Variant report

Variant	esv8289
Chromosome Location	chr12:11144397-11222359
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:356)
CpG islands
(count:1039)
Chromatin interactive
region (count:11)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:356 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:11168444-11168649	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:11176072-11176303	HepG2	liver:	n/a	n/a
3	BATF	chr12:11186566-11186883	GM12878	blood:	n/a	n/a
4	BATF	chr12:11186631-11186911	GM12878	blood:	n/a	n/a
5	BATF	chr12:11216721-11217010	GM12878	blood:	n/a	n/a
6	BCL11A	chr12:11186584-11186913	GM12878	blood:	n/a	n/a
7	BHLHE40	chr12:11168360-11168714	HepG2	liver:	n/a	n/a
8	BRCA1	chr12:11168480-11168660	HepG2	liver:	n/a	n/a
9	CEBPB	chr12:11148042-11148079	K562	blood:	n/a	n/a
10	CEBPB	chr12:11170024-11170162	HepG2	liver:	n/a	chr12:11170139-11170150
11	CEBPB	chr12:11167458-11167736	HepG2	liver:	n/a	chr12:11167582-11167593
12	CTCF	chr12:11178880-11179030	HPAF	blood vessel:	n/a	n/a
13	CTCF	chr12:11169080-11169230	RPTEC	kidney:	n/a	n/a
14	CTCF	chr12:11206452-11206523	Kidney_OC	kidney:	n/a	n/a
15	CTCF	chr12:11178807-11179031	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr12:11178880-11179030	MCF-7	breast:	n/a	n/a
17	CTCF	chr12:11178831-11178990	Gliobla	brain:	n/a	n/a
18	CTCF	chr12:11178880-11179030	AoAF	blood vessel:	n/a	n/a
19	CTCF	chr12:11169160-11169310	HEK293	kidney:	n/a	n/a
20	CTCF	chr12:11178720-11178870	NHDF-neo	bronchial:	n/a	n/a
21	CTCF	chr12:11178800-11178950	GM12864	blood:	n/a	n/a
22	CTCF	chr12:11178800-11178950	AG09319	gingival:	n/a	n/a
23	CTCF	chr12:11178840-11178990	GM12873	blood:	n/a	n/a
24	CTCF	chr12:11178820-11178970	HFF-Myc	foreskin:	n/a	n/a
25	CTCF	chr12:11178740-11178890	HMEC	breast:	n/a	n/a
26	CTCF	chr12:11178785-11179055	MCF-7	breast:	n/a	n/a
27	CTCF	chr12:11209700-11209850	MCF-7	breast:	n/a	n/a
28	CTCF	chr12:11178820-11178970	HepG2	liver:	n/a	n/a
29	CTCF	chr12:11178820-11178970	GM12866	blood:	n/a	n/a
30	CTCF	chr12:11178800-11178950	HVMF	connective:	n/a	n/a
31	CTCF	chr12:11178840-11178990	AG04449	skin:	n/a	n/a
32	CTCF	chr12:11178862-11178967	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr12:11178920-11179070	GM12868	blood:	n/a	n/a
34	CTCF	chr12:11178820-11178970	SAEC	small airway:	n/a	n/a
35	CTCF	chr12:11178920-11179070	BE2_C	brain:	n/a	n/a
36	CTCF	chr12:11178780-11178930	WERI-Rb-1	eye:	n/a	n/a
37	CTCF	chr12:11178840-11178990	K562	blood:	n/a	n/a
38	CTCF	chr12:11178840-11178990	BE2_C	brain:	n/a	n/a
39	CTCF	chr12:11178840-11178990	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr12:11178700-11178990	HPF	lung:	n/a	n/a
41	CTCF	chr12:11178800-11178950	HFF-Myc	foreskin:	n/a	n/a
42	CTCF	chr12:11178820-11178970	HCFaa	heart:	n/a	n/a
43	CTCF	chr12:11178840-11178990	HUVEC	blood vessel:	n/a	n/a
44	CTCF	chr12:11178880-11179030	GM12873	blood:	n/a	n/a
45	CTCF	chr12:11178746-11178994	HepG2	liver:	n/a	n/a
46	CTCF	chr12:11178820-11178970	NB4	blood:	n/a	n/a
47	CTCF	chr12:11178780-11178930	WI-38	lung:	n/a	n/a
48	CTCF	chr12:11183077-11183136	GM10248	blood:	n/a	n/a
49	CTCF	chr12:11209872-11209908	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr12:11178819-11178997	A549	lung:	n/a	n/a

(count:1039 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:11184149-11184199	U87	brain:	n/a
2	chr12:11216351-11216401	BE2_C	brain:	n/a
3	chr12:11184149-11184199	U87	brain:	n/a
4	chr12:11216351-11216401	BE2_C	brain:	n/a
5	chr12:11184415-11184465	HCF	heart:	n/a
6	chr12:11185058-11185108	HUVEC	blood vessel:	n/a
7	chr12:11215083-11215133	NB4	blood:	n/a
8	chr12:11184415-11184465	NB4	blood:	n/a
9	chr12:11151622-11151672	CMK	blood:	n/a
10	chr12:11151224-11151274	CMK	blood:	n/a
11	chr12:11184005-11184055	HCM	heart:	n/a
12	chr12:11151430-11151480	PrEC	prostate:	n/a
13	chr12:11151224-11151274	IMR90	lung:	fetal
14	chr12:11216351-11216401	PANC-1	pancreas:	n/a
15	chr12:11176386-11176436	GM12892	blood:	n/a
16	chr12:11184037-11184087	AG10803	skin:	n/a
17	chr12:11151522-11151572	AG04449	skin:	fetal
18	chr12:11151478-11151528	BJ	skin:	n/a
19	chr12:11151224-11151274	Jurkat	blood:	n/a
20	chr12:11151622-11151672	HUVEC	blood vessel:	n/a
21	chr12:11149362-11149412	U87	brain:	n/a
