Variant report

Variant	nsv869466
Chromosome Location	chr21:15482572-15683385
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1545)
CpG islands
(count:1282)
Chromatin interactive
region (count:75)
LncRNA
region (count:20)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1545 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr21:15643398-15643769	K562	blood:	n/a	n/a
2	ARID3A	chr21:15669056-15669343	K562	blood:	n/a	n/a
3	ARID3A	chr21:15632046-15632350	HepG2	liver:	n/a	n/a
4	ARID3A	chr21:15636185-15636385	K562	blood:	n/a	n/a
5	ARID3A	chr21:15656994-15657207	K562	blood:	n/a	n/a
6	ARID3A	chr21:15632038-15632466	K562	blood:	n/a	n/a
7	ARID3A	chr21:15678881-15679135	K562	blood:	n/a	n/a
8	ARID3A	chr21:15583357-15583367	HepG2	liver:	n/a	n/a
9	ATF1	chr21:15580497-15580694	K562	blood:	n/a	n/a
10	ATF1	chr21:15643368-15643726	K562	blood:	n/a	n/a
11	ATF1	chr21:15636259-15636544	K562	blood:	n/a	n/a
12	ATF2	chr21:15488328-15488936	GM12878	blood:	n/a	n/a
13	ATF3	chr21:15636281-15636574	K562	blood:	n/a	n/a
14	BACH1	chr21:15632039-15632366	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr21:15588533-15589188	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr21:15662884-15663269	K562	blood:	n/a	n/a
17	BCL11A	chr21:15486659-15486847	H1-hESC	embryonic stem cell:	n/a	n/a
18	BCLAF1	chr21:15492361-15492757	GM12878	blood:	n/a	n/a
19	BCLAF1	chr21:15488385-15488957	GM12878	blood:	n/a	n/a
20	BHLHE40	chr21:15613395-15613514	K562	blood:	n/a	n/a
21	BHLHE40	chr21:15488497-15488954	GM12878	blood:	n/a	n/a
22	BHLHE40	chr21:15646919-15647015	HepG2	liver:	n/a	chr21:15646984-15646993 chr21:15646984-15646993 chr21:15646983-15646992
23	BHLHE40	chr21:15643413-15643717	K562	blood:	n/a	n/a
24	BHLHE40	chr21:15646763-15647064	K562	blood:	n/a	chr21:15646984-15646993 chr21:15646984-15646993 chr21:15646983-15646992
25	BHLHE40	chr21:15673530-15673565	K562	blood:	n/a	n/a
26	BHLHE40	chr21:15588525-15588576	K562	blood:	n/a	n/a
27	BHLHE40	chr21:15646075-15646422	K562	blood:	n/a	n/a
28	BHLHE40	chr21:15492443-15492754	GM12878	blood:	n/a	n/a
29	BHLHE40	chr21:15626679-15626685	GM12878	blood:	n/a	n/a
30	BRCA1	chr21:15492774-15492860	GM12878	blood:	n/a	n/a
31	BRCA1	chr21:15660289-15660306	GM12878	blood:	n/a	n/a
32	BRCA1	chr21:15633651-15633671	GM12878	blood:	n/a	n/a
33	CBX3	chr21:15646066-15646407	K562	blood:	n/a	n/a
34	CBX3	chr21:15601768-15601981	K562	blood:	n/a	n/a
35	CCNT2	chr21:15643026-15643838	K562	blood:	n/a	chr21:15643572-15643592
36	CCNT2	chr21:15588227-15588771	K562	blood:	n/a	n/a
37	CCNT2	chr21:15646221-15646874	K562	blood:	n/a	n/a
38	CEBPB	chr21:15616272-15616511	K562	blood:	n/a	chr21:15616395-15616406
39	CEBPB	chr21:15551618-15551892	K562	blood:	n/a	chr21:15551765-15551776
40	CEBPB	chr21:15647260-15647457	H1-hESC	embryonic stem cell:	n/a	chr21:15647385-15647398
41	CEBPB	chr21:15643370-15643730	K562	blood:	n/a	chr21:15643550-15643567
42	CEBPB	chr21:15564243-15564490	HepG2	liver:	n/a	n/a
43	CEBPB	chr21:15607494-15607721	HepG2	liver:	n/a	chr21:15607615-15607626
44	CEBPB	chr21:15644175-15644343	K562	blood:	n/a	chr21:15644246-15644259
45	CEBPB	chr21:15616219-15616581	Hela-S3	cervix:	n/a	chr21:15616395-15616406
46	CEBPB	chr21:15616286-15616521	K562	blood:	n/a	chr21:15616395-15616406
47	CEBPB	chr21:15616281-15616480	H1-hESC	embryonic stem cell:	n/a	chr21:15616395-15616406
48	CEBPB	chr21:15676434-15676819	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr21:15592805-15593066	A549	lung:	n/a	chr21:15592892-15592903 chr21:15592876-15592893
50	CEBPB	chr21:15669697-15669826	H1-hESC	embryonic stem cell:	n/a	chr21:15669752-15669765 chr21:15669752-15669765

