Variant report

Variant	nsv897518
Chromosome Location	chr11:50297005-51093950
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2439)
CpG islands
(count:122)
Chromatin interactive
region (count:2)
LncRNA
region (count:25)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2439 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:50712564-50712666	K562	blood:	n/a	n/a
2	ATF1	chr11:50757990-50758182	K562	blood:	n/a	n/a
3	ATF1	chr11:50676160-50676529	K562	blood:	n/a	n/a
4	ATF1	chr11:50755176-50755720	K562	blood:	n/a	n/a
5	ATF1	chr11:50381201-50381204	K562	blood:	n/a	n/a
6	ATF1	chr11:50767721-50767932	K562	blood:	n/a	n/a
7	ATF1	chr11:50728352-50728528	K562	blood:	n/a	n/a
8	ATF1	chr11:50721580-50721799	K562	blood:	n/a	n/a
9	ATF1	chr11:50741510-50741536	K562	blood:	n/a	n/a
10	ATF1	chr11:50771363-50771551	K562	blood:	n/a	n/a
11	ATF1	chr11:50409411-50409611	K562	blood:	n/a	n/a
12	BACH1	chr11:50780465-50780837	K562	blood:	n/a	n/a
13	BACH1	chr11:50759699-50760188	K562	blood:	n/a	n/a
14	BACH1	chr11:50744265-50744293	K562	blood:	n/a	n/a
15	BACH1	chr11:50699638-50700011	K562	blood:	n/a	n/a
16	BACH1	chr11:50739007-50739300	K562	blood:	n/a	n/a
17	BACH1	chr11:50765324-50765524	K562	blood:	n/a	n/a
18	BACH1	chr11:50741715-50742187	K562	blood:	n/a	n/a
19	BACH1	chr11:50769674-50770049	K562	blood:	n/a	n/a
20	BACH1	chr11:50762679-50763056	K562	blood:	n/a	n/a
21	BACH1	chr11:50767401-50767428	K562	blood:	n/a	n/a
22	BATF	chr11:50670735-50670974	GM12878	blood:	n/a	n/a
23	BATF	chr11:50649412-50649706	GM12878	blood:	n/a	n/a
24	BATF	chr11:50756360-50756521	GM12878	blood:	n/a	n/a
25	BATF	chr11:50761809-50762209	GM12878	blood:	n/a	n/a
26	BATF	chr11:50772285-50772433	GM12878	blood:	n/a	n/a
27	BATF	chr11:50670092-50670325	GM12878	blood:	n/a	n/a
28	BATF	chr11:50779460-50779823	GM12878	blood:	n/a	n/a
29	BATF	chr11:50686999-50687394	GM12878	blood:	n/a	n/a
30	BATF	chr11:50668601-50668765	GM12878	blood:	n/a	n/a
31	BATF	chr11:50764084-50764312	GM12878	blood:	n/a	n/a
32	BATF	chr11:50757466-50757719	GM12878	blood:	n/a	n/a
33	BATF	chr11:50711202-50711412	GM12878	blood:	n/a	n/a
34	BATF	chr11:50700733-50700935	GM12878	blood:	n/a	n/a
35	BATF	chr11:50742992-50743342	GM12878	blood:	n/a	n/a
36	BATF	chr11:50711195-50711416	GM12878	blood:	n/a	n/a
37	BATF	chr11:50772283-50772434	GM12878	blood:	n/a	n/a
38	BATF	chr11:50767583-50768188	GM12878	blood:	n/a	n/a
39	BATF	chr11:50755495-50755763	GM12878	blood:	n/a	n/a
40	BATF	chr11:50687048-50687278	GM12878	blood:	n/a	n/a
41	BATF	chr11:50676209-50676542	GM12878	blood:	n/a	n/a
42	BATF	chr11:50676256-50676541	GM12878	blood:	n/a	n/a
43	BATF	chr11:50768336-50768651	GM12878	blood:	n/a	n/a
44	BATF	chr11:50782290-50782554	GM12878	blood:	n/a	n/a
