Variant report

Variant	nsv1049443
Chromosome Location	chr12:86185887-86272493
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	chr12:86215439-86216042	HepG2	liver:	n/a	n/a
2	ATF2	chr12:86267833-86268209	GM12878	blood:	n/a	n/a
3	ATF2	chr12:86267846-86268296	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr12:86198461-86198632	GM12878	blood:	n/a	n/a
5	BCL3	chr12:86215330-86216088	A549	lung:	n/a	chr12:86215353-86215362
6	BHLHE40	chr12:86261009-86261260	GM12878	blood:	n/a	n/a
7	BHLHE40	chr12:86215633-86215635	HepG2	liver:	n/a	n/a
8	BRCA1	chr12:86261140-86261219	GM12878	blood:	n/a	n/a
9	BRCA1	chr12:86215072-86216259	Hela-S3	cervix:	n/a	n/a
10	BRCA1	chr12:86268124-86268259	GM12878	blood:	n/a	n/a
11	BRCA1	chr12:86227791-86228570	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr12:86229275-86230390	Hela-S3	cervix:	n/a	chr12:86229554-86229561
13	BRCA1	chr12:86217593-86217944	Hela-S3	cervix:	n/a	n/a
14	CBX3	chr12:86198470-86198858	HCT-116	colon:	n/a	n/a
15	CEBPB	chr12:86201477-86201788	Hela-S3	cervix:	n/a	chr12:86201645-86201662
16	CEBPB	chr12:86230000-86230366	HepG2	liver:	n/a	chr12:86230145-86230156 chr12:86230146-86230155 chr12:86230144-86230155
17	CEBPB	chr12:86229999-86230279	HepG2	liver:	n/a	chr12:86230145-86230156 chr12:86230146-86230155 chr12:86230144-86230155
18	CEBPB	chr12:86229803-86230626	A549	lung:	n/a	chr12:86230145-86230156 chr12:86230146-86230155 chr12:86230144-86230155
19	CEBPB	chr12:86196893-86197551	HCT-116	colon:	n/a	chr12:86197208-86197219
20	CEBPB	chr12:86229989-86230326	IMR90	lung:	n/a	chr12:86230145-86230156 chr12:86230146-86230155 chr12:86230144-86230155
21	CEBPB	chr12:86215416-86216160	A549	lung:	n/a	chr12:86215834-86215843 chr12:86215832-86215843
22	CEBPB	chr12:86227642-86228559	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr12:86229902-86230485	A549	lung:	n/a	chr12:86230145-86230156 chr12:86230146-86230155 chr12:86230144-86230155
24	CEBPB	chr12:86204534-86204695	HepG2	liver:	n/a	chr12:86204547-86204558 chr12:86204638-86204651
25	CEBPB	chr12:86216928-86217980	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr12:86225435-86225784	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr12:86214106-86214370	IMR90	lung:	n/a	chr12:86214283-86214296
28	CEBPB	chr12:86197080-86197333	HepG2	liver:	n/a	chr12:86197208-86197219
29	CEBPB	chr12:86215613-86216011	HepG2	liver:	n/a	chr12:86215834-86215843 chr12:86215832-86215843
30	CEBPB	chr12:86215658-86216029	IMR90	lung:	n/a	chr12:86215834-86215843 chr12:86215832-86215843
31	CEBPB	chr12:86229967-86230337	HepG2	liver:	n/a	chr12:86230145-86230156 chr12:86230146-86230155 chr12:86230144-86230155
32	CEBPB	chr12:86214056-86214384	A549	lung:	n/a	chr12:86214283-86214296
33	CEBPB	chr12:86214101-86214384	HepG2	liver:	n/a	chr12:86214283-86214296
34	CEBPB	chr12:86242279-86242603	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr12:86222891-86223471	Hela-S3	cervix:	n/a	chr12:86223285-86223296 chr12:86223280-86223297
36	CEBPB	chr12:86215602-86216110	MCF-7	breast:	n/a	chr12:86215834-86215843 chr12:86215832-86215843
37	CEBPB	chr12:86215647-86216083	H1-hESC	embryonic stem cell:	n/a	chr12:86215834-86215843 chr12:86215832-86215843
38	CEBPB	chr12:86229901-86230389	A549	lung:	n/a	chr12:86230145-86230156 chr12:86230146-86230155 chr12:86230144-86230155
39	CEBPB	chr12:86229126-86230531	Hela-S3	cervix:	n/a	chr12:86230145-86230156 chr12:86230146-86230155 chr12:86230144-86230155
40	CEBPB	chr12:86229778-86230418	ECC-1	luminal epithelium:	n/a	chr12:86230145-86230156 chr12:86230146-86230155 chr12:86230144-86230155
41	CEBPB	chr12:86215613-86216055	A549	lung:	n/a	chr12:86215834-86215843 chr12:86215832-86215843
42	CEBPB	chr12:86213417-86213616	HepG2	liver:	n/a	n/a
43	CEBPB	chr12:86229965-86230311	H1-hESC	embryonic stem cell:	n/a	chr12:86230145-86230156 chr12:86230146-86230155 chr12:86230144-86230155
44	CEBPB	chr12:86203810-86203816	A549	lung:	n/a	n/a
45	CEBPB	chr12:86197022-86197515	Hela-S3	cervix:	n/a	chr12:86197208-86197219
46	CEBPB	chr12:86272459-86272539	A549	lung:	n/a	n/a
47	CEBPB	chr12:86227052-86227437	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr12:86235090-86235358	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr12:86229956-86230339	HepG2	liver:	n/a	chr12:86230145-86230156 chr12:86230146-86230155 chr12:86230144-86230155
