Variant report

Variant	nsv436149
Chromosome Location	chr12:11183745-11251095
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:199)
CpG islands
(count:610)
Chromatin interactive
region (count:2)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:199 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:11224069-11224255	HepG2	liver:	n/a	n/a
2	ATF2	chr12:11237956-11238445	GM12878	blood:	n/a	n/a
3	ATF2	chr12:11238009-11238486	GM12878	blood:	n/a	n/a
4	BATF	chr12:11186631-11186911	GM12878	blood:	n/a	n/a
5	BATF	chr12:11238084-11238352	GM12878	blood:	n/a	n/a
6	BATF	chr12:11216721-11217010	GM12878	blood:	n/a	n/a
7	BATF	chr12:11225254-11225547	GM12878	blood:	n/a	n/a
8	BATF	chr12:11247547-11247827	GM12878	blood:	n/a	n/a
9	BATF	chr12:11247482-11247799	GM12878	blood:	n/a	n/a
10	BATF	chr12:11238012-11238373	GM12878	blood:	n/a	n/a
11	BATF	chr12:11228218-11228560	GM12878	blood:	n/a	n/a
12	BATF	chr12:11186566-11186883	GM12878	blood:	n/a	n/a
13	BCL11A	chr12:11247500-11247829	GM12878	blood:	n/a	n/a
14	BCL11A	chr12:11238061-11238356	GM12878	blood:	n/a	chr12:11238263-11238272
15	BCL11A	chr12:11228248-11228517	GM12878	blood:	n/a	n/a
16	BCL11A	chr12:11186584-11186913	GM12878	blood:	n/a	n/a
17	BHLHE40	chr12:11228293-11228667	GM12878	blood:	n/a	n/a
18	CEBPB	chr12:11222658-11222813	HepG2	liver:	n/a	n/a
19	CEBPB	chr12:11223987-11224332	HepG2	liver:	n/a	n/a
20	CEBPB	chr12:11226186-11226481	HepG2	liver:	n/a	n/a
21	CHD2	chr12:11238132-11238304	GM12878	blood:	n/a	n/a
22	CTCF	chr12:11209700-11209850	MCF-7	breast:	n/a	n/a
23	CTCF	chr12:11247641-11247704	GM20000	blood:	n/a	n/a
24	CTCF	chr12:11206452-11206523	Kidney_OC	kidney:	n/a	n/a
25	CTCF	chr12:11209820-11209970	HEK293	kidney:	n/a	n/a
26	CTCF	chr12:11186759-11186855	Spleen_OC	spleen:	n/a	n/a
27	CTCF	chr12:11230498-11230623	Lung_OC	lung:	n/a	n/a
28	CTCF	chr12:11187719-11187757	GM13976	blood:	n/a	n/a
29	CTCF	chr12:11209872-11209908	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr12:11207523-11207552	GM10248	blood:	n/a	n/a
31	CTCF	chr12:11209880-11210030	GM12872	blood:	n/a	n/a
32	CTCF	chr12:11248748-11248798	Kidney_OC	kidney:	n/a	n/a
33	CTCF	chr12:11209740-11209890	HepG2	liver:	n/a	n/a
34	CUX1	chr12:11238241-11238349	GM12878	blood:	n/a	n/a
35	E2F4	chr12:11220752-11221188	MCF10A-Er-Src	breast:	n/a	n/a
36	E2F4	chr12:11205619-11205672	MCF10A-Er-Src	breast:	n/a	n/a
37	EBF1	chr12:11226243-11226583	GM12878	blood:	n/a	chr12:11226441-11226451 chr12:11226441-11226450 chr12:11226439-11226452
38	ELK1	chr12:11201299-11201328	Hela-S3	cervix:	n/a	n/a
39	EP300	chr12:11223962-11224277	HepG2	liver:	n/a	n/a
40	EP300	chr12:11228364-11228516	GM12878	blood:	n/a	n/a
41	EP300	chr12:11238104-11238440	GM12878	blood:	n/a	n/a
42	EP300	chr12:11238133-11238438	GM12878	blood:	n/a	n/a
43	FOXA1	chr12:11223974-11224466	HepG2	liver:	n/a	n/a