22	chr12:11215083-11215133	PrEC	prostate:	n/a
23	chr12:11149362-11149412	HRCEpiC	kidney:	n/a
24	chr12:11215083-11215133	HEK293	kidney:	embryo
25	chr12:11151478-11151528	NT2-D1	testis:	n/a
26	chr12:11184005-11184055	K562	blood:	n/a
27	chr12:11151430-11151480	HEK293	kidney:	embryo
28	chr12:11176386-11176436	HAEpiC	amniotic membrane:	n/a
29	chr12:11151522-11151572	HUVEC	blood vessel:	n/a
30	chr12:11184347-11184397	HPAEpiC	pulmonary alveolar:	n/a
31	chr12:11151478-11151528	PANC-1	pancreas:	n/a
32	chr12:11151224-11151274	T-47D	breast:	n/a
33	chr12:11151430-11151480	ECC-1	luminal epithelium:	n/a
34	chr12:11151430-11151480	AG10803	skin:	n/a
35	chr12:11151430-11151480	HAEpiC	amniotic membrane:	n/a
36	chr12:11151430-11151480	AG09319	gingival:	n/a
37	chr12:11215083-11215133	BJ	skin:	n/a
38	chr12:11149362-11149412	SAEC	small airway:	n/a
39	chr12:11215083-11215133	HCF	heart:	n/a
40	chr12:11151622-11151672	GM12892	blood:	n/a
41	chr12:11151224-11151274	Hepatocyte	liver:	n/a
42	chr12:11151224-11151274	HCT-116	colon:	n/a
43	chr12:11184005-11184055	PrEC	prostate:	n/a
44	chr12:11149362-11149412	PANC-1	pancreas:	n/a
45	chr12:11185058-11185108	AG09309	skin:	n/a
46	chr12:11184149-11184199	ProgFib	skin:	n/a
47	chr12:11215083-11215133	HUVEC	blood vessel:	n/a
48	chr12:11216351-11216401	A549	lung:	n/a
49	chr12:11184005-11184055	NHDF-neo	bronchial:	n/a
50	chr12:11151478-11151528	HL-60	blood:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:11158423..11160257-chr12:11164352..11165951,2	MCF-7	breast:
2	chr12:11154648..11156385-chr12:11157901..11159498,2	K562	blood:
3	chr12:11153714..11156559-chr12:11162296..11164278,2	MCF-7	breast:
4	chr12:11157746..11159406-chr12:11165545..11167423,2	K562	blood:
5	chr12:11169301..11171201-chr12:11322573..11325255,2	MCF-7	breast:
6	chr12:11009323..11011109-chr12:11168207..11170860,2	K562	blood:
7	chr12:11153714..11156559-chr12:11162296..11164278,2	MCF-7	breast:
8	chr12:11158423..11160257-chr12:11164352..11165951,2	MCF-7	breast:
9	chr12:11210669..11211248-chr5:109800405..109801099,2	MCF-7	breast:
10	chr12:11157746..11159406-chr12:11165545..11167423,2	K562	blood:
11	chr12:11154648..11156385-chr12:11157901..11159498,2	K562	blood:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRH1-1	chr12:11187381-11187484	NR_037918
2	lnc-PRH1-1	chr12:11199619-11199787	NR_037918
3	lnc-PRH1-1	chr12:11199619-11199787	NONHSAT026912
4	lnc-PRH1-1	chr12:11199619-11199640	NONHSAT026908
5	lnc-PRH1-1	chr12:11187381-11187484	NONHSAT026912
6	lnc-PRH1-1	chr12:11199619-11199736	NONHSAT026915
7	lnc-PRH1-1	chr12:11199619-11199713	NONHSAT026914
8	lnc-PRH1-1	chr12:11199612-11199787	NONHSAT026916
9	lnc-PRH1-1	chr12:11158533-11158868	NONHSAT026915
10	lnc-TAS2R46-1	chr12:11200931-11201855	NONHSAT026917
11	lnc-PRH1-1	chr12:11199619-11199787	NONHSAT026907

No data

Variant related genes	Relation type
TAS2R46	TF binding region
TAS2R19	TF binding region
TAS2R31	TF binding region
ENSG00000268301	TF binding region
TAS2R20	TF binding region
TAS2R50	TF binding region
PRR4	TF binding region
TAS2R63P	TF binding region
TAS2R46	CpG island
TAS2R19	CpG island
TAS2R31	CpG island
ENSG00000268301	CpG island
TAS2R20	CpG island
TAS2R50	CpG island
PRR4	CpG island
TAS2R63P	CpG island
ENSG00000111215	chromatin interactions
ENSG00000256712	chromatin interactions
ENSG00000256537	chromatin interactions
ENSG00000212127	chromatin interactions

Extended variants
information (count: 4044 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:4044 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73051613	chr12:11144424-11144425	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs7306372	chr12:11144449-11144450	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
