Variant report

Variant	nsv1040846
Chromosome Location	chr12:74033679-74295583
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:392)
CpG islands
(count:61)
Chromatin interactive
region (count:12)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:392 , 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	ARID3A	chr12:74163177-74163418	HepG2	liver:	n/a	n/a
2	ATF1	chr12:74128867-74129001	K562	blood:	n/a	n/a
3	ATF1	chr12:74119709-74119780	K562	blood:	n/a	n/a
4	ATF1	chr12:74282572-74282667	K562	blood:	n/a	n/a
5	BACH1	chr12:74053673-74053952	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr12:74163092-74163473	HepG2	liver:	n/a	n/a
7	CBX3	chr12:74195079-74195462	HCT-116	colon:	n/a	n/a
8	CEBPB	chr12:74191001-74191343	A549	lung:	n/a	n/a
9	CEBPB	chr12:74210954-74211331	HepG2	liver:	n/a	chr12:74211135-74211144 chr12:74211135-74211144 chr12:74211166-74211179 chr12:74211133-74211146 chr12:74210965-74210978 chr12:74211135-74211144
10	CEBPB	chr12:74035798-74036052	A549	lung:	n/a	n/a
11	CEBPB	chr12:74130762-74131024	IMR90	lung:	n/a	chr12:74130863-74130874
12	CEBPB	chr12:74286000-74286226	A549	lung:	n/a	n/a
13	CEBPB	chr12:74146197-74146414	A549	lung:	n/a	n/a
14	CEBPB	chr12:74218793-74219021	HepG2	liver:	n/a	chr12:74218871-74218882
15	CEBPB	chr12:74211002-74211280	ECC-1	luminal epithelium:	n/a	chr12:74211135-74211144 chr12:74211135-74211144 chr12:74211166-74211179 chr12:74211133-74211146 chr12:74211135-74211144
16	CEBPB	chr12:74211018-74211307	H1-hESC	embryonic stem cell:	n/a	chr12:74211135-74211144 chr12:74211135-74211144 chr12:74211166-74211179 chr12:74211133-74211146 chr12:74211135-74211144
17	CEBPB	chr12:74211006-74211309	K562	blood:	n/a	chr12:74211135-74211144 chr12:74211135-74211144 chr12:74211166-74211179 chr12:74211133-74211146 chr12:74211135-74211144
18	CEBPB	chr12:74210959-74211325	IMR90	lung:	n/a	chr12:74211135-74211144 chr12:74211135-74211144 chr12:74211166-74211179 chr12:74211133-74211146 chr12:74210965-74210978 chr12:74211135-74211144
19	CEBPB	chr12:74287654-74287786	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr12:74191128-74191271	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr12:74287777-74287783	K562	blood:	n/a	n/a
22	CEBPB	chr12:74211017-74211328	MCF-7	breast:	n/a	chr12:74211135-74211144 chr12:74211135-74211144 chr12:74211166-74211179 chr12:74211133-74211146 chr12:74211135-74211144
23	CEBPB	chr12:74191006-74191336	IMR90	lung:	n/a	n/a
24	CEBPB	chr12:74210956-74211329	A549	lung:	n/a	chr12:74211135-74211144 chr12:74211135-74211144 chr12:74211166-74211179 chr12:74211133-74211146 chr12:74210965-74210978 chr12:74211135-74211144
25	CEBPB	chr12:74190991-74191321	HepG2	liver:	n/a	n/a
26	CTCF	chr12:74096060-74096210	Hela-S3	cervix:	n/a	n/a
27	CTCF	chr12:74175351-74175439	GM20000	blood:	n/a	n/a
28	CTCF	chr12:74085471-74085524	GM10266	blood:	n/a	n/a
29	CTCF	chr12:74050275-74050479	MCF-7	breast:	n/a	n/a
30	CTCF	chr12:74050227-74050497	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr12:74050280-74050430	MCF-7	breast:	n/a	n/a
32	CTCF	chr12:74050139-74050519	MCF-7	breast:	n/a	n/a
33	CTCF	chr12:74050260-74050410	SK-N-SH_RA	brain:	n/a	n/a
34	CTCF	chr12:74173713-74173737	GM10248	blood:	n/a	n/a
35	CTCF	chr12:74129185-74129225	GM10248	blood:	n/a	n/a
36	CTCF	chr12:74050296-74050452	Gliobla	brain:	n/a	n/a
37	CTCF	chr12:74050240-74050390	HCT-116	colon:	n/a	n/a
38	CTCF	chr12:74285580-74285730	HCPEpiC	choroid plexus:	n/a	n/a
39	CTCF	chr12:74050293-74050485	MCF-7	breast:	n/a	n/a
40	CTCF	chr12:74250511-74250576	K562	blood:	n/a	n/a
41	CTCF	chr12:74096120-74096270	MCF-7	breast:	n/a	n/a
42	CTCF	chr12:74173060-74173087	Lung_OC	lung:	n/a	n/a
43	CTCF	chr12:74050260-74050410	HBMEC	blood vessel:	n/a	n/a
44	CTCF	chr12:74197540-74197690	HMEC	breast:	n/a	n/a
45	CTCF	chr12:74050296-74050469	MCF-7	breast:	n/a	n/a
46	CTCF	chr12:74050372-74050402	Fibrobl	skin:	n/a	n/a
47	CTCF	chr12:74120160-74120310	GM06990	blood:	n/a	n/a
48	CTCF	chr12:74106132-74106176	GM13976	blood:	n/a	n/a
49	CTCF	chr12:74065480-74065553	Lung_OC	lung:	n/a	n/a
50	CTCF	chr12:74250502-74250565	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:74072114-74072164	AoSMC	blood vessel:	n/a
2	chr12:74072114-74072164	ProgFib	skin:	n/a
3	chr12:74072114-74072164	HNPCEpiC	eye:	n/a
