Variant report

Variant	nsv1047257
Chromosome Location	chr12:59444966-59520330
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:843)
CpG islands
(count:183)
Chromatin interactive
region (count:25)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:843 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr12:59482441-59482833	H1-hESC	embryonic stem cell:	n/a	chr12:59482636-59482650
2	BATF	chr12:59449276-59449566	GM12878	blood:	n/a	chr12:59449406-59449417
3	BATF	chr12:59449304-59449598	GM12878	blood:	n/a	chr12:59449406-59449417
4	BHLHE40	chr12:59460962-59461087	GM12878	blood:	n/a	n/a
5	BHLHE40	chr12:59507587-59507787	GM12878	blood:	n/a	n/a
6	BHLHE40	chr12:59507676-59507746	K562	blood:	n/a	n/a
7	BRCA1	chr12:59514134-59514158	GM12878	blood:	n/a	n/a
8	BRCA1	chr12:59484047-59484096	GM12878	blood:	n/a	n/a
9	CBX3	chr12:59449051-59449681	HCT-116	colon:	n/a	n/a
10	CEBPB	chr12:59489526-59489800	IMR90	lung:	n/a	n/a
11	CEBPB	chr12:59472897-59473169	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr12:59489628-59489698	HepG2	liver:	n/a	n/a
13	CEBPB	chr12:59486875-59487478	IMR90	lung:	n/a	chr12:59487323-59487334
14	CEBPB	chr12:59449316-59449698	IMR90	lung:	n/a	chr12:59449548-59449561
15	CEBPB	chr12:59450762-59451085	IMR90	lung:	n/a	chr12:59450809-59450820
16	CEBPB	chr12:59510930-59511142	HepG2	liver:	n/a	n/a
17	CEBPB	chr12:59449096-59449787	HCT-116	colon:	n/a	chr12:59449548-59449561 chr12:59449711-59449724
18	CEBPB	chr12:59449357-59449678	A549	lung:	n/a	chr12:59449548-59449561
19	CEBPB	chr12:59508412-59508602	A549	lung:	n/a	n/a
20	CEBPB	chr12:59449154-59449707	Hela-S3	cervix:	n/a	chr12:59449548-59449561
21	CEBPB	chr12:59508155-59508587	HepG2	liver:	n/a	n/a
22	CEBPB	chr12:59489620-59489708	A549	lung:	n/a	n/a
23	CEBPB	chr12:59472934-59473166	A549	lung:	n/a	n/a
24	CEBPB	chr12:59449130-59449771	HCT-116	colon:	n/a	chr12:59449548-59449561 chr12:59449711-59449724
25	CHD1	chr12:59507445-59507924	IMR90	lung:	n/a	n/a
26	CHD2	chr12:59454135-59454171	HepG2	liver:	n/a	n/a
27	CHD2	chr12:59507719-59507920	HepG2	liver:	n/a	n/a
28	CTCF	chr12:59507680-59507830	GM12871	blood:	n/a	n/a
29	CTCF	chr12:59478560-59478710	HFF	foreskin:	n/a	n/a
30	CTCF	chr12:59480497-59481993	A549	lung:	n/a	chr12:59481044-59481062 chr12:59481045-59481061 chr12:59481039-59481060
31	CTCF	chr12:59507584-59507856	Pancreas_OC	pancreas:	n/a	n/a
32	CTCF	chr12:59507458-59507960	HepG2	liver:	n/a	n/a
33	CTCF	chr12:59507604-59507875	SK-N-SH_RA	brain:	n/a	n/a
34	CTCF	chr12:59507660-59507810	AG09319	gingival:	n/a	n/a
35	CTCF	chr12:59507640-59507790	BJ	skin:	n/a	n/a
36	CTCF	chr12:59507586-59507837	K562	blood:	n/a	n/a
37	CTCF	chr12:59507620-59507770	AG09319	gingival:	n/a	n/a
38	CTCF	chr12:59480984-59481168	Spleen_OC	spleen:	n/a	chr12:59481044-59481062 chr12:59481045-59481061 chr12:59481039-59481060
39	CTCF	chr12:59507631-59508060	MCF-7	breast:	n/a	n/a
40	CTCF	chr12:59470000-59470150	NHDF-neo	bronchial:	n/a	n/a
41	CTCF	chr12:59480940-59481090	GM12864	blood:	n/a	chr12:59481044-59481062 chr12:59481045-59481061 chr12:59481039-59481060
42	CTCF	chr12:59507640-59507790	BE2_C	brain:	n/a	n/a
43	CTCF	chr12:59507548-59507893	K562	blood:	n/a	n/a
44	CTCF	chr12:59478800-59478950	NHDF-neo	bronchial:	n/a	chr12:59478843-59478852
45	CTCF	chr12:59469880-59470030	RPTEC	kidney:	n/a	n/a
46	CTCF	chr12:59507640-59507790	AG09309	skin:	n/a	n/a
47	CTCF	chr12:59469800-59469950	HA-sp	spinal cord:	n/a	n/a
48	CTCF	chr12:59480967-59481141	A549	lung:	n/a	chr12:59481044-59481062 chr12:59481045-59481061 chr12:59481039-59481060
49	CTCF	chr12:59507640-59507790	GM12867	blood:	n/a	n/a
50	CTCF	chr12:59507700-59507850	GM12866	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:59478783-59478833	SKMC	muscle:	n/a
2	chr12:59508147-59508197	IMR90	lung:	fetal
3	chr12:59508147-59508197	HPAEpiC	pulmonary alveolar:	n/a
4	chr12:59478783-59478833	ovcar-3	ovarian:	n/a
5	chr12:59508147-59508197	AG09319	gingival:	n/a
6	chr12:59508147-59508197	GM19239	blood:	n/a
7	chr12:59478957-59479007	AG09319	gingival:	n/a
8	chr12:59478783-59478833	HCM	heart:	n/a
9	chr12:59478783-59478833	HUVEC	blood vessel:	n/a
10	chr12:59478783-59478833	SAEC	small airway:	n/a
