Variant report

Variant	nsv1004604
Chromosome Location	chr2:133658116-133761794
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:333)
CpG islands
(count:244)
Chromatin interactive
region (count:10)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:333 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL11A	chr2:133736400-133736844	GM12878	blood:	n/a	n/a
2	BCL11A	chr2:133711370-133711688	GM12878	blood:	n/a	n/a
3	BHLHE40	chr2:133694444-133694688	GM12878	blood:	n/a	n/a
4	BHLHE40	chr2:133727257-133727412	GM12878	blood:	n/a	n/a
5	BHLHE40	chr2:133736509-133736513	GM12878	blood:	n/a	n/a
6	CCNT2	chr2:133676696-133676742	K562	blood:	n/a	n/a
7	CEBPB	chr2:133748918-133749459	HepG2	liver:	n/a	chr2:133749057-133749070 chr2:133749057-133749068 chr2:133749056-133749073 chr2:133749057-133749070 chr2:133749057-133749070
8	CEBPB	chr2:133752193-133752411	HepG2	liver:	n/a	n/a
9	CEBPB	chr2:133735747-133736076	IMR90	lung:	n/a	n/a
10	CEBPB	chr2:133690013-133690065	HepG2	liver:	n/a	chr2:133690026-133690039 chr2:133690028-133690039 chr2:133690026-133690037
11	CEBPB	chr2:133698906-133699025	HepG2	liver:	n/a	chr2:133698963-133698974
12	CEBPB	chr2:133659336-133659561	HepG2	liver:	n/a	chr2:133659455-133659466
13	CEBPB	chr2:133689986-133690100	IMR90	lung:	n/a	chr2:133690026-133690039 chr2:133690028-133690039 chr2:133690026-133690037
14	CEBPB	chr2:133667172-133667379	IMR90	lung:	n/a	n/a
15	CEBPB	chr2:133665111-133665208	HepG2	liver:	n/a	chr2:133665148-133665159
16	CEBPB	chr2:133724477-133724677	IMR90	lung:	n/a	n/a
17	CEBPB	chr2:133748993-133749121	Hela-S3	cervix:	n/a	chr2:133749057-133749070 chr2:133749057-133749068 chr2:133749056-133749073 chr2:133749057-133749070 chr2:133749057-133749070
18	CEBPB	chr2:133748145-133748354	HepG2	liver:	n/a	chr2:133748232-133748243
19	CEBPB	chr2:133748166-133748284	A549	lung:	n/a	chr2:133748232-133748243
20	CEBPB	chr2:133752167-133752449	A549	lung:	n/a	n/a
21	CEBPB	chr2:133723194-133723273	HepG2	liver:	n/a	chr2:133723220-133723231
22	CEBPB	chr2:133752159-133752432	IMR90	lung:	n/a	n/a
23	CHD2	chr2:133737450-133737503	GM12878	blood:	n/a	n/a
24	CHD2	chr2:133711486-133711703	GM12878	blood:	n/a	n/a
25	CHD2	chr2:133736475-133736717	GM12878	blood:	n/a	n/a
26	CHD2	chr2:133694464-133694732	GM12878	blood:	n/a	n/a
27	CTCF	chr2:133688020-133688170	A549	lung:	n/a	n/a
28	CTCF	chr2:133688860-133689010	WERI-Rb-1	eye:	n/a	n/a
29	CTCF	chr2:133688906-133689030	GM19238	blood:	n/a	n/a
30	CTCF	chr2:133669530-133669869	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr2:133669578-133669848	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr2:133669700-133669850	HRPEpiC	eye:	n/a	n/a
33	CTCF	chr2:133681500-133681650	AG04450	lung:	n/a	n/a
34	CTCF	chr2:133714300-133714450	GM12866	blood:	n/a	n/a
35	CTCF	chr2:133669600-133669899	GM12878	blood:	n/a	n/a
36	CTCF	chr2:133669670-133669820	SK-N-SH_RA	brain:	n/a	n/a
37	CTCF	chr2:133669628-133669838	HepG2	liver:	n/a	n/a
38	CTCF	chr2:133669620-133669770	HVMF	connective:	n/a	n/a
39	CTCF	chr2:133660400-133660550	SK-N-SH_RA	brain:	n/a	n/a
40	CTCF	chr2:133669660-133669810	RPTEC	kidney:	n/a	n/a
41	CTCF	chr2:133669705-133669824	NHEK	skin:	n/a	n/a
42	CTCF	chr2:133689460-133689610	Caco-2	colon:	n/a	n/a
43	CTCF	chr2:133669651-133669851	Fibrobl	skin:	n/a	n/a
44	CTCF	chr2:133669720-133669870	WERI-Rb-1	eye:	n/a	n/a
45	CTCF	chr2:133669660-133669810	GM12874	blood:	n/a	n/a
46	CTCF	chr2:133669640-133669790	BJ	skin:	n/a	n/a
47	CTCF	chr2:133669672-133669786	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr2:133669600-133669750	AG10803	skin:	n/a	n/a
49	CTCF	chr2:133669710-133669800	Medullo	brain:	n/a	n/a
50	CTCF	chr2:133669660-133669810	WERI-Rb-1	eye:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:133733241-133733291	HCF	heart:	n/a
2	chr2:133672682-133672732	PrEC	prostate:	n/a
3	chr2:133695582-133695632	MCF10A-Er-Src	breast:	n/a
4	chr2:133670347-133670397	U87	brain:	n/a