44	FOXA1	chr12:11223940-11224452	HepG2	liver:	n/a	n/a
45	FOXA1	chr12:11223802-11224380	HepG2	liver:	n/a	n/a
46	FOXA1	chr12:11193258-11193557	HepG2	liver:	n/a	n/a
47	FOXA1	chr12:11223913-11224415	HepG2	liver:	n/a	n/a
48	FOXA2	chr12:11194068-11194219	HepG2	liver:	n/a	n/a
49	FOXA2	chr12:11223920-11224357	HepG2	liver:	n/a	n/a
50	FOXA2	chr12:11223986-11224245	A549	lung:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:11244939-11244989	A549	lung:	n/a
2	chr12:11244899-11244949	HPAEpiC	pulmonary alveolar:	n/a
3	chr12:11184149-11184199	LNCaP	prostate:	n/a
4	chr12:11184037-11184087	HCT-116	colon:	n/a
5	chr12:11244939-11244989	NT2-D1	testis:	n/a
6	chr12:11216351-11216401	LNCaP	prostate:	n/a
7	chr12:11185058-11185108	NT2-D1	testis:	n/a
8	chr12:11215083-11215133	NB4	blood:	n/a
9	chr12:11244899-11244949	K562	blood:	n/a
10	chr12:11185058-11185108	RPTEC	kidney:	n/a
11	chr12:11184415-11184465	ECC-1	luminal epithelium:	n/a
12	chr12:11185058-11185108	AG04449	skin:	fetal
13	chr12:11185058-11185108	HPAEpiC	pulmonary alveolar:	n/a
14	chr12:11215083-11215133	BE2_C	brain:	n/a
15	chr12:11184005-11184055	PFSK-1	brain:	n/a
16	chr12:11185058-11185108	AG09309	skin:	n/a
17	chr12:11184037-11184087	HUVEC	blood vessel:	n/a
18	chr12:11184005-11184055	GM12891	blood:	n/a
19	chr12:11184037-11184087	NT2-D1	testis:	n/a
20	chr12:11184005-11184055	IMR90	lung:	fetal
21	chr12:11184415-11184465	SAEC	small airway:	n/a
22	chr12:11216351-11216401	Caco-2	colon:	n/a
23	chr12:11184037-11184087	ovcar-3	ovarian:	n/a
24	chr12:11244939-11244989	MCF10A-Er-Src	breast:	n/a
25	chr12:11215083-11215133	HRPEpiC	eye:	n/a
26	chr12:11215083-11215133	GM12878	blood:	n/a
27	chr12:11184149-11184199	T-47D	breast:	n/a
28	chr12:11244899-11244949	GM06990	blood:	n/a
29	chr12:11185058-11185108	GM12891	blood:	n/a
30	chr12:11184005-11184055	HIPEpiC	eye:	n/a
31	chr12:11184415-11184465	HIPEpiC	eye:	n/a
32	chr12:11216351-11216401	NB4	blood:	n/a
33	chr12:11215083-11215133	IMR90	lung:	fetal
34	chr12:11215083-11215133	HIPEpiC	eye:	n/a
35	chr12:11184005-11184055	GM19239	blood:	n/a
36	chr12:11216351-11216401	HRPEpiC	eye:	n/a
37	chr12:11184037-11184087	HAEpiC	amniotic membrane:	n/a
38	chr12:11184037-11184087	HCM	heart:	n/a
39	chr12:11184037-11184087	CMK	blood:	n/a
40	chr12:11184415-11184465	ovcar-3	ovarian:	n/a
41	chr12:11184149-11184199	SK-N-SH_RA	brain:	n/a
42	chr12:11184347-11184397	HRCEpiC	kidney:	n/a
43	chr12:11215083-11215133	MCF10A-Er-Src	breast:	n/a
44	chr12:11184415-11184465	NHDF-neo	bronchial:	n/a
45	chr12:11244939-11244989	MCF-7	breast:	n/a
46	chr12:11184347-11184397	GM12892	blood:	n/a
47	chr12:11184005-11184055	NH-A	brain:	n/a
48	chr12:11184347-11184397	HPAEpiC	pulmonary alveolar:	n/a
49	chr12:11185058-11185108	SKMC	muscle:	n/a
50	chr12:11244899-11244949	HRPEpiC	eye:	n/a

