Variant report

Variant	nsv1048678
Chromosome Location	chr12:8520544-8584660
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	BACH1	chr12:8549275-8549403	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr12:8529405-8529600	GM12878	blood:	n/a	n/a
3	BATF	chr12:8572227-8572466	GM12878	blood:	n/a	n/a
4	BCL11A	chr12:8529324-8529698	GM12878	blood:	n/a	n/a
5	BCL11A	chr12:8529379-8529680	GM12878	blood:	n/a	n/a
6	BHLHE40	chr12:8549365-8549435	GM12878	blood:	n/a	n/a
7	BHLHE40	chr12:8543218-8543226	GM12878	blood:	n/a	n/a
8	CEBPB	chr12:8550591-8550718	IMR90	lung:	n/a	chr12:8550656-8550665 chr12:8550654-8550665 chr12:8550654-8550667
9	CEBPB	chr12:8550579-8550720	HepG2	liver:	n/a	chr12:8550656-8550665 chr12:8550654-8550665 chr12:8550654-8550667
10	CHD2	chr12:8543173-8543243	GM12878	blood:	n/a	n/a
11	CTCF	chr12:8530922-8531009	MCF-7	breast:	n/a	n/a
12	CTCF	chr12:8543005-8543439	K562	blood:	n/a	n/a
13	CTCF	chr12:8549360-8549510	NHLF	lung:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
14	CTCF	chr12:8523680-8523830	HEK293	kidney:	n/a	n/a
15	CTCF	chr12:8549360-8549510	HMEC	breast:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
16	CTCF	chr12:8526540-8526580	GM20000	blood:	n/a	n/a
17	CTCF	chr12:8549380-8549530	HUVEC	blood vessel:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
18	CTCF	chr12:8572221-8572419	K562	blood:	n/a	n/a
19	CTCF	chr12:8543260-8543410	AG10803	skin:	n/a	n/a
20	CTCF	chr12:8543180-8543330	HEEpiC	esophagus:	n/a	n/a
21	CTCF	chr12:8543220-8543370	GM12867	blood:	n/a	n/a
22	CTCF	chr12:8543300-8543450	A549	lung:	n/a	n/a
23	CTCF	chr12:8542957-8543462	A549	lung:	n/a	n/a
24	CTCF	chr12:8526440-8526590	BJ	skin:	n/a	n/a
25	CTCF	chr12:8526460-8526610	GM12871	blood:	n/a	n/a
26	CTCF	chr12:8549676-8549794	GM10266	blood:	n/a	n/a
27	CTCF	chr12:8526480-8526630	GM12872	blood:	n/a	n/a
28	CTCF	chr12:8549520-8549670	WI-38	lung:	n/a	n/a
29	CTCF	chr12:8549380-8549530	WI-38	lung:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
30	CTCF	chr12:8526440-8526590	AG09319	gingival:	n/a	n/a
31	CTCF	chr12:8526445-8526589	SK-N-SH_RA	brain:	n/a	n/a
32	CTCF	chr12:8549360-8549510	HAc	cerebellar:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
33	CTCF	chr12:8526460-8526610	GM12864	blood:	n/a	n/a
34	CTCF	chr12:8543107-8543340	HepG2	liver:	n/a	n/a
35	CTCF	chr12:8549265-8549565	HepG2	liver:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
36	CTCF	chr12:8543112-8543340	HepG2	liver:	n/a	n/a
37	CTCF	chr12:8543220-8543370	HCFaa	heart:	n/a	n/a
38	CTCF	chr12:8549292-8549582	K562	blood:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
39	CTCF	chr12:8526460-8526610	HEK293	kidney:	n/a	n/a
40	CTCF	chr12:8549267-8549610	GM12891	blood:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
41	CTCF	chr12:8543200-8543350	WI-38	lung:	n/a	n/a
42	CTCF	chr12:8549460-8549610	NHEK	skin:	n/a	n/a
43	CTCF	chr12:8572215-8572507	K562	blood:	n/a	n/a
44	CTCF	chr12:8543065-8543450	IMR90	lung:	n/a	n/a
45	CTCF	chr12:8549340-8549490	GM12870	blood:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
46	CTCF	chr12:8526460-8526610	GM12867	blood:	n/a	n/a
47	CTCF	chr12:8526421-8526645	HCT-116	colon:	n/a	n/a
48	CTCF	chr12:8549228-8549561	HepG2	liver:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
49	CTCF	chr12:8549360-8549510	GM12870	blood:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
50	CTCF	chr12:8526460-8526610	AG09309	skin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:8546330-8546380	RPTEC	kidney:	n/a
2	chr12:8575533-8575583	NT2-D1	testis:	n/a
3	chr12:8571692-8571742	SAEC	small airway:	n/a
4	chr12:8546330-8546380	RPTEC	kidney:	n/a
5	chr12:8575533-8575583	NT2-D1	testis:	n/a
6	chr12:8571692-8571742	SAEC	small airway:	n/a
7	chr12:8549457-8549507	Hela-S3	cervix:	n/a
8	chr12:8575139-8575189	HRPEpiC	eye:	n/a
9	chr12:8544796-8544846	MCF10A-Er-Src	breast:	n/a
10	chr12:8559779-8559829	K562	blood:	n/a
11	chr12:8576728-8576778	HUVEC	blood vessel:	n/a
12	chr12:8549457-8549507	HCM	heart:	n/a
