Variant report

Variant	esv1827245
Chromosome Location	chr2:11385834-11442583
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:388)
CpG islands
(count:184)
Chromatin interactive
region (count:42)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:388 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:11413824-11413997	K562	blood:	n/a	n/a
2	ARID3A	chr2:11394130-11394529	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:11437410-11437793	K562	blood:	n/a	n/a
4	ARID3A	chr2:11414239-11414545	K562	blood:	n/a	n/a
5	ARID3A	chr2:11401273-11401437	K562	blood:	n/a	n/a
6	ARID3A	chr2:11436003-11436311	K562	blood:	n/a	n/a
7	ARID3A	chr2:11419261-11420073	K562	blood:	n/a	n/a
8	ATF1	chr2:11419498-11419968	K562	blood:	n/a	n/a
9	BACH1	chr2:11433742-11433763	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr2:11419436-11419654	K562	blood:	n/a	n/a
11	BHLHE40	chr2:11419680-11419901	K562	blood:	n/a	n/a
12	BHLHE40	chr2:11415460-11415682	GM12878	blood:	n/a	n/a
13	CBX3	chr2:11432761-11433357	K562	blood:	n/a	n/a
14	CBX3	chr2:11402557-11402864	K562	blood:	n/a	n/a
15	CCNT2	chr2:11413906-11414098	K562	blood:	n/a	n/a
16	CCNT2	chr2:11419541-11419881	K562	blood:	n/a	n/a
17	CEBPB	chr2:11436582-11436912	HepG2	liver:	n/a	n/a
18	CEBPB	chr2:11425455-11425637	A549	lung:	n/a	n/a
19	CEBPB	chr2:11394119-11394545	A549	lung:	n/a	n/a
20	CEBPB	chr2:11436588-11436925	K562	blood:	n/a	n/a
21	CEBPB	chr2:11427331-11427382	HepG2	liver:	n/a	chr2:11427365-11427377 chr2:11427334-11427345
22	CEBPB	chr2:11419378-11419937	K562	blood:	n/a	n/a
23	CEBPB	chr2:11394135-11394487	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr2:11436598-11436906	A549	lung:	n/a	n/a
25	CEBPB	chr2:11394128-11394664	MCF-7	breast:	n/a	n/a
26	CEBPB	chr2:11433210-11433471	A549	lung:	n/a	n/a
27	CEBPB	chr2:11413473-11414250	K562	blood:	n/a	n/a
28	CEBPB	chr2:11393990-11394583	A549	lung:	n/a	n/a
29	CEBPB	chr2:11419470-11419946	K562	blood:	n/a	n/a
30	CEBPB	chr2:11433002-11433383	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr2:11436609-11436901	IMR90	lung:	n/a	n/a
32	CEBPB	chr2:11413694-11414207	K562	blood:	n/a	n/a
33	CEBPB	chr2:11433197-11433478	K562	blood:	n/a	n/a
34	CEBPB	chr2:11394109-11394562	A549	lung:	n/a	n/a
35	CEBPB	chr2:11426923-11427462	IMR90	lung:	n/a	chr2:11427365-11427377 chr2:11427334-11427345
36	CEBPB	chr2:11394124-11394568	HepG2	liver:	n/a	n/a
37	CEBPB	chr2:11433174-11433476	K562	blood:	n/a	n/a
38	CEBPB	chr2:11413538-11413738	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr2:11433266-11433466	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr2:11433208-11433418	HepG2	liver:	n/a	n/a
41	CEBPB	chr2:11433227-11433439	IMR90	lung:	n/a	n/a
42	CEBPD	chr2:11419347-11420057	K562	blood:	n/a	n/a
43	CEBPD	chr2:11419474-11420066	K562	blood:	n/a	n/a
44	CHD2	chr2:11436009-11436278	K562	blood:	n/a	n/a
45	CREB1	chr2:11419293-11420093	K562	blood:	n/a	n/a
46	CREB1	chr2:11397978-11398526	GM12878	blood:	n/a	n/a
47	CREB1	chr2:11398174-11398563	GM12878	blood:	n/a	n/a
48	CTCF	chr2:11431430-11431488	GM13976	blood:	n/a	n/a
49	CTCF	chr2:11397851-11397923	GM13976	blood:	n/a	n/a
50	CTCF	chr2:11422606-11422656	Kidney_OC	kidney:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:11397475-11397525	GM06990	blood:	n/a
2	chr2:11397475-11397525	GM06990	blood:	n/a
3	chr2:11430093-11430143	U87	brain:	n/a
4	chr2:11397475-11397525	SK-N-SH	brain:	n/a
5	chr2:11430093-11430143	K562	blood:	n/a
6	chr2:11397351-11397401	Jurkat	blood:	n/a
7	chr2:11397351-11397401	HAEpiC	amniotic membrane:	n/a
8	chr2:11430093-11430143	HRCEpiC	kidney:	n/a
9	chr2:11397475-11397525	RPTEC	kidney:	n/a
10	chr2:11430093-11430143	GM06990	blood:	n/a
11	chr2:11430093-11430143	PrEC	prostate:	n/a
12	chr2:11397475-11397525	ovcar-3	ovarian:	n/a
13	chr2:11430093-11430143	HCF	heart:	n/a
14	chr2:11397351-11397401	Hepatocyte	liver:	n/a
15	chr2:11397351-11397401	HCT-116	colon:	n/a
16	chr2:11430093-11430143	ProgFib	skin:	n/a
17	chr2:11430093-11430143	MCF10A-Er-Src	breast:	n/a
18	chr2:11397351-11397401	T-47D	breast:	n/a
19	chr2:11430093-11430143	T-47D	breast:	n/a
20	chr2:11397351-11397401	PANC-1	pancreas:	n/a
21	chr2:11397475-11397525	HCPEpiC	choroid plexus:	n/a
22	chr2:11397475-11397525	AG09319	gingival:	n/a
23	chr2:11397475-11397525	HCM	heart:	n/a
24	chr2:11430093-11430143	NT2-D1	testis:	n/a
25	chr2:11397351-11397401	NHBE	bronchial:	n/a
