Variant report

Variant	nsv719
Chromosome Location	chr12:56246405-56290812
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:102)
CpG islands
(count:61)
Chromatin interactive
region (count:31)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:102 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:56259246-56259443	K562	blood:	n/a	n/a
2	CBX3	chr12:56271609-56272019	K562	blood:	n/a	n/a
3	CBX3	chr12:56271594-56272011	K562	blood:	n/a	n/a
4	CBX3	chr12:56259052-56259561	HCT-116	colon:	n/a	n/a
5	CEBPB	chr12:56260270-56260609	A549	lung:	n/a	n/a
6	CEBPB	chr12:56260269-56260517	K562	blood:	n/a	n/a
7	CEBPB	chr12:56260240-56260546	A549	lung:	n/a	n/a
8	CEBPB	chr12:56260357-56260558	HepG2	liver:	n/a	n/a
9	CEBPB	chr12:56260259-56260616	IMR90	lung:	n/a	n/a
10	CEBPB	chr12:56282392-56282592	HepG2	liver:	n/a	n/a
11	CEBPB	chr12:56260269-56260596	K562	blood:	n/a	n/a
12	CEBPB	chr12:56260311-56260527	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr12:56260225-56260576	MCF-7	breast:	n/a	n/a
14	CEBPB	chr12:56260244-56260546	ECC-1	luminal epithelium:	n/a	n/a
15	CEBPB	chr12:56260285-56260590	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr12:56260240-56260588	ECC-1	luminal epithelium:	n/a	n/a
17	CEBPB	chr12:56260269-56260615	HepG2	liver:	n/a	n/a
18	CEBPB	chr12:56260301-56260573	MCF-7	breast:	n/a	n/a
19	CEBPB	chr12:56260360-56260515	HepG2	liver:	n/a	n/a
20	CEBPB	chr12:56260240-56260553	A549	lung:	n/a	n/a
21	CEBPD	chr12:56246414-56247093	K562	blood:	n/a	n/a
22	CEBPD	chr12:56246441-56246979	K562	blood:	n/a	n/a
23	CTCF	chr12:56287140-56287290	HEK293	kidney:	n/a	chr12:56287280-56287287
24	CTCF	chr12:56285217-56285251	MCF-7	breast:	n/a	n/a
25	CTCF	chr12:56250100-56250250	Hela-S3	cervix:	n/a	n/a
26	CTCF	chr12:56287217-56287330	Hela-S3	cervix:	n/a	chr12:56287280-56287287
27	CTCF	chr12:56287260-56287410	NHEK	skin:	n/a	chr12:56287280-56287287
28	CTCF	chr12:56287260-56287410	Hela-S3	cervix:	n/a	chr12:56287280-56287287
29	CTCF	chr12:56270738-56270787	LNCaP	prostate:	n/a	n/a
30	CTCF	chr12:56287200-56287350	MCF-7	breast:	n/a	chr12:56287280-56287287
31	CTCF	chr12:56250160-56250310	HBMEC	blood vessel:	n/a	n/a
32	CUX1	chr12:56274909-56274919	GM12878	blood:	n/a	n/a
33	EBF1	chr12:56274877-56275113	GM12878	blood:	n/a	n/a
34	FOS	chr12:56274815-56275195	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr12:56268389-56268630	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr12:56274819-56275205	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr12:56274820-56275137	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr12:56274864-56275168	MCF10A-Er-Src	breast:	n/a	n/a
39	GATA1	chr12:56246304-56247199	K562	blood:	n/a	n/a
40	GATA2	chr12:56246456-56247137	K562	blood:	n/a	n/a
41	GATA3	chr12:56246701-56246852	MCF-7	breast:	n/a	n/a
42	GATA3	chr12:56246544-56246871	SH-SY5Y	brain:	n/a	n/a
43	HNF4A	chr12:56282282-56282682	HepG2	liver:	n/a	chr12:56282549-56282564
44	HNF4A	chr12:56282414-56282699	HepG2	liver:	n/a	chr12:56282549-56282564
45	HNF4G	chr12:56282386-56282702	HepG2	liver:	n/a	chr12:56282548-56282563
46	IRF1	chr12:56271562-56271574	K562	blood:	n/a	n/a
47	JUND	chr12:56274426-56274447	HepG2	liver:	n/a	n/a
48	JUND	chr12:56269241-56269394	H1-hESC	embryonic stem cell:	n/a	n/a
49	KAP1	chr12:56255894-56256294	K562	blood:	n/a	n/a
50	KAP1	chr12:56259088-56259619	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:56269767-56269817	AG09319	gingival:	n/a
2	chr12:56269767-56269817	SK-N-MC	brain:	n/a
3	chr12:56269767-56269817	AG04449	skin:	fetal
4	chr12:56269767-56269817	Hepatocyte	liver:	n/a
5	chr12:56269767-56269817	SAEC	small airway:	n/a
6	chr12:56269767-56269817	HPAEpiC	pulmonary alveolar:	n/a
7	chr12:56269767-56269817	HIPEpiC	eye:	n/a
8	chr12:56269767-56269817	HNPCEpiC	eye:	n/a
9	chr12:56269767-56269817	AG09309	skin:	n/a
10	chr12:56269767-56269817	T-47D	breast:	n/a
11	chr12:56269767-56269817	HCPEpiC	choroid plexus:	n/a
12	chr12:56269767-56269817	Caco-2	colon:	n/a
13	chr12:56269767-56269817	HUVEC	blood vessel:	n/a
14	chr12:56269767-56269817	HCF	heart:	n/a
15	chr12:56269767-56269817	AG04450	lung:	fetal
16	chr12:56269767-56269817	SK-N-SH	brain:	n/a
17	chr12:56269767-56269817	K562	blood:	n/a
18	chr12:56269767-56269817	HRCEpiC	kidney:	n/a
19	chr12:56269767-56269817	NT2-D1	testis:	n/a
20	chr12:56269767-56269817	HEEpiC	esophagus:	n/a
21	chr12:56269767-56269817	NHDF-neo	bronchial:	n/a
22	chr12:56269767-56269817	MCF10A-Er-Src	breast:	n/a
23	chr12:56269767-56269817	GM06990	blood:	n/a
24	chr12:56269767-56269817	MCF-7	breast:	n/a
25	chr12:56269767-56269817	HAEpiC	amniotic membrane:	n/a
