Variant report

Variant	nsv1060151
Chromosome Location	chr21:16295713-16435497
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1479)
CpG islands
(count:305)
Chromatin interactive
region (count:175)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:1479 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr21:16432881-16433903	K562	blood:	n/a	n/a
2	ARID3A	chr21:16430227-16430555	K562	blood:	n/a	n/a
3	ARID3A	chr21:16429812-16430010	K562	blood:	n/a	n/a
4	ARID3A	chr21:16434127-16435157	K562	blood:	n/a	chr21:16434401-16434417 chr21:16434402-16434418
5	ARID3A	chr21:16315068-16315951	HepG2	liver:	n/a	n/a
6	ARID3A	chr21:16317602-16317884	HepG2	liver:	n/a	n/a
7	ARID3A	chr21:16431284-16431893	K562	blood:	n/a	n/a
8	BACH1	chr21:16336728-16336893	K562	blood:	n/a	n/a
9	BACH1	chr21:16337799-16337865	K562	blood:	n/a	n/a
10	BACH1	chr21:16412374-16412466	K562	blood:	n/a	n/a
11	BATF	chr21:16428937-16429245	GM12878	blood:	n/a	n/a
12	BATF	chr21:16424351-16424627	GM12878	blood:	n/a	chr21:16424493-16424504
13	BATF	chr21:16404307-16404523	GM12878	blood:	n/a	n/a
14	BATF	chr21:16424329-16424712	GM12878	blood:	n/a	chr21:16424493-16424504
15	BATF	chr21:16404278-16404597	GM12878	blood:	n/a	n/a
16	BATF	chr21:16317540-16317736	GM12878	blood:	n/a	n/a
17	BATF	chr21:16374109-16374409	GM12878	blood:	n/a	n/a
18	BATF	chr21:16374132-16374442	GM12878	blood:	n/a	n/a
19	BCL11A	chr21:16377785-16378065	H1-hESC	embryonic stem cell:	n/a	n/a
20	BCL3	chr21:16330386-16331728	A549	lung:	n/a	n/a
21	BCLAF1	chr21:16424054-16424998	GM12878	blood:	n/a	n/a
22	BHLHE40	chr21:16423436-16423685	GM12878	blood:	n/a	n/a
23	BHLHE40	chr21:16422838-16423174	HepG2	liver:	n/a	chr21:16422950-16422959 chr21:16422945-16422966 chr21:16422951-16422960 chr21:16422952-16422961 chr21:16422951-16422960 chr21:16422949-16422962
24	BHLHE40	chr21:16434968-16435218	GM12878	blood:	n/a	n/a
25	BHLHE40	chr21:16374139-16374809	GM12878	blood:	n/a	chr21:16374418-16374427 chr21:16374419-16374428 chr21:16374418-16374427
26	BHLHE40	chr21:16395346-16395398	GM12878	blood:	n/a	n/a
27	BHLHE40	chr21:16340688-16340736	GM12878	blood:	n/a	n/a
28	BRCA1	chr21:16368651-16368746	HepG2	liver:	n/a	n/a
29	CCNT2	chr21:16433097-16433493	K562	blood:	n/a	chr21:16433316-16433336 chr21:16433354-16433363
30	CCNT2	chr21:16434268-16434545	K562	blood:	n/a	n/a
31	CEBPB	chr21:16358048-16358061	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr21:16359529-16359806	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr21:16315313-16315687	HepG2	liver:	n/a	chr21:16315588-16315599
34	CEBPB	chr21:16295868-16296284	IMR90	lung:	n/a	n/a
35	CEBPB	chr21:16376977-16377246	A549	lung:	n/a	chr21:16377127-16377138 chr21:16377127-16377140 chr21:16377182-16377193
36	CEBPB	chr21:16334912-16335499	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr21:16416011-16416026	A549	lung:	n/a	n/a
38	CEBPB	chr21:16377081-16377292	HepG2	liver:	n/a	chr21:16377127-16377138 chr21:16377127-16377140 chr21:16377182-16377193
39	CEBPB	chr21:16334908-16335502	A549	lung:	n/a	n/a
40	CEBPB	chr21:16330204-16330549	IMR90	lung:	n/a	n/a
41	CEBPB	chr21:16347893-16348146	K562	blood:	n/a	n/a
42	CEBPB	chr21:16382261-16382655	IMR90	lung:	n/a	n/a
43	CEBPB	chr21:16334887-16335545	K562	blood:	n/a	n/a
44	CEBPB	chr21:16336788-16336989	A549	lung:	n/a	n/a
45	CEBPB	chr21:16409446-16409784	IMR90	lung:	n/a	n/a
46	CEBPB	chr21:16359485-16359785	HepG2	liver:	n/a	n/a
47	CEBPB	chr21:16346716-16346849	K562	blood:	n/a	n/a
48	CEBPB	chr21:16400157-16400369	HepG2	liver:	n/a	chr21:16400320-16400331 chr21:16400216-16400227
49	CEBPB	chr21:16336760-16336960	IMR90	lung:	n/a	n/a
50	CEBPB	chr21:16431734-16432078	IMR90	lung:	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	chr21:16340625-16340675	AoSMC	blood vessel:	n/a
2	chr21:16340722-16340772	HEK293	kidney:	embryo
3	chr21:16340625-16340675	HepG2	liver:	n/a
4	chr21:16340722-16340772	NB4	blood:	n/a
5	chr21:16434067-16434117	AG09309	skin:	n/a
6	chr21:16340625-16340675	HCM	heart:	n/a
7	chr21:16335810-16335860	HRPEpiC	eye:	n/a
