Variant report

Variant	nsv898379
Chromosome Location	chr11:107649026-107673300
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	chr11:107658025-107658157	K562	blood:	n/a	n/a
2	ARID3A	chr11:107670016-107670309	K562	blood:	n/a	n/a
3	ARID3A	chr11:107670088-107670292	HepG2	liver:	n/a	n/a
4	ATF2	chr11:107656107-107656546	GM12878	blood:	n/a	n/a
5	BACH1	chr11:107649876-107650025	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr11:107669987-107670260	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr11:107658543-107658622	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr11:107656116-107656405	GM12878	blood:	n/a	n/a
9	BATF	chr11:107656068-107656457	GM12878	blood:	n/a	n/a
10	BCL11A	chr11:107656119-107656430	GM12878	blood:	n/a	n/a
11	BCLAF1	chr11:107669922-107670287	GM12878	blood:	n/a	n/a
12	CCNT2	chr11:107651637-107651830	K562	blood:	n/a	n/a
13	CEBPB	chr11:107672371-107672629	HepG2	liver:	n/a	chr11:107672475-107672486
14	CEBPB	chr11:107672348-107672657	IMR90	lung:	n/a	chr11:107672475-107672486
15	CTCF	chr11:107670050-107670297	NHEK	skin:	n/a	chr11:107670165-107670174
16	CTCF	chr11:107670080-107670230	HRPEpiC	eye:	n/a	chr11:107670165-107670174
17	CTCF	chr11:107670080-107670230	AG09309	skin:	n/a	chr11:107670165-107670174
18	CTCF	chr11:107651540-107651690	GM12866	blood:	n/a	n/a
19	CTCF	chr11:107669931-107670363	H1-hESC	embryonic stem cell:	n/a	chr11:107670165-107670174
20	CTCF	chr11:107651652-107651772	Gliobla	brain:	n/a	chr11:107651689-107651707 chr11:107651684-107651705 chr11:107651690-107651706 chr11:107651696-107651704 chr11:107651691-107651704
21	CTCF	chr11:107670060-107670210	NHEK	skin:	n/a	chr11:107670165-107670174
22	CTCF	chr11:107651640-107651790	HEEpiC	esophagus:	n/a	chr11:107651689-107651707 chr11:107651684-107651705 chr11:107651690-107651706 chr11:107651696-107651704 chr11:107651691-107651704
23	CTCF	chr11:107651640-107651790	HMEC	breast:	n/a	chr11:107651689-107651707 chr11:107651684-107651705 chr11:107651690-107651706 chr11:107651696-107651704 chr11:107651691-107651704
24	CTCF	chr11:107670080-107670230	HEEpiC	esophagus:	n/a	chr11:107670165-107670174
25	CTCF	chr11:107670065-107670268	GM12891	blood:	n/a	chr11:107670165-107670174
26	CTCF	chr11:107651626-107651762	IMR90	lung:	n/a	chr11:107651689-107651707 chr11:107651684-107651705 chr11:107651690-107651706 chr11:107651696-107651704 chr11:107651691-107651704
27	CTCF	chr11:107669498-107669593	GM20000	blood:	n/a	n/a
28	CTCF	chr11:107670120-107670270	SK-N-SH_RA	brain:	n/a	chr11:107670165-107670174
29	CTCF	chr11:107669959-107670286	A549	lung:	n/a	chr11:107670165-107670174
30	CTCF	chr11:107670080-107670230	HVMF	connective:	n/a	chr11:107670165-107670174
31	CTCF	chr11:107670051-107670299	MCF-7	breast:	n/a	chr11:107670165-107670174
32	CTCF	chr11:107651993-107652017	GM19239	blood:	n/a	n/a
33	CTCF	chr11:107669943-107670389	GM12878	blood:	n/a	chr11:107670165-107670174
34	CTCF	chr11:107670060-107670210	HL-60	blood:	n/a	chr11:107670165-107670174
35	CTCF	chr11:107651645-107651751	Medullo	brain:	n/a	chr11:107651689-107651707 chr11:107651684-107651705 chr11:107651690-107651706 chr11:107651696-107651704 chr11:107651691-107651704
36	CTCF	chr11:107670120-107670270	GM12864	blood:	n/a	chr11:107670165-107670174
37	CTCF	chr11:107670100-107670250	HBMEC	blood vessel:	n/a	chr11:107670165-107670174
38	CTCF	chr11:107670100-107670250	GM12872	blood:	n/a	chr11:107670165-107670174
39	CTCF	chr11:107670100-107670250	NHDF-neo	bronchial:	n/a	chr11:107670165-107670174
40	CTCF	chr11:107670100-107670250	HCFaa	heart:	n/a	chr11:107670165-107670174
41	CTCF	chr11:107670080-107670230	GM12874	blood:	n/a	chr11:107670165-107670174
42	CTCF	chr11:107670040-107670305	LNCaP	prostate:	n/a	chr11:107670165-107670174
43	CTCF	chr11:107651580-107651730	GM12864	blood:	n/a	chr11:107651689-107651707 chr11:107651684-107651705 chr11:107651690-107651706 chr11:107651696-107651704 chr11:107651691-107651704
44	CTCF	chr11:107670100-107670250	GM12878	blood:	n/a	chr11:107670165-107670174
45	CTCF	chr11:107669919-107670372	IMR90	lung:	n/a	chr11:107670165-107670174
