Variant report

Variant	nsv914473
Chromosome Location	chr22:22266577-22349088
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3900)
CpG islands
(count:2685)
Chromatin interactive
region (count:210)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:3900 , 50 per page) page: 1 2 3 4 5 6 7 ... 78

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr22:22307655-22307768	HepG2	liver:	n/a	n/a
2	ARID3A	chr22:22307263-22307486	K562	blood:	n/a	n/a
3	ARID3A	chr22:22337039-22337516	K562	blood:	n/a	n/a
4	ARID3A	chr22:22292460-22293156	HepG2	liver:	n/a	n/a
5	ARID3A	chr22:22339268-22339597	K562	blood:	n/a	n/a
6	ARID3A	chr22:22302093-22302226	HepG2	liver:	n/a	n/a
7	ARID3A	chr22:22306577-22306630	HepG2	liver:	n/a	n/a
8	ARID3A	chr22:22337105-22337394	HepG2	liver:	n/a	n/a
9	ARID3A	chr22:22292407-22293273	K562	blood:	n/a	n/a
10	ARID3A	chr22:22302000-22302519	K562	blood:	n/a	n/a
11	ATF2	chr22:22292364-22293180	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr22:22337013-22337406	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr22:22336963-22337512	GM12878	blood:	n/a	n/a
14	ATF2	chr22:22337046-22337443	GM12878	blood:	n/a	n/a
15	ATF3	chr22:22282384-22282756	K562	blood:	n/a	n/a
16	ATF3	chr22:22337022-22337431	A549	lung:	n/a	n/a
17	ATF3	chr22:22336920-22337450	K562	blood:	n/a	n/a
18	ATF3	chr22:22292081-22293278	K562	blood:	n/a	n/a
19	ATF3	chr22:22306866-22307977	K562	blood:	n/a	n/a
20	ATF3	chr22:22328320-22329148	K562	blood:	n/a	n/a
21	ATF3	chr22:22336622-22337455	K562	blood:	n/a	n/a
22	ATF3	chr22:22339054-22340019	K562	blood:	n/a	n/a
23	ATF3	chr22:22326711-22327539	K562	blood:	n/a	n/a
24	BACH1	chr22:22307058-22307324	K562	blood:	n/a	n/a
25	BACH1	chr22:22307119-22307441	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr22:22337071-22337345	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr22:22292421-22293206	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr22:22301982-22302288	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr22:22292333-22293152	K562	blood:	n/a	n/a
30	BACH1	chr22:22337067-22337481	K562	blood:	n/a	n/a
31	BATF	chr22:22292460-22292722	GM12878	blood:	n/a	n/a
32	BATF	chr22:22337088-22337392	GM12878	blood:	n/a	n/a
33	BCL3	chr22:22313952-22315920	K562	blood:	n/a	chr22:22315179-22315192 chr22:22315274-22315283 chr22:22315390-22315399
34	BCL3	chr22:22320187-22321216	K562	blood:	n/a	n/a
35	BCL3	chr22:22292392-22293207	A549	lung:	n/a	n/a
36	BCL3	chr22:22292737-22293192	A549	lung:	n/a	n/a
37	BCL3	chr22:22336978-22337514	A549	lung:	n/a	chr22:22337114-22337127
38	BCLAF1	chr22:22336890-22337545	GM12878	blood:	n/a	chr22:22337114-22337127
39	BCLAF1	chr22:22336985-22337436	GM12878	blood:	n/a	chr22:22337114-22337127
40	BCLAF1	chr22:22292337-22292849	GM12878	blood:	n/a	n/a
41	BCLAF1	chr22:22336162-22337594	K562	blood:	n/a	chr22:22336598-22336607 chr22:22337114-22337127
42	BCLAF1	chr22:22336752-22337612	K562	blood:	n/a	chr22:22337114-22337127
43	BCLAF1	chr22:22307022-22307505	GM12878	blood:	n/a	n/a
44	BCLAF1	chr22:22292363-22293140	GM12878	blood:	n/a	n/a
45	BHLHE40	chr22:22290696-22291118	K562	blood:	n/a	n/a
46	BHLHE40	chr22:22292171-22293376	K562	blood:	n/a	n/a
47	BHLHE40	chr22:22301242-22302464	K562	blood:	n/a	n/a
48	BHLHE40	chr22:22306971-22307800	K562	blood:	n/a	chr22:22307216-22307232
49	BHLHE40	chr22:22307024-22307474	GM12878	blood:	n/a	chr22:22307216-22307232
50	BHLHE40	chr22:22306452-22306681	K562	blood:	n/a	n/a

(count:2685 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:22292241-22292291	AG04449	skin:	fetal
2	chr22:22292241-22292291	AG04449	skin:	fetal
3	chr22:22337171-22337221	HAEpiC	amniotic membrane:	n/a
4	chr22:22337034-22337084	IMR90	lung:	fetal
5	chr22:22307395-22307445	HUVEC	blood vessel:	n/a
