Variant report

Variant	nsv897498
Chromosome Location	chr11:49997431-50325741
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	chr11:50017185-50017430	HepG2	liver:	n/a	n/a
2	ATF1	chr11:50257555-50257921	K562	blood:	n/a	n/a
3	ATF3	chr11:50257564-50257818	K562	blood:	n/a	chr11:50257726-50257746 chr11:50257724-50257737 chr11:50257584-50257592 chr11:50257723-50257738 chr11:50257725-50257736
4	BATF	chr11:50251866-50252053	GM12878	blood:	n/a	n/a
5	BHLHE40	chr11:50017239-50017377	K562	blood:	n/a	n/a
6	BHLHE40	chr11:50257408-50257634	K562	blood:	n/a	chr11:50257599-50257615
7	CBX3	chr11:50017158-50017392	K562	blood:	n/a	n/a
8	CBX3	chr11:50017099-50017442	K562	blood:	n/a	n/a
9	CCNT2	chr11:50257299-50257888	K562	blood:	n/a	n/a
10	CCNT2	chr11:50134957-50135155	K562	blood:	n/a	n/a
11	CEBPB	chr11:50132313-50132582	IMR90	lung:	n/a	n/a
12	CEBPB	chr11:50185206-50185319	A549	lung:	n/a	chr11:50185257-50185274 chr11:50185258-50185271 chr11:50185259-50185270 chr11:50185258-50185269
13	CEBPB	chr11:50134957-50135324	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr11:50180269-50180536	MCF-7	breast:	n/a	n/a
15	CEBPB	chr11:50202172-50202422	IMR90	lung:	n/a	chr11:50202284-50202295
16	CEBPB	chr11:50114752-50114922	K562	blood:	n/a	chr11:50114830-50114843 chr11:50114830-50114843 chr11:50114832-50114841 chr11:50114830-50114841 chr11:50114832-50114843
17	CEBPB	chr11:50256005-50256238	K562	blood:	n/a	chr11:50256104-50256115
18	CEBPB	chr11:50062636-50062814	HepG2	liver:	n/a	chr11:50062715-50062726
19	CEBPB	chr11:50230060-50230405	MCF-7	breast:	n/a	n/a
20	CEBPB	chr11:50185114-50185392	HepG2	liver:	n/a	chr11:50185257-50185274 chr11:50185258-50185271 chr11:50185259-50185270 chr11:50185258-50185269
21	CEBPB	chr11:50105602-50105814	IMR90	lung:	n/a	n/a
22	CEBPB	chr11:50202142-50202359	HepG2	liver:	n/a	chr11:50202284-50202295
23	CEBPB	chr11:50056041-50056226	HepG2	liver:	n/a	chr11:50056106-50056117
24	CEBPB	chr11:50233638-50233794	HepG2	liver:	n/a	n/a
25	CEBPB	chr11:50145990-50146140	HepG2	liver:	n/a	chr11:50146064-50146075
26	CEBPB	chr11:50114607-50115033	MCF-7	breast:	n/a	chr11:50114830-50114843 chr11:50114830-50114843 chr11:50114832-50114841 chr11:50114830-50114841 chr11:50114832-50114843
27	CEBPB	chr11:50256020-50256220	HepG2	liver:	n/a	chr11:50256104-50256115
28	CEBPB	chr11:50114701-50115022	MCF-7	breast:	n/a	chr11:50114830-50114843 chr11:50114830-50114843 chr11:50114832-50114841 chr11:50114830-50114841 chr11:50114832-50114843
29	CEBPB	chr11:50132343-50132599	HepG2	liver:	n/a	n/a
30	CEBPB	chr11:50062165-50062194	HepG2	liver:	n/a	chr11:50062170-50062183 chr11:50062171-50062182 chr11:50062170-50062183
31	CEBPB	chr11:50114681-50114996	HepG2	liver:	n/a	chr11:50114830-50114843 chr11:50114830-50114843 chr11:50114832-50114841 chr11:50114830-50114841 chr11:50114832-50114843
32	CEBPB	chr11:50047487-50047664	A549	lung:	n/a	n/a
33	CEBPB	chr11:50182673-50182737	HepG2	liver:	n/a	chr11:50182687-50182698
34	CEBPB	chr11:50114658-50114986	IMR90	lung:	n/a	chr11:50114830-50114843 chr11:50114830-50114843 chr11:50114832-50114841 chr11:50114830-50114841 chr11:50114832-50114843
35	CEBPB	chr11:50114698-50115007	A549	lung:	n/a	chr11:50114830-50114843 chr11:50114830-50114843 chr11:50114832-50114841 chr11:50114830-50114841 chr11:50114832-50114843
36	CEBPB	chr11:50114776-50115008	Hela-S3	cervix:	n/a	chr11:50114830-50114843 chr11:50114830-50114843 chr11:50114832-50114841 chr11:50114830-50114841 chr11:50114832-50114843
37	CHD1	chr11:50134958-50135158	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD2	chr11:50017167-50017356	K562	blood:	n/a	n/a
39	CREB1	chr11:50257411-50258094	K562	blood:	n/a	chr11:50257724-50257737
40	CREB1	chr11:50257549-50258023	K562	blood:	n/a	chr11:50257724-50257737
41	CTCF	chr11:50017240-50017390	BE2_C	brain:	n/a	n/a
42	CTCF	chr11:50133600-50133750	GM06990	blood:	n/a	chr11:50133670-50133686 chr11:50133672-50133681 chr11:50133669-50133687
43	CTCF	chr11:50097823-50097863	GM20000	blood:	n/a	n/a
44	CTCF	chr11:50017200-50017350	GM12872	blood:	n/a	n/a
45	CTCF	chr11:50017101-50017393	A549	lung:	n/a	n/a
46	CTCF	chr11:50017320-50017470	MCF-7	breast:	n/a	n/a
47	CTCF	chr11:50017320-50017470	HAc	cerebellar:	n/a	n/a
48	CTCF	chr11:50017180-50017330	GM12871	blood:	n/a	n/a
49	CTCF	chr11:50017120-50017270	HCT-116	colon:	n/a	n/a
50	CTCF	chr11:49999104-49999175	Spleen_OC	spleen:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:50005399-50005449	HepG2	liver:	n/a
2	chr11:50260762-50260812	MCF10A-Er-Src	breast:	n/a
3	chr11:50227102-50227152	LNCaP	prostate:	n/a
