Variant report

Variant	nsv1041397
Chromosome Location	chr12:86438607-86737558
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:875)
CpG islands
(count:488)
Chromatin interactive
region (count:15)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:875 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr12:86520872-86521057	K562	blood:	n/a	n/a
2	BACH1	chr12:86503495-86503527	K562	blood:	n/a	n/a
3	BATF	chr12:86643692-86643942	GM12878	blood:	n/a	n/a
4	BATF	chr12:86643693-86643934	GM12878	blood:	n/a	n/a
5	BRCA1	chr12:86624079-86624702	Hela-S3	cervix:	n/a	n/a
6	BRCA1	chr12:86705709-86705766	Hela-S3	cervix:	n/a	n/a
7	BRCA1	chr12:86519275-86519309	HepG2	liver:	n/a	n/a
8	BRCA1	chr12:86617529-86617530	GM12878	blood:	n/a	n/a
9	CBX3	chr12:86531638-86532059	HCT-116	colon:	n/a	n/a
10	CEBPB	chr12:86654936-86655271	IMR90	lung:	n/a	n/a
11	CEBPB	chr12:86608569-86608828	IMR90	lung:	n/a	chr12:86608708-86608721 chr12:86608708-86608719 chr12:86608809-86608822 chr12:86608708-86608721
12	CEBPB	chr12:86620344-86620573	MCF-7	breast:	n/a	n/a
13	CEBPB	chr12:86530235-86530421	HepG2	liver:	n/a	chr12:86530309-86530322 chr12:86530309-86530322 chr12:86530310-86530321
14	CEBPB	chr12:86487913-86488003	Hela-S3	cervix:	n/a	chr12:86487944-86487955 chr12:86487944-86487957 chr12:86487944-86487957
15	CEBPB	chr12:86568024-86568281	ECC-1	luminal epithelium:	n/a	n/a
16	CEBPB	chr12:86646079-86646091	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr12:86531721-86532212	IMR90	lung:	n/a	n/a
18	CEBPB	chr12:86736448-86736846	Hela-S3	cervix:	n/a	chr12:86736661-86736673
19	CEBPB	chr12:86529118-86529215	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr12:86645972-86646254	HepG2	liver:	n/a	chr12:86646082-86646093 chr12:86646081-86646094 chr12:86646081-86646092
21	CEBPB	chr12:86568018-86568312	A549	lung:	n/a	n/a
22	CEBPB	chr12:86521848-86522071	HepG2	liver:	n/a	chr12:86522008-86522019
23	CEBPB	chr12:86729535-86729923	A549	lung:	n/a	n/a
24	CEBPB	chr12:86558160-86558369	HepG2	liver:	n/a	chr12:86558244-86558255
25	CEBPB	chr12:86558172-86558218	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr12:86528767-86528967	HepG2	liver:	n/a	chr12:86528886-86528899 chr12:86528888-86528899 chr12:86528886-86528899 chr12:86528886-86528897 chr12:86528886-86528899
27	CEBPB	chr12:86647213-86647291	HepG2	liver:	n/a	chr12:86647273-86647284
28	CEBPB	chr12:86707089-86707289	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr12:86608580-86608852	A549	lung:	n/a	chr12:86608708-86608721 chr12:86608708-86608719 chr12:86608809-86608822 chr12:86608708-86608721
30	CEBPB	chr12:86654940-86655288	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr12:86716434-86716725	Hela-S3	cervix:	n/a	chr12:86716572-86716585 chr12:86716574-86716585 chr12:86716572-86716585 chr12:86716574-86716585
32	CEBPB	chr12:86558127-86558402	IMR90	lung:	n/a	chr12:86558244-86558255 chr12:86558131-86558142
33	CEBPB	chr12:86567983-86568332	IMR90	lung:	n/a	n/a
34	CEBPB	chr12:86542454-86542728	IMR90	lung:	n/a	n/a
35	CEBPB	chr12:86645929-86646233	IMR90	lung:	n/a	chr12:86646082-86646093 chr12:86646081-86646094 chr12:86646081-86646092
36	CEBPB	chr12:86568042-86568280	HepG2	liver:	n/a	n/a
37	CEBPB	chr12:86530289-86530354	Hela-S3	cervix:	n/a	chr12:86530309-86530322 chr12:86530309-86530322 chr12:86530310-86530321
38	CEBPB	chr12:86608533-86608837	HepG2	liver:	n/a	chr12:86608708-86608721 chr12:86608708-86608719 chr12:86608809-86608822 chr12:86608708-86608721
39	CEBPB	chr12:86521887-86522111	IMR90	lung:	n/a	chr12:86522008-86522019
40	CEBPB	chr12:86654966-86655213	A549	lung:	n/a	n/a
41	CEBPB	chr12:86624082-86624737	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr12:86568011-86568326	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD2	chr12:86477352-86477433	GM12878	blood:	n/a	n/a
44	CHD2	chr12:86544643-86544699	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr12:86580380-86580530	NHEK	skin:	n/a	n/a
46	CTCF	chr12:86580248-86580480	A549	lung:	n/a	n/a
47	CTCF	chr12:86580363-86580485	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr12:86580353-86580491	LNCaP	prostate:	n/a	n/a
49	CTCF	chr12:86580420-86580570	HBMEC	blood vessel:	n/a	n/a
