Variant report

Variant	esv17877
Chromosome Location	chr12:8544884-8601829
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	CEBPB	chr12:8550579-8550720	HepG2	liver:	n/a	chr12:8550656-8550665 chr12:8550654-8550665 chr12:8550654-8550667
5	CEBPB	chr12:8550591-8550718	IMR90	lung:	n/a	chr12:8550656-8550665 chr12:8550654-8550665 chr12:8550654-8550667
6	CTCF	chr12:8549275-8549592	Lung_OC	lung:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
7	CTCF	chr12:8549288-8549565	GM13977	blood:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
8	CTCF	chr12:8549281-8549616	GM19239	blood:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
9	CTCF	chr12:8575566-8575634	Lung_OC	lung:	n/a	n/a
10	CTCF	chr12:8549360-8549510	HBMEC	blood vessel:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
11	CTCF	chr12:8572330-8572427	Fibrobl	skin:	n/a	n/a
12	CTCF	chr12:8572320-8572470	HFF	foreskin:	n/a	n/a
13	CTCF	chr12:8549380-8549530	NHEK	skin:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
14	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
15	CTCF	chr12:8549400-8549550	SAEC	small airway:	n/a	chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
16	CTCF	chr12:8572661-8572667	GM19239	blood:	n/a	n/a
17	CTCF	chr12:8572203-8572435	A549	lung:	n/a	n/a
18	CTCF	chr12:8549185-8549759	K562	blood:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
19	CTCF	chr12:8549262-8549599	GM19240	blood:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
20	CTCF	chr12:8549300-8549588	ProgFib	skin:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
21	CTCF	chr12:8549239-8549593	A549	lung:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
22	CTCF	chr12:8549360-8549510	HCFaa	heart:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
23	CTCF	chr12:8549360-8549510	GM12865	blood:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
24	CTCF	chr12:8598717-8598801	Kidney_OC	kidney:	n/a	n/a
25	CTCF	chr12:8549720-8549870	GM12872	blood:	n/a	n/a
26	CTCF	chr12:8572198-8572492	GM19240	blood:	n/a	n/a
27	CTCF	chr12:8549289-8549572	Kidney_OC	kidney:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
28	CTCF	chr12:8549288-8549586	MCF-7	breast:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
29	CTCF	chr12:8549323-8549566	MCF-7	breast:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
30	CTCF	chr12:8596656-8596747	GM13976	blood:	n/a	n/a
31	CTCF	chr12:8549380-8549530	WERI-Rb-1	eye:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
32	CTCF	chr12:8549312-8549521	SK-N-SH_RA	brain:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
33	CTCF	chr12:8549283-8549582	GM10266	blood:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
34	CTCF	chr12:8572220-8572370	HRE	kidney:	n/a	n/a
35	CTCF	chr12:8549340-8549490	A549	lung:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
36	CTCF	chr12:8549189-8549641	K562	blood:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
37	CTCF	chr12:8572280-8572430	HRE	kidney:	n/a	n/a
38	CTCF	chr12:8549270-8549598	Gliobla	brain:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
39	CTCF	chr12:8549298-8549564	LNCaP	prostate:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
40	CTCF	chr12:8591390-8591459	GM10248	blood:	n/a	n/a
41	CTCF	chr12:8548920-8549070	GM12866	blood:	n/a	n/a
42	CTCF	chr12:8550840-8550892	Lung_OC	lung:	n/a	n/a
43	CTCF	chr12:8549292-8549582	K562	blood:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
44	CTCF	chr12:8549320-8549559	GM20000	blood:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
45	CTCF	chr12:8549297-8549581	GM13976	blood:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
46	CTCF	chr12:8549380-8549530	Caco-2	colon:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
47	CTCF	chr12:8549292-8549587	GM10248	blood:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
48	CTCF	chr12:8549340-8549490	GM12870	blood:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
49	CTCF	chr12:8549320-8549470	HepG2	liver:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
50	CTCF	chr12:8549265-8549565	HepG2	liver:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:8551501-8551551	Jurkat	blood:	n/a
2	chr12:8601421-8601471	CMK	blood:	n/a
3	chr12:8596201-8596251	GM12878	blood:	n/a
4	chr12:8571692-8571742	ProgFib	skin:	n/a
5	chr12:8599952-8600002	HCT-116	colon:	n/a
6	chr12:8551501-8551551	Jurkat	blood:	n/a
7	chr12:8601421-8601471	CMK	blood:	n/a
8	chr12:8596201-8596251	GM12878	blood:	n/a
9	chr12:8571692-8571742	ProgFib	skin:	n/a
10	chr12:8599952-8600002	HCT-116	colon:	n/a
11	chr12:8575533-8575583	ECC-1	luminal epithelium:	n/a
12	chr12:8557855-8557905	BJ	skin:	n/a
13	chr12:8596201-8596251	ECC-1	luminal epithelium:	n/a
14	chr12:8600287-8600337	HIPEpiC	eye:	n/a
15	chr12:8599671-8599721	GM19239	blood:	n/a
16	chr12:8570268-8570318	GM12891	blood:	n/a
17	chr12:8596320-8596370	HPAEpiC	pulmonary alveolar:	n/a
18	chr12:8559701-8559751	A549	lung:	n/a
19	chr12:8601160-8601210	HUVEC	blood vessel:	n/a
20	chr12:8551501-8551551	SK-N-MC	brain:	n/a
