Variant report

Variant	nsv554395
Chromosome Location	chr11:50008258-50642550
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1151)
CpG islands
(count:2381)
Chromatin interactive
region (count:4)
LncRNA
region (count:50)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1151 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

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	chr11:50409411-50409611	K562	blood:	n/a	n/a
3	ATF1	chr11:50381201-50381204	K562	blood:	n/a	n/a
4	ATF1	chr11:50257555-50257921	K562	blood:	n/a	n/a
5	ATF3	chr11:50257564-50257818	K562	blood:	n/a	chr11:50257726-50257746 chr11:50257724-50257737 chr11:50257584-50257592 chr11:50257723-50257738 chr11:50257725-50257736
6	BATF	chr11:50251866-50252053	GM12878	blood:	n/a	n/a
7	BHLHE40	chr11:50609960-50609990	GM12878	blood:	n/a	n/a
8	BHLHE40	chr11:50017239-50017377	K562	blood:	n/a	n/a
9	BHLHE40	chr11:50257408-50257634	K562	blood:	n/a	chr11:50257599-50257615
10	BRCA1	chr11:50609964-50609989	GM12878	blood:	n/a	n/a
11	CBX3	chr11:50017158-50017392	K562	blood:	n/a	n/a
12	CBX3	chr11:50017099-50017442	K562	blood:	n/a	n/a
13	CCNT2	chr11:50134957-50135155	K562	blood:	n/a	n/a
14	CCNT2	chr11:50257299-50257888	K562	blood:	n/a	n/a
15	CEBPB	chr11:50114607-50115033	MCF-7	breast:	n/a	chr11:50114830-50114843 chr11:50114830-50114843 chr11:50114832-50114841 chr11:50114830-50114841 chr11:50114832-50114843
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	chr11:50132343-50132599	HepG2	liver:	n/a	n/a
18	CEBPB	chr11:50202172-50202422	IMR90	lung:	n/a	chr11:50202284-50202295
19	CEBPB	chr11:50105602-50105814	IMR90	lung:	n/a	n/a
20	CEBPB	chr11:50114681-50114996	HepG2	liver:	n/a	chr11:50114830-50114843 chr11:50114830-50114843 chr11:50114832-50114841 chr11:50114830-50114841 chr11:50114832-50114843
21	CEBPB	chr11:50230060-50230405	MCF-7	breast:	n/a	n/a
22	CEBPB	chr11:50182673-50182737	HepG2	liver:	n/a	chr11:50182687-50182698
23	CEBPB	chr11:50134957-50135324	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr11:50062165-50062194	HepG2	liver:	n/a	chr11:50062170-50062183 chr11:50062171-50062182 chr11:50062170-50062183
25	CEBPB	chr11:50256020-50256220	HepG2	liver:	n/a	chr11:50256104-50256115
26	CEBPB	chr11:50185206-50185319	A549	lung:	n/a	chr11:50185257-50185274 chr11:50185258-50185271 chr11:50185259-50185270 chr11:50185258-50185269
27	CEBPB	chr11:50202142-50202359	HepG2	liver:	n/a	chr11:50202284-50202295
28	CEBPB	chr11:50062636-50062814	HepG2	liver:	n/a	chr11:50062715-50062726
29	CEBPB	chr11:50132313-50132582	IMR90	lung:	n/a	n/a
30	CEBPB	chr11:50056041-50056226	HepG2	liver:	n/a	chr11:50056106-50056117
31	CEBPB	chr11:50180269-50180536	MCF-7	breast:	n/a	n/a
32	CEBPB	chr11:50185114-50185392	HepG2	liver:	n/a	chr11:50185257-50185274 chr11:50185258-50185271 chr11:50185259-50185270 chr11:50185258-50185269
33	CEBPB	chr11:50256005-50256238	K562	blood:	n/a	chr11:50256104-50256115
34	CEBPB	chr11:50114701-50115022	MCF-7	breast:	n/a	chr11:50114830-50114843 chr11:50114830-50114843 chr11:50114832-50114841 chr11:50114830-50114841 chr11:50114832-50114843
35	CEBPB	chr11:50145990-50146140	HepG2	liver:	n/a	chr11:50146064-50146075
36	CEBPB	chr11:50409463-50409610	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr11:50233638-50233794	HepG2	liver:	n/a	n/a
38	CEBPB	chr11:50114752-50114922	K562	blood:	n/a	chr11:50114830-50114843 chr11:50114830-50114843 chr11:50114832-50114841 chr11:50114830-50114841 chr11:50114832-50114843
39	CEBPB	chr11:50114658-50114986	IMR90	lung:	n/a	chr11:50114830-50114843 chr11:50114830-50114843 chr11:50114832-50114841 chr11:50114830-50114841 chr11:50114832-50114843
40	CEBPB	chr11:50114698-50115007	A549	lung:	n/a	chr11:50114830-50114843 chr11:50114830-50114843 chr11:50114832-50114841 chr11:50114830-50114841 chr11:50114832-50114843
41	CEBPB	chr11:50047487-50047664	A549	lung:	n/a	n/a
42	CHD1	chr11:50409410-50409777	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD1	chr11:50382847-50382977	GM12878	blood:	n/a	n/a
44	CHD1	chr11:50609964-50609986	GM12878	blood:	n/a	n/a
45	CHD1	chr11:50134958-50135158	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD2	chr11:50522282-50522663	Hela-S3	cervix:	n/a	n/a
47	CHD2	chr11:50614701-50614706	HepG2	liver:	n/a	n/a
48	CHD2	chr11:50491957-50491986	Hela-S3	cervix:	n/a	n/a
49	CHD2	chr11:50609872-50609989	GM12878	blood:	n/a	n/a
50	CHD2	chr11:50017167-50017356	K562	blood:	n/a	n/a

