Variant report

Variant	nsv1054278
Chromosome Location	chr11:104317164-104562129
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1168)
CpG islands
(count:244)
Chromatin interactive
region (count:20)
LncRNA
region (count:22)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1168 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:104539807-104540209	HepG2	liver:	n/a	n/a
2	BACH1	chr11:104404978-104405409	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL11A	chr11:104452026-104452271	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL11A	chr11:104451956-104452294	H1-hESC	embryonic stem cell:	n/a	n/a
5	BRCA1	chr11:104336495-104336518	Hela-S3	cervix:	n/a	n/a
6	CBX3	chr11:104322981-104323720	HCT-116	colon:	n/a	n/a
7	CBX3	chr11:104539778-104540232	HCT-116	colon:	n/a	n/a
8	CBX3	chr11:104520974-104521253	HCT-116	colon:	n/a	n/a
9	CEBPB	chr11:104539700-104540315	HCT-116	colon:	n/a	n/a
10	CEBPB	chr11:104322583-104322867	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr11:104489254-104489482	HepG2	liver:	n/a	n/a
12	CEBPB	chr11:104479994-104480282	Hela-S3	cervix:	n/a	chr11:104480194-104480207
13	CEBPB	chr11:104536365-104536737	IMR90	lung:	n/a	n/a
14	CEBPB	chr11:104444109-104444452	IMR90	lung:	n/a	chr11:104444139-104444152
15	CEBPB	chr11:104418796-104419073	Hela-S3	cervix:	n/a	chr11:104418932-104418943
16	CEBPB	chr11:104404965-104405432	IMR90	lung:	n/a	n/a
17	CEBPB	chr11:104539824-104540164	A549	lung:	n/a	n/a
18	CEBPB	chr11:104494200-104494571	Hela-S3	cervix:	n/a	chr11:104494285-104494296 chr11:104494285-104494296
19	CEBPB	chr11:104365021-104365243	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr11:104539749-104540204	HCT-116	colon:	n/a	n/a
21	CEBPB	chr11:104539817-104540111	HepG2	liver:	n/a	n/a
22	CEBPB	chr11:104365000-104365259	HepG2	liver:	n/a	n/a
23	CEBPB	chr11:104537036-104537358	HepG2	liver:	n/a	chr11:104537185-104537196
24	CEBPB	chr11:104335721-104335846	HepG2	liver:	n/a	chr11:104335766-104335777
25	CEBPB	chr11:104442981-104443405	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr11:104322526-104322825	A549	lung:	n/a	n/a
27	CEBPB	chr11:104355702-104355911	HepG2	liver:	n/a	chr11:104355849-104355860
28	CEBPB	chr11:104341857-104341865	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr11:104539759-104540264	A549	lung:	n/a	n/a
30	CEBPB	chr11:104335648-104335888	A549	lung:	n/a	chr11:104335766-104335777
31	CEBPB	chr11:104537084-104537209	H1-hESC	embryonic stem cell:	n/a	chr11:104537185-104537196
32	CEBPB	chr11:104418823-104419081	HepG2	liver:	n/a	chr11:104418932-104418943
33	CEBPB	chr11:104333165-104333473	IMR90	lung:	n/a	chr11:104333312-104333324
34	CEBPB	chr11:104474341-104474571	Hela-S3	cervix:	n/a	chr11:104474423-104474434
35	CEBPB	chr11:104474275-104474597	HepG2	liver:	n/a	chr11:104474423-104474434
36	CEBPB	chr11:104539680-104540284	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr11:104536453-104536685	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr11:104525090-104525327	K562	blood:	n/a	chr11:104525181-104525194 chr11:104525181-104525194 chr11:104525181-104525194 chr11:104525181-104525192
39	CEBPB	chr11:104534104-104534298	HepG2	liver:	n/a	chr11:104534205-104534216
40	CEBPB	chr11:104442251-104442397	HepG2	liver:	n/a	chr11:104442293-104442304
41	CEBPB	chr11:104512648-104512834	IMR90	lung:	n/a	chr11:104512746-104512757
42	CEBPB	chr11:104418775-104419061	A549	lung:	n/a	chr11:104418932-104418943
43	CEBPB	chr11:104539838-104540124	A549	lung:	n/a	n/a
44	CEBPB	chr11:104323015-104323790	HCT-116	colon:	n/a	n/a
45	CEBPB	chr11:104550013-104550355	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr11:104365047-104365362	A549	lung:	n/a	n/a
47	CEBPB	chr11:104365015-104365286	IMR90	lung:	n/a	n/a
48	CEBPB	chr11:104450617-104450780	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr11:104452414-104452693	IMR90	lung:	n/a	chr11:104452534-104452547
50	CEBPB	chr11:104525013-104525262	A549	lung:	n/a	chr11:104525181-104525194 chr11:104525181-104525194 chr11:104525181-104525194 chr11:104525181-104525192