13	chr12:8544796-8544846	Hela-S3	cervix:	n/a
14	chr12:8541476-8541526	MCF10A-Er-Src	breast:	n/a
15	chr12:8559779-8559829	GM19239	blood:	n/a
16	chr12:8542524-8542574	U87	brain:	n/a
17	chr12:8562937-8562987	GM12892	blood:	n/a
18	chr12:8543333-8543383	MCF10A-Er-Src	breast:	n/a
19	chr12:8571692-8571742	GM19239	blood:	n/a
20	chr12:8551501-8551551	NB4	blood:	n/a
21	chr12:8548618-8548668	NT2-D1	testis:	n/a
22	chr12:8575691-8575741	NH-A	brain:	n/a
23	chr12:8570268-8570318	SK-N-SH	brain:	n/a
24	chr12:8548923-8548973	Hela-S3	cervix:	n/a
25	chr12:8548618-8548668	ECC-1	luminal epithelium:	n/a
26	chr12:8548618-8548668	HepG2	liver:	n/a
27	chr12:8543302-8543352	CMK	blood:	n/a
28	chr12:8575533-8575583	HIPEpiC	eye:	n/a
29	chr12:8542839-8542889	A549	lung:	n/a
30	chr12:8559779-8559829	T-47D	breast:	n/a
31	chr12:8571692-8571742	H1-hESC	embryonic stem cell:	embryo
32	chr12:8546330-8546380	AG10803	skin:	n/a
33	chr12:8557855-8557905	Jurkat	blood:	n/a
34	chr12:8539716-8539766	SKMC	muscle:	n/a
35	chr12:8575139-8575189	T-47D	breast:	n/a
36	chr12:8575139-8575189	PrEC	prostate:	n/a
37	chr12:8559628-8559678	SK-N-SH_RA	brain:	n/a
38	chr12:8557855-8557905	PFSK-1	brain:	n/a
39	chr12:8549243-8549293	HCPEpiC	choroid plexus:	n/a
40	chr12:8575139-8575189	HRCEpiC	kidney:	n/a
41	chr12:8570210-8570260	PFSK-1	brain:	n/a
42	chr12:8542839-8542889	PFSK-1	brain:	n/a
43	chr12:8543333-8543383	AG04449	skin:	fetal
44	chr12:8571692-8571742	HCPEpiC	choroid plexus:	n/a
45	chr12:8549446-8549496	K562	blood:	n/a
46	chr12:8549457-8549507	T-47D	breast:	n/a
47	chr12:8543302-8543352	HUVEC	blood vessel:	n/a
48	chr12:8575533-8575583	SAEC	small airway:	n/a
49	chr12:8557855-8557905	HRE	kidney:	n/a
50	chr12:8548618-8548668	GM19239	blood:	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CLEC4E-2	chr12:8536701-8537017	ENSG00000226091.2
2	lnc-CLEC4E-2	chr12:8527013-8527109	ENSG00000226091.2
3	lnc-CLEC6A-2	chr12:8521578-8522151	ENSG00000256552.1
4	lnc-CLEC4E-2	chr12:8535440-8535671	ENSG00000226091.2
5	lnc-CLEC4E-2	chr12:8542866-8543107	NONHSAT026335
6	lnc-CLEC4E-2	chr12:8522809-8523025	ENSG00000226091.2
7	lnc-CLEC4E-2	chr12:8522809-8523025	ENSG00000226091.2
8	lnc-CLEC4E-2	chr12:8542866-8543348	NR_024420
9	lnc-CLEC4E-2	chr12:8538284-8538323	ENSG00000226091.2
10	lnc-CLEC4E-2	chr12:8539359-8540500	ENSG00000226091.2
11	lnc-CLEC4E-2	chr12:8542883-8542933	ENSG00000226091.2
12	lnc-CLEC4E-2	chr12:8542866-8543398	NONHSAT026332
13	lnc-CLEC4E-2	chr12:8542866-8543348	ENSG00000226091.2
14	lnc-CLEC4E-2	chr12:8549019-8549212	NONHSAT026335
15	lnc-CLEC4E-2	chr12:8538284-8538442	ENSG00000226091.2
16	lnc-CLEC4E-2	chr12:8543498-8543565	ENSG00000226091.2
17	lnc-CLEC4E-2	chr12:8542866-8543107	ENSG00000226091.2
18	lnc-CLEC4E-2	chr12:8523906-8524036	ENSG00000226091.2
19	lnc-CLEC4E-2	chr12:8522809-8523025	NONHSAT026332
20	lnc-CLEC4E-2	chr12:8549019-8549091	ENSG00000226091.2
21	lnc-CLEC4E-2	chr12:8537740-8537895	ENSG00000226091.2
22	lnc-CLEC4E-2	chr12:8522931-8523025	NONHSAT026335
23	lnc-CLEC6A-2	chr12:8521588-8521956	NONHSAT026334

Variant related genes	Relation type
LINC00937	TF binding region
OR7E148P	TF binding region
OR7E140P	TF binding region
ENSG00000256552	TF binding region
ENSG00000266218	TF binding region
ENSG00000256136	TF binding region
LINC00937	CpG island
OR7E148P	CpG island
OR7E140P	CpG island
ENSG00000256552	CpG island
ENSG00000266218	CpG island
ENSG00000256136	CpG island

Extended variants
