Variant report

Variant	esv1836738
Chromosome Location	chr12:1344141-1374396
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	CEBPB	chr12:1355759-1356204	HCT-116	colon:	n/a	n/a
2	CEBPB	chr12:1355879-1356175	K562	blood:	n/a	n/a
3	CEBPB	chr12:1355868-1356196	Hela-S3	cervix:	n/a	n/a
4	CTCF	chr12:1357080-1357230	A549	lung:	n/a	n/a
5	CUX1	chr12:1367912-1367961	GM12878	blood:	n/a	n/a
6	EBF1	chr12:1348914-1349234	GM12878	blood:	n/a	chr12:1349050-1349061
7	EBF1	chr12:1348941-1349156	GM12878	blood:	n/a	chr12:1349050-1349061
8	EP300	chr12:1361751-1362501	SK-N-SH_RA	brain:	n/a	n/a
9	EP300	chr12:1355858-1356194	K562	blood:	n/a	n/a
10	EP300	chr12:1359657-1360174	SK-N-SH_RA	brain:	n/a	n/a
11	EP300	chr12:1359059-1359336	SK-N-SH_RA	brain:	n/a	n/a
12	EP300	chr12:1359097-1359381	SK-N-SH_RA	brain:	n/a	n/a
13	EP300	chr12:1361764-1362445	SK-N-SH_RA	brain:	n/a	n/a
14	EP300	chr12:1355787-1356182	SK-N-SH_RA	brain:	n/a	n/a
15	EP300	chr12:1355645-1356354	SK-N-SH	brain:	n/a	n/a
16	EP300	chr12:1360535-1362598	SK-N-SH	brain:	n/a	chr12:1360535-1360549
17	EP300	chr12:1359768-1360152	SK-N-SH_RA	brain:	n/a	n/a
18	EP300	chr12:1355811-1356214	SK-N-SH_RA	brain:	n/a	n/a
19	FOS	chr12:1369014-1369217	MCF10A-Er-Src	breast:	n/a	n/a
20	GATA2	chr12:1362229-1362529	SH-SY5Y	brain:	n/a	n/a
21	GATA2	chr12:1359107-1359305	SH-SY5Y	brain:	n/a	n/a
22	GATA3	chr12:1359646-1360355	SK-N-SH	brain:	n/a	chr12:1360007-1360016 chr12:1360269-1360285 chr12:1359834-1359844 chr12:1359998-1360015
23	GATA3	chr12:1359847-1360076	SH-SY5Y	brain:	n/a	chr12:1360007-1360016 chr12:1359998-1360015
24	GATA3	chr12:1361736-1362586	SK-N-SH	brain:	n/a	n/a
25	GATA3	chr12:1361529-1361713	SH-SY5Y	brain:	n/a	n/a
26	GATA3	chr12:1361651-1362701	SK-N-SH	brain:	n/a	n/a
27	GATA3	chr12:1362212-1362512	SH-SY5Y	brain:	n/a	n/a
28	GATA3	chr12:1359588-1360344	SK-N-SH	brain:	n/a	chr12:1360007-1360016 chr12:1360269-1360285 chr12:1359834-1359844 chr12:1359998-1360015
29	IRF1	chr12:1358450-1358456	K562	blood:	n/a	n/a
30	JUND	chr12:1361853-1362505	SK-N-SH	brain:	n/a	n/a
31	JUND	chr12:1355940-1356140	K562	blood:	n/a	n/a
32	JUND	chr12:1344219-1344293	HepG2	liver:	n/a	chr12:1344262-1344273
33	MAFF	chr12:1365463-1365837	HepG2	liver:	n/a	chr12:1365637-1365655
34	MAFF	chr12:1365489-1365825	K562	blood:	n/a	chr12:1365637-1365655
35	MAFK	chr12:1371530-1371651	HepG2	liver:	n/a	n/a
36	MAFK	chr12:1365467-1365822	IMR90	lung:	n/a	chr12:1365638-1365652 chr12:1365642-1365658 chr12:1365639-1365655 chr12:1365639-1365654 chr12:1365640-1365660
37	MAFK	chr12:1365487-1365824	K562	blood:	n/a	chr12:1365638-1365652 chr12:1365642-1365658 chr12:1365639-1365655 chr12:1365639-1365654 chr12:1365640-1365660
38	MAFK	chr12:1365479-1365830	HepG2	liver:	n/a	chr12:1365638-1365652 chr12:1365642-1365658 chr12:1365639-1365655 chr12:1365639-1365654 chr12:1365640-1365660
39	MAFK	chr12:1365465-1365838	HepG2	liver:	n/a	chr12:1365638-1365652 chr12:1365642-1365658 chr12:1365639-1365655 chr12:1365639-1365654 chr12:1365640-1365660
40	MAFK	chr12:1365480-1365834	H1-hESC	embryonic stem cell:	n/a	chr12:1365638-1365652 chr12:1365642-1365658 chr12:1365639-1365655 chr12:1365639-1365654 chr12:1365640-1365660
41	MAFK	chr12:1365519-1365817	Hela-S3	cervix:	n/a	chr12:1365638-1365652 chr12:1365642-1365658 chr12:1365639-1365655 chr12:1365639-1365654 chr12:1365640-1365660
42	MXI1	chr12:1346808-1346819	H1-hESC	embryonic stem cell:	n/a	n/a
43	MXI1	chr12:1365976-1366048	GM12878	blood:	n/a	n/a
44	NFIC	chr12:1361860-1362435	SK-N-SH	brain:	n/a	n/a
45	PBX3	chr12:1359709-1360278	SK-N-SH	brain:	n/a	n/a
46	PBX3	chr12:1361876-1362533	SK-N-SH	brain:	n/a	n/a
47	PBX3	chr12:1359778-1360278	SK-N-SH	brain:	n/a	n/a
48	PBX3	chr12:1361773-1362460	SK-N-SH	brain:	n/a	n/a
49	POLR2A	chr12:1350306-1350344	MCF10A-Er-Src	breast:	n/a	n/a