6	chr22:22292638-22292688	AG09309	skin:	n/a
7	chr22:22292729-22292779	NB4	blood:	n/a
8	chr22:22288352-22288402	PFSK-1	brain:	n/a
9	chr22:22293118-22293168	AG09319	gingival:	n/a
10	chr22:22292241-22292291	T-47D	breast:	n/a
11	chr22:22307395-22307445	HIPEpiC	eye:	n/a
12	chr22:22309769-22309819	U87	brain:	n/a
13	chr22:22337332-22337382	PFSK-1	brain:	n/a
14	chr22:22339538-22339588	BJ	skin:	n/a
15	chr22:22289520-22289570	Jurkat	blood:	n/a
16	chr22:22336396-22336446	HCM	heart:	n/a
17	chr22:22337171-22337221	NB4	blood:	n/a
18	chr22:22307378-22307428	HUVEC	blood vessel:	n/a
19	chr22:22337374-22337424	HIPEpiC	eye:	n/a
20	chr22:22337153-22337203	A549	lung:	n/a
21	chr22:22337468-22337518	GM12891	blood:	n/a
22	chr22:22275386-22275436	HCPEpiC	choroid plexus:	n/a
23	chr22:22337178-22337228	PFSK-1	brain:	n/a
24	chr22:22292729-22292779	NT2-D1	testis:	n/a
25	chr22:22287697-22287747	BJ	skin:	n/a
26	chr22:22292638-22292688	NT2-D1	testis:	n/a
27	chr22:22337332-22337382	ovcar-3	ovarian:	n/a
28	chr22:22307070-22307120	MCF-7	breast:	n/a
29	chr22:22307070-22307120	GM19239	blood:	n/a
30	chr22:22337327-22337377	ProgFib	skin:	n/a
31	chr22:22290866-22290916	HUVEC	blood vessel:	n/a
32	chr22:22311698-22311748	PFSK-1	brain:	n/a
33	chr22:22288352-22288402	AG10803	skin:	n/a
34	chr22:22292729-22292779	Hepatocyte	liver:	n/a
35	chr22:22296625-22296675	PFSK-1	brain:	n/a
36	chr22:22337327-22337377	HRPEpiC	eye:	n/a
37	chr22:22307573-22307623	A549	lung:	n/a
38	chr22:22337369-22337419	RPTEC	kidney:	n/a
39	chr22:22307378-22307428	MCF-7	breast:	n/a
40	chr22:22306651-22306701	BE2_C	brain:	n/a
41	chr22:22307395-22307445	NT2-D1	testis:	n/a
42	chr22:22337141-22337191	HRE	kidney:	n/a
43	chr22:22290866-22290916	MCF10A-Er-Src	breast:	n/a
44	chr22:22307482-22307532	HCF	heart:	n/a
45	chr22:22290866-22290916	NB4	blood:	n/a
46	chr22:22337171-22337221	H1-hESC	embryonic stem cell:	embryo
47	chr22:22306651-22306701	AG09319	gingival:	n/a
48	chr22:22293118-22293168	H1-hESC	embryonic stem cell:	embryo
49	chr22:22302600-22302650	NHBE	bronchial:	n/a
50	chr22:22337034-22337084	SK-N-SH_RA	brain:	n/a

(count:210 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr22:22290664..22292935-chr22:22346867..22348436,2	K562	blood:
2	chr22:21982930..21985503-chr22:22298209..22299787,2	K562	blood:
3	chr22:22329308..22331029-chr22:22335214..22337114,2	MCF-7	breast:
4	chr22:22088545..22090754-chr22:22292290..22294479,2	MCF-7	breast:
5	chr22:22001170..22003842-chr22:22303847..22305574,2	K562	blood:
6	chr22:22292166..22293064-chr22:22414699..22415634,3	K562	blood:
7	chr22:21981288..21984493-chr22:22304068..22306404,3	K562	blood:
8	chr22:22149149..22152103-chr22:22281667..22284130,2	K562	blood:
9	chr22:22071322..22073400-chr22:22269185..22271638,3	K562	blood:
10	chr22:22292535..22295844-chr22:22301877..22304014,4	MCF-7	breast:
11	chr22:22067689..22069822-chr22:22273194..22275247,2	K562	blood:
12	chr22:22315227..22317746-chr22:22319787..22322237,2	MCF-7	breast:
13	chr22:22342384..22345359-chr22:22398039..22400395,2	K562	blood:
14	chr22:22307185..22307826-chr22:22315287..22316233,2	K562	blood:
15	chr22:22080235..22082660-chr22:22313495..22315266,2	K562	blood:
16	chr22:22081098..22081614-chr22:22292958..22293509,2	MCF-7	breast:
17	chr22:22221148..22221961-chr22:22292763..22293453,2	K562	blood:
18	chr22:22109453..22112191-chr22:22307233..22308989,2	K562	blood:
19	chr22:22291707..22294409-chr22:22295547..22298448,3	MCF-7	breast:
20	chr22:22218339..22225021-chr22:22291070..22294784,16	K562	blood:
21	chr22:22292531..22293584-chr22:22326371..22327337,3	K562	blood:
22	chr22:22292249..22292768-chr6:36853269..36853777,2	K562	blood:
23	chr22:22328328..22330386-chr22:22400402..22403039,2	K562	blood:
24	chr22:22337908..22340571-chr22:22464076..22466498,2	K562	blood:
25	chr22:22326791..22328773-chr22:22331790..22334833,5	MCF-7	breast:
26	chr22:22312865..22314736-chr22:22395820..22398625,2	K562	blood:
27	chr22:22335671..22337946-chr22:22899521..22901593,2	K562	blood:
28	chr22:22320427..22322900-chr22:22335647..22337789,2	MCF-7	breast:
29	chr22:22214377..22217269-chr22:22270465..22272236,2	K562	blood:
30	chr22:22251681..22254057-chr22:22299774..22302552,2	K562	blood:
31	chr22:22306382..22307926-chrX:12992863..12994802,2	MCF-7	breast:
32	chr22:22292154..22292772-chr22:22301837..22302500,2	MCF-7	breast:
33	chr22:22053860..22056327-chr22:22270499..22272537,2	K562	blood:
34	chr22:22326791..22328773-chr22:22331790..22334833,5	MCF-7	breast:
35	chr22:22306982..22308543-chr22:22325097..22327409,2	MCF-7	breast:
36	chr22:22068299..22069266-chr22:22301656..22302231,2	K562	blood:
37	chr22:22015152..22017176-chr22:22303779..22306519,2	K562	blood:
38	chr22:22067733..22069469-chr22:22300683..22303045,3	MCF-7	breast:
39	chr22:22037368..22040740-chr22:22291546..22294238,3	K562	blood:
40	chr22:22014013..22016208-chr22:22290767..22292528,2	K562	blood:
41	chr22:22326670..22328362-chr22:22335678..22338446,2	MCF-7	breast:
42	chr22:21996385..21999011-chr22:22290359..22293088,2	K562	blood:
43	chr22:22068963..22071183-chr22:22300868..22303636,2	K562	blood:
44	chr22:21996404..21998024-chr22:22293546..22295195,2	K562	blood:
45	chr22:21976586..21979474-chr22:22290804..22292395,2	K562	blood:
46	chr22:22053698..22055287-chr22:22332085..22334698,2	K562	blood:
47	chr22:22295757..22298107-chr4:82520720..82523521,2	MCF-7	breast:
48	chr22:22219525..22222944-chr22:22304293..22307333,4	K562	blood:
49	chr22:22296163..22299761-chr22:22300679..22303627,3	MCF-7	breast:
50	chr22:22334819..22337137-chr22:22380026..22382739,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PPIL2-1	chr22:22295474-22297799	ENSG00000224086.3
2	lnc-TOP3B-2	chr22:22292576-22292903	NONHSAT083723
3	lnc-PPIL2-1	chr22:22292609-22294263	ENSG00000224086.3
4	lnc-TOP3B-2	chr22:22291334-22291588	NONHSAT083723
5	lnc-PPIL2-1	chr22:22292665-22292934	NONHSAT083725
6	lnc-PPIL2-1	chr22:22292665-22293985	ENSG00000224086.3
7	lnc-PPIL2-1	chr22:22295474-22297794	NONHSAT083725

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PPM1F	hsa-miR-186-5p	chr22:22276653-22276674

Variant related genes	Relation type
ENSG00000224086	TF binding region
PPM1F	TF binding region
TOP3B	TF binding region
ENSG00000224086	CpG island
PPM1F	CpG island
TOP3B	CpG island
ENSG00000128228	chromatin interactions
ENSG00000100038	chromatin interactions
ENSG00000253794	chromatin interactions
ENSG00000228161	chromatin interactions
ENSG00000272954	chromatin interactions
ENSG00000223461	chromatin interactions
ENSG00000197549	chromatin interactions
ENSG00000161179	chromatin interactions
ENSG00000253823	chromatin interactions
ENSG00000249333	chromatin interactions
ENSG00000100023	chromatin interactions
ENSG00000253239	chromatin interactions
ENSG00000225741	chromatin interactions
ENSG00000100030	chromatin interactions
ENSG00000112972	chromatin interactions
ENSG00000227710	chromatin interactions
ENSG00000070413	chromatin interactions
ENSG00000205542	chromatin interactions
ENSG00000224086	chromatin interactions
ENSG00000212102	chromatin interactions
ENSG00000207751	chromatin interactions
ENSG00000211637	chromatin interactions
ENSG00000254075	chromatin interactions
ENSG00000100034	chromatin interactions
ENSG00000185651	chromatin interactions
ENSG00000185686	chromatin interactions
ENSG00000253752	chromatin interactions
ENSG00000198663	chromatin interactions
ENSG00000254355	chromatin interactions