(count:1282 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:15645810-15645860	HL-60	blood:	n/a
2	chr21:15645810-15645860	HL-60	blood:	n/a
3	chr21:15588571-15588621	GM12878	blood:	n/a
4	chr21:15588372-15588422	SK-N-SH	brain:	n/a
5	chr21:15588608-15588658	SK-N-MC	brain:	n/a
6	chr21:15646635-15646685	HCT-116	colon:	n/a
7	chr21:15645649-15645699	HNPCEpiC	eye:	n/a
8	chr21:15645810-15645860	HRPEpiC	eye:	n/a
9	chr21:15646635-15646685	RPTEC	kidney:	n/a
10	chr21:15589441-15589491	SK-N-SH	brain:	n/a
11	chr21:15645649-15645699	PrEC	prostate:	n/a
12	chr21:15589441-15589491	PFSK-1	brain:	n/a
13	chr21:15588349-15588399	ECC-1	luminal epithelium:	n/a
14	chr21:15588349-15588399	SK-N-SH	brain:	n/a
15	chr21:15588038-15588088	HepG2	liver:	n/a
16	chr21:15646312-15646362	K562	blood:	n/a
17	chr21:15487742-15487792	AoSMC	blood vessel:	n/a
18	chr21:15588349-15588399	HAEpiC	amniotic membrane:	n/a
19	chr21:15645787-15645837	HCT-116	colon:	n/a
20	chr21:15588571-15588621	H1-hESC	embryonic stem cell:	embryo
21	chr21:15588349-15588399	PFSK-1	brain:	n/a
22	chr21:15645649-15645699	NH-A	brain:	n/a
23	chr21:15645649-15645699	HIPEpiC	eye:	n/a
24	chr21:15647368-15647418	GM12878	blood:	n/a
25	chr21:15588120-15588170	HRE	kidney:	n/a
26	chr21:15588830-15588880	HCT-116	colon:	n/a
27	chr21:15588372-15588422	HUVEC	blood vessel:	n/a
28	chr21:15645787-15645837	HUVEC	blood vessel:	n/a
29	chr21:15487742-15487792	NB4	blood:	n/a
30	chr21:15588038-15588088	Caco-2	colon:	n/a
31	chr21:15588571-15588621	K562	blood:	n/a
32	chr21:15588848-15588898	U87	brain:	n/a
33	chr21:15646635-15646685	IMR90	lung:	fetal
34	chr21:15588120-15588170	SK-N-MC	brain:	n/a
35	chr21:15645787-15645837	HRPEpiC	eye:	n/a
36	chr21:15645810-15645860	K562	blood:	n/a
37	chr21:15588571-15588621	NHDF-neo	bronchial:	n/a
38	chr21:15588120-15588170	U87	brain:	n/a
39	chr21:15588848-15588898	BJ	skin:	n/a
40	chr21:15589441-15589491	HRPEpiC	eye:	n/a
41	chr21:15588571-15588621	NT2-D1	testis:	n/a
42	chr21:15647368-15647418	A549	lung:	n/a
43	chr21:15645787-15645837	NH-A	brain:	n/a
44	chr21:15588038-15588088	AoSMC	blood vessel:	n/a
45	chr21:15588038-15588088	ProgFib	skin:	n/a
46	chr21:15588571-15588621	HUVEC	blood vessel:	n/a
47	chr21:15487742-15487792	K562	blood:	n/a
48	chr21:15588848-15588898	HEEpiC	esophagus:	n/a
49	chr21:15587812-15587862	MCF-7	breast:	n/a
50	chr21:15588571-15588621	Caco-2	colon:	n/a

