2	liver:	n/a	chr6:163067696-163067707
41	CEBPB	chr6:163036133-163036384	Hela-S3	cervix:	n/a	chr6:163036237-163036246 chr6:163036237-163036246 chr6:163036235-163036248 chr6:163036235-163036248 chr6:163036237-163036246 chr6:163036236-163036247
42	CEBPB	chr6:162857291-162857590	HepG2	liver:	n/a	chr6:162857420-162857431
43	CEBPB	chr6:163036076-163036363	H1-hESC	embryonic stem cell:	n/a	chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036235-163036248 chr6:163036235-163036248 chr6:163036237-163036246 chr6:163036116-163036129 chr6:163036236-163036247
44	CEBPB	chr6:162943679-162943865	HepG2	liver:	n/a	n/a
45	CEBPB	chr6:162910422-162910805	HepG2	liver:	n/a	n/a
46	CEBPB	chr6:162636016-162636253	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr6:162671584-162671889	IMR90	lung:	n/a	n/a
48	CEBPB	chr6:162779076-162779247	A549	lung:	n/a	chr6:162779118-162779129
49	CEBPB	chr6:162839236-162839248	A549	lung:	n/a	n/a
50	CEBPB	chr6:162939387-162939585	HepG2	liver:	n/a	chr6:162939453-162939464

(count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:162684526-162684576	GM12891	blood:	n/a
2	chr6:162831837-162831887	HRCEpiC	kidney:	n/a
3	chr6:162684526-162684576	GM12891	blood:	n/a
4	chr6:162831837-162831887	HRCEpiC	kidney:	n/a
5	chr6:162831837-162831887	GM12892	blood:	n/a
6	chr6:162865258-162865308	HCF	heart:	n/a
7	chr6:162864586-162864636	A549	lung:	n/a
8	chr6:162683857-162683907	NH-A	brain:	n/a
9	chr6:163024624-163024674	HRCEpiC	kidney:	n/a
10	chr6:162865258-162865308	MCF10A-Er-Src	breast:	n/a
11	chr6:162683857-162683907	K562	blood:	n/a
12	chr6:162964378-162964428	K562	blood:	n/a
13	chr6:162831837-162831887	PFSK-1	brain:	n/a
14	chr6:162864586-162864636	SK-N-SH_RA	brain:	n/a
15	chr6:163110854-163110904	AG10803	skin:	n/a
16	chr6:162863505-162863555	IMR90	lung:	fetal
17	chr6:162683857-162683907	AG04449	skin:	fetal
18	chr6:162831837-162831887	SKMC	muscle:	n/a
19	chr6:163024624-163024674	GM06990	blood:	n/a
20	chr6:162684441-162684491	GM12878	blood:	n/a
21	chr6:162865171-162865221	HPAEpiC	pulmonary alveolar:	n/a
22	chr6:162684441-162684491	K562	blood:	n/a
23	chr6:162683881-162683931	HUVEC	blood vessel:	n/a
24	chr6:162684526-162684576	K562	blood:	n/a
25	chr6:162683857-162683907	HUVEC	blood vessel:	n/a
26	chr6:162865171-162865221	H1-hESC	embryonic stem cell:	embryo
27	chr6:162831837-162831887	HCPEpiC	choroid plexus:	n/a
28	chr6:163024624-163024674	NT2-D1	testis:	n/a
29	chr6:162683961-162684011	LNCaP	prostate:	n/a
30	chr6:162864586-162864636	SK-N-SH	brain:	n/a
31	chr6:162684526-162684576	SKMC	muscle:	n/a
32	chr6:162683881-162683931	HIPEpiC	eye:	n/a
33	chr6:162683881-162683931	SKMC	muscle:	n/a
34	chr6:162684526-162684576	MCF10A-Er-Src	breast:	n/a
35	chr6:162863505-162863555	SK-N-SH_RA	brain:	n/a
36	chr6:162865171-162865221	HUVEC	blood vessel:	n/a
37	chr6:162683881-162683931	AG04449	skin:	fetal
38	chr6:163110854-163110904	HCF	heart:	n/a
39	chr6:162864586-162864636	BJ	skin:	n/a
40	chr6:162964378-162964428	GM12892	blood:	n/a
41	chr6:162865171-162865221	ProgFib	skin:	n/a
42	chr6:162683961-162684011	HEK293	kidney:	embryo
43	chr6:162831837-162831887	SK-N-SH_RA	brain:	n/a
44	chr6:162684441-162684491	Jurkat	blood:	n/a
45	chr6:162684441-162684491	HCM	heart:	n/a
46	chr6:163024624-163024674	GM19239	blood:	n/a
47	chr6:162864586-162864636	HUVEC	blood vessel:	n/a
48	chr6:162863505-162863555	NT2-D1	testis:	n/a
49	chr6:162865258-162865308	H1-hESC	embryonic stem cell:	embryo
50	chr6:162964378-162964428	MCF10A-Er-Src	breast:	n/a

