Variant report

Variant	esv1839295
Chromosome Location	chr12:1305357-1372114
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:377)
CpG islands
(count:307)
Chromatin interactive
region (count:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:377 , 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	BATF	chr12:1336135-1336446	GM12878	blood:	n/a	chr12:1336325-1336336
2	BATF	chr12:1336172-1336455	GM12878	blood:	n/a	chr12:1336325-1336336
3	BATF	chr12:1335695-1335957	GM12878	blood:	n/a	n/a
4	BATF	chr12:1335617-1335994	GM12878	blood:	n/a	n/a
5	BATF	chr12:1314041-1314260	GM12878	blood:	n/a	n/a
6	BCLAF1	chr12:1313895-1314388	GM12878	blood:	n/a	n/a
7	BRCA1	chr12:1312967-1313007	H1-hESC	embryonic stem cell:	n/a	n/a
8	BRCA1	chr12:1326108-1327006	Hela-S3	cervix:	n/a	n/a
9	CBX3	chr12:1307829-1308562	K562	blood:	n/a	n/a
10	CBX3	chr12:1307963-1308462	K562	blood:	n/a	n/a
11	CEBPB	chr12:1326237-1326703	MCF-7	breast:	n/a	n/a
12	CEBPB	chr12:1324865-1325159	IMR90	lung:	n/a	n/a
13	CEBPB	chr12:1311608-1311947	MCF-7	breast:	n/a	n/a
14	CEBPB	chr12:1324819-1325149	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr12:1326280-1326651	IMR90	lung:	n/a	n/a
16	CEBPB	chr12:1355868-1356196	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr12:1326215-1327174	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr12:1355759-1356204	HCT-116	colon:	n/a	n/a
19	CEBPB	chr12:1311671-1311821	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr12:1355879-1356175	K562	blood:	n/a	n/a
21	CEBPB	chr12:1324913-1325149	HepG2	liver:	n/a	n/a
22	CEBPB	chr12:1326297-1326684	MCF-7	breast:	n/a	n/a
23	CEBPB	chr12:1327544-1327921	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr12:1311684-1311881	K562	blood:	n/a	n/a
25	CEBPB	chr12:1327636-1327849	HepG2	liver:	n/a	n/a
26	CEBPB	chr12:1317917-1318120	K562	blood:	n/a	n/a
27	CEBPB	chr12:1311674-1311853	A549	lung:	n/a	n/a
28	CHD1	chr12:1313725-1314426	GM12878	blood:	n/a	n/a
29	CHD2	chr12:1326226-1327060	Hela-S3	cervix:	n/a	n/a
30	CTCF	chr12:1313740-1313890	HPAF	blood vessel:	n/a	n/a
31	CTCF	chr12:1322866-1322903	GM10248	blood:	n/a	n/a
32	CTCF	chr12:1357080-1357230	A549	lung:	n/a	n/a
33	CUX1	chr12:1367912-1367961	GM12878	blood:	n/a	n/a
34	E2F4	chr12:1314768-1314968	MCF10A-Er-Src	breast:	n/a	n/a
35	E2F4	chr12:1326131-1326520	MCF10A-Er-Src	breast:	n/a	n/a
36	E2F4	chr12:1330925-1331253	MCF10A-Er-Src	breast:	n/a	n/a
37	E2F4	chr12:1331989-1332189	MCF10A-Er-Src	breast:	n/a	n/a
38	EBF1	chr12:1348914-1349234	GM12878	blood:	n/a	chr12:1349050-1349061
39	EBF1	chr12:1335809-1335822	GM12878	blood:	n/a	n/a
40	EBF1	chr12:1348941-1349156	GM12878	blood:	n/a	chr12:1349050-1349061
41	EBF1	chr12:1314085-1314366	GM12878	blood:	n/a	n/a
42	EP300	chr12:1343295-1343553	SK-N-SH_RA	brain:	n/a	n/a
43	EP300	chr12:1332867-1333249	SK-N-SH_RA	brain:	n/a	n/a
44	EP300	chr12:1326097-1327372	SK-N-SH_RA	brain:	n/a	chr12:1326454-1326461
45	EP300	chr12:1355645-1356354	SK-N-SH	brain:	n/a	n/a
46	EP300	chr12:1361751-1362501	SK-N-SH_RA	brain:	n/a	n/a
47	EP300	chr12:1355811-1356214	SK-N-SH_RA	brain:	n/a	n/a
48	EP300	chr12:1325936-1327142	Hela-S3	cervix:	n/a	chr12:1326454-1326461
49	EP300	chr12:1359097-1359381	SK-N-SH_RA	brain:	n/a	n/a
50	EP300	chr12:1359657-1360174	SK-N-SH_RA	brain:	n/a	n/a

(count:307 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:1352911-1352961	ProgFib	skin:	n/a
2	chr12:1352875-1352925	SAEC	small airway:	n/a
3	chr12:1352911-1352961	ProgFib	skin:	n/a
4	chr12:1352875-1352925	SAEC	small airway:	n/a
5	chr12:1327264-1327314	HCM	heart:	n/a
6	chr12:1327264-1327314	Jurkat	blood:	n/a
7	chr12:1352875-1352925	PFSK-1	brain:	n/a
8	chr12:1351149-1351199	HRPEpiC	eye:	n/a
9	chr12:1327264-1327314	HCPEpiC	choroid plexus:	n/a
10	chr12:1327264-1327314	LNCaP	prostate:	n/a
11	chr12:1327264-1327314	BJ	skin:	n/a
12	chr12:1327264-1327314	NH-A	brain:	n/a
13	chr12:1352926-1352976	GM06990	blood:	n/a
14	chr12:1352875-1352925	NB4	blood:	n/a
15	chr12:1352875-1352925	HRCEpiC	kidney:	n/a
16	chr12:1352911-1352961	IMR90	lung:	fetal
17	chr12:1351149-1351199	GM12892	blood:	n/a
18	chr12:1352926-1352976	CMK	blood:	n/a
19	chr12:1352926-1352976	GM12891	blood:	n/a
20	chr12:1352926-1352976	HL-60	blood:	n/a
21	chr12:1327264-1327314	HRCEpiC	kidney:	n/a
22	chr12:1352926-1352976	A549	lung:	n/a
