Variant report

Variant	nsv898390
Chromosome Location	chr11:108893765-109003536
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:606)
CpG islands
(count:427)
Chromatin interactive
region (count:13)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:606 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:108979879-108980350	HepG2	liver:	n/a	n/a
2	ATF2	chr11:108910987-108911437	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr11:108976753-108977364	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr11:108911022-108911451	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr11:108976878-108977607	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr11:108914217-108914418	GM12878	blood:	n/a	n/a
7	BATF	chr11:108914188-108914419	GM12878	blood:	n/a	n/a
8	BCL11A	chr11:108914180-108914452	GM12878	blood:	n/a	chr11:108914250-108914259
9	BHLHE40	chr11:108979895-108980135	HepG2	liver:	n/a	n/a
10	BHLHE40	chr11:108979897-108980294	HepG2	liver:	n/a	n/a
11	CEBPB	chr11:108939447-108939579	K562	blood:	n/a	chr11:108939510-108939521
12	CEBPB	chr11:108906187-108906219	HepG2	liver:	n/a	chr11:108906201-108906212
13	CEBPB	chr11:108906092-108906392	H1-hESC	embryonic stem cell:	n/a	chr11:108906201-108906212
14	CEBPB	chr11:108933204-108933537	IMR90	lung:	n/a	n/a
15	CEBPB	chr11:108939439-108939612	HepG2	liver:	n/a	chr11:108939510-108939521
16	CEBPB	chr11:108997869-108998011	A549	lung:	n/a	chr11:108997936-108997947
17	CEBPB	chr11:108997876-108998093	HepG2	liver:	n/a	chr11:108997936-108997947
18	CEBPB	chr11:108961566-108961568	IMR90	lung:	n/a	n/a
19	CEBPB	chr11:108918761-108919039	IMR90	lung:	n/a	chr11:108918880-108918891 chr11:108918878-108918891 chr11:108918880-108918891
20	CEBPB	chr11:108933263-108933534	HepG2	liver:	n/a	n/a
21	CHD2	chr11:109003242-109003633	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD2	chr11:108994901-108995043	HepG2	liver:	n/a	n/a
23	CHD2	chr11:108976790-108977395	H1-hESC	embryonic stem cell:	n/a	n/a
24	CREB1	chr11:108911088-108911360	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTBP2	chr11:108976914-108977735	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr11:108911200-108911350	HAc	cerebellar:	n/a	n/a
27	CTCF	chr11:108924043-108924098	GM20000	blood:	n/a	n/a
28	CTCF	chr11:108911180-108911330	GM12875	blood:	n/a	n/a
29	CTCF	chr11:108911120-108911270	GM12872	blood:	n/a	n/a
30	CTCF	chr11:108911200-108911350	HMF	breast:	n/a	n/a
31	CTCF	chr11:108911220-108911370	AoAF	blood vessel:	n/a	n/a
32	CTCF	chr11:108988780-108988930	HFF-Myc	foreskin:	n/a	n/a
33	CTCF	chr11:108911080-108911230	GM12869	blood:	n/a	n/a
34	CTCF	chr11:108911120-108911270	HBMEC	blood vessel:	n/a	n/a
35	CTCF	chr11:108911195-108911275	GM13977	blood:	n/a	n/a
36	CTCF	chr11:108911200-108911350	RPTEC	kidney:	n/a	n/a
37	CTCF	chr11:108991140-108991290	HCPEpiC	choroid plexus:	n/a	n/a
38	CTCF	chr11:108911140-108911290	NHEK	skin:	n/a	n/a
39	CTCF	chr11:108989014-108989079	HepG2	liver:	n/a	chr11:108989059-108989066 chr11:108989055-108989073
40	CTCF	chr11:108911200-108911350	HA-sp	spinal cord:	n/a	n/a
41	CTCF	chr11:108911140-108911290	GM06990	blood:	n/a	n/a
42	CTCF	chr11:108911180-108911330	GM12878	blood:	n/a	n/a
43	CTCF	chr11:108978021-108978098	GM10248	blood:	n/a	n/a
44	CTCF	chr11:108988940-108989090	HepG2	liver:	n/a	chr11:108989059-108989066 chr11:108989055-108989073
45	CTCF	chr11:108911200-108911350	HPF	lung:	n/a	n/a
46	CTCF	chr11:108911132-108911318	Gliobla	brain:	n/a	n/a
47	CTCF	chr11:108911220-108911370	GM12864	blood:	n/a	n/a
48	CTCF	chr11:108911200-108911350	AG04450	lung:	n/a	n/a
