Variant report

Variant	nsv897351
Chromosome Location	chr11:48576961-48958687
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3469)
CpG islands
(count:794)
Chromatin interactive
region (count:5)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3469 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

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	chr11:48895975-48896341	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:48600198-48600306	K562	blood:	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	chr11:48940082-48940286	K562	blood:	n/a	n/a
7	ATF1	chr11:48867583-48867993	K562	blood:	n/a	n/a
8	ATF1	chr11:48849264-48849333	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	chr11:48883351-48883720	K562	blood:	n/a	n/a
12	ATF1	chr11:48895825-48896343	K562	blood:	n/a	n/a
13	ATF1	chr11:48859189-48859770	K562	blood:	n/a	n/a
14	ATF1	chr11:48796111-48796444	K562	blood:	n/a	n/a
15	ATF1	chr11:48892890-48893270	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	chr11:48814467-48814498	K562	blood:	n/a	n/a
19	BACH1	chr11:48881669-48882080	K562	blood:	n/a	n/a
20	BACH1	chr11:48956270-48956471	K562	blood:	n/a	n/a
21	BATF	chr11:48854717-48855191	GM12878	blood:	n/a	n/a
22	BATF	chr11:48886811-48887099	GM12878	blood:	n/a	n/a
23	BATF	chr11:48775372-48775512	GM12878	blood:	n/a	n/a
24	BATF	chr11:48828245-48828584	GM12878	blood:	n/a	n/a
25	BATF	chr11:48943793-48944288	GM12878	blood:	n/a	n/a
26	BATF	chr11:48934446-48934684	GM12878	blood:	n/a	n/a
27	BATF	chr11:48844664-48844887	GM12878	blood:	n/a	n/a
28	BATF	chr11:48775367-48775560	GM12878	blood:	n/a	n/a
29	BATF	chr11:48940420-48940720	GM12878	blood:	n/a	n/a
30	BATF	chr11:48883215-48883597	GM12878	blood:	n/a	n/a
31	BATF	chr11:48834286-48834608	GM12878	blood:	n/a	n/a
32	BATF	chr11:48776572-48776725	GM12878	blood:	n/a	n/a
33	BATF	chr11:48804986-48805223	GM12878	blood:	n/a	n/a
34	BATF	chr11:48856700-48857102	GM12878	blood:	n/a	n/a
35	BATF	chr11:48931968-48932274	GM12878	blood:	n/a	n/a
36	BATF	chr11:48877440-48877803	GM12878	blood:	n/a	n/a
37	BATF	chr11:48817733-48818014	GM12878	blood:	n/a	n/a
38	BATF	chr11:48953227-48953611	GM12878	blood:	n/a	n/a
39	BATF	chr11:48834403-48834545	GM12878	blood:	n/a	n/a
40	BATF	chr11:48877883-48878085	GM12878	blood:	n/a	n/a
41	BATF	chr11:48859171-48859730	GM12878	blood:	n/a	n/a
42	BATF	chr11:48885554-48885939	GM12878	blood:	n/a	n/a
43	BATF	chr11:48906491-48906775	GM12878	blood:	n/a	chr11:48906618-48906628
44	BATF	chr11:48945095-48945310	GM12878	blood:	n/a	n/a
45	BATF	chr11:48839569-48839852	GM12878	blood:	n/a	n/a
46	BATF	chr11:48946780-48947152	GM12878	blood:	n/a	n/a
47	BATF	chr11:48955305-48955628	GM12878	blood:	n/a	n/a
48	BATF	chr11:48810099-48810738	GM12878	blood:	n/a	n/a
49	BATF	chr11:48945011-48945390	GM12878	blood:	n/a	n/a
50	BATF	chr11:48934181-48934321	GM12878	blood:	n/a	n/a

