Variant report

Variant	esv3419217
Chromosome Location	chr11:67265931-67267818
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:32)
CpG islands
(count:183)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:32 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr11:67267736-67268107	Hela-S3	cervix:	n/a	n/a
2	POLR2A	chr11:67266350-67266498	HepG2	liver:	n/a	n/a
3	POLR2A	chr11:67265877-67266235	K562	blood:	n/a	n/a
4	POLR2A	chr11:67266136-67266292	Hela-S3	cervix:	n/a	n/a
5	POLR2A	chr11:67267429-67267435	K562	blood:	n/a	n/a
6	POLR2A	chr11:67267742-67268240	GM12878	blood:	n/a	n/a
7	POLR2A	chr11:67267084-67268162	A549	lung:	n/a	n/a
8	POLR2A	chr11:67267059-67268291	SK-N-MC	brain:	n/a	n/a
9	POLR2A	chr11:67267453-67267483	K562	blood:	n/a	n/a
10	POLR2A	chr11:67266197-67266209	K562	blood:	n/a	n/a
11	POLR2A	chr11:67267573-67267707	HepG2	liver:	n/a	n/a
12	POLR2A	chr11:67267512-67267533	K562	blood:	n/a	n/a
13	POLR2A	chr11:67267344-67267419	K562	blood:	n/a	n/a
14	POLR2A	chr11:67266300-67266631	K562	blood:	n/a	n/a
15	POLR2A	chr11:67266010-67266111	A549	lung:	n/a	n/a
16	POLR2A	chr11:67267656-67268060	GM12878	blood:	n/a	n/a
17	POLR2A	chr11:67266169-67266198	H1-hESC	embryonic stem cell:	n/a	n/a
18	POLR2A	chr11:67265968-67266531	SK-N-MC	brain:	n/a	n/a
19	POLR2A	chr11:67267317-67267488	K562	blood:	n/a	n/a
20	POLR2A	chr11:67267182-67267765	HL-60	blood:	n/a	n/a
21	POLR2A	chr11:67265699-67265955	K562	blood:	n/a	n/a
22	POLR2A	chr11:67267571-67267944	K562	blood:	n/a	n/a
23	POLR2A	chr11:67267765-67267932	A549	lung:	n/a	n/a
24	POLR2A	chr11:67267689-67268153	K562	blood:	n/a	n/a
25	POLR2A	chr11:67267219-67267263	Hela-S3	cervix:	n/a	n/a
26	POLR2A	chr11:67266261-67266282	K562	blood:	n/a	n/a
27	POLR2A	chr11:67266333-67266929	K562	blood:	n/a	n/a
28	POLR2A	chr11:67266109-67266157	H1-hESC	embryonic stem cell:	n/a	n/a
29	POLR2A	chr11:67267270-67268102	GM12878	blood:	n/a	n/a
30	POLR2A	chr11:67267404-67268085	K562	blood:	n/a	n/a
31	POLR2A	chr11:67267542-67267560	HepG2	liver:	n/a	n/a
32	STAT5A	chr11:67266317-67266873	GM12878	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:67266089-67266139	HRE	kidney:	n/a
2	chr11:67266128-67266178	H1-hESC	embryonic stem cell:	embryo
3	chr11:67266089-67266139	PrEC	prostate:	n/a
4	chr11:67266089-67266139	BJ	skin:	n/a
5	chr11:67266176-67266226	HUVEC	blood vessel:	n/a
6	chr11:67266128-67266178	BJ	skin:	n/a
7	chr11:67266128-67266178	K562	blood:	n/a
