Variant report

Variant	nsv1054279
Chromosome Location	chr12:8536600-8584660
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	chr12:8572227-8572466	GM12878	blood:	n/a	n/a
3	BHLHE40	chr12:8549365-8549435	GM12878	blood:	n/a	n/a
4	BHLHE40	chr12:8543218-8543226	GM12878	blood:	n/a	n/a
5	CEBPB	chr12:8550591-8550718	IMR90	lung:	n/a	chr12:8550656-8550665 chr12:8550654-8550665 chr12:8550654-8550667
6	CEBPB	chr12:8550579-8550720	HepG2	liver:	n/a	chr12:8550656-8550665 chr12:8550654-8550665 chr12:8550654-8550667
7	CHD2	chr12:8543173-8543243	GM12878	blood:	n/a	n/a
8	CTCF	chr12:8549380-8549530	GM12873	blood:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
9	CTCF	chr12:8549400-8549550	GM12874	blood:	n/a	chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
10	CTCF	chr12:8543220-8543370	HepG2	liver:	n/a	n/a
11	CTCF	chr12:8549340-8549490	HFF-Myc	foreskin:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
12	CTCF	chr12:8549380-8549530	AG04450	lung:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
13	CTCF	chr12:8543220-8543370	GM06990	blood:	n/a	n/a
14	CTCF	chr12:8543220-8543370	HBMEC	blood vessel:	n/a	n/a
15	CTCF	chr12:8549360-8549510	GM12873	blood:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
16	CTCF	chr12:8549307-8549657	MCF-7	breast:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
17	CTCF	chr12:8548960-8549110	AG04449	skin:	n/a	n/a
18	CTCF	chr12:8543116-8543408	LNCaP	prostate:	n/a	n/a
19	CTCF	chr12:8543214-8543321	GM20000	blood:	n/a	n/a
20	CTCF	chr12:8549320-8549470	HepG2	liver:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
21	CTCF	chr12:8549267-8549610	GM12891	blood:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
22	CTCF	chr12:8549380-8549530	K562	blood:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
23	CTCF	chr12:8549340-8549490	GM12870	blood:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
24	CTCF	chr12:8549323-8549566	MCF-7	breast:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
25	CTCF	chr12:8549320-8549470	K562	blood:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
26	CTCF	chr12:8549400-8549550	GM12864	blood:	n/a	chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
27	CTCF	chr12:8550318-8550393	LNCaP	prostate:	n/a	n/a
28	CTCF	chr12:8549400-8549550	Caco-2	colon:	n/a	chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
29	CTCF	chr12:8549360-8549510	GM12871	blood:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
30	CTCF	chr12:8543112-8543379	Lung_OC	lung:	n/a	n/a
31	CTCF	chr12:8543132-8543401	GM13977	blood:	n/a	n/a
32	CTCF	chr12:8542980-8543130	NHLF	lung:	n/a	n/a
33	CTCF	chr12:8548980-8549648	SK-N-SH	brain:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
34	CTCF	chr12:8543220-8543370	HCPEpiC	choroid plexus:	n/a	n/a
35	CTCF	chr12:8549189-8549641	K562	blood:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
36	CTCF	chr12:8543240-8543390	GM12872	blood:	n/a	n/a
37	CTCF	chr12:8549300-8549529	T-47D	breast:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
38	CTCF	chr12:8549360-8549510	NHLF	lung:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
39	CTCF	chr12:8543106-8543433	GM19238	blood:	n/a	n/a
40	CTCF	chr12:8549400-8549550	HMF	breast:	n/a	chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
41	CTCF	chr12:8543240-8543390	MCF-7	breast:	n/a	n/a
42	CTCF	chr12:8549676-8549794	GM10266	blood:	n/a	n/a
43	CTCF	chr12:8543220-8543370	HCFaa	heart:	n/a	n/a
44	CTCF	chr12:8543135-8543421	Fibrobl	skin:	n/a	n/a
45	CTCF	chr12:8543200-8543350	HA-sp	spinal cord:	n/a	n/a
46	CTCF	chr12:8543200-8543350	HMEC	breast:	n/a	n/a
47	CTCF	chr12:8543220-8543370	GM12870	blood:	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	chr12:8549380-8549530	SK-N-SH_RA	brain:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
50	CTCF	chr12:8543240-8543390	HCM	heart:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:8575139-8575189	GM12891	blood:	n/a
2	chr12:8575139-8575189	GM12891	blood:	n/a
3	chr12:8557855-8557905	NT2-D1	testis:	n/a
4	chr12:8549243-8549293	HNPCEpiC	eye:	n/a
5	chr12:8543302-8543352	GM06990	blood:	n/a
6	chr12:8570268-8570318	HUVEC	blood vessel:	n/a
7	chr12:8557855-8557905	AG04450	lung:	fetal
8	chr12:8549446-8549496	HRPEpiC	eye:	n/a
9	chr12:8557855-8557905	AG04449	skin:	fetal
10	chr12:8575533-8575583	HCPEpiC	choroid plexus:	n/a
11	chr12:8539716-8539766	ProgFib	skin:	n/a
12	chr12:8562937-8562987	T-47D	breast:	n/a
13	chr12:8571692-8571742	NHDF-neo	bronchial:	n/a
14	chr12:8559779-8559829	NT2-D1	testis:	n/a
15	chr12:8559701-8559751	ProgFib	skin:	n/a
16	chr12:8549511-8549561	SKMC	muscle:	n/a
17	chr12:8575691-8575741	PANC-1	pancreas:	n/a
18	chr12:8559701-8559751	AG09319	gingival:	n/a
19	chr12:8559701-8559751	SK-N-SH	brain:	n/a
20	chr12:8548978-8549028	NH-A	brain:	n/a
21	chr12:8541476-8541526	Hepatocyte	liver:	n/a
22	chr12:8546330-8546380	T-47D	breast:	n/a
23	chr12:8541476-8541526	HCPEpiC	choroid plexus:	n/a
24	chr12:8548618-8548668	BJ	skin:	n/a
25	chr12:8549511-8549561	GM12878	blood:	n/a
26	chr12:8559628-8559678	HCPEpiC	choroid plexus:	n/a
27	chr12:8576728-8576778	GM12878	blood:	n/a
28	chr12:8548978-8549028	HMEC	breast:	n/a
29	chr12:8575139-8575189	HMEC	breast:	n/a