46	CTCF	chr11:107651600-107651750	HBMEC	blood vessel:	n/a	chr11:107651689-107651707 chr11:107651684-107651705 chr11:107651690-107651706 chr11:107651696-107651704 chr11:107651691-107651704
47	CTCF	chr11:107670021-107670317	K562	blood:	n/a	chr11:107670165-107670174
48	CTCF	chr11:107670100-107670250	AG09319	gingival:	n/a	chr11:107670165-107670174
49	CTCF	chr11:107651599-107651772	LNCaP	prostate:	n/a	chr11:107651689-107651707 chr11:107651684-107651705 chr11:107651690-107651706 chr11:107651696-107651704 chr11:107651691-107651704
50	CTCF	chr11:107651460-107651610	HRE	kidney:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:107662133-107662183	SK-N-SH	brain:	n/a
2	chr11:107662133-107662183	ovcar-3	ovarian:	n/a
3	chr11:107662133-107662183	SK-N-SH_RA	brain:	n/a
4	chr11:107662133-107662183	U87	brain:	n/a
5	chr11:107662133-107662183	NH-A	brain:	n/a
6	chr11:107662133-107662183	NB4	blood:	n/a
7	chr11:107662133-107662183	SKMC	muscle:	n/a
8	chr11:107662133-107662183	AG04449	skin:	fetal
9	chr11:107662133-107662183	HCT-116	colon:	n/a
10	chr11:107662133-107662183	BE2_C	brain:	n/a
11	chr11:107662133-107662183	A549	lung:	n/a
12	chr11:107662133-107662183	MCF10A-Er-Src	breast:	n/a
13	chr11:107662133-107662183	HEEpiC	esophagus:	n/a
14	chr11:107662133-107662183	HEK293	kidney:	embryo
15	chr11:107662133-107662183	GM19239	blood:	n/a
16	chr11:107662133-107662183	HepG2	liver:	n/a
17	chr11:107662133-107662183	HPAEpiC	pulmonary alveolar:	n/a
18	chr11:107662133-107662183	SAEC	small airway:	n/a
19	chr11:107662133-107662183	PFSK-1	brain:	n/a
20	chr11:107662133-107662183	NHDF-neo	bronchial:	n/a
21	chr11:107662133-107662183	HRPEpiC	eye:	n/a
22	chr11:107662133-107662183	AG09319	gingival:	n/a
23	chr11:107662133-107662183	HRCEpiC	kidney:	n/a
24	chr11:107662133-107662183	K562	blood:	n/a
25	chr11:107662133-107662183	AG09309	skin:	n/a
26	chr11:107662133-107662183	Jurkat	blood:	n/a
27	chr11:107662133-107662183	SK-N-MC	brain:	n/a
28	chr11:107662133-107662183	GM12878	blood:	n/a
29	chr11:107662133-107662183	PrEC	prostate:	n/a
30	chr11:107662133-107662183	HUVEC	blood vessel:	n/a
31	chr11:107662133-107662183	CMK	blood:	n/a
32	chr11:107662133-107662183	ProgFib	skin:	n/a
33	chr11:107662133-107662183	RPTEC	kidney:	n/a
34	chr11:107662133-107662183	T-47D	breast:	n/a
35	chr11:107662133-107662183	GM12892	blood:	n/a
36	chr11:107662133-107662183	HIPEpiC	eye:	n/a
37	chr11:107662133-107662183	Hepatocyte	liver:	n/a
38	chr11:107662133-107662183	LNCaP	prostate:	n/a
39	chr11:107662133-107662183	GM06990	blood:	n/a
40	chr11:107662133-107662183	HMEC	breast:	n/a
41	chr11:107662133-107662183	H1-hESC	embryonic stem cell:	embryo
42	chr11:107662133-107662183	AG10803	skin:	n/a
43	chr11:107662133-107662183	HNPCEpiC	eye:	n/a
44	chr11:107662133-107662183	NT2-D1	testis:	n/a
45	chr11:107662133-107662183	HAEpiC	amniotic membrane:	n/a
46	chr11:107662133-107662183	HL-60	blood:	n/a
47	chr11:107662133-107662183	HCPEpiC	choroid plexus:	n/a
48	chr11:107662133-107662183	PANC-1	pancreas:	n/a
49	chr11:107662133-107662183	HCF	heart:	n/a
50	chr11:107662133-107662183	Hela-S3	cervix:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:201191728..201192238-chr11:107650401..107650990,2	MCF-7	breast:
2	chr11:107636795..107638295-chr11:107651566..107653122,2	K562	blood:
3	chr11:107646046..107648383-chr11:107654593..107656210,2	MCF-7	breast:
4	chr11:107670081..107670628-chr11:107695151..107695710,2	K562	blood:
5	chr11:107663159..107665072-chr11:107667163..107669875,2	MCF-7	breast:
6	chr11:107663159..107665072-chr11:107667163..107669875,2	MCF-7	breast:
7	chr11:107670116..107670647-chr11:107768751..107769447,2	MCF-7	breast:
8	chr11:107641920..107642539-chr11:107651250..107651774,2	K562	blood:

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	SLC35F2	hsa-miR-155-5p	chr11:107662756-107662777

Variant related genes	Relation type
ENSG00000214305	TF binding region
ENSG00000214305	CpG island

Extended variants
