Variant report

Variant	nsv1053886
Chromosome Location	chr11:104328822-104562129
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1117)
CpG islands
(count:244)
Chromatin interactive
region (count:17)
LncRNA
region (count:22)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1117 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

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	chr11:104451956-104452294	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL11A	chr11:104452026-104452271	H1-hESC	embryonic stem cell:	n/a	n/a
5	BRCA1	chr11:104336495-104336518	Hela-S3	cervix:	n/a	n/a
6	CBX3	chr11:104539778-104540232	HCT-116	colon:	n/a	n/a
7	CBX3	chr11:104520974-104521253	HCT-116	colon:	n/a	n/a
8	CEBPB	chr11:104474341-104474571	Hela-S3	cervix:	n/a	chr11:104474423-104474434
9	CEBPB	chr11:104418754-104419111	IMR90	lung:	n/a	chr11:104418932-104418943
10	CEBPB	chr11:104418796-104419073	Hela-S3	cervix:	n/a	chr11:104418932-104418943
11	CEBPB	chr11:104480012-104480256	H1-hESC	embryonic stem cell:	n/a	chr11:104480194-104480207
12	CEBPB	chr11:104550013-104550355	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr11:104444109-104444452	IMR90	lung:	n/a	chr11:104444139-104444152
14	CEBPB	chr11:104442981-104443405	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr11:104442251-104442397	HepG2	liver:	n/a	chr11:104442293-104442304
16	CEBPB	chr11:104474320-104474546	A549	lung:	n/a	chr11:104474423-104474434
17	CEBPB	chr11:104365021-104365243	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr11:104365000-104365259	HepG2	liver:	n/a	n/a
19	CEBPB	chr11:104512599-104512892	HepG2	liver:	n/a	chr11:104512746-104512757
20	CEBPB	chr11:104512648-104512834	IMR90	lung:	n/a	chr11:104512746-104512757
21	CEBPB	chr11:104537084-104537209	H1-hESC	embryonic stem cell:	n/a	chr11:104537185-104537196
22	CEBPB	chr11:104418775-104419061	A549	lung:	n/a	chr11:104418932-104418943
23	CEBPB	chr11:104418823-104419081	HepG2	liver:	n/a	chr11:104418932-104418943
24	CEBPB	chr11:104539817-104540111	HepG2	liver:	n/a	n/a
25	CEBPB	chr11:104539824-104540164	A549	lung:	n/a	n/a
26	CEBPB	chr11:104355702-104355911	HepG2	liver:	n/a	chr11:104355849-104355860
27	CEBPB	chr11:104539700-104540315	HCT-116	colon:	n/a	n/a
28	CEBPB	chr11:104489254-104489482	HepG2	liver:	n/a	n/a
29	CEBPB	chr11:104494255-104494393	A549	lung:	n/a	chr11:104494285-104494296 chr11:104494285-104494296
30	CEBPB	chr11:104335721-104335846	HepG2	liver:	n/a	chr11:104335766-104335777
31	CEBPB	chr11:104365015-104365286	IMR90	lung:	n/a	n/a
32	CEBPB	chr11:104537036-104537358	HepG2	liver:	n/a	chr11:104537185-104537196
33	CEBPB	chr11:104452414-104452693	IMR90	lung:	n/a	chr11:104452534-104452547
34	CEBPB	chr11:104534113-104534393	IMR90	lung:	n/a	chr11:104534205-104534216
35	CEBPB	chr11:104494200-104494571	Hela-S3	cervix:	n/a	chr11:104494285-104494296 chr11:104494285-104494296
36	CEBPB	chr11:104539838-104540124	A549	lung:	n/a	n/a
37	CEBPB	chr11:104534104-104534298	HepG2	liver:	n/a	chr11:104534205-104534216
38	CEBPB	chr11:104365047-104365362	A549	lung:	n/a	n/a
39	CEBPB	chr11:104450058-104450309	HepG2	liver:	n/a	chr11:104450182-104450193 chr11:104450182-104450195 chr11:104450183-104450194
40	CEBPB	chr11:104404965-104405432	IMR90	lung:	n/a	n/a
41	CEBPB	chr11:104450617-104450780	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr11:104539749-104540204	HCT-116	colon:	n/a	n/a
