Variant report

Variant	esv1804003
Chromosome Location	chr11:71512115-71563035
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	chr11:71532357-71532883	GM12878	blood:	n/a	n/a
3	BATF	chr11:71524810-71525112	GM12878	blood:	n/a	n/a
4	BATF	chr11:71527794-71528002	GM12878	blood:	n/a	chr11:71527879-71527890
5	BCL11A	chr11:71532424-71532928	GM12878	blood:	n/a	n/a
6	BCL11A	chr11:71532549-71532834	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	chr11:71541854-71542142	K562	blood:	n/a	n/a
10	BHLHE40	chr11:71532638-71532832	GM12878	blood:	n/a	n/a
11	BHLHE40	chr11:71540852-71541062	GM12878	blood:	n/a	n/a
12	BHLHE40	chr11:71541847-71542211	GM12878	blood:	n/a	n/a
13	CBX3	chr11:71561489-71561676	K562	blood:	n/a	n/a
14	CBX3	chr11:71561434-71561699	K562	blood:	n/a	n/a
15	CEBPB	chr11:71549344-71549406	Hela-S3	cervix:	n/a	chr11:71549347-71549358 chr11:71549347-71549356
16	CEBPB	chr11:71549210-71549469	IMR90	lung:	n/a	chr11:71549347-71549358 chr11:71549347-71549356
17	CEBPB	chr11:71549258-71549410	HepG2	liver:	n/a	chr11:71549347-71549358 chr11:71549347-71549356
18	CEBPB	chr11:71549235-71549396	K562	blood:	n/a	chr11:71549347-71549358 chr11:71549347-71549356
19	CEBPB	chr11:71549224-71549424	A549	lung:	n/a	chr11:71549347-71549358 chr11:71549347-71549356
20	CHD1	chr11:71524751-71525147	IMR90	lung:	n/a	n/a
21	CTCF	chr11:71524860-71525010	Caco-2	colon:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
22	CTCF	chr11:71524825-71525127	Medullo	brain:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
23	CTCF	chr11:71524880-71525030	GM12873	blood:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
24	CTCF	chr11:71524824-71525112	LNCaP	prostate:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
25	CTCF	chr11:71524940-71525090	GM12870	blood:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
26	CTCF	chr11:71524920-71525070	HBMEC	blood vessel:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
27	CTCF	chr11:71524920-71525070	Hela-S3	cervix:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
28	CTCF	chr11:71524920-71525070	HRPEpiC	eye:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
29	CTCF	chr11:71531470-71531524	Spleen_OC	spleen:	n/a	n/a
30	CTCF	chr11:71560307-71560339	GM10266	blood:	n/a	n/a
31	CTCF	chr11:71547574-71547581	GM20000	blood:	n/a	n/a
32	CTCF	chr11:71524800-71524950	HAc	cerebellar:	n/a	n/a
33	CTCF	chr11:71524826-71525101	NHEK	skin:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
34	CTCF	chr11:71514202-71514226	GM20000	blood:	n/a	n/a
35	CTCF	chr11:71513891-71513972	GM20000	blood:	n/a	n/a
36	CTCF	chr11:71524960-71525110	HCM	heart:	n/a	chr11:71524973-71524994 chr11:71524971-71524989
37	CTCF	chr11:71524780-71524930	A549	lung:	n/a	n/a
38	CTCF	chr11:71513754-71513842	A549	lung:	n/a	n/a
39	CTCF	chr11:71524960-71525110	WI-38	lung:	n/a	chr11:71524973-71524994 chr11:71524971-71524989
40	CTCF	chr11:71524844-71525100	MCF-7	breast:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
41	CTCF	chr11:71524848-71525108	LNCaP	prostate:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
42	CTCF	chr11:71524766-71525168	A549	lung:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
