Variant report

Variant	nsv554220
Chromosome Location	chr11:48416423-48958687
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3603)
CpG islands
(count:976)
Chromatin interactive
region (count:6)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3603 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:48600198-48600306	K562	blood:	n/a	n/a
2	ARID3A	chr11:48880376-48880748	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:48895975-48896341	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:48892892-48893269	HepG2	liver:	n/a	n/a
5	ATF1	chr11:48880374-48880748	K562	blood:	n/a	n/a
6	ATF1	chr11:48895825-48896343	K562	blood:	n/a	n/a
7	ATF1	chr11:48859189-48859770	K562	blood:	n/a	n/a
8	ATF1	chr11:48896850-48897050	K562	blood:	n/a	n/a
9	ATF1	chr11:48940082-48940286	K562	blood:	n/a	n/a
10	ATF1	chr11:48892890-48893270	K562	blood:	n/a	n/a
11	ATF1	chr11:48867583-48867993	K562	blood:	n/a	n/a
12	ATF1	chr11:48845364-48845733	K562	blood:	n/a	n/a
13	ATF1	chr11:48849264-48849333	K562	blood:	n/a	n/a
14	ATF1	chr11:48883351-48883720	K562	blood:	n/a	n/a
15	ATF1	chr11:48796111-48796444	K562	blood:	n/a	n/a
16	ATF3	chr11:48892858-48893151	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF3	chr11:48845439-48845653	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr11:48956270-48956471	K562	blood:	n/a	n/a
19	BACH1	chr11:48814467-48814498	K562	blood:	n/a	n/a
20	BACH1	chr11:48881669-48882080	K562	blood:	n/a	n/a
21	BATF	chr11:48932107-48932317	GM12878	blood:	n/a	n/a
22	BATF	chr11:48817733-48818014	GM12878	blood:	n/a	n/a
23	BATF	chr11:48931968-48932274	GM12878	blood:	n/a	n/a
24	BATF	chr11:48877440-48877803	GM12878	blood:	n/a	n/a
25	BATF	chr11:48946780-48947152	GM12878	blood:	n/a	n/a
26	BATF	chr11:48953209-48953631	GM12878	blood:	n/a	n/a
27	BATF	chr11:48867677-48867900	GM12878	blood:	n/a	n/a
28	BATF	chr11:48945095-48945310	GM12878	blood:	n/a	n/a
29	BATF	chr11:48906491-48906775	GM12878	blood:	n/a	chr11:48906618-48906628
30	BATF	chr11:48883215-48883597	GM12878	blood:	n/a	n/a
31	BATF	chr11:48834403-48834545	GM12878	blood:	n/a	n/a
32	BATF	chr11:48940420-48940720	GM12878	blood:	n/a	n/a
33	BATF	chr11:48883213-48883919	GM12878	blood:	n/a	n/a
34	BATF	chr11:48828245-48828584	GM12878	blood:	n/a	n/a
35	BATF	chr11:48898982-48899252	GM12878	blood:	n/a	n/a
36	BATF	chr11:48842846-48843034	GM12878	blood:	n/a	n/a
37	BATF	chr11:48894524-48895290	GM12878	blood:	n/a	n/a
38	BATF	chr11:48854717-48855191	GM12878	blood:	n/a	n/a
39	BATF	chr11:48892880-48893156	GM12878	blood:	n/a	n/a
40	BATF	chr11:48866749-48866988	GM12878	blood:	n/a	n/a
41	BATF	chr11:48934117-48934343	GM12878	blood:	n/a	n/a
42	BATF	chr11:48953227-48953611	GM12878	blood:	n/a	n/a
43	BATF	chr11:48906543-48906879	GM12878	blood:	n/a	chr11:48906618-48906628
44	BATF	chr11:48810099-48810738	GM12878	blood:	n/a	n/a
45	BATF	chr11:48834286-48834608	GM12878	blood:	n/a	n/a
46	BATF	chr11:48861796-48862105	GM12878	blood:	n/a	n/a
47	BATF	chr11:48916722-48917006	GM12878	blood:	n/a	chr11:48916904-48916914
48	BATF	chr11:48859171-48859730	GM12878	blood:	n/a	n/a
49	BATF	chr11:48810174-48810367	GM12878	blood:	n/a	n/a
50	BATF	chr11:48856700-48857102	GM12878	blood:	n/a	n/a

