Variant report

Variant	nsv431757
Chromosome Location	chr2:140931289-141098020
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:302)
CpG islands
(count:61)
Chromatin interactive
region (count:9)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:302 , 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	BACH1	chr2:141045829-141046086	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr2:140945882-140946199	IMR90	lung:	n/a	n/a
3	CEBPB	chr2:140970085-140970250	A549	lung:	n/a	chr2:140970145-140970154
4	CEBPB	chr2:141006315-141006515	A549	lung:	n/a	chr2:141006393-141006404 chr2:141006394-141006405
5	CEBPB	chr2:141059497-141059710	A549	lung:	n/a	chr2:141059596-141059607
6	CEBPB	chr2:141015270-141015702	HepG2	liver:	n/a	chr2:141015372-141015383 chr2:141015618-141015631 chr2:141015374-141015385
7	CEBPB	chr2:141067348-141067570	HepG2	liver:	n/a	chr2:141067445-141067454 chr2:141067445-141067454
8	CEBPB	chr2:140972064-140972178	HepG2	liver:	n/a	n/a
9	CEBPB	chr2:141067429-141067576	A549	lung:	n/a	chr2:141067445-141067454 chr2:141067445-141067454
10	CEBPB	chr2:140955696-140955802	A549	lung:	n/a	n/a
11	CEBPB	chr2:141067332-141067618	IMR90	lung:	n/a	chr2:141067445-141067454 chr2:141067445-141067454
12	CEBPB	chr2:141059459-141059780	HepG2	liver:	n/a	chr2:141059596-141059607
13	CEBPB	chr2:141060359-141060467	HepG2	liver:	n/a	n/a
14	CEBPB	chr2:140969981-140970326	HepG2	liver:	n/a	chr2:140970145-140970154
15	CEBPB	chr2:141006267-141006547	HepG2	liver:	n/a	chr2:141006393-141006404 chr2:141006394-141006405
16	CEBPB	chr2:141015040-141015528	A549	lung:	n/a	chr2:141015372-141015383 chr2:141015374-141015385
17	CHD2	chr2:141040648-141040666	H1-hESC	embryonic stem cell:	n/a	n/a
18	CREB1	chr2:140944679-140945049	K562	blood:	n/a	n/a
19	CTCF	chr2:140935926-140935973	Lung_OC	lung:	n/a	n/a
20	CTCF	chr2:141000551-141000767	MCF-7	breast:	n/a	n/a
21	CTCF	chr2:141000620-141000770	HMEC	breast:	n/a	n/a
22	CTCF	chr2:141000600-141000750	SK-N-SH_RA	brain:	n/a	n/a
23	CTCF	chr2:141000560-141000710	HBMEC	blood vessel:	n/a	n/a
24	CTCF	chr2:140985145-140985194	GM20000	blood:	n/a	n/a
25	CTCF	chr2:141000680-141000830	HepG2	liver:	n/a	n/a
26	CTCF	chr2:141000540-141000690	HepG2	liver:	n/a	n/a
27	CTCF	chr2:141000600-141000750	HMEC	breast:	n/a	n/a
28	CTCF	chr2:141000620-141000770	HRE	kidney:	n/a	n/a
29	CTCF	chr2:141090200-141090350	HPF	lung:	n/a	n/a
30	CTCF	chr2:141070518-141070545	GM20000	blood:	n/a	n/a
31	CTCF	chr2:141000554-141000837	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr2:141000573-141000762	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr2:141000580-141000730	MCF-7	breast:	n/a	n/a
34	CTCF	chr2:141000600-141000750	Caco-2	colon:	n/a	n/a
35	CTCF	chr2:141000568-141000741	MCF-7	breast:	n/a	n/a
36	CTCF	chr2:141000580-141000730	HMF	breast:	n/a	n/a
37	CTCF	chr2:141000520-141000670	AG04450	lung:	n/a	n/a
38	CTCF	chr2:141000580-141000730	HEK293	kidney:	n/a	n/a
39	CTCF	chr2:141044823-141044854	Lung_OC	lung:	n/a	n/a
40	CTCF	chr2:140971493-140971536	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr2:140939000-140939078	LNCaP	prostate:	n/a	chr2:140939009-140939030 chr2:140939014-140939032 chr2:140939021-140939029
42	CTCF	chr2:141000500-141000650	RPTEC	kidney:	n/a	n/a
43	CTCF	chr2:141000588-141000723	Gliobla	brain:	n/a	n/a
44	CTCF	chr2:141000600-141000750	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr2:141000580-141000730	HPAF	blood vessel:	n/a	n/a
46	CTCF	chr2:141000600-141000750	BE2_C	brain:	n/a	n/a
47	CTCF	chr2:141000514-141000804	HepG2	liver:	n/a	n/a
48	CTCF	chr2:140934115-140934163	GM10266	blood:	n/a	n/a
49	CTCF	chr2:141000600-141000750	MCF-7	breast:	n/a	n/a
50	CTCF	chr2:141000500-141000650	HCPEpiC	choroid plexus:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:141039361-141039411	HEEpiC	esophagus:	n/a
2	chr2:141039361-141039411	HMEC	breast:	n/a
3	chr2:141039361-141039411	SK-N-SH_RA	brain:	n/a
4	chr2:141039361-141039411	HL-60	blood:	n/a
5	chr2:141039361-141039411	GM12891	blood:	n/a
6	chr2:141039361-141039411	PANC-1	pancreas:	n/a
7	chr2:141039361-141039411	HNPCEpiC	eye:	n/a
8	chr2:141039361-141039411	NHBE	bronchial:	n/a
