Variant report

Variant	nsv585
Chromosome Location	chr12:4514249-4559242
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	ATF2	chr12:4550662-4551109	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF3	chr12:4544736-4545063	GM12878	blood:	n/a	n/a
3	BHLHE40	chr12:4524274-4524639	K562	blood:	n/a	n/a
4	CEBPB	chr12:4526413-4526599	HepG2	liver:	n/a	chr12:4526513-4526524
5	CEBPB	chr12:4550863-4551038	H1-hESC	embryonic stem cell:	n/a	n/a
6	CHD2	chr12:4550768-4550991	H1-hESC	embryonic stem cell:	n/a	n/a
7	CHD2	chr12:4558990-4559009	H1-hESC	embryonic stem cell:	n/a	n/a
8	CREB1	chr12:4530802-4531004	A549	lung:	n/a	n/a
9	CTBP2	chr12:4550465-4551555	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr12:4530788-4530997	GM19238	blood:	n/a	chr12:4530843-4530856 chr12:4530842-4530863 chr12:4530841-4530857 chr12:4530840-4530858
11	CTCF	chr12:4530760-4530910	HUVEC	blood vessel:	n/a	chr12:4530843-4530856 chr12:4530842-4530863 chr12:4530841-4530857 chr12:4530840-4530858
12	CTCF	chr12:4530760-4530910	BE2_C	brain:	n/a	chr12:4530843-4530856 chr12:4530842-4530863 chr12:4530841-4530857 chr12:4530840-4530858
13	CTCF	chr12:4530714-4530982	K562	blood:	n/a	chr12:4530843-4530856 chr12:4530842-4530863 chr12:4530841-4530857 chr12:4530840-4530858
14	CTCF	chr12:4530800-4530950	BJ	skin:	n/a	chr12:4530843-4530856 chr12:4530842-4530863 chr12:4530841-4530857 chr12:4530840-4530858
15	CTCF	chr12:4530732-4530926	SK-N-SH_RA	brain:	n/a	chr12:4530843-4530856 chr12:4530842-4530863 chr12:4530841-4530857 chr12:4530840-4530858
16	CTCF	chr12:4530819-4530967	GM12891	blood:	n/a	chr12:4530843-4530856 chr12:4530842-4530863 chr12:4530841-4530857 chr12:4530840-4530858
17	CTCF	chr12:4530760-4530910	HepG2	liver:	n/a	chr12:4530843-4530856 chr12:4530842-4530863 chr12:4530841-4530857 chr12:4530840-4530858
18	CTCF	chr12:4550660-4550810	GM12871	blood:	n/a	n/a
19	CTCF	chr12:4550512-4550672	GM12892	blood:	n/a	n/a
20	CTCF	chr12:4530800-4530950	HCT-116	colon:	n/a	chr12:4530843-4530856 chr12:4530842-4530863 chr12:4530841-4530857 chr12:4530840-4530858
21	CTCF	chr12:4550500-4550650	NB4	blood:	n/a	n/a
22	CTCF	chr12:4529880-4530030	GM12871	blood:	n/a	n/a
23	CTCF	chr12:4530678-4530998	K562	blood:	n/a	chr12:4530843-4530856 chr12:4530842-4530863 chr12:4530841-4530857 chr12:4530840-4530858
24	CTCF	chr12:4530740-4530890	HEEpiC	esophagus:	n/a	chr12:4530843-4530856 chr12:4530842-4530863 chr12:4530841-4530857 chr12:4530840-4530858
25	CTCF	chr12:4530507-4530592	Spleen_OC	spleen:	n/a	n/a
26	CTCF	chr12:4530760-4530910	SK-N-SH_RA	brain:	n/a	chr12:4530843-4530856 chr12:4530842-4530863 chr12:4530841-4530857 chr12:4530840-4530858
27	CTCF	chr12:4550586-4550628	GM10266	blood:	n/a	n/a
28	CTCF	chr12:4530734-4530958	LNCaP	prostate:	n/a	chr12:4530843-4530856 chr12:4530842-4530863 chr12:4530841-4530857 chr12:4530840-4530858
29	CTCF	chr12:4530780-4530930	HMF	breast:	n/a	chr12:4530843-4530856 chr12:4530842-4530863 chr12:4530841-4530857 chr12:4530840-4530858
30	CTCF	chr12:4530760-4530910	WERI-Rb-1	eye:	n/a	chr12:4530843-4530856 chr12:4530842-4530863 chr12:4530841-4530857 chr12:4530840-4530858
31	CTCF	chr12:4534950-4534984	Spleen_OC	spleen:	n/a	n/a
32	CTCF	chr12:4530776-4530976	GM19239	blood:	n/a	chr12:4530843-4530856 chr12:4530842-4530863 chr12:4530841-4530857 chr12:4530840-4530858
33	CTCF	chr12:4550557-4550634	K562	blood:	n/a	n/a
34	CTCF	chr12:4530840-4530990	HMEC	breast:	n/a	chr12:4530843-4530856 chr12:4530842-4530863 chr12:4530841-4530857 chr12:4530840-4530858
35	CTCF	chr12:4530780-4530930	AoAF	blood vessel:	n/a	chr12:4530843-4530856 chr12:4530842-4530863 chr12:4530841-4530857 chr12:4530840-4530858
36	CTCF	chr12:4530780-4530930	GM12865	blood:	n/a	chr12:4530843-4530856 chr12:4530842-4530863 chr12:4530841-4530857 chr12:4530840-4530858
37	CTCF	chr12:4530729-4530953	Pancreas_OC	pancreas:	n/a	chr12:4530843-4530856 chr12:4530842-4530863 chr12:4530841-4530857 chr12:4530840-4530858
38	CTCF	chr12:4530687-4531018	MCF-7	breast:	n/a	chr12:4530843-4530856 chr12:4530842-4530863 chr12:4530841-4530857 chr12:4530840-4530858
39	CTCF	chr12:4530799-4531000	GM12892	blood:	n/a	chr12:4530843-4530856 chr12:4530842-4530863 chr12:4530841-4530857 chr12:4530840-4530858
40	CTCF	chr12:4530664-4531040	K562	blood:	n/a	chr12:4530843-4530856 chr12:4530842-4530863 chr12:4530841-4530857 chr12:4530840-4530858
41	CTCF	chr12:4530960-4531110	WI-38	lung:	n/a	n/a