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:104501066-104501116	NHBE	bronchial:	n/a
2	chr11:104405198-104405248	SAEC	small airway:	n/a
3	chr11:104435867-104435917	GM12891	blood:	n/a
4	chr11:104501066-104501116	HEK293	kidney:	embryo
5	chr11:104501066-104501116	HCT-116	colon:	n/a
6	chr11:104501066-104501116	SAEC	small airway:	n/a
7	chr11:104405198-104405248	HCPEpiC	choroid plexus:	n/a
8	chr11:104508637-104508687	AG09309	skin:	n/a
9	chr11:104435867-104435917	HAEpiC	amniotic membrane:	n/a
10	chr11:104508637-104508687	GM12891	blood:	n/a
11	chr11:104508637-104508687	SK-N-SH	brain:	n/a
12	chr11:104405198-104405248	HPAEpiC	pulmonary alveolar:	n/a
13	chr11:104501066-104501116	MCF10A-Er-Src	breast:	n/a
14	chr11:104501066-104501116	SKMC	muscle:	n/a
15	chr11:104405198-104405248	NB4	blood:	n/a
16	chr11:104501066-104501116	NB4	blood:	n/a
17	chr11:104501066-104501116	HL-60	blood:	n/a
18	chr11:104508637-104508687	GM12892	blood:	n/a
19	chr11:104405198-104405248	H1-hESC	embryonic stem cell:	embryo
20	chr11:104405198-104405248	HCF	heart:	n/a
21	chr11:104405198-104405248	PANC-1	pancreas:	n/a
22	chr11:104435867-104435917	MCF-7	breast:	n/a
23	chr11:104435867-104435917	AG04449	skin:	fetal
24	chr11:104508637-104508687	GM19239	blood:	n/a
25	chr11:104435867-104435917	K562	blood:	n/a
26	chr11:104508637-104508687	NHBE	bronchial:	n/a
27	chr11:104405198-104405248	HIPEpiC	eye:	n/a
28	chr11:104405198-104405248	HL-60	blood:	n/a
29	chr11:104435867-104435917	GM06990	blood:	n/a
30	chr11:104405198-104405248	U87	brain:	n/a
31	chr11:104501066-104501116	A549	lung:	n/a
32	chr11:104405198-104405248	AG09309	skin:	n/a
33	chr11:104501066-104501116	Hepatocyte	liver:	n/a
34	chr11:104508637-104508687	HCPEpiC	choroid plexus:	n/a
35	chr11:104405198-104405248	BE2_C	brain:	n/a
36	chr11:104435867-104435917	T-47D	breast:	n/a
37	chr11:104501066-104501116	GM12878	blood:	n/a
38	chr11:104405198-104405248	GM19239	blood:	n/a
39	chr11:104508637-104508687	A549	lung:	n/a
40	chr11:104501066-104501116	PrEC	prostate:	n/a
41	chr11:104508637-104508687	SK-N-SH_RA	brain:	n/a
42	chr11:104508637-104508687	HMEC	breast:	n/a
43	chr11:104501066-104501116	MCF-7	breast:	n/a
44	chr11:104501066-104501116	AG10803	skin:	n/a
45	chr11:104501066-104501116	BJ	skin:	n/a
46	chr11:104435867-104435917	HepG2	liver:	n/a
47	chr11:104435867-104435917	PFSK-1	brain:	n/a
48	chr11:104508637-104508687	PrEC	prostate:	n/a
49	chr11:104405198-104405248	PFSK-1	brain:	n/a
50	chr11:104501066-104501116	LNCaP	prostate:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:104318241..104320528-chr11:104331933..104333593,2	K562	blood:
2	chr11:104516723..104519201-chr11:104522234..104524667,2	K562	blood:
3	chr11:104372355..104372989-chr5:37799043..37799937,2	MCF-7	breast:
4	chr11:104331867..104333415-chr11:104336822..104339133,2	K562	blood:
5	chr11:104524242..104527061-chr11:104559725..104562588,2	K562	blood:
6	chr11:104321181..104323172-chr11:104324922..104326441,2	K562	blood:
7	chr11:104481943..104484005-chr11:104508194..104510818,2	K562	blood:
8	chr11:104505386..104506145-chr7:1705158..1706031,2	MCF-7	breast:
9	chr11:104318241..104320528-chr11:104331933..104333593,2	K562	blood:
10	chr11:104242893..104244741-chr11:104376136..104378191,2	K562	blood:
11	chr11:104481697..104482494-chr17:63790105..63790828,2	MCF-7	breast:
12	chr11:104380583..104383114-chr11:104384527..104386564,2	K562	blood:
13	chr11:104331867..104333415-chr11:104336822..104339133,2	K562	blood:
14	chr11:104377912..104380713-chr11:104411485..104413500,2	MCF-7	breast:
15	chr11:104321181..104323172-chr11:104324922..104326441,2	K562	blood:
16	chr11:104516723..104519201-chr11:104522234..104524667,2	K562	blood:
17	chr11:104380583..104383114-chr11:104384527..104386564,2	K562	blood:
18	chr11:104377912..104380713-chr11:104411485..104413500,2	MCF-7	breast:
19	chr11:104481943..104484005-chr11:104508194..104510818,2	K562	blood:
20	chr11:104524242..104527061-chr11:104559725..104562588,2	K562	blood:

(count:22 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CASP12-1	chr11:104439776-104439859	ENSG00000256422
2	lnc-CASP12-1	chr11:104442804-104443213	NONHSAT023935
3	lnc-CASP12-1	chr11:104439083-104439649	XLOC_009538
4	lnc-CASP12-1	chr11:104479965-104480102	NONHSAT023934
5	lnc-CASP12-1	chr11:104443285-104443325	XLOC_009538
6	lnc-CASP12-1	chr11:104479965-104480049	ENSG00000256422
7	lnc-CASP12-1	chr11:104439776-104439859	XLOC_009538
8	lnc-CASP12-1	chr11:104415604-104415877	ENSG00000256422
9	lnc-CASP12-1	chr11:104443285-104443325	ENSG00000256422
10	lnc-CASP12-1	chr11:104439776-104439859	NONHSAT023934
11	lnc-CASP12-1	chr11:104479965-104480030	ENSG00000256422
12	lnc-CASP12-1	chr11:104439240-104439649	NONHSAT023935
13	lnc-CASP12-1	chr11:104479965-104480024	ENSG00000256422
14	lnc-CASP12-1	chr11:104415427-104415514	ENSG00000256422
15	lnc-CASP12-1	chr11:104439221-104439649	NONHSAT023934
16	lnc-CASP12-1	chr11:104382877-104382961	ENSG00000256422
17	lnc-CASP12-1	chr11:104479965-104480062	XLOC_009538
18	lnc-CASP12-1	chr11:104410659-104410753	ENSG00000256422
19	lnc-CASP12-1	chr11:104439776-104439859	NONHSAT023935
20	lnc-CASP12-1	chr11:104415427-104415514	ENSG00000256422
21	lnc-CASP12-1	chr11:104439258-104439649	ENSG00000256422
22	lnc-CASP12-1	chr11:104415604-104415877	ENSG00000256422

No data

Variant related genes	Relation type
ENSG00000270449	TF binding region
ENSG00000256422	TF binding region
ENSG00000270449	CpG island
ENSG00000256422	CpG island

Extended variants
information (count: 7025 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:7025 , 50 per page) page: 1 2 3 4 5 6 7 ... 141

