Variant report

Variant	nsv516042
Chromosome Location	chr12:60354307-60459370
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BRCA1	chr12:60366741-60367760	Hela-S3	cervix:	n/a	n/a
2	CEBPB	chr12:60361958-60362309	MCF-7	breast:	n/a	chr12:60362082-60362091 chr12:60362080-60362091 chr12:60362082-60362091 chr12:60362077-60362094 chr12:60362082-60362091 chr12:60362080-60362093 chr12:60362039-60362050
3	CEBPB	chr12:60366750-60367211	MCF-7	breast:	n/a	n/a
4	CEBPB	chr12:60366716-60367184	A549	lung:	n/a	n/a
5	CEBPB	chr12:60367288-60367859	MCF-7	breast:	n/a	n/a
6	CEBPB	chr12:60366835-60367090	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr12:60394344-60394410	A549	lung:	n/a	n/a
8	CEBPB	chr12:60366788-60367144	HepG2	liver:	n/a	n/a
9	CEBPB	chr12:60369658-60369876	Hela-S3	cervix:	n/a	chr12:60369754-60369765 chr12:60369752-60369763
10	CEBPB	chr12:60361924-60362269	Hela-S3	cervix:	n/a	chr12:60362082-60362091 chr12:60362080-60362091 chr12:60362082-60362091 chr12:60362077-60362094 chr12:60362082-60362091 chr12:60362080-60362093 chr12:60362039-60362050
11	CEBPB	chr12:60361925-60362243	A549	lung:	n/a	chr12:60362082-60362091 chr12:60362080-60362091 chr12:60362082-60362091 chr12:60362077-60362094 chr12:60362082-60362091 chr12:60362080-60362093 chr12:60362039-60362050
12	CEBPB	chr12:60366734-60367137	ECC-1	luminal epithelium:	n/a	n/a
13	CEBPB	chr12:60428205-60428348	A549	lung:	n/a	chr12:60428277-60428288
14	CEBPB	chr12:60361922-60362355	A549	lung:	n/a	chr12:60362082-60362091 chr12:60362080-60362091 chr12:60362082-60362091 chr12:60362077-60362094 chr12:60362082-60362091 chr12:60362080-60362093 chr12:60362039-60362050
15	CEBPB	chr12:60361929-60362221	K562	blood:	n/a	chr12:60362082-60362091 chr12:60362080-60362091 chr12:60362082-60362091 chr12:60362077-60362094 chr12:60362082-60362091 chr12:60362080-60362093 chr12:60362039-60362050
16	CEBPB	chr12:60361902-60362363	MCF-7	breast:	n/a	chr12:60362082-60362091 chr12:60362080-60362091 chr12:60362082-60362091 chr12:60362077-60362094 chr12:60362082-60362091 chr12:60362080-60362093 chr12:60362039-60362050
17	CEBPB	chr12:60399603-60399803	A549	lung:	n/a	n/a
18	CEBPB	chr12:60369597-60369913	IMR90	lung:	n/a	chr12:60369754-60369765 chr12:60369752-60369763
19	CEBPB	chr12:60366635-60367322	HCT-116	colon:	n/a	n/a
20	CEBPB	chr12:60361926-60362239	H1-hESC	embryonic stem cell:	n/a	chr12:60362082-60362091 chr12:60362080-60362091 chr12:60362082-60362091 chr12:60362077-60362094 chr12:60362082-60362091 chr12:60362080-60362093 chr12:60362039-60362050
21	CEBPB	chr12:60366496-60367846	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr12:60366792-60367130	A549	lung:	n/a	n/a
23	CEBPB	chr12:60361890-60362272	ECC-1	luminal epithelium:	n/a	chr12:60362082-60362091 chr12:60362080-60362091 chr12:60362082-60362091 chr12:60362077-60362094 chr12:60362082-60362091 chr12:60362080-60362093 chr12:60362039-60362050
24	CEBPB	chr12:60366669-60367241	ECC-1	luminal epithelium:	n/a	n/a
25	CEBPB	chr12:60366778-60367703	IMR90	lung:	n/a	n/a
26	CEBPB	chr12:60366789-60367037	HepG2	liver:	n/a	n/a
27	CEBPB	chr12:60361906-60362273	A549	lung:	n/a	chr12:60362082-60362091 chr12:60362080-60362091 chr12:60362082-60362091 chr12:60362077-60362094 chr12:60362082-60362091 chr12:60362080-60362093 chr12:60362039-60362050
28	CEBPB	chr12:60428211-60428406	HepG2	liver:	n/a	chr12:60428277-60428288
29	CEBPB	chr12:60361957-60362273	ECC-1	luminal epithelium:	n/a	chr12:60362082-60362091 chr12:60362080-60362091 chr12:60362082-60362091 chr12:60362077-60362094 chr12:60362082-60362091 chr12:60362080-60362093 chr12:60362039-60362050
30	CEBPB	chr12:60361898-60362267	HepG2	liver:	n/a	chr12:60362082-60362091 chr12:60362080-60362091 chr12:60362082-60362091 chr12:60362077-60362094 chr12:60362082-60362091 chr12:60362080-60362093 chr12:60362039-60362050
31	CEBPB	chr12:60366667-60367794	MCF-7	breast:	n/a	n/a
32	CEBPB	chr12:60366670-60367249	HCT-116	colon:	n/a	n/a
33	CEBPB	chr12:60369580-60369859	A549	lung:	n/a	chr12:60369754-60369765 chr12:60369752-60369763
34	CEBPB	chr12:60361900-60362274	IMR90	lung:	n/a	chr12:60362082-60362091 chr12:60362080-60362091 chr12:60362082-60362091 chr12:60362077-60362094 chr12:60362082-60362091 chr12:60362080-60362093 chr12:60362039-60362050
35	CEBPB	chr12:60369671-60369898	HepG2	liver:	n/a	chr12:60369754-60369765 chr12:60369752-60369763
36	CHD2	chr12:60366693-60367114	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr12:60415080-60415230	MCF-7	breast:	n/a	n/a
38	CTCF	chr12:60453060-60453210	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr12:60453060-60453210	HMF	breast:	n/a	n/a