(count:75 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr21:15518340..15522108-chr21:15524344..15527724,3	K562	blood:
2	chr21:15618985..15621962-chr21:15624169..15625950,3	K562	blood:
3	chr21:15493769..15495607-chr21:15500118..15502421,2	K562	blood:
4	chr21:15639101..15641621-chr21:15642019..15644892,2	MCF-7	breast:
5	chr21:15612009..15614501-chr21:15615453..15618275,2	K562	blood:
6	chr21:15652280..15654566-chr21:15773386..15776181,2	MCF-7	breast:
7	chr21:15591982..15594612-chr21:15596999..15599183,2	K562	blood:
8	chr21:15677584..15679731-chr21:15681094..15683819,2	MCF-7	breast:
9	chr21:15637737..15639634-chr21:15641854..15644729,2	K562	blood:
10	chr21:15494107..15496665-chr21:15500921..15502468,2	K562	blood:
11	chr21:15647599..15649902-chr21:15656709..15659445,2	K562	blood:
12	chr21:15590624..15592860-chr21:15594760..15596779,2	K562	blood:
13	chr21:15498829..15500815-chr21:15502377..15504055,2	K562	blood:
14	chr21:15650981..15652853-chr21:15655632..15658875,3	K562	blood:
15	chr21:15576826..15579345-chr21:15583403..15585435,2	K562	blood:
16	chr21:15611898..15613509-chr21:15614140..15616953,2	K562	blood:
17	chr21:15642365..15645973-chr21:15647939..15652510,4	K562	blood:
18	chr21:15650981..15652853-chr21:15655632..15658875,3	K562	blood:
19	chr21:15652023..15652746-chr7:152811109..152812098,2	MCF-7	breast:
20	chr21:15642588..15643574-chr21:15678270..15679033,2	MCF-7	breast:
21	chr21:15591982..15594612-chr21:15596999..15599183,2	K562	blood:
22	chr21:15677109..15679201-chr21:16581226..16583119,2	MCF-7	breast:
23	chr21:15637216..15639622-chr21:15681292..15683772,2	MCF-7	breast:
24	chr21:15518340..15522108-chr21:15524344..15527724,3	K562	blood:
25	chr21:15639101..15641621-chr21:15642019..15644892,2	MCF-7	breast:
26	chr21:15675259..15676017-chr3:64232863..64233717,2	MCF-7	breast:
27	chr21:15494107..15496665-chr21:15500921..15502468,2	K562	blood:
28	chr21:15584053..15586326-chr21:15587304..15590158,2	K562	blood:
29	chr21:15642588..15643376-chr21:15678270..15679084,2	MCF-7	breast:
30	chr21:15678758..15680789-chr21:15681192..15683321,2	K562	blood:
31	chr21:15645251..15647400-chr21:15754351..15756122,2	K562	blood:
32	chr21:15612009..15614501-chr21:15615453..15618275,2	K562	blood:
33	chr21:15637824..15639860-chr21:15661262..15662859,2	MCF-7	breast:
34	chr21:15678412..15679071-chr21:15688646..15689192,2	MCF-7	breast:
35	chr21:15656047..15658961-chr21:16165584..16168436,2	K562	blood:
36	chr21:15669627..15671972-chr21:15676907..15679063,2	MCF-7	breast:
37	chr21:15681814..15683687-chr21:15754179..15756305,2	MCF-7	breast:
38	chr21:15510246..15512237-chr21:15537714..15540194,2	MCF-7	breast:
39	chr21:15493769..15495607-chr21:15500118..15502421,2	K562	blood:
40	chr21:15572112..15574456-chr21:15577631..15579440,2	K562	blood:
41	chr21:15676809..15681316-chr21:16435213..16438529,7	MCF-7	breast:
42	chr21:15642365..15645973-chr21:15647939..15652510,4	K562	blood:
43	chr21:15498829..15500815-chr21:15502377..15504055,2	K562	blood:
44	chr21:15611898..15613509-chr21:15614140..15616953,2	K562	blood:
45	chr21:15644504..15646965-chr21:15652945..15655779,2	K562	blood:
46	chr21:15638970..15641725-chr21:15734559..15736787,2	K562	blood:
47	chr21:15642588..15643574-chr21:15678270..15679033,2	MCF-7	breast:
48	chr21:15642588..15643376-chr21:15678270..15679084,2	MCF-7	breast:
49	chr21:15678758..15680789-chr21:15681192..15683321,2	K562	blood:
50	chr21:15669596..15672076-chr21:15673281..15675239,2	K562	blood:

(count:20 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RBM11-5	chr21:15678017-15678163	NONHSAT081154
2	lnc-RBM11-5	chr21:15646120-15646478	NONHSAT081156
3	lnc-RBM11-5	chr21:15642846-15642930	NONHSAT081153
4	lnc-RBM11-5	chr21:15659871-15660018	NONHSAT081156
5	lnc-RBM11-2	chr21:15515902-15516479	NONHSAT081148
6	lnc-RBM11-5	chr21:15651917-15651978	NONHSAT081153
7	lnc-RBM11-5	chr21:15646120-15646478	NONHSAT081154
8	lnc-RBM11-5	chr21:15663891-15664068	NONHSAT081154
9	lnc-RBM11-5	chr21:15651917-15651978	NONHSAT081154
10	lnc-RBM11-5	chr21:15659871-15660018	NONHSAT081154
11	lnc-RBM11-5	chr21:15660725-15660867	NONHSAT081156
12	lnc-RBM11-5	chr21:15663607-15663706	NONHSAT081156
13	lnc-HSPA13-2	chr21:15664712-15665101	NONHSAT081159
14	lnc-RBM11-5	chr21:15651917-15651978	NONHSAT081156
15	lnc-RBM11-5	chr21:15640724-15640913	NONHSAT081153
16	lnc-RBM11-5	chr21:15608527-15608627	NONHSAT081153
17	lnc-RBM11-5	chr21:15660725-15660867	NONHSAT081154
18	lnc-RBM11-5	chr21:15641808-15641980	NONHSAT081153
19	lnc-RBM11-5	chr21:15680692-15680776	NONHSAT081154
20	lnc-RBM11-5	chr21:15680874-15680940	NONHSAT081154

No data

Variant related genes	Relation type
LIPI	TF binding region
ABCC13	TF binding region
RBM11	TF binding region
ERLEC1P1	TF binding region
LIPI	CpG island
ABCC13	CpG island
RBM11	CpG island
ERLEC1P1	CpG island
ENSG00000185272	chromatin interactions
ENSG00000243064	chromatin interactions
ENSG00000155304	chromatin interactions
ENSG00000180530	chromatin interactions
ENSG00000188992	chromatin interactions

Extended variants
information (count: 4810 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:4810 , 50 per page) page: 1 2 3 4 5 6 7 ... 97

