Variant report

Variant	nsv1022618
Chromosome Location	chr6:86465365-87432069
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2472)
CpG islands
(count:489)
Chromatin interactive
region (count:65)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2472 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:86965769-86966016	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:87392792-87393956	K562	blood:	n/a	n/a
3	ARID3A	chr6:86466649-86467010	K562	blood:	n/a	n/a
4	ARID3A	chr6:87394843-87395342	K562	blood:	n/a	n/a
5	ARID3A	chr6:86466750-86467021	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:86632675-86632979	HepG2	liver:	n/a	n/a
7	ATF1	chr6:87394954-87395205	K562	blood:	n/a	n/a
8	ATF1	chr6:86919119-86919208	K562	blood:	n/a	n/a
9	ATF1	chr6:87392891-87393627	K562	blood:	n/a	n/a
10	ATF1	chr6:87410117-87410320	K562	blood:	n/a	n/a
11	ATF3	chr6:86901866-86902226	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr6:86901939-86902219	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr6:86576041-86576233	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr6:86901914-86902069	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr6:86898846-86898863	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr6:87347416-87347417	K562	blood:	n/a	n/a
17	BACH1	chr6:87187567-87187831	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr6:86578018-86578101	K562	blood:	n/a	n/a
19	BCL11A	chr6:87198812-87199065	H1-hESC	embryonic stem cell:	n/a	n/a
20	BDP1	chr6:86552462-86552680	Hela-S3	cervix:	n/a	n/a
21	BHLHE40	chr6:86901978-86902056	GM12878	blood:	n/a	n/a
22	BHLHE40	chr6:87225876-87226119	GM12878	blood:	n/a	chr6:87225988-87226001 chr6:87225984-87226005 chr6:87225990-87225999 chr6:87225989-87225998 chr6:87225990-87225999 chr6:87225991-87226000
23	BHLHE40	chr6:87394959-87395310	K562	blood:	n/a	n/a
24	BHLHE40	chr6:87392836-87393518	K562	blood:	n/a	n/a
25	BHLHE40	chr6:86700819-86701140	GM12878	blood:	n/a	n/a
26	BHLHE40	chr6:86685736-86685780	GM12878	blood:	n/a	n/a
27	BRCA1	chr6:86779162-86779163	HepG2	liver:	n/a	n/a
28	BRCA1	chr6:87368528-87368609	Hela-S3	cervix:	n/a	n/a
29	BRF1	chr6:86552462-86552681	Hela-S3	cervix:	n/a	n/a
30	CBX3	chr6:87382089-87382437	K562	blood:	n/a	n/a
31	CBX3	chr6:86538698-86539019	K562	blood:	n/a	n/a
32	CBX3	chr6:87302409-87302725	K562	blood:	n/a	n/a
33	CBX3	chr6:87382079-87382469	K562	blood:	n/a	n/a
34	CBX3	chr6:86538752-86539012	K562	blood:	n/a	n/a
35	CBX3	chr6:87392924-87393577	K562	blood:	n/a	n/a
36	CBX3	chr6:87392934-87393686	K562	blood:	n/a	n/a
37	CCNT2	chr6:87392719-87393684	K562	blood:	n/a	n/a
38	CCNT2	chr6:87242777-87242902	K562	blood:	n/a	n/a
39	CCNT2	chr6:86922703-86922903	K562	blood:	n/a	n/a
40	CEBPB	chr6:87425344-87425752	ECC-1	luminal epithelium:	n/a	n/a
41	CEBPB	chr6:87173887-87173910	K562	blood:	n/a	chr6:87173895-87173906 chr6:87173894-87173907
42	CEBPB	chr6:87431910-87432114	A549	lung:	n/a	n/a
43	CEBPB	chr6:87209815-87210240	MCF-7	breast:	n/a	chr6:87210019-87210030
44	CEBPB	chr6:87244691-87244981	K562	blood:	n/a	chr6:87244814-87244825
45	CEBPB	chr6:87245887-87246207	IMR90	lung:	n/a	chr6:87246039-87246050
46	CEBPB	chr6:87296212-87296438	K562	blood:	n/a	chr6:87296422-87296433 chr6:87296299-87296310 chr6:87296301-87296310
47	CEBPB	chr6:87295698-87295900	HepG2	liver:	n/a	chr6:87295821-87295832 chr6:87295821-87295834 chr6:87295821-87295834 chr6:87295823-87295834
48	CEBPB	chr6:87245888-87246198	K562	blood:	n/a	chr6:87246039-87246050
49	CEBPB	chr6:87425232-87425884	MCF-7	breast:	n/a	n/a
50	CEBPB	chr6:86646714-86646969	Hela-S3	cervix:	n/a	chr6:86646818-86646827 chr6:86646817-86646828

