Variant report

Variant	nsv559645
Chromosome Location	chr12:85224141-85330496
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1075)
CpG islands
(count:1589)
Chromatin interactive
region (count:22)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:1075 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:85236213-85236485	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:85268279-85268603	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:85268354-85268642	K562	blood:	n/a	n/a
4	ATF2	chr12:85304904-85305500	H1-hESC	embryonic stem cell:	n/a	chr12:85305196-85305207
5	ATF2	chr12:85304987-85305439	H1-hESC	embryonic stem cell:	n/a	chr12:85305196-85305207
6	BACH1	chr12:85318786-85319125	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr12:85251635-85251968	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr12:85306376-85307360	H1-hESC	embryonic stem cell:	n/a	n/a
9	BRCA1	chr12:85314034-85314408	Hela-S3	cervix:	n/a	n/a
10	BRCA1	chr12:85307093-85307218	Hela-S3	cervix:	n/a	n/a
11	BRCA1	chr12:85236243-85236478	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr12:85305066-85305337	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr12:85306516-85306552	H1-hESC	embryonic stem cell:	n/a	n/a
14	CCNT2	chr12:85267940-85268140	K562	blood:	n/a	n/a
15	CEBPB	chr12:85312319-85312504	K562	blood:	n/a	chr12:85312380-85312391 chr12:85312378-85312391 chr12:85312378-85312391 chr12:85312378-85312389 chr12:85312378-85312391
16	CEBPB	chr12:85306754-85307282	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr12:85283148-85283255	HepG2	liver:	n/a	chr12:85283223-85283234
18	CEBPB	chr12:85312202-85312559	Hela-S3	cervix:	n/a	chr12:85312380-85312391 chr12:85312378-85312391 chr12:85312378-85312391 chr12:85312378-85312389 chr12:85312378-85312391
19	CEBPB	chr12:85293930-85294083	A549	lung:	n/a	chr12:85293967-85293978
20	CEBPB	chr12:85268226-85268641	HepG2	liver:	n/a	n/a
21	CEBPB	chr12:85316431-85316947	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr12:85273336-85273604	HepG2	liver:	n/a	chr12:85273466-85273477 chr12:85273465-85273478
23	CEBPB	chr12:85312228-85312506	A549	lung:	n/a	chr12:85312380-85312391 chr12:85312378-85312391 chr12:85312378-85312391 chr12:85312378-85312389 chr12:85312378-85312391
24	CEBPB	chr12:85268297-85268666	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr12:85312217-85312538	IMR90	lung:	n/a	chr12:85312380-85312391 chr12:85312378-85312391 chr12:85312378-85312391 chr12:85312378-85312389 chr12:85312378-85312391
26	CEBPB	chr12:85305055-85305369	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr12:85268175-85268753	A549	lung:	n/a	n/a
28	CEBPB	chr12:85268226-85268674	HCT-116	colon:	n/a	n/a
29	CEBPB	chr12:85268353-85268653	MCF-7	breast:	n/a	n/a
30	CEBPB	chr12:85306919-85307191	HepG2	liver:	n/a	n/a
31	CEBPB	chr12:85261428-85261650	HepG2	liver:	n/a	chr12:85261574-85261587 chr12:85261574-85261587 chr12:85261575-85261586
32	CEBPB	chr12:85306502-85307327	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr12:85306923-85307295	A549	lung:	n/a	n/a
34	CEBPB	chr12:85293832-85294105	HepG2	liver:	n/a	chr12:85293967-85293978
35	CEBPB	chr12:85268323-85268623	K562	blood:	n/a	n/a
36	CEBPB	chr12:85273382-85273621	IMR90	lung:	n/a	chr12:85273466-85273477 chr12:85273465-85273478
37	CEBPB	chr12:85268313-85268684	IMR90	lung:	n/a	n/a
38	CEBPB	chr12:85306902-85307256	A549	lung:	n/a	n/a
39	CEBPB	chr12:85312197-85312540	HepG2	liver:	n/a	chr12:85312380-85312391 chr12:85312378-85312391 chr12:85312378-85312391 chr12:85312378-85312389 chr12:85312378-85312391
40	CEBPB	chr12:85306847-85307357	A549	lung:	n/a	n/a
41	CEBPB	chr12:85268104-85268751	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr12:85283076-85283339	H1-hESC	embryonic stem cell:	n/a	chr12:85283223-85283234
43	CEBPB	chr12:85313948-85314603	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr12:85312245-85312403	H1-hESC	embryonic stem cell:	n/a	chr12:85312380-85312391 chr12:85312378-85312391 chr12:85312378-85312391 chr12:85312378-85312389 chr12:85312378-85312391
45	CEBPB	chr12:85268168-85268658	A549	lung:	n/a	n/a
46	CEBPB	chr12:85305037-85305389	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr12:85260209-85260382	A549	lung:	n/a	n/a
48	CEBPB	chr12:85285233-85285419	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr12:85273318-85273635	A549	lung:	n/a	chr12:85273466-85273477 chr12:85273465-85273478
50	CEBPB	chr12:85273326-85273578	Hela-S3	cervix:	n/a	chr12:85273466-85273477 chr12:85273465-85273478

