Variant report

Variant	nsv1036651
Chromosome Location	chr11:58809985-58847365
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	chr11:58831671-58832143	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	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	chr11:58818940-58819193	GM12878	blood:	n/a	n/a
7	BATF	chr11:58831416-58832275	GM12878	blood:	n/a	chr11:58831926-58831934
8	BATF	chr11:58831471-58831776	GM12878	blood:	n/a	n/a
9	BATF	chr11:58826199-58826498	GM12878	blood:	n/a	n/a
10	BCL11A	chr11:58818899-58819262	GM12878	blood:	n/a	chr11:58819091-58819100
11	BCL11A	chr11:58818878-58819275	GM12878	blood:	n/a	chr11:58819091-58819100
12	BCL11A	chr11:58831528-58832157	GM12878	blood:	n/a	n/a
13	BCL11A	chr11:58831483-58831904	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	chr11:58827942-58827984	H1-hESC	embryonic stem cell:	n/a	n/a
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	chr11:58835714-58835923	HepG2	liver:	n/a	chr11:58835780-58835791
23	CEBPB	chr11:58825987-58826187	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr11:58835627-58835890	IMR90	lung:	n/a	chr11:58835780-58835791
25	CHD1	chr11:58825963-58826312	GM12878	blood:	n/a	n/a
26	CHD1	chr11:58821218-58821270	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr11:58825891-58826300	GM12878	blood:	n/a	n/a
28	CHD2	chr11:58825822-58826232	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr11:58826018-58826077	K562	blood:	n/a	n/a
30	CREB1	chr11:58845805-58846333	GM12878	blood:	n/a	n/a
31	CREB1	chr11:58845766-58846361	GM12878	blood:	n/a	n/a
32	CTCF	chr11:58820880-58821030	GM12874	blood:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
33	CTCF	chr11:58820920-58821070	HCT-116	colon:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
34	CTCF	chr11:58825980-58826130	HMEC	breast:	n/a	n/a
35	CTCF	chr11:58820840-58820990	GM12868	blood:	n/a	chr11:58820969-58820985 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
36	CTCF	chr11:58825938-58826176	HepG2	liver:	n/a	n/a
37	CTCF	chr11:58825924-58826243	NHEK	skin:	n/a	n/a
38	CTCF	chr11:58820860-58821010	HRPEpiC	eye:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
39	CTCF	chr11:58825939-58826206	K562	blood:	n/a	n/a
40	CTCF	chr11:58820880-58821030	HMEC	breast:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
41	CTCF	chr11:58820771-58821119	K562	blood:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
42	CTCF	chr11:58825968-58826201	GM13976	blood:	n/a	n/a
43	CTCF	chr11:58820880-58821030	NHDF-neo	bronchial:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
44	CTCF	chr11:58820754-58821158	H1-hESC	embryonic stem cell:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
45	CTCF	chr11:58820860-58821010	MCF-7	breast:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