45	BATF	chr11:50671779-50671988	GM12878	blood:	n/a	n/a
46	BATF	chr11:50764082-50764319	GM12878	blood:	n/a	n/a
47	BATF	chr11:50770838-50771135	GM12878	blood:	n/a	n/a
48	BATF	chr11:50749839-50750367	GM12878	blood:	n/a	n/a
49	BATF	chr11:50756315-50756627	GM12878	blood:	n/a	n/a
50	BATF	chr11:50685636-50685821	GM12878	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:50368251-50368301	NHDF-neo	bronchial:	n/a
2	chr11:50371681-50371731	ProgFib	skin:	n/a
3	chr11:50368251-50368301	AG09309	skin:	n/a
4	chr11:50368251-50368301	HIPEpiC	eye:	n/a
5	chr11:50368251-50368301	HUVEC	blood vessel:	n/a
6	chr11:50371681-50371731	HPAEpiC	pulmonary alveolar:	n/a
7	chr11:50371681-50371731	HRPEpiC	eye:	n/a
8	chr11:50371681-50371731	PANC-1	pancreas:	n/a
9	chr11:50371681-50371731	HRCEpiC	kidney:	n/a
10	chr11:50371681-50371731	PFSK-1	brain:	n/a
11	chr11:50368251-50368301	PFSK-1	brain:	n/a
12	chr11:50371681-50371731	Caco-2	colon:	n/a
13	chr11:50371681-50371731	GM12878	blood:	n/a
14	chr11:50371681-50371731	AG04450	lung:	fetal
15	chr11:50368251-50368301	LNCaP	prostate:	n/a
16	chr11:50371681-50371731	K562	blood:	n/a
17	chr11:50368251-50368301	MCF-7	breast:	n/a
18	chr11:50368251-50368301	NHBE	bronchial:	n/a
19	chr11:50368251-50368301	SAEC	small airway:	n/a
20	chr11:50368251-50368301	SK-N-MC	brain:	n/a
21	chr11:50368251-50368301	HCM	heart:	n/a
22	chr11:50368251-50368301	NB4	blood:	n/a
23	chr11:50371681-50371731	NHDF-neo	bronchial:	n/a
24	chr11:50368251-50368301	HRCEpiC	kidney:	n/a
25	chr11:50368251-50368301	GM06990	blood:	n/a
26	chr11:50371681-50371731	U87	brain:	n/a
27	chr11:50371681-50371731	Jurkat	blood:	n/a
28	chr11:50368251-50368301	Jurkat	blood:	n/a
29	chr11:50371681-50371731	MCF10A-Er-Src	breast:	n/a
30	chr11:50371681-50371731	AG04449	skin:	fetal
31	chr11:50371681-50371731	HEEpiC	esophagus:	n/a
32	chr11:50368251-50368301	HEEpiC	esophagus:	n/a
33	chr11:50368251-50368301	AG10803	skin:	n/a
34	chr11:50371681-50371731	HRE	kidney:	n/a
35	chr11:50368251-50368301	GM12891	blood:	n/a
36	chr11:50368251-50368301	HRE	kidney:	n/a
37	chr11:50371681-50371731	SK-N-MC	brain:	n/a
38	chr11:50371681-50371731	AG09319	gingival:	n/a
39	chr11:50368251-50368301	T-47D	breast:	n/a
40	chr11:50371681-50371731	HEK293	kidney:	embryo
41	chr11:50371681-50371731	NHBE	bronchial:	n/a
42	chr11:50368251-50368301	AG04449	skin:	fetal
43	chr11:50368251-50368301	PANC-1	pancreas:	n/a
44	chr11:50371681-50371731	Hela-S3	cervix:	n/a
45	chr11:50368251-50368301	HPAEpiC	pulmonary alveolar:	n/a
46	chr11:50371681-50371731	GM19239	blood:	n/a
47	chr11:50371681-50371731	PrEC	prostate:	n/a
48	chr11:50368251-50368301	HRPEpiC	eye:	n/a
49	chr11:50368251-50368301	SK-N-SH	brain:	n/a
50	chr11:50368251-50368301	IMR90	lung:	fetal

