Variant report

Variant	nsv897502
Chromosome Location	chr11:50121285-50235107
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	CCNT2	chr11:50134957-50135155	K562	blood:	n/a	n/a
2	CEBPB	chr11:50185114-50185392	HepG2	liver:	n/a	chr11:50185257-50185274 chr11:50185258-50185271 chr11:50185259-50185270 chr11:50185258-50185269
3	CEBPB	chr11:50132343-50132599	HepG2	liver:	n/a	n/a
4	CEBPB	chr11:50230060-50230405	MCF-7	breast:	n/a	n/a
5	CEBPB	chr11:50233638-50233794	HepG2	liver:	n/a	n/a
6	CEBPB	chr11:50145990-50146140	HepG2	liver:	n/a	chr11:50146064-50146075
7	CEBPB	chr11:50134957-50135324	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr11:50180269-50180536	MCF-7	breast:	n/a	n/a
9	CEBPB	chr11:50182673-50182737	HepG2	liver:	n/a	chr11:50182687-50182698
10	CEBPB	chr11:50132313-50132582	IMR90	lung:	n/a	n/a
11	CEBPB	chr11:50202172-50202422	IMR90	lung:	n/a	chr11:50202284-50202295
12	CEBPB	chr11:50202142-50202359	HepG2	liver:	n/a	chr11:50202284-50202295
13	CEBPB	chr11:50185206-50185319	A549	lung:	n/a	chr11:50185257-50185274 chr11:50185258-50185271 chr11:50185259-50185270 chr11:50185258-50185269
14	CHD1	chr11:50134958-50135158	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr11:50133540-50133690	SAEC	small airway:	n/a	chr11:50133670-50133686 chr11:50133672-50133681 chr11:50133669-50133687
16	CTCF	chr11:50165390-50165477	LNCaP	prostate:	n/a	n/a
17	CTCF	chr11:50133580-50133730	HEK293	kidney:	n/a	chr11:50133670-50133686 chr11:50133672-50133681 chr11:50133669-50133687
18	CTCF	chr11:50133628-50133712	HepG2	liver:	n/a	chr11:50133670-50133686 chr11:50133672-50133681 chr11:50133669-50133687
19	CTCF	chr11:50133660-50133810	HMF	breast:	n/a	chr11:50133670-50133686 chr11:50133672-50133681 chr11:50133669-50133687
20	CTCF	chr11:50207190-50207225	Pancreas_OC	pancreas:	n/a	n/a
21	CTCF	chr11:50133600-50133750	HBMEC	blood vessel:	n/a	chr11:50133670-50133686 chr11:50133672-50133681 chr11:50133669-50133687
22	CTCF	chr11:50133580-50133730	HFF	foreskin:	n/a	chr11:50133670-50133686 chr11:50133672-50133681 chr11:50133669-50133687
23	CTCF	chr11:50133560-50133710	HL-60	blood:	n/a	chr11:50133670-50133686 chr11:50133672-50133681 chr11:50133669-50133687
24	CTCF	chr11:50220602-50220640	MCF-7	breast:	n/a	n/a
25	CTCF	chr11:50133512-50133811	T-47D	breast:	n/a	chr11:50133670-50133686 chr11:50133672-50133681 chr11:50133669-50133687
26	CTCF	chr11:50133740-50133890	NHEK	skin:	n/a	n/a
27	CTCF	chr11:50133680-50133830	AG10803	skin:	n/a	n/a
28	CTCF	chr11:50133580-50133730	HVMF	connective:	n/a	chr11:50133670-50133686 chr11:50133672-50133681 chr11:50133669-50133687
29	CTCF	chr11:50133520-50133670	NB4	blood:	n/a	n/a
30	CTCF	chr11:50129940-50130090	MCF-7	breast:	n/a	chr11:50129945-50129958
31	CTCF	chr11:50189348-50189444	GM13976	blood:	n/a	n/a
32	CTCF	chr11:50133540-50133690	Hela-S3	cervix:	n/a	chr11:50133670-50133686 chr11:50133672-50133681 chr11:50133669-50133687
33	CTCF	chr11:50133552-50133779	MCF-7	breast:	n/a	chr11:50133670-50133686 chr11:50133672-50133681 chr11:50133669-50133687
34	CTCF	chr11:50133600-50133750	HMEC	breast:	n/a	chr11:50133670-50133686 chr11:50133672-50133681 chr11:50133669-50133687
35	CTCF	chr11:50133412-50133884	T-47D	breast:	n/a	chr11:50133670-50133686 chr11:50133672-50133681 chr11:50133669-50133687
36	CTCF	chr11:50133580-50133730	MCF-7	breast:	n/a	chr11:50133670-50133686 chr11:50133672-50133681 chr11:50133669-50133687
37	CTCF	chr11:50129884-50129976	MCF-7	breast:	n/a	chr11:50129945-50129958
38	CTCF	chr11:50227575-50227627	LNCaP	prostate:	n/a	n/a
39	CTCF	chr11:50203704-50203730	Fibrobl	skin:	n/a	n/a
40	CTCF	chr11:50133600-50133750	GM06990	blood:	n/a	chr11:50133670-50133686 chr11:50133672-50133681 chr11:50133669-50133687
41	CTCF	chr11:50162853-50162864	GM20000	blood:	n/a	n/a
42	CTCF	chr11:50133520-50133670	HVMF	connective:	n/a	n/a
43	CTCF	chr11:50143702-50143807	Gliobla	brain:	n/a	n/a
44	CTCF	chr11:50133619-50133706	NHEK	skin:	n/a	chr11:50133670-50133686 chr11:50133672-50133681 chr11:50133669-50133687