4	chr11:50257256-50257306	IMR90	lung:	fetal
5	chr11:50219952-50220002	HNPCEpiC	eye:	n/a
6	chr11:50005399-50005449	ovcar-3	ovarian:	n/a
7	chr11:50005457-50005507	HL-60	blood:	n/a
8	chr11:50005399-50005449	HepG2	liver:	n/a
9	chr11:50260762-50260812	MCF10A-Er-Src	breast:	n/a
10	chr11:50227102-50227152	LNCaP	prostate:	n/a
11	chr11:50257256-50257306	IMR90	lung:	fetal
12	chr11:50219952-50220002	HNPCEpiC	eye:	n/a
13	chr11:50005399-50005449	ovcar-3	ovarian:	n/a
14	chr11:50005457-50005507	HL-60	blood:	n/a
15	chr11:50257256-50257306	HCT-116	colon:	n/a
16	chr11:50227199-50227249	AG09309	skin:	n/a
17	chr11:50234973-50235023	MCF10A-Er-Src	breast:	n/a
18	chr11:50257771-50257821	Hepatocyte	liver:	n/a
19	chr11:50257256-50257306	PANC-1	pancreas:	n/a
20	chr11:50231261-50231311	HL-60	blood:	n/a
21	chr11:50257830-50257880	Jurkat	blood:	n/a
22	chr11:50220426-50220476	HRE	kidney:	n/a
23	chr11:50206606-50206656	HUVEC	blood vessel:	n/a
24	chr11:50004210-50004260	LNCaP	prostate:	n/a
25	chr11:50257625-50257675	HAEpiC	amniotic membrane:	n/a
26	chr11:50238009-50238059	SK-N-SH_RA	brain:	n/a
27	chr11:50257496-50257546	NB4	blood:	n/a
28	chr11:50238214-50238264	GM19239	blood:	n/a
29	chr11:50257633-50257683	PANC-1	pancreas:	n/a
30	chr11:50231261-50231311	AG10803	skin:	n/a
31	chr11:50220055-50220105	SKMC	muscle:	n/a
32	chr11:50003963-50004013	HPAEpiC	pulmonary alveolar:	n/a
33	chr11:50257752-50257802	HAEpiC	amniotic membrane:	n/a
34	chr11:50005457-50005507	HRCEpiC	kidney:	n/a
35	chr11:50256574-50256624	Hela-S3	cervix:	n/a
36	chr11:50220426-50220476	HepG2	liver:	n/a
37	chr11:50257979-50258029	HCM	heart:	n/a
38	chr11:50239550-50239600	HCPEpiC	choroid plexus:	n/a
39	chr11:50258750-50258800	Hela-S3	cervix:	n/a
40	chr11:50206606-50206656	H1-hESC	embryonic stem cell:	embryo
41	chr11:50206561-50206611	NHBE	bronchial:	n/a
42	chr11:50257625-50257675	HRE	kidney:	n/a
43	chr11:50206530-50206580	HEK293	kidney:	embryo
44	chr11:50238214-50238264	IMR90	lung:	fetal
45	chr11:50129456-50129506	K562	blood:	n/a
46	chr11:50226789-50226839	PFSK-1	brain:	n/a
47	chr11:50257771-50257821	AG09309	skin:	n/a
48	chr11:50238214-50238264	HRPEpiC	eye:	n/a
49	chr11:50220426-50220476	U87	brain:	n/a
50	chr11:50257830-50257880	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:50256839..50259422-chr11:50261676..50263683,2	K562	blood:
2	chr11:50172306..50174473-chr11:50176469..50178865,2	K562	blood:
3	chr11:49547545..49548055-chr11:50016701..50017446,2	MCF-7	breast:
4	chr11:50172306..50174473-chr11:50176469..50178865,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR4C13-7	chr11:50274586-50274778	NONHSAT021338
2	lnc-OR4C13-1	chr11:50257750-50258088	ENSG00000254518
3	lnc-OR4C13-7	chr11:50280085-50280169	NONHSAT021340
4	lnc-OR4C13-1	chr11:50262310-50262433	ENSG00000254518
5	lnc-OR4C13-7	chr11:50279538-50279677	NONHSAT021340
6	lnc-OR4C12-2	chr11:50060551-50060604	NONHSAT021327
7	lnc-OR4C13-1	chr11:50257789-50258088	ENSG00000254518
8	lnc-OR4C13-7	chr11:50274586-50274767	NONHSAT021340
9	lnc-OR4C13-7	chr11:50266852-50266898	NONHSAT021340
10	lnc-OR4C13-1	chr11:50257750-50258210	NONHSAT021336
11	lnc-OR4C13-7	chr11:50302810-50303035	NONHSAT021343
12	lnc-OR4C13-7	chr11:50313156-50313246	NONHSAT021340
13	lnc-OR4C13-7	chr11:50266792-50266965	NONHSAT021338
14	lnc-OR4C13-7	chr11:50279839-50280169	NONHSAT021342
15	lnc-OR4C13-7	chr11:50274586-50274767	NONHSAT021339
16	lnc-OR4C13-1	chr11:50263752-50263827	NONHSAT021336
17	lnc-OR4C13-7	chr11:50301870-50302020	NONHSAT021343
18	lnc-OR4C13-7	chr11:50266792-50266898	NONHSAT021339
19	lnc-OR4C13-7	chr11:50302810-50302996	NONHSAT021339
20	lnc-OR4C13-1	chr11:50263752-50263827	ENSG00000254518
21	lnc-OR4C12-2	chr11:50061788-50062069	NONHSAT021327
22	lnc-OR4C13-7	chr11:50320143-50320239	NONHSAT021340
23	lnc-OR4C12-1	chr11:50231598-50231759	XLOC_009440
24	lnc-OR4C13-1	chr11:50262310-50262433	NONHSAT021336
25	lnc-OR4C13-7	chr11:50279538-50279677	NONHSAT021339
26	lnc-OR4C13-7	chr11:50280085-50280169	NONHSAT021339
27	lnc-OR4C13-7	chr11:50320710-50320877	NONHSAT021340
28	lnc-OR4C13-1	chr11:50261115-50261299	NONHSAT021336
29	lnc-OR4C12-1	chr11:50232840-50233106	XLOC_009440
30	lnc-OR4C13-1	chr11:50261115-50261299	ENSG00000254518
31	lnc-OR4C13-7	chr11:50301079-50301142	NONHSAT021343
32	lnc-OR4C12-2	chr11:50060063-50060146	NONHSAT021327
33	lnc-OR4C13-7	chr11:50302810-50303098	NONHSAT021342

Variant related genes	Relation type
ENSG00000255442	TF binding region
ENSG00000254518	TF binding region
ENSG00000255042	TF binding region
ENSG00000255500	TF binding region