5	chr2:133670347-133670397	CMK	blood:	n/a
6	chr2:133695582-133695632	HCF	heart:	n/a
7	chr2:133670347-133670397	MCF10A-Er-Src	breast:	n/a
8	chr2:133670347-133670397	HEEpiC	esophagus:	n/a
9	chr2:133733241-133733291	HNPCEpiC	eye:	n/a
10	chr2:133733241-133733291	GM12891	blood:	n/a
11	chr2:133672682-133672732	CMK	blood:	n/a
12	chr2:133670347-133670397	AG04449	skin:	fetal
13	chr2:133670347-133670397	SKMC	muscle:	n/a
14	chr2:133695582-133695632	GM06990	blood:	n/a
15	chr2:133695582-133695632	K562	blood:	n/a
16	chr2:133733241-133733291	ECC-1	luminal epithelium:	n/a
17	chr2:133670347-133670397	HRPEpiC	eye:	n/a
18	chr2:133670347-133670397	ECC-1	luminal epithelium:	n/a
19	chr2:133670347-133670397	SAEC	small airway:	n/a
20	chr2:133672682-133672732	AG09319	gingival:	n/a
21	chr2:133670347-133670397	AG09319	gingival:	n/a
22	chr2:133733241-133733291	PFSK-1	brain:	n/a
23	chr2:133695582-133695632	Caco-2	colon:	n/a
24	chr2:133733241-133733291	SAEC	small airway:	n/a
25	chr2:133672682-133672732	ovcar-3	ovarian:	n/a
26	chr2:133733241-133733291	HIPEpiC	eye:	n/a
27	chr2:133672682-133672732	K562	blood:	n/a
28	chr2:133695582-133695632	PFSK-1	brain:	n/a
29	chr2:133672682-133672732	SK-N-MC	brain:	n/a
30	chr2:133670347-133670397	AG04450	lung:	fetal
31	chr2:133733241-133733291	HMEC	breast:	n/a
32	chr2:133695582-133695632	HNPCEpiC	eye:	n/a
33	chr2:133670347-133670397	HEK293	kidney:	embryo
34	chr2:133670347-133670397	Hepatocyte	liver:	n/a
35	chr2:133695582-133695632	GM12878	blood:	n/a
36	chr2:133672682-133672732	BE2_C	brain:	n/a
37	chr2:133733241-133733291	SK-N-SH_RA	brain:	n/a
38	chr2:133695582-133695632	SK-N-SH_RA	brain:	n/a
39	chr2:133695582-133695632	HCT-116	colon:	n/a
40	chr2:133695582-133695632	HPAEpiC	pulmonary alveolar:	n/a
41	chr2:133695582-133695632	IMR90	lung:	fetal
42	chr2:133670347-133670397	T-47D	breast:	n/a
43	chr2:133695582-133695632	ovcar-3	ovarian:	n/a
44	chr2:133672682-133672732	MCF-7	breast:	n/a
45	chr2:133672682-133672732	NHDF-neo	bronchial:	n/a
46	chr2:133672682-133672732	HRE	kidney:	n/a
47	chr2:133672682-133672732	HCT-116	colon:	n/a
48	chr2:133670347-133670397	NT2-D1	testis:	n/a
49	chr2:133670347-133670397	AG09309	skin:	n/a
50	chr2:133733241-133733291	HCPEpiC	choroid plexus:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:133710364..133712250-chr2:133715085..133717070,2	K562	blood:
2	chr2:133737097..133739714-chr2:133742077..133743742,2	MCF-7	breast:
3	chr2:133722484..133724496-chr2:133727279..133729057,2	K562	blood:
4	chr2:133737230..133740275-chr2:133741296..133743711,3	K562	blood:
5	chr2:133661857..133663730-chr2:133665052..133667903,2	K562	blood:
6	chr2:133710364..133712250-chr2:133715085..133717070,2	K562	blood:
7	chr2:133737097..133739714-chr2:133742077..133743742,2	MCF-7	breast:
8	chr2:133661857..133663730-chr2:133665052..133667903,2	K562	blood:
9	chr2:133722484..133724496-chr2:133727279..133729057,2	K562	blood:
10	chr2:133737230..133740275-chr2:133741296..133743711,3	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPR39-3	chr2:133673130-133673224	ENSG00000233729.1
2	lnc-GPR39-12	chr2:133740284-133740478	ucscGeneNc_uc002ttu_1
3	lnc-GPR39-12	chr2:133741315-133741466	ucscGeneNc_uc002ttu_1
4	lnc-GPR39-3	chr2:133687452-133689067	ENSG00000233729.1
5	lnc-GPR39-12	chr2:133742958-133743083	ucscGeneNc_uc002ttu_1
6	lnc-GPR39-12	chr2:133742398-133742484	ucscGeneNc_uc002ttu_1

No data

Variant related genes	Relation type
ENSG00000228721	TF binding region
ENSG00000233729	TF binding region
ENSG00000228721	CpG island
ENSG00000233729	CpG island

Extended variants