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs137941409	chr21:15482572-15482573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs112051692	chr21:15482589-15482590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs1556276	chr21:15482605-15482606	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs144617068	chr21:15482607-15482608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs560256821	chr21:15482619-15482620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs551787673	chr21:15482644-15482645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs548040435	chr21:15482663-15482664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs202163360	chr21:15482667-15482668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs5842468	chr21:15482672-15482673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs200082051	chr21:15482675-15482676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs1556277	chr21:15482718-15482719	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs186066720	chr21:15482720-15482721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs189837667	chr21:15482738-15482739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs547398318	chr21:15482817-15482818	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs61422874	chr21:15482850-15482851	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs138511638	chr21:15482925-15482926	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs181430725	chr21:15482932-15482933	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs111238502	chr21:15482965-15482966	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs567397756	chr21:15482989-15482990	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs566310499	chr21:15483045-15483046	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs372690725	chr21:15483112-15483113	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs77862035	chr21:15483122-15483123	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs556051398	chr21:15483123-15483124	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs2187062	chr21:15483143-15483144	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs150848512	chr21:15483173-15483174	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs75628106	chr21:15483183-15483184	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs78031660	chr21:15483199-15483200	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs185500903	chr21:15483201-15483202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs578062875	chr21:15483206-15483207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs118034967	chr21:15483270-15483271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs560545243	chr21:15483280-15483281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs149238924	chr21:15483286-15483287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs542608773	chr21:15483287-15483288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs62208637	chr21:15483306-15483307	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs530698093	chr21:15483323-15483324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs8127547	chr21:15483324-15483325	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs564099886	chr21:15483379-15483380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs533063911	chr21:15483405-15483406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs144649749	chr21:15483417-15483418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs566469365	chr21:15483438-15483439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs148479335	chr21:15483441-15483442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs111648867	chr21:15483445-15483446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs548992617	chr21:15483477-15483478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs190315781	chr21:15483496-15483497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs569597829	chr21:15483515-15483516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs538509188	chr21:15483561-15483562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs182957377	chr21:15483562-15483563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs9978470	chr21:15483570-15483571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs534303905	chr21:15483578-15483579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs79490739	chr21:15483580-15483581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

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	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:842 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:15457600-15487400	Weak transcription	Fetal Brain Male	brain
2	chr21:15457800-15486200	Weak transcription	Thymus	Thymus
3	chr21:15470400-15487200	Weak transcription	Ovary	ovary
4	chr21:15470800-15483600	Weak transcription	Fetal Lung	lung
5	chr21:15470800-15484800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr21:15470800-15486200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr21:15471000-15484200	Weak transcription	Fetal Brain Female	brain
8	chr21:15474000-15489200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr21:15474600-15489600	Weak transcription	Duodenum Smooth Muscle	Duodenum
10	chr21:15475000-15486600	Weak transcription	Fetal Stomach	stomach
11	chr21:15475400-15485200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr21:15475800-15494600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr21:15477000-15482800	Weak transcription	Dnd41	blood
14	chr21:15477600-15498000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr21:15478000-15495200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr21:15479600-15485200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr21:15480400-15482800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr21:15480400-15497200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr21:15482800-15483200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr21:15482800-15483200	Strong transcription	Dnd41	blood
21	chr21:15483200-15485000	Weak transcription	Dnd41	blood
22	chr21:15483200-15485400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr21:15484200-15484400	ZNF genes & repeats	Fetal Brain Female	brain
24	chr21:15485000-15488600	Strong transcription	Dnd41	blood
25	chr21:15485200-15485400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr21:15485200-15486200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr21:15485400-15486000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr21:15485400-15486400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr21:15485800-15486600	Weak transcription	GM12878-XiMat	blood
30	chr21:15486000-15494000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr21:15486200-15487200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr21:15486200-15496600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr21:15486600-15486800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr21:15486600-15487000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr21:15486600-15487000	Enhancers	Esophagus	oesophagus
36	chr21:15486600-15487000	ZNF genes & repeats	Fetal Stomach	stomach
37	chr21:15486600-15487000	ZNF genes & repeats	GM12878-XiMat	blood
38	chr21:15486600-15487000	Enhancers	HMEC	breast
39	chr21:15486600-15487200	Enhancers	Placenta	Placenta
40	chr21:15486600-15487600	Enhancers	H1 Cell Line	embryonic stem cell
41	chr21:15486800-15487000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr21:15487000-15487200	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr21:15487000-15487800	Weak transcription	Esophagus	oesophagus
44	chr21:15487000-15487800	Weak transcription	Fetal Stomach	stomach
45	chr21:15487000-15487800	Weak transcription	GM12878-XiMat	blood
46	chr21:15487000-15488000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr21:15487200-15488000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr21:15487400-15489600	Enhancers	Primary B cells from peripheral blood	blood
49	chr21:15487800-15488000	Enhancers	GM12878-XiMat	blood
50	chr21:15487800-15488600	Strong transcription	Fetal Stomach	stomach

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