Variant report

Variant	nsv1040060
Chromosome Location	chr11:50271324-50450684
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:180)
CpG islands
(count:122)
Chromatin interactive
region (count:0)
LncRNA
region (count:33)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:180 , 50 per page) page: 1 2 3 4

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	CEBPB	chr11:50409463-50409610	H1-hESC	embryonic stem cell:	n/a	n/a
4	CHD1	chr11:50409410-50409777	H1-hESC	embryonic stem cell:	n/a	n/a
5	CHD1	chr11:50382847-50382977	GM12878	blood:	n/a	n/a
6	CTCF	chr11:50305210-50305247	GM20000	blood:	n/a	n/a
7	CTCF	chr11:50312320-50312366	Kidney_OC	kidney:	n/a	n/a
8	CTCF	chr11:50304509-50304621	Kidney_OC	kidney:	n/a	n/a
9	CTCF	chr11:50318115-50318201	GM10266	blood:	n/a	n/a
10	CTCF	chr11:50417864-50417915	LNCaP	prostate:	n/a	n/a
11	CTCF	chr11:50277249-50277334	Spleen_OC	spleen:	n/a	n/a
12	CTCF	chr11:50372648-50372696	LNCaP	prostate:	n/a	n/a
13	CTCF	chr11:50382479-50382654	K562	blood:	n/a	n/a
14	CTCF	chr11:50305777-50305808	Lung_OC	lung:	n/a	n/a
15	CTCF	chr11:50294779-50294808	GM20000	blood:	n/a	n/a
16	CTCF	chr11:50316423-50316519	GM10266	blood:	n/a	n/a
17	CTCF	chr11:50317679-50317740	GM13976	blood:	n/a	n/a
18	CTCF	chr11:50284186-50284275	GM20000	blood:	n/a	n/a
19	CTCF	chr11:50401027-50401059	GM20000	blood:	n/a	n/a
20	CTCF	chr11:50291325-50291378	LNCaP	prostate:	n/a	n/a
21	CTCF	chr11:50376015-50376061	Pancreas_OC	pancreas:	n/a	n/a
22	CTCF	chr11:50382446-50382672	IMR90	lung:	n/a	n/a
23	CTCF	chr11:50293200-50293350	SAEC	small airway:	n/a	n/a
24	CTCF	chr11:50293189-50293335	NHEK	skin:	n/a	n/a
25	CTCF	chr11:50399914-50399973	GM20000	blood:	n/a	n/a
26	CTCF	chr11:50300095-50300112	GM10248	blood:	n/a	n/a
27	CUX1	chr11:50360922-50360959	GM12878	blood:	n/a	n/a
28	E2F4	chr11:50448625-50448638	MCF10A-Er-Src	breast:	n/a	n/a
29	E2F4	chr11:50369680-50369722	MCF10A-Er-Src	breast:	n/a	n/a
30	E2F4	chr11:50437701-50438072	MCF10A-Er-Src	breast:	n/a	n/a
31	E2F4	chr11:50426467-50426646	MCF10A-Er-Src	breast:	n/a	n/a
32	ELK1	chr11:50412353-50412521	GM12878	blood:	n/a	n/a
33	EP300	chr11:50412481-50412512	GM12878	blood:	n/a	n/a
34	EP300	chr11:50337674-50337737	GM12878	blood:	n/a	n/a
35	FAM48A	chr11:50409409-50409777	GM12878	blood:	n/a	n/a
36	FOS	chr11:50276547-50276647	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr11:50293136-50293277	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr11:50276555-50276756	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr11:50293131-50293138	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr11:50291698-50291895	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr11:50437701-50438072	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr11:50276556-50276677	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr11:50291697-50291896	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr11:50437702-50438072	MCF10A-Er-Src	breast:	n/a	n/a