26	chr2:11397475-11397525	NB4	blood:	n/a
27	chr2:11397351-11397401	SK-N-SH	brain:	n/a
28	chr2:11397475-11397525	PFSK-1	brain:	n/a
29	chr2:11397475-11397525	SKMC	muscle:	n/a
30	chr2:11397475-11397525	GM19239	blood:	n/a
31	chr2:11397475-11397525	CMK	blood:	n/a
32	chr2:11397351-11397401	ovcar-3	ovarian:	n/a
33	chr2:11430093-11430143	AG09309	skin:	n/a
34	chr2:11430093-11430143	PANC-1	pancreas:	n/a
35	chr2:11430093-11430143	Hepatocyte	liver:	n/a
36	chr2:11430093-11430143	GM12892	blood:	n/a
37	chr2:11430093-11430143	NH-A	brain:	n/a
38	chr2:11397351-11397401	NHDF-neo	bronchial:	n/a
39	chr2:11397475-11397525	H1-hESC	embryonic stem cell:	embryo
40	chr2:11397351-11397401	SAEC	small airway:	n/a
41	chr2:11397475-11397525	SAEC	small airway:	n/a
42	chr2:11397351-11397401	NT2-D1	testis:	n/a
43	chr2:11397351-11397401	AG04450	lung:	fetal
44	chr2:11397351-11397401	HRE	kidney:	n/a
45	chr2:11397475-11397525	HepG2	liver:	n/a
46	chr2:11430093-11430143	NHBE	bronchial:	n/a
47	chr2:11397351-11397401	Caco-2	colon:	n/a
48	chr2:11397475-11397525	LNCaP	prostate:	n/a
49	chr2:11430093-11430143	IMR90	lung:	fetal
50	chr2:11397351-11397401	NH-A	brain:	n/a

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:11430627..11432341-chr2:11435403..11437501,2	K562	blood:
2	chr2:11410844..11413119-chr2:11416854..11418715,2	K562	blood:
3	chr2:11420942..11423564-chr2:11424238..11426360,2	K562	blood:
4	chr2:11429835..11432089-chr2:11450828..11453411,2	K562	blood:
5	chr2:11394019..11396921-chr2:11397879..11400612,3	MCF-7	breast:
6	chr2:11437034..11438737-chr2:11483029..11485386,2	K562	blood:
7	chr2:11435130..11436816-chr2:11483332..11486230,2	MCF-7	breast:
8	chr2:11436708..11439216-chr2:11441108..11443775,3	K562	blood:
9	chr2:11420998..11422528-chr2:11427283..11429692,2	K562	blood:
10	chr2:11407368..11409021-chr2:11484083..11485849,2	K562	blood:
11	chr2:11436411..11439216-chr2:11442275..11444665,2	K562	blood:
12	chr2:11411018..11413119-chr2:11416854..11418915,2	K562	blood:
13	chr2:11422735..11425372-chr2:11448792..11450664,2	MCF-7	breast:
14	chr2:11390471..11392521-chr2:11397410..11399091,2	MCF-7	breast:
15	chr2:11420942..11423564-chr2:11424238..11426360,2	K562	blood:
16	chr2:11411018..11413119-chr2:11416854..11418915,2	K562	blood:
17	chr2:11437773..11439523-chr2:11445218..11447388,2	K562	blood:
18	chr2:11430627..11432341-chr2:11435403..11437501,2	K562	blood:
19	chr2:11425026..11427134-chr2:11483302..11485357,2	K562	blood:
20	chr2:11336489..11338486-chr2:11405089..11406642,2	K562	blood:
21	chr2:11378197..11380031-chr2:11396489..11398532,2	K562	blood:
22	chr2:11405281..11407608-chr2:11412695..11415283,2	K562	blood:
23	chr2:11436411..11439216-chr2:11442275..11444665,2	K562	blood:
24	chr2:11390471..11392521-chr2:11397410..11399091,2	MCF-7	breast:
25	chr2:11410844..11413119-chr2:11416854..11418715,2	K562	blood:
26	chr2:11435116..11437284-chr2:11481697..11485588,4	K562	blood:
27	chr2:11432453..11434936-chr2:11435134..11437192,2	MCF-7	breast:
28	chr2:11436708..11439216-chr2:11441108..11443775,3	K562	blood:
29	chr2:11434738..11436289-chr2:11444236..11445981,2	K562	blood:
30	chr2:11431258..11433262-chr2:11441914..11443504,2	K562	blood:
31	chr2:11382499..11384208-chr2:11387400..11389311,2	K562	blood:
32	chr2:11414827..11416965-chr2:11482213..11484758,3	K562	blood:
33	chr2:11435287..11437143-chr2:11445238..11447670,2	K562	blood:
34	chr2:11431258..11433262-chr2:11441914..11443504,2	K562	blood:
35	chr2:11433437..11435472-chr2:11482925..11485031,2	MCF-7	breast:
36	chr2:11394019..11396921-chr2:11397879..11400612,3	MCF-7	breast:
37	chr2:11405281..11407608-chr2:11412695..11415283,2	K562	blood:
38	chr2:11428310..11431014-chr2:11439661..11442646,2	MCF-7	breast:
39	chr2:11428310..11431014-chr2:11439661..11442646,2	MCF-7	breast:
40	chr2:11376107..11377665-chr2:11385146..11388088,2	K562	blood:
41	chr2:11432453..11434936-chr2:11435134..11437192,2	MCF-7	breast:
42	chr2:11394169..11396145-chr2:11484229..11486145,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PQLC3-2	chr2:11402605-11403266	l_1777_chr2:11402604-11406864_testes
2	lnc-PQLC3-2	chr2:11406634-11406864	l_1777_chr2:11402604-11406864_testes

No data

Variant related genes	Relation type
ROCK2	TF binding region
ROCK2	CpG island
ENSG00000134318	chromatin interactions

Extended variants