ENSG00000100027	chromatin interactions

Extended variants
information (count: 3523 )
Associated
traits (count: 217 )

Variant overlapped rSNPs/rCNVs (count:3523 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs240054	chr22:22266577-22266578	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs561677443	chr22:22266644-22266645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs572066806	chr22:22266748-22266749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs568736059	chr22:22266795-22266796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs240055	chr22:22266808-22266809	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs150605092	chr22:22266818-22266819	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs369314484	chr22:22266847-22266848	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs139701546	chr22:22266883-22266884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs549714117	chr22:22266900-22266901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs373085105	chr22:22266928-22266929	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs8139622	chr22:22266938-22266939	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs374873051	chr22:22266944-22266945	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs201977186	chr22:22266945-22266946	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs529114540	chr22:22266973-22266974	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs143081735	chr22:22266988-22266989	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs240056	chr22:22266995-22266996	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs539859625	chr22:22267010-22267011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs370805394	chr22:22267011-22267012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs534050356	chr22:22267019-22267020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs547855630	chr22:22267110-22267111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs140016634	chr22:22267114-22267115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs540028247	chr22:22267127-22267128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs374422806	chr22:22267138-22267139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs185629133	chr22:22267145-22267146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs536125397	chr22:22267150-22267151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs113366054	chr22:22267184-22267185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs553719997	chr22:22267192-22267193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs540794852	chr22:22267202-22267203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs190738350	chr22:22267247-22267248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs560402697	chr22:22267274-22267275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs113109654	chr22:22267280-22267281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs114986945	chr22:22267303-22267304	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
33	rs543226050	chr22:22267320-22267321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs144256743	chr22:22267323-22267324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs145351580	chr22:22267334-22267335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs71197628	chr22:22267340-22267341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs131669	chr22:22267342-22267343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs5756043	chr22:22267359-22267360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs71318737	chr22:22267360-22267361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs376696648	chr22:22267361-22267362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs150323422	