Variant report

Variant	nsv554396
Chromosome Location	chr11:50057854-50642550
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	ATF1	chr11:50381201-50381204	K562	blood:	n/a	n/a
2	ATF1	chr11:50409411-50409611	K562	blood:	n/a	n/a
3	ATF1	chr11:50257555-50257921	K562	blood:	n/a	n/a
4	ATF3	chr11:50257564-50257818	K562	blood:	n/a	chr11:50257726-50257746 chr11:50257724-50257737 chr11:50257584-50257592 chr11:50257723-50257738 chr11:50257725-50257736
5	BATF	chr11:50251866-50252053	GM12878	blood:	n/a	n/a
6	BHLHE40	chr11:50257408-50257634	K562	blood:	n/a	chr11:50257599-50257615
7	BHLHE40	chr11:50609960-50609990	GM12878	blood:	n/a	n/a
8	BRCA1	chr11:50609964-50609989	GM12878	blood:	n/a	n/a
9	CCNT2	chr11:50134957-50135155	K562	blood:	n/a	n/a
10	CCNT2	chr11:50257299-50257888	K562	blood:	n/a	n/a
11	CEBPB	chr11:50114698-50115007	A549	lung:	n/a	chr11:50114830-50114843 chr11:50114830-50114843 chr11:50114832-50114841 chr11:50114830-50114841 chr11:50114832-50114843
12	CEBPB	chr11:50145990-50146140	HepG2	liver:	n/a	chr11:50146064-50146075
13	CEBPB	chr11:50409463-50409610	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr11:50233638-50233794	HepG2	liver:	n/a	n/a
15	CEBPB	chr11:50105602-50105814	IMR90	lung:	n/a	n/a
16	CEBPB	chr11:50114776-50115008	Hela-S3	cervix:	n/a	chr11:50114830-50114843 chr11:50114830-50114843 chr11:50114832-50114841 chr11:50114830-50114841 chr11:50114832-50114843
17	CEBPB	chr11:50230060-50230405	MCF-7	breast:	n/a	n/a
18	CEBPB	chr11:50132313-50132582	IMR90	lung:	n/a	n/a
19	CEBPB	chr11:50185206-50185319	A549	lung:	n/a	chr11:50185257-50185274 chr11:50185258-50185271 chr11:50185259-50185270 chr11:50185258-50185269
20	CEBPB	chr11:50132343-50132599	HepG2	liver:	n/a	n/a
21	CEBPB	chr11:50256005-50256238	K562	blood:	n/a	chr11:50256104-50256115
22	CEBPB	chr11:50256020-50256220	HepG2	liver:	n/a	chr11:50256104-50256115
23	CEBPB	chr11:50180269-50180536	MCF-7	breast:	n/a	n/a
24	CEBPB	chr11:50182673-50182737	HepG2	liver:	n/a	chr11:50182687-50182698
25	CEBPB	chr11:50114681-50114996	HepG2	liver:	n/a	chr11:50114830-50114843 chr11:50114830-50114843 chr11:50114832-50114841 chr11:50114830-50114841 chr11:50114832-50114843
26	CEBPB	chr11:50202142-50202359	HepG2	liver:	n/a	chr11:50202284-50202295
27	CEBPB	chr11:50114701-50115022	MCF-7	breast:	n/a	chr11:50114830-50114843 chr11:50114830-50114843 chr11:50114832-50114841 chr11:50114830-50114841 chr11:50114832-50114843
28	CEBPB	chr11:50114752-50114922	K562	blood:	n/a	chr11:50114830-50114843 chr11:50114830-50114843 chr11:50114832-50114841 chr11:50114830-50114841 chr11:50114832-50114843
29	CEBPB	chr11:50185114-50185392	HepG2	liver:	n/a	chr11:50185257-50185274 chr11:50185258-50185271 chr11:50185259-50185270 chr11:50185258-50185269
30	CEBPB	chr11:50062165-50062194	HepG2	liver:	n/a	chr11:50062170-50062183 chr11:50062171-50062182 chr11:50062170-50062183
31	CEBPB	chr11:50202172-50202422	IMR90	lung:	n/a	chr11:50202284-50202295
32	CEBPB	chr11:50114658-50114986	IMR90	lung:	n/a	chr11:50114830-50114843 chr11:50114830-50114843 chr11:50114832-50114841 chr11:50114830-50114841 chr11:50114832-50114843
33	CEBPB	chr11:50134957-50135324	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr11:50062636-50062814	HepG2	liver:	n/a	chr11:50062715-50062726
35	CEBPB	chr11:50114607-50115033	MCF-7	breast:	n/a	chr11:50114830-50114843 chr11:50114830-50114843 chr11:50114832-50114841 chr11:50114830-50114841 chr11:50114832-50114843
36	CHD1	chr11:50409410-50409777	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD1	chr11:50382847-50382977	GM12878	blood:	n/a	n/a
38	CHD1	chr11:50134958-50135158	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD1	chr11:50609964-50609986	GM12878	blood:	n/a	n/a
40	CHD2	chr11:50522282-50522663	Hela-S3	cervix:	n/a	n/a
