Variant report

Variant	esv21276
Chromosome Location	chr22:23771503-23774165
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:53)
CpG islands
(count:0)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:53 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr22:23773469-23773794	K562	blood:	n/a	n/a
2	CBX3	chr22:23773490-23773804	K562	blood:	n/a	n/a
3	CEBPB	chr22:23773733-23773799	HepG2	liver:	n/a	n/a
4	CHD2	chr22:23773688-23773725	HepG2	liver:	n/a	n/a
5	E2F6	chr22:23773501-23773825	K562	blood:	n/a	n/a
6	EP300	chr22:23773344-23774154	ECC-1	luminal epithelium:	n/a	n/a
7	ESR1	chr22:23773340-23773907	ECC-1	luminal epithelium:	n/a	chr22:23773599-23773614
8	ESR1	chr22:23773354-23773702	T-47D	breast:	n/a	chr22:23773599-23773614
9	ESR1	chr22:23773352-23773778	ECC-1	luminal epithelium:	n/a	chr22:23773599-23773614
10	ESR1	chr22:23773298-23773869	ECC-1	luminal epithelium:	n/a	chr22:23773599-23773614
11	FOXA1	chr22:23774152-23774547	HepG2	liver:	n/a	chr22:23774485-23774497
12	FOXP2	chr22:23773673-23774033	SK-N-MC	brain:	n/a	n/a
13	FOXP2	chr22:23773459-23774017	SK-N-MC	brain:	n/a	n/a
14	JUND	chr22:23773685-23773874	K562	blood:	n/a	n/a
15	MAFF	chr22:23773179-23773735	HepG2	liver:	n/a	n/a
16	MAFK	chr22:23773193-23773543	HepG2	liver:	n/a	n/a
17	MAFK	chr22:23773557-23773864	HepG2	liver:	n/a	n/a
18	MAX	chr22:23773542-23773839	NB4	blood:	n/a	n/a
19	MAX	chr22:23773417-23773971	ECC-1	luminal epithelium:	n/a	n/a
20	MAX	chr22:23773558-23773747	K562	blood:	n/a	n/a
21	MAX	chr22:23773394-23773878	K562	blood:	n/a	n/a
22	MAX	chr22:23773391-23773975	ECC-1	luminal epithelium:	n/a	n/a
23	MYC	chr22:23773611-23773723	K562	blood:	n/a	n/a
24	MYC	chr22:23773637-23773651	MCF-7	breast:	n/a	n/a
25	MYC	chr22:23773640-23773682	K562	blood:	n/a	n/a
26	MYC	chr22:23773590-23773624	MCF-7	breast:	n/a	n/a
27	NFIC	chr22:23773394-23774062	ECC-1	luminal epithelium:	n/a	n/a
28	NFIC	chr22:23773416-23774072	ECC-1	luminal epithelium:	n/a	n/a
29	POLR2A	chr22:23773075-23773167	K562	blood:	n/a	n/a
30	POLR2A	chr22:23773913-23773929	MCF10A-Er-Src	breast:	n/a	n/a
31	POLR2A	chr22:23773549-23773720	MCF-7	breast:	n/a	n/a
32	POLR2A	chr22:23773738-23773806	MCF-7	breast:	n/a	n/a
33	POLR2A	chr22:23772636-23772836	MCF10A-Er-Src	breast:	n/a	n/a
34	POLR2A	chr22:23773903-23773905	K562	blood:	n/a	n/a
35	POLR2A	chr22:23774024-23774272	MCF-7	breast:	n/a	n/a
36	POLR2A	chr22:23773722-23773725	MCF-7	breast:	n/a	n/a
37	POLR2A	chr22:23773631-23773636	MCF-7	breast:	n/a	n/a
38	POLR2A	chr22:23773646-23773650	MCF-7	breast:	n/a	n/a
39	POLR2A	chr22:23773323-23774200	SK-N-MC	brain:	n/a	n/a
40	POLR2A	chr22:23773062-23773103	MCF-7	breast:	n/a	n/a
41	POLR2A	chr22:23773059-23773091	MCF-7	breast:	n/a	n/a
42	POLR2A	chr22:23773564-23773628	MCF-7	breast:	n/a	n/a
43	POLR2A	chr22:23773538-23773861	K562	blood:	n/a	n/a
44	RCOR1	chr22:23773549-23773996	HepG2	liver:	n/a	n/a
45	RCOR1	chr22:23773693-23773699	K562	blood:	n/a	n/a
46	RFX5	chr22:23773691-23773694	HepG2	liver:	n/a	n/a
47	RXRA	chr22:23774134-23774483	HepG2	liver:	n/a	chr22:23774421-23774443
48	SETDB1	chr22:23771652-23772360	U2OS	brain:	n/a	n/a
49	SP1	chr22:23774051-23774512	HepG2	liver:	n/a	n/a
50	TCF12	chr22:23773395-23774083	ECC-1	luminal epithelium:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	chr22:23772556..23774777-chr7:1920577..1922999,2	K562	blood:
2	chr22:23769141..23771372-chr22:23773918..23775518,2	MCF-7	breast:
3	chr22:23771574..23774271-chr7:1915099..1916676,3	K562	blood:
4	chr22:23770302..23775681-chr7:1914349..1918723,8	MCF-7	breast:
5	chr22:23771574..23774271-chr7:1915104..1916676,2	K562	blood:
6	chr22:23767599..23770526-chr22:23770883..23773096,2	K562	blood:
7	chr22:23773942..23774594-chr7:1915027..1915991,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000234928	TF binding region

