Variant report

Variant	nsv949546
Chromosome Location	chr2:133798832-133933491
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:133929022-133929350	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:133915573-133916005	HepG2	liver:	n/a	n/a
3	BATF	chr2:133892668-133892866	GM12878	blood:	n/a	n/a
4	BCL11A	chr2:133897445-133897743	H1-hESC	embryonic stem cell:	n/a	chr2:133897635-133897644 chr2:133897634-133897643
5	CEBPB	chr2:133819747-133820083	IMR90	lung:	n/a	n/a
6	CEBPB	chr2:133821436-133821710	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr2:133927616-133927977	MCF-7	breast:	n/a	chr2:133927787-133927798 chr2:133927786-133927797 chr2:133927788-133927797
8	CEBPB	chr2:133867421-133867772	IMR90	lung:	n/a	n/a
9	CEBPB	chr2:133867453-133867754	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr2:133884649-133884917	IMR90	lung:	n/a	chr2:133884879-133884890 chr2:133884881-133884890
11	CEBPB	chr2:133821434-133821709	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr2:133821440-133821725	IMR90	lung:	n/a	n/a
13	CEBPB	chr2:133927441-133927955	HepG2	liver:	n/a	chr2:133927787-133927798 chr2:133927786-133927797 chr2:133927788-133927797
14	CEBPB	chr2:133911651-133911930	IMR90	lung:	n/a	chr2:133911792-133911803
15	CEBPB	chr2:133923387-133923427	HepG2	liver:	n/a	n/a
16	CEBPB	chr2:133924811-133925135	IMR90	lung:	n/a	chr2:133924973-133924984
17	CEBPB	chr2:133911787-133911835	H1-hESC	embryonic stem cell:	n/a	chr2:133911792-133911803
18	CEBPB	chr2:133911637-133911956	Hela-S3	cervix:	n/a	chr2:133911792-133911803
19	CEBPB	chr2:133862229-133862527	A549	lung:	n/a	chr2:133862250-133862261 chr2:133862250-133862263
20	CEBPB	chr2:133836739-133836849	HepG2	liver:	n/a	n/a
21	CEBPB	chr2:133911620-133911962	HepG2	liver:	n/a	chr2:133911792-133911803
22	CEBPB	chr2:133927773-133927830	H1-hESC	embryonic stem cell:	n/a	chr2:133927787-133927798 chr2:133927786-133927797 chr2:133927788-133927797
23	CEBPB	chr2:133924821-133925142	HepG2	liver:	n/a	chr2:133924973-133924984
24	CEBPB	chr2:133808972-133809055	HepG2	liver:	n/a	chr2:133809011-133809022 chr2:133809010-133809023
25	CEBPB	chr2:133834945-133835142	IMR90	lung:	n/a	chr2:133835029-133835040 chr2:133835029-133835042
26	CEBPB	chr2:133862268-133862515	HepG2	liver:	n/a	n/a
27	CEBPB	chr2:133888428-133888781	IMR90	lung:	n/a	n/a
28	CEBPB	chr2:133927644-133927947	MCF-7	breast:	n/a	chr2:133927787-133927798 chr2:133927786-133927797 chr2:133927788-133927797
29	CEBPB	chr2:133820511-133821222	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr2:133862217-133862515	IMR90	lung:	n/a	chr2:133862250-133862261 chr2:133862250-133862263
31	CEBPB	chr2:133927438-133927952	A549	lung:	n/a	chr2:133927787-133927798 chr2:133927786-133927797 chr2:133927788-133927797
32	CEBPB	chr2:133897405-133897664	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr2:133884617-133885020	HepG2	liver:	n/a	chr2:133884879-133884890 chr2:133884881-133884890
34	CEBPB	chr2:133821472-133821768	MCF-7	breast:	n/a	n/a
35	CEBPB	chr2:133927649-133927954	IMR90	lung:	n/a	chr2:133927787-133927798 chr2:133927786-133927797 chr2:133927788-133927797
36	CEBPB	chr2:133911687-133911964	A549	lung:	n/a	chr2:133911792-133911803
37	CEBPB	chr2:133808875-133809161	IMR90	lung:	n/a	chr2:133809011-133809022 chr2:133809010-133809023
38	CEBPB	chr2:133911686-133911964	MCF-7	breast:	n/a	chr2:133911792-133911803
39	CEBPB	chr2:133836687-133836898	IMR90	lung:	n/a	n/a
40	CEBPB	chr2:133924899-133925138	A549	lung:	n/a	chr2:133924973-133924984
41	CEBPB	chr2:133927367-133927908	Hela-S3	cervix:	n/a	chr2:133927787-133927798 chr2:133927786-133927797 chr2:133927788-133927797
42	CEBPB	chr2:133833598-133833686	HepG2	liver:	n/a	chr2:133833672-133833683 chr2:133833611-133833622
43	CEBPB	chr2:133836703-133836940	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr2:133835003-133835062	HepG2	liver:	n/a	chr2:133835029-133835040 chr2:133835029-133835042
45	CEBPB	chr2:133888455-133888729	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr2:133819724-133820116	Hela-S3	cervix:	n/a	n/a
47	CHD2	chr2:133897550-133897741	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr2:133928780-133928930	GM12871	blood:	n/a	n/a
49	CTCF	chr2:133929120-133929270	HepG2	liver:	n/a	chr2:133929165-133929181 chr2:133929164-133929182 chr2:133929166-133929179 chr2:133929159-133929180
50	CTCF	chr2:133929080-133929230	AG04449	skin:	n/a	chr2:133929165-133929181 chr2:133929164-133929182 chr2:133929166-133929179 chr2:133929159-133929180

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:133834998-133835048	HEEpiC	esophagus:	n/a