43	CEBPB	chr11:104330837-104331040	Hela-S3	cervix:	n/a	chr11:104330940-104330953 chr11:104330942-104330953
44	CEBPB	chr11:104525013-104525262	A549	lung:	n/a	chr11:104525181-104525194 chr11:104525181-104525194 chr11:104525181-104525194 chr11:104525181-104525192
45	CEBPB	chr11:104536365-104536737	IMR90	lung:	n/a	n/a
46	CEBPB	chr11:104489291-104489495	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr11:104525090-104525327	K562	blood:	n/a	chr11:104525181-104525194 chr11:104525181-104525194 chr11:104525181-104525194 chr11:104525181-104525192
48	CEBPB	chr11:104479994-104480282	Hela-S3	cervix:	n/a	chr11:104480194-104480207
49	CEBPB	chr11:104539774-104540189	IMR90	lung:	n/a	n/a
50	CEBPB	chr11:104539759-104540264	A549	lung:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:104435867-104435917	NH-A	brain:	n/a
2	chr11:104435867-104435917	HCT-116	colon:	n/a
3	chr11:104405198-104405248	IMR90	lung:	fetal
4	chr11:104501066-104501116	T-47D	breast:	n/a
5	chr11:104405198-104405248	ProgFib	skin:	n/a
6	chr11:104501066-104501116	Hela-S3	cervix:	n/a
7	chr11:104435867-104435917	ovcar-3	ovarian:	n/a
8	chr11:104508637-104508687	SK-N-MC	brain:	n/a
9	chr11:104435867-104435917	Hela-S3	cervix:	n/a
10	chr11:104435867-104435917	HRE	kidney:	n/a
11	chr11:104501066-104501116	PANC-1	pancreas:	n/a
12	chr11:104501066-104501116	HAEpiC	amniotic membrane:	n/a
13	chr11:104435867-104435917	HPAEpiC	pulmonary alveolar:	n/a
14	chr11:104501066-104501116	GM12878	blood:	n/a
15	chr11:104501066-104501116	BE2_C	brain:	n/a
16	chr11:104501066-104501116	GM06990	blood:	n/a
17	chr11:104508637-104508687	LNCaP	prostate:	n/a
18	chr11:104435867-104435917	GM12878	blood:	n/a
19	chr11:104405198-104405248	U87	brain:	n/a
20	chr11:104501066-104501116	PFSK-1	brain:	n/a
21	chr11:104501066-104501116	RPTEC	kidney:	n/a
22	chr11:104405198-104405248	RPTEC	kidney:	n/a
23	chr11:104508637-104508687	NHBE	bronchial:	n/a
24	chr11:104508637-104508687	GM06990	blood:	n/a
25	chr11:104508637-104508687	SKMC	muscle:	n/a
26	chr11:104405198-104405248	ovcar-3	ovarian:	n/a
27	chr11:104405198-104405248	Hepatocyte	liver:	n/a
28	chr11:104508637-104508687	CMK	blood:	n/a
29	chr11:104508637-104508687	ECC-1	luminal epithelium:	n/a
30	chr11:104508637-104508687	AG10803	skin:	n/a
31	chr11:104435867-104435917	AG09319	gingival:	n/a
32	chr11:104501066-104501116	HRE	kidney:	n/a
33	chr11:104508637-104508687	GM19239	blood:	n/a
34	chr11:104405198-104405248	Hela-S3	cervix:	n/a
35	chr11:104501066-104501116	SKMC	muscle:	n/a
36	chr11:104508637-104508687	AG09309	skin:	n/a
37	chr11:104501066-104501116	K562	blood:	n/a
38	chr11:104501066-104501116	HCPEpiC	choroid plexus:	n/a
39	chr11:104405198-104405248	GM06990	blood:	n/a
40	chr11:104501066-104501116	SAEC	small airway:	n/a
41	chr11:104501066-104501116	CMK	blood:	n/a
42	chr11:104435867-104435917	GM12891	blood:	n/a
43	chr11:104501066-104501116	SK-N-SH	brain:	n/a
44	chr11:104405198-104405248	NHBE	bronchial:	n/a
45	chr11:104508637-104508687	MCF10A-Er-Src	breast:	n/a
46	chr11:104508637-104508687	HEEpiC	esophagus:	n/a
47	chr11:104501066-104501116	Jurkat	blood:	n/a
48	chr11:104405198-104405248	HEEpiC	esophagus:	n/a
49	chr11:104435867-104435917	HUVEC	blood vessel:	n/a
50	chr11:104405198-104405248	PANC-1	pancreas:	n/a