3	rs7305429	chr12:11144451-11144452	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs139426858	chr12:11144465-11144466	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs546028241	chr12:11144467-11144468	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs182096297	chr12:11144486-11144487	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs559277050	chr12:11144494-11144495	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs187672544	chr12:11144538-11144539	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs541538567	chr12:11144541-11144542	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs7305587	chr12:11144579-11144580	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs149980175	chr12:11144583-11144584	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs7305588	chr12:11144584-11144585	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs144242274	chr12:11144738-11144739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs191940990	chr12:11144749-11144750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs140062199	chr12:11144767-11144768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs566123191	chr12:11144822-11144823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs74692886	chr12:11144832-11144833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs555071050	chr12:11144837-11144838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs554099490	chr12:11144880-11144881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs568478219	chr12:11144889-11144890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs537397894	chr12:11144942-11144943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs35101759	chr12:11144947-11144948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs7307031	chr12:11144994-11144995	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs577253262	chr12:11145000-11145001	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs73051617	chr12:11145002-11145003	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs200531568	chr12:11145004-11145005	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs375116799	chr12:11145012-11145013	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs202176700	chr12:11145013-11145014	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs372904129	chr12:11145038-11145039	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs115320511	chr12:11145067-11145068	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs34946638	chr12:11145068-11145069	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs541925347	chr12:11145089-11145090	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs561406591	chr12:11145103-11145104	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs530427520	chr12:11145113-11145114	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs146475047	chr12:11145121-11145122	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs183811909	chr12:11145125-11145126	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs4132154	chr12:11145191-11145192	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs369026631	chr12:11145197-11145198	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs10845274	chr12:11145232-11145233	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs117382710	chr12:11145249-11145250	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs10845275	chr12:11145309-11145310	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs568618323	chr12:11145338-11145339	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs10845276	chr12:11145463-11145464	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs557428297	chr12:11145468-11145469	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs141003860	chr12:11145477-11145478	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs539743037	chr12:11145482-11145483	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs113591142	chr12:11145486-11145487	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs188299611	chr12:11145496-11145497	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs374226042	chr12:11145515-11145516	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs573003827	chr12:11145516-11145517	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
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
Acute lymphoblastic leukemia	22237106	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21611746	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Squamous cell cancer	19607727	CNVD
Prostate cancer	16573809	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16461572	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian cancer	21720365	CNVD
