Variant report

Variant	nsv1052475
Chromosome Location	chr11:50283977-50524009
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:267)
CpG islands
(count:122)
Chromatin interactive
region (count:0)
LncRNA
region (count:25)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:267 , 50 per page) page: 1 2 3 4 5 6

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	chr11:50382847-50382977	GM12878	blood:	n/a	n/a
5	CHD1	chr11:50409410-50409777	H1-hESC	embryonic stem cell:	n/a	n/a
6	CHD2	chr11:50522282-50522663	Hela-S3	cervix:	n/a	n/a
7	CHD2	chr11:50491957-50491986	Hela-S3	cervix:	n/a	n/a
8	CTCF	chr11:50382446-50382672	IMR90	lung:	n/a	n/a
9	CTCF	chr11:50304509-50304621	Kidney_OC	kidney:	n/a	n/a
10	CTCF	chr11:50372648-50372696	LNCaP	prostate:	n/a	n/a
11	CTCF	chr11:50294779-50294808	GM20000	blood:	n/a	n/a
12	CTCF	chr11:50318115-50318201	GM10266	blood:	n/a	n/a
13	CTCF	chr11:50305210-50305247	GM20000	blood:	n/a	n/a
14	CTCF	chr11:50417864-50417915	LNCaP	prostate:	n/a	n/a
15	CTCF	chr11:50399914-50399973	GM20000	blood:	n/a	n/a
16	CTCF	chr11:50472977-50473050	GM13976	blood:	n/a	n/a
17	CTCF	chr11:50376015-50376061	Pancreas_OC	pancreas:	n/a	n/a
18	CTCF	chr11:50505847-50505946	HepG2	liver:	n/a	n/a
19	CTCF	chr11:50505637-50505695	GM10248	blood:	n/a	n/a
20	CTCF	chr11:50284186-50284275	GM20000	blood:	n/a	n/a
21	CTCF	chr11:50382479-50382654	K562	blood:	n/a	n/a
22	CTCF	chr11:50317679-50317740	GM13976	blood:	n/a	n/a
23	CTCF	chr11:50312320-50312366	Kidney_OC	kidney:	n/a	n/a
24	CTCF	chr11:50293200-50293350	SAEC	small airway:	n/a	n/a
25	CTCF	chr11:50316423-50316519	GM10266	blood:	n/a	n/a
26	CTCF	chr11:50305777-50305808	Lung_OC	lung:	n/a	n/a
27	CTCF	chr11:50470750-50470789	Lung_OC	lung:	n/a	n/a
28	CTCF	chr11:50505847-50505946	Hela-S3	cervix:	n/a	n/a
29	CTCF	chr11:50300095-50300112	GM10248	blood:	n/a	n/a
30	CTCF	chr11:50401027-50401059	GM20000	blood:	n/a	n/a
31	CTCF	chr11:50291325-50291378	LNCaP	prostate:	n/a	n/a
32	CTCF	chr11:50293189-50293335	NHEK	skin:	n/a	n/a
33	CUX1	chr11:50360922-50360959	GM12878	blood:	n/a	n/a
34	E2F4	chr11:50426467-50426646	MCF10A-Er-Src	breast:	n/a	n/a
35	E2F4	chr11:50474624-50474734	MCF10A-Er-Src	breast:	n/a	n/a
36	E2F4	chr11:50448625-50448638	MCF10A-Er-Src	breast:	n/a	n/a
37	E2F4	chr11:50437701-50438072	MCF10A-Er-Src	breast:	n/a	n/a
38	E2F4	chr11:50522286-50522659	MCF10A-Er-Src	breast:	n/a	n/a
39	E2F4	chr11:50369680-50369722	MCF10A-Er-Src	breast:	n/a	n/a
40	ELK1	chr11:50412353-50412521	GM12878	blood:	n/a	n/a
41	ELK1	chr11:50522282-50522663	Hela-S3	cervix:	n/a	n/a
42	EP300	chr11:50522282-50522663	Hela-S3	cervix:	n/a	n/a
43	EP300	chr11:50337674-50337737	GM12878	blood:	n/a	n/a
44	EP300	chr11:50412481-50412512	GM12878	blood:	n/a	n/a
45	FAM48A	chr11:50475217-50475585	GM12878	blood:	n/a	n/a
46	FAM48A	chr11:50409409-50409777	GM12878	blood:	n/a	n/a
47	FOS	chr11:50522286-50522658	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr11:50437702-50438072	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr11:50291697-50291896	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr11:50291698-50291895	MCF10A-Er-Src	breast:	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	HepG2	liver:	n/a
2	chr11:50371681-50371731	U87	brain:	n/a
3	chr11:50371681-50371731	HRE	kidney:	n/a
4	chr11:50371681-50371731	LNCaP	prostate:	n/a
5	chr11:50368251-50368301	MCF10A-Er-Src	breast:	n/a
6	chr11:50368251-50368301	AG04450	lung:	fetal
7	chr11:50368251-50368301	RPTEC	kidney:	n/a
8	chr11:50368251-50368301	NHDF-neo	bronchial:	n/a
9	chr11:50368251-50368301	Jurkat	blood:	n/a
10	chr11:50371681-50371731	GM19239	blood:	n/a
11	chr11:50368251-50368301	MCF-7	breast:	n/a
12	chr11:50371681-50371731	IMR90	lung:	fetal
13	chr11:50368251-50368301	NHBE	bronchial:	n/a
14	chr11:50371681-50371731	HCPEpiC	choroid plexus:	n/a
15	chr11:50368251-50368301	GM12891	blood:	n/a
16	chr11:50371681-50371731	SK-N-MC	brain:	n/a
17	chr11:50368251-50368301	HPAEpiC	pulmonary alveolar:	n/a
18	chr11:50371681-50371731	AG09319	gingival:	n/a
19	chr11:50371681-50371731	SK-N-SH_RA	brain:	n/a
20	chr11:50368251-50368301	HUVEC	blood vessel:	n/a
21	chr11:50371681-50371731	ECC-1	luminal epithelium:	n/a
22	chr11:50371681-50371731	HNPCEpiC	eye:	n/a
23	chr11:50371681-50371731	HCT-116	colon:	n/a
24	chr11:50371681-50371731	GM12891	blood:	n/a
25	chr11:50368251-50368301	ECC-1	luminal epithelium:	n/a
26	chr11:50368251-50368301	Caco-2	colon:	n/a
27	chr11:50371681-50371731	PrEC	prostate:	n/a
28	chr11:50371681-50371731	HMEC	breast:	n/a
29	chr11:50368251-50368301	ovcar-3	ovarian:	n/a
30	chr11:50371681-50371731	GM12892	blood:	n/a
31	chr11:50368251-50368301	NH-A	brain:	n/a
32	chr11:50368251-50368301	AG09319	gingival:	n/a
33	chr11:50368251-50368301	A549	lung:	n/a
34	chr11:50368251-50368301	HCM	heart:	n/a
35	chr11:50368251-50368301	NB4	blood:	n/a
36	chr11:50368251-50368301	HMEC	breast:	n/a
37	chr11:50371681-50371731	MCF10A-Er-Src	breast:	n/a
38	chr11:50368251-50368301	HepG2	liver:	n/a
39	chr11:50371681-50371731	HL-60	blood:	n/a
40	chr11:50368251-50368301	CMK	blood:	n/a
41	chr11:50371681-50371731	T-47D	breast:	n/a
42	chr11:50368251-50368301	Hela-S3	cervix:	n/a
43	chr11:50368251-50368301	HRCEpiC	kidney:	n/a
44	chr11:50371681-50371731	AG10803	skin:	n/a
45	chr11:50371681-50371731	MCF-7	breast:	n/a
46	chr11:50371681-50371731	NH-A	brain:	n/a
47	chr11:50371681-50371731	BJ	skin:	n/a
48	chr11:50368251-50368301	HIPEpiC	eye:	n/a
49	chr11:50371681-50371731	BE2_C	brain:	n/a
50	chr11:50371681-50371731	GM06990	blood:	n/a

