Variant report

Variant	nsv8837
Chromosome Location	chr11:71517340-71559915
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr11:71540829-71541073	GM12878	blood:	n/a	n/a
2	BATF	chr11:71527794-71528002	GM12878	blood:	n/a	chr11:71527879-71527890
3	BATF	chr11:71524810-71525112	GM12878	blood:	n/a	n/a
4	BATF	chr11:71532357-71532883	GM12878	blood:	n/a	n/a
5	BCL11A	chr11:71532549-71532834	GM12878	blood:	n/a	n/a
6	BCL11A	chr11:71532424-71532928	GM12878	blood:	n/a	n/a
7	BCL11A	chr11:71540694-71541007	GM12878	blood:	n/a	n/a
8	BHLHE40	chr11:71524868-71525086	GM12878	blood:	n/a	n/a
9	BHLHE40	chr11:71541847-71542211	GM12878	blood:	n/a	n/a
10	BHLHE40	chr11:71541854-71542142	K562	blood:	n/a	n/a
11	BHLHE40	chr11:71540852-71541062	GM12878	blood:	n/a	n/a
12	BHLHE40	chr11:71532638-71532832	GM12878	blood:	n/a	n/a
13	CEBPB	chr11:71549235-71549396	K562	blood:	n/a	chr11:71549347-71549358 chr11:71549347-71549356
14	CEBPB	chr11:71549210-71549469	IMR90	lung:	n/a	chr11:71549347-71549358 chr11:71549347-71549356
15	CEBPB	chr11:71549344-71549406	Hela-S3	cervix:	n/a	chr11:71549347-71549358 chr11:71549347-71549356
16	CEBPB	chr11:71549258-71549410	HepG2	liver:	n/a	chr11:71549347-71549358 chr11:71549347-71549356
17	CEBPB	chr11:71549224-71549424	A549	lung:	n/a	chr11:71549347-71549358 chr11:71549347-71549356
18	CHD1	chr11:71524751-71525147	IMR90	lung:	n/a	n/a
19	CTCF	chr11:71524811-71525106	MCF-7	breast:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
20	CTCF	chr11:71553140-71553290	HMEC	breast:	n/a	n/a
21	CTCF	chr11:71524826-71525068	MCF-7	breast:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
22	CTCF	chr11:71524610-71524672	GM10266	blood:	n/a	n/a
23	CTCF	chr11:71524766-71525060	H1-hESC	embryonic stem cell:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
24	CTCF	chr11:71524860-71525010	HPAF	blood vessel:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
25	CTCF	chr11:71524860-71525010	GM12865	blood:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
26	CTCF	chr11:71524860-71525010	HUVEC	blood vessel:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
27	CTCF	chr11:71524844-71525100	MCF-7	breast:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
28	CTCF	chr11:71524630-71525108	A549	lung:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
29	CTCF	chr11:71524820-71524970	BE2_C	brain:	n/a	n/a
30	CTCF	chr11:71524820-71524970	HCT-116	colon:	n/a	n/a
31	CTCF	chr11:71524820-71524970	HRPEpiC	eye:	n/a	n/a
32	CTCF	chr11:71524824-71525112	LNCaP	prostate:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
33	CTCF	chr11:71524920-71525070	HCPEpiC	choroid plexus:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
34	CTCF	chr11:71524900-71525050	GM12866	blood:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
35	CTCF	chr11:71553220-71553370	HEEpiC	esophagus:	n/a	n/a
36	CTCF	chr11:71524769-71525135	Spleen_OC	spleen:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
37	CTCF	chr11:71518805-71519082	A549	lung:	n/a	chr11:71518921-71518942
38	CTCF	chr11:71544457-71544524	GM13976	blood:	n/a	n/a
39	CTCF	chr11:71524900-71525050	HUVEC	blood vessel:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
40	CTCF	chr11:71555060-71555210	GM12871	blood:	n/a	n/a
41	CTCF	chr11:71524800-71524950	GM12868	blood:	n/a	n/a
42	CTCF	chr11:71518643-71519202	K562	blood:	n/a	chr11:71518921-71518942
43	CTCF	chr11:71524870-71525081	Hela-S3	cervix:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
44	CTCF	chr11:71524840-71524990	BE2_C	brain:	n/a	chr11:71524959-71524975 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
45	CTCF	chr11:71524820-71524970	MCF-7	breast:	n/a	n/a
46	CTCF	chr11:71547587-71547663	GM20000	blood:	n/a	n/a
47	CTCF	chr11:71524800-71524950	A549	lung:	n/a	n/a
48	CTCF	chr11:71524860-71525010	HCFaa	heart:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
49	CTCF	chr11:71524920-71525070	HPF	lung:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
50	CTCF	chr11:71524826-71525101	NHEK	skin:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:71524971-71525021	GM06990	blood:	n/a
2	chr11:71524971-71525021	GM06990	blood:	n/a