(count:2381 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:50257625-50257675	GM19239	blood:	n/a
2	chr11:50227265-50227315	Caco-2	colon:	n/a
3	chr11:50257625-50257675	GM19239	blood:	n/a
4	chr11:50227265-50227315	Caco-2	colon:	n/a
5	chr11:50236153-50236203	GM12878	blood:	n/a
6	chr11:50219952-50220002	NB4	blood:	n/a
7	chr11:50220343-50220393	ProgFib	skin:	n/a
8	chr11:50219952-50220002	RPTEC	kidney:	n/a
9	chr11:50260762-50260812	HCF	heart:	n/a
10	chr11:50206530-50206580	MCF-7	breast:	n/a
11	chr11:50220055-50220105	HNPCEpiC	eye:	n/a
12	chr11:50239550-50239600	NB4	blood:	n/a
13	chr11:50220343-50220393	PANC-1	pancreas:	n/a
14	chr11:50257633-50257683	NB4	blood:	n/a
15	chr11:50254503-50254553	HAEpiC	amniotic membrane:	n/a
16	chr11:50219952-50220002	AG09319	gingival:	n/a
17	chr11:50257496-50257546	MCF-7	breast:	n/a
18	chr11:50220343-50220393	SAEC	small airway:	n/a
19	chr11:50227476-50227526	ProgFib	skin:	n/a
20	chr11:50227265-50227315	SK-N-SH_RA	brain:	n/a
21	chr11:50238009-50238059	HIPEpiC	eye:	n/a
22	chr11:50227265-50227315	SK-N-SH	brain:	n/a
23	chr11:50257496-50257546	U87	brain:	n/a
24	chr11:50371681-50371731	MCF-7	breast:	n/a
25	chr11:50239550-50239600	ProgFib	skin:	n/a
26	chr11:50234973-50235023	AG04449	skin:	fetal
27	chr11:50226789-50226839	HRE	kidney:	n/a
28	chr11:50231261-50231311	GM12891	blood:	n/a
29	chr11:50257752-50257802	AoSMC	blood vessel:	n/a
30	chr11:50256574-50256624	NB4	blood:	n/a
31	chr11:50238107-50238157	ProgFib	skin:	n/a
32	chr11:50257752-50257802	A549	lung:	n/a
33	chr11:50239550-50239600	ECC-1	luminal epithelium:	n/a
34	chr11:50227199-50227249	NHDF-neo	bronchial:	n/a
35	chr11:50220426-50220476	SK-N-SH	brain:	n/a
36	chr11:50206606-50206656	HRPEpiC	eye:	n/a
37	chr11:50227476-50227526	HRE	kidney:	n/a
38	chr11:50257256-50257306	CMK	blood:	n/a
39	chr11:50227199-50227249	PFSK-1	brain:	n/a
40	chr11:50257771-50257821	LNCaP	prostate:	n/a
41	chr11:50368251-50368301	SK-N-SH_RA	brain:	n/a
42	chr11:50236153-50236203	NB4	blood:	n/a
43	chr11:50258750-50258800	BE2_C	brain:	n/a
44	chr11:50220389-50220439	HIPEpiC	eye:	n/a
45	chr11:50227102-50227152	RPTEC	kidney:	n/a
46	chr11:50227199-50227249	NH-A	brain:	n/a
47	chr11:50257752-50257802	PANC-1	pancreas:	n/a
48	chr11:50257752-50257802	SK-N-MC	brain:	n/a
49	chr11:50258750-50258800	NHDF-neo	bronchial:	n/a
50	chr11:50206561-50206611	ProgFib	skin:	n/a

(count:4 , 50 per page) page: 1

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

(count:50 , 50 per page) page: 1

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

No data

Variant related genes	Relation type
ENSG00000255500	TF binding region
ENSG00000254840	TF binding region
ENSG00000255199	TF binding region
ENSG00000255001	TF binding region
ENSG00000255442	TF binding region
ENSG00000254518	TF binding region
ENSG00000255042	TF binding region
OR4C12	TF binding region
ENSG00000236919	TF binding region
ENSG00000214883	TF binding region
ENSG00000255500	CpG island
ENSG00000254840	CpG island
ENSG00000255199	CpG island
ENSG00000255001	CpG island
ENSG00000255442	CpG island
ENSG00000254518	CpG island
ENSG00000255042	CpG island
OR4C12	CpG island
ENSG00000236919	CpG island
ENSG00000214883	CpG island
ENSG00000254518	chromatin interactions

