Variant report

Variant	nsv897204
Chromosome Location	chr11:34248229-34271712
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:796)
CpG islands
(count:184)
Chromatin interactive
region (count:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:796 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:34263663-34263838	K562	blood:	n/a	n/a
2	ARID3A	chr11:34258144-34258360	K562	blood:	n/a	n/a
3	ATF1	chr11:34271202-34271360	K562	blood:	n/a	n/a
4	ATF1	chr11:34255636-34255924	K562	blood:	n/a	n/a
5	ATF1	chr11:34263622-34264047	K562	blood:	n/a	n/a
6	ATF1	chr11:34258159-34258470	K562	blood:	n/a	n/a
7	ATF1	chr11:34264548-34264774	K562	blood:	n/a	n/a
8	ATF2	chr11:34263526-34263963	GM12878	blood:	n/a	n/a
9	ATF2	chr11:34255380-34256269	GM12878	blood:	n/a	n/a
10	ATF2	chr11:34256641-34257339	GM12878	blood:	n/a	n/a
11	ATF2	chr11:34255540-34255940	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr11:34261244-34261828	GM12878	blood:	n/a	n/a
13	ATF2	chr11:34265540-34266147	GM12878	blood:	n/a	n/a
14	ATF2	chr11:34265488-34266211	GM12878	blood:	n/a	n/a
15	ATF2	chr11:34253173-34253663	GM12878	blood:	n/a	n/a
16	ATF2	chr11:34256665-34257227	GM12878	blood:	n/a	n/a
17	ATF2	chr11:34255499-34256159	GM12878	blood:	n/a	n/a
18	ATF3	chr11:34264947-34265689	A549	lung:	n/a	n/a
19	BACH1	chr11:34265215-34265539	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr11:34255562-34255974	H1-hESC	embryonic stem cell:	n/a	n/a
21	BATF	chr11:34255571-34256220	GM12878	blood:	n/a	n/a
22	BATF	chr11:34270025-34270281	GM12878	blood:	n/a	n/a
23	BATF	chr11:34256722-34257234	GM12878	blood:	n/a	n/a
24	BATF	chr11:34261472-34261820	GM12878	blood:	n/a	n/a
25	BATF	chr11:34256617-34257256	GM12878	blood:	n/a	n/a
26	BATF	chr11:34265565-34266061	GM12878	blood:	n/a	n/a
27	BATF	chr11:34265298-34266102	GM12878	blood:	n/a	n/a
28	BATF	chr11:34253222-34253532	GM12878	blood:	n/a	n/a
29	BCL11A	chr11:34255514-34256163	GM12878	blood:	n/a	chr11:34255960-34255969 chr11:34255961-34255970 chr11:34255679-34255688
30	BCL11A	chr11:34261392-34261842	GM12878	blood:	n/a	chr11:34261556-34261565
31	BCL11A	chr11:34256644-34257202	GM12878	blood:	n/a	n/a
32	BCL11A	chr11:34265602-34266021	GM12878	blood:	n/a	n/a
33	BCL11A	chr11:34269963-34270339	GM12878	blood:	n/a	n/a
34	BCL11A	chr11:34256783-34257188	GM12878	blood:	n/a	n/a
35	BCL11A	chr11:34255701-34256085	GM12878	blood:	n/a	chr11:34255960-34255969 chr11:34255961-34255970
36	BCL11A	chr11:34265561-34266037	GM12878	blood:	n/a	n/a
37	BCL11A	chr11:34269972-34270387	GM12878	blood:	n/a	n/a
38	BCL11A	chr11:34253175-34253472	GM12878	blood:	n/a	n/a
39	BCL3	chr11:34253205-34253551	GM12878	blood:	n/a	n/a
40	BCL3	chr11:34264863-34265664	A549	lung:	n/a	chr11:34265439-34265448
41	BCL3	chr11:34255404-34256085	A549	lung:	n/a	chr11:34255960-34255969 chr11:34255961-34255970 chr11:34255679-34255688
42	BCL3	chr11:34265620-34266076	GM12878	blood:	n/a	n/a
43	BCL3	chr11:34264858-34265821	A549	lung:	n/a	chr11:34265439-34265448
44	BCL3	chr11:34256725-34257134	GM12878	blood:	n/a	n/a
45	BCL3	chr11:34255500-34256150	GM12878	blood:	n/a	chr11:34255960-34255969 chr11:34255961-34255970 chr11:34255679-34255688
46	BCL3	chr11:34263551-34264064	GM12878	blood:	n/a	n/a
47	BCL3	chr11:34261474-34261883	GM12878	blood:	n/a	chr11:34261556-34261565
48	BCLAF1	chr11:34255432-34256233	GM12878	blood:	n/a	chr11:34255960-34255969 chr11:34255961-34255970 chr11:34255679-34255688
49	BCLAF1	chr11:34255534-34256221	GM12878	blood:	n/a	chr11:34255960-34255969 chr11:34255961-34255970 chr11:34255679-34255688
50	BCLAF1	chr11:34265528-34266191	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:34265361-34265411	HEEpiC	esophagus:	n/a
2	chr11:34265361-34265411	HEEpiC	esophagus:	n/a
3	chr11:34265361-34265411	PFSK-1	brain:	n/a
4	chr11:34256703-34256753	HRE	kidney:	n/a
5	chr11:34255733-34255783	AG09309	skin:	n/a
6	chr11:34256703-34256753	ECC-1	luminal epithelium:	n/a
7	chr11:34256703-34256753	ovcar-3	ovarian:	n/a
8	chr11:34265361-34265411	PANC-1	pancreas:	n/a
9	chr11:34256703-34256753	Hela-S3	cervix:	n/a
10	chr11:34255733-34255783	HCM	heart:	n/a
11	chr11:34255733-34255783	H1-hESC	embryonic stem cell:	embryo
12	chr11:34256703-34256753	HUVEC	blood vessel:	n/a
13	chr11:34255733-34255783	NH-A	brain:	n/a
