Variant report

Variant	nsv1064554
Chromosome Location	chr21:15676222-15809321
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1473)
CpG islands
(count:916)
Chromatin interactive
region (count:76)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:8)

(count:1473 , 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	chr21:15755268-15756109	HepG2	liver:	n/a	n/a
2	ARID3A	chr21:15758299-15758479	K562	blood:	n/a	n/a
3	ARID3A	chr21:15753998-15754080	K562	blood:	n/a	n/a
4	ARID3A	chr21:15755173-15756571	K562	blood:	n/a	n/a
5	ARID3A	chr21:15678881-15679135	K562	blood:	n/a	n/a
6	ARID3A	chr21:15776002-15776346	K562	blood:	n/a	n/a
7	ATF1	chr21:15693445-15693715	K562	blood:	n/a	n/a
8	ATF1	chr21:15755085-15755946	K562	blood:	n/a	n/a
9	ATF2	chr21:15755202-15755652	GM12878	blood:	n/a	n/a
10	ATF3	chr21:15734278-15734672	K562	blood:	n/a	n/a
11	ATF3	chr21:15755249-15755657	K562	blood:	n/a	chr21:15755481-15755495
12	BACH1	chr21:15755261-15755431	K562	blood:	n/a	n/a
13	BACH1	chr21:15755021-15755056	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr21:15755338-15756042	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr21:15760631-15760949	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr21:15760675-15760968	K562	blood:	n/a	n/a
17	BACH1	chr21:15742480-15742584	K562	blood:	n/a	n/a
18	BATF	chr21:15787301-15787516	GM12878	blood:	n/a	n/a
19	BATF	chr21:15755303-15755640	GM12878	blood:	n/a	chr21:15755330-15755340
20	BATF	chr21:15755145-15755665	GM12878	blood:	n/a	chr21:15755330-15755340
21	BCLAF1	chr21:15755292-15756207	GM12878	blood:	n/a	n/a
22	BCLAF1	chr21:15755245-15755807	GM12878	blood:	n/a	n/a
23	BHLHE40	chr21:15755029-15756177	HepG2	liver:	n/a	chr21:15755215-15755231
24	BHLHE40	chr21:15755011-15756441	K562	blood:	n/a	chr21:15755215-15755231
25	BHLHE40	chr21:15755039-15756420	GM12878	blood:	n/a	chr21:15755215-15755231
26	BRCA1	chr21:15755310-15755866	HepG2	liver:	n/a	n/a
27	BRCA1	chr21:15755164-15756426	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr21:15708190-15708206	H1-hESC	embryonic stem cell:	n/a	n/a
29	BRCA1	chr21:15755229-15756067	GM12878	blood:	n/a	n/a
30	BRCA1	chr21:15730137-15730553	Hela-S3	cervix:	n/a	n/a
31	BRCA1	chr21:15776084-15776399	Hela-S3	cervix:	n/a	n/a
32	BRCA1	chr21:15755348-15756047	H1-hESC	embryonic stem cell:	n/a	n/a
33	CBX3	chr21:15791230-15791584	K562	blood:	n/a	n/a
34	CBX3	chr21:15791238-15791580	K562	blood:	n/a	n/a
35	CCNT2	chr21:15757539-15757977	K562	blood:	n/a	n/a
36	CCNT2	chr21:15755282-15756426	K562	blood:	n/a	n/a
37	CCNT2	chr21:15776143-15776343	K562	blood:	n/a	n/a
38	CEBPB	chr21:15755409-15755730	A549	lung:	n/a	n/a
39	CEBPB	chr21:15676434-15676819	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr21:15770341-15770581	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr21:15734315-15734686	HepG2	liver:	n/a	chr21:15734491-15734502
42	CEBPB	chr21:15756026-15756585	GM12878	blood:	n/a	n/a
43	CEBPB	chr21:15689872-15690147	K562	blood:	n/a	chr21:15690014-15690023 chr21:15690014-15690023 chr21:15690012-15690025 chr21:15690014-15690023
44	CEBPB	chr21:15755315-15755801	MCF-7	breast:	n/a	n/a
45	CEBPB	chr21:15754813-15755089	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr21:15734332-15734638	A549	lung:	n/a	chr21:15734491-15734502
47	CEBPB	chr21:15755379-15755740	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr21:15689907-15690144	H1-hESC	embryonic stem cell:	n/a	chr21:15690014-15690023 chr21:15690014-15690023 chr21:15690012-15690025 chr21:15690014-15690023
49	CEBPB	chr21:15754739-15755070	K562	blood:	n/a	n/a
50	CEBPB	chr21:15770324-15770766	A549	lung:	n/a	n/a

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:15755706-15755756	BJ	skin:	n/a
2	chr21:15755706-15755756	BJ	skin:	n/a
3	chr21:15756122-15756172	NT2-D1	testis:	n/a
4	chr21:15755644-15755694	AG10803	skin:	n/a
5	chr21:15755449-15755499	ovcar-3	ovarian:	n/a
6	chr21:15755706-15755756	Hepatocyte	liver:	n/a
