Variant report

Variant	nsv897192
Chromosome Location	chr11:32828760-32903263
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	ARID3A	chr11:32851965-32852404	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:32850824-32851272	HepG2	liver:	n/a	n/a
3	ATF1	chr11:32888538-32888562	K562	blood:	n/a	n/a
4	ATF1	chr11:32878012-32878101	K562	blood:	n/a	n/a
5	ATF2	chr11:32850720-32851321	GM12878	blood:	n/a	n/a
6	ATF2	chr11:32850594-32851339	GM12878	blood:	n/a	n/a
7	BACH1	chr11:32862150-32862517	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL3	chr11:32902869-32903255	GM12878	blood:	n/a	n/a
9	BHLHE40	chr11:32846405-32846534	K562	blood:	n/a	n/a
10	BHLHE40	chr11:32830791-32831195	GM12878	blood:	n/a	n/a
11	BRCA1	chr11:32850715-32851268	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr11:32897267-32897327	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr11:32851255-32851263	H1-hESC	embryonic stem cell:	n/a	n/a
14	BRCA1	chr11:32851524-32851531	GM12878	blood:	n/a	n/a
15	CCNT2	chr11:32860829-32861008	K562	blood:	n/a	n/a
16	CEBPB	chr11:32851061-32851240	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr11:32851833-32852432	HCT-116	colon:	n/a	chr11:32852309-32852320 chr11:32852133-32852144 chr11:32852309-32852322
18	CEBPB	chr11:32865173-32865425	A549	lung:	n/a	chr11:32865248-32865259 chr11:32865290-32865301
19	CEBPB	chr11:32873897-32874252	K562	blood:	n/a	chr11:32874038-32874049
20	CEBPB	chr11:32851911-32852361	ECC-1	luminal epithelium:	n/a	chr11:32852309-32852320 chr11:32852133-32852144 chr11:32852309-32852322
21	CEBPB	chr11:32851856-32852380	MCF-7	breast:	n/a	chr11:32852309-32852320 chr11:32852133-32852144 chr11:32852309-32852322
22	CEBPB	chr11:32860372-32860755	HepG2	liver:	n/a	chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860560-32860573 chr11:32860560-32860571
23	CEBPB	chr11:32892291-32892555	K562	blood:	n/a	n/a
24	CEBPB	chr11:32860342-32860804	K562	blood:	n/a	chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860560-32860573 chr11:32860560-32860571
25	CEBPB	chr11:32860025-32860806	HCT-116	colon:	n/a	chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860560-32860573 chr11:32860560-32860571
26	CEBPB	chr11:32860199-32860800	MCF-7	breast:	n/a	chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860560-32860573 chr11:32860560-32860571
27	CEBPB	chr11:32860052-32861142	Hela-S3	cervix:	n/a	chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860560-32860573 chr11:32860560-32860571
28	CEBPB	chr11:32851907-32852432	A549	lung:	n/a	chr11:32852309-32852320 chr11:32852133-32852144 chr11:32852309-32852322
29	CEBPB	chr11:32873859-32874214	Hela-S3	cervix:	n/a	chr11:32874038-32874049
30	CEBPB	chr11:32845183-32845559	Hela-S3	cervix:	n/a	chr11:32845341-32845352
31	CEBPB	chr11:32860376-32860759	IMR90	lung:	n/a	chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860560-32860573 chr11:32860560-32860571
32	CEBPB	chr11:32902896-32903471	IMR90	lung:	n/a	chr11:32903447-32903460
33	CEBPB	chr11:32860503-32860617	HepG2	liver:	n/a	chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860560-32860573 chr11:32860560-32860571
34	CEBPB	chr11:32840455-32840633	HepG2	liver:	n/a	chr11:32840539-32840550
35	CEBPB	chr11:32865136-32865413	K562	blood:	n/a	chr11:32865248-32865259 chr11:32865290-32865301
36	CEBPB	chr11:32851870-32852240	HepG2	liver:	n/a	chr11:32852133-32852144
37	CEBPB	chr11:32865153-32865353	HepG2	liver:	n/a	chr11:32865248-32865259 chr11:32865290-32865301
38	CEBPB	chr11:32860402-32860698	K562	blood:	n/a	chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860560-32860573 chr11:32860560-32860571
39	CEBPB	chr11:32845218-32845505	HepG2	liver:	n/a	chr11:32845341-32845352
40	CEBPB	chr11:32860134-32860823	ECC-1	luminal epithelium:	n/a	chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860560-32860573 chr11:32860560-32860571
41	CEBPB	chr11:32873889-32874204	H1-hESC	embryonic stem cell:	n/a	chr11:32874038-32874049
42	CEBPB	chr11:32845248-32845397	HepG2	liver:	n/a	chr11:32845341-32845352