4	chr12:74072114-74072164	GM12891	blood:	n/a
5	chr12:74072114-74072164	HCPEpiC	choroid plexus:	n/a
6	chr12:74072114-74072164	HCM	heart:	n/a
7	chr12:74072114-74072164	SK-N-MC	brain:	n/a
8	chr12:74072114-74072164	HCT-116	colon:	n/a
9	chr12:74072114-74072164	Hela-S3	cervix:	n/a
10	chr12:74072114-74072164	LNCaP	prostate:	n/a
11	chr12:74072114-74072164	HAEpiC	amniotic membrane:	n/a
12	chr12:74072114-74072164	A549	lung:	n/a
13	chr12:74072114-74072164	HCF	heart:	n/a
14	chr12:74072114-74072164	ovcar-3	ovarian:	n/a
15	chr12:74072114-74072164	AG10803	skin:	n/a
16	chr12:74072114-74072164	H1-hESC	embryonic stem cell:	embryo
17	chr12:74072114-74072164	GM12892	blood:	n/a
18	chr12:74072114-74072164	RPTEC	kidney:	n/a
19	chr12:74072114-74072164	PFSK-1	brain:	n/a
20	chr12:74072114-74072164	AG09319	gingival:	n/a
21	chr12:74072114-74072164	GM19239	blood:	n/a
22	chr12:74072114-74072164	SAEC	small airway:	n/a
23	chr12:74072114-74072164	NH-A	brain:	n/a
24	chr12:74072114-74072164	Jurkat	blood:	n/a
25	chr12:74072114-74072164	Caco-2	colon:	n/a
26	chr12:74072114-74072164	HRCEpiC	kidney:	n/a
27	chr12:74072114-74072164	AG04449	skin:	fetal
28	chr12:74072114-74072164	PrEC	prostate:	n/a
29	chr12:74072114-74072164	MCF10A-Er-Src	breast:	n/a
30	chr12:74072114-74072164	HRPEpiC	eye:	n/a
31	chr12:74072114-74072164	BJ	skin:	n/a
32	chr12:74072114-74072164	AG09309	skin:	n/a
33	chr12:74072114-74072164	SK-N-SH	brain:	n/a
34	chr12:74072114-74072164	HEK293	kidney:	embryo
35	chr12:74072114-74072164	SKMC	muscle:	n/a
36	chr12:74072114-74072164	GM06990	blood:	n/a
37	chr12:74072114-74072164	HPAEpiC	pulmonary alveolar:	n/a
38	chr12:74072114-74072164	IMR90	lung:	fetal
39	chr12:74072114-74072164	NB4	blood:	n/a
40	chr12:74072114-74072164	K562	blood:	n/a
41	chr12:74072114-74072164	HRE	kidney:	n/a
42	chr12:74072114-74072164	NT2-D1	testis:	n/a
43	chr12:74072114-74072164	AG04450	lung:	fetal
44	chr12:74072114-74072164	HepG2	liver:	n/a
45	chr12:74072114-74072164	MCF-7	breast:	n/a
46	chr12:74072114-74072164	HMEC	breast:	n/a
47	chr12:74072114-74072164	HL-60	blood:	n/a
48	chr12:74072114-74072164	NHDF-neo	bronchial:	n/a
49	chr12:74072114-74072164	Hepatocyte	liver:	n/a
50	chr12:74072114-74072164	SK-N-SH_RA	brain:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:74101710..74104445-chr12:74107767..74109671,2	MCF-7	breast:
2	chr11:832244..834955-chr12:74130847..74132651,2	MCF-7	breast:
3	chr12:74217471..74219715-chr12:74230543..74232076,2	K562	blood:
4	chr12:74157785..74160249-chr12:74160573..74162864,2	K562	blood:
5	chr12:74132246..74134294-chr12:74150416..74152196,2	K562	blood:
6	chr12:74101710..74104445-chr12:74107767..74109671,2	MCF-7	breast:
7	chr12:74217471..74219715-chr12:74230543..74232076,2	K562	blood:
8	chr12:74294795..74296655-chr12:74314771..74316525,2	K562	blood:
9	chr12:74132246..74134294-chr12:74150416..74152196,2	K562	blood:
10	chr12:74035671..74038050-chr12:74931309..74933975,2	K562	blood:
11	chr12:74287229..74290045-chr12:74297410..74300071,2	K562	blood:
12	chr12:73908195..73908905-chr12:74049929..74050461,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATXN7L3B-3	chr12:74189878-74189940	ENSG00000257750
2	lnc-ATXN7L3B-3	chr12:74154469-74154540	ENSG00000257750
3	lnc-ATXN7L3B-3	chr12:74165366-74165507	ENSG00000257750
4	lnc-ATXN7L3B-3	chr12:74192458-74192507	ENSG00000257750
5	lnc-ATXN7L3B-3	chr12:74161396-74161527	ENSG00000257750
6	lnc-KCNC2-4	chr12:74231887-74231923	ENSG00000258109
7	lnc-KCNC2-9	chr12:74174310-74176146	predAs_engstrom06_BX350135_1

No data

Variant related genes	Relation type
ENSG00000257750	TF binding region
RNU6-1012P	TF binding region
ENSG00000201809	TF binding region
ENSG00000243164	TF binding region
ENSG00000272231	TF binding region
ENSG00000257750	CpG island
RNU6-1012P	CpG island
ENSG00000201809	CpG island
ENSG00000243164	CpG island
ENSG00000272231	CpG island
ENSG00000253719	chromatin interactions
ENSG00000255108	chromatin interactions
ENSG00000177697	chromatin interactions
ENSG00000257386	chromatin interactions
ENSG00000201809	chromatin interactions
PPP6C	miRNA target sites

Extended variants