14	chr11:34256703-34256753	HIPEpiC	eye:	n/a
15	chr11:34255733-34255783	PFSK-1	brain:	n/a
16	chr11:34265361-34265411	HCT-116	colon:	n/a
17	chr11:34265361-34265411	LNCaP	prostate:	n/a
18	chr11:34256703-34256753	PANC-1	pancreas:	n/a
19	chr11:34256703-34256753	T-47D	breast:	n/a
20	chr11:34255733-34255783	BE2_C	brain:	n/a
21	chr11:34265361-34265411	ECC-1	luminal epithelium:	n/a
22	chr11:34256703-34256753	AG09319	gingival:	n/a
23	chr11:34255733-34255783	K562	blood:	n/a
24	chr11:34255733-34255783	NHBE	bronchial:	n/a
25	chr11:34265361-34265411	HPAEpiC	pulmonary alveolar:	n/a
26	chr11:34265361-34265411	GM12878	blood:	n/a
27	chr11:34256703-34256753	BE2_C	brain:	n/a
28	chr11:34256703-34256753	SK-N-MC	brain:	n/a
29	chr11:34255733-34255783	NB4	blood:	n/a
30	chr11:34265361-34265411	MCF10A-Er-Src	breast:	n/a
31	chr11:34255733-34255783	HUVEC	blood vessel:	n/a
32	chr11:34265361-34265411	H1-hESC	embryonic stem cell:	embryo
33	chr11:34255733-34255783	GM12892	blood:	n/a
34	chr11:34265361-34265411	AG09309	skin:	n/a
35	chr11:34255733-34255783	HMEC	breast:	n/a
36	chr11:34255733-34255783	HRCEpiC	kidney:	n/a
37	chr11:34265361-34265411	IMR90	lung:	fetal
38	chr11:34255733-34255783	RPTEC	kidney:	n/a
39	chr11:34265361-34265411	Hela-S3	cervix:	n/a
40	chr11:34255733-34255783	SAEC	small airway:	n/a
41	chr11:34256703-34256753	AG09309	skin:	n/a
42	chr11:34265361-34265411	GM06990	blood:	n/a
43	chr11:34256703-34256753	SK-N-SH	brain:	n/a
44	chr11:34255733-34255783	HL-60	blood:	n/a
45	chr11:34265361-34265411	HEK293	kidney:	embryo
46	chr11:34256703-34256753	NH-A	brain:	n/a
47	chr11:34256703-34256753	LNCaP	prostate:	n/a
48	chr11:34256703-34256753	NHBE	bronchial:	n/a
49	chr11:34256703-34256753	HepG2	liver:	n/a
50	chr11:34255733-34255783	BJ	skin:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:34244635..34246968-chr11:34254432..34256180,2	K562	blood:
2	chr11:34261414..34263986-chr11:34271757..34273793,2	K562	blood:
3	chr11:34229883..34232389-chr11:34271160..34273308,2	K562	blood:
4	chr11:34244635..34246968-chr11:34254314..34256180,3	K562	blood:
5	chr11:34265214..34267176-chr11:34283077..34285328,3	MCF-7	breast:
6	chr11:34260780..34263020-chr11:34279926..34282268,2	MCF-7	breast:
7	chr11:34268801..34271707-chr11:34290725..34293055,2	K562	blood:
8	chr11:34267721..34270365-chr11:34272865..34274585,2	MCF-7	breast:
9	chr11:34264193..34265705-chr11:34292865..34295828,2	K562	blood:
10	chr11:34270206..34274230-chr11:34378598..34380931,3	MCF-7	breast:
11	chr11:34256033..34257760-chr11:34260641..34262431,2	K562	blood:
12	chr11:34231932..34233684-chr11:34247435..34249545,2	K562	blood:
13	chr11:34256786..34259420-chr11:34262602..34265053,3	K562	blood:
14	chr11:34256033..34257760-chr11:34260641..34262431,2	K562	blood:
15	chr11:34229441..34231710-chr11:34255472..34258756,3	MCF-7	breast:
16	chr11:34254769..34257518-chr11:34263900..34266853,2	K562	blood:
17	chr11:34269717..34273624-chr11:34376687..34380089,5	MCF-7	breast:
18	chr11:34257238..34258836-chr11:34262928..34265413,2	MCF-7	breast:
19	chr11:34263600..34266230-chr11:34266603..34268167,2	MCF-7	breast:

No data

Variant related genes	Relation type
ABTB2	TF binding region
ABTB2	CpG island
ENSG00000166016	chromatin interactions

Extended variants
information (count: 1014 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:1014 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4755363	chr11:34248229-34248230	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs547476016	chr11:34248325-34248326	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs200056906	chr11:34248378-34248379	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs536383168	chr11:34248478-34248479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs289983	chr11:34248540-34248541	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs289984	chr11:34248566-34248567	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs538057273	chr11:34248584-34248585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs6484701	chr11:34248586-34248587	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs578001418	chr11:34248590-34248591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs7118745	chr11:34248619-34248620	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs553528985	chr11:34248624-34248625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs543901575	chr11:34248641-34248642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs9783356	chr11:34248689-34248690	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs575733426	chr11:34248690-34248691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs370637530	chr11:34248724-34248725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs542384607	chr11:34248748-34248749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs562624574	chr11:34248756-34248757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs189317345	chr11:34248802-34248803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs372284660	chr11:34248820-34248821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs372031668	chr11:34248833-34248834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs200772478	chr11:34248834-34248835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs74739876	chr11:34248846-34248847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs371366218	chr11:34248848-34248849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs374993462	chr11:34248903-34248904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs139672252	chr11:34248936-34248937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs73493563	chr11:34248941-34248942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs146807995	chr11:34248949-34248950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs167054	chr11:34249011-34249012	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs547774021	chr11:34249012-34249013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs567583830	chr11:34249032-34249033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs139633114	chr11:34249036-34249037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs566777178	chr11:34249065-34249066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs144385221	chr11:34249076-34249077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs10836161	chr11:34249091-34249092	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs182013039	chr11:34249238-34249239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs2473899	chr11:34249265-34249266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs547325310	chr11:34249273-34249274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs533878776	chr11:34249285-34249286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs565268465	chr11:34249297-34249298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs553704987	chr11:34249303-34249304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs573527638	chr11:34249304-34249305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs149217200	chr11:34249305-34249306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs555799363	chr11:34249312-34249313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs12801390	chr11:34249338-34249339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs12801895	chr11:34249340-34249341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs185807104	chr11:34249344-34249345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs111950300	chr11:34249370-34249371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs111946794	chr11:34249374-34249375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs143414231	chr11:34249375-34249376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs112956545	chr11:34249384-34249385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	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
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	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
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	21364760	CNVD
Aniridia syndrome	21572526	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Retinoblastoma	22278416	CNVD
Denys-drash syndrome	21085971	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
WAGR syndrome	16773131	CNVD
Disorders of sex development	22290220	CNVD
Aniridia syndrome	17204608	CNVD
Mental retardation	17204608	CNVD
WAGR syndrome	19617690	CNVD
genitourinary abnormalities	17204608	CNVD
Breast cancer	16397240	CNVD
