Variant report

Variant	nsv559367
Chromosome Location	chr12:73130815-73385096
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:400)
CpG islands
(count:61)
Chromatin interactive
region (count:20)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:400 , 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	ATF1	chr12:73374122-73374322	K562	blood:	n/a	n/a
2	BACH1	chr12:73208970-73209323	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr12:73212115-73212362	GM12878	blood:	n/a	n/a
4	BCL11A	chr12:73249185-73249390	GM12878	blood:	n/a	n/a
5	BRCA1	chr12:73184254-73184360	Hela-S3	cervix:	n/a	n/a
6	CBX3	chr12:73153067-73153380	HCT-116	colon:	n/a	n/a
7	CEBPB	chr12:73217928-73217981	HepG2	liver:	n/a	chr12:73217954-73217965
8	CEBPB	chr12:73200699-73200856	HepG2	liver:	n/a	chr12:73200811-73200822
9	CEBPB	chr12:73351574-73351777	HepG2	liver:	n/a	chr12:73351723-73351734 chr12:73351720-73351737 chr12:73351723-73351736
10	CEBPB	chr12:73282158-73282341	H1-hESC	embryonic stem cell:	n/a	chr12:73282238-73282249
11	CEBPB	chr12:73193952-73194101	K562	blood:	n/a	chr12:73194021-73194032
12	CEBPB	chr12:73367300-73367563	HepG2	liver:	n/a	n/a
13	CEBPB	chr12:73157951-73158107	A549	lung:	n/a	n/a
14	CEBPB	chr12:73230494-73230590	A549	lung:	n/a	chr12:73230521-73230532 chr12:73230519-73230532
15	CEBPB	chr12:73200677-73201003	A549	lung:	n/a	chr12:73200811-73200822
16	CEBPB	chr12:73282088-73282352	HepG2	liver:	n/a	chr12:73282238-73282249
17	CEBPB	chr12:73184092-73184484	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr12:73298090-73298349	HepG2	liver:	n/a	chr12:73298180-73298191 chr12:73298182-73298193 chr12:73298182-73298191 chr12:73298180-73298193
19	CEBPB	chr12:73298119-73298319	A549	lung:	n/a	chr12:73298180-73298191 chr12:73298182-73298193 chr12:73298182-73298191 chr12:73298180-73298193
20	CEBPB	chr12:73193897-73194188	HepG2	liver:	n/a	chr12:73194021-73194032
21	CEBPB	chr12:73350231-73350466	HepG2	liver:	n/a	chr12:73350345-73350354 chr12:73350343-73350354 chr12:73350345-73350356 chr12:73350343-73350356 chr12:73350345-73350354 chr12:73350345-73350354 chr12:73350343-73350356 chr12:73350345-73350356 chr12:73350345-73350354
22	CEBPB	chr12:73196692-73196836	HepG2	liver:	n/a	n/a
23	CEBPB	chr12:73369644-73369858	A549	lung:	n/a	chr12:73369724-73369735 chr12:73369682-73369695
24	CEBPB	chr12:73184115-73184468	MCF-7	breast:	n/a	n/a
25	CEBPB	chr12:73282160-73282379	K562	blood:	n/a	chr12:73282238-73282249
26	CEBPB	chr12:73152789-73152830	K562	blood:	n/a	n/a
27	CEBPB	chr12:73310435-73310652	HepG2	liver:	n/a	chr12:73310520-73310531
28	CEBPB	chr12:73282533-73282852	A549	lung:	n/a	chr12:73282765-73282776 chr12:73282763-73282776 chr12:73282763-73282776 chr12:73282763-73282776 chr12:73282765-73282776