3	chr11:71524734-71524784	GM12891	blood:	n/a
4	chr11:71524971-71525021	ovcar-3	ovarian:	n/a
5	chr11:71524540-71524590	ProgFib	skin:	n/a
6	chr11:71554504-71554554	SK-N-MC	brain:	n/a
7	chr11:71554504-71554554	GM19239	blood:	n/a
8	chr11:71524734-71524784	AG09319	gingival:	n/a
9	chr11:71527895-71527945	Caco-2	colon:	n/a
10	chr11:71524734-71524784	HNPCEpiC	eye:	n/a
11	chr11:71527895-71527945	AoSMC	blood vessel:	n/a
12	chr11:71543583-71543633	HRE	kidney:	n/a
13	chr11:71524540-71524590	HRCEpiC	kidney:	n/a
14	chr11:71524971-71525021	HAEpiC	amniotic membrane:	n/a
15	chr11:71545243-71545293	ProgFib	skin:	n/a
16	chr11:71522461-71522511	AG04450	lung:	fetal
17	chr11:71524540-71524590	SK-N-MC	brain:	n/a
18	chr11:71545243-71545293	HL-60	blood:	n/a
19	chr11:71527895-71527945	ovcar-3	ovarian:	n/a
20	chr11:71545243-71545293	SAEC	small airway:	n/a
21	chr11:71527895-71527945	NH-A	brain:	n/a
22	chr11:71524852-71524902	SKMC	muscle:	n/a
23	chr11:71524734-71524784	HRPEpiC	eye:	n/a
24	chr11:71543471-71543521	HRCEpiC	kidney:	n/a
25	chr11:71524500-71524550	HIPEpiC	eye:	n/a
26	chr11:71522461-71522511	SAEC	small airway:	n/a
27	chr11:71543583-71543633	GM06990	blood:	n/a
28	chr11:71522461-71522511	SK-N-MC	brain:	n/a
29	chr11:71524500-71524550	AG09319	gingival:	n/a
30	chr11:71524852-71524902	AoSMC	blood vessel:	n/a
31	chr11:71527895-71527945	SKMC	muscle:	n/a
32	chr11:71524540-71524590	HNPCEpiC	eye:	n/a
33	chr11:71545243-71545293	AoSMC	blood vessel:	n/a
34	chr11:71524500-71524550	A549	lung:	n/a
35	chr11:71524852-71524902	HCPEpiC	choroid plexus:	n/a
36	chr11:71524852-71524902	NHDF-neo	bronchial:	n/a
37	chr11:71524540-71524590	HCM	heart:	n/a
38	chr11:71524852-71524902	GM12892	blood:	n/a
39	chr11:71524500-71524550	HAEpiC	amniotic membrane:	n/a
40	chr11:71527895-71527945	GM19239	blood:	n/a
41	chr11:71524540-71524590	HCF	heart:	n/a
42	chr11:71524971-71525021	BE2_C	brain:	n/a
43	chr11:71527895-71527945	A549	lung:	n/a
44	chr11:71524500-71524550	GM12878	blood:	n/a
45	chr11:71522461-71522511	RPTEC	kidney:	n/a
46	chr11:71543583-71543633	NB4	blood:	n/a
47	chr11:71524971-71525021	Hela-S3	cervix:	n/a
48	chr11:71522461-71522511	MCF10A-Er-Src	breast:	n/a
49	chr11:71524734-71524784	PANC-1	pancreas:	n/a
50	chr11:71543471-71543521	IMR90	lung:	fetal

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-849H4.2.1-1	chr11:71517696-71518702	NONHSAT022713
2	lnc-RP11-849H4.2.1-1	chr11:71529199-71529284	ENSG00000248671.3
3	lnc-RP11-849H4.2.1-1	chr11:71518637-71518702	ENSG00000248671.3
4	lnc-DEFB108B-2	chr11:71548445-71548756	NONHSAT022717
5	lnc-DEFB108B-2	chr11:71545758-71545904	NONHSAT022717
6	lnc-DEFB108B-2	chr11:71548070-71548218	NONHSAT022717
7	lnc-RP11-849H4.2.1-1	chr11:71524389-71524529	NONHSAT022713
8	lnc-RP11-849H4.2.1-1	chr11:71527956-71528142	ENSG00000248671.3

Variant related genes	Relation type
ENSG00000248671	TF binding region
ZNF705E	TF binding region
ENSG00000264091	TF binding region
ALG1L9P	TF binding region
DEFB108B	TF binding region
RNA5SP342	TF binding region
ENSG00000248671	CpG island
ZNF705E	CpG island
ENSG00000264091	CpG island
ALG1L9P	CpG island
DEFB108B	CpG island
RNA5SP342	CpG island

Extended variants
information (count: 1628 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:1628 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs200511483	chr11:71517341-71517342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs7951127	chr11:71517342-71517343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs183566149	chr11:71517348-71517349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs534426954	chr11:71517404-71517405	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs553918442	chr11:71517449-71517450	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs565959209	chr11:71517493-71517494	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs535717635	chr11:71517517-71517518	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs539735765	chr11:71517548-71517549	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs558476428	chr11:71517556-71517557	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs576667546	