45	FOSL2	chr11:50296224-50296441	HepG2	liver:	n/a	chr11:50296386-50296395 chr11:50296388-50296397
46	FOXA2	chr11:50296123-50296491	A549	lung:	n/a	n/a
47	FOXP2	chr11:50437694-50438023	SK-N-MC	brain:	n/a	n/a
48	GABPA	chr11:50296318-50296402	HepG2	liver:	n/a	n/a
49	GATA2	chr11:50346724-50347094	HUVEC	blood vessel:	n/a	n/a
50	GATA3	chr11:50437701-50438072	SH-SY5Y	brain:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:50371681-50371731	A549	lung:	n/a
2	chr11:50368251-50368301	GM19239	blood:	n/a
3	chr11:50371681-50371731	Jurkat	blood:	n/a
4	chr11:50371681-50371731	ProgFib	skin:	n/a
5	chr11:50371681-50371731	HCF	heart:	n/a
6	chr11:50371681-50371731	BJ	skin:	n/a
7	chr11:50368251-50368301	AG04450	lung:	fetal
8	chr11:50371681-50371731	AG04449	skin:	fetal
9	chr11:50368251-50368301	K562	blood:	n/a
10	chr11:50371681-50371731	HUVEC	blood vessel:	n/a
11	chr11:50371681-50371731	BE2_C	brain:	n/a
12	chr11:50368251-50368301	HCPEpiC	choroid plexus:	n/a
13	chr11:50368251-50368301	LNCaP	prostate:	n/a
14	chr11:50368251-50368301	SKMC	muscle:	n/a
15	chr11:50368251-50368301	SK-N-SH_RA	brain:	n/a
16	chr11:50371681-50371731	HAEpiC	amniotic membrane:	n/a
17	chr11:50368251-50368301	ProgFib	skin:	n/a
18	chr11:50368251-50368301	HRPEpiC	eye:	n/a
19	chr11:50371681-50371731	AG04450	lung:	fetal
20	chr11:50371681-50371731	SK-N-SH	brain:	n/a
21	chr11:50368251-50368301	Jurkat	blood:	n/a
22	chr11:50371681-50371731	MCF10A-Er-Src	breast:	n/a
23	chr11:50368251-50368301	MCF10A-Er-Src	breast:	n/a
24	chr11:50371681-50371731	NT2-D1	testis:	n/a
25	chr11:50371681-50371731	HCPEpiC	choroid plexus:	n/a
26	chr11:50371681-50371731	GM19239	blood:	n/a
27	chr11:50371681-50371731	PANC-1	pancreas:	n/a
28	chr11:50371681-50371731	NB4	blood:	n/a
29	chr11:50371681-50371731	HRE	kidney:	n/a
30	chr11:50368251-50368301	H1-hESC	embryonic stem cell:	embryo
31	chr11:50368251-50368301	U87	brain:	n/a
32	chr11:50368251-50368301	T-47D	breast:	n/a
33	chr11:50368251-50368301	AoSMC	blood vessel:	n/a
34	chr11:50368251-50368301	Hepatocyte	liver:	n/a
35	chr11:50368251-50368301	BE2_C	brain:	n/a
36	chr11:50368251-50368301	CMK	blood:	n/a
37	chr11:50371681-50371731	Caco-2	colon:	n/a
38	chr11:50368251-50368301	GM12891	blood:	n/a
39	chr11:50368251-50368301	SK-N-SH	brain:	n/a
40	chr11:50368251-50368301	PFSK-1	brain:	n/a
41	chr11:50368251-50368301	HUVEC	blood vessel:	n/a
42	chr11:50371681-50371731	SK-N-MC	brain:	n/a
43	chr11:50371681-50371731	GM12878	blood:	n/a
44	chr11:50371681-50371731	HCM	heart:	n/a
45	chr11:50371681-50371731	HRPEpiC	eye:	n/a
46	chr11:50371681-50371731	PFSK-1	brain:	n/a
47	chr11:50368251-50368301	HepG2	liver:	n/a
48	chr11:50368251-50368301	PANC-1	pancreas:	n/a
49	chr11:50368251-50368301	HEK293	kidney:	embryo
50	chr11:50371681-50371731	ECC-1	luminal epithelium:	n/a