43	CTCF	chr11:71524780-71524930	HA-sp	spinal cord:	n/a	n/a
44	CTCF	chr11:71518817-71518991	A549	lung:	n/a	chr11:71518921-71518942
45	CTCF	chr11:71524920-71525070	HRE	kidney:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
46	CTCF	chr11:71524900-71525050	AoAF	blood vessel:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
47	CTCF	chr11:71524860-71525010	HCFaa	heart:	n/a	chr11:71524959-71524975 chr11:71524973-71524994 chr11:71524958-71524976 chr11:71524971-71524989 chr11:71524953-71524974
48	CTCF	chr11:71524800-71524950	GM12868	blood:	n/a	n/a
49	CTCF	chr11:71553240-71553390	Caco-2	colon:	n/a	n/a
50	CTCF	chr11:71524782-71525102	HepG2	liver:	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	chr11:71524540-71524590	U87	brain:	n/a
2	chr11:71543471-71543521	T-47D	breast:	n/a
3	chr11:71524734-71524784	AG09309	skin:	n/a
4	chr11:71524852-71524902	AG04449	skin:	fetal
5	chr11:71522461-71522511	GM06990	blood:	n/a
6	chr11:71543471-71543521	GM12891	blood:	n/a
7	chr11:71524971-71525021	HIPEpiC	eye:	n/a
8	chr11:71545243-71545293	HL-60	blood:	n/a
9	chr11:71554504-71554554	NH-A	brain:	n/a
10	chr11:71524500-71524550	AG09319	gingival:	n/a
11	chr11:71543471-71543521	GM19239	blood:	n/a
12	chr11:71543583-71543633	GM12892	blood:	n/a
13	chr11:71524852-71524902	AG10803	skin:	n/a
14	chr11:71522461-71522511	HAEpiC	amniotic membrane:	n/a
15	chr11:71524500-71524550	NH-A	brain:	n/a
16	chr11:71524852-71524902	PrEC	prostate:	n/a
17	chr11:71522461-71522511	HRPEpiC	eye:	n/a
18	chr11:71524971-71525021	HEEpiC	esophagus:	n/a
19	chr11:71545243-71545293	K562	blood:	n/a
20	chr11:71527895-71527945	SK-N-MC	brain:	n/a
21	chr11:71522461-71522511	SAEC	small airway:	n/a
22	chr11:71522461-71522511	T-47D	breast:	n/a
23	chr11:71545243-71545293	NHDF-neo	bronchial:	n/a
24	chr11:71524734-71524784	GM12892	blood:	n/a
25	chr11:71524734-71524784	HCT-116	colon:	n/a
26	chr11:71524971-71525021	H1-hESC	embryonic stem cell:	embryo
27	chr11:71545243-71545293	MCF10A-Er-Src	breast:	n/a
28	chr11:71524852-71524902	U87	brain:	n/a
29	chr11:71522461-71522511	A549	lung:	n/a
30	chr11:71543583-71543633	SAEC	small airway:	n/a
31	chr11:71522461-71522511	HCF	heart:	n/a
32	chr11:71524540-71524590	Jurkat	blood:	n/a
33	chr11:71545243-71545293	HNPCEpiC	eye:	n/a
34	chr11:71524500-71524550	SAEC	small airway:	n/a
35	chr11:71543471-71543521	GM06990	blood:	n/a
36	chr11:71524971-71525021	SAEC	small airway:	n/a
37	chr11:71543583-71543633	SK-N-SH_RA	brain:	n/a
38	chr11:71522461-71522511	MCF10A-Er-Src	breast:	n/a
39	chr11:71543471-71543521	HAEpiC	amniotic membrane:	n/a
40	chr11:71524971-71525021	HMEC	breast:	n/a
41	chr11:71524500-71524550	A549	lung:	n/a
42	chr11:71543471-71543521	AG04450	lung:	fetal
43	chr11:71524734-71524784	HCPEpiC	choroid plexus:	n/a
44	chr11:71554504-71554554	NHDF-neo	bronchial:	n/a
45	chr11:71524500-71524550	AG04450	lung:	fetal
46	chr11:71527895-71527945	HPAEpiC	pulmonary alveolar:	n/a
47	chr11:71522461-71522511	HEK293	kidney:	embryo
48	chr11:71524971-71525021	SK-N-MC	brain:	n/a
49	chr11:71543471-71543521	HL-60	blood:	n/a
50	chr11:71524500-71524550	ECC-1	luminal epithelium:	n/a

