Variant report

Variant	esv2759827
Chromosome Location	chr11:50056424-50449192
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	chr11:50257555-50257921	K562	blood:	n/a	n/a
2	ATF1	chr11:50409411-50409611	K562	blood:	n/a	n/a
3	ATF1	chr11:50381201-50381204	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	CCNT2	chr11:50257299-50257888	K562	blood:	n/a	n/a
8	CCNT2	chr11:50134957-50135155	K562	blood:	n/a	n/a
9	CEBPB	chr11:50202172-50202422	IMR90	lung:	n/a	chr11:50202284-50202295
10	CEBPB	chr11:50114752-50114922	K562	blood:	n/a	chr11:50114830-50114843 chr11:50114830-50114843 chr11:50114832-50114841 chr11:50114830-50114841 chr11:50114832-50114843
11	CEBPB	chr11:50202142-50202359	HepG2	liver:	n/a	chr11:50202284-50202295
12	CEBPB	chr11:50230060-50230405	MCF-7	breast:	n/a	n/a
13	CEBPB	chr11:50233638-50233794	HepG2	liver:	n/a	n/a
14	CEBPB	chr11:50256020-50256220	HepG2	liver:	n/a	chr11:50256104-50256115
15	CEBPB	chr11:50062636-50062814	HepG2	liver:	n/a	chr11:50062715-50062726
16	CEBPB	chr11:50180269-50180536	MCF-7	breast:	n/a	n/a
17	CEBPB	chr11:50185114-50185392	HepG2	liver:	n/a	chr11:50185257-50185274 chr11:50185258-50185271 chr11:50185259-50185270 chr11:50185258-50185269
18	CEBPB	chr11:50132313-50132582	IMR90	lung:	n/a	n/a
19	CEBPB	chr11:50134957-50135324	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr11:50182673-50182737	HepG2	liver:	n/a	chr11:50182687-50182698
21	CEBPB	chr11:50256005-50256238	K562	blood:	n/a	chr11:50256104-50256115
22	CEBPB	chr11:50409463-50409610	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr11:50185206-50185319	A549	lung:	n/a	chr11:50185257-50185274 chr11:50185258-50185271 chr11:50185259-50185270 chr11:50185258-50185269
24	CEBPB	chr11:50114607-50115033	MCF-7	breast:	n/a	chr11:50114830-50114843 chr11:50114830-50114843 chr11:50114832-50114841 chr11:50114830-50114841 chr11:50114832-50114843
25	CEBPB	chr11:50062165-50062194	HepG2	liver:	n/a	chr11:50062170-50062183 chr11:50062171-50062182 chr11:50062170-50062183
26	CEBPB	chr11:50145990-50146140	HepG2	liver:	n/a	chr11:50146064-50146075
27	CEBPB	chr11:50114658-50114986	IMR90	lung:	n/a	chr11:50114830-50114843 chr11:50114830-50114843 chr11:50114832-50114841 chr11:50114830-50114841 chr11:50114832-50114843
28	CEBPB	chr11:50132343-50132599	HepG2	liver:	n/a	n/a
29	CEBPB	chr11:50114681-50114996	HepG2	liver:	n/a	chr11:50114830-50114843 chr11:50114830-50114843 chr11:50114832-50114841 chr11:50114830-50114841 chr11:50114832-50114843
30	CEBPB	chr11:50114698-50115007	A549	lung:	n/a	chr11:50114830-50114843 chr11:50114830-50114843 chr11:50114832-50114841 chr11:50114830-50114841 chr11:50114832-50114843
31	CEBPB	chr11:50114701-50115022	MCF-7	breast:	n/a	chr11:50114830-50114843 chr11:50114830-50114843 chr11:50114832-50114841 chr11:50114830-50114841 chr11:50114832-50114843
32	CEBPB	chr11:50105602-50105814	IMR90	lung:	n/a	n/a
33	CEBPB	chr11:50114776-50115008	Hela-S3	cervix:	n/a	chr11:50114830-50114843 chr11:50114830-50114843 chr11:50114832-50114841 chr11:50114830-50114841 chr11:50114832-50114843
34	CHD1	chr11:50382847-50382977	GM12878	blood:	n/a	n/a
35	CHD1	chr11:50409410-50409777	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD1	chr11:50134958-50135158	H1-hESC	embryonic stem cell:	n/a	n/a
37	CREB1	chr11:50257549-50258023	K562	blood:	n/a	chr11:50257724-50257737
38	CREB1	chr11:50257411-50258094	K562	blood:	n/a	chr11:50257724-50257737
39	CTCF	chr11:50133500-50133650	HMF	breast:	n/a	n/a
40	CTCF	chr11:50133600-50133750	GM06990	blood:	n/a	chr11:50133670-50133686 chr11:50133672-50133681 chr11:50133669-50133687
41	CTCF	chr11:50089327-50089361	Medullo	brain:	n/a	n/a
42	CTCF	chr11:50133560-50133710	HepG2	liver:	n/a	chr11:50133670-50133686 chr11:50133672-50133681 chr11:50133669-50133687
43	CTCF	chr11:50133520-50133670	NHEK	skin:	n/a	n/a
44	CTCF	chr11:50133628-50133712	HepG2	liver:	n/a	chr11:50133670-50133686 chr11:50133672-50133681 chr11:50133669-50133687
45	CTCF	chr11:50133680-50133830	A549	lung:	n/a	n/a
46	CTCF	chr11:50133560-50133710	AG10803	skin:	n/a	chr11:50133670-50133686 chr11:50133672-50133681 chr11:50133669-50133687
47	CTCF	chr11:50291325-50291378	LNCaP	prostate:	n/a	n/a
48	CTCF	chr11:50248936-50248972	Spleen_OC	spleen:	n/a	n/a
49	CTCF	chr11:50133600-50133750	HPAF	blood vessel:	n/a	chr11:50133670-50133686 chr11:50133672-50133681 chr11:50133669-50133687
50	CTCF	chr11:50133599-50133728	LNCaP	prostate:	n/a	chr11:50133670-50133686 chr11:50133672-50133681 chr11:50133669-50133687