43	CEBPB	chr11:32892285-32892603	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr11:32851052-32852610	HCT-116	colon:	n/a	chr11:32852309-32852320 chr11:32852133-32852144 chr11:32852309-32852322
45	CEBPB	chr11:32840508-32840570	A549	lung:	n/a	chr11:32840539-32840550
46	CEBPB	chr11:32851962-32852298	K562	blood:	n/a	chr11:32852133-32852144
47	CEBPB	chr11:32851855-32852473	ECC-1	luminal epithelium:	n/a	chr11:32852309-32852320 chr11:32852133-32852144 chr11:32852309-32852322
48	CEBPB	chr11:32892287-32892573	A549	lung:	n/a	n/a
49	CEBPB	chr11:32892363-32892495	HepG2	liver:	n/a	n/a
50	CEBPB	chr11:32851943-32852334	A549	lung:	n/a	chr11:32852309-32852320 chr11:32852133-32852144 chr11:32852309-32852322

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:32851371-32851421	HCT-116	colon:	n/a
2	chr11:32851371-32851421	HCT-116	colon:	n/a
3	chr11:32851177-32851227	SKMC	muscle:	n/a
4	chr11:32847480-32847530	HAEpiC	amniotic membrane:	n/a
5	chr11:32851378-32851428	HCF	heart:	n/a
6	chr11:32853267-32853317	NHBE	bronchial:	n/a
7	chr11:32851240-32851290	SK-N-MC	brain:	n/a
8	chr11:32851378-32851428	HUVEC	blood vessel:	n/a
9	chr11:32851361-32851411	HepG2	liver:	n/a
10	chr11:32851950-32852000	SAEC	small airway:	n/a
11	chr11:32851371-32851421	AG09309	skin:	n/a
12	chr11:32847480-32847530	CMK	blood:	n/a
13	chr11:32854320-32854370	GM12891	blood:	n/a
14	chr11:32875930-32875980	T-47D	breast:	n/a
15	chr11:32851371-32851421	H1-hESC	embryonic stem cell:	embryo
16	chr11:32847480-32847530	AG09319	gingival:	n/a
17	chr11:32854320-32854370	HepG2	liver:	n/a
18	chr11:32851260-32851310	HMEC	breast:	n/a
19	chr11:32851087-32851137	HCM	heart:	n/a
20	chr11:32854320-32854370	HIPEpiC	eye:	n/a
21	chr11:32853267-32853317	HEK293	kidney:	embryo
22	chr11:32851950-32852000	HEK293	kidney:	embryo
23	chr11:32851240-32851290	ECC-1	luminal epithelium:	n/a
24	chr11:32875930-32875980	GM12892	blood:	n/a
25	chr11:32847480-32847530	NHDF-neo	bronchial:	n/a
26	chr11:32851531-32851581	PANC-1	pancreas:	n/a
27	chr11:32851177-32851227	MCF10A-Er-Src	breast:	n/a
28	chr11:32854320-32854370	SK-N-MC	brain:	n/a
29	chr11:32851177-32851227	H1-hESC	embryonic stem cell:	embryo
30	chr11:32851356-32851406	SKMC	muscle:	n/a
31	chr11:32875930-32875980	MCF-7	breast:	n/a
32	chr11:32853267-32853317	K562	blood:	n/a
33	chr11:32851378-32851428	RPTEC	kidney:	n/a
34	chr11:32851371-32851421	HIPEpiC	eye:	n/a
35	chr11:32851950-32852000	NHBE	bronchial:	n/a
36	chr11:32851346-32851396	AoSMC	blood vessel:	n/a
37	chr11:32851378-32851428	MCF10A-Er-Src	breast:	n/a
38	chr11:32851240-32851290	HCF	heart:	n/a
39	chr11:32851531-32851581	SKMC	muscle:	n/a
40	chr11:32851378-32851428	Jurkat	blood:	n/a
41	chr11:32847480-32847530	Caco-2	colon:	n/a
42	chr11:32851177-32851227	HCT-116	colon:	n/a
43	chr11:32851260-32851310	Jurkat	blood:	n/a
44	chr11:32851260-32851310	ECC-1	luminal epithelium:	n/a
45	chr11:32851531-32851581	ECC-1	luminal epithelium:	n/a
46	chr11:32851177-32851227	PrEC	prostate:	n/a
47	chr11:32875930-32875980	HL-60	blood:	n/a
48	chr11:32851240-32851290	ProgFib	skin:	n/a
49	chr11:32851346-32851396	MCF10A-Er-Src	breast:	n/a
50	chr11:32851240-32851290	HCT-116	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:32851461..32852210-chr3:49058647..49059440,2	NB4	blood:
2	chr11:32851187..32853645-chr11:32854709..32858523,6	MCF-7	breast:
3	chr11:32843099..32845929-chr11:32851383..32853799,2	MCF-7	breast:
4	chr11:32861977..32862713-chr14:65386776..65387380,2	MCF-7	breast:
5	chr11:32850955..32851927-chr16:89752956..89753523,2	Hela-S3	cervix:
6	chr11:32825967..32829445-chr11:32834509..32837119,3	K562	blood:
7	chr11:32900766..32903313-chr11:32912451..32914688,2	K562	blood:
8	chr11:32854588..32857057-chr11:32860540..32862429,2	K562	blood:
9	chr11:32849868..32852880-chr11:32911360..32916794,6	MCF-7	breast:
10	chr11:32862183..32864294-chr11:32914218..32916079,2	K562	blood:
11	chr11:32892015..32892872-chr11:32914554..32915403,2	MCF-7	breast:
12	chr11:32847589..32849311-chr11:32913725..32915620,2	K562	blood:
13	chr11:32851501..32854370-chr11:32879596..32881538,2	MCF-7	breast:
14	chr11:32850866..32853799-chr11:32862127..32863701,2	MCF-7	breast:
15	chr11:32835440..32837233-chr11:32841490..32844292,2	K562	blood:
16	chr11:32851420..32852136-chr5:36606640..36607218,2	Hela-S3	cervix:
17	chr11:32854588..32857057-chr11:32860540..32862429,2	K562	blood:
18	chr11:32851501..32854370-chr11:32879596..32881538,2	MCF-7	breast:
19	chr11:32892094..32893817-chr11:32914118..32916253,2	K562	blood:
20	chr11:32830572..32833021-chr11:32913903..32915593,2	MCF-7	breast:
21	chr11:32850121..32852277-chr11:33088797..33091531,2	MCF-7	breast:
22	chr11:32851076..32851981-chr12:123011655..123012268,2	Hela-S3	cervix:
23	chr11:32873372..32875504-chr11:32882412..32884075,2	K562	blood:
24	chr11:32873372..32875504-chr11:32882412..32884075,2	K562	blood:
25	chr11:32845133..32847624-chr11:32847772..32849617,2	MCF-7	breast:
26	chr11:32850001..32854483-chr11:32912810..32915962,5	MCF-7	breast:
27	chr11:32845133..32847624-chr11:32847772..32849617,2	MCF-7	breast:
28	chr11:32858756..32863139-chr11:32912593..32915314,4	MCF-7	breast:
29	chr11:32835440..32837233-chr11:32841490..32844292,2	K562	blood:
30	chr11:32862368..32865112-chr11:32868900..32870710,2	K562	blood:
31	chr11:32862368..32865112-chr11:32868900..32870710,2	K562	blood:
32	chr11:32851440..32852221-chr2:173420119..173420696,2	Hela-S3	cervix:
33	chr11:32830676..32831274-chr11:33709287..33709961,2	K562	blood:
34	chr11:32825967..32829445-chr11:32834509..32837119,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-QSER1-1	chr11:32878980-32879666	NONHSAT018678
2	lnc-CCDC73-1	chr11:32878982-32879665	ENSG00000248689
3	lnc-PRRG4-1	chr11:32846016-32846832	NONHSAT018677
4	lnc-QSER1-1	chr11:32875249-32875808	NONHSAT018678
5	lnc-PRRG4-2	chr11:32839176-32839252	NONHSAT018676
6	lnc-PRRG4-2	chr11:32839485-32839664	NONHSAT018676
7	lnc-CCDC73-1	chr11:32875249-32875810	ENSG00000248689

Variant related genes	Relation type
PRRG4	TF binding region
PRRG4	CpG island
ENSG00000184445	chromatin interactions
ENSG00000060749	chromatin interactions
ENSG00000178149	chromatin interactions
ENSG00000185324	chromatin interactions
ENSG00000079215	chromatin interactions
ENSG00000176148	chromatin interactions
ENSG00000178057	chromatin interactions
ENSG00000135378	chromatin interactions
ENSG00000152256	chromatin interactions
ENSG00000260259	chromatin interactions
FBXW7	miRNA target sites
LMAN2L	miRNA target sites

Extended variants
information (count: 2062 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:2062 , 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	rs186041545	chr11:32830578-32830579	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs190948971	chr11:32830584-32830585	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs567247128	chr11:32830621-32830622	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs147799521	chr11:32830668-32830669	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs555980009	chr11:32830705-32830706	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs141307833	chr11:32830784-32830785	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs79307307	chr11:32830800-32830801	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs558837587	chr11:32830817-32830818	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs143559568	chr11:32830861-32830862	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs182802029	chr11:32830868-32830869	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs560976082	chr11:32830875-32830876	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs148043242	chr11:32830896-32830897	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs550838168	chr11:32830965-32830966	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs117284177	chr11:32831012-32831013	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs563584608	chr11:32831016-32831017	