40	CTCF	chr12:60453040-60453190	HEEpiC	esophagus:	n/a	n/a
41	CTCF	chr12:60453000-60453150	AoAF	blood vessel:	n/a	n/a
42	CTCF	chr12:60453040-60453190	AG04450	lung:	n/a	n/a
43	CTCF	chr12:60452960-60453110	HCT-116	colon:	n/a	n/a
44	CTCF	chr12:60399040-60399190	GM06990	blood:	n/a	n/a
45	CTCF	chr12:60431540-60431690	HCT-116	colon:	n/a	n/a
46	CTCF	chr12:60393364-60393506	GM12878	blood:	n/a	n/a
47	CTCF	chr12:60453060-60453210	SAEC	small airway:	n/a	n/a
48	CTCF	chr12:60453060-60453210	HMEC	breast:	n/a	n/a
49	CTCF	chr12:60431569-60431633	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr12:60453060-60453210	AoAF	blood vessel:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:60358617-60358667	SK-N-SH	brain:	n/a
2	chr12:60358617-60358667	IMR90	lung:	fetal
3	chr12:60358617-60358667	NHBE	bronchial:	n/a
4	chr12:60358617-60358667	K562	blood:	n/a
5	chr12:60358617-60358667	NT2-D1	testis:	n/a
6	chr12:60358617-60358667	HPAEpiC	pulmonary alveolar:	n/a
7	chr12:60358617-60358667	GM12878	blood:	n/a
8	chr12:60358617-60358667	HAEpiC	amniotic membrane:	n/a
9	chr12:60358617-60358667	PANC-1	pancreas:	n/a
10	chr12:60358617-60358667	AoSMC	blood vessel:	n/a
11	chr12:60358617-60358667	GM12892	blood:	n/a
12	chr12:60358617-60358667	ovcar-3	ovarian:	n/a
13	chr12:60358617-60358667	BJ	skin:	n/a
14	chr12:60358617-60358667	AG10803	skin:	n/a
15	chr12:60358617-60358667	LNCaP	prostate:	n/a
16	chr12:60358617-60358667	HCT-116	colon:	n/a
17	chr12:60358617-60358667	PFSK-1	brain:	n/a
18	chr12:60358617-60358667	MCF10A-Er-Src	breast:	n/a
19	chr12:60358617-60358667	HEEpiC	esophagus:	n/a
20	chr12:60358617-60358667	ProgFib	skin:	n/a
21	chr12:60358617-60358667	ECC-1	luminal epithelium:	n/a
22	chr12:60358617-60358667	Hela-S3	cervix:	n/a
23	chr12:60358617-60358667	HNPCEpiC	eye:	n/a
24	chr12:60358617-60358667	HCF	heart:	n/a
25	chr12:60358617-60358667	AG04449	skin:	fetal
26	chr12:60358617-60358667	NHDF-neo	bronchial:	n/a
27	chr12:60358617-60358667	HMEC	breast:	n/a
28	chr12:60358617-60358667	SKMC	muscle:	n/a
29	chr12:60358617-60358667	HRPEpiC	eye:	n/a
30	chr12:60358617-60358667	MCF-7	breast:	n/a
31	chr12:60358617-60358667	A549	lung:	n/a
32	chr12:60358617-60358667	SK-N-MC	brain:	n/a
33	chr12:60358617-60358667	HIPEpiC	eye:	n/a
34	chr12:60358617-60358667	SAEC	small airway:	n/a
35	chr12:60358617-60358667	U87	brain:	n/a
36	chr12:60358617-60358667	NH-A	brain:	n/a
37	chr12:60358617-60358667	GM12891	blood:	n/a
38	chr12:60358617-60358667	AG04450	lung:	fetal
39	chr12:60358617-60358667	Caco-2	colon:	n/a
40	chr12:60358617-60358667	GM19239	blood:	n/a
41	chr12:60358617-60358667	HepG2	liver:	n/a
42	chr12:60358617-60358667	GM06990	blood:	n/a
43	chr12:60358617-60358667	HUVEC	blood vessel:	n/a
44	chr12:60358617-60358667	T-47D	breast:	n/a
45	chr12:60358617-60358667	NB4	blood:	n/a
46	chr12:60358617-60358667	RPTEC	kidney:	n/a
47	chr12:60358617-60358667	SK-N-SH_RA	brain:	n/a
48	chr12:60358617-60358667	HCM	heart:	n/a
49	chr12:60358617-60358667	HCPEpiC	choroid plexus:	n/a
50	chr12:60358617-60358667	HEK293	kidney:	embryo

No.	Distal block	Cell Line	Cell type
1	chr12:60439937..60442180-chr12:60446699..60448272,2	MCF-7	breast:
2	chr12:60424657..60427143-chr12:60427851..60429693,2	MCF-7	breast:
3	chr12:60454406..60456057-chr12:60465200..60468132,2	MCF-7	breast:
4	chr12:60442817..60444737-chr12:60445729..60447893,2	K562	blood:
5	chr12:60424657..60427143-chr12:60427851..60429693,2	MCF-7	breast:
6	chr12:60355837..60358640-chr12:60365883..60368050,2	MCF-7	breast:
7	chr12:60448484..60450647-chr12:60452739..60455616,2	K562	blood:
8	chr1:107703503..107704327-chr12:60399253..60400075,2	MCF-7	breast:
9	chr12:60362230..60364908-chr12:60365705..60369063,3	MCF-7	breast:
10	chr12:60366694..60369623-chr12:60371578..60373431,2	MCF-7	breast:
11	chr12:60355837..60358640-chr12:60365883..60368050,2	MCF-7	breast:
12	chr12:60419898..60420453-chr14:61344505..61345184,2	MCF-7	breast:
13	chr12:60442817..60444737-chr12:60445729..60447893,2	K562	blood:
14	chr12:60439937..60442180-chr12:60446699..60448272,2	MCF-7	breast:
15	chr12:60448484..60450647-chr12:60452739..60455616,2	K562	blood:
16	chr12:60366694..60369623-chr12:60371578..60373431,2	MCF-7	breast:
17	chr12:60437721..60438429-chr8:43096750..43097250,2	MCF-7	breast:
18	chr12:60362230..60364908-chr12:60365705..60369063,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000264437	TF binding region
ENSG00000264437	CpG island

Extended variants