50	CEBPB	chr12:86229921-86230267	MCF-7	breast:	n/a	chr12:86230145-86230156 chr12:86230146-86230155 chr12:86230144-86230155

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:86230093-86230143	AG09309	skin:	n/a
2	chr12:86268154-86268204	PFSK-1	brain:	n/a
3	chr12:86230957-86231007	Jurkat	blood:	n/a
4	chr12:86230557-86230607	AG04449	skin:	fetal
5	chr12:86267881-86267931	HEK293	kidney:	embryo
6	chr12:86240461-86240511	LNCaP	prostate:	n/a
7	chr12:86268154-86268204	LNCaP	prostate:	n/a
8	chr12:86268154-86268204	PrEC	prostate:	n/a
9	chr12:86230557-86230607	BE2_C	brain:	n/a
10	chr12:86230957-86231007	Caco-2	colon:	n/a
11	chr12:86230176-86230226	Hepatocyte	liver:	n/a
12	chr12:86268154-86268204	ECC-1	luminal epithelium:	n/a
13	chr12:86230957-86231007	HCT-116	colon:	n/a
14	chr12:86230093-86230143	HAEpiC	amniotic membrane:	n/a
15	chr12:86230825-86230875	Jurkat	blood:	n/a
16	chr12:86230557-86230607	GM12878	blood:	n/a
17	chr12:86230825-86230875	U87	brain:	n/a
18	chr12:86230093-86230143	AoSMC	blood vessel:	n/a
19	chr12:86230557-86230607	Caco-2	colon:	n/a
20	chr12:86230176-86230226	HUVEC	blood vessel:	n/a
21	chr12:86268154-86268204	HEK293	kidney:	embryo
22	chr12:86240461-86240511	HRE	kidney:	n/a
23	chr12:86229804-86229854	SK-N-SH_RA	brain:	n/a
24	chr12:86230825-86230875	GM19239	blood:	n/a
25	chr12:86230557-86230607	HRPEpiC	eye:	n/a
26	chr12:86267881-86267931	MCF-7	breast:	n/a
27	chr12:86230825-86230875	HEK293	kidney:	embryo
28	chr12:86230825-86230875	PANC-1	pancreas:	n/a
29	chr12:86267839-86267889	U87	brain:	n/a
30	chr12:86230176-86230226	IMR90	lung:	fetal
31	chr12:86230825-86230875	NHBE	bronchial:	n/a
32	chr12:86240461-86240511	GM12891	blood:	n/a
33	chr12:86230176-86230226	MCF-7	breast:	n/a
34	chr12:86230957-86231007	BJ	skin:	n/a
35	chr12:86268154-86268204	NT2-D1	testis:	n/a
36	chr12:86268154-86268204	HEEpiC	esophagus:	n/a
37	chr12:86267881-86267931	NHBE	bronchial:	n/a
38	chr12:86267839-86267889	PFSK-1	brain:	n/a
39	chr12:86230367-86230417	ProgFib	skin:	n/a
40	chr12:86230367-86230417	NHBE	bronchial:	n/a
41	chr12:86230176-86230226	AG09319	gingival:	n/a
42	chr12:86230957-86231007	RPTEC	kidney:	n/a
43	chr12:86230557-86230607	HepG2	liver:	n/a
44	chr12:86267839-86267889	HCT-116	colon:	n/a
45	chr12:86230367-86230417	BE2_C	brain:	n/a
46	chr12:86240461-86240511	GM12878	blood:	n/a
47	chr12:86230957-86231007	AG04450	lung:	fetal
48	chr12:86230557-86230607	NT2-D1	testis:	n/a
49	chr12:86230093-86230143	HEEpiC	esophagus:	n/a
50	chr12:86230367-86230417	SAEC	small airway:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:85870834..85871570-chr12:86260678..86261344,3	MCF-7	breast:
2	chr12:85861848..85863045-chr12:86266253..86266913,4	MCF-7	breast:
3	chr12:86229619..86230190-chr5:141302910..141303768,2	Hela-S3	cervix:
4	chr12:86243212..86244125-chr15:53990318..53991124,2	MCF-7	breast:
5	chr12:86212969..86215091-chr12:86229770..86232108,2	K562	blood:
6	chr12:85969245..85970171-chr12:86260729..86261622,3	MCF-7	breast:
7	chr12:86210558..86212149-chr21:9825340..9827489,2	MCF-7	breast:
8	chr12:86207996..86208525-chr12:86266396..86266910,2	MCF-7	breast:
9	chr12:85870710..85871639-chr12:86266180..86266857,2	MCF-7	breast:
10	chr12:85470481..85471011-chr12:86260831..86261575,2	MCF-7	breast:
11	chr12:85968890..85970646-chr12:86260113..86261752,8	MCF-7	breast:
12	chr12:85972333..85972969-chr12:86260657..86261419,2	MCF-7	breast:
13	chr11:110316530..110317353-chr12:86192071..86192576,2	MCF-7	breast:
14	chr12:86207996..86208525-chr12:86266396..86266910,2	MCF-7	breast:
15	chr12:85549530..85550247-chr12:86266080..86266618,2	MCF-7	breast:

Variant related genes	Relation type
RASSF9	TF binding region
NTS	TF binding region
RASSF9	CpG island
NTS	CpG island
ENSG00000198774	chromatin interactions
ENSG00000081791	chromatin interactions
ENSG00000264063	chromatin interactions
ENSG00000264462	chromatin interactions

Extended variants
