Variant report

Variant	nsv518059
Chromosome Location	chr12:86416212-86747726
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:918)
CpG islands
(count:489)
Chromatin interactive
region (count:17)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:918 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

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	chr12:86519275-86519309	HepG2	liver:	n/a	n/a
6	BRCA1	chr12:86617529-86617530	GM12878	blood:	n/a	n/a
7	BRCA1	chr12:86705709-86705766	Hela-S3	cervix:	n/a	n/a
8	BRCA1	chr12:86624079-86624702	Hela-S3	cervix:	n/a	n/a
9	CBX3	chr12:86531638-86532059	HCT-116	colon:	n/a	n/a
10	CEBPB	chr12:86647213-86647291	HepG2	liver:	n/a	chr12:86647273-86647284
11	CEBPB	chr12:86521887-86522111	IMR90	lung:	n/a	chr12:86522008-86522019
12	CEBPB	chr12:86558172-86558218	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr12:86608533-86608837	HepG2	liver:	n/a	chr12:86608708-86608721 chr12:86608708-86608719 chr12:86608809-86608822 chr12:86608708-86608721
14	CEBPB	chr12:86654966-86655213	A549	lung:	n/a	n/a
15	CEBPB	chr12:86530289-86530354	Hela-S3	cervix:	n/a	chr12:86530309-86530322 chr12:86530309-86530322 chr12:86530310-86530321
16	CEBPB	chr12:86521848-86522071	HepG2	liver:	n/a	chr12:86522008-86522019
17	CEBPB	chr12:86528767-86528967	HepG2	liver:	n/a	chr12:86528886-86528899 chr12:86528888-86528899 chr12:86528886-86528899 chr12:86528886-86528897 chr12:86528886-86528899
18	CEBPB	chr12:86736448-86736846	Hela-S3	cervix:	n/a	chr12:86736661-86736673
19	CEBPB	chr12:86542454-86542728	IMR90	lung:	n/a	n/a
20	CEBPB	chr12:86558160-86558369	HepG2	liver:	n/a	chr12:86558244-86558255
21	CEBPB	chr12:86624082-86624737	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr12:86568024-86568281	ECC-1	luminal epithelium:	n/a	n/a
23	CEBPB	chr12:86487913-86488003	Hela-S3	cervix:	n/a	chr12:86487944-86487955 chr12:86487944-86487957 chr12:86487944-86487957
24	CEBPB	chr12:86568018-86568312	A549	lung:	n/a	n/a
25	CEBPB	chr12:86729535-86729923	A549	lung:	n/a	n/a
26	CEBPB	chr12:86608580-86608852	A549	lung:	n/a	chr12:86608708-86608721 chr12:86608708-86608719 chr12:86608809-86608822 chr12:86608708-86608721
27	CEBPB	chr12:86568042-86568280	HepG2	liver:	n/a	n/a
28	CEBPB	chr12:86645929-86646233	IMR90	lung:	n/a	chr12:86646082-86646093 chr12:86646081-86646094 chr12:86646081-86646092
29	CEBPB	chr12:86620344-86620573	MCF-7	breast:	n/a	n/a
30	CEBPB	chr12:86420707-86420864	IMR90	lung:	n/a	n/a
31	CEBPB	chr12:86742139-86742513	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr12:86529118-86529215	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr12:86654936-86655271	IMR90	lung:	n/a	n/a
34	CEBPB	chr12:86608569-86608828	IMR90	lung:	n/a	chr12:86608708-86608721 chr12:86608708-86608719 chr12:86608809-86608822 chr12:86608708-86608721
