Variant report

Variant	esv3503763
Chromosome Location	chr12:11161162-11275828
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:476)
CpG islands
(count:794)
Chromatin interactive
region (count:11)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:476 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

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	ARID3A	chr12:11224069-11224255	HepG2	liver:	n/a	n/a
4	ATF2	chr12:11237956-11238445	GM12878	blood:	n/a	n/a
5	ATF2	chr12:11238009-11238486	GM12878	blood:	n/a	n/a
6	BATF	chr12:11186631-11186911	GM12878	blood:	n/a	n/a
7	BATF	chr12:11216721-11217010	GM12878	blood:	n/a	n/a
8	BATF	chr12:11225254-11225547	GM12878	blood:	n/a	n/a
9	BATF	chr12:11186566-11186883	GM12878	blood:	n/a	n/a
10	BATF	chr12:11263857-11264113	GM12878	blood:	n/a	n/a
11	BATF	chr12:11238084-11238352	GM12878	blood:	n/a	n/a
12	BATF	chr12:11238012-11238373	GM12878	blood:	n/a	n/a
13	BATF	chr12:11247482-11247799	GM12878	blood:	n/a	n/a
14	BATF	chr12:11263799-11264109	GM12878	blood:	n/a	n/a
15	BATF	chr12:11247547-11247827	GM12878	blood:	n/a	n/a
16	BATF	chr12:11228218-11228560	GM12878	blood:	n/a	n/a
17	BCL11A	chr12:11238061-11238356	GM12878	blood:	n/a	chr12:11238263-11238272
18	BCL11A	chr12:11263900-11264159	GM12878	blood:	n/a	n/a
19	BCL11A	chr12:11247500-11247829	GM12878	blood:	n/a	n/a
20	BCL11A	chr12:11228248-11228517	GM12878	blood:	n/a	n/a
21	BCL11A	chr12:11186584-11186913	GM12878	blood:	n/a	n/a
22	BHLHE40	chr12:11168360-11168714	HepG2	liver:	n/a	n/a
23	BHLHE40	chr12:11228293-11228667	GM12878	blood:	n/a	n/a
24	BRCA1	chr12:11168480-11168660	HepG2	liver:	n/a	n/a
25	CEBPB	chr12:11170024-11170162	HepG2	liver:	n/a	chr12:11170139-11170150
26	CEBPB	chr12:11167458-11167736	HepG2	liver:	n/a	chr12:11167582-11167593
27	CEBPB	chr12:11226186-11226481	HepG2	liver:	n/a	n/a
28	CEBPB	chr12:11260954-11260970	HepG2	liver:	n/a	n/a
29	CEBPB	chr12:11223987-11224332	HepG2	liver:	n/a	n/a
30	CEBPB	chr12:11222658-11222813	HepG2	liver:	n/a	n/a
31	CHD2	chr12:11238132-11238304	GM12878	blood:	n/a	n/a
32	CTCF	chr12:11187719-11187757	GM13976	blood:	n/a	n/a
33	CTCF	chr12:11270380-11270463	GM13977	blood:	n/a	n/a
34	CTCF	chr12:11178780-11178930	WI-38	lung:	n/a	n/a
35	CTCF	chr12:11178800-11178950	AG04450	lung:	n/a	n/a
36	CTCF	chr12:11178860-11179010	HPF	lung:	n/a	n/a
37	CTCF	chr12:11169160-11169310	HEK293	kidney:	n/a	n/a
38	CTCF	chr12:11178902-11178949	HepG2	liver:	n/a	n/a
39	CTCF	chr12:11178840-11178990	HMF	breast:	n/a	n/a
40	CTCF	chr12:11178880-11179030	GM12864	blood:	n/a	n/a
41	CTCF	chr12:11178800-11178950	GM12864	blood:	n/a	n/a
42	CTCF	chr12:11207523-11207552	GM10248	blood:	n/a	n/a
43	CTCF	chr12:11257042-11257094	GM20000	blood:	n/a	n/a
44	CTCF	chr12:11209880-11210030	GM12872	blood:	n/a	n/a
45	CTCF	chr12:11178690-11179157	MCF-7	breast:	n/a	n/a
46	CTCF	chr12:11169160-11169310	Caco-2	colon:	n/a	n/a
47	CTCF	chr12:11178880-11179030	BJ	skin:	n/a	n/a
48	CTCF	chr12:11178840-11178990	HEK293	kidney:	n/a	n/a
49	CTCF	chr12:11178760-11178910	GM12869	blood:	n/a	n/a
50	CTCF	chr12:11183077-11183136	GM10248	blood:	n/a	n/a

