Variant report

Variant	nsv875139
Chromosome Location	chr2:133777866-133929225
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	chr2:133915573-133916005	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:133929022-133929350	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	chr2:133820511-133821222	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr2:133884617-133885020	HepG2	liver:	n/a	chr2:133884879-133884890 chr2:133884881-133884890
7	CEBPB	chr2:133862229-133862527	A549	lung:	n/a	chr2:133862250-133862261 chr2:133862250-133862263
8	CEBPB	chr2:133821440-133821725	IMR90	lung:	n/a	n/a
9	CEBPB	chr2:133923387-133923427	HepG2	liver:	n/a	n/a
10	CEBPB	chr2:133927367-133927908	Hela-S3	cervix:	n/a	chr2:133927787-133927798 chr2:133927786-133927797 chr2:133927788-133927797
11	CEBPB	chr2:133911686-133911964	MCF-7	breast:	n/a	chr2:133911792-133911803
12	CEBPB	chr2:133797830-133798092	HepG2	liver:	n/a	chr2:133797955-133797966
13	CEBPB	chr2:133862268-133862515	HepG2	liver:	n/a	n/a
14	CEBPB	chr2:133782590-133782918	IMR90	lung:	n/a	n/a
15	CEBPB	chr2:133911637-133911956	Hela-S3	cervix:	n/a	chr2:133911792-133911803
16	CEBPB	chr2:133792922-133793196	HepG2	liver:	n/a	n/a
17	CEBPB	chr2:133927616-133927977	MCF-7	breast:	n/a	chr2:133927787-133927798 chr2:133927786-133927797 chr2:133927788-133927797
18	CEBPB	chr2:133797791-133798131	Hela-S3	cervix:	n/a	chr2:133797955-133797966
19	CEBPB	chr2:133888455-133888729	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr2:133862217-133862515	IMR90	lung:	n/a	chr2:133862250-133862261 chr2:133862250-133862263
21	CEBPB	chr2:133835003-133835062	HepG2	liver:	n/a	chr2:133835029-133835040 chr2:133835029-133835042
22	CEBPB	chr2:133797903-133797994	H1-hESC	embryonic stem cell:	n/a	chr2:133797955-133797966
23	CEBPB	chr2:133792934-133793194	IMR90	lung:	n/a	n/a
24	CEBPB	chr2:133792877-133793234	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr2:133819724-133820116	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr2:133833598-133833686	HepG2	liver:	n/a	chr2:133833672-133833683 chr2:133833611-133833622
27	CEBPB	chr2:133792973-133793173	A549	lung:	n/a	n/a
28	CEBPB	chr2:133836739-133836849	HepG2	liver:	n/a	n/a
29	CEBPB	chr2:133867453-133867754	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr2:133897405-133897664	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr2:133927649-133927954	IMR90	lung:	n/a	chr2:133927787-133927798 chr2:133927786-133927797 chr2:133927788-133927797
32	CEBPB	chr2:133821434-133821709	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr2:133924821-133925142	HepG2	liver:	n/a	chr2:133924973-133924984
34	CEBPB	chr2:133884649-133884917	IMR90	lung:	n/a	chr2:133884879-133884890 chr2:133884881-133884890
35	CEBPB	chr2:133927438-133927952	A549	lung:	n/a	chr2:133927787-133927798 chr2:133927786-133927797 chr2:133927788-133927797
36	CEBPB	chr2:133927441-133927955	HepG2	liver:	n/a	chr2:133927787-133927798 chr2:133927786-133927797 chr2:133927788-133927797
37	CEBPB	chr2:133836703-133836940	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr2:133834945-133835142	IMR90	lung:	n/a	chr2:133835029-133835040 chr2:133835029-133835042
39	CEBPB	chr2:133867421-133867772	IMR90	lung:	n/a	n/a
40	CEBPB	chr2:133821436-133821710	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr2:133819747-133820083	IMR90	lung:	n/a	n/a
42	CEBPB	chr2:133911687-133911964	A549	lung:	n/a	chr2:133911792-133911803
43	CEBPB	chr2:133797821-133798110	A549	lung:	n/a	chr2:133797955-133797966
44	CEBPB	chr2:133836687-133836898	IMR90	lung:	n/a	n/a
45	CEBPB	chr2:133924899-133925138	A549	lung:	n/a	chr2:133924973-133924984
46	CEBPB	chr2:133808972-133809055	HepG2	liver:	n/a	chr2:133809011-133809022 chr2:133809010-133809023
47	CEBPB	chr2:133821472-133821768	MCF-7	breast:	n/a	n/a
48	CEBPB	chr2:133927773-133927830	H1-hESC	embryonic stem cell:	n/a	chr2:133927787-133927798 chr2:133927786-133927797 chr2:133927788-133927797
49	CEBPB	chr2:133911651-133911930	IMR90	lung:	n/a	chr2:133911792-133911803
50	CEBPB	chr2:133927644-133927947	MCF-7	breast:	n/a	chr2:133927787-133927798 chr2:133927786-133927797 chr2:133927788-133927797

