Variant report

Variant	nsv899396
Chromosome Location	chr12:86863041-87276957
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1384)
CpG islands
(count:549)
Chromatin interactive
region (count:14)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1384 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr12:87129390-87130163	GM12878	blood:	n/a	n/a
2	ATF2	chr12:87129495-87130047	GM12878	blood:	n/a	n/a
3	ATF3	chr12:87106039-87106609	A549	lung:	n/a	chr12:87106339-87106352
4	ATF3	chr12:87054387-87055009	A549	lung:	n/a	n/a
5	ATF3	chr12:87054426-87055001	HCT-116	colon:	n/a	n/a
6	ATF3	chr12:87106001-87106627	HCT-116	colon:	n/a	chr12:87106339-87106352
7	ATF3	chr12:87106056-87106583	A549	lung:	n/a	chr12:87106339-87106352
8	ATF3	chr12:87054371-87054987	A549	lung:	n/a	n/a
9	ATF3	chr12:87054428-87054989	HCT-116	colon:	n/a	n/a
10	BACH1	chr12:87077208-87077425	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr12:87128909-87129147	GM12878	blood:	n/a	chr12:87129029-87129040 chr12:87129124-87129137
12	BATF	chr12:87128924-87129189	GM12878	blood:	n/a	chr12:87129029-87129040 chr12:87129124-87129137
13	BATF	chr12:87129616-87130068	GM12878	blood:	n/a	n/a
14	BATF	chr12:87129654-87130011	GM12878	blood:	n/a	n/a
15	BATF	chr12:87106192-87106389	GM12878	blood:	n/a	chr12:87106276-87106287 chr12:87106273-87106283 chr12:87106277-87106287
16	BCL11A	chr12:87129719-87130045	GM12878	blood:	n/a	n/a
17	BCL3	chr12:87105926-87106732	A549	lung:	n/a	chr12:87106275-87106284 chr12:87106276-87106285
18	BCL3	chr12:87053492-87055044	A549	lung:	n/a	chr12:87053948-87053957
19	BCL3	chr12:87106135-87106543	A549	lung:	n/a	chr12:87106275-87106284 chr12:87106276-87106285
20	BCL3	chr12:87129614-87129994	GM12878	blood:	n/a	n/a
21	BCL3	chr12:87220989-87221712	A549	lung:	n/a	n/a
22	BHLHE40	chr12:86907623-86907945	GM12878	blood:	n/a	n/a
23	BHLHE40	chr12:87222440-87222493	GM12878	blood:	n/a	n/a
24	BHLHE40	chr12:87219939-87220108	A549	lung:	n/a	n/a
25	BRCA1	chr12:87106043-87106541	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr12:87054526-87054996	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr12:87120957-87121494	Hela-S3	cervix:	n/a	n/a
28	CBX3	chr12:87105981-87106752	HCT-116	colon:	n/a	chr12:87106072-87106083
29	CBX3	chr12:87028429-87028928	HCT-116	colon:	n/a	n/a
30	CBX3	chr12:87106000-87106729	HCT-116	colon:	n/a	chr12:87106072-87106083
31	CBX3	chr12:87054474-87054921	HCT-116	colon:	n/a	n/a
32	CEBPB	chr12:87062677-87063178	ECC-1	luminal epithelium:	n/a	n/a
33	CEBPB	chr12:86901393-86901548	A549	lung:	n/a	chr12:86901493-86901506 chr12:86901494-86901505
34	CEBPB	chr12:87115497-87115839	HepG2	liver:	n/a	chr12:87115669-87115680
35	CEBPB	chr12:87271055-87271397	HepG2	liver:	n/a	chr12:87271223-87271236 chr12:87271225-87271234 chr12:87271223-87271236 chr12:87271225-87271236 chr12:87271223-87271234
36	CEBPB	chr12:87004120-87004441	Hela-S3	cervix:	n/a	chr12:87004269-87004280 chr12:87004269-87004282
37	CEBPB	chr12:87038569-87038889	A549	lung:	n/a	n/a
38	CEBPB	chr12:87040173-87040305	HepG2	liver:	n/a	n/a
39	CEBPB	chr12:87103955-87104202	K562	blood:	n/a	chr12:87104071-87104082
40	CEBPB	chr12:87077538-87077814	IMR90	lung:	n/a	n/a
41	CEBPB	chr12:86969245-86969329	HepG2	liver:	n/a	chr12:86969264-86969275
42	CEBPB	chr12:87115548-87115786	H1-hESC	embryonic stem cell:	n/a	chr12:87115669-87115680
43	CEBPB	chr12:87058724-87058725	K562	blood:	n/a	n/a
44	CEBPB	chr12:86924820-86925108	A549	lung:	n/a	chr12:86924980-86924991
45	CEBPB	chr12:87105927-87106719	A549	lung:	n/a	n/a
46	CEBPB	chr12:87054495-87054913	A549	lung:	n/a	n/a
47	CEBPB	chr12:87129495-87130079	GM12878	blood:	n/a	n/a
48	CEBPB	chr12:87062792-87063130	MCF-7	breast:	n/a	n/a
49	CEBPB	chr12:87009163-87009278	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr12:87004145-87004345	H1-hESC	embryonic stem cell:	n/a	chr12:87004269-87004280 chr12:87004269-87004282