information (count: 1382 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:1382 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs181863254	chr12:8520578-8520579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs9738812	chr12:8520621-8520622	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs186354759	chr12:8520653-8520654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs374316025	chr12:8520749-8520750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs192007311	chr12:8520760-8520761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs368612923	chr12:8520816-8520817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs183490711	chr12:8520857-8520858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs138063850	chr12:8520882-8520883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs375805196	chr12:8520905-8520906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs386760095	chr12:8520946-8520947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs9705980	chr12:8520947-8520948	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs371855474	chr12:8520968-8520969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs10770566	chr12:8520980-8520981	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs369227369	chr12:8520992-8520993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs9705982	chr12:8521001-8521002	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs191398990	chr12:8521002-8521003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs112606052	chr12:8521027-8521028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs35975891	chr12:8521033-8521034	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs55821468	chr12:8521076-8521077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs182675750	chr12:8521084-8521085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs397932767	chr12:8521091-8521092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs369641395	chr12:8521092-8521093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs10770567	chr12:8521104-8521105	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs139868997	chr12:8521256-8521257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs186607012	chr12:8521264-8521265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs554186272	chr12:8521272-8521273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs373524314	chr12:8521314-8521315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs377523454	chr12:8521324-8521325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs116500139	chr12:8521338-8521339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs191387244	chr12:8521368-8521369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs55757212	chr12:8521390-8521391	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs117602415	chr12:8521409-8521410	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs386760096	chr12:8521481-8521482	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs10841393	chr12:8521482-8521483	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs183690002	chr12:8521493-8521494	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs114431122	chr12:8521519-8521520	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs556112464	chr12:8521526-8521527	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs372273898	chr12:8521537-8521538	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs376382728	chr12:8521542-8521543	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs187570360	chr12:8521564-8521565	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs113127129	chr12:8521586-8521587	Strong transcription Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs185273526	chr12:8521599-8521600	Strong transcription Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs145704258	chr12:8521654-8521655	Strong transcription Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs12827982	chr12:8521677-8521678	Strong transcription Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs553892573	chr12:8521784-8521785	Strong transcription Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs370575593	chr12:8521867-8521868	Strong transcription Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
47	rs12828426	chr12:8521916-8521917	Strong transcription Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs545480412	chr12:8522050-8522051	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
49	rs368421153	chr12:8522100-8522101	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs148777297	chr12:8522115-8522116	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

