Variant report

Variant	nsv554268
Chromosome Location	chr11:48735395-48912139
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2554)
CpG islands
(count:245)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2554 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:48895975-48896341	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:48880376-48880748	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:48892892-48893269	HepG2	liver:	n/a	n/a
4	ATF1	chr11:48859189-48859770	K562	blood:	n/a	n/a
5	ATF1	chr11:48883351-48883720	K562	blood:	n/a	n/a
6	ATF1	chr11:48892890-48893270	K562	blood:	n/a	n/a
7	ATF1	chr11:48867583-48867993	K562	blood:	n/a	n/a
8	ATF1	chr11:48895825-48896343	K562	blood:	n/a	n/a
9	ATF1	chr11:48896850-48897050	K562	blood:	n/a	n/a
10	ATF1	chr11:48845364-48845733	K562	blood:	n/a	n/a
11	ATF1	chr11:48849264-48849333	K562	blood:	n/a	n/a
12	ATF1	chr11:48880374-48880748	K562	blood:	n/a	n/a
13	ATF1	chr11:48796111-48796444	K562	blood:	n/a	n/a
14	ATF3	chr11:48892858-48893151	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF3	chr11:48845439-48845653	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr11:48881669-48882080	K562	blood:	n/a	n/a
17	BACH1	chr11:48814467-48814498	K562	blood:	n/a	n/a
18	BATF	chr11:48906543-48906879	GM12878	blood:	n/a	chr11:48906618-48906628
19	BATF	chr11:48885554-48885939	GM12878	blood:	n/a	n/a
20	BATF	chr11:48775372-48775512	GM12878	blood:	n/a	n/a
21	BATF	chr11:48776572-48776725	GM12878	blood:	n/a	n/a
22	BATF	chr11:48810099-48810738	GM12878	blood:	n/a	n/a
23	BATF	chr11:48887996-48888565	GM12878	blood:	n/a	n/a
24	BATF	chr11:48804986-48805223	GM12878	blood:	n/a	n/a
25	BATF	chr11:48817733-48818014	GM12878	blood:	n/a	n/a
26	BATF	chr11:48839569-48839852	GM12878	blood:	n/a	n/a
27	BATF	chr11:48844664-48844887	GM12878	blood:	n/a	n/a
28	BATF	chr11:48810174-48810367	GM12878	blood:	n/a	n/a
29	BATF	chr11:48894608-48895288	GM12878	blood:	n/a	n/a
30	BATF	chr11:48776576-48776723	GM12878	blood:	n/a	n/a
31	BATF	chr11:48854717-48855191	GM12878	blood:	n/a	n/a
32	BATF	chr11:48894524-48895290	GM12878	blood:	n/a	n/a
33	BATF	chr11:48866749-48866988	GM12878	blood:	n/a	n/a
34	BATF	chr11:48805015-48805320	GM12878	blood:	n/a	n/a
35	BATF	chr11:48883213-48883919	GM12878	blood:	n/a	n/a
36	BATF	chr11:48898958-48899437	GM12878	blood:	n/a	n/a
37	BATF	chr11:48741581-48741798	GM12878	blood:	n/a	n/a
38	BATF	chr11:48885664-48885889	GM12878	blood:	n/a	n/a
39	BATF	chr11:48856704-48856991	GM12878	blood:	n/a	n/a
40	BATF	chr11:48844232-48844479	GM12878	blood:	n/a	n/a
41	BATF	chr11:48877883-48878085	GM12878	blood:	n/a	n/a
42	BATF	chr11:48861740-48862096	GM12878	blood:	n/a	n/a
43	BATF	chr11:48906491-48906775	GM12878	blood:	n/a	chr11:48906618-48906628
44	BATF	chr11:48867677-48867900	GM12878	blood:	n/a	n/a
45	BATF	chr11:48895948-48896327	GM12878	blood:	n/a	n/a
46	BATF	chr11:48775367-48775560	GM12878	blood:	n/a	n/a
47	BATF	chr11:48844167-48844436	GM12878	blood:	n/a	n/a
48	BATF	chr11:48854637-48855193	GM12878	blood:	n/a	n/a
49	BATF	chr11:48831050-48831447	GM12878	blood:	n/a	n/a
50	BATF	chr11:48895950-48896265	GM12878	blood:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:48902014-48902064	HCF	heart:	n/a
2	chr11:48902014-48902064	HCF	heart:	n/a
3	chr11:48902014-48902064	GM06990	blood:	n/a
4	chr11:48901705-48901755	HUVEC	blood vessel:	n/a
5	chr11:48902014-48902064	HPAEpiC	pulmonary alveolar:	n/a
6	chr11:48901914-48901964	NB4	blood:	n/a
7	chr11:48880009-48880059	Caco-2	colon:	n/a
8	chr11:48901705-48901755	NHBE	bronchial:	n/a
9	chr11:48880009-48880059	SK-N-SH	brain:	n/a
10	chr11:48901914-48901964	NHDF-neo	bronchial:	n/a
11	chr11:48901705-48901755	AG04449	skin:	fetal
12	chr11:48901914-48901964	AG04450	lung:	fetal
13	chr11:48901914-48901964	HNPCEpiC	eye:	n/a
14	chr11:48901914-48901964	HRE	kidney:	n/a
15	chr11:48901914-48901964	AG04449	skin:	fetal
16	chr11:48901705-48901755	Jurkat	blood:	n/a
17	chr11:48901705-48901755	HCPEpiC	choroid plexus:	n/a
18	chr11:48901914-48901964	K562	blood:	n/a
19	chr11:48880009-48880059	K562	blood:	n/a
20	chr11:48880009-48880059	HRPEpiC	eye:	n/a
21	chr11:48880009-48880059	RPTEC	kidney:	n/a
22	chr11:48901914-48901964	SK-N-SH_RA	brain:	n/a
23	chr11:48902014-48902064	K562	blood:	n/a
24	chr11:48901705-48901755	AoSMC	blood vessel:	n/a
25	chr11:48880009-48880059	MCF10A-Er-Src	breast:	n/a
26	chr11:48901705-48901755	HCT-116	colon:	n/a
27	chr11:48901914-48901964	Jurkat	blood:	n/a
28	chr11:48902014-48902064	HIPEpiC	eye:	n/a
29	chr11:48902014-48902064	IMR90	lung:	fetal
30	chr11:48880009-48880059	BE2_C	brain:	n/a
31	chr11:48880009-48880059	IMR90	lung:	fetal
32	chr11:48901914-48901964	HepG2	liver:	n/a
33	chr11:48901914-48901964	HCF	heart:	n/a
34	chr11:48901914-48901964	Hela-S3	cervix:	n/a
35	chr11:48902014-48902064	NT2-D1	testis:	n/a
36	chr11:48902014-48902064	AG09319	gingival:	n/a
37	chr11:48880009-48880059	HCT-116	colon:	n/a
38	chr11:48901914-48901964	HRCEpiC	kidney:	n/a
39	chr11:48902014-48902064	NHDF-neo	bronchial:	n/a
40	chr11:48901914-48901964	LNCaP	prostate:	n/a
41	chr11:48902014-48902064	SK-N-SH	brain:	n/a
42	chr11:48902014-48902064	Hela-S3	cervix:	n/a
43	chr11:48902014-48902064	Jurkat	blood:	n/a
44	chr11:48901914-48901964	CMK	blood:	n/a