(count:1589 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:85285441-85285491	MCF-7	breast:	n/a
2	chr12:85306916-85306966	NT2-D1	testis:	n/a
3	chr12:85305087-85305137	HL-60	blood:	n/a
4	chr12:85285441-85285491	MCF-7	breast:	n/a
5	chr12:85306916-85306966	NT2-D1	testis:	n/a
6	chr12:85305087-85305137	HL-60	blood:	n/a
7	chr12:85305677-85305727	ovcar-3	ovarian:	n/a
8	chr12:85306648-85306698	PFSK-1	brain:	n/a
9	chr12:85305219-85305269	Jurkat	blood:	n/a
10	chr12:85282560-85282610	SK-N-SH_RA	brain:	n/a
11	chr12:85307152-85307202	ProgFib	skin:	n/a
12	chr12:85285441-85285491	ProgFib	skin:	n/a
13	chr12:85305677-85305727	HRE	kidney:	n/a
14	chr12:85307080-85307130	HPAEpiC	pulmonary alveolar:	n/a
15	chr12:85305742-85305792	GM06990	blood:	n/a
16	chr12:85306021-85306071	GM12891	blood:	n/a
17	chr12:85304696-85304746	Hela-S3	cervix:	n/a
18	chr12:85306474-85306524	SK-N-SH_RA	brain:	n/a
19	chr12:85305742-85305792	HCF	heart:	n/a
20	chr12:85305219-85305269	AG04449	skin:	fetal
21	chr12:85285441-85285491	Jurkat	blood:	n/a
22	chr12:85285441-85285491	AG04449	skin:	fetal
23	chr12:85305677-85305727	AG09319	gingival:	n/a
24	chr12:85305677-85305727	H1-hESC	embryonic stem cell:	embryo
25	chr12:85306021-85306071	HNPCEpiC	eye:	n/a
26	chr12:85306916-85306966	ovcar-3	ovarian:	n/a
27	chr12:85306474-85306524	PFSK-1	brain:	n/a
28	chr12:85306021-85306071	NB4	blood:	n/a
29	chr12:85307152-85307202	GM06990	blood:	n/a
30	chr12:85306916-85306966	SKMC	muscle:	n/a
31	chr12:85306854-85306904	LNCaP	prostate:	n/a
32	chr12:85305742-85305792	HPAEpiC	pulmonary alveolar:	n/a
33	chr12:85307424-85307474	AG09319	gingival:	n/a
34	chr12:85306474-85306524	Jurkat	blood:	n/a
35	chr12:85305087-85305137	HAEpiC	amniotic membrane:	n/a
36	chr12:85306797-85306847	PANC-1	pancreas:	n/a
37	chr12:85306916-85306966	HRE	kidney:	n/a
38	chr12:85302937-85302987	AG04450	lung:	fetal
39	chr12:85306548-85306598	HRPEpiC	eye:	n/a
40	chr12:85304514-85304564	SK-N-MC	brain:	n/a
41	chr12:85305742-85305792	MCF-7	breast:	n/a
42	chr12:85302937-85302987	T-47D	breast:	n/a
43	chr12:85306741-85306791	Caco-2	colon:	n/a
44	chr12:85306741-85306791	BE2_C	brain:	n/a
45	chr12:85305677-85305727	GM12878	blood:	n/a
46	chr12:85306323-85306373	HRE	kidney:	n/a
47	chr12:85305219-85305269	HCM	heart:	n/a
48	chr12:85306797-85306847	HCF	heart:	n/a
49	chr12:85306916-85306966	HUVEC	blood vessel:	n/a
50	chr12:85305219-85305269	NH-A	brain:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:85328199..85330648-chr17:56736325..56738042,2	MCF-7	breast:
2	chr12:85287799..85288304-chr17:41465245..41465882,2	Hela-S3	cervix:
3	chr11:10315577..10316374-chr12:85304790..85305756,2	Hela-S3	cervix:
4	chr12:50222179..50223090-chr12:85304791..85305560,2	Hela-S3	cervix:
5	chr12:85270876..85273150-chr12:85276094..85278154,2	MCF-7	breast:
6	chr12:85232820..85235309-chr12:85237518..85239463,2	K562	blood:
7	chr1:47779341..47780185-chr12:85304853..85305718,2	Hela-S3	cervix:
8	chr12:85287797..85288304-chr3:73159863..73160610,2	Hela-S3	cervix:
9	chr12:85031251..85032044-chr12:85236099..85236834,2	MCF-7	breast:
10	chr12:85270876..85273150-chr12:85276094..85278154,2	MCF-7	breast:
11	chr12:85275674..85277179-chr12:85300709..85303261,2	K562	blood:
12	chr11:62609070..62609626-chr12:85287765..85288304,2	NB4	blood:
13	chr12:85217121..85219586-chr12:85222343..85224592,2	MCF-7	breast:
14	chr12:85232820..85235309-chr12:85237518..85239463,2	K562	blood:
15	chr12:85275674..85277179-chr12:85300709..85303261,2	K562	blood:
16	chr12:85305841..85306396-chr17:26988797..26989434,2	Hela-S3	cervix:
17	chr12:84896709..84897539-chr12:85236279..85236879,3	MCF-7	breast:
18	chr12:85269198..85269791-chr12:85451134..85451813,2	MCF-7	breast:
19	chr12:85268551..85271336-chr12:85421363..85424699,4	MCF-7	breast:
20	chr12:85287784..85288299-chr17:41465185..41465702,2	NB4	blood:
21	chr12:85257218..85259275-chr12:85261171..85263278,2	K562	blood:
22	chr12:84901925..84902765-chr12:85235880..85236805,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRRIQ1-1	chr12:85306659-85306683	XLOC_009819
2	lnc-TSPAN19-2	chr12:85258120-85259169	NONHSAT029740
3	lnc-LRRIQ1-1	chr12:85306655-85306683	XLOC_009819
4	lnc-LRRIQ1-1	chr12:85308536-85308641	XLOC_009819
5	lnc-LRRIQ1-1	chr12:85308536-85308641	XLOC_009819

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	SLC6A15	hsa-miR-23b-3p	chr12:85277173-85277193
2	SLC6A15	hsa-miR-23a-3p	chr12:85277173-85277191

Variant related genes	Relation type
SLC6A15	TF binding region
SLC6A15	CpG island