No data

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR4C13-7	chr11:50320143-50320239	NONHSAT021340
2	lnc-OR4C13-9	chr11:50368318-50368359	NR_024504
3	lnc-OR4C13-9	chr11:50375235-50375391	NONHSAT021345
4	lnc-OR4C13-7	chr11:50320710-50320877	NONHSAT021340
5	lnc-OR4C13-7	chr11:50302810-50303035	NONHSAT021343
6	lnc-OR4C13-9	chr11:50379313-50379548	NR_024504
7	lnc-OR4C13-7	chr11:50301079-50301142	NONHSAT021343
8	lnc-OR4C13-9	chr11:50378065-50378165	NONHSAT021344
9	lnc-OR4C13-9	chr11:50378065-50378165	NR_024504
10	lnc-OR4C13-9	chr11:50379313-50379548	NONHSAT021345
11	lnc-OR4C13-9	chr11:50379775-50379803	NONHSAT021345
12	lnc-OR4C13-9	chr11:50378065-50378165	NONHSAT021345
13	lnc-OR4C13-7	chr11:50302810-50303098	NONHSAT021342
14	lnc-OR4C13-9	chr11:50368318-50368359	NONHSAT021344
15	lnc-OR4C13-7	chr11:50302810-50302996	NONHSAT021339
16	lnc-OR4C13-9	chr11:50375235-50375391	NONHSAT021344
17	lnc-OR4C13-7	chr11:50301870-50302020	NONHSAT021343
18	lnc-OR4C13-9	chr11:50376439-50376850	NONHSAT021344
19	lnc-OR4C13-9	chr11:50368739-50368821	NONHSAT021344
20	lnc-OR4C13-7	chr11:50313156-50313246	NONHSAT021340
21	lnc-OR4C13-9	chr11:50376439-50376850	NONHSAT021345
22	lnc-OR4C13-9	chr11:50379313-50379802	NONHSAT021344
23	lnc-OR4C13-9	chr11:50375274-50375391	NR_024504
24	lnc-OR4C13-9	chr11:50368739-50368821	NR_024504
25	lnc-OR4C13-9	chr11:50379775-50379802	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: 9660 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:9660 , 50 per page) page: 1 2 3 4 5 6 7 ... 194

