Variant report

Variant	esv1819852
Chromosome Location	chr11:46971012-47064542
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:688)
CpG islands
(count:183)
Chromatin interactive
region (count:34)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:688 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:46999635-46999887	K562	blood:	n/a	n/a
2	ARID3A	chr11:47006385-47006912	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:47024831-47025538	K562	blood:	n/a	n/a
4	ARID3A	chr11:47026205-47026655	K562	blood:	n/a	n/a
5	ARID3A	chr11:47050001-47050005	K562	blood:	n/a	n/a
6	ARID3A	chr11:47027131-47027477	HepG2	liver:	n/a	n/a
7	ARID3A	chr11:47026311-47026723	HepG2	liver:	n/a	n/a
8	ATF1	chr11:47026214-47026689	K562	blood:	n/a	n/a
9	ATF1	chr11:47025100-47025431	K562	blood:	n/a	n/a
10	ATF1	chr11:46999565-46999720	K562	blood:	n/a	n/a
11	ATF1	chr11:47056675-47056990	K562	blood:	n/a	n/a
12	ATF1	chr11:47050378-47050512	K562	blood:	n/a	n/a
13	ATF1	chr11:47027111-47027303	K562	blood:	n/a	n/a
14	ATF2	chr11:47039423-47039895	GM12878	blood:	n/a	n/a
15	ATF2	chr11:46997734-46998178	GM12878	blood:	n/a	n/a
16	ATF2	chr11:46997613-46998189	GM12878	blood:	n/a	n/a
17	ATF2	chr11:47039487-47039885	GM12878	blood:	n/a	n/a
18	ATF3	chr11:47026167-47026559	K562	blood:	n/a	n/a
19	BACH1	chr11:46985406-46985820	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr11:46985399-46985791	K562	blood:	n/a	n/a
21	BATF	chr11:46997758-46998075	GM12878	blood:	n/a	n/a
22	BATF	chr11:46997692-46998117	GM12878	blood:	n/a	n/a
23	BATF	chr11:47039566-47039808	GM12878	blood:	n/a	n/a
24	BATF	chr11:47039455-47039820	GM12878	blood:	n/a	n/a
25	BATF	chr11:47042527-47042928	GM12878	blood:	n/a	n/a
26	BCL11A	chr11:46997716-46998141	GM12878	blood:	n/a	n/a
27	BCL3	chr11:46997723-46998149	GM12878	blood:	n/a	n/a
28	BCL3	chr11:47039486-47039818	GM12878	blood:	n/a	n/a
29	BCLAF1	chr11:46997594-46998229	GM12878	blood:	n/a	n/a
30	BCLAF1	chr11:47026145-47026721	K562	blood:	n/a	chr11:47026204-47026213 chr11:47026207-47026216
31	BDP1	chr11:46999782-47000178	Hela-S3	cervix:	n/a	n/a
32	BHLHE40	chr11:46997781-46998102	GM12878	blood:	n/a	n/a
33	BHLHE40	chr11:47025138-47025389	K562	blood:	n/a	n/a
34	BHLHE40	chr11:47039635-47039686	GM12878	blood:	n/a	n/a
35	BHLHE40	chr11:47026305-47026607	K562	blood:	n/a	n/a
36	BRCA1	chr11:47023516-47023556	GM12878	blood:	n/a	n/a
37	BRF1	chr11:46993894-46994223	Hela-S3	cervix:	n/a	n/a
38	BRF1	chr11:46973785-46974303	Hela-S3	cervix:	n/a	n/a
39	CBX3	chr11:47026119-47026742	K562	blood:	n/a	n/a
40	CCNT2	chr11:47026284-47026570	K562	blood:	n/a	n/a
41	CCNT2	chr11:47025042-47025436	K562	blood:	n/a	chr11:47025219-47025239
42	CEBPB	chr11:47063595-47063754	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr11:46999779-47000111	A549	lung:	n/a	chr11:46999942-46999955 chr11:46999942-46999953
44	CEBPB	chr11:47026277-47026671	HepG2	liver:	n/a	chr11:47026332-47026340
45	CEBPB	chr11:47026340-47026543	HepG2	liver:	n/a	n/a
46	CEBPB	chr11:46999832-47000043	K562	blood:	n/a	chr11:46999942-46999955 chr11:46999942-46999953
47	CEBPB	chr11:47026278-47026634	HepG2	liver:	n/a	chr11:47026332-47026340
48	CEBPB	chr11:47026110-47026657	K562	blood:	n/a	chr11:47026332-47026340
49	CEBPB	chr11:47050142-47050517	K562	blood:	n/a	chr11:47050243-47050254 chr11:47050243-47050254
50	CEBPB	chr11:46999754-47000093	IMR90	lung:	n/a	chr11:46999942-46999955 chr11:46999942-46999953

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:47024513-47024563	HNPCEpiC	eye:	n/a
2	chr11:47024513-47024563	GM12891	blood:	n/a
3	chr11:47024513-47024563	AoSMC	blood vessel:	n/a
4	chr11:47042656-47042706	SKMC	muscle:	n/a
5	chr11:47024513-47024563	AG09309	skin:	n/a
6	chr11:47042656-47042706	U87	brain:	n/a
7	chr11:46998965-46999015	HCPEpiC	choroid plexus:	n/a
8	chr11:47042656-47042706	AoSMC	blood vessel:	n/a
9	chr11:47024513-47024563	HCT-116	colon:	n/a
10	chr11:46998965-46999015	HCT-116	colon:	n/a
11	chr11:47042656-47042706	HCF	heart:	n/a
12	chr11:47042656-47042706	AG10803	skin:	n/a
13	chr11:46998965-46999015	NHBE	bronchial:	n/a
14	chr11:47024513-47024563	HRE	kidney:	n/a
15	chr11:47042656-47042706	HCM	heart:	n/a
16	chr11:46998965-46999015	NH-A	brain:	n/a
17	chr11:47024513-47024563	NHBE	bronchial:	n/a
18	chr11:47024513-47024563	HUVEC	blood vessel:	n/a
19	chr11:47042656-47042706	Jurkat	blood:	n/a
20	chr11:47024513-47024563	NH-A	brain:	n/a