41	CHD2	chr11:50609872-50609989	GM12878	blood:	n/a	n/a
42	CHD2	chr11:50491957-50491986	Hela-S3	cervix:	n/a	n/a
43	CHD2	chr11:50614701-50614706	HepG2	liver:	n/a	n/a
44	CREB1	chr11:50257411-50258094	K562	blood:	n/a	chr11:50257724-50257737
45	CREB1	chr11:50257549-50258023	K562	blood:	n/a	chr11:50257724-50257737
46	CTCF	chr11:50316423-50316519	GM10266	blood:	n/a	n/a
47	CTCF	chr11:50133580-50133730	HCFaa	heart:	n/a	chr11:50133670-50133686 chr11:50133672-50133681 chr11:50133669-50133687
48	CTCF	chr11:50382479-50382654	K562	blood:	n/a	n/a
49	CTCF	chr11:50133600-50133750	AoAF	blood vessel:	n/a	chr11:50133670-50133686 chr11:50133672-50133681 chr11:50133669-50133687
50	CTCF	chr11:50133560-50133710	HepG2	liver:	n/a	chr11:50133670-50133686 chr11:50133672-50133681 chr11:50133669-50133687

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:50219952-50220002	NHBE	bronchial:	n/a
2	chr11:50239550-50239600	BJ	skin:	n/a
3	chr11:50227265-50227315	SK-N-SH	brain:	n/a
4	chr11:50129456-50129506	IMR90	lung:	fetal
5	chr11:50219952-50220002	NHBE	bronchial:	n/a
6	chr11:50239550-50239600	BJ	skin:	n/a
7	chr11:50227265-50227315	SK-N-SH	brain:	n/a
8	chr11:50129456-50129506	IMR90	lung:	fetal
9	chr11:50238214-50238264	T-47D	breast:	n/a
10	chr11:50206530-50206580	HPAEpiC	pulmonary alveolar:	n/a
11	chr11:50371681-50371731	NT2-D1	testis:	n/a
12	chr11:50371681-50371731	AG04449	skin:	fetal
13	chr11:50256574-50256624	HRE	kidney:	n/a
14	chr11:50220343-50220393	NH-A	brain:	n/a
15	chr11:50227079-50227129	Jurkat	blood:	n/a
16	chr11:50257752-50257802	HUVEC	blood vessel:	n/a
17	chr11:50227265-50227315	ECC-1	luminal epithelium:	n/a
18	chr11:50257256-50257306	IMR90	lung:	fetal
19	chr11:50219952-50220002	PFSK-1	brain:	n/a
20	chr11:50257633-50257683	NHDF-neo	bronchial:	n/a
21	chr11:50220426-50220476	ovcar-3	ovarian:	n/a
22	chr11:50258750-50258800	SK-N-MC	brain:	n/a
23	chr11:50206530-50206580	HCPEpiC	choroid plexus:	n/a
24	chr11:50227102-50227152	NH-A	brain:	n/a
25	chr11:50257633-50257683	HRCEpiC	kidney:	n/a
26	chr11:50238214-50238264	NT2-D1	testis:	n/a
27	chr11:50257771-50257821	K562	blood:	n/a
28	chr11:50226789-50226839	HRCEpiC	kidney:	n/a
29	chr11:50227102-50227152	NHDF-neo	bronchial:	n/a
30	chr11:50226789-50226839	HCPEpiC	choroid plexus:	n/a
31	chr11:50226789-50226839	AG04450	lung:	fetal
32	chr11:50231261-50231311	SAEC	small airway:	n/a
33	chr11:50231261-50231311	GM12878	blood:	n/a
34	chr11:50238214-50238264	SK-N-MC	brain:	n/a
35	chr11:50129456-50129506	GM12892	blood:	n/a
36	chr11:50226789-50226839	A549	lung:	n/a
37	chr11:50220107-50220157	NH-A	brain:	n/a
38	chr11:50371681-50371731	SK-N-SH	brain:	n/a
39	chr11:50258273-50258323	NHDF-neo	bronchial:	n/a
40	chr11:50206606-50206656	HIPEpiC	eye:	n/a
41	chr11:50206561-50206611	PANC-1	pancreas:	n/a
42	chr11:50239550-50239600	MCF10A-Er-Src	breast:	n/a
43	chr11:50227265-50227315	MCF-7	breast:	n/a
44	chr11:50227102-50227152	Hepatocyte	liver:	n/a
45	chr11:50226789-50226839	AG04449	skin:	fetal
46	chr11:50254503-50254553	HCM	heart:	n/a
47	chr11:50227265-50227315	ovcar-3	ovarian:	n/a
48	chr11:50254503-50254553	MCF10A-Er-Src	breast:	n/a
49	chr11:50129456-50129506	PrEC	prostate:	n/a
50	chr11:50257830-50257880	BE2_C	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:50172306..50174473-chr11:50176469..50178865,2	K562	blood:
2	chr11:50172306..50174473-chr11:50176469..50178865,2	K562	blood:
3	chr11:50256839..50259422-chr11:50261676..50263683,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR4C13-7	chr11:50302810-50302996	NONHSAT021339
2	lnc-OR4C13-9	chr11:50376439-50376850	NONHSAT021344
3	lnc-OR4C13-9	chr11:50375274-50375391	NR_024504
4	lnc-OR4C13-7	chr11:50313156-50313246	NONHSAT021340
5	lnc-OR4C13-9	chr11:50379313-50379548	NR_024504
