Variant report

Variant	nsv1052610
Chromosome Location	chr12:8401834-8584660
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1378)
CpG islands
(count:2079)
Chromatin interactive
region (count:0)
LncRNA
region (count:38)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1378 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:8477801-8477893	K562	blood:	n/a	n/a
2	ATF1	chr12:8477835-8478036	K562	blood:	n/a	n/a
3	ATF3	chr12:8447388-8447568	HepG2	liver:	n/a	n/a
4	BACH1	chr12:8549275-8549403	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr12:8472837-8473049	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr12:8465483-8465876	GM12878	blood:	n/a	chr12:8465611-8465619
7	BATF	chr12:8495383-8495701	GM12878	blood:	n/a	n/a
8	BATF	chr12:8516441-8516876	GM12878	blood:	n/a	n/a
9	BATF	chr12:8486977-8487298	GM12878	blood:	n/a	n/a
10	BATF	chr12:8572227-8572466	GM12878	blood:	n/a	n/a
11	BATF	chr12:8468641-8469136	GM12878	blood:	n/a	n/a
12	BATF	chr12:8472176-8472570	GM12878	blood:	n/a	n/a
13	BATF	chr12:8529405-8529600	GM12878	blood:	n/a	n/a
14	BATF	chr12:8495427-8495677	GM12878	blood:	n/a	n/a
15	BATF	chr12:8449447-8449770	GM12878	blood:	n/a	n/a
16	BATF	chr12:8437659-8437860	GM12878	blood:	n/a	n/a
17	BATF	chr12:8465287-8465850	GM12878	blood:	n/a	chr12:8465611-8465619
18	BATF	chr12:8472172-8472739	GM12878	blood:	n/a	n/a
19	BATF	chr12:8468528-8469314	GM12878	blood:	n/a	n/a
20	BATF	chr12:8473299-8473507	GM12878	blood:	n/a	n/a
21	BCL11A	chr12:8449593-8449779	GM12878	blood:	n/a	n/a
22	BCL11A	chr12:8487014-8487435	GM12878	blood:	n/a	n/a
23	BCL11A	chr12:8449416-8449699	GM12878	blood:	n/a	n/a
24	BCL11A	chr12:8468528-8469107	GM12878	blood:	n/a	n/a
25	BCL11A	chr12:8516727-8516902	GM12878	blood:	n/a	n/a
26	BCL11A	chr12:8465466-8465929	GM12878	blood:	n/a	chr12:8465696-8465705
27	BCL11A	chr12:8495513-8495666	GM12878	blood:	n/a	chr12:8495622-8495631
28	BCL11A	chr12:8465300-8465536	GM12878	blood:	n/a	n/a
29	BCL11A	chr12:8529324-8529698	GM12878	blood:	n/a	n/a
30	BCL11A	chr12:8471330-8471501	GM12878	blood:	n/a	n/a
31	BCL11A	chr12:8437663-8437885	GM12878	blood:	n/a	n/a
32	BCL11A	chr12:8473294-8473468	GM12878	blood:	n/a	n/a
33	BCL11A	chr12:8464258-8464453	GM12878	blood:	n/a	n/a
34	BCL11A	chr12:8495462-8495734	GM12878	blood:	n/a	chr12:8495622-8495631
35	BCL11A	chr12:8468494-8469161	GM12878	blood:	n/a	n/a
36	BCL11A	chr12:8472450-8472705	GM12878	blood:	n/a	n/a
37	BCL11A	chr12:8472509-8472704	GM12878	blood:	n/a	n/a
38	BCL11A	chr12:8474618-8474785	GM12878	blood:	n/a	n/a
39	BCL11A	chr12:8529379-8529680	GM12878	blood:	n/a	n/a
40	BHLHE40	chr12:8543218-8543226	GM12878	blood:	n/a	n/a
41	BHLHE40	chr12:8468724-8468924	GM12878	blood:	n/a	n/a
42	BHLHE40	chr12:8549365-8549435	GM12878	blood:	n/a	n/a
43	CBX3	chr12:8466618-8466989	K562	blood:	n/a	chr12:8466977-8466988
44	CBX3	chr12:8481269-8481471	K562	blood:	n/a	n/a
45	CBX3	chr12:8481207-8481769	K562	blood:	n/a	n/a
46	CBX3	chr12:8477654-8478198	K562	blood:	n/a	n/a
47	CEBPB	chr12:8447478-8447503	IMR90	lung:	n/a	chr12:8447480-8447491
48	CEBPB	chr12:8447422-8447576	H1-hESC	embryonic stem cell:	n/a	chr12:8447480-8447491
49	CEBPB	chr12:8477125-8477527	K562	blood:	n/a	n/a
50	CEBPB	chr12:8447299-8447667	HepG2	liver:	n/a	chr12:8447480-8447491