information (count: 2042 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:2042 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6716817	chr2:11385834-11385835	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs137952000	chr2:11385901-11385902	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs530138795	chr2:11385916-11385917	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs193227273	chr2:11386006-11386007	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs183949402	chr2:11386012-11386013	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs567083950	chr2:11386152-11386153	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs527875216	chr2:11386163-11386164	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs115692845	chr2:11386206-11386207	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs571280508	chr2:11386238-11386239	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs571025948	chr2:11386243-11386244	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs538304049	chr2:11386250-11386251	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs189194998	chr2:11386305-11386306	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs572932446	chr2:11386363-11386364	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs568494014	chr2:11386390-11386391	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs117830014	chr2:11386400-11386401	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs142612933	chr2:11386417-11386418	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs374815434	chr2:11386443-11386444	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs557047436	chr2:11386549-11386550	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs573102539	chr2:11386552-11386553	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs573652562	chr2:11386709-11386710	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs367762295	chr2:11386760-11386761	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs542666563	chr2:11386774-11386775	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs144769260	chr2:11386812-11386813	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs371475571	chr2:11386843-11386844	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs191195439	chr2:11386854-11386855	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs577127457	chr2:11386964-11386965	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs553153903	chr2:11387103-11387104	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs183793199	chr2:11387106-11387107	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs531408540	chr2:11387121-11387122	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs374966532	chr2:11387249-11387250	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs114078244	chr2:11387253-11387254	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs116450097	chr2:11387261-11387262	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs542282906	chr2:11387317-11387318	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs575256931	chr2:11387319-11387320	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs188506650	chr2:11387325-11387326	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs527931707	chr2:11387334-11387335	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs75111986	chr2:11387367-11387368	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs56393775	chr2:11387450-11387451	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs369347443	chr2:11387452-11387453	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs373120009	chr2:11387454-11387455	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs530962013	chr2:11387523-11387524	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs550401707	chr2:11387532-11387533	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs191716902	chr2:11387542-11387543	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs148282455	chr2:11387548-11387549	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs544275059	chr2:11387587-11387588	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs535843192	chr2:11387589-11387590	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs547829273	chr2:11387617-11387618	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs571830972	chr2:11387669-11387670	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs533812367	chr2:11387687-11387688	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs558835554	chr2:11387705-11387706	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Mental retardation	17847001	CNVD