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:86995758-86995808	SK-N-SH	brain:	n/a
2	chr12:87232821-87232871	GM12891	blood:	n/a
3	chr12:86995819-86995869	AG09309	skin:	n/a
4	chr12:87106229-87106279	NT2-D1	testis:	n/a
5	chr12:87106229-87106279	GM06990	blood:	n/a
6	chr12:87232821-87232871	Hepatocyte	liver:	n/a
7	chr12:87106229-87106279	K562	blood:	n/a
8	chr12:87232692-87232742	AG04450	lung:	fetal
9	chr12:87119199-87119249	PrEC	prostate:	n/a
10	chr12:87232692-87232742	PFSK-1	brain:	n/a
11	chr12:87232821-87232871	AG09309	skin:	n/a
12	chr12:86995819-86995869	MCF-7	breast:	n/a
13	chr12:87232511-87232561	ovcar-3	ovarian:	n/a
14	chr12:87232821-87232871	T-47D	breast:	n/a
15	chr12:87119199-87119249	T-47D	breast:	n/a
16	chr12:86995758-86995808	Hepatocyte	liver:	n/a
17	chr12:86994755-86994805	HCM	heart:	n/a
18	chr12:87232821-87232871	HCPEpiC	choroid plexus:	n/a
19	chr12:87232821-87232871	PANC-1	pancreas:	n/a
20	chr12:87232821-87232871	HIPEpiC	eye:	n/a
21	chr12:86994755-86994805	HEK293	kidney:	embryo
22	chr12:86994755-86994805	SAEC	small airway:	n/a
23	chr12:86995758-86995808	HEEpiC	esophagus:	n/a
24	chr12:87232821-87232871	SK-N-SH	brain:	n/a
25	chr12:87106229-87106279	SK-N-SH_RA	brain:	n/a
26	chr12:87106229-87106279	T-47D	breast:	n/a
27	chr12:87232692-87232742	HCF	heart:	n/a
28	chr12:86995819-86995869	NHDF-neo	bronchial:	n/a
29	chr12:87119199-87119249	AG04450	lung:	fetal
30	chr12:87232511-87232561	AG04449	skin:	fetal
31	chr12:86994755-86994805	U87	brain:	n/a
32	chr12:87232821-87232871	SKMC	muscle:	n/a
33	chr12:87232692-87232742	AG09319	gingival:	n/a
34	chr12:86994815-86994865	PANC-1	pancreas:	n/a
35	chr12:87119199-87119249	HepG2	liver:	n/a
36	chr12:87119199-87119249	Hela-S3	cervix:	n/a
37	chr12:86995758-86995808	MCF10A-Er-Src	breast:	n/a
38	chr12:86994815-86994865	HMEC	breast:	n/a
39	chr12:86994815-86994865	HPAEpiC	pulmonary alveolar:	n/a
40	chr12:86995819-86995869	T-47D	breast:	n/a
41	chr12:86995819-86995869	AG04449	skin:	fetal
42	chr12:87119199-87119249	NH-A	brain:	n/a
43	chr12:86994755-86994805	SK-N-SH	brain:	n/a