8	chr21:16434067-16434117	AoSMC	blood vessel:	n/a
9	chr21:16434067-16434117	NHBE	bronchial:	n/a
10	chr21:16340722-16340772	SK-N-SH	brain:	n/a
11	chr21:16335810-16335860	MCF10A-Er-Src	breast:	n/a
12	chr21:16337172-16337222	HL-60	blood:	n/a
13	chr21:16337172-16337222	MCF-7	breast:	n/a
14	chr21:16340625-16340675	IMR90	lung:	fetal
15	chr21:16340722-16340772	Jurkat	blood:	n/a
16	chr21:16434067-16434117	AG04449	skin:	fetal
17	chr21:16434067-16434117	HCT-116	colon:	n/a
18	chr21:16337172-16337222	GM19239	blood:	n/a
19	chr21:16340625-16340675	HEK293	kidney:	embryo
20	chr21:16335810-16335860	AG09319	gingival:	n/a
21	chr21:16340722-16340772	ECC-1	luminal epithelium:	n/a
22	chr21:16340722-16340772	PFSK-1	brain:	n/a
23	chr21:16335810-16335860	Hepatocyte	liver:	n/a
24	chr21:16340722-16340772	U87	brain:	n/a
25	chr21:16340722-16340772	SAEC	small airway:	n/a
26	chr21:16434067-16434117	HCM	heart:	n/a
27	chr21:16340722-16340772	HRPEpiC	eye:	n/a
28	chr21:16337172-16337222	HRCEpiC	kidney:	n/a
29	chr21:16340625-16340675	GM12891	blood:	n/a
30	chr21:16434067-16434117	AG10803	skin:	n/a
31	chr21:16337172-16337222	Jurkat	blood:	n/a
32	chr21:16337172-16337222	BE2_C	brain:	n/a
33	chr21:16340722-16340772	GM06990	blood:	n/a
34	chr21:16434067-16434117	HRPEpiC	eye:	n/a
35	chr21:16434067-16434117	HPAEpiC	pulmonary alveolar:	n/a
36	chr21:16335810-16335860	SKMC	muscle:	n/a
37	chr21:16434067-16434117	Caco-2	colon:	n/a
38	chr21:16434067-16434117	GM12891	blood:	n/a
39	chr21:16340722-16340772	HNPCEpiC	eye:	n/a
40	chr21:16340722-16340772	MCF-7	breast:	n/a
41	chr21:16340722-16340772	HepG2	liver:	n/a
42	chr21:16340625-16340675	HMEC	breast:	n/a
43	chr21:16335810-16335860	GM12892	blood:	n/a
44	chr21:16340722-16340772	HPAEpiC	pulmonary alveolar:	n/a
45	chr21:16337172-16337222	AG09309	skin:	n/a
46	chr21:16337172-16337222	AoSMC	blood vessel:	n/a
47	chr21:16340625-16340675	U87	brain:	n/a
48	chr21:16340625-16340675	NH-A	brain:	n/a
49	chr21:16335810-16335860	NB4	blood:	n/a
50	chr21:16434067-16434117	K562	blood:	n/a

(count:175 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr21:16431111..16433395-chr21:16603127..16605498,2	MCF-7	breast:
2	chr21:16326244..16328555-chr21:16431229..16433465,2	MCF-7	breast:
3	chr21:16331957..16335486-chr21:16435819..16438054,3	MCF-7	breast:
4	chr21:16358929..16361068-chr21:16362393..16365514,4	K562	blood:
5	chr21:16377405..16378014-chr21:16493921..16494784,3	MCF-7	breast:
6	chr21:16390155..16392486-chr21:16399376..16401448,2	MCF-7	breast:
7	chr21:16358423..16361021-chr21:16428563..16430076,2	K562	blood:
8	chr21:16311490..16313439-chr21:16315470..16318449,2	MCF-7	breast:
9	chr21:16377426..16379495-chr21:16381579..16384387,2	MCF-7	breast:
10	chr21:16348445..16350792-chr21:16351626..16354922,3	K562	blood:
11	chr21:16377401..16378315-chr21:16714678..16715347,3	MCF-7	breast:
12	chr21:16375307..16377965-chr21:16378343..16380044,2	K562	blood:
13	chr21:16404641..16407621-chr21:16410737..16413727,2	K562	blood:
14	chr21:16422646..16426145-chr21:16428439..16434126,5	K562	blood:
15	chr21:16348445..16350792-chr21:16351626..16354922,3	K562	blood:
16	chr21:16384405..16386106-chr21:16392542..16394997,2	K562	blood:
17	chr21:16235181..16239841-chr21:16427951..16432204,4	MCF-7	breast:
18	chr21:16363309..16365664-chr21:16374179..16376018,2	K562	blood:
19	chr20:52812014..52814070-chr21:16432051..16434117,2	MCF-7	breast:
20	chr21:16370323..16372974-chr21:16375206..16377799,2	K562	blood:
21	chr21:16423642..16425341-chr21:16436698..16438268,2	K562	blood:
22	chr21:16401518..16403961-chr21:16435811..16437558,2	MCF-7	breast:
23	chr21:16327250..16329548-chr21:16336657..16339565,2	K562	blood:
24	chr21:16397947..16400507-chr21:16406341..16409146,2	MCF-7	breast:
25	chr21:16394934..16397671-chr21:16408444..16410714,3	MCF-7	breast:
26	chr21:16356082..16358745-chr21:16434038..16436986,2	MCF-7	breast:
27	chr21:16234362..16237223-chr21:16420995..16422874,2	MCF-7	breast:
28	chr21:16291414..16294345-chr21:16297800..16300613,2	MCF-7	breast:
29	chr21:16336657..16338695-chr21:16343721..16346197,3	MCF-7	breast:
30	chr21:16377309..16378284-chr21:16582106..16583282,23	MCF-7	breast:
31	chr21:16377421..16378235-chr21:16545003..16546153,5	MCF-7	breast:
32	chr21:16384405..16386106-chr21:16392542..16394997,2	K562	blood:
33	chr21:16334780..16336550-chr21:16340369..16342276,2	MCF-7	breast:
34	chr21:16327250..16329548-chr21:16336657..16339565,2	K562	blood:
35	chr21:16365404..16367302-chr21:16367721..16370714,2	K562	blood:
36	chr21:16326039..16327819-chr21:16329413..16331941,2	K562	blood:
37	chr21:16371773..16374195-chr21:16375368..16377855,2	K562	blood:
38	chr21:16377238..16378235-chr21:16544902..16545602,3	MCF-7	breast:
39	chr21:16383232..16385485-chr21:16435985..16437706,2	MCF-7	breast:
40	chr21:16377480..16378305-chr21:16571594..16572768,5	MCF-7	breast:
41	chr21:16415623..16417157-chr21:16436047..16437880,2	MCF-7	breast:
42	chr21:16397267..16399986-chr21:16410765..16412488,2	K562	blood:
43	chr21:16377411..16378027-chr21:16572053..16572593,2	MCF-7	breast:
44	chr21:16422646..16426145-chr21:16428439..16434126,5	K562	blood:
45	chr21:16381268..16384536-chr21:16390453..16394487,3	MCF-7	breast:
46	chr21:16311490..16313439-chr21:16315470..16318449,2	MCF-7	breast:
47	chr21:16404641..16407621-chr21:16410737..16413727,2	K562	blood:
48	chr21:16395351..16397728-chr21:16427292..16429201,2	MCF-7	breast:
49	chr21:16376922..16379315-chr21:16436281..16439109,2	MCF-7	breast:
50	chr21:16358929..16361068-chr21:16362393..16365514,4	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AF127577.1-2	chr21:16346536-16346638	ENSG00000231201.1
2	lnc-AF127577.1-2	chr21:16343791-16343890	ENSG00000231201.1
3	lnc-AF127577.1-4	chr21:16318876-16319417	XLOC_013864
4	lnc-AF165138.7.1-7	chr21:16351553-16351591	NONHSAT081193
5	lnc-AF127577.1-3	chr21:16336406-16336554	ENSG00000229047.1
6	lnc-AF165138.7.1-7	chr21:16363279-16363310	NONHSAT081193
7	lnc-AF127577.1-3	chr21:16333630-16334042	ENSG00000229047.1
8	lnc-AF127577.1-2	chr21:16364555-16365175	ENSG00000231201.1
9	lnc-AF165138.7.1-7	chr21:16360063-16360513	NONHSAT081193

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	NRIP1	hsa-miR-590-3p	chr21:16335199-16335221
2	NRIP1	hsa-miR-590-3p	chr21:16335003-16335027

Variant related genes	Relation type
ENSG00000231201	TF binding region
ENSG00000236471	TF binding region
ENSG00000229047	TF binding region
NRIP1	TF binding region
ENSG00000231201	CpG island
ENSG00000236471	CpG island
ENSG00000229047	CpG island
NRIP1	CpG island
ENSG00000229047	chromatin interactions
ENSG00000180530	chromatin interactions
ENSG00000155304	chromatin interactions
ENSG00000236471	chromatin interactions
ENSG00000231201	chromatin interactions

Extended variants
information (count: 4733 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:4733 , 50 per page) page: 1 2 3 4 5 6 7 ... 95

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555973516	chr21:16295757-16295758	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs564865227	chr21:16295759-16295760	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs544908904	chr21:16295916-16295917	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs75528184	chr21:16295918-16295919	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs201727033	chr21:16295921-16295922	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs577519823	chr21:16295925-16295926	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs540344468	chr21:16295934-16295935	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs560024966	chr21:16296004-16296005	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs57070884	chr21:16296018-16296019	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs548812843	chr21:16296094-16296095	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs562334948	chr21:16296097-16296098	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs371303652	chr21:16296113-16296114	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs531513623	