50	POLR2A	chr12:1364512-1364559	ProgFib	skin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:1352911-1352961	NH-A	brain:	n/a
2	chr12:1352911-1352961	NH-A	brain:	n/a
3	chr12:1352926-1352976	HNPCEpiC	eye:	n/a
4	chr12:1351149-1351199	Hela-S3	cervix:	n/a
5	chr12:1352911-1352961	U87	brain:	n/a
6	chr12:1351149-1351199	SK-N-SH_RA	brain:	n/a
7	chr12:1351149-1351199	PANC-1	pancreas:	n/a
8	chr12:1352911-1352961	AG04449	skin:	fetal
9	chr12:1352911-1352961	H1-hESC	embryonic stem cell:	embryo
10	chr12:1352911-1352961	AG09309	skin:	n/a
11	chr12:1351149-1351199	HEEpiC	esophagus:	n/a
12	chr12:1352911-1352961	HPAEpiC	pulmonary alveolar:	n/a
13	chr12:1352911-1352961	NT2-D1	testis:	n/a
14	chr12:1352911-1352961	NHBE	bronchial:	n/a
15	chr12:1352911-1352961	HRCEpiC	kidney:	n/a
16	chr12:1352911-1352961	HCM	heart:	n/a
17	chr12:1352926-1352976	K562	blood:	n/a
18	chr12:1352926-1352976	HRPEpiC	eye:	n/a
19	chr12:1352875-1352925	U87	brain:	n/a
20	chr12:1352875-1352925	HMEC	breast:	n/a
21	chr12:1351149-1351199	HMEC	breast:	n/a
22	chr12:1351149-1351199	MCF-7	breast:	n/a
23	chr12:1351149-1351199	NB4	blood:	n/a
24	chr12:1352911-1352961	HNPCEpiC	eye:	n/a
25	chr12:1352875-1352925	Hela-S3	cervix:	n/a
26	chr12:1352875-1352925	BE2_C	brain:	n/a
27	chr12:1351149-1351199	AG09319	gingival:	n/a
28	chr12:1351149-1351199	HAEpiC	amniotic membrane:	n/a
29	chr12:1352926-1352976	HCM	heart:	n/a
30	chr12:1352911-1352961	HCT-116	colon:	n/a
31	chr12:1352911-1352961	LNCaP	prostate:	n/a
32	chr12:1352926-1352976	HEK293	kidney:	embryo
33	chr12:1352875-1352925	Jurkat	blood:	n/a
34	chr12:1352926-1352976	T-47D	breast:	n/a
35	chr12:1351149-1351199	PFSK-1	brain:	n/a
36	chr12:1352926-1352976	SK-N-SH_RA	brain:	n/a
37	chr12:1352875-1352925	GM06990	blood:	n/a
38	chr12:1352911-1352961	AoSMC	blood vessel:	n/a
39	chr12:1352926-1352976	Hela-S3	cervix:	n/a
40	chr12:1351149-1351199	HL-60	blood:	n/a
41	chr12:1351149-1351199	HCT-116	colon:	n/a
42	chr12:1352911-1352961	HepG2	liver:	n/a
43	chr12:1352926-1352976	HCT-116	colon:	n/a
44	chr12:1351149-1351199	GM12891	blood:	n/a
45	chr12:1352926-1352976	GM12878	blood:	n/a
46	chr12:1352875-1352925	A549	lung:	n/a
47	chr12:1352875-1352925	HCM	heart:	n/a
48	chr12:1352875-1352925	LNCaP	prostate:	n/a
49	chr12:1351149-1351199	AG10803	skin:	n/a
50	chr12:1352926-1352976	HCPEpiC	choroid plexus:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:1365739..1369161-chr12:1369581..1373916,5	K562	blood:
2	chr12:1343229..1344970-chr12:1348640..1350399,2	K562	blood:
3	chr12:1350007..1350508-chr6:80690705..80691205,2	Hela-S3	cervix:
4	chr12:1345086..1347706-chr12:1348677..1351190,2	K562	blood:
5	chr12:1343229..1344970-chr12:1348640..1350399,2	K562	blood:
6	chr12:1357106..1358885-chr12:1361378..1363992,2	MCF-7	breast:
7	chr12:1345086..1347706-chr12:1348677..1351190,2	K562	blood:
8	chr12:1365739..1368747-chr12:1369581..1372843,3	K562	blood:
9	chr12:1360740..1362305-chr12:1366547..1369167,2	K562	blood:
10	chr12:1360740..1362305-chr12:1366547..1369167,2	K562	blood:
11	chr12:1357106..1358885-chr12:1361378..1363992,2	MCF-7	breast:

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

Extended variants
information (count: 1266 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:1266 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12423086	chr12:1344141-1344142	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs35939871	chr12:1344146-1344147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs558872645	chr12:1344181-1344182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs180882415	chr12:1344187-1344188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs373031324	chr12:1344229-1344230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs547966977	chr12:1344230-1344231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs183675306	