Variant report

Variant	esv2757434
Chromosome Location	chr11:32792784-32958609
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2863)
CpG islands
(count:2631)
Chromatin interactive
region (count:132)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2863 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:32915738-32916200	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:32814471-32814880	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:32913132-32913996	K562	blood:	n/a	chr11:32913597-32913613
4	ARID3A	chr11:32851965-32852404	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:32913427-32913694	HepG2	liver:	n/a	chr11:32913597-32913613
6	ARID3A	chr11:32906515-32906528	K562	blood:	n/a	n/a
7	ARID3A	chr11:32850824-32851272	HepG2	liver:	n/a	n/a
8	ATF1	chr11:32888538-32888562	K562	blood:	n/a	n/a
9	ATF1	chr11:32915664-32916142	K562	blood:	n/a	n/a
10	ATF1	chr11:32878012-32878101	K562	blood:	n/a	n/a
11	ATF2	chr11:32913742-32914213	GM12878	blood:	n/a	n/a
12	ATF2	chr11:32850720-32851321	GM12878	blood:	n/a	n/a
13	ATF2	chr11:32913292-32914128	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr11:32850594-32851339	GM12878	blood:	n/a	n/a
15	ATF2	chr11:32913808-32914188	GM12878	blood:	n/a	n/a
16	ATF2	chr11:32915625-32916189	GM12878	blood:	n/a	n/a
17	ATF2	chr11:32914760-32915526	GM12878	blood:	n/a	n/a
18	ATF2	chr11:32913700-32914254	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF2	chr11:32915613-32916188	GM12878	blood:	n/a	n/a
20	ATF3	chr11:32915769-32916187	K562	blood:	n/a	n/a
21	BACH1	chr11:32862150-32862517	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr11:32928699-32928715	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr11:32913665-32914328	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr11:32913936-32914116	K562	blood:	n/a	n/a
25	BACH1	chr11:32935881-32935887	K562	blood:	n/a	n/a
26	BACH1	chr11:32915078-32915472	H1-hESC	embryonic stem cell:	n/a	n/a
27	BCL3	chr11:32902869-32903255	GM12878	blood:	n/a	n/a
28	BCL3	chr11:32914015-32914566	GM12878	blood:	n/a	chr11:32914267-32914280 chr11:32914323-32914336 chr11:32914107-32914115 chr11:32914333-32914342
29	BCLAF1	chr11:32913588-32914237	GM12878	blood:	n/a	chr11:32914107-32914115
30	BCLAF1	chr11:32914768-32915512	GM12878	blood:	n/a	chr11:32914772-32914781 chr11:32914805-32914818 chr11:32914799-32914812 chr11:32914811-32914820 chr11:32914808-32914817 chr11:32914806-32914819 chr11:32914889-32914902 chr11:32915061-32915074 chr11:32914805-32914814
31	BCLAF1	chr11:32914715-32915492	GM12878	blood:	n/a	chr11:32914772-32914781 chr11:32914805-32914818 chr11:32914799-32914812 chr11:32914811-32914820 chr11:32914808-32914817 chr11:32914806-32914819 chr11:32914889-32914902 chr11:32915061-32915074 chr11:32914805-32914814
32	BHLHE40	chr11:32846405-32846534	K562	blood:	n/a	n/a
33	BHLHE40	chr11:32920967-32921453	GM12878	blood:	n/a	n/a
34	BHLHE40	chr11:32830791-32831195	GM12878	blood:	n/a	n/a
35	BHLHE40	chr11:32942198-32942441	GM12878	blood:	n/a	n/a
36	BHLHE40	chr11:32915128-32915967	K562	blood:	n/a	n/a