No data

(count:33 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR4C13-7	chr11:50279839-50280169	NONHSAT021342
2	lnc-OR4C13-7	chr11:50280085-50280169	NONHSAT021339
3	lnc-OR4C13-7	chr11:50274586-50274778	NONHSAT021338
4	lnc-OR4C13-7	chr11:50301079-50301142	NONHSAT021343
5	lnc-OR4C13-7	chr11:50302810-50302996	NONHSAT021339
6	lnc-OR4C13-9	chr11:50375274-50375391	NR_024504
7	lnc-OR4C13-9	chr11:50376439-50376850	NONHSAT021344
8	lnc-OR4C13-9	chr11:50376439-50376850	NONHSAT021345
9	lnc-OR4C13-7	chr11:50279538-50279677	NONHSAT021339
10	lnc-OR4C13-9	chr11:50368739-50368821	NONHSAT021344
11	lnc-OR4C13-9	chr11:50378065-50378165	NONHSAT021344
12	lnc-OR4C13-9	chr11:50368318-50368359	NONHSAT021344
13	lnc-OR4C13-7	chr11:50302810-50303035	NONHSAT021343
14	lnc-OR4C13-7	chr11:50302810-50303098	NONHSAT021342
15	lnc-OR4C13-9	chr11:50375235-50375391	NONHSAT021344
16	lnc-OR4C13-9	chr11:50379313-50379802	NONHSAT021344
17	lnc-OR4C13-9	chr11:50378065-50378165	NONHSAT021345
18	lnc-OR4C13-9	chr11:50379775-50379802	NR_024504
19	lnc-OR4C13-7	chr11:50274586-50274767	NONHSAT021339
20	lnc-OR4C13-9	chr11:50375235-50375391	NONHSAT021345
21	lnc-OR4C13-9	chr11:50368318-50368359	NR_024504
22	lnc-OR4C13-9	chr11:50379313-50379548	NONHSAT021345
23	lnc-OR4C13-7	chr11:50313156-50313246	NONHSAT021340
24	lnc-OR4C13-7	chr11:50274586-50274767	NONHSAT021340
25	lnc-OR4C13-7	chr11:50279538-50279677	NONHSAT021340
26	lnc-OR4C13-9	chr11:50379313-50379548	NR_024504
27	lnc-OR4C13-7	chr11:50280085-50280169	NONHSAT021340
28	lnc-OR4C13-7	chr11:50301870-50302020	NONHSAT021343
29	lnc-OR4C13-7	chr11:50320710-50320877	NONHSAT021340
30	lnc-OR4C13-9	chr11:50368739-50368821	NR_024504
31	lnc-OR4C13-9	chr11:50379775-50379803	NONHSAT021345
32	lnc-OR4C13-7	chr11:50320143-50320239	NONHSAT021340
33	lnc-OR4C13-9	chr11:50378065-50378165	NR_024504

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: 6588 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:6588 , 50 per page) page: 1 2 3 4 5 6 7 ... 132