11	chr12:59478783-59478833	GM19239	blood:	n/a
12	chr12:59478783-59478833	HL-60	blood:	n/a
13	chr12:59508147-59508197	Hela-S3	cervix:	n/a
14	chr12:59478957-59479007	GM06990	blood:	n/a
15	chr12:59508147-59508197	SKMC	muscle:	n/a
16	chr12:59508147-59508197	PrEC	prostate:	n/a
17	chr12:59478957-59479007	HCPEpiC	choroid plexus:	n/a
18	chr12:59478783-59478833	AoSMC	blood vessel:	n/a
19	chr12:59478957-59479007	ovcar-3	ovarian:	n/a
20	chr12:59508147-59508197	SK-N-MC	brain:	n/a
21	chr12:59508147-59508197	Hepatocyte	liver:	n/a
22	chr12:59478783-59478833	BJ	skin:	n/a
23	chr12:59508147-59508197	SAEC	small airway:	n/a
24	chr12:59508147-59508197	K562	blood:	n/a
25	chr12:59478783-59478833	HAEpiC	amniotic membrane:	n/a
26	chr12:59478783-59478833	GM12892	blood:	n/a
27	chr12:59508147-59508197	GM12892	blood:	n/a
28	chr12:59508147-59508197	NHBE	bronchial:	n/a
29	chr12:59478783-59478833	NHDF-neo	bronchial:	n/a
30	chr12:59478957-59479007	HepG2	liver:	n/a
31	chr12:59478957-59479007	SAEC	small airway:	n/a
32	chr12:59478957-59479007	Hepatocyte	liver:	n/a
33	chr12:59478957-59479007	PANC-1	pancreas:	n/a
34	chr12:59508147-59508197	HRCEpiC	kidney:	n/a
35	chr12:59478957-59479007	NHDF-neo	bronchial:	n/a
36	chr12:59508147-59508197	HRPEpiC	eye:	n/a
37	chr12:59478957-59479007	PFSK-1	brain:	n/a
38	chr12:59478783-59478833	AG04449	skin:	fetal
39	chr12:59508147-59508197	AG10803	skin:	n/a
40	chr12:59478957-59479007	AG10803	skin:	n/a
41	chr12:59508147-59508197	MCF10A-Er-Src	breast:	n/a
42	chr12:59478783-59478833	H1-hESC	embryonic stem cell:	embryo
43	chr12:59478957-59479007	HL-60	blood:	n/a
44	chr12:59478783-59478833	ProgFib	skin:	n/a
45	chr12:59478783-59478833	HCPEpiC	choroid plexus:	n/a
46	chr12:59508147-59508197	HCM	heart:	n/a
47	chr12:59478783-59478833	NT2-D1	testis:	n/a
48	chr12:59508147-59508197	HMEC	breast:	n/a
49	chr12:59478957-59479007	HCT-116	colon:	n/a
50	chr12:59478783-59478833	GM06990	blood:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:59301538..59302531-chr12:59480961..59481505,2	MCF-7	breast:
2	chr12:59506527..59507272-chr12:59543925..59544447,2	MCF-7	breast:
3	chr12:59450782..59453219-chr12:59453673..59455796,2	MCF-7	breast:
4	chr12:59301019..59303651-chr12:59478405..59481329,2	MCF-7	breast:
5	chr12:59506961..59508922-chr12:59510527..59512982,3	MCF-7	breast:
6	chr12:59507288..59508240-chr12:61932726..61933441,2	MCF-7	breast:
7	chr12:59227368..59228360-chr12:59480589..59481215,3	MCF-7	breast:
8	chr12:59507415..59508147-chr12:59543545..59544473,6	MCF-7	breast:
9	chr12:59312732..59314963-chr12:59478479..59481283,2	MCF-7	breast:
10	chr12:58583843..58585417-chr12:59486387..59488506,2	MCF-7	breast:
11	chr12:56121872..56123886-chr12:59449553..59451460,2	MCF-7	breast:
12	chr12:58933996..58934513-chr12:59480494..59481170,2	MCF-7	breast:
13	chr12:59450782..59453219-chr12:59453673..59455796,2	MCF-7	breast:
14	chr12:59443922..59445981-chr12:59446568..59448120,2	MCF-7	breast:
15	chr12:59507234..59507853-chr12:59766386..59767199,2	MCF-7	breast:
16	chr12:59507135..59508358-chr12:59543262..59544671,18	MCF-7	breast:
17	chr12:59455363..59458271-chr12:59461574..59463083,2	MCF-7	breast:
18	chr12:59507468..59508144-chr12:59801341..59801884,3	MCF-7	breast:
19	chr12:59312784..59314392-chr12:59448916..59450725,2	MCF-7	breast:
20	chr12:59455363..59458271-chr12:59461574..59463083,2	MCF-7	breast:
21	chr12:59479101..59479887-chr6:136172579..136173303,2	MCF-7	breast:
22	chr12:58934165..58934990-chr12:59480959..59481541,2	MCF-7	breast:
23	chr12:59506961..59508922-chr12:59510527..59512982,3	MCF-7	breast:
24	chr12:58934011..58934535-chr12:59507466..59507984,2	MCF-7	breast:
25	chr12:59507585..59508107-chr12:59766521..59767200,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-362K2.2.1-1	chr12:59449787-59449889	ENSG00000257443.1
2	lnc-RP11-362K2.2.1-1	chr12:59457794-59458019	ENSG00000257443.1

No data

Variant related genes	Relation type
ENSG00000257288	TF binding region
ENSG00000257288	CpG island
ENSG00000257443	chromatin interactions
ENSG00000258056	chromatin interactions
ENSG00000139263	chromatin interactions
ENSG00000257288	chromatin interactions
ENSG00000135404	chromatin interactions