6	lnc-OR4C13-9	chr11:50379775-50379803	NONHSAT021345
7	lnc-OR4C13-1	chr11:50257789-50258088	ENSG00000254518
8	lnc-OR4C13-7	chr11:50302810-50303098	NONHSAT021342
9	lnc-OR4C13-9	chr11:50376439-50376850	NONHSAT021345
10	lnc-OR4C13-7	chr11:50301079-50301142	NONHSAT021343
11	lnc-OR4C12-2	chr11:50060063-50060146	NONHSAT021327
12	lnc-OR4C13-9	chr11:50375235-50375391	NONHSAT021345
13	lnc-OR4C13-7	chr11:50266792-50266965	NONHSAT021338
14	lnc-OR4C13-7	chr11:50280085-50280169	NONHSAT021339
15	lnc-OR4C13-9	chr11:50368318-50368359	NONHSAT021344
16	lnc-OR4C13-9	chr11:50379775-50379802	NR_024504
17	lnc-OR4C13-7	chr11:50274586-50274767	NONHSAT021339
18	lnc-OR4C13-7	chr11:50279839-50280169	NONHSAT021342
19	lnc-OR4C13-7	chr11:50279538-50279677	NONHSAT021339
20	lnc-OR4C13-7	chr11:50320710-50320877	NONHSAT021340
21	lnc-OR4C13-1	chr11:50263752-50263827	ENSG00000254518
22	lnc-OR4C13-7	chr11:50280085-50280169	NONHSAT021340
23	lnc-OR4C13-1	chr11:50262310-50262433	ENSG00000254518
24	lnc-OR4C13-9	chr11:50368318-50368359	NR_024504
25	lnc-OR4C13-9	chr11:50378065-50378165	NONHSAT021344
26	lnc-OR4C13-9	chr11:50378065-50378165	NONHSAT021345
27	lnc-OR4C13-7	chr11:50320143-50320239	NONHSAT021340
28	lnc-OR4C13-7	chr11:50279538-50279677	NONHSAT021340
29	lnc-OR4C13-9	chr11:50378065-50378165	NR_024504
30	lnc-OR4C12-2	chr11:50060551-50060604	NONHSAT021327
31	lnc-OR4C13-7	chr11:50302810-50303035	NONHSAT021343
32	lnc-OR4C13-1	chr11:50257750-50258088	ENSG00000254518
33	lnc-OR4C13-9	chr11:50379313-50379802	NONHSAT021344
34	lnc-OR4C13-7	chr11:50301870-50302020	NONHSAT021343
35	lnc-OR4C13-1	chr11:50261115-50261299	NONHSAT021336
36	lnc-OR4C13-9	chr11:50375235-50375391	NONHSAT021344
37	lnc-OR4C13-1	chr11:50261115-50261299	ENSG00000254518
38	lnc-OR4C13-7	chr11:50274586-50274767	NONHSAT021340
39	lnc-OR4C13-1	chr11:50262310-50262433	NONHSAT021336
40	lnc-OR4C12-2	chr11:50061788-50062069	NONHSAT021327
41	lnc-OR4C13-1	chr11:50257750-50258210	NONHSAT021336
42	lnc-OR4C13-7	chr11:50266852-50266898	NONHSAT021340
43	lnc-OR4C13-7	chr11:50274586-50274778	NONHSAT021338
44	lnc-OR4C12-1	chr11:50231598-50231759	XLOC_009440
45	lnc-OR4C13-9	chr11:50368739-50368821	NR_024504
46	lnc-OR4C13-9	chr11:50368739-50368821	NONHSAT021344
47	lnc-OR4C12-1	chr11:50232840-50233106	XLOC_009440
48	lnc-OR4C13-7	chr11:50266792-50266898	NONHSAT021339
49	lnc-OR4C13-9	chr11:50379313-50379548	NONHSAT021345
50	lnc-OR4C13-1	chr11:50263752-50263827	NONHSAT021336

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
ENSG00000214883	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
ENSG00000214883	CpG island
ENSG00000254518	chromatin interactions

Extended variants
information (count: 20445 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:20445 , 50 per page) page: 1 2 3 4 5 6 7 ... 409

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11245582	chr11:50057854-50057855	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs140407596	chr11:50057861-50057862	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs540667571	chr11:50057901-50057902	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs73472886	chr11:50057903-50057904	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs147005638	chr11:50057906-50057907	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs374580057	chr11:50057934-50057935	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs540662389	chr11:50057971-50057972	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs186086399	chr11:50058021-50058022	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs115309351	chr11:50058051-50058052	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs191200917	chr11:50058064-50058065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs138129510	