Variant report

Variant	nsv1002838
Chromosome Location	chr2:185035277-185289130
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	chr2:185136996-185137081	K562	blood:	n/a	n/a
2	ARID3A	chr2:185060541-185060558	K562	blood:	n/a	n/a
3	ARID3A	chr2:185234055-185234428	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:185060092-185060099	K562	blood:	n/a	n/a
5	ARID3A	chr2:185068347-185068808	K562	blood:	n/a	n/a
6	ARID3A	chr2:185069593-185070127	K562	blood:	n/a	n/a
7	ATF1	chr2:185039540-185039740	K562	blood:	n/a	n/a
8	ATF2	chr2:185187340-185187651	GM12878	blood:	n/a	n/a
9	BACH1	chr2:185051246-185051364	K562	blood:	n/a	n/a
10	BACH1	chr2:185068420-185068484	K562	blood:	n/a	n/a
11	BATF	chr2:185187318-185187665	GM12878	blood:	n/a	n/a
12	BHLHE40	chr2:185137191-185137291	K562	blood:	n/a	n/a
13	BHLHE40	chr2:185251589-185251715	K562	blood:	n/a	n/a
14	BHLHE40	chr2:185227990-185228275	HepG2	liver:	n/a	n/a
15	BRCA1	chr2:185234005-185234016	HepG2	liver:	n/a	n/a
16	CBX3	chr2:185271763-185272041	K562	blood:	n/a	n/a
17	CCNT2	chr2:185075725-185075820	K562	blood:	n/a	n/a
18	CCNT2	chr2:185106876-185106964	K562	blood:	n/a	n/a
19	CEBPB	chr2:185070782-185071136	HepG2	liver:	n/a	chr2:185070950-185070959 chr2:185070950-185070961 chr2:185070948-185070959 chr2:185070950-185070959 chr2:185070950-185070959 chr2:185070948-185070961 chr2:185070950-185070959 chr2:185070948-185070961
20	CEBPB	chr2:185135546-185135816	H1-hESC	embryonic stem cell:	n/a	chr2:185135672-185135689 chr2:185135675-185135686
21	CEBPB	chr2:185072144-185072389	HepG2	liver:	n/a	chr2:185072268-185072279
22	CEBPB	chr2:185234153-185234367	HepG2	liver:	n/a	chr2:185234227-185234240 chr2:185234228-185234239 chr2:185234227-185234240 chr2:185234205-185234216
23	CEBPB	chr2:185069857-185070431	K562	blood:	n/a	chr2:185070115-185070128 chr2:185070115-185070126
24	CEBPB	chr2:185274251-185274354	K562	blood:	n/a	n/a
25	CEBPB	chr2:185225898-185226098	K562	blood:	n/a	n/a
26	CEBPB	chr2:185147218-185147526	IMR90	lung:	n/a	chr2:185147372-185147383
27	CEBPB	chr2:185284749-185284771	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr2:185251635-185251802	K562	blood:	n/a	chr2:185251752-185251763
29	CEBPB	chr2:185070797-185071127	IMR90	lung:	n/a	chr2:185070950-185070959 chr2:185070950-185070961 chr2:185070948-185070959 chr2:185070950-185070959 chr2:185070950-185070959 chr2:185070948-185070961 chr2:185070950-185070959 chr2:185070948-185070961
30	CEBPB	chr2:185251568-185251928	HepG2	liver:	n/a	chr2:185251752-185251763
31	CEBPB	chr2:185147241-185147522	HepG2	liver:	n/a	chr2:185147372-185147383
32	CEBPB	chr2:185135564-185135804	HepG2	liver:	n/a	chr2:185135672-185135689 chr2:185135675-185135686
33	CEBPB	chr2:185255484-185255530	HepG2	liver:	n/a	chr2:185255514-185255525
34	CEBPB	chr2:185057464-185057806	K562	blood:	n/a	chr2:185057476-185057489 chr2:185057618-185057629
35	CEBPB	chr2:185220639-185220873	HepG2	liver:	n/a	n/a
36	CEBPB	chr2:185069970-185070132	K562	blood:	n/a	chr2:185070115-185070128 chr2:185070115-185070126
37	CEBPB	chr2:185173271-185173521	Hela-S3	cervix:	n/a	chr2:185173409-185173420
38	CEBPB	chr2:185112478-185112662	HepG2	liver:	n/a	n/a
39	CEBPB	chr2:185072166-185072441	K562	blood:	n/a	chr2:185072268-185072279
40	CEBPB	chr2:185173289-185173559	HepG2	liver:	n/a	chr2:185173409-185173420
41	CEBPB	chr2:185067380-185067637	K562	blood:	n/a	n/a
42	CEBPB	chr2:185167273-185167627	Hela-S3	cervix:	n/a	chr2:185167453-185167464
43	CEBPB	chr2:185234071-185234445	HepG2	liver:	n/a	chr2:185234227-185234240 chr2:185234228-185234239 chr2:185234227-185234240 chr2:185234205-185234216
44	CEBPB	chr2:185207055-185207352	Hela-S3	cervix:	n/a	chr2:185207173-185207184 chr2:185207208-185207219 chr2:185207173-185207182
45	CEBPB	chr2:185251698-185251921	Hela-S3	cervix:	n/a	chr2:185251752-185251763
46	CEBPB	chr2:185057502-185057747	K562	blood:	n/a	chr2:185057618-185057629
47	CEBPB	chr2:185070724-185071141	K562	blood:	n/a	chr2:185070950-185070959 chr2:185070950-185070961 chr2:185070948-185070959 chr2:185070950-185070959 chr2:185070950-185070959 chr2:185070948-185070961 chr2:185070950-185070959 chr2:185070948-185070961
48	CEBPB	chr2:185207011-185207394	HepG2	liver:	n/a	chr2:185207173-185207184 chr2:185207208-185207219 chr2:185207173-185207182
49	CEBPB	chr2:185152684-185152884	K562	blood:	n/a	chr2:185152760-185152771 chr2:185152760-185152773