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

Variant related genes	Relation type
DEFB108B	TF binding region
ENSG00000248671	TF binding region
ZNF705E	TF binding region
ENSG00000255157	TF binding region
ENSG00000264091	TF binding region
ALG1L9P	TF binding region
RNA5SP342	TF binding region
DEFB108B	CpG island
ENSG00000248671	CpG island
ZNF705E	CpG island
ENSG00000255157	CpG island
ENSG00000264091	CpG island
ALG1L9P	CpG island
RNA5SP342	CpG island

Extended variants
information (count: 2063 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:2063 , 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	rs553936948	chr11:71512134-71512135	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs191413595	chr11:71512139-71512140	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs17151306	chr11:71512164-71512165	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs112380757	chr11:71512168-71512169	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs367799378	chr11:71512169-71512170	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs557758981	chr11:71512183-71512184	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs17151227	chr11:71512194-71512195	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs576134282	chr11:71512203-71512204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs543489880	chr11:71512219-71512220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs371457029	chr11:71512235-71512236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs555211128	chr11:71512243-71512244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs574972509	chr11:71512254-71512255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs542010215	chr11:71512271-71512272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs151053441	chr11:71512287-71512288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs527942592	chr11:71512343-71512344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs550516042	chr11:71512349-71512350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs546108469	chr11:71512358-71512359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs564116711	chr11:71512436-71512437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs531627615	chr11:71512455-71512456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs202063230	chr11:71512464-71512465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs368653606	chr11:71512483-71512484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs199881620	chr11:71512512-71512513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs56231977	chr11:71512519-71512520	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs200572746	chr11:71512535-71512536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs529401007	chr11:71512539-71512540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs200444593	chr11:71512558-71512559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs547244004	chr11:71512568-71512569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs59283006	chr11:71512625-71512626	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs138743560	chr11:71512629-71512630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs551735013	chr11:71512641-71512642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs569660380	chr11:71512706-71512707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs536693234	chr11:71512711-71512712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs555344487	chr11:71512720-71512721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs573614259	chr11:71512721-71512722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs184272696	chr11:71512730-71512731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs117401089	chr11:71512740-71512741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs553918124	chr11:71512747-71512748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs188611315	chr11:71512769-71512770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs546071749	chr11:71512791-71512792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs56328938	chr11:71512809-71512810	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs200568703	chr11:71512822-71512823	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs576678995	chr11:71512831-71512832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs543413239	chr11:71512857-71512858	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs369226402	chr11:71512868-71512869	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs181811708	chr11:71512869-71512870	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs547898780	chr11:71512894-71512895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs185098816	chr11:71512904-71512905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs531970364	chr11:71512923-71512924	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs533204474	chr11:71512931-71512932	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs551697456	chr11:71512938-71512939	Weak transcription Enhancers	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:311 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:71499200-71515200	Weak transcription	Lung	lung
2	chr11:71499400-71512800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr11:71499400-71515200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr11:71499400-71515600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr11:71499800-71512800	Weak transcription	Fetal Muscle Leg	muscle
6	chr11:71499800-71515200	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr11:71500400-71515200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr11:71500400-71515200	Weak transcription	Fetal Intestine Large	intestine
9	chr11:71500400-71515600	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr11:71500800-71515200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr11:71506000-71515600	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr11:71506200-71514000	Weak transcription	NHLF	lung
13	chr11:71506400-71515600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
14	chr11:71506600-71513400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr11:71506600-71515200	Weak transcription	Spleen	Spleen
16	chr11:71506600-71515600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr11:71506800-71513200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr11:71507000-71513400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
19	chr11:71508200-71514000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr11:71508200-71524400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr11:71508400-71512800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr11:71508800-71524400	Weak transcription	Fetal Intestine Small	intestine
23	chr11:71510200-71512200	Enhancers	HSMM	muscle
24	chr11:71511400-71513200	Weak transcription	Osteobl	bone
25	chr11:71511600-71513200	Weak transcription	HSMMtube	muscle
26	chr11:71511600-71514000	Weak transcription	Fetal Stomach	stomach
27	chr11:71511600-71515200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr11:71511600-71515200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr11:71511600-71523600	Weak transcription	Brain Inferior Temporal Lobe	brain
30	chr11:71511600-71524400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr11:71511600-71524400	Weak transcription	Brain Angular Gyrus	brain
32	chr11:71512000-71515200	Weak transcription	Fetal Muscle Trunk	muscle
33	chr11:71512800-71513200	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr11:71512800-71513600	Enhancers	Fetal Muscle Leg	muscle
35	chr11:71512800-71514200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr11:71513200-71513600	Enhancers	Osteobl	bone
37	chr11:71513200-71514000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
38	chr11:71513400-71513600	Enhancers	Primary hematopoietic stem cells short term culture	blood
39	chr11:71513600-71515600	Weak transcription	Fetal Muscle Leg	muscle
40	chr11:71514000-71514200	Enhancers	Breast Myoepithelial Primary Cells	Breast
41	chr11:71514000-71514200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr11:71515200-71515400	Enhancers	H1 Cell Line	embryonic stem cell
43	chr11:71515200-71515400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr11:71515200-71515400	Enhancers	Fetal Muscle Trunk	muscle
45	chr11:71515200-71515400	Enhancers	Spleen	Spleen
46	chr11:71515200-71515800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr11:71515200-71515800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr11:71515200-71515800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr11:71515200-71515800	Enhancers	Fetal Intestine Large	intestine
50	chr11:71515200-71515800	Enhancers	Lung	lung

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