chr21:16296192-16296193	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs149513045	chr21:16296198-16296199	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs185902052	chr21:16296284-16296285	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs539419136	chr21:16296320-16296321	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs546955015	chr21:16296481-16296482	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs566997421	chr21:16296489-16296490	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs144030306	chr21:16296541-16296542	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs572106861	chr21:16296550-16296551	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs34113073	chr21:16296572-16296573	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs574635595	chr21:16296602-16296603	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs190317560	chr21:16296606-16296607	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs540746005	chr21:16296609-16296610	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs73170266	chr21:16296647-16296648	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs112665577	chr21:16296718-16296719	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs369701477	chr21:16296896-16296897	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs577580392	chr21:16296897-16296898	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs182878390	chr21:16296902-16296903	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs117207509	chr21:16296941-16296942	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs75078099	chr21:16296961-16296962	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs2245317	chr21:16296967-16296968	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs562349133	chr21:16297033-16297034	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs77323824	chr21:16297038-16297039	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs551671837	chr21:16297044-16297045	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs565069815	chr21:16297047-16297048	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs554821580	chr21:16297081-16297082	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs370587840	chr21:16297093-16297094	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs112755030	chr21:16297108-16297109	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs187386148	chr21:16297109-16297110	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs574831380	chr21:16297149-16297150	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs543603605	chr21:16297168-16297169	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs2245411	chr21:16297181-16297182	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs535960248	chr21:16297244-16297245	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs549451661	chr21:16297271-16297272	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs569494237	chr21:16297289-16297290	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs9978697	chr21:16297290-16297291	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs370845680	chr21:16297313-16297314	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs144701542	chr21:16297337-16297338	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs192229166	chr21:16297339-16297340	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
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
Sudden cardiac death	19188705	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell lymphomas	19863542	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
Acute lymphoblastic leukemia	21980252	CNVD
Metanephric adenoma	20802469	CNVD
Neuroblastoma	18923191	CNVD
Prostate cancer	19156837	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	20409316	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
lymphocytic leukemia	21291569	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute myeloid leukemia	21251322	CNVD