Extended variants
information (count: 208 )
Associated
traits (count: 213 )

Variant overlapped rSNPs/rCNVs (count:208 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556972823	chr22:23771525-23771526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs573591403	chr22:23771557-23771558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs542956954	chr22:23771560-23771561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs113640320	chr22:23771562-23771563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs552847716	chr22:23771563-23771564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs186624628	chr22:23771565-23771566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs79835574	chr22:23771567-23771568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs151284972	chr22:23771570-23771571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs200638233	chr22:23771585-23771586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs74511811	chr22:23771588-23771589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs550735301	chr22:23771598-23771599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs71320709	chr22:23771645-23771646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs140490761	chr22:23771649-23771650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs80022615	chr22:23771659-23771660	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs78127678	chr22:23771671-23771672	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs142759123	chr22:23771677-23771678	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs73155032	chr22:23771686-23771687	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs139944913	chr22:23771747-23771748	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs528008754	chr22:23771748-23771749	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs575439618	chr22:23771750-23771751	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs76154451	chr22:23771751-23771752	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs560905684	chr22:23771761-23771762	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs78267600	chr22:23771795-23771796	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs373997044	chr22:23771799-23771800	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs529556462	chr22:23771818-23771819	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs369527755	chr22:23771821-23771822	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs77232309	chr22:23771835-23771836	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs76654449	chr22:23771853-23771854	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs191418882	chr22:23771877-23771878	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs74646059	chr22:23771878-23771879	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs551432075	chr22:23771887-23771888	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs78305362	chr22:23771899-23771900	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs541327677	chr22:23771900-23771901	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs183878585	chr22:23771910-23771911	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs73155034	chr22:23771917-23771918	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs189904916	chr22:23771919-23771920	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs78070553	chr22:23771930-23771931	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs567656998	chr22:23771949-23771950	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs560690368	chr22:23771978-23771979	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs146949250	chr22:23771991-23771992	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs80343412	chr22:23772003-23772004	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs529476566	chr22:23772007-23772008	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs372997485	chr22:23772023-23772024	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs192820880	chr22:23772026-23772027	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs575402065	chr22:23772037-23772038	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs77434229	chr22:23772041-23772042	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs9624153	chr22:23772068-23772069	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs75381322	chr22:23772074-23772075	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs544369196	chr22:23772104-23772105	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs73155036	chr22:23772122-23772123	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:213)

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
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
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
Hodgkin''s lymphoma	17606441	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
low-grade B-cell lymphoma tumor	18367492	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	21248843	CNVD
Chronic myeloid leukemia	21384125	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Schizophrenia	17989066	CNVD
Cancer	20164919	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Li-fraumeni syndrome	18685109	CNVD
Breast cancer	20409316	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Cancer	19424424	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:72 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:23758000-23773000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr22:23759000-23773400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr22:23771400-23773600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr22:23771800-23773200	ZNF genes & repeats	Primary Natural Killer cells fromperipheralblood	blood
5	chr22:23772200-23772600	ZNF genes & repeats	Primary T cells fromperipheralblood	blood
6	chr22:23772200-23773200	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr22:23772200-23773400	Weak transcription	Primary T cells from cord blood	blood
8	chr22:23772600-23773000	Enhancers	Primary T cells fromperipheralblood	blood
9	chr22:23772600-23773000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
10	chr22:23772800-23775200	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr22:23773000-23773400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr22:23773000-23773400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
13	chr22:23773000-23773400	Enhancers	HepG2	liver
14	chr22:23773000-23773600	ZNF genes & repeats	Spleen	Spleen
15	chr22:23773000-23774000	Enhancers	Gastric	stomach
16	chr22:23773000-23774000	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
17	chr22:23773000-23774400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr22:23773000-23774400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
19	chr22:23773000-23775800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
20	chr22:23773000-23775800	Enhancers	Fetal Thymus	thymus
21	chr22:23773000-23776200	Enhancers	K562	blood
22	chr22:23773200-23773800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
23	chr22:23773200-23774000	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr22:23773200-23774200	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
25	chr22:23773200-23775400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
26	chr22:23773200-23775600	Enhancers	Primary T killer memory cells from peripheral blood	blood
27	chr22:23773400-23773800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr22:23773400-23773800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr22:23773400-23773800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
30	chr22:23773400-23773800	Flanking Bivalent TSS/Enh	Skeletal Muscle Female	skeletal muscle
31	chr22:23773400-23774000	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr22:23773400-23774000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
33	chr22:23773400-23774200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr22:23773400-23774200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr22:23773400-23774200	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr22:23773400-23774200	Strong transcription	Primary T cells from cord blood	blood
37	chr22:23773400-23774200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
38	chr22:23773400-23774200	Flanking Active TSS	HepG2	liver
39	chr22:23773400-23774400	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr22:23773400-23775600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr22:23773600-23773800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr22:23773600-23773800	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr22:23773600-23773800	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr22:23773600-23773800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
45	chr22:23773600-23773800	ZNF genes & repeats	Brain Cingulate Gyrus	brain
46	chr22:23773600-23773800	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
47	chr22:23773600-23773800	Enhancers	A549	lung
48	chr22:23773600-23774000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr22:23773600-23774000	Enhancers	H9 Cell Line	embryonic stem cell
50	chr22:23773600-23774000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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