44	chr12:87232511-87232561	Caco-2	colon:	n/a
45	chr12:86994815-86994865	HEEpiC	esophagus:	n/a
46	chr12:87232821-87232871	BJ	skin:	n/a
47	chr12:87232692-87232742	SK-N-SH_RA	brain:	n/a
48	chr12:87106229-87106279	HEK293	kidney:	embryo
49	chr12:87232511-87232561	ProgFib	skin:	n/a
50	chr12:87232692-87232742	GM06990	blood:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:87039746..87040275-chr20:55849330..55849889,2	MCF-7	breast:
2	chr12:87190903..87192895-chr12:87193374..87195934,2	K562	blood:
3	chr12:87039292..87041386-chr12:87052095..87053649,2	MCF-7	breast:
4	chr12:87132936..87135299-chr12:87145575..87148336,2	K562	blood:
5	chr12:87237467..87238342-chr7:40961627..40962369,2	MCF-7	breast:
6	chr12:86873477..86875774-chr12:86880255..86882982,2	K562	blood:
7	chr12:87071567..87073233-chr12:87073299..87075080,2	MCF-7	breast:
8	chr12:87148253..87150354-chr12:87164115..87166023,2	MCF-7	breast:
9	chr12:87039292..87041386-chr12:87052095..87053649,2	MCF-7	breast:
10	chr12:86873477..86875774-chr12:86880255..86882982,2	K562	blood:
11	chr12:87071567..87073233-chr12:87073299..87075080,2	MCF-7	breast:
12	chr12:87148253..87150354-chr12:87164115..87166023,2	MCF-7	breast:
13	chr12:87132936..87135299-chr12:87145575..87148336,2	K562	blood:
14	chr12:87190903..87192895-chr12:87193374..87195934,2	K562	blood:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MGAT4C-1	chr12:86993355-86993438	ENSG00000258185
2	lnc-MGAT4C-1	chr12:87232443-87232681	NONHSAT029762
3	lnc-MGAT4C-1	chr12:87120986-87121018	NONHSAT029762
4	lnc-MGAT4C-1	chr12:86995005-86995081	NONHSAT029759
5	lnc-MGAT4C-1	chr12:86889028-86889092	NONHSAT029762
6	lnc-MGAT4C-1	chr12:87232443-87232775	ENSG00000258185
7	lnc-MGAT4C-1	chr12:87120986-87121018	ENSG00000258185
8	lnc-MGAT4C-1	chr12:87120982-87121018	ENSG00000258185
9	lnc-MGAT4C-1	chr12:86993355-86993438	NONHSAT029759
10	lnc-MGAT4C-2	chr12:86953025-86953268	l_687_chr12:86951511-86953159_testes
11	lnc-MGAT4C-1	chr12:87232443-87232905	ENSG00000258185
12	lnc-MGAT4C-2	chr12:86951512-86952255	l_687_chr12:86951511-86953159_testes

