Variant report

Variant	nsv897354
Chromosome Location	chr11:48616694-48958687
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3443)
CpG islands
(count:793)
Chromatin interactive
region (count:5)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3443 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

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	chr11:48880374-48880748	K562	blood:	n/a	n/a
5	ATF1	chr11:48849264-48849333	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	chr11:48845364-48845733	K562	blood:	n/a	n/a
9	ATF1	chr11:48896850-48897050	K562	blood:	n/a	n/a
10	ATF1	chr11:48895825-48896343	K562	blood:	n/a	n/a
11	ATF1	chr11:48796111-48796444	K562	blood:	n/a	n/a
12	ATF1	chr11:48940082-48940286	K562	blood:	n/a	n/a
13	ATF1	chr11:48859189-48859770	K562	blood:	n/a	n/a
14	ATF1	chr11:48883351-48883720	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	chr11:48956270-48956471	K562	blood:	n/a	n/a
18	BACH1	chr11:48814467-48814498	K562	blood:	n/a	n/a
19	BACH1	chr11:48881669-48882080	K562	blood:	n/a	n/a
20	BATF	chr11:48885664-48885889	GM12878	blood:	n/a	n/a
21	BATF	chr11:48894608-48895288	GM12878	blood:	n/a	n/a
22	BATF	chr11:48844664-48844887	GM12878	blood:	n/a	n/a
23	BATF	chr11:48886811-48887099	GM12878	blood:	n/a	n/a
24	BATF	chr11:48776576-48776723	GM12878	blood:	n/a	n/a
25	BATF	chr11:48842846-48843034	GM12878	blood:	n/a	n/a
26	BATF	chr11:48931968-48932274	GM12878	blood:	n/a	n/a
27	BATF	chr11:48955305-48955628	GM12878	blood:	n/a	n/a
28	BATF	chr11:48859171-48859730	GM12878	blood:	n/a	n/a
29	BATF	chr11:48839569-48839852	GM12878	blood:	n/a	n/a
30	BATF	chr11:48934117-48934343	GM12878	blood:	n/a	n/a
31	BATF	chr11:48906491-48906775	GM12878	blood:	n/a	chr11:48906618-48906628
32	BATF	chr11:48916722-48917006	GM12878	blood:	n/a	chr11:48916904-48916914
33	BATF	chr11:48861740-48862096	GM12878	blood:	n/a	n/a
34	BATF	chr11:48888085-48888631	GM12878	blood:	n/a	n/a
35	BATF	chr11:48856700-48857102	GM12878	blood:	n/a	n/a
36	BATF	chr11:48860990-48861237	GM12878	blood:	n/a	n/a
37	BATF	chr11:48945011-48945390	GM12878	blood:	n/a	n/a
38	BATF	chr11:48856704-48856991	GM12878	blood:	n/a	n/a
39	BATF	chr11:48828245-48828541	GM12878	blood:	n/a	n/a
40	BATF	chr11:48775372-48775512	GM12878	blood:	n/a	n/a
41	BATF	chr11:48775367-48775560	GM12878	blood:	n/a	n/a
42	BATF	chr11:48887996-48888565	GM12878	blood:	n/a	n/a
43	BATF	chr11:48877878-48878291	GM12878	blood:	n/a	n/a
44	BATF	chr11:48916618-48916954	GM12878	blood:	n/a	chr11:48916904-48916914
45	BATF	chr11:48834403-48834545	GM12878	blood:	n/a	n/a
46	BATF	chr11:48932107-48932317	GM12878	blood:	n/a	n/a
47	BATF	chr11:48894524-48895290	GM12878	blood:	n/a	n/a
48	BATF	chr11:48805015-48805320	GM12878	blood:	n/a	n/a
49	BATF	chr11:48898982-48899252	GM12878	blood:	n/a	n/a
50	BATF	chr11:48934181-48934321	GM12878	blood:	n/a	n/a

