Variant report

Variant	esv1802222
Chromosome Location	chr11:76683305-76709407
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:70)
CpG islands
(count:61)
Chromatin interactive
region (count:11)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:70 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr11:76698288-76698423	K562	blood:	n/a	n/a
2	CBX3	chr11:76683051-76683513	HCT-116	colon:	n/a	n/a
3	CBX3	chr11:76689231-76689598	K562	blood:	n/a	n/a
4	CEBPB	chr11:76684751-76684965	K562	blood:	n/a	n/a
5	CTCF	chr11:76685351-76685417	Hela-S3	cervix:	n/a	n/a
6	CTCF	chr11:76685460-76685610	HMEC	breast:	n/a	n/a
7	CTCF	chr11:76684499-76684553	Fibrobl	skin:	n/a	n/a
8	CTCF	chr11:76683700-76683850	HepG2	liver:	n/a	chr11:76683828-76683838
9	CTCF	chr11:76685322-76685471	Pancreas_OC	pancreas:	n/a	n/a
10	CTCF	chr11:76685289-76685392	MCF-7	breast:	n/a	n/a
11	E2F4	chr11:76685046-76685172	MCF10A-Er-Src	breast:	n/a	n/a
12	ELF1	chr11:76695803-76696213	MCF-7	breast:	n/a	n/a
13	EP300	chr11:76698234-76698549	K562	blood:	n/a	n/a
14	FOS	chr11:76686596-76686864	MCF10A-Er-Src	breast:	n/a	chr11:76686756-76686764
15	FOXA1	chr11:76698795-76699180	HepG2	liver:	n/a	n/a
16	FOXA1	chr11:76698825-76699151	HepG2	liver:	n/a	n/a
17	FOXA1	chr11:76698729-76699082	HepG2	liver:	n/a	n/a
18	FOXA1	chr11:76698704-76699067	HepG2	liver:	n/a	n/a
19	FOXA2	chr11:76698803-76699046	HepG2	liver:	n/a	n/a
20	GATA2	chr11:76698228-76698621	K562	blood:	n/a	n/a
21	KAP1	chr11:76689233-76689618	HEK293	kidney:	n/a	n/a
22	MAFK	chr11:76706845-76706975	HepG2	liver:	n/a	n/a
23	MAX	chr11:76695877-76696251	MCF-7	breast:	n/a	n/a
24	MAZ	chr11:76687534-76687734	HepG2	liver:	n/a	n/a
25	MYC	chr11:76689904-76690055	MCF-7	breast:	n/a	n/a
26	MYC	chr11:76695992-76696053	MCF-7	breast:	n/a	n/a
27	MYC	chr11:76689118-76689205	MCF-7	breast:	n/a	n/a
28	POLR2A	chr11:76689883-76689892	MCF-7	breast:	n/a	n/a
29	POLR2A	chr11:76684160-76684248	MCF-7	breast:	n/a	n/a
30	POLR2A	chr11:76689051-76689061	MCF-7	breast:	n/a	n/a
31	POLR2A	chr11:76684526-76684540	MCF-7	breast:	n/a	n/a
32	POLR2A	chr11:76694535-76694547	A549	lung:	n/a	n/a
33	POLR2A	chr11:76689003-76689020	MCF-7	breast:	n/a	n/a
34	POLR2A	chr11:76684585-76684703	ProgFib	skin:	n/a	n/a
35	POLR2A	chr11:76689914-76689926	MCF-7	breast:	n/a	n/a
36	POLR2A	chr11:76689032-76689054	A549	lung:	n/a	n/a
37	POLR2A	chr11:76685239-76685394	MCF10A-Er-Src	breast:	n/a	n/a
38	POLR2A	chr11:76683804-76683808	MCF-7	breast:	n/a	n/a
39	POLR2A	chr11:76694466-76694513	A549	lung:	n/a	n/a
40	POLR2A	chr11:76694913-76695005	MCF-7	breast:	n/a	n/a
41	POLR2A	chr11:76689923-76690151	MCF-7	breast:	n/a	n/a
42	POLR2A	chr11:76689995-76690143	A549	lung:	n/a	n/a
43	POLR2A	chr11:76684099-76684222	A549	lung:	n/a	n/a
44	POLR2A	chr11:76703622-76703715	MCF10A-Er-Src	breast:	n/a	n/a
45	POLR2A	chr11:76704030-76704165	MCF-7	breast:	n/a	n/a
46	POLR2A	chr11:76689101-76689186	MCF-7	breast:	n/a	n/a
47	POLR2A	chr11:76700841-76700858	HUVEC	blood vessel:	n/a	n/a
48	POLR2A	chr11:76684312-76684458	MCF-7	breast:	n/a	n/a
49	POLR2A	chr11:76689947-76690011	MCF-7	breast:	n/a	n/a
50	POLR2A	chr11:76683838-76683894	MCF-7	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:76709256-76709306	CMK	blood:	n/a