35	CEBPB	chr12:86645972-86646254	HepG2	liver:	n/a	chr12:86646082-86646093 chr12:86646081-86646094 chr12:86646081-86646092
36	CEBPB	chr12:86707089-86707289	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr12:86646079-86646091	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr12:86558127-86558402	IMR90	lung:	n/a	chr12:86558244-86558255 chr12:86558131-86558142
39	CEBPB	chr12:86716434-86716725	Hela-S3	cervix:	n/a	chr12:86716572-86716585 chr12:86716574-86716585 chr12:86716572-86716585 chr12:86716574-86716585
40	CEBPB	chr12:86654940-86655288	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr12:86530235-86530421	HepG2	liver:	n/a	chr12:86530309-86530322 chr12:86530309-86530322 chr12:86530310-86530321
42	CEBPB	chr12:86568011-86568326	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr12:86531721-86532212	IMR90	lung:	n/a	n/a
44	CEBPB	chr12:86567983-86568332	IMR90	lung:	n/a	n/a
45	CHD2	chr12:86477352-86477433	GM12878	blood:	n/a	n/a
46	CHD2	chr12:86544643-86544699	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr12:86580320-86580470	HBMEC	blood vessel:	n/a	n/a
48	CTCF	chr12:86643680-86643830	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr12:86617800-86617950	HBMEC	blood vessel:	n/a	n/a
50	CTCF	chr12:86438318-86438349	ProgFib	skin:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:86651249-86651299	SK-N-SH_RA	brain:	n/a
2	chr12:86651249-86651299	SK-N-SH_RA	brain:	n/a
3	chr12:86690485-86690535	GM12891	blood:	n/a
4	chr12:86650107-86650157	GM19239	blood:	n/a
5	chr12:86658745-86658795	AoSMC	blood vessel:	n/a
6	chr12:86658745-86658795	SK-N-MC	brain:	n/a
7	chr12:86658385-86658435	PANC-1	pancreas:	n/a
8	chr12:86651249-86651299	H1-hESC	embryonic stem cell:	embryo
9	chr12:86650107-86650157	AoSMC	blood vessel:	n/a
10	chr12:86658745-86658795	RPTEC	kidney:	n/a
11	chr12:86650107-86650157	PrEC	prostate:	n/a
12	chr12:86650107-86650157	NH-A	brain:	n/a
13	chr12:86727874-86727924	T-47D	breast:	n/a
14	chr12:86658385-86658435	RPTEC	kidney:	n/a
15	chr12:86727874-86727924	ECC-1	luminal epithelium:	n/a
16	chr12:86658385-86658435	PrEC	prostate:	n/a
17	chr12:86659008-86659058	HIPEpiC	eye:	n/a
18	chr12:86658860-86658910	NHBE	bronchial:	n/a
19	chr12:86659008-86659058	LNCaP	prostate:	n/a
20	chr12:86658385-86658435	HEK293	kidney:	embryo
21	chr12:86651249-86651299	AG10803	skin:	n/a
22	chr12:86651249-86651299	HRCEpiC	kidney:	n/a
23	chr12:86690485-86690535	AG10803	skin:	n/a
24	chr12:86727874-86727924	ProgFib	skin:	n/a
25	chr12:86658860-86658910	HRPEpiC	eye:	n/a
26	chr12:86658745-86658795	HCPEpiC	choroid plexus:	n/a
27	chr12:86658745-86658795	NHDF-neo	bronchial:	n/a
28	chr12:86658385-86658435	HNPCEpiC	eye:	n/a
