Variant report

Variant	nsv899398
Chromosome Location	chr12:86880442-87051310
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:388)
CpG islands
(count:244)
Chromatin interactive
region (count:3)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:388 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr12:86907623-86907945	GM12878	blood:	n/a	n/a
2	CBX3	chr12:87028429-87028928	HCT-116	colon:	n/a	n/a
3	CEBPB	chr12:87007056-87007537	Hela-S3	cervix:	n/a	chr12:87007313-87007324
4	CEBPB	chr12:87032800-87033051	IMR90	lung:	n/a	chr12:87033003-87033016 chr12:87032911-87032920
5	CEBPB	chr12:87007152-87007478	IMR90	lung:	n/a	chr12:87007313-87007324
6	CEBPB	chr12:87038569-87038889	A549	lung:	n/a	n/a
7	CEBPB	chr12:86969097-86969442	A549	lung:	n/a	chr12:86969264-86969275
8	CEBPB	chr12:86978450-86978649	A549	lung:	n/a	n/a
9	CEBPB	chr12:87041590-87041949	A549	lung:	n/a	n/a
10	CEBPB	chr12:87004145-87004345	H1-hESC	embryonic stem cell:	n/a	chr12:87004269-87004280 chr12:87004269-87004282
11	CEBPB	chr12:87007174-87007477	HepG2	liver:	n/a	chr12:87007313-87007324
12	CEBPB	chr12:87004119-87004420	HepG2	liver:	n/a	chr12:87004269-87004280 chr12:87004269-87004282
13	CEBPB	chr12:87029847-87030037	HepG2	liver:	n/a	chr12:87030001-87030012
14	CEBPB	chr12:87040173-87040305	HepG2	liver:	n/a	n/a
15	CEBPB	chr12:87038583-87038879	HepG2	liver:	n/a	n/a
16	CEBPB	chr12:86901393-86901548	A549	lung:	n/a	chr12:86901493-86901506 chr12:86901494-86901505
17	CEBPB	chr12:87028522-87028945	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr12:86951563-86951595	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr12:87004112-87004399	IMR90	lung:	n/a	chr12:87004269-87004280 chr12:87004269-87004282
20	CEBPB	chr12:86924383-86925166	Hela-S3	cervix:	n/a	chr12:86924980-86924991
21	CEBPB	chr12:86924820-86925108	A549	lung:	n/a	chr12:86924980-86924991
22	CEBPB	chr12:86924838-86925112	HepG2	liver:	n/a	chr12:86924980-86924991
23	CEBPB	chr12:87041512-87041964	A549	lung:	n/a	n/a
24	CEBPB	chr12:87004130-87004403	A549	lung:	n/a	chr12:87004269-87004280 chr12:87004269-87004282
25	CEBPB	chr12:87007136-87007499	ECC-1	luminal epithelium:	n/a	chr12:87007313-87007324
26	CEBPB	chr12:86901427-86901620	HepG2	liver:	n/a	chr12:86901493-86901506 chr12:86901494-86901505
27	CEBPB	chr12:87009163-87009278	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr12:86887592-86887783	A549	lung:	n/a	n/a
29	CEBPB	chr12:87007164-87007459	A549	lung:	n/a	chr12:87007313-87007324
30	CEBPB	chr12:87038592-87038865	IMR90	lung:	n/a	n/a
31	CEBPB	chr12:87004120-87004441	Hela-S3	cervix:	n/a	chr12:87004269-87004280 chr12:87004269-87004282
32	CEBPB	chr12:87041635-87041919	A549	lung:	n/a	n/a
33	CEBPB	chr12:86969245-86969329	HepG2	liver:	n/a	chr12:86969264-86969275
34	CHD2	chr12:86907575-86907975	GM12878	blood:	n/a	n/a
35	CHD2	chr12:87007085-87007413	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr12:86944920-86945070	BE2_C	brain:	n/a	n/a
37	CTCF	chr12:86995930-86996042	LNCaP	prostate:	n/a	n/a
38	CTCF	chr12:87014560-87014710	GM12871	blood:	n/a	n/a
39	CTCF	chr12:86945000-86945150	BE2_C	brain:	n/a	n/a
40	CTCF	chr12:86995926-86996080	LNCaP	prostate:	n/a	n/a
41	CTCF	chr12:86948742-86948761	GM10248	blood:	n/a	n/a
42	CTCF	chr12:86908160-86908310	GM12864	blood:	n/a	n/a
43	CTCF	chr12:87021842-87021887	LNCaP	prostate:	n/a	n/a
44	CTCF	chr12:86971800-86971950	NHEK	skin:	n/a	n/a