information (count: 3719 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:3719 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566680501	chr2:133658127-133658128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs533926661	chr2:133658141-133658142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs186953699	chr2:133658205-133658206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs191696168	chr2:133658223-133658224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs182793062	chr2:133658274-133658275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs557353844	chr2:133658278-133658279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs575207065	chr2:133658301-133658302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs1989735	chr2:133658324-133658325	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs188315502	chr2:133658325-133658326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs192842072	chr2:133658404-133658405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs370930166	chr2:133658447-133658448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs185297191	chr2:133658448-133658449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs376244679	chr2:133658449-133658450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs190221903	chr2:133658450-133658451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs192658297	chr2:133658513-133658514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs547438374	chr2:133658550-133658551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs60142401	chr2:133658568-133658569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs142234514	chr2:133658608-133658609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs34169086	chr2:133658632-133658633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs551503696	chr2:133658654-133658655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs566617223	chr2:133658669-133658670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs34899378	chr2:133658679-133658680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs533862713	chr2:133658687-133658688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs115576757	chr2:133658772-133658773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs567327466	chr2:133658840-133658841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs538164110	chr2:133658967-133658968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs117832551	chr2:133658986-133658987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs566113718	chr2:133659017-133659018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs114440255	chr2:133659027-133659028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs539403812	chr2:133659028-133659029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs557728975	chr2:133659054-133659055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs573044138	chr2:133659127-133659128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs183608457	chr2:133659154-133659155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs562325918	chr2:133659155-133659156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs375653164	chr2:133659170-133659171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs574114310	chr2:133659192-133659193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs544896944	chr2:133659220-133659221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs372312622	chr2:133659272-133659273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs530195659	chr2:133659279-133659280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs533662417	chr2:133659358-133659359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs371797394	chr2:133659360-133659361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs551435026	chr2:133659387-133659388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs561368245	chr2:133659407-133659408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs560174928	chr2:133659489-133659490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs548439321	chr2:133659495-133659496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs146378156	chr2:133659564-133659565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs548775755	chr2:133659685-133659686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs375727240	chr2:133659752-133659753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs567470422	chr2:133659760-133659761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs537603805	chr2:133659766-133659767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