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563563330	chr11:50271336-50271337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs528902964	chr11:50271345-50271346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs370337553	chr11:50271388-50271389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs79792046	chr11:50271389-50271390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs79923323	chr11:50271400-50271401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs559189894	chr11:50271424-50271425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs529748238	chr11:50271472-50271473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs528210711	chr11:50271522-50271523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs374338067	chr11:50271539-50271540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs551055926	chr11:50271555-50271556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs369984676	chr11:50271597-50271598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs188556087	chr11:50271637-50271638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs570738274	chr11:50271658-50271659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs181178750	chr11:50271746-50271747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs137871610	chr11:50271779-50271780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs187102857	chr11:50271818-50271819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs191539119	chr11:50271828-50271829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs149029265	chr11:50271864-50271865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs7481328	chr11:50271896-50271897	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs535151792	chr11:50271927-50271928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs558268679	chr11:50271978-50271979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs577927019	chr11:50271985-50271986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs543573845	chr11:50272104-50272105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs13328893	chr11:50272145-50272146	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs573212276	chr11:50272148-50272149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs184232139	chr11:50272162-50272163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs542544733	chr11:50272189-50272190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs558967185	chr11:50272205-50272206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs528053903	chr11:50272211-50272212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs142486667	chr11:50272238-50272239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs564612372	chr11:50272244-50272245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs146109382	chr11:50272287-50272288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs138867253	chr11:50272323-50272324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs550312475	chr11:50272326-50272327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs570141427	chr11:50272359-50272360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs529639328	chr11:50272367-50272368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs549390487	chr11:50272372-50272373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs186992062	chr11:50272375-50272376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs369317789	chr11:50272392-50272393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs189748395	chr11:50272411-50272412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs142010476	chr11:50272415-50272416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs182095641	chr11:50272481-50272482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs536863163	chr11:50272482-50272483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs375967109	chr11:50272499-50272500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs370056968	chr11:50272550-50272551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs369865520	chr11:50272576-50272577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs569595679	chr11:50272598-50272599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs573748914	chr11:50272618-50272619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs187091695	chr11:50272645-50272646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs2890925	chr11:50272662-50272663	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:55)

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

Chromatin state (count:108 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:50258800-50274600	Weak transcription	Placenta	Placenta
2	chr11:50274600-50275400	Strong transcription	Placenta	Placenta
3	chr11:50275400-50277000	Weak transcription	Placenta	Placenta
4	chr11:50295800-50296200	Enhancers	Adipose Nuclei	Adipose
5	chr11:50324400-50325400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
6	chr11:50326400-50345800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr11:50326600-50328800	ZNF genes & repeats	Liver	Liver
8	chr11:50330000-50331600	ZNF genes & repeats	Liver	Liver
9	chr11:50337400-50343400	ZNF genes & repeats	Liver	Liver
10	chr11:50337600-50341800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
11	chr11:50340600-50341400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr11:50341600-50345800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
13	chr11:50342800-50343200	Active TSS	Right Atrium	heart
14	chr11:50344800-50345600	Active TSS	Fetal Heart	heart
15	chr11:50345400-50345600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
16	chr11:50345800-50346800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr11:50346600-50347000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
18	chr11:50346800-50347000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
19	chr11:50346800-50347000	ZNF genes & repeats	ES-WA7 Cell Line	embryonic stem cell
20	chr11:50346800-50347000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr11:50346800-50347000	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
22	chr11:50349200-50357800	ZNF genes & repeats	Adipose Nuclei	Adipose
23	chr11:50350000-50351800	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
24	chr11:50350800-50361200	ZNF genes & repeats	Liver	Liver
25	chr11:50351000-50367200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr11:50352200-50355600	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr11:50353200-50354600	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
28	chr11:50354600-50359000	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
29	chr11:50360600-50361000	Active TSS	Fetal Heart	heart
30	chr11:50360600-50363000	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr11:50360600-50363000	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
32	chr11:50364800-50365200	ZNF genes & repeats	Adipose Nuclei	Adipose
33	chr11:50371000-50371600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
34	chr11:50371400-50372600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr11:50378000-50378600	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
36	chr11:50384600-50385800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr11:50385000-50395000	ZNF genes & repeats	Liver	Liver
38	chr11:50386400-50387000	Active TSS	Right Atrium	heart
39	chr11:50386600-50394400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
40	chr11:50387200-50393600	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
41	chr11:50388000-50391000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
42	chr11:50388000-50392600	ZNF genes & repeats	Adipose Nuclei	Adipose
43	chr11:50388800-50390400	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
44	chr11:50391600-50393600	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr11:50393600-50398600	ZNF genes & repeats	Adipose Nuclei	Adipose
46	chr11:50394400-50398000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr11:50400200-50400800	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
48	chr11:50406200-50417200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr11:50406600-50411800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
50	chr11:50408200-50417200	ZNF genes & repeats	Liver	Liver

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