7	chr21:15755538-15755588	AG04449	skin:	fetal
8	chr21:15755986-15756036	HRPEpiC	eye:	n/a
9	chr21:15755538-15755588	IMR90	lung:	fetal
10	chr21:15756122-15756172	PFSK-1	brain:	n/a
11	chr21:15755449-15755499	HMEC	breast:	n/a
12	chr21:15752932-15752982	NT2-D1	testis:	n/a
13	chr21:15755608-15755658	AG04449	skin:	fetal
14	chr21:15755538-15755588	A549	lung:	n/a
15	chr21:15755538-15755588	Hepatocyte	liver:	n/a
16	chr21:15755644-15755694	Jurkat	blood:	n/a
17	chr21:15755606-15755656	AG09309	skin:	n/a
18	chr21:15756085-15756135	PrEC	prostate:	n/a
19	chr21:15755931-15755981	Hepatocyte	liver:	n/a
20	chr21:15753565-15753615	MCF-7	breast:	n/a
21	chr21:15755986-15756036	NT2-D1	testis:	n/a
22	chr21:15755380-15755430	A549	lung:	n/a
23	chr21:15755380-15755430	AG10803	skin:	n/a
24	chr21:15756062-15756112	NH-A	brain:	n/a
25	chr21:15755608-15755658	GM12878	blood:	n/a
26	chr21:15755538-15755588	AG09319	gingival:	n/a
27	chr21:15755452-15755502	AoSMC	blood vessel:	n/a
28	chr21:15755706-15755756	PFSK-1	brain:	n/a
29	chr21:15755449-15755499	CMK	blood:	n/a
30	chr21:15755706-15755756	NT2-D1	testis:	n/a
31	chr21:15755608-15755658	NT2-D1	testis:	n/a
32	chr21:15756085-15756135	ECC-1	luminal epithelium:	n/a
33	chr21:15755644-15755694	HCT-116	colon:	n/a
34	chr21:15755452-15755502	AG09319	gingival:	n/a
35	chr21:15755931-15755981	HRPEpiC	eye:	n/a
36	chr21:15752932-15752982	HCPEpiC	choroid plexus:	n/a
37	chr21:15755449-15755499	MCF-7	breast:	n/a
38	chr21:15755449-15755499	HRE	kidney:	n/a
39	chr21:15755608-15755658	Hepatocyte	liver:	n/a
40	chr21:15755538-15755588	U87	brain:	n/a
41	chr21:15755931-15755981	HCT-116	colon:	n/a
42	chr21:15755606-15755656	GM06990	blood:	n/a
43	chr21:15755644-15755694	NB4	blood:	n/a
44	chr21:15755452-15755502	Caco-2	colon:	n/a
45	chr21:15755986-15756036	RPTEC	kidney:	n/a
46	chr21:15755986-15756036	Caco-2	colon:	n/a
47	chr21:15755931-15755981	SK-N-SH_RA	brain:	n/a
48	chr21:15753565-15753615	HRPEpiC	eye:	n/a
49	chr21:15755606-15755656	SK-N-SH	brain:	n/a
50	chr21:15756062-15756112	PrEC	prostate:	n/a

(count:76 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr21:15725447..15727391-chr21:15735609..15737943,2	K562	blood:
2	chr21:15677109..15679201-chr21:16581226..16583119,2	MCF-7	breast:
3	chr21:15725447..15727391-chr21:15735609..15737943,2	K562	blood:
4	chr21:15733062..15735967-chr21:15740026..15741975,2	MCF-7	breast:
5	chr21:15738341..15740358-chr21:15745168..15748188,3	MCF-7	breast:
6	chr11:65265638..65266483-chr21:15738427..15738927,2	NB4	blood:
7	chr21:15693896..15695521-chr21:15703441..15704959,2	K562	blood:
8	chr21:15751469..15753501-chr21:15755651..15758117,2	K562	blood:
9	chr21:15755580..15758807-chr21:15770098..15773208,3	K562	blood:
10	chr21:15732454..15736809-chr21:15737344..15740819,4	K562	blood:
11	chr21:15645251..15647400-chr21:15754351..15756122,2	K562	blood:
12	chr21:15743793..15747020-chr21:15754018..15757060,4	K562	blood:
13	chr21:15800225..15803025-chr21:15808190..15810823,2	K562	blood:
14	chr21:15755786..15757968-chr21:15767216..15769064,2	K562	blood:
15	chr21:15638970..15641725-chr21:15734559..15736787,2	K562	blood:
16	chr21:15754870..15757296-chr21:16435942..16438083,2	K562	blood:
17	chr21:15741032..15742950-chr21:15746679..15748662,2	MCF-7	breast:
18	chr21:15738717..15742131-chr21:15743462..15746963,4	K562	blood:
19	chr21:15740980..15743787-chr21:15748039..15750871,3	K562	blood:
20	chr21:15669627..15671972-chr21:15676907..15679063,2	MCF-7	breast:
21	chr21:15652280..15654566-chr21:15773386..15776181,2	MCF-7	breast:
22	chr21:15748798..15750660-chr21:15754088..15755961,2	K562	blood:
23	chr21:15708032..15710641-chr21:15713125..15715543,2	K562	blood:
24	chr21:15738236..15741206-chr21:15753262..15755404,2	K562	blood:
25	chr21:15681814..15683687-chr21:15754179..15756305,2	MCF-7	breast:
26	chr21:15787706..15790405-chr21:16436901..16438934,2	MCF-7	breast:
27	chr21:15738236..15741206-chr21:15753262..15755404,2	K562	blood:
28	chr21:15678412..15679071-chr21:15688646..15689192,2	MCF-7	breast:
29	chr21:15642588..15643376-chr21:15678270..15679084,2	MCF-7	breast:
30	chr21:15764391..15766947-chr21:15768713..15771374,3	K562	blood:
31	chr21:15676809..15681316-chr21:16435213..16438529,7	MCF-7	breast:
32	chr21:15678758..15680789-chr21:15681192..15683321,2	K562	blood:
33	chr21:15693896..15695521-chr21:15703441..15704959,2	K562	blood:
34	chr21:15753396..15756217-chr21:15770461..15772950,2	K562	blood:
35	chr21:15750689..15753216-chr21:15754882..15756987,2	MCF-7	breast:
36	chr21:15754842..15757143-chr21:15757991..15759672,2	MCF-7	breast:
37	chr21:15678271..15679097-chr21:16582211..16583261,3	MCF-7	breast:
38	chr21:15764391..15766947-chr21:15768713..15771374,3	K562	blood:
39	chr21:15753622..15756331-chr21:15761576..15764249,2	MCF-7	breast:
40	chr21:15761527..15763962-chr21:15764673..15767332,2	K562	blood:
41	chr21:15738236..15741507-chr21:15753904..15757362,3	K562	blood:
42	chr21:15678412..15679071-chr21:15688646..15689192,2	MCF-7	breast:
43	chr21:15757559..15759154-chr21:16437032..16438993,2	K562	blood:
44	chr21:15677584..15679731-chr21:15681094..15683819,2	MCF-7	breast:
45	chr21:15725007..15727450-chr21:15727478..15730890,3	K562	blood:
46	chr21:15733246..15736908-chr21:15755835..15758351,3	K562	blood:
47	chr21:15800225..15803025-chr21:15808190..15810823,2	K562	blood:
48	chr21:15739043..15741032-chr21:15755736..15757362,2	K562	blood:
49	chr21:15738341..15740358-chr21:15745168..15748188,3	MCF-7	breast:
50	chr21:15738717..15742131-chr21:15743462..15746963,4	K562	blood:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RBM11-5	chr21:15688522-15689956	NONHSAT081154
2	lnc-RBM11-5	chr21:15709501-15709561	NONHSAT081154
3	lnc-RBM11-5	chr21:15710102-15710338	NONHSAT081154
4	lnc-RBM11-5	chr21:15680692-15680776	NONHSAT081154
5	lnc-RBM11-1	chr21:15765643-15765753	ENSG00000242342
6	lnc-HSPA13-2	chr21:15688663-15688696	NONHSAT081159
7	lnc-RBM11-5	chr21:15685265-15685452	NONHSAT081154
8	lnc-HSPA13-1	chr21:15788122-15789088	NONHSAT081162
9	lnc-RBM11-5	chr21:15678017-15678163	NONHSAT081154
10	lnc-RBM11-1	chr21:15764891-15764967	ENSG00000242342
11	lnc-HSPA13-2	chr21:15684768-15684808	NONHSAT081159
12	lnc-HSPA13-2	chr21:15694688-15694739	NONHSAT081159
13	lnc-HSPA13-1	chr21:15789906-15790314	NONHSAT081162
14	lnc-RBM11-5	chr21:15708401-15708578	NONHSAT081154
15	lnc-HSPA13-2	chr21:15689190-15689319	NONHSAT081159
16	lnc-RBM11-5	chr21:15695833-15695908	NONHSAT081154
17	lnc-RBM11-5	chr21:15680874-15680940	NONHSAT081154
18	lnc-HSPA13-2	chr21:15696178-15696495	NONHSAT081159
19	lnc-HSPA13-2	chr21:15689653-15689687	NONHSAT081159

No data

(count:8 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	HSPA13	hsa-miR-374b-5p	chr21:15743825-15743845
2	HSPA13	hsa-miR-181a-5p	chr21:15744415-15744438
3	HSPA13	hsa-miR-590-3p	chr21:15743724-15743744
4	HSPA13	hsa-miR-590-3p	chr21:15743537-15743557
5	HSPA13	hsa-miR-590-3p	chr21:15745175-15745195
6	HSPA13	hsa-miR-374b-5p	chr21:15744626-15744647
7	HSPA13	hsa-miR-590-3p	chr21:15745703-15745724
8	HSPA13	hsa-miR-374b-5p	chr21:15745406-15745427

Variant related genes	Relation type
HSPA13	TF binding region
HSPA13	CpG island
ENSG00000258056	chromatin interactions
ENSG00000225502	chromatin interactions
ENSG00000113407	chromatin interactions
ENSG00000243064	chromatin interactions
ENSG00000155304	chromatin interactions
ENSG00000135404	chromatin interactions
ENSG00000270117	chromatin interactions
ENSG00000180530	chromatin interactions

Extended variants