21	chr12:8548978-8549028	PrEC	prostate:	n/a
22	chr12:8599149-8599199	HMEC	breast:	n/a
23	chr12:8548618-8548668	AG04450	lung:	fetal
24	chr12:8600287-8600337	Jurkat	blood:	n/a
25	chr12:8548978-8549028	PFSK-1	brain:	n/a
26	chr12:8599404-8599454	ProgFib	skin:	n/a
27	chr12:8559628-8559678	HPAEpiC	pulmonary alveolar:	n/a
28	chr12:8600287-8600337	HMEC	breast:	n/a
29	chr12:8570210-8570260	LNCaP	prostate:	n/a
30	chr12:8557855-8557905	SKMC	muscle:	n/a
31	chr12:8597596-8597646	ovcar-3	ovarian:	n/a
32	chr12:8549243-8549293	HIPEpiC	eye:	n/a
33	chr12:8562937-8562987	PFSK-1	brain:	n/a
34	chr12:8594653-8594703	LNCaP	prostate:	n/a
35	chr12:8548923-8548973	NT2-D1	testis:	n/a
36	chr12:8597997-8598047	U87	brain:	n/a
37	chr12:8562937-8562987	NB4	blood:	n/a
38	chr12:8549511-8549561	NHDF-neo	bronchial:	n/a
39	chr12:8559628-8559678	U87	brain:	n/a
40	chr12:8596320-8596370	BE2_C	brain:	n/a
41	chr12:8551501-8551551	U87	brain:	n/a
42	chr12:8549243-8549293	T-47D	breast:	n/a
43	chr12:8559628-8559678	Hepatocyte	liver:	n/a
44	chr12:8596892-8596942	ECC-1	luminal epithelium:	n/a
45	chr12:8600287-8600337	NHBE	bronchial:	n/a
46	chr12:8549243-8549293	RPTEC	kidney:	n/a
47	chr12:8548978-8549028	Jurkat	blood:	n/a
48	chr12:8570210-8570260	SK-N-SH_RA	brain:	n/a
49	chr12:8570210-8570260	AoSMC	blood vessel:	n/a
50	chr12:8549511-8549561	AG09309	skin:	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CLEC4E-2	chr12:8549019-8549212	NONHSAT026335
2	lnc-CLEC4E-2	chr12:8549019-8549091	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
OR7E149P	TF binding region
OR7E140P	CpG island
ENSG00000266218	CpG island
LINC00937	CpG island
OR7E148P	CpG island
ENSG00000256136	CpG island
OR7E149P	CpG island

Extended variants
information (count: 1030 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:1030 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs74582604	chr12:8544919-8544920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs199557229	chr12:8544921-8544922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs188071450	chr12:8544929-8544930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs549678587	chr12:8544930-8544931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs142029711	chr12:8544945-8544946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs200942162	chr12:8544965-8544966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs201453964	chr12:8544966-8544967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs180701078	chr12:8544997-8544998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs371183162	chr12:8545028-8545029	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs11045058	chr12:8545060-8545061	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs79616631	chr12:8545078-8545079	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs11045059	chr12:8545097-8545098	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs145972604	chr12:8545104-8545105	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs551738178	chr12:8545112-8545113	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs113771152	chr12:8545128-8545129	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs200817565	chr12:8545155-8545156	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs187411055	chr12:8545158-8545159	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs571817734	chr12:8545187-8545188	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs192596078	chr12:8545219-8545220	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs139841726	chr12:8545232-8545233	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs11045060	chr12:8545256-8545257	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs184391826	chr12:8545261-8545262	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs369074138	chr12:8545295-8545296	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs112839498	chr12:8545305-8545306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs143266732	chr12:8545316-8545317	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs555860518	chr12:8545319-8545320	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs146677626	chr12:8545345-8545346	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs201311878	chr12:8545365-8545366	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs190454113	chr12:8545402-8545403	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs148399512	chr12:8545450-8545451	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs182039083	chr12:8545453-8545454	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs372358715	chr12:8545456-8545457	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs142722595	chr12:8545467-8545468	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs9300142	chr12:8545472-8545473	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs184309494	chr12:8545484-8545485	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs189062340	chr12:8545507-8545508	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs555625900	chr12:8545527-8545528	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs9300143	chr12:8545528-8545529	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs376018042	chr12:8545542-8545543	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs144365618	chr12:8545565-8545566	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs9300144	chr12:8545572-8545573	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs9300145	chr12:8545582-8545583	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs577783821	chr12:8545585-8545586	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs9300146	chr12:8545586-8545587	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