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:133927261-133927311	SKMC	muscle:	n/a
2	chr2:133927261-133927311	SKMC	muscle:	n/a
3	chr2:133855847-133855897	AoSMC	blood vessel:	n/a
4	chr2:133888263-133888313	HUVEC	blood vessel:	n/a
5	chr2:133888263-133888313	GM12891	blood:	n/a
6	chr2:133888263-133888313	BE2_C	brain:	n/a
7	chr2:133923604-133923654	H1-hESC	embryonic stem cell:	embryo
8	chr2:133855847-133855897	NB4	blood:	n/a
9	chr2:133923604-133923654	Hepatocyte	liver:	n/a
10	chr2:133923604-133923654	SK-N-SH_RA	brain:	n/a
11	chr2:133888263-133888313	A549	lung:	n/a
12	chr2:133923604-133923654	HCM	heart:	n/a
13	chr2:133923604-133923654	PrEC	prostate:	n/a
14	chr2:133923604-133923654	AG09309	skin:	n/a
15	chr2:133855847-133855897	HCF	heart:	n/a
16	chr2:133923604-133923654	NH-A	brain:	n/a
17	chr2:133855847-133855897	PrEC	prostate:	n/a
18	chr2:133888263-133888313	H1-hESC	embryonic stem cell:	embryo
19	chr2:133923604-133923654	ovcar-3	ovarian:	n/a
20	chr2:133927261-133927311	AG04450	lung:	fetal
21	chr2:133927261-133927311	GM06990	blood:	n/a
22	chr2:133927261-133927311	SAEC	small airway:	n/a
23	chr2:133855847-133855897	LNCaP	prostate:	n/a
24	chr2:133927261-133927311	A549	lung:	n/a
25	chr2:133855847-133855897	AG09319	gingival:	n/a
26	chr2:133923604-133923654	A549	lung:	n/a
27	chr2:133868449-133868499	A549	lung:	n/a
28	chr2:133834998-133835048	AoSMC	blood vessel:	n/a
29	chr2:133927261-133927311	HAEpiC	amniotic membrane:	n/a
30	chr2:133927261-133927311	T-47D	breast:	n/a
31	chr2:133834998-133835048	PANC-1	pancreas:	n/a
32	chr2:133868449-133868499	MCF-7	breast:	n/a
33	chr2:133868449-133868499	ECC-1	luminal epithelium:	n/a
34	chr2:133855847-133855897	NT2-D1	testis:	n/a
35	chr2:133927261-133927311	HL-60	blood:	n/a
36	chr2:133927261-133927311	AG09319	gingival:	n/a
37	chr2:133868449-133868499	HMEC	breast:	n/a
38	chr2:133868449-133868499	U87	brain:	n/a
39	chr2:133923604-133923654	NB4	blood:	n/a
40	chr2:133855847-133855897	K562	blood:	n/a
41	chr2:133927261-133927311	RPTEC	kidney:	n/a
42	chr2:133923604-133923654	RPTEC	kidney:	n/a
43	chr2:133834998-133835048	HCPEpiC	choroid plexus:	n/a
44	chr2:133868449-133868499	HRCEpiC	kidney:	n/a
45	chr2:133923604-133923654	HRE	kidney:	n/a
46	chr2:133888263-133888313	U87	brain:	n/a
47	chr2:133888263-133888313	NT2-D1	testis:	n/a
48	chr2:133927261-133927311	ECC-1	luminal epithelium:	n/a
49	chr2:133923604-133923654	AG04450	lung:	fetal
50	chr2:133834998-133835048	NHDF-neo	bronchial:	n/a