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
early-passage human iPS cells	21368824	CNVD
Schizophrenia	20967226	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:485 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:8510200-8521400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr12:8519400-8530600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr12:8521400-8522000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr12:8522000-8523800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr12:8527200-8542600	Weak transcription	Right Atrium	heart
6	chr12:8527800-8530400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr12:8528000-8531400	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr12:8530400-8531600	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr12:8530400-8531600	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr12:8530600-8530800	Enhancers	H9 Cell Line	embryonic stem cell
11	chr12:8530600-8531000	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr12:8530600-8531000	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr12:8530600-8531800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr12:8530800-8531600	Enhancers	H1 Cell Line	embryonic stem cell
15	chr12:8530800-8531600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr12:8530800-8532400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr12:8531400-8531600	Enhancers	H9 Cell Line	embryonic stem cell
18	chr12:8531400-8531600	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr12:8531600-8533600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
20	chr12:8531600-8537400	Weak transcription	HUES6 Cell Line	embryonic stem cell
21	chr12:8531800-8532200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr12:8532200-8532400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr12:8532400-8533600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr12:8533600-8533800	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr12:8533600-8533800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr12:8533800-8534400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr12:8534400-8535000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr12:8535000-8541600	Weak transcription	Monocytes-CD14+_RO01746	blood
29	chr12:8535000-8542000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr12:8535400-8541600	Weak transcription	Primary neutrophils fromperipheralblood	blood
31	chr12:8537400-8537800	Strong transcription	HUES6 Cell Line	embryonic stem cell
32	chr12:8537400-8538200	Enhancers	HUVEC	blood vessel
33	chr12:8537800-8542000	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr12:8541200-8542000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
35	chr12:8541600-8542000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr12:8541800-8542000	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
37	chr12:8542000-8542200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
38	chr12:8542000-8542200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr12:8542000-8542200	Enhancers	H9 Cell Line	embryonic stem cell
40	chr12:8542000-8542200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
41	chr12:8542000-8542200	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
42	chr12:8542000-8542200	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
43	chr12:8542000-8542200	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
44	chr12:8542000-8542200	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
45	chr12:8542000-8542200	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr12:8542000-8542200	Flanking Bivalent TSS/Enh	Primary neutrophils fromperipheralblood	blood
47	chr12:8542000-8542200	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
48	chr12:8542000-8542200	Enhancers	Esophagus	oesophagus
49	chr12:8542000-8542200	Enhancers	Pancreas	Pancrea
50	chr12:8542000-8542200	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle

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