45	CTCF	chr11:50133640-50133790	HEEpiC	esophagus:	n/a	chr11:50133670-50133686 chr11:50133672-50133681 chr11:50133669-50133687
46	CTCF	chr11:50133680-50133830	A549	lung:	n/a	n/a
47	CTCF	chr11:50129886-50129984	MCF-7	breast:	n/a	chr11:50129945-50129958
48	CTCF	chr11:50133611-50133724	ProgFib	skin:	n/a	chr11:50133670-50133686 chr11:50133672-50133681 chr11:50133669-50133687
49	CTCF	chr11:50129939-50129971	MCF-7	breast:	n/a	chr11:50129945-50129958
50	CTCF	chr11:50174400-50174550	WI-38	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:50227079-50227129	HUVEC	blood vessel:	n/a
2	chr11:50227476-50227526	HUVEC	blood vessel:	n/a
3	chr11:50227476-50227526	Jurkat	blood:	n/a
4	chr11:50227079-50227129	HUVEC	blood vessel:	n/a
5	chr11:50227476-50227526	HUVEC	blood vessel:	n/a
6	chr11:50227476-50227526	Jurkat	blood:	n/a
7	chr11:50129456-50129506	BE2_C	brain:	n/a
8	chr11:50206561-50206611	HepG2	liver:	n/a
9	chr11:50220389-50220439	Jurkat	blood:	n/a
10	chr11:50220107-50220157	BE2_C	brain:	n/a
11	chr11:50234973-50235023	SAEC	small airway:	n/a
12	chr11:50227476-50227526	AoSMC	blood vessel:	n/a
13	chr11:50227079-50227129	ovcar-3	ovarian:	n/a
14	chr11:50220426-50220476	GM12878	blood:	n/a
15	chr11:50226789-50226839	T-47D	breast:	n/a
16	chr11:50220426-50220476	NH-A	brain:	n/a
17	chr11:50220055-50220105	HRPEpiC	eye:	n/a
18	chr11:50227265-50227315	SK-N-SH_RA	brain:	n/a
19	chr11:50220426-50220476	AoSMC	blood vessel:	n/a
20	chr11:50231261-50231311	NB4	blood:	n/a
21	chr11:50227102-50227152	ProgFib	skin:	n/a
22	chr11:50129456-50129506	NHDF-neo	bronchial:	n/a
23	chr11:50206606-50206656	SKMC	muscle:	n/a
24	chr11:50206606-50206656	BE2_C	brain:	n/a
25	chr11:50219952-50220002	HAEpiC	amniotic membrane:	n/a
26	chr11:50231261-50231311	Hela-S3	cervix:	n/a
27	chr11:50234973-50235023	NH-A	brain:	n/a
28	chr11:50231261-50231311	AG04450	lung:	fetal
29	chr11:50206606-50206656	AG04450	lung:	fetal
30	chr11:50206530-50206580	A549	lung:	n/a
31	chr11:50227079-50227129	H1-hESC	embryonic stem cell:	embryo
32	chr11:50206561-50206611	Jurkat	blood:	n/a
33	chr11:50129456-50129506	HIPEpiC	eye:	n/a
34	chr11:50227199-50227249	AG04450	lung:	fetal
35	chr11:50220343-50220393	HRE	kidney:	n/a
36	chr11:50206561-50206611	GM12878	blood:	n/a
37	chr11:50220107-50220157	HCF	heart:	n/a
38	chr11:50206530-50206580	GM19239	blood:	n/a
39	chr11:50129456-50129506	GM12891	blood:	n/a
40	chr11:50206606-50206656	HEK293	kidney:	embryo
41	chr11:50227476-50227526	ovcar-3	ovarian:	n/a
42	chr11:50206530-50206580	LNCaP	prostate:	n/a
43	chr11:50129456-50129506	SK-N-SH	brain:	n/a
44	chr11:50206606-50206656	BJ	skin:	n/a
45	chr11:50220055-50220105	Caco-2	colon:	n/a
46	chr11:50220389-50220439	HCT-116	colon:	n/a
47	chr11:50129456-50129506	AG09319	gingival:	n/a
48	chr11:50219952-50220002	SKMC	muscle:	n/a
49	chr11:50219952-50220002	NH-A	brain:	n/a
50	chr11:50220426-50220476	NHDF-neo	bronchial:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:50172306..50174473-chr11:50176469..50178865,2	K562	blood:
2	chr11:50172306..50174473-chr11:50176469..50178865,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR4C12-1	chr11:50232840-50233106	XLOC_009440
2	lnc-OR4C12-1	chr11:50231598-50231759	XLOC_009440

Variant related genes	Relation type
ENSG00000255500	TF binding region
ENSG00000236919	TF binding region
ENSG00000255442	TF binding region
ENSG00000255500	CpG island
ENSG00000236919	CpG island
ENSG00000255442	CpG island

Extended variants
information (count: 1429 )
Associated
traits (count: 49 )