26	chr12:56269767-56269817	NHBE	bronchial:	n/a
27	chr12:56269767-56269817	GM12892	blood:	n/a
28	chr12:56269767-56269817	RPTEC	kidney:	n/a
29	chr12:56269767-56269817	SK-N-SH_RA	brain:	n/a
30	chr12:56269767-56269817	H1-hESC	embryonic stem cell:	embryo
31	chr12:56269767-56269817	ProgFib	skin:	n/a
32	chr12:56269767-56269817	HMEC	breast:	n/a
33	chr12:56269767-56269817	AG10803	skin:	n/a
34	chr12:56269767-56269817	BJ	skin:	n/a
35	chr12:56269767-56269817	GM12878	blood:	n/a
36	chr12:56269767-56269817	ECC-1	luminal epithelium:	n/a
37	chr12:56269767-56269817	PrEC	prostate:	n/a
38	chr12:56269767-56269817	HCM	heart:	n/a
39	chr12:56269767-56269817	HepG2	liver:	n/a
40	chr12:56269767-56269817	Hela-S3	cervix:	n/a
41	chr12:56269767-56269817	AoSMC	blood vessel:	n/a
42	chr12:56269767-56269817	BE2_C	brain:	n/a
43	chr12:56269767-56269817	NH-A	brain:	n/a
44	chr12:56269767-56269817	PFSK-1	brain:	n/a
45	chr12:56269767-56269817	U87	brain:	n/a
46	chr12:56269767-56269817	HRPEpiC	eye:	n/a
47	chr12:56269767-56269817	ovcar-3	ovarian:	n/a
48	chr12:56269767-56269817	HRE	kidney:	n/a
49	chr12:56269767-56269817	GM19239	blood:	n/a
50	chr12:56269767-56269817	HL-60	blood:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:56259043..56260903-chr12:56264083..56266148,2	MCF-7	breast:
2	chr12:56239688..56242373-chr12:56243822..56246712,2	K562	blood:
3	chr12:56222329..56224581-chr12:56249574..56252234,3	MCF-7	breast:
4	chr12:56279349..56281773-chr12:56292727..56294743,2	MCF-7	breast:
5	chr12:56239254..56241526-chr12:56250178..56252605,2	MCF-7	breast:
6	chr12:56276249..56278200-chr12:56283079..56285139,3	K562	blood:
7	chr12:56251018..56252886-chr12:56269364..56271809,2	MCF-7	breast:
8	chr12:56220693..56225301-chr12:56284725..56289550,5	MCF-7	breast:
9	chr12:56212052..56214479-chr12:56262564..56265253,2	MCF-7	breast:
10	chr12:56221810..56225034-chr12:56267373..56269273,5	MCF-7	breast:
11	chr12:56222854..56224376-chr12:56275059..56277720,2	MCF-7	breast:
12	chr12:56250854..56253503-chr12:56253508..56255759,2	MCF-7	breast:
13	chr12:56276249..56278200-chr12:56283079..56285139,3	K562	blood:
14	chr12:56250854..56253503-chr12:56253508..56255759,2	MCF-7	breast:
15	chr12:56252528..56254672-chr12:56323921..56326010,2	K562	blood:
16	chr12:56222856..56225509-chr12:56248097..56250014,2	MCF-7	breast:
17	chr12:56259043..56260903-chr12:56264083..56266148,2	MCF-7	breast:
18	chr12:56210407..56211916-chr12:56266892..56269258,2	MCF-7	breast:
19	chr12:56235527..56238350-chr12:56244319..56246655,2	K562	blood:
20	chr12:56253710..56255659-chr12:56256074..56259018,2	K562	blood:
21	chr12:56264439..56267013-chr12:56319966..56322100,2	MCF-7	breast:
22	chr12:56222158..56225126-chr12:56264832..56267063,2	MCF-7	breast:
23	chr12:56222008..56224355-chr12:56264663..56266225,2	MCF-7	breast:
24	chr12:56253710..56255659-chr12:56256074..56259018,2	K562	blood:
25	chr12:56262911..56265585-chr12:56266786..56268671,2	MCF-7	breast:
26	chr12:56210774..56212897-chr12:56262378..56264339,2	MCF-7	breast:
27	chr12:56251018..56252886-chr12:56269364..56271809,2	MCF-7	breast:
28	chr12:56239542..56242387-chr12:56243822..56247751,5	K562	blood:
29	chr12:56262709..56264327-chr12:56267681..56270079,2	K562	blood:
30	chr12:56258284..56260527-chr12:56321024..56323288,2	MCF-7	breast:
31	chr12:56265141..56267648-chr12:56273330..56275768,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DGKA-2	chr12:56275021-56275253	NONHSAT028711
2	lnc-ORMDL2-2	chr12:56263361-56263633	expReg_chr12_6155_+
3	lnc-ORMDL2-3	chr12:56264956-56266676	ucscGeneNc_uc001sos_2

No data

Variant related genes	Relation type
OLA1P3	TF binding region
GSTP1P1	TF binding region
RNU1-69P	TF binding region
OLA1P3	CpG island
GSTP1P1	CpG island
RNU1-69P	CpG island
ENSG00000257966	chromatin interactions
ENSG00000123353	chromatin interactions
ENSG00000205323	chromatin interactions
ENSG00000065357	chromatin interactions
ENSG00000123342	chromatin interactions
ENSG00000207339	chromatin interactions
ENSG00000170473	chromatin interactions
ENSG00000257390	chromatin interactions
ENSG00000257569	chromatin interactions
ENSG00000182796	chromatin interactions
ENSG00000135392	chromatin interactions

Extended variants
