Variant report

Variant	esv3347626
Chromosome Location	chr12:11167851-11223280
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:333)
CpG islands
(count:673)
Chromatin interactive
region (count:3)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:333 , 50 per page) page: 1 2 3 4 5 6 7

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	chr12:11186631-11186911	GM12878	blood:	n/a	n/a
4	BATF	chr12:11186566-11186883	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	chr12:11222658-11222813	HepG2	liver:	n/a	n/a
10	CEBPB	chr12:11170024-11170162	HepG2	liver:	n/a	chr12:11170139-11170150
11	CTCF	chr12:11178880-11179030	HPAF	blood vessel:	n/a	n/a
12	CTCF	chr12:11178795-11179005	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr12:11209880-11210030	GM12872	blood:	n/a	n/a
14	CTCF	chr12:11168980-11169130	HAc	cerebellar:	n/a	n/a
15	CTCF	chr12:11178820-11178970	HCFaa	heart:	n/a	n/a
16	CTCF	chr12:11178740-11178890	HMEC	breast:	n/a	n/a
17	CTCF	chr12:11178840-11178990	GM12865	blood:	n/a	n/a
18	CTCF	chr12:11178780-11178930	GM12878	blood:	n/a	n/a
19	CTCF	chr12:11178792-11179011	MCF-7	breast:	n/a	n/a
20	CTCF	chr12:11178820-11178970	HUVEC	blood vessel:	n/a	n/a
21	CTCF	chr12:11178800-11178950	HBMEC	blood vessel:	n/a	n/a
22	CTCF	chr12:11178872-11178912	GM12891	blood:	n/a	n/a
23	CTCF	chr12:11178800-11178950	AG04450	lung:	n/a	n/a
24	CTCF	chr12:11176040-11176190	BE2_C	brain:	n/a	n/a
25	CTCF	chr12:11178840-11178990	BE2_C	brain:	n/a	n/a
26	CTCF	chr12:11178858-11178977	ProgFib	skin:	n/a	n/a
27	CTCF	chr12:11178869-11178995	LNCaP	prostate:	n/a	n/a
28	CTCF	chr12:11178800-11178950	AG09319	gingival:	n/a	n/a
29	CTCF	chr12:11178860-11179010	Caco-2	colon:	n/a	n/a
30	CTCF	chr12:11178820-11178970	HAc	cerebellar:	n/a	n/a
31	CTCF	chr12:11178800-11178950	HFF-Myc	foreskin:	n/a	n/a
32	CTCF	chr12:11178700-11178990	HPF	lung:	n/a	n/a
33	CTCF	chr12:11178840-11178990	A549	lung:	n/a	n/a
34	CTCF	chr12:11178880-11179030	MCF-7	breast:	n/a	n/a
35	CTCF	chr12:11178800-11178950	HMF	breast:	n/a	n/a
36	CTCF	chr12:11178820-11178970	HFF-Myc	foreskin:	n/a	n/a
37	CTCF	chr12:11209872-11209908	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr12:11178780-11178930	HRPEpiC	eye:	n/a	n/a
39	CTCF	chr12:11183077-11183136	GM10248	blood:	n/a	n/a
40	CTCF	chr12:11178880-11179030	AoAF	blood vessel:	n/a	n/a
41	CTCF	chr12:11178902-11178949	HepG2	liver:	n/a	n/a
42	CTCF	chr12:11178820-11178970	GM12866	blood:	n/a	n/a
43	CTCF	chr12:11178857-11178967	Fibrobl	skin:	n/a	n/a
44	CTCF	chr12:11178940-11179090	GM06990	blood:	n/a	n/a
45	CTCF	chr12:11178700-11178850	K562	blood:	n/a	n/a
46	CTCF	chr12:11187719-11187757	GM13976	blood:	n/a	n/a
47	CTCF	chr12:11178840-11178990	HRPEpiC	eye:	n/a	n/a
48	CTCF	chr12:11178840-11178990	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr12:11178860-11179010	HCPEpiC	choroid plexus:	n/a	n/a
50	CTCF	chr12:11178770-11179057	MCF-7	breast:	n/a	n/a

