Variant report

Variant	nsv916953
Chromosome Location	chr11:58792126-58846911
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	ARID3A	chr11:58792609-58792905	HepG2	liver:	n/a	n/a
2	ATF2	chr11:58831671-58832143	GM12878	blood:	n/a	n/a
3	ATF2	chr11:58825833-58826405	GM12878	blood:	n/a	n/a
4	ATF2	chr11:58831402-58832419	GM12878	blood:	n/a	n/a
5	BACH1	chr11:58825972-58826213	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr11:58831786-58832150	GM12878	blood:	n/a	chr11:58831926-58831934
7	BATF	chr11:58818940-58819193	GM12878	blood:	n/a	n/a
8	BATF	chr11:58831471-58831776	GM12878	blood:	n/a	n/a
9	BATF	chr11:58831416-58832275	GM12878	blood:	n/a	chr11:58831926-58831934
10	BATF	chr11:58826199-58826498	GM12878	blood:	n/a	n/a
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	chr11:58818899-58819262	GM12878	blood:	n/a	chr11:58819091-58819100
14	BCL11A	chr11:58831483-58831904	GM12878	blood:	n/a	n/a
15	BCL3	chr11:58831794-58832281	GM12878	blood:	n/a	n/a
16	BHLHE40	chr11:58820953-58821000	K562	blood:	n/a	n/a
17	BHLHE40	chr11:58792570-58792935	HepG2	liver:	n/a	chr11:58792752-58792765 chr11:58792748-58792769
18	BHLHE40	chr11:58826040-58826162	K562	blood:	n/a	n/a
19	BHLHE40	chr11:58825938-58826278	GM12878	blood:	n/a	n/a
20	BRCA1	chr11:58825950-58826184	GM12878	blood:	n/a	n/a
21	CEBPB	chr11:58835627-58835890	IMR90	lung:	n/a	chr11:58835780-58835791
22	CEBPB	chr11:58825987-58826187	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr11:58835714-58835923	HepG2	liver:	n/a	chr11:58835780-58835791
24	CEBPB	chr11:58835676-58835875	K562	blood:	n/a	chr11:58835780-58835791
25	CEBPB	chr11:58841369-58841519	IMR90	lung:	n/a	n/a
26	CEBPB	chr11:58827942-58827984	H1-hESC	embryonic stem cell:	n/a	n/a
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	chr11:58825822-58826232	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	chr11:58845766-58846361	GM12878	blood:	n/a	n/a
33	CREB1	chr11:58845805-58846333	GM12878	blood:	n/a	n/a
34	CTCF	chr11:58820920-58821070	HCT-116	colon:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
35	CTCF	chr11:58825960-58826110	HFF-Myc	foreskin:	n/a	n/a
36	CTCF	chr11:58825931-58826235	A549	lung:	n/a	n/a
37	CTCF	chr11:58826000-58826150	BJ	skin:	n/a	n/a
38	CTCF	chr11:58820880-58821030	NHDF-neo	bronchial:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
39	CTCF	chr11:58825980-58826130	HMF	breast:	n/a	n/a
40	CTCF	chr11:58825870-58826180	T-47D	breast:	n/a	n/a
41	CTCF	chr11:58820858-58821084	HepG2	liver:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
42	CTCF	chr11:58820826-58821117	HUVEC	blood vessel:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
43	CTCF	chr11:58820787-58821172	K562	blood:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
44	CTCF	chr11:58820880-58821030	BE2_C	brain:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
45	CTCF	chr11:58825980-58826130	BJ	skin:	n/a	n/a
46	CTCF	chr11:58825777-58826296	A549	lung:	n/a	n/a
47	CTCF	chr11:58820920-58821070	Hela-S3	cervix:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
48	CTCF	chr11:58820840-58820990	HA-sp	spinal cord:	n/a	chr11:58820969-58820985 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
49	CTCF	chr11:58820780-58821155	GM12878	blood:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986
50	CTCF	chr11:58820878-58821091	H1-hESC	embryonic stem cell:	n/a	chr11:58820969-58820985 chr11:58820970-58820991 chr11:58820971-58820980 chr11:58820971-58820984 chr11:58820968-58820986

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:58830191-58830241	HNPCEpiC	eye:	n/a
2	chr11:58826073-58826123	HCT-116	colon:	n/a
3	chr11:58826110-58826160	NT2-D1	testis:	n/a
4	chr11:58825714-58825764	Hepatocyte	liver:	n/a
5	chr11:58830191-58830241	HNPCEpiC	eye:	n/a
6	chr11:58826073-58826123	HCT-116	colon:	n/a
7	chr11:58826110-58826160	NT2-D1	testis:	n/a
8	chr11:58825714-58825764	Hepatocyte	liver:	n/a
9	chr11:58825870-58825920	HNPCEpiC	eye:	n/a
10	chr11:58826414-58826464	AG09309	skin:	n/a
11	chr11:58826073-58826123	HAEpiC	amniotic membrane:	n/a
12	chr11:58830610-58830660	AG09309	skin:	n/a
13	chr11:58826475-58826525	NHBE	bronchial:	n/a
14	chr11:58830610-58830660	BJ	skin:	n/a
15	chr11:58830610-58830660	Hela-S3	cervix:	n/a
16	chr11:58828174-58828224	AG09319	gingival:	n/a
17	chr11:58830191-58830241	SAEC	small airway:	n/a
18	chr11:58826414-58826464	IMR90	lung:	fetal
19	chr11:58833356-58833406	RPTEC	kidney:	n/a
20	chr11:58833356-58833406	AG04450	lung:	fetal
21	chr11:58806952-58807002	T-47D	breast:	n/a
22	chr11:58826475-58826525	HCF	heart:	n/a
23	chr11:58828174-58828224	T-47D	breast:	n/a
24	chr11:58825714-58825764	HEK293	kidney:	embryo
25	chr11:58826073-58826123	MCF10A-Er-Src	breast:	n/a
26	chr11:58826475-58826525	RPTEC	kidney:	n/a
27	chr11:58830424-58830474	SAEC	small airway:	n/a
28	chr11:58833356-58833406	GM12878	blood:	n/a
29	chr11:58825714-58825764	NB4	blood:	n/a
30	chr11:58830857-58830907	HRPEpiC	eye:	n/a
31	chr11:58833356-58833406	HRPEpiC	eye:	n/a