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:87041914-87041964	SK-N-SH	brain:	n/a
2	chr6:87041914-87041964	SK-N-SH	brain:	n/a
3	chr6:87380615-87380665	RPTEC	kidney:	n/a
4	chr6:86548232-86548282	SK-N-SH_RA	brain:	n/a
5	chr6:86548232-86548282	HIPEpiC	eye:	n/a
6	chr6:87041914-87041964	HIPEpiC	eye:	n/a
7	chr6:87380615-87380665	PrEC	prostate:	n/a
8	chr6:87041914-87041964	A549	lung:	n/a
9	chr6:86862059-86862109	HCM	heart:	n/a
10	chr6:87222174-87222224	U87	brain:	n/a
11	chr6:86547801-86547851	AG09319	gingival:	n/a
12	chr6:87196595-87196645	U87	brain:	n/a
13	chr6:86862059-86862109	AG10803	skin:	n/a
14	chr6:86547801-86547851	AoSMC	blood vessel:	n/a
15	chr6:87380615-87380665	ECC-1	luminal epithelium:	n/a
16	chr6:86548232-86548282	HAEpiC	amniotic membrane:	n/a
17	chr6:87196595-87196645	HL-60	blood:	n/a
18	chr6:87196595-87196645	HAEpiC	amniotic membrane:	n/a
19	chr6:86547801-86547851	AG09309	skin:	n/a
20	chr6:86862059-86862109	PANC-1	pancreas:	n/a
21	chr6:86862059-86862109	HIPEpiC	eye:	n/a
22	chr6:86547801-86547851	ECC-1	luminal epithelium:	n/a
23	chr6:86548232-86548282	HPAEpiC	pulmonary alveolar:	n/a
24	chr6:87222174-87222224	T-47D	breast:	n/a
25	chr6:87196595-87196645	Hepatocyte	liver:	n/a
26	chr6:86547801-86547851	HRPEpiC	eye:	n/a
27	chr6:86548232-86548282	U87	brain:	n/a
28	chr6:87041914-87041964	AG09319	gingival:	n/a
29	chr6:87380671-87380721	RPTEC	kidney:	n/a
30	chr6:87041914-87041964	SK-N-MC	brain:	n/a
31	chr6:87380615-87380665	GM12892	blood:	n/a
32	chr6:87196595-87196645	HEEpiC	esophagus:	n/a
33	chr6:87380671-87380721	HRE	kidney:	n/a
34	chr6:86862059-86862109	BE2_C	brain:	n/a
35	chr6:87222174-87222224	HCPEpiC	choroid plexus:	n/a
36	chr6:86548232-86548282	AG04450	lung:	fetal
37	chr6:87380615-87380665	NT2-D1	testis:	n/a
38	chr6:87041914-87041964	RPTEC	kidney:	n/a
39	chr6:87222174-87222224	ECC-1	luminal epithelium:	n/a
40	chr6:86548232-86548282	AG04449	skin:	fetal
41	chr6:87196595-87196645	HIPEpiC	eye:	n/a
42	chr6:87222174-87222224	BJ	skin:	n/a
43	chr6:87041914-87041964	SK-N-SH_RA	brain:	n/a
44	chr6:87041914-87041964	HPAEpiC	pulmonary alveolar:	n/a
45	chr6:87380615-87380665	Hela-S3	cervix:	n/a
46	chr6:87380615-87380665	HCF	heart:	n/a
47	chr6:86548232-86548282	T-47D	breast:	n/a
48	chr6:86548232-86548282	AG09309	skin:	n/a
49	chr6:86862059-86862109	T-47D	breast:	n/a
50	chr6:87380615-87380665	SK-N-MC	brain:	n/a