information (count: 3084 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:3084 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs140029681	chr12:86188025-86188026	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs183858477	chr12:86188069-86188070	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs531546377	chr12:86188116-86188117	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs549522266	chr12:86188117-86188118	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs571210412	chr12:86188146-86188147	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs189360135	chr12:86188148-86188149	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs553391027	chr12:86188160-86188161	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs556882434	chr12:86188163-86188164	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs567089667	chr12:86188186-86188187	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs201622947	chr12:86188206-86188207	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs141024974	chr12:86188207-86188208	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs77971371	chr12:86188208-86188209	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs182011799	chr12:86188305-86188306	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs143539202	chr12:86188321-86188322	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs577021940	chr12:86188365-86188366	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs544507392	chr12:86188368-86188369	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs186034973	chr12:86188376-86188377	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs191749930	chr12:86188380-86188381	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs151280171	chr12:86188412-86188413	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs181932652	chr12:86188413-86188414	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs186188060	chr12:86188435-86188436	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs140480601	chr12:86188469-86188470	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs150044687	chr12:86188497-86188498	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs560315651	chr12:86188527-86188528	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs145324144	chr12:86188542-86188543	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs527710504	chr12:86188548-86188549	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs191478045	chr12:86188583-86188584	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs561440783	chr12:86188590-86188591	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs117321741	chr12:86188635-86188636	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs549610062	chr12:86188638-86188639	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs369463524	chr12:86188640-86188641	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs79448030	chr12:86188702-86188703	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs532305779	chr12:86188714-86188715	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs61928894	chr12:86188740-86188741	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs540525534	chr12:86188897-86188898	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs565808272	chr12:86188906-86188907	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs370280881	chr12:86188920-86188921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs75792753	chr12:86188922-86188923	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs548685056	chr12:86188971-86188972	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs569779905	chr12:86188976-86188977	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs182107466	chr12:86188977-86188978	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs556832480	chr12:86188987-86188988	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs34018236	chr12:86189006-86189007	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs578203704	chr12:86189011-86189012	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs186744823	chr12:86189052-86189053	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs554460509	chr12:86189074-86189075	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs572608049	chr12:86189090-86189091	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs190821469	chr12:86189112-86189113	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs149230682	chr12:86189170-86189171	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs7399276	chr12:86189219-86189220	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17899364	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	22032731	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