Variant overlapped rSNPs/rCNVs (count:1429 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs374403775	chr11:50124781-50124782	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs567323457	chr11:50124790-50124791	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs536453141	chr11:50124796-50124797	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs368514516	chr11:50124797-50124798	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs116327800	chr11:50124810-50124811	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs143694102	chr11:50124857-50124858	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs189956986	chr11:50124869-50124870	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs114926767	chr11:50129008-50129009	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs529494050	chr11:50129012-50129013	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs11245894	chr11:50129033-50129034	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs559412557	chr11:50129040-50129041	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs186011377	chr11:50129060-50129061	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs145508901	chr11:50129093-50129094	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs568551621	chr11:50129112-50129113	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs534007787	chr11:50129130-50129131	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs113682456	chr11:50129175-50129176	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs537265728	chr11:50129188-50129189	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs550584042	chr11:50129203-50129204	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs145257215	chr11:50129217-50129218	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs373378117	chr11:50129241-50129242	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs567591849	chr11:50129257-50129258	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs536248113	chr11:50129260-50129261	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs1995041	chr11:50129261-50129262	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs138031910	chr11:50129277-50129278	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs538711537	chr11:50129324-50129325	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs16926834	chr11:50129325-50129326	ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs189574434	chr11:50129388-50129389	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs544023501	chr11:50129408-50129409	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs563825954	chr11:50129413-50129414	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs180808185	chr11:50129454-50129455	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs542923637	chr11:50129456-50129457	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs577343319	chr11:50129483-50129484	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs559275696	chr11:50129500-50129501	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs570499675	chr11:50129510-50129511	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs150562363	chr11:50129513-50129514	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs546207068	chr11:50129522-50129523	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs372348367	chr11:50129543-50129544	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs186728827	chr11:50129553-50129554	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs530595719	chr11:50129561-50129562	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs7104653	chr11:50129598-50129599	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs567555810	chr11:50129633-50129634	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs58677382	chr11:50129655-50129656	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs546940267	chr11:50129664-50129665	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs566444260	chr11:50129673-50129674	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs538664134	chr11:50129689-50129690	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs58447209	chr11:50129708-50129709	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs149267806	chr11:50129718-50129719	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs368235824	chr11:50129723-50129724	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs557093030	chr11:50129746-50129747	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs573899800	chr11:50129751-50129752	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:49)

