Variant report

Variant	nsv834099
Chromosome Location	chr21:41076873-41206030
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1011)
CpG islands
(count:305)
Chromatin interactive
region (count:103)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1011 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr21:41087775-41088050	HepG2	liver:	n/a	n/a
2	ARID3A	chr21:41160290-41160508	K562	blood:	n/a	n/a
3	ARID3A	chr21:41087730-41088079	K562	blood:	n/a	n/a
4	ARID3A	chr21:41160360-41160603	HepG2	liver:	n/a	n/a
5	ATF1	chr21:41180803-41180907	K562	blood:	n/a	n/a
6	BACH1	chr21:41087881-41088094	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr21:41160279-41160720	HepG2	liver:	n/a	chr21:41160530-41160543 chr21:41160532-41160541 chr21:41160531-41160540 chr21:41160526-41160547
8	BHLHE40	chr21:41085895-41086147	K562	blood:	n/a	n/a
9	BHLHE40	chr21:41160253-41160679	K562	blood:	n/a	chr21:41160530-41160543 chr21:41160532-41160541 chr21:41160531-41160540 chr21:41160526-41160547
10	BRCA1	chr21:41195062-41195198	H1-hESC	embryonic stem cell:	n/a	n/a
11	BRCA1	chr21:41160429-41160440	HepG2	liver:	n/a	n/a
12	CCNT2	chr21:41160383-41160650	K562	blood:	n/a	n/a
13	CEBPB	chr21:41205781-41205890	K562	blood:	n/a	n/a
14	CEBPB	chr21:41080603-41080800	HepG2	liver:	n/a	n/a
15	CEBPB	chr21:41082240-41082537	A549	lung:	n/a	chr21:41082457-41082468
16	CEBPB	chr21:41167025-41167332	K562	blood:	n/a	chr21:41167166-41167177
17	CEBPB	chr21:41109305-41110101	MCF-7	breast:	n/a	n/a
18	CEBPB	chr21:41152923-41153354	IMR90	lung:	n/a	chr21:41153062-41153073 chr21:41153335-41153346
19	CEBPB	chr21:41160393-41160469	HepG2	liver:	n/a	n/a
20	CEBPB	chr21:41151921-41152189	IMR90	lung:	n/a	n/a
21	CEBPB	chr21:41109358-41110069	MCF-7	breast:	n/a	n/a
22	CEBPB	chr21:41152960-41153574	HepG2	liver:	n/a	chr21:41153353-41153364 chr21:41153062-41153073 chr21:41153335-41153346
23	CEBPB	chr21:41153273-41153491	A549	lung:	n/a	chr21:41153353-41153364 chr21:41153335-41153346
24	CEBPB	chr21:41082367-41082611	HepG2	liver:	n/a	chr21:41082457-41082468
25	CEBPB	chr21:41167080-41167349	HepG2	liver:	n/a	chr21:41167166-41167177
26	CEBPB	chr21:41205675-41206013	IMR90	lung:	n/a	n/a
27	CEBPB	chr21:41110633-41110673	HepG2	liver:	n/a	n/a
28	CHD1	chr21:41079191-41079193	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr21:41160412-41160523	HepG2	liver:	n/a	n/a
30	CTCF	chr21:41077900-41078050	HCPEpiC	choroid plexus:	n/a	n/a
31	CTCF	chr21:41098200-41098350	HEK293	kidney:	n/a	n/a
32	CTCF	chr21:41135300-41135450	MCF-7	breast:	n/a	n/a
33	CTCF	chr21:41087820-41087970	GM12865	blood:	n/a	chr21:41087909-41087925 chr21:41087908-41087926 chr21:41087910-41087923 chr21:41087903-41087924
34	CTCF	chr21:41077920-41078070	HA-sp	spinal cord:	n/a	n/a
35	CTCF	chr21:41160285-41160516	SK-N-SH_RA	brain:	n/a	chr21:41160400-41160418 chr21:41160402-41160423
36	CTCF	chr21:41087940-41088090	HFF-Myc	foreskin:	n/a	n/a
37	CTCF	chr21:41160340-41160490	HepG2	liver:	n/a	chr21:41160400-41160418 chr21:41160402-41160423
38	CTCF	chr21:41160340-41160490	SK-N-SH_RA	brain:	n/a	chr21:41160400-41160418 chr21:41160402-41160423
39	CTCF	chr21:41098109-41098386	IMR90	lung:	n/a	n/a
40	CTCF	chr21:41085080-41085230	SK-N-SH_RA	brain:	n/a	n/a
41	CTCF	chr21:41098194-41098345	ProgFib	skin:	n/a	n/a
42	CTCF	chr21:41098180-41098330	AG04449	skin:	n/a	n/a
43	CTCF	chr21:41078405-41078445	Lung_OC	lung:	n/a	n/a
44	CTCF	chr21:41160220-41160370	GM12866	blood:	n/a	n/a
45	CTCF	chr21:41087827-41088078	GM13977	blood:	n/a	chr21:41087909-41087925 chr21:41087908-41087926 chr21:41087910-41087923 chr21:41087903-41087924
46	CTCF	chr21:41160213-41160644	K562	blood:	n/a	chr21:41160400-41160418 chr21:41160402-41160423
47	CTCF	chr21:41160360-41160510	HRE	kidney:	n/a	chr21:41160400-41160418 chr21:41160402-41160423
48	CTCF	chr21:41084920-41085070	HAc	cerebellar:	n/a	n/a
49	CTCF	chr21:41098160-41098310	AoAF	blood vessel:	n/a	n/a
50	CTCF	chr21:41098013-41098473	MCF-7	breast:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:41170358-41170408	NHBE	bronchial:	n/a
2	chr21:41129855-41129905	AoSMC	blood vessel:	n/a
3	chr21:41173950-41174000	AG04449	skin:	fetal
4	chr21:41116522-41116572	BJ	skin:	n/a