(count:65 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:86679171..86681936-chr6:86686395..86689125,2	K562	blood:
2	chr6:86632367..86633291-chr6:86884579..86885474,2	MCF-7	breast:
3	chr6:86722649..86724742-chr6:86768609..86770800,2	MCF-7	breast:
4	chr6:86463941..86466706-chr6:87565460..87567312,2	MCF-7	breast:
5	chr6:87317696..87319542-chr6:87392510..87394797,2	K562	blood:
6	chr2:199112345..199112956-chr6:87088425..87089218,2	MCF-7	breast:
7	chr6:86632253..86632927-chr6:87646756..87647373,2	K562	blood:
8	chr6:87423786..87425445-chr6:87431347..87433792,2	MCF-7	breast:
9	chr6:86741107..86743196-chr6:86766246..86768757,2	MCF-7	breast:
10	chr6:87314634..87318988-chr6:87322106..87325054,3	K562	blood:
11	chr6:87317696..87319542-chr6:87392510..87394797,2	K562	blood:
12	chr6:86352318..86354176-chr6:87391935..87394056,2	K562	blood:
13	chr6:87137565..87139106-chr6:87140631..87142698,2	K562	blood:
14	chr6:86632071..86633265-chr6:86884594..86886454,5	MCF-7	breast:
15	chr6:87059757..87062290-chr6:87067357..87069140,2	K562	blood:
16	chr6:86389006..86390560-chr6:86474592..86476523,2	K562	blood:
17	chr6:87045137..87047941-chr6:87049643..87052368,2	K562	blood:
18	chr6:86350073..86353077-chr6:86464784..86467330,3	MCF-7	breast:
19	chr6:87225517..87227389-chr6:87237269..87238777,2	K562	blood:
20	chr6:87137847..87140371-chr6:87144269..87146494,2	K562	blood:
21	chr6:87343553..87345245-chr6:87346173..87348745,2	K562	blood:
22	chr6:87121819..87123929-chr6:87125096..87127462,2	MCF-7	breast:
23	chr6:87321780..87323458-chr6:87325338..87327123,2	K562	blood:
24	chr6:86351778..86354255-chr6:86511973..86513723,2	MCF-7	breast:
25	chr6:87423786..87425445-chr6:87431347..87433792,2	MCF-7	breast:
26	chr6:86386226..86389765-chr6:86463703..86468308,5	MCF-7	breast:
27	chr6:86632071..86633265-chr6:86884594..86886454,5	MCF-7	breast:
28	chr6:87313812..87315954-chr6:87317958..87322098,3	K562	blood:
29	chr6:86741107..86743196-chr6:86766246..86768757,2	MCF-7	breast:
30	chr6:87322046..87324306-chr6:87330179..87333097,2	K562	blood:
31	chr6:86501351..86504380-chr6:86507013..86510023,3	K562	blood:
32	chr6:87424582..87427120-chr6:87432105..87434756,2	MCF-7	breast:
33	chr6:86466808..86467382-chr6:87646548..87647385,2	K562	blood:
34	chr6:87300183..87302534-chr6:87323211..87326101,2	K562	blood:
35	chr6:86897792..86900051-chr6:86901438..86903650,2	K562	blood:
36	chr6:86387031..86390064-chr6:86464060..86466977,4	MCF-7	breast:
37	chr6:87225517..87227389-chr6:87237269..87238777,2	K562	blood:
38	chr6:86679171..86681936-chr6:86686395..86689125,2	K562	blood:
39	chr6:86386556..86388965-chr6:87417224..87418892,2	MCF-7	breast:
40	chr10:3371371..3371930-chr6:86798182..86798788,2	MCF-7	breast:
41	chr6:87059757..87062290-chr6:87067357..87069140,2	K562	blood:
42	chr6:86657984..86660030-chr6:86660418..86662554,2	MCF-7	breast:
43	chr6:87313812..87315954-chr6:87317958..87322098,3	K562	blood:
44	chr6:87045137..87047941-chr6:87049643..87052368,2	K562	blood:
45	chr6:87321780..87323458-chr6:87325338..87327123,2	K562	blood:
46	chr6:87322046..87324306-chr6:87330179..87333097,2	K562	blood:
47	chr6:86722649..86724742-chr6:86768609..86770800,2	MCF-7	breast:
48	chr6:86534169..86534685-chr6:86574198..86574815,2	MCF-7	breast:
49	chr6:86597171..86598674-chr6:86601290..86603346,2	K562	blood:
50	chr6:87300183..87302534-chr6:87323211..87326101,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NT5E-8	chr6:86578671-86579182	NONHSAT113874
2	lnc-NT5E-7	chr6:86565538-86565836	NONHSAT113873
3	lnc-HTR1E-3	chr6:87145570-87145854	NONHSAT113881
4	lnc-FAM165A-2	chr6:86482026-86482088	NONHSAT113871
5	lnc-NT5E-7	chr6:86571835-86571903	NONHSAT113873
6	lnc-HTR1E-4	chr6:87141962-87142387	NONHSAT113880
7	lnc-FAM165A-3	chr6:86880165-86880736	NONHSAT113876

