Variant report

Variant	nsv1041669
Chromosome Location	chr11:109085822-109282528
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:391)
CpG islands
(count:123)
Chromatin interactive
region (count:18)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:391 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr11:109261429-109261951	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr11:109162375-109162631	GM12878	blood:	n/a	chr11:109162484-109162495
3	CBX3	chr11:109191222-109191841	HCT-116	colon:	n/a	n/a
4	CEBPB	chr11:109235044-109235223	A549	lung:	n/a	n/a
5	CEBPB	chr11:109211878-109212092	HepG2	liver:	n/a	chr11:109211947-109211958
6	CEBPB	chr11:109138162-109138362	HepG2	liver:	n/a	chr11:109138213-109138224 chr11:109138236-109138247
7	CEBPB	chr11:109245200-109245433	HepG2	liver:	n/a	chr11:109245381-109245394 chr11:109245310-109245321
8	CEBPB	chr11:109138067-109138403	A549	lung:	n/a	chr11:109138213-109138224 chr11:109138236-109138247
9	CEBPB	chr11:109211822-109212057	IMR90	lung:	n/a	chr11:109211947-109211958
10	CEBPB	chr11:109093162-109093293	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr11:109138052-109138427	Hela-S3	cervix:	n/a	chr11:109138213-109138224 chr11:109138236-109138247
12	CEBPB	chr11:109093060-109093402	HepG2	liver:	n/a	n/a
13	CEBPB	chr11:109277467-109277665	HepG2	liver:	n/a	chr11:109277603-109277614
14	CEBPB	chr11:109211804-109211995	A549	lung:	n/a	chr11:109211947-109211958
15	CEBPB	chr11:109204638-109204929	MCF-7	breast:	n/a	chr11:109204806-109204817
16	CEBPB	chr11:109204691-109204962	HepG2	liver:	n/a	chr11:109204806-109204817
17	CHD1	chr11:109220096-109220161	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr11:109191280-109191430	AG04449	skin:	n/a	n/a
19	CTCF	chr11:109191360-109191510	HAc	cerebellar:	n/a	n/a
20	CTCF	chr11:109112700-109112850	SAEC	small airway:	n/a	n/a
21	CTCF	chr11:109138180-109138330	NHEK	skin:	n/a	n/a
22	CTCF	chr11:109191413-109191466	NHEK	skin:	n/a	n/a
23	CTCF	chr11:109190910-109190928	GM13976	blood:	n/a	n/a
24	CTCF	chr11:109119485-109119537	GM20000	blood:	n/a	n/a
25	CTCF	chr11:109191260-109191410	HMEC	breast:	n/a	n/a
26	CTCF	chr11:109191280-109191430	AG09309	skin:	n/a	n/a
27	CTCF	chr11:109150527-109150568	GM13977	blood:	n/a	n/a
28	CTCF	chr11:109165117-109165197	Spleen_OC	spleen:	n/a	n/a
29	CTCF	chr11:109191280-109191430	SK-N-SH_RA	brain:	n/a	n/a
30	CTCF	chr11:109191374-109191379	Fibrobl	skin:	n/a	n/a
31	CTCF	chr11:109150476-109150516	GM13977	blood:	n/a	n/a
32	CTCF	chr11:109191320-109191470	AoAF	blood vessel:	n/a	n/a
33	CTCF	chr11:109191280-109191430	HRPEpiC	eye:	n/a	n/a
34	CTCF	chr11:109191240-109191390	NHEK	skin:	n/a	n/a
35	CTCF	chr11:109191320-109191470	HCT-116	colon:	n/a	n/a
36	CTCF	chr11:109256860-109257010	HL-60	blood:	n/a	n/a
37	CTCF	chr11:109198820-109198875	GM10248	blood:	n/a	n/a
38	CTCF	chr11:109138160-109138310	HMEC	breast:	n/a	n/a
39	CTCF	chr11:109138200-109138350	SAEC	small airway:	n/a	n/a
40	CTCF	chr11:109191385-109191419	Fibrobl	skin:	n/a	n/a
41	CTCF	chr11:109171320-109171470	Caco-2	colon:	n/a	n/a
42	CTCF	chr11:109191340-109191351	Fibrobl	skin:	n/a	n/a
43	CTCF	chr11:109216980-109217130	BE2_C	brain:	n/a	n/a
44	CTCF	chr11:109261680-109261830	GM12871	blood:	n/a	n/a
45	CTCF	chr11:109161078-109161168	Lung_OC	lung:	n/a	n/a
46	CTCF	chr11:109191240-109191390	SAEC	small airway:	n/a	n/a
47	CTCF	chr11:109179200-109179350	NB4	blood:	n/a	n/a
48	CTCF	chr11:109191260-109191410	HPAF	blood vessel:	n/a	n/a
49	CTCF	chr11:109253580-109253730	GM12869	blood:	n/a	n/a
50	E2F4	chr11:109107589-109107636	MCF10A-Er-Src	breast:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:109259766-109259816	MCF10A-Er-Src	breast:	n/a
2	chr11:109259766-109259816	MCF10A-Er-Src	breast:	n/a
3	chr11:109259766-109259816	ProgFib	skin:	n/a
4	chr11:109172798-109172848	HCM	heart:	n/a
5	chr11:109259766-109259816	T-47D	breast:	n/a
6	chr11:109259766-109259816	HCT-116	colon:	n/a
7	chr11:109259766-109259816	NT2-D1	testis:	n/a
8	chr11:109172798-109172848	NT2-D1	testis:	n/a
9	chr11:109259766-109259816	K562	blood:	n/a
10	chr11:109259766-109259816	HPAEpiC	pulmonary alveolar:	n/a
11	chr11:109259766-109259816	BJ	skin:	n/a
12	chr11:109259766-109259816	AG04449	skin:	fetal
13	chr11:109259766-109259816	NHBE	bronchial:	n/a