information (count: 2733 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:2733 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs569873539	chr21:15676234-15676235	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs140102126	chr21:15676259-15676260	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs536754490	chr21:15676261-15676262	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs558624412	chr21:15676312-15676313	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs980268	chr21:15676336-15676337	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs535003621	chr21:15676357-15676358	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs553810185	chr21:15676379-15676380	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs374940289	chr21:15676385-15676386	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs67532512	chr21:15676444-15676445	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs201100788	chr21:15676463-15676464	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs79236598	chr21:15676467-15676468	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs200687431	chr21:15676468-15676469	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs397867073	chr21:15676469-15676470	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs1153316	chr21:15676470-15676471	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs548790882	chr21:15676489-15676490	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs78850266	chr21:15676527-15676528	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs142909575	chr21:15676541-15676542	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs2822561	chr21:15676583-15676584	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs112102817	chr21:15676598-15676599	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs564954643	chr21:15676599-15676600	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs527315136	chr21:15676609-15676610	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs542518005	chr21:15676613-15676614	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs547389725	chr21:15676619-15676620	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs556116510	chr21:15676676-15676677	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs560686920	chr21:15676691-15676692	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs73344378	chr21:15676770-15676771	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs550014804	chr21:15676782-15676783	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs569962459	chr21:15676849-15676850	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs538838416	chr21:15676851-15676852	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs552288304	chr21:15676902-15676903	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs575714958	chr21:15676917-15676918	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs62228673	chr21:15676946-15676947	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs185821666	chr21:15676977-15676978	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs189084051	chr21:15677065-15677066	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs9974847	chr21:15677183-15677184	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs536553259	chr21:15677219-15677220	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs556485550	chr21:15677230-15677231	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs1153317	chr21:15677231-15677232	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs1153318	chr21:15677245-15677246	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs558755078	chr21:15677252-15677253	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs572120982	chr21:15677277-15677278	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs35719953	chr21:15677306-15677307	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs540727495	chr21:15677334-15677335	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs151084785	chr21:15677425-15677426	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs369304331	chr21:15677462-15677463	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs563835294	chr21:15677487-15677488	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs529654485	chr21:15677495-15677496	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs34880884	chr21:15677497-15677498	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs543747370	chr21:15677498-15677499	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs548833179	chr21:15677509-15677510	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1137 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:15676000-15676600	Enhancers	HUVEC	blood vessel