ENSG00000171408	chromatin interactions

Extended variants
information (count: 2708 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:2708 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7303996	chr12:59444966-59444967	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs191834064	chr12:59444987-59444988	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs151117981	chr12:59444990-59444991	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs562059576	chr12:59445046-59445047	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs529418824	chr12:59445055-59445056	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs34639416	chr12:59445075-59445076	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs185086694	chr12:59445178-59445179	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs562599325	chr12:59445202-59445203	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs190423056	chr12:59445213-59445214	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs551747872	chr12:59445246-59445247	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs542432654	chr12:59445299-59445300	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs551235458	chr12:59445303-59445304	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs566782439	chr12:59445400-59445401	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs534081194	chr12:59445446-59445447	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs12422372	chr12:59445461-59445462	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs182069570	chr12:59445597-59445598	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs537992640	chr12:59445611-59445612	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs531813671	chr12:59445671-59445672	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs187222619	chr12:59445723-59445724	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs556403704	chr12:59445752-59445753	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs577659683	chr12:59445754-59445755	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs58975592	chr12:59445807-59445808	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs189344201	chr12:59445833-59445834	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs571607698	chr12:59445842-59445843	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs527696113	chr12:59445849-59445850	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs376764272	chr12:59445883-59445884	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs542236464	chr12:59445892-59445893	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs561998100	chr12:59445970-59445971	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs554917858	chr12:59445975-59445976	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs11172887	chr12:59445990-59445991	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs141077377	chr12:59445995-59445996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs562985000	chr12:59446027-59446028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs567983845	chr12:59446030-59446031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs180745531	chr12:59446092-59446093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs74620330	chr12:59446093-59446094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs560653311	chr12:59446115-59446116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs34385338	chr12:59446136-59446137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs536808812	chr12:59446137-59446138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs373900132	chr12:59446217-59446218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs185149927	chr12:59446218-59446219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs531677685	chr12:59446267-59446268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs556779623	chr12:59446274-59446275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs141463835	chr12:59446336-59446337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs571381854	chr12:59446355-59446356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs538841283	chr12:59446372-59446373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs553557515	chr12:59446381-59446382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs537944107	chr12:59446383-59446384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs182622078	chr12:59446393-59446394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs2166038	chr12:59446455-59446456	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs535803175	chr12:59446483-59446484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
