Variant report

Variant	esv1830655
Chromosome Location	chr22:23472954-23479163
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:38)
CpG islands
(count:0)
Chromatin interactive
region (count:1)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:38 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr22:23473568-23473599	K562	blood:	n/a	n/a
2	ATF1	chr22:23474991-23475521	K562	blood:	n/a	n/a
3	ATF3	chr22:23474006-23474686	K562	blood:	n/a	n/a
4	BACH1	chr22:23478063-23478066	K562	blood:	n/a	n/a
5	CEBPB	chr22:23474461-23474635	HepG2	liver:	n/a	chr22:23474522-23474533
6	CEBPB	chr22:23474361-23474700	K562	blood:	n/a	chr22:23474522-23474533
7	CEBPB	chr22:23473212-23473425	K562	blood:	n/a	n/a
8	EBF1	chr22:23478222-23478604	GM12878	blood:	n/a	n/a
9	EBF1	chr22:23478198-23478592	GM12878	blood:	n/a	n/a
10	EBF1	chr22:23477884-23478144	GM12878	blood:	n/a	n/a
11	EBF1	chr22:23478079-23478093	GM12878	blood:	n/a	n/a
12	ELF1	chr22:23472915-23473377	K562	blood:	n/a	n/a
13	ELK1	chr22:23477978-23477988	GM12878	blood:	n/a	n/a
14	EP300	chr22:23477768-23478126	K562	blood:	n/a	n/a
15	EP300	chr22:23474470-23474612	K562	blood:	n/a	n/a
16	EP300	chr22:23475324-23475645	GM12878	blood:	n/a	n/a
17	GABPA	chr22:23476015-23476617	K562	blood:	n/a	n/a
18	IRF3	chr22:23477963-23477973	GM12878	blood:	n/a	n/a
19	MAX	chr22:23478037-23478167	GM12878	blood:	n/a	n/a
20	MYC	chr22:23474586-23474589	NB4	blood:	n/a	n/a
21	POLR2A	chr22:23478412-23478481	Hela-S3	cervix:	n/a	n/a
22	POLR2A	chr22:23478294-23478636	GM12878	blood:	n/a	n/a
23	POU2F2	chr22:23478211-23478663	GM12878	blood:	n/a	n/a
24	RCOR1	chr22:23474490-23474580	K562	blood:	n/a	n/a
25	RUNX3	chr22:23478712-23478972	GM12878	blood:	n/a	n/a
26	RUNX3	chr22:23477841-23478156	GM12878	blood:	n/a	n/a
27	SMC3	chr22:23474516-23474556	K562	blood:	n/a	n/a
28	SP2	chr22:23473707-23474706	K562	blood:	n/a	n/a
29	STAT5A	chr22:23474911-23475682	K562	blood:	n/a	n/a
30	STAT5A	chr22:23472683-23473157	K562	blood:	n/a	n/a
31	TBL1XR1	chr22:23474371-23474877	K562	blood:	n/a	n/a
32	TBP	chr22:23474471-23474501	K562	blood:	n/a	n/a
33	THAP1	chr22:23472892-23473281	K562	blood:	n/a	n/a
34	THAP1	chr22:23473847-23474368	K562	blood:	n/a	n/a
35	THAP1	chr22:23476122-23476583	K562	blood:	n/a	n/a
36	ZBTB7A	chr22:23476121-23476564	K562	blood:	n/a	n/a
37	ZC3H11A	chr22:23474133-23474214	K562	blood:	n/a	n/a
38	ZNF384	chr22:23477198-23477310	K562	blood:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr22:23301147..23302267-chr22:23472305..23473430,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IGLL1-6	chr22:23474917-23475187	NONHSAT083854

No data

Variant related genes	Relation type
ENSG00000221069	TF binding region
RTDR1	TF binding region
ENSG00000272019	TF binding region

Extended variants
information (count: 226 )
Associated
traits (count: 206 )