14	chr11:109172798-109172848	AG04450	lung:	fetal
15	chr11:109172798-109172848	HCPEpiC	choroid plexus:	n/a
16	chr11:109172798-109172848	HIPEpiC	eye:	n/a
17	chr11:109259766-109259816	NHDF-neo	bronchial:	n/a
18	chr11:109172798-109172848	T-47D	breast:	n/a
19	chr11:109259766-109259816	HCF	heart:	n/a
20	chr11:109259766-109259816	NB4	blood:	n/a
21	chr11:109172798-109172848	GM06990	blood:	n/a
22	chr11:109172798-109172848	HRE	kidney:	n/a
23	chr11:109172798-109172848	GM12891	blood:	n/a
24	chr11:109172798-109172848	HRCEpiC	kidney:	n/a
25	chr11:109259766-109259816	H1-hESC	embryonic stem cell:	embryo
26	chr11:109259766-109259816	HUVEC	blood vessel:	n/a
27	chr11:109172798-109172848	SKMC	muscle:	n/a
28	chr11:109172798-109172848	Hepatocyte	liver:	n/a
29	chr11:109172798-109172848	HCF	heart:	n/a
30	chr11:109259766-109259816	LNCaP	prostate:	n/a
31	chr11:109259766-109259816	GM06990	blood:	n/a
32	chr11:109259766-109259816	HAEpiC	amniotic membrane:	n/a
33	chr11:109172798-109172848	AG10803	skin:	n/a
34	chr11:109172798-109172848	SK-N-MC	brain:	n/a
35	chr11:109259766-109259816	PrEC	prostate:	n/a
36	chr11:109259766-109259816	SK-N-SH_RA	brain:	n/a
37	chr11:109259766-109259816	ovcar-3	ovarian:	n/a
38	chr11:109259766-109259816	HRCEpiC	kidney:	n/a
39	chr11:109259766-109259816	AG10803	skin:	n/a
40	chr11:109259766-109259816	GM19239	blood:	n/a
41	chr11:109172798-109172848	HUVEC	blood vessel:	n/a
42	chr11:109259766-109259816	Caco-2	colon:	n/a
43	chr11:109172798-109172848	SAEC	small airway:	n/a
44	chr11:109259766-109259816	SK-N-MC	brain:	n/a
45	chr11:109172798-109172848	HMEC	breast:	n/a
46	chr11:109259766-109259816	AoSMC	blood vessel:	n/a
47	chr11:109172798-109172848	GM12878	blood:	n/a
48	chr11:109172798-109172848	AoSMC	blood vessel:	n/a
49	chr11:109172798-109172848	AG09309	skin:	n/a
50	chr11:109172798-109172848	PFSK-1	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr11:109222828..109225348-chr11:109227908..109230189,3	K562	blood:
2	chr11:109204590..109206135-chr11:109207677..109210571,2	K562	blood:
3	chr11:109204590..109206135-chr11:109207677..109210571,2	K562	blood:
4	chr11:109211476..109214893-chr11:109215512..109220497,5	K562	blood:
5	chr11:109127805..109129868-chr11:109133707..109135749,2	K562	blood:
6	chr11:109192870..109196198-chr11:109196275..109199852,4	K562	blood:
7	chr11:109125816..109127319-chr11:109129668..109132140,2	K562	blood:
8	chr11:109118774..109120383-chr11:109121444..109124055,2	K562	blood:
9	chr11:109212379..109214893-chr11:109216911..109218598,2	K562	blood:
10	chr11:109118774..109120383-chr11:109121444..109124055,2	K562	blood:
11	chr11:109212379..109214893-chr11:109216911..109218598,2	K562	blood:
12	chr11:109279005..109280963-chr11:109282959..109284752,2	K562	blood:
13	chr11:109222828..109225348-chr11:109227908..109230189,3	K562	blood:
14	chr11:109192870..109196198-chr11:109196275..109199852,4	K562	blood:
15	chr11:109210973..109212916-chr11:109213284..109215225,2	K562	blood:
16	chr11:109125816..109127319-chr11:109129668..109132140,2	K562	blood:
17	chr11:109211476..109214893-chr11:109215512..109220497,5	K562	blood:
18	chr11:109210973..109212916-chr11:109213284..109215225,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RDX-2	chr11:109235733-109235795	ENSG00000255028.1
2	lnc-RDX-2	chr11:109225812-109225861	ENSG00000255028.1

No data

Variant related genes	Relation type
ENSG00000264997	TF binding region
ENSG00000264997	CpG island
ENSG00000264997	chromatin interactions

Extended variants
information (count: 5424 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:5424 , 50 per page) page: 1 2 3 4 5 6 7 ... 109

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11212989	chr11:109085822-109085823	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs34811846	chr11:109085823-109085824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs148350551	chr11:109085849-109085850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs550688429	chr11:109085852-109085853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs114307015	chr11:109085880-109085881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs112311031	chr11:109085884-109085885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs77246381	chr11:109085916-109085917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs551119092	