information (count: 3047 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:3047 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs145136394	chr12:74035709-74035710	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs377295894	chr12:74035773-74035774	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs139012325	chr12:74035775-74035776	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs370558175	chr12:74035794-74035795	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs183395151	chr12:74035795-74035796	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs568491413	chr12:74035841-74035842	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs151136811	chr12:74035851-74035852	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs551779377	chr12:74035879-74035880	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs371308583	chr12:74035883-74035884	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs573449823	chr12:74035901-74035902	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs63190861	chr12:74035902-74035903	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs562405877	chr12:74035903-74035904	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs577274731	chr12:74035926-74035927	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs201194660	chr12:74035927-74035928	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs141988172	chr12:74035947-74035948	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs537350049	chr12:74035977-74035978	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs373452095	chr12:74036084-74036085	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs549322582	chr12:74036085-74036086	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs569323802	chr12:74036244-74036245	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs531019650	chr12:74036270-74036271	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs555466680	chr12:74036281-74036282	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs2586912	chr12:74036323-74036324	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs150819774	chr12:74036342-74036343	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs76292070	chr12:74036395-74036396	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs201533480	chr12:74036495-74036496	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs187248094	chr12:74036500-74036501	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs539748596	chr12:74036504-74036505	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs563645732	chr12:74036578-74036579	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs193174322	chr12:74036580-74036581	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs553211010	chr12:74036626-74036627	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs138233991	chr12:74036642-74036643	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs567070642	chr12:74036651-74036652	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs374814871	chr12:74036657-74036658	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs528677752	chr12:74036692-74036693	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs149581121	chr12:74036737-74036738	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs565345291	chr12:74036756-74036757	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs35141969	chr12:74036775-74036776	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs531073877	chr12:74036780-74036781	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs550881887	chr12:74036795-74036796	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs35622394	chr12:74036847-74036848	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs981632	chr12:74036855-74036856	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs528890288	chr12:74036908-74036909	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs548794080	chr12:74036916-74036917	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs565813045	chr12:74036943-74036944	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs144054458	chr12:74037038-74037039	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs112906466	chr12:74037056-74037057	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs571489526	chr12:74037071-74037072	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs184555820	chr12:74037146-74037147	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs557328966	chr12:74037184-74037185	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs574075326	chr12:74037187-74037188	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