chr22:22267365-22267366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs143834970	chr22:22267366-22267367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs71197629	chr22:22267380-22267381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs201153821	chr22:22267385-22267386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs131670	chr22:22267392-22267393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs563099300	chr22:22267417-22267418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs374449616	chr22:22267440-22267441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs147803405	chr22:22267461-22267462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs529173024	chr22:22267463-22267464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs542873121	chr22:22267500-22267501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:217)

Disease	PMID	Source
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Velocardiofacial syndrome	20111667	CNVD
Medulloblastoma	21979893	CNVD
sporadic solitary meningiomas	19589153	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Emanuel syndrome	21549014	CNVD
Digeorge syndrome	22283845	CNVD
Schizophrenia	17504246	CNVD
Digeorge syndrome	18033723	CNVD
22q11 deletion syndrome	17034021	CNVD
22q11 deletion syndrome	22511897	CNVD
22q11 deletion syndrome	16829213	CNVD
Autism	22067053	CNVD
Autism	19218893	CNVD
Biliary cancer	22067053	CNVD
Congenital heart defect	21390462	CNVD
Digeorge syndrome	16617304	CNVD
Emanuel syndrome	18184694	CNVD
Non-syndromic sensorineural hearing loss	18184694	CNVD
Obsessive-compulsive disorder	22067053	CNVD
Psychosis	22067053	CNVD
Schizophrenia	19415332	CNVD
Schizophrenia	20587603	CNVD
Shprintzen syndrome	19443537	CNVD
absent pulmonary valve syndrome	16795129	CNVD
language delay	22067053	CNVD
periventricular nodular heterotopia	20648244	CNVD
renal disease	17924346	CNVD
Schizophrenia	20433910	CNVD
22q11 deletion syndrome	17028864	CNVD
Schizophrenia	16969581	CNVD
Non-syndromic sensorineural hearing loss	17135275	CNVD
velo-cardio-facial syndrome	17135275	CNVD
Digeorge syndrome	18787571	CNVD
Autism	18925931	CNVD
Non-small cell lung cancer	21829676	CNVD
22q11.2 microdeletion syndrome	21547621	CNVD
Congenital heart defect	21308838	CNVD
Digeorge syndrome	16512914	CNVD
Digeorge syndrome	20954168	CNVD
Nuchal translucency	21837766	CNVD
Right aortic arch in the fetus	17066500	CNVD
Shprintzen syndrome	17117043	CNVD
Tetralogy of fallot	17405110	CNVD
Velocardiofacial syndrome	20140301	CNVD
Velocardiofacial syndrome	16512914	CNVD
bone mass and metabolism	20516202	CNVD
choanal atresia	18209138	CNVD
extracardiac malformations	17086578	CNVD
fetal heart defects	21308838	CNVD
parathyroid gland dysfunction	16793949	CNVD
prenatal diagnosis	20453657	CNVD
velopharyngeal insufficiency	19620585	CNVD
Prader-willi syndrome	20942916	CNVD
22q11 deletion syndrome	17653112	CNVD
Chronic myelomonocytic leukemia	16760666	CNVD
Non-syndromic sensorineural hearing loss	16829213	CNVD
Non-syndromic sensorineural hearing loss	16760666	CNVD
Chordoma	21602918	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Congenital heart defect	22511896	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Seminomas	18059402	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Metachromatic leukodystrophy	18421352	CNVD
Basal cell lymphoma	17170743	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Cat eye syndrome	21549014	CNVD
Digeorge syndrome	21549014	CNVD
22q11.2 microdeletion syndrome	22051516	CNVD
22q11.2 microdeletion syndrome	18483005	CNVD
22q11.2 microdeletion syndrome	19565140	CNVD
22q11.2 microdeletion syndrome	20396437	CNVD
22q11.2 microdeletion syndrome	21390462	CNVD
