Variant report

Variant	nsv825772
Chromosome Location	chr11:17723530-17783128
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1653)
CpG islands
(count:2504)
Chromatin interactive
region (count:64)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1653 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:17752734-17752850	HepG2	liver:	n/a	n/a
2	ATF1	chr11:17738453-17738597	K562	blood:	n/a	n/a
3	ATF3	chr11:17725592-17725911	GM12878	blood:	n/a	n/a
4	ATF3	chr11:17725652-17725838	K562	blood:	n/a	n/a
5	BACH1	chr11:17743740-17743870	K562	blood:	n/a	n/a
6	BACH1	chr11:17735827-17736024	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr11:17756192-17756315	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr11:17781684-17782192	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr11:17743545-17743911	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr11:17781712-17781838	K562	blood:	n/a	n/a
11	BACH1	chr11:17740034-17740383	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr11:17741849-17741864	H1-hESC	embryonic stem cell:	n/a	n/a
13	BHLHE40	chr11:17782021-17782165	GM12878	blood:	n/a	n/a
14	BHLHE40	chr11:17752607-17752898	GM12878	blood:	n/a	n/a
15	BHLHE40	chr11:17756560-17756818	HepG2	liver:	n/a	chr11:17756644-17756660
16	BHLHE40	chr11:17756573-17756763	GM12878	blood:	n/a	chr11:17756644-17756660
17	BHLHE40	chr11:17781973-17782310	K562	blood:	n/a	n/a
18	BHLHE40	chr11:17756580-17756727	K562	blood:	n/a	chr11:17756644-17756660
19	BRCA1	chr11:17781963-17782291	HepG2	liver:	n/a	n/a
20	BRCA1	chr11:17752729-17752836	HepG2	liver:	n/a	n/a
21	BRCA1	chr11:17741781-17741867	H1-hESC	embryonic stem cell:	n/a	n/a
22	BRCA1	chr11:17752601-17752887	H1-hESC	embryonic stem cell:	n/a	n/a
23	BRCA1	chr11:17752773-17752833	GM12878	blood:	n/a	n/a
24	CBX3	chr11:17781908-17782256	K562	blood:	n/a	n/a
25	CCNT2	chr11:17738413-17738634	K562	blood:	n/a	n/a
26	CEBPB	chr11:17772354-17772618	HepG2	liver:	n/a	chr11:17772511-17772522
27	CEBPB	chr11:17741695-17741950	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr11:17752607-17752941	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr11:17741618-17741818	HepG2	liver:	n/a	n/a
30	CEBPB	chr11:17772452-17772532	H1-hESC	embryonic stem cell:	n/a	chr11:17772511-17772522
31	CEBPB	chr11:17772409-17772648	HepG2	liver:	n/a	chr11:17772511-17772522
32	CEBPB	chr11:17772414-17772625	Hela-S3	cervix:	n/a	chr11:17772511-17772522
33	CEBPB	chr11:17725560-17725583	A549	lung:	n/a	n/a
34	CEBPB	chr11:17779238-17779303	HepG2	liver:	n/a	n/a
35	CEBPB	chr11:17776105-17776129	HepG2	liver:	n/a	n/a
36	CEBPB	chr11:17782011-17782346	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr11:17743677-17743912	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr11:17772348-17772662	HepG2	liver:	n/a	chr11:17772511-17772522
39	CEBPB	chr11:17772343-17772697	HepG2	liver:	n/a	chr11:17772511-17772522
40	CEBPB	chr11:17752652-17752914	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr11:17752665-17752866	HepG2	liver:	n/a	n/a
42	CEBPB	chr11:17772512-17772518	K562	blood:	n/a	n/a
43	CEBPB	chr11:17779188-17779456	IMR90	lung:	n/a	chr11:17779294-17779305
44	CEBPB	chr11:17756623-17756736	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr11:17725586-17725830	K562	blood:	n/a	n/a
46	CHD1	chr11:17756611-17756687	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD1	chr11:17752489-17753087	IMR90	lung:	n/a	n/a
48	CHD1	chr11:17741837-17741948	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD1	chr11:17752611-17752799	GM12878	blood:	n/a	n/a
50	CHD2	chr11:17740541-17740608	H1-hESC	embryonic stem cell:	n/a	n/a

