Variant report

Variant	nsv897342
Chromosome Location	chr11:48485877-48924826
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2841)
CpG islands
(count:977)
Chromatin interactive
region (count:4)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2841 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:48880376-48880748	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:48600198-48600306	K562	blood:	n/a	n/a
3	ARID3A	chr11:48892892-48893269	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:48895975-48896341	HepG2	liver:	n/a	n/a
5	ATF1	chr11:48883351-48883720	K562	blood:	n/a	n/a
6	ATF1	chr11:48896850-48897050	K562	blood:	n/a	n/a
7	ATF1	chr11:48796111-48796444	K562	blood:	n/a	n/a
8	ATF1	chr11:48849264-48849333	K562	blood:	n/a	n/a
9	ATF1	chr11:48867583-48867993	K562	blood:	n/a	n/a
10	ATF1	chr11:48892890-48893270	K562	blood:	n/a	n/a
11	ATF1	chr11:48895825-48896343	K562	blood:	n/a	n/a
12	ATF1	chr11:48880374-48880748	K562	blood:	n/a	n/a
13	ATF1	chr11:48845364-48845733	K562	blood:	n/a	n/a
14	ATF1	chr11:48859189-48859770	K562	blood:	n/a	n/a
15	ATF3	chr11:48892858-48893151	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF3	chr11:48845439-48845653	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr11:48881669-48882080	K562	blood:	n/a	n/a
18	BACH1	chr11:48814467-48814498	K562	blood:	n/a	n/a
19	BATF	chr11:48844232-48844479	GM12878	blood:	n/a	n/a
20	BATF	chr11:48828245-48828584	GM12878	blood:	n/a	n/a
21	BATF	chr11:48894524-48895290	GM12878	blood:	n/a	n/a
22	BATF	chr11:48861796-48862105	GM12878	blood:	n/a	n/a
23	BATF	chr11:48805015-48805320	GM12878	blood:	n/a	n/a
24	BATF	chr11:48885554-48885939	GM12878	blood:	n/a	n/a
25	BATF	chr11:48898958-48899437	GM12878	blood:	n/a	n/a
26	BATF	chr11:48885664-48885889	GM12878	blood:	n/a	n/a
27	BATF	chr11:48867677-48867900	GM12878	blood:	n/a	n/a
28	BATF	chr11:48892880-48893156	GM12878	blood:	n/a	n/a
29	BATF	chr11:48895948-48896327	GM12878	blood:	n/a	n/a
30	BATF	chr11:48834403-48834545	GM12878	blood:	n/a	n/a
31	BATF	chr11:48894608-48895288	GM12878	blood:	n/a	n/a
32	BATF	chr11:48860990-48861237	GM12878	blood:	n/a	n/a
33	BATF	chr11:48866749-48866988	GM12878	blood:	n/a	n/a
34	BATF	chr11:48854717-48855191	GM12878	blood:	n/a	n/a
35	BATF	chr11:48887996-48888565	GM12878	blood:	n/a	n/a
36	BATF	chr11:48916722-48917006	GM12878	blood:	n/a	chr11:48916904-48916914
37	BATF	chr11:48828245-48828541	GM12878	blood:	n/a	n/a
38	BATF	chr11:48775372-48775512	GM12878	blood:	n/a	n/a
39	BATF	chr11:48895950-48896265	GM12878	blood:	n/a	n/a
40	BATF	chr11:48856704-48856991	GM12878	blood:	n/a	n/a
41	BATF	chr11:48831050-48831447	GM12878	blood:	n/a	n/a
42	BATF	chr11:48776576-48776723	GM12878	blood:	n/a	n/a
43	BATF	chr11:48810099-48810738	GM12878	blood:	n/a	n/a
44	BATF	chr11:48834286-48834608	GM12878	blood:	n/a	n/a
45	BATF	chr11:48916618-48916954	GM12878	blood:	n/a	chr11:48916904-48916914
46	BATF	chr11:48776572-48776725	GM12878	blood:	n/a	n/a
47	BATF	chr11:48804986-48805223	GM12878	blood:	n/a	n/a
48	BATF	chr11:48861740-48862096	GM12878	blood:	n/a	n/a
49	BATF	chr11:48741581-48741798	GM12878	blood:	n/a	n/a
50	BATF	chr11:48883215-48883597	GM12878	blood:	n/a	n/a