2	chr2:133834998-133835048	HEEpiC	esophagus:	n/a
3	chr2:133923604-133923654	HCT-116	colon:	n/a
4	chr2:133868449-133868499	ProgFib	skin:	n/a
5	chr2:133868449-133868499	ovcar-3	ovarian:	n/a
6	chr2:133927261-133927311	ProgFib	skin:	n/a
7	chr2:133927261-133927311	HRE	kidney:	n/a
8	chr2:133834998-133835048	ovcar-3	ovarian:	n/a
9	chr2:133834998-133835048	PANC-1	pancreas:	n/a
10	chr2:133888263-133888313	K562	blood:	n/a
11	chr2:133927261-133927311	HPAEpiC	pulmonary alveolar:	n/a
12	chr2:133927261-133927311	IMR90	lung:	fetal
13	chr2:133868449-133868499	HRE	kidney:	n/a
14	chr2:133927261-133927311	HL-60	blood:	n/a
15	chr2:133834998-133835048	MCF-7	breast:	n/a
16	chr2:133927261-133927311	ovcar-3	ovarian:	n/a
17	chr2:133855847-133855897	HCT-116	colon:	n/a
18	chr2:133923604-133923654	MCF10A-Er-Src	breast:	n/a
19	chr2:133855847-133855897	H1-hESC	embryonic stem cell:	embryo
20	chr2:133923604-133923654	HNPCEpiC	eye:	n/a
21	chr2:133923604-133923654	CMK	blood:	n/a
22	chr2:133923604-133923654	HCM	heart:	n/a
23	chr2:133834998-133835048	NHBE	bronchial:	n/a
24	chr2:133834998-133835048	GM06990	blood:	n/a
25	chr2:133834998-133835048	BE2_C	brain:	n/a
26	chr2:133834998-133835048	SK-N-MC	brain:	n/a
27	chr2:133888263-133888313	NH-A	brain:	n/a
28	chr2:133888263-133888313	MCF10A-Er-Src	breast:	n/a
29	chr2:133834998-133835048	HCT-116	colon:	n/a
30	chr2:133834998-133835048	IMR90	lung:	fetal
31	chr2:133855847-133855897	GM12891	blood:	n/a
32	chr2:133868449-133868499	NB4	blood:	n/a
33	chr2:133923604-133923654	AG04450	lung:	fetal
34	chr2:133868449-133868499	PrEC	prostate:	n/a
35	chr2:133855847-133855897	SAEC	small airway:	n/a
36	chr2:133855847-133855897	AG10803	skin:	n/a
37	chr2:133868449-133868499	NH-A	brain:	n/a
38	chr2:133868449-133868499	PANC-1	pancreas:	n/a
39	chr2:133923604-133923654	PrEC	prostate:	n/a
40	chr2:133927261-133927311	HCF	heart:	n/a
41	chr2:133923604-133923654	GM12891	blood:	n/a
42	chr2:133923604-133923654	A549	lung:	n/a
43	chr2:133923604-133923654	BE2_C	brain:	n/a
44	chr2:133888263-133888313	HUVEC	blood vessel:	n/a
45	chr2:133855847-133855897	HAEpiC	amniotic membrane:	n/a
46	chr2:133855847-133855897	HepG2	liver:	n/a
47	chr2:133923604-133923654	Hepatocyte	liver:	n/a
48	chr2:133888263-133888313	Hela-S3	cervix:	n/a
49	chr2:133868449-133868499	PFSK-1	brain:	n/a
50	chr2:133834998-133835048	AG09309	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:133932748..133934866-chr2:133936195..133938875,2	MCF-7	breast:
2	chr2:133850084..133851752-chr2:133851774..133853791,2	MCF-7	breast:
3	chr2:133426257..133428194-chr2:133927974..133930516,2	MCF-7	breast:
4	chr2:133865556..133868534-chr2:133870878..133873548,2	K562	blood:
5	chr2:133434344..133435258-chr2:133928761..133929306,2	MCF-7	breast:
6	chr2:133828442..133830137-chr2:133831672..133833496,2	MCF-7	breast:
7	chr2:133836968..133839255-chr2:133840150..133841905,2	K562	blood:
8	chr2:133428080..133428797-chr2:133928852..133929367,2	MCF-7	breast:
9	chr2:133922662..133923182-chr20:49410946..49412118,12	MCF-7	breast:
10	chr2:133850171..133852489-chr2:133854080..133856768,2	MCF-7	breast:
11	chr2:133106208..133106974-chr2:133928762..133929385,2	MCF-7	breast:
12	chr2:133408307..133409298-chr2:133928740..133929575,3	MCF-7	breast:
13	chr2:133865556..133868534-chr2:133870878..133873548,2	K562	blood:
14	chr2:133795860..133798019-chr2:133803076..133805297,2	MCF-7	breast:
15	chr2:133907650..133909821-chr2:133911613..133914505,3	MCF-7	breast:
16	chr2:133831745..133832436-chr8:97637034..97637925,2	MCF-7	breast:
17	chr2:133850084..133851752-chr2:133851774..133853791,2	MCF-7	breast:
18	chr2:133826353..133828506-chr2:133839741..133842653,2	MCF-7	breast:
19	chr2:133427399..133430167-chr2:133804238..133806785,2	MCF-7	breast:
20	chr2:133811077..133813218-chr2:133838444..133841047,2	MCF-7	breast:
21	chr2:133304640..133305382-chr2:133928983..133929651,2	MCF-7	breast:
22	chr2:133850171..133852489-chr2:133854080..133856768,2	MCF-7	breast:
23	chr2:133828442..133830137-chr2:133831672..133833496,2	MCF-7	breast:
24	chr2:133907650..133909821-chr2:133911613..133914505,3	MCF-7	breast:
25	chr2:133427195..133430167-chr2:133854644..133856509,2	MCF-7	breast:
26	chr2:133836968..133839255-chr2:133840150..133841905,2	K562	blood:
27	chr2:133826353..133828506-chr2:133839741..133842653,2	MCF-7	breast:
28	chr2:133922662..133923182-chr20:49410992..49411888,4	MCF-7	breast:
29	chr2:133811077..133813218-chr2:133838444..133841047,2	MCF-7	breast:
30	chr2:133427423..133430466-chr2:133927227..133930556,4	MCF-7	breast:
31	chr2:133304031..133305145-chr2:133928594..133929580,6	MCF-7	breast:

Variant related genes	Relation type
ENSG00000269686	TF binding region
ENSG00000269686	CpG island
ENSG00000124243	chromatin interactions
ENSG00000150551	chromatin interactions

Extended variants
information (count: 5095 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:5095 , 50 per page) page: 1 2 3 4 5 6 7 ... 102

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7608610	chr2:133798832-133798833	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs183064506	chr2:133798854-133798855	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs151034115	chr2:133798880-133798881	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs141177613	chr2:133798902-133798903	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs573464381	chr2:133798910-133798911	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs572482733	chr2:133798912-133798913	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs187246117	chr2:133798917-133798918	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs75024454	chr2:133798931-133798932	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs528904179	chr2:133798960-133798961	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs550275836	chr2:133799088-133799089	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs192101905	chr2:133799107-133799108	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs111802195	chr2:133799120-133799121	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs184651841	chr2:133799127-133799128	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs531937718	chr2:133799260-133799261	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs550019086	chr2:133799263-133799264	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs567046372	chr2:133799281-133799282	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs539273235	chr2:133799292-133799293	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs187892408	chr2:133799303-133799304	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs78572672	chr2:133799325-133799326	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs566370032	chr2:133799332-133799333	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs565251888	chr2:133799338-133799339	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs79277721	chr2:133799365-133799366	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs16846041	chr2:133799388-133799389	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs567187654	chr2:133799389-133799390	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs193296408	chr2:133799456-133799457	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs566543628	chr2:133799462-133799463	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs557104501	chr2:133799468-133799469	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs575579010	chr2:133799556-133799557	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs185591600	chr2:133799579-133799580	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs189272849	chr2:133799581-133799582	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs34942366	chr2:133799607-133799608	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs573476827	chr2:133799656-133799657	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs180955991	chr2:133799678-133799679	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs369074440	chr2:133799715-133799716	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs372961571	chr2:133799767-133799768	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs184750925	chr2:133799798-133799799	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs75737590	chr2:133799815-133799816	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs79626300	chr2:133799895-133799896	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs114750783	chr2:133799915-133799916	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs556645013	chr2:133800058-133800059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs549155809	chr2:133800059-133800060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs530854933	chr2:133800116-133800117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs138744515	chr2:133800135-133800136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs16846080	chr2:133800200-133800201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs200684321	chr2:133800216-133800217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs527494307	chr2:133800220-133800221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs548738391	chr2:133800238-133800239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs956343	chr2:133800240-133800241	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs373983225	chr2:133800256-133800257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs556471286	chr2:133800280-133800281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Developmental delay	21147756	CNVD
