Variant report

Variant	nsv898356
Chromosome Location	chr11:104779195-104838471
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:449)
CpG islands
(count:672)
Chromatin interactive
region (count:1)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:449 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:104817646-104818039	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:104814897-104815170	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:104814360-104814630	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:104827306-104827643	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:104838331-104838340	HepG2	liver:	n/a	n/a
6	BRCA1	chr11:104838120-104838701	Hela-S3	cervix:	n/a	n/a
7	CBX3	chr11:104817608-104818133	HCT-116	colon:	n/a	n/a
8	CEBPB	chr11:104827235-104827625	A549	lung:	n/a	chr11:104827468-104827479
9	CEBPB	chr11:104827075-104827789	HCT-116	colon:	n/a	chr11:104827468-104827479
10	CEBPB	chr11:104827272-104827658	H1-hESC	embryonic stem cell:	n/a	chr11:104827468-104827479
11	CEBPB	chr11:104837727-104839837	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr11:104827292-104827597	HepG2	liver:	n/a	chr11:104827468-104827479
13	CEBPB	chr11:104789758-104789850	A549	lung:	n/a	n/a
14	CEBPB	chr11:104827178-104827731	Hela-S3	cervix:	n/a	chr11:104827468-104827479
15	CEBPB	chr11:104814408-104814668	Hela-S3	cervix:	n/a	chr11:104814576-104814588 chr11:104814528-104814541 chr11:104814528-104814541 chr11:104814528-104814539 chr11:104814529-104814540
16	CEBPB	chr11:104827299-104827601	HepG2	liver:	n/a	chr11:104827468-104827479
17	CEBPB	chr11:104828023-104828380	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr11:104827300-104827618	K562	blood:	n/a	chr11:104827468-104827479
19	CEBPB	chr11:104784953-104785176	HepG2	liver:	n/a	chr11:104785067-104785078
20	CEBPB	chr11:104827200-104827640	ECC-1	luminal epithelium:	n/a	chr11:104827468-104827479
21	CEBPB	chr11:104827192-104827735	A549	lung:	n/a	chr11:104827468-104827479
22	CEBPB	chr11:104827256-104827673	HepG2	liver:	n/a	chr11:104827468-104827479
23	CEBPB	chr11:104780576-104780776	HepG2	liver:	n/a	chr11:104780651-104780664 chr11:104780651-104780662
24	CEBPB	chr11:104827214-104827637	ECC-1	luminal epithelium:	n/a	chr11:104827468-104827479
25	CEBPB	chr11:104827194-104827678	MCF-7	breast:	n/a	chr11:104827468-104827479
26	CEBPB	chr11:104827256-104827636	MCF-7	breast:	n/a	chr11:104827468-104827479
27	CEBPB	chr11:104814346-104815203	HepG2	liver:	n/a	chr11:104814576-104814588 chr11:104814528-104814541 chr11:104814528-104814541 chr11:104814528-104814539 chr11:104814529-104814540
28	CEBPB	chr11:104814361-104814678	IMR90	lung:	n/a	chr11:104814576-104814588 chr11:104814528-104814541 chr11:104814528-104814541 chr11:104814528-104814539 chr11:104814529-104814540
29	CEBPB	chr11:104827278-104827652	HepG2	liver:	n/a	chr11:104827468-104827479
30	CEBPB	chr11:104827282-104827644	IMR90	lung:	n/a	chr11:104827468-104827479
31	CEBPB	chr11:104817693-104817982	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr11:104827278-104827653	A549	lung:	n/a	chr11:104827468-104827479
33	CEBPB	chr11:104785033-104785128	Hela-S3	cervix:	n/a	chr11:104785067-104785078
34	CEBPB	chr11:104827216-104827712	HCT-116	colon:	n/a	chr11:104827468-104827479
35	CEBPD	chr11:104827306-104827641	HepG2	liver:	n/a	chr11:104827467-104827478
36	CHD2	chr11:104838217-104838662	Hela-S3	cervix:	n/a	n/a
37	CHD2	chr11:104796787-104796814	HepG2	liver:	n/a	n/a
38	CTCF	chr11:104817760-104817910	HBMEC	blood vessel:	n/a	n/a
39	CTCF	chr11:104817679-104817981	HUVEC	blood vessel:	n/a	n/a
40	CTCF	chr11:104818020-104818170	HA-sp	spinal cord:	n/a	n/a
41	CTCF	chr11:104817760-104817910	HPF	lung:	n/a	n/a
42	CTCF	chr11:104818080-104818230	HCM	heart:	n/a	n/a
43	CTCF	chr11:104817740-104817890	SK-N-SH_RA	brain:	n/a	n/a
44	CTCF	chr11:104817740-104817890	GM12869	blood:	n/a	n/a
45	CTCF	chr11:104817574-104818173	SK-N-SH	brain:	n/a	n/a
46	CTCF	chr11:104817751-104817905	A549	lung:	n/a	n/a
47	CTCF	chr11:104817740-104817890	HMF	breast:	n/a	n/a
48	CTCF	chr11:104817740-104817890	AG09309	skin:	n/a	n/a
49	CTCF	chr11:104817680-104817830	HFF-Myc	foreskin:	n/a	n/a
50	CTCF	chr11:104817800-104817950	HEK293	kidney:	n/a	n/a