21	chr11:47042656-47042706	GM12878	blood:	n/a
22	chr11:47024513-47024563	GM06990	blood:	n/a
23	chr11:47024513-47024563	A549	lung:	n/a
24	chr11:46998965-46999015	AG09319	gingival:	n/a
25	chr11:47042656-47042706	AG04450	lung:	fetal
26	chr11:47042656-47042706	HAEpiC	amniotic membrane:	n/a
27	chr11:47024513-47024563	SAEC	small airway:	n/a
28	chr11:47024513-47024563	GM19239	blood:	n/a
29	chr11:46998965-46999015	NB4	blood:	n/a
30	chr11:47024513-47024563	BJ	skin:	n/a
31	chr11:47024513-47024563	HCPEpiC	choroid plexus:	n/a
32	chr11:47024513-47024563	SKMC	muscle:	n/a
33	chr11:46998965-46999015	RPTEC	kidney:	n/a
34	chr11:47024513-47024563	SK-N-SH_RA	brain:	n/a
35	chr11:47024513-47024563	AG04450	lung:	fetal
36	chr11:47024513-47024563	NHDF-neo	bronchial:	n/a
37	chr11:46998965-46999015	PrEC	prostate:	n/a
38	chr11:46998965-46999015	U87	brain:	n/a
39	chr11:46998965-46999015	BJ	skin:	n/a
40	chr11:47024513-47024563	HCM	heart:	n/a
41	chr11:47024513-47024563	AG09319	gingival:	n/a
42	chr11:47042656-47042706	AG04449	skin:	fetal
43	chr11:46998965-46999015	HUVEC	blood vessel:	n/a
44	chr11:47024513-47024563	HEK293	kidney:	embryo
45	chr11:46998965-46999015	MCF10A-Er-Src	breast:	n/a
46	chr11:47042656-47042706	SK-N-SH_RA	brain:	n/a
47	chr11:47024513-47024563	HCF	heart:	n/a
48	chr11:47042656-47042706	HRPEpiC	eye:	n/a
49	chr11:46998965-46999015	T-47D	breast:	n/a
50	chr11:47024513-47024563	PFSK-1	brain:	n/a

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:47043884..47045816-chr11:47048717..47051419,2	K562	blood:
2	chr11:46993954..46995802-chr11:46998173..47000292,2	K562	blood:
3	chr11:46969609..46972208-chr11:46975485..46977882,2	MCF-7	breast:
4	chr11:46970587..46973185-chr11:47182326..47184987,2	MCF-7	breast:
5	chr11:46867290..46869103-chr11:47036825..47039117,2	MCF-7	breast:
6	chr11:47002891..47005569-chr11:47007322..47009966,3	MCF-7	breast:
7	chr11:47041841..47045384-chr11:47049919..47053840,3	K562	blood:
8	chr11:47008492..47009359-chr11:47174486..47175315,3	MCF-7	breast:
9	chr11:46983981..46985605-chr11:46987399..46989528,2	K562	blood:
10	chr11:47002186..47004329-chr11:47006169..47008025,2	K562	blood:
11	chr11:47019891..47022627-chr11:47029015..47030790,2	MCF-7	breast:
12	chr11:46968606..46971099-chr11:46973035..46974708,2	MCF-7	breast:
13	chr11:46969609..46972208-chr11:46975485..46977882,2	MCF-7	breast:
14	chr11:47002891..47005569-chr11:47007322..47009966,3	MCF-7	breast:
15	chr11:47021984..47023996-chr11:47024940..47028464,4	K562	blood:
16	chr11:46938649..46940580-chr11:46969206..46971125,2	MCF-7	breast:
17	chr11:46993954..46995802-chr11:46998173..47000292,2	K562	blood:
18	chr11:47026518..47028545-chr11:47034520..47036509,2	K562	blood:
19	chr11:47025033..47028147-chr11:47030692..47034126,5	K562	blood:
20	chr11:46963455..46964222-chr11:47006540..47007193,2	MCF-7	breast:
21	chr11:46969116..46970652-chr11:46978768..46980520,2	K562	blood:
22	chr11:46968606..46971099-chr11:46973035..46974708,2	MCF-7	breast:
23	chr11:47048648..47051358-chr11:47053601..47056863,3	K562	blood:
24	chr11:47002186..47004329-chr11:47006169..47008025,2	K562	blood:
25	chr11:47048648..47051358-chr11:47053601..47056863,3	K562	blood:
26	chr11:46941107..46942004-chr11:47044229..47044846,2	K562	blood:
27	chr11:47021984..47023996-chr11:47024940..47028464,4	K562	blood:
28	chr11:46964914..46967746-chr11:46969560..46971972,2	K562	blood:
29	chr11:47041841..47045384-chr11:47049919..47053840,3	K562	blood:
30	chr11:46983981..46985605-chr11:46987399..46989528,2	K562	blood:
31	chr11:47025033..47028147-chr11:47030692..47034126,5	K562	blood:
32	chr11:47019891..47022627-chr11:47029015..47030790,2	MCF-7	breast:
33	chr11:47026518..47028545-chr11:47034520..47036509,2	K562	blood:
34	chr11:47043884..47045816-chr11:47048717..47051419,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000271350	TF binding region
ENSG00000271350	CpG island
ENSG00000175216	chromatin interactions
ENSG00000247675	chromatin interactions
ENSG00000134569	chromatin interactions

Extended variants
