Variant report

Variant	nsv559392
Chromosome Location	chr12:74456882-74565295
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:425)
CpG islands
(count:366)
Chromatin interactive
region (count:46)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:425 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:74562651-74562972	K562	blood:	n/a	n/a
2	ATF1	chr12:74562685-74562943	K562	blood:	n/a	n/a
3	ATF1	chr12:74505524-74505833	K562	blood:	n/a	n/a
4	BHLHE40	chr12:74564438-74565831	K562	blood:	n/a	n/a
5	CBX3	chr12:74564451-74565685	K562	blood:	n/a	n/a
6	CBX3	chr12:74505433-74505896	HCT-116	colon:	n/a	n/a
7	CCNT2	chr12:74564372-74564872	K562	blood:	n/a	n/a
8	CEBPB	chr12:74538300-74538814	K562	blood:	n/a	n/a
9	CEBPB	chr12:74523898-74524098	HepG2	liver:	n/a	chr12:74524027-74524038
10	CEBPB	chr12:74523593-74523771	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr12:74456774-74456982	HepG2	liver:	n/a	chr12:74456926-74456937
12	CEBPB	chr12:74523983-74524169	A549	lung:	n/a	chr12:74524027-74524038
13	CEBPB	chr12:74456800-74457031	A549	lung:	n/a	chr12:74456926-74456937
14	CEBPB	chr12:74505523-74505779	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr12:74543240-74543419	HepG2	liver:	n/a	chr12:74543280-74543291
16	CHD2	chr12:74564446-74565068	K562	blood:	n/a	chr12:74564765-74564775
17	CHD2	chr12:74505628-74505708	GM12878	blood:	n/a	n/a
18	CTCF	chr12:74505620-74505770	GM12866	blood:	n/a	n/a
19	CTCF	chr12:74505579-74505776	Kidney_OC	kidney:	n/a	n/a
20	CTCF	chr12:74505640-74505790	AG09319	gingival:	n/a	n/a
21	CTCF	chr12:74505600-74505750	MCF-7	breast:	n/a	n/a
22	CTCF	chr12:74505538-74505851	K562	blood:	n/a	n/a
23	CTCF	chr12:74505551-74505803	NHEK	skin:	n/a	n/a
24	CTCF	chr12:74505620-74505770	GM12869	blood:	n/a	n/a
25	CTCF	chr12:74505497-74505847	T-47D	breast:	n/a	n/a
26	CTCF	chr12:74505600-74505750	HMF	breast:	n/a	n/a
27	CTCF	chr12:74505604-74505748	GM10248	blood:	n/a	n/a
28	CTCF	chr12:74505473-74505960	MCF-7	breast:	n/a	n/a
29	CTCF	chr12:74505680-74505830	HUVEC	blood vessel:	n/a	n/a
30	CTCF	chr12:74505660-74505810	SAEC	small airway:	n/a	n/a
31	CTCF	chr12:74505580-74505730	NB4	blood:	n/a	n/a
32	CTCF	chr12:74505612-74505757	GM19240	blood:	n/a	n/a
33	CTCF	chr12:74505510-74505858	T-47D	breast:	n/a	n/a
34	CTCF	chr12:74505588-74505783	HepG2	liver:	n/a	n/a
35	CTCF	chr12:74505582-74505737	A549	lung:	n/a	n/a
36	CTCF	chr12:74505580-74505730	BE2_C	brain:	n/a	n/a
37	CTCF	chr12:74505560-74505710	HVMF	connective:	n/a	n/a
38	CTCF	chr12:74470977-74471243	MCF-7	breast:	n/a	n/a
39	CTCF	chr12:74564355-74564551	K562	blood:	n/a	n/a
40	CTCF	chr12:74505620-74505770	HEEpiC	esophagus:	n/a	n/a
41	CTCF	chr12:74505536-74505809	K562	blood:	n/a	n/a
42	CTCF	chr12:74505608-74505751	GM10266	blood:	n/a	n/a
43	CTCF	chr12:74505580-74505730	HCT-116	colon:	n/a	n/a
44	CTCF	chr12:74505532-74505783	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr12:74505515-74505796	ECC-1	luminal epithelium:	n/a	n/a
46	CTCF	chr12:74505601-74505737	Medullo	brain:	n/a	n/a
47	CTCF	chr12:74470996-74471165	MCF-7	breast:	n/a	n/a
48	CTCF	chr12:74505578-74505794	MCF-7	breast:	n/a	n/a
49	CTCF	chr12:74505623-74505773	GM12891	blood:	n/a	n/a
50	CTCF	chr12:74507519-74507622	MCF-7	breast:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:74564523-74564573	AoSMC	blood vessel:	n/a
2	chr12:74564847-74564897	Caco-2	colon:	n/a
3	chr12:74565116-74565166	ProgFib	skin:	n/a
4	chr12:74561645-74561695	HMEC	breast:	n/a
5	chr12:74564856-74564906	MCF10A-Er-Src	breast:	n/a
6	chr12:74564847-74564897	H1-hESC	embryonic stem cell:	embryo
7	chr12:74565116-74565166	GM12892	blood:	n/a
8	chr12:74564847-74564897	HL-60	blood:	n/a
9	chr12:74564847-74564897	ovcar-3	ovarian:	n/a
10	chr12:74564523-74564573	Hela-S3	cervix:	n/a
11	chr12:74564847-74564897	PrEC	prostate:	n/a
12	chr12:74564856-74564906	U87	brain:	n/a
13	chr12:74564856-74564906	HCM	heart:	n/a
14	chr12:74564523-74564573	ovcar-3	ovarian:	n/a
15	chr12:74564523-74564573	GM12891	blood:	n/a
16	chr12:74564932-74564982	AoSMC	blood vessel:	n/a
17	chr12:74564523-74564573	U87	brain:	n/a