ENSG00000133812	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000072041	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000258057	chromatin interactions
ENSG00000109111	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000123473	chromatin interactions
ENSG00000132581	chromatin interactions
ENSG00000167566	chromatin interactions

Extended variants
information (count: 3577 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:3577 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7968335	chr12:85224141-85224142	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs73170032	chr12:85224150-85224151	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs539023820	chr12:85224249-85224250	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs537389062	chr12:85224306-85224307	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs187563562	chr12:85224364-85224365	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs116763906	chr12:85224395-85224396	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs561526555	chr12:85224859-85224860	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs530168951	chr12:85224862-85224863	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs117200495	chr12:85224890-85224891	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs563391516	chr12:85224912-85224913	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs530889509	chr12:85224920-85224921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs552609381	chr12:85224965-85224966	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs368342207	chr12:85224998-85224999	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs372326886	chr12:85225108-85225109	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs537144825	chr12:85225111-85225112	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs539789335	chr12:85225122-85225123	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs547248835	chr12:85225130-85225131	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs7954075	chr12:85225236-85225237	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs535589548	chr12:85225262-85225263	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs141485282	chr12:85225282-85225283	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs56267901	chr12:85225305-85225306	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs537495846	chr12:85225306-85225307	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs112522055	chr12:85225358-85225359	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs539386226	chr12:85225369-85225370	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs150849479	chr12:85225528-85225529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs573121962	chr12:85225550-85225551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs540143281	chr12:85225561-85225562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs370084200	chr12:85225585-85225586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs12582385	chr12:85225603-85225604	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs574318561	chr12:85225620-85225621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs17012447	chr12:85225677-85225678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs1376987	chr12:85225699-85225700	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs553831940	chr12:85225701-85225702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs563402083	chr12:85225711-85225712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs143944885	chr12:85225724-85225725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs147328791	chr12:85225730-85225731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs35906675	chr12:85225739-85225740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs546162050	chr12:85225743-85225744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs377374591	chr12:85225812-85225813	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs547307109	chr12:85225827-85225828	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs76727105	chr12:85225828-85225829	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs568671149	chr12:85225840-85225841	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs529465677	chr12:85225920-85225921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs550713260	chr12:85225947-85225948	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs368862281	chr12:85225948-85225949	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs140989084	chr12:85226023-85226024	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs539140869	chr12:85226038-85226039	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs186985603	chr12:85226041-85226042	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs566335192	chr12:85226102-85226103	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs534143758	chr12:85226106-85226107	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