Extended variants
information (count: 21419 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:21419 , 50 per page) page: 1 2 3 4 5 6 7 ... 429

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190262285	chr11:50039211-50039212	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs182395209	chr11:50039237-50039238	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs574678132	chr11:50039258-50039259	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs530988689	chr11:50039279-50039280	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs201831370	chr11:50039358-50039359	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs75388644	chr11:50039359-50039360	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs28411228	chr11:50039363-50039364	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs202163031	chr11:50039365-50039366	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs550798187	chr11:50039370-50039371	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs187394240	chr11:50039406-50039407	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs536550079	chr11:50039458-50039459	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs191724797	chr11:50039463-50039464	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs533900234	chr11:50039491-50039492	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs150370720	chr11:50039505-50039506	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs566288066	chr11:50039513-50039514	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs145024458	chr11:50039531-50039532	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs149076744	chr11:50039534-50039535	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs113087310	chr11:50039540-50039541	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs372280135	chr11:50039586-50039587	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs375111677	chr11:50039605-50039606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs183956652	chr11:50039623-50039624	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs574740277	chr11:50039669-50039670	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs371587437	chr11:50039704-50039705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs144696986	chr11:50039710-50039711	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs558073432	chr11:50039744-50039745	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs554199140	chr11:50039774-50039775	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs28560250	chr11:50039796-50039797	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs138555056	chr11:50039811-50039812	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs28430465	chr11:50039832-50039833	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs189205635	chr11:50039886-50039887	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs374841346	chr11:50039916-50039917	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs141540656	chr11:50039945-50039946	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs117728889	chr11:50040018-50040019	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs561155459	chr11:50040019-50040020	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs557463314	chr11:50040034-50040035	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs376614794	chr11:50040041-50040042	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs530291992	chr11:50040047-50040048	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs547000293	chr11:50040060-50040061	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs567180552	chr11:50040082-50040083	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs574160623	chr11:50040091-50040092	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs193061800	chr11:50040092-50040093	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs552580120	chr11:50040106-50040107	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs569372781	chr11:50040138-50040139	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs183968129	chr11:50040142-50040143	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs28417656	chr11:50040152-50040153	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs72920451	chr11:50040153-50040154	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs377746771	chr11:50040154-50040155	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs71455954	chr11:50040155-50040156	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs145553208	chr11:50040158-50040159	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs142874265	chr11:50040166-50040167	Enhancers	n/a	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:336 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:50039200-50040600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr11:50040600-50049200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr11:50047400-50047600	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr11:50049200-50049600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr11:50049600-50054400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr11:50054400-50058600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr11:50056000-50056400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr11:50057400-50058000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr11:50066200-50067400	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
10	chr11:50100600-50101400	Enhancers	Adipose Nuclei	Adipose
11	chr11:50101400-50103600	Weak transcription	Adipose Nuclei	Adipose
12	chr11:50103200-50103400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr11:50103600-50103800	Enhancers	Adipose Nuclei	Adipose
14	chr11:50103600-50105200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr11:50105200-50106400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr11:50114800-50115200	Enhancers	Adipose Nuclei	Adipose
17	chr11:50129000-50130400	ZNF genes & repeats	Placenta	Placenta
18	chr11:50129400-50129800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr11:50130400-50131000	Active TSS	Placenta	Placenta
20	chr11:50133000-50133200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr11:50133000-50133800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr11:50133200-50133600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr11:50133200-50134200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr11:50133200-50134400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr11:50133200-50134400	Enhancers	Adipose Nuclei	Adipose
26	chr11:50133600-50133800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr11:50133800-50134000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr11:50133800-50134000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr11:50134000-50134400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr11:50134000-50135000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr11:50134200-50134400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr11:50134400-50140400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr11:50134400-50146200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr11:50136600-50136800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
35	chr11:50140400-50142200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr11:50140400-50142600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr11:50141800-50142000	Weak transcription	Adipose Nuclei	Adipose
38	chr11:50142000-50142200	Enhancers	Adipose Nuclei	Adipose
39	chr11:50142200-50144600	Weak transcription	Adipose Nuclei	Adipose
40	chr11:50142200-50145600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr11:50142600-50147000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr11:50144600-50147200	Enhancers	Adipose Nuclei	Adipose
43	chr11:50145600-50146000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr11:50145800-50147400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr11:50146000-50147000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr11:50146200-50147400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr11:50147000-50147400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr11:50147000-50147600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr11:50151800-50152200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr11:50155000-50155200	Active TSS	HMEC	breast

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