Variant report

Variant	esv1850948
Chromosome Location	chr22:23806269-23829443
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:416)
CpG islands
(count:0)
Chromatin interactive
region (count:2)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:416 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr22:23810108-23810480	HepG2	liver:	n/a	n/a
2	BATF	chr22:23819974-23820417	GM12878	blood:	n/a	n/a
3	BATF	chr22:23815225-23815371	GM12878	blood:	n/a	n/a
4	BATF	chr22:23814219-23814432	GM12878	blood:	n/a	n/a
5	BATF	chr22:23827789-23828067	GM12878	blood:	n/a	n/a
6	BATF	chr22:23828883-23829053	GM12878	blood:	n/a	n/a
7	BATF	chr22:23817542-23817698	GM12878	blood:	n/a	n/a
8	BATF	chr22:23827783-23828060	GM12878	blood:	n/a	n/a
9	BCL11A	chr22:23814300-23814538	GM12878	blood:	n/a	n/a
10	BCL11A	chr22:23828873-23829061	GM12878	blood:	n/a	n/a
11	BCL11A	chr22:23814796-23814963	GM12878	blood:	n/a	n/a
12	BCL11A	chr22:23827775-23828065	GM12878	blood:	n/a	n/a
13	BCL11A	chr22:23820122-23820430	GM12878	blood:	n/a	n/a
14	BCL11A	chr22:23819918-23820441	GM12878	blood:	n/a	n/a
15	BCL11A	chr22:23827797-23828034	GM12878	blood:	n/a	n/a
16	BHLHE40	chr22:23828739-23829217	HepG2	liver:	n/a	n/a
17	BHLHE40	chr22:23810980-23811147	HepG2	liver:	n/a	n/a
18	BHLHE40	chr22:23810151-23810450	HepG2	liver:	n/a	n/a
19	BHLHE40	chr22:23810125-23810453	HepG2	liver:	n/a	n/a
20	BHLHE40	chr22:23810674-23810961	HepG2	liver:	n/a	n/a
21	BHLHE40	chr22:23827779-23827957	HepG2	liver:	n/a	n/a
22	CEBPB	chr22:23817889-23818034	HepG2	liver:	n/a	chr22:23817946-23817957
23	CEBPB	chr22:23814003-23814182	HepG2	liver:	n/a	n/a
24	CHD2	chr22:23825339-23825347	GM12878	blood:	n/a	n/a
25	CTCF	chr22:23809394-23809477	MCF-7	breast:	n/a	chr22:23809436-23809457 chr22:23809434-23809452
26	CTCF	chr22:23827801-23827897	MCF-7	breast:	n/a	n/a
27	CTCF	chr22:23828961-23829054	GM10266	blood:	n/a	n/a
28	CTCF	chr22:23827839-23827856	Pancreas_OC	pancreas:	n/a	n/a
29	CTCF	chr22:23828955-23829077	Medullo	brain:	n/a	n/a
30	CTCF	chr22:23809429-23809445	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr22:23827834-23827853	MCF-7	breast:	n/a	n/a
32	CTCF	chr22:23827867-23828004	GM10266	blood:	n/a	n/a
33	CTCF	chr22:23827867-23828008	GM20000	blood:	n/a	n/a
34	CTCF	chr22:23827856-23827895	MCF-7	breast:	n/a	n/a
35	CTCF	chr22:23827867-23828014	GM10248	blood:	n/a	n/a
36	CTCF	chr22:23828965-23829012	GM20000	blood:	n/a	n/a
37	CTCF	chr22:23827859-23827896	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr22:23827860-23827974	Gliobla	brain:	n/a	n/a
39	CTCF	chr22:23827858-23827895	GM12892	blood:	n/a	n/a
40	CTCF	chr22:23827868-23828006	Kidney_OC	kidney:	n/a	n/a
41	CTCF	chr22:23827867-23828013	LNCaP	prostate:	n/a	n/a
42	CTCF	chr22:23827858-23827957	GM19239	blood:	n/a	n/a
43	CTCF	chr22:23828962-23829049	LNCaP	prostate:	n/a	n/a
44	CTCF	chr22:23809426-23809441	MCF-7	breast:	n/a	n/a
45	CTCF	chr22:23828955-23829079	LNCaP	prostate:	n/a	n/a
46	CTCF	chr22:23828908-23829070	GM10248	blood:	n/a	n/a
47	CTCF	chr22:23827861-23827946	GM12891	blood:	n/a	n/a
48	CTCF	chr22:23827857-23827897	Pancreas_OC	pancreas:	n/a	n/a
49	CTCF	chr22:23827868-23828017	LNCaP	prostate:	n/a	n/a
50	CTCF	chr22:23827869-23828003	Medullo	brain:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr22:23804034..23806130-chr22:23807353..23810139,2	K562	blood:
2	chr22:23811117..23813674-chr22:23862180..23864787,2	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IGLL1-2	chr22:23812995-23813350	ENSG00000178248
2	lnc-IGLL1-2	chr22:23816064-23816125	ENSG00000178248
3	lnc-IGLL1-2	chr22:23815565-23815598	ENSG00000178248
4	lnc-IGLL1-2	chr22:23812502-23812523	ENSG00000178248
5	lnc-IGLL1-2	chr22:23825255-23825313	ENSG00000178248
6	lnc-IGLL1-2	chr22:23829066-23829093	ENSG00000178248
7	lnc-IGLL1-2	chr22:23824762-23824792	ENSG00000178248
8	lnc-IGLL1-2	chr22:23812181-23812224	ENSG00000178248
9	lnc-IGLL1-2	chr22:23822604-23822687	ENSG00000178248

