Variant report

Variant	nsv1036053
Chromosome Location	chr11:48342863-48388686
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:228)
CpG islands
(count:307)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:228 , 50 per page) page: 1 2 3 4 5

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	chr11:48367014-48367428	HCT-116	colon:	n/a	n/a
5	CEBPB	chr11:48367027-48367324	HCT-116	colon:	n/a	n/a
6	CEBPB	chr11:48374701-48375094	Hela-S3	cervix:	n/a	chr11:48374900-48374913
7	CEBPB	chr11:48367044-48367318	HepG2	liver:	n/a	n/a
8	CEBPB	chr11:48376639-48376671	H1-hESC	embryonic stem cell:	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	chr11:48377806-48377814	Hela-S3	cervix:	n/a	n/a
12	CHD2	chr11:48344566-48344658	K562	blood:	n/a	n/a
13	CTCF	chr11:48386557-48386854	K562	blood:	n/a	n/a
14	CTCF	chr11:48353060-48353210	HCPEpiC	choroid plexus:	n/a	n/a
15	CTCF	chr11:48361940-48362090	NB4	blood:	n/a	n/a
16	CTCF	chr11:48367644-48367692	Fibrobl	skin:	n/a	n/a
17	CTCF	chr11:48361960-48362110	GM12873	blood:	n/a	n/a
18	CTCF	chr11:48387640-48387790	GM12878	blood:	n/a	n/a
19	CTCF	chr11:48361860-48362010	GM12873	blood:	n/a	n/a
20	CTCF	chr11:48387426-48387586	MCF-7	breast:	n/a	n/a
21	CTCF	chr11:48387380-48387530	MCF-7	breast:	n/a	n/a
22	CTCF	chr11:48387420-48387570	HepG2	liver:	n/a	n/a
23	CTCF	chr11:48387400-48387550	A549	lung:	n/a	n/a
24	CTCF	chr11:48387500-48387650	HepG2	liver:	n/a	n/a
25	CTCF	chr11:48367060-48367210	K562	blood:	n/a	n/a
26	CTCF	chr11:48361920-48362070	GM06990	blood:	n/a	n/a
27	CTCF	chr11:48387380-48387530	GM12873	blood:	n/a	n/a
28	CTCF	chr11:48387460-48387610	GM12873	blood:	n/a	n/a
29	CTCF	chr11:48361980-48362130	MCF-7	breast:	n/a	n/a
30	CTCF	chr11:48347233-48347255	Fibrobl	skin:	n/a	n/a
31	CTCF	chr11:48387460-48387610	HEK293	kidney:	n/a	n/a
32	CTCF	chr11:48384480-48384630	GM12869	blood:	n/a	n/a
33	CTCF	chr11:48387460-48387610	GM12875	blood:	n/a	n/a
34	CTCF	chr11:48387456-48387593	MCF-7	breast:	n/a	n/a
35	CTCF	chr11:48353120-48353270	AoAF	blood vessel:	n/a	n/a
36	CTCF	chr11:48361860-48362010	A549	lung:	n/a	n/a
37	CTCF	chr11:48387474-48387580	MCF-7	breast:	n/a	n/a
38	CTCF	chr11:48382500-48382650	HPF	lung:	n/a	n/a
39	CTCF	chr11:48362100-48362250	A549	lung:	n/a	n/a
40	CTCF	chr11:48377200-48377350	GM12866	blood:	n/a	n/a
41	CTCF	chr11:48387503-48387527	LNCaP	prostate:	n/a	n/a
42	CTCF	chr11:48387420-48387570	Caco-2	colon:	n/a	n/a
43	CTCF	chr11:48361820-48361970	MCF-7	breast:	n/a	n/a
44	CTCF	chr11:48361920-48362070	GM12864	blood:	n/a	n/a
45	CTCF	chr11:48387501-48387576	A549	lung:	n/a	n/a
46	CTCF	chr11:48361920-48362070	HepG2	liver:	n/a	n/a
47	CTCF	chr11:48387540-48387690	GM12870	blood:	n/a	n/a
48	CTCF	chr11:48355180-48355330	HFF-Myc	foreskin:	n/a	n/a
49	CTCF	chr11:48387445-48387596	MCF-7	breast:	n/a	n/a
50	CTCF	chr11:48377730-48377792	A549	lung:	n/a	n/a