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:163103043..163104996-chr6:163109382..163111025,2	K562	blood:
2	chr6:162960178..162962006-chr6:162962880..162965078,2	K562	blood:
3	chr6:162721411..162723925-chr6:162726328..162729326,2	K562	blood:
4	chr6:162902802..162905070-chr6:162905406..162907332,2	K562	blood:
5	chr6:163103043..163104996-chr6:163109382..163111025,2	K562	blood:
6	chr6:163111769..163114753-chr6:163116374..163118174,2	K562	blood:
7	chr6:163100762..163102270-chr6:163108804..163111519,2	K562	blood:
8	chr6:162902802..162905070-chr6:162905406..162907332,2	K562	blood:
9	chr6:162613600..162615384-chr6:162617227..162618872,2	K562	blood:
10	chr6:162671180..162673472-chr6:162808694..162811227,2	K562	blood:
11	chr6:162620407..162622935-chr6:162623040..162625617,2	K562	blood:
12	chr6:163111769..163114753-chr6:163116374..163118174,2	K562	blood:
13	chr6:162763017..162765353-chr6:162767098..162769301,2	K562	blood:
14	chr6:162863816..162864618-chr6:163271757..163272511,2	MCF-7	breast:
15	chr6:163002877..163005708-chr6:163021910..163024946,3	K562	blood:
16	chr6:162643217..162645721-chr6:162646719..162648950,2	K562	blood:
17	chr6:162666890..162668464-chr6:162670216..162671922,2	K562	blood:
18	chr6:163117200..163118947-chr6:163123211..163125034,2	K562	blood:
19	chr6:163002877..163005708-chr6:163021910..163024946,3	K562	blood:
20	chr6:162661286..162663139-chr6:162673530..162675376,2	K562	blood:
21	chr6:162960178..162962006-chr6:162962880..162965078,2	K562	blood:
22	chr6:162768506..162770213-chr6:162786241..162788330,2	K562	blood:
23	chr6:162661286..162663139-chr6:162673530..162675376,2	K562	blood:
24	chr6:162666890..162668464-chr6:162670216..162671922,2	K562	blood:
25	chr6:162643217..162645721-chr6:162646719..162648950,2	K562	blood:
26	chr6:163080104..163081787-chr6:163082227..163083951,2	K562	blood:
27	chr6:162863367..162864320-chr6:163157771..163158572,4	MCF-7	breast:
28	chr6:162799485..162803733-chr6:162804296..162807777,5	K562	blood:
29	chr6:162799485..162803733-chr6:162804296..162807777,5	K562	blood:
30	chr6:163100762..163102270-chr6:163108804..163111519,2	K562	blood:
31	chr6:162820265..162823089-chr6:162827852..162829559,2	K562	blood:
32	chr6:162721411..162723925-chr6:162726328..162729326,2	K562	blood:
33	chr6:162613600..162615384-chr6:162617227..162618872,2	K562	blood:
34	chr6:163077595..163080176-chr6:163085064..163087575,2	K562	blood:
35	chr6:163077595..163080176-chr6:163085064..163087575,2	K562	blood:
36	chr6:162768506..162770213-chr6:162786241..162788330,2	K562	blood:
37	chr6:162820265..162823089-chr6:162827852..162829559,2	K562	blood:
38	chr6:163080104..163081787-chr6:163082227..163083951,2	K562	blood:
39	chr6:162671180..162673472-chr6:162808694..162811227,2	K562	blood:
40	chr6:162763017..162765353-chr6:162767098..162769301,2	K562	blood:
41	chr6:162620407..162622935-chr6:162623040..162625617,2	K562	blood:

No data

Variant related genes	Relation type
KRT8P44	TF binding region
KRT8P44	CpG island

Extended variants
information (count: 20854 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:20854 , 50 per page) page: 1 2 3 4 5 6 7 ... 418

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs147826497	chr6:162611342-162611343	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs555532139	chr6:162611413-162611414	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs115794244	chr6:162611425-162611426	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs573539191	chr6:162611429-162611430	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs533768736	chr6:162611449-162611450	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs529750268	chr6:162611510-162611511	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs113668168	chr6:162611520-162611521	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs375335066	chr6:162611546-162611547	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs566595321	chr6:162611549-162611550	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs113489750	chr6:162611555-162611556	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs140190325	chr6:162611559-162611560	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs187486205	chr6:162611562-162611563	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs73594248	chr6:162611569-162611570	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs537638460	chr6:162611579-162611580	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs192153369	chr6:162611591-162611592	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs143936446	chr6:162611635-162611636	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs115162651	chr6:162611659-162611660	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs552920622	chr6:162611719-162611720	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs573015543	chr6:162611751-162611752	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs184232336	chr6:162611753-162611754	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs144828403	chr6:162611754-162611755	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs575835337	chr6:162611767-162611768	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs367934980	chr6:162611772-162611773	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs544464019	chr6:162611809-162611810	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs75215200	chr6:162611813-162611814	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs118183748	chr6:162611817-162611818	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs540250343	chr6:162611876-162611877	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs560151621	chr6:162611879-162611880	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs9347599	chr6:162611892-162611893	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs117175592	chr6:162611937-162611938	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs368262207	chr6:162611993-162611994	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs545400936	chr6:162611997-162611998	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs386708036	chr6:162612002-162612003	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs9355988	chr6:162612003-162612004	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs531567486	chr6:162612024-162612025	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs531013227	chr6:162612044-162612045	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs9365383	chr6:162612073-162612074	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs114312450	chr6:162612089-162612090	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs549257585	chr6:162612097-162612098	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs58841741	chr6:162612107-162612108	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs7764353	chr6:162612119-162612120	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs148520925	chr6:162612133-162612134	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs538648436	chr6:162612134-162612135	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs372649620	chr6:162612136-162612137	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs575629210	chr6:162612174-162612175	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs142789089	chr6:162612175-162612176	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs151066149	chr6:162612198-162612199	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs116325789	chr6:162612202-162612203	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs540885646	chr6:162612222-162612223	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs560761939	chr6:162612223-162612224	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