(count:2504 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:17740967-17741017	K562	blood:	n/a
2	chr11:17756435-17756485	HCT-116	colon:	n/a
3	chr11:17760602-17760652	AG04450	lung:	fetal
4	chr11:17740967-17741017	K562	blood:	n/a
5	chr11:17756435-17756485	HCT-116	colon:	n/a
6	chr11:17760602-17760652	AG04450	lung:	fetal
7	chr11:17752634-17752684	SAEC	small airway:	n/a
8	chr11:17743667-17743717	H1-hESC	embryonic stem cell:	embryo
9	chr11:17743761-17743811	Hela-S3	cervix:	n/a
10	chr11:17758537-17758587	NB4	blood:	n/a
11	chr11:17742741-17742791	HIPEpiC	eye:	n/a
12	chr11:17740430-17740480	HEK293	kidney:	embryo
13	chr11:17741243-17741293	SKMC	muscle:	n/a
14	chr11:17757129-17757179	AG04450	lung:	fetal
15	chr11:17743080-17743130	Jurkat	blood:	n/a
16	chr11:17741243-17741293	NH-A	brain:	n/a
17	chr11:17756750-17756800	MCF10A-Er-Src	breast:	n/a
18	chr11:17756761-17756811	RPTEC	kidney:	n/a
19	chr11:17758285-17758335	SK-N-MC	brain:	n/a
20	chr11:17757415-17757465	SKMC	muscle:	n/a
21	chr11:17756479-17756529	BJ	skin:	n/a
22	chr11:17738031-17738081	U87	brain:	n/a
23	chr11:17743080-17743130	HCF	heart:	n/a
24	chr11:17757415-17757465	Hela-S3	cervix:	n/a
25	chr11:17756435-17756485	IMR90	lung:	fetal
26	chr11:17740430-17740480	HMEC	breast:	n/a
27	chr11:17757342-17757392	GM12892	blood:	n/a
28	chr11:17758537-17758587	Hepatocyte	liver:	n/a
29	chr11:17742741-17742791	AG10803	skin:	n/a
30	chr11:17757415-17757465	HUVEC	blood vessel:	n/a
31	chr11:17760602-17760652	SK-N-SH_RA	brain:	n/a
32	chr11:17741925-17741975	HCM	heart:	n/a
33	chr11:17761718-17761768	NHBE	bronchial:	n/a
34	chr11:17747289-17747339	IMR90	lung:	fetal
35	chr11:17761718-17761768	Hepatocyte	liver:	n/a
36	chr11:17756986-17757036	AoSMC	blood vessel:	n/a
37	chr11:17740977-17741027	PrEC	prostate:	n/a
38	chr11:17752634-17752684	HPAEpiC	pulmonary alveolar:	n/a
39	chr11:17741925-17741975	T-47D	breast:	n/a
40	chr11:17756479-17756529	AG09309	skin:	n/a
41	chr11:17757129-17757179	MCF10A-Er-Src	breast:	n/a
42	chr11:17741070-17741120	H1-hESC	embryonic stem cell:	embryo
43	chr11:17755937-17755987	HepG2	liver:	n/a
44	chr11:17743840-17743890	HCM	heart:	n/a
45	chr11:17743946-17743996	AG09309	skin:	n/a
46	chr11:17741925-17741975	HIPEpiC	eye:	n/a
47	chr11:17741070-17741120	GM12892	blood:	n/a
48	chr11:17747289-17747339	HRPEpiC	eye:	n/a
49	chr11:17760574-17760624	PFSK-1	brain:	n/a
50	chr11:17760602-17760652	HL-60	blood:	n/a