(count:2079 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:8544796-8544846	AG09309	skin:	n/a
2	chr12:8549511-8549561	ECC-1	luminal epithelium:	n/a
3	chr12:8575139-8575189	HL-60	blood:	n/a
4	chr12:8546330-8546380	GM12878	blood:	n/a
5	chr12:8571692-8571742	ovcar-3	ovarian:	n/a
6	chr12:8544796-8544846	AG09309	skin:	n/a
7	chr12:8549511-8549561	ECC-1	luminal epithelium:	n/a
8	chr12:8575139-8575189	HL-60	blood:	n/a
9	chr12:8546330-8546380	GM12878	blood:	n/a
10	chr12:8571692-8571742	ovcar-3	ovarian:	n/a
11	chr12:8570210-8570260	T-47D	breast:	n/a
12	chr12:8557855-8557905	ovcar-3	ovarian:	n/a
13	chr12:8542756-8542806	HL-60	blood:	n/a
14	chr12:8549446-8549496	CMK	blood:	n/a
15	chr12:8576728-8576778	AG09309	skin:	n/a
16	chr12:8539716-8539766	GM12891	blood:	n/a
17	chr12:8542839-8542889	ProgFib	skin:	n/a
18	chr12:8557855-8557905	HMEC	breast:	n/a
19	chr12:8571692-8571742	HCF	heart:	n/a
20	chr12:8433230-8433280	CMK	blood:	n/a
21	chr12:8542756-8542806	T-47D	breast:	n/a
22	chr12:8548978-8549028	NB4	blood:	n/a
23	chr12:8559779-8559829	HUVEC	blood vessel:	n/a
24	chr12:8542756-8542806	HCPEpiC	choroid plexus:	n/a
25	chr12:8548978-8549028	BJ	skin:	n/a
26	chr12:8570268-8570318	NT2-D1	testis:	n/a
27	chr12:8543302-8543352	GM12892	blood:	n/a
28	chr12:8575533-8575583	HRPEpiC	eye:	n/a
29	chr12:8474082-8474132	HPAEpiC	pulmonary alveolar:	n/a
30	chr12:8546330-8546380	NT2-D1	testis:	n/a
31	chr12:8559779-8559829	AG09319	gingival:	n/a
32	chr12:8403616-8403666	H1-hESC	embryonic stem cell:	embryo
33	chr12:8542524-8542574	HMEC	breast:	n/a
34	chr12:8548618-8548668	HAEpiC	amniotic membrane:	n/a
35	chr12:8474082-8474132	GM19239	blood:	n/a
36	chr12:8571692-8571742	HNPCEpiC	eye:	n/a
37	chr12:8474082-8474132	Hela-S3	cervix:	n/a
38	chr12:8551501-8551551	NHBE	bronchial:	n/a
39	chr12:8570268-8570318	HAEpiC	amniotic membrane:	n/a
40	chr12:8549446-8549496	AG04449	skin:	fetal
41	chr12:8433230-8433280	ovcar-3	ovarian:	n/a
42	chr12:8541476-8541526	HIPEpiC	eye:	n/a
43	chr12:8548978-8549028	HRPEpiC	eye:	n/a
44	chr12:8562937-8562987	SK-N-SH_RA	brain:	n/a
45	chr12:8542524-8542574	HCPEpiC	choroid plexus:	n/a
46	chr12:8549457-8549507	NHDF-neo	bronchial:	n/a
47	chr12:8546330-8546380	HMEC	breast:	n/a
48	chr12:8549243-8549293	GM12878	blood:	n/a
49	chr12:8474082-8474132	HNPCEpiC	eye:	n/a
50	chr12:8548978-8549028	HCT-116	colon:	n/a

