Variant report

Variant	esv2422406
Chromosome Location	chr11:26329870-26473641
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:26353554-26353760	HepG2	liver:	n/a	n/a
2	BACH1	chr11:26353420-26353701	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL11A	chr11:26337942-26338233	GM12878	blood:	n/a	n/a
4	CBX3	chr11:26386870-26387186	K562	blood:	n/a	n/a
5	CBX3	chr11:26399212-26399510	K562	blood:	n/a	n/a
6	CBX3	chr11:26399220-26399538	K562	blood:	n/a	n/a
7	CEBPB	chr11:26370346-26370626	Hela-S3	cervix:	n/a	chr11:26370499-26370510 chr11:26370498-26370511
8	CEBPB	chr11:26405224-26405299	HepG2	liver:	n/a	chr11:26405279-26405290 chr11:26405278-26405289 chr11:26405278-26405291
9	CEBPB	chr11:26355467-26355859	Hela-S3	cervix:	n/a	chr11:26355659-26355670 chr11:26355660-26355669 chr11:26355660-26355669 chr11:26355658-26355669 chr11:26355660-26355669 chr11:26355658-26355669 chr11:26355660-26355669 chr11:26355658-26355671
10	CEBPB	chr11:26449130-26449301	Hela-S3	cervix:	n/a	chr11:26449189-26449198 chr11:26449187-26449198
11	CEBPB	chr11:26341492-26342016	ECC-1	luminal epithelium:	n/a	chr11:26341627-26341638
12	CEBPB	chr11:26449069-26449341	IMR90	lung:	n/a	chr11:26449189-26449198 chr11:26449187-26449198
13	CEBPB	chr11:26386313-26386526	Hela-S3	cervix:	n/a	chr11:26386427-26386438
14	CEBPB	chr11:26355501-26355731	H1-hESC	embryonic stem cell:	n/a	chr11:26355659-26355670 chr11:26355660-26355669 chr11:26355660-26355669 chr11:26355658-26355669 chr11:26355660-26355669 chr11:26355658-26355669 chr11:26355660-26355669 chr11:26355658-26355671
15	CEBPB	chr11:26341447-26342010	HepG2	liver:	n/a	chr11:26341627-26341638
16	CEBPB	chr11:26341440-26342026	Hela-S3	cervix:	n/a	chr11:26341627-26341638
17	CEBPB	chr11:26370367-26370604	HepG2	liver:	n/a	chr11:26370499-26370510 chr11:26370498-26370511
18	CEBPB	chr11:26355521-26355796	HepG2	liver:	n/a	chr11:26355659-26355670 chr11:26355660-26355669 chr11:26355660-26355669 chr11:26355658-26355669 chr11:26355660-26355669 chr11:26355658-26355669 chr11:26355660-26355669 chr11:26355658-26355671
19	CEBPB	chr11:26386261-26386572	HepG2	liver:	n/a	chr11:26386427-26386438
20	CEBPB	chr11:26370392-26370605	A549	lung:	n/a	chr11:26370499-26370510 chr11:26370498-26370511
21	CEBPB	chr11:26464650-26464825	Hela-S3	cervix:	n/a	chr11:26464731-26464742
22	CEBPB	chr11:26449001-26449357	HepG2	liver:	n/a	chr11:26449054-26449067 chr11:26449189-26449198 chr11:26449187-26449198
23	CEBPB	chr11:26386264-26386577	IMR90	lung:	n/a	chr11:26386427-26386438
24	CEBPB	chr11:26353545-26353852	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr11:26464620-26464892	HepG2	liver:	n/a	chr11:26464731-26464742
26	CEBPB	chr11:26449002-26449304	A549	lung:	n/a	chr11:26449054-26449067 chr11:26449189-26449198 chr11:26449187-26449198
27	CEBPB	chr11:26341451-26342002	A549	lung:	n/a	chr11:26341627-26341638
28	CEBPB	chr11:26353559-26353847	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr11:26355522-26355823	IMR90	lung:	n/a	chr11:26355659-26355670 chr11:26355660-26355669 chr11:26355660-26355669 chr11:26355658-26355669 chr11:26355660-26355669 chr11:26355658-26355669 chr11:26355660-26355669 chr11:26355658-26355671
30	CEBPB	chr11:26344265-26344447	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr11:26341466-26342019	H1-hESC	embryonic stem cell:	n/a	chr11:26341627-26341638
32	CEBPB	chr11:26386296-26386584	A549	lung:	n/a	chr11:26386427-26386438
33	CEBPB	chr11:26464614-26464915	IMR90	lung:	n/a	chr11:26464731-26464742
34	CEBPB	chr11:26341469-26341997	IMR90	lung:	n/a	chr11:26341627-26341638
35	CEBPB	chr11:26349976-26350242	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr11:26451887-26452079	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr11:26386348-26386454	H1-hESC	embryonic stem cell:	n/a	chr11:26386427-26386438