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:104789052-104789102	HEEpiC	esophagus:	n/a
2	chr11:104789052-104789102	HEEpiC	esophagus:	n/a
3	chr11:104780712-104780762	HRPEpiC	eye:	n/a
4	chr11:104779518-104779568	GM12878	blood:	n/a
5	chr11:104780712-104780762	PrEC	prostate:	n/a
6	chr11:104789052-104789102	PANC-1	pancreas:	n/a
7	chr11:104817914-104817964	HEEpiC	esophagus:	n/a
8	chr11:104827238-104827288	IMR90	lung:	fetal
9	chr11:104814390-104814440	ECC-1	luminal epithelium:	n/a
10	chr11:104780795-104780845	HEEpiC	esophagus:	n/a
11	chr11:104789337-104789387	NB4	blood:	n/a
12	chr11:104789052-104789102	HepG2	liver:	n/a
13	chr11:104827790-104827840	GM12892	blood:	n/a
14	chr11:104779518-104779568	GM12892	blood:	n/a
15	chr11:104827238-104827288	HRPEpiC	eye:	n/a
16	chr11:104817914-104817964	GM12891	blood:	n/a
17	chr11:104781259-104781309	HL-60	blood:	n/a
18	chr11:104789052-104789102	Jurkat	blood:	n/a
19	chr11:104814390-104814440	BJ	skin:	n/a
20	chr11:104789337-104789387	Hepatocyte	liver:	n/a
21	chr11:104827790-104827840	GM12891	blood:	n/a
22	chr11:104789337-104789387	Caco-2	colon:	n/a
23	chr11:104789337-104789387	HNPCEpiC	eye:	n/a
24	chr11:104814390-104814440	Hela-S3	cervix:	n/a
25	chr11:104817914-104817964	NH-A	brain:	n/a
26	chr11:104827790-104827840	Caco-2	colon:	n/a
27	chr11:104779518-104779568	MCF10A-Er-Src	breast:	n/a
28	chr11:104781259-104781309	MCF-7	breast:	n/a
29	chr11:104828060-104828110	MCF-7	breast:	n/a
30	chr11:104779518-104779568	NHDF-neo	bronchial:	n/a
31	chr11:104780795-104780845	LNCaP	prostate:	n/a
32	chr11:104779518-104779568	AG09319	gingival:	n/a
33	chr11:104827238-104827288	Jurkat	blood:	n/a
34	chr11:104781259-104781309	AoSMC	blood vessel:	n/a
35	chr11:104814390-104814440	PFSK-1	brain:	n/a
36	chr11:104817914-104817964	Jurkat	blood:	n/a
37	chr11:104789337-104789387	HCT-116	colon:	n/a
38	chr11:104780712-104780762	NHBE	bronchial:	n/a
39	chr11:104814390-104814440	Jurkat	blood:	n/a
40	chr11:104828060-104828110	H1-hESC	embryonic stem cell:	embryo
41	chr11:104827790-104827840	LNCaP	prostate:	n/a
42	chr11:104827238-104827288	A549	lung:	n/a
43	chr11:104827790-104827840	CMK	blood:	n/a
44	chr11:104827790-104827840	PANC-1	pancreas:	n/a
45	chr11:104789337-104789387	SKMC	muscle:	n/a
46	chr11:104827238-104827288	PANC-1	pancreas:	n/a
47	chr11:104779518-104779568	NT2-D1	testis:	n/a
48	chr11:104827238-104827288	AG09319	gingival:	n/a
49	chr11:104789052-104789102	HUVEC	blood vessel:	n/a
50	chr11:104789052-104789102	AG04449	skin:	fetal