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:48922035-48922085	T-47D	breast:	n/a
2	chr11:48901914-48901964	ECC-1	luminal epithelium:	n/a
3	chr11:48922674-48922724	Jurkat	blood:	n/a
4	chr11:48924804-48924854	PFSK-1	brain:	n/a
5	chr11:48901705-48901755	ovcar-3	ovarian:	n/a
6	chr11:48922674-48922724	HUVEC	blood vessel:	n/a
7	chr11:48923577-48923627	MCF10A-Er-Src	breast:	n/a
8	chr11:48922741-48922791	AG10803	skin:	n/a
9	chr11:48923577-48923627	BE2_C	brain:	n/a
10	chr11:48922035-48922085	Hela-S3	cervix:	n/a
11	chr11:48923577-48923627	U87	brain:	n/a
12	chr11:48922035-48922085	HUVEC	blood vessel:	n/a
13	chr11:48922674-48922724	HIPEpiC	eye:	n/a
14	chr11:48922269-48922319	PFSK-1	brain:	n/a
15	chr11:48922674-48922724	HAEpiC	amniotic membrane:	n/a
16	chr11:48901914-48901964	ProgFib	skin:	n/a
17	chr11:48922035-48922085	GM12892	blood:	n/a
18	chr11:48924804-48924854	HRE	kidney:	n/a
19	chr11:48901914-48901964	SK-N-MC	brain:	n/a
20	chr11:48923668-48923718	IMR90	lung:	fetal
21	chr11:48922035-48922085	HCT-116	colon:	n/a
22	chr11:48901705-48901755	GM12892	blood:	n/a
23	chr11:48922741-48922791	NHDF-neo	bronchial:	n/a
24	chr11:48924804-48924854	A549	lung:	n/a
25	chr11:48922271-48922321	MCF-7	breast:	n/a
26	chr11:48923668-48923718	NT2-D1	testis:	n/a
27	chr11:48901914-48901964	GM12892	blood:	n/a
28	chr11:48922269-48922319	NB4	blood:	n/a
29	chr11:48924804-48924854	IMR90	lung:	fetal
30	chr11:48923392-48923442	ECC-1	luminal epithelium:	n/a
31	chr11:48922674-48922724	PrEC	prostate:	n/a
32	chr11:48880009-48880059	HCT-116	colon:	n/a
33	chr11:48922269-48922319	SAEC	small airway:	n/a
34	chr11:48922674-48922724	SAEC	small airway:	n/a
35	chr11:48923392-48923442	SK-N-SH	brain:	n/a
36	chr11:48922674-48922724	AG09309	skin:	n/a
37	chr11:48901914-48901964	PrEC	prostate:	n/a
38	chr11:48901914-48901964	AoSMC	blood vessel:	n/a
39	chr11:48922035-48922085	BJ	skin:	n/a
40	chr11:48923577-48923627	AG04449	skin:	fetal
41	chr11:48923392-48923442	GM12878	blood:	n/a
42	chr11:48901914-48901964	AG09309	skin:	n/a
43	chr11:48901914-48901964	HL-60	blood:	n/a
44	chr11:48922271-48922321	A549	lung:	n/a
45	chr11:48922035-48922085	Hepatocyte	liver:	n/a
46	chr11:48880009-48880059	MCF-7	breast:	n/a
47	chr11:48922741-48922791	SK-N-SH_RA	brain:	n/a
48	chr11:48923668-48923718	HAEpiC	amniotic membrane:	n/a
49	chr11:48922674-48922724	ProgFib	skin:	n/a
50	chr11:48923392-48923442	HEEpiC	esophagus:	n/a

(count:5 , 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	chr1:121484902..121485419-chr11:48946286..48946806,2	MCF-7	breast:
4	chr11:48811378..48811898-chr8:46850618..46851141,2	MCF-7	breast:
5	chr1:121484496..121485051-chr11:48865024..48865528,2	K562	blood:

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

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

No data

Variant related genes	Relation type
ENSG00000255551	TF binding region
ENSG00000254920	TF binding region
ENSG00000255527	TF binding region
OR4A44P	TF binding region
ENSG00000254728	TF binding region
OR4A42P	TF binding region
ENSG00000255551	CpG island
ENSG00000254920	CpG island
ENSG00000255527	CpG island
OR4A44P	CpG island
ENSG00000254728	CpG island
OR4A42P	CpG island

Extended variants
information (count: 19443 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:19443 , 50 per page) page: 1 2 3 4 5 6 7 ... 389

