Variant report

Variant	nsv897591
Chromosome Location	chr11:58807241-58854169
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	ATF2	chr11:58825833-58826405	GM12878	blood:	n/a	n/a
2	ATF2	chr11:58831671-58832143	GM12878	blood:	n/a	n/a
3	ATF2	chr11:58831402-58832419	GM12878	blood:	n/a	n/a
4	BACH1	chr11:58825972-58826213	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr11:58831786-58832150	GM12878	blood:	n/a	chr11:58831926-58831934
6	BATF	chr11:58831416-58832275	GM12878	blood:	n/a	chr11:58831926-58831934
7	BATF	chr11:58831471-58831776	GM12878	blood:	n/a	n/a
8	BATF	chr11:58826199-58826498	GM12878	blood:	n/a	n/a
9	BATF	chr11:58818940-58819193	GM12878	blood:	n/a	n/a
10	BCL11A	chr11:58818878-58819275	GM12878	blood:	n/a	chr11:58819091-58819100
11	BCL11A	chr11:58818899-58819262	GM12878	blood:	n/a	chr11:58819091-58819100
12	BCL11A	chr11:58831483-58831904	GM12878	blood:	n/a	n/a
13	BCL11A	chr11:58831528-58832157	GM12878	blood:	n/a	n/a
14	BCL3	chr11:58831794-58832281	GM12878	blood:	n/a	n/a
15	BHLHE40	chr11:58826040-58826162	K562	blood:	n/a	n/a
16	BHLHE40	chr11:58825938-58826278	GM12878	blood:	n/a	n/a
17	BHLHE40	chr11:58820953-58821000	K562	blood:	n/a	n/a
18	BRCA1	chr11:58825950-58826184	GM12878	blood:	n/a	n/a
19	CEBPB	chr11:58835714-58835923	HepG2	liver:	n/a	chr11:58835780-58835791
20	CEBPB	chr11:58835676-58835875	K562	blood:	n/a	chr11:58835780-58835791
21	CEBPB	chr11:58841369-58841519	IMR90	lung:	n/a	n/a
22	CEBPB	chr11:58852160-58852235	HepG2	liver:	n/a	n/a
23	CEBPB	chr11:58850700-58850889	HepG2	liver:	n/a	n/a
24	CEBPB	chr11:58825987-58826187	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr11:58835627-58835890	IMR90	lung:	n/a	chr11:58835780-58835791
26	CEBPB	chr11:58827942-58827984	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD1	chr11:58821218-58821270	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD1	chr11:58825963-58826312	GM12878	blood:	n/a	n/a
29	CHD2	chr11:58825822-58826232	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr11:58826018-58826077	K562	blood:	n/a	n/a
31	CHD2	chr11:58825891-58826300	GM12878	blood:	n/a	n/a
32	CREB1	chr11:58845805-58846333	GM12878	blood:	n/a	n/a
33	CREB1	chr11:58845766-58846361	GM12878	blood:	n/a	n/a
34	CTCF	chr11:58825980-58826130	BJ	skin:	n/a	n/a
35	CTCF	chr11:58820830-58821114	MCF-7	breast:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
36	CTCF	chr11:58826000-58826150	BE2_C	brain:	n/a	n/a
37	CTCF	chr11:58825881-58826206	A549	lung:	n/a	n/a
38	CTCF	chr11:58826000-58826150	GM12867	blood:	n/a	n/a
39	CTCF	chr11:58826020-58826170	GM12864	blood:	n/a	n/a
40	CTCF	chr11:58820780-58821155	GM12878	blood:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
41	CTCF	chr11:58825968-58826201	GM13976	blood:	n/a	n/a
42	CTCF	chr11:58820875-58821066	GM20000	blood:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
43	CTCF	chr11:58825980-58826130	HMEC	breast:	n/a	n/a
44	CTCF	chr11:58820840-58820990	Caco-2	colon:	n/a	chr11:58820969-58820985 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
45	CTCF	chr11:58825980-58826130	MCF-7	breast:	n/a	n/a
46	CTCF	chr11:58820860-58821010	GM12869	blood:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
47	CTCF	chr11:58825883-58826276	K562	blood:	n/a	n/a
48	CTCF	chr11:58825919-58826227	HUVEC	blood vessel:	n/a	n/a
