Variant report

Variant	nsv975104
Chromosome Location	chr11:48343977-48384914
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:179)
CpG islands
(count:305)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:179 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr11:48356437-48356637	K562	blood:	n/a	n/a
2	BACH1	chr11:48356973-48356986	K562	blood:	n/a	n/a
3	BRCA1	chr11:48361931-48361935	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr11:48367027-48367324	HCT-116	colon:	n/a	n/a
5	CEBPB	chr11:48374701-48375094	Hela-S3	cervix:	n/a	chr11:48374900-48374913
6	CEBPB	chr11:48367044-48367318	HepG2	liver:	n/a	n/a
7	CEBPB	chr11:48376639-48376671	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr11:48367014-48367428	HCT-116	colon:	n/a	n/a
9	CEBPB	chr11:48367001-48367415	Hela-S3	cervix:	n/a	n/a
10	CEBPZ	chr11:48360331-48360376	HepG2	liver:	n/a	n/a
11	CHD2	chr11:48344566-48344658	K562	blood:	n/a	n/a
12	CHD2	chr11:48377806-48377814	Hela-S3	cervix:	n/a	n/a
13	CTCF	chr11:48382500-48382650	HPF	lung:	n/a	n/a
14	CTCF	chr11:48361860-48362010	A549	lung:	n/a	n/a
15	CTCF	chr11:48377200-48377350	GM12866	blood:	n/a	n/a
16	CTCF	chr11:48361960-48362110	GM12873	blood:	n/a	n/a
17	CTCF	chr11:48384480-48384630	GM12869	blood:	n/a	n/a
18	CTCF	chr11:48367060-48367210	K562	blood:	n/a	n/a
19	CTCF	chr11:48362002-48362026	MCF-7	breast:	n/a	n/a
20	CTCF	chr11:48361920-48362070	HepG2	liver:	n/a	n/a
21	CTCF	chr11:48353120-48353270	AoAF	blood vessel:	n/a	n/a
22	CTCF	chr11:48367644-48367692	Fibrobl	skin:	n/a	n/a
23	CTCF	chr11:48378591-48378684	Kidney_OC	kidney:	n/a	n/a
24	CTCF	chr11:48361860-48362010	GM12873	blood:	n/a	n/a
25	CTCF	chr11:48360411-48360480	Fibrobl	skin:	n/a	n/a
26	CTCF	chr11:48347233-48347255	Fibrobl	skin:	n/a	n/a
27	CTCF	chr11:48362900-48363050	A549	lung:	n/a	n/a
28	CTCF	chr11:48361920-48362070	GM12864	blood:	n/a	n/a
29	CTCF	chr11:48361820-48361970	MCF-7	breast:	n/a	n/a
30	CTCF	chr11:48361980-48362130	MCF-7	breast:	n/a	n/a
31	CTCF	chr11:48361920-48362070	GM06990	blood:	n/a	n/a
32	CTCF	chr11:48361940-48362090	NB4	blood:	n/a	n/a
33	CTCF	chr11:48362100-48362250	A549	lung:	n/a	n/a
34	CTCF	chr11:48361900-48362050	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr11:48377730-48377792	A549	lung:	n/a	n/a
36	CTCF	chr11:48361940-48362090	HEK293	kidney:	n/a	n/a
37	CTCF	chr11:48353060-48353210	HCPEpiC	choroid plexus:	n/a	n/a
38	CTCF	chr11:48355180-48355330	HFF-Myc	foreskin:	n/a	n/a
39	CTCF	chr11:48362000-48362150	GM12875	blood:	n/a	n/a
40	E2F4	chr11:48374623-48375377	MCF10A-Er-Src	breast:	n/a	n/a
41	E2F4	chr11:48347512-48347672	MCF10A-Er-Src	breast:	n/a	n/a
42	E2F4	chr11:48352506-48352706	MCF10A-Er-Src	breast:	n/a	n/a
43	E2F4	chr11:48345431-48345631	MCF10A-Er-Src	breast:	n/a	n/a
44	ELK1	chr11:48347070-48347169	Hela-S3	cervix:	n/a	n/a
45	ELK1	chr11:48362984-48363095	Hela-S3	cervix:	n/a	n/a
46	EP300	chr11:48356678-48357328	T-47D	breast:	n/a	chr11:48356774-48356781
