Variant report

Variant	nsv541481
Chromosome Location	chr12:40226283-40439843
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1426)
CpG islands
(count:488)
Chromatin interactive
region (count:62)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1426 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:40396426-40396943	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:40384336-40384600	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:40404985-40405299	K562	blood:	n/a	n/a
4	ARID3A	chr12:40365978-40366241	K562	blood:	n/a	n/a
5	ARID3A	chr12:40404969-40405289	HepG2	liver:	n/a	n/a
6	ATF1	chr12:40233006-40233117	K562	blood:	n/a	n/a
7	ATF1	chr12:40433849-40433966	K562	blood:	n/a	n/a
8	ATF2	chr12:40229614-40229974	GM12878	blood:	n/a	n/a
9	ATF3	chr12:40296568-40297063	HCT-116	colon:	n/a	n/a
10	BACH1	chr12:40436921-40436927	K562	blood:	n/a	n/a
11	BATF	chr12:40229548-40229926	GM12878	blood:	n/a	n/a
12	BATF	chr12:40229525-40229935	GM12878	blood:	n/a	n/a
13	BCL11A	chr12:40229655-40229889	GM12878	blood:	n/a	n/a
14	BCL11A	chr12:40414180-40414488	H1-hESC	embryonic stem cell:	n/a	n/a
15	BHLHE40	chr12:40394891-40395051	K562	blood:	n/a	n/a
16	BHLHE40	chr12:40352291-40352347	K562	blood:	n/a	n/a
17	BHLHE40	chr12:40329756-40329949	K562	blood:	n/a	n/a
18	BHLHE40	chr12:40229588-40229877	GM12878	blood:	n/a	n/a
19	BHLHE40	chr12:40405034-40405200	K562	blood:	n/a	n/a
20	CBX3	chr12:40272533-40272815	K562	blood:	n/a	n/a
21	CBX3	chr12:40296552-40297169	HCT-116	colon:	n/a	n/a
22	CBX3	chr12:40393094-40393454	K562	blood:	n/a	n/a
23	CBX3	chr12:40393144-40393402	K562	blood:	n/a	n/a
24	CCNT2	chr12:40330926-40331240	K562	blood:	n/a	n/a
25	CEBPB	chr12:40378249-40378366	HepG2	liver:	n/a	chr12:40378314-40378323 chr12:40378311-40378328 chr12:40378312-40378323 chr12:40378313-40378324 chr12:40378312-40378325
26	CEBPB	chr12:40310947-40311180	HepG2	liver:	n/a	chr12:40311034-40311045
27	CEBPB	chr12:40426721-40427016	H1-hESC	embryonic stem cell:	n/a	chr12:40426877-40426888
28	CEBPB	chr12:40317211-40317549	A549	lung:	n/a	chr12:40317385-40317396
29	CEBPB	chr12:40323810-40324010	K562	blood:	n/a	chr12:40323883-40323894
30	CEBPB	chr12:40317199-40317568	IMR90	lung:	n/a	chr12:40317385-40317396
31	CEBPB	chr12:40365993-40366373	ECC-1	luminal epithelium:	n/a	chr12:40366103-40366112 chr12:40366103-40366112 chr12:40366101-40366112 chr12:40366101-40366114 chr12:40366103-40366112
32	CEBPB	chr12:40396212-40396998	A549	lung:	n/a	n/a
33	CEBPB	chr12:40325733-40326009	Hela-S3	cervix:	n/a	chr12:40325816-40325829 chr12:40325816-40325827 chr12:40325818-40325829
34	CEBPB	chr12:40296557-40297148	HCT-116	colon:	n/a	n/a
35	CEBPB	chr12:40317140-40317561	K562	blood:	n/a	chr12:40317385-40317396
36	CEBPB	chr12:40317248-40317411	HepG2	liver:	n/a	chr12:40317385-40317396
37	CEBPB	chr12:40384337-40384654	HepG2	liver:	n/a	n/a
38	CEBPB	chr12:40426722-40427029	Hela-S3	cervix:	n/a	chr12:40426877-40426888
39	CEBPB	chr12:40291029-40291240	K562	blood:	n/a	chr12:40291139-40291152
40	CEBPB	chr12:40317209-40317567	HepG2	liver:	n/a	chr12:40317385-40317396
41	CEBPB	chr12:40384318-40384643	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr12:40317186-40317488	A549	lung:	n/a	chr12:40317385-40317396
43	CEBPB	chr12:40316543-40316782	HepG2	liver:	n/a	chr12:40316601-40316614 chr12:40316601-40316614 chr12:40316603-40316614 chr12:40316673-40316686 chr12:40316613-40316624 chr12:40316675-40316686
44	CEBPB	chr12:40404952-40405387	A549	lung:	n/a	n/a
45	CEBPB	chr12:40384305-40384660	K562	blood:	n/a	n/a
46	CEBPB	chr12:40426710-40427032	IMR90	lung:	n/a	chr12:40426877-40426888
47	CEBPB	chr12:40365930-40366322	ECC-1	luminal epithelium:	n/a	chr12:40366103-40366112 chr12:40366103-40366112 chr12:40366101-40366112 chr12:40366101-40366114 chr12:40366103-40366112
48	CEBPB	chr12:40396321-40396643	HepG2	liver:	n/a	n/a