49	CTCF	chr11:58820860-58821010	HAc	cerebellar:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
50	CTCF	chr11:58826040-58826190	GM12865	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:58833356-58833406	AG09319	gingival:	n/a
2	chr11:58830424-58830474	AG10803	skin:	n/a
3	chr11:58830424-58830474	NB4	blood:	n/a
4	chr11:58833356-58833406	AG09319	gingival:	n/a
5	chr11:58830424-58830474	AG10803	skin:	n/a
6	chr11:58830424-58830474	NB4	blood:	n/a
7	chr11:58828174-58828224	ProgFib	skin:	n/a
8	chr11:58830191-58830241	GM12892	blood:	n/a
9	chr11:58825870-58825920	IMR90	lung:	fetal
10	chr11:58826110-58826160	HCPEpiC	choroid plexus:	n/a
11	chr11:58826475-58826525	GM12892	blood:	n/a
12	chr11:58825870-58825920	MCF10A-Er-Src	breast:	n/a
13	chr11:58826414-58826464	MCF10A-Er-Src	breast:	n/a
14	chr11:58828174-58828224	NB4	blood:	n/a
15	chr11:58825714-58825764	K562	blood:	n/a
16	chr11:58826073-58826123	SK-N-SH_RA	brain:	n/a
17	chr11:58825870-58825920	AG04449	skin:	fetal
18	chr11:58830857-58830907	GM12878	blood:	n/a
19	chr11:58830191-58830241	ECC-1	luminal epithelium:	n/a
20	chr11:58826110-58826160	HNPCEpiC	eye:	n/a
21	chr11:58828174-58828224	ovcar-3	ovarian:	n/a
22	chr11:58810187-58810237	HRPEpiC	eye:	n/a
23	chr11:58826414-58826464	BJ	skin:	n/a
24	chr11:58830424-58830474	MCF-7	breast:	n/a
25	chr11:58826414-58826464	BE2_C	brain:	n/a
26	chr11:58833356-58833406	Jurkat	blood:	n/a
27	chr11:58825870-58825920	SAEC	small airway:	n/a
28	chr11:58828174-58828224	HepG2	liver:	n/a
29	chr11:58826073-58826123	HCPEpiC	choroid plexus:	n/a
30	chr11:58830355-58830405	HRCEpiC	kidney:	n/a
31	chr11:58826110-58826160	HEK293	kidney:	embryo
32	chr11:58830191-58830241	AG10803	skin:	n/a
33	chr11:58826414-58826464	LNCaP	prostate:	n/a
34	chr11:58828174-58828224	GM06990	blood:	n/a
35	chr11:58810187-58810237	HNPCEpiC	eye:	n/a
36	chr11:58833356-58833406	AG04450	lung:	fetal
37	chr11:58828174-58828224	AG09319	gingival:	n/a
38	chr11:58826073-58826123	Caco-2	colon:	n/a
39	chr11:58828174-58828224	HCPEpiC	choroid plexus:	n/a
40	chr11:58828174-58828224	PrEC	prostate:	n/a
41	chr11:58826475-58826525	HCPEpiC	choroid plexus:	n/a
42	chr11:58830424-58830474	HEK293	kidney:	embryo
43	chr11:58830355-58830405	ECC-1	luminal epithelium:	n/a
44	chr11:58825870-58825920	ECC-1	luminal epithelium:	n/a
45	chr11:58833356-58833406	Hela-S3	cervix:	n/a
46	chr11:58830610-58830660	GM12878	blood:	n/a
47	chr11:58830191-58830241	HCPEpiC	choroid plexus:	n/a
48	chr11:58826073-58826123	GM12891	blood:	n/a
49	chr11:58833356-58833406	AG10803	skin:	n/a
50	chr11:58825870-58825920	U87	brain:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:58399679..58402149-chr11:58838160..58840024,2	K562	blood:
2	chr11:58830364..58831268-chr11:58873992..58874927,2	HCT-116	colon:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GLYATL2-2	chr11:58820930-58821099	NR_033853
2	lnc-GLYATL2-2	chr11:58822768-58822919	ENSG00000255240.1
3	lnc-GLYATL2-2	chr11:58825845-58825925	NR_033853
4	lnc-GLYATL2-2	chr11:58818733-58818781	NR_033853
5	lnc-GLYATL2-2	chr11:58825845-58825923	ENSG00000255240.1
6	lnc-GLYATL2-2	chr11:58818733-58818781	ENSG00000255240.1
7	lnc-GLYATL2-2	chr11:58820930-58821099	ENSG00000255240.1
8	lnc-GLYATL2-2	chr11:58825845-58826132	ENSG00000255240.1
9	lnc-GLYATL2-2	chr11:58818733-58818781	ENSG00000255240.1
10	lnc-GLYATL2-2	chr11:58820930-58821099	ENSG00000255240.1

Variant related genes	Relation type
ENSG00000255240	TF binding region
GLYATL1P3	TF binding region
GLYATL1P4	TF binding region
ENSG00000255240	CpG island
GLYATL1P3	CpG island
GLYATL1P4	CpG island
ENSG00000189057	chromatin interactions

Extended variants
information (count: 1715 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:1715 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11602551	chr11:58807241-58807242	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs376717579	chr11:58807246-58807247	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs143609446	chr11:58807293-58807294	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs558200781	chr11:58807296-58807297	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs533370889	chr11:58807303-58807304	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs543989355	chr11:58807309-58807310	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs563384457	chr11:58807349-58807350	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs187079495	chr11:58807358-58807359	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs528991612	chr11:58807384-58807385	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs560488085	chr11:58807412-58807413	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs369607481	chr11:58807437-58807438	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs527816682	chr11:58807448-58807449	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs549433999	chr11:58807456-58807457	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs191050784	chr11:58807483-58807484	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs148022517	chr11:58807486-58807487	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs549815498	chr11:58807500-58807501	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs559060734	chr11:58807501-58807502	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs372274604	chr11:58807509-58807510	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs141733568	chr11:58807511-58807512	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs565319086	chr11:58807530-58807531	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs150573421	chr11:58807538-58807539	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs554617881	chr11:58807554-58807555	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs180710485	chr11:58807586-58807587	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs528419224	chr11:58807619-58807620	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs185287373	chr11:58807627-58807628	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs556793621	chr11:58807634-58807635	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs377273821	chr11:58807637-58807638	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs544133079	chr11:58807647-58807648	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs370176087	chr11:58807670-58807671	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs190041899	chr11:58807684-58807685	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs140801480	chr11:58807688-58807689	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs527656925	chr11:58807755-58807756	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs552258950	chr11:58807760-58807761	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs143132699	chr11:58807822-58807823	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs571488745	chr11:58807823-58807824	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs373386743	chr11:58807841-58807842	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs182905946	chr11:58807857-58807858	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs531407900	chr11:58807887-58807888	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs147447986	chr11:58807902-58807903	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs372965370	chr11:58807912-58807913	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs139881397	chr11:58807946-58807947	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs116781623	chr11:58807948-58807949	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs188392540	chr11:58807978-58807979	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs565558668	chr11:58807996-58807997	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs191437628	chr11:58808017-58808018	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs536206777	chr11:58808036-58808037	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs550321374	chr11:58808039-58808040	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs150049495	chr11:58808044-58808045	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs183748019	chr11:58808048-58808049	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs536739842	chr11:58808054-58808055	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:53)

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
Esophageal cancer	21851588	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Glioblastoma multiforme	22286061	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
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Pituitary adenoma	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Autism	22495309	CNVD
Autism	20808228	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:344 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:58782800-58810600	Weak transcription	Primary B cells from cord blood	blood
2	chr11:58804600-58807400	Weak transcription	Primary B cells from peripheral blood	blood
3	chr11:58805000-58825200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr11:58805200-58825400	Weak transcription	Primary hematopoietic stem cells	blood
5	chr11:58806200-58807400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
6	chr11:58806200-58807800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr11:58807400-58808000	Strong transcription	Primary B cells from peripheral blood	blood
8	chr11:58808000-58808200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr11:58808000-58808600	Enhancers	Stomach Mucosa	stomach
10	chr11:58808000-58810800	Weak transcription	Primary B cells from peripheral blood	blood
11	chr11:58810600-58811400	Strong transcription	Primary B cells from cord blood	blood
12	chr11:58810800-58811800	Strong transcription	Primary B cells from peripheral blood	blood
13	chr11:58811400-58818200	Weak transcription	Primary B cells from cord blood	blood
14	chr11:58811800-58816200	Weak transcription	Primary B cells from peripheral blood	blood
15	chr11:58813600-58825200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr11:58815400-58824400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr11:58816200-58818200	Strong transcription	Primary B cells from peripheral blood	blood
18	chr11:58816600-58816800	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr11:58816800-58817000	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr11:58817000-58817200	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr11:58817000-58817200	Enhancers	Fetal Intestine Large	intestine
22	chr11:58817000-58818200	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr11:58817200-58821800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr11:58817200-58825200	Weak transcription	Liver	Liver
25	chr11:58817200-58825400	Weak transcription	Fetal Intestine Large	intestine
26	chr11:58817400-58819400	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr11:58817400-58822000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
28	chr11:58818200-58818600	Genic enhancers	Primary B cells from peripheral blood	blood
29	chr11:58818200-58819400	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr11:58818200-58820200	Enhancers	Primary B cells from cord blood	blood
31	chr11:58818600-58825200	Enhancers	Primary B cells from peripheral blood	blood
32	chr11:58818800-58819400	Enhancers	GM12878-XiMat	blood
33	chr11:58819200-58819400	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr11:58819400-58820600	Weak transcription	GM12878-XiMat	blood
35	chr11:58819400-58821200	Weak transcription	HUES48 Cell Line	embryonic stem cell
36	chr11:58819400-58822000	Weak transcription	HUES6 Cell Line	embryonic stem cell
37	chr11:58819400-58822600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
38	chr11:58820200-58820800	Weak transcription	Primary B cells from cord blood	blood
39	chr11:58820600-58821200	Enhancers	GM12878-XiMat	blood
40	chr11:58820800-58822200	Enhancers	Primary B cells from cord blood	blood
41	chr11:58821200-58821400	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr11:58821200-58821600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr11:58821200-58825400	Weak transcription	GM12878-XiMat	blood
44	chr11:58821400-58822200	Weak transcription	HUES48 Cell Line	embryonic stem cell
45	chr11:58821600-58822400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr11:58821800-58822600	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr11:58821800-58822800	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr11:58822000-58822600	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr11:58822000-58822800	Enhancers	iPS-20b Cell Line	embryonic stem cell
50	chr11:58822200-58823200	Enhancers	HUES48 Cell Line	embryonic stem cell

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