18	chr12:74564523-74564573	AG10803	skin:	n/a
19	chr12:74564847-74564897	BJ	skin:	n/a
20	chr12:74564847-74564897	NHBE	bronchial:	n/a
21	chr12:74561645-74561695	T-47D	breast:	n/a
22	chr12:74564523-74564573	HCT-116	colon:	n/a
23	chr12:74564523-74564573	HRPEpiC	eye:	n/a
24	chr12:74564523-74564573	HIPEpiC	eye:	n/a
25	chr12:74565116-74565166	Jurkat	blood:	n/a
26	chr12:74564847-74564897	U87	brain:	n/a
27	chr12:74564932-74564982	HCF	heart:	n/a
28	chr12:74564523-74564573	HCPEpiC	choroid plexus:	n/a
29	chr12:74565116-74565166	NT2-D1	testis:	n/a
30	chr12:74561645-74561695	SK-N-SH	brain:	n/a
31	chr12:74564932-74564982	SK-N-MC	brain:	n/a
32	chr12:74564932-74564982	GM12892	blood:	n/a
33	chr12:74565116-74565166	AG04450	lung:	fetal
34	chr12:74565116-74565166	K562	blood:	n/a
35	chr12:74565116-74565166	GM12878	blood:	n/a
36	chr12:74564523-74564573	AG09309	skin:	n/a
37	chr12:74565116-74565166	HRE	kidney:	n/a
38	chr12:74561645-74561695	GM12878	blood:	n/a
39	chr12:74564856-74564906	GM19239	blood:	n/a
40	chr12:74564932-74564982	PrEC	prostate:	n/a
41	chr12:74564932-74564982	HAEpiC	amniotic membrane:	n/a
42	chr12:74565116-74565166	AoSMC	blood vessel:	n/a
43	chr12:74564523-74564573	SK-N-SH	brain:	n/a
44	chr12:74564932-74564982	A549	lung:	n/a
45	chr12:74564847-74564897	SKMC	muscle:	n/a
46	chr12:74564856-74564906	SAEC	small airway:	n/a
47	chr12:74561645-74561695	RPTEC	kidney:	n/a
48	chr12:74561645-74561695	ECC-1	luminal epithelium:	n/a
49	chr12:74564856-74564906	AG09319	gingival:	n/a
50	chr12:74565116-74565166	SK-N-SH	brain:	n/a

(count:46 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:74505546..74506081-chr12:74710850..74711455,2	MCF-7	breast:
2	chr12:74505191..74505755-chr12:74710574..74711440,3	MCF-7	breast:
3	chr12:74531548..74535089-chr12:74542302..74547555,5	K562	blood:
4	chr12:74517100..74519637-chr12:74522625..74525226,2	K562	blood:
5	chr12:74489819..74492327-chr12:74494030..74495535,2	K562	blood:
6	chr12:74540805..74543327-chr12:74544789..74546497,2	K562	blood:
7	chr12:74536886..74539098-chr12:74541490..74544013,2	MCF-7	breast:
8	chr12:74505239..74506034-chr12:74759124..74759988,3	MCF-7	breast:
9	chr12:74505591..74506415-chr18:8130965..8131756,2	MCF-7	breast:
10	chr12:74443201..74445435-chr12:74461454..74463551,2	MCF-7	breast:
11	chr12:74545641..74548768-chr12:74554696..74557729,3	K562	blood:
12	chr12:74489819..74492327-chr12:74494030..74495535,2	K562	blood:
13	chr12:74560053..74562479-chr12:74564625..74566537,2	K562	blood:
14	chr12:74540805..74543327-chr12:74544789..74546497,2	K562	blood:
15	chr12:74545641..74548957-chr12:74555890..74557729,3	K562	blood:
16	chr12:74526468..74528133-chr12:74535792..74537959,2	MCF-7	breast:
17	chr12:74564480..74567461-chr12:74575954..74578864,3	K562	blood:
18	chr12:74545641..74548957-chr12:74555890..74557729,3	K562	blood:
19	chr12:74560053..74562479-chr12:74564625..74566537,2	K562	blood:
20	chr12:74517100..74519637-chr12:74522625..74525226,2	K562	blood:
21	chr12:74522697..74525336-chr12:74527749..74530439,2	K562	blood:
22	chr12:74564462..74568132-chr12:74683426..74687604,5	K562	blood:
23	chr12:74505235..74505774-chr12:74710528..74711393,3	K562	blood:
24	chr12:74545641..74548768-chr12:74554696..74557729,3	K562	blood:
25	chr12:74539088..74540893-chr12:74543258..74546036,3	K562	blood:
26	chr12:74491549..74494531-chr12:74496083..74497929,2	K562	blood:
27	chr12:74528403..74529928-chr12:74531825..74534781,2	K562	blood:
28	chr12:74547425..74549185-chr12:74551970..74554441,2	MCF-7	breast:
29	chr12:74564280..74566761-chr12:74606459..74609033,2	K562	blood:
30	chr12:74447256..74448968-chr12:74473500..74476491,2	MCF-7	breast:
31	chr12:74531548..74535089-chr12:74542302..74547555,5	K562	blood:
32	chr12:74415701..74416228-chr12:74504378..74504925,2	MCF-7	breast:
33	chr12:74508582..74510560-chr12:74931489..74932997,2	MCF-7	breast:
34	chr12:74505591..74506172-chr12:74759484..74759999,2	MCF-7	breast:
35	chr12:74528403..74529928-chr12:74531825..74534781,2	K562	blood:
36	chr12:74527061..74530059-chr12:74931122..74933872,2	MCF-7	breast:
37	chr12:74526468..74528133-chr12:74535792..74537959,2	MCF-7	breast:
38	chr12:74535843..74538591-chr12:74539511..74542141,2	K562	blood:
39	chr12:74415229..74416317-chr12:74501474..74502787,6	MCF-7	breast:
40	chr12:74547425..74549185-chr12:74551970..74554441,2	MCF-7	breast:
41	chr12:74536886..74539098-chr12:74541490..74544013,2	MCF-7	breast:
42	chr12:74491549..74494531-chr12:74496083..74497929,2	K562	blood:
43	chr12:74552737..74556720-chr12:74559479..74564261,5	K562	blood:
44	chr12:74539088..74540893-chr12:74543258..74546036,3	K562	blood:
45	chr12:74535843..74538591-chr12:74539511..74542141,2	K562	blood:
46	chr12:74522697..74525336-chr12:74527749..74530439,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000258320	TF binding region
ENSG00000258320	CpG island
ENSG00000257364	chromatin interactions
ENSG00000251138	chromatin interactions
ENSG00000253719	chromatin interactions
ENSG00000258320	chromatin interactions
ENSG00000257386	chromatin interactions

Extended variants
information (count: 1561 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:1561 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2365430	chr12:74460203-74460204	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs2365429	chr12:74460213-74460214	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs207473088	chr12:74460217-74460218	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs142770666	chr12:74460224-74460225	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs548708410	chr12:74460242-74460243	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs559019905	chr12:74460251-74460252	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs115819813	chr12:74460275-74460276	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs377077650	chr12:74460287-74460288	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs551294337	chr12:74460291-74460292	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs368889890	chr12:74460329-74460330	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs571382892	chr12:74460382-74460383	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs541956893	chr12:74460383-74460384	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs550838256	chr12:74460388-74460389	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs567596365	chr12:74460423-74460424	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs12316659	chr12:74460431-74460432	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs75617695	chr12:74460439-74460440	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs543212510	chr12:74460446-74460447	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs200117450	chr12:74460460-74460461	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs115550583	chr12:74460502-74460503	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs539101602	chr12:74460584-74460585	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs146948737	chr12:74460596-74460597	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs146258756	chr12:74482005-74482006	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs574771498	chr12:74482012-74482013	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs540186216	chr12:74482051-74482052	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs11179911	chr12:74482079-74482080	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs181275849	chr12:74482096-74482097	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs370399424	chr12:74482107-74482108	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs576895011	chr12:74482117-74482118	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs78335054	chr12:74482130-74482131	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs137894568	chr12:74482152-74482153	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs562055344	chr12:74482181-74482182	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs185491659	chr12:74482218-74482219	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs189562650	chr12:74482311-74482312	