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:48922741-48922791	MCF10A-Er-Src	breast:	n/a
2	chr11:48922741-48922791	MCF10A-Er-Src	breast:	n/a
3	chr11:48922035-48922085	HEEpiC	esophagus:	n/a
4	chr11:48901705-48901755	HCT-116	colon:	n/a
5	chr11:48924804-48924854	SK-N-SH_RA	brain:	n/a
6	chr11:48880009-48880059	GM19239	blood:	n/a
7	chr11:48923668-48923718	NH-A	brain:	n/a
8	chr11:48922035-48922085	NT2-D1	testis:	n/a
9	chr11:48922674-48922724	HCT-116	colon:	n/a
10	chr11:48901705-48901755	A549	lung:	n/a
11	chr11:48901914-48901964	SAEC	small airway:	n/a
12	chr11:48922271-48922321	NHDF-neo	bronchial:	n/a
13	chr11:48880009-48880059	GM06990	blood:	n/a
14	chr11:48924804-48924854	GM12891	blood:	n/a
15	chr11:48880009-48880059	SK-N-SH_RA	brain:	n/a
16	chr11:48923577-48923627	AG10803	skin:	n/a
17	chr11:48922741-48922791	NHDF-neo	bronchial:	n/a
18	chr11:48922674-48922724	GM12878	blood:	n/a
19	chr11:48923577-48923627	H1-hESC	embryonic stem cell:	embryo
20	chr11:48922271-48922321	AoSMC	blood vessel:	n/a
21	chr11:48923577-48923627	HPAEpiC	pulmonary alveolar:	n/a
22	chr11:48922741-48922791	PFSK-1	brain:	n/a
23	chr11:48902014-48902064	GM06990	blood:	n/a
24	chr11:48880009-48880059	SK-N-MC	brain:	n/a
25	chr11:48923392-48923442	MCF10A-Er-Src	breast:	n/a
26	chr11:48924804-48924854	CMK	blood:	n/a
27	chr11:48922741-48922791	MCF-7	breast:	n/a
28	chr11:48901914-48901964	NHDF-neo	bronchial:	n/a
29	chr11:48923668-48923718	U87	brain:	n/a
30	chr11:48924804-48924854	H1-hESC	embryonic stem cell:	embryo
31	chr11:48922271-48922321	SKMC	muscle:	n/a
32	chr11:48902014-48902064	LNCaP	prostate:	n/a
33	chr11:48924804-48924854	HPAEpiC	pulmonary alveolar:	n/a
34	chr11:48901914-48901964	HRCEpiC	kidney:	n/a
35	chr11:48924804-48924854	HRCEpiC	kidney:	n/a
36	chr11:48922741-48922791	AG10803	skin:	n/a
37	chr11:48922674-48922724	HMEC	breast:	n/a
38	chr11:48923668-48923718	T-47D	breast:	n/a
39	chr11:48924804-48924854	HRE	kidney:	n/a
40	chr11:48901914-48901964	PANC-1	pancreas:	n/a
41	chr11:48922035-48922085	IMR90	lung:	fetal
42	chr11:48923577-48923627	NHBE	bronchial:	n/a
43	chr11:48924804-48924854	SK-N-SH	brain:	n/a
44	chr11:48901914-48901964	HCF	heart:	n/a
45	chr11:48922674-48922724	U87	brain:	n/a
46	chr11:48902014-48902064	HIPEpiC	eye:	n/a
47	chr11:48923668-48923718	HRCEpiC	kidney:	n/a
48	chr11:48922741-48922791	GM12878	blood:	n/a
49	chr11:48923577-48923627	AG09309	skin:	n/a
50	chr11:48923392-48923442	MCF-7	breast:	n/a

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

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

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

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

No data

Variant related genes	Relation type
OR4A41P	TF binding region
ENSG00000255551	TF binding region
OR4A45P	TF binding region
ENSG00000254920	TF binding region
ENSG00000255527	TF binding region
OR4A44P	TF binding region
ENSG00000254728	TF binding region
OR4A42P	TF binding region
OR4A41P	CpG island
ENSG00000255551	CpG island
OR4A45P	CpG island
ENSG00000254920	CpG island
ENSG00000255527	CpG island
OR4A44P	CpG island
ENSG00000254728	CpG island
OR4A42P	CpG island

Extended variants
information (count: 19497 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:19497 , 50 per page) page: 1 2 3 4 5 6 7 ... 390