2	chr11:76709256-76709306	GM12891	blood:	n/a
3	chr11:76709256-76709306	ProgFib	skin:	n/a
4	chr11:76709256-76709306	NHDF-neo	bronchial:	n/a
5	chr11:76709256-76709306	HPAEpiC	pulmonary alveolar:	n/a
6	chr11:76709256-76709306	A549	lung:	n/a
7	chr11:76709256-76709306	SK-N-SH	brain:	n/a
8	chr11:76709256-76709306	HNPCEpiC	eye:	n/a
9	chr11:76709256-76709306	MCF-7	breast:	n/a
10	chr11:76709256-76709306	AG09309	skin:	n/a
11	chr11:76709256-76709306	SAEC	small airway:	n/a
12	chr11:76709256-76709306	SKMC	muscle:	n/a
13	chr11:76709256-76709306	HIPEpiC	eye:	n/a
14	chr11:76709256-76709306	GM12892	blood:	n/a
15	chr11:76709256-76709306	MCF10A-Er-Src	breast:	n/a
16	chr11:76709256-76709306	Hela-S3	cervix:	n/a
17	chr11:76709256-76709306	NH-A	brain:	n/a
18	chr11:76709256-76709306	BJ	skin:	n/a
19	chr11:76709256-76709306	K562	blood:	n/a
20	chr11:76709256-76709306	RPTEC	kidney:	n/a
21	chr11:76709256-76709306	HL-60	blood:	n/a
22	chr11:76709256-76709306	SK-N-MC	brain:	n/a
23	chr11:76709256-76709306	PrEC	prostate:	n/a
24	chr11:76709256-76709306	PFSK-1	brain:	n/a
25	chr11:76709256-76709306	HCPEpiC	choroid plexus:	n/a
26	chr11:76709256-76709306	HepG2	liver:	n/a
27	chr11:76709256-76709306	PANC-1	pancreas:	n/a
28	chr11:76709256-76709306	NHBE	bronchial:	n/a
29	chr11:76709256-76709306	SK-N-SH_RA	brain:	n/a
30	chr11:76709256-76709306	GM19239	blood:	n/a
31	chr11:76709256-76709306	GM12878	blood:	n/a
32	chr11:76709256-76709306	BE2_C	brain:	n/a
33	chr11:76709256-76709306	HRCEpiC	kidney:	n/a
34	chr11:76709256-76709306	ECC-1	luminal epithelium:	n/a
35	chr11:76709256-76709306	AG10803	skin:	n/a
36	chr11:76709256-76709306	U87	brain:	n/a
37	chr11:76709256-76709306	Jurkat	blood:	n/a
38	chr11:76709256-76709306	LNCaP	prostate:	n/a
39	chr11:76709256-76709306	HMEC	breast:	n/a
40	chr11:76709256-76709306	HCT-116	colon:	n/a
41	chr11:76709256-76709306	AG04450	lung:	fetal
42	chr11:76709256-76709306	HAEpiC	amniotic membrane:	n/a
43	chr11:76709256-76709306	HEEpiC	esophagus:	n/a
44	chr11:76709256-76709306	HCM	heart:	n/a
45	chr11:76709256-76709306	HRE	kidney:	n/a
46	chr11:76709256-76709306	T-47D	breast:	n/a
47	chr11:76709256-76709306	HUVEC	blood vessel:	n/a
48	chr11:76709256-76709306	HEK293	kidney:	embryo
49	chr11:76709256-76709306	NB4	blood:	n/a
50	chr11:76709256-76709306	AG09319	gingival:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:76684575..76686730-chr11:76722373..76724667,2	MCF-7	breast:
2	chr11:76691402..76695270-chr11:76696975..76699875,3	K562	blood:
3	chr11:76699145..76701750-chr11:76703493..76705984,2	K562	blood:
4	chr11:76693879..76696563-chr11:76699673..76701721,2	MCF-7	breast:
5	chr11:76693879..76696563-chr11:76699673..76701721,2	MCF-7	breast:
6	chr11:76691341..76694336-chr11:76696975..76699945,2	K562	blood:
7	chr11:76686294..76687888-chr11:76690773..76692768,2	K562	blood:
8	chr11:76691402..76695270-chr11:76696975..76699875,3	K562	blood:
9	chr11:76684953..76685685-chr11:76756997..76757683,2	MCF-7	breast:
10	chr11:76686294..76687888-chr11:76690773..76692768,2	K562	blood:
11	chr11:76691341..76694336-chr11:76696975..76699945,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GDPD4-2	chr11:76689445-76689663	ENSG00000254988.1