22q11.2 microdeletion syndrome	21573985	CNVD
Austim spectrum disorder	21302340	CNVD
Autism	20970697	CNVD
Bipolar disorder	19114987	CNVD
Congenital heart defect	21257016	CNVD
Developmental delay	18414209	CNVD
DiGeorge-Velo cardiofacial	19284877	CNVD
Epilepsy	20970697	CNVD
Heart disease	20551144	CNVD
Hughes'' syndrome	16595601	CNVD
Mental retardation	18414209	CNVD
Okamoto syndrome	19046188	CNVD
Primary immunodeficiency	22566803	CNVD
Schizophrenia	20877625	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	21956041	CNVD
Schizophrenia	20970697	CNVD
Tetralogy of Fallot	22912587	CNVD
Velocardiofacial syndrome	17556857	CNVD
Velocardiofacial syndrome	20206275	CNVD
Velocardiofacial syndrome	20970697	CNVD
delayed speech development	21274400	CNVD
velo-cardio-facial syndrome	16511839	CNVD
velo-cardio-facial syndrome	21763005	CNVD
22q11.2 microdeletion syndrome	18799940	CNVD
Digeorge syndrome	20877625	CNVD
22q11.2 microdeletion syndrome	18923514	CNVD
Congenital heart defect	22185286	CNVD
DiGeorge-Velo cardiofacial	16773131	CNVD
Digeorge syndrome	20186050	CNVD
velo-cardio-facial conotruncal-face syndrome	20186050	CNVD
22q11.2 microdeletion syndrome	22116936	CNVD
Disorders of sex development	22290220	CNVD
22q11.2 duplication syndrome	18923514	CNVD
Autism	22095694	CNVD
Mental retardation	19951919	CNVD
Honadal dysgenesis	21048976	CNVD
Mental retardation	16773131	CNVD
22q11.2 microdeletion syndrome	22395003	CNVD
22q11.2 microdeletion syndrome	18691436	CNVD
22q11.2 microdeletion syndrome	18053182	CNVD
22q11.2 microdeletion syndrome	18324686	CNVD
22q11.2 microdeletion syndrome	20074913	CNVD
Congenital heart defect	20802965	CNVD
Congenital heart defect	21134246	CNVD
DiGeorge syndrome	19040613	CNVD
DiGeorge-Velo cardiofacial	18179902	CNVD
Digeorge syndrome	18172682	CNVD
Digeorge syndrome	22470819	CNVD
Digeorge syndrome	21364285	CNVD
Neuroendocrine carcinoma	22470819	CNVD
Non-syndromic sensorineural hearing loss	20069674	CNVD
Smith-Magenis syndrome	18301319	CNVD
Tetralogy of fallot	19144126	CNVD
Velo-cardio-facial syndrome	21364285	CNVD
Velocardiofacial syndrome	18788013	CNVD
cardiac malformation	20573211	CNVD
cardiac malformation	18172682	CNVD
velo-cardio-facial syndrome	18636631	CNVD
Schizophrenia	21822266	CNVD
synaptic plasticity	21368174	CNVD
Schizophrenia	18043741	CNVD
sporadic birth defects	19047251	CNVD
Autism	19046189	CNVD
DiGeorge-Velo cardiofacial	19047251	CNVD
Hypernasal speech	21968682	CNVD
Mental retardation	17339581	CNVD
diverse phenotype	16760730	CNVD
Mental retardation	20152051	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	22174824	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Wilms tumour	21544195	CNVD
Acute myeloid leukemia	21251322	CNVD
DiGeorge-Velo cardiofacial	17597781	CNVD
Digeorge syndrome	17576883	CNVD
Schizophrenia	18806272	CNVD
Schizophrenia	18990708	CNVD
Velocardiofacial syndrome	17576883	CNVD
Schizophrenia	20075378	CNVD
Neurodevelopmental disorder	17015230	CNVD
Neuropsychiatric disorder	20069037	CNVD
Williams-beuren syndrome	18553513	CNVD
Emphysema	19352772	CNVD
Cancer	17440070	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Disease	21346257	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Developmental delay	21147756	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Asthma	21956041	CNVD
Glioblastoma multiforme	22286061	CNVD
Colorectal cancer	21128281	CNVD
Systemic lupus erythematosus	21956041	CNVD
Primary central nervous system lymphoma	21088137	CNVD
22q11.23 microdeletion syndrome	19193630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Urothelial carcinoma	21177765	CNVD
Chronic myeloid leukemia	21384125	CNVD