(count:307 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:48345815-48345865	NHBE	bronchial:	n/a
2	chr11:48374446-48374496	MCF-7	breast:	n/a
3	chr11:48345815-48345865	NHBE	bronchial:	n/a
4	chr11:48374446-48374496	MCF-7	breast:	n/a
5	chr11:48374446-48374496	HCT-116	colon:	n/a
6	chr11:48345361-48345411	HL-60	blood:	n/a
7	chr11:48346680-48346730	SK-N-SH_RA	brain:	n/a
8	chr11:48367974-48368024	BE2_C	brain:	n/a
9	chr11:48345361-48345411	K562	blood:	n/a
10	chr11:48345361-48345411	HNPCEpiC	eye:	n/a
11	chr11:48346680-48346730	HRPEpiC	eye:	n/a
12	chr11:48367974-48368024	HRCEpiC	kidney:	n/a
13	chr11:48345815-48345865	NH-A	brain:	n/a
14	chr11:48367974-48368024	K562	blood:	n/a
15	chr11:48367974-48368024	RPTEC	kidney:	n/a
16	chr11:48346680-48346730	HMEC	breast:	n/a
17	chr11:48345361-48345411	BJ	skin:	n/a
18	chr11:48367974-48368024	HPAEpiC	pulmonary alveolar:	n/a
19	chr11:48345361-48345411	SKMC	muscle:	n/a
20	chr11:48367974-48368024	NH-A	brain:	n/a
21	chr11:48374446-48374496	HepG2	liver:	n/a
22	chr11:48345815-48345865	Caco-2	colon:	n/a
23	chr11:48345361-48345411	HPAEpiC	pulmonary alveolar:	n/a
24	chr11:48345815-48345865	SKMC	muscle:	n/a
25	chr11:48346680-48346730	HEEpiC	esophagus:	n/a
26	chr11:48374446-48374496	HEEpiC	esophagus:	n/a
27	chr11:48345815-48345865	HCF	heart:	n/a
28	chr11:48374446-48374496	GM12891	blood:	n/a
29	chr11:48346680-48346730	NB4	blood:	n/a
30	chr11:48345361-48345411	NHBE	bronchial:	n/a
31	chr11:48367974-48368024	H1-hESC	embryonic stem cell:	embryo
32	chr11:48367974-48368024	HIPEpiC	eye:	n/a
33	chr11:48345815-48345865	SK-N-MC	brain:	n/a
34	chr11:48345815-48345865	AoSMC	blood vessel:	n/a
35	chr11:48345815-48345865	NB4	blood:	n/a
36	chr11:48345815-48345865	HIPEpiC	eye:	n/a
37	chr11:48345815-48345865	GM06990	blood:	n/a
38	chr11:48367974-48368024	HRE	kidney:	n/a
39	chr11:48346680-48346730	HUVEC	blood vessel:	n/a
40	chr11:48345815-48345865	CMK	blood:	n/a
41	chr11:48367974-48368024	NB4	blood:	n/a
42	chr11:48346680-48346730	HRE	kidney:	n/a
43	chr11:48345815-48345865	LNCaP	prostate:	n/a
44	chr11:48345815-48345865	PrEC	prostate:	n/a
45	chr11:48346680-48346730	H1-hESC	embryonic stem cell:	embryo
46	chr11:48345361-48345411	HRE	kidney:	n/a
47	chr11:48345361-48345411	HRPEpiC	eye:	n/a
48	chr11:48346680-48346730	SK-N-SH	brain:	n/a
49	chr11:48345815-48345865	MCF10A-Er-Src	breast:	n/a
50	chr11:48374446-48374496	NHDF-neo	bronchial:	n/a

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

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

No data

Variant related genes	Relation type
OR4C5	TF binding region
OR4C4P	TF binding region
OR4C3	TF binding region
OR4C5	CpG island
OR4C4P	CpG island
OR4C3	CpG island
ENSG00000197161	chromatin interactions

Extended variants
information (count: 3698 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:3698 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs80066896	chr11:48342868-48342869	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs533707692	chr11:48342877-48342878	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs72911411	chr11:48342887-48342888	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs72911412	chr11:48342894-48342895	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs553532174	chr11:48342906-48342907	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs77569786	chr11:48342910-48342911	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs576555119	chr11:48342915-48342916	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs73461937	chr11:48342931-48342932	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs573173822	chr11:48342943-48342944	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs545488517	chr11:48342970-48342971	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs79215901	chr11:48342971-48342972	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs33929742	chr11:48342972-48342973	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs372667968	chr11:48343016-48343017	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs55841115	chr11:48343056-48343057	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs151187769	chr11:48343065-48343066	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs542512606	chr11:48343067-48343068	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs562216351	chr11:48343068-48343069	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs73461938	chr11:48343084-48343085	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs527904123	chr11:48343106-48343107	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs61915350	chr11:48343117-48343118	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs541674176	chr11:48343121-48343122	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs564666887	chr11:48343136-48343137	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs533507744	chr11:48343153-48343154	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs73463955	chr11:48343157-48343158	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs72473365	chr11:48343204-48343205	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs549968636	chr11:48343218-48343219	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs563705990	chr11:48343223-48343224	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs72473366	chr11:48343224-48343225	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs11039677	chr11:48343246-48343247	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs73463957	chr11:48343285-48343286	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs73463958	chr11:48343301-48343302	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs76574733	chr11:48343331-48343332	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs79998505	chr11:48343344-48343345	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs71851029	chr11:48343351-48343352	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs557452155	chr11:48343354-48343355	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs35749815	chr11:48343382-48343383	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs548483215	chr11:48343389-48343390	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs190169114	chr11:48343391-48343392	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs75118371	chr11:48343398-48343399	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs79604292	chr11:48343399-48343400	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs78770820	chr11:48343403-48343404	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs145753152	chr11:48343422-48343423	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs67611064	chr11:48343438-48343439	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs114318316	chr11:48343447-48343448	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs78484269	chr11:48343477-48343478	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs386753289	chr11:48343490-48343491	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs77009342	chr11:48343491-48343492	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs570301541	chr11:48343501-48343502	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs76648777	chr11:48343504-48343505	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs539154517	chr11:48343511-48343512	ZNF genes & repeats Weak transcription	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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