(count:976 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:48923668-48923718	GM12878	blood:	n/a
2	chr11:48901914-48901964	PrEC	prostate:	n/a
3	chr11:48509778-48509828	HRE	kidney:	n/a
4	chr11:48923392-48923442	SK-N-SH	brain:	n/a
5	chr11:48880009-48880059	HCPEpiC	choroid plexus:	n/a
6	chr11:48922741-48922791	HEEpiC	esophagus:	n/a
7	chr11:48922035-48922085	Caco-2	colon:	n/a
8	chr11:48509488-48509538	IMR90	lung:	fetal
9	chr11:48922674-48922724	PFSK-1	brain:	n/a
10	chr11:48509488-48509538	HRPEpiC	eye:	n/a
11	chr11:48880009-48880059	Hela-S3	cervix:	n/a
12	chr11:48922271-48922321	NT2-D1	testis:	n/a
13	chr11:48922674-48922724	HIPEpiC	eye:	n/a
14	chr11:48922035-48922085	HEK293	kidney:	embryo
15	chr11:48922271-48922321	PFSK-1	brain:	n/a
16	chr11:48902014-48902064	SAEC	small airway:	n/a
17	chr11:48510647-48510697	HCM	heart:	n/a
18	chr11:48923668-48923718	NB4	blood:	n/a
19	chr11:48880009-48880059	Jurkat	blood:	n/a
20	chr11:48924804-48924854	NHDF-neo	bronchial:	n/a
21	chr11:48509778-48509828	SAEC	small airway:	n/a
22	chr11:48922271-48922321	T-47D	breast:	n/a
23	chr11:48922269-48922319	HCF	heart:	n/a
24	chr11:48901705-48901755	Hela-S3	cervix:	n/a
25	chr11:48880009-48880059	HepG2	liver:	n/a
26	chr11:48510647-48510697	NHBE	bronchial:	n/a
27	chr11:48923577-48923627	NT2-D1	testis:	n/a
28	chr11:48509778-48509828	NT2-D1	testis:	n/a
29	chr11:48922269-48922319	SKMC	muscle:	n/a
30	chr11:48923668-48923718	HCT-116	colon:	n/a
31	chr11:48880009-48880059	NHBE	bronchial:	n/a
32	chr11:48922035-48922085	NHDF-neo	bronchial:	n/a
33	chr11:48922271-48922321	ovcar-3	ovarian:	n/a
34	chr11:48901914-48901964	AG04450	lung:	fetal
35	chr11:48922269-48922319	ECC-1	luminal epithelium:	n/a
36	chr11:48922035-48922085	HCM	heart:	n/a
37	chr11:48924804-48924854	PFSK-1	brain:	n/a
38	chr11:48901705-48901755	H1-hESC	embryonic stem cell:	embryo
39	chr11:48880009-48880059	LNCaP	prostate:	n/a
40	chr11:48509488-48509538	MCF10A-Er-Src	breast:	n/a
41	chr11:48922674-48922724	HCT-116	colon:	n/a
42	chr11:48923392-48923442	MCF-7	breast:	n/a
43	chr11:48923577-48923627	PrEC	prostate:	n/a
44	chr11:48922035-48922085	Hela-S3	cervix:	n/a
45	chr11:48922674-48922724	MCF10A-Er-Src	breast:	n/a
46	chr11:48902014-48902064	HEEpiC	esophagus:	n/a
47	chr11:48509778-48509828	HMEC	breast:	n/a
48	chr11:48922035-48922085	GM19239	blood:	n/a
49	chr11:48922035-48922085	HCT-116	colon:	n/a
50	chr11:48880009-48880059	ovcar-3	ovarian:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:121484902..121485419-chr11:48946286..48946806,2	MCF-7	breast:
2	chr1:121484040..121484766-chr11:48865024..48865526,2	MCF-7	breast:
3	chr11:48862246..48863766-chr12:38036979..38038502,2	MCF-7	breast:
4	chr11:48478071..48478587-chr11:49191267..49191777,2	MCF-7	breast:
5	chr1:121484496..121485051-chr11:48865024..48865528,2	K562	blood:
6	chr11:48811378..48811898-chr8:46850618..46851141,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC084851.1-4	chr11:48929840-48930498	NONHSAT021302
2	lnc-AC084851.1-5	chr11:48919940-48920255	NONHSAT021301
3	lnc-OR4C5-1	chr11:48507915-48508377	NONHSAT021297
4	lnc-AC084851.1-4	chr11:48928655-48928750	NONHSAT021302
5	lnc-AC084851.1-5	chr11:48916513-48916636	NONHSAT021301
6	lnc-AC084851.1-5	chr11:48919540-48919822	NONHSAT021301
7	lnc-AC084851.1-5	chr11:48914808-48914900	NONHSAT021301

