Variant report

Variant	esv21271
Chromosome Location	chr12:11142157-11169458
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:88)
CpG islands
(count:368)
Chromatin interactive
region (count:10)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:88 , 50 per page) page: 1 2

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	BHLHE40	chr12:11168360-11168714	HepG2	liver:	n/a	n/a
3	BRCA1	chr12:11168480-11168660	HepG2	liver:	n/a	n/a
4	CEBPB	chr12:11167458-11167736	HepG2	liver:	n/a	chr12:11167582-11167593
5	CEBPB	chr12:11148042-11148079	K562	blood:	n/a	n/a
6	CTCF	chr12:11169160-11169310	Caco-2	colon:	n/a	n/a
7	CTCF	chr12:11143647-11143668	GM13977	blood:	n/a	n/a
8	CTCF	chr12:11169160-11169310	HEK293	kidney:	n/a	n/a
9	CTCF	chr12:11169160-11169310	HepG2	liver:	n/a	n/a
10	CTCF	chr12:11147020-11147170	GM12869	blood:	n/a	n/a
11	CTCF	chr12:11168980-11169130	HAc	cerebellar:	n/a	n/a
12	CTCF	chr12:11169080-11169230	RPTEC	kidney:	n/a	n/a
13	E2F4	chr12:11152173-11152390	MCF10A-Er-Src	breast:	n/a	n/a
14	E2F4	chr12:11155484-11155547	MCF10A-Er-Src	breast:	n/a	n/a
15	ELF1	chr12:11168373-11168750	HepG2	liver:	n/a	n/a
16	EP300	chr12:11167186-11167211	K562	blood:	n/a	n/a
17	EP300	chr12:11168480-11168651	HepG2	liver:	n/a	n/a
18	EP300	chr12:11168317-11168866	HepG2	liver:	n/a	n/a
19	EP300	chr12:11168276-11168877	HepG2	liver:	n/a	n/a
20	FOXA1	chr12:11168275-11168843	HepG2	liver:	n/a	n/a
21	FOXA1	chr12:11168229-11168882	HepG2	liver:	n/a	n/a
22	FOXA1	chr12:11168099-11168858	HepG2	liver:	n/a	n/a
23	FOXA1	chr12:11168230-11168849	HepG2	liver:	n/a	n/a
24	FOXA2	chr12:11168394-11168826	HepG2	liver:	n/a	n/a
25	GATA2	chr12:11168114-11168760	HUVEC	blood vessel:	n/a	n/a
26	GATA3	chr12:11143062-11143262	SH-SY5Y	brain:	n/a	n/a
27	HDAC2	chr12:11168257-11168879	HepG2	liver:	n/a	n/a
28	HDAC2	chr12:11168351-11168795	HepG2	liver:	n/a	n/a
29	HEY1	chr12:11168466-11168892	HepG2	liver:	n/a	n/a
30	HNF4A	chr12:11168343-11168835	HepG2	liver:	n/a	chr12:11168634-11168649
31	HNF4A	chr12:11168259-11168819	HepG2	liver:	n/a	chr12:11168634-11168649
32	HNF4G	chr12:11168264-11168911	HepG2	liver:	n/a	n/a
33	HNF4G	chr12:11168316-11168857	HepG2	liver:	n/a	n/a
34	JUND	chr12:11166774-11167165	HepG2	liver:	n/a	chr12:11166993-11167004
35	MAFK	chr12:11162847-11162877	HepG2	liver:	n/a	n/a
36	MAFK	chr12:11152587-11152722	IMR90	lung:	n/a	n/a
37	MAFK	chr12:11152481-11152777	HepG2	liver:	n/a	n/a
38	MAFK	chr12:11168515-11168781	HepG2	liver:	n/a	n/a
39	MAX	chr12:11146604-11146792	NB4	blood:	n/a	chr12:11146721-11146731
40	MAZ	chr12:11168408-11168578	HepG2	liver:	n/a	n/a
41	MBD4	chr12:11168239-11168837	HepG2	liver:	n/a	n/a
42	MBD4	chr12:11168355-11168882	HepG2	liver:	n/a	n/a
43	MYBL2	chr12:11168286-11168895	HepG2	liver:	n/a	n/a
44	MYBL2	chr12:11168220-11168823	HepG2	liver:	n/a	n/a
45	MYC	chr12:11168686-11168718	HepG2	liver:	n/a	n/a
46	MYC	chr12:11168616-11168683	HepG2	liver:	n/a	n/a
47	NFIC	chr12:11168427-11168789	HepG2	liver:	n/a	n/a
48	NFIC	chr12:11168177-11168831	HepG2	liver:	n/a	n/a
49	NFYA	chr12:11164861-11165030	GM12878	blood:	n/a	n/a
50	NFYB	chr12:11161436-11161555	GM12878	blood:	n/a	n/a