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:48880009-48880059	NT2-D1	testis:	n/a
2	chr11:48880009-48880059	NT2-D1	testis:	n/a
3	chr11:48510647-48510697	AG04450	lung:	fetal
4	chr11:48923668-48923718	T-47D	breast:	n/a
5	chr11:48922035-48922085	GM06990	blood:	n/a
6	chr11:48901914-48901964	GM12891	blood:	n/a
7	chr11:48922271-48922321	SK-N-MC	brain:	n/a
8	chr11:48901705-48901755	ECC-1	luminal epithelium:	n/a
9	chr11:48509488-48509538	AG04449	skin:	fetal
10	chr11:48924804-48924854	GM12878	blood:	n/a
11	chr11:48922741-48922791	HRE	kidney:	n/a
12	chr11:48901914-48901964	Jurkat	blood:	n/a
13	chr11:48923577-48923627	HRE	kidney:	n/a
14	chr11:48922271-48922321	GM12891	blood:	n/a
15	chr11:48922035-48922085	ECC-1	luminal epithelium:	n/a
16	chr11:48924804-48924854	NB4	blood:	n/a
17	chr11:48922269-48922319	Hepatocyte	liver:	n/a
18	chr11:48922741-48922791	RPTEC	kidney:	n/a
19	chr11:48923668-48923718	HAEpiC	amniotic membrane:	n/a
20	chr11:48922741-48922791	GM12891	blood:	n/a
21	chr11:48880009-48880059	HCT-116	colon:	n/a
22	chr11:48510647-48510697	PrEC	prostate:	n/a
23	chr11:48901705-48901755	Hela-S3	cervix:	n/a
24	chr11:48922269-48922319	ovcar-3	ovarian:	n/a
25	chr11:48510647-48510697	HepG2	liver:	n/a
26	chr11:48902014-48902064	SK-N-MC	brain:	n/a
27	chr11:48923577-48923627	K562	blood:	n/a
28	chr11:48922271-48922321	ovcar-3	ovarian:	n/a
29	chr11:48880009-48880059	Caco-2	colon:	n/a
30	chr11:48924804-48924854	AG04449	skin:	fetal
31	chr11:48923577-48923627	AG09319	gingival:	n/a
32	chr11:48509488-48509538	HCPEpiC	choroid plexus:	n/a
33	chr11:48901914-48901964	A549	lung:	n/a
34	chr11:48902014-48902064	SK-N-SH	brain:	n/a
35	chr11:48901914-48901964	HEK293	kidney:	embryo
36	chr11:48902014-48902064	Hepatocyte	liver:	n/a
37	chr11:48922674-48922724	HMEC	breast:	n/a
38	chr11:48902014-48902064	CMK	blood:	n/a
39	chr11:48923668-48923718	HL-60	blood:	n/a
40	chr11:48901705-48901755	HRE	kidney:	n/a
41	chr11:48923668-48923718	AG04449	skin:	fetal
42	chr11:48510647-48510697	BJ	skin:	n/a
43	chr11:48923392-48923442	HRCEpiC	kidney:	n/a
44	chr11:48924804-48924854	IMR90	lung:	fetal
45	chr11:48922674-48922724	SK-N-SH_RA	brain:	n/a
46	chr11:48923668-48923718	NHDF-neo	bronchial:	n/a
47	chr11:48880009-48880059	H1-hESC	embryonic stem cell:	embryo
48	chr11:48924804-48924854	HCF	heart:	n/a
49	chr11:48922674-48922724	PFSK-1	brain:	n/a
50	chr11:48922741-48922791	NHBE	bronchial:	n/a

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

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

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR4C5-1	chr11:48507915-48508377	NONHSAT021297
2	lnc-AC084851.1-5	chr11:48919540-48919822	NONHSAT021301
3	lnc-AC084851.1-5	chr11:48919940-48920255	NONHSAT021301
4	lnc-AC084851.1-5	chr11:48916513-48916636	NONHSAT021301
5	lnc-AC084851.1-5	chr11:48914808-48914900	NONHSAT021301

No data

Variant related genes	Relation type
OR4C9P	TF binding region
OR4A47	TF binding region
OR4A41P	TF binding region
OR4A46P	TF binding region
ENSG00000255551	TF binding region
OR4A45P	TF binding region
ENSG00000254920	TF binding region
OR4R1P	TF binding region
OR4A43P	TF binding region
ENSG00000255527	TF binding region
OR4A40P	TF binding region
OR4A44P	TF binding region
OR4A48P	TF binding region
ENSG00000254728	TF binding region
OR4A42P	TF binding region
OR4C9P	CpG island
OR4A47	CpG island
OR4A41P	CpG island
OR4A46P	CpG island
ENSG00000255551	CpG island
OR4A45P	CpG island
ENSG00000254920	CpG island
OR4R1P	CpG island
OR4A43P	CpG island
ENSG00000255527	CpG island
OR4A40P	CpG island
OR4A44P	CpG island
OR4A48P	CpG island
ENSG00000254728	CpG island
OR4A42P	CpG island

Extended variants
information (count: 16326 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:16326 , 50 per page) page: 1 2 3 4 5 6 7 ... 327