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs78656390	chr11:32831058-32831059	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs552459915	chr11:32831073-32831074	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs566260400	chr11:32831103-32831104	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs75346603	chr11:32831113-32831114	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs528820508	chr11:32831144-32831145	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs568741461	chr11:32831152-32831153	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs548892894	chr11:32831179-32831180	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs2175209	chr11:32831254-32831255	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs543158452	chr11:32831275-32831276	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs535834740	chr11:32831329-32831330	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs80061060	chr11:32831365-32831366	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs528909615	chr11:32831380-32831381	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs572613763	chr11:32831404-32831405	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs113864991	chr11:32831412-32831413	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs565636092	chr11:32831432-32831433	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs533112931	chr11:32831440-32831441	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs185672574	chr11:32831514-32831515	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs540975089	chr11:32831517-32831518	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs114947478	chr11:32831690-32831691	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs190829129	chr11:32831734-32831735	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs543423506	chr11:32831751-32831752	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs563819047	chr11:32831830-32831831	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs2175210	chr11:32832033-32832034	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs77167246	chr11:32832071-32832072	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs115137818	chr11:32832084-32832085	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs528683851	chr11:32832091-32832092	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs374259622	chr11:32832122-32832123	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs183055152	chr11:32832145-32832146	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs71034621	chr11:32832150-32832151	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs397829920	chr11:32832153-32832154	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs117004133	chr11:32832164-32832165	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs542379978	chr11:32832219-32832220	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs529716901	chr11:32832221-32832222	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs188509671	chr11:32832228-32832229	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs192024515	chr11:32832243-32832244	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
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
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	16783165	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21364760	CNVD
Glioblastoma multiforme	22286061	CNVD
Aniridia syndrome	21572526	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Retinoblastoma	22278416	CNVD
Denys-drash syndrome	21085971	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
WAGR syndrome	16773131	CNVD
Disorders of sex development	22290220	CNVD
Aniridia syndrome	17204608	CNVD
Mental retardation	17204608	CNVD
WAGR syndrome	19617690	CNVD
genitourinary abnormalities	17204608	CNVD
Breast cancer	16397240	CNVD
Mental retardation	16773131	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Cancer	21183584	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