Variant overlapped rSNPs/rCNVs (count:226 , 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	rs9612237	chr22:23472954-23472955	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs576467407	chr22:23472982-23472983	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs190024795	chr22:23472999-23473000	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs574088321	chr22:23473006-23473007	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs375209524	chr22:23473008-23473009	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs545351213	chr22:23473059-23473060	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs5996469	chr22:23473060-23473061	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs559283428	chr22:23473109-23473110	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs74738584	chr22:23473123-23473124	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs77916443	chr22:23473145-23473146	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs144229068	chr22:23473149-23473150	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs181285202	chr22:23473161-23473162	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs4822357	chr22:23473231-23473232	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs73386679	chr22:23473250-23473251	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs74879436	chr22:23473259-23473260	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs546628810	chr22:23473297-23473298	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs566153469	chr22:23473317-23473318	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs542423022	chr22:23473343-23473344	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs148729824	chr22:23473354-23473355	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs552127554	chr22:23473393-23473394	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs572000247	chr22:23473435-23473436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs562177720	chr22:23473488-23473489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs142275896	chr22:23473491-23473492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs186331031	chr22:23473537-23473538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs554841440	chr22:23473577-23473578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs11309131	chr22:23473578-23473579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs573929376	chr22:23473584-23473585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs151264453	chr22:23473632-23473633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs553396388	chr22:23473721-23473722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs572973136	chr22:23473798-23473799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs544827002	chr22:23473804-23473805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs140619734	chr22:23473833-23473834	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs77136519	chr22:23473839-23473840	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs9612238	chr22:23473848-23473849	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs6003520	chr22:23473849-23473850	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs9620217	chr22:23473862-23473863	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs560767904	chr22:23473874-23473875	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs143348780	chr22:23473913-23473914	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs530230419	chr22:23473968-23473969	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs13055979	chr22:23474085-23474086	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs180730585	chr22:23474114-23474115	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs564542969	chr22:23474115-23474116	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs373643287	chr22:23474120-23474121	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs533368972	chr22:23474201-23474202	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs186372613	chr22:23474210-23474211	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs552017269	chr22:23474244-23474245	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs571826647	chr22:23474282-23474283	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs537791157	chr22:23474283-23474284	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs55638709	chr22:23474284-23474285	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs569719995	chr22:23474352-23474353	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:206)

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 cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:87 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:23453200-23484800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr22:23470600-23476400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr22:23470800-23483600	Weak transcription	Fetal Intestine Small	intestine
4	chr22:23471000-23474200	Weak transcription	HepG2	liver
5	chr22:23471000-23476200	Weak transcription	Fetal Stomach	stomach
6	chr22:23471200-23474000	Weak transcription	Pancreas	Pancrea
7	chr22:23471400-23476200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr22:23471400-23483600	Weak transcription	Brain Anterior Caudate	brain
9	chr22:23471400-23483600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr22:23471800-23473200	Weak transcription	Fetal Brain Male	brain
11	chr22:23472800-23473400	Strong transcription	Right Atrium	heart
12	chr22:23473000-23473200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr22:23473200-23473400	Enhancers	Fetal Brain Male	brain
14	chr22:23473400-23476200	Weak transcription	Right Atrium	heart
15	chr22:23474000-23474400	Enhancers	Skeletal Muscle Male	skeletal muscle
16	chr22:23474200-23474400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr22:23474200-23474400	Enhancers	HepG2	liver
18	chr22:23474400-23478200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr22:23476200-23476400	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr22:23476200-23476600	ZNF genes & repeats	Fetal Stomach	stomach
21	chr22:23476200-23478400	Strong transcription	Right Atrium	heart
22	chr22:23476200-23479600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
23	chr22:23476200-23483800	Enhancers	Primary T cells fromperipheralblood	blood
24	chr22:23476400-23476600	Enhancers	H1 Cell Line	embryonic stem cell
25	chr22:23476400-23476600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr22:23476600-23478200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr22:23476600-23483600	Weak transcription	Fetal Stomach	stomach
28	chr22:23476800-23477800	Weak transcription	H1 Cell Line	embryonic stem cell
29	chr22:23476800-23483800	Weak transcription	Right Ventricle	heart
30	chr22:23477000-23483800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
31	chr22:23477200-23477800	Enhancers	GM12878-XiMat	blood
32	chr22:23477800-23478000	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr22:23477800-23478000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
34	chr22:23477800-23478000	Flanking Active TSS	GM12878-XiMat	blood
35	chr22:23477800-23478200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr22:23477800-23478400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr22:23477800-23478400	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr22:23477800-23479000	Enhancers	Dnd41	blood
39	chr22:23477800-23479400	Enhancers	H1 Cell Line	embryonic stem cell
40	chr22:23477800-23479600	Enhancers	Primary T helper naive cells from peripheral blood	blood
41	chr22:23477800-23480000	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr22:23477800-23481400	Enhancers	Primary T killer memory cells from peripheral blood	blood
43	chr22:23477800-23481600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
44	chr22:23477800-23481800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
45	chr22:23477800-23483600	Enhancers	Primary T helper cells PMA-I stimulated	--
46	chr22:23477800-23484200	Enhancers	Primary B cells from cord blood	blood
47	chr22:23477800-23485000	Enhancers	Primary hematopoietic stem cells short term culture	blood
48	chr22:23478000-23478200	Enhancers	GM12878-XiMat	blood
49	chr22:23478000-23478400	Bivalent Enhancer	K562	blood
50	chr22:23478000-23479600	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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