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:151511788..151512678-chr11:104838165..104838828,2	Hela-S3	cervix:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CASP12-3	chr11:104789658-104789800	NONHSAT023943
2	lnc-CASP12-3	chr11:104779415-104779735	NONHSAT023944
3	lnc-CASP12-3	chr11:104788840-104788870	NONHSAT023944
4	lnc-CASP12-3	chr11:104779562-104779735	NR_034078
5	lnc-CASP12-3	chr11:104779562-104779735	NONHSAT023943
6	lnc-CASP12-3	chr11:104788840-104788902	NR_034079
7	lnc-CASP4-1	chr11:104815475-104815578	NONHSAT023946
8	lnc-CASP12-3	chr11:104788840-104788902	NR_034078
9	lnc-CASP12-3	chr11:104779562-104779735	NR_034079
10	lnc-CASP4-1	chr11:104819260-104819461	NONHSAT023947
11	lnc-CASP4-1	chr11:104817351-104817919	NONHSAT023947
12	lnc-CASP4-1	chr11:104817810-104818085	NONHSAT023946
13	lnc-CASP4-1	chr11:104813600-104813700	NONHSAT023946

No data

(count:2 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	CASP4	hsa-miR-26b-5p	chr11:104822275-104822295
2	CASP4	hsa-miR-26b-5p	chr11:104822249-104822272

Variant related genes	Relation type
ENSG00000235505	TF binding region
CASP4	TF binding region
ENSG00000235505	CpG island
CASP4	CpG island