No data

Variant related genes	Relation type
ENSG00000217272	TF binding region
ENSG00000200427	TF binding region
ENSG00000221101	TF binding region
NDUFA5P9	TF binding region
RPL7P27	TF binding region
ENSG00000219500	TF binding region
ENSG00000218766	TF binding region
RNU4-12P	TF binding region
RN7SL643P	TF binding region
ENSG00000217272	CpG island
ENSG00000200427	CpG island
ENSG00000221101	CpG island
NDUFA5P9	CpG island
RPL7P27	CpG island
ENSG00000219500	CpG island
ENSG00000218766	CpG island
RNU4-12P	CpG island
RN7SL643P	CpG island
ENSG00000243124	chromatin interactions
ENSG00000135316	chromatin interactions
ENSG00000219500	chromatin interactions
ENSG00000203875	chromatin interactions
ENSG00000168830	chromatin interactions

Extended variants
information (count: 22205 )
Associated
traits (count: 111 )

Variant overlapped rSNPs/rCNVs (count:22205 , 50 per page) page: 1 2 3 4 5 6 7 ... 445

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556151000	chr6:86465365-86465366	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs551813222	chr6:86465370-86465371	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs186307437	chr6:86465385-86465386	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs538704062	chr6:86465403-86465404	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs368881323	chr6:86465435-86465436	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs73487447	chr6:86465441-86465442	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs368151759	chr6:86465447-86465448	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs149916419	chr6:86465478-86465479	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs543255356	chr6:86465528-86465529	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs189957806	chr6:86465551-86465552	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs75717544	chr6:86465553-86465554	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs543433455	chr6:86465626-86465627	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs565246778	chr6:86465662-86465663	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs532390985	chr6:86465701-86465702	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs547436444	chr6:86465702-86465703	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs146450656	chr6:86465752-86465753	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs527473915	chr6:86465756-86465757	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs548098496	chr6:86465759-86465760	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs568327261	chr6:86465782-86465783	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs181353334	chr6:86465814-86465815	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs200764100	chr6:86465827-86465828	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs140810685	chr6:86465840-86465841	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs570896045	chr6:86465847-86465848	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs144563655	chr6:86465877-86465878	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs569248091	chr6:86465892-86465893	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs539846616	chr6:86465940-86465941	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs34014430	chr6:86465986-86465987	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs139024962	chr6:86465992-86465993	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs186839171	chr6:86466032-86466033	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs116353236	chr6:86466049-86466050	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs548288944	chr6:86466050-86466051	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs34678410	chr6:86466107-86466108	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs374581838	chr6:86466122-86466123	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs9450320	chr6:86466139-86466140	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs112497482	chr6:86466167-86466168	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs190679331	chr6:86466168-86466169	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs544064108	chr6:86466183-86466184	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs576629532	chr6:86466220-86466221	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs565440986	chr6:86466254-86466255	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs576783506	chr6:86466292-86466293	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs7758708	chr6:86466331-86466332	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs181911567	chr6:86466343-86466344	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs530161729	chr6:86466394-86466395	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs542441682	chr6:86466404-86466405	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs542396315	chr6:86466498-86466499	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs561103658	chr6:86466550-86466551	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs186560320	chr6:86466568-86466569	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs555712767	chr6:86466681-86466682	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs1335442	chr6:86466692-86466693	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs571575058	chr6:86466743-86466744	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:111)