(count:673 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:11176386-11176436	HRE	kidney:	n/a
2	chr12:11216351-11216401	ovcar-3	ovarian:	n/a
3	chr12:11176386-11176436	HRE	kidney:	n/a
4	chr12:11216351-11216401	ovcar-3	ovarian:	n/a
5	chr12:11184005-11184055	U87	brain:	n/a
6	chr12:11176386-11176436	NHBE	bronchial:	n/a
7	chr12:11184037-11184087	HCT-116	colon:	n/a
8	chr12:11174898-11174948	Hepatocyte	liver:	n/a
9	chr12:11184149-11184199	K562	blood:	n/a
10	chr12:11184005-11184055	GM19239	blood:	n/a
11	chr12:11184149-11184199	AG10803	skin:	n/a
12	chr12:11184149-11184199	HPAEpiC	pulmonary alveolar:	n/a
13	chr12:11184347-11184397	ovcar-3	ovarian:	n/a
14	chr12:11174898-11174948	HUVEC	blood vessel:	n/a
15	chr12:11174898-11174948	BJ	skin:	n/a
16	chr12:11185058-11185108	HUVEC	blood vessel:	n/a
17	chr12:11176574-11176624	A549	lung:	n/a
18	chr12:11184149-11184199	BE2_C	brain:	n/a
19	chr12:11176386-11176436	HAEpiC	amniotic membrane:	n/a
20	chr12:11176574-11176624	NT2-D1	testis:	n/a
21	chr12:11184347-11184397	ProgFib	skin:	n/a
22	chr12:11184149-11184199	GM12892	blood:	n/a
23	chr12:11176386-11176436	MCF-7	breast:	n/a
24	chr12:11185058-11185108	A549	lung:	n/a
25	chr12:11174898-11174948	GM12891	blood:	n/a
26	chr12:11185058-11185108	SKMC	muscle:	n/a
27	chr12:11176386-11176436	AG09309	skin:	n/a
28	chr12:11215083-11215133	HCF	heart:	n/a
29	chr12:11185058-11185108	HPAEpiC	pulmonary alveolar:	n/a
30	chr12:11176574-11176624	HRCEpiC	kidney:	n/a
31	chr12:11184005-11184055	NHDF-neo	bronchial:	n/a
32	chr12:11216351-11216401	HUVEC	blood vessel:	n/a
33	chr12:11184005-11184055	HCT-116	colon:	n/a
34	chr12:11184347-11184397	HepG2	liver:	n/a
35	chr12:11216351-11216401	Caco-2	colon:	n/a
36	chr12:11215083-11215133	Hepatocyte	liver:	n/a
37	chr12:11176574-11176624	BE2_C	brain:	n/a
38	chr12:11184005-11184055	Hela-S3	cervix:	n/a
39	chr12:11176386-11176436	T-47D	breast:	n/a
40	chr12:11176574-11176624	SK-N-SH	brain:	n/a
41	chr12:11176386-11176436	GM06990	blood:	n/a
42	chr12:11215083-11215133	SAEC	small airway:	n/a
43	chr12:11184149-11184199	HCT-116	colon:	n/a
44	chr12:11176574-11176624	SK-N-MC	brain:	n/a
45	chr12:11174898-11174948	LNCaP	prostate:	n/a
46	chr12:11176386-11176436	HCF	heart:	n/a
47	chr12:11184149-11184199	SKMC	muscle:	n/a
48	chr12:11184149-11184199	HEK293	kidney:	embryo
49	chr12:11174898-11174948	HEK293	kidney:	embryo
50	chr12:11184149-11184199	PrEC	prostate:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:11210669..11211248-chr5:109800405..109801099,2	MCF-7	breast:
2	chr12:11009323..11011109-chr12:11168207..11170860,2	K562	blood:
3	chr12:11169301..11171201-chr12:11322573..11325255,2	MCF-7	breast:

(count:10 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 3188 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:3188 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs72475460	chr12:11167858-11167859	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs570183815	chr12:11167891-11167892	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs542066220	chr12:11167906-11167907	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs188904836	chr12:11167924-11167925	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs73047108	chr12:11167928-11167929	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs73047109	chr12:11167930-11167931	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs73047112	chr12:11167947-11167948	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs529520928	chr12:11167983-11167984	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs549185438	chr12:11168045-11168046	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs569077456	chr12:11168130-11168131	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs537959544	chr12:11168140-11168141	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs551417979	chr12:11168169-11168170	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs571713844	chr12:11168238-11168239	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs540661730	chr12:11168261-11168262	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs193233489	chr12:11168262-11168263	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs533979942	chr12:11168319-11168320	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs200535634	chr12:11168357-11168358	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs145888183	chr12:11168372-11168373	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs573882451	chr12:11168379-11168380	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs536515347	chr12:11168455-11168456	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs556401689	chr12:11168456-11168457	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs576257778	chr12:11168458-11168459	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs112397044	chr12:11168505-11168506	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs200068285	chr12:11168527-11168528	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs564869367	chr12:11168549-11168550	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs563817367	chr12:11168555-11168556	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs370969083	chr12:11168566-11168567	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs532909216	chr12:11168573-11168574	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs73254827	chr12:11168578-11168579	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs574582040	chr12:11168653-11168654	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs540695946	chr12:11168663-11168664	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs560908454	chr12:11168742-11168743	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs529560987	chr12:11168745-11168746	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs542874601	chr12:11168749-11168750	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs185452753	chr12:11168765-11168766	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs367871725	chr12:11168843-11168844	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs543603691	chr12:11168852-11168853	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs112996296	chr12:11168892-11168893	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs112628123	chr12:11168896-11168897	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs531834546	chr12:11168897-11168898	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs147684021	chr12:11168902-11168903	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs113277001	chr12:11168905-11168906	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs571684629	chr12:11168978-11168979	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs527765286	chr12:11168982-11168983	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs547496681	chr12:11168999-11169000	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs563867608	chr12:11169001-11169002	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs375601255	chr12:11169003-11169004	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs190310787	chr12:11169054-11169055	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs73047117	chr12:11169067-11169068	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs536551652	chr12:11169101-11169102	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:97)