9	chr2:141039361-141039411	T-47D	breast:	n/a
10	chr2:141039361-141039411	PrEC	prostate:	n/a
11	chr2:141039361-141039411	BJ	skin:	n/a
12	chr2:141039361-141039411	HRE	kidney:	n/a
13	chr2:141039361-141039411	Hepatocyte	liver:	n/a
14	chr2:141039361-141039411	HCT-116	colon:	n/a
15	chr2:141039361-141039411	HRCEpiC	kidney:	n/a
16	chr2:141039361-141039411	Caco-2	colon:	n/a
17	chr2:141039361-141039411	SAEC	small airway:	n/a
18	chr2:141039361-141039411	HAEpiC	amniotic membrane:	n/a
19	chr2:141039361-141039411	K562	blood:	n/a
20	chr2:141039361-141039411	GM06990	blood:	n/a
21	chr2:141039361-141039411	IMR90	lung:	fetal
22	chr2:141039361-141039411	A549	lung:	n/a
23	chr2:141039361-141039411	AoSMC	blood vessel:	n/a
24	chr2:141039361-141039411	HEK293	kidney:	embryo
25	chr2:141039361-141039411	NH-A	brain:	n/a
26	chr2:141039361-141039411	SKMC	muscle:	n/a
27	chr2:141039361-141039411	AG04449	skin:	fetal
28	chr2:141039361-141039411	LNCaP	prostate:	n/a
29	chr2:141039361-141039411	MCF-7	breast:	n/a
30	chr2:141039361-141039411	ECC-1	luminal epithelium:	n/a
31	chr2:141039361-141039411	NB4	blood:	n/a
32	chr2:141039361-141039411	H1-hESC	embryonic stem cell:	embryo
33	chr2:141039361-141039411	AG09309	skin:	n/a
34	chr2:141039361-141039411	Jurkat	blood:	n/a
35	chr2:141039361-141039411	HIPEpiC	eye:	n/a
36	chr2:141039361-141039411	HUVEC	blood vessel:	n/a
37	chr2:141039361-141039411	ProgFib	skin:	n/a
38	chr2:141039361-141039411	HCF	heart:	n/a
39	chr2:141039361-141039411	PFSK-1	brain:	n/a
40	chr2:141039361-141039411	SK-N-MC	brain:	n/a
41	chr2:141039361-141039411	RPTEC	kidney:	n/a
42	chr2:141039361-141039411	MCF10A-Er-Src	breast:	n/a
43	chr2:141039361-141039411	HRPEpiC	eye:	n/a
44	chr2:141039361-141039411	AG09319	gingival:	n/a
45	chr2:141039361-141039411	HCM	heart:	n/a
46	chr2:141039361-141039411	HPAEpiC	pulmonary alveolar:	n/a
47	chr2:141039361-141039411	NT2-D1	testis:	n/a
48	chr2:141039361-141039411	Hela-S3	cervix:	n/a
49	chr2:141039361-141039411	BE2_C	brain:	n/a
50	chr2:141039361-141039411	AG04450	lung:	fetal

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

No.	Distal block	Cell Line	Cell type
1	chr2:141030971..141033718-chr2:141035593..141037981,2	MCF-7	breast:
2	chr2:140987688..140989881-chr2:140993819..140996733,2	K562	blood:
3	chr2:140988006..140990694-chr2:140993986..140995615,2	MCF-7	breast:
4	chr2:141030971..141033718-chr2:141035593..141037981,2	MCF-7	breast:
5	chr2:140989005..140991875-chr2:140992469..140995241,2	MCF-7	breast:
6	chr2:140987688..140989881-chr2:140993819..140996733,2	K562	blood:
7	chr2:141096050..141098665-chr2:141100590..141102243,2	MCF-7	breast:
8	chr2:140988006..140990694-chr2:140993986..140995615,2	MCF-7	breast:
9	chr2:140989005..140991875-chr2:140992469..140995241,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRP1B-6	chr2:140977233-140977937	NONHSAT074700
2	lnc-LRP1B-5	chr2:140978153-140979054	NONHSAT074701
3	lnc-LRP1B-7	chr2:140974566-140974808	NONHSAT074699
4	lnc-LRP1B-6	chr2:140975220-140975526	NONHSAT074700

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	LRP1B	hsa-miR-335-5p	chr2:140989321-140989343

Variant related genes	Relation type
MTND1P27	TF binding region
ENSG00000227149	TF binding region
MTND2P19	TF binding region
LRP1B	TF binding region
MTND1P27	CpG island
ENSG00000227149	CpG island
MTND2P19	CpG island
LRP1B	CpG island

Extended variants
information (count: 2137 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:2137 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs569446418	chr2:140931411-140931412	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs145376553	chr2:140931447-140931448	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs558232932	chr2:140931456-140931457	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs183718420	chr2:140931466-140931467	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs536899228	chr2:140931469-140931470	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs534568265	chr2:140931475-140931476	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs74881161	chr2:140931482-140931483	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs574539297	