42	CTCF	chr12:4530780-4530930	GM12874	blood:	n/a	chr12:4530843-4530856 chr12:4530842-4530863 chr12:4530841-4530857 chr12:4530840-4530858
43	CTCF	chr12:4530800-4530950	GM12864	blood:	n/a	chr12:4530843-4530856 chr12:4530842-4530863 chr12:4530841-4530857 chr12:4530840-4530858
44	CTCF	chr12:4530740-4530890	HBMEC	blood vessel:	n/a	chr12:4530843-4530856 chr12:4530842-4530863 chr12:4530841-4530857 chr12:4530840-4530858
45	CTCF	chr12:4559060-4559210	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr12:4530761-4530973	MCF-7	breast:	n/a	chr12:4530843-4530856 chr12:4530842-4530863 chr12:4530841-4530857 chr12:4530840-4530858
47	CTCF	chr12:4530603-4531089	HCT-116	colon:	n/a	chr12:4530843-4530856 chr12:4530842-4530863 chr12:4530841-4530857 chr12:4530840-4530858
48	CTCF	chr12:4530780-4530930	AG10803	skin:	n/a	chr12:4530843-4530856 chr12:4530842-4530863 chr12:4530841-4530857 chr12:4530840-4530858
49	CTCF	chr12:4543120-4543270	HBMEC	blood vessel:	n/a	n/a
50	CTCF	chr12:4530714-4530931	A549	lung:	n/a	chr12:4530843-4530856 chr12:4530842-4530863 chr12:4530841-4530857 chr12:4530840-4530858

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:4554480-4554530	PrEC	prostate:	n/a
2	chr12:4554480-4554530	PrEC	prostate:	n/a
3	chr12:4549503-4549553	HRPEpiC	eye:	n/a
4	chr12:4554756-4554806	BE2_C	brain:	n/a
5	chr12:4554480-4554530	PANC-1	pancreas:	n/a
6	chr12:4543316-4543366	HEEpiC	esophagus:	n/a
7	chr12:4554971-4555021	HUVEC	blood vessel:	n/a
8	chr12:4554786-4554836	HMEC	breast:	n/a
9	chr12:4543316-4543366	H1-hESC	embryonic stem cell:	embryo
10	chr12:4554623-4554673	NHDF-neo	bronchial:	n/a
11	chr12:4556149-4556199	Jurkat	blood:	n/a
12	chr12:4554962-4555012	HEK293	kidney:	embryo
13	chr12:4554756-4554806	NT2-D1	testis:	n/a
14	chr12:4554878-4554928	HCM	heart:	n/a
15	chr12:4554480-4554530	HCPEpiC	choroid plexus:	n/a
16	chr12:4554962-4555012	AoSMC	blood vessel:	n/a
17	chr12:4556149-4556199	HIPEpiC	eye:	n/a
18	chr12:4554962-4555012	SAEC	small airway:	n/a
19	chr12:4554756-4554806	MCF-7	breast:	n/a
20	chr12:4554596-4554646	IMR90	lung:	fetal
21	chr12:4554463-4554513	NT2-D1	testis:	n/a
22	chr12:4555720-4555770	HRPEpiC	eye:	n/a
23	chr12:4554962-4555012	BJ	skin:	n/a
24	chr12:4554971-4555021	AG10803	skin:	n/a
25	chr12:4543316-4543366	HEK293	kidney:	embryo
26	chr12:4554756-4554806	NHDF-neo	bronchial:	n/a
27	chr12:4556149-4556199	HEEpiC	esophagus:	n/a
28	chr12:4554295-4554345	AG10803	skin:	n/a
29	chr12:4554596-4554646	HIPEpiC	eye:	n/a
30	chr12:4543316-4543366	HL-60	blood:	n/a
31	chr12:4554809-4554859	ovcar-3	ovarian:	n/a
32	chr12:4553029-4553079	BJ	skin:	n/a
33	chr12:4554962-4555012	MCF-7	breast:	n/a
34	chr12:4554623-4554673	HAEpiC	amniotic membrane:	n/a
35	chr12:4554971-4555021	GM12878	blood:	n/a
36	chr12:4554623-4554673	HNPCEpiC	eye:	n/a
37	chr12:4554623-4554673	HCM	heart:	n/a
38	chr12:4555311-4555361	AG10803	skin:	n/a
39	chr12:4555311-4555361	BJ	skin:	n/a
40	chr12:4554463-4554513	BJ	skin:	n/a
41	chr12:4553029-4553079	ovcar-3	ovarian:	n/a
42	chr12:4556149-4556199	HepG2	liver:	n/a
43	chr12:4554786-4554836	HRCEpiC	kidney:	n/a
44	chr12:4554962-4555012	ECC-1	luminal epithelium:	n/a
45	chr12:4557277-4557327	AG10803	skin:	n/a
46	chr12:4554786-4554836	AG10803	skin:	n/a
47	chr12:4550927-4550977	SKMC	muscle:	n/a
48	chr12:4554295-4554345	HRCEpiC	kidney:	n/a
49	chr12:4555720-4555770	MCF10A-Er-Src	breast:	n/a
50	chr12:4549503-4549553	GM19239	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:4530409..4532083-chr12:4533762..4536051,2	K562	blood:
2	chr12:4465014..4465763-chr12:4530635..4531275,2	K562	blood:
3	chr12:4556951..4558618-chr12:4562621..4564423,2	K562	blood:
4	chr12:4550824..4553664-chr12:4554520..4557456,3	K562	blood:
5	chr12:4530453..4531092-chr12:4635858..4636763,3	MCF-7	breast:
6	chr12:4493639..4495339-chr12:4512124..4514965,2	K562	blood:
7	chr12:4464912..4465712-chr12:4530622..4531249,2	MCF-7	breast:
8	chr12:4530354..4531235-chr12:4867040..4867907,2	K562	blood:
9	chr12:4549549..4551778-chr12:4554163..4556191,2	MCF-7	breast:
10	chr12:4495347..4499076-chr12:4544187..4545933,3	K562	blood:
11	chr12:4366467..4368180-chr12:4540128..4541713,2	K562	blood:
12	chr12:4550824..4553664-chr12:4554520..4557456,3	K562	blood:
13	chr12:4530409..4532083-chr12:4533762..4536051,2	K562	blood:
14	chr12:4536252..4538511-chr12:4543376..4545742,2	K562	blood:
15	chr12:4541324..4542846-chr12:4646030..4648242,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FGF6-1	chr12:4537665-4537881	NONHSAT025953