No data

(count:38 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CLEC4E-2	chr12:8542866-8543398	NONHSAT026332
2	lnc-CLEC4E-2	chr12:8522809-8523025	ENSG00000226091.2
3	lnc-CLEC4E-2	chr12:8527013-8527109	ENSG00000226091.2
4	lnc-ZNF705A-3	chr12:8430651-8430757	ENSG00000250937
5	lnc-ZNF705A-3	chr12:8404007-8404103	ENSG00000250937
6	lnc-CLEC4E-2	chr12:8509559-8509737	ENSG00000226091.2
7	lnc-CLEC4E-2	chr12:8538284-8538442	ENSG00000226091.2
8	lnc-CLEC4E-2	chr12:8509559-8509737	ENSG00000226091.2
9	lnc-ZNF705A-3	chr12:8447315-8447576	ENSG00000250937
10	lnc-CLEC4E-2	chr12:8523906-8524036	ENSG00000226091.2
11	lnc-CLEC4E-2	chr12:8542866-8543348	NR_024420
12	lnc-CLEC4E-2	chr12:8543498-8543565	ENSG00000226091.2
13	lnc-ZNF705A-3	chr12:8444364-8444483	ENSG00000250937
14	lnc-CLEC4E-2	chr12:8509708-8509737	NONHSAT026332
15	lnc-CLEC6A-2	chr12:8521588-8521956	NONHSAT026334
16	lnc-CLEC4E-2	chr12:8535440-8535671	ENSG00000226091.2
17	lnc-CLEC4E-2	chr12:8542866-8543107	NONHSAT026335
18	lnc-CLEC4E-2	chr12:8537740-8537895	ENSG00000226091.2
19	lnc-CLEC4E-2	chr12:8522809-8523025	ENSG00000226091.2
20	lnc-CLEC6A-2	chr12:8521578-8522151	ENSG00000256552.1
21	lnc-CLEC4E-2	chr12:8549019-8549212	NONHSAT026335
22	lnc-CLEC4E-2	chr12:8549019-8549091	ENSG00000226091.2
23	lnc-ZNF705A-3	chr12:8449260-8450140	ENSG00000250937
24	lnc-CLEC4E-2	chr12:8538284-8538323	ENSG00000226091.2
25	lnc-CLEC4E-2	chr12:8522809-8523025	NONHSAT026332
26	lnc-CLEC4E-2	chr12:8542866-8543107	ENSG00000226091.2
27	lnc-CLEC6A-1	chr12:8475457-8475704	ENSG00000256101
28	lnc-CLEC4E-2	chr12:8509559-8509737	ENSG00000226091.2
29	lnc-CLEC6A-2	chr12:8472977-8473022	ENSG00000256552.1
30	lnc-CLEC4E-2	chr12:8542866-8543348	ENSG00000226091.2
31	lnc-CLEC6A-1	chr12:8481993-8482210	ENSG00000256101
32	lnc-ZNF705A-3	chr12:8448589-8448704	ENSG00000250937
33	lnc-CLEC6A-1	chr12:8474549-8474684	ENSG00000256101
34	lnc-CLEC4E-2	chr12:8509560-8509737	NR_024420
35	lnc-CLEC4E-2	chr12:8522931-8523025	NONHSAT026335
36	lnc-CLEC4E-2	chr12:8539359-8540500	ENSG00000226091.2
37	lnc-CLEC4E-2	chr12:8536701-8537017	ENSG00000226091.2
38	lnc-CLEC4E-2	chr12:8542883-8542933	ENSG00000226091.2

No data

Variant related genes	Relation type
OR7E140P	TF binding region
ENPP7P5	TF binding region
ENSG00000256552	TF binding region
ENSG00000256101	TF binding region
ENSG00000266218	TF binding region
ENSG00000221104	TF binding region
LINC00937	TF binding region
ENSG00000221307	TF binding region
OR7E148P	TF binding region
ENSG00000256136	TF binding region
RPS3AP43	TF binding region
OR7E140P	CpG island
ENPP7P5	CpG island
ENSG00000256552	CpG island
ENSG00000256101	CpG island
ENSG00000266218	CpG island
ENSG00000221104	CpG island
LINC00937	CpG island
ENSG00000221307	CpG island
OR7E148P	CpG island
ENSG00000256136	CpG island
RPS3AP43	CpG island

Extended variants
information (count: 4825 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:4825 , 50 per page) page: 1 2 3 4 5 6 7 ... 97