5	chr21:41116522-41116572	HCPEpiC	choroid plexus:	n/a
6	chr21:41170358-41170408	BJ	skin:	n/a
7	chr21:41170358-41170408	MCF10A-Er-Src	breast:	n/a
8	chr21:41116522-41116572	GM12878	blood:	n/a
9	chr21:41129855-41129905	GM19239	blood:	n/a
10	chr21:41129855-41129905	NHDF-neo	bronchial:	n/a
11	chr21:41116522-41116572	SK-N-MC	brain:	n/a
12	chr21:41173950-41174000	PANC-1	pancreas:	n/a
13	chr21:41170358-41170408	A549	lung:	n/a
14	chr21:41117225-41117275	HAEpiC	amniotic membrane:	n/a
15	chr21:41129855-41129905	HEK293	kidney:	embryo
16	chr21:41117225-41117275	U87	brain:	n/a
17	chr21:41173950-41174000	HRE	kidney:	n/a
18	chr21:41117225-41117275	NHDF-neo	bronchial:	n/a
19	chr21:41117225-41117275	NH-A	brain:	n/a
20	chr21:41173950-41174000	HL-60	blood:	n/a
21	chr21:41173950-41174000	GM06990	blood:	n/a
22	chr21:41129855-41129905	MCF10A-Er-Src	breast:	n/a
23	chr21:41173950-41174000	SK-N-SH	brain:	n/a
24	chr21:41117225-41117275	IMR90	lung:	fetal
25	chr21:41129855-41129905	HCM	heart:	n/a
26	chr21:41116522-41116572	Jurkat	blood:	n/a
27	chr21:41116522-41116572	AG09319	gingival:	n/a
28	chr21:41117225-41117275	HL-60	blood:	n/a
29	chr21:41173950-41174000	NT2-D1	testis:	n/a
30	chr21:41129855-41129905	HEEpiC	esophagus:	n/a
31	chr21:41170358-41170408	HCF	heart:	n/a
32	chr21:41129855-41129905	Caco-2	colon:	n/a
33	chr21:41170358-41170408	NH-A	brain:	n/a
34	chr21:41173950-41174000	PrEC	prostate:	n/a
35	chr21:41170358-41170408	HAEpiC	amniotic membrane:	n/a
36	chr21:41116522-41116572	T-47D	breast:	n/a
37	chr21:41117225-41117275	SK-N-MC	brain:	n/a
38	chr21:41116522-41116572	ovcar-3	ovarian:	n/a
39	chr21:41170358-41170408	GM19239	blood:	n/a
40	chr21:41129855-41129905	CMK	blood:	n/a
41	chr21:41170358-41170408	Hepatocyte	liver:	n/a
42	chr21:41117225-41117275	HEK293	kidney:	embryo
43	chr21:41170358-41170408	HL-60	blood:	n/a
44	chr21:41173950-41174000	AG09309	skin:	n/a
45	chr21:41129855-41129905	AG04449	skin:	fetal
46	chr21:41116522-41116572	HCM	heart:	n/a
47	chr21:41129855-41129905	SK-N-MC	brain:	n/a
48	chr21:41116522-41116572	GM12891	blood:	n/a
49	chr21:41129855-41129905	BJ	skin:	n/a
50	chr21:41129855-41129905	GM12891	blood:	n/a

(count:103 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr21:41159969..41160584-chr21:41227809..41228464,2	MCF-7	breast:
2	chr21:41144717..41146805-chr21:41147192..41149848,2	MCF-7	breast:
3	chr21:41128004..41130584-chr21:41132045..41133967,2	K562	blood:
4	chr21:41108059..41110631-chr21:41112030..41114431,2	MCF-7	breast:
5	chr21:40888055..40890382-chr21:41107871..41110600,2	MCF-7	breast:
6	chr21:41182267..41183782-chr21:41185681..41187493,2	K562	blood:
7	chr21:41159877..41161605-chr21:41224829..41226757,2	MCF-7	breast:
8	chr20:52556347..52557088-chr21:41160097..41160766,2	MCF-7	breast:
9	chr21:41159989..41160905-chr21:41238798..41240091,5	MCF-7	breast:
10	chr21:40903746..40904291-chr21:41077595..41078460,2	MCF-7	breast:
11	chr21:41159761..41160935-chr21:41492511..41493448,9	MCF-7	breast:
12	chr21:41160014..41161121-chr21:41238636..41239761,13	MCF-7	breast:
13	chr21:41142349..41144750-chr21:41149538..41151762,2	MCF-7	breast:
14	chr21:41000433..41001034-chr21:41095112..41095627,2	MCF-7	breast:
15	chr21:40889881..40890913-chr21:41087416..41088456,10	K562	blood:
16	chr21:40951212..40954090-chr21:41083007..41085637,2	MCF-7	breast:
17	chr21:41180463..41183269-chr21:41209070..41212997,3	MCF-7	breast:
18	chr21:41164154..41166617-chr21:41178349..41181058,2	MCF-7	breast:
19	chr21:41085205..41088011-chr21:41112686..41115638,2	MCF-7	breast:
20	chr21:41161226..41165062-chr21:41165469..41170017,6	MCF-7	breast:
21	chr21:41159977..41160541-chr21:41415064..41415828,3	MCF-7	breast:
22	chr21:41159565..41161270-chr21:41282682..41284025,38	MCF-7	breast:
23	chr21:41115743..41118299-chr21:41125237..41128060,2	MCF-7	breast:
24	chr21:40889992..40890995-chr21:41087409..41088601,6	MCF-7	breast:
25	chr21:41082155..41084385-chr21:41086359..41088868,2	K562	blood:
26	chr21:41038787..41039328-chr21:41095472..41096012,2	MCF-7	breast:
27	chr21:41160054..41160775-chr21:41284759..41285609,3	MCF-7	breast:
28	chr21:41159985..41160557-chr21:41226622..41227128,2	MCF-7	breast:
29	chr21:41197122..41199779-chr21:41222569..41224970,2	MCF-7	breast:
30	chr21:41082155..41084385-chr21:41086359..41088868,2	K562	blood:
31	chr21:40895962..40896593-chr21:41095361..41096036,2	MCF-7	breast:
32	chr21:41160024..41160878-chr21:41233096..41233742,2	MCF-7	breast:
33	chr21:41159272..41160801-chr21:41162335..41164635,2	MCF-7	breast:
34	chr21:40890014..40890661-chr21:41083159..41083881,2	MCF-7	breast:
35	chr21:40889963..40891050-chr21:41077484..41078432,7	MCF-7	breast:
36	chr21:41162459..41164745-chr21:41169799..41171557,2	K562	blood:
37	chr21:41173962..41176069-chr21:41178013..41180055,3	MCF-7	breast:
38	chr21:41160070..41160863-chr21:41223917..41224517,2	MCF-7	breast:
39	chr21:41160001..41160898-chr21:41492571..41493083,2	K562	blood:
40	chr21:41159987..41160858-chr21:41490256..41491059,2	MCF-7	breast:
41	chr21:41159939..41160492-chr21:42441112..42441880,2	K562	blood:
42	chr21:41041438..41042040-chr21:41077540..41078289,2	MCF-7	breast:
43	chr21:41169026..41172002-chr21:41176222..41177881,2	MCF-7	breast:
44	chr21:40899345..40899885-chr21:41095454..41095987,2	MCF-7	breast:
45	chr21:40889947..40890880-chr21:41084564..41085517,6	MCF-7	breast:
46	chr21:41078662..41082504-chr21:41085801..41089448,3	MCF-7	breast:
47	chr21:41159990..41160890-chr21:41235008..41236199,4	MCF-7	breast:
48	chr21:41135857..41138503-chr21:41140415..41142272,2	MCF-7	breast:
49	chr21:41178535..41181156-chr21:41183661..41185952,2	MCF-7	breast:
50	chr21:41145481..41148000-chr21:41151829..41153726,2	MCF-7	breast:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-B3GALT5-1	chr21:41086098-41086146	NONHSAT082208
2	lnc-IGSF5-1	chr21:41101431-41102607	XLOC_013946
3	lnc-IGSF5-1	chr21:41101059-41101611	XLOC_013946
4	lnc-IGSF5-1	chr21:41099773-41099919	ENSG00000231713
5	lnc-B3GALT5-1	chr21:41097765-41098012	ENSG00000225330.1
6	lnc-IGSF5-1	chr21:41101060-41101611	ENSG00000231713
7	lnc-B3GALT5-1	chr21:41097822-41098012	XLOC_013945
8	lnc-IGSF5-1	chr21:41099773-41099919	XLOC_013946
9	lnc-B3GALT5-1	chr21:41097765-41098012	NONHSAT082208
10	lnc-IGSF5-1	chr21:41099682-41099919	XLOC_013946
11	lnc-B3GALT5-1	chr21:41094403-41094478	ENSG00000225330.1
12	lnc-IGSF5-1	chr21:41101060-41101186	XLOC_013946
13	lnc-B3GALT5-1	chr21:41098691-41098875	NONHSAT082208
14	lnc-B3GALT5-1	chr21:41098692-41098875	XLOC_013945

No data

Variant related genes	Relation type
ENSG00000231713	TF binding region
IGSF5	TF binding region
ENSG00000231713	CpG island
IGSF5	CpG island
ENSG00000184809	chromatin interactions
ENSG00000163636	chromatin interactions
ENSG00000231713	chromatin interactions
ENSG00000183067	chromatin interactions
ENSG00000183036	chromatin interactions
ENSG00000236352	chromatin interactions
ENSG00000180879	chromatin interactions

Extended variants
information (count: 5528 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:5528 , 50 per page) page: 1 2 3 4 5 6 7 ... 111

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8133930	chr21:41076994-41076995	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs187641074	chr21:41077008-41077009	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs539867910	chr21:41077048-41077049	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs546767552	chr21:41077062-41077063	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs566986904	chr21:41077063-41077064	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs191910568	chr21:41077078-41077079	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs78825587	chr21:41077101-41077102	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs575922578	chr21:41077183-41077184	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs200044707	chr21:41077184-41077185	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs571942385	chr21:41077192-41077193	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs114937194	chr21:41077206-41077207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs558433944	chr21:41077235-41077236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs8128755	chr21:41077248-41077249	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs540265096	chr21:41077267-41077268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs559978582	