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
Endometrioid adenocarcinoma	16974079	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
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	17443227	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
Prostate cancer	16573809	CNVD
Breast cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Follicular lymphoma	17699855	CNVD
Breast cancer	17133270	CNVD
Leukemia	18688285	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
Prostate cancer	16461572	CNVD
Mental retardation	21045960	CNVD
Obesity	21045960	CNVD
learning difficulties	21045960	CNVD
Prostate cancer	17245344	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Cancer	20164920	CNVD
Burkitt''s lymphoma	20823134	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
craniofacial dysmorphism	21918468	CNVD
Myelofibrosis	22110671	CNVD
Neurodevelopmental disorder	22521361	CNVD
abnormal development	18461090	CNVD
Myelodysplastic syndrome	18508791	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD
Schizophrenia	23813976	CNVD
Developmental delay	19490664	CNVD

Chromatin state (count:1023 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:86464800-86465600	Enhancers	Fetal Lung	lung
2	chr6:86473800-86475600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr6:86474000-86475200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr6:86474200-86475800	Enhancers	Ovary	ovary
5	chr6:86474400-86475600	Enhancers	Adipose Nuclei	Adipose
6	chr6:86474600-86475200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr6:86474600-86475200	Enhancers	Aorta	Aorta
8	chr6:86474600-86475200	Enhancers	HepG2	liver
9	chr6:86474800-86475200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr6:86475200-86478200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr6:86475200-86485600	Weak transcription	Aorta	Aorta
12	chr6:86481400-86481600	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr6:86481400-86482200	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr6:86481400-86482200	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr6:86481400-86482400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr6:86481600-86481800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
17	chr6:86481600-86482200	Enhancers	H1 Cell Line	embryonic stem cell
18	chr6:86481600-86482200	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr6:86481600-86482200	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr6:86481600-86482600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr6:86481800-86482000	Active TSS	iPS-20b Cell Line	embryonic stem cell
22	chr6:86481800-86482200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr6:86481800-86482400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr6:86481800-86482600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr6:86482200-86482600	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr6:86482600-86482800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr6:86485600-86486400	Enhancers	Aorta	Aorta
28	chr6:86505400-86505600	Enhancers	Psoas Muscle	Psoas
29	chr6:86505600-86506200	Enhancers	Brain Germinal Matrix	brain
30	chr6:86505600-86512000	Weak transcription	Psoas Muscle	Psoas
31	chr6:86507800-86508000	Enhancers	Brain Germinal Matrix	brain
32	chr6:86507800-86508400	Enhancers	Esophagus	oesophagus
33	chr6:86508000-86509400	Enhancers	Fetal Lung	lung
34	chr6:86508200-86508600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr6:86508400-86509200	Enhancers	Adipose Nuclei	Adipose
36	chr6:86512000-86512200	Enhancers	Psoas Muscle	Psoas
37	chr6:86513400-86513800	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr6:86517000-86517600	Weak transcription	Aorta	Aorta
39	chr6:86518000-86518200	ZNF genes & repeats	Aorta	Aorta
40	chr6:86525600-86526000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr6:86534400-86534800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr6:86537600-86537800	ZNF genes & repeats	Ovary	ovary
43	chr6:86537800-86550000	Weak transcription	Ovary	ovary
44	chr6:86546800-86556800	Weak transcription	Right Atrium	heart
45	chr6:86550000-86550400	ZNF genes & repeats	Ovary	ovary
46	chr6:86551400-86552800	Enhancers	Dnd41	blood
47	chr6:86552400-86552600	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
48	chr6:86552400-86552600	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr6:86552400-86552600	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr6:86552400-86552600	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived

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