chr11:50058087-50058088	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs1874474	chr11:50058095-50058096	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs537519541	chr11:50058131-50058132	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs369419070	chr11:50058156-50058157	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs554261532	chr11:50058182-50058183	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs183253165	chr11:50058219-50058220	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs542815227	chr11:50058227-50058228	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs78506321	chr11:50058232-50058233	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs554947883	chr11:50058255-50058256	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs200161139	chr11:50058273-50058274	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs559991161	chr11:50058287-50058288	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs200733041	chr11:50058297-50058298	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs574916510	chr11:50058304-50058305	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs573498005	chr11:50058306-50058307	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs375168732	chr11:50058307-50058308	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs545371226	chr11:50058329-50058330	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs565161215	chr11:50058354-50058355	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs530948247	chr11:50058388-50058389	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs201539422	chr11:50058390-50058391	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs185976605	chr11:50058391-50058392	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs561372795	chr11:50058392-50058393	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs75503204	chr11:50058400-50058401	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs529914450	chr11:50058403-50058404	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs372112052	chr11:50058429-50058430	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs546520303	chr11:50058434-50058435	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs540879382	chr11:50058488-50058489	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs566746089	chr11:50058497-50058498	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs145871175	chr11:50058509-50058510	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs552467132	chr11:50058599-50058600	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs541685747	chr11:50060076-50060077	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
41	rs561657686	chr11:50060080-50060081	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
42	rs146386109	chr11:50060085-50060086	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
43	rs547414502	chr11:50060115-50060116	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
44	rs564011539	chr11:50060123-50060124	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
45	rs181994002	chr11:50060134-50060135	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
46	rs185909887	chr11:50060570-50060571	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
47	rs566547056	chr11:50061819-50061820	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
48	rs193094421	chr11:50061832-50061833	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
49	rs374035443	chr11:50061855-50061856	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
50	rs553028925	chr11:50061918-50061919	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

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
Breast cancer	17142309	CNVD
Bipolar disorder	19214233	CNVD
Medulloblastoma	21163964	CNVD
