Variant report

Variant	nsv899013
Chromosome Location	chr12:39567945-39732430
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:919)
CpG islands
(count:244)
Chromatin interactive
region (count:42)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:919 , 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	ARID3A	chr12:39713017-39713303	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:39726981-39727045	K562	blood:	n/a	n/a
3	ARID3A	chr12:39708632-39708643	K562	blood:	n/a	n/a
4	ATF1	chr12:39681654-39681982	K562	blood:	n/a	n/a
5	ATF2	chr12:39599817-39600262	GM12878	blood:	n/a	n/a
6	ATF2	chr12:39567500-39567998	GM12878	blood:	n/a	n/a
7	BACH1	chr12:39713137-39713293	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr12:39693284-39693435	GM12878	blood:	n/a	n/a
9	BATF	chr12:39626976-39627170	GM12878	blood:	n/a	chr12:39627086-39627097
10	BATF	chr12:39599839-39600242	GM12878	blood:	n/a	n/a
11	BATF	chr12:39626610-39626815	GM12878	blood:	n/a	n/a
12	BATF	chr12:39671281-39671667	GM12878	blood:	n/a	n/a
13	BATF	chr12:39671306-39671625	GM12878	blood:	n/a	n/a
14	BATF	chr12:39626959-39627154	GM12878	blood:	n/a	chr12:39627086-39627097
15	BATF	chr12:39693282-39693429	GM12878	blood:	n/a	n/a
16	BATF	chr12:39599781-39600204	GM12878	blood:	n/a	n/a
17	BCL3	chr12:39630714-39631296	A549	lung:	n/a	n/a
18	BCL3	chr12:39630667-39631248	A549	lung:	n/a	n/a
19	BHLHE40	chr12:39599801-39600047	GM12878	blood:	n/a	n/a
20	BHLHE40	chr12:39667041-39667224	GM12878	blood:	n/a	n/a
21	BHLHE40	chr12:39671371-39671521	GM12878	blood:	n/a	n/a
22	BRCA1	chr12:39694055-39694061	GM12878	blood:	n/a	n/a
23	BRCA1	chr12:39618264-39618265	GM12878	blood:	n/a	n/a
24	CEBPB	chr12:39707718-39707730	K562	blood:	n/a	n/a
25	CEBPB	chr12:39681644-39682034	A549	lung:	n/a	chr12:39681826-39681837
26	CEBPB	chr12:39612419-39612607	A549	lung:	n/a	n/a
27	CEBPB	chr12:39681567-39682036	ECC-1	luminal epithelium:	n/a	chr12:39681826-39681837
28	CEBPB	chr12:39681602-39681955	A549	lung:	n/a	chr12:39681826-39681837
29	CEBPB	chr12:39681618-39681998	MCF-7	breast:	n/a	chr12:39681826-39681837
30	CEBPB	chr12:39681640-39682014	H1-hESC	embryonic stem cell:	n/a	chr12:39681826-39681837
31	CEBPB	chr12:39681542-39682062	K562	blood:	n/a	chr12:39681826-39681837
32	CEBPB	chr12:39724202-39724401	HepG2	liver:	n/a	chr12:39724314-39724325 chr12:39724316-39724327
33	CEBPB	chr12:39671251-39671626	K562	blood:	n/a	chr12:39671434-39671447 chr12:39671434-39671447 chr12:39671434-39671445 chr12:39671436-39671447
34	CEBPB	chr12:39681750-39681908	HepG2	liver:	n/a	chr12:39681826-39681837
35	CEBPB	chr12:39671094-39671647	Hela-S3	cervix:	n/a	chr12:39671434-39671447 chr12:39671239-39671252 chr12:39671434-39671447 chr12:39671434-39671445 chr12:39671436-39671447
36	CEBPB	chr12:39681629-39681971	K562	blood:	n/a	chr12:39681826-39681837
37	CEBPB	chr12:39681650-39682021	IMR90	lung:	n/a	chr12:39681826-39681837
38	CEBPB	chr12:39630887-39631318	A549	lung:	n/a	n/a
39	CEBPB	chr12:39681689-39681935	HepG2	liver:	n/a	chr12:39681826-39681837
40	CEBPB	chr12:39708432-39708620	A549	lung:	n/a	chr12:39708518-39708529
41	CEBPB	chr12:39712949-39713260	HepG2	liver:	n/a	chr12:39713116-39713127
42	CEBPB	chr12:39681660-39682018	K562	blood:	n/a	chr12:39681826-39681837
43	CEBPB	chr12:39598766-39599081	IMR90	lung:	n/a	chr12:39598896-39598909 chr12:39598898-39598909 chr12:39599036-39599047 chr12:39598921-39598934 chr12:39598896-39598907 chr12:39598918-39598935 chr12:39599034-39599047
44	CEBPB	chr12:39671272-39671617	A549	lung:	n/a	chr12:39671434-39671447 chr12:39671434-39671447 chr12:39671434-39671445 chr12:39671436-39671447
45	CEBPB	chr12:39681603-39682092	MCF-7	breast:	n/a	chr12:39681826-39681837
46	CEBPB	chr12:39630745-39631303	A549	lung:	n/a	n/a
47	CEBPB	chr12:39712964-39713245	MCF-7	breast:	n/a	chr12:39713116-39713127