45	chr11:48901914-48901964	IMR90	lung:	fetal
46	chr11:48901914-48901964	ECC-1	luminal epithelium:	n/a
47	chr11:48880009-48880059	T-47D	breast:	n/a
48	chr11:48901705-48901755	HRE	kidney:	n/a
49	chr11:48901705-48901755	Hela-S3	cervix:	n/a
50	chr11:48901914-48901964	PANC-1	pancreas:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr11:48862246..48863766-chr12:38036979..38038502,2	MCF-7	breast:
2	chr1:121484040..121484766-chr11:48865024..48865526,2	MCF-7	breast:
3	chr1:121484496..121485051-chr11:48865024..48865528,2	K562	blood:
4	chr11:48811378..48811898-chr8:46850618..46851141,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000255551	TF binding region
ENSG00000254920	TF binding region
ENSG00000255551	CpG island
ENSG00000254920	CpG island

Extended variants
information (count: 14210 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:14210 , 50 per page) page: 1 2 3 4 5 6 7 ... 285

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs187080260	chr11:48735413-48735414	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs112792112	chr11:48735438-48735439	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs564273083	chr11:48735441-48735442	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs373491097	chr11:48735447-48735448	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs142533078	chr11:48735462-48735463	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs573908799	chr11:48735466-48735467	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs373051786	chr11:48735479-48735480	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs536529504	chr11:48735484-48735485	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs146851363	chr11:48735486-48735487	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs192852268	chr11:48735491-48735492	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs8189319	chr11:48735499-48735500	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs544950845	chr11:48735506-48735507	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs12274623	chr11:48735507-48735508	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs115607289	chr11:48735518-48735519	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs183699973	chr11:48735555-48735556	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs550030441	chr11:48735567-48735568	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs78761277	chr11:48735589-48735590	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs561047504	chr11:48735636-48735637	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs569753803	chr11:48735637-48735638	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs2135687	chr11:48735660-48735661	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs548999015	chr11:48735665-48735666	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs529941956	chr11:48735667-48735668	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs565544802	chr11:48735671-48735672	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs546573395	chr11:48735689-48735690	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs2135686	chr11:48735702-48735703	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs375254851	chr11:48735704-48735705	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs532312799	chr11:48735741-48735742	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs193294749	chr11:48735817-48735818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs144150808	chr11:48735855-48735856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs78608213	chr11:48735856-48735857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs74806954	chr11:48735860-48735861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs75365829	chr11:48735863-48735864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs530875463	chr11:48735864-48735865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs80089656	chr11:48735866-48735867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs77644476	chr11:48735872-48735873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs550692701	chr11:48735875-48735876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs112435356	chr11:48735876-48735877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs111824156	chr11:48735886-48735887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs76436782	chr11:48735887-48735888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs76664065	chr11:48735891-48735892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs3942786	chr11:48735892-48735893	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs79114764	chr11:48735893-48735894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs79312104	chr11:48735895-48735896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs537225464	chr11:48735896-48735897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs536893055	chr11:48735900-48735901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs77774115	chr11:48735901-48735902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs76526392	chr11:48735910-48735911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs193076650	chr11:48735913-48735914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs76656731	chr11:48735918-48735919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs111512443	chr11:48735921-48735922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Parathyroid adenoma	22454399	CNVD