45	CTCF	chr12:86961884-86961951	GM10266	blood:	n/a	n/a
46	CTCF	chr12:87006492-87006547	GM13976	blood:	n/a	n/a
47	CTCF	chr12:86960736-86960790	Lung_OC	lung:	n/a	n/a
48	CTCF	chr12:86883120-86883270	GM12871	blood:	n/a	n/a
49	CTCF	chr12:86920100-86920250	GM12873	blood:	n/a	n/a
50	CTCF	chr12:86944840-86944990	AoAF	blood vessel:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:86995758-86995808	HEK293	kidney:	embryo
2	chr12:86994815-86994865	AG04449	skin:	fetal
3	chr12:86994755-86994805	K562	blood:	n/a
4	chr12:86994755-86994805	GM06990	blood:	n/a
5	chr12:86994755-86994805	ECC-1	luminal epithelium:	n/a
6	chr12:86994815-86994865	GM19239	blood:	n/a
7	chr12:86994815-86994865	HIPEpiC	eye:	n/a
8	chr12:86995758-86995808	Hepatocyte	liver:	n/a
9	chr12:86995758-86995808	PrEC	prostate:	n/a
10	chr12:86995819-86995869	IMR90	lung:	fetal
11	chr12:86994755-86994805	PFSK-1	brain:	n/a
12	chr12:86994755-86994805	HepG2	liver:	n/a
13	chr12:86995819-86995869	NT2-D1	testis:	n/a
14	chr12:86994755-86994805	NHBE	bronchial:	n/a
15	chr12:86994815-86994865	SAEC	small airway:	n/a
16	chr12:86995758-86995808	GM12891	blood:	n/a
17	chr12:86995819-86995869	ProgFib	skin:	n/a
18	chr12:86995819-86995869	GM19239	blood:	n/a
19	chr12:86994815-86994865	NHDF-neo	bronchial:	n/a
20	chr12:86994815-86994865	MCF-7	breast:	n/a
21	chr12:86995819-86995869	Caco-2	colon:	n/a
22	chr12:86994755-86994805	PrEC	prostate:	n/a
23	chr12:86994815-86994865	HPAEpiC	pulmonary alveolar:	n/a
24	chr12:86995758-86995808	AG09319	gingival:	n/a
25	chr12:86994755-86994805	HPAEpiC	pulmonary alveolar:	n/a
26	chr12:86995819-86995869	HepG2	liver:	n/a
27	chr12:86994755-86994805	GM12892	blood:	n/a
28	chr12:86994755-86994805	SAEC	small airway:	n/a
29	chr12:86994755-86994805	RPTEC	kidney:	n/a
30	chr12:86994815-86994865	HRPEpiC	eye:	n/a
31	chr12:86995758-86995808	NH-A	brain:	n/a
32	chr12:86994815-86994865	HNPCEpiC	eye:	n/a
33	chr12:86995819-86995869	GM12891	blood:	n/a
34	chr12:86994815-86994865	HMEC	breast:	n/a
35	chr12:86995819-86995869	HEK293	kidney:	embryo
36	chr12:86995758-86995808	GM19239	blood:	n/a
37	chr12:86995819-86995869	LNCaP	prostate:	n/a
38	chr12:86995819-86995869	HEEpiC	esophagus:	n/a
39	chr12:86994815-86994865	NH-A	brain:	n/a
40	chr12:86995819-86995869	Hela-S3	cervix:	n/a
41	chr12:86995819-86995869	SK-N-SH	brain:	n/a
42	chr12:86994815-86994865	BE2_C	brain:	n/a
43	chr12:86995758-86995808	T-47D	breast:	n/a
44	chr12:86995758-86995808	IMR90	lung:	fetal
45	chr12:86995819-86995869	SK-N-MC	brain:	n/a
46	chr12:86994755-86994805	Caco-2	colon:	n/a
47	chr12:86994815-86994865	NHBE	bronchial:	n/a
48	chr12:86994755-86994805	BE2_C	brain:	n/a
49	chr12:86995758-86995808	GM12878	blood:	n/a
50	chr12:86994755-86994805	NB4	blood:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:87039292..87041386-chr12:87052095..87053649,2	MCF-7	breast:
2	chr12:86873477..86875774-chr12:86880255..86882982,2	K562	blood:
3	chr12:87039746..87040275-chr20:55849330..55849889,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MGAT4C-1	chr12:86995005-86995081	NONHSAT029759
2	lnc-MGAT4C-1	chr12:86889028-86889092	NONHSAT029762
3	lnc-MGAT4C-1	chr12:86993355-86993438	ENSG00000258185
4	lnc-MGAT4C-1	chr12:86993355-86993438	NONHSAT029759
5	lnc-MGAT4C-2	chr12:86951512-86952255	l_687_chr12:86951511-86953159_testes
6	lnc-MGAT4C-2	chr12:86953025-86953268	l_687_chr12:86951511-86953159_testes