Melanoma	20877625	CNVD
Ovarian cancer	21781307	CNVD
Acute myeloid leukemia	17237825	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Breast cancer	22522925	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Bipolar disorder	19114987	CNVD
early-passage human iPS cells	21368824	CNVD
Incontinentia Pigmenti	22033527	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1053 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:11095200-11148800	Weak transcription	HepG2	liver
2	chr12:11114000-11149200	Weak transcription	GM12878-XiMat	blood
3	chr12:11114400-11180200	Weak transcription	Primary B cells from peripheral blood	blood
4	chr12:11114600-11146400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
5	chr12:11114600-11146800	Weak transcription	Ovary	ovary
6	chr12:11122000-11146200	Weak transcription	Left Ventricle	heart
7	chr12:11122000-11170200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr12:11122200-11168000	Weak transcription	HUVEC	blood vessel
9	chr12:11129200-11167600	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr12:11132000-11154800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr12:11132400-11146200	Weak transcription	Adipose Nuclei	Adipose
12	chr12:11134800-11166800	Weak transcription	NHDF-Ad	bronchial
13	chr12:11135200-11162200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr12:11135600-11146000	Weak transcription	Stomach Smooth Muscle	stomach
15	chr12:11136400-11146600	Weak transcription	Aorta	Aorta
16	chr12:11136400-11146600	Weak transcription	Lung	lung
17	chr12:11136400-11180200	Weak transcription	Primary T cells fromperipheralblood	blood
18	chr12:11136600-11153600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
19	chr12:11136600-11180200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
20	chr12:11136600-11196400	Weak transcription	Primary T helper cells PMA-I stimulated	--
21	chr12:11137400-11203000	Weak transcription	Hela-S3	cervix
22	chr12:11139000-11149000	Weak transcription	HUES64 Cell Line	embryonic stem cell
23	chr12:11140200-11146600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr12:11140800-11152800	Weak transcription	Fetal Thymus	thymus
25	chr12:11141600-11146400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr12:11141800-11148200	Weak transcription	Primary T helper cells fromperipheralblood	blood
27	chr12:11142200-11146600	Weak transcription	Esophagus	oesophagus
28	chr12:11142200-11151200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
29	chr12:11142200-11153400	Weak transcription	Rectal Smooth Muscle	rectum
30	chr12:11142400-11146200	Weak transcription	Fetal Heart	heart
31	chr12:11142800-11144600	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr12:11142800-11146400	Weak transcription	Pancreas	Pancrea
33	chr12:11143000-11148600	Weak transcription	Duodenum Mucosa	Duodenum
34	chr12:11143200-11145400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
35	chr12:11143200-11146000	Weak transcription	Brain Cingulate Gyrus	brain
36	chr12:11143200-11146000	Weak transcription	Brain Substantia Nigra	brain
37	chr12:11143200-11146200	Weak transcription	Brain Anterior Caudate	brain
38	chr12:11143200-11147800	Weak transcription	HSMMtube	muscle
39	chr12:11143400-11145200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr12:11143400-11145200	Weak transcription	Fetal Muscle Leg	muscle
41	chr12:11143400-11146400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
42	chr12:11143400-11146400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
43	chr12:11143400-11146400	Weak transcription	Liver	Liver
44	chr12:11143400-11146600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr12:11143400-11146600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr12:11143400-11147000	Weak transcription	Fetal Lung	lung
47	chr12:11143400-11147200	Weak transcription	HUES6 Cell Line	embryonic stem cell
48	chr12:11143400-11151200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr12:11143400-11161000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr12:11143400-11167600	Weak transcription	Fetal Intestine Small	intestine

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