(count:64 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:17726249..17728928-chr11:17732573..17735083,2	MCF-7	breast:
2	chr11:17722486..17724717-chr11:17727954..17730842,2	K562	blood:
3	chr11:17722486..17724717-chr11:17727954..17730842,2	K562	blood:
4	chr11:17735220..17735764-chr11:17743713..17744525,2	MCF-7	breast:
5	chr11:17620217..17621179-chr11:17742829..17744247,6	MCF-7	breast:
6	chr11:17752325..17753223-chr11:18001001..18001982,6	K562	blood:
7	chr11:17764908..17766462-chr11:17767114..17769351,2	K562	blood:
8	chr11:17781854..17784746-chr11:17785272..17786871,2	MCF-7	breast:
9	chr11:17781675..17782374-chr11:17994338..17995285,3	MCF-7	breast:
10	chr11:17751795..17753232-chr11:17999934..18001786,19	MCF-7	breast:
11	chr11:17622892..17623600-chr11:17752018..17752807,2	MCF-7	breast:
12	chr11:17782031..17782545-chr11:17865700..17866358,2	MCF-7	breast:
13	chr11:17781047..17783603-chr11:17891179..17893367,2	K562	blood:
14	chr11:17755705..17757483-chr11:17762543..17764877,2	K562	blood:
15	chr11:17735220..17735764-chr11:17743713..17744525,2	MCF-7	breast:
16	chr11:17781544..17782571-chr11:17999973..18000867,4	K562	blood:
17	chr11:17757319..17757897-chr11:17781730..17782258,2	K562	blood:
18	chr11:17781701..17782562-chr11:17868027..17868986,3	MCF-7	breast:
19	chr11:17762630..17764298-chr11:17768234..17770289,2	MCF-7	breast:
20	chr11:17620215..17621250-chr11:17751773..17752935,12	MCF-7	breast:
21	chr11:17588922..17590478-chr11:17766034..17768818,2	K562	blood:
22	chr11:17752483..17753383-chr11:17994354..17995164,3	MCF-7	breast:
23	chr11:17764908..17766462-chr11:17767114..17769351,2	K562	blood:
24	chr11:17622678..17623570-chr11:17743313..17743816,2	MCF-7	breast:
25	chr11:17781843..17782605-chr11:17868062..17868630,2	MCF-7	breast:
26	chr11:17762630..17764298-chr11:17768234..17770289,2	MCF-7	breast:
27	chr11:17769238..17771607-chr11:17779598..17782123,2	K562	blood:
28	chr11:17752436..17753246-chr11:17868432..17868961,2	MCF-7	breast:
29	chr11:17751921..17752763-chr19:36040271..36040795,2	MCF-7	breast:
30	chr11:17752076..17753447-chr11:17867688..17868717,4	MCF-7	breast:
31	chr11:17614764..17616023-chr11:17751704..17752684,3	MCF-7	breast:
32	chr11:17781823..17782570-chr11:18001193..18001905,2	MCF-7	breast:
33	chr11:17725619..17727703-chr11:17740365..17742924,2	K562	blood:
34	chr11:17752308..17753219-chr11:18785582..18786221,2	K562	blood:
35	chr11:17620244..17621142-chr11:17752157..17753016,5	MCF-7	breast:
36	chr11:17726249..17728928-chr11:17732573..17735083,2	MCF-7	breast:
37	chr11:17751864..17753212-chr11:17999973..18001949,7	MCF-7	breast:
38	chr11:17622422..17624117-chr11:17750393..17752396,2	MCF-7	breast:
39	chr11:17769238..17771607-chr11:17779598..17782123,2	K562	blood:
40	chr11:17757117..17759964-chr11:17765393..17768099,2	MCF-7	breast:
41	chr11:17782032..17782544-chr11:17801368..17801871,2	MCF-7	breast:
42	chr11:17781836..17782575-chr11:17999957..18000865,3	MCF-7	breast:
43	chr11:17768263..17770539-chr11:17771638..17773890,2	MCF-7	breast:
44	chr11:17753668..17754453-chr6:57615850..57616702,2	MCF-7	breast:
45	chr11:17619891..17621109-chr11:17743288..17744431,5	MCF-7	breast:
46	chr11:17752308..17752866-chr11:17774705..17775593,2	MCF-7	breast:
47	chr11:17752064..17753282-chr11:17994336..17995305,5	MCF-7	breast:
48	chr11:17622618..17623441-chr11:17752027..17752742,2	K562	blood:
49	chr11:17752292..17753246-chr11:17999986..18000903,4	K562	blood:
50	chr11:17768263..17770539-chr11:17771638..17773890,2	MCF-7	breast:

No data

Variant related genes	Relation type
KCNC1	TF binding region
MYOD1	TF binding region
KCNC1	CpG island
MYOD1	CpG island
ENSG00000129159	chromatin interactions
ENSG00000129152	chromatin interactions