information (count: 1120 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:1120 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553663	chr11:107649026-107649027	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs116091267	chr11:107649046-107649047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs11212367	chr11:107649079-107649080	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs666751	chr11:107649162-107649163	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs535263866	chr11:107649210-107649211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs561159676	chr11:107649218-107649219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs191769468	chr11:107649248-107649249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs143945632	chr11:107649291-107649292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs36173954	chr11:107649305-107649306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs77330697	chr11:107649355-107649356	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs78842968	chr11:107649369-107649370	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs145671147	chr11:107649388-107649389	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs547807567	chr11:107649402-107649403	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs566752633	chr11:107649415-107649416	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs534104064	chr11:107649416-107649417	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs149858596	chr11:107649421-107649422	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs10693839	chr11:107649422-107649423	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs375755793	chr11:107649424-107649425	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs370196170	chr11:107649425-107649426	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs558901277	chr11:107649431-107649432	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs572559863	chr11:107649432-107649433	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs541871159	chr11:107649436-107649437	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs377010194	chr11:107649439-107649440	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs12222649	chr11:107649440-107649441	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs555567370	chr11:107649445-107649446	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs573890781	chr11:107649465-107649466	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs183871091	chr11:107649494-107649495	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs374180026	chr11:107649504-107649505	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs1680250	chr11:107649539-107649540	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs540166933	chr11:107649544-107649545	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs117125407	chr11:107649560-107649561	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs559737416	chr11:107649586-107649587	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs572367499	chr11:107649604-107649605	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs188819643	chr11:107649664-107649665	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs542921395	chr11:107649722-107649723	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs59048491	chr11:107649731-107649732	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs145259406	chr11:107649777-107649778	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs116385151	chr11:107649779-107649780	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs192590876	chr11:107649855-107649856	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs532669243	chr11:107649958-107649959	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs182373975	chr11:107649966-107649967	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs76175234	chr11:107649985-107649986	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs149171622	chr11:107650126-107650127	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs186911976	chr11:107650153-107650154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs111788501	chr11:107650158-107650159	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs150288322	chr11:107650161-107650162	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs4754250	chr11:107650164-107650165	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs539914773	chr11:107650168-107650169	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs190236792	chr11:107650180-107650181	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs368832092	chr11:107650182-107650183	Weak transcription 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