23	chr12:1351149-1351199	HCM	heart:	n/a
24	chr12:1352875-1352925	HNPCEpiC	eye:	n/a
25	chr12:1327264-1327314	AG09319	gingival:	n/a
26	chr12:1327264-1327314	SAEC	small airway:	n/a
27	chr12:1352926-1352976	SK-N-SH	brain:	n/a
28	chr12:1351149-1351199	SAEC	small airway:	n/a
29	chr12:1327264-1327314	A549	lung:	n/a
30	chr12:1327264-1327314	RPTEC	kidney:	n/a
31	chr12:1351149-1351199	HIPEpiC	eye:	n/a
32	chr12:1351149-1351199	AG09319	gingival:	n/a
33	chr12:1352926-1352976	Jurkat	blood:	n/a
34	chr12:1352875-1352925	AoSMC	blood vessel:	n/a
35	chr12:1352875-1352925	BJ	skin:	n/a
36	chr12:1352926-1352976	HCF	heart:	n/a
37	chr12:1327264-1327314	ECC-1	luminal epithelium:	n/a
38	chr12:1352926-1352976	AoSMC	blood vessel:	n/a
39	chr12:1352926-1352976	BJ	skin:	n/a
40	chr12:1352911-1352961	A549	lung:	n/a
41	chr12:1352926-1352976	HEK293	kidney:	embryo
42	chr12:1327264-1327314	GM12891	blood:	n/a
43	chr12:1352911-1352961	GM12878	blood:	n/a
44	chr12:1352875-1352925	GM12891	blood:	n/a
45	chr12:1327264-1327314	Caco-2	colon:	n/a
46	chr12:1351149-1351199	NHDF-neo	bronchial:	n/a
47	chr12:1327264-1327314	GM19239	blood:	n/a
48	chr12:1327264-1327314	SK-N-SH_RA	brain:	n/a
49	chr12:1352875-1352925	GM06990	blood:	n/a
50	chr12:1352911-1352961	SK-N-SH_RA	brain:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:1365739..1369161-chr12:1369581..1373916,5	K562	blood:
2	chr12:1323691..1326096-chr12:1328110..1330887,3	K562	blood:
3	chr12:1357106..1358885-chr12:1361378..1363992,2	MCF-7	breast:
4	chr12:1343229..1344970-chr12:1348640..1350399,2	K562	blood:
5	chr12:1285165..1287754-chr12:1303919..1306724,2	K562	blood:
6	chr12:1360740..1362305-chr12:1366547..1369167,2	K562	blood:
7	chr12:1350007..1350508-chr6:80690705..80691205,2	Hela-S3	cervix:
8	chr12:1343229..1344970-chr12:1348640..1350399,2	K562	blood:
9	chr12:1299686..1301198-chr12:1315494..1317236,2	K562	blood:
10	chr12:1335548..1337986-chr12:1340753..1343719,2	K562	blood:
11	chr12:1345086..1347706-chr12:1348677..1351190,2	K562	blood:
12	chr12:1322894..1325087-chr12:1546213..1548025,2	K562	blood:
13	chr12:1365739..1368747-chr12:1369581..1372843,3	K562	blood:
14	chr12:1316163..1318272-chr12:1321850..1324062,2	MCF-7	breast:
15	chr12:1316163..1318272-chr12:1321850..1324062,2	MCF-7	breast:
16	chr12:1345086..1347706-chr12:1348677..1351190,2	K562	blood:
17	chr12:1357106..1358885-chr12:1361378..1363992,2	MCF-7	breast:
18	chr12:1360740..1362305-chr12:1366547..1369167,2	K562	blood:
19	chr12:1335548..1337986-chr12:1340753..1343719,2	K562	blood:
20	chr12:1323691..1326096-chr12:1328110..1330887,3	K562	blood:

No data

Variant related genes	Relation type
ERC1	TF binding region
ERC1	CpG island
ENSG00000082805	chromatin interactions

Extended variants
information (count: 2630 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:2630 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs569673679	chr12:1305370-1305371	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs183309833	chr12:1305379-1305380	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs541133295	chr12:1305431-1305432	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs147332721	chr12:1305462-1305463	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs558781459	chr12:1305480-1305481	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs577238610	chr12:1305528-1305529	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs16928273	chr12:1305542-1305543	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs528627839	chr12:1305571-1305572	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs7301231	chr12:1305592-1305593	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs574393117	chr12:1305616-1305617	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs142573969	chr12:1305664-1305665	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs368116412	chr12:1305698-1305699	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs372300671	chr12:1305709-1305710	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs186190984	chr12:1305720-1305721	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs563050985	chr12:1305721-1305722	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs574993854	chr12:1305762-1305763	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs190616513	