chr21:41077287-41077288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs573431330	chr21:41077335-41077336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs542336500	chr21:41077364-41077365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs562301766	chr21:41077370-41077371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs371602389	chr21:41077388-41077389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs551382265	chr21:41077490-41077491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs9976947	chr21:41077512-41077513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs543664226	chr21:41077527-41077528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs561698922	chr21:41077545-41077546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs75060250	chr21:41077581-41077582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs546997531	chr21:41077583-41077584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs115560722	chr21:41077590-41077591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs535913941	chr21:41077595-41077596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs183774740	chr21:41077628-41077629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs148180914	chr21:41077721-41077722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs538489342	chr21:41077755-41077756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs77698535	chr21:41077767-41077768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs59348631	chr21:41077770-41077771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs397946588	chr21:41077771-41077772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs62235478	chr21:41077773-41077774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs117699353	chr21:41077776-41077777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs578223577	chr21:41077808-41077809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs368086532	chr21:41077867-41077868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs141154901	chr21:41077971-41077972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs553700834	chr21:41078009-41078010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs150683854	chr21:41078048-41078049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs186631513	chr21:41078063-41078064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs190296648	chr21:41078183-41078184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs575821429	chr21:41078192-41078193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs73907335	chr21:41078257-41078258	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs565009084	chr21:41078262-41078263	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs527553072	chr21:41078325-41078326	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs536310604	chr21:41078328-41078329	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs552489090	chr21:41078329-41078330	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs547388605	chr21:41078356-41078357	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs11088492	chr21:41078367-41078368	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:72)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Down syndrome	17412756	CNVD
Down syndrome	17576883	CNVD
Acute promyelocytic leukemia	19109227	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Renal cell carcinoma	19461508	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Prostate cancer	19156837	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
lymphocytic leukemia	21291569	CNVD
Melanoma	18172304	CNVD
Autism	22958593	CNVD
Schizophrenia	22958593	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Wilms tumour	21544195	CNVD
Ewing''s sarcoma	17952124	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute myeloid leukemia	16864856	CNVD
Mental retardation	21031080	CNVD
Polymicrogyria	21031080	CNVD
periventricular nodular heterotopia	21031080	CNVD
Myelodysplastic syndrome	21606161	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Autism	18414403	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21858162	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17899364	CNVD
