Variant report

Variant	esv10686
Chromosome Location	chr22:20693740-20708427
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:467)
CpG islands
(count:61)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:467 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr22:20705452-20705653	GM12878	blood:	n/a	chr22:20705604-20705614
2	BATF	chr22:20695109-20695381	GM12878	blood:	n/a	chr22:20695212-20695223
3	BATF	chr22:20704837-20705151	GM12878	blood:	n/a	n/a
4	BATF	chr22:20700720-20701058	GM12878	blood:	n/a	n/a
5	BATF	chr22:20707505-20707718	GM12878	blood:	n/a	n/a
6	BATF	chr22:20701125-20701590	GM12878	blood:	n/a	n/a
7	BATF	chr22:20697648-20697855	GM12878	blood:	n/a	n/a
8	BATF	chr22:20705491-20705797	GM12878	blood:	n/a	chr22:20705604-20705614
9	BATF	chr22:20704152-20704420	GM12878	blood:	n/a	n/a
10	BATF	chr22:20706564-20706772	GM12878	blood:	n/a	n/a
11	BATF	chr22:20695672-20695836	GM12878	blood:	n/a	n/a
12	BCL11A	chr22:20703665-20703934	GM12878	blood:	n/a	n/a
13	BCL11A	chr22:20706545-20706782	GM12878	blood:	n/a	n/a
14	BCL11A	chr22:20700654-20701413	GM12878	blood:	n/a	n/a
15	BCL11A	chr22:20697151-20697358	GM12878	blood:	n/a	n/a
16	BCL11A	chr22:20694397-20694737	GM12878	blood:	n/a	chr22:20694629-20694638
17	BCL11A	chr22:20707623-20707920	GM12878	blood:	n/a	n/a
18	BCL11A	chr22:20695093-20695286	GM12878	blood:	n/a	chr22:20695103-20695112 chr22:20695212-20695221
19	BCL11A	chr22:20696767-20697036	GM12878	blood:	n/a	n/a
20	BCL11A	chr22:20700742-20701651	GM12878	blood:	n/a	n/a
21	BHLHE40	chr22:20694394-20694642	HepG2	liver:	n/a	n/a
22	BHLHE40	chr22:20704919-20705283	HepG2	liver:	n/a	n/a
23	CEBPB	chr22:20707163-20707365	HepG2	liver:	n/a	n/a
24	CTCF	chr22:20696691-20696736	Pancreas_OC	pancreas:	n/a	n/a
25	CTCF	chr22:20696665-20696689	Pancreas_OC	pancreas:	n/a	n/a
26	EBF1	chr22:20704847-20705151	GM12878	blood:	n/a	n/a
27	EBF1	chr22:20706291-20706801	GM12878	blood:	n/a	chr22:20706555-20706564 chr22:20706554-20706564 chr22:20706553-20706566 chr22:20706555-20706564
28	EBF1	chr22:20706339-20706807	GM12878	blood:	n/a	chr22:20706555-20706564 chr22:20706554-20706564 chr22:20706553-20706566 chr22:20706555-20706564
29	EBF1	chr22:20700713-20701605	GM12878	blood:	n/a	n/a
30	EBF1	chr22:20694346-20694706	GM12878	blood:	n/a	n/a
31	EBF1	chr22:20700685-20701671	GM12878	blood:	n/a	n/a
32	EBF1	chr22:20694935-20695353	GM12878	blood:	n/a	n/a
33	EP300	chr22:20697514-20698589	GM12878	blood:	n/a	n/a
34	EP300	chr22:20695708-20695873	GM12878	blood:	n/a	n/a
35	EP300	chr22:20701406-20701594	GM12878	blood:	n/a	n/a
36	EP300	chr22:20703329-20704193	GM12878	blood:	n/a	n/a
37	EP300	chr22:20696338-20697437	GM12878	blood:	n/a	chr22:20697153-20697160
38	EP300	chr22:20704436-20704748	GM12878	blood:	n/a	n/a
39	EP300	chr22:20705321-20705868	GM12878	blood:	n/a	n/a
40	EP300	chr22:20704816-20705241	GM12878	blood:	n/a	n/a
41	EP300	chr22:20707403-20708116	GM12878	blood:	n/a	chr22:20707974-20707988
