Variant report

Variant	nsv468776
Chromosome Location	chr11:86788716-86826422
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:487)
CpG islands
(count:61)
Chromatin interactive
region (count:18)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:487 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:86808596-86809092	K562	blood:	n/a	n/a
2	ARID3A	chr11:86808565-86809024	HepG2	liver:	n/a	n/a
3	ATF1	chr11:86808580-86808925	K562	blood:	n/a	n/a
4	ATF3	chr11:86803222-86803489	K562	blood:	n/a	n/a
5	BACH1	chr11:86805450-86805451	K562	blood:	n/a	n/a
6	BACH1	chr11:86808725-86808892	K562	blood:	n/a	n/a
7	BCL11A	chr11:86794117-86794402	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL11A	chr11:86794104-86794296	H1-hESC	embryonic stem cell:	n/a	n/a
9	BHLHE40	chr11:86808720-86808888	K562	blood:	n/a	n/a
10	BRCA1	chr11:86794111-86794566	H1-hESC	embryonic stem cell:	n/a	n/a
11	CBX3	chr11:86797796-86798165	K562	blood:	n/a	n/a
12	CBX3	chr11:86808476-86808990	K562	blood:	n/a	n/a
13	CCNT2	chr11:86808679-86808904	K562	blood:	n/a	n/a
14	CEBPB	chr11:86803287-86803608	K562	blood:	n/a	n/a
15	CEBPB	chr11:86814685-86814880	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr11:86803289-86803589	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr11:86814348-86814868	K562	blood:	n/a	n/a
18	CEBPB	chr11:86811816-86811879	K562	blood:	n/a	n/a
19	CEBPB	chr11:86823041-86823150	HepG2	liver:	n/a	n/a
20	CHD1	chr11:86794598-86794704	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr11:86808615-86808994	K562	blood:	n/a	n/a
22	CTCF	chr11:86808660-86808810	NB4	blood:	n/a	n/a
23	CTCF	chr11:86808635-86808841	LNCaP	prostate:	n/a	n/a
24	CTCF	chr11:86807020-86807170	AG04450	lung:	n/a	n/a
25	CTCF	chr11:86807058-86807224	K562	blood:	n/a	n/a
26	CTCF	chr11:86808600-86808750	GM12872	blood:	n/a	n/a
27	CTCF	chr11:86808660-86808810	Hela-S3	cervix:	n/a	n/a
28	CTCF	chr11:86808611-86808887	Gliobla	brain:	n/a	n/a
29	CTCF	chr11:86808605-86808870	A549	lung:	n/a	n/a
30	CTCF	chr11:86807040-86807190	HPAF	blood vessel:	n/a	n/a
31	CTCF	chr11:86807060-86807210	HCPEpiC	choroid plexus:	n/a	n/a
32	CTCF	chr11:86808660-86808810	WERI-Rb-1	eye:	n/a	n/a
33	CTCF	chr11:86806966-86807293	K562	blood:	n/a	n/a
34	CTCF	chr11:86808680-86808830	GM12870	blood:	n/a	n/a
35	CTCF	chr11:86808647-86808845	GM10266	blood:	n/a	n/a
36	CTCF	chr11:86808700-86808850	GM12865	blood:	n/a	n/a
37	CTCF	chr11:86808579-86808878	HepG2	liver:	n/a	n/a
38	CTCF	chr11:86808636-86808844	GM13977	blood:	n/a	n/a
39	CTCF	chr11:86808680-86808830	HA-sp	spinal cord:	n/a	n/a
40	CTCF	chr11:86808640-86808790	NHEK	skin:	n/a	n/a
41	CTCF	chr11:86808653-86808843	GM20000	blood:	n/a	n/a
42	CTCF	chr11:86808640-86808790	HCM	heart:	n/a	n/a
43	CTCF	chr11:86807040-86807190	HepG2	liver:	n/a	n/a
44	CTCF	chr11:86807060-86807210	HVMF	connective:	n/a	n/a
45	CTCF	chr11:86808660-86808810	NHDF-neo	bronchial:	n/a	n/a
46	CTCF	chr11:86808637-86808846	Lung_OC	lung:	n/a	n/a
47	CTCF	chr11:86808680-86808830	HUVEC	blood vessel:	n/a	n/a
48	CTCF	chr11:86808640-86808790	GM12866	blood:	n/a	n/a
49	CTCF	chr11:86807020-86807170	HA-sp	spinal cord:	n/a	n/a
50	CTCF	chr11:86808576-86808985	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:86793667-86793717	CMK	blood:	n/a
2	chr11:86793667-86793717	U87	brain:	n/a
3	chr11:86793667-86793717	RPTEC	kidney:	n/a
4	chr11:86793667-86793717	LNCaP	prostate:	n/a
5	chr11:86793667-86793717	AG04450	lung:	fetal
6	chr11:86793667-86793717	Hela-S3	cervix:	n/a
7	chr11:86793667-86793717	PANC-1	pancreas:	n/a
8	chr11:86793667-86793717	HCF	heart:	n/a
9	chr11:86793667-86793717	GM19239	blood:	n/a
10	chr11:86793667-86793717	H1-hESC	embryonic stem cell:	embryo
11	chr11:86793667-86793717	SK-N-SH	brain:	n/a
12	chr11:86793667-86793717	GM12878	blood:	n/a
13	chr11:86793667-86793717	AG09319	gingival:	n/a
14	chr11:86793667-86793717	SAEC	small airway:	n/a
15	chr11:86793667-86793717	T-47D	breast:	n/a
16	chr11:86793667-86793717	K562	blood:	n/a
17	chr11:86793667-86793717	HRE	kidney:	n/a
18	chr11:86793667-86793717	AG04449	skin:	fetal
19	chr11:86793667-86793717	HCT-116	colon:	n/a