Glioblastoma multiforme	21080181	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Cancer	20164920	CNVD
Neuroblastoma	21508638	CNVD
Breast cancer	17603634	CNVD
Cancer	16751803	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Ependymoma	16718352	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Glioma	17123091	CNVD
Breast cancer	20409316	CNVD
Multiple myeloma	16616336	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1255 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:11296200-11412600	Weak transcription	Aorta	Aorta
2	chr2:11297600-11394400	Weak transcription	Right Ventricle	heart
3	chr2:11310600-11433000	Weak transcription	Pancreas	Pancrea
4	chr2:11333400-11386200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr2:11352600-11411200	Weak transcription	Thymus	Thymus
6	chr2:11352800-11424000	Weak transcription	HSMMtube	muscle
7	chr2:11354400-11388000	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr2:11354600-11423800	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr2:11360400-11396400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr2:11361000-11397000	Weak transcription	Fetal Muscle Trunk	muscle
11	chr2:11361000-11397400	Weak transcription	Left Ventricle	heart
12	chr2:11361000-11399200	Weak transcription	Primary neutrophils fromperipheralblood	blood
13	chr2:11361000-11400200	Weak transcription	Gastric	stomach
14	chr2:11361000-11410800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
15	chr2:11361000-11411200	Weak transcription	Fetal Thymus	thymus
16	chr2:11361000-11416600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
17	chr2:11361200-11425600	Weak transcription	Stomach Smooth Muscle	stomach
18	chr2:11361600-11396800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr2:11364000-11387000	Weak transcription	Primary T helper cells fromperipheralblood	blood
20	chr2:11364400-11387600	Weak transcription	Rectal Mucosa Donor 31	rectum
21	chr2:11364400-11423800	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr2:11364800-11397400	Weak transcription	Primary T cells fromperipheralblood	blood
23	chr2:11365400-11387400	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr2:11366000-11391000	Weak transcription	HUES6 Cell Line	embryonic stem cell
25	chr2:11366400-11396800	Weak transcription	Fetal Muscle Leg	muscle
26	chr2:11366600-11390800	Weak transcription	NHLF	lung
27	chr2:11367600-11387000	Weak transcription	Duodenum Mucosa	Duodenum
28	chr2:11367600-11387000	Weak transcription	Placenta	Placenta
29	chr2:11367600-11388200	Weak transcription	Primary B cells from peripheral blood	blood
30	chr2:11367800-11387000	Weak transcription	Dnd41	blood
31	chr2:11368200-11387000	Weak transcription	Rectal Mucosa Donor 29	rectum
32	chr2:11368400-11394400	Weak transcription	Brain Angular Gyrus	brain
33	chr2:11369600-11388000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr2:11370400-11394200	Weak transcription	Fetal Lung	lung
35	chr2:11372600-11397200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr2:11372600-11423800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr2:11373400-11387200	Weak transcription	Fetal Intestine Small	intestine
38	chr2:11375400-11390600	Weak transcription	Primary T helper cells PMA-I stimulated	--
39	chr2:11375600-11387200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
40	chr2:11376000-11387000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr2:11376200-11387200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr2:11376200-11410800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
43	chr2:11376800-11387000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr2:11376800-11387000	Weak transcription	Skeletal Muscle Female	skeletal muscle
45	chr2:11376800-11387600	Weak transcription	Skeletal Muscle Male	skeletal muscle
46	chr2:11376800-11394200	Weak transcription	Rectal Smooth Muscle	rectum
47	chr2:11376800-11395000	Weak transcription	Fetal Heart	heart
48	chr2:11376800-11399000	Weak transcription	Brain Anterior Caudate	brain
49	chr2:11378800-11428600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr2:11379800-11387200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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