chr12:1344251-1344252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs538032356	chr12:1344254-1344255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs114221453	chr12:1344261-1344262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs571862609	chr12:1344283-1344284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs539310974	chr12:1344295-1344296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs564480982	chr12:1344304-1344305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs531774199	chr12:1344341-1344342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs12425793	chr12:1344359-1344360	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs189526523	chr12:1344368-1344369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs181877753	chr12:1344372-1344373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs186197528	chr12:1344374-1344375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs189980737	chr12:1344448-1344449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs543239596	chr12:1344451-1344452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs562014010	chr12:1344473-1344474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs34350531	chr12:1344522-1344523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs558688316	chr12:1344544-1344545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs112327298	chr12:1344551-1344552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs540885107	chr12:1344582-1344583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs558962808	chr12:1344591-1344592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs529636653	chr12:1344609-1344610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs74059707	chr12:1344628-1344629	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs75799865	chr12:1344647-1344648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs530594120	chr12:1344668-1344669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs181572161	chr12:1344720-1344721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs186383327	chr12:1344730-1344731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs146750224	chr12:1344744-1344745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs548101319	chr12:1344771-1344772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs566128014	chr12:1344782-1344783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs148888903	chr12:1344790-1344791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs143545300	chr12:1344818-1344819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs150973265	chr12:1344839-1344840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs140778619	chr12:1344948-1344949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs558479588	chr12:1344990-1344991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs576616501	chr12:1345035-1345036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs540973003	chr12:1345054-1345055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs145839597	chr12:1345058-1345059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs574129308	chr12:1345064-1345065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs541475199	chr12:1345090-1345091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs146019529	chr12:1345182-1345183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs191239978	chr12:1345206-1345207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs182279944	chr12:1345231-1345232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs545843182	chr12:1345268-1345269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs145732175	chr12:1345293-1345294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs369202275	chr12:1345294-1345295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