45	rs186391987	chr12:8545625-8545626	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs9300147	chr12:8545638-8545639	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs191240897	chr12:8545640-8545641	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs4357771	chr12:8545645-8545646	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
49	rs180710115	chr12:8545716-8545717	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs7953991	chr12:8545721-8545722	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:264 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:8542200-8548600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr12:8543000-8548400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr12:8543200-8545200	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr12:8543200-8545200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr12:8543200-8545200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr12:8543200-8545200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr12:8543200-8545400	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr12:8543200-8545400	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr12:8543200-8548400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr12:8543200-8548400	Weak transcription	Monocytes-CD14+_RO01746	blood
11	chr12:8543200-8548800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr12:8543200-8549000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr12:8543400-8549000	Weak transcription	Pancreas	Pancrea
14	chr12:8543600-8548000	Weak transcription	Primary neutrophils fromperipheralblood	blood
15	chr12:8543600-8548800	Weak transcription	Primary B cells from cord blood	blood
16	chr12:8545000-8546400	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr12:8545200-8545400	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr12:8545200-8545600	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr12:8545200-8545600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr12:8545200-8545800	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr12:8545200-8546000	Enhancers	H1 Cell Line	embryonic stem cell
22	chr12:8545400-8546000	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr12:8545400-8546400	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr12:8545400-8546400	Enhancers	H9 Cell Line	embryonic stem cell
25	chr12:8545600-8548400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
26	chr12:8545600-8548800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr12:8545800-8546200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
28	chr12:8546000-8546200	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr12:8546400-8546600	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr12:8546400-8548600	Weak transcription	H9 Cell Line	embryonic stem cell
31	chr12:8546400-8548800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr12:8548000-8548400	Enhancers	Primary neutrophils fromperipheralblood	blood
33	chr12:8548200-8549400	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
34	chr12:8548400-8548600	Active TSS	iPS-15b Cell Line	embryonic stem cell
35	chr12:8548400-8548600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
36	chr12:8548400-8548600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
37	chr12:8548400-8549000	Flanking Bivalent TSS/Enh	Primary monocytes fromperipheralblood	blood
38	chr12:8548400-8549000	Bivalent/Poised TSS	Colonic Mucosa	Colon
39	chr12:8548400-8549200	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
40	chr12:8548400-8549200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr12:8548400-8549400	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
42	chr12:8548400-8549400	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
43	chr12:8548400-8549400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
44	chr12:8548400-8549400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr12:8548400-8549400	Active TSS	Primary hematopoietic stem cells	blood
46	chr12:8548600-8548800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr12:8548600-8548800	Weak transcription	Brain Cingulate Gyrus	brain
48	chr12:8548600-8548800	Enhancers	Stomach Smooth Muscle	stomach
49	chr12:8548600-8548800	Active TSS	Monocytes-CD14+_RO01746	blood
50	chr12:8548600-8549000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell

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