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
Bipolar disorder	19114987	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:11114400-11180200	Weak transcription	Primary B cells from peripheral blood	blood
2	chr12:11122000-11170200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr12:11122200-11168000	Weak transcription	HUVEC	blood vessel
4	chr12:11136400-11180200	Weak transcription	Primary T cells fromperipheralblood	blood
5	chr12:11136600-11180200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
6	chr12:11136600-11196400	Weak transcription	Primary T helper cells PMA-I stimulated	--
7	chr12:11137400-11203000	Weak transcription	Hela-S3	cervix
8	chr12:11143400-11178800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr12:11145400-11177600	Weak transcription	Primary monocytes fromperipheralblood	blood
10	chr12:11147000-11168400	Weak transcription	Liver	Liver
11	chr12:11147000-11178600	Weak transcription	Fetal Stomach	stomach
12	chr12:11147000-11185400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr12:11147200-11168600	Weak transcription	Spleen	Spleen
14	chr12:11147200-11169200	Weak transcription	Skeletal Muscle Female	skeletal muscle
15	chr12:11147200-11171200	Weak transcription	Primary hematopoietic stem cells	blood
16	chr12:11147200-11176200	Weak transcription	Aorta	Aorta
17	chr12:11147200-11180400	Weak transcription	Pancreas	Pancrea
18	chr12:11148400-11178200	Weak transcription	Dnd41	blood
19	chr12:11149000-11168600	Weak transcription	Left Ventricle	heart
20	chr12:11154000-11169000	Weak transcription	Primary T cells from cord blood	blood
21	chr12:11154200-11168000	Weak transcription	Fetal Muscle Leg	muscle
22	chr12:11154200-11174200	Weak transcription	Primary B cells from cord blood	blood
23	chr12:11154200-11178000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr12:11154200-11178200	Weak transcription	A549	lung
25	chr12:11154200-11178800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr12:11154400-11168000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr12:11159400-11168600	Weak transcription	Gastric	stomach
28	chr12:11159400-11182000	Weak transcription	NHEK	skin
29	chr12:11159600-11178200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
30	chr12:11161400-11178200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr12:11161400-11179200	Weak transcription	Fetal Kidney	kidney
32	chr12:11162400-11172800	Weak transcription	Fetal Brain Female	brain
33	chr12:11163400-11177600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr12:11163400-11178000	Weak transcription	GM12878-XiMat	blood
35	chr12:11163600-11178800	Weak transcription	Ovary	ovary
36	chr12:11163800-11178000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr12:11164400-11178600	Weak transcription	Fetal Thymus	thymus
38	chr12:11164600-11168200	Weak transcription	Stomach Mucosa	stomach
39	chr12:11164800-11171800	Weak transcription	Lung	lung
40	chr12:11165000-11170000	Weak transcription	Fetal Muscle Trunk	muscle
41	chr12:11165000-11180800	Weak transcription	HSMM	muscle
42	chr12:11165200-11170800	Enhancers	Brain Substantia Nigra	brain
43	chr12:11165400-11180200	Weak transcription	Esophagus	oesophagus
44	chr12:11165600-11174200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr12:11166000-11192000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
46	chr12:11166200-11210000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
47	chr12:11166400-11168600	Enhancers	HepG2	liver
48	chr12:11166400-11170600	Enhancers	Brain Hippocampus Middle	brain
49	chr12:11166400-11170800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
50	chr12:11166600-11168800	Weak transcription	Right Ventricle	heart

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