chr11:109085917-109085918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs566443677	chr11:109085919-109085920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs75445764	chr11:109085928-109085929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs76995331	chr11:109085929-109085930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs201116019	chr11:109086061-109086062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs533807592	chr11:109086174-109086175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs55987348	chr11:109086214-109086215	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs568150672	chr11:109086216-109086217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs76449309	chr11:109086236-109086237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs557476994	chr11:109086278-109086279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs575604530	chr11:109086320-109086321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs185513793	chr11:109086343-109086344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs558366035	chr11:109086361-109086362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs567354442	chr11:109086370-109086371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs188371206	chr11:109086377-109086378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs540947017	chr11:109086379-109086380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs556059198	chr11:109086429-109086430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs535989903	chr11:109086444-109086445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs573586907	chr11:109086468-109086469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs543863699	chr11:109086485-109086486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs562645274	chr11:109086501-109086502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs532871898	chr11:109086575-109086576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs544833130	chr11:109086592-109086593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs559937564	chr11:109086607-109086608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs555911254	chr11:109086690-109086691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs181196538	chr11:109086708-109086709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs186036307	chr11:109086713-109086714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs60455184	chr11:109086722-109086723	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs529333332	chr11:109086728-109086729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs538509129	chr11:109086787-109086788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs111921849	chr11:109086788-109086789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs191527166	chr11:109086811-109086812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs569365570	chr11:109086814-109086815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs539917327	chr11:109086877-109086878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs141599110	chr11:109086897-109086898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs567083176	chr11:109086920-109086921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs534345641	chr11:109086928-109086929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs556145137	chr11:109086940-109086941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs147532818	chr11:109086946-109086947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs544230424	chr11:109086954-109086955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs558492370	chr11:109086977-109086978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs555865679	chr11:109086980-109086981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs577539191	chr11:109087009-109087010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	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
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	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
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	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
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17603634	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	16790693	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Mental retardation	19966786	CNVD