(count:368 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:11151622-11151672	GM12891	blood:	n/a
2	chr12:11151522-11151572	HCT-116	colon:	n/a
3	chr12:11151622-11151672	GM12891	blood:	n/a
4	chr12:11151522-11151572	HCT-116	colon:	n/a
5	chr12:11151478-11151528	U87	brain:	n/a
6	chr12:11151622-11151672	T-47D	breast:	n/a
7	chr12:11151478-11151528	CMK	blood:	n/a
8	chr12:11151522-11151572	Jurkat	blood:	n/a
9	chr12:11151224-11151274	HMEC	breast:	n/a
10	chr12:11149362-11149412	SKMC	muscle:	n/a
11	chr12:11151522-11151572	IMR90	lung:	fetal
12	chr12:11149362-11149412	NT2-D1	testis:	n/a
13	chr12:11149362-11149412	Hela-S3	cervix:	n/a
14	chr12:11151478-11151528	IMR90	lung:	fetal
15	chr12:11151430-11151480	Caco-2	colon:	n/a
16	chr12:11149362-11149412	U87	brain:	n/a
17	chr12:11151522-11151572	Caco-2	colon:	n/a
18	chr12:11151430-11151480	HEK293	kidney:	embryo
19	chr12:11151478-11151528	HCT-116	colon:	n/a
20	chr12:11151478-11151528	HCM	heart:	n/a
21	chr12:11151430-11151480	GM12878	blood:	n/a
22	chr12:11151478-11151528	BJ	skin:	n/a
23	chr12:11151622-11151672	HCM	heart:	n/a
24	chr12:11151478-11151528	RPTEC	kidney:	n/a
25	chr12:11151478-11151528	GM06990	blood:	n/a
26	chr12:11151622-11151672	AG09309	skin:	n/a
27	chr12:11151522-11151572	HIPEpiC	eye:	n/a
28	chr12:11151478-11151528	HepG2	liver:	n/a
29	chr12:11151224-11151274	PrEC	prostate:	n/a
30	chr12:11151224-11151274	AG04450	lung:	fetal
31	chr12:11151224-11151274	HRE	kidney:	n/a
32	chr12:11151622-11151672	HRPEpiC	eye:	n/a
33	chr12:11149362-11149412	HMEC	breast:	n/a
34	chr12:11149362-11149412	Hepatocyte	liver:	n/a
35	chr12:11151478-11151528	GM19239	blood:	n/a
36	chr12:11151430-11151480	IMR90	lung:	fetal
37	chr12:11151478-11151528	ECC-1	luminal epithelium:	n/a
38	chr12:11151522-11151572	NH-A	brain:	n/a
39	chr12:11151522-11151572	SK-N-MC	brain:	n/a
40	chr12:11151522-11151572	ProgFib	skin:	n/a
41	chr12:11151430-11151480	AG04450	lung:	fetal
42	chr12:11151430-11151480	CMK	blood:	n/a
43	chr12:11151622-11151672	A549	lung:	n/a
44	chr12:11151622-11151672	MCF10A-Er-Src	breast:	n/a
45	chr12:11149362-11149412	AG09309	skin:	n/a
46	chr12:11151430-11151480	AG10803	skin:	n/a
47	chr12:11151622-11151672	Caco-2	colon:	n/a
48	chr12:11151478-11151528	HRCEpiC	kidney:	n/a
49	chr12:11151478-11151528	T-47D	breast:	n/a
50	chr12:11151622-11151672	AG10803	skin:	n/a

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

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

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRH1-1	chr12:11158533-11158868	NONHSAT026915

No data

Variant related genes	Relation type
TAS2R20	TF binding region
TAS2R50	TF binding region
TAS2R20	CpG island
TAS2R50	CpG island
ENSG00000256712	chromatin interactions
ENSG00000256537	chromatin interactions
ENSG00000212127	chromatin interactions
ENSG00000111215	chromatin interactions