37	BHLHE40	chr11:32913436-32914499	K562	blood:	n/a	n/a
38	BHLHE40	chr11:32913929-32914459	GM12878	blood:	n/a	n/a
39	BHLHE40	chr11:32914929-32915449	GM12878	blood:	n/a	chr11:32915058-32915074
40	BRCA1	chr11:32851255-32851263	H1-hESC	embryonic stem cell:	n/a	n/a
41	BRCA1	chr11:32913363-32914293	Hela-S3	cervix:	n/a	chr11:32913451-32913458
42	BRCA1	chr11:32850715-32851268	Hela-S3	cervix:	n/a	n/a
43	BRCA1	chr11:32851524-32851531	GM12878	blood:	n/a	n/a
44	BRCA1	chr11:32897267-32897327	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chr11:32915646-32916155	Hela-S3	cervix:	n/a	n/a
46	CBX3	chr11:32913686-32914284	K562	blood:	n/a	n/a
47	CBX3	chr11:32932943-32933388	K562	blood:	n/a	n/a
48	CBX3	chr11:32915588-32916050	K562	blood:	n/a	n/a
49	CCNT2	chr11:32860829-32861008	K562	blood:	n/a	n/a
50	CCNT2	chr11:32808701-32808880	K562	blood:	n/a	n/a

(count:2631 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:32817614-32817664	BE2_C	brain:	n/a
2	chr11:32851087-32851137	AG09319	gingival:	n/a
3	chr11:32851260-32851310	HAEpiC	amniotic membrane:	n/a
4	chr11:32815865-32815915	AG04450	lung:	fetal
5	chr11:32816885-32816935	Caco-2	colon:	n/a
6	chr11:32816885-32816935	HCT-116	colon:	n/a
7	chr11:32853267-32853317	HIPEpiC	eye:	n/a
8	chr11:32932059-32932109	HRCEpiC	kidney:	n/a
9	chr11:32817614-32817664	BE2_C	brain:	n/a
10	chr11:32851087-32851137	AG09319	gingival:	n/a
11	chr11:32851260-32851310	HAEpiC	amniotic membrane:	n/a
12	chr11:32815865-32815915	AG04450	lung:	fetal
13	chr11:32816885-32816935	Caco-2	colon:	n/a
14	chr11:32816885-32816935	HCT-116	colon:	n/a
15	chr11:32853267-32853317	HIPEpiC	eye:	n/a
16	chr11:32932059-32932109	HRCEpiC	kidney:	n/a
17	chr11:32875930-32875980	BE2_C	brain:	n/a
18	chr11:32851371-32851421	AG04449	skin:	fetal
19	chr11:32916120-32916170	IMR90	lung:	fetal
20	chr11:32816227-32816277	BE2_C	brain:	n/a
21	chr11:32914648-32914698	ECC-1	luminal epithelium:	n/a
22	chr11:32815896-32815946	Caco-2	colon:	n/a
23	chr11:32851950-32852000	PFSK-1	brain:	n/a
24	chr11:32817614-32817664	SK-N-SH_RA	brain:	n/a
25	chr11:32926880-32926930	HL-60	blood:	n/a
26	chr11:32851531-32851581	HIPEpiC	eye:	n/a
27	chr11:32914638-32914688	NB4	blood:	n/a
28	chr11:32815896-32815946	AG04450	lung:	fetal
29	chr11:32913990-32914040	AG09319	gingival:	n/a
30	chr11:32851240-32851290	GM12878	blood:	n/a
31	chr11:32919083-32919133	HL-60	blood:	n/a
32	chr11:32851950-32852000	HRE	kidney:	n/a
33	chr11:32816227-32816277	ECC-1	luminal epithelium:	n/a
34	chr11:32851087-32851137	Jurkat	blood:	n/a
35	chr11:32914648-32914698	SKMC	muscle:	n/a
36	chr11:32851378-32851428	RPTEC	kidney:	n/a
37	chr11:32851378-32851428	SKMC	muscle:	n/a
38	chr11:32851361-32851411	GM12878	blood:	n/a
39	chr11:32851087-32851137	SAEC	small airway:	n/a
40	chr11:32915497-32915547	SK-N-SH	brain:	n/a
41	chr11:32816885-32816935	HNPCEpiC	eye:	n/a
42	chr11:32816254-32816304	ProgFib	skin:	n/a
43	chr11:32815896-32815946	Hela-S3	cervix:	n/a
44	chr11:32932059-32932109	AG10803	skin:	n/a
45	chr11:32816080-32816130	ProgFib	skin:	n/a
46	chr11:32851378-32851428