2	lnc-FGF6-1	chr12:4537321-4537569	NONHSAT025953

Variant related genes	Relation type
FGF6	TF binding region
FGF6	CpG island
ENSG00000111247	chromatin interactions
ENSG00000111241	chromatin interactions
ENSG00000047621	chromatin interactions

Extended variants
information (count: 1703 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:1703 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs540584927	chr12:4514318-4514319	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs142273990	chr12:4514319-4514320	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs574019500	chr12:4514338-4514339	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs11063136	chr12:4514388-4514389	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs139861020	chr12:4514478-4514479	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs571236179	chr12:4514496-4514497	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs145479112	chr12:4514512-4514513	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs10735034	chr12:4514529-4514530	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs564634415	chr12:4514530-4514531	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs563796777	chr12:4514536-4514537	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs147689471	chr12:4514537-4514538	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs538353459	chr12:4514546-4514547	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs374042017	chr12:4514549-4514550	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs546337332	chr12:4514561-4514562	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs566337359	chr12:4514562-4514563	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs546128614	chr12:4520200-4520201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs559275325	chr12:4520228-4520229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs540344960	chr12:4520265-4520266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs145208975	chr12:4520281-4520282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs74061616	chr12:4520331-4520332	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs532651869	chr12:4520345-4520346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs568161394	chr12:4520347-4520348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs74061617	chr12:4520362-4520363	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs74061619	chr12:4520395-4520396	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs570159317	chr12:4520467-4520468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs539734452	chr12:4520495-4520496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs143073891	chr12:4520547-4520548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs566928387	chr12:4520548-4520549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs148259012	chr12:4520555-4520556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs186553876	chr12:4520577-4520578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs370695194	chr12:4520585-4520586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs191369399	chr12:4520605-4520606	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs115790485	chr12:4520606-4520607	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs544571038	chr12:4520614-4520615	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs558182784	chr12:4520695-4520696	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs71458098	chr12:4520740-4520741	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs141821159	chr12:4520842-4520843	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs545765872	chr12:4520858-4520859	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs559628912	chr12:4520893-4520894	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs74061620	chr12:4520916-4520917	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs150380633	chr12:4520919-4520920	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs561396405	chr12:4520936-4520937	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs74061621	chr12:4520942-4520943	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs35900789	chr12:4520949-4520950	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs550301055	chr12:4520975-4520976	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs34317131	chr12:4521001-4521002	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs7968988	chr12:4521044-4521045	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs74061622	chr12:4521050-4521051	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs368213690	chr12:4521061-4521062	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs546951358	chr12:4521112-4521113	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Ovarian cancer	20844748	CNVD