ENSG00000254840	TF binding region
ENSG00000255001	TF binding region
ENSG00000236919	TF binding region
ENSG00000255199	TF binding region
OR4C12	TF binding region
ENSG00000255442	CpG island
ENSG00000254518	CpG island
ENSG00000255042	CpG island
ENSG00000255500	CpG island
ENSG00000254840	CpG island
ENSG00000255001	CpG island
ENSG00000236919	CpG island
ENSG00000255199	CpG island
OR4C12	CpG island
ENSG00000254518	chromatin interactions

Extended variants
information (count: 4665 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:4665 , 50 per page) page: 1 2 3 4 5 6 7 ... 94

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs369617851	chr11:50003413-50003414	Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs147181422	chr11:50003428-50003429	Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs374542319	chr11:50003431-50003432	Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs545187798	chr11:50003443-50003444	Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs201564751	chr11:50003448-50003449	Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs377698711	chr11:50003461-50003462	Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs147895623	chr11:50003469-50003470	Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs114706080	chr11:50003508-50003509	Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs371209365	chr11:50003523-50003524	Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs144596966	chr11:50003527-50003528	Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs267602935	chr11:50003581-50003582	Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs568189298	chr11:50003596-50003597	Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs374949660	chr11:50003625-50003626	Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs139887616	chr11:50003627-50003628	Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs377392786	chr11:50003636-50003637	Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs370533796	chr11:50003651-50003652	Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs374549077	chr11:50003736-50003737	Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs368427781	chr11:50003769-50003770	Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs553820430	chr11:50003795-50003796	Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs181521994	chr11:50004233-50004234	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
21	rs61893962	chr11:50005400-50005401	Inactive region	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs569628938	chr11:50005406-50005407	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
23	rs150164676	chr11:50005458-50005459	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
24	rs373586596	chr11:50005921-50005922	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs117539803	chr11:50005939-50005940	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs569858171	chr11:50005947-50005948	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs533897754	chr11:50005962-50005963	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs112828389	chr11:50005983-50005984	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs565705808	chr11:50005991-50005992	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs534405515	chr11:50006058-50006059	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs367763930	chr11:50006063-50006064	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs550690508	chr11:50007290-50007291	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs570145698	chr11:50007325-50007326	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs192864913	chr11:50007334-50007335	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs190262285	chr11:50039211-50039212	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs182395209	chr11:50039237-50039238	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs574678132	chr11:50039258-50039259	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs530988689	chr11:50039279-50039280	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs201831370	chr11:50039358-50039359	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs75388644	chr11:50039359-50039360	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs28411228	chr11:50039363-50039364	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs202163031	chr11:50039365-50039366	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs550798187	chr11:50039370-50039371	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs187394240	chr11:50039406-50039407	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs536550079	chr11:50039458-50039459	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs191724797	chr11:50039463-50039464	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs533900234	chr11:50039491-50039492	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs150370720	chr11:50039505-50039506	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs566288066	chr11:50039513-50039514	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs145024458	chr11:50039531-50039532	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:53)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Autism	22495309	CNVD