49	CEBPB	chr12:40365919-40366292	HepG2	liver:	n/a	chr12:40366103-40366112 chr12:40366103-40366112 chr12:40366101-40366112 chr12:40366101-40366114 chr12:40366103-40366112
50	CEBPB	chr12:40426741-40427008	A549	lung:	n/a	chr12:40426877-40426888

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:40372396-40372446	HRPEpiC	eye:	n/a
2	chr12:40415007-40415057	NB4	blood:	n/a
3	chr12:40364819-40364869	HRPEpiC	eye:	n/a
4	chr12:40415007-40415057	T-47D	breast:	n/a
5	chr12:40410965-40411015	ovcar-3	ovarian:	n/a
6	chr12:40280075-40280125	BJ	skin:	n/a
7	chr12:40372396-40372446	AG09309	skin:	n/a
8	chr12:40268790-40268840	SK-N-MC	brain:	n/a
9	chr12:40268790-40268840	NHBE	bronchial:	n/a
10	chr12:40280075-40280125	SKMC	muscle:	n/a
11	chr12:40372396-40372446	GM12878	blood:	n/a
12	chr12:40268790-40268840	ECC-1	luminal epithelium:	n/a
13	chr12:40372396-40372446	PANC-1	pancreas:	n/a
14	chr12:40410965-40411015	PANC-1	pancreas:	n/a
15	chr12:40427762-40427812	A549	lung:	n/a
16	chr12:40383732-40383782	HCPEpiC	choroid plexus:	n/a
17	chr12:40427762-40427812	H1-hESC	embryonic stem cell:	embryo
18	chr12:40372396-40372446	A549	lung:	n/a
19	chr12:40410965-40411015	GM19239	blood:	n/a
20	chr12:40383732-40383782	NHDF-neo	bronchial:	n/a
21	chr12:40383732-40383782	HEEpiC	esophagus:	n/a
22	chr12:40372396-40372446	SK-N-SH	brain:	n/a
23	chr12:40415007-40415057	AG04449	skin:	fetal
24	chr12:40410965-40411015	SAEC	small airway:	n/a
25	chr12:40268790-40268840	SAEC	small airway:	n/a
26	chr12:40410965-40411015	SK-N-SH	brain:	n/a
27	chr12:40280075-40280125	GM19239	blood:	n/a
28	chr12:40410965-40411015	CMK	blood:	n/a
29	chr12:40364819-40364869	ECC-1	luminal epithelium:	n/a
30	chr12:40280075-40280125	RPTEC	kidney:	n/a
31	chr12:40372396-40372446	HepG2	liver:	n/a
32	chr12:40364819-40364869	SKMC	muscle:	n/a
33	chr12:40427762-40427812	HAEpiC	amniotic membrane:	n/a
34	chr12:40383732-40383782	HRPEpiC	eye:	n/a
35	chr12:40410965-40411015	IMR90	lung:	fetal
36	chr12:40268790-40268840	AG04449	skin:	fetal
37	chr12:40372396-40372446	HCT-116	colon:	n/a
38	chr12:40268790-40268840	MCF-7	breast:	n/a
39	chr12:40280075-40280125	MCF10A-Er-Src	breast:	n/a
40	chr12:40383732-40383782	HCT-116	colon:	n/a
41	chr12:40280075-40280125	HRCEpiC	kidney:	n/a
42	chr12:40268790-40268840	GM12891	blood:	n/a
43	chr12:40415007-40415057	HMEC	breast:	n/a
44	chr12:40427762-40427812	MCF10A-Er-Src	breast:	n/a
45	chr12:40372396-40372446	NH-A	brain:	n/a
46	chr12:40415007-40415057	HRPEpiC	eye:	n/a
47	chr12:40410965-40411015	AG10803	skin:	n/a
48	chr12:40427762-40427812	HCF	heart:	n/a
49	chr12:40427762-40427812	ovcar-3	ovarian:	n/a
50	chr12:40410965-40411015	AoSMC	blood vessel:	n/a

(count:62 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	12:40350301-40351146..12:40703633-40711447	GM12878	blood:
2	chr12:40280351..40282903-chr12:40497485..40499923,2	K562	blood:
3	chr12:40404668..40405271-chr12:40503732..40504617,2	MCF-7	breast:
4	chr12:40233400..40236371-chr12:40236570..40239035,2	MCF-7	breast:
5	chr12:40400651..40403072-chr12:40497922..40501179,3	MCF-7	breast:
6	chr12:40154023..40155558-chr12:40243257..40245766,2	MCF-7	breast:
7	chr12:40404779..40405544-chr12:40501079..40501769,2	K562	blood:
8	chr12:40365099..40366790-chr12:40368418..40370454,2	K562	blood:
9	chr12:40266748..40268583-chr12:40273608..40276021,2	K562	blood:
10	chr12:40233400..40236371-chr12:40236570..40239035,2	MCF-7	breast:
11	chr12:40428243..40430877-chr12:40432067..40435027,3	K562	blood:
12	chr12:40158493..40159396-chr12:40384037..40384925,5	MCF-7	breast:
13	chr12:40428243..40430877-chr12:40432067..40435027,3	K562	blood:
14	chr12:40324481..40326427-chr12:40398894..40400439,2	MCF-7	breast:
15	chr12:40324732..40326472-chr12:40398965..40400889,3	MCF-7	breast:
16	chr12:40261148..40263319-chr12:40264058..40266162,2	MCF-7	breast:
17	chr12:40224533..40225359-chr12:40351916..40352430,2	MCF-7	breast:
18	chr12:40324480..40325465-chr12:40399923..40400479,2	MCF-7	breast:
19	chr12:40419862..40422582-chr12:40493466..40495715,2	K562	blood:
20	chr12:40158540..40159495-chr12:40351942..40352752,5	MCF-7	breast:
21	chr12:40239652..40241691-chr12:40246024..40247653,2	K562	blood:
22	chr12:40427544..40429854-chr12:40484526..40486904,2	MCF-7	breast:
23	chr12:40399921..40402831-chr12:40405268..40407402,2	MCF-7	breast:
24	chr12:40218165..40218758-chr12:40352165..40352674,2	MCF-7	breast:
25	chr12:40401380..40404194-chr12:40458458..40460119,2	K562	blood:
26	chr12:40301225..40304048-chr12:40312812..40315442,2	K562	blood:
27	chr12:40245063..40247132-chr12:40258548..40261407,2	K562	blood:
28	chr12:40425499..40426450-chr12:40706505..40707111,2	MCF-7	breast:
29	chr12:40266748..40268583-chr12:40273608..40276021,2	K562	blood:
30	chr12:40200606..40201630-chr12:40404872..40405807,3	MCF-7	breast:
31	chr12:40313077..40313679-chr12:59990152..59990853,2	Hela-S3	cervix:
32	chr12:40324480..40325465-chr12:40399923..40400479,2	MCF-7	breast:
33	chr12:40365099..40366790-chr12:40368418..40370454,2	K562	blood:
34	chr12:40404217..40405558-chr12:40500388..40503110,15	MCF-7	breast:
35	chr12:40272751..40275551-chr12:46121726..46124669,2	MCF-7	breast:
36	chr12:40239652..40241691-chr12:40246024..40247653,2	K562	blood:
37	chr12:40399921..40402831-chr12:40405268..40407402,2	MCF-7	breast:
38	chr12:40158566..40159336-chr12:40404675..40405547,2	MCF-7	breast:
39	12:40400312-40401438..12:40703633-40711447	GM12878	blood:
40	chr12:40271089..40271943-chr15:34306615..34307212,2	MCF-7	breast:
41	chr12:40158893..40159412-chr12:40383653..40384584,2	K562	blood:
42	chr12:40366212..40368701-chr12:40371213..40373110,2	K562	blood:
43	chr12:40434942..40437888-chr12:40438406..40442021,3	MCF-7	breast:
44	chr12:40413403..40416172-chr12:40500145..40501731,2	K562	blood:
45	chr12:40161730..40164453-chr12:40368546..40370092,2	K562	blood:
46	chr12:40434942..40437888-chr12:40438406..40442021,3	MCF-7	breast:
47	chr12:40366212..40368701-chr12:40371213..40373110,2	K562	blood:
48	chr12:40301225..40304048-chr12:40312812..40315442,2	K562	blood:
49	chr12:40424834..40427522-chr12:40498279..40501048,3	MCF-7	breast:
50	chr12:40324481..40326427-chr12:40398894..40400439,2	MCF-7	breast:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	SLC2A13	hsa-miR-335-5p	chr12:40344059-40344081

Variant related genes	Relation type
SLC2A13	TF binding region
SLC2A13	CpG island
ENSG00000223082	chromatin interactions
ENSG00000189079	chromatin interactions
ENSG00000188906	chromatin interactions
ENSG00000151229	chromatin interactions
ENSG00000118596	chromatin interactions
ENSG00000205592	chromatin interactions

Extended variants
information (count: 7359 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:7359 , 50 per page) page: 1 2 3 4 5 6 7 ... 148

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556477559	chr12:40226290-40226291	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs574811387	chr12:40226399-40226400	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs116891204	chr12:40226410-40226411	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs560683970	chr12:40226515-40226516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs201330796	chr12:40226516-40226517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs199520373	chr12:40226517-40226518	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs35907589	chr12:40226518-40226519	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs58277175	chr12:40226519-40226520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs200763892	chr12:40226520-40226521	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs62957760	chr12:40226539-40226540	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs572407535	chr12:40226563-40226564	