48	CEBPB	chr12:39671277-39671610	HepG2	liver:	n/a	chr12:39671434-39671447 chr12:39671434-39671447 chr12:39671434-39671445 chr12:39671436-39671447
49	CEBPB	chr12:39681643-39682028	HepG2	liver:	n/a	chr12:39681826-39681837
50	CEBPB	chr12:39681203-39682057	Hela-S3	cervix:	n/a	chr12:39681826-39681837

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:39727030-39727080	SAEC	small airway:	n/a
2	chr12:39706834-39706884	MCF10A-Er-Src	breast:	n/a
3	chr12:39727030-39727080	MCF-7	breast:	n/a
4	chr12:39706834-39706884	NH-A	brain:	n/a
5	chr12:39687917-39687967	MCF10A-Er-Src	breast:	n/a
6	chr12:39687917-39687967	HRPEpiC	eye:	n/a
7	chr12:39706834-39706884	HL-60	blood:	n/a
8	chr12:39726715-39726765	ovcar-3	ovarian:	n/a
9	chr12:39687917-39687967	HCF	heart:	n/a
10	chr12:39727030-39727080	NH-A	brain:	n/a
11	chr12:39726715-39726765	AoSMC	blood vessel:	n/a
12	chr12:39727030-39727080	HAEpiC	amniotic membrane:	n/a
13	chr12:39706834-39706884	AoSMC	blood vessel:	n/a
14	chr12:39706834-39706884	SK-N-SH_RA	brain:	n/a
15	chr12:39726715-39726765	HL-60	blood:	n/a
16	chr12:39727030-39727080	AG04450	lung:	fetal
17	chr12:39687917-39687967	HepG2	liver:	n/a
18	chr12:39727030-39727080	HCT-116	colon:	n/a
19	chr12:39706834-39706884	SKMC	muscle:	n/a
20	chr12:39706834-39706884	HCM	heart:	n/a
21	chr12:39727030-39727080	AG09319	gingival:	n/a
22	chr12:39727030-39727080	GM12892	blood:	n/a
23	chr12:39726715-39726765	HRE	kidney:	n/a
24	chr12:39726715-39726765	MCF-7	breast:	n/a
25	chr12:39687917-39687967	NHBE	bronchial:	n/a
26	chr12:39727030-39727080	PFSK-1	brain:	n/a
27	chr12:39727030-39727080	NT2-D1	testis:	n/a
28	chr12:39727030-39727080	GM06990	blood:	n/a
29	chr12:39727030-39727080	LNCaP	prostate:	n/a
30	chr12:39687917-39687967	ProgFib	skin:	n/a
31	chr12:39726715-39726765	CMK	blood:	n/a
32	chr12:39727030-39727080	HRE	kidney:	n/a
33	chr12:39726715-39726765	SKMC	muscle:	n/a
34	chr12:39687917-39687967	RPTEC	kidney:	n/a
35	chr12:39687917-39687967	MCF-7	breast:	n/a
36	chr12:39727030-39727080	SKMC	muscle:	n/a
37	chr12:39706834-39706884	T-47D	breast:	n/a
38	chr12:39727030-39727080	Hepatocyte	liver:	n/a
39	chr12:39727030-39727080	Jurkat	blood:	n/a
40	chr12:39727030-39727080	H1-hESC	embryonic stem cell:	embryo
41	chr12:39706834-39706884	GM12878	blood:	n/a
42	chr12:39687917-39687967	LNCaP	prostate:	n/a
43	chr12:39726715-39726765	HUVEC	blood vessel:	n/a
44	chr12:39727030-39727080	PrEC	prostate:	n/a
45	chr12:39726715-39726765	GM12891	blood:	n/a
46	chr12:39706834-39706884	CMK	blood:	n/a
47	chr12:39706834-39706884	HPAEpiC	pulmonary alveolar:	n/a
48	chr12:39727030-39727080	HCPEpiC	choroid plexus:	n/a
49	chr12:39727030-39727080	Hela-S3	cervix:	n/a
50	chr12:39706834-39706884	NB4	blood:	n/a

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:39607982..39610891-chr12:39612624..39615291,2	K562	blood:
2	chr12:39705679..39708570-chr12:39709976..39712207,2	MCF-7	breast:
3	chr12:39723120..39728244-chr12:39834929..39837982,4	MCF-7	breast:
4	chr12:39709526..39712296-chr12:39716470..39718844,2	MCF-7	breast:
5	chr12:39701621..39703209-chr12:39709361..39712125,2	K562	blood:
6	chr12:39711735..39712649-chr12:40077357..40078312,2	K562	blood:
7	chr12:39713760..39716372-chr12:39835448..39837014,2	MCF-7	breast:
8	chr12:39708828..39711217-chr12:39835849..39838225,2	K562	blood:
9	chr12:39690972..39693239-chr12:39694761..39697625,2	MCF-7	breast:
10	chr12:39729399..39730971-chr12:39733599..39736235,2	MCF-7	breast:
11	chr12:39685600..39687183-chr12:39700503..39702703,2	K562	blood:
12	chr12:39725322..39729241-chr12:39730380..39734731,5	K562	blood:
13	chr12:39716315..39719529-chr12:39835472..39838157,3	K562	blood:
14	chr12:39690972..39693239-chr12:39694761..39697625,2	MCF-7	breast:
15	chr12:38532568..38533113-chr12:39666750..39667387,2	K562	blood:
16	chr12:39708256..39710912-chr12:39833762..39835679,2	MCF-7	breast:
17	chr12:39708222..39708926-chr12:39836719..39837524,2	MCF-7	breast:
18	chr12:39707343..39709850-chr12:39833796..39835957,2	K562	blood:
19	chr12:39708198..39710149-chr12:39835781..39837977,2	MCF-7	breast:
20	chr12:39701709..39705031-chr12:39707216..39710861,3	K562	blood:
21	chr12:39721304..39723929-chr12:39731222..39733567,2	K562	blood:
22	chr12:39701435..39705436-chr12:39706649..39711644,6	MCF-7	breast:
23	chr12:39706735..39709135-chr12:39713252..39715316,2	K562	blood:
24	chr12:39701435..39705436-chr12:39706649..39711644,6	MCF-7	breast:
25	chr12:39607982..39610891-chr12:39612624..39615291,2	K562	blood:
26	chr12:39706735..39709135-chr12:39713252..39715316,2	K562	blood:
27	chr12:39698698..39701515-chr12:39705485..39708006,2	K562	blood:
28	chr12:39708405..39711742-chr12:39713944..39715751,3	K562	blood:
29	chr12:39725322..39729241-chr12:39730380..39734731,5	K562	blood:
30	chr12:39707021..39709923-chr12:39830984..39833005,2	K562	blood:
31	chr12:39701709..39705031-chr12:39707216..39710861,3	K562	blood:
32	chr12:39679471..39682455-chr12:39683067..39685661,2	MCF-7	breast:
33	chr12:38722084..38722866-chr12:39667246..39667987,2	MCF-7	breast:
34	chr12:39685600..39687183-chr12:39700503..39702703,2	K562	blood:
35	chr12:39701621..39703209-chr12:39709361..39712125,2	K562	blood:
36	chr12:39694207..39696152-chr12:39837237..39840087,2	K562	blood:
37	chr12:39300107..39301045-chr12:39666439..39667709,7	MCF-7	breast:
38	chr12:39582358..39584719-chr20:55839448..55841740,2	MCF-7	breast:
39	chr12:39709526..39712296-chr12:39716470..39718844,2	MCF-7	breast:
40	chr12:39679471..39682455-chr12:39683067..39685661,2	MCF-7	breast:
41	chr12:39727146..39729804-chr12:39835867..39838331,2	K562	blood:
42	chr12:39719395..39721529-chr12:39835962..39838768,2	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C12orf40-3	chr12:39720075-39720147	NONHSAT027700
2	lnc-C12orf40-3	chr12:39720338-39720424	NONHSAT027701
3	lnc-C12orf40-4	chr12:39667024-39667150	NONHSAT027698
4	lnc-C12orf40-3	chr12:39721472-39721634	NONHSAT027701
5	lnc-C12orf40-3	chr12:39721864-39722713	NONHSAT027702
6	lnc-C12orf40-3	chr12:39721472-39721634	NONHSAT027700
7	lnc-C12orf40-4	chr12:39667587-39667691	NONHSAT027698
8	lnc-C12orf40-3	chr12:39721864-39722713	NONHSAT027700
9	lnc-C12orf40-3	chr12:39721864-39722713	NONHSAT027701
10	lnc-C12orf40-3	chr12:39721452-39721634	NONHSAT027702

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	KIF21A	hsa-miR-186-5p	chr12:39688170-39688191
2	KIF21A	hsa-miR-186-5p	chr12:39687380-39687401

Variant related genes	Relation type
KIF21A	TF binding region
KIF21A	CpG island
ENSG00000101144	chromatin interactions
ENSG00000257718	chromatin interactions
ENSG00000252974	chromatin interactions
ENSG00000139116	chromatin interactions

Extended variants
information (count: 3447 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:3447 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11170975	chr12:39567945-39567946	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs137889058	chr12:39567946-39567947	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs535816696	chr12:39567973-39567974	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs75964120	chr12:39568013-39568014	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs560103964	chr12:39568076-39568077	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs76271689	chr12:39568077-39568078	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs181380046	chr12:39568112-39568113	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs557531274	chr12:39568159-39568160	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs577387680	chr12:39568173-39568174	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs149447817	