46	CTCF	chr11:58820880-58821030	HCPEpiC	choroid plexus:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
47	CTCF	chr11:58820820-58820970	RPTEC	kidney:	n/a	n/a
48	CTCF	chr11:58820920-58821070	GM12865	blood:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
49	CTCF	chr11:58820940-58821090	HFF	foreskin:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
50	CTCF	chr11:58826020-58826170	HFF-Myc	foreskin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:58830191-58830241	MCF10A-Er-Src	breast:	n/a
2	chr11:58830191-58830241	MCF10A-Er-Src	breast:	n/a
3	chr11:58830191-58830241	AG10803	skin:	n/a
4	chr11:58830424-58830474	K562	blood:	n/a
5	chr11:58830424-58830474	HEK293	kidney:	embryo
6	chr11:58830424-58830474	GM12891	blood:	n/a
7	chr11:58828174-58828224	HIPEpiC	eye:	n/a
8	chr11:58825714-58825764	PANC-1	pancreas:	n/a
9	chr11:58826414-58826464	HMEC	breast:	n/a
10	chr11:58830355-58830405	Jurkat	blood:	n/a
11	chr11:58826414-58826464	H1-hESC	embryonic stem cell:	embryo
12	chr11:58830355-58830405	HRE	kidney:	n/a
13	chr11:58830857-58830907	NHDF-neo	bronchial:	n/a
14	chr11:58830610-58830660	A549	lung:	n/a
15	chr11:58828174-58828224	PFSK-1	brain:	n/a
16	chr11:58826110-58826160	H1-hESC	embryonic stem cell:	embryo
17	chr11:58830424-58830474	T-47D	breast:	n/a
18	chr11:58810187-58810237	K562	blood:	n/a
19	chr11:58830610-58830660	HRCEpiC	kidney:	n/a
20	chr11:58825714-58825764	NT2-D1	testis:	n/a
21	chr11:58833356-58833406	SK-N-SH	brain:	n/a
22	chr11:58830355-58830405	HCM	heart:	n/a
23	chr11:58826475-58826525	SKMC	muscle:	n/a
24	chr11:58830355-58830405	CMK	blood:	n/a
25	chr11:58826073-58826123	NH-A	brain:	n/a
26	chr11:58830355-58830405	HPAEpiC	pulmonary alveolar:	n/a
27	chr11:58830610-58830660	HepG2	liver:	n/a
28	chr11:58825714-58825764	HPAEpiC	pulmonary alveolar:	n/a
29	chr11:58825714-58825764	HepG2	liver:	n/a
30	chr11:58830355-58830405	GM12891	blood:	n/a
31	chr11:58826414-58826464	ovcar-3	ovarian:	n/a
32	chr11:58828174-58828224	HepG2	liver:	n/a
33	chr11:58826110-58826160	Caco-2	colon:	n/a
34	chr11:58830857-58830907	SK-N-SH	brain:	n/a
35	chr11:58830191-58830241	HMEC	breast:	n/a
36	chr11:58826110-58826160	HCF	heart:	n/a
37	chr11:58810187-58810237	GM19239	blood:	n/a
38	chr11:58830424-58830474	IMR90	lung:	fetal
39	chr11:58830857-58830907	HAEpiC	amniotic membrane:	n/a
40	chr11:58826475-58826525	SK-N-MC	brain:	n/a
41	chr11:58825714-58825764	AG10803	skin:	n/a
42	chr11:58826414-58826464	HepG2	liver:	n/a
43	chr11:58830424-58830474	AoSMC	blood vessel:	n/a
44	chr11:58830355-58830405	SK-N-MC	brain:	n/a
45	chr11:58830610-58830660	NHBE	bronchial:	n/a
46	chr11:58830355-58830405	NT2-D1	testis:	n/a
47	chr11:58826110-58826160	GM12892	blood:	n/a
48	chr11:58825714-58825764	HL-60	blood:	n/a
49	chr11:58826110-58826160	HEK293	kidney:	embryo
50	chr11:58826414-58826464	Hela-S3	cervix:	n/a

