Variant report

Variant	nsv1039379
Chromosome Location	chr11:58800374-58864544
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:775)
CpG islands
(count:915)
Chromatin interactive
region (count:3)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:775 , 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	chr11:58825833-58826405	GM12878	blood:	n/a	n/a
2	ATF2	chr11:58864502-58864964	GM12878	blood:	n/a	n/a
3	ATF2	chr11:58831402-58832419	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	chr11:58862752-58863071	GM12878	blood:	n/a	n/a
7	BATF	chr11:58818940-58819193	GM12878	blood:	n/a	n/a
8	BATF	chr11:58826199-58826498	GM12878	blood:	n/a	n/a
9	BATF	chr11:58831786-58832150	GM12878	blood:	n/a	chr11:58831926-58831934
10	BATF	chr11:58831416-58832275	GM12878	blood:	n/a	chr11:58831926-58831934
11	BATF	chr11:58831471-58831776	GM12878	blood:	n/a	n/a
12	BCL11A	chr11:58862711-58863079	GM12878	blood:	n/a	chr11:58862903-58862912
13	BCL11A	chr11:58818899-58819262	GM12878	blood:	n/a	chr11:58819091-58819100
14	BCL11A	chr11:58818878-58819275	GM12878	blood:	n/a	chr11:58819091-58819100
15	BCL11A	chr11:58862690-58863069	GM12878	blood:	n/a	chr11:58862903-58862912
16	BCL11A	chr11:58831528-58832157	GM12878	blood:	n/a	n/a
17	BCL11A	chr11:58831483-58831904	GM12878	blood:	n/a	n/a
18	BCL3	chr11:58831794-58832281	GM12878	blood:	n/a	n/a
19	BHLHE40	chr11:58820953-58821000	K562	blood:	n/a	n/a
20	BHLHE40	chr11:58862780-58863126	GM12878	blood:	n/a	n/a
21	BHLHE40	chr11:58825938-58826278	GM12878	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	chr11:58827942-58827984	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr11:58825987-58826187	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr11:58852160-58852235	HepG2	liver:	n/a	n/a
27	CEBPB	chr11:58861212-58861364	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr11:58850700-58850889	HepG2	liver:	n/a	n/a
29	CEBPB	chr11:58835627-58835890	IMR90	lung:	n/a	chr11:58835780-58835791
30	CEBPB	chr11:58835676-58835875	K562	blood:	n/a	chr11:58835780-58835791
31	CEBPB	chr11:58835714-58835923	HepG2	liver:	n/a	chr11:58835780-58835791
32	CEBPB	chr11:58841369-58841519	IMR90	lung:	n/a	n/a
33	CHD1	chr11:58821218-58821270	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD1	chr11:58825963-58826312	GM12878	blood:	n/a	n/a
35	CHD2	chr11:58825891-58826300	GM12878	blood:	n/a	n/a
36	CHD2	chr11:58825822-58826232	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD2	chr11:58826018-58826077	K562	blood:	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	chr11:58825960-58826197	LNCaP	prostate:	n/a	n/a
41	CTCF	chr11:58826020-58826170	HFF-Myc	foreskin:	n/a	n/a
42	CTCF	chr11:58825980-58826130	GM12866	blood:	n/a	n/a
43	CTCF	chr11:58820920-58821070	GM12865	blood:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
44	CTCF	chr11:58825938-58826176	HepG2	liver:	n/a	n/a
45	CTCF	chr11:58820860-58821010	GM12870	blood:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
46	CTCF	chr11:58820040-58820123	GM10248	blood:	n/a	n/a
47	CTCF	chr11:58825891-58826269	GM19238	blood:	n/a	n/a
48	CTCF	chr11:58826000-58826150	HCFaa	heart:	n/a	n/a
49	CTCF	chr11:58820880-58821030	HPAF	blood vessel:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
50	CTCF	chr11:58825917-58826236	Lung_OC	lung:	n/a	n/a