Extended variants
information (count: 1087 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:1087 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538596208	chr12:11142177-11142178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs74062416	chr12:11142178-11142179	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs11054136	chr12:11142222-11142223	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs540908855	chr12:11142225-11142226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs554103804	chr12:11142257-11142258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs11054137	chr12:11142306-11142307	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs111569284	chr12:11142360-11142361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs7489266	chr12:11142370-11142371	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs531602175	chr12:11142373-11142374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs10772400	chr12:11142376-11142377	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs11054138	chr12:11142481-11142482	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs527625766	chr12:11142483-11142484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs58064634	chr12:11142497-11142498	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs79407772	chr12:11142511-11142512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs529879849	chr12:11142573-11142574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs549912369	chr12:11142577-11142578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs147997671	chr12:11142578-11142579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs376761963	chr12:11142595-11142596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs143545430	chr12:11142627-11142628	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs558624068	chr12:11142642-11142643	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs565652610	chr12:11142655-11142656	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs10772401	chr12:11142656-11142657	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs550356253	chr12:11142668-11142669	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs10772402	chr12:11142675-11142676	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs10772403	chr12:11142682-11142683	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs147286077	chr12:11142695-11142696	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs556338405	chr12:11142716-11142717	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs369897589	chr12:11142736-11142737	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs10845266	chr12:11142742-11142743	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs139251644	chr12:11142771-11142772	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs545082883	chr12:11142790-11142791	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs4270005	chr12:11142797-11142798	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs572377742	chr12:11142801-11142802	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs563647143	chr12:11142883-11142884	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs557248620	chr12:11142886-11142887	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs561194890	chr12:11142942-11142943	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs529918461	chr12:11142945-11142946	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs368843841	chr12:11142974-11142975	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs550046856	chr12:11143012-11143013	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs563460819	chr12:11143067-11143068	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs532277302	chr12:11143080-11143081	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs552225581	chr12:11143117-11143118	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs10845267	chr12:11143121-11143122	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs534572030	chr12:11143158-11143159	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs545403536	chr12:11143162-11143163	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs547780546	chr12:11143180-11143181	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs567999356	chr12:11143207-11143208	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs12296784	chr12:11143223-11143224	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs537980276	chr12:11143248-11143249	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs12305080	chr12:11143251-11143252	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:102)

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
Ovarian clear cell carcinoma	21343371	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:393 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:11095200-11148800	Weak transcription	HepG2	liver
2	chr12:11111800-11142800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr12:11114000-11149200	Weak transcription	GM12878-XiMat	blood
4	chr12:11114400-11180200	Weak transcription	Primary B cells from peripheral blood	blood
5	chr12:11114600-11142800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr12:11114600-11146400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
7	chr12:11114600-11146800	Weak transcription	Ovary	ovary
8	chr12:11121800-11142800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr12:11122000-11142600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr12:11122000-11146200	Weak transcription	Left Ventricle	heart
11	chr12:11122000-11170200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr12:11122200-11168000	Weak transcription	HUVEC	blood vessel
13	chr12:11126400-11142800	Weak transcription	Primary B cells from cord blood	blood
14	chr12:11126400-11143000	Weak transcription	HSMM	muscle
15	chr12:11128200-11142800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr12:11129200-11167600	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr12:11132000-11154800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr12:11132400-11146200	Weak transcription	Adipose Nuclei	Adipose
19	chr12:11133800-11142600	Weak transcription	Brain Substantia Nigra	brain
20	chr12:11134000-11142800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr12:11134800-11166800	Weak transcription	NHDF-Ad	bronchial
22	chr12:11135200-11162200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr12:11135600-11143200	Weak transcription	Fetal Lung	lung
24	chr12:11135600-11146000	Weak transcription	Stomach Smooth Muscle	stomach
25	chr12:11136400-11142600	Weak transcription	Primary hematopoietic stem cells	blood
26	chr12:11136400-11146600	Weak transcription	Aorta	Aorta
27	chr12:11136400-11146600	Weak transcription	Lung	lung
28	chr12:11136400-11180200	Weak transcription	Primary T cells fromperipheralblood	blood
29	chr12:11136600-11142800	Weak transcription	Dnd41	blood
30	chr12:11136600-11143400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
31	chr12:11136600-11153600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
32	chr12:11136600-11180200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
33	chr12:11136600-11196400	Weak transcription	Primary T helper cells PMA-I stimulated	--
34	chr12:11137400-11203000	Weak transcription	Hela-S3	cervix
35	chr12:11139000-11149000	Weak transcription	HUES64 Cell Line	embryonic stem cell
36	chr12:11140200-11146600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr12:11140800-11152800	Weak transcription	Fetal Thymus	thymus
38	chr12:11141600-11146400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr12:11141800-11142600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr12:11141800-11148200	Weak transcription	Primary T helper cells fromperipheralblood	blood
41	chr12:11142200-11143200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr12:11142200-11146600	Weak transcription	Esophagus	oesophagus
43	chr12:11142200-11151200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
44	chr12:11142200-11153400	Weak transcription	Rectal Smooth Muscle	rectum
45	chr12:11142400-11142600	Weak transcription	Primary T cells from cord blood	blood
46	chr12:11142400-11143000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
47	chr12:11142400-11143000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr12:11142400-11146200	Weak transcription	Fetal Heart	heart
49	chr12:11142600-11142800	Strong transcription	Primary hematopoietic stem cells	blood
50	chr12:11142600-11142800	Weak transcription	Duodenum Mucosa	Duodenum

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