WAGR syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Denys-drash syndrome	19566914	CNVD
Familial wilms tumor	19566914	CNVD
Frasier syndrome	19566914	CNVD
Non-small cell lung cancer	21829676	CNVD
WAGR syndrome	20603712	CNVD
Autism	17322880	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21858162	CNVD
Cancer	20164920	CNVD
Breast cancer	16620391	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Ependymoma	20639864	CNVD

Chromatin state (count:674 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:32830600-32831400	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chr11:32831000-32831400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
3	chr11:32837400-32850800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr11:32837600-32839800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr11:32838800-32839800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr11:32838800-32839800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr11:32838800-32839800	Enhancers	NHEK	skin
8	chr11:32839000-32839800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr11:32839200-32839800	Enhancers	Hela-S3	cervix
10	chr11:32839200-32840000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr11:32839400-32839600	Enhancers	HSMM	muscle
12	chr11:32839400-32839600	Enhancers	Monocytes-CD14+_RO01746	blood
13	chr11:32839400-32839800	Enhancers	Primary monocytes fromperipheralblood	blood
14	chr11:32839400-32840000	Enhancers	Liver	Liver
15	chr11:32839800-32841200	Weak transcription	HSMM	muscle
16	chr11:32839800-32841800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr11:32839800-32841800	Weak transcription	Primary monocytes fromperipheralblood	blood
18	chr11:32839800-32841800	Weak transcription	Hela-S3	cervix
19	chr11:32839800-32842000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr11:32839800-32842200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr11:32839800-32842200	Weak transcription	NHEK	skin
22	chr11:32839800-32843400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr11:32840000-32841800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr11:32840000-32850200	Weak transcription	Liver	Liver
25	chr11:32841600-32844000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr11:32841800-32843200	Enhancers	Monocytes-CD14+_RO01746	blood
27	chr11:32841800-32843800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr11:32841800-32844000	Enhancers	Hela-S3	cervix
29	chr11:32841800-32844200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr11:32841800-32846400	Enhancers	Primary monocytes fromperipheralblood	blood
31	chr11:32842000-32842400	Enhancers	HMEC	breast
32	chr11:32842000-32843200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr11:32842200-32843800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr11:32842200-32844000	Enhancers	NHEK	skin
35	chr11:32842400-32843400	Weak transcription	HMEC	breast
36	chr11:32843000-32843200	Enhancers	GM12878-XiMat	blood
37	chr11:32843200-32843600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr11:32843200-32844000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr11:32843200-32844000	Flanking Active TSS	GM12878-XiMat	blood
40	chr11:32843200-32844000	Enhancers	HSMM	muscle
41	chr11:32843200-32844600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
42	chr11:32843200-32846600	Enhancers	Primary neutrophils fromperipheralblood	blood
43	chr11:32843200-32850800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr11:32843400-32843600	Enhancers	Primary hematopoietic stem cells	blood
45	chr11:32843400-32843800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr11:32843400-32844000	Enhancers	HMEC	breast
47	chr11:32843600-32850200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr11:32843800-32850600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr11:32844000-32844200	Enhancers	GM12878-XiMat	blood
50	chr11:32844000-32848800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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