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
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
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	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
Malignant peripheral nerve sheath tumor	18522746	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	20729466	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Renal cell carcinoma	18194544	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21364760	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:646 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:85223400-85224400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr12:85224800-85225400	Enhancers	Fetal Heart	heart
3	chr12:85225400-85225800	Weak transcription	Fetal Heart	heart
4	chr12:85225800-85226400	Enhancers	Fetal Heart	heart
5	chr12:85234000-85234400	Enhancers	NHDF-Ad	bronchial
6	chr12:85234000-85235800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr12:85234200-85236000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr12:85237400-85237600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr12:85238000-85238400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
10	chr12:85243000-85250200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr12:85249600-85251000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr12:85249600-85251000	Enhancers	NHEK	skin
13	chr12:85249800-85252200	Enhancers	HMEC	breast
14	chr12:85250000-85271400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr12:85250200-85250600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr12:85250200-85250600	Enhancers	Muscle Satellite Cultured Cells	--
17	chr12:85250200-85251000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr12:85250200-85251400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr12:85250400-85250600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr12:85250400-85250600	Enhancers	NHDF-Ad	bronchial
21	chr12:85250400-85251200	Enhancers	Esophagus	oesophagus
22	chr12:85250400-85251600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr12:85250600-85250800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr12:85250600-85251800	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr12:85250600-85264400	Weak transcription	NHDF-Ad	bronchial
26	chr12:85250800-85251400	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr12:85251000-85251400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr12:85251000-85251600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr12:85251000-85303000	Weak transcription	NHEK	skin
30	chr12:85251200-85251400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr12:85251400-85251600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr12:85251400-85251600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr12:85251400-85252000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr12:85251400-85255400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr12:85251400-85256800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr12:85251600-85251800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr12:85251600-85255400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr12:85251600-85267200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr12:85251800-85257600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr12:85251800-85285400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr12:85252000-85255200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr12:85252000-85263400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
43	chr12:85252200-85254000	Weak transcription	HMEC	breast
44	chr12:85253800-85271200	Weak transcription	Brain Inferior Temporal Lobe	brain
45	chr12:85254000-85257200	Strong transcription	HMEC	breast
46	chr12:85254000-85276800	Weak transcription	Fetal Brain Male	brain
47	chr12:85254000-85289800	Weak transcription	Brain Angular Gyrus	brain
48	chr12:85254600-85270600	Weak transcription	Brain Substantia Nigra	brain
49	chr12:85254800-85271200	Weak transcription	Brain Hippocampus Middle	brain
50	chr12:85255000-85257600	Weak transcription	Brain Germinal Matrix	brain

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