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs11611143	chr12:40226577-40226578	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs553215008	chr12:40226610-40226611	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs6581365	chr12:40226614-40226615	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs182523017	chr12:40226617-40226618	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs78719252	chr12:40226638-40226639	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs188439548	chr12:40226706-40226707	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs142648786	chr12:40226717-40226718	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs566574133	chr12:40226769-40226770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs533839667	chr12:40226875-40226876	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs369014474	chr12:40226962-40226963	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs7966294	chr12:40226978-40226979	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs191780328	chr12:40226990-40226991	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs7980988	chr12:40227020-40227021	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs148356278	chr12:40227073-40227074	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs535845931	chr12:40227089-40227090	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs567614943	chr12:40227120-40227121	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs553844995	chr12:40227138-40227139	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs572522507	chr12:40227144-40227145	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs77570167	chr12:40227154-40227155	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs564225482	chr12:40227162-40227163	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs183974943	chr12:40227169-40227170	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs73101286	chr12:40227174-40227175	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs189097900	chr12:40227278-40227279	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs562407450	chr12:40227353-40227354	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs113237355	chr12:40227364-40227365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs548185963	chr12:40227525-40227526	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs559867137	chr12:40227562-40227563	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs192010686	chr12:40227582-40227583	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs552337895	chr12:40227630-40227631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs7358574	chr12:40227688-40227689	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs80219958	chr12:40227694-40227695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs538086136	chr12:40227736-40227737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs73101291	chr12:40227747-40227748	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs530421368	chr12:40227793-40227794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs78763409	chr12:40227806-40227807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs535357800	chr12:40227857-40227858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs73101294	chr12:40227861-40227862	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs572140774	chr12:40227885-40227886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs539436032	chr12:40227950-40227951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	CNVD
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
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Neurodevelopmental disorder	22521361	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Renal cell carcinoma	18194544	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