information (count: 1380 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:1380 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs112268752	chr12:56246425-56246426	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs566878675	chr12:56246494-56246495	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs374304639	chr12:56246502-56246503	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs547447352	chr12:56246572-56246573	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs149431613	chr12:56246579-56246580	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs373293943	chr12:56246641-56246642	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs113694152	chr12:56246777-56246778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs376331494	chr12:56246797-56246798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs180938297	chr12:56246798-56246799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs147610516	chr12:56246799-56246800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs537800405	chr12:56246829-56246830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs556882789	chr12:56246858-56246859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs117837756	chr12:56246885-56246886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs572472707	chr12:56246983-56246984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs185982822	chr12:56247056-56247057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs372127004	chr12:56247069-56247070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs541820705	chr12:56247116-56247117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs540340473	chr12:56247123-56247124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs561727422	chr12:56247133-56247134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs117123108	chr12:56247148-56247149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs544226673	chr12:56247230-56247231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs563219422	chr12:56247244-56247245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs73119300	chr12:56247251-56247252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs367839672	chr12:56247284-56247285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs372026503	chr12:56247321-56247322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs575345446	chr12:56247322-56247323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs551756851	chr12:56247364-56247365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs560750944	chr12:56247411-56247412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs113309523	chr12:56247454-56247455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs190910915	chr12:56247486-56247487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs112977682	chr12:56247493-56247494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs567417088	chr12:56247498-56247499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs78100674	chr12:56247504-56247505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs537889294	chr12:56247505-56247506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs4759013	chr12:56247566-56247567	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
36	rs569085332	chr12:56247603-56247604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs183100536	chr12:56247632-56247633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs536866987	chr12:56247653-56247654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs79861330	chr12:56247654-56247655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs564300612	chr12:56247693-56247694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs573005511	chr12:56247700-56247701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs533704984	chr12:56247737-56247738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs555550850	chr12:56247774-56247775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs7315755	chr12:56247828-56247829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs544250385	chr12:56247857-56247858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs187516470	chr12:56247858-56247859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs190493872	chr12:56247874-56247875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs368042134	chr12:56247900-56247901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs183382191	chr12:56248015-56248016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs546879000	chr12:56248025-56248026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
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
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
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	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
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	20505157	CNVD
Hepatocellular carcinoma	16750200	CNVD