Medulloblastoma	21979893	CNVD
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
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
Breast cancer	17603634	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Lung cancer	18438408	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Myelofibrosis	22110671	CNVD
Melanoma	18172304	CNVD
Intracranial ependymoma	16609018	CNVD
Myxofibrosarcoma	16751306	CNVD
Potocki-Shaffer syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	16608533	CNVD
Hirschsprung''s Disease	21712996	CNVD
Follicular lymphoma	20505157	CNVD
Colorectal cancer	21128281	CNVD
Breast cancer	20409316	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Mantle cell lymphoma	19029149	CNVD
Glioblastoma multiforme	21138945	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22581003	CNVD
Breast cancer	21990379	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	20967226	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
early-passage human iPS cells	21368824	CNVD
Medulloblastoma	21163964	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Intellectual disability	22045946	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:710 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:48731400-48735600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr11:48733200-48735800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
3	chr11:48734200-48738400	Weak transcription	Right Atrium	heart
4	chr11:48736600-48742600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr11:48738000-48739600	ZNF genes & repeats	Adipose Nuclei	Adipose
6	chr11:48738400-48739200	Active TSS	Right Atrium	heart
7	chr11:48738800-48742000	ZNF genes & repeats	Liver	Liver
8	chr11:48741200-48742400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr11:48743800-48744600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
10	chr11:48744200-48744800	ZNF genes & repeats	Liver	Liver
11	chr11:48750800-48751400	ZNF genes & repeats	Adipose Nuclei	Adipose
12	chr11:48762000-48763800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
13	chr11:48762600-48764200	ZNF genes & repeats	Liver	Liver
14	chr11:48763000-48763600	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr11:48763000-48765600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
16	chr11:48763200-48763400	ZNF genes & repeats	Brain Cingulate Gyrus	brain
17	chr11:48763200-48763600	Active TSS	Aorta	Aorta
18	chr11:48763200-48763600	ZNF genes & repeats	Brain Anterior Caudate	brain
19	chr11:48763200-48763600	ZNF genes & repeats	Brain Hippocampus Middle	brain
20	chr11:48763200-48763600	ZNF genes & repeats	Brain Substantia Nigra	brain
21	chr11:48763200-48766200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr11:48763200-48766200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
23	chr11:48771800-48772200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr11:48774600-48774800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr11:48774800-48776400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr11:48775400-48776000	Active TSS	Aorta	Aorta
27	chr11:48775800-48776600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr11:48776400-48776600	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr11:48777400-48780800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
30	chr11:48778200-48781800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
31	chr11:48779600-48782600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr11:48787200-48792800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr11:48789200-48789800	Active TSS	Fetal Heart	heart
34	chr11:48789800-48796200	Weak transcription	Fetal Heart	heart
35	chr11:48791000-48791200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr11:48791200-48796200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr11:48793000-48793200	Enhancers	Pancreatic Islets	Pancreatic Islet
38	chr11:48793200-48793400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr11:48793200-48796200	Weak transcription	Pancreatic Islets	Pancreatic Islet
40	chr11:48794800-48796200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr11:48795400-48796200	Weak transcription	Duodenum Smooth Muscle	Duodenum
42	chr11:48796000-48797600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
43	chr11:48796000-48802600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr11:48796200-48796400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
45	chr11:48796200-48796400	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr11:48796200-48796400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr11:48796200-48796400	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
48	chr11:48796200-48796400	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
49	chr11:48796200-48796400	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr11:48796200-48796400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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