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs80003098	chr11:104317249-104317250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs369423510	chr11:104317272-104317273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs187421501	chr11:104317292-104317293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs140762486	chr11:104317322-104317323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs576240966	chr11:104317375-104317376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs191791316	chr11:104317390-104317391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs563044235	chr11:104317391-104317392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs531949829	chr11:104317408-104317409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs149686714	chr11:104317471-104317472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs543234927	chr11:104317476-104317477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs369266060	chr11:104317477-104317478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs568521239	chr11:104317492-104317493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs2450963	chr11:104317496-104317497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs114031487	chr11:104317525-104317526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs182526887	chr11:104317557-104317558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs146675819	chr11:104317596-104317597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs2220445	chr11:104317629-104317630	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs377721830	chr11:104317639-104317640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs569715347	chr11:104317647-104317648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs371206676	chr11:104317691-104317692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs370066027	chr11:104317709-104317710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs187122483	chr11:104317716-104317717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs555300441	chr11:104317717-104317718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs572103712	chr11:104317727-104317728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs192805934	chr11:104317729-104317730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs557738822	chr11:104317737-104317738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs145608056	chr11:104317767-104317768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs138080192	chr11:104317805-104317806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs184220529	chr11:104317823-104317824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs531941332	chr11:104317842-104317843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs542408444	chr11:104317845-104317846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs562187733	chr11:104317864-104317865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs527748304	chr11:104317880-104317881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs11604545	chr11:104317897-104317898	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs376085995	chr11:104317904-104317905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs564747824	chr11:104317910-104317911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs11226365	chr11:104317911-104317912	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs533167889	chr11:104317918-104317919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs569324364	chr11:104317921-104317922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs2200753	chr11:104317936-104317937	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs569909186	chr11:104317995-104317996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs539049024	chr11:104318010-104318011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs111381434	chr11:104318011-104318012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs140075159	chr11:104318019-104318020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs190763681	chr11:104318042-104318043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs116265812	chr11:104318113-104318114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs549151661	chr11:104318123-104318124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs193027160	chr11:104318131-104318132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs75613859	chr11:104318134-104318135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs184400324	chr11:104318146-104318147	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
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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:749 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:104314600-104323200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr11:104316000-104320200	Weak transcription	Fetal Heart	heart
3	chr11:104316800-104321400	Weak transcription	Stomach Mucosa	stomach
4	chr11:104319400-104320200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr11:104320200-104320600	Enhancers	Fetal Heart	heart
6	chr11:104320200-104322000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr11:104320600-104320800	Weak transcription	Fetal Heart	heart
8	chr11:104320800-104321800	Enhancers	Fetal Heart	heart
9	chr11:104321400-104322800	Enhancers	Stomach Mucosa	stomach
10	chr11:104321800-104322200	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr11:104321800-104322200	Flanking Active TSS	Fetal Heart	heart
12	chr11:104322000-104322200	Enhancers	Aorta	Aorta
13	chr11:104322000-104322200	Enhancers	Ovary	ovary
14	chr11:104322000-104323200	Enhancers	NHEK	skin
15	chr11:104322000-104324000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr11:104322000-104324000	Enhancers	Hela-S3	cervix
17	chr11:104322000-104324000	Enhancers	HMEC	breast
18	chr11:104322200-104322800	Weak transcription	Aorta	Aorta
19	chr11:104322200-104322800	Weak transcription	Ovary	ovary
20	chr11:104322200-104323800	Enhancers	Fetal Heart	heart
21	chr11:104322200-104324000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr11:104322800-104323200	Weak transcription	Stomach Mucosa	stomach
23	chr11:104322800-104323600	Enhancers	Aorta	Aorta
24	chr11:104322800-104323800	Enhancers	Ovary	ovary
25	chr11:104323000-104323800	Enhancers	Muscle Satellite Cultured Cells	--
26	chr11:104323200-104323600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr11:104323200-104323600	Flanking Active TSS	NHEK	skin
28	chr11:104323200-104323800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr11:104323200-104324000	Enhancers	Stomach Mucosa	stomach
30	chr11:104323400-104323800	Enhancers	Placenta Amnion	Placenta Amnion
31	chr11:104323600-104324400	Enhancers	NHEK	skin
32	chr11:104323800-104334000	Weak transcription	Fetal Heart	heart
33	chr11:104324000-104328800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr11:104328800-104329000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr11:104332600-104333400	Enhancers	Psoas Muscle	Psoas
36	chr11:104332800-104333000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr11:104332800-104333200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr11:104333000-104333400	Enhancers	Skeletal Muscle Female	skeletal muscle
39	chr11:104333000-104333800	Enhancers	Muscle Satellite Cultured Cells	--
40	chr11:104333600-104333800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr11:104333800-104336200	Weak transcription	Muscle Satellite Cultured Cells	--
42	chr11:104334000-104334600	Enhancers	Fetal Heart	heart
43	chr11:104335000-104335800	Enhancers	Fetal Muscle Leg	muscle
44	chr11:104336200-104336600	Enhancers	Muscle Satellite Cultured Cells	--
45	chr11:104336200-104336800	Enhancers	Cortex derived primary cultured neurospheres	brain
46	chr11:104336600-104336800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr11:104336600-104337000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr11:104336600-104338200	Weak transcription	Muscle Satellite Cultured Cells	--
49	chr11:104336800-104338000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr11:104338000-104339600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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