Malignant peripheral nerve sheath tumor	18522746	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	20729466	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Renal cell carcinoma	18194544	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21364760	CNVD

Chromatin state (count:819 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:86188000-86189000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr12:86188000-86189000	Enhancers	Osteobl	bone
3	chr12:86188000-86190200	Enhancers	NH-A	brain
4	chr12:86188000-86190600	Enhancers	Hela-S3	cervix
5	chr12:86188200-86188800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr12:86188200-86189000	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr12:86188200-86189000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr12:86188200-86189000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr12:86188200-86189600	Enhancers	Cortex derived primary cultured neurospheres	brain
10	chr12:86188400-86188800	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr12:86188400-86188800	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr12:86188400-86188800	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr12:86188400-86188800	Enhancers	NHDF-Ad	bronchial
14	chr12:86188400-86190000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr12:86188400-86190200	Enhancers	Muscle Satellite Cultured Cells	--
16	chr12:86188800-86189200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr12:86188800-86190200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr12:86189000-86189800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr12:86189000-86189800	Weak transcription	Osteobl	bone
20	chr12:86189200-86190000	Enhancers	Primary hematopoietic stem cells	blood
21	chr12:86189400-86190200	Enhancers	HUVEC	blood vessel
22	chr12:86189600-86189800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr12:86189800-86190000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr12:86189800-86190000	Enhancers	Osteobl	bone
25	chr12:86190000-86190200	Weak transcription	Osteobl	bone
26	chr12:86190000-86196800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr12:86190200-86196400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr12:86190600-86196200	Weak transcription	Hela-S3	cervix
29	chr12:86191200-86191400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr12:86191400-86207400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr12:86194200-86214000	Weak transcription	HMEC	breast
32	chr12:86196000-86197200	Active TSS	NHEK	skin
33	chr12:86196000-86197400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr12:86196000-86197800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
35	chr12:86196200-86196400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr12:86196200-86197200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr12:86196200-86197600	Enhancers	Hela-S3	cervix
38	chr12:86196400-86196600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr12:86196400-86196800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr12:86196400-86198800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr12:86196600-86198400	Enhancers	Muscle Satellite Cultured Cells	--
42	chr12:86196600-86199200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr12:86196800-86197200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr12:86196800-86197600	Enhancers	HUVEC	blood vessel
45	chr12:86196800-86198400	Weak transcription	Adipose Nuclei	Adipose
46	chr12:86196800-86198800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr12:86197000-86199200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr12:86197000-86199800	Enhancers	NH-A	brain
49	chr12:86197000-86207800	Weak transcription	Fetal Heart	heart
50	chr12:86197200-86197400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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