No data

Variant related genes	Relation type
ACER3	TF binding region
ENSG00000254988	TF binding region
ACER3	CpG island
ENSG00000254988	CpG island
ENSG00000078124	chromatin interactions

Extended variants
information (count: 888 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:888 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2187499	chr11:76683305-76683306	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs543464765	chr11:76683317-76683318	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs5792750	chr11:76683325-76683326	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs141637896	chr11:76683355-76683356	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs529431668	chr11:76683444-76683445	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs79949665	chr11:76683519-76683520	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs566218988	chr11:76683529-76683530	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs374881197	chr11:76683549-76683550	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs34239659	chr11:76683595-76683596	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs2156770	chr11:76683700-76683701	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs573997009	chr11:76683722-76683723	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs111942555	chr11:76683749-76683750	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs181810845	chr11:76683756-76683757	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs571307674	chr11:76683775-76683776	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs537049396	chr11:76683777-76683778	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs556743170	chr11:76683783-76683784	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs186169615	chr11:76683802-76683803	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs12791998	chr11:76683806-76683807	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs147051748	chr11:76683812-76683813	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs144717065	chr11:76683831-76683832	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs116695875	chr11:76683876-76683877	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs544943097	chr11:76683877-76683878	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs563830860	chr11:76683885-76683886	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs75320312	chr11:76683981-76683982	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs531129276	chr11:76683990-76683991	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs190489658	chr11:76683994-76683995	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs183640104	chr11:76683996-76683997	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs188170985	chr11:76683997-76683998	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs75246872	chr11:76684035-76684036	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs7943913	chr11:76684046-76684047	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs114233139	chr11:76684065-76684066	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs528789689	chr11:76684117-76684118	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs552060152	chr11:76684142-76684143	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs571981749	chr11:76684166-76684167	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs191344432	chr11:76684177-76684178	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs141895030	chr11:76684190-76684191	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs113308886	chr11:76684194-76684195	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs370668569	chr11:76684216-76684217	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs536382251	chr11:76684229-76684230	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs552882706	chr11:76684271-76684272	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs147694744	chr11:76684280-76684281	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs182714419	chr11:76684298-76684299	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs61086262	chr11:76684357-76684358	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs186546208	chr11:76684359-76684360	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs537024251	chr11:76684375-76684376	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs557357870	chr11:76684378-76684379	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs192594834	chr11:76684420-76684421	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs112494190	chr11:76684437-76684438	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs139021322	chr11:76684456-76684457	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs575365423	chr11:76684457-76684458	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

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
Acute myeloid leukemia	20729466	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
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Glioblastoma multiforme	21080181	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Melanoma	18172304	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Breast cancer	16620391	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21482786	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	16608533	CNVD
Usher syndrome	18421352	CNVD
Ovarian cancer	21240255	CNVD
Ovarian cancer	22355333	CNVD
Breast cancer	20932292	CNVD
Cancer	20164920	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Acute lymphoblastic leukemia	17690704	CNVD

Chromatin state (count:381 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:76631400-76688400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr11:76645800-76683800	Weak transcription	Esophagus	oesophagus
3	chr11:76646600-76688000	Weak transcription	HMEC	breast
4	chr11:76657200-76688400	Weak transcription	Gastric	stomach
5	chr11:76660000-76710800	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr11:76665800-76688400	Weak transcription	Right Ventricle	heart
7	chr11:76666800-76695400	Weak transcription	NHEK	skin
8	chr11:76672200-76697800	Weak transcription	Left Ventricle	heart
9	chr11:76672400-76696000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr11:76673000-76689600	Weak transcription	Skeletal Muscle Male	skeletal muscle
11	chr11:76673800-76690400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr11:76674000-76688600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
13	chr11:76674200-76683800	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr11:76674400-76696000	Weak transcription	Small Intestine	intestine
15	chr11:76675000-76683800	Weak transcription	Placenta	Placenta
16	chr11:76675000-76688600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr11:76675000-76689800	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr11:76675000-76691600	Weak transcription	Fetal Lung	lung
19	chr11:76675000-76721800	Weak transcription	Stomach Smooth Muscle	stomach
20	chr11:76675000-76725600	Weak transcription	A549	lung
21	chr11:76675000-76729600	Weak transcription	Brain Angular Gyrus	brain
22	chr11:76675200-76684000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr11:76675200-76688000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr11:76675200-76688000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr11:76675200-76688200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr11:76675400-76688600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr11:76675400-76688800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr11:76675400-76689000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr11:76681600-76684200	Weak transcription	Duodenum Mucosa	Duodenum
30	chr11:76681800-76683400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr11:76681800-76683400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
32	chr11:76682000-76683400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr11:76682800-76683400	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr11:76683000-76683800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
35	chr11:76683000-76684200	Strong transcription	Cortex derived primary cultured neurospheres	brain
36	chr11:76683000-76684200	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr11:76683000-76688000	Weak transcription	Primary B cells from cord blood	blood
38	chr11:76683000-76736400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
39	chr11:76683200-76683400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr11:76683200-76688000	Weak transcription	Primary neutrophils fromperipheralblood	blood
41	chr11:76683200-76688600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr11:76683200-76729200	Weak transcription	Brain Hippocampus Middle	brain
43	chr11:76683400-76684600	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr11:76683400-76684600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr11:76683400-76688000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr11:76683400-76688200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr11:76683400-76689600	Weak transcription	Fetal Brain Male	brain
48	chr11:76683400-76690600	Strong transcription	Monocytes-CD14+_RO01746	blood
49	chr11:76683600-76688400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
50	chr11:76683600-76720400	Weak transcription	Brain Cingulate Gyrus	brain

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