29	chr12:86650107-86650157	LNCaP	prostate:	n/a
30	chr12:86658860-86658910	AG04450	lung:	fetal
31	chr12:86659008-86659058	SK-N-SH_RA	brain:	n/a
32	chr12:86690485-86690535	HEK293	kidney:	embryo
33	chr12:86651249-86651299	NH-A	brain:	n/a
34	chr12:86651249-86651299	RPTEC	kidney:	n/a
35	chr12:86658860-86658910	HEEpiC	esophagus:	n/a
36	chr12:86658745-86658795	MCF10A-Er-Src	breast:	n/a
37	chr12:86727874-86727924	HUVEC	blood vessel:	n/a
38	chr12:86658385-86658435	A549	lung:	n/a
39	chr12:86658860-86658910	SAEC	small airway:	n/a
40	chr12:86658385-86658435	AoSMC	blood vessel:	n/a
41	chr12:86658385-86658435	PFSK-1	brain:	n/a
42	chr12:86690485-86690535	NT2-D1	testis:	n/a
43	chr12:86727874-86727924	NT2-D1	testis:	n/a
44	chr12:86658860-86658910	HUVEC	blood vessel:	n/a
45	chr12:86658860-86658910	K562	blood:	n/a
46	chr12:86651249-86651299	HMEC	breast:	n/a
47	chr12:86658385-86658435	HAEpiC	amniotic membrane:	n/a
48	chr12:86658745-86658795	GM06990	blood:	n/a
49	chr12:86650107-86650157	T-47D	breast:	n/a
50	chr12:86690485-86690535	AG09309	skin:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:86633057..86634931-chr12:86636880..86638760,2	K562	blood:
2	chr12:86626187..86628759-chr12:86629956..86631967,2	K562	blood:
3	chr12:86633057..86634931-chr12:86636880..86638760,2	K562	blood:
4	chr12:86511451..86513760-chr12:86516670..86519004,2	K562	blood:
5	chr12:86723150..86725256-chr12:86785265..86787177,2	MCF-7	breast:
6	chr12:86416679..86418710-chr12:86418948..86421586,2	MCF-7	breast:
7	chr12:86559122..86560912-chr12:86565276..86567562,2	K562	blood:
8	chr12:86629307..86629807-chr7:120030191..120030808,2	MCF-7	breast:
9	chr12:86559122..86560912-chr12:86565276..86567562,2	K562	blood:
10	chr12:86626187..86628759-chr12:86629956..86631967,2	K562	blood:
11	chr12:86416679..86418710-chr12:86418948..86421586,2	MCF-7	breast:
12	chr12:86661669..86664440-chr12:86664812..86667661,2	MCF-7	breast:
13	chr12:86661669..86664440-chr12:86664812..86667661,2	MCF-7	breast:
14	chr12:86511451..86513760-chr12:86516670..86519004,2	K562	blood:
15	chr12:86543597..86545688-chr12:86546239..86548183,2	K562	blood:
16	chr12:86365669..86366250-chr12:86579981..86580554,2	MCF-7	breast:
17	chr12:86543597..86545688-chr12:86546239..86548183,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MGAT4C-1	chr12:86461869-86462285	NONHSAT029763
2	lnc-MGAT4C-1	chr12:86650017-86650192	NONHSAT029760
3	lnc-MGAT4C-1	chr12:86443452-86443501	NONHSAT029759
4	lnc-MGAT4C-1	chr12:86443453-86443501	NONHSAT029762
5	lnc-MGAT4C-1	chr12:86650017-86650101	NONHSAT029763
6	lnc-MGAT4C-1	chr12:86421882-86421982	NONHSAT029760
7	lnc-MGAT4C-1	chr12:86443452-86443501	NONHSAT029760
8	lnc-MGAT4C-1	chr12:86727843-86727905	NONHSAT029762
9	lnc-MGAT4C-1	chr12:86727843-86727905	NONHSAT029759