8	chr11:67266089-67266139	NB4	blood:	n/a
9	chr11:67266176-67266226	SKMC	muscle:	n/a
10	chr11:67266176-67266226	AG09309	skin:	n/a
11	chr11:67266176-67266226	ProgFib	skin:	n/a
12	chr11:67266089-67266139	AG04449	skin:	fetal
13	chr11:67266128-67266178	HNPCEpiC	eye:	n/a
14	chr11:67266128-67266178	NH-A	brain:	n/a
15	chr11:67266176-67266226	HRE	kidney:	n/a
16	chr11:67266089-67266139	HMEC	breast:	n/a
17	chr11:67266128-67266178	ProgFib	skin:	n/a
18	chr11:67266128-67266178	AG10803	skin:	n/a
19	chr11:67266128-67266178	HRE	kidney:	n/a
20	chr11:67266089-67266139	NHDF-neo	bronchial:	n/a
21	chr11:67266128-67266178	AG04449	skin:	fetal
22	chr11:67266089-67266139	AG04450	lung:	fetal
23	chr11:67266089-67266139	ProgFib	skin:	n/a
24	chr11:67266089-67266139	GM12892	blood:	n/a
25	chr11:67266089-67266139	GM12878	blood:	n/a
26	chr11:67266128-67266178	Caco-2	colon:	n/a
27	chr11:67266128-67266178	PANC-1	pancreas:	n/a
28	chr11:67266089-67266139	CMK	blood:	n/a
29	chr11:67266089-67266139	MCF-7	breast:	n/a
30	chr11:67266176-67266226	NH-A	brain:	n/a
31	chr11:67266128-67266178	HRPEpiC	eye:	n/a
32	chr11:67266176-67266226	HNPCEpiC	eye:	n/a
33	chr11:67266176-67266226	SK-N-SH	brain:	n/a
34	chr11:67266089-67266139	SAEC	small airway:	n/a
35	chr11:67266089-67266139	U87	brain:	n/a
36	chr11:67266128-67266178	AG04450	lung:	fetal
37	chr11:67266176-67266226	MCF10A-Er-Src	breast:	n/a
38	chr11:67266089-67266139	NT2-D1	testis:	n/a
39	chr11:67266089-67266139	MCF10A-Er-Src	breast:	n/a
40	chr11:67266089-67266139	SKMC	muscle:	n/a
41	chr11:67266128-67266178	HepG2	liver:	n/a
42	chr11:67266176-67266226	SK-N-SH_RA	brain:	n/a
43	chr11:67266176-67266226	AG10803	skin:	n/a
44	chr11:67266176-67266226	RPTEC	kidney:	n/a
45	chr11:67266128-67266178	HAEpiC	amniotic membrane:	n/a
46	chr11:67266176-67266226	PrEC	prostate:	n/a
47	chr11:67266128-67266178	HCM	heart:	n/a
48	chr11:67266176-67266226	HAEpiC	amniotic membrane:	n/a
49	chr11:67266128-67266178	GM19239	blood:	n/a
50	chr11:67266089-67266139	HCF	heart:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:67263850..67266105-chr11:67266792..67269183,3	MCF-7	breast:
2	chr11:67201761..67204037-chr11:67264926..67266855,2	K562	blood:
3	chr11:67263850..67266105-chr11:67266792..67269183,3	MCF-7	breast:
4	chr11:67161312..67163125-chr11:67265626..67268296,2	MCF-7	breast:
5	chr11:67266460..67268680-chr11:67274631..67276596,2	MCF-7	breast:
6	chr11:67249113..67250802-chr11:67267518..67269287,2	MCF-7	breast:

No data

Variant related genes	Relation type
PITPNM1	TF binding region
PITPNM1	CpG island
ENSG00000253024	chromatin interactions
ENSG00000110711	chromatin interactions
ENSG00000167797	chromatin interactions
ENSG00000255949	chromatin interactions
ENSG00000110697	chromatin interactions

Extended variants
information (count: 118 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:118 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs375911692	chr11:67265949-67265950	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs535664043	chr11:67265957-67265958	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs547575410	chr11:67265959-67265960	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs565981829	chr11:67266003-67266004	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs539788660	chr11:67266008-67266009	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs377280148	chr11:67266015-67266016	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs576415886	chr11:67266035-67266036	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs200868833	chr11:67266077-67266078	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs61749182	chr11:67266090-67266091	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs372455862	chr11:67266092-67266093	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs573761696	chr11:67266093-67266094	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs200449321	chr11:67266096-67266097	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs202168402	chr11:67266118-67266119	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs142903253	chr11:67266120-67266121	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs139654702	chr11:67266155-67266156	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs370369107	chr11:67266157-67266158	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs1551883	chr11:67266162-67266163	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs61755426	chr11:67266164-67266165	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs201664682	chr11:67266165-67266166	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs115377785	chr11:67266171-67266172	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs151117956	chr11:67266176-67266177	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs139703605	chr11:67266186-67266187	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs373396510	chr11:67266187-67266188	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs373983783	chr11:67266199-67266200	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs377079742	chr11:67266215-67266216	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs2276121	chr11:67266270-67266271	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs370162006	chr11:67266278-67266279	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs149766151	chr11:67266279-67266280	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs528951501	chr11:67266290-67266291	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs200367071	chr11:67266292-67266293	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs17847837	chr11:67266322-67266323	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs199607704	chr11:67266327-67266328	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs141123505	chr11:67266340-67266341	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs372614770	chr11:67266343-67266344	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs145158021	chr11:67266346-67266347	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs17847836	chr11:67266360-67266361	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs372256167	chr11:67266361-67266362	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs34341689	chr11:67266363-67266364	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs537467937	chr11:67266375-67266376	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs192293629	chr11:67266392-67266393	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs369254513	chr11:67266408-67266409	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs573696007	chr11:67266424-67266425	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs145780148	chr11:67266438-67266439	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs141637904	chr11:67266439-67266440	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs61731773	chr11:67266453-67266454	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs17847835	chr11:67266466-67266467	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs140488259	chr11:67266484-67266485	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs145713580	chr11:67266502-67266503	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs557654029	chr11:67266564-67266565	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs138190231	chr11:67266569-67266570	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Metanephric adenoma	20802469	CNVD
Chordoma	21602918	CNVD
Melanoma	18172304	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	21251322	CNVD
Lung cancer	19153074	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	22860045	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	21399695	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
small cell lung cancer	20016488	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:185 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67251000-67271000	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr11:67251400-67268000	Weak transcription	HSMMtube	muscle
3	chr11:67251400-67271200	Weak transcription	HSMM	muscle
4	chr11:67251400-67271400	Weak transcription	HUVEC	blood vessel
5	chr11:67251600-67268400	Weak transcription	NH-A	brain
6	chr11:67251600-67268600	Strong transcription	Fetal Intestine Small	intestine
7	chr11:67251600-67270600	Weak transcription	Fetal Heart	heart
8	chr11:67251600-67271400	Weak transcription	NHDF-Ad	bronchial
9	chr11:67252600-67270000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr11:67252600-67270200	Strong transcription	Fetal Stomach	stomach
11	chr11:67252600-67271600	Weak transcription	Psoas Muscle	Psoas
12	chr11:67252800-67270000	Weak transcription	Fetal Brain Male	brain
13	chr11:67252800-67271400	Weak transcription	Right Atrium	heart
14	chr11:67253800-67269600	Strong transcription	Cortex derived primary cultured neurospheres	brain
15	chr11:67254000-67268000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
16	chr11:67254000-67268000	Strong transcription	Brain Germinal Matrix	brain
17	chr11:67254000-67268000	Strong transcription	Monocytes-CD14+_RO01746	blood
18	chr11:67254000-67270000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr11:67254000-67270800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr11:67254000-67271000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr11:67254200-67266400	Strong transcription	Brain Inferior Temporal Lobe	brain
22	chr11:67254200-67266400	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr11:67254200-67268600	Strong transcription	Gastric	stomach
24	chr11:67254400-67268000	Strong transcription	Primary monocytes fromperipheralblood	blood
25	chr11:67254400-67268000	Strong transcription	Primary neutrophils fromperipheralblood	blood
26	chr11:67254400-67270600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr11:67254400-67271200	Weak transcription	K562	blood
28	chr11:67254600-67266000	Strong transcription	Left Ventricle	heart
29	chr11:67254600-67266800	Strong transcription	Primary T cells from cord blood	blood
30	chr11:67254600-67267000	Strong transcription	Fetal Brain Female	brain
31	chr11:67254600-67270600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
32	chr11:67254800-67267400	Strong transcription	Thymus	Thymus
33	chr11:67254800-67270800	Strong transcription	Duodenum Mucosa	Duodenum
34	chr11:67254800-67271000	Weak transcription	HepG2	liver
35	chr11:67255000-67268000	Strong transcription	Placenta Amnion	Placenta Amnion
36	chr11:67255800-67270200	Strong transcription	Dnd41	blood
37	chr11:67255800-67272000	Weak transcription	Fetal Kidney	kidney
38	chr11:67256000-67270400	Strong transcription	Primary B cells from peripheral blood	blood
39	chr11:67256400-67270800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr11:67256600-67267000	Strong transcription	HUES6 Cell Line	embryonic stem cell
41	chr11:67256600-67270200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
42	chr11:67256600-67270400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
43	chr11:67256600-67270600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
44	chr11:67257000-67270200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
45	chr11:67257200-67266400	Strong transcription	Brain Cingulate Gyrus	brain
46	chr11:67257200-67268000	Strong transcription	Primary T helper cells fromperipheralblood	blood
47	chr11:67257400-67267400	Strong transcription	Esophagus	oesophagus
48	chr11:67257400-67269800	Strong transcription	Primary T helper cells PMA-I stimulated	--
49	chr11:67257400-67270800	Strong transcription	Fetal Thymus	thymus
50	chr11:67257400-67270800	Strong transcription	Sigmoid Colon	Sigmoid Colon

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