20	chr11:86793667-86793717	NHDF-neo	bronchial:	n/a
21	chr11:86793667-86793717	NHBE	bronchial:	n/a
22	chr11:86793667-86793717	HAEpiC	amniotic membrane:	n/a
23	chr11:86793667-86793717	NH-A	brain:	n/a
24	chr11:86793667-86793717	GM12891	blood:	n/a
25	chr11:86793667-86793717	HCM	heart:	n/a
26	chr11:86793667-86793717	PFSK-1	brain:	n/a
27	chr11:86793667-86793717	AoSMC	blood vessel:	n/a
28	chr11:86793667-86793717	HMEC	breast:	n/a
29	chr11:86793667-86793717	MCF10A-Er-Src	breast:	n/a
30	chr11:86793667-86793717	NB4	blood:	n/a
31	chr11:86793667-86793717	HEK293	kidney:	embryo
32	chr11:86793667-86793717	GM06990	blood:	n/a
33	chr11:86793667-86793717	HepG2	liver:	n/a
34	chr11:86793667-86793717	HIPEpiC	eye:	n/a
35	chr11:86793667-86793717	SK-N-SH_RA	brain:	n/a
36	chr11:86793667-86793717	Caco-2	colon:	n/a
37	chr11:86793667-86793717	ProgFib	skin:	n/a
38	chr11:86793667-86793717	AG09309	skin:	n/a
39	chr11:86793667-86793717	HL-60	blood:	n/a
40	chr11:86793667-86793717	MCF-7	breast:	n/a
41	chr11:86793667-86793717	BJ	skin:	n/a
42	chr11:86793667-86793717	NT2-D1	testis:	n/a
43	chr11:86793667-86793717	HUVEC	blood vessel:	n/a
44	chr11:86793667-86793717	HNPCEpiC	eye:	n/a
45	chr11:86793667-86793717	A549	lung:	n/a
46	chr11:86793667-86793717	Jurkat	blood:	n/a
47	chr11:86793667-86793717	IMR90	lung:	fetal
48	chr11:86793667-86793717	GM12892	blood:	n/a
49	chr11:86793667-86793717	ECC-1	luminal epithelium:	n/a
50	chr11:86793667-86793717	SK-N-MC	brain:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:86664322..86666678-chr11:86802389..86805418,3	MCF-7	breast:
2	chr11:86791713..86794335-chr11:86807155..86810110,2	K562	blood:
3	chr11:86810025..86812420-chr11:86813811..86815830,2	K562	blood:
4	chr11:86798772..86800664-chr11:86801632..86803429,2	K562	blood:
5	chr11:86706337..86706967-chr11:86808249..86808967,2	K562	blood:
6	chr11:86809033..86811037-chr11:86814602..86817030,2	K562	blood:
7	chr11:86666646..86669098-chr11:86793601..86796453,2	MCF-7	breast:
8	chr11:86805484..86807360-chr11:87007311..87009404,2	MCF-7	breast:
9	chr11:86803340..86806124-chr11:86810035..86812567,2	K562	blood:
10	chr11:86810025..86812420-chr11:86813811..86815830,2	K562	blood:
11	chr11:86664821..86667112-chr11:86824827..86827318,2	MCF-7	breast:
12	chr11:86798772..86800664-chr11:86801632..86803429,2	K562	blood:
13	chr11:86818728..86820494-chr11:86831907..86834474,2	K562	blood:
14	chr11:86779436..86781916-chr11:86820681..86823632,2	K562	blood:
15	chr11:86773350..86775874-chr11:86786933..86789262,2	K562	blood:
16	chr11:86809033..86811037-chr11:86814602..86817030,2	K562	blood:
17	chr11:86803340..86806124-chr11:86810035..86812567,2	K562	blood:
18	chr11:86806619..86807569-chr11:86992272..86993052,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FZD4-6	chr11:86805776-86807627	NONHSAT023514

No data

Variant related genes	Relation type
ENSG00000254843	TF binding region
ENSG00000254843	CpG island
ENSG00000174804	chromatin interactions
ENSG00000254843	chromatin interactions
ENSG00000246523	chromatin interactions

Extended variants
information (count: 1535 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:1535 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11234958	chr11:86788716-86788717	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs535161546	chr11:86788724-86788725	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs112853233	chr11:86788756-86788757	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs75520519	chr11:86788789-86788790	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs76292319	chr11:86788833-86788834	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs541438251	chr11:86788841-86788842	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs561756965	chr11:86788843-86788844	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs144043366	chr11:86788875-86788876	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs377195131	chr11:86788886-86788887	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs550506026	chr11:86788937-86788938	