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
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
low-grade B-cell lymphoma tumor	18367492	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
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Epilepsy	21858020	CNVD
Colorectal cancer	19359472	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	21509527	CNVD
Breast cancer	22522925	CNVD
Prostate cancer	18632612	CNVD
Pancreatic cancer	17952125	CNVD
Chordoma	18071362	CNVD

Chromatin state (count:472 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:4513400-4514600	Enhancers	Duodenum Mucosa	Duodenum
2	chr12:4520200-4524000	Weak transcription	Fetal Brain Male	brain
3	chr12:4520600-4522400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr12:4520800-4522400	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr12:4521200-4522000	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr12:4521600-4522000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr12:4521600-4522200	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr12:4521600-4522400	Enhancers	Brain Germinal Matrix	brain
9	chr12:4521600-4524200	Enhancers	Primary hematopoietic stem cells short term culture	blood
10	chr12:4522000-4523200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr12:4522400-4522600	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr12:4522400-4524000	Weak transcription	Brain Germinal Matrix	brain
13	chr12:4522600-4522800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr12:4523200-4524000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr12:4523200-4524000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr12:4523200-4524000	Enhancers	Dnd41	blood
17	chr12:4523200-4526600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr12:4523600-4524200	Enhancers	Primary hematopoietic stem cells	blood
19	chr12:4523800-4524000	Enhancers	Fetal Muscle Trunk	muscle
20	chr12:4523800-4524600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr12:4523800-4525000	Enhancers	Fetal Thymus	thymus
22	chr12:4524000-4524200	Enhancers	Duodenum Mucosa	Duodenum
23	chr12:4524000-4524400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
24	chr12:4524000-4524400	Enhancers	Fetal Brain Male	brain
25	chr12:4524000-4524600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr12:4524000-4524600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
27	chr12:4524000-4524600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr12:4524000-4524600	Enhancers	Fetal Intestine Small	intestine
29	chr12:4524000-4524600	Bivalent Enhancer	Fetal Stomach	stomach
30	chr12:4524000-4524600	Enhancers	Lung	lung
31	chr12:4524000-4524800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
32	chr12:4524000-4524800	Enhancers	Left Ventricle	heart
33	chr12:4524000-4524800	Enhancers	Right Atrium	heart
34	chr12:4524000-4524800	Enhancers	Thymus	Thymus
35	chr12:4524000-4524800	Enhancers	HSMM	muscle
36	chr12:4524000-4524800	Enhancers	K562	blood
37	chr12:4524000-4525000	Flanking Active TSS	Dnd41	blood
38	chr12:4524000-4525200	Enhancers	Brain Germinal Matrix	brain
39	chr12:4524000-4525200	Enhancers	Fetal Intestine Large	intestine
40	chr12:4524000-4525200	Bivalent Enhancer	Fetal Muscle Leg	muscle
41	chr12:4524000-4525600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr12:4524200-4524400	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
43	chr12:4524200-4524400	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
44	chr12:4524200-4524400	Bivalent Enhancer	NHEK	skin
45	chr12:4524200-4524600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
46	chr12:4524200-4524600	Enhancers	Gastric	stomach
47	chr12:4524200-4524600	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
48	chr12:4524200-4524600	Flanking Active TSS	HSMMtube	muscle
49	chr12:4524200-4524800	Flanking Active TSS	Primary hematopoietic stem cells	blood
50	chr12:4524200-4524800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood

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