Melanoma	20877625	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21785460	CNVD
Esophageal cancer	21851588	CNVD
Acute myeloid leukemia	20729466	CNVD

Chromatin state (count:101 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:50003400-50003800	Active TSS	Brain Substantia Nigra	brain
2	chr11:50039200-50040600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr11:50040600-50049200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr11:50047400-50047600	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr11:50049200-50049600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr11:50049600-50054400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr11:50054400-50058600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr11:50056000-50056400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr11:50057400-50058000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr11:50066200-50067400	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
11	chr11:50100600-50101400	Enhancers	Adipose Nuclei	Adipose
12	chr11:50101400-50103600	Weak transcription	Adipose Nuclei	Adipose
13	chr11:50103200-50103400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr11:50103600-50103800	Enhancers	Adipose Nuclei	Adipose
15	chr11:50103600-50105200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr11:50105200-50106400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr11:50114800-50115200	Enhancers	Adipose Nuclei	Adipose
18	chr11:50129000-50130400	ZNF genes & repeats	Placenta	Placenta
19	chr11:50129400-50129800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr11:50130400-50131000	Active TSS	Placenta	Placenta
21	chr11:50133000-50133200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr11:50133000-50133800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr11:50133200-50133600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr11:50133200-50134200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr11:50133200-50134400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr11:50133200-50134400	Enhancers	Adipose Nuclei	Adipose
27	chr11:50133600-50133800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr11:50133800-50134000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr11:50133800-50134000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr11:50134000-50134400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr11:50134000-50135000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr11:50134200-50134400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr11:50134400-50140400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr11:50134400-50146200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr11:50136600-50136800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
36	chr11:50140400-50142200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr11:50140400-50142600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr11:50141800-50142000	Weak transcription	Adipose Nuclei	Adipose
39	chr11:50142000-50142200	Enhancers	Adipose Nuclei	Adipose
40	chr11:50142200-50144600	Weak transcription	Adipose Nuclei	Adipose
41	chr11:50142200-50145600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr11:50142600-50147000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr11:50144600-50147200	Enhancers	Adipose Nuclei	Adipose
44	chr11:50145600-50146000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr11:50145800-50147400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr11:50146000-50147000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr11:50146200-50147400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr11:50147000-50147400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr11:50147000-50147600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr11:50151800-50152200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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