Extended variants
information (count: 2284 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:2284 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs528146953	chr11:17723557-17723558	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs7109765	chr11:17723577-17723578	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs368517784	chr11:17723607-17723608	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs112867948	chr11:17723629-17723630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs182314218	chr11:17723669-17723670	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs113605954	chr11:17723680-17723681	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs201138472	chr11:17723681-17723682	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs138946282	chr11:17723688-17723689	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs72212574	chr11:17723707-17723708	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs3051799	chr11:17723717-17723718	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs550477227	chr11:17723759-17723760	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs569107141	chr11:17723764-17723765	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs6416179	chr11:17723798-17723799	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs548327027	chr11:17723843-17723844	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs567697571	chr11:17723871-17723872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs186711230	chr11:17723984-17723985	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs535122567	chr11:17723985-17723986	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs112261208	chr11:17724037-17724038	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs553428483	chr11:17724050-17724051	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs571649658	chr11:17724118-17724119	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs191175023	chr11:17724129-17724130	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs550438424	chr11:17724137-17724138	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs184065605	chr11:17724156-17724157	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs542861195	chr11:17724189-17724190	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs117631832	chr11:17724200-17724201	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs572648488	chr11:17724254-17724255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs539924755	chr11:17724256-17724257	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs139531715	chr11:17724258-17724259	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs532003087	chr11:17724303-17724304	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs544148643	chr11:17724331-17724332	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs527841483	chr11:17724361-17724362	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs529993044	chr11:17724385-17724386	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs144476609	chr11:17724394-17724395	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs2336846	chr11:17724426-17724427	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs548043529	chr11:17724433-17724434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs146636573	chr11:17724465-17724466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs6416180	chr11:17724491-17724492	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs571740813	chr11:17724495-17724496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs527317908	chr11:17724511-17724512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs188612119	chr11:17724537-17724538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs557280921	chr11:17724569-17724570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs551864462	chr11:17724636-17724637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs569488723	chr11:17724644-17724645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs373119321	chr11:17724682-17724683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs536948228	chr11:17724715-17724716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs61880587	chr11:17724718-17724719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs372793875	chr11:17724733-17724734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs534099155	chr11:17724740-17724741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs558234437	chr11:17724763-17724764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs576489914	chr11:17724769-17724770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Multiple myeloma	16461302	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Lung adenocarcinoma	17086460	CNVD
Urothelial cell carcinoma	18451213	CNVD
Lung cancer	17086460	CNVD
Uterine serous papillary cancer	19536090	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Medulloblastoma	16783165	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:968 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:17719000-17724400	Enhancers	Fetal Muscle Leg	muscle
2	chr11:17721200-17723600	Enhancers	Skeletal Muscle Female	skeletal muscle
3	chr11:17721800-17729000	Weak transcription	Fetal Muscle Trunk	muscle
4	chr11:17721800-17729400	Weak transcription	Psoas Muscle	Psoas
5	chr11:17723600-17729000	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr11:17728800-17735600	Enhancers	Fetal Muscle Leg	muscle
7	chr11:17729000-17729400	Enhancers	Placenta	Placenta
8	chr11:17729000-17730200	Enhancers	Fetal Lung	lung
9	chr11:17729000-17730600	Enhancers	Fetal Muscle Trunk	muscle
10	chr11:17729000-17730800	Enhancers	Skeletal Muscle Female	skeletal muscle
11	chr11:17729200-17730200	Enhancers	HSMMtube	muscle
12	chr11:17729200-17730800	Enhancers	Skeletal Muscle Male	skeletal muscle
13	chr11:17729400-17729800	Bivalent Enhancer	Fetal Stomach	stomach
14	chr11:17729400-17729800	Enhancers	Right Atrium	heart
15	chr11:17729400-17730200	Enhancers	Psoas Muscle	Psoas
16	chr11:17729600-17729800	Bivalent Enhancer	Placenta	Placenta
17	chr11:17729800-17736000	Weak transcription	Right Atrium	heart
18	chr11:17730200-17730400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr11:17730200-17730400	Bivalent Enhancer	Placenta	Placenta
20	chr11:17730200-17735600	Weak transcription	Psoas Muscle	Psoas
21	chr11:17730200-17735600	Weak transcription	HSMMtube	muscle
22	chr11:17730600-17731800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
23	chr11:17732000-17735800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr11:17732000-17736200	Enhancers	Skeletal Muscle Male	skeletal muscle
25	chr11:17732000-17736200	Enhancers	Skeletal Muscle Female	skeletal muscle
26	chr11:17732600-17733000	Enhancers	Fetal Muscle Trunk	muscle
27	chr11:17733000-17734000	Weak transcription	Fetal Muscle Trunk	muscle
28	chr11:17733600-17733800	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr11:17733600-17734000	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
30	chr11:17733800-17734000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
31	chr11:17734000-17734200	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr11:17734000-17734200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
33	chr11:17734000-17734200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
34	chr11:17734000-17734200	Enhancers	Fetal Muscle Trunk	muscle
35	chr11:17734200-17734800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
36	chr11:17735400-17736800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
37	chr11:17735600-17735800	Enhancers	Psoas Muscle	Psoas
38	chr11:17735600-17736200	Enhancers	HSMMtube	muscle
39	chr11:17735600-17736800	Bivalent Enhancer	Fetal Muscle Leg	muscle
40	chr11:17735600-17736800	Enhancers	HSMM	muscle
41	chr11:17735600-17737000	Enhancers	Fetal Heart	heart
42	chr11:17735800-17736200	Weak transcription	Psoas Muscle	Psoas
43	chr11:17735800-17736400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr11:17735800-17736600	Enhancers	Right Ventricle	heart
45	chr11:17735800-17736800	Enhancers	Left Ventricle	heart
46	chr11:17736000-17736400	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr11:17736000-17736800	Enhancers	Right Atrium	heart
48	chr11:17736200-17736600	Flanking Active TSS	HSMMtube	muscle
49	chr11:17736200-17736800	Enhancers	Psoas Muscle	Psoas
50	chr11:17736200-17736800	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle

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