(count:17 , 50 per page) page: 1

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

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CASP12-1	chr11:104410659-104410753	ENSG00000256422
2	lnc-CASP12-1	chr11:104479965-104480049	ENSG00000256422
3	lnc-CASP12-1	chr11:104479965-104480062	XLOC_009538
4	lnc-CASP12-1	chr11:104439240-104439649	NONHSAT023935
5	lnc-CASP12-1	chr11:104439221-104439649	NONHSAT023934
6	lnc-CASP12-1	chr11:104479965-104480030	ENSG00000256422
7	lnc-CASP12-1	chr11:104439776-104439859	NONHSAT023934
8	lnc-CASP12-1	chr11:104415604-104415877	ENSG00000256422
9	lnc-CASP12-1	chr11:104439258-104439649	ENSG00000256422
10	lnc-CASP12-1	chr11:104415427-104415514	ENSG00000256422
11	lnc-CASP12-1	chr11:104415427-104415514	ENSG00000256422
12	lnc-CASP12-1	chr11:104439776-104439859	XLOC_009538
13	lnc-CASP12-1	chr11:104382877-104382961	ENSG00000256422
14	lnc-CASP12-1	chr11:104415604-104415877	ENSG00000256422
15	lnc-CASP12-1	chr11:104439776-104439859	NONHSAT023935
16	lnc-CASP12-1	chr11:104443285-104443325	ENSG00000256422
17	lnc-CASP12-1	chr11:104479965-104480024	ENSG00000256422
18	lnc-CASP12-1	chr11:104443285-104443325	XLOC_009538
19	lnc-CASP12-1	chr11:104439083-104439649	XLOC_009538
20	lnc-CASP12-1	chr11:104479965-104480102	NONHSAT023934
21	lnc-CASP12-1	chr11:104442804-104443213	NONHSAT023935
22	lnc-CASP12-1	chr11:104439776-104439859	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: 6576 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:6576 , 50 per page) page: 1 2 3 4 5 6 7 ... 132