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:11184347-11184397	PANC-1	pancreas:	n/a
2	chr12:11184347-11184397	PANC-1	pancreas:	n/a
3	chr12:11184415-11184465	MCF10A-Er-Src	breast:	n/a
4	chr12:11184415-11184465	HCM	heart:	n/a
5	chr12:11184005-11184055	BE2_C	brain:	n/a
6	chr12:11215083-11215133	NHDF-neo	bronchial:	n/a
7	chr12:11215083-11215133	H1-hESC	embryonic stem cell:	embryo
8	chr12:11184037-11184087	HAEpiC	amniotic membrane:	n/a
9	chr12:11184149-11184199	AoSMC	blood vessel:	n/a
10	chr12:11184149-11184199	HMEC	breast:	n/a
11	chr12:11184037-11184087	T-47D	breast:	n/a
12	chr12:11184149-11184199	LNCaP	prostate:	n/a
13	chr12:11184005-11184055	GM12878	blood:	n/a
14	chr12:11244899-11244949	HRPEpiC	eye:	n/a
15	chr12:11176386-11176436	HAEpiC	amniotic membrane:	n/a
16	chr12:11184415-11184465	Caco-2	colon:	n/a
17	chr12:11176386-11176436	RPTEC	kidney:	n/a
18	chr12:11176386-11176436	HRE	kidney:	n/a
19	chr12:11216351-11216401	GM12892	blood:	n/a
20	chr12:11184415-11184465	HepG2	liver:	n/a
21	chr12:11215083-11215133	HEK293	kidney:	embryo
22	chr12:11174898-11174948	Hepatocyte	liver:	n/a
23	chr12:11244939-11244989	NB4	blood:	n/a
24	chr12:11176574-11176624	HL-60	blood:	n/a
25	chr12:11176574-11176624	AoSMC	blood vessel:	n/a
26	chr12:11244899-11244949	HCM	heart:	n/a
27	chr12:11184149-11184199	HCF	heart:	n/a
28	chr12:11184005-11184055	ovcar-3	ovarian:	n/a
29	chr12:11185058-11185108	HUVEC	blood vessel:	n/a
30	chr12:11174898-11174948	PrEC	prostate:	n/a
31	chr12:11184415-11184465	RPTEC	kidney:	n/a
32	chr12:11185058-11185108	HCPEpiC	choroid plexus:	n/a
33	chr12:11184005-11184055	PANC-1	pancreas:	n/a
34	chr12:11174898-11174948	HRPEpiC	eye:	n/a
35	chr12:11184149-11184199	BJ	skin:	n/a
36	chr12:11176386-11176436	AG04449	skin:	fetal
37	chr12:11176386-11176436	HCPEpiC	choroid plexus:	n/a
38	chr12:11176574-11176624	H1-hESC	embryonic stem cell:	embryo
39	chr12:11184149-11184199	Hepatocyte	liver:	n/a
40	chr12:11184005-11184055	AG09319	gingival:	n/a
41	chr12:11174898-11174948	SK-N-MC	brain:	n/a
42	chr12:11244899-11244949	SAEC	small airway:	n/a
43	chr12:11184149-11184199	ovcar-3	ovarian:	n/a
44	chr12:11184149-11184199	AG10803	skin:	n/a
45	chr12:11216351-11216401	HCM	heart:	n/a
46	chr12:11184347-11184397	PrEC	prostate:	n/a
47	chr12:11176574-11176624	GM06990	blood:	n/a
48	chr12:11216351-11216401	Hela-S3	cervix:	n/a
49	chr12:11244899-11244949	NHBE	bronchial:	n/a
50	chr12:11244899-11244949	HL-60	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr12:11157746..11159406-chr12:11165545..11167423,2	K562	blood:
2	chr12:11169301..11171201-chr12:11322573..11325255,2	MCF-7	breast:
3	chr12:11158423..11160257-chr12:11164352..11165951,2	MCF-7	breast:
4	chr12:11153714..11156559-chr12:11162296..11164278,2	MCF-7	breast:
5	chr12:11237724..11239418-chr12:11252570..11254241,2	MCF-7	breast:
6	chr12:11210669..11211248-chr5:109800405..109801099,2	MCF-7	breast:
7	chr12:11271454..11274346-chr12:11279643..11282306,2	MCF-7	breast:
8	chr12:11253040..11255708-chr12:11259363..11262255,2	K562	blood:
9	chr12:11237724..11239418-chr12:11252570..11254241,2	MCF-7	breast:
10	chr12:11009323..11011109-chr12:11168207..11170860,2	K562	blood:
11	chr12:11253040..11255708-chr12:11259363..11262255,2	K562	blood:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRH1-1	chr12:11199612-11199787	NONHSAT026916
2	lnc-PRH1-1	chr12:11187381-11187484	NR_037918
3	lnc-TAS2R43-1	chr12:11229368-11231770	NONHSAT026918
4	lnc-PRH1-1	chr12:11273435-11273779	NONHSAT026920
5	lnc-TAS2R46-1	chr12:11200931-11201855	NONHSAT026917
6	lnc-PRH1-1	chr12:11273609-11273779	NONHSAT026916
7	lnc-PRH1-1	chr12:11199619-11199787	NONHSAT026907
8	lnc-PRH1-1	chr12:11199619-11199640	NONHSAT026908
9	lnc-TAS2R43-1	chr12:11229915-11230841	NONHSAT140056
10	lnc-PRH1-1	chr12:11187381-11187484	NONHSAT026912
11	lnc-PRH1-1	chr12:11199619-11199736	NONHSAT026915
12	lnc-PRH1-1	chr12:11199619-11199713	NONHSAT026914
13	lnc-PRH1-1	chr12:11199619-11199787	NR_037918
14	lnc-PRH1-1	chr12:11199619-11199787	NONHSAT026912