Mental retardation	16773131	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Cancer	21183584	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
WAGR syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Denys-drash syndrome	19566914	CNVD
Familial wilms tumor	19566914	CNVD
Frasier syndrome	19566914	CNVD
Non-small cell lung cancer	21829676	CNVD
WAGR syndrome	20603712	CNVD
Autism	17322880	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21858162	CNVD
Cancer	20164920	CNVD
Breast cancer	16620391	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD

Chromatin state (count:681 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:34237200-34255600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr11:34245200-34254600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr11:34245200-34255400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr11:34245200-34255600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr11:34245200-34255800	Weak transcription	HSMMtube	muscle
6	chr11:34245200-34263800	Weak transcription	Right Atrium	heart
7	chr11:34245200-34264200	Weak transcription	Aorta	Aorta
8	chr11:34245400-34251400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr11:34245400-34254600	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr11:34245400-34255600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr11:34245400-34255600	Weak transcription	NHLF	lung
12	chr11:34245600-34263600	Weak transcription	Right Ventricle	heart
13	chr11:34246200-34255600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr11:34246800-34255800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr11:34247000-34254800	Weak transcription	Fetal Intestine Small	intestine
16	chr11:34247000-34255800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr11:34247000-34257400	Weak transcription	Fetal Stomach	stomach
18	chr11:34247800-34248400	Enhancers	Rectal Mucosa Donor 29	rectum
19	chr11:34248200-34249400	Weak transcription	Duodenum Mucosa	Duodenum
20	chr11:34248200-34251600	Weak transcription	GM12878-XiMat	blood
21	chr11:34248200-34254600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
22	chr11:34249600-34263600	Weak transcription	Gastric	stomach
23	chr11:34251600-34252000	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr11:34251600-34252000	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr11:34251600-34255400	Enhancers	GM12878-XiMat	blood
26	chr11:34251800-34255400	Weak transcription	H1 Cell Line	embryonic stem cell
27	chr11:34251800-34255600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr11:34252000-34255400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr11:34252000-34255600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
30	chr11:34252600-34253800	Enhancers	A549	lung
31	chr11:34252800-34253200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
32	chr11:34253200-34253600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
33	chr11:34253600-34256000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
34	chr11:34253800-34254600	Weak transcription	A549	lung
35	chr11:34254000-34256400	Enhancers	Primary B cells from peripheral blood	blood
36	chr11:34254200-34255800	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr11:34254400-34254600	Weak transcription	Brain Substantia Nigra	brain
38	chr11:34254400-34256200	Enhancers	Primary B cells from cord blood	blood
39	chr11:34254600-34254800	Enhancers	Brain Substantia Nigra	brain
40	chr11:34254600-34255400	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr11:34254600-34255400	Enhancers	A549	lung
42	chr11:34254600-34256200	Enhancers	HepG2	liver
43	chr11:34254600-34256400	Enhancers	Primary hematopoietic stem cells short term culture	blood
44	chr11:34254600-34258800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr11:34254800-34255600	Enhancers	Hela-S3	cervix
46	chr11:34254800-34256400	Enhancers	Fetal Intestine Small	intestine
47	chr11:34254800-34257200	Weak transcription	Brain Substantia Nigra	brain
48	chr11:34254800-34257600	Enhancers	Primary T helper cells PMA-I stimulated	--
49	chr11:34255000-34257600	Enhancers	Fetal Thymus	thymus
50	chr11:34255400-34255600	Enhancers	Duodenum Mucosa	Duodenum

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