information (count: 3044 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:3044 , 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	rs186700096	chr12:60356225-60356226	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs535716936	chr12:60356256-60356257	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs200803042	chr12:60356266-60356267	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs567941448	chr12:60356283-60356284	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs190813928	chr12:60356291-60356292	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs373059332	chr12:60356339-60356340	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs182001178	chr12:60356340-60356341	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs186155732	chr12:60356358-60356359	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs73354417	chr12:60356384-60356385	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs142784515	chr12:60356442-60356443	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs553167210	chr12:60356461-60356462	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs573106872	chr12:60356513-60356514	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs189612967	chr12:60356519-60356520	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs182545735	chr12:60356541-60356542	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs115647207	chr12:60356548-60356549	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs147379988	chr12:60356550-60356551	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs564326753	chr12:60356624-60356625	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs114165471	chr12:60356651-60356652	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs567879816	chr12:60356672-60356673	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs560297804	chr12:60356703-60356704	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs529473855	chr12:60356731-60356732	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs555652907	chr12:60356739-60356740	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs541358979	chr12:60356747-60356748	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs148422489	chr12:60356771-60356772	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs10877374	chr12:60356799-60356800	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs538166829	chr12:60356804-60356805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs141046532	chr12:60356815-60356816	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs142520509	chr12:60356859-60356860	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs372958648	chr12:60356949-60356950	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs150504696	chr12:60357005-60357006	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs529949965	chr12:60357043-60357044	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs373352854	chr12:60357089-60357090	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs140013608	chr12:60357096-60357097	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs143895982	chr12:60357140-60357141	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs78244209	chr12:60357150-60357151	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs535677921	chr12:60357169-60357170	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs532394561	chr12:60357177-60357178	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs555280716	chr12:60357180-60357181	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs575448830	chr12:60357198-60357199	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs552506022	chr12:60357222-60357223	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs146859290	chr12:60357227-60357228	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs80136278	chr12:60357255-60357256	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs140668443	chr12:60357261-60357262	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs185318918	chr12:60357298-60357299	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs7135268	chr12:60357338-60357339	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs35977726	chr12:60357367-60357368	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs144351269	chr12:60357378-60357379	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs554874806	chr12:60357428-60357429	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs377711329	chr12:60357460-60357461	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs568290715	chr12:60357483-60357484	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

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