(count:2 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:50670378..50671219-chr4:101762576..101763076,2	MCF-7	breast:
2	chr11:50731452..50731974-chr8:46856234..46856754,2	MCF-7	breast:

(count:25 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR4C13-9	chr11:50368739-50368821	NR_024504
2	lnc-OR4C13-9	chr11:50379775-50379803	NONHSAT021345
3	lnc-OR4C13-9	chr11:50379313-50379548	NONHSAT021345
4	lnc-OR4C13-7	chr11:50320143-50320239	NONHSAT021340
5	lnc-OR4C13-7	chr11:50320710-50320877	NONHSAT021340
6	lnc-OR4C13-9	chr11:50376439-50376850	NONHSAT021345
7	lnc-OR4C13-7	chr11:50302810-50303035	NONHSAT021343
8	lnc-OR4C13-7	chr11:50302810-50303098	NONHSAT021342
9	lnc-OR4C13-9	chr11:50375235-50375391	NONHSAT021345
10	lnc-OR4C13-9	chr11:50379313-50379802	NONHSAT021344
11	lnc-OR4C13-9	chr11:50375274-50375391	NR_024504
12	lnc-OR4C13-7	chr11:50301870-50302020	NONHSAT021343
13	lnc-OR4C13-9	chr11:50378065-50378165	NR_024504
14	lnc-OR4C13-9	chr11:50378065-50378165	NONHSAT021345
15	lnc-OR4C13-9	chr11:50378065-50378165	NONHSAT021344
16	lnc-OR4C13-7	chr11:50301079-50301142	NONHSAT021343
17	lnc-OR4C13-9	chr11:50368318-50368359	NR_024504
18	lnc-OR4C13-9	chr11:50375235-50375391	NONHSAT021344
19	lnc-OR4C13-9	chr11:50368318-50368359	NONHSAT021344
20	lnc-OR4C13-7	chr11:50302810-50302996	NONHSAT021339
21	lnc-OR4C13-9	chr11:50376439-50376850	NONHSAT021344
22	lnc-OR4C13-9	chr11:50379775-50379802	NR_024504
23	lnc-OR4C13-7	chr11:50313156-50313246	NONHSAT021340
24	lnc-OR4C13-9	chr11:50379313-50379548	NR_024504
25	lnc-OR4C13-9	chr11:50368739-50368821	NONHSAT021344

No data

Variant related genes	Relation type
ENSG00000254840	TF binding region
ENSG00000214883	TF binding region
ENSG00000254840	CpG island
ENSG00000214883	CpG island

Extended variants
information (count: 31487 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:31487 , 50 per page) page: 1 2 3 4 5 6 7 ... 630