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:50260762-50260812	SK-N-SH	brain:	n/a
2	chr11:50257771-50257821	HRCEpiC	kidney:	n/a
3	chr11:50220343-50220393	A549	lung:	n/a
4	chr11:50258750-50258800	MCF-7	breast:	n/a
5	chr11:50234973-50235023	MCF-7	breast:	n/a
6	chr11:50257830-50257880	HMEC	breast:	n/a
7	chr11:50260762-50260812	SK-N-SH	brain:	n/a
8	chr11:50257771-50257821	HRCEpiC	kidney:	n/a
9	chr11:50220343-50220393	A549	lung:	n/a
10	chr11:50258750-50258800	MCF-7	breast:	n/a
11	chr11:50234973-50235023	MCF-7	breast:	n/a
12	chr11:50257830-50257880	HMEC	breast:	n/a
13	chr11:50220107-50220157	SK-N-MC	brain:	n/a
14	chr11:50371681-50371731	HPAEpiC	pulmonary alveolar:	n/a
15	chr11:50257771-50257821	HIPEpiC	eye:	n/a
16	chr11:50257256-50257306	Jurkat	blood:	n/a
17	chr11:50227199-50227249	GM12878	blood:	n/a
18	chr11:50220107-50220157	PFSK-1	brain:	n/a
19	chr11:50257625-50257675	NHBE	bronchial:	n/a
20	chr11:50231261-50231311	NHBE	bronchial:	n/a
21	chr11:50241016-50241066	GM12891	blood:	n/a
22	chr11:50227265-50227315	HEEpiC	esophagus:	n/a
23	chr11:50206561-50206611	HCPEpiC	choroid plexus:	n/a
24	chr11:50227199-50227249	SK-N-SH_RA	brain:	n/a
25	chr11:50257752-50257802	GM12892	blood:	n/a
26	chr11:50257771-50257821	ProgFib	skin:	n/a
27	chr11:50260762-50260812	HEK293	kidney:	embryo
28	chr11:50220389-50220439	SK-N-MC	brain:	n/a
29	chr11:50227265-50227315	BE2_C	brain:	n/a
30	chr11:50220343-50220393	HNPCEpiC	eye:	n/a
31	chr11:50260762-50260812	Hela-S3	cervix:	n/a
32	chr11:50206606-50206656	HMEC	breast:	n/a
33	chr11:50220389-50220439	HUVEC	blood vessel:	n/a
34	chr11:50220055-50220105	NB4	blood:	n/a
35	chr11:50220343-50220393	SKMC	muscle:	n/a
36	chr11:50257830-50257880	MCF-7	breast:	n/a
37	chr11:50238214-50238264	HMEC	breast:	n/a
38	chr11:50220107-50220157	ProgFib	skin:	n/a
39	chr11:50129456-50129506	ProgFib	skin:	n/a
40	chr11:50129456-50129506	AG10803	skin:	n/a
41	chr11:50254503-50254553	AG04449	skin:	fetal
42	chr11:50257752-50257802	PrEC	prostate:	n/a
43	chr11:50231261-50231311	AG04450	lung:	fetal
44	chr11:50227102-50227152	HepG2	liver:	n/a
45	chr11:50238214-50238264	SKMC	muscle:	n/a
46	chr11:50257752-50257802	T-47D	breast:	n/a
47	chr11:50238107-50238157	SK-N-SH	brain:	n/a
48	chr11:50257633-50257683	HPAEpiC	pulmonary alveolar:	n/a
49	chr11:50206606-50206656	RPTEC	kidney:	n/a
50	chr11:50220343-50220393	AoSMC	blood vessel:	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	chr11:50266852-50266898	NONHSAT021340
2	lnc-OR4C13-7	chr11:50266792-50266965	NONHSAT021338
3	lnc-OR4C13-7	chr11:50266792-50266898	NONHSAT021339