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
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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Chronic lymphocytic leukemia	21215367	CNVD

Chromatin state (count:676 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:59441000-59450800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr12:59442000-59446400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr12:59442000-59446800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr12:59442000-59446800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr12:59442000-59446800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr12:59442000-59446800	Weak transcription	HMEC	breast
7	chr12:59442000-59446800	Weak transcription	NHEK	skin
8	chr12:59446400-59451000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr12:59446400-59451200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr12:59446800-59449200	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr12:59446800-59449200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr12:59446800-59450000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr12:59446800-59450200	Enhancers	HMEC	breast
14	chr12:59446800-59450200	Enhancers	NHEK	skin
15	chr12:59447200-59447400	Enhancers	Brain Substantia Nigra	brain
16	chr12:59447200-59447600	Enhancers	Fetal Muscle Leg	muscle
17	chr12:59447600-59448200	Enhancers	Fetal Stomach	stomach
18	chr12:59448000-59450000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr12:59448200-59448400	Enhancers	Sigmoid Colon	Sigmoid Colon
20	chr12:59448200-59449000	Enhancers	Esophagus	oesophagus
21	chr12:59448200-59452600	Weak transcription	Fetal Stomach	stomach
22	chr12:59448400-59450000	Enhancers	Hela-S3	cervix
23	chr12:59448400-59453600	Weak transcription	Sigmoid Colon	Sigmoid Colon
24	chr12:59448600-59448800	Enhancers	Aorta	Aorta
25	chr12:59448600-59449000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr12:59448600-59449000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr12:59448600-59449000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr12:59448600-59449200	Enhancers	Stomach Mucosa	stomach
29	chr12:59448600-59449600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr12:59448600-59450000	Enhancers	Muscle Satellite Cultured Cells	--
31	chr12:59448600-59450000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr12:59448600-59450000	Enhancers	Pancreatic Islets	Pancreatic Islet
33	chr12:59448600-59451200	Enhancers	HUVEC	blood vessel
34	chr12:59448800-59449200	Enhancers	A549	lung
35	chr12:59448800-59449800	Enhancers	Osteobl	bone
36	chr12:59448800-59450000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr12:59448800-59450000	Enhancers	Placenta Amnion	Placenta Amnion
38	chr12:59448800-59450000	Enhancers	HSMMtube	muscle
39	chr12:59448800-59450000	Enhancers	NH-A	brain
40	chr12:59449000-59449600	Enhancers	HSMM	muscle
41	chr12:59449000-59449800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr12:59449000-59450000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr12:59449000-59450000	Enhancers	NHDF-Ad	bronchial
44	chr12:59449000-59459800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr12:59449200-59449400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr12:59449200-59449600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr12:59449200-59449600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr12:59449200-59449600	Enhancers	Fetal Intestine Large	intestine
49	chr12:59449200-59449800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
50	chr12:59449200-59449800	Weak transcription	Stomach Mucosa	stomach

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