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs113900099	chr11:48576961-48576962	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs112257736	chr11:48576970-48576971	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs373153634	chr11:48576973-48576974	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs34967308	chr11:48596644-48596645	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs189984961	chr11:48596661-48596662	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs530551341	chr11:48596689-48596690	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs367619160	chr11:48596751-48596752	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs182166003	chr11:48596756-48596757	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs536522837	chr11:48596766-48596767	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs546919863	chr11:48596768-48596769	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs71479920	chr11:48596780-48596781	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs566811967	chr11:48596793-48596794	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs535014196	chr11:48596796-48596797	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs557895314	chr11:48596817-48596818	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs10742856	chr11:48596818-48596819	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs10838969	chr11:48596837-48596838	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs557101515	chr11:48596860-48596861	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs187139338	chr11:48596900-48596901	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs554946231	chr11:48596901-48596902	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs542870536	chr11:48596917-48596918	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs559611008	chr11:48596927-48596928	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs372607365	chr11:48596928-48596929	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs143060771	chr11:48596929-48596930	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs138264552	chr11:48596930-48596931	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs36134860	chr11:48596932-48596933	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs10742857	chr11:48596955-48596956	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs36176069	chr11:48596959-48596960	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs10742858	chr11:48596962-48596963	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs11825197	chr11:48596986-48596987	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs546862517	chr11:48596997-48596998	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs566750440	chr11:48597037-48597038	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs112286102	chr11:48597040-48597041	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs578122563	chr11:48597075-48597076	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs532338738	chr11:48597082-48597083	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs551717410	chr11:48597084-48597085	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs183474044	chr11:48597098-48597099	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs74403804	chr11:48606371-48606372	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs540526809	chr11:48606418-48606419	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs560054538	chr11:48606436-48606437	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs116329055	chr11:48606495-48606496	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs545026625	chr11:48606510-48606511	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs565022272	chr11:48606520-48606521	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs145951279	chr11:48608583-48608584	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs549000610	chr11:48608659-48608660	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs548275363	chr11:48608661-48608662	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs566006386	chr11:48608670-48608671	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs144079928	chr11:48608685-48608686	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs186636218	chr11:48608696-48608697	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs564654084	chr11:48608715-48608716	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs190298956	chr11:48608717-48608718	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:798 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:48576800-48577000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr11:48632800-48633200	Active TSS	Fetal Heart	heart
3	chr11:48670600-48672800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
4	chr11:48671600-48672200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
5	chr11:48671600-48674000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
6	chr11:48679800-48680400	ZNF genes & repeats	Adipose Nuclei	Adipose
7	chr11:48680200-48688400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr11:48681200-48684000	ZNF genes & repeats	Liver	Liver
9	chr11:48685000-48686400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr11:48686800-48688000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
11	chr11:48688200-48691800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
12	chr11:48694000-48695400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
13	chr11:48694200-48695800	ZNF genes & repeats	Adipose Nuclei	Adipose
14	chr11:48695400-48695800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr11:48696800-48698200	ZNF genes & repeats	Liver	Liver
16	chr11:48697200-48699000	ZNF genes & repeats	Adipose Nuclei	Adipose
17	chr11:48698200-48698800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr11:48704600-48705400	ZNF genes & repeats	Adipose Nuclei	Adipose
19	chr11:48711000-48712200	ZNF genes & repeats	Liver	Liver
20	chr11:48717600-48718400	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
21	chr11:48718000-48718200	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
22	chr11:48718000-48718200	ZNF genes & repeats	Primary T cells effector/memory enriched fromperipheralblood	blood
23	chr11:48718000-48718200	ZNF genes & repeats	HUVEC	blood vessel
24	chr11:48718000-48718200	ZNF genes & repeats	NH-A	brain
25	chr11:48718000-48718400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
26	chr11:48718000-48718400	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
27	chr11:48718000-48718600	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
28	chr11:48718000-48719000	ZNF genes & repeats	Adipose Nuclei	Adipose
29	chr11:48718200-48718400	ZNF genes & repeats	Brain Inferior Temporal Lobe	brain
30	chr11:48728000-48728800	ZNF genes & repeats	Liver	Liver
31	chr11:48728400-48728800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
32	chr11:48731000-48732600	ZNF genes & repeats	Liver	Liver
33	chr11:48731400-48733000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
34	chr11:48731400-48735600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr11:48732600-48733400	Weak transcription	Liver	Liver
36	chr11:48733200-48734600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
37	chr11:48733200-48735800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
38	chr11:48733400-48734200	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
39	chr11:48733400-48734200	ZNF genes & repeats	Liver	Liver
40	chr11:48733400-48734400	ZNF genes & repeats	Adipose Nuclei	Adipose
41	chr11:48733800-48734200	Active TSS	Right Atrium	heart
42	chr11:48734200-48738400	Weak transcription	Right Atrium	heart
43	chr11:48736600-48742600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr11:48738000-48739600	ZNF genes & repeats	Adipose Nuclei	Adipose
45	chr11:48738400-48739200	Active TSS	Right Atrium	heart
46	chr11:48738800-48742000	ZNF genes & repeats	Liver	Liver
47	chr11:48741200-48742400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr11:48743800-48744600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
49	chr11:48744200-48744800	ZNF genes & repeats	Liver	Liver
50	chr11:48750800-48751400	ZNF genes & repeats	Adipose Nuclei	Adipose

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