No data

Variant related genes	Relation type
ENSG00000178248	TF binding region

Extended variants
information (count: 1086 )
Associated
traits (count: 214 )

Variant overlapped rSNPs/rCNVs (count:1086 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs376946607	chr22:23806332-23806333	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs181597741	chr22:23806412-23806413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs73389497	chr22:23806428-23806429	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs531050418	chr22:23806490-23806491	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs572043048	chr22:23806507-23806508	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs17615162	chr22:23806564-23806565	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs3057969	chr22:23806569-23806570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs200328384	chr22:23806571-23806572	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs200902242	chr22:23806572-23806573	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs2330420	chr22:23806573-23806574	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs551123912	chr22:23806589-23806590	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs186101063	chr22:23806598-23806599	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs190904731	chr22:23806600-23806601	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs546577383	chr22:23806624-23806625	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs140960977	chr22:23806625-23806626	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs201876491	chr22:23806627-23806628	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs370001847	chr22:23806628-23806629	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs566765690	chr22:23806647-23806648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs183449619	chr22:23806749-23806750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs62238840	chr22:23806781-23806782	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs568737427	chr22:23806811-23806812	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs535959489	chr22:23806836-23806837	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs537529738	chr22:23806906-23806907	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs554284070	chr22:23806970-23806971	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs574346720	chr22:23806973-23806974	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs540226523	chr22:23806983-23806984	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs375332862	chr22:23807008-23807009	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs567491035	chr22:23807020-23807021	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs143053308	chr22:23807029-23807030	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs565457737	chr22:23807079-23807080	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs6003727	chr22:23807100-23807101	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs531165361	chr22:23807128-23807129	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs544710174	chr22:23807142-23807143	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs114028250	chr22:23807174-23807175	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs553328892	chr22:23807175-23807176	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs529999280	chr22:23807199-23807200	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs112310483	chr22:23807304-23807305	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs546985431	chr22:23807308-23807309	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs566623382	chr22:23807368-23807369	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs73391303	chr22:23807446-23807447	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs568700468	chr22:23807511-23807512	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs537694012	chr22:23807522-23807523	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs538899601	chr22:23807525-23807526	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs187835400	chr22:23807527-23807528	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs568157183	chr22:23807561-23807562	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs12168060	chr22:23807581-23807582	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs9624182	chr22:23807603-23807604	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs576792860	chr22:23807632-23807633	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs545701577	chr22:23807639-23807640	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs190887487	chr22:23807671-23807672	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:214)