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
Cancer	20164920	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	20838587	CNVD
Early-onset parkinson disease	21993715	CNVD
Glioblastoma	18772890	CNVD
Pancreatic cancer	20981101	CNVD
Autism	21360662	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Intellectual disability	22102821	CNVD
Parkinson disease	0	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21720365	CNVD
Parkinson disease	21829596	CNVD
Schizophrenia	20967226	CNVD
Schizophrenia	21346763	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Attention deficit hyperactivity disorder	19546859	CNVD
Autism	22495309	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian cancer	22355333	CNVD
Schizophrenia	19805367	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:1644 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:162605800-162624200	Weak transcription	Pancreas	Pancrea
2	chr6:162609600-162612000	Weak transcription	Right Atrium	heart
3	chr6:162609600-162622000	Weak transcription	Left Ventricle	heart
4	chr6:162609600-162622400	Weak transcription	Psoas Muscle	Psoas
5	chr6:162610800-162612400	Enhancers	Fetal Heart	heart
6	chr6:162612000-162613000	Enhancers	Right Atrium	heart
7	chr6:162612400-162615800	Weak transcription	Fetal Heart	heart
8	chr6:162613000-162621600	Weak transcription	Spleen	Spleen
9	chr6:162613000-162622000	Weak transcription	Right Atrium	heart
10	chr6:162615800-162617200	Enhancers	Fetal Heart	heart
11	chr6:162616200-162616400	Weak transcription	Aorta	Aorta
12	chr6:162616200-162617200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr6:162617200-162621800	Weak transcription	Fetal Heart	heart
14	chr6:162618800-162619200	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr6:162619000-162619400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr6:162619000-162619400	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr6:162619200-162622000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr6:162619800-162620000	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr6:162620600-162620800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr6:162620800-162621400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr6:162620800-162623000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr6:162620800-162623000	Enhancers	Adipose Nuclei	Adipose
23	chr6:162621000-162622800	Enhancers	Skeletal Muscle Female	skeletal muscle
24	chr6:162621200-162622200	Enhancers	Skeletal Muscle Male	skeletal muscle
25	chr6:162621600-162622000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr6:162621600-162622400	Enhancers	Fetal Stomach	stomach
27	chr6:162621800-162622200	Enhancers	Fetal Kidney	kidney
28	chr6:162621800-162623000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr6:162621800-162623000	Enhancers	Fetal Heart	heart
30	chr6:162622000-162622200	Enhancers	Right Ventricle	heart
31	chr6:162622000-162622400	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr6:162622000-162622400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr6:162622000-162622400	Enhancers	Cortex derived primary cultured neurospheres	brain
34	chr6:162622000-162622400	Enhancers	Fetal Brain Male	brain
35	chr6:162622000-162622400	Enhancers	Left Ventricle	heart
36	chr6:162622000-162622400	Enhancers	Rectal Smooth Muscle	rectum
37	chr6:162622000-162622400	Enhancers	Right Atrium	heart
38	chr6:162622000-162622400	Active TSS	Stomach Smooth Muscle	stomach
39	chr6:162622000-162622600	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr6:162622000-162623000	Enhancers	Colon Smooth Muscle	Colon
41	chr6:162622200-162622800	Weak transcription	Skeletal Muscle Male	skeletal muscle
42	chr6:162622400-162622600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr6:162622400-162622800	Enhancers	Psoas Muscle	Psoas
44	chr6:162622400-162624200	Weak transcription	Cortex derived primary cultured neurospheres	brain
45	chr6:162622400-162624400	Weak transcription	Aorta	Aorta
46	chr6:162622400-162624400	Weak transcription	Fetal Stomach	stomach
47	chr6:162622400-162632000	Weak transcription	Left Ventricle	heart
48	chr6:162622400-162636000	Weak transcription	Right Atrium	heart
49	chr6:162622600-162623000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr6:162622800-162623000	Enhancers	Skeletal Muscle Male	skeletal muscle

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