50	CTCF	chr12:86580360-86580510	GM12875	blood:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:86659008-86659058	PANC-1	pancreas:	n/a
2	chr12:86727874-86727924	Caco-2	colon:	n/a
3	chr12:86659008-86659058	HCM	heart:	n/a
4	chr12:86658860-86658910	AG09309	skin:	n/a
5	chr12:86727874-86727924	BJ	skin:	n/a
6	chr12:86659008-86659058	PFSK-1	brain:	n/a
7	chr12:86658385-86658435	AG04450	lung:	fetal
8	chr12:86658385-86658435	HL-60	blood:	n/a
9	chr12:86727874-86727924	CMK	blood:	n/a
10	chr12:86658385-86658435	NB4	blood:	n/a
11	chr12:86690485-86690535	SK-N-SH	brain:	n/a
12	chr12:86690485-86690535	HRE	kidney:	n/a
13	chr12:86658860-86658910	HepG2	liver:	n/a
14	chr12:86727874-86727924	PANC-1	pancreas:	n/a
15	chr12:86658745-86658795	PFSK-1	brain:	n/a
16	chr12:86659008-86659058	Jurkat	blood:	n/a
17	chr12:86727874-86727924	NT2-D1	testis:	n/a
18	chr12:86658745-86658795	GM12892	blood:	n/a
19	chr12:86690485-86690535	HEEpiC	esophagus:	n/a
20	chr12:86727874-86727924	HPAEpiC	pulmonary alveolar:	n/a
21	chr12:86651249-86651299	GM12891	blood:	n/a
22	chr12:86658860-86658910	BJ	skin:	n/a
23	chr12:86690485-86690535	PANC-1	pancreas:	n/a
24	chr12:86658385-86658435	GM06990	blood:	n/a
25	chr12:86651249-86651299	PrEC	prostate:	n/a
26	chr12:86658860-86658910	GM12891	blood:	n/a
27	chr12:86658860-86658910	NT2-D1	testis:	n/a
28	chr12:86650107-86650157	HAEpiC	amniotic membrane:	n/a
29	chr12:86650107-86650157	HRCEpiC	kidney:	n/a
30	chr12:86658385-86658435	MCF10A-Er-Src	breast:	n/a
31	chr12:86658860-86658910	HCF	heart:	n/a
32	chr12:86650107-86650157	HRE	kidney:	n/a
33	chr12:86659008-86659058	AG04450	lung:	fetal
34	chr12:86659008-86659058	HPAEpiC	pulmonary alveolar:	n/a
35	chr12:86650107-86650157	Hela-S3	cervix:	n/a
36	chr12:86659008-86659058	HL-60	blood:	n/a
37	chr12:86658860-86658910	Caco-2	colon:	n/a
38	chr12:86659008-86659058	HCPEpiC	choroid plexus:	n/a
39	chr12:86658745-86658795	K562	blood:	n/a
40	chr12:86651249-86651299	Caco-2	colon:	n/a
41	chr12:86651249-86651299	Hela-S3	cervix:	n/a
42	chr12:86658860-86658910	AG04450	lung:	fetal
43	chr12:86650107-86650157	A549	lung:	n/a
44	chr12:86658385-86658435	BE2_C	brain:	n/a
45	chr12:86690485-86690535	MCF-7	breast:	n/a
46	chr12:86658385-86658435	ProgFib	skin:	n/a
47	chr12:86727874-86727924	PFSK-1	brain:	n/a
48	chr12:86650107-86650157	NHBE	bronchial:	n/a
49	chr12:86651249-86651299	SK-N-MC	brain:	n/a
50	chr12:86658860-86658910	LNCaP	prostate:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:86629307..86629807-chr7:120030191..120030808,2	MCF-7	breast:
2	chr12:86633057..86634931-chr12:86636880..86638760,2	K562	blood:
3	chr12:86633057..86634931-chr12:86636880..86638760,2	K562	blood:
4	chr12:86626187..86628759-chr12:86629956..86631967,2	K562	blood:
5	chr12:86723150..86725256-chr12:86785265..86787177,2	MCF-7	breast:
6	chr12:86511451..86513760-chr12:86516670..86519004,2	K562	blood:
7	chr12:86626187..86628759-chr12:86629956..86631967,2	K562	blood:
8	chr12:86543597..86545688-chr12:86546239..86548183,2	K562	blood:
9	chr12:86365669..86366250-chr12:86579981..86580554,2	MCF-7	breast:
10	chr12:86661669..86664440-chr12:86664812..86667661,2	MCF-7	breast:
11	chr12:86543597..86545688-chr12:86546239..86548183,2	K562	blood:
12	chr12:86559122..86560912-chr12:86565276..86567562,2	K562	blood:
13	chr12:86661669..86664440-chr12:86664812..86667661,2	MCF-7	breast:
14	chr12:86511451..86513760-chr12:86516670..86519004,2	K562	blood:
15	chr12:86559122..86560912-chr12:86565276..86567562,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MGAT4C-1	chr12:86727843-86727905	NONHSAT029762
2	lnc-MGAT4C-1	chr12:86650017-86650101	NONHSAT029763
3	lnc-MGAT4C-1	chr12:86461869-86462285	NONHSAT029763
4	lnc-MGAT4C-1	chr12:86443452-86443501	NONHSAT029759
5	lnc-MGAT4C-1	chr12:86443452-86443501	NONHSAT029760
6	lnc-MGAT4C-1	chr12:86727843-86727905	NONHSAT029759
7	lnc-MGAT4C-1	chr12:86443453-86443501	NONHSAT029762
8	lnc-MGAT4C-1	chr12:86650017-86650192	NONHSAT029760

No data

Variant related genes	Relation type
MGAT4C	TF binding region
MGAT4C	CpG island

Extended variants
information (count: 5141 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:5141 , 50 per page) page: 1 2 3 4 5 6 7 ... 103