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

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

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

Extended variants
information (count: 1240 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:1240 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2020038	chr11:58809985-58809986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs138082957	chr11:58809995-58809996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs149545776	chr11:58810046-58810047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs528982500	chr11:58810047-58810048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs548543514	chr11:58810063-58810064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs569901915	chr11:58810078-58810079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs531137916	chr11:58810089-58810090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs558120856	chr11:58810102-58810103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs552425231	chr11:58810103-58810104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs570528911	chr11:58810144-58810145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs534671292	chr11:58810150-58810151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs181918790	chr11:58810154-58810155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs556815541	chr11:58810169-58810170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs373735864	chr11:58810175-58810176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs186530157	chr11:58810187-58810188	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
16	rs535935503	chr11:58810188-58810189	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
17	rs189776184	chr11:58810229-58810230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs143120975	chr11:58810230-58810231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs539763910	chr11:58810234-58810235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs138842163	chr11:58810235-58810236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs143065540	chr11:58810248-58810249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs375639957	chr11:58810249-58810250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs539897182	chr11:58810259-58810260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs543180621	chr11:58810281-58810282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs369546863	chr11:58810306-58810307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs573691628	chr11:58810307-58810308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs372205457	chr11:58810318-58810319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs563562500	chr11:58810325-58810326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs113920315	chr11:58810343-58810344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs372806723	chr11:58810351-58810352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs56915834	chr11:58810352-58810353	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs578409	chr11:58810355-58810356	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs528777247	chr11:58810362-58810363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs564536854	chr11:58810363-58810364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs180963445	chr11:58810377-58810378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs535601421	chr11:58810379-58810380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs530741572	chr11:58810385-58810386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs551064390	chr11:58810453-58810454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs370658457	chr11:58810462-58810463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs113027908	chr11:58810513-58810514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs186228794	chr11:58810591-58810592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs539602038	chr11:58810599-58810600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs580918	chr11:58810605-58810606	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs560820844	chr11:58810612-58810613	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs114338251	chr11:58810627-58810628	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs12794062	chr11:58810634-58810635	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs115273986	chr11:58810642-58810643	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs386753967	chr11:58810668-58810669	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs562205132	chr11:58810670-58810671	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs11229769	chr11:58810675-58810676	Strong transcription 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:332 , 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	chr11:58805000-58825200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr11:58805200-58825400	Weak transcription	Primary hematopoietic stem cells	blood
4	chr11:58808000-58810800	Weak transcription	Primary B cells from peripheral blood	blood
5	chr11:58810600-58811400	Strong transcription	Primary B cells from cord blood	blood
6	chr11:58810800-58811800	Strong transcription	Primary B cells from peripheral blood	blood
7	chr11:58811400-58818200	Weak transcription	Primary B cells from cord blood	blood
8	chr11:58811800-58816200	Weak transcription	Primary B cells from peripheral blood	blood
9	chr11:58813600-58825200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr11:58815400-58824400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr11:58816200-58818200	Strong transcription	Primary B cells from peripheral blood	blood
12	chr11:58816600-58816800	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr11:58816800-58817000	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr11:58817000-58817200	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr11:58817000-58817200	Enhancers	Fetal Intestine Large	intestine
16	chr11:58817000-58818200	Weak transcription	HUES6 Cell Line	embryonic stem cell
17	chr11:58817200-58821800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr11:58817200-58825200	Weak transcription	Liver	Liver
19	chr11:58817200-58825400	Weak transcription	Fetal Intestine Large	intestine
20	chr11:58817400-58819400	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr11:58817400-58822000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
22	chr11:58818200-58818600	Genic enhancers	Primary B cells from peripheral blood	blood
23	chr11:58818200-58819400	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr11:58818200-58820200	Enhancers	Primary B cells from cord blood	blood
25	chr11:58818600-58825200	Enhancers	Primary B cells from peripheral blood	blood
26	chr11:58818800-58819400	Enhancers	GM12878-XiMat	blood
27	chr11:58819200-58819400	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr11:58819400-58820600	Weak transcription	GM12878-XiMat	blood
29	chr11:58819400-58821200	Weak transcription	HUES48 Cell Line	embryonic stem cell
30	chr11:58819400-58822000	Weak transcription	HUES6 Cell Line	embryonic stem cell
31	chr11:58819400-58822600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
32	chr11:58820200-58820800	Weak transcription	Primary B cells from cord blood	blood
33	chr11:58820600-58821200	Enhancers	GM12878-XiMat	blood
34	chr11:58820800-58822200	Enhancers	Primary B cells from cord blood	blood
35	chr11:58821200-58821400	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr11:58821200-58821600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr11:58821200-58825400	Weak transcription	GM12878-XiMat	blood
38	chr11:58821400-58822200	Weak transcription	HUES48 Cell Line	embryonic stem cell
39	chr11:58821600-58822400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr11:58821800-58822600	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr11:58821800-58822800	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr11:58822000-58822600	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr11:58822000-58822800	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr11:58822200-58823200	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr11:58822200-58824400	Weak transcription	Primary B cells from cord blood	blood
46	chr11:58822400-58823200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr11:58822600-58823200	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr11:58822600-58825200	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr11:58822800-58825200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
50	chr11:58822800-58825200	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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