38	CEBPB	chr11:26464604-26464813	K562	blood:	n/a	chr11:26464731-26464742
39	CHD1	chr11:26353789-26354030	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr11:26353491-26353926	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD2	chr11:26353496-26353861	Hela-S3	cervix:	n/a	n/a
42	CREB1	chr11:26353505-26353801	A549	lung:	n/a	n/a
43	CTCF	chr11:26353540-26353690	AoAF	blood vessel:	n/a	n/a
44	CTCF	chr11:26353540-26353690	HRPEpiC	eye:	n/a	n/a
45	CTCF	chr11:26353560-26353710	K562	blood:	n/a	chr11:26353696-26353704
46	CTCF	chr11:26353479-26353725	NHEK	skin:	n/a	chr11:26353696-26353704
47	CTCF	chr11:26353420-26353570	K562	blood:	n/a	n/a
48	CTCF	chr11:26353500-26353650	GM12867	blood:	n/a	n/a
49	CTCF	chr11:26353481-26353753	A549	lung:	n/a	chr11:26353696-26353704
50	CTCF	chr11:26353500-26353650	GM12872	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:26353484-26353534	GM12891	blood:	n/a
2	chr11:26353811-26353861	AG09309	skin:	n/a
3	chr11:26353484-26353534	GM12891	blood:	n/a
4	chr11:26353811-26353861	AG09309	skin:	n/a
5	chr11:26353622-26353672	HAEpiC	amniotic membrane:	n/a
6	chr11:26353630-26353680	HRCEpiC	kidney:	n/a
7	chr11:26353622-26353672	Hepatocyte	liver:	n/a
8	chr11:26350473-26350523	GM12892	blood:	n/a
9	chr11:26353723-26353773	NHDF-neo	bronchial:	n/a
10	chr11:26353622-26353672	SK-N-SH_RA	brain:	n/a
11	chr11:26353484-26353534	SAEC	small airway:	n/a
12	chr11:26353094-26353144	HL-60	blood:	n/a
13	chr11:26353723-26353773	PrEC	prostate:	n/a
14	chr11:26353811-26353861	HIPEpiC	eye:	n/a
15	chr11:26353630-26353680	MCF-7	breast:	n/a
16	chr11:26353800-26353850	AG04449	skin:	fetal
17	chr11:26353605-26353655	Jurkat	blood:	n/a
18	chr11:26353800-26353850	HRE	kidney:	n/a
19	chr11:26353618-26353668	SAEC	small airway:	n/a
20	chr11:26353800-26353850	MCF10A-Er-Src	breast:	n/a
21	chr11:26353800-26353850	GM12878	blood:	n/a
22	chr11:26353811-26353861	Jurkat	blood:	n/a
23	chr11:26353723-26353773	HPAEpiC	pulmonary alveolar:	n/a
24	chr11:26353723-26353773	NHBE	bronchial:	n/a
25	chr11:26353605-26353655	HRCEpiC	kidney:	n/a
26	chr11:26353622-26353672	NHDF-neo	bronchial:	n/a
27	chr11:26353094-26353144	K562	blood:	n/a
28	chr11:26353622-26353672	SAEC	small airway:	n/a
29	chr11:26353618-26353668	HNPCEpiC	eye:	n/a
30	chr11:26353094-26353144	MCF10A-Er-Src	breast:	n/a
31	chr11:26353622-26353672	K562	blood:	n/a
32	chr11:26353094-26353144	HCT-116	colon:	n/a
33	chr11:26355628-26355678	H1-hESC	embryonic stem cell:	embryo
34	chr11:26353811-26353861	HRCEpiC	kidney:	n/a
35	chr11:26354057-26354107	HAEpiC	amniotic membrane:	n/a
36	chr11:26353094-26353144	PFSK-1	brain:	n/a
37	chr11:26353484-26353534	HCF	heart:	n/a
38	chr11:26353484-26353534	SK-N-MC	brain:	n/a
39	chr11:26353094-26353144	Caco-2	colon:	n/a
40	chr11:26354057-26354107	U87	brain:	n/a
41	chr11:26353811-26353861	SK-N-SH	brain:	n/a
42	chr11:26353605-26353655	ProgFib	skin:	n/a
43	chr11:26353723-26353773	HRCEpiC	kidney:	n/a
44	chr11:26353618-26353668	PFSK-1	brain:	n/a
45	chr11:26353094-26353144	LNCaP	prostate:	n/a
46	chr11:26354057-26354107	LNCaP	prostate:	n/a
47	chr11:26353630-26353680	HL-60	blood:	n/a
48	chr11:26350473-26350523	LNCaP	prostate:	n/a
49	chr11:26353605-26353655	HCF	heart:	n/a
50	chr11:26355628-26355678	HRCEpiC	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:26396905..26399519-chr11:26402915..26404778,2	K562	blood:
2	chr11:26396905..26399519-chr11:26402915..26404778,2	K562	blood:
3	chr11:26353156..26354057-chr9:139137195..139137941,2	Hela-S3	cervix:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FIBIN-5	chr11:26448598-26448959	NONHSAT018459