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567195012	chr12:86438607-86438608	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs146768305	chr12:86438608-86438609	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs7966352	chr12:86438705-86438706	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs575870582	chr12:86438748-86438749	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs540044443	chr12:86438792-86438793	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs139418406	chr12:86438815-86438816	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs573368039	chr12:86438823-86438824	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs562141915	chr12:86438855-86438856	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs551645056	chr12:86438858-86438859	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs114610940	chr12:86438869-86438870	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs562092829	chr12:86438884-86438885	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs377197741	chr12:86438901-86438902	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs115256836	chr12:86438915-86438916	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs375029421	chr12:86438933-86438934	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs191199701	chr12:86438939-86438940	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs76183430	chr12:86438949-86438950	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs548066328	chr12:86438963-86438964	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs149945547	chr12:86439001-86439002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs551170004	chr12:86439008-86439009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs372004922	chr12:86439053-86439054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs74851459	chr12:86439073-86439074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs567266276	chr12:86439081-86439082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs527376984	chr12:86439109-86439110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs145207318	chr12:86439184-86439185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs115540044	chr12:86439187-86439188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs113159143	chr12:86439215-86439216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs549652532	chr12:86439216-86439217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs185633184	chr12:86439322-86439323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs143307973	chr12:86439372-86439373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs540178755	chr12:86439415-86439416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs558382630	chr12:86439434-86439435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs573385927	chr12:86439437-86439438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs534285075	chr12:86439467-86439468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs555596983	chr12:86439478-86439479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs147898479	chr12:86439515-86439516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs147086413	chr12:86439591-86439592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs77974258	chr12:86439619-86439620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs117831422	chr12:86439624-86439625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs577505273	chr12:86439692-86439693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs138446405	chr12:86439696-86439697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs559890522	chr12:86439697-86439698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs142019152	chr12:86439742-86439743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs373682000	chr12:86439806-86439807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs117938878	chr12:86439854-86439855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs560839840	chr12:86439859-86439860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs190488824	chr12:86439937-86439938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs570810740	