Variant report

Variant	nsv1045695
Chromosome Location	chr11:58811241-58864544
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:766)
CpG islands
(count:793)
Chromatin interactive
region (count:3)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:766 , 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	ATF2	chr11:58864502-58864964	GM12878	blood:	n/a	n/a
2	ATF2	chr11:58831402-58832419	GM12878	blood:	n/a	n/a
3	ATF2	chr11:58825833-58826405	GM12878	blood:	n/a	n/a
4	ATF2	chr11:58831671-58832143	GM12878	blood:	n/a	n/a
5	BACH1	chr11:58825972-58826213	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr11:58831471-58831776	GM12878	blood:	n/a	n/a
7	BATF	chr11:58862752-58863071	GM12878	blood:	n/a	n/a
8	BATF	chr11:58818940-58819193	GM12878	blood:	n/a	n/a
9	BATF	chr11:58826199-58826498	GM12878	blood:	n/a	n/a
10	BATF	chr11:58831786-58832150	GM12878	blood:	n/a	chr11:58831926-58831934
11	BATF	chr11:58831416-58832275	GM12878	blood:	n/a	chr11:58831926-58831934
12	BCL11A	chr11:58831528-58832157	GM12878	blood:	n/a	n/a
13	BCL11A	chr11:58831483-58831904	GM12878	blood:	n/a	n/a
14	BCL11A	chr11:58862711-58863079	GM12878	blood:	n/a	chr11:58862903-58862912
15	BCL11A	chr11:58862690-58863069	GM12878	blood:	n/a	chr11:58862903-58862912
16	BCL11A	chr11:58818899-58819262	GM12878	blood:	n/a	chr11:58819091-58819100
17	BCL11A	chr11:58818878-58819275	GM12878	blood:	n/a	chr11:58819091-58819100
18	BCL3	chr11:58831794-58832281	GM12878	blood:	n/a	n/a
19	BHLHE40	chr11:58825938-58826278	GM12878	blood:	n/a	n/a
20	BHLHE40	chr11:58862780-58863126	GM12878	blood:	n/a	n/a
21	BHLHE40	chr11:58820953-58821000	K562	blood:	n/a	n/a
22	BHLHE40	chr11:58826040-58826162	K562	blood:	n/a	n/a
23	BRCA1	chr11:58825950-58826184	GM12878	blood:	n/a	n/a
24	CEBPB	chr11:58825987-58826187	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr11:58841369-58841519	IMR90	lung:	n/a	n/a
26	CEBPB	chr11:58850700-58850889	HepG2	liver:	n/a	n/a
27	CEBPB	chr11:58835676-58835875	K562	blood:	n/a	chr11:58835780-58835791
28	CEBPB	chr11:58835627-58835890	IMR90	lung:	n/a	chr11:58835780-58835791
29	CEBPB	chr11:58861212-58861364	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr11:58827942-58827984	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr11:58835714-58835923	HepG2	liver:	n/a	chr11:58835780-58835791
32	CEBPB	chr11:58852160-58852235	HepG2	liver:	n/a	n/a
33	CHD1	chr11:58825963-58826312	GM12878	blood:	n/a	n/a
34	CHD1	chr11:58821218-58821270	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr11:58825891-58826300	GM12878	blood:	n/a	n/a
36	CHD2	chr11:58826018-58826077	K562	blood:	n/a	n/a
37	CHD2	chr11:58825822-58826232	H1-hESC	embryonic stem cell:	n/a	n/a
38	CREB1	chr11:58845805-58846333	GM12878	blood:	n/a	n/a
39	CREB1	chr11:58845766-58846361	GM12878	blood:	n/a	n/a
40	CTCF	chr11:58826000-58826150	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr11:58825980-58826130	GM12874	blood:	n/a	n/a
42	CTCF	chr11:58825931-58826299	HCT-116	colon:	n/a	n/a
43	CTCF	chr11:58820860-58821010	GM12867	blood:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
44	CTCF	chr11:58820642-58820718	GM10266	blood:	n/a	n/a
45	CTCF	chr11:58825980-58826130	HMF	breast:	n/a	n/a
46	CTCF	chr11:58864280-58864430	HPF	lung:	n/a	n/a
47	CTCF	chr11:58820500-58820650	GM12873	blood:	n/a	n/a
48	CTCF	chr11:58825854-58826335	GM12878	blood:	n/a	n/a
49	CTCF	chr11:58820880-58821030	HPF	lung:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
50	CTCF	chr11:58825956-58826189	MCF-7	breast:	n/a	n/a