30	chr12:8559779-8559829	H1-hESC	embryonic stem cell:	embryo
31	chr12:8559779-8559829	GM12891	blood:	n/a
32	chr12:8541476-8541526	HEK293	kidney:	embryo
33	chr12:8546330-8546380	GM19239	blood:	n/a
34	chr12:8546330-8546380	A549	lung:	n/a
35	chr12:8543302-8543352	HRE	kidney:	n/a
36	chr12:8542524-8542574	GM06990	blood:	n/a
37	chr12:8557855-8557905	ovcar-3	ovarian:	n/a
38	chr12:8551501-8551551	PrEC	prostate:	n/a
39	chr12:8542839-8542889	GM12878	blood:	n/a
40	chr12:8541476-8541526	ProgFib	skin:	n/a
41	chr12:8575691-8575741	AG04450	lung:	fetal
42	chr12:8542756-8542806	HL-60	blood:	n/a
43	chr12:8548618-8548668	HEEpiC	esophagus:	n/a
44	chr12:8548978-8549028	HepG2	liver:	n/a
45	chr12:8559701-8559751	AG09309	skin:	n/a
46	chr12:8571374-8571424	HL-60	blood:	n/a
47	chr12:8575691-8575741	T-47D	breast:	n/a
48	chr12:8549243-8549293	HMEC	breast:	n/a
49	chr12:8542839-8542889	AG04450	lung:	fetal
50	chr12:8548618-8548668	AG09319	gingival:	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CLEC4E-2	chr12:8537740-8537895	ENSG00000226091.2
2	lnc-CLEC4E-2	chr12:8539359-8540500	ENSG00000226091.2
3	lnc-CLEC4E-2	chr12:8542866-8543348	ENSG00000226091.2
4	lnc-CLEC4E-2	chr12:8549019-8549212	NONHSAT026335
5	lnc-CLEC4E-2	chr12:8542866-8543348	NR_024420
6	lnc-CLEC4E-2	chr12:8542866-8543398	NONHSAT026332
7	lnc-CLEC4E-2	chr12:8542866-8543107	NONHSAT026335
8	lnc-CLEC4E-2	chr12:8542866-8543107	ENSG00000226091.2
9	lnc-CLEC4E-2	chr12:8536701-8537017	ENSG00000226091.2
10	lnc-CLEC4E-2	chr12:8542883-8542933	ENSG00000226091.2
11	lnc-CLEC4E-2	chr12:8543498-8543565	ENSG00000226091.2
12	lnc-CLEC4E-2	chr12:8538284-8538323	ENSG00000226091.2
13	lnc-CLEC4E-2	chr12:8549019-8549091	ENSG00000226091.2
14	lnc-CLEC4E-2	chr12:8538284-8538442	ENSG00000226091.2

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

Extended variants
information (count: 916 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9988949	chr12:8536678-8536679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs143589240	chr12:8536875-8536876	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
3	rs146800813	chr12:8536911-8536912	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
4	rs61920476	chr12:8536935-8536936	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
5	rs35419240	chr12:8536955-8536956	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
6	rs183530636	chr12:8536964-8536965	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
7	rs61920477	chr12:8536967-8536968	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
8	rs138374118	chr12:8537017-8537018	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
9	rs199813096	chr12:8537107-8537108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs200727669	chr12:8537120-8537121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs10770610	chr12:8537152-8537153	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs375619043	chr12:8537214-8537215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs368360783	chr12:8537268-8537269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs61920478	chr12:8537285-8537286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs370022994	chr12:8537375-8537376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs12826588	chr12:8537394-8537395	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs200828486	chr12:8537398-8537399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs368955163	chr12:8537504-8537505	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs577510697	chr12:8537507-8537508	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs149196431	chr12:8537535-8537536	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs546181049	chr12:8537629-8537630	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs368858677	chr12:8537640-8537641	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs147589587	chr12:8537751-8537752	Strong transcription Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
24	rs12367659	chr12:8537765-8537766	Strong transcription Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
25	rs145862241	chr12:8537798-8537799	Strong transcription Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
26	rs576723349	chr12:8537819-8537820	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
27	rs185340830	chr12:8537821-8537822	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
28	rs190148889	chr12:8537891-8537892	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