Down syndrome	20877625	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Prostate cancer	21147910	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Prostate cancer	17245344	CNVD
Prostate cancer	20473283	CNVD
Chordoma	18071362	CNVD
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Cancer	20164919	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:407 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:41064800-41078600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
2	chr21:41069000-41095000	Weak transcription	Pancreas	Pancrea
3	chr21:41071800-41078200	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr21:41072800-41078400	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr21:41075200-41077200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
6	chr21:41075800-41101800	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr21:41076000-41078200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr21:41076000-41078600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr21:41076600-41077000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr21:41076600-41077000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr21:41076800-41078400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr21:41077000-41078600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr21:41077000-41078600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr21:41077400-41078200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
15	chr21:41078200-41078400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
16	chr21:41078200-41078600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
17	chr21:41078200-41078600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
18	chr21:41078400-41081000	Enhancers	H1 Cell Line	embryonic stem cell
19	chr21:41078400-41081000	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr21:41078400-41081200	Enhancers	H9 Cell Line	embryonic stem cell
21	chr21:41078600-41078800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr21:41078600-41079000	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr21:41078600-41079000	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr21:41078600-41079200	Enhancers	Stomach Mucosa	stomach
25	chr21:41078600-41079400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr21:41078600-41079600	Enhancers	Fetal Intestine Large	intestine
27	chr21:41078600-41079600	Enhancers	Fetal Intestine Small	intestine
28	chr21:41078600-41079800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr21:41078600-41080400	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr21:41078600-41080800	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr21:41078600-41080800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr21:41078600-41081200	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr21:41078600-41081200	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr21:41078800-41079200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr21:41078800-41084200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr21:41079000-41079200	Enhancers	Duodenum Mucosa	Duodenum
37	chr21:41079000-41079400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
38	chr21:41079000-41079400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
39	chr21:41079200-41080400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr21:41079400-41081400	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr21:41079400-41081400	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr21:41079400-41109600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr21:41079600-41082000	Weak transcription	Fetal Intestine Large	intestine
44	chr21:41079600-41087400	Weak transcription	Fetal Intestine Small	intestine
45	chr21:41080600-41080800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr21:41081200-41088000	Weak transcription	H9 Cell Line	embryonic stem cell
47	chr21:41081400-41083600	Enhancers	Placenta	Placenta
48	chr21:41081400-41087400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
49	chr21:41081400-41088000	Weak transcription	HUES6 Cell Line	embryonic stem cell
50	chr21:41082000-41082200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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