No data

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

Extended variants
information (count: 1681 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:1681 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2406158	chr12:86880442-86880443	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs546333715	chr12:86880456-86880457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs185466797	chr12:86880531-86880532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs534559054	chr12:86880615-86880616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs199682300	chr12:86880622-86880623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs189834412	chr12:86880695-86880696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs114228385	chr12:86880696-86880697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs183500459	chr12:86880697-86880698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs112557187	chr12:86880737-86880738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs543531728	chr12:86880754-86880755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs17014026	chr12:86880778-86880779	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs531295392	chr12:86880821-86880822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs369577820	chr12:86880842-86880843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs148055777	chr12:86880883-86880884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs193167297	chr12:86880934-86880935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs559693751	chr12:86880961-86880962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs529970723	chr12:86880970-86880971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs183313344	chr12:86880980-86880981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs188266514	chr12:86880990-86880991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs530679614	chr12:86881029-86881030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs552313378	chr12:86881078-86881079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs570601546	chr12:86881133-86881134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs528192815	chr12:86881154-86881155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs192567176	chr12:86881233-86881234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs568033729	chr12:86881241-86881242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs112676416	chr12:86881248-86881249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs78377937	chr12:86881283-86881284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs555215621	chr12:86881321-86881322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs560468412	chr12:86881322-86881323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs570156968	chr12:86881329-86881330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs537204708	chr12:86881371-86881372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs558715396	chr12:86881373-86881374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs1955399	chr12:86881383-86881384	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs541103799	chr12:86881396-86881397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs553109586	chr12:86881461-86881462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs183960614	chr12:86881505-86881506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs371289359	chr12:86881534-86881535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs541764587	chr12:86881569-86881570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs150499524	chr12:86881626-86881627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs563561352	chr12:86881628-86881629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs369943510	chr12:86881631-86881632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs188350008	chr12:86881641-86881642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs371316306	chr12:86881728-86881729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs191204433	chr12:86881749-86881750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs577067167	chr12:86881776-86881777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs184823264	chr12:86881785-86881786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs7961251	chr12:86881828-86881829	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs546639152	chr12:86881847-86881848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs190250483	chr12:86881906-86881907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs550133565	chr12:86881915-86881916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

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

Chromatin state (count:111 , 50 per page) page: 1 2 3

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

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