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370271210	chr11:50300101-50300102	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs564380397	chr11:50300105-50300106	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs551354110	chr11:50301097-50301098	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs564859221	chr11:50301108-50301109	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs530607831	chr11:50301112-50301113	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs77874937	chr11:50301130-50301131	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs186009371	chr11:50301137-50301138	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs12226313	chr11:50301874-50301875	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs577887764	chr11:50301884-50301885	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs529778030	chr11:50301890-50301891	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs544433335	chr11:50301898-50301899	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs559867389	chr11:50301899-50301900	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs191102550	chr11:50301934-50301935	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs369566926	chr11:50301949-50301950	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs551616688	chr11:50301950-50301951	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs543621824	chr11:50301955-50301956	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs571598735	chr11:50301984-50301985	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs183899566	chr11:50301986-50301987	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs550538717	chr11:50302002-50302003	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs141375991	chr11:50302006-50302007	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs374606024	chr11:50302821-50302822	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs372225043	chr11:50302859-50302860	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs2635611	chr11:50302877-50302878	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs189351680	chr11:50302878-50302879	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs376657208	chr11:50302908-50302909	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs2644999	chr11:50302917-50302918	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs548501031	chr11:50302957-50302958	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs4111475	chr11:50302990-50302991	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs11828181	chr11:50302996-50302997	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
30	rs553479909	chr11:50303082-50303083	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
31	rs1188214	chr11:50320173-50320174	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
32	rs201486388	chr11:50320238-50320239	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs542017295	chr11:50320814-50320815	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
34	rs112934717	chr11:50320825-50320826	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
35	rs34187548	chr11:50324413-50324414	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs80141250	chr11:50324414-50324415	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs184086695	chr11:50324416-50324417	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs528217875	chr11:50324432-50324433	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs545091707	chr11:50324456-50324457	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs550046231	chr11:50324460-50324461	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs564957737	chr11:50324480-50324481	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs533593994	chr11:50324516-50324517	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs148590608	chr11:50324526-50324527	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs570292164	chr11:50324561-50324562	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs529549197	chr11:50324584-50324585	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs553997389	chr11:50324591-50324592	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs113193125	chr11:50324597-50324598	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs566033841	chr11:50324599-50324600	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs112207213	chr11:50324603-50324604	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs76358814	chr11:50324623-50324624	ZNF genes & repeats	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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Mortal	21835882	CNVD
Autism	22495309	CNVD
Breast cancer	21785460	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Esophageal cancer	21851588	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	22522925	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
Cancer	20164919	CNVD
Williams Syndrome	20824207	CNVD

Chromatin state (count:633 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:50324400-50325400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
2	chr11:50326400-50345800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr11:50326600-50328800	ZNF genes & repeats	Liver	Liver
4	chr11:50330000-50331600	ZNF genes & repeats	Liver	Liver
5	chr11:50337400-50343400	ZNF genes & repeats	Liver	Liver
6	chr11:50337600-50341800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
7	chr11:50340600-50341400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr11:50341600-50345800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
9	chr11:50342800-50343200	Active TSS	Right Atrium	heart
10	chr11:50344800-50345600	Active TSS	Fetal Heart	heart
11	chr11:50345400-50345600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
12	chr11:50345800-50346800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr11:50346600-50347000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
14	chr11:50346800-50347000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
15	chr11:50346800-50347000	ZNF genes & repeats	ES-WA7 Cell Line	embryonic stem cell
16	chr11:50346800-50347000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr11:50346800-50347000	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
18	chr11:50349200-50357800	ZNF genes & repeats	Adipose Nuclei	Adipose
19	chr11:50350000-50351800	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
20	chr11:50350800-50361200	ZNF genes & repeats	Liver	Liver
21	chr11:50351000-50367200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr11:50352200-50355600	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr11:50353200-50354600	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
24	chr11:50354600-50359000	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
25	chr11:50360600-50361000	Active TSS	Fetal Heart	heart
26	chr11:50360600-50363000	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr11:50360600-50363000	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
28	chr11:50364800-50365200	ZNF genes & repeats	Adipose Nuclei	Adipose
29	chr11:50371000-50371600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
30	chr11:50371400-50372600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr11:50378000-50378600	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
32	chr11:50384600-50385800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr11:50385000-50395000	ZNF genes & repeats	Liver	Liver
34	chr11:50386400-50387000	Active TSS	Right Atrium	heart
35	chr11:50386600-50394400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
36	chr11:50387200-50393600	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
37	chr11:50388000-50391000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
38	chr11:50388000-50392600	ZNF genes & repeats	Adipose Nuclei	Adipose
39	chr11:50388800-50390400	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
40	chr11:50391600-50393600	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr11:50393600-50398600	ZNF genes & repeats	Adipose Nuclei	Adipose
42	chr11:50394400-50398000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr11:50400200-50400800	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
44	chr11:50406200-50417200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr11:50406600-50411800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
46	chr11:50408200-50417200	ZNF genes & repeats	Liver	Liver
47	chr11:50409800-50410400	Active TSS	Aorta	Aorta
48	chr11:50409800-50412600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
49	chr11:50410200-50417400	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
50	chr11:50410200-50417800	ZNF genes & repeats	Adipose Nuclei	Adipose

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