Mental retardation	17621639	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Breast cancer	21509527	CNVD
Mental retardation	17124404	CNVD
Colorectal cancer	20459617	CNVD
Neuroticism	17667963	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	22522925	CNVD
Oral cancer	21386901	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:499 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:133797800-133800000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:133797800-133802200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr2:133798200-133801800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr2:133800000-133802200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr2:133801800-133802600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr2:133801800-133803000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr2:133802000-133802600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr2:133802000-133802600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr2:133802200-133802600	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr2:133802200-133802600	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr2:133802200-133802600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr2:133802200-133802600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr2:133802200-133802600	Enhancers	HMEC	breast
14	chr2:133802200-133802600	Enhancers	NHEK	skin
15	chr2:133802200-133803800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr2:133802400-133802600	Enhancers	Brain Hippocampus Middle	brain
17	chr2:133802400-133802600	Enhancers	Ovary	ovary
18	chr2:133802600-133803400	Weak transcription	Brain Hippocampus Middle	brain
19	chr2:133802600-133807200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr2:133802600-133811000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
21	chr2:133802600-133813600	Weak transcription	Ovary	ovary
22	chr2:133803000-133803400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr2:133803400-133803800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr2:133803400-133803800	Enhancers	Brain Hippocampus Middle	brain
25	chr2:133803600-133804000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr2:133803600-133804000	Enhancers	Brain Anterior Caudate	brain
27	chr2:133803800-133804000	Weak transcription	Brain Hippocampus Middle	brain
28	chr2:133803800-133807400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr2:133804000-133804400	Weak transcription	Brain Anterior Caudate	brain
30	chr2:133804000-133805000	Enhancers	Brain Hippocampus Middle	brain
31	chr2:133804400-133804600	Enhancers	Brain Anterior Caudate	brain
32	chr2:133804400-133805400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr2:133804600-133805000	Enhancers	Brain Substantia Nigra	brain
34	chr2:133804600-133811800	Weak transcription	Brain Anterior Caudate	brain
35	chr2:133805000-133805200	Weak transcription	Brain Substantia Nigra	brain
36	chr2:133805000-133811200	Weak transcription	Brain Hippocampus Middle	brain
37	chr2:133805200-133805600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr2:133805200-133805600	Enhancers	Brain Substantia Nigra	brain
39	chr2:133805400-133810600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr2:133805600-133805800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr2:133805600-133811800	Weak transcription	Brain Substantia Nigra	brain
42	chr2:133805800-133811200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr2:133807200-133807600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr2:133807400-133807600	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr2:133807600-133811000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr2:133807600-133812000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr2:133808800-133809000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr2:133809000-133809200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr2:133809000-133810800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr2:133810400-133812000	Enhancers	Cortex derived primary cultured neurospheres	brain

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