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560878713	chr11:50295803-50295804	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs143401472	chr11:50295807-50295808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs539947694	chr11:50295814-50295815	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs548591334	chr11:50295847-50295848	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs560230155	chr11:50295895-50295896	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs191994026	chr11:50295896-50295897	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs376368019	chr11:50295956-50295957	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs145547299	chr11:50295964-50295965	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs148872553	chr11:50296006-50296007	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs186565838	chr11:50296007-50296008	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs191751240	chr11:50296038-50296039	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs539376315	chr11:50296042-50296043	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs4090123	chr11:50296059-50296060	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs182394716	chr11:50296088-50296089	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs199974326	chr11:50296121-50296122	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs200930393	chr11:50296132-50296133	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs563193748	chr11:50296142-50296143	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs188672575	chr11:50296147-50296148	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs61893105	chr11:50296155-50296156	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs144432644	chr11:50296183-50296184	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs148006595	chr11:50296202-50296203	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs554091400	chr11:50296203-50296204	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs1854691	chr11:50296210-50296211	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs549476083	chr11:50296223-50296224	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs145659354	chr11:50296239-50296240	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs192895745	chr11:50296284-50296285	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs111621618	chr11:50296328-50296329	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs185846534	chr11:50296331-50296332	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs12225736	chr11:50296355-50296356	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs1995048	chr11:50296358-50296359	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs58037290	chr11:50296381-50296382	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs71051745	chr11:50296384-50296385	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs200404488	chr11:50296386-50296387	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs200934491	chr11:50296387-50296388	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs374863150	chr11:50296388-50296389	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs60819379	chr11:50296397-50296398	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs28695554	chr11:50296401-50296402	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs377213031	chr11:50296402-50296403	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs1928731	chr11:50296403-50296404	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs370071413	chr11:50296409-50296410	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs527803212	chr11:50296484-50296485	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs547884771	chr11:50296486-50296487	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs552011107	chr11:50296710-50296711	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs377708155	chr11:50296726-50296727	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs368057350	chr11:50296739-50296740	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs370271210	chr11:50300101-50300102	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs564380397	chr11:50300105-50300106	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs551354110	chr11:50301097-50301098	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
49	rs564859221	chr11:50301108-50301109	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
50	rs530607831	chr11:50301112-50301113	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

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

Chromatin state (count:173 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:50295800-50296200	Enhancers	Adipose Nuclei	Adipose
2	chr11:50324400-50325400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
3	chr11:50326400-50345800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr11:50326600-50328800	ZNF genes & repeats	Liver	Liver
5	chr11:50330000-50331600	ZNF genes & repeats	Liver	Liver
6	chr11:50337400-50343400	ZNF genes & repeats	Liver	Liver
7	chr11:50337600-50341800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
8	chr11:50340600-50341400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr11:50341600-50345800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
10	chr11:50342800-50343200	Active TSS	Right Atrium	heart
11	chr11:50344800-50345600	Active TSS	Fetal Heart	heart
12	chr11:50345400-50345600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
13	chr11:50345800-50346800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr11:50346600-50347000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
15	chr11:50346800-50347000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
16	chr11:50346800-50347000	ZNF genes & repeats	ES-WA7 Cell Line	embryonic stem cell
17	chr11:50346800-50347000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr11:50346800-50347000	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
19	chr11:50349200-50357800	ZNF genes & repeats	Adipose Nuclei	Adipose
20	chr11:50350000-50351800	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
21	chr11:50350800-50361200	ZNF genes & repeats	Liver	Liver
22	chr11:50351000-50367200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr11:50352200-50355600	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr11:50353200-50354600	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
25	chr11:50354600-50359000	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
26	chr11:50360600-50361000	Active TSS	Fetal Heart	heart
27	chr11:50360600-50363000	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr11:50360600-50363000	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
29	chr11:50364800-50365200	ZNF genes & repeats	Adipose Nuclei	Adipose
30	chr11:50371000-50371600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
31	chr11:50371400-50372600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr11:50378000-50378600	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
33	chr11:50384600-50385800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr11:50385000-50395000	ZNF genes & repeats	Liver	Liver
35	chr11:50386400-50387000	Active TSS	Right Atrium	heart
36	chr11:50386600-50394400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
37	chr11:50387200-50393600	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
38	chr11:50388000-50391000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
39	chr11:50388000-50392600	ZNF genes & repeats	Adipose Nuclei	Adipose
40	chr11:50388800-50390400	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
41	chr11:50391600-50393600	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr11:50393600-50398600	ZNF genes & repeats	Adipose Nuclei	Adipose
43	chr11:50394400-50398000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr11:50400200-50400800	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
45	chr11:50406200-50417200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr11:50406600-50411800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
47	chr11:50408200-50417200	ZNF genes & repeats	Liver	Liver
48	chr11:50409800-50410400	Active TSS	Aorta	Aorta
49	chr11:50409800-50412600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
50	chr11:50410200-50417400	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum

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