chr11:71517561-71517562	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs539641746	chr11:71517569-71517570	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs4122051	chr11:71517581-71517582	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs543760002	chr11:71517585-71517586	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs4122052	chr11:71517621-71517622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs555816283	chr11:71517624-71517625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs530130908	chr11:71517645-71517646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs574156454	chr11:71517662-71517663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs541567688	chr11:71517694-71517695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs559573226	chr11:71517702-71517703	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
20	rs35601081	chr11:71517718-71517719	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs544970484	chr11:71517719-71517720	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
22	rs187117728	chr11:71517741-71517742	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
23	rs191171865	chr11:71517756-71517757	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
24	rs548928503	chr11:71517775-71517776	Weak transcription	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
25	rs372514995	chr11:71517777-71517778	Weak transcription	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
26	rs528150867	chr11:71517785-71517786	Weak transcription	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
27	rs570009046	chr11:71517792-71517793	Weak transcription	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
28	rs182445157	chr11:71517831-71517832	Weak transcription	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
29	rs539976894	chr11:71517842-71517843	Weak transcription	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
30	rs537376098	chr11:71517844-71517845	Weak transcription	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
31	rs570295569	chr11:71517891-71517892	Weak transcription	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
32	rs114796766	chr11:71517892-71517893	Weak transcription	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
33	rs570342985	chr11:71517908-71517909	Weak transcription	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
34	rs188359817	chr11:71517937-71517938	Weak transcription	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
35	rs535114670	chr11:71517957-71517958	Weak transcription	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
36	rs553548909	chr11:71517976-71517977	Weak transcription	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
37	rs374474492	chr11:71517990-71517991	Weak transcription	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
38	rs4519118	chr11:71518035-71518036	Weak transcription	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
39	rs578034262	chr11:71518049-71518050	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
40	rs151010819	chr11:71518064-71518065	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs7104538	chr11:71518072-71518073	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs7104541	chr11:71518078-71518079	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs374393288	chr11:71518091-71518092	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs542540932	chr11:71518143-71518144	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs7120359	chr11:71518179-71518180	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs141665527	chr11:71518271-71518272	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
47	rs546193065	chr11:71518278-71518279	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
48	rs192526354	chr11:71518290-71518291	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
49	rs532124976	chr11:71518298-71518299	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs7927726	chr11:71518349-71518350	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:104)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	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