32	chr11:58810187-58810237	GM19239	blood:	n/a
33	chr11:58830424-58830474	SK-N-SH_RA	brain:	n/a
34	chr11:58828174-58828224	HRE	kidney:	n/a
35	chr11:58830355-58830405	GM12892	blood:	n/a
36	chr11:58830610-58830660	IMR90	lung:	fetal
37	chr11:58826073-58826123	GM12892	blood:	n/a
38	chr11:58825870-58825920	IMR90	lung:	fetal
39	chr11:58830191-58830241	SK-N-MC	brain:	n/a
40	chr11:58830610-58830660	Jurkat	blood:	n/a
41	chr11:58806952-58807002	HCPEpiC	choroid plexus:	n/a
42	chr11:58830424-58830474	MCF10A-Er-Src	breast:	n/a
43	chr11:58830355-58830405	HAEpiC	amniotic membrane:	n/a
44	chr11:58826110-58826160	PrEC	prostate:	n/a
45	chr11:58830191-58830241	ECC-1	luminal epithelium:	n/a
46	chr11:58825870-58825920	MCF-7	breast:	n/a
47	chr11:58830857-58830907	SK-N-MC	brain:	n/a
48	chr11:58825870-58825920	HUVEC	blood vessel:	n/a
49	chr11:58830355-58830405	ovcar-3	ovarian:	n/a
50	chr11:58830191-58830241	NHDF-neo	bronchial:	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	chr11:58825845-58826132	ENSG00000255240.1
2	lnc-GLYATL2-2	chr11:58825845-58825923	ENSG00000255240.1
3	lnc-GLYATL2-2	chr11:58822768-58822919	ENSG00000255240.1
4	lnc-GLYATL2-2	chr11:58818733-58818781	ENSG00000255240.1
5	lnc-GLYATL2-2	chr11:58820930-58821099	ENSG00000255240.1
6	lnc-GLYATL2-2	chr11:58825845-58825925	NR_033853
7	lnc-GLYATL2-2	chr11:58818733-58818781	ENSG00000255240.1
8	lnc-GLYATL2-2	chr11:58820930-58821099	NR_033853
9	lnc-GLYATL2-2	chr11:58820930-58821099	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: 2028 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:2028 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs147133455	chr11:58792133-58792134	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs193245135	chr11:58792154-58792155	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs185742993	chr11:58792160-58792161	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs189369184	chr11:58792178-58792179	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs565603852	chr11:58792188-58792189	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs574297211	chr11:58792207-58792208	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs180977487	chr11:58792240-58792241	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs77753798	chr11:58792251-58792252	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs77786331	chr11:58792260-58792261	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs547511611	chr11:58792279-58792280	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs559794607	chr11:58792329-58792330	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs74879826	chr11:58792358-58792359	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs72919107	chr11:58792399-58792400	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs185340984	chr11:58792503-58792504	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs9630212	chr11:58792519-58792520	Active TSS Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs112413973	chr11:58792521-58792522	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs552033048	chr11:58792559-58792560	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs376191323	chr11:58792588-58792589	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs188639645	chr11:58792589-58792590	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs9630208	chr11:58792615-58792616	Active TSS Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs552743470	chr11:58792619-58792620	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs574379502	chr11:58792637-58792638	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs564722352	chr11:58792641-58792642	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs181378267	chr11:58792650-58792651	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs557110062	chr11:58792663-58792664	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs576686493	chr11:58792670-58792671	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs530862454	chr11:58792671-58792672	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs10896900	chr11:58792681-58792682	Active TSS Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs572071414	chr11:58792700-58792701	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs369442655	chr11:58792702-58792703	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs12418002	chr11:58792723-58792724	Active TSS Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs140313953	chr11:58792731-58792732	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs556648696	chr11:58792759-58792760	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs34462670	chr11:58792829-58792830	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs186998255	chr11:58792856-58792857	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs117322776	chr11:58792886-58792887	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs530121866	chr11:58792901-58792902	