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
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Urothelial cell carcinoma	18451213	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Myelofibrosis	22110671	CNVD
Phyllodes tumor	17334353	CNVD
Glaucoma	21310917	CNVD
Breast cancer	16272173	CNVD
Mental retardation	19951919	CNVD
Glaucoma	21447600	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Developmental delay	21267005	CNVD
12q14 microdeletion syndrome	21267005	CNVD
Developmental delay	19277063	CNVD
Dwarfism	19277063	CNVD
Fibroblasts	20926602	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	20080666	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	17133270	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Glioblastoma	17090523	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	16773561	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Breast cancer	21364760	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Osteosarcoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:114 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:60356200-60357000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr12:60357000-60357400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr12:60357200-60357400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr12:60357200-60357800	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr12:60357400-60357800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr12:60357600-60359000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr12:60357800-60358000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr12:60357800-60358800	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr12:60358000-60358400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr12:60358000-60360400	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr12:60358400-60359000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr12:60358400-60359000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr12:60358400-60359600	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr12:60358400-60360200	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr12:60358400-60360400	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr12:60358600-60359000	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr12:60358600-60360400	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr12:60358800-60359200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
19	chr12:60358800-60359600	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr12:60359000-60360000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr12:60359000-60360000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
22	chr12:60359000-60360600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr12:60359800-60360400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr12:60360000-60360200	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr12:60363600-60364200	Enhancers	HUVEC	blood vessel
26	chr12:60363800-60364000	Enhancers	HMEC	breast
27	chr12:60364200-60366400	Weak transcription	HUVEC	blood vessel
28	chr12:60364400-60365600	Weak transcription	HMEC	breast
29	chr12:60365600-60366600	Enhancers	HMEC	breast
30	chr12:60365600-60367600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr12:60366000-60366600	Enhancers	Hela-S3	cervix
32	chr12:60366000-60368200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr12:60366200-60366600	Enhancers	NHEK	skin
34	chr12:60366400-60368200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr12:60366400-60368200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr12:60366400-60368200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr12:60366400-60368400	Enhancers	HUVEC	blood vessel
38	chr12:60366600-60367000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr12:60366600-60367000	Flanking Active TSS	Hela-S3	cervix
40	chr12:60366600-60367000	Flanking Active TSS	HMEC	breast
41	chr12:60366600-60367000	Flanking Active TSS	NHEK	skin
42	chr12:60366600-60367800	Enhancers	NHLF	lung
43	chr12:60366600-60368000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr12:60366600-60368200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr12:60366600-60368200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr12:60366600-60368200	Enhancers	NH-A	brain
47	chr12:60366600-60368200	Enhancers	NHDF-Ad	bronchial
48	chr12:60367000-60367600	Active TSS	HMEC	breast
49	chr12:60367000-60368400	Enhancers	Hela-S3	cervix
50	chr12:60367000-60368400	Enhancers	NHEK	skin

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