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:58826073-58826123	NHBE	bronchial:	n/a
2	chr11:58830857-58830907	GM19239	blood:	n/a
3	chr11:58826073-58826123	BJ	skin:	n/a
4	chr11:58826414-58826464	ECC-1	luminal epithelium:	n/a
5	chr11:58825714-58825764	HIPEpiC	eye:	n/a
6	chr11:58825870-58825920	HPAEpiC	pulmonary alveolar:	n/a
7	chr11:58830610-58830660	HAEpiC	amniotic membrane:	n/a
8	chr11:58825714-58825764	AG09319	gingival:	n/a
9	chr11:58830355-58830405	Hepatocyte	liver:	n/a
10	chr11:58826073-58826123	HIPEpiC	eye:	n/a
11	chr11:58830857-58830907	HEK293	kidney:	embryo
12	chr11:58828174-58828224	NT2-D1	testis:	n/a
13	chr11:58826073-58826123	A549	lung:	n/a
14	chr11:58825870-58825920	AG09319	gingival:	n/a
15	chr11:58825714-58825764	IMR90	lung:	fetal
16	chr11:58826414-58826464	BJ	skin:	n/a
17	chr11:58825714-58825764	LNCaP	prostate:	n/a
18	chr11:58826073-58826123	IMR90	lung:	fetal
19	chr11:58825870-58825920	NHDF-neo	bronchial:	n/a
20	chr11:58826110-58826160	BE2_C	brain:	n/a
21	chr11:58830610-58830660	AG09319	gingival:	n/a
22	chr11:58825870-58825920	HCT-116	colon:	n/a
23	chr11:58828174-58828224	BE2_C	brain:	n/a
24	chr11:58826414-58826464	Caco-2	colon:	n/a
25	chr11:58830424-58830474	GM12892	blood:	n/a
26	chr11:58826110-58826160	NB4	blood:	n/a
27	chr11:58830857-58830907	GM12878	blood:	n/a
28	chr11:58826110-58826160	NT2-D1	testis:	n/a
29	chr11:58830857-58830907	CMK	blood:	n/a
30	chr11:58825870-58825920	MCF10A-Er-Src	breast:	n/a
31	chr11:58828174-58828224	HCPEpiC	choroid plexus:	n/a
32	chr11:58830355-58830405	HCF	heart:	n/a
33	chr11:58825870-58825920	PrEC	prostate:	n/a
34	chr11:58826073-58826123	Jurkat	blood:	n/a
35	chr11:58830857-58830907	PANC-1	pancreas:	n/a
36	chr11:58830424-58830474	U87	brain:	n/a
37	chr11:58830610-58830660	GM12892	blood:	n/a
38	chr11:58826110-58826160	RPTEC	kidney:	n/a
39	chr11:58826414-58826464	HL-60	blood:	n/a
40	chr11:58825714-58825764	U87	brain:	n/a
41	chr11:58830424-58830474	GM12878	blood:	n/a
42	chr11:58830610-58830660	HUVEC	blood vessel:	n/a
43	chr11:58825714-58825764	HCF	heart:	n/a
44	chr11:58826073-58826123	HCT-116	colon:	n/a
45	chr11:58826073-58826123	AG04450	lung:	fetal
46	chr11:58830191-58830241	BJ	skin:	n/a
47	chr11:58825870-58825920	Caco-2	colon:	n/a
48	chr11:58830191-58830241	MCF10A-Er-Src	breast:	n/a
49	chr11:58830610-58830660	SK-N-MC	brain:	n/a
50	chr11:58830857-58830907	MCF10A-Er-Src	breast:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:58863409..58866220-chr11:58910202..58912249,2	K562	blood:
2	chr11:58399679..58402149-chr11:58838160..58840024,2	K562	blood:
3	chr11:58830364..58831268-chr11:58873992..58874927,2	HCT-116	colon:

(count:10 , 50 per page) page: 1

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

No data

Variant related genes	Relation type
ENSG00000255240	TF binding region
GLYATL1P3	TF binding region
ENSG00000255240	CpG island
GLYATL1P3	CpG island
ENSG00000245571	chromatin interactions
ENSG00000166801	chromatin interactions
ENSG00000189057	chromatin interactions

Extended variants
information (count: 1997 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:1997 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10160600	chr11:58811241-58811242	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs540583655	chr11:58811251-58811252	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs187820636	chr11:58811252-58811253	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs529306586	chr11:58811261-58811262	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs143222512	chr11:58811271-58811272	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs7479623	chr11:58811310-58811311	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs376102878	chr11:58811317-58811318	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs148861723	chr11:58811335-58811336	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs551827780	chr11:58811393-58811394	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs558195469	chr11:58811395-58811396	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs574915247	chr11:58811425-58811426	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs571680189	chr11:58811429-58811430	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs1943142	chr11:58811441-58811442	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs527441287	chr11:58811452-58811453	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs142504011	chr11:58811455-58811456	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs150939234	chr11:58811464-58811465	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs372247808	chr11:58811507-58811508	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs555772919	chr11:58811515-58811516	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs570888082	chr11:58811532-58811533	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs557392184	chr11:58811602-58811603	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs538367764	chr11:58811613-58811614	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs113435190	chr11:58811625-58811626	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs553792773	chr11:58811660-58811661	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs573363599	chr11:58811747-58811748	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs77609816	chr11:58811756-58811757	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs540772008	chr11:58811794-58811795	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs529990704	chr11:58811807-58811808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs555676853	chr11:58811817-58811818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs117997538	chr11:58811820-58811821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs192213805	chr11:58811833-58811834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs560269769	chr11:58811837-58811838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs562894252	chr11:58811849-58811850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs533334185	chr11:58811889-58811890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs545180487	chr11:58811925-58811926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs182870991	chr11:58811951-58811952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs527782542	chr11:58811992-58811993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs549202689	chr11:58812111-58812112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs115862494	chr11:58812125-58812126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs187824803	chr11:58812155-58812156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs549636525	chr11:58812178-58812179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs570923041	chr11:58812294-58812295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs10750909	chr11:58812308-58812309	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs140868978	chr11:58812334-58812335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs192899179	chr11:58812335-58812336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs535951561	chr11:58812343-58812344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs3133049	chr11:58812369-58812370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs3133050	chr11:58812398-58812399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs555958079	chr11:58812401-58812402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs372173510	chr11:58812405-58812406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs538557140	chr11:58812427-58812428	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:405 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

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

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