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs548249552	chr11:58792912-58792913	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs191740333	chr11:58792922-58792923	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs531669507	chr11:58792943-58792944	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs530604868	chr11:58792996-58792997	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs112540860	chr11:58793061-58793062	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs570724322	chr11:58793067-58793068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs11229741	chr11:58793078-58793079	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs11822599	chr11:58793080-58793081	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs184027567	chr11:58793207-58793208	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs535468869	chr11:58793289-58793290	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs375065286	chr11:58793410-58793411	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs151223260	chr11:58793424-58793425	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs569010454	chr11:58793488-58793489	Weak transcription Enhancers	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:382 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:58782800-58810600	Weak transcription	Primary B cells from cord blood	blood
2	chr11:58791800-58793600	Enhancers	Fetal Intestine Large	intestine
3	chr11:58792200-58792400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr11:58792200-58792600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr11:58792200-58792600	Enhancers	Fetal Intestine Small	intestine
6	chr11:58792200-58792600	Enhancers	Rectal Mucosa Donor 29	rectum
7	chr11:58792200-58792600	Enhancers	Rectal Mucosa Donor 31	rectum
8	chr11:58792200-58792800	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr11:58792200-58792800	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr11:58792200-58793000	Enhancers	Duodenum Mucosa	Duodenum
11	chr11:58792400-58793000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr11:58792400-58793000	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr11:58792400-58793000	Enhancers	HepG2	liver
14	chr11:58792400-58793600	Enhancers	Liver	Liver
15	chr11:58792600-58793400	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr11:58792600-58796600	Weak transcription	Rectal Mucosa Donor 29	rectum
17	chr11:58793000-58796400	Weak transcription	Duodenum Mucosa	Duodenum
18	chr11:58793400-58794200	Enhancers	Rectal Mucosa Donor 31	rectum
19	chr11:58793600-58795800	Weak transcription	Fetal Intestine Large	intestine
20	chr11:58794200-58796400	Weak transcription	Rectal Mucosa Donor 31	rectum
21	chr11:58795600-58796000	Enhancers	Primary monocytes fromperipheralblood	blood
22	chr11:58795800-58797800	Enhancers	Fetal Intestine Large	intestine
23	chr11:58796000-58796200	Enhancers	Sigmoid Colon	Sigmoid Colon
24	chr11:58796000-58797400	Weak transcription	Primary monocytes fromperipheralblood	blood
25	chr11:58796000-58798600	Enhancers	Fetal Intestine Small	intestine
26	chr11:58796400-58797200	Enhancers	Duodenum Mucosa	Duodenum
27	chr11:58796400-58797200	Enhancers	Rectal Mucosa Donor 31	rectum
28	chr11:58796400-58797400	Weak transcription	Sigmoid Colon	Sigmoid Colon
29	chr11:58796600-58796800	Enhancers	Rectal Mucosa Donor 29	rectum
30	chr11:58796600-58797400	Enhancers	Stomach Mucosa	stomach
31	chr11:58796600-58797600	Enhancers	Colonic Mucosa	Colon
32	chr11:58797200-58797600	Flanking Active TSS	Duodenum Mucosa	Duodenum
33	chr11:58797200-58797800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
34	chr11:58797400-58797800	Enhancers	Primary monocytes fromperipheralblood	blood
35	chr11:58797400-58797800	Enhancers	Sigmoid Colon	Sigmoid Colon
36	chr11:58797600-58797800	Flanking Active TSS	Colonic Mucosa	Colon
37	chr11:58797600-58797800	Enhancers	Duodenum Mucosa	Duodenum
38	chr11:58801400-58803200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr11:58803200-58804600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr11:58804400-58804600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr11:58804400-58804600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
42	chr11:58804600-58805000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr11:58804600-58806200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
44	chr11:58804600-58807400	Weak transcription	Primary B cells from peripheral blood	blood
45	chr11:58804800-58805000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr11:58804800-58805200	Enhancers	Primary hematopoietic stem cells	blood
47	chr11:58804800-58805200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr11:58805000-58805200	Enhancers	Rectal Mucosa Donor 31	rectum
49	chr11:58805000-58806200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr11:58805000-58825200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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