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
abnormal development	18461090	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:76 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:23792800-23812800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr22:23800400-23815200	Weak transcription	Primary B cells from cord blood	blood
3	chr22:23801600-23806800	Weak transcription	Ovary	ovary
4	chr22:23803200-23806800	Weak transcription	Thymus	Thymus
5	chr22:23804800-23806400	Weak transcription	Fetal Thymus	thymus
6	chr22:23806000-23808600	Enhancers	Dnd41	blood
7	chr22:23806400-23807200	Enhancers	Fetal Thymus	thymus
8	chr22:23806800-23807000	Enhancers	Ovary	ovary
9	chr22:23806800-23807000	Enhancers	Thymus	Thymus
10	chr22:23807000-23808200	Weak transcription	Ovary	ovary
11	chr22:23807200-23808000	Weak transcription	Fetal Thymus	thymus
12	chr22:23808000-23808800	Enhancers	Fetal Thymus	thymus
13	chr22:23808800-23813000	Weak transcription	A549	lung
14	chr22:23809400-23810600	Enhancers	HepG2	liver
15	chr22:23812200-23812400	Enhancers	HepG2	liver
16	chr22:23812800-23813000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr22:23813000-23814400	Enhancers	HepG2	liver
18	chr22:23813200-23813400	Enhancers	A549	lung
19	chr22:23813400-23814000	Enhancers	Fetal Brain Male	brain
20	chr22:23813800-23814200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr22:23814000-23815600	Enhancers	Primary B cells from peripheral blood	blood
22	chr22:23814000-23815600	Weak transcription	Fetal Brain Male	brain
23	chr22:23814200-23815400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
24	chr22:23815200-23815400	Enhancers	Primary B cells from cord blood	blood
25	chr22:23815400-23817000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
26	chr22:23815600-23816400	Enhancers	Fetal Brain Male	brain
27	chr22:23816000-23816200	Enhancers	Brain Cingulate Gyrus	brain
28	chr22:23816000-23817200	Enhancers	Brain Germinal Matrix	brain
29	chr22:23816200-23817000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr22:23816200-23817000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr22:23816200-23817000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr22:23816200-23817000	Enhancers	Brain Inferior Temporal Lobe	brain
33	chr22:23819600-23821400	Enhancers	Dnd41	blood
34	chr22:23820400-23820600	Enhancers	Small Intestine	intestine
35	chr22:23820400-23820800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
36	chr22:23820400-23820800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
37	chr22:23820600-23821200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
38	chr22:23821400-23825200	Weak transcription	Dnd41	blood
39	chr22:23823600-23824200	Enhancers	Fetal Thymus	thymus
40	chr22:23825200-23825800	Enhancers	Dnd41	blood
41	chr22:23825800-23827800	Weak transcription	Dnd41	blood
42	chr22:23826600-23827000	Bivalent Enhancer	HepG2	liver
43	chr22:23827800-23828000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
44	chr22:23827800-23828000	ZNF genes & repeats	Primary B cells from cord blood	blood
45	chr22:23827800-23828000	ZNF genes & repeats	Primary hematopoietic stem cells	blood
46	chr22:23827800-23828000	ZNF genes & repeats	Primary T killer naive cells fromperipheralblood	blood
47	chr22:23827800-23828000	ZNF genes & repeats	Primary mononuclear cells fromperipheralblood	Blood
48	chr22:23827800-23828000	Flanking Active TSS	Esophagus	oesophagus
49	chr22:23827800-23828000	Enhancers	Gastric	stomach
50	chr22:23827800-23828000	Enhancers	Pancreas	Pancrea

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