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

Chromatin state (count:400 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:133652600-133668400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr2:133657800-133660400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr2:133660000-133660400	Enhancers	Brain Substantia Nigra	brain
4	chr2:133660000-133660800	Enhancers	Brain Hippocampus Middle	brain
5	chr2:133660200-133660600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr2:133660400-133661400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr2:133661400-133668000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr2:133666400-133666600	Enhancers	Adipose Nuclei	Adipose
9	chr2:133666600-133667600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr2:133666600-133669200	Weak transcription	Adipose Nuclei	Adipose
11	chr2:133666800-133667600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr2:133667000-133667400	Enhancers	NHDF-Ad	bronchial
13	chr2:133667200-133681600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr2:133667600-133669600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr2:133667600-133673000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr2:133668000-133668800	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr2:133668400-133668600	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr2:133668600-133669400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr2:133668800-133676400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr2:133669200-133669800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr2:133669200-133669800	Enhancers	Adipose Nuclei	Adipose
22	chr2:133669200-133669800	Enhancers	Colon Smooth Muscle	Colon
23	chr2:133669200-133669800	Enhancers	Fetal Lung	lung
24	chr2:133669200-133670200	Enhancers	Fetal Stomach	stomach
25	chr2:133669400-133669800	Enhancers	Fetal Muscle Trunk	muscle
26	chr2:133669400-133669800	Enhancers	Lung	lung
27	chr2:133669400-133670200	Enhancers	Fetal Muscle Leg	muscle
28	chr2:133669400-133670400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr2:133669600-133670400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr2:133669800-133672600	Weak transcription	Adipose Nuclei	Adipose
31	chr2:133669800-133672800	Weak transcription	Fetal Lung	lung
32	chr2:133669800-133672800	Weak transcription	Fetal Muscle Trunk	muscle
33	chr2:133670200-133672800	Weak transcription	Fetal Muscle Leg	muscle
34	chr2:133670400-133672600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr2:133670400-133673400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr2:133672200-133673600	Enhancers	Fetal Heart	heart
37	chr2:133672600-133673000	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr2:133672600-133674200	Enhancers	Adipose Nuclei	Adipose
39	chr2:133672800-133673000	Enhancers	Lung	lung
40	chr2:133672800-133673200	Enhancers	Fetal Muscle Trunk	muscle
41	chr2:133672800-133673400	Enhancers	Fetal Muscle Leg	muscle
42	chr2:133672800-133673400	Enhancers	Right Atrium	heart
43	chr2:133672800-133674000	Enhancers	Fetal Lung	lung
44	chr2:133672800-133674000	Enhancers	Right Ventricle	heart
45	chr2:133672800-133674400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr2:133673000-133674200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr2:133673000-133681000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr2:133673200-133674000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr2:133673400-133674000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr2:133673600-133688800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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