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs533735122	chr11:104328825-104328826	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs553724264	chr11:104328891-104328892	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs576828224	chr11:104328902-104328903	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs539160987	chr11:104328922-104328923	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs183674633	chr11:104328931-104328932	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs111235137	chr11:104328972-104328973	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs562510078	chr11:104328987-104328988	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs541882812	chr11:104328990-104328991	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs561545851	chr11:104328999-104329000	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs74796790	chr11:104329098-104329099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs376228249	chr11:104329110-104329111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs540822667	chr11:104329112-104329113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs367600238	chr11:104329153-104329154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs560529777	chr11:104329183-104329184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs61339041	chr11:104329214-104329215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs532592172	chr11:104329218-104329219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs561491829	chr11:104329233-104329234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs531334692	chr11:104329236-104329237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs76502620	chr11:104329271-104329272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs77022477	chr11:104329279-104329280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs527514672	chr11:104329339-104329340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs189017441	chr11:104329345-104329346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs376710710	chr11:104329350-104329351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs114496913	chr11:104329354-104329355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs192995163	chr11:104329366-104329367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs142501538	chr11:104329371-104329372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs183575970	chr11:104329374-104329375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs547142780	chr11:104329407-104329408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs570573032	chr11:104329423-104329424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs187299969	chr11:104329460-104329461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs555972062	chr11:104329556-104329557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs191657856	chr11:104329570-104329571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs183867180	chr11:104329653-104329654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs188092969	chr11:104329666-104329667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs575145816	chr11:104329672-104329673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs79608255	chr11:104329673-104329674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs564231463	chr11:104329682-104329683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs564868557	chr11:104329690-104329691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs554315523	chr11:104329699-104329700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs577383453	chr11:104329706-104329707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs548639172	chr11:104329714-104329715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs546404211	chr11:104329725-104329726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs562639345	chr11:104329727-104329728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs113882583	chr11:104329767-104329768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs35184287	chr11:104329770-104329771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs531730845	chr11:104329788-104329789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs532014225	chr11:104329790-104329791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs192540671	chr11:104329797-104329798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs145969790	chr11:104329843-104329844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs547388774	chr11:104329861-104329862	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:717 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:104323800-104334000	Weak transcription	Fetal Heart	heart
2	chr11:104328800-104329000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr11:104332600-104333400	Enhancers	Psoas Muscle	Psoas
4	chr11:104332800-104333000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr11:104332800-104333200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr11:104333000-104333400	Enhancers	Skeletal Muscle Female	skeletal muscle
7	chr11:104333000-104333800	Enhancers	Muscle Satellite Cultured Cells	--
8	chr11:104333600-104333800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr11:104333800-104336200	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr11:104334000-104334600	Enhancers	Fetal Heart	heart
11	chr11:104335000-104335800	Enhancers	Fetal Muscle Leg	muscle
12	chr11:104336200-104336600	Enhancers	Muscle Satellite Cultured Cells	--
13	chr11:104336200-104336800	Enhancers	Cortex derived primary cultured neurospheres	brain
14	chr11:104336600-104336800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr11:104336600-104337000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr11:104336600-104338200	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr11:104336800-104338000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr11:104338000-104339600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr11:104338200-104338400	Enhancers	Muscle Satellite Cultured Cells	--
20	chr11:104338200-104338600	Enhancers	Dnd41	blood
21	chr11:104338200-104338600	Enhancers	HSMMtube	muscle
22	chr11:104340400-104340800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr11:104342200-104342600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr11:104342200-104342600	Enhancers	NHEK	skin
25	chr11:104344800-104345000	Enhancers	Ovary	ovary
26	chr11:104345200-104346800	Weak transcription	Ovary	ovary
27	chr11:104345800-104346000	Enhancers	Stomach Mucosa	stomach
28	chr11:104346000-104346600	Weak transcription	Stomach Mucosa	stomach
29	chr11:104346600-104347200	Enhancers	Stomach Mucosa	stomach
30	chr11:104346800-104347200	Enhancers	Ovary	ovary
31	chr11:104347000-104347600	Enhancers	Muscle Satellite Cultured Cells	--
32	chr11:104347200-104348400	Weak transcription	Stomach Mucosa	stomach
33	chr11:104347200-104357800	Weak transcription	Ovary	ovary
34	chr11:104348400-104348600	Enhancers	Stomach Mucosa	stomach
35	chr11:104348400-104349200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr11:104355600-104355800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr11:104355600-104357000	Enhancers	Fetal Lung	lung
38	chr11:104355600-104358400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr11:104356000-104356200	Enhancers	Brain Germinal Matrix	brain
40	chr11:104356400-104356800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr11:104356400-104357400	Weak transcription	Brain Germinal Matrix	brain
42	chr11:104356600-104358200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr11:104356800-104357200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr11:104357000-104357800	Weak transcription	Fetal Lung	lung
45	chr11:104357200-104358400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr11:104357200-104358400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr11:104357400-104358400	Enhancers	Brain Germinal Matrix	brain
48	chr11:104357600-104358000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr11:104357600-104359600	Enhancers	Fetal Heart	heart
50	chr11:104357800-104358000	Enhancers	Ovary	ovary

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