Variant related genes	Relation type
ENSG00000255505	TF binding region
ANO3	TF binding region
ENSG00000255505	CpG island
ANO3	CpG island
ENSG00000165661	chromatin interactions

Extended variants
information (count: 3356 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:3356 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs187582734	chr11:26329894-26329895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs550994390	chr11:26329938-26329939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs560002516	chr11:26329965-26329966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs535703214	chr11:26329966-26329967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs527624153	chr11:26329985-26329986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs7945792	chr11:26329993-26329994	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs567466336	chr11:26330072-26330073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs143728983	chr11:26330139-26330140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs377446493	chr11:26330176-26330177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs533896782	chr11:26330179-26330180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs571678808	chr11:26330215-26330216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs35521594	chr11:26330232-26330233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs373941444	chr11:26330258-26330259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs539020959	chr11:26330272-26330273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs554248657	chr11:26330273-26330274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs558466736	chr11:26330286-26330287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs17308992	chr11:26330289-26330290	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs544056042	chr11:26330297-26330298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs374917727	chr11:26330307-26330308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs576597524	chr11:26330325-26330326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs543681980	chr11:26330331-26330332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs562586427	chr11:26330341-26330342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs577356445	chr11:26330365-26330366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs193256500	chr11:26330378-26330379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs73441544	chr11:26330430-26330431	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs184750421	chr11:26330451-26330452	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs112371018	chr11:26330504-26330505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs560893109	chr11:26330514-26330515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs558218642	chr11:26330533-26330534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs531512692	chr11:26330534-26330535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs187559202	chr11:26330572-26330573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs541567677	chr11:26330583-26330584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs151030827	chr11:26330586-26330587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs539182727	chr11:26330634-26330635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs547772162	chr11:26330681-26330682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs192276164	chr11:26330727-26330728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs140943695	chr11:26330791-26330792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs555221667	chr11:26330792-26330793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs10501044	chr11:26330810-26330811	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs537640785	chr11:26330839-26330840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs376121065	chr11:26330850-26330851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs558929411	chr11:26330855-26330856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs116179506	chr11:26330880-26330881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs150365524	chr11:26330916-26330917	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs544716615	chr11:26330942-26330943	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs138204934	chr11:26330949-26330950	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs571733226	chr11:26330957-26330958	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs117757022	chr11:26330982-26330983	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs184472392	chr11:26330983-26330984	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs190008314	chr11:26330984-26330985	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:53)

Disease	PMID	Source
Burkitt''s lymphoma	19759907	CNVD
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
Congenital diaphragmatic hernia	21525063	CNVD
Renal cell carcinoma	18194544	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Chordoma	18071362	CNVD
Autism	22102821	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Neuroticism	17667963	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:319 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:26328400-26337600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr11:26332000-26332400	Enhancers	Fetal Intestine Small	intestine
3	chr11:26337000-26340000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr11:26337600-26338800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr11:26338000-26338400	Enhancers	Primary B cells from peripheral blood	blood
6	chr11:26338000-26338800	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr11:26338200-26338800	Enhancers	H1 Cell Line	embryonic stem cell
8	chr11:26338200-26338800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr11:26338600-26341600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr11:26338800-26341000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr11:26338800-26341600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
12	chr11:26338800-26341600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr11:26341000-26342000	Enhancers	Hela-S3	cervix
14	chr11:26341400-26341800	Enhancers	Pancreas	Pancrea
15	chr11:26341400-26342000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr11:26341600-26341800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
17	chr11:26341600-26342000	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr11:26341600-26342000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr11:26341600-26342000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr11:26341600-26342000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr11:26341600-26342000	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr11:26341600-26342000	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr11:26341600-26342000	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr11:26341600-26342200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr11:26341800-26353200	Weak transcription	Pancreas	Pancrea
26	chr11:26344200-26344400	Enhancers	Fetal Intestine Small	intestine
27	chr11:26344600-26346200	Enhancers	Hela-S3	cervix
28	chr11:26348200-26349000	Enhancers	Stomach Mucosa	stomach
29	chr11:26349600-26349800	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr11:26349600-26350200	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr11:26349600-26350800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr11:26349800-26350000	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr11:26349800-26350400	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr11:26349800-26351800	Enhancers	Fetal Brain Male	brain
35	chr11:26349800-26353200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr11:26350000-26351200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr11:26350000-26352000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
38	chr11:26350000-26353200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr11:26350000-26353200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr11:26350200-26352000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
41	chr11:26350400-26352000	Weak transcription	HUES48 Cell Line	embryonic stem cell
42	chr11:26350600-26351800	Weak transcription	HUES64 Cell Line	embryonic stem cell
43	chr11:26350800-26351800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr11:26351200-26353200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr11:26351400-26353400	Weak transcription	Spleen	Spleen
46	chr11:26351800-26352200	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr11:26351800-26353000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
48	chr11:26351800-26353400	Weak transcription	Fetal Brain Male	brain
49	chr11:26352000-26352400	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr11:26352000-26352600	Enhancers	iPS-20b Cell Line	embryonic stem cell

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