Chronic lymphocytic leukemia	21546498	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
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
Obesity	19966786	CNVD
Renal cell carcinoma	21668985	CNVD
Cancer	20164920	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Attention deficit hyperactivity disorder	19546859	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	17440070	CNVD

Chromatin state (count:268 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:107648400-107656000	Weak transcription	GM12878-XiMat	blood
2	chr11:107649600-107649800	Enhancers	Fetal Kidney	kidney
3	chr11:107649600-107650800	Enhancers	Liver	Liver
4	chr11:107649800-107650000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr11:107649800-107650000	Enhancers	Fetal Lung	lung
6	chr11:107649800-107651000	Weak transcription	Fetal Kidney	kidney
7	chr11:107650000-107650600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr11:107650400-107651400	Weak transcription	Fetal Lung	lung
9	chr11:107650600-107651200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr11:107650600-107651200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr11:107651000-107651800	Enhancers	Fetal Kidney	kidney
12	chr11:107651400-107651600	Enhancers	Rectal Mucosa Donor 31	rectum
13	chr11:107651400-107651800	Enhancers	Fetal Lung	lung
14	chr11:107651600-107652000	Active TSS	A549	lung
15	chr11:107652000-107665000	Weak transcription	A549	lung
16	chr11:107653600-107654600	Enhancers	Osteobl	bone
17	chr11:107653800-107654000	Enhancers	NH-A	brain
18	chr11:107654000-107676800	Weak transcription	NH-A	brain
19	chr11:107654600-107655800	Weak transcription	Osteobl	bone
20	chr11:107655400-107657000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr11:107655400-107662800	Weak transcription	Rectal Mucosa Donor 31	rectum
22	chr11:107655800-107656600	Enhancers	Osteobl	bone
23	chr11:107655800-107657000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr11:107656000-107656200	Enhancers	GM12878-XiMat	blood
25	chr11:107656200-107656400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr11:107656200-107656600	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr11:107656200-107656800	Enhancers	K562	blood
28	chr11:107656200-107662200	Weak transcription	GM12878-XiMat	blood
29	chr11:107656400-107656600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr11:107656400-107656600	Enhancers	Muscle Satellite Cultured Cells	--
31	chr11:107656400-107657800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr11:107656600-107658000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
33	chr11:107656600-107663000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr11:107656600-107673400	Weak transcription	Muscle Satellite Cultured Cells	--
35	chr11:107656600-107679800	Weak transcription	Osteobl	bone
36	chr11:107656800-107657000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr11:107656800-107673800	Weak transcription	K562	blood
38	chr11:107657000-107662200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr11:107657000-107662200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr11:107657000-107662600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr11:107657800-107658000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr11:107658000-107658800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr11:107658000-107659000	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr11:107658200-107658600	Enhancers	Placenta Amnion	Placenta Amnion
45	chr11:107658200-107658800	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr11:107658200-107658800	Enhancers	NHEK	skin
47	chr11:107658200-107659200	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chr11:107658200-107659200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr11:107658200-107659400	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr11:107658400-107658600	Enhancers	ES-WA7 Cell Line	embryonic stem cell

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