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370496922	chr11:48628770-48628771	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs577216921	chr11:48628783-48628784	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs199609923	chr11:48632809-48632810	Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs577252709	chr11:48632818-48632819	Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs545924263	chr11:48632820-48632821	Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs7481141	chr11:48632821-48632822	Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs562741938	chr11:48632824-48632825	Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs576272399	chr11:48632833-48632834	Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs542079842	chr11:48632917-48632918	Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs374241537	chr11:48632918-48632919	Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs527255391	chr11:48632948-48632949	Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs368953656	chr11:48632950-48632951	Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs12416716	chr11:48632976-48632977	Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs146478361	chr11:48632977-48632978	Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs532603844	chr11:48632985-48632986	Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs141012902	chr11:48633006-48633007	Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs190710030	chr11:48633034-48633035	Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs535647233	chr11:48633041-48633042	Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs548979942	chr11:48633074-48633075	Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs138438606	chr11:48633080-48633081	Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs182953708	chr11:48633089-48633090	Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs187660583	chr11:48633107-48633108	Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs191654461	chr11:48633109-48633110	Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs182709542	chr11:48633114-48633115	Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs11039875	chr11:48633117-48633118	Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs72906652	chr11:48633120-48633121	Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs576184543	chr11:48633129-48633130	Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs542032812	chr11:48633147-48633148	Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs557448748	chr11:48633151-48633152	Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs187365925	chr11:48633184-48633185	Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs115275826	chr11:48633194-48633195	Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs377166879	chr11:48633197-48633198	Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs572171691	chr11:48644136-48644137	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs541127267	chr11:48644143-48644144	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs113707670	chr11:48644163-48644164	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs577783622	chr11:48644171-48644172	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs543325345	chr11:48644207-48644208	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs188286901	chr11:48644228-48644229	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs529183536	chr11:48644230-48644231	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs541810363	chr11:48644231-48644232	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs146639015	chr11:48644251-48644252	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs527736470	chr11:48644254-48644255	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs547876368	chr11:48644284-48644285	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs139370329	chr11:48646673-48646674	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs370694970	chr11:48646704-48646705	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs536227475	chr11:48646711-48646712	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs573976490	chr11:48647795-48647796	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs201472181	chr11:48647804-48647805	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs186411569	chr11:48647849-48647850	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs560260734	chr11:48647884-48647885	Inactive region	TF binding region	1 gene(s)	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
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Medulloblastoma	21163964	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
early-passage human iPS cells	21368824	CNVD
Intellectual disability	22045946	CNVD
Breast cancer	22522925	CNVD
small cell lung cancer	17426248	CNVD

Chromatin state (count:797 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:48632800-48633200	Active TSS	Fetal Heart	heart
2	chr11:48670600-48672800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
3	chr11:48671600-48672200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
4	chr11:48671600-48674000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
5	chr11:48679800-48680400	ZNF genes & repeats	Adipose Nuclei	Adipose
6	chr11:48680200-48688400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr11:48681200-48684000	ZNF genes & repeats	Liver	Liver
8	chr11:48685000-48686400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr11:48686800-48688000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
10	chr11:48688200-48691800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
11	chr11:48694000-48695400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
12	chr11:48694200-48695800	ZNF genes & repeats	Adipose Nuclei	Adipose
13	chr11:48695400-48695800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr11:48696800-48698200	ZNF genes & repeats	Liver	Liver
15	chr11:48697200-48699000	ZNF genes & repeats	Adipose Nuclei	Adipose
16	chr11:48698200-48698800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr11:48704600-48705400	ZNF genes & repeats	Adipose Nuclei	Adipose
18	chr11:48711000-48712200	ZNF genes & repeats	Liver	Liver
19	chr11:48717600-48718400	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
20	chr11:48718000-48718200	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
21	chr11:48718000-48718200	ZNF genes & repeats	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr11:48718000-48718200	ZNF genes & repeats	HUVEC	blood vessel
23	chr11:48718000-48718200	ZNF genes & repeats	NH-A	brain
24	chr11:48718000-48718400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
25	chr11:48718000-48718400	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
26	chr11:48718000-48718600	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
27	chr11:48718000-48719000	ZNF genes & repeats	Adipose Nuclei	Adipose
28	chr11:48718200-48718400	ZNF genes & repeats	Brain Inferior Temporal Lobe	brain
29	chr11:48728000-48728800	ZNF genes & repeats	Liver	Liver
30	chr11:48728400-48728800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
31	chr11:48731000-48732600	ZNF genes & repeats	Liver	Liver
32	chr11:48731400-48733000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
33	chr11:48731400-48735600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr11:48732600-48733400	Weak transcription	Liver	Liver
35	chr11:48733200-48734600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
36	chr11:48733200-48735800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
37	chr11:48733400-48734200	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
38	chr11:48733400-48734200	ZNF genes & repeats	Liver	Liver
39	chr11:48733400-48734400	ZNF genes & repeats	Adipose Nuclei	Adipose
40	chr11:48733800-48734200	Active TSS	Right Atrium	heart
41	chr11:48734200-48738400	Weak transcription	Right Atrium	heart
42	chr11:48736600-48742600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr11:48738000-48739600	ZNF genes & repeats	Adipose Nuclei	Adipose
44	chr11:48738400-48739200	Active TSS	Right Atrium	heart
45	chr11:48738800-48742000	ZNF genes & repeats	Liver	Liver
46	chr11:48741200-48742400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr11:48743800-48744600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
48	chr11:48744200-48744800	ZNF genes & repeats	Liver	Liver
49	chr11:48750800-48751400	ZNF genes & repeats	Adipose Nuclei	Adipose
50	chr11:48762000-48763800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum

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