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs370304407	chr12:74482348-74482349	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs11503767	chr12:74482371-74482372	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs544666055	chr12:74504651-74504652	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs565205306	chr12:74504656-74504657	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs193050837	chr12:74504778-74504779	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs549491989	chr12:74504822-74504823	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs144506304	chr12:74504828-74504829	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs376624206	chr12:74504840-74504841	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs184257450	chr12:74504846-74504847	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs145464722	chr12:74504852-74504853	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs4397930	chr12:74504869-74504870	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs534773621	chr12:74504882-74504883	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs551720367	chr12:74504900-74504901	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs571542856	chr12:74504918-74504919	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs559628311	chr12:74504951-74504952	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs550827673	chr12:74505051-74505052	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs189068672	chr12:74505065-74505066	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
craniofacial dysmorphism	21918468	CNVD
Breast cancer	21364760	CNVD
Breast cancer	17133270	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
Urothelial cell carcinoma	18451213	CNVD
Myelofibrosis	22110671	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:74460200-74460600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr12:74482000-74482400	Enhancers	Esophagus	oesophagus
3	chr12:74504600-74505400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr12:74504600-74505800	Enhancers	HMEC	breast
5	chr12:74504600-74506200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr12:74504800-74505600	Enhancers	NHEK	skin
7	chr12:74505800-74513600	Weak transcription	HMEC	breast
8	chr12:74513600-74513800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr12:74513600-74514200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr12:74513600-74514200	Enhancers	HMEC	breast
11	chr12:74514400-74514600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr12:74520000-74528200	Weak transcription	K562	blood
13	chr12:74523600-74524000	Enhancers	Brain Cingulate Gyrus	brain
14	chr12:74523600-74524000	Active TSS	Ovary	ovary
15	chr12:74531200-74531600	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr12:74544000-74544400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr12:74545400-74545600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr12:74545600-74546600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr12:74545600-74547400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr12:74546000-74546400	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr12:74546000-74546800	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr12:74546000-74546800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr12:74546200-74546800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
24	chr12:74546200-74547000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr12:74546400-74546800	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr12:74546400-74546800	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
27	chr12:74546600-74547200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr12:74548800-74563400	Weak transcription	K562	blood
29	chr12:74561200-74561600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr12:74563400-74565200	Active TSS	K562	blood
31	chr12:74564600-74565400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr12:74565200-74565400	Transcr. at gene 5' and 3'	K562	blood

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