Variant report

Variant	nsv1058282
Chromosome Location	chr22:22263018-22334795
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3053)
CpG islands
(count:1893)
Chromatin interactive
region (count:184)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:3053 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr22:22302093-22302226	HepG2	liver:	n/a	n/a
2	ARID3A	chr22:22302000-22302519	K562	blood:	n/a	n/a
3	ARID3A	chr22:22306577-22306630	HepG2	liver:	n/a	n/a
4	ARID3A	chr22:22292460-22293156	HepG2	liver:	n/a	n/a
5	ARID3A	chr22:22307263-22307486	K562	blood:	n/a	n/a
6	ARID3A	chr22:22307655-22307768	HepG2	liver:	n/a	n/a
7	ARID3A	chr22:22292407-22293273	K562	blood:	n/a	n/a
8	ATF1	chr22:22264747-22264931	K562	blood:	n/a	n/a
9	ATF2	chr22:22292364-22293180	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chr22:22306866-22307977	K562	blood:	n/a	n/a
11	ATF3	chr22:22292081-22293278	K562	blood:	n/a	n/a
12	ATF3	chr22:22282384-22282756	K562	blood:	n/a	n/a
13	ATF3	chr22:22326711-22327539	K562	blood:	n/a	n/a
14	ATF3	chr22:22328320-22329148	K562	blood:	n/a	n/a
15	BACH1	chr22:22292421-22293206	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr22:22307119-22307441	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr22:22301982-22302288	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr22:22292333-22293152	K562	blood:	n/a	n/a
19	BACH1	chr22:22307058-22307324	K562	blood:	n/a	n/a
20	BATF	chr22:22292460-22292722	GM12878	blood:	n/a	n/a
21	BCL3	chr22:22313952-22315920	K562	blood:	n/a	chr22:22315179-22315192 chr22:22315274-22315283 chr22:22315390-22315399
22	BCL3	chr22:22320187-22321216	K562	blood:	n/a	n/a
23	BCL3	chr22:22292737-22293192	A549	lung:	n/a	n/a
24	BCL3	chr22:22292392-22293207	A549	lung:	n/a	n/a
25	BCLAF1	chr22:22292363-22293140	GM12878	blood:	n/a	n/a
26	BCLAF1	chr22:22307022-22307505	GM12878	blood:	n/a	n/a
27	BCLAF1	chr22:22292337-22292849	GM12878	blood:	n/a	n/a
28	BHLHE40	chr22:22306971-22307800	K562	blood:	n/a	chr22:22307216-22307232
29	BHLHE40	chr22:22306452-22306681	K562	blood:	n/a	n/a
30	BHLHE40	chr22:22326701-22326993	K562	blood:	n/a	n/a
31	BHLHE40	chr22:22301242-22302464	K562	blood:	n/a	n/a
32	BHLHE40	chr22:22328626-22328822	K562	blood:	n/a	n/a
33	BHLHE40	chr22:22290696-22291118	K562	blood:	n/a	n/a
34	BHLHE40	chr22:22292408-22293180	GM12878	blood:	n/a	n/a
35	BHLHE40	chr22:22307024-22307474	GM12878	blood:	n/a	chr22:22307216-22307232
36	BHLHE40	chr22:22292171-22293376	K562	blood:	n/a	n/a
37	BRCA1	chr22:22292575-22292676	HepG2	liver:	n/a	n/a
38	BRCA1	chr22:22293444-22293447	GM12878	blood:	n/a	n/a
39	BRCA1	chr22:22280044-22280205	H1-hESC	embryonic stem cell:	n/a	n/a
40	BRCA1	chr22:22292226-22293082	GM12878	blood:	n/a	n/a
41	BRCA1	chr22:22292443-22293184	H1-hESC	embryonic stem cell:	n/a	n/a
42	BRCA1	chr22:22292338-22292766	Hela-S3	cervix:	n/a	n/a
43	BRCA1	chr22:22285196-22285214	GM12878	blood:	n/a	n/a
44	BRCA1	chr22:22306220-22306226	HepG2	liver:	n/a	n/a
45	BRCA1	chr22:22292942-22293146	HepG2	liver:	n/a	n/a
46	BRCA1	chr22:22307211-22307385	H1-hESC	embryonic stem cell:	n/a	n/a
47	BRCA1	chr22:22307265-22307461	Hela-S3	cervix:	n/a	n/a
48	CBX3	chr22:22305316-22305720	K562	blood:	n/a	n/a
49	CBX3	chr22:22306901-22308020	K562	blood:	n/a	n/a
50	CBX3	chr22:22305825-22308076	K562	blood:	n/a	n/a