Extended variants
information (count: 2059 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:2059 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs478650	chr11:104779195-104779196	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs516574	chr11:104779226-104779227	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs543004686	chr11:104779239-104779240	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs112446010	chr11:104779355-104779356	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs369096286	chr11:104779415-104779416	Weak transcription Enhancers Genic enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
6	rs58526794	chr11:104779451-104779452	Weak transcription Enhancers Genic enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
7	rs56215529	chr11:104779454-104779455	Weak transcription Enhancers Genic enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
8	rs518553	chr11:104779466-104779467	Weak transcription Enhancers Genic enhancers Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs554443199	chr11:104779491-104779492	Weak transcription Enhancers Genic enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs545300560	chr11:104779518-104779519	Weak transcription Enhancers Genic enhancers Strong transcription	CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
11	rs564966402	chr11:104779519-104779520	Weak transcription Enhancers Genic enhancers Strong transcription	CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
12	rs78679482	chr11:104779543-104779544	Weak transcription Enhancers Genic enhancers Strong transcription	CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
13	rs530720561	chr11:104779544-104779545	Weak transcription Enhancers Genic enhancers Strong transcription	CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs189452256	chr11:104779565-104779566	Weak transcription Enhancers Genic enhancers Strong transcription	CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
15	rs182140418	chr11:104779566-104779567	Weak transcription Enhancers Genic enhancers Strong transcription	CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
16	rs570375645	chr11:104779674-104779675	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
17	rs114885915	chr11:104779707-104779708	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
18	rs72976989	chr11:104779712-104779713	Weak transcription Enhancers Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs566051549	chr11:104779733-104779734	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
20	rs142377968	chr11:104779756-104779757	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs552044893	chr11:104779783-104779784	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs186574205	chr11:104779789-104779790	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs150969303	chr11:104779793-104779794	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs557184358	chr11:104779864-104779865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs71037283	chr11:104779867-104779868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs3831467	chr11:104779871-104779872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs398017416	chr11:104779872-104779873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs554291615	chr11:104779873-104779874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs201721798	chr11:104779874-104779875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs376819796	chr11:104779920-104779921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs12422201	chr11:104779924-104779925	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs140770574	chr11:104779975-104779976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs562305480	chr11:104779985-104779986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs79263449	chr11:104780031-104780032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs150096954	chr11:104780064-104780065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs524060	chr11:104780081-104780082	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs545529562	chr11:104780109-104780110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs575347363	chr11:104780126-104780127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs529006981	chr11:104780129-104780130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs560833743	chr11:104780200-104780201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs509899	chr11:104780213-104780214	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs546265416	chr11:104780220-104780221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs559760023	chr11:104780231-104780232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs138516941	chr11:104780236-104780237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs551791736	chr11:104780247-104780248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs571872194	chr11:104780280-104780281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs140219201	chr11:104780307-104780308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs72976991	chr11:104780320-104780321	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs112256350	chr11:104780324-104780325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs547452543	chr11:104780341-104780342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	22429812	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17603634	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	16790693	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Mental retardation	19966786	CNVD
Non-small cell lung cancer	21829676	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Intracranial aneurysm	16715129	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Ovarian cancer	21720365	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Neuroblastoma	17327916	CNVD
Melanoma	17363583	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Mantle cell lymphoma	19029149	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant melanoma	17260012	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Prostate cancer	16573809	CNVD
Obesity	19966786	CNVD
Tetralogy of Fallot	22912587	CNVD
Prostate cancer	18632612	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1285 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:104769200-104786400	Weak transcription	Lung	lung
2	chr11:104769200-104786600	Weak transcription	Fetal Muscle Leg	muscle
3	chr11:104769200-104787800	Weak transcription	Fetal Lung	lung
4	chr11:104769400-104785400	Weak transcription	Psoas Muscle	Psoas
5	chr11:104769400-104786800	Weak transcription	Duodenum Mucosa	Duodenum
6	chr11:104769600-104785800	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr11:104769600-104786800	Weak transcription	Adipose Nuclei	Adipose
8	chr11:104769600-104788000	Weak transcription	Fetal Stomach	stomach
9	chr11:104770400-104786600	Weak transcription	Ovary	ovary
10	chr11:104772200-104782000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
11	chr11:104772600-104783600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr11:104773600-104779800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr11:104773800-104785600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
14	chr11:104776400-104787200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr11:104777600-104779200	Enhancers	Primary T helper cells fromperipheralblood	blood
16	chr11:104778000-104779600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
17	chr11:104778000-104779800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
18	chr11:104778200-104779200	Strong transcription	Fetal Muscle Trunk	muscle
19	chr11:104778200-104779800	Strong transcription	Left Ventricle	heart
20	chr11:104778400-104786800	Weak transcription	Aorta	Aorta
21	chr11:104778400-104788800	Weak transcription	Pancreas	Pancrea
22	chr11:104778800-104779200	Enhancers	Primary T helper cells PMA-I stimulated	--
23	chr11:104779000-104779200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr11:104779000-104779600	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
25	chr11:104779000-104783800	Weak transcription	Primary T cells fromperipheralblood	blood
26	chr11:104779000-104784600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
27	chr11:104779000-104785400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
28	chr11:104779000-104786800	Weak transcription	NHLF	lung
29	chr11:104779200-104782000	Weak transcription	Primary T helper cells PMA-I stimulated	--
30	chr11:104779200-104782000	Weak transcription	Primary T helper cells fromperipheralblood	blood
31	chr11:104779200-104788000	Weak transcription	Fetal Muscle Trunk	muscle
32	chr11:104779600-104783600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
33	chr11:104779600-104784600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
34	chr11:104779800-104782200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
35	chr11:104779800-104786600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
36	chr11:104779800-104786600	Weak transcription	Left Ventricle	heart
37	chr11:104782000-104782400	Enhancers	Primary T helper naive cells from peripheral blood	blood
38	chr11:104782000-104782600	Enhancers	Primary T helper cells fromperipheralblood	blood
39	chr11:104782000-104782800	Enhancers	Primary T helper cells PMA-I stimulated	--
40	chr11:104782000-104783400	Enhancers	Dnd41	blood
41	chr11:104782200-104786600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
42	chr11:104782400-104784200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
43	chr11:104782600-104783000	Weak transcription	Primary T helper cells fromperipheralblood	blood
44	chr11:104782800-104784400	Weak transcription	Primary T helper cells PMA-I stimulated	--
45	chr11:104783000-104783200	Enhancers	Primary T helper cells fromperipheralblood	blood
46	chr11:104783200-104784400	Weak transcription	Primary T helper cells fromperipheralblood	blood
47	chr11:104783400-104786800	Weak transcription	Dnd41	blood
48	chr11:104783600-104784600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
49	chr11:104783600-104786600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
50	chr11:104783800-104784200	Enhancers	Primary T cells fromperipheralblood	blood

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