Variant report

Variant	esv1803631
Chromosome Location	chr11:71521288-71560091
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	chr11:71540694-71541007	GM12878	blood:	n/a	n/a
7	BCL11A	chr11:71532424-71532928	GM12878	blood:	n/a	n/a
8	BHLHE40	chr11:71532638-71532832	GM12878	blood:	n/a	n/a
9	BHLHE40	chr11:71524868-71525086	GM12878	blood:	n/a	n/a
10	BHLHE40	chr11:71541854-71542142	K562	blood:	n/a	n/a
11	BHLHE40	chr11:71541847-71542211	GM12878	blood:	n/a	n/a
12	BHLHE40	chr11:71540852-71541062	GM12878	blood:	n/a	n/a
13	CEBPB	chr11:71549210-71549469	IMR90	lung:	n/a	chr11:71549347-71549358 chr11:71549347-71549356
14	CEBPB	chr11:71549258-71549410	HepG2	liver:	n/a	chr11:71549347-71549358 chr11:71549347-71549356
15	CEBPB	chr11:71549224-71549424	A549	lung:	n/a	chr11:71549347-71549358 chr11:71549347-71549356
16	CEBPB	chr11:71549235-71549396	K562	blood:	n/a	chr11:71549347-71549358 chr11:71549347-71549356
17	CEBPB	chr11:71549344-71549406	Hela-S3	cervix:	n/a	chr11:71549347-71549358 chr11:71549347-71549356
18	CHD1	chr11:71524751-71525147	IMR90	lung:	n/a	n/a
19	CTCF	chr11:71524900-71525050	GM12872	blood:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
20	CTCF	chr11:71524920-71525070	HCPEpiC	choroid plexus:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
21	CTCF	chr11:71524920-71525070	GM12801	blood:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
22	CTCF	chr11:71524840-71524990	GM12869	blood:	n/a	chr11:71524959-71524975 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
23	CTCF	chr11:71524837-71525101	GM13976	blood:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
24	CTCF	chr11:71524900-71525050	HEK293	kidney:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
25	CTCF	chr11:71524780-71524930	GM12868	blood:	n/a	n/a
26	CTCF	chr11:71524672-71525123	H1-hESC	embryonic stem cell:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
27	CTCF	chr11:71524834-71525090	MCF-7	breast:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
28	CTCF	chr11:71524880-71525030	GM12869	blood:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
29	CTCF	chr11:71524643-71525076	HCT-116	colon:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
30	CTCF	chr11:71524814-71525050	SK-N-SH_RA	brain:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
31	CTCF	chr11:71524920-71525070	HPF	lung:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
32	CTCF	chr11:71524900-71525050	AG04449	skin:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
33	CTCF	chr11:71524860-71525010	AG10803	skin:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
34	CTCF	chr11:71524820-71524970	HFF	foreskin:	n/a	n/a
35	CTCF	chr11:71550289-71550348	GM10248	blood:	n/a	n/a
36	CTCF	chr11:71524900-71525050	GM12866	blood:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
37	CTCF	chr11:71524811-71525106	MCF-7	breast:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
38	CTCF	chr11:71524860-71525010	BJ	skin:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
39	CTCF	chr11:71524920-71525070	HRE	kidney:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
40	CTCF	chr11:71524900-71525050	GM12865	blood:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
41	CTCF	chr11:71524824-71525112	LNCaP	prostate:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
42	CTCF	chr11:71524813-71525123	K562	blood:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
43	CTCF	chr11:71524729-71525131	T-47D	breast:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
44	CTCF	chr11:71524820-71524970	BE2_C	brain:	n/a	n/a
45	CTCF	chr11:71524832-71525109	MCF-7	breast:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
46	CTCF	chr11:71524880-71525030	HL-60	blood:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
47	CTCF	chr11:71524800-71524950	A549	lung:	n/a	n/a
48	CTCF	chr11:71553225-71553288	NHEK	skin:	n/a	n/a
49	CTCF	chr11:71524820-71524970	NHDF-neo	bronchial:	n/a	n/a
50	CTCF	chr11:71524630-71525108	A549	lung:	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	chr11:71524852-71524902	GM06990	blood:	n/a
2	chr11:71543471-71543521	AG04449	skin:	fetal
3	chr11:71524734-71524784	HCT-116	colon:	n/a
4	chr11:71543583-71543633	HRE	kidney:	n/a
5	chr11:71527895-71527945	HCM	heart:	n/a
6	chr11:71524852-71524902	LNCaP	prostate:	n/a
7	chr11:71524971-71525021	SK-N-SH_RA	brain:	n/a
8	chr11:71554504-71554554	HNPCEpiC	eye:	n/a
9	chr11:71524852-71524902	SK-N-SH	brain:	n/a
10	chr11:71524734-71524784	HCM	heart:	n/a
11	chr11:71522461-71522511	MCF10A-Er-Src	breast:	n/a
12	chr11:71524734-71524784	AG09319	gingival:	n/a
13	chr11:71554504-71554554	SK-N-SH	brain:	n/a
14	chr11:71545243-71545293	MCF-7	breast:	n/a
15	chr11:71524734-71524784	SKMC	muscle:	n/a
16	chr11:71554504-71554554	AG04450	lung:	fetal
17	chr11:71522461-71522511	PANC-1	pancreas:	n/a
18	chr11:71524852-71524902	Hepatocyte	liver:	n/a
19	chr11:71554504-71554554	SAEC	small airway:	n/a
20	chr11:71524971-71525021	HepG2	liver:	n/a
21	chr11:71522461-71522511	Jurkat	blood:	n/a
22	chr11:71524540-71524590	HCM	heart:	n/a
23	chr11:71524852-71524902	NHBE	bronchial:	n/a
24	chr11:71527895-71527945	Jurkat	blood:	n/a
25	chr11:71545243-71545293	MCF10A-Er-Src	breast:	n/a
26	chr11:71545243-71545293	NB4	blood:	n/a
27	chr11:71524540-71524590	SKMC	muscle:	n/a
28	chr11:71524540-71524590	HNPCEpiC	eye:	n/a
29	chr11:71545243-71545293	ProgFib	skin:	n/a
30	chr11:71545243-71545293	HCPEpiC	choroid plexus:	n/a
31	chr11:71545243-71545293	SK-N-SH_RA	brain:	n/a
32	chr11:71545243-71545293	Caco-2	colon:	n/a
33	chr11:71522461-71522511	HRPEpiC	eye:	n/a
34	chr11:71527895-71527945	NB4	blood:	n/a
35	chr11:71524540-71524590	MCF-7	breast:	n/a
36	chr11:71554504-71554554	Hepatocyte	liver:	n/a
37	chr11:71527895-71527945	GM06990	blood:	n/a
38	chr11:71545243-71545293	NHDF-neo	bronchial:	n/a
39	chr11:71524540-71524590	GM12892	blood:	n/a
40	chr11:71524852-71524902	CMK	blood:	n/a
41	chr11:71524852-71524902	HEK293	kidney:	embryo
42	chr11:71543471-71543521	NT2-D1	testis:	n/a
43	chr11:71543583-71543633	HepG2	liver:	n/a
44	chr11:71524971-71525021	AG04450	lung:	fetal
45	chr11:71522461-71522511	NHDF-neo	bronchial:	n/a
46	chr11:71522461-71522511	AG04450	lung:	fetal
47	chr11:71524500-71524550	K562	blood:	n/a
48	chr11:71524734-71524784	Jurkat	blood:	n/a
49	chr11:71543471-71543521	RPTEC	kidney:	n/a
50	chr11:71554504-71554554	AoSMC	blood vessel:	n/a