chr2:140931492-140931493	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs114877910	chr2:140931511-140931512	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs527713117	chr2:140931529-140931530	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs188662359	chr2:140931531-140931532	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs78729930	chr2:140931546-140931547	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs541313785	chr2:140931562-140931563	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs545531800	chr2:140931589-140931590	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs538266241	chr2:140931595-140931596	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs191552213	chr2:140931596-140931597	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs574452797	chr2:140931615-140931616	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs139557517	chr2:140931616-140931617	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs547768091	chr2:140931621-140931622	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs549381510	chr2:140931622-140931623	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs541956333	chr2:140931638-140931639	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs10197564	chr2:140931650-140931651	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs10205678	chr2:140931667-140931668	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs145137696	chr2:140931681-140931682	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs538306392	chr2:140931686-140931687	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs552253858	chr2:140931704-140931705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs563190381	chr2:140931777-140931778	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs560221491	chr2:140934407-140934408	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs16843460	chr2:140934415-140934416	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs79480176	chr2:140934418-140934419	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs568724990	chr2:140934424-140934425	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs182420910	chr2:140934470-140934471	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs553167004	chr2:140934481-140934482	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs550667230	chr2:140934497-140934498	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs563752371	chr2:140934513-140934514	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs201574868	chr2:140934538-140934539	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs200787827	chr2:140934539-140934540	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs146276479	chr2:140934543-140934544	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs199759173	chr2:140934545-140934546	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs199813427	chr2:140934548-140934549	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs539492571	chr2:140934549-140934550	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs6430876	chr2:140934550-140934551	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs112108581	chr2:140934555-140934556	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs535483118	chr2:140934606-140934607	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs76509428	chr2:140934654-140934655	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs115225390	chr2:140934673-140934674	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs17384762	chr2:140934692-140934693	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs575920257	chr2:140934695-140934696	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs187182021	chr2:140934709-140934710	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs373843415	chr2:140934727-140934728	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
Breast cancer	16272173	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	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	18632612	CNVD