chr12:39568177-39568178	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs559800384	chr12:39568213-39568214	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs561179072	chr12:39568215-39568216	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs184231323	chr12:39568224-39568225	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs549289619	chr12:39568327-39568328	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs145905932	chr12:39568361-39568362	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs540951170	chr12:39570005-39570006	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs554148888	chr12:39570047-39570048	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs574211499	chr12:39570051-39570052	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs542843161	chr12:39570052-39570053	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs563045710	chr12:39570053-39570054	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs74345465	chr12:39570095-39570096	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs189777917	chr12:39570133-39570134	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs73084866	chr12:39570134-39570135	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs145553461	chr12:39570176-39570177	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs547696230	chr12:39570233-39570234	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs148859172	chr12:39570276-39570277	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs372894816	chr12:39570299-39570300	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs112628072	chr12:39570308-39570309	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs549715061	chr12:39570316-39570317	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs182115592	chr12:39570437-39570438	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs150949370	chr12:39570475-39570476	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs558658886	chr12:39570478-39570479	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs140708225	chr12:39570534-39570535	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs534585223	chr12:39570563-39570564	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs17483228	chr12:39570573-39570574	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs574247888	chr12:39570579-39570580	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs536902699	chr12:39570591-39570592	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs77942240	chr12:39570637-39570638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs576195172	chr12:39570651-39570652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs545118052	chr12:39570720-39570721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs4332558	chr12:39570724-39570725	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs537780764	chr12:39570772-39570773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs541054540	chr12:39570793-39570794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs144569559	chr12:39570800-39570801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs371937564	chr12:39570858-39570859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs529957573	chr12:39570892-39570893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs187033185	chr12:39570906-39570907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs189958355	chr12:39570957-39570958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs532325570	chr12:39571026-39571027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs552335963	chr12:39571047-39571048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

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
Breast cancer	21509527	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