information (count: 2667 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:2667 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577695856	chr11:46971136-46971137	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs368835754	chr11:46971137-46971138	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs565808371	chr11:46971219-46971220	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs150952576	chr11:46971220-46971221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs11329243	chr11:46971221-46971222	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs34668154	chr11:46971229-46971230	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs76856843	chr11:46971235-46971236	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs398015976	chr11:46971236-46971237	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs369490799	chr11:46971252-46971253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs536023710	chr11:46971276-46971277	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs543518104	chr11:46971310-46971311	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs563917152	chr11:46971338-46971339	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs572490683	chr11:46971348-46971349	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs544622649	chr11:46971439-46971440	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs187847597	chr11:46971440-46971441	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs374105537	chr11:46971466-46971467	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs549707121	chr11:46971470-46971471	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs544441427	chr11:46971471-46971472	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs7938169	chr11:46971539-46971540	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs192771266	chr11:46971549-46971550	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs375685415	chr11:46971575-46971576	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs369884604	chr11:46971630-46971631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs530343979	chr11:46971643-46971644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs185026605	chr11:46971727-46971728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs11441023	chr11:46971742-46971743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs184336274	chr11:46971780-46971781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs528507995	chr11:46971786-46971787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs551451766	chr11:46971822-46971823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs571596237	chr11:46971882-46971883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs113342680	chr11:46971894-46971895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs34096686	chr11:46971905-46971906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs552545127	chr11:46971908-46971909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs569212256	chr11:46971914-46971915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs538327798	chr11:46971917-46971918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs554812601	chr11:46971945-46971946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs567102354	chr11:46972019-46972020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs373277824	chr11:46972020-46972021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs189479851	chr11:46972050-46972051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs192530520	chr11:46972076-46972077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs184520190	chr11:46972098-46972099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs201666667	chr11:46972158-46972159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs199957475	chr11:46972165-46972166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs572826146	chr11:46972257-46972258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs544633695	chr11:46972288-46972289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs558536531	chr11:46972299-46972300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs145375377	chr11:46972307-46972308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs564435723	chr11:46972320-46972321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs148766498	chr11:46972321-46972322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs544271517	chr11:46972375-46972376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs560852002	chr11:46972411-46972412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Parathyroid adenoma	22454399	CNVD
Medulloblastoma	21979893	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	16783165	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Myelofibrosis	22110671	CNVD