49	CTCF	chr11:108911140-108911290	HEK293	kidney:	n/a	n/a
50	CTCF	chr11:108911127-108911318	HepG2	liver:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:109002818-109002868	PrEC	prostate:	n/a
2	chr11:108983607-108983657	HRCEpiC	kidney:	n/a
3	chr11:108983607-108983657	AG04449	skin:	fetal
4	chr11:108994504-108994554	AG10803	skin:	n/a
5	chr11:108906099-108906149	HepG2	liver:	n/a
6	chr11:108906099-108906149	HAEpiC	amniotic membrane:	n/a
7	chr11:108918285-108918335	HMEC	breast:	n/a
8	chr11:108909215-108909265	T-47D	breast:	n/a
9	chr11:108918285-108918335	HEK293	kidney:	embryo
10	chr11:108909215-108909265	MCF-7	breast:	n/a
11	chr11:108909215-108909265	HCT-116	colon:	n/a
12	chr11:108918285-108918335	HEEpiC	esophagus:	n/a
13	chr11:108983607-108983657	BE2_C	brain:	n/a
14	chr11:108994504-108994554	GM19239	blood:	n/a
15	chr11:108906099-108906149	NT2-D1	testis:	n/a
16	chr11:108918285-108918335	ECC-1	luminal epithelium:	n/a
17	chr11:108994504-108994554	Hepatocyte	liver:	n/a
18	chr11:108994504-108994554	NHDF-neo	bronchial:	n/a
19	chr11:108909215-108909265	HEK293	kidney:	embryo
20	chr11:108918285-108918335	HCF	heart:	n/a
21	chr11:108991744-108991794	HIPEpiC	eye:	n/a
22	chr11:108991744-108991794	SK-N-SH	brain:	n/a
23	chr11:108909215-108909265	IMR90	lung:	fetal
24	chr11:108983607-108983657	HCF	heart:	n/a
25	chr11:108906099-108906149	HCM	heart:	n/a
26	chr11:108994504-108994554	GM06990	blood:	n/a
27	chr11:108918285-108918335	NHBE	bronchial:	n/a
28	chr11:108906099-108906149	BE2_C	brain:	n/a
29	chr11:108994504-108994554	HCT-116	colon:	n/a
30	chr11:108991744-108991794	A549	lung:	n/a
31	chr11:109002818-109002868	HL-60	blood:	n/a
32	chr11:108918285-108918335	SKMC	muscle:	n/a
33	chr11:108983607-108983657	PANC-1	pancreas:	n/a
34	chr11:108906099-108906149	HCF	heart:	n/a
35	chr11:108909215-108909265	Jurkat	blood:	n/a
36	chr11:108994504-108994554	BJ	skin:	n/a
37	chr11:108909215-108909265	HepG2	liver:	n/a
38	chr11:109002818-109002868	SK-N-SH_RA	brain:	n/a
39	chr11:108918285-108918335	Jurkat	blood:	n/a
40	chr11:108983607-108983657	NHDF-neo	bronchial:	n/a
41	chr11:108983607-108983657	LNCaP	prostate:	n/a
42	chr11:108983607-108983657	HL-60	blood:	n/a
43	chr11:108994504-108994554	GM12891	blood:	n/a
44	chr11:109002818-109002868	Hela-S3	cervix:	n/a
45	chr11:108918285-108918335	GM12891	blood:	n/a
46	chr11:108906099-108906149	K562	blood:	n/a
47	chr11:108906099-108906149	AG04449	skin:	fetal
48	chr11:108909215-108909265	GM06990	blood:	n/a
49	chr11:108991744-108991794	GM19239	blood:	n/a
50	chr11:109002818-109002868	MCF-7	breast:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:108905168..108907464-chr11:108909151..108912288,3	K562	blood:
2	chr11:108989018..108990754-chr11:108993164..108995394,2	K562	blood:
3	chr11:108899961..108902009-chr11:108909481..108912314,2	K562	blood:
4	chr11:108936870..108939701-chr11:108941192..108943026,2	K562	blood:
5	chr11:108905168..108907464-chr11:108909151..108912288,3	K562	blood:
6	chr11:108927357..108928938-chr11:108932482..108934210,2	K562	blood:
7	chr11:108936870..108939701-chr11:108941192..108943026,2	K562	blood:
8	chr11:108899961..108902009-chr11:108909481..108912314,2	K562	blood:
9	chr11:108905323..108906917-chr11:108910788..108913428,2	K562	blood:
10	chr11:108927357..108928938-chr11:108932482..108934210,2	K562	blood:
11	chr11:108989018..108990754-chr11:108993164..108995394,2	K562	blood:
12	chr11:108905323..108906917-chr11:108910788..108913428,2	K562	blood:
13	chr11:108873859..108875938-chr11:108935111..108937056,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EXPH5-1	chr11:108908470-108908694	ENSG00000255528