50	CEBPB	chr2:185069957-185070381	HepG2	liver:	n/a	chr2:185070115-185070128 chr2:185070115-185070126

No.	Distal block	Cell Line	Cell type
1	chr2:185204369..185206130-chr2:185218623..185221505,2	K562	blood:
2	chr2:185103488..185105465-chr2:185244326..185245928,2	K562	blood:
3	chr2:185073490..185075521-chr2:185077251..185078979,2	K562	blood:
4	chr2:185128748..185131745-chr2:185134110..185138355,3	K562	blood:
5	chr2:185053723..185055741-chr2:185058684..185061541,2	K562	blood:
6	chr2:127533916..127534758-chr2:185187632..185188334,2	MCF-7	breast:
7	chr2:185073976..185076039-chr2:185080302..185082080,2	K562	blood:
8	chr2:185223918..185225918-chr2:185227977..185230621,2	K562	blood:
9	chr2:185169023..185171389-chr2:185175264..185178248,2	K562	blood:
10	chr2:185068138..185070964-chr2:185088334..185090815,2	K562	blood:
11	chr2:185063557..185066298-chr2:185074059..185077042,2	K562	blood:
12	chr2:185160917..185163331-chr2:185190953..185193318,2	K562	blood:
13	chr2:185046979..185048851-chr2:185065608..185068607,2	K562	blood:
14	chr2:185048995..185051495-chr2:185054071..185055731,2	K562	blood:
15	chr2:185115001..185116702-chr2:185121013..185123546,2	K562	blood:
16	chr2:185223918..185225918-chr2:185227977..185230621,2	K562	blood:
17	chr2:185048995..185051495-chr2:185054071..185055731,2	K562	blood:
18	chr2:185052728..185055643-chr2:185086397..185088845,2	K562	blood:
19	chr2:185065862..185068679-chr2:185266062..185268642,2	K562	blood:
20	chr2:185066479..185068495-chr2:185209496..185211402,2	K562	blood:
21	chr2:185032130..185034735-chr2:185068262..185070242,2	K562	blood:
22	chr2:185073976..185076039-chr2:185080302..185082080,2	K562	blood:
23	chr2:185046979..185048851-chr2:185065608..185068607,2	K562	blood:
24	chr2:185069331..185071140-chr2:185086941..185089740,2	K562	blood:
25	chr2:185086289..185087889-chr2:185091229..185094182,2	K562	blood:
26	chr2:185017202..185019755-chr2:185059188..185062172,2	K562	blood:
27	chr2:185056201..185058976-chr2:185059740..185064773,6	K562	blood:
28	chr2:185230131..185232758-chr2:185233211..185235341,2	MCF-7	breast:
29	chr2:185039098..185041209-chr2:185044660..185047313,2	K562	blood:
30	chr2:185073490..185075521-chr2:185077251..185078979,2	K562	blood:
31	chr2:185160917..185163331-chr2:185190953..185193318,2	K562	blood:
32	chr2:185086289..185087889-chr2:185091229..185094182,2	K562	blood:
33	chr2:185265120..185267657-chr2:185268029..185269760,2	K562	blood:
34	chr2:185050606..185053529-chr2:185055758..185057591,2	K562	blood:
35	chr2:185201237..185203817-chr2:185332460..185335138,2	K562	blood:
36	chr2:185208077..185209998-chr2:185211977..185213608,2	K562	blood:
37	chr2:185056201..185058411-chr2:185059740..185062010,3	K562	blood:
38	chr2:185027163..185028822-chr2:185041434..185043457,2	K562	blood:
39	chr2:185115001..185116702-chr2:185121013..185123546,2	K562	blood:
40	chr2:185128748..185131745-chr2:185134110..185138355,3	K562	blood:
41	chr2:185267016..185267836-chr3:27870668..27871485,2	MCF-7	breast:
42	chr2:185052728..185055643-chr2:185086397..185088845,2	K562	blood:
43	chr2:185039098..185041209-chr2:185044660..185047313,2	K562	blood:
44	chr2:185052029..185054073-chr2:185054906..185057591,2	K562	blood:
45	chr2:185230131..185232758-chr2:185233211..185235341,2	MCF-7	breast:
46	chr2:185103488..185105465-chr2:185244326..185245928,2	K562	blood:
47	chr2:185204369..185206130-chr2:185218623..185221505,2	K562	blood:
48	chr2:185169023..185171389-chr2:185175264..185178248,2	K562	blood:
49	chr2:185050606..185053529-chr2:185055758..185057591,2	K562	blood:
50	chr2:185030205..185032507-chr2:185041818..185044084,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NCKAP1-4	chr2:185169077-185169159	l_2003_chr2:185169076-185171314_76bGuttman_hLF
2	lnc-ZNF804A-3	chr2:185246875-185247280	NONHSAT075951
3	lnc-NCKAP1-4	chr2:185169187-185169348	l_2003_chr2:185169076-185171314_76bGuttman_hLF
4	lnc-NCKAP1-4	chr2:185171240-185171314	l_2003_chr2:185169076-185171314_76bGuttman_hLF
5	lnc-ZNF804A-3	chr2:185244856-185245013	NONHSAT075951

miRNA name	Chromosome Location	mirBase accession
hsa-miR-548ae	chr2:185243744-185243764	MIMAT0018954

Variant related genes	Relation type
MIR548AE1	TF binding region
ENSG00000104142	chromatin interactions

Extended variants