(count:2 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:11237724..11239418-chr12:11252570..11254241,2	MCF-7	breast:
2	chr12:11210669..11211248-chr5:109800405..109801099,2	MCF-7	breast:

(count:12 , 50 per page) page: 1

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

No data

Variant related genes	Relation type
TAS2R46	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
TAS2R31	CpG island
ENSG00000256400	CpG island
ENSG00000268301	CpG island
PRR4	CpG island
TAS2R63P	CpG island
TAS2R43	CpG island
TAS2R64P	CpG island

Extended variants
information (count: 3896 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:3896 , 50 per page) page: 1 2 3 4 5 6 7 ... 78

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs371468130	chr12:11183745-11183746	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs72475489	chr12:11183752-11183753	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs374745478	chr12:11183754-11183755	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs577784067	chr12:11183779-11183780	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs143614038	chr12:11183802-11183803	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs370880260	chr12:11183805-11183806	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs375751426	chr12:11183811-11183812	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs560053968	chr12:11183820-11183821	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs367928248	chr12:11183829-11183830	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs372174270	chr12:11183831-11183832	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs10845295	chr12:11183832-11183833	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs367891409	chr12:11183863-11183864	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs370188504	chr12:11183895-11183896	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs542557800	chr12:11183898-11183899	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs201034225	chr12:11183920-11183921	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs562236488	chr12:11183934-11183935	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs371809022	chr12:11183941-11183942	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs552840755	chr12:11183946-11183947	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs73254862	chr12:11183977-11183978	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs375736512	chr12:11183980-11183981	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs550742960	chr12:11183981-11183982	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs564264735	chr12:11184047-11184048	Weak transcription ZNF genes & repeats Strong transcription	CpG island	2 gene(s)	Overlapped CNVs	n/a
23	rs533209722	chr12:11184061-11184062	Weak transcription ZNF genes & repeats Strong transcription	CpG island	2 gene(s)	Overlapped CNVs	n/a
24	rs374486657	chr12:11184088-11184089	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs145988287	chr12:11184108-11184109	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs568266189	chr12:11184116-11184117	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs566902777	chr12:11184138-11184139	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs10845296	chr12:11184140-11184141	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs547649472	chr12:11184149-11184150	Weak transcription ZNF genes & repeats Strong transcription	CpG island	2 gene(s)	Overlapped CNVs	n/a
30	rs569034251	chr12:11184150-11184151	Weak transcription ZNF genes & repeats Strong transcription	CpG island	2 gene(s)	Overlapped CNVs	n/a
31	rs538059514	chr12:11184157-11184158	Weak transcription ZNF genes & repeats Strong transcription	CpG island	2 gene(s)	Overlapped CNVs	n/a
32	rs184724248	chr12:11184168-11184169	Weak transcription ZNF genes & repeats Strong transcription	CpG island	2 gene(s)	Overlapped CNVs	n/a
33	rs189311532	chr12:11184169-11184170	Weak transcription ZNF genes & repeats Strong transcription	CpG island	2 gene(s)	Overlapped CNVs	n/a
34	rs138630191	chr12:11184176-11184177	Weak transcription ZNF genes & repeats Strong transcription	CpG island	2 gene(s)	Overlapped CNVs	n/a
35	rs553584091	chr12:11184187-11184188	Weak transcription ZNF genes & repeats Strong transcription	CpG island	2 gene(s)	Overlapped CNVs	n/a
36	rs182165838	chr12:11184268-11184269	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs186695742	chr12:11184308-11184309	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs77847958	chr12:11184347-11184348	Weak transcription ZNF genes & repeats Strong transcription	CpG island	2 gene(s)	Overlapped CNVs	n/a
39	rs562436022	chr12:11184411-11184412	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs575507084	chr12:11184433-11184434	Weak transcription Strong transcription	CpG island	2 gene(s)	Overlapped CNVs	n/a
41	rs189965332	chr12:11184453-11184454	Weak transcription Strong transcription	CpG island	2 gene(s)	Overlapped CNVs	n/a
42	rs564291062	chr12:11184475-11184476	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs533343579	chr12:11184494-11184495	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs35241999	chr12:11184504-11184505	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs560366570	chr12:11184520-11184521	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs556562263	chr12:11184548-11184549	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs7315079	chr12:11184565-11184566	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs549079469	chr12:11184584-11184585	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs56242278	chr12:11184594-11184595	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs538091939	chr12:11184665-11184666	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