Breast cancer	21364760	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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:691 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:39567200-39568400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr12:39567400-39568000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr12:39570000-39570600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr12:39570600-39575200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr12:39575200-39575800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr12:39577600-39578400	Enhancers	Fetal Lung	lung
7	chr12:39592800-39593000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr12:39592800-39593400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr12:39592800-39593800	Enhancers	HUVEC	blood vessel
10	chr12:39592800-39594200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr12:39593000-39593400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr12:39593000-39593400	Enhancers	Cortex derived primary cultured neurospheres	brain
13	chr12:39593000-39593600	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr12:39593000-39593600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr12:39593000-39593800	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr12:39593000-39593800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
17	chr12:39593200-39593600	Enhancers	Fetal Lung	lung
18	chr12:39593400-39593600	Enhancers	Rectal Mucosa Donor 29	rectum
19	chr12:39593400-39595000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr12:39595200-39595400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr12:39611400-39611800	Enhancers	Esophagus	oesophagus
22	chr12:39620800-39622000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr12:39621000-39621400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr12:39621000-39621600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr12:39621200-39621400	Enhancers	Cortex derived primary cultured neurospheres	brain
26	chr12:39622000-39624000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr12:39624000-39624600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr12:39624600-39629600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr12:39629400-39630200	Enhancers	Colon Smooth Muscle	Colon
30	chr12:39629600-39631400	Enhancers	NH-A	brain
31	chr12:39629600-39635000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr12:39629800-39630000	Enhancers	Sigmoid Colon	Sigmoid Colon
33	chr12:39629800-39630400	Enhancers	A549	lung
34	chr12:39629800-39631200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr12:39630000-39634000	Weak transcription	Sigmoid Colon	Sigmoid Colon
36	chr12:39630200-39631200	Enhancers	Hela-S3	cervix
37	chr12:39630200-39631400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr12:39630200-39631400	Enhancers	Muscle Satellite Cultured Cells	--
39	chr12:39630400-39631200	Flanking Active TSS	A549	lung
40	chr12:39630600-39631000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr12:39630600-39631000	Enhancers	HSMMtube	muscle
42	chr12:39630800-39631200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr12:39630800-39631600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr12:39631200-39631400	Enhancers	Cortex derived primary cultured neurospheres	brain
45	chr12:39631200-39631400	Enhancers	A549	lung
46	chr12:39631200-39632600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr12:39631200-39632600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr12:39631400-39632600	Weak transcription	Cortex derived primary cultured neurospheres	brain
49	chr12:39631400-39633200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr12:39631600-39632200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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