chr12:1305763-1305764	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs9943709	chr12:1305777-1305778	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs371117235	chr12:1305785-1305786	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs548091884	chr12:1305798-1305799	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs559749445	chr12:1305821-1305822	Strong transcription Enhancers Genic enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs530117768	chr12:1305822-1305823	Strong transcription Enhancers Genic enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs548595085	chr12:1305963-1305964	Strong transcription Enhancers Genic enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs570208981	chr12:1305966-1305967	Strong transcription Enhancers Genic enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs144748398	chr12:1305973-1305974	Strong transcription Enhancers Genic enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs375141672	chr12:1305994-1305995	Strong transcription Enhancers Genic enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs543962575	chr12:1305997-1305998	Strong transcription Enhancers Genic enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs146685159	chr12:1305998-1305999	Strong transcription Enhancers Genic enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs199928314	chr12:1306001-1306002	Strong transcription Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs151087402	chr12:1306002-1306003	Strong transcription Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs373521450	chr12:1306003-1306004	Strong transcription Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs369394950	chr12:1306004-1306005	Strong transcription Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs537519860	chr12:1306006-1306007	Strong transcription Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs200729487	chr12:1306025-1306026	Strong transcription Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs552436186	chr12:1306029-1306030	Strong transcription Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs570638737	chr12:1306034-1306035	Strong transcription Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs76071513	chr12:1306043-1306044	Strong transcription Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs200123069	chr12:1306048-1306049	Strong transcription Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs141802047	chr12:1306052-1306053	Strong transcription Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs112575014	chr12:1306056-1306057	Strong transcription Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs534487600	chr12:1306062-1306063	Strong transcription Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs111722160	chr12:1306064-1306065	Strong transcription Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs55948839	chr12:1306140-1306141	Strong transcription Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs11061661	chr12:1306142-1306143	Strong transcription Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs71435023	chr12:1306144-1306145	Strong transcription Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs143122459	chr12:1306154-1306155	Strong transcription Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs537115154	chr12:1306156-1306157	Strong transcription Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs71055139	chr12:1306179-1306180	Strong transcription Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs182811284	chr12:1306239-1306240	Strong transcription Enhancers Weak transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs112837574	chr12:1306255-1306256	Strong transcription Enhancers Weak transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Glaucoma	21310917	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Squamous cell cancer	19607727	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Mental retardation	17847001	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ovarian cancer	20844748	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Breast cancer	22032731	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	21965145	CNVD
Acute myeloid leukemia	16864856	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Disorders of sex development	21048976	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Prostate cancer	19156837	CNVD
Emphysema	19352772	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	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
Testicular germ cell tumor	18059402	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21509527	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Ovarian cancer	21720365	CNVD
Myelodysplastic syndrome	21251322	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Cancer	17440070	CNVD
Autism	22495311	CNVD
Pancreatic cancer	17952125	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
small cell lung cancer	20016488	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1447 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:1237400-1313800	Weak transcription	Small Intestine	intestine
2	chr12:1241200-1306400	Weak transcription	Dnd41	blood
3	chr12:1241200-1307200	Weak transcription	Duodenum Mucosa	Duodenum
4	chr12:1241400-1307800	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr12:1241800-1326600	Weak transcription	Pancreas	Pancrea
6	chr12:1263200-1306600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
7	chr12:1263400-1305800	Weak transcription	Thymus	Thymus
8	chr12:1268800-1313600	Weak transcription	Ovary	ovary
9	chr12:1276600-1305600	Weak transcription	Fetal Brain Female	brain
10	chr12:1277600-1305600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr12:1278600-1306000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr12:1281200-1313600	Weak transcription	Fetal Kidney	kidney
13	chr12:1282200-1313800	Weak transcription	Hela-S3	cervix
14	chr12:1283200-1313600	Weak transcription	Aorta	Aorta
15	chr12:1283400-1308000	Weak transcription	Esophagus	oesophagus
16	chr12:1283400-1309600	Weak transcription	Gastric	stomach
17	chr12:1283400-1312600	Weak transcription	Brain Germinal Matrix	brain
18	chr12:1283400-1313600	Weak transcription	Right Ventricle	heart
19	chr12:1283400-1313600	Weak transcription	Skeletal Muscle Male	skeletal muscle
20	chr12:1283600-1313000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
21	chr12:1283800-1313600	Weak transcription	Brain Substantia Nigra	brain
22	chr12:1283800-1315200	Weak transcription	HSMMtube	muscle
23	chr12:1284000-1312600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
24	chr12:1284000-1313800	Weak transcription	Brain Angular Gyrus	brain
25	chr12:1286000-1313600	Weak transcription	Psoas Muscle	Psoas
26	chr12:1287200-1312600	Weak transcription	Spleen	Spleen
27	chr12:1290200-1306600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr12:1290800-1305400	Weak transcription	H1 Cell Line	embryonic stem cell
29	chr12:1293000-1306600	Weak transcription	A549	lung
30	chr12:1293200-1305400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr12:1294400-1305600	Weak transcription	Fetal Intestine Small	intestine
32	chr12:1294400-1313600	Weak transcription	Duodenum Smooth Muscle	Duodenum
33	chr12:1294600-1306400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr12:1294600-1311600	Weak transcription	Left Ventricle	heart
35	chr12:1294800-1306400	Weak transcription	NH-A	brain
36	chr12:1295800-1307400	Weak transcription	HepG2	liver
37	chr12:1296000-1306400	Weak transcription	GM12878-XiMat	blood
38	chr12:1296400-1306200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr12:1296800-1305600	Weak transcription	Fetal Stomach	stomach
40	chr12:1297200-1305800	Weak transcription	Placenta Amnion	Placenta Amnion
41	chr12:1297400-1312600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr12:1297600-1312400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
43	chr12:1298200-1307400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
44	chr12:1298600-1305800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr12:1298600-1306600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
46	chr12:1299200-1307800	Weak transcription	Lung	lung
47	chr12:1299200-1313600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
48	chr12:1299400-1306600	Weak transcription	Fetal Muscle Leg	muscle
49	chr12:1299400-1313800	Weak transcription	Skeletal Muscle Female	skeletal muscle
50	chr12:1299800-1306600	Weak transcription	NHLF	lung

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