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

Chromatin state (count:648 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:11136600-11196400	Weak transcription	Primary T helper cells PMA-I stimulated	--
2	chr12:11137400-11203000	Weak transcription	Hela-S3	cervix
3	chr12:11147000-11185400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr12:11166000-11192000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
5	chr12:11166200-11210000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr12:11166600-11199600	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr12:11167400-11201800	Weak transcription	Stomach Smooth Muscle	stomach
8	chr12:11168800-11201000	Weak transcription	Colon Smooth Muscle	Colon
9	chr12:11168800-11205800	Weak transcription	Osteobl	bone
10	chr12:11169400-11201600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr12:11169400-11219400	Weak transcription	HUVEC	blood vessel
12	chr12:11169800-11198800	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr12:11171000-11225600	Weak transcription	HSMMtube	muscle
14	chr12:11174400-11200800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr12:11174600-11192000	Weak transcription	Brain Angular Gyrus	brain
16	chr12:11175000-11204600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
17	chr12:11176400-11203000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr12:11176400-11211200	Weak transcription	Aorta	Aorta
19	chr12:11177000-11200200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
20	chr12:11177400-11187000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr12:11178400-11201000	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr12:11178400-11201000	Weak transcription	Brain Anterior Caudate	brain
23	chr12:11178400-11203400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
24	chr12:11178600-11191400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
25	chr12:11178800-11197400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr12:11179000-11185600	Weak transcription	Ovary	ovary
27	chr12:11179000-11190000	Weak transcription	Fetal Brain Female	brain
28	chr12:11179000-11191400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr12:11179000-11195200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
30	chr12:11179000-11198200	Weak transcription	Placenta	Placenta
31	chr12:11179000-11201000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr12:11179000-11203400	Weak transcription	Duodenum Smooth Muscle	Duodenum
33	chr12:11179000-11223800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr12:11179200-11190800	Weak transcription	Fetal Lung	lung
35	chr12:11179200-11203200	Weak transcription	Fetal Muscle Trunk	muscle
36	chr12:11179400-11185000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr12:11179400-11222000	Weak transcription	Fetal Kidney	kidney
38	chr12:11180200-11203200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr12:11180600-11191800	Weak transcription	Brain Hippocampus Middle	brain
40	chr12:11180600-11202600	Weak transcription	Cortex derived primary cultured neurospheres	brain
41	chr12:11181000-11184800	Weak transcription	Pancreas	Pancrea
42	chr12:11181000-11190800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr12:11181000-11196200	Weak transcription	Primary T helper cells fromperipheralblood	blood
44	chr12:11181000-11196800	Weak transcription	Adipose Nuclei	Adipose
45	chr12:11181000-11197000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr12:11181000-11197400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr12:11181000-11197400	Weak transcription	Rectal Mucosa Donor 29	rectum
48	chr12:11181000-11198800	Weak transcription	HepG2	liver
49	chr12:11181000-11199000	Weak transcription	Primary B cells from peripheral blood	blood
50	chr12:11181000-11201000	Weak transcription	Brain Cingulate Gyrus	brain

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