information (count: 2670 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:2670 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553161017	chr2:185039206-185039207	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs115636211	chr2:185039207-185039208	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs375086958	chr2:185039223-185039224	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs538325333	chr2:185039224-185039225	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs539767833	chr2:185039257-185039258	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs558550919	chr2:185039260-185039261	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs575115463	chr2:185039282-185039283	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs557393844	chr2:185039318-185039319	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs146028870	chr2:185039324-185039325	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs17731073	chr2:185039398-185039399	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs542823352	chr2:185039407-185039408	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs559488035	chr2:185039423-185039424	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs16825569	chr2:185039546-185039547	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs16825573	chr2:185039605-185039606	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs189799712	chr2:185039606-185039607	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs530804861	chr2:185039621-185039622	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs550943835	chr2:185039629-185039630	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs139951346	chr2:185039640-185039641	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs567573673	chr2:185039645-185039646	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs555920515	chr2:185039687-185039688	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs529979989	chr2:185039696-185039697	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs546835973	chr2:185039731-185039732	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs77644427	chr2:185039777-185039778	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs181891483	chr2:185039804-185039805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs567337806	chr2:185039805-185039806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs558359341	chr2:185039817-185039818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs142275783	chr2:185039879-185039880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs537446601	chr2:185039951-185039952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs541272598	chr2:185039965-185039966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs10931121	chr2:185039972-185039973	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs577484009	chr2:185039973-185039974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs574011638	chr2:185039979-185039980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs186873083	chr2:185039982-185039983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs369900423	chr2:185040033-185040034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs191015802	chr2:185040039-185040040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs545526405	chr2:185040041-185040042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs565234712	chr2:185040048-185040049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs181769413	chr2:185040063-185040064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs185158891	chr2:185040073-185040074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs189531234	chr2:185040085-185040086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs572529650	chr2:185040094-185040095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs557846207	chr2:185040149-185040150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs539823486	chr2:185040162-185040163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs73048923	chr2:185040170-185040171	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs532203743	chr2:185040184-185040185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs552301746	chr2:185040218-185040219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs568869641	chr2:185040272-185040273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs537513403	chr2:185040277-185040278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs151240138	chr2:185040364-185040365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs1526199	chr2:185040380-185040381	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	18522746	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	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