47	EP300	chr11:48383988-48384019	GM12878	blood:	n/a	n/a
48	EP300	chr11:48353150-48353292	GM12878	blood:	n/a	n/a
49	ESR1	chr11:48356715-48357255	T-47D	breast:	n/a	n/a
50	ESR1	chr11:48355104-48355467	T-47D	breast:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:48374446-48374496	LNCaP	prostate:	n/a
2	chr11:48374446-48374496	PANC-1	pancreas:	n/a
3	chr11:48345361-48345411	NB4	blood:	n/a
4	chr11:48346680-48346730	HEK293	kidney:	embryo
5	chr11:48367974-48368024	PFSK-1	brain:	n/a
6	chr11:48345815-48345865	PFSK-1	brain:	n/a
7	chr11:48346680-48346730	ovcar-3	ovarian:	n/a
8	chr11:48346680-48346730	BE2_C	brain:	n/a
9	chr11:48374446-48374496	AoSMC	blood vessel:	n/a
10	chr11:48367974-48368024	Jurkat	blood:	n/a
11	chr11:48367974-48368024	AG09309	skin:	n/a
12	chr11:48346680-48346730	NT2-D1	testis:	n/a
13	chr11:48374446-48374496	HNPCEpiC	eye:	n/a
14	chr11:48345361-48345411	HMEC	breast:	n/a
15	chr11:48374446-48374496	AG09309	skin:	n/a
16	chr11:48346680-48346730	A549	lung:	n/a
17	chr11:48345361-48345411	PrEC	prostate:	n/a
18	chr11:48346680-48346730	GM19239	blood:	n/a
19	chr11:48345361-48345411	CMK	blood:	n/a
20	chr11:48374446-48374496	BE2_C	brain:	n/a
21	chr11:48346680-48346730	BJ	skin:	n/a
22	chr11:48374446-48374496	HUVEC	blood vessel:	n/a
23	chr11:48345361-48345411	SK-N-SH	brain:	n/a
24	chr11:48374446-48374496	K562	blood:	n/a
25	chr11:48346680-48346730	HPAEpiC	pulmonary alveolar:	n/a
26	chr11:48367974-48368024	HCPEpiC	choroid plexus:	n/a
27	chr11:48346680-48346730	HCM	heart:	n/a
28	chr11:48345361-48345411	BJ	skin:	n/a
29	chr11:48345815-48345865	AG09319	gingival:	n/a
30	chr11:48346680-48346730	GM12891	blood:	n/a
31	chr11:48345361-48345411	MCF10A-Er-Src	breast:	n/a
32	chr11:48367974-48368024	ovcar-3	ovarian:	n/a
33	chr11:48345361-48345411	A549	lung:	n/a
34	chr11:48345815-48345865	ProgFib	skin:	n/a
35	chr11:48345815-48345865	HAEpiC	amniotic membrane:	n/a
36	chr11:48345815-48345865	U87	brain:	n/a
37	chr11:48367974-48368024	SAEC	small airway:	n/a
38	chr11:48367974-48368024	HRPEpiC	eye:	n/a
39	chr11:48345361-48345411	HPAEpiC	pulmonary alveolar:	n/a
40	chr11:48374446-48374496	HCPEpiC	choroid plexus:	n/a
41	chr11:48367974-48368024	AG04449	skin:	fetal
42	chr11:48346680-48346730	HUVEC	blood vessel:	n/a
43	chr11:48345361-48345411	HNPCEpiC	eye:	n/a
44	chr11:48345361-48345411	SK-N-MC	brain:	n/a
45	chr11:48345361-48345411	GM12878	blood:	n/a
46	chr11:48367974-48368024	HRE	kidney:	n/a
47	chr11:48374446-48374496	GM12891	blood:	n/a
48	chr11:48345361-48345411	HCM	heart:	n/a
49	chr11:48345361-48345411	HUVEC	blood vessel:	n/a
50	chr11:48345815-48345865	K562	blood:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:48366878..48368914-chr11:48372533..48375413,2	MCF-7	breast:
2	chr11:48361908..48364233-chr11:48365831..48368223,2	MCF-7	breast:
3	chr11:48361908..48364233-chr11:48365831..48368223,2	MCF-7	breast:

No data

Variant related genes	Relation type
OR4C4P	TF binding region
OR4C3	TF binding region
OR4C4P	CpG island
OR4C3	CpG island
ENSG00000197161	chromatin interactions

Extended variants
information (count: 3287 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:3287 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs72911431	chr11:48343993-48343994	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs549863135	chr11:48344013-48344014	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs72911433	chr11:48344015-48344016	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs569685571	chr11:48344021-48344022	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs76653117	chr11:48344030-48344031	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs74768201	chr11:48344033-48344034	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs79528922	chr11:48344044-48344045	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs79519652	chr11:48344047-48344048	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs75720891	chr11:48344053-48344054	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs80319807	chr11:48344059-48344060	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs10839500	chr11:48344072-48344073	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs76638052	chr11:48344083-48344084	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs144065904	chr11:48344096-48344097	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs72911435	chr11:48344097-48344098	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs72911436	chr11:48344103-48344104	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs190688534	chr11:48344109-48344110	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs183092270	chr11:48344117-48344118	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs78700933	chr11:48344132-48344133	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs7936042	chr11:48344136-48344137	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs72911437	chr11:48344146-48344147	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs11040735	chr11:48344156-48344157	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs374709507	chr11:48344172-48344173	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs200803128	chr11:48344173-48344174	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs572030867	chr11:48344178-48344179	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs80066030	chr11:48344189-48344190	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs77374030	chr11:48344200-48344201	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs538033294	chr11:48344218-48344219	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs558463622	chr11:48344229-48344230	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs548399204	chr11:48344288-48344289	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs578228228	chr11:48344298-48344299	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs77633787	chr11:48344303-48344304	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs76322433	chr11:48344310-48344311	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs76928424	chr11:48344315-48344316	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs543692141	chr11:48344316-48344317	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs78543242	chr11:48344321-48344322	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs79009747	chr11:48344323-48344324	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs74479872	chr11:48344326-48344327	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs543095824	chr11:48344327-48344328	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs368532539	chr11:48344333-48344334	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs80177179	chr11:48344334-48344335	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs559330081	chr11:48344335-48344336	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs75100815	chr11:48344360-48344361	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs12222372	chr11:48344370-48344371	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs76871611	chr11:48344381-48344382	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs112109491	chr11:48344386-48344387	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs12281554	chr11:48344395-48344396	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs79861837	chr11:48344412-48344413	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs564004382	chr11:48344451-48344452	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs79435678	chr11:48344461-48344462	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs78091290	chr11:48344462-48344463	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

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
small cell lung cancer	20016488	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
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Schizophrenia	20967226	CNVD

Chromatin state (count:95 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:48341400-48345800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
2	chr11:48342600-48344400	Weak transcription	Stomach Mucosa	stomach
3	chr11:48344400-48344800	Enhancers	Stomach Mucosa	stomach
4	chr11:48344800-48349800	Weak transcription	Stomach Mucosa	stomach
5	chr11:48346600-48346800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
6	chr11:48346600-48347000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
7	chr11:48346600-48347400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
8	chr11:48346600-48348600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
9	chr11:48346800-48347400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr11:48348800-48350000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr11:48350000-48355600	Weak transcription	Stomach Mucosa	stomach
12	chr11:48352400-48353400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
13	chr11:48352400-48353800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
14	chr11:48353000-48359800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
15	chr11:48355200-48363800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
16	chr11:48355600-48357000	Enhancers	Stomach Mucosa	stomach
17	chr11:48357000-48358000	Weak transcription	Stomach Mucosa	stomach
18	chr11:48358000-48358200	Enhancers	Stomach Mucosa	stomach
19	chr11:48362000-48362200	Enhancers	Primary T helper naive cells from peripheral blood	blood
20	chr11:48362400-48362800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
21	chr11:48362800-48363200	Enhancers	Primary T helper naive cells from peripheral blood	blood
22	chr11:48362800-48363200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
23	chr11:48362800-48363600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
24	chr11:48362800-48363800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
25	chr11:48363000-48363200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
26	chr11:48363000-48363400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
27	chr11:48363000-48363400	Active TSS	A549	lung
28	chr11:48363000-48363600	Active TSS	Hela-S3	cervix
29	chr11:48363000-48363800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
30	chr11:48363000-48363800	Enhancers	Primary T helper cells PMA-I stimulated	--
31	chr11:48363200-48363600	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
32	chr11:48363200-48363600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
33	chr11:48363200-48363600	Enhancers	Primary T helper cells fromperipheralblood	blood
34	chr11:48363200-48363600	Enhancers	Primary T killer memory cells from peripheral blood	blood
35	chr11:48363200-48363600	Enhancers	Liver	Liver
36	chr11:48363200-48363600	Enhancers	Dnd41	blood
37	chr11:48363200-48363800	Enhancers	Primary T cells fromperipheralblood	blood
38	chr11:48363200-48366400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
39	chr11:48363600-48363800	Enhancers	Primary T helper naive cells from peripheral blood	blood
40	chr11:48363600-48363800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
41	chr11:48363600-48363800	Enhancers	Hela-S3	cervix
42	chr11:48363600-48366800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
43	chr11:48363600-48367000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
44	chr11:48363800-48366600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
45	chr11:48363800-48366800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
46	chr11:48363800-48367000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
47	chr11:48364200-48364600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
48	chr11:48364800-48367400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
49	chr11:48365000-48366400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
50	chr11:48365200-48365600	Weak transcription	Primary T helper cells PMA-I stimulated	--

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