abnormal development	18461090	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Alzheimer''s disease	18923514	CNVD
Alzheimer''s disease	20877625	CNVD
Follicular lymphoma	20505157	CNVD
Alzheimer''s disease	21956041	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Invasive pancreatic ductal carcinoma	16982739	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
Epilepsy	20502679	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
22q11.2 microdeletion syndrome	19750312	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:4093 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:16294200-16296400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr21:16294400-16296000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr21:16294800-16296000	Enhancers	HSMM	muscle
4	chr21:16294800-16296200	Enhancers	NHLF	lung
5	chr21:16295000-16295800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr21:16295000-16296600	Enhancers	NHDF-Ad	bronchial
7	chr21:16295200-16296000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr21:16295200-16296600	Enhancers	Muscle Satellite Cultured Cells	--
9	chr21:16295400-16296400	Enhancers	Osteobl	bone
10	chr21:16295600-16296000	Enhancers	Adipose Nuclei	Adipose
11	chr21:16295800-16298200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr21:16296000-16298200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr21:16296000-16298200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr21:16296000-16298400	Weak transcription	Adipose Nuclei	Adipose
15	chr21:16296400-16298400	Weak transcription	Osteobl	bone
16	chr21:16298200-16298600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr21:16298200-16298800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr21:16298200-16299000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr21:16298400-16298800	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr21:16298400-16298800	Enhancers	Adipose Nuclei	Adipose
21	chr21:16298400-16299000	Enhancers	Osteobl	bone
22	chr21:16298600-16298800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr21:16298800-16299000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr21:16312800-16313200	ZNF genes & repeats	Primary hematopoietic stem cells	blood
25	chr21:16312800-16315200	Weak transcription	HSMM	muscle
26	chr21:16313200-16334800	Weak transcription	Primary hematopoietic stem cells	blood
27	chr21:16314400-16318800	Enhancers	HepG2	liver
28	chr21:16314600-16316400	Enhancers	Osteobl	bone
29	chr21:16314600-16317600	Enhancers	Pancreatic Islets	Pancreatic Islet
30	chr21:16314800-16315000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr21:16314800-16315400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr21:16314800-16316000	Enhancers	NHLF	lung
33	chr21:16314800-16318200	Enhancers	Liver	Liver
34	chr21:16315000-16315400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr21:16315000-16315400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr21:16315000-16315400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr21:16315000-16315400	Enhancers	Muscle Satellite Cultured Cells	--
38	chr21:16315000-16316800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr21:16315000-16316800	Enhancers	Fetal Kidney	kidney
40	chr21:16315200-16315600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr21:16315200-16315600	Enhancers	Brain Hippocampus Middle	brain
42	chr21:16315200-16315600	Enhancers	HSMM	muscle
43	chr21:16315200-16315800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
44	chr21:16315200-16316000	Enhancers	Brain Substantia Nigra	brain
45	chr21:16315200-16316200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr21:16315400-16316200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr21:16315400-16316600	Enhancers	Fetal Lung	lung
48	chr21:16315600-16316400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr21:16315600-16338000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr21:16315800-16316200	Enhancers	HUES48 Cell Line	embryonic stem cell

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