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Sudden cardiac death	19188705	CNVD
Autism	19329560	CNVD
Autism	22543975	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Psychiatric disorder	20548289	CNVD
Psychosis	20048749	CNVD
Rectal cancer	20877625	CNVD
Schizophrenia	20548289	CNVD
anxiety disorder	20548289	CNVD
Autism	20548289	CNVD
Bipolar disorder	20548289	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:154 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:185039200-185039800	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr2:185039400-185039800	Active TSS	Hela-S3	cervix
3	chr2:185039400-185039800	Active TSS	K562	blood
4	chr2:185039800-185043000	Weak transcription	Hela-S3	cervix
5	chr2:185043000-185043400	Enhancers	Liver	Liver
6	chr2:185043000-185043800	Enhancers	Hela-S3	cervix
7	chr2:185052200-185052600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr2:185052400-185052600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr2:185055400-185057600	Active TSS	K562	blood
10	chr2:185057600-185063400	Weak transcription	K562	blood
11	chr2:185060600-185061200	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr2:185060800-185063400	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr2:185061000-185061200	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr2:185061200-185062200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr2:185061600-185063600	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr2:185061600-185063600	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr2:185061800-185063800	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr2:185062200-185062600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr2:185062200-185063600	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr2:185062400-185063400	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr2:185062600-185063000	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr2:185063200-185063600	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr2:185063400-185063800	Enhancers	K562	blood
24	chr2:185063800-185067000	Weak transcription	K562	blood
25	chr2:185067000-185070800	Active TSS	K562	blood
26	chr2:185068600-185069000	Enhancers	Pancreatic Islets	Pancreatic Islet
27	chr2:185070800-185071800	Weak transcription	K562	blood
28	chr2:185071800-185072000	Enhancers	K562	blood
29	chr2:185100000-185100200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
30	chr2:185100200-185100800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
31	chr2:185116200-185116600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr2:185116200-185117000	Enhancers	Adipose Nuclei	Adipose
33	chr2:185117000-185118800	Weak transcription	Adipose Nuclei	Adipose
34	chr2:185118800-185119000	Enhancers	Adipose Nuclei	Adipose
35	chr2:185121400-185121800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr2:185125000-185125600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr2:185125400-185127400	Enhancers	Liver	Liver
38	chr2:185125600-185127000	Enhancers	Adipose Nuclei	Adipose
39	chr2:185126000-185126800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr2:185126800-185128600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr2:185127000-185134200	Weak transcription	Adipose Nuclei	Adipose
42	chr2:185128600-185129200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr2:185129000-185129200	Enhancers	Liver	Liver
44	chr2:185129200-185134800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr2:185133800-185134200	Enhancers	Psoas Muscle	Psoas
46	chr2:185134200-185134600	Weak transcription	Psoas Muscle	Psoas
47	chr2:185134200-185136600	Enhancers	Adipose Nuclei	Adipose
48	chr2:185134600-185134800	Enhancers	Psoas Muscle	Psoas
49	chr2:185134600-185134800	Enhancers	Skeletal Muscle Female	skeletal muscle
50	chr2:185134800-185136200	Weak transcription	Psoas Muscle	Psoas

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