29	CEBPB	chr12:73200612-73201101	H1-hESC	embryonic stem cell:	n/a	chr12:73200811-73200822
30	CEBPB	chr12:73369686-73369713	K562	blood:	n/a	n/a
31	CHD2	chr12:73222605-73222617	GM12878	blood:	n/a	n/a
32	CTCF	chr12:73381589-73381620	GM10248	blood:	n/a	n/a
33	CTCF	chr12:73207056-73207117	GM13976	blood:	n/a	n/a
34	CTCF	chr12:73248391-73248426	Lung_OC	lung:	n/a	n/a
35	CTCF	chr12:73233380-73233530	GM12865	blood:	n/a	n/a
36	CTCF	chr12:73273920-73274070	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr12:73167240-73167390	RPTEC	kidney:	n/a	n/a
38	CTCF	chr12:73272698-73272752	Lung_OC	lung:	n/a	n/a
39	CTCF	chr12:73167506-73167615	LNCaP	prostate:	n/a	n/a
40	CTCF	chr12:73167440-73167590	SK-N-SH_RA	brain:	n/a	n/a
41	CTCF	chr12:73207692-73207761	Lung_OC	lung:	n/a	n/a
42	CTCF	chr12:73239070-73239097	Spleen_OC	spleen:	n/a	n/a
43	CTCF	chr12:73339412-73339451	GM20000	blood:	n/a	n/a
44	CTCF	chr12:73251007-73251078	Lung_OC	lung:	n/a	n/a
45	CTCF	chr12:73157949-73158020	GM10248	blood:	n/a	n/a
46	CTCF	chr12:73239098-73239114	Spleen_OC	spleen:	n/a	n/a
47	CTCF	chr12:73212285-73212364	LNCaP	prostate:	n/a	n/a
48	CTCF	chr12:73167560-73167710	RPTEC	kidney:	n/a	n/a
49	CTCF	chr12:73242574-73242624	HepG2	liver:	n/a	n/a
50	CTCF	chr12:73356662-73356743	Kidney_OC	kidney:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:73266969-73267019	BJ	skin:	n/a
2	chr12:73266969-73267019	AG04449	skin:	fetal
3	chr12:73266969-73267019	NHBE	bronchial:	n/a
4	chr12:73266969-73267019	HEK293	kidney:	embryo
5	chr12:73266969-73267019	HCT-116	colon:	n/a
6	chr12:73266969-73267019	HRPEpiC	eye:	n/a
7	chr12:73266969-73267019	GM12892	blood:	n/a
8	chr12:73266969-73267019	T-47D	breast:	n/a
9	chr12:73266969-73267019	HIPEpiC	eye:	n/a
10	chr12:73266969-73267019	HMEC	breast:	n/a
11	chr12:73266969-73267019	NT2-D1	testis:	n/a
12	chr12:73266969-73267019	HRE	kidney:	n/a
13	chr12:73266969-73267019	HAEpiC	amniotic membrane:	n/a
14	chr12:73266969-73267019	MCF10A-Er-Src	breast:	n/a
15	chr12:73266969-73267019	LNCaP	prostate:	n/a
16	chr12:73266969-73267019	AG10803	skin:	n/a
17	chr12:73266969-73267019	ECC-1	luminal epithelium:	n/a
18	chr12:73266969-73267019	AG09319	gingival:	n/a
19	chr12:73266969-73267019	ProgFib	skin:	n/a
20	chr12:73266969-73267019	IMR90	lung:	fetal
21	chr12:73266969-73267019	HPAEpiC	pulmonary alveolar:	n/a
22	chr12:73266969-73267019	CMK	blood:	n/a
23	chr12:73266969-73267019	GM12891	blood:	n/a
24	chr12:73266969-73267019	GM06990	blood:	n/a
25	chr12:73266969-73267019	GM12878	blood:	n/a
26	chr12:73266969-73267019	Jurkat	blood:	n/a
27	chr12:73266969-73267019	AG04450	lung:	fetal
28	chr12:73266969-73267019	K562	blood:	n/a
29	chr12:73266969-73267019	HCM	heart:	n/a