(count:1893 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:22288352-22288402	SKMC	muscle:	n/a
2	chr22:22309769-22309819	Caco-2	colon:	n/a
3	chr22:22288352-22288402	SKMC	muscle:	n/a
4	chr22:22309769-22309819	Caco-2	colon:	n/a
5	chr22:22287697-22287747	U87	brain:	n/a
6	chr22:22285359-22285409	NH-A	brain:	n/a
7	chr22:22287697-22287747	HMEC	breast:	n/a
8	chr22:22292774-22292824	HCT-116	colon:	n/a
9	chr22:22285359-22285409	RPTEC	kidney:	n/a
10	chr22:22311698-22311748	GM12891	blood:	n/a
11	chr22:22290866-22290916	SK-N-MC	brain:	n/a
12	chr22:22307684-22307734	GM12878	blood:	n/a
13	chr22:22312957-22313007	HL-60	blood:	n/a
14	chr22:22315643-22315693	HEEpiC	esophagus:	n/a
15	chr22:22311698-22311748	NHDF-neo	bronchial:	n/a
16	chr22:22306651-22306701	HPAEpiC	pulmonary alveolar:	n/a
17	chr22:22288473-22288523	PrEC	prostate:	n/a
18	chr22:22292241-22292291	HEEpiC	esophagus:	n/a
19	chr22:22334553-22334603	NHBE	bronchial:	n/a
20	chr22:22287697-22287747	BE2_C	brain:	n/a
21	chr22:22307378-22307428	AG04450	lung:	fetal
22	chr22:22292241-22292291	SAEC	small airway:	n/a
23	chr22:22292241-22292291	RPTEC	kidney:	n/a
24	chr22:22288352-22288402	HEEpiC	esophagus:	n/a
25	chr22:22306651-22306701	SK-N-MC	brain:	n/a
26	chr22:22306263-22306313	AoSMC	blood vessel:	n/a
27	chr22:22292729-22292779	K562	blood:	n/a
28	chr22:22292638-22292688	HCPEpiC	choroid plexus:	n/a
29	chr22:22292774-22292824	AG04449	skin:	fetal
30	chr22:22285359-22285409	BJ	skin:	n/a
31	chr22:22307395-22307445	GM06990	blood:	n/a
32	chr22:22306651-22306701	BJ	skin:	n/a
33	chr22:22307395-22307445	IMR90	lung:	fetal
34	chr22:22306263-22306313	ProgFib	skin:	n/a
35	chr22:22292241-22292291	ECC-1	luminal epithelium:	n/a
36	chr22:22307371-22307421	HCT-116	colon:	n/a
37	chr22:22307378-22307428	AoSMC	blood vessel:	n/a
38	chr22:22288559-22288609	H1-hESC	embryonic stem cell:	embryo
39	chr22:22296625-22296675	K562	blood:	n/a
40	chr22:22292241-22292291	U87	brain:	n/a
41	chr22:22309769-22309819	ovcar-3	ovarian:	n/a
42	chr22:22307395-22307445	PFSK-1	brain:	n/a
43	chr22:22292638-22292688	AG09309	skin:	n/a
44	chr22:22288508-22288558	SKMC	muscle:	n/a
45	chr22:22311698-22311748	NHBE	bronchial:	n/a
46	chr22:22334553-22334603	BE2_C	brain:	n/a
47	chr22:22288559-22288609	NHDF-neo	bronchial:	n/a
48	chr22:22306651-22306701	LNCaP	prostate:	n/a
49	chr22:22290866-22290916	PANC-1	pancreas:	n/a
50	chr22:22288352-22288402	SK-N-SH	brain:	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr22:22292610..22297899-chr22:22316736..22322432,6	K562	blood:
2	chr22:22037368..22040740-chr22:22291546..22294238,3	K562	blood:
3	chr22:22055923..22058133-chr22:22298564..22300939,2	K562	blood:
4	chr22:22306115..22309049-chr22:22314797..22317582,3	MCF-7	breast:
5	chr22:22068963..22071183-chr22:22300868..22303636,2	K562	blood:
6	chr22:22334793..22336573-chr22:22401804..22404443,2	K562	blood:
7	chr22:22291063..22292706-chr22:22313114..22314633,2	K562	blood:
8	chr22:22067136..22068163-chr22:22300753..22302623,8	K562	blood:
9	chr22:22006264..22009261-chr22:22291037..22293088,2	K562	blood:
10	chr22:22274411..22276355-chr22:22316813..22318418,2	K562	blood:
11	chr22:22089169..22091453-chr22:22299864..22302320,3	K562	blood:
12	chr22:22280478..22282568-chr22:22285578..22287154,2	MCF-7	breast:
13	chr22:22292026..22293306-chr22:22304101..22305516,4	K562	blood:
14	chr22:22333715..22337365-chr22:22437629..22441288,4	K562	blood:
15	chr22:22306382..22307926-chrX:12992863..12994802,2	MCF-7	breast:
16	chr22:21976586..21979474-chr22:22290804..22292395,2	K562	blood:
17	chr22:22088545..22090754-chr22:22292290..22294479,2	MCF-7	breast:
18	chr22:22130696..22132847-chr22:22280604..22282994,2	K562	blood:
19	chr22:22307419..22309124-chr22:22395144..22396659,2	K562	blood:
20	chr22:22255775..22257984-chr22:22276245..22278618,2	K562	blood:
21	chr22:22299166..22301404-chr22:22302950..22305296,2	MCF-7	breast:
22	chr22:22301568..22303769-chr22:22443867..22445458,2	K562	blood:
23	chr22:22065172..22068892-chr22:22301220..22303855,4	K562	blood:
24	chr22:22089192..22091927-chr22:22279825..22282512,2	K562	blood:
25	chr22:22306982..22308543-chr22:22325097..22327409,2	MCF-7	breast:
26	chr22:22303827..22304626-chr22:22326823..22327382,2	K562	blood:
27	chr22:22292535..22295844-chr22:22301877..22304014,4	MCF-7	breast:
28	chr22:22219761..22223642-chr22:22333943..22337946,5	K562	blood:
29	chr22:22106788..22109532-chr22:22300482..22301999,2	K562	blood:
30	chr22:22053860..22056327-chr22:22270499..22272537,2	K562	blood:
31	chr22:22014013..22016208-chr22:22290767..22292528,2	K562	blood:
32	chr22:22071322..22073400-chr22:22269185..22271638,3	K562	blood:
33	chr22:22083663..22085506-chr22:22275492..22277482,2	K562	blood:
34	chr22:22251681..22254057-chr22:22299774..22302552,2	K562	blood:
35	chr22:22242609..22244247-chr22:22272159..22274753,3	K562	blood:
36	chr22:22290645..22292893-chr22:22385193..22387835,2	K562	blood:
37	chr22:22328328..22330386-chr22:22400402..22403039,2	K562	blood:
38	chr22:22129393..22130914-chr22:22299587..22301892,2	K562	blood:
39	chr22:22316437..22317944-chr22:22319379..22321751,2	MCF-7	breast:
40	chr22:22290671..22292913-chr22:22304916..22307695,3	MCF-7	breast:
41	chr22:22292249..22292768-chr6:36853269..36853777,2	K562	blood:
42	chr22:22292166..22293064-chr22:22414699..22415634,3	K562	blood:
43	chr22:21981138..21983094-chr22:22301398..22303697,2	K562	blood:
44	chr22:22307185..22307826-chr22:22315287..22316233,2	K562	blood:
45	chr22:19108558..19111368-chr22:22312314..22314926,2	K562	blood:
46	chr22:22289966..22298336-chr22:22332694..22342462,17	K562	blood:
47	chr22:22255129..22259166-chr22:22267129..22272472,7	K562	blood:
48	chr22:22292531..22293584-chr22:22326371..22327337,3	K562	blood:
49	chr22:21981288..21984493-chr22:22304068..22306404,3	K562	blood:
50	chr22:22306115..22309049-chr22:22314797..22317582,3	MCF-7	breast:

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

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

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
ENSG00000227710	chromatin interactions
ENSG00000100030	chromatin interactions
ENSG00000161179	chromatin interactions
ENSG00000224086	chromatin interactions
ENSG00000100027	chromatin interactions
ENSG00000228161	chromatin interactions
ENSG00000205542	chromatin interactions
ENSG00000100038	chromatin interactions
ENSG00000207751	chromatin interactions
ENSG00000197549	chromatin interactions
ENSG00000272954	chromatin interactions
ENSG00000253794	chromatin interactions
ENSG00000212102	chromatin interactions
ENSG00000254075	chromatin interactions
ENSG00000223461	chromatin interactions
ENSG00000211637	chromatin interactions
ENSG00000198663	chromatin interactions
ENSG00000254355	chromatin interactions
ENSG00000100023	chromatin interactions
ENSG00000253823	chromatin interactions
ENSG00000100034	chromatin interactions
ENSG00000112972	chromatin interactions
ENSG00000070413	chromatin interactions
ENSG00000128228	chromatin interactions

Extended variants
information (count: 3072 )
Associated
traits (count: 217 )

Variant overlapped rSNPs/rCNVs (count:3072 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs559794998	chr22:22263077-22263078	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs144443360	chr22:22263091-22263092	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs184838477	chr22:22263131-22263132	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs571702738	chr22:22263170-22263171	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs531124904	chr22:22263211-22263212	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs528974528	chr22:22263215-22263216	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs550225345	chr22:22263267-22263268	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs566950087	chr22:22263291-22263292	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs540671728	chr22:22263312-22263313	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs189733644	chr22:22263337-22263338	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs191618378	chr22:22263356-22263357	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs566570008	chr22:22263402-22263403	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs12167687	chr22:22263473-22263474	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs171254	chr22:22263575-22263576	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs575478113	chr22:22263588-22263589	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs370715426	chr22:22263597-22263598	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs577436450	chr22:22263605-22263606	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs538178515	chr22:22263618-22263619	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs569109762	chr22:22263652-22263653	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs183761598	chr22:22263658-22263659	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs537228481	chr22:22263659-22263660	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs552883450	chr22:22263660-22263661	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs374415647	chr22:22263661-22263662	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs188139632	chr22:22263669-22263670	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs559447866	chr22:22263680-22263681	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs79381748	chr22:22263700-22263701	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs377239545	chr22:22263707-22263708	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs461833	chr22:22263711-22263712	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs461024	chr22:22263723-22263724	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs545137275	chr22:22263798-22263799	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs565508854	chr22:22263870-22263871	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs530986570	chr22:22263901-22263902	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs73386291	chr22:22263937-22263938	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs150296523	chr22:22263947-22263948	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs530287672	chr22:22263997-22263998	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs6000051	chr22:22264027-22264028	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs550596192	chr22:22264037-22264038	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs574749185	chr22:22264038-22264039	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs551973075	chr22:22264054-22264055	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs535970490	chr22:22264055-22264056	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs569102652	chr22:22264088-22264089	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs240050	chr22:22264089-22264090	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs240051	chr22:22264103-22264104	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs240052	chr22:22264119-22264120	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs6000052	chr22:22264137-22264138	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs181885082	chr22:22264171-22264172	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs142032664	chr22:22264175-22264176	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs573139037	chr22:22264186-22264187	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs117116696	chr22:22264199-22264200	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs565034485	chr22:22264214-22264215	Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	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:3222 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

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	chr22:22259200-22263600	Weak transcription	Stomach Smooth Muscle	stomach
16	chr22:22259200-22269600	Weak transcription	Right Atrium	heart
17	chr22:22259200-22270600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr22:22259200-22271600	Weak transcription	Right Ventricle	heart
19	chr22:22259200-22271600	Weak transcription	Spleen	Spleen
20	chr22:22262800-22270400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr22:22264200-22264400	Bivalent Enhancer	K562	blood
22	chr22:22264400-22264600	Enhancers	HSMM	muscle
23	chr22:22264400-22265000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr22:22264400-22265200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr22:22264400-22265800	Enhancers	K562	blood
26	chr22:22264600-22271600	Weak transcription	HSMM	muscle
27	chr22:22266200-22266600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr22:22266800-22267000	Enhancers	Primary neutrophils fromperipheralblood	blood
29	chr22:22267000-22273400	Weak transcription	Primary neutrophils fromperipheralblood	blood
30	chr22:22268000-22271000	Weak transcription	Placenta	Placenta
31	chr22:22268800-22273600	Weak transcription	Primary T cells from cord blood	blood
32	chr22:22269200-22271600	Weak transcription	Gastric	stomach
33	chr22:22269200-22274800	Weak transcription	Fetal Intestine Small	intestine
34	chr22:22269600-22269800	Enhancers	Fetal Brain Male	brain
35	chr22:22269600-22271600	Strong transcription	Right Atrium	heart
36	chr22:22270000-22270200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr22:22270000-22271400	Weak transcription	Brain Anterior Caudate	brain
38	chr22:22270000-22272600	Enhancers	Fetal Muscle Trunk	muscle
39	chr22:22270000-22275800	Weak transcription	Fetal Brain Male	brain
40	chr22:22270200-22274400	Weak transcription	Primary monocytes fromperipheralblood	blood
41	chr22:22270400-22270600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr22:22270400-22271600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr22:22270400-22272600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr22:22270400-22272800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
45	chr22:22270600-22270800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr22:22270600-22271800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr22:22270600-22272600	Enhancers	Ovary	ovary
48	chr22:22270600-22272600	Enhancers	Pancreas	Pancrea
49	chr22:22270600-22276600	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr22:22270800-22273000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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