4	lnc-OR4C13-9	chr11:50379775-50379802	NR_024504
5	lnc-OR4C13-9	chr11:50378065-50378165	NR_024504
6	lnc-OR4C13-9	chr11:50378065-50378165	NONHSAT021344
7	lnc-OR4C13-1	chr11:50263752-50263827	NONHSAT021336
8	lnc-OR4C12-2	chr11:50060063-50060146	NONHSAT021327
9	lnc-OR4C13-7	chr11:50274586-50274767	NONHSAT021340
10	lnc-OR4C13-1	chr11:50263752-50263827	ENSG00000254518
11	lnc-OR4C12-2	chr11:50060551-50060604	NONHSAT021327
12	lnc-OR4C13-7	chr11:50274586-50274778	NONHSAT021338
13	lnc-OR4C13-9	chr11:50379313-50379548	NR_024504
14	lnc-OR4C13-1	chr11:50261115-50261299	ENSG00000254518
15	lnc-OR4C13-9	chr11:50378065-50378165	NONHSAT021345
16	lnc-OR4C13-1	chr11:50257750-50258088	ENSG00000254518
17	lnc-OR4C13-9	chr11:50379313-50379548	NONHSAT021345
18	lnc-OR4C13-9	chr11:50375235-50375391	NONHSAT021344
19	lnc-OR4C13-1	chr11:50257750-50258210	NONHSAT021336
20	lnc-OR4C13-9	chr11:50375235-50375391	NONHSAT021345
21	lnc-OR4C13-9	chr11:50375274-50375391	NR_024504
22	lnc-OR4C13-9	chr11:50368739-50368821	NONHSAT021344
23	lnc-OR4C13-7	chr11:50279538-50279677	NONHSAT021340
24	lnc-OR4C13-7	chr11:50280085-50280169	NONHSAT021339
25	lnc-OR4C13-7	chr11:50320143-50320239	NONHSAT021340
26	lnc-OR4C13-1	chr11:50261115-50261299	NONHSAT021336
27	lnc-OR4C13-1	chr11:50262310-50262433	NONHSAT021336
28	lnc-OR4C13-7	chr11:50302810-50303035	NONHSAT021343
29	lnc-OR4C13-7	chr11:50320710-50320877	NONHSAT021340
30	lnc-OR4C12-2	chr11:50061788-50062069	NONHSAT021327
31	lnc-OR4C13-9	chr11:50368318-50368359	NR_024504
32	lnc-OR4C13-9	chr11:50368739-50368821	NR_024504
33	lnc-OR4C13-7	chr11:50313156-50313246	NONHSAT021340
34	lnc-OR4C13-7	chr11:50301079-50301142	NONHSAT021343
35	lnc-OR4C13-7	chr11:50301870-50302020	NONHSAT021343
36	lnc-OR4C13-7	chr11:50279538-50279677	NONHSAT021339
37	lnc-OR4C13-1	chr11:50257789-50258088	ENSG00000254518
38	lnc-OR4C13-7	chr11:50302810-50303098	NONHSAT021342
39	lnc-OR4C13-7	chr11:50274586-50274767	NONHSAT021339
40	lnc-OR4C13-7	chr11:50280085-50280169	NONHSAT021340
41	lnc-OR4C13-7	chr11:50302810-50302996	NONHSAT021339
42	lnc-OR4C12-1	chr11:50232840-50233106	XLOC_009440
43	lnc-OR4C13-7	chr11:50279839-50280169	NONHSAT021342
44	lnc-OR4C13-9	chr11:50379313-50379802	NONHSAT021344
45	lnc-OR4C13-1	chr11:50262310-50262433	ENSG00000254518
46	lnc-OR4C13-9	chr11:50368318-50368359	NONHSAT021344
47	lnc-OR4C12-1	chr11:50231598-50231759	XLOC_009440
48	lnc-OR4C13-9	chr11:50376439-50376850	NONHSAT021344
49	lnc-OR4C13-9	chr11:50376439-50376850	NONHSAT021345
50	lnc-OR4C13-9	chr11:50379775-50379803	NONHSAT021345