No data

Variant related genes	Relation type
TAS2R46	TF binding region
TAS2R19	TF binding region
TAS2R31	TF binding region
ENSG00000256400	TF binding region
ENSG00000268301	TF binding region
PRR4	TF binding region
TAS2R63P	TF binding region
TAS2R43	TF binding region
TAS2R64P	TF binding region
TAS2R46	CpG island
TAS2R19	CpG island
TAS2R31	CpG island
ENSG00000256400	CpG island
ENSG00000268301	CpG island
PRR4	CpG island
TAS2R63P	CpG island
TAS2R43	CpG island
TAS2R64P	CpG island
ENSG00000212127	chromatin interactions
ENSG00000256712	chromatin interactions
ENSG00000111215	chromatin interactions
ENSG00000256537	chromatin interactions

Extended variants
information (count: 6266 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:6266 , 50 per page) page: 1 2 3 4 5 6 7 ... 126

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs375299536	chr12:11161163-11161164	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs529164774	chr12:11161171-11161172	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs201461637	chr12:11161172-11161173	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs368623756	chr12:11161176-11161177	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs72475458	chr12:11161202-11161203	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs187722733	chr12:11161216-11161217	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs560323863	chr12:11161219-11161220	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs66945954	chr12:11161227-11161228	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs150202369	chr12:11161230-11161231	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs192910330	chr12:11161273-11161274	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs527329698	chr12:11161285-11161286	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs146078990	chr12:11161315-11161316	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs7133669	chr12:11161343-11161344	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs567190363	chr12:11161346-11161347	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs111422775	chr12:11161378-11161379	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs7303382	chr12:11161382-11161383	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs7302419	chr12:11161385-11161386	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs112377198	chr12:11161396-11161397	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs557780209	chr12:11161422-11161423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs36104587	chr12:11161448-11161449	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs34292055	chr12:11161478-11161479	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs34211071	chr12:11161483-11161484	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs573905779	chr12:11161490-11161491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs35653945	chr12:11161496-11161497	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs562718777	chr12:11161504-11161505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs147181236	chr12:11161606-11161607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs545222432	chr12:11161622-11161623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs200849202	chr12:11161630-11161631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs72120591	chr12:11161632-11161633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs183663001	chr12:11161648-11161649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs67443370	chr12:11161663-11161664	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs545316980	chr12:11161667-11161668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs67420003	chr12:11161675-11161676	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs34179102	chr12:11161717-11161718	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs35977481	chr12:11161766-11161767	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs118035012	chr12:11161772-11161773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs35941350	chr12:11161784-11161785	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs538099165	chr12:11161808-11161809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs138840044	chr12:11161811-11161812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs28414974	chr12:11161817-11161818	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs28569398	chr12:11161838-11161839	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs534008381	chr12:11161898-11161899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs142835168	chr12:11161899-11161900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs202126563	chr12:11161915-11161916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs28654530	chr12:11161936-11161937	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs12366595	chr12:11161948-11161949	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs28498385	chr12:11161976-11161977	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs147430824	chr12:11161991-11161992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs28630880	chr12:11162014-11162015	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs553857042	chr12:11162084-11162085	Weak transcription	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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Bipolar disorder	19114987	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD

Chromatin state (count:1411 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

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	chr12:11129200-11167600	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr12:11134800-11166800	Weak transcription	NHDF-Ad	bronchial
6	chr12:11135200-11162200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr12:11136400-11180200	Weak transcription	Primary T cells fromperipheralblood	blood
8	chr12:11136600-11180200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
9	chr12:11136600-11196400	Weak transcription	Primary T helper cells PMA-I stimulated	--
10	chr12:11137400-11203000	Weak transcription	Hela-S3	cervix
11	chr12:11143400-11167600	Weak transcription	Fetal Intestine Small	intestine
12	chr12:11143400-11178800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr12:11145400-11177600	Weak transcription	Primary monocytes fromperipheralblood	blood
14	chr12:11146200-11167400	Weak transcription	Fetal Intestine Large	intestine
15	chr12:11147000-11165200	Weak transcription	Esophagus	oesophagus
16	chr12:11147000-11166400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
17	chr12:11147000-11168400	Weak transcription	Liver	Liver
18	chr12:11147000-11178600	Weak transcription	Fetal Stomach	stomach
19	chr12:11147000-11185400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr12:11147200-11168600	Weak transcription	Spleen	Spleen
21	chr12:11147200-11169200	Weak transcription	Skeletal Muscle Female	skeletal muscle
22	chr12:11147200-11171200	Weak transcription	Primary hematopoietic stem cells	blood
23	chr12:11147200-11176200	Weak transcription	Aorta	Aorta
24	chr12:11147200-11180400	Weak transcription	Pancreas	Pancrea
25	chr12:11148400-11178200	Weak transcription	Dnd41	blood
26	chr12:11149000-11168600	Weak transcription	Left Ventricle	heart
27	chr12:11154000-11169000	Weak transcription	Primary T cells from cord blood	blood
28	chr12:11154200-11167400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr12:11154200-11168000	Weak transcription	Fetal Muscle Leg	muscle
30	chr12:11154200-11174200	Weak transcription	Primary B cells from cord blood	blood
31	chr12:11154200-11178000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr12:11154200-11178200	Weak transcription	A549	lung
33	chr12:11154200-11178800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr12:11154400-11168000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr12:11159400-11168600	Weak transcription	Gastric	stomach
36	chr12:11159400-11182000	Weak transcription	NHEK	skin
37	chr12:11159600-11178200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
38	chr12:11160400-11163800	Weak transcription	Psoas Muscle	Psoas
39	chr12:11160800-11165800	Weak transcription	NH-A	brain
40	chr12:11161000-11161400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr12:11161000-11161400	ZNF genes & repeats	Fetal Kidney	kidney
42	chr12:11161400-11178200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr12:11161400-11179200	Weak transcription	Fetal Kidney	kidney
44	chr12:11162200-11162600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr12:11162400-11172800	Weak transcription	Fetal Brain Female	brain
46	chr12:11162600-11167800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr12:11163400-11177600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr12:11163400-11178000	Weak transcription	GM12878-XiMat	blood
49	chr12:11163600-11178800	Weak transcription	Ovary	ovary
50	chr12:11163800-11164000	Enhancers	Brain Substantia Nigra	brain

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