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
Breast cancer	21509527	CNVD
Breast cancer	22522925	CNVD
Osteosarcoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Ovarian cancer	21720365	CNVD

Chromatin state (count:129 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:74037600-74039200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr12:74038400-74041200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr12:74038600-74039000	Weak transcription	Brain Hippocampus Middle	brain
4	chr12:74038600-74040600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
5	chr12:74039000-74039800	ZNF genes & repeats	Brain Hippocampus Middle	brain
6	chr12:74039200-74039400	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr12:74039200-74040400	ZNF genes & repeats	Liver	Liver
8	chr12:74039800-74041800	Weak transcription	Brain Hippocampus Middle	brain
9	chr12:74045800-74046400	Weak transcription	Brain Hippocampus Middle	brain
10	chr12:74046400-74047800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
11	chr12:74046600-74047400	ZNF genes & repeats	Brain Hippocampus Middle	brain
12	chr12:74046600-74048200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr12:74058000-74059200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr12:74059000-74059400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr12:74059200-74059400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr12:74059600-74061000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr12:74061000-74061600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr12:74061600-74062600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr12:74064400-74065400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr12:74065000-74065400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr12:74065000-74066000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr12:74065000-74066000	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr12:74065400-74065600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr12:74066000-74071400	Weak transcription	HUES6 Cell Line	embryonic stem cell
25	chr12:74070800-74072200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr12:74071200-74072200	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr12:74071200-74072200	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr12:74071200-74072600	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr12:74071400-74072000	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr12:74071600-74072000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr12:74071600-74072200	Enhancers	H9 Cell Line	embryonic stem cell
32	chr12:74071600-74072200	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr12:74071600-74072600	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr12:74071800-74072600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr12:74072000-74072400	Enhancers	H1 Cell Line	embryonic stem cell
36	chr12:74072200-74074800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr12:74074800-74075600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr12:74078200-74078800	ZNF genes & repeats	Pancreas	Pancrea
39	chr12:74107200-74107400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr12:74107400-74108400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr12:74108400-74108800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr12:74108800-74110000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr12:74109600-74110000	Enhancers	Breast Myoepithelial Primary Cells	Breast
44	chr12:74110000-74110400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
45	chr12:74110200-74110400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr12:74110400-74110600	Enhancers	Breast Myoepithelial Primary Cells	Breast
47	chr12:74110600-74119000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
48	chr12:74119000-74121400	Enhancers	Breast Myoepithelial Primary Cells	Breast
49	chr12:74119200-74121000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr12:74119200-74121000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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