No data

Variant related genes	Relation type
ENSG00000264077	TF binding region
MGAT4C	TF binding region
ENSG00000258185	TF binding region
ENSG00000264077	CpG island
MGAT4C	CpG island
ENSG00000258185	CpG island

Extended variants
information (count: 5023 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:5023 , 50 per page) page: 1 2 3 4 5 6 7 ... 101

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4300451	chr12:86863041-86863042	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs181759634	chr12:86863050-86863051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs369539082	chr12:86863078-86863079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs111865332	chr12:86863103-86863104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs547797730	chr12:86863124-86863125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs551477325	chr12:86863137-86863138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs566483237	chr12:86863144-86863145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs533517179	chr12:86863187-86863188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs186441616	chr12:86863196-86863197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs150413331	chr12:86863244-86863245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs61949559	chr12:86863245-86863246	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs191324089	chr12:86863339-86863340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs536505623	chr12:86863340-86863341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs113462086	chr12:86863371-86863372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs545922263	chr12:86863373-86863374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs564397529	chr12:86863391-86863392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs371851657	chr12:86863401-86863402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs573205546	chr12:86863409-86863410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs112429424	chr12:86863465-86863466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs182316058	chr12:86863493-86863494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs529253668	chr12:86863556-86863557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs568477216	chr12:86863617-86863618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs186640537	chr12:86863661-86863662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs144124973	chr12:86863662-86863663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs551467173	chr12:86863674-86863675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs75991433	chr12:86863690-86863691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs533785831	chr12:86863706-86863707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs548749302	chr12:86863735-86863736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs147291345	chr12:86863753-86863754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs140935026	chr12:86863800-86863801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs557211537	chr12:86863803-86863804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs575455589	chr12:86863808-86863809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs111832645	chr12:86863809-86863810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs558241501	chr12:86863810-86863811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs534200671	chr12:86863852-86863853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs573213022	chr12:86863935-86863936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs73387880	chr12:86864012-86864013	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs143952176	chr12:86864045-86864046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs61950760	chr12:86864052-86864053	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs544538288	chr12:86864086-86864087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs562736562	chr12:86864090-86864091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs533168460	chr12:86864101-86864102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs551238968	chr12:86864102-86864103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs201963530	chr12:86864105-86864106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs73189394	chr12:86864106-86864107	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs577792306	chr12:86864108-86864109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs199578307	chr12:86864109-86864110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs370536055	chr12:86864127-86864128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs566950082	chr12:86864129-86864130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs112646795	chr12:86864136-86864137	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
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
Multiple myeloma	17550852	CNVD
Breast cancer	22522925	CNVD
Recurrent pregnancy loss	19789632	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Melanoma	17363583	CNVD

Chromatin state (count:462 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:86861200-86867000	Weak transcription	Fetal Lung	lung
2	chr12:86867000-86867800	Enhancers	Fetal Lung	lung
3	chr12:86872400-86878200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr12:86878000-86878200	Enhancers	Pancreas	Pancrea
5	chr12:86878200-86878400	ZNF genes & repeats	Pancreas	Pancrea
6	chr12:86878200-86878600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr12:86878200-86878600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr12:86878200-86878800	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr12:86878200-86878800	Enhancers	H1 Cell Line	embryonic stem cell
10	chr12:86878400-86879800	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr12:86878600-86879200	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr12:86878600-86882800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr12:86878800-86879600	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr12:86879000-86879600	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr12:86882800-86883600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
16	chr12:86888600-86890000	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr12:86888800-86889400	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr12:86889000-86889400	Enhancers	Brain Germinal Matrix	brain
19	chr12:86889200-86890000	Enhancers	H9 Cell Line	embryonic stem cell
20	chr12:86889200-86890000	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr12:86906800-86907000	Enhancers	Fetal Lung	lung
22	chr12:86907000-86907400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr12:86907000-86907400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr12:86907000-86907400	Flanking Active TSS	Fetal Lung	lung
25	chr12:86907000-86907400	Enhancers	Dnd41	blood
26	chr12:86907200-86907400	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr12:86907200-86907400	Enhancers	Adipose Nuclei	Adipose
28	chr12:86907200-86907600	Enhancers	Muscle Satellite Cultured Cells	--
29	chr12:86907200-86907800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
30	chr12:86907200-86908000	Active TSS	Brain Anterior Caudate	brain
31	chr12:86907200-86908200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
32	chr12:86907200-86908200	Enhancers	GM12878-XiMat	blood
33	chr12:86907200-86908400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr12:86907400-86907600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr12:86907400-86907600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr12:86907400-86907600	Enhancers	Brain Hippocampus Middle	brain
37	chr12:86907400-86907600	Enhancers	Brain Inferior Temporal Lobe	brain
38	chr12:86907400-86907600	Enhancers	Fetal Lung	lung
39	chr12:86907400-86907600	Enhancers	A549	lung
40	chr12:86907400-86907800	Flanking Active TSS	Adipose Nuclei	Adipose
41	chr12:86907400-86907800	Active TSS	Brain Substantia Nigra	brain
42	chr12:86907400-86908000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr12:86907400-86908000	Flanking Active TSS	Dnd41	blood
44	chr12:86907400-86908200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr12:86907400-86908400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr12:86907400-86908600	Enhancers	Fetal Heart	heart
47	chr12:86907600-86907800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr12:86907600-86907800	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
49	chr12:86907600-86908000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr12:86907600-86908000	Flanking Active TSS	Muscle Satellite Cultured Cells	--

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