Melanoma	18172304	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Bladder cancer	21909424	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	17661082	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	20531469	CNVD
Multiple myeloma	16616336	CNVD
Rhabdomyosarcoma	16790082	CNVD
Renal cell carcinoma	18765545	CNVD
Urothelial cell carcinoma	18451213	CNVD
Glioblastoma multiforme	21138945	CNVD
Glioblastoma multiforme	21569311	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Glioblastoma multiforme	19115005	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Breast cancer	21509527	CNVD
Lung adenocarcinoma	17982442	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Leukemia	18628472	CNVD
Breast cancer	21804112	CNVD

Chromatin state (count:132 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:56245000-56249800	Weak transcription	Muscle Satellite Cultured Cells	--
2	chr12:56245000-56250000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr12:56245000-56250000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr12:56245200-56250000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr12:56249800-56250400	Enhancers	Muscle Satellite Cultured Cells	--
6	chr12:56249800-56251200	Enhancers	Hela-S3	cervix
7	chr12:56250000-56250400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr12:56250000-56250400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr12:56250000-56250600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr12:56250000-56251000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr12:56250200-56251000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr12:56250800-56251200	Enhancers	Cortex derived primary cultured neurospheres	brain
13	chr12:56250800-56251200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr12:56256400-56256600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr12:56256600-56257200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr12:56257200-56257400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr12:56266600-56267400	Enhancers	Fetal Thymus	thymus
18	chr12:56267400-56268000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr12:56267400-56269000	Weak transcription	Fetal Thymus	thymus
20	chr12:56267800-56268000	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr12:56267800-56268200	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr12:56267800-56268400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr12:56267800-56268400	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr12:56267800-56268600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr12:56267800-56268600	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr12:56267800-56268600	Enhancers	Brain Cingulate Gyrus	brain
27	chr12:56267800-56268800	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr12:56268000-56268200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr12:56268000-56268600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr12:56268000-56268600	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr12:56268000-56270200	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr12:56268000-56270200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr12:56268200-56268400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr12:56268200-56269200	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr12:56268200-56269200	Weak transcription	HUES64 Cell Line	embryonic stem cell
36	chr12:56268200-56269800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr12:56268200-56270200	Enhancers	Breast Myoepithelial Primary Cells	Breast
38	chr12:56268400-56269600	Weak transcription	Cortex derived primary cultured neurospheres	brain
39	chr12:56268400-56272200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr12:56268600-56269000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr12:56268600-56269000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
42	chr12:56268600-56269800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
43	chr12:56268600-56271000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr12:56268800-56269200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr12:56269000-56269800	Enhancers	Fetal Thymus	thymus
46	chr12:56269000-56270000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr12:56269000-56270000	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr12:56269200-56269400	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr12:56269200-56269800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr12:56269200-56269800	Enhancers	HUES48 Cell Line	embryonic stem cell

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