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Autism	20858243	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Cancer	20164920	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Osteosarcoma	21215367	CNVD

Chromatin state (count:1057 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:40193800-40255800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr12:40194600-40232600	Weak transcription	Right Ventricle	heart
3	chr12:40199200-40265400	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr12:40209200-40268800	Weak transcription	Duodenum Smooth Muscle	Duodenum
5	chr12:40209400-40249800	Weak transcription	Aorta	Aorta
6	chr12:40213000-40248200	Weak transcription	Fetal Intestine Large	intestine
7	chr12:40216000-40246600	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr12:40219800-40272600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr12:40221800-40232400	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr12:40222000-40239600	Weak transcription	Monocytes-CD14+_RO01746	blood
11	chr12:40222200-40259400	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr12:40224000-40226400	Enhancers	Liver	Liver
13	chr12:40224400-40232800	Weak transcription	Stomach Smooth Muscle	stomach
14	chr12:40224400-40240400	Weak transcription	Left Ventricle	heart
15	chr12:40224400-40246600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr12:40224600-40226400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr12:40224600-40226800	Enhancers	HepG2	liver
18	chr12:40225000-40226600	Enhancers	Pancreas	Pancrea
19	chr12:40225200-40226400	Enhancers	Hela-S3	cervix
20	chr12:40225400-40226400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr12:40225400-40226400	Enhancers	NH-A	brain
22	chr12:40225600-40226600	Enhancers	A549	lung
23	chr12:40225800-40226400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr12:40225800-40227600	Enhancers	Pancreatic Islets	Pancreatic Islet
25	chr12:40226400-40227600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr12:40226400-40275000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr12:40228000-40228200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr12:40229400-40230200	Enhancers	GM12878-XiMat	blood
29	chr12:40229400-40232800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
30	chr12:40232400-40233000	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
31	chr12:40232600-40233600	Strong transcription	Right Ventricle	heart
32	chr12:40232600-40267800	Weak transcription	Liver	Liver
33	chr12:40232800-40233000	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
34	chr12:40232800-40233000	ZNF genes & repeats	Stomach Smooth Muscle	stomach
35	chr12:40232800-40233000	Enhancers	Spleen	Spleen
36	chr12:40232800-40233200	ZNF genes & repeats	Fetal Intestine Small	intestine
37	chr12:40233000-40235200	Strong transcription	Cortex derived primary cultured neurospheres	brain
38	chr12:40233000-40259400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
39	chr12:40233000-40259800	Weak transcription	Stomach Smooth Muscle	stomach
40	chr12:40233200-40250400	Weak transcription	Fetal Intestine Small	intestine
41	chr12:40233600-40235000	Enhancers	HUVEC	blood vessel
42	chr12:40233600-40257400	Weak transcription	Right Ventricle	heart
43	chr12:40234800-40235000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr12:40234800-40245400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr12:40235200-40269200	Weak transcription	Cortex derived primary cultured neurospheres	brain
46	chr12:40239400-40240600	Enhancers	Primary monocytes fromperipheralblood	blood
47	chr12:40239400-40242000	Enhancers	Primary B cells from peripheral blood	blood
48	chr12:40239600-40240400	Enhancers	Monocytes-CD14+_RO01746	blood
49	chr12:40239600-40241600	Enhancers	Primary B cells from cord blood	blood
50	chr12:40240400-40240600	ZNF genes & repeats	Left Ventricle	heart

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