Lung cancer	18438408	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Glioblastoma multiforme	21080181	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chordoma	21602918	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Multiple myeloma	16616336	CNVD
Urothelial cell carcinoma	18451213	CNVD
Leukoplakia	24403051	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	17142309	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:260 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:71508200-71524400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr11:71508800-71524400	Weak transcription	Fetal Intestine Small	intestine
3	chr11:71511600-71523600	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr11:71511600-71524400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr11:71511600-71524400	Weak transcription	Brain Angular Gyrus	brain
6	chr11:71522000-71523600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr11:71523200-71524000	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr11:71523400-71523600	Enhancers	Brain Hippocampus Middle	brain
9	chr11:71523400-71523600	Enhancers	Rectal Smooth Muscle	rectum
10	chr11:71523400-71523800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
11	chr11:71523400-71524400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr11:71523600-71523800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr11:71523600-71523800	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr11:71523600-71523800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr11:71523600-71523800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr11:71523600-71523800	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr11:71523600-71523800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr11:71523600-71523800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr11:71523600-71523800	Enhancers	Brain Anterior Caudate	brain
20	chr11:71523600-71523800	Enhancers	Brain Cingulate Gyrus	brain
21	chr11:71523600-71523800	Enhancers	Brain Substantia Nigra	brain
22	chr11:71523600-71523800	Enhancers	Fetal Brain Female	brain
23	chr11:71523600-71523800	Enhancers	Fetal Stomach	stomach
24	chr11:71523600-71523800	Enhancers	Left Ventricle	heart
25	chr11:71523600-71523800	Enhancers	Lung	lung
26	chr11:71523600-71523800	Enhancers	Rectal Mucosa Donor 29	rectum
27	chr11:71523600-71523800	Enhancers	Skeletal Muscle Male	skeletal muscle
28	chr11:71523600-71523800	Enhancers	HSMMtube	muscle
29	chr11:71523600-71524000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr11:71523600-71524200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr11:71523600-71524200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr11:71523600-71524200	Enhancers	Brain Inferior Temporal Lobe	brain
33	chr11:71523600-71524200	Enhancers	Osteobl	bone
34	chr11:71523600-71524400	Enhancers	Primary T cells fromperipheralblood	blood
35	chr11:71523600-71524400	Enhancers	Skeletal Muscle Female	skeletal muscle
36	chr11:71523600-71524400	Enhancers	HMEC	breast
37	chr11:71523600-71525000	Active TSS	Brain Hippocampus Middle	brain
38	chr11:71523600-71525000	Active TSS	Stomach Smooth Muscle	stomach
39	chr11:71523800-71524200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr11:71523800-71524200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr11:71523800-71524400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr11:71523800-71524400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
43	chr11:71523800-71524400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr11:71523800-71524400	Weak transcription	Brain Anterior Caudate	brain
45	chr11:71523800-71524400	Weak transcription	Brain Cingulate Gyrus	brain
46	chr11:71523800-71524400	Weak transcription	Fetal Stomach	stomach
47	chr11:71523800-71524400	Weak transcription	Lung	lung
48	chr11:71523800-71524400	Weak transcription	Rectal Smooth Muscle	rectum
49	chr11:71523800-71524400	Weak transcription	HSMMtube	muscle
50	chr11:71524000-71524200	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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