Disease	PMID	Source
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Wilms tumour	21544195	CNVD
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Renal cell carcinoma	18194544	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Hirschsprung''s Disease	21712996	CNVD
Follicular lymphoma	20505157	CNVD
Colorectal cancer	21128281	CNVD
Glioblastoma multiforme	21138945	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
small cell lung cancer	20016488	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Mortal	21835882	CNVD
Autism	22495309	CNVD
Melanoma	20877625	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:46 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:50129000-50130400	ZNF genes & repeats	Placenta	Placenta
2	chr11:50129400-50129800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr11:50130400-50131000	Active TSS	Placenta	Placenta
4	chr11:50133000-50133200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr11:50133000-50133800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr11:50133200-50133600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr11:50133200-50134200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr11:50133200-50134400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr11:50133200-50134400	Enhancers	Adipose Nuclei	Adipose
10	chr11:50133600-50133800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr11:50133800-50134000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr11:50133800-50134000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr11:50134000-50134400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr11:50134000-50135000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr11:50134200-50134400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr11:50134400-50140400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr11:50134400-50146200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr11:50136600-50136800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
19	chr11:50140400-50142200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr11:50140400-50142600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr11:50141800-50142000	Weak transcription	Adipose Nuclei	Adipose
22	chr11:50142000-50142200	Enhancers	Adipose Nuclei	Adipose
23	chr11:50142200-50144600	Weak transcription	Adipose Nuclei	Adipose
24	chr11:50142200-50145600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr11:50142600-50147000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr11:50144600-50147200	Enhancers	Adipose Nuclei	Adipose
27	chr11:50145600-50146000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr11:50145800-50147400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr11:50146000-50147000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr11:50146200-50147400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr11:50147000-50147400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr11:50147000-50147600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr11:50151800-50152200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr11:50155000-50155200	Active TSS	HMEC	breast
35	chr11:50155000-50155200	Enhancers	HSMMtube	muscle
36	chr11:50155000-50155200	Enhancers	NH-A	brain
37	chr11:50188200-50189000	Enhancers	Adipose Nuclei	Adipose
38	chr11:50191600-50191800	ZNF genes & repeats	Right Atrium	heart
39	chr11:50191800-50194400	Weak transcription	Right Atrium	heart
40	chr11:50192600-50195800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
41	chr11:50193600-50193800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr11:50202200-50204200	Weak transcription	Pancreatic Islets	Pancreatic Islet
43	chr11:50206200-50207200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr11:50217000-50218200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
45	chr11:50220000-50220800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr11:50220600-50221200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell

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