No data

Variant related genes	Relation type
ENSG00000255528	TF binding region
RNA5SP349	TF binding region
ENSG00000255528	CpG island
RNA5SP349	CpG island

Extended variants
information (count: 3478 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:3478 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10502107	chr11:108893765-108893766	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs117530825	chr11:108893798-108893799	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs544851788	chr11:108893800-108893801	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs150990638	chr11:108893816-108893817	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs532154238	chr11:108893851-108893852	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs558022223	chr11:108893889-108893890	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs368319592	chr11:108893911-108893912	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs542577092	chr11:108893912-108893913	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs540512538	chr11:108893925-108893926	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs139612846	chr11:108893945-108893946	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs118010968	chr11:108893953-108893954	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs551082904	chr11:108893987-108893988	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs148464301	chr11:108893993-108893994	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs569420838	chr11:108894040-108894041	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs533466722	chr11:108894106-108894107	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs73010594	chr11:108894107-108894108	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs149755355	chr11:108894135-108894136	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs59484602	chr11:108894159-108894160	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs534478945	chr11:108894164-108894165	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs555814967	chr11:108894272-108894273	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs4753858	chr11:108894273-108894274	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs537488902	chr11:108894275-108894276	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs555840055	chr11:108894327-108894328	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs145461203	chr11:108894406-108894407	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs368021723	chr11:108894412-108894413	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs544716616	chr11:108894486-108894487	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs4370904	chr11:108894516-108894517	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs572172838	chr11:108894518-108894519	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs186196381	chr11:108894530-108894531	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs190326360	chr11:108894553-108894554	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs538494463	chr11:108894570-108894571	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs574077403	chr11:108894640-108894641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs544569272	chr11:108894641-108894642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs182952204	chr11:108894678-108894679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs11600306	chr11:108894705-108894706	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs560695894	chr11:108894713-108894714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs551927400	chr11:108894789-108894790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs4586113	chr11:108894798-108894799	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs527915577	chr11:108894805-108894806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs11212863	chr11:108894809-108894810	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs528128504	chr11:108894845-108894846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs567913083	chr11:108894861-108894862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs10789708	chr11:108894875-108894876	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs10890931	chr11:108894917-108894918	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs10890932	chr11:108894922-108894923	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs141077905	chr11:108894955-108894956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs553617032	chr11:108894956-108894957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs61484998	chr11:108894959-108894960	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs536102393	chr11:108894995-108894996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs554750871	chr11:108895000-108895001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

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

Chromatin state (count:497 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:108892600-108894600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr11:108893600-108894000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
3	chr11:108893600-108894200	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr11:108893600-108894200	Enhancers	Osteobl	bone
5	chr11:108893800-108894200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr11:108894000-108894400	Enhancers	Monocytes-CD14+_RO01746	blood
7	chr11:108894200-108903800	Weak transcription	Osteobl	bone
8	chr11:108897000-108898000	Enhancers	HSMM	muscle
9	chr11:108897200-108899000	Enhancers	Muscle Satellite Cultured Cells	--
10	chr11:108897600-108897800	Enhancers	A549	lung
11	chr11:108897800-108898800	Weak transcription	A549	lung
12	chr11:108898800-108899000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr11:108898800-108899200	Enhancers	A549	lung
14	chr11:108899000-108904200	Weak transcription	Muscle Satellite Cultured Cells	--
15	chr11:108899200-108900600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr11:108899800-108901000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr11:108900600-108900800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr11:108900600-108901000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr11:108900800-108901400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr11:108901000-108904000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr11:108901000-108908800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr11:108901400-108902000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr11:108901600-108901800	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr11:108901600-108902000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr11:108901600-108902000	Enhancers	HMEC	breast
26	chr11:108901600-108902200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr11:108901800-108902200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr11:108901800-108902200	Enhancers	NHEK	skin
29	chr11:108901800-108904800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr11:108902000-108904400	Weak transcription	HMEC	breast
31	chr11:108902000-108904600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr11:108902200-108904600	Weak transcription	NHEK	skin
33	chr11:108902600-108905800	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr11:108902800-108903600	Enhancers	HUVEC	blood vessel
35	chr11:108903400-108904600	Enhancers	NH-A	brain
36	chr11:108903600-108904600	Weak transcription	HUVEC	blood vessel
37	chr11:108903800-108904800	Enhancers	Osteobl	bone
38	chr11:108904000-108904800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr11:108904000-108906000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr11:108904200-108905400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
41	chr11:108904400-108905600	Enhancers	HMEC	breast
42	chr11:108904600-108905000	Flanking Active TSS	NHEK	skin
43	chr11:108904600-108905400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr11:108904600-108905400	Enhancers	HSMMtube	muscle
45	chr11:108904600-108905400	Flanking Active TSS	NH-A	brain
46	chr11:108904600-108905600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr11:108904600-108906400	Enhancers	HUVEC	blood vessel
48	chr11:108904800-108905400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr11:108904800-108905400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr11:108904800-108905400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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