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs150690499	chr11:86788945-86788946	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs2445576	chr11:86788952-86788953	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs148898868	chr11:86788980-86788981	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs190896757	chr11:86788985-86788986	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs566876885	chr11:86789004-86789005	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs112488492	chr11:86789142-86789143	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs12279443	chr11:86789266-86789267	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs376393940	chr11:86789281-86789282	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs10898593	chr11:86789285-86789286	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs138923648	chr11:86789302-86789303	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs538154200	chr11:86789323-86789324	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs149432054	chr11:86789387-86789388	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs568491368	chr11:86789401-86789402	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs76990034	chr11:86789426-86789427	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs377025399	chr11:86789431-86789432	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs75579348	chr11:86789464-86789465	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs534415849	chr11:86789582-86789583	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs535823785	chr11:86789696-86789697	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs554434426	chr11:86789705-86789706	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs139531706	chr11:86789743-86789744	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs112952957	chr11:86789778-86789779	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs555063807	chr11:86789817-86789818	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs555927363	chr11:86789832-86789833	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs35962056	chr11:86789834-86789835	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs575196933	chr11:86789850-86789851	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs374567916	chr11:86789883-86789884	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs146099200	chr11:86789943-86789944	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs564051686	chr11:86789977-86789978	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs532936934	chr11:86789981-86789982	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs534981943	chr11:86789982-86789983	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs2512390	chr11:86790003-86790004	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs386755845	chr11:86790081-86790082	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs3133319	chr11:86790083-86790084	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs371979896	chr11:86790101-86790102	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs549503438	chr11:86790102-86790103	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs569111748	chr11:86790125-86790126	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs139915671	chr11:86790152-86790153	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs552068643	chr11:86790194-86790195	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs571948739	chr11:86790211-86790212	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs142186978	chr11:86790299-86790300	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	20729466	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
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	22429812	CNVD
Breast cancer	21364760	CNVD
Ovarian neoplasms	16753589	CNVD
Breast cancer	16608533	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Sudden cardiac death	19188705	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Ductal carcinoma	22052326	CNVD
small cell lung cancer	20016488	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Attention deficit hyperactivity disorder	22241247	CNVD