30	chr12:73266969-73267019	HL-60	blood:	n/a
31	chr12:73266969-73267019	PrEC	prostate:	n/a
32	chr12:73266969-73267019	Hela-S3	cervix:	n/a
33	chr12:73266969-73267019	NHDF-neo	bronchial:	n/a
34	chr12:73266969-73267019	HRCEpiC	kidney:	n/a
35	chr12:73266969-73267019	HUVEC	blood vessel:	n/a
36	chr12:73266969-73267019	ovcar-3	ovarian:	n/a
37	chr12:73266969-73267019	SKMC	muscle:	n/a
38	chr12:73266969-73267019	A549	lung:	n/a
39	chr12:73266969-73267019	Caco-2	colon:	n/a
40	chr12:73266969-73267019	HEEpiC	esophagus:	n/a
41	chr12:73266969-73267019	SK-N-SH_RA	brain:	n/a
42	chr12:73266969-73267019	HCPEpiC	choroid plexus:	n/a
43	chr12:73266969-73267019	H1-hESC	embryonic stem cell:	embryo
44	chr12:73266969-73267019	SK-N-MC	brain:	n/a
45	chr12:73266969-73267019	NB4	blood:	n/a
46	chr12:73266969-73267019	MCF-7	breast:	n/a
47	chr12:73266969-73267019	NH-A	brain:	n/a
48	chr12:73266969-73267019	AoSMC	blood vessel:	n/a
49	chr12:73266969-73267019	BE2_C	brain:	n/a
50	chr12:73266969-73267019	AG09309	skin:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:73279960..73282832-chr12:73288146..73290237,2	K562	blood:
2	chr12:73360278..73363130-chr12:73365904..73367534,2	K562	blood:
3	chr12:73162846..73164376-chr12:73166429..73169138,2	MCF-7	breast:
4	chr12:73329562..73331929-chr12:73334253..73335865,2	MCF-7	breast:
5	chr12:73276124..73278278-chr12:73280088..73282013,2	K562	blood:
6	chr12:73279960..73282832-chr12:73288146..73290237,2	K562	blood:
7	chr1:53191543..53194375-chr12:73227297..73229475,2	MCF-7	breast:
8	chr12:73276124..73278278-chr12:73280088..73282013,2	K562	blood:
9	chr12:73360278..73363130-chr12:73365904..73367534,2	K562	blood:
10	chr12:73279777..73282647-chr12:73282776..73285810,4	K562	blood:
11	chr12:73361630..73364620-chr12:73364832..73367404,2	K562	blood:
12	chr12:73177952..73180851-chr12:73182448..73184176,2	K562	blood:
13	chr12:73279777..73282647-chr12:73282776..73285810,4	K562	blood:
14	chr12:73162846..73164376-chr12:73166429..73169138,2	MCF-7	breast:
15	chr12:73177952..73180851-chr12:73182448..73184176,2	K562	blood:
16	chr12:73280330..73282647-chr12:73282776..73285288,2	K562	blood:
17	chr12:73361630..73364620-chr12:73364832..73367404,2	K562	blood:
18	chr12:73329562..73331929-chr12:73334253..73335865,2	MCF-7	breast:
19	chr12:73280330..73282647-chr12:73282776..73285288,2	K562	blood:
20	chr12:73278361..73280409-chr12:73393211..73395574,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRHDE-1	chr12:73362033-73362097	XLOC_009803
2	lnc-TRHDE-1	chr12:73362420-73362470	XLOC_009803
3	lnc-TRHDE-1	chr12:73318544-73318675	XLOC_009803
4	lnc-TRHDE-1	chr12:73352845-73352944	XLOC_009803
5	lnc-TRHDE-1	chr12:73367333-73367380	XLOC_009803