42	EP300	chr22:20699987-20700362	GM12878	blood:	n/a	n/a
43	EP300	chr22:20705913-20706863	GM12878	blood:	n/a	n/a
44	EP300	chr22:20694328-20696063	GM12878	blood:	n/a	chr22:20695103-20695117 chr22:20694784-20694798
45	EP300	chr22:20700422-20701683	GM12878	blood:	n/a	n/a
46	EP300	chr22:20700807-20701381	GM12878	blood:	n/a	n/a
47	EP300	chr22:20696763-20696937	GM12878	blood:	n/a	n/a
48	EP300	chr22:20707579-20707735	GM12878	blood:	n/a	n/a
49	EP300	chr22:20704175-20704310	GM12878	blood:	n/a	n/a
50	FOS	chr22:20706809-20707193	MCF10A-Er-Src	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:20706928-20706978	RPTEC	kidney:	n/a
2	chr22:20706928-20706978	PFSK-1	brain:	n/a
3	chr22:20706928-20706978	HIPEpiC	eye:	n/a
4	chr22:20706928-20706978	AG04450	lung:	fetal
5	chr22:20706928-20706978	BJ	skin:	n/a
6	chr22:20706928-20706978	HRPEpiC	eye:	n/a
7	chr22:20706928-20706978	GM19239	blood:	n/a
8	chr22:20706928-20706978	BE2_C	brain:	n/a
9	chr22:20706928-20706978	HCM	heart:	n/a
10	chr22:20706928-20706978	MCF-7	breast:	n/a
11	chr22:20706928-20706978	GM06990	blood:	n/a
12	chr22:20706928-20706978	HUVEC	blood vessel:	n/a
13	chr22:20706928-20706978	HNPCEpiC	eye:	n/a
14	chr22:20706928-20706978	SK-N-SH_RA	brain:	n/a
15	chr22:20706928-20706978	NH-A	brain:	n/a
16	chr22:20706928-20706978	PrEC	prostate:	n/a
17	chr22:20706928-20706978	H1-hESC	embryonic stem cell:	embryo
18	chr22:20706928-20706978	GM12892	blood:	n/a
19	chr22:20706928-20706978	HEK293	kidney:	embryo
20	chr22:20706928-20706978	SKMC	muscle:	n/a
21	chr22:20706928-20706978	NB4	blood:	n/a
22	chr22:20706928-20706978	HCPEpiC	choroid plexus:	n/a
23	chr22:20706928-20706978	AoSMC	blood vessel:	n/a
24	chr22:20706928-20706978	HL-60	blood:	n/a
25	chr22:20706928-20706978	HCF	heart:	n/a
26	chr22:20706928-20706978	SK-N-SH	brain:	n/a
27	chr22:20706928-20706978	Caco-2	colon:	n/a
28	chr22:20706928-20706978	HAEpiC	amniotic membrane:	n/a
29	chr22:20706928-20706978	HCT-116	colon:	n/a
30	chr22:20706928-20706978	HRCEpiC	kidney:	n/a
31	chr22:20706928-20706978	U87	brain:	n/a
32	chr22:20706928-20706978	GM12878	blood:	n/a
33	chr22:20706928-20706978	Hepatocyte	liver:	n/a
34	chr22:20706928-20706978	GM12891	blood:	n/a
35	chr22:20706928-20706978	SK-N-MC	brain:	n/a
36	chr22:20706928-20706978	Hela-S3	cervix:	n/a
37	chr22:20706928-20706978	ovcar-3	ovarian:	n/a
38	chr22:20706928-20706978	HEEpiC	esophagus:	n/a
39	chr22:20706928-20706978	Jurkat	blood:	n/a
40	chr22:20706928-20706978	IMR90	lung:	fetal
41	chr22:20706928-20706978	AG09309	skin:	n/a
42	chr22:20706928-20706978	PANC-1	pancreas:	n/a
43	chr22:20706928-20706978	NHBE	bronchial:	n/a
44	chr22:20706928-20706978	ECC-1	luminal epithelium:	n/a
45	chr22:20706928-20706978	HPAEpiC	pulmonary alveolar:	n/a
46	chr22:20706928-20706978	CMK	blood:	n/a
47	chr22:20706928-20706978	HepG2	liver:	n/a
48	chr22:20706928-20706978	NT2-D1	testis:	n/a
49	chr22:20706928-20706978	ProgFib	skin:	n/a
50	chr22:20706928-20706978	K562	blood:	n/a