Melanoma	18172304	CNVD
Intracranial ependymoma	16609018	CNVD
Myxofibrosarcoma	16751306	CNVD
Potocki-Shaffer syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	16608533	CNVD
Hirschsprung''s Disease	21712996	CNVD
Follicular lymphoma	20505157	CNVD
Colorectal cancer	21128281	CNVD
Breast cancer	20409316	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Mantle cell lymphoma	19029149	CNVD
Glioblastoma multiforme	21138945	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:1178 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:46958600-46973800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr11:46959000-46973400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr11:46959000-46973600	Weak transcription	HUVEC	blood vessel
4	chr11:46959000-46973800	Weak transcription	Primary T cells from cord blood	blood
5	chr11:46959000-46973800	Weak transcription	Primary hematopoietic stem cells	blood
6	chr11:46959000-46973800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
7	chr11:46959000-46975600	Weak transcription	Fetal Muscle Trunk	muscle
8	chr11:46959000-46977000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr11:46959000-46980000	Weak transcription	Aorta	Aorta
10	chr11:46959000-46980000	Weak transcription	Fetal Muscle Leg	muscle
11	chr11:46959000-46980000	Weak transcription	Ovary	ovary
12	chr11:46959000-46980200	Weak transcription	Primary B cells from cord blood	blood
13	chr11:46959000-46980200	Weak transcription	Gastric	stomach
14	chr11:46959000-46980200	Weak transcription	Lung	lung
15	chr11:46959000-46980200	Weak transcription	Thymus	Thymus
16	chr11:46959000-46981000	Weak transcription	Primary T cells fromperipheralblood	blood
17	chr11:46959000-46982200	Weak transcription	Fetal Kidney	kidney
18	chr11:46959000-46982400	Weak transcription	Primary T helper cells fromperipheralblood	blood
19	chr11:46959000-46982600	Weak transcription	Fetal Thymus	thymus
20	chr11:46959000-46998600	Weak transcription	Left Ventricle	heart
21	chr11:46959200-46973400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr11:46959200-46973600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
23	chr11:46959200-46973600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr11:46959200-46973600	Weak transcription	Brain Cingulate Gyrus	brain
25	chr11:46959200-46973800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr11:46959200-46980200	Weak transcription	Duodenum Smooth Muscle	Duodenum
27	chr11:46959200-46980200	Weak transcription	Dnd41	blood
28	chr11:46959200-46985000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr11:46959200-46990600	Weak transcription	Brain Angular Gyrus	brain
30	chr11:46959200-46990600	Weak transcription	Brain Inferior Temporal Lobe	brain
31	chr11:46959200-46993800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
32	chr11:46959600-46978800	Weak transcription	Fetal Brain Male	brain
33	chr11:46959600-46980000	Weak transcription	Fetal Brain Female	brain
34	chr11:46964000-46973400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr11:46965200-46975200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
36	chr11:46965200-46975400	Weak transcription	Stomach Smooth Muscle	stomach
37	chr11:46965200-46984600	Weak transcription	Primary T helper cells PMA-I stimulated	--
38	chr11:46967200-46978800	Weak transcription	H9 Cell Line	embryonic stem cell
39	chr11:46968800-46971600	Enhancers	Duodenum Mucosa	Duodenum
40	chr11:46968800-46971600	Enhancers	Stomach Mucosa	stomach
41	chr11:46969000-46980200	Weak transcription	Fetal Lung	lung
42	chr11:46969200-46973600	Weak transcription	Brain Hippocampus Middle	brain
43	chr11:46969400-46971600	Enhancers	Sigmoid Colon	Sigmoid Colon
44	chr11:46969400-46972800	Weak transcription	HUES48 Cell Line	embryonic stem cell
45	chr11:46969400-46980000	Weak transcription	HUES6 Cell Line	embryonic stem cell
46	chr11:46969400-46980200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
47	chr11:46969600-46973600	Weak transcription	Brain Substantia Nigra	brain
48	chr11:46969800-46980000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr11:46970000-46971200	Enhancers	Pancreatic Islets	Pancreatic Islet
50	chr11:46970000-46973400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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