29	rs182060720	chr12:8537914-8537915	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs148203227	chr12:8537929-8537930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs560991805	chr12:8537930-8537931	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs375853785	chr12:8537936-8537937	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs201977848	chr12:8538005-8538006	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs111424084	chr12:8538016-8538017	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs116444100	chr12:8538030-8538031	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs140069704	chr12:8538046-8538047	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs150381861	chr12:8538076-8538077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs186808887	chr12:8538078-8538079	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs373631400	chr12:8538103-8538104	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs9737617	chr12:8538213-8538214	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs140480957	chr12:8538226-8538227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs34363881	chr12:8538240-8538241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs193078243	chr12:8538251-8538252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs113546417	chr12:8538319-8538320	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs9705683	chr12:8538497-8538498	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs374477823	chr12:8538523-8538524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs184178700	chr12:8538623-8538624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs562354334	chr12:8538652-8538653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs552197946	chr12:8538660-8538661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs188283811	chr12:8538715-8538716	Weak transcription	n/a	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
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:460 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:8527200-8542600	Weak transcription	Right Atrium	heart
2	chr12:8531600-8537400	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr12:8535000-8541600	Weak transcription	Monocytes-CD14+_RO01746	blood
4	chr12:8535000-8542000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr12:8535400-8541600	Weak transcription	Primary neutrophils fromperipheralblood	blood
6	chr12:8537400-8537800	Strong transcription	HUES6 Cell Line	embryonic stem cell
7	chr12:8537400-8538200	Enhancers	HUVEC	blood vessel
8	chr12:8537800-8542000	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr12:8541200-8542000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr12:8541600-8542000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr12:8541800-8542000	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
12	chr12:8542000-8542200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
13	chr12:8542000-8542200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr12:8542000-8542200	Enhancers	H9 Cell Line	embryonic stem cell
15	chr12:8542000-8542200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
16	chr12:8542000-8542200	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
17	chr12:8542000-8542200	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
18	chr12:8542000-8542200	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
19	chr12:8542000-8542200	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
20	chr12:8542000-8542200	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr12:8542000-8542200	Flanking Bivalent TSS/Enh	Primary neutrophils fromperipheralblood	blood
22	chr12:8542000-8542200	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
23	chr12:8542000-8542200	Enhancers	Esophagus	oesophagus
24	chr12:8542000-8542200	Enhancers	Pancreas	Pancrea
25	chr12:8542000-8542200	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
26	chr12:8542000-8542400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
27	chr12:8542000-8542400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr12:8542000-8542400	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr12:8542000-8542400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr12:8542000-8542400	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
31	chr12:8542000-8542600	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
32	chr12:8542000-8542600	Bivalent Enhancer	Primary hematopoietic stem cells	blood
33	chr12:8542000-8542600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr12:8542000-8542600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr12:8542000-8542600	Bivalent Enhancer	Adipose Nuclei	Adipose
36	chr12:8542000-8542600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
37	chr12:8542000-8543200	Active TSS	iPS-15b Cell Line	embryonic stem cell
38	chr12:8542000-8543200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr12:8542200-8542400	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr12:8542200-8542400	Bivalent/Poised TSS	Primary neutrophils fromperipheralblood	blood
41	chr12:8542200-8542600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr12:8542200-8542600	Weak transcription	Pancreas	Pancrea
43	chr12:8542200-8542800	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
44	chr12:8542200-8542800	Enhancers	Primary hematopoietic stem cells short term culture	blood
45	chr12:8542200-8543000	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
46	chr12:8542200-8543000	Enhancers	Spleen	Spleen
47	chr12:8542200-8543200	Active TSS	H9 Cell Line	embryonic stem cell
48	chr12:8542200-8543200	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
49	chr12:8542200-8543200	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
50	chr12:8542200-8548600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell

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