No data

Variant related genes	Relation type
FAM230A	TF binding region
FAM230A	CpG island

Extended variants
information (count: 99 )
Associated
traits (count: 228 )

Variant overlapped rSNPs/rCNVs (count:99 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs28641548	chr22:20699016-20699017	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs28517714	chr22:20699051-20699052	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs566160630	chr22:20699222-20699223	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs3966543	chr22:20699690-20699691	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs9605574	chr22:20700102-20700103	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs579287	chr22:20701769-20701770	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs9625802	chr22:20701824-20701825	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs472485	chr22:20702138-20702139	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs9620901	chr22:20702257-20702258	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs200855967	chr22:20702272-20702273	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs577606	chr22:20702628-20702629	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs9620904	chr22:20702787-20702788	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs670654	chr22:20702832-20702833	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs58407922	chr22:20702889-20702890	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs57325120	chr22:20703076-20703077	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs61625249	chr22:20703324-20703325	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs3984722	chr22:20703356-20703357	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs5992196	chr22:20703490-20703491	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs3984717	chr22:20703496-20703497	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs9614015	chr22:20703530-20703531	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs3984715	chr22:20703566-20703567	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs3984714	chr22:20703596-20703597	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs9614020	chr22:20703627-20703628	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs5993063	chr22:20703675-20703676	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs518868	chr22:20703685-20703686	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs199633272	chr22:20703772-20703773	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs4052354	chr22:20707007-20707008	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs542848143	chr22:20707019-20707020	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs2329337	chr22:20707021-20707022	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs200252764	chr22:20707028-20707029	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs528676041	chr22:20707052-20707053	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs4141818	chr22:20707076-20707077	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs147334439	chr22:20707081-20707082	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs4141817	chr22:20707097-20707098	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs2876820	chr22:20707110-20707111	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs542803476	chr22:20707112-20707113	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs2329338	chr22:20707123-20707124	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs571635591	chr22:20707129-20707130	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs4141816	chr22:20707187-20707188	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs112916507	chr22:20707191-20707192	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs554887243	chr22:20707192-20707193	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs537579768	chr22:20707204-20707205	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs377134786	chr22:20707234-20707235	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs201037125	chr22:20707262-20707263	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs376426152	chr22:20707272-20707273	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs2329339	chr22:20707284-20707285	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs112446297	chr22:20707311-20707312	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs112930875	chr22:20707321-20707322	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs111603322	chr22:20707329-20707330	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs368786015	chr22:20707333-20707334	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:228)

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	22102821	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
Acute lymphoblastic leukemia	19100363	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
Acute lymphoblastic leukemia	21248843	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
Glioblastoma multiforme	22286061	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
Acute lymphoblastic leukemia	20435627	CNVD
Autism	19521722	CNVD
Digeorge syndrome	19521722	CNVD
Autism	19955444	CNVD
Schizophrenia	19955444	CNVD
Mental retardation	17124404	CNVD
Tourette syndrome	20069037	CNVD
Williams-beuren syndrome	18553513	CNVD
Emphysema	19352772	CNVD
Schizophrenia	17160897	CNVD
Cancer	17160897	CNVD
Neuropsychiatric disorder	20069037	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
Cancer	17440070	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
22q11.2 deletion syndrome	22563040	CNVD
cardiac septal defect	19239688	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
Type 2 diabetes	21526130	CNVD
Ependymoma	20639864	CNVD
Cancer	20164919	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Neuroblastoma	18923191	CNVD
Prader-willi syndrome	20588305	CNVD
T-cell acute lymphoblastic leukemia	21980252	CNVD
22q11.22 microdeletion syndrome	19193630	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	17989066	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:20707000-20707400	Enhancers	HMEC	breast
2	chr22:20707600-20721200	Weak transcription	Right Atrium	heart

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