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2953209	chr12:8401834-8401835	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs139032516	chr12:8401844-8401845	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs186274643	chr12:8401863-8401864	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs60654192	chr12:8401895-8401896	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs539099009	chr12:8401896-8401897	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs544724121	chr12:8402052-8402053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs552650820	chr12:8402063-8402064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs561242697	chr12:8402120-8402121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs530161347	chr12:8402133-8402134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs2953210	chr12:8402187-8402188	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs2965696	chr12:8402194-8402195	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs190357676	chr12:8402227-8402228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs2965695	chr12:8402252-8402253	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs182952251	chr12:8402256-8402257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs61922584	chr12:8402269-8402270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs61922585	chr12:8402275-8402276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs200313645	chr12:8402372-8402373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs75223136	chr12:8402373-8402374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs35610600	chr12:8402382-8402383	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs4883093	chr12:8402388-8402389	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs187464794	chr12:8402461-8402462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs10466780	chr12:8402499-8402500	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs79155253	chr12:8402530-8402531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs74794468	chr12:8402532-8402533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs78930892	chr12:8402540-8402541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs367684179	chr12:8402544-8402545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs550678271	chr12:8402580-8402581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs192647001	chr12:8402595-8402596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs12819495	chr12:8402605-8402606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs11044260	chr12:8402611-8402612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs80138172	chr12:8402663-8402664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs183428862	chr12:8402678-8402679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs10841069	chr12:8402713-8402714	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs187582867	chr12:8402718-8402719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs148885299	chr12:8402731-8402732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs192717906	chr12:8402732-8402733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs184750477	chr12:8402738-8402739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs76910539	chr12:8402788-8402789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs566384196	chr12:8402815-8402816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs189532278	chr12:8402834-8402835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs114977271	chr12:8402835-8402836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs558455335	chr12:8402844-8402845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs201324034	chr12:8402853-8402854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs10770388	chr12:8402856-8402857	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs10743283	chr12:8402867-8402868	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs113175053	chr12:8402919-8402920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs10770389	chr12:8402936-8402937	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs199993952	chr12:8403001-8403002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs201101449	chr12:8403039-8403040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs201861452	chr12:8403091-8403092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	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
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Epilepsy	21858020	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
craniofacial dysmorphism	21918468	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Alzheimer''s disease	17160897	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
early-passage human iPS cells	21368824	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Schizophrenia	20967226	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:689 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:8396800-8417000	Weak transcription	Ovary	ovary
2	chr12:8396800-8422800	Weak transcription	Pancreas	Pancrea
3	chr12:8397000-8413600	Weak transcription	Brain Anterior Caudate	brain
4	chr12:8397000-8414800	Weak transcription	Brain Angular Gyrus	brain
5	chr12:8399400-8412400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr12:8400000-8412400	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr12:8401200-8402000	Enhancers	Primary neutrophils fromperipheralblood	blood
8	chr12:8402600-8404600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr12:8403400-8408400	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr12:8404600-8404800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr12:8404800-8405000	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr12:8405000-8405400	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr12:8405400-8409400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr12:8405600-8412000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr12:8407600-8413800	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr12:8412000-8412600	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr12:8412400-8412800	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr12:8412400-8412800	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr12:8413200-8413800	Enhancers	Fetal Muscle Leg	muscle
20	chr12:8413200-8414800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr12:8413400-8414000	Enhancers	Fetal Muscle Trunk	muscle
22	chr12:8413600-8413800	Enhancers	Brain Anterior Caudate	brain
23	chr12:8413600-8414200	Enhancers	Right Atrium	heart
24	chr12:8413600-8414400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr12:8413600-8414400	Enhancers	Fetal Lung	lung
26	chr12:8413800-8414000	Active TSS	Brain Inferior Temporal Lobe	brain
27	chr12:8413800-8417600	Weak transcription	Brain Anterior Caudate	brain
28	chr12:8414000-8414200	Bivalent Enhancer	A549	lung
29	chr12:8414000-8414400	Enhancers	Primary monocytes fromperipheralblood	blood
30	chr12:8414400-8418600	Weak transcription	Primary monocytes fromperipheralblood	blood
31	chr12:8417000-8417400	Enhancers	Ovary	ovary
32	chr12:8417000-8418200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
33	chr12:8418600-8421600	Enhancers	Monocytes-CD14+_RO01746	blood
34	chr12:8418600-8423400	Enhancers	Primary monocytes fromperipheralblood	blood
35	chr12:8419600-8419800	Enhancers	Primary neutrophils fromperipheralblood	blood
36	chr12:8419800-8420800	Weak transcription	Primary neutrophils fromperipheralblood	blood
37	chr12:8420800-8422400	Enhancers	Primary neutrophils fromperipheralblood	blood
38	chr12:8421600-8422000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
39	chr12:8422000-8423400	Enhancers	Monocytes-CD14+_RO01746	blood
40	chr12:8430800-8431200	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr12:8431200-8432400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
42	chr12:8432400-8432600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr12:8432400-8432600	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr12:8432400-8432800	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr12:8432400-8432800	Enhancers	iPS-20b Cell Line	embryonic stem cell
46	chr12:8432600-8433000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
47	chr12:8432600-8433400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr12:8432800-8433200	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr12:8432800-8433400	Enhancers	H9 Cell Line	embryonic stem cell
50	chr12:8432800-8433800	Weak transcription	HUES48 Cell Line	embryonic stem cell

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