(count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:58830424-58830474	HepG2	liver:	n/a
2	chr11:58830610-58830660	HCM	heart:	n/a
3	chr11:58830424-58830474	GM06990	blood:	n/a
4	chr11:58830424-58830474	RPTEC	kidney:	n/a
5	chr11:58826110-58826160	PFSK-1	brain:	n/a
6	chr11:58830355-58830405	H1-hESC	embryonic stem cell:	embryo
7	chr11:58810187-58810237	PANC-1	pancreas:	n/a
8	chr11:58826110-58826160	HNPCEpiC	eye:	n/a
9	chr11:58830610-58830660	AG09309	skin:	n/a
10	chr11:58826475-58826525	NH-A	brain:	n/a
11	chr11:58830857-58830907	HRE	kidney:	n/a
12	chr11:58826475-58826525	ProgFib	skin:	n/a
13	chr11:58830355-58830405	T-47D	breast:	n/a
14	chr11:58826073-58826123	HPAEpiC	pulmonary alveolar:	n/a
15	chr11:58828174-58828224	HRE	kidney:	n/a
16	chr11:58830355-58830405	PrEC	prostate:	n/a
17	chr11:58825870-58825920	HL-60	blood:	n/a
18	chr11:58830610-58830660	PFSK-1	brain:	n/a
19	chr11:58828174-58828224	GM12892	blood:	n/a
20	chr11:58828174-58828224	SKMC	muscle:	n/a
21	chr11:58826073-58826123	HMEC	breast:	n/a
22	chr11:58825714-58825764	Hela-S3	cervix:	n/a
23	chr11:58833356-58833406	SKMC	muscle:	n/a
24	chr11:58826073-58826123	SK-N-SH	brain:	n/a
25	chr11:58830857-58830907	HEK293	kidney:	embryo
26	chr11:58830355-58830405	PFSK-1	brain:	n/a
27	chr11:58828174-58828224	Hela-S3	cervix:	n/a
28	chr11:58830191-58830241	SKMC	muscle:	n/a
29	chr11:58810187-58810237	AoSMC	blood vessel:	n/a
30	chr11:58830424-58830474	HNPCEpiC	eye:	n/a
31	chr11:58830857-58830907	Hepatocyte	liver:	n/a
32	chr11:58830610-58830660	GM12878	blood:	n/a
33	chr11:58830610-58830660	HL-60	blood:	n/a
34	chr11:58826073-58826123	MCF-7	breast:	n/a
35	chr11:58826110-58826160	HCT-116	colon:	n/a
36	chr11:58810187-58810237	MCF10A-Er-Src	breast:	n/a
37	chr11:58830424-58830474	HL-60	blood:	n/a
38	chr11:58830355-58830405	BJ	skin:	n/a
39	chr11:58826414-58826464	PANC-1	pancreas:	n/a
40	chr11:58830191-58830241	NB4	blood:	n/a
41	chr11:58830610-58830660	Hela-S3	cervix:	n/a
42	chr11:58830355-58830405	SK-N-SH_RA	brain:	n/a
43	chr11:58825870-58825920	NH-A	brain:	n/a
44	chr11:58830191-58830241	GM06990	blood:	n/a
45	chr11:58833356-58833406	A549	lung:	n/a
46	chr11:58830191-58830241	BE2_C	brain:	n/a
47	chr11:58830424-58830474	LNCaP	prostate:	n/a
48	chr11:58826073-58826123	HUVEC	blood vessel:	n/a
49	chr11:58806952-58807002	HAEpiC	amniotic membrane:	n/a
50	chr11:58826475-58826525	HIPEpiC	eye:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr11:58399679..58402149-chr11:58838160..58840024,2	K562	blood:
2	chr11:58863409..58866220-chr11:58910202..58912249,2	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	chr11:58818733-58818781	ENSG00000255240.1
3	lnc-GLYATL2-2	chr11:58820930-58821099	ENSG00000255240.1
4	lnc-GLYATL2-2	chr11:58818733-58818781	NR_033853
5	lnc-GLYATL2-2	chr11:58825845-58825923	ENSG00000255240.1
6	lnc-GLYATL2-2	chr11:58820930-58821099	NR_033853
7	lnc-GLYATL2-2	chr11:58820930-58821099	ENSG00000255240.1
8	lnc-GLYATL2-2	chr11:58822768-58822919	ENSG00000255240.1
9	lnc-GLYATL2-2	chr11:58818733-58818781	ENSG00000255240.1
10	lnc-GLYATL2-2	chr11:58825845-58825925	NR_033853

No data

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
ENSG00000245571	chromatin interactions
ENSG00000189057	chromatin interactions
ENSG00000166801	chromatin interactions