Non-small cell lung cancer	21829676	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Intracranial aneurysm	16715129	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Ovarian cancer	21720365	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Neuroblastoma	17327916	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Mantle cell lymphoma	19029149	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant melanoma	17260012	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Renal cell carcinoma	21668985	CNVD
Cancer	20164920	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Developmental delay	21147756	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:224 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:109068800-109108600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr11:109092600-109095600	Enhancers	Brain Germinal Matrix	brain
3	chr11:109093200-109095000	Enhancers	Fetal Brain Female	brain
4	chr11:109093600-109094800	Enhancers	Fetal Brain Male	brain
5	chr11:109107600-109108000	Active TSS	A549	lung
6	chr11:109108600-109111000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr11:109111000-109112600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr11:109112200-109113600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr11:109112600-109113400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr11:109112600-109113400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr11:109112600-109113600	Enhancers	HMEC	breast
12	chr11:109112600-109114600	Enhancers	NHEK	skin
13	chr11:109112800-109113000	Active TSS	Gastric	stomach
14	chr11:109112800-109113200	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr11:109112800-109113200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr11:109112800-109113200	ZNF genes & repeats	Pancreas	Pancrea
17	chr11:109112800-109113200	Enhancers	Osteobl	bone
18	chr11:109113000-109113200	Flanking Active TSS	Gastric	stomach
19	chr11:109113200-109117000	Weak transcription	Osteobl	bone
20	chr11:109113400-109113800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr11:109113400-109117400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr11:109113600-109117400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr11:109113600-109117400	Weak transcription	HMEC	breast
24	chr11:109113800-109114400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr11:109114600-109117400	Weak transcription	NHEK	skin
26	chr11:109117000-109118200	Enhancers	Osteobl	bone
27	chr11:109117200-109118000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr11:109117200-109118200	Enhancers	Muscle Satellite Cultured Cells	--
29	chr11:109117400-109117800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr11:109117400-109117800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr11:109117400-109118000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr11:109117400-109118000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr11:109117400-109118200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr11:109117400-109118200	Enhancers	NHEK	skin
35	chr11:109117400-109118400	Enhancers	HMEC	breast
36	chr11:109117800-109120200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr11:109118000-109119400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr11:109118000-109119600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr11:109118200-109119600	Weak transcription	Osteobl	bone
40	chr11:109118200-109120200	Weak transcription	NHEK	skin
41	chr11:109118200-109120400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr11:109118400-109120600	Weak transcription	HMEC	breast
43	chr11:109119400-109121000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr11:109119600-109120400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr11:109119600-109120800	Enhancers	Osteobl	bone
46	chr11:109119800-109120600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr11:109120200-109120800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr11:109120400-109121000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr11:109120600-109120800	Enhancers	NHEK	skin
50	chr11:109120600-109121000	Enhancers	HMEC	breast

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