No data

Variant related genes	Relation type
OR4C9P	TF binding region
OR4C10P	TF binding region
OR4A47	TF binding region
OR4C2P	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
OR4C10P	CpG island
OR4A47	CpG island
OR4C2P	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: 19736 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:19736 , 50 per page) page: 1 2 3 4 5 6 7 ... 395

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs184018331	chr11:48436948-48436949	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs613838	chr11:48439807-48439808	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs186915414	chr11:48439902-48439903	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs532019408	chr11:48440763-48440764	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs151129707	chr11:48455643-48455644	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs544470165	chr11:48455665-48455666	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs551877577	chr11:48455685-48455686	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs571635475	chr11:48455687-48455688	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs4882064	chr11:48455757-48455758	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs535790161	chr11:48455772-48455773	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs555697726	chr11:48455790-48455791	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs530092064	chr11:48455791-48455792	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs574328381	chr11:48487751-48487752	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs371144119	chr11:48487757-48487758	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs554006216	chr11:48487763-48487764	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs539904605	chr11:48487773-48487774	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs559835083	chr11:48487780-48487781	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs36105506	chr11:48488845-48488846	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs141858706	chr11:48488896-48488897	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs185455714	chr11:48488901-48488902	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs368635166	chr11:48488973-48488974	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs556297304	chr11:48488995-48488996	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs570240203	chr11:48488998-48488999	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs200545698	chr11:48489014-48489015	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs190377088	chr11:48489023-48489024	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs193258689	chr11:48489033-48489034	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs576388622	chr11:48489036-48489037	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs113784301	chr11:48489069-48489070	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs138114797	chr11:48489084-48489085	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs183646568	chr11:48489118-48489119	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs537488376	chr11:48490069-48490070	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs557049678	chr11:48490093-48490094	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs182311875	chr11:48490098-48490099	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs73464765	chr11:48490110-48490111	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs535351174	chr11:48490114-48490115	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs545626641	chr11:48490150-48490151	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs555198569	chr11:48490160-48490161	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs186973215	chr11:48490193-48490194	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs540799397	chr11:48490222-48490223	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs183243013	chr11:48491258-48491259	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs4882076	chr11:48491270-48491271	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs530050704	chr11:48491271-48491272	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs371119854	chr11:48491281-48491282	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs146284381	chr11:48491320-48491321	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs565663890	chr11:48491323-48491324	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs573165138	chr11:48507969-48507970	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
47	rs538884728	chr11:48507981-48507982	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
48	rs532028336	chr11:48507982-48507983	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
49	rs182597874	chr11:48507995-48507996	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
50	rs187106158	chr11:48508046-48508047	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Glioma	20126413	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
small cell lung cancer	17426248	CNVD

Chromatin state (count:801 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

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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