early-passage human iPS cells	21368824	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:330 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:50054400-50058600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr11:50057400-50058000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr11:50066200-50067400	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
4	chr11:50100600-50101400	Enhancers	Adipose Nuclei	Adipose
5	chr11:50101400-50103600	Weak transcription	Adipose Nuclei	Adipose
6	chr11:50103200-50103400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr11:50103600-50103800	Enhancers	Adipose Nuclei	Adipose
8	chr11:50103600-50105200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr11:50105200-50106400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr11:50114800-50115200	Enhancers	Adipose Nuclei	Adipose
11	chr11:50129000-50130400	ZNF genes & repeats	Placenta	Placenta
12	chr11:50129400-50129800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr11:50130400-50131000	Active TSS	Placenta	Placenta
14	chr11:50133000-50133200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr11:50133000-50133800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr11:50133200-50133600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr11:50133200-50134200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr11:50133200-50134400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr11:50133200-50134400	Enhancers	Adipose Nuclei	Adipose
20	chr11:50133600-50133800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr11:50133800-50134000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr11:50133800-50134000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr11:50134000-50134400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr11:50134000-50135000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr11:50134200-50134400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr11:50134400-50140400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr11:50134400-50146200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr11:50136600-50136800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
29	chr11:50140400-50142200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr11:50140400-50142600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr11:50141800-50142000	Weak transcription	Adipose Nuclei	Adipose
32	chr11:50142000-50142200	Enhancers	Adipose Nuclei	Adipose
33	chr11:50142200-50144600	Weak transcription	Adipose Nuclei	Adipose
34	chr11:50142200-50145600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr11:50142600-50147000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr11:50144600-50147200	Enhancers	Adipose Nuclei	Adipose
37	chr11:50145600-50146000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr11:50145800-50147400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr11:50146000-50147000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr11:50146200-50147400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr11:50147000-50147400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr11:50147000-50147600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr11:50151800-50152200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr11:50155000-50155200	Active TSS	HMEC	breast
45	chr11:50155000-50155200	Enhancers	HSMMtube	muscle
46	chr11:50155000-50155200	Enhancers	NH-A	brain
47	chr11:50188200-50189000	Enhancers	Adipose Nuclei	Adipose
48	chr11:50191600-50191800	ZNF genes & repeats	Right Atrium	heart
49	chr11:50191800-50194400	Weak transcription	Right Atrium	heart
50	chr11:50192600-50195800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell

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