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: 9937 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:9937 , 50 per page) page: 1 2 3 4 5 6 7 ... 199

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs557306459	chr11:50056456-50056457	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs573637885	chr11:50056468-50056469	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs541781146	chr11:50056472-50056473	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs372864458	chr11:50056473-50056474	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs559487210	chr11:50056559-50056560	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs528227773	chr11:50056577-50056578	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs541248067	chr11:50056604-50056605	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs564729077	chr11:50056610-50056611	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs533378373	chr11:50056715-50056716	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs143880923	chr11:50056716-50056717	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs146858526	chr11:50056739-50056740	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs540779411	chr11:50056763-50056764	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs1390676	chr11:50056778-50056779	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs549007447	chr11:50056789-50056790	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs565821422	chr11:50056796-50056797	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs377523719	chr11:50056802-50056803	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs3028502	chr11:50056803-50056804	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs535149070	chr11:50056814-50056815	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs79456307	chr11:50056853-50056854	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs571992317	chr11:50056944-50056945	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs369651987	chr11:50056950-50056951	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs79484193	chr11:50056974-50056975	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs184251558	chr11:50056978-50056979	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs114541779	chr11:50057012-50057013	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs140647707	chr11:50057017-50057018	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs113174728	chr11:50057031-50057032	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs372830038	chr11:50057056-50057057	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs189500298	chr11:50057074-50057075	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs192450591	chr11:50057079-50057080	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs572827346	chr11:50057098-50057099	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs137859041	chr11:50057150-50057151	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs375366762	chr11:50057151-50057152	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs59769741	chr11:50057155-50057156	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs115331491	chr11:50057172-50057173	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs376042586	chr11:50057184-50057185	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs528850846	chr11:50057280-50057281	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs564839901	chr11:50057285-50057286	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs548688601	chr11:50057289-50057290	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs543658378	chr11:50057309-50057310	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs12804225	chr11:50057326-50057327	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs58486096	chr11:50057336-50057337	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs566037816	chr11:50057339-50057340	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs112225166	chr11:50057368-50057369	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs149140952	chr11:50057391-50057392	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs377378525	chr11:50057402-50057403	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs183644597	chr11:50057415-50057416	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs12803798	chr11:50057456-50057457	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs143259205	chr11:50057474-50057475	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs370505786	chr11:50057476-50057477	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs537240131	chr11:50057543-50057544	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

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

Chromatin state (count:197 , 50 per page) page: 1 2 3 4

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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