Breast cancer	21958427	CNVD
Breast cancer	17133270	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Obesity	20622171	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:692 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:86769200-86791200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
2	chr11:86769200-86792400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr11:86770400-86808200	Weak transcription	HUVEC	blood vessel
4	chr11:86773000-86790800	Weak transcription	NHLF	lung
5	chr11:86773000-86792000	Weak transcription	Primary T helper cells PMA-I stimulated	--
6	chr11:86774600-86792400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
7	chr11:86774800-86806400	Weak transcription	Small Intestine	intestine
8	chr11:86775600-86791400	Weak transcription	HSMM	muscle
9	chr11:86776400-86792400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
10	chr11:86776600-86793000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr11:86776600-86815600	Weak transcription	HSMMtube	muscle
12	chr11:86777400-86792400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
13	chr11:86778400-86792400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
14	chr11:86778800-86789000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr11:86778800-86789600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr11:86778800-86791800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr11:86778800-86792400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
18	chr11:86779000-86790200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr11:86779400-86792400	Weak transcription	GM12878-XiMat	blood
20	chr11:86779600-86792200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
21	chr11:86780200-86789400	Strong transcription	Adipose Nuclei	Adipose
22	chr11:86782600-86795400	Weak transcription	Fetal Heart	heart
23	chr11:86783000-86814000	Weak transcription	Hela-S3	cervix
24	chr11:86783200-86799000	Weak transcription	Psoas Muscle	Psoas
25	chr11:86784000-86792000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
26	chr11:86785600-86789200	Strong transcription	Dnd41	blood
27	chr11:86786400-86791400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr11:86786600-86789000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
29	chr11:86786600-86789000	Genic enhancers	HepG2	liver
30	chr11:86786600-86789400	Strong transcription	Duodenum Smooth Muscle	Duodenum
31	chr11:86786800-86788800	Strong transcription	Duodenum Mucosa	Duodenum
32	chr11:86786800-86789000	Strong transcription	Cortex derived primary cultured neurospheres	brain
33	chr11:86786800-86789200	Strong transcription	Stomach Smooth Muscle	stomach
34	chr11:86786800-86789400	Strong transcription	Primary hematopoietic stem cells	blood
35	chr11:86787000-86789000	Strong transcription	K562	blood
36	chr11:86787200-86791800	Weak transcription	Colonic Mucosa	Colon
37	chr11:86787200-86794200	Weak transcription	Brain Anterior Caudate	brain
38	chr11:86787200-86795400	Weak transcription	H9 Cell Line	embryonic stem cell
39	chr11:86787400-86819600	Weak transcription	NH-A	brain
40	chr11:86787600-86788800	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr11:86787600-86789200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr11:86787600-86791800	Weak transcription	Primary T helper cells fromperipheralblood	blood
43	chr11:86787600-86792000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
44	chr11:86787600-86804200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr11:86787600-86825200	Weak transcription	Brain Substantia Nigra	brain
46	chr11:86787800-86792400	Weak transcription	Primary T cells fromperipheralblood	blood
47	chr11:86787800-86792400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
48	chr11:86787800-86797200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr11:86787800-86797200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr11:86787800-86798200	Weak transcription	Spleen	Spleen

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