Mental retardation	17621639	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Mental retardation	22214275	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Glioblastoma multiforme	19435819	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma	21080181	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Autism	22543975	CNVD
Cancer	20164920	CNVD
Hypertension	22686481	CNVD
Hypospadia	22686481	CNVD
Intellectual disability	22686481	CNVD
Omphalocele	22686481	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	22522925	CNVD
Ependymoma	20639864	CNVD
Pancreatic cancer	17952125	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:104 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:140931400-140931800	Enhancers	Gastric	stomach
2	chr2:140934400-140936400	Enhancers	Fetal Heart	heart
3	chr2:140935400-140936400	Enhancers	Muscle Satellite Cultured Cells	--
4	chr2:140935400-140936400	Enhancers	Fetal Lung	lung
5	chr2:140935800-140936200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr2:140935800-140936200	Enhancers	Adipose Nuclei	Adipose
7	chr2:140935800-140936200	Active TSS	Right Ventricle	heart
8	chr2:140936000-140936400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr2:140936000-140936400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr2:140939600-140940000	Enhancers	Aorta	Aorta
11	chr2:140940600-140941200	Enhancers	Gastric	stomach
12	chr2:140941200-140944200	Enhancers	Fetal Brain Male	brain
13	chr2:140942000-140942200	Enhancers	Fetal Brain Female	brain
14	chr2:140942400-140943400	Weak transcription	Fetal Brain Female	brain
15	chr2:140943400-140944200	Enhancers	Fetal Brain Female	brain
16	chr2:140943600-140943800	Enhancers	Ovary	ovary
17	chr2:140944000-140944400	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr2:140944000-140944600	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr2:140944000-140944600	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr2:140944000-140944800	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr2:140944000-140944800	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr2:140968200-140968600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr2:140968200-140968600	Enhancers	Fetal Kidney	kidney
24	chr2:140968200-140969200	Enhancers	Cortex derived primary cultured neurospheres	brain
25	chr2:140968200-140969600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr2:140972200-140973800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr2:140972600-140973000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr2:140991000-140992400	Enhancers	Fetal Lung	lung
29	chr2:140997200-140997400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr2:140997400-140997600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr2:140997600-140998000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr2:141002400-141003400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr2:141003400-141004400	Active TSS	Adipose Nuclei	Adipose
34	chr2:141003400-141005400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr2:141003600-141005800	Active TSS	Skeletal Muscle Female	skeletal muscle
36	chr2:141004400-141004600	Flanking Active TSS	Adipose Nuclei	Adipose
37	chr2:141004400-141005800	Active TSS	Psoas Muscle	Psoas
38	chr2:141004600-141005400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr2:141004600-141005800	Enhancers	Adipose Nuclei	Adipose
40	chr2:141005400-141005600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr2:141005400-141005800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr2:141005400-141005800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr2:141005400-141005800	Enhancers	Fetal Lung	lung
44	chr2:141005600-141006200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr2:141005800-141006600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr2:141005800-141007200	Weak transcription	Adipose Nuclei	Adipose
47	chr2:141006200-141008000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr2:141007200-141007800	Enhancers	Adipose Nuclei	Adipose
49	chr2:141015000-141015200	Enhancers	Adipose Nuclei	Adipose
50	chr2:141015000-141015600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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