Autism	20841430	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:3640 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:22255800-22271000	Weak transcription	Fetal Muscle Leg	muscle
2	chr22:22256000-22267000	Weak transcription	Brain Anterior Caudate	brain
3	chr22:22256200-22271200	Weak transcription	Fetal Stomach	stomach
4	chr22:22256200-22271600	Weak transcription	Brain Germinal Matrix	brain
5	chr22:22256600-22273600	Weak transcription	Lung	lung
6	chr22:22256800-22271600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr22:22257000-22277600	Weak transcription	Aorta	Aorta
8	chr22:22257200-22273400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr22:22257600-22270000	Weak transcription	Fetal Muscle Trunk	muscle
10	chr22:22257600-22271200	Weak transcription	Adipose Nuclei	Adipose
11	chr22:22257600-22273400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
12	chr22:22258600-22271600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr22:22258800-22274400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr22:22259000-22271600	Weak transcription	Skeletal Muscle Male	skeletal muscle
15	chr22:22259200-22269600	Weak transcription	Right Atrium	heart
16	chr22:22259200-22270600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr22:22259200-22271600	Weak transcription	Right Ventricle	heart
18	chr22:22259200-22271600	Weak transcription	Spleen	Spleen
19	chr22:22262800-22270400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
20	chr22:22264600-22271600	Weak transcription	HSMM	muscle
21	chr22:22266200-22266600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr22:22266800-22267000	Enhancers	Primary neutrophils fromperipheralblood	blood
23	chr22:22267000-22273400	Weak transcription	Primary neutrophils fromperipheralblood	blood
24	chr22:22268000-22271000	Weak transcription	Placenta	Placenta
25	chr22:22268800-22273600	Weak transcription	Primary T cells from cord blood	blood
26	chr22:22269200-22271600	Weak transcription	Gastric	stomach
27	chr22:22269200-22274800	Weak transcription	Fetal Intestine Small	intestine
28	chr22:22269600-22269800	Enhancers	Fetal Brain Male	brain
29	chr22:22269600-22271600	Strong transcription	Right Atrium	heart
30	chr22:22270000-22270200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr22:22270000-22271400	Weak transcription	Brain Anterior Caudate	brain
32	chr22:22270000-22272600	Enhancers	Fetal Muscle Trunk	muscle
33	chr22:22270000-22275800	Weak transcription	Fetal Brain Male	brain
34	chr22:22270200-22274400	Weak transcription	Primary monocytes fromperipheralblood	blood
35	chr22:22270400-22270600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr22:22270400-22271600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr22:22270400-22272600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr22:22270400-22272800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
39	chr22:22270600-22270800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr22:22270600-22271800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr22:22270600-22272600	Enhancers	Ovary	ovary
42	chr22:22270600-22272600	Enhancers	Pancreas	Pancrea
43	chr22:22270600-22276600	Enhancers	Breast Myoepithelial Primary Cells	Breast
44	chr22:22270800-22273000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr22:22270800-22274400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr22:22271000-22272200	Enhancers	Brain Inferior Temporal Lobe	brain
47	chr22:22271000-22272200	Enhancers	Placenta	Placenta
48	chr22:22271000-22272400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr22:22271000-22272600	Enhancers	Fetal Muscle Leg	muscle
50	chr22:22271000-22273000	Enhancers	Cortex derived primary cultured neurospheres	brain

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