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574328381	chr11:48487751-48487752	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs371144119	chr11:48487757-48487758	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs554006216	chr11:48487763-48487764	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs539904605	chr11:48487773-48487774	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs559835083	chr11:48487780-48487781	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs36105506	chr11:48488845-48488846	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs141858706	chr11:48488896-48488897	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs185455714	chr11:48488901-48488902	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs368635166	chr11:48488973-48488974	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs556297304	chr11:48488995-48488996	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs570240203	chr11:48488998-48488999	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs200545698	chr11:48489014-48489015	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs190377088	chr11:48489023-48489024	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs193258689	chr11:48489033-48489034	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs576388622	chr11:48489036-48489037	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs113784301	chr11:48489069-48489070	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs138114797	chr11:48489084-48489085	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs183646568	chr11:48489118-48489119	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs537488376	chr11:48490069-48490070	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs557049678	chr11:48490093-48490094	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs182311875	chr11:48490098-48490099	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs73464765	chr11:48490110-48490111	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs535351174	chr11:48490114-48490115	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs545626641	chr11:48490150-48490151	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs555198569	chr11:48490160-48490161	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs186973215	chr11:48490193-48490194	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs540799397	chr11:48490222-48490223	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs183243013	chr11:48491258-48491259	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs4882076	chr11:48491270-48491271	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs530050704	chr11:48491271-48491272	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs371119854	chr11:48491281-48491282	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs146284381	chr11:48491320-48491321	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs565663890	chr11:48491323-48491324	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs573165138	chr11:48507969-48507970	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
35	rs538884728	chr11:48507981-48507982	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs532028336	chr11:48507982-48507983	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
37	rs182597874	chr11:48507995-48507996	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
38	rs187106158	chr11:48508046-48508047	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
39	rs150949989	chr11:48508073-48508074	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
40	rs543988692	chr11:48508088-48508089	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
41	rs192022201	chr11:48508116-48508117	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
42	rs368896113	chr11:48508122-48508123	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
43	rs542289416	chr11:48508143-48508144	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
44	rs546450913	chr11:48508166-48508167	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
45	rs539841979	chr11:48508217-48508218	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
46	rs560455772	chr11:48508240-48508241	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
47	rs532677683	chr11:48508250-48508251	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
48	rs185446737	chr11:48508251-48508252	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
49	rs562954422	chr11:48508264-48508265	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
50	rs531916637	chr11:48508271-48508272	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

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	21293372	CNVD
Glioma	20126413	CNVD
Breast cancer	22522925	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Medulloblastoma	21163964	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
early-passage human iPS cells	21368824	CNVD
Intellectual disability	22045946	CNVD

Chromatin state (count:753 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:48515600-48516600	Enhancers	Pancreatic Islets	Pancreatic Islet
2	chr11:48569000-48569600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
3	chr11:48569200-48569600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
4	chr11:48576800-48577000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr11:48632800-48633200	Active TSS	Fetal Heart	heart
6	chr11:48670600-48672800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
7	chr11:48671600-48672200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
8	chr11:48671600-48674000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
9	chr11:48679800-48680400	ZNF genes & repeats	Adipose Nuclei	Adipose
10	chr11:48680200-48688400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr11:48681200-48684000	ZNF genes & repeats	Liver	Liver
12	chr11:48685000-48686400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr11:48686800-48688000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
14	chr11:48688200-48691800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
15	chr11:48694000-48695400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
16	chr11:48694200-48695800	ZNF genes & repeats	Adipose Nuclei	Adipose
17	chr11:48695400-48695800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr11:48696800-48698200	ZNF genes & repeats	Liver	Liver
19	chr11:48697200-48699000	ZNF genes & repeats	Adipose Nuclei	Adipose
20	chr11:48698200-48698800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr11:48704600-48705400	ZNF genes & repeats	Adipose Nuclei	Adipose
22	chr11:48711000-48712200	ZNF genes & repeats	Liver	Liver
23	chr11:48717600-48718400	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
24	chr11:48718000-48718200	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
25	chr11:48718000-48718200	ZNF genes & repeats	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr11:48718000-48718200	ZNF genes & repeats	HUVEC	blood vessel
27	chr11:48718000-48718200	ZNF genes & repeats	NH-A	brain
28	chr11:48718000-48718400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
29	chr11:48718000-48718400	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
30	chr11:48718000-48718600	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
31	chr11:48718000-48719000	ZNF genes & repeats	Adipose Nuclei	Adipose
32	chr11:48718200-48718400	ZNF genes & repeats	Brain Inferior Temporal Lobe	brain
33	chr11:48728000-48728800	ZNF genes & repeats	Liver	Liver
34	chr11:48728400-48728800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
35	chr11:48731000-48732600	ZNF genes & repeats	Liver	Liver
36	chr11:48731400-48733000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
37	chr11:48731400-48735600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr11:48732600-48733400	Weak transcription	Liver	Liver
39	chr11:48733200-48734600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
40	chr11:48733200-48735800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
41	chr11:48733400-48734200	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
42	chr11:48733400-48734200	ZNF genes & repeats	Liver	Liver
43	chr11:48733400-48734400	ZNF genes & repeats	Adipose Nuclei	Adipose
44	chr11:48733800-48734200	Active TSS	Right Atrium	heart
45	chr11:48734200-48738400	Weak transcription	Right Atrium	heart
46	chr11:48736600-48742600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr11:48738000-48739600	ZNF genes & repeats	Adipose Nuclei	Adipose
48	chr11:48738400-48739200	Active TSS	Right Atrium	heart
49	chr11:48738800-48742000	ZNF genes & repeats	Liver	Liver
50	chr11:48741200-48742400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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