chr12:86439983-86439984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs577323066	chr12:86444006-86444007	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs7961367	chr12:86444015-86444016	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs527627245	chr12:86444063-86444064	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:681 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:86438000-86439000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr12:86439000-86440000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr12:86452800-86453400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr12:86453400-86457600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr12:86470600-86473800	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr12:86473800-86474000	Enhancers	Brain Germinal Matrix	brain
7	chr12:86473800-86474200	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr12:86473800-86476400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr12:86473800-86476400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr12:86473800-86477000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr12:86474200-86474400	Weak transcription	Cortex derived primary cultured neurospheres	brain
12	chr12:86474200-86474600	Enhancers	Fetal Brain Male	brain
13	chr12:86474200-86474600	Enhancers	Fetal Heart	heart
14	chr12:86474200-86475400	Weak transcription	Brain Germinal Matrix	brain
15	chr12:86474400-86476400	Enhancers	Cortex derived primary cultured neurospheres	brain
16	chr12:86474600-86475000	Weak transcription	Fetal Heart	heart
17	chr12:86474600-86475600	Weak transcription	Fetal Brain Male	brain
18	chr12:86474600-86475800	Enhancers	Brain Anterior Caudate	brain
19	chr12:86474800-86476000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr12:86474800-86476000	Enhancers	Brain Hippocampus Middle	brain
21	chr12:86474800-86476000	Enhancers	Brain Substantia Nigra	brain
22	chr12:86475000-86476200	Enhancers	Brain Inferior Temporal Lobe	brain
23	chr12:86475000-86476200	Enhancers	Fetal Heart	heart
24	chr12:86475000-86476400	Enhancers	Brain Cingulate Gyrus	brain
25	chr12:86475400-86476200	Enhancers	Fetal Brain Female	brain
26	chr12:86475400-86476400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr12:86475400-86476600	Enhancers	Brain Germinal Matrix	brain
28	chr12:86475600-86476200	Enhancers	Fetal Brain Male	brain
29	chr12:86476200-86477200	Weak transcription	Brain Inferior Temporal Lobe	brain
30	chr12:86476600-86477400	Weak transcription	Brain Germinal Matrix	brain
31	chr12:86477200-86477600	Enhancers	Fetal Lung	lung
32	chr12:86477400-86477600	Enhancers	Brain Inferior Temporal Lobe	brain
33	chr12:86477400-86477800	Enhancers	Brain Germinal Matrix	brain
34	chr12:86484400-86486000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr12:86485000-86486000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr12:86485200-86485800	Enhancers	Pancreatic Islets	Pancreatic Islet
37	chr12:86485200-86486000	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr12:86486000-86487800	Weak transcription	HUES48 Cell Line	embryonic stem cell
39	chr12:86487800-86488000	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr12:86488000-86488400	Weak transcription	HUES48 Cell Line	embryonic stem cell
41	chr12:86488400-86488600	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr12:86488400-86489400	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr12:86488600-86489400	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr12:86488600-86489800	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr12:86489400-86490400	Weak transcription	HUES48 Cell Line	embryonic stem cell
46	chr12:86489400-86490400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
47	chr12:86489800-86491400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
48	chr12:86490400-86491000	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr12:86490400-86491400	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr12:86490400-86491600	Enhancers	HUES48 Cell Line	embryonic stem cell

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