No data

Variant related genes	Relation type
ENSG00000216084	TF binding region
ENSG00000216084	CpG island
ENSG00000162378	chromatin interactions
UBE2Q1	miRNA target sites
UBE2W	miRNA target sites
UBE2R2	miRNA target sites

Extended variants
information (count: 3642 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:3642 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs537955110	chr12:73131407-73131408	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs549769630	chr12:73131425-73131426	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs149806485	chr12:73131439-73131440	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs115147632	chr12:73131441-73131442	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs548610795	chr12:73131442-73131443	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs567047892	chr12:73131453-73131454	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs114093707	chr12:73131467-73131468	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs557704582	chr12:73131506-73131507	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs558606327	chr12:73131559-73131560	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs570647620	chr12:73131603-73131604	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs542654635	chr12:73131611-73131612	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs111954681	chr12:73131627-73131628	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs574740757	chr12:73131658-73131659	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs542064230	chr12:73131661-73131662	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs553822044	chr12:73131670-73131671	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs146820559	chr12:73131675-73131676	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs187060594	chr12:73131715-73131716	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs376538002	chr12:73131764-73131765	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs191118111	chr12:73131772-73131773	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs531406866	chr12:73131784-73131785	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs180787891	chr12:73131804-73131805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs577628592	chr12:73131810-73131811	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs572264848	chr12:73131819-73131820	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs543546057	chr12:73131828-73131829	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs561628390	chr12:73131865-73131866	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs186709323	chr12:73131889-73131890	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs548862857	chr12:73131899-73131900	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs567081694	chr12:73131913-73131914	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs551215627	chr12:73131931-73131932	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs112677197	chr12:73131946-73131947	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs554193941	chr12:73131994-73131995	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs140325649	chr12:73132008-73132009	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs570730414	chr12:73132034-73132035	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs537899405	chr12:73132073-73132074	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs556246522	chr12:73132079-73132080	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs145453106	chr12:73132092-73132093	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs190075164	chr12:73132096-73132097	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs12297767	chr12:73132107-73132108	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs542891828	chr12:73132108-73132109	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs554010828	chr12:73132141-73132142	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs572284994	chr12:73132151-73132152	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs564300875	chr12:73132161-73132162	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs183046751	chr12:73132174-73132175	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs138085810	chr12:73132194-73132195	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs112681909	chr12:73132205-73132206	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs143025828	chr12:73132214-73132215	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs187370987	chr12:73132223-73132224	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs190337893	chr12:73132233-73132234	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs528861047	chr12:73132257-73132258	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs117564197	chr12:73132265-73132266	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

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
Neurodevelopmental disorder	22521361	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
Colorectal cancer	16272173	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
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Burkitt''s lymphoma	20823134	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16620391	CNVD
Disease	21505450	CNVD
craniofacial dysmorphism	21918468	CNVD
Breast cancer	21364760	CNVD
Breast cancer	17133270	CNVD
Autism	20685689	CNVD
Urothelial cell carcinoma	18451213	CNVD
Myelofibrosis	22110671	CNVD
Cutaneous T-cell lymphoma	21881587	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
Hodgkin''s lymphoma	18641027	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Osteosarcoma	21215367	CNVD

Chromatin state (count:144 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:73131400-73131600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr12:73131400-73131800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
3	chr12:73131600-73132800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr12:73132000-73132600	Enhancers	Primary hematopoietic stem cells	blood
5	chr12:73132000-73132800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr12:73132000-73134600	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr12:73132200-73132800	Enhancers	Primary hematopoietic stem cells short term culture	blood
8	chr12:73132600-73133600	Weak transcription	Primary hematopoietic stem cells	blood
9	chr12:73132600-73134400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr12:73133600-73133800	ZNF genes & repeats	Primary hematopoietic stem cells	blood
11	chr12:73134200-73134600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr12:73134400-73134800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr12:73134600-73140600	Weak transcription	Primary monocytes fromperipheralblood	blood
14	chr12:73140600-73143200	Enhancers	Primary monocytes fromperipheralblood	blood
15	chr12:73141000-73141800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr12:73141000-73143000	Enhancers	Monocytes-CD14+_RO01746	blood
17	chr12:73141200-73142000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr12:73141400-73141800	Enhancers	Fetal Stomach	stomach
19	chr12:73141400-73142000	Enhancers	Fetal Lung	lung
20	chr12:73142000-73144000	Weak transcription	Fetal Lung	lung
21	chr12:73144000-73144600	Enhancers	Fetal Lung	lung
22	chr12:73149200-73150200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr12:73150000-73150600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr12:73150600-73151400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr12:73150600-73152200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr12:73150800-73151200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr12:73183800-73184800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr12:73199600-73200800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr12:73200000-73201200	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr12:73200400-73200800	Enhancers	Brain Germinal Matrix	brain
31	chr12:73200600-73200800	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr12:73200800-73207000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
33	chr12:73206400-73212400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr12:73207000-73207800	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
35	chr12:73207000-73208000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
36	chr12:73207000-73208000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
37	chr12:73207400-73208800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
38	chr12:73208600-73209000	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr12:73208600-73209200	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr12:73209000-73209400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
41	chr12:73209400-73209800	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr12:73210400-73211200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
43	chr12:73215200-73221000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr12:73216000-73227000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr12:73218000-73219400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr12:73218600-73219400	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
47	chr12:73219400-73219600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chr12:73219400-73221400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr12:73219600-73220200	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr12:73220000-73220600	Enhancers	iPS-18 Cell Line	embryonic stem cell

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