2	chr21:15676000-15677400	Enhancers	Hela-S3	cervix
3	chr21:15676600-15678200	Weak transcription	HUVEC	blood vessel
4	chr21:15677200-15677600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr21:15677400-15678400	Weak transcription	Hela-S3	cervix
6	chr21:15677600-15678600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr21:15678200-15678400	Enhancers	Primary hematopoietic stem cells	blood
8	chr21:15678200-15679200	Enhancers	HUVEC	blood vessel
9	chr21:15678400-15678800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr21:15678400-15678800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr21:15678400-15678800	Enhancers	Fetal Kidney	kidney
12	chr21:15678400-15678800	Enhancers	Hela-S3	cervix
13	chr21:15678400-15679200	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr21:15678600-15678800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr21:15678600-15678800	Enhancers	Rectal Mucosa Donor 31	rectum
16	chr21:15678600-15679000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr21:15678600-15680600	Weak transcription	Primary hematopoietic stem cells	blood
18	chr21:15678800-15680600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr21:15678800-15680600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr21:15678800-15681200	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr21:15678800-15688600	Weak transcription	Rectal Mucosa Donor 31	rectum
22	chr21:15679200-15684600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
23	chr21:15680600-15681000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr21:15680600-15681000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr21:15680600-15681200	Enhancers	Primary hematopoietic stem cells	blood
26	chr21:15681000-15685200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr21:15681200-15682400	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr21:15681200-15691000	Weak transcription	Primary hematopoietic stem cells	blood
29	chr21:15684600-15686000	Enhancers	Primary hematopoietic stem cells short term culture	blood
30	chr21:15685400-15686000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr21:15686000-15690600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
32	chr21:15690000-15690800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr21:15690600-15691400	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr21:15690800-15691400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr21:15690800-15691400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr21:15691000-15691200	Enhancers	Primary hematopoietic stem cells	blood
37	chr21:15691000-15691400	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr21:15692000-15692600	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr21:15692800-15693800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr21:15693200-15693800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr21:15693200-15693800	Enhancers	HMEC	breast
42	chr21:15725600-15726600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr21:15725800-15726000	Enhancers	Fetal Stomach	stomach
44	chr21:15726000-15726400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
45	chr21:15729000-15729400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr21:15729000-15729600	Enhancers	HMEC	breast
47	chr21:15729000-15729600	Enhancers	NHEK	skin
48	chr21:15729200-15729600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr21:15729200-15729600	Enhancers	Esophagus	oesophagus
50	chr21:15729400-15730000	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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