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

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

Extended variants
information (count: 5751 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:5751 , 50 per page) page: 1 2 3 4 5 6 7 ... 116

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6725800	chr2:133777866-133777867	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs554743121	chr2:133777882-133777883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs373393231	chr2:133777897-133777898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs576609669	chr2:133777923-133777924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs4954022	chr2:133777989-133777990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs142152378	chr2:133778006-133778007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs72996838	chr2:133778113-133778114	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs532647285	chr2:133778170-133778171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs151172896	chr2:133778181-133778182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs186461612	chr2:133778242-133778243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs572608883	chr2:133778287-133778288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs149135434	chr2:133778320-133778321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs16845619	chr2:133778324-133778325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs569644118	chr2:133778325-133778326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs530783350	chr2:133778356-133778357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs140178546	chr2:133778472-133778473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs552042388	chr2:133778476-133778477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs570734016	chr2:133778483-133778484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs571422005	chr2:133778508-133778509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs114796559	chr2:133778513-133778514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs554232007	chr2:133778522-133778523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs538847803	chr2:133778529-133778530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs566105859	chr2:133778539-133778540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs370143492	chr2:133778556-133778557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs180952815	chr2:133778565-133778566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs554074673	chr2:133778628-133778629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs373352784	chr2:133778639-133778640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs368008815	chr2:133778715-133778716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs150303748	chr2:133778758-133778759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs186363821	chr2:133778781-133778782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs115255988	chr2:133778782-133778783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs370784231	chr2:133778807-133778808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs80204952	chr2:133778811-133778812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs559604807	chr2:133778843-133778844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs35615951	chr2:133778855-133778856	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs144889778	chr2:133778874-133778875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs563402673	chr2:133778881-133778882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs370761588	chr2:133778888-133778889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs536627037	chr2:133778912-133778913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs530482380	chr2:133779008-133779009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs552364974	chr2:133779019-133779020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs564099852	chr2:133779021-133779022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs528274474	chr2:133779086-133779087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs546948467	chr2:133779096-133779097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs191311203	chr2:133779200-133779201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs201505635	chr2:133779208-133779209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs116558895	chr2:133779227-133779228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs76121294	chr2:133779244-133779245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs570140204	chr2:133779251-133779252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs576470843	chr2:133779257-133779258	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:519 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:133759800-133784400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:133762600-133797200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr2:133779800-133780200	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr2:133779800-133780400	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr2:133780200-133783800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr2:133783000-133783200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr2:133783200-133784400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr2:133783800-133784600	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr2:133784000-133784600	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr2:133784000-133784600	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr2:133784200-133784800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr2:133784400-133784600	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr2:133784400-133784600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr2:133784400-133784800	Enhancers	H1 Cell Line	embryonic stem cell
15	chr2:133784400-133784800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr2:133784400-133784800	Enhancers	H9 Cell Line	embryonic stem cell
17	chr2:133784400-133784800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr2:133784600-133787600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr2:133784600-133789200	Weak transcription	HUES6 Cell Line	embryonic stem cell
20	chr2:133784800-133789000	Weak transcription	H1 Cell Line	embryonic stem cell
21	chr2:133784800-133789000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr2:133787600-133789200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr2:133787800-133788000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr2:133788000-133788600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr2:133788600-133789400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr2:133789000-133789400	Enhancers	H1 Cell Line	embryonic stem cell
27	chr2:133789000-133789600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr2:133789200-133789800	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr2:133789200-133790400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr2:133797000-133797800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr2:133797200-133797800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr2:133797800-133798200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr2:133797800-133800000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr2:133797800-133802200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr2:133798200-133801800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr2:133800000-133802200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr2:133801800-133802600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr2:133801800-133803000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr2:133802000-133802600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr2:133802000-133802600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr2:133802200-133802600	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr2:133802200-133802600	Enhancers	Breast Myoepithelial Primary Cells	Breast
43	chr2:133802200-133802600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr2:133802200-133802600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr2:133802200-133802600	Enhancers	HMEC	breast
46	chr2:133802200-133802600	Enhancers	NHEK	skin
47	chr2:133802200-133803800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr2:133802400-133802600	Enhancers	Brain Hippocampus Middle	brain
49	chr2:133802400-133802600	Enhancers	Ovary	ovary
50	chr2:133802600-133803400	Weak transcription	Brain Hippocampus Middle	brain

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