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

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

Extended variants
information (count: 1456 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:1456 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183299694	chr11:71521325-71521326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs4245457	chr11:71521364-71521365	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs4245458	chr11:71521378-71521379	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs137939545	chr11:71521388-71521389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs538011150	chr11:71521393-71521394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs550168830	chr11:71521418-71521419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs556356869	chr11:71521437-71521438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs80132553	chr11:71521444-71521445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs189140847	chr11:71521473-71521474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs553863145	chr11:71521474-71521475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs193021841	chr11:71521600-71521601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs545976624	chr11:71521616-71521617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs564556386	chr11:71521671-71521672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs531721883	chr11:71521672-71521673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs543607427	chr11:71521679-71521680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs150092522	chr11:71521680-71521681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs113425917	chr11:71521686-71521687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs564462539	chr11:71521695-71521696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs138929921	chr11:71521696-71521697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs111949989	chr11:71521707-71521708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs565538603	chr11:71521722-71521723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs532894954	chr11:71521723-71521724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs551102203	chr11:71521738-71521739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs569702403	chr11:71521740-71521741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs7946426	chr11:71521744-71521745	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs185650985	chr11:71521785-71521786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs568348839	chr11:71521800-71521801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs7947421	chr11:71521826-71521827	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs187778138	chr11:71521833-71521834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs536047261	chr11:71521835-71521836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs547985924	chr11:71521873-71521874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs569694612	chr11:71521939-71521940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs370420452	chr11:71521987-71521988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs373723609	chr11:71521988-71521989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs536668274	chr11:71521991-71521992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs375752294	chr11:71522016-71522017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs61067004	chr11:71522018-71522019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs529348405	chr11:71522019-71522020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs200869986	chr11:71522020-71522021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs368031717	chr11:71522022-71522023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs371606920	chr11:71522028-71522029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs111994158	chr11:71522061-71522062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs184303073	chr11:71522087-71522088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs1945055	chr11:71522099-71522100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs557881371	chr11:71522117-71522118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs576584274	chr11:71522153-71522154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs1945056	chr11:71522171-71522172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs543968934	chr11:71522185-71522186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs188549921	chr11:71522225-71522226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs9666822	chr11:71522253-71522254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

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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