No data

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

Extended variants
information (count: 5383 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:5383 , 50 per page) page: 1 2 3 4 5 6 7 ... 108

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543297194	chr12:86421920-86421921	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs564862144	chr12:86421945-86421946	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs576006353	chr12:86422368-86422369	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs543432178	chr12:86422395-86422396	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs376993319	chr12:86422434-86422435	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs138359405	chr12:86422510-86422511	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs115131380	chr12:86425149-86425150	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs143793026	chr12:86425157-86425158	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs557798771	chr12:86425198-86425199	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs572860266	chr12:86425241-86425242	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs554714263	chr12:86425305-86425306	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs369083148	chr12:86430816-86430817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs539198270	chr12:86430852-86430853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs12818675	chr12:86430891-86430892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs553203707	chr12:86430917-86430918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs189855329	chr12:86430920-86430921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs142059879	chr12:86430922-86430923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs536646990	chr12:86430990-86430991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs530488824	chr12:86430997-86430998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs374603397	chr12:86431043-86431044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs144714172	chr12:86431053-86431054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs565524623	chr12:86431071-86431072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs532689506	chr12:86431116-86431117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs547723851	chr12:86431132-86431133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs565917887	chr12:86431157-86431158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs530258821	chr12:86431192-86431193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs548249144	chr12:86431195-86431196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs570067143	chr12:86431222-86431223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs373339654	chr12:86431255-86431256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs537413339	chr12:86431257-86431258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs558684953	chr12:86431296-86431297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs555441313	chr12:86431297-86431298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs192796381	chr12:86431326-86431327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs534944386	chr12:86431336-86431337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs386764957	chr12:86431363-86431364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs6539937	chr12:86431374-86431375	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs184846227	chr12:86431395-86431396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs542058565	chr12:86431406-86431407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs556973693	chr12:86431412-86431413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs569528678	chr12:86431416-86431417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs61931120	chr12:86431417-86431418	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs189290492	chr12:86431457-86431458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs139858882	chr12:86431467-86431468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs528104286	chr12:86431514-86431515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs541310985	chr12:86431516-86431517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs559636357	chr12:86431535-86431536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs530204642	chr12:86431542-86431543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs548500639	chr12:86431544-86431545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs563761202	chr12:86431550-86431551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs530898755	chr12:86431570-86431571	Weak transcription	n/a	n/a	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:688 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:86430800-86433800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr12:86431600-86431800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr12:86433800-86434600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr12:86436200-86436400	ZNF genes & repeats	Fetal Heart	heart
5	chr12:86438000-86438400	ZNF genes & repeats	Pancreas	Pancrea
6	chr12:86438000-86439000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr12:86438200-86438400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr12:86439000-86440000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr12:86452800-86453400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr12:86453400-86457600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr12:86470600-86473800	Weak transcription	Cortex derived primary cultured neurospheres	brain
12	chr12:86473800-86474000	Enhancers	Brain Germinal Matrix	brain
13	chr12:86473800-86474200	Enhancers	Cortex derived primary cultured neurospheres	brain
14	chr12:86473800-86476400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr12:86473800-86476400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr12:86473800-86477000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr12:86474200-86474400	Weak transcription	Cortex derived primary cultured neurospheres	brain
18	chr12:86474200-86474600	Enhancers	Fetal Brain Male	brain
19	chr12:86474200-86474600	Enhancers	Fetal Heart	heart
20	chr12:86474200-86475400	Weak transcription	Brain Germinal Matrix	brain
21	chr12:86474400-86476400	Enhancers	Cortex derived primary cultured neurospheres	brain
22	chr12:86474600-86475000	Weak transcription	Fetal Heart	heart
23	chr12:86474600-86475600	Weak transcription	Fetal Brain Male	brain
24	chr12:86474600-86475800	Enhancers	Brain Anterior Caudate	brain
25	chr12:86474800-86476000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr12:86474800-86476000	Enhancers	Brain Hippocampus Middle	brain
27	chr12:86474800-86476000	Enhancers	Brain Substantia Nigra	brain
28	chr12:86475000-86476200	Enhancers	Brain Inferior Temporal Lobe	brain
29	chr12:86475000-86476200	Enhancers	Fetal Heart	heart
30	chr12:86475000-86476400	Enhancers	Brain Cingulate Gyrus	brain
31	chr12:86475400-86476200	Enhancers	Fetal Brain Female	brain
32	chr12:86475400-86476400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr12:86475400-86476600	Enhancers	Brain Germinal Matrix	brain
34	chr12:86475600-86476200	Enhancers	Fetal Brain Male	brain
35	chr12:86476200-86477200	Weak transcription	Brain Inferior Temporal Lobe	brain
36	chr12:86476600-86477400	Weak transcription	Brain Germinal Matrix	brain
37	chr12:86477200-86477600	Enhancers	Fetal Lung	lung
38	chr12:86477400-86477600	Enhancers	Brain Inferior Temporal Lobe	brain
39	chr12:86477400-86477800	Enhancers	Brain Germinal Matrix	brain
40	chr12:86484400-86486000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr12:86485000-86486000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr12:86485200-86485800	Enhancers	Pancreatic Islets	Pancreatic Islet
43	chr12:86485200-86486000	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr12:86486000-86487800	Weak transcription	HUES48 Cell Line	embryonic stem cell
45	chr12:86487800-86488000	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr12:86488000-86488400	Weak transcription	HUES48 Cell Line	embryonic stem cell
47	chr12:86488400-86488600	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr12:86488400-86489400	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr12:86488600-86489400	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr12:86488600-86489800	Enhancers	iPS-15b Cell Line	embryonic stem cell

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