Extended variants
information (count: 2540 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:2540 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1943141	chr11:58800374-58800375	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs550642144	chr11:58800384-58800385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs4616060	chr11:58800434-58800435	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs139204045	chr11:58800493-58800494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs61891785	chr11:58800509-58800510	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs192576805	chr11:58800510-58800511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs141754290	chr11:58800516-58800517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs534916238	chr11:58800580-58800581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs12786168	chr11:58800594-58800595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs147100664	chr11:58800633-58800634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs568456694	chr11:58800647-58800648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs148218092	chr11:58800663-58800664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs557278530	chr11:58800705-58800706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs575561716	chr11:58800856-58800857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs553514580	chr11:58800875-58800876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs182654504	chr11:58800902-58800903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs188076032	chr11:58800909-58800910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs573056021	chr11:58800937-58800938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs141218234	chr11:58801021-58801022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs555695446	chr11:58801083-58801084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs573934539	chr11:58801141-58801142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs192727574	chr11:58801143-58801144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs2510229	chr11:58801160-58801161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs184340241	chr11:58801193-58801194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs188992921	chr11:58801201-58801202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs192296361	chr11:58801202-58801203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs184774418	chr11:58801249-58801250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs150711239	chr11:58801283-58801284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs2510230	chr11:58801288-58801289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs528653141	chr11:58801302-58801303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs546837654	chr11:58801362-58801363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs371190088	chr11:58801397-58801398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs529505452	chr11:58801407-58801408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs551010125	chr11:58801433-58801434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs12276995	chr11:58801443-58801444	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs539480708	chr11:58801447-58801448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs190483613	chr11:58801486-58801487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs556441885	chr11:58801509-58801510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs11229755	chr11:58801536-58801537	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs76039980	chr11:58801572-58801573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs555559247	chr11:58801573-58801574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs573896681	chr11:58801625-58801626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs565019333	chr11:58801632-58801633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs74237937	chr11:58801633-58801634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs556213210	chr11:58801653-58801654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs180701075	chr11:58801659-58801660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs185998690	chr11:58801697-58801698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs559814574	chr11:58801698-58801699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs201144613	chr11:58801709-58801710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs189629016	chr11:58801722-58801723	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:424 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:58782800-58810600	Weak transcription	Primary B cells from cord blood	blood
2	chr11:58801400-58803200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr11:58803200-58804600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr11:58804400-58804600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr11:58804400-58804600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
6	chr11:58804600-58805000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr11:58804600-58806200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr11:58804600-58807400	Weak transcription	Primary B cells from peripheral blood	blood
9	chr11:58804800-58805000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr11:58804800-58805200	Enhancers	Primary hematopoietic stem cells	blood
11	chr11:58804800-58805200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr11:58805000-58805200	Enhancers	Rectal Mucosa Donor 31	rectum
13	chr11:58805000-58806200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr11:58805000-58825200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr11:58805200-58825400	Weak transcription	Primary hematopoietic stem cells	blood
16	chr11:58806200-58807400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
17	chr11:58806200-58807800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr11:58807400-58808000	Strong transcription	Primary B cells from peripheral blood	blood
19	chr11:58808000-58808200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr11:58808000-58808600	Enhancers	Stomach Mucosa	stomach
21	chr11:58808000-58810800	Weak transcription	Primary B cells from peripheral blood	blood
22	chr11:58810600-58811400	Strong transcription	Primary B cells from cord blood	blood
23	chr11:58810800-58811800	Strong transcription	Primary B cells from peripheral blood	blood
24	chr11:58811400-58818200	Weak transcription	Primary B cells from cord blood	blood
25	chr11:58811800-58816200	Weak transcription	Primary B cells from peripheral blood	blood
26	chr11:58813600-58825200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr11:58815400-58824400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr11:58816200-58818200	Strong transcription	Primary B cells from peripheral blood	blood
29	chr11:58816600-58816800	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr11:58816800-58817000	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr11:58817000-58817200	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr11:58817000-58817200	Enhancers	Fetal Intestine Large	intestine
33	chr11:58817000-58818200	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr11:58817200-58821800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr11:58817200-58825200	Weak transcription	Liver	Liver
36	chr11:58817200-58825400	Weak transcription	Fetal Intestine Large	intestine
37	chr11:58817400-58819400	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr11:58817400-58822000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
39	chr11:58818200-58818600	Genic enhancers	Primary B cells from peripheral blood	blood
40	chr11:58818200-58819400	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr11:58818200-58820200	Enhancers	Primary B cells from cord blood	blood
42	chr11:58818600-58825200	Enhancers	Primary B cells from peripheral blood	blood
43	chr11:58818800-58819400	Enhancers	GM12878-XiMat	blood
44	chr11:58819200-58819400	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr11:58819400-58820600	Weak transcription	GM12878-XiMat	blood
46	chr11:58819400-58821200	Weak transcription	HUES48 Cell Line	embryonic stem cell
47	chr11:58819400-58822000	Weak transcription	HUES6 Cell Line	embryonic stem cell
48	chr11:58819400-58822600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
49	chr11:58820200-58820800	Weak transcription	Primary B cells from cord blood	blood
50	chr11:58820600-58821200	Enhancers	GM12878-XiMat	blood

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