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

Chromatin state (count:483 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:1314600-1346200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr12:1315000-1345800	Weak transcription	Primary hematopoietic stem cells	blood
3	chr12:1315400-1345800	Weak transcription	Primary T cells from cord blood	blood
4	chr12:1316800-1366200	Weak transcription	Primary B cells from cord blood	blood
5	chr12:1326200-1346800	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr12:1327200-1346000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr12:1327200-1346000	Weak transcription	NHDF-Ad	bronchial
8	chr12:1327200-1391200	Weak transcription	Aorta	Aorta
9	chr12:1327400-1345800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr12:1327400-1346000	Weak transcription	Primary B cells from peripheral blood	blood
11	chr12:1327600-1345800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr12:1327600-1345800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr12:1327600-1346200	Weak transcription	HMEC	breast
14	chr12:1327600-1352400	Weak transcription	HSMM	muscle
15	chr12:1327600-1354200	Weak transcription	Osteobl	bone
16	chr12:1327800-1348400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr12:1328000-1346000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr12:1328000-1359200	Weak transcription	HUVEC	blood vessel
19	chr12:1328600-1346000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr12:1329200-1345800	Weak transcription	Left Ventricle	heart
21	chr12:1329200-1366200	Weak transcription	Lung	lung
22	chr12:1329800-1346000	Weak transcription	Fetal Brain Female	brain
23	chr12:1330200-1346600	Weak transcription	Muscle Satellite Cultured Cells	--
24	chr12:1330200-1348200	Weak transcription	Fetal Muscle Trunk	muscle
25	chr12:1330200-1348200	Weak transcription	Fetal Stomach	stomach
26	chr12:1330200-1353800	Weak transcription	Pancreas	Pancrea
27	chr12:1330200-1358800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr12:1330200-1390600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr12:1330200-1391400	Weak transcription	Fetal Muscle Leg	muscle
30	chr12:1330400-1372200	Weak transcription	Stomach Smooth Muscle	stomach
31	chr12:1330400-1373200	Weak transcription	Hela-S3	cervix
32	chr12:1330600-1346200	Weak transcription	Colon Smooth Muscle	Colon
33	chr12:1333000-1346400	Weak transcription	Primary T helper cells PMA-I stimulated	--
34	chr12:1334200-1425000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr12:1334800-1346000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr12:1335800-1352600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
37	chr12:1336000-1360400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
38	chr12:1336600-1345800	Weak transcription	Monocytes-CD14+_RO01746	blood
39	chr12:1336800-1346200	Weak transcription	Primary monocytes fromperipheralblood	blood
40	chr12:1337800-1347800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
41	chr12:1338400-1345800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
42	chr12:1339800-1358600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr12:1340400-1346000	Weak transcription	Brain Anterior Caudate	brain
44	chr12:1340800-1345800	Weak transcription	Sigmoid Colon	Sigmoid Colon
45	chr12:1341400-1348200	Weak transcription	Ovary	ovary
46	chr12:1341400-1373000	Weak transcription	Fetal Intestine Small	intestine
47	chr12:1341600-1346600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
48	chr12:1341800-1347800	Weak transcription	Dnd41	blood
49	chr12:1341800-1420000	Weak transcription	Esophagus	oesophagus
50	chr12:1342000-1345800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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