Variant report

Variant	nsv897594
Chromosome Location	chr11:58810634-58858722
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	chr11:58825833-58826405	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	chr11:58818940-58819193	GM12878	blood:	n/a	n/a
6	BATF	chr11:58831471-58831776	GM12878	blood:	n/a	n/a
7	BATF	chr11:58831416-58832275	GM12878	blood:	n/a	chr11:58831926-58831934
8	BATF	chr11:58831786-58832150	GM12878	blood:	n/a	chr11:58831926-58831934
9	BATF	chr11:58826199-58826498	GM12878	blood:	n/a	n/a
10	BCL11A	chr11:58818878-58819275	GM12878	blood:	n/a	chr11:58819091-58819100
11	BCL11A	chr11:58831483-58831904	GM12878	blood:	n/a	n/a
12	BCL11A	chr11:58818899-58819262	GM12878	blood:	n/a	chr11:58819091-58819100
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	chr11:58835627-58835890	IMR90	lung:	n/a	chr11:58835780-58835791
20	CEBPB	chr11:58852160-58852235	HepG2	liver:	n/a	n/a
21	CEBPB	chr11:58827942-58827984	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr11:58850700-58850889	HepG2	liver:	n/a	n/a
23	CEBPB	chr11:58835676-58835875	K562	blood:	n/a	chr11:58835780-58835791
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	chr11:58835714-58835923	HepG2	liver:	n/a	chr11:58835780-58835791
27	CHD1	chr11:58825963-58826312	GM12878	blood:	n/a	n/a
28	CHD1	chr11:58821218-58821270	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr11:58825891-58826300	GM12878	blood:	n/a	n/a
30	CHD2	chr11:58825822-58826232	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr11:58826018-58826077	K562	blood:	n/a	n/a
32	CREB1	chr11:58845766-58846361	GM12878	blood:	n/a	n/a
33	CREB1	chr11:58845805-58846333	GM12878	blood:	n/a	n/a
34	CTCF	chr11:58820861-58821027	SK-N-SH_RA	brain:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
35	CTCF	chr11:58825914-58826215	MCF-7	breast:	n/a	n/a
36	CTCF	chr11:58826000-58826150	GM12872	blood:	n/a	n/a
37	CTCF	chr11:58825881-58826206	A549	lung:	n/a	n/a
38	CTCF	chr11:58826040-58826190	AG09309	skin:	n/a	n/a
39	CTCF	chr11:58826000-58826150	HBMEC	blood vessel:	n/a	n/a
40	CTCF	chr11:58820820-58820970	WI-38	lung:	n/a	n/a
41	CTCF	chr11:58826000-58826150	K562	blood:	n/a	n/a
42	CTCF	chr11:58820860-58821010	GM12864	blood:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
43	CTCF	chr11:58820940-58821090	AoAF	blood vessel:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
44	CTCF	chr11:58825980-58826130	WERI-Rb-1	eye:	n/a	n/a
45	CTCF	chr11:58820790-58821140	A549	lung:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
46	CTCF	chr11:58820880-58821030	GM12874	blood:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
47	CTCF	chr11:58820860-58821010	HVMF	connective:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
48	CTCF	chr11:58826040-58826190	GM12868	blood:	n/a	n/a
49	CTCF	chr11:58820840-58820990	HUVEC	blood vessel:	n/a	chr11:58820969-58820985 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
50	CTCF	chr11:58825962-58826217	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:58826073-58826123	HIPEpiC	eye:	n/a
2	chr11:58826073-58826123	HIPEpiC	eye:	n/a
3	chr11:58830424-58830474	HepG2	liver:	n/a
4	chr11:58830191-58830241	K562	blood:	n/a
5	chr11:58830610-58830660	AG09319	gingival:	n/a
6	chr11:58830610-58830660	H1-hESC	embryonic stem cell:	embryo
7	chr11:58828174-58828224	PrEC	prostate:	n/a
8	chr11:58826073-58826123	A549	lung:	n/a
9	chr11:58830355-58830405	HepG2	liver:	n/a
10	chr11:58825870-58825920	ECC-1	luminal epithelium:	n/a
11	chr11:58825870-58825920	HMEC	breast:	n/a
12	chr11:58833356-58833406	NHDF-neo	bronchial:	n/a
13	chr11:58830857-58830907	AoSMC	blood vessel:	n/a
14	chr11:58828174-58828224	HPAEpiC	pulmonary alveolar:	n/a
15	chr11:58825870-58825920	SAEC	small airway:	n/a
16	chr11:58826110-58826160	AG09309	skin:	n/a
17	chr11:58830857-58830907	BJ	skin:	n/a
18	chr11:58830424-58830474	BJ	skin:	n/a
19	chr11:58826475-58826525	SK-N-MC	brain:	n/a
20	chr11:58830610-58830660	NHBE	bronchial:	n/a
21	chr11:58830610-58830660	Hepatocyte	liver:	n/a
22	chr11:58825714-58825764	GM19239	blood:	n/a
23	chr11:58826073-58826123	Hepatocyte	liver:	n/a
24	chr11:58826073-58826123	AG04449	skin:	fetal
25	chr11:58833356-58833406	GM12892	blood:	n/a
26	chr11:58828174-58828224	HCF	heart:	n/a
27	chr11:58830857-58830907	HRPEpiC	eye:	n/a
28	chr11:58825870-58825920	MCF10A-Er-Src	breast:	n/a
29	chr11:58825870-58825920	HRCEpiC	kidney:	n/a
30	chr11:58830610-58830660	HMEC	breast:	n/a
31	chr11:58826110-58826160	HL-60	blood:	n/a
32	chr11:58828174-58828224	GM19239	blood:	n/a
33	chr11:58825714-58825764	AG04450	lung:	fetal
34	chr11:58826414-58826464	SKMC	muscle:	n/a
35	chr11:58830424-58830474	Hepatocyte	liver:	n/a
36	chr11:58833356-58833406	Hepatocyte	liver:	n/a
37	chr11:58826414-58826464	GM06990	blood:	n/a
38	chr11:58830857-58830907	MCF10A-Er-Src	breast:	n/a
39	chr11:58830424-58830474	ECC-1	luminal epithelium:	n/a
40	chr11:58830191-58830241	SK-N-MC	brain:	n/a
41	chr11:58825714-58825764	HepG2	liver:	n/a
42	chr11:58826414-58826464	Caco-2	colon:	n/a
43	chr11:58830191-58830241	HIPEpiC	eye:	n/a
44	chr11:58830857-58830907	HCT-116	colon:	n/a
45	chr11:58830191-58830241	PrEC	prostate:	n/a
46	chr11:58825714-58825764	NHBE	bronchial:	n/a
47	chr11:58830610-58830660	MCF-7	breast:	n/a
48	chr11:58830355-58830405	MCF10A-Er-Src	breast:	n/a
49	chr11:58833356-58833406	PANC-1	pancreas:	n/a
50	chr11:58825870-58825920	HUVEC	blood vessel:	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	ENSG00000255240.1
2	lnc-GLYATL2-2	chr11:58818733-58818781	NR_033853
3	lnc-GLYATL2-2	chr11:58822768-58822919	ENSG00000255240.1
4	lnc-GLYATL2-2	chr11:58825845-58826132	ENSG00000255240.1
5	lnc-GLYATL2-2	chr11:58818733-58818781	ENSG00000255240.1
6	lnc-GLYATL2-2	chr11:58818733-58818781	ENSG00000255240.1
7	lnc-GLYATL2-2	chr11:58820930-58821099	ENSG00000255240.1
8	lnc-GLYATL2-2	chr11:58820930-58821099	NR_033853
9	lnc-GLYATL2-2	chr11:58825845-58825923	ENSG00000255240.1
10	lnc-GLYATL2-2	chr11:58825845-58825925	NR_033853

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

Extended variants
information (count: 1739 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:1739 , 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	rs12794062	chr11:58810634-58810635	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs115273986	chr11:58810642-58810643	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs386753967	chr11:58810668-58810669	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs562205132	chr11:58810670-58810671	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs11229769	chr11:58810675-58810676	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs546033210	chr11:58810704-58810705	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs150623341	chr11:58810724-58810725	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs386753968	chr11:58810731-58810732	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs11229771	chr11:58810732-58810733	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs2844344	chr11:58810775-58810776	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs2720350	chr11:58810787-58810788	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs3017462	chr11:58810816-58810817	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs551509206	chr11:58810836-58810837	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs375865784	chr11:58810845-58810846	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs529249554	chr11:58810853-58810854	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs3017463	chr11:58810862-58810863	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs551101410	chr11:58810912-58810913	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs191423408	chr11:58810913-58810914	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs183255392	chr11:58810927-58810928	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs185824860	chr11:58810941-58810942	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs566639772	chr11:58811016-58811017	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs533867880	chr11:58811023-58811024	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs3017464	chr11:58811046-58811047	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs190684300	chr11:58811066-58811067	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs537403640	chr11:58811080-58811081	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs10160428	chr11:58811136-58811137	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs577358166	chr11:58811146-58811147	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs544687959	chr11:58811154-58811155	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs567912757	chr11:58811165-58811166	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs183161552	chr11:58811228-58811229	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs10160600	chr11:58811241-58811242	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs540583655	chr11:58811251-58811252	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs187820636	chr11:58811252-58811253	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs529306586	chr11:58811261-58811262	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs143222512	chr11:58811271-58811272	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs7479623	chr11:58811310-58811311	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs376102878	chr11:58811317-58811318	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs148861723	chr11:58811335-58811336	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs551827780	chr11:58811393-58811394	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs558195469	chr11:58811395-58811396	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs574915247	chr11:58811425-58811426	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs571680189	chr11:58811429-58811430	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs1943142	chr11:58811441-58811442	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs527441287	chr11:58811452-58811453	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs142504011	chr11:58811455-58811456	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs150939234	chr11:58811464-58811465	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs372247808	chr11:58811507-58811508	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs555772919	chr11:58811515-58811516	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs570888082	chr11:58811532-58811533	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs557392184	chr11:58811602-58811603	Weak transcription Strong 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:343 , 50 per page) page: 1 2 3 4 5 6 7

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	chr11:58808000-58810800	Weak transcription	Primary B cells from peripheral blood	blood
4	chr11:58810600-58811400	Strong transcription	Primary B cells from cord blood	blood
5	chr11:58810800-58811800	Strong transcription	Primary B cells from peripheral blood	blood
6	chr11:58811400-58818200	Weak transcription	Primary B cells from cord blood	blood
7	chr11:58811800-58816200	Weak transcription	Primary B cells from peripheral blood	blood
8	chr11:58813600-58825200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr11:58815400-58824400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr11:58816200-58818200	Strong transcription	Primary B cells from peripheral blood	blood
11	chr11:58816600-58816800	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr11:58816800-58817000	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr11:58817000-58817200	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr11:58817000-58817200	Enhancers	Fetal Intestine Large	intestine
15	chr11:58817000-58818200	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr11:58817200-58821800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr11:58817200-58825200	Weak transcription	Liver	Liver
18	chr11:58817200-58825400	Weak transcription	Fetal Intestine Large	intestine
19	chr11:58817400-58819400	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr11:58817400-58822000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
21	chr11:58818200-58818600	Genic enhancers	Primary B cells from peripheral blood	blood
22	chr11:58818200-58819400	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr11:58818200-58820200	Enhancers	Primary B cells from cord blood	blood
24	chr11:58818600-58825200	Enhancers	Primary B cells from peripheral blood	blood
25	chr11:58818800-58819400	Enhancers	GM12878-XiMat	blood
26	chr11:58819200-58819400	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr11:58819400-58820600	Weak transcription	GM12878-XiMat	blood
28	chr11:58819400-58821200	Weak transcription	HUES48 Cell Line	embryonic stem cell
29	chr11:58819400-58822000	Weak transcription	HUES6 Cell Line	embryonic stem cell
30	chr11:58819400-58822600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
31	chr11:58820200-58820800	Weak transcription	Primary B cells from cord blood	blood
32	chr11:58820600-58821200	Enhancers	GM12878-XiMat	blood
33	chr11:58820800-58822200	Enhancers	Primary B cells from cord blood	blood
34	chr11:58821200-58821400	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr11:58821200-58821600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr11:58821200-58825400	Weak transcription	GM12878-XiMat	blood
37	chr11:58821400-58822200	Weak transcription	HUES48 Cell Line	embryonic stem cell
38	chr11:58821600-58822400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
39	chr11:58821800-58822600	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr11:58821800-58822800	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr11:58822000-58822600	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr11:58822000-58822800	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr11:58822200-58823200	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr11:58822200-58824400	Weak transcription	Primary B cells from cord blood	blood
45	chr11:58822400-58823200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr11:58822600-58823200	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr11:58822600-58825200	Weak transcription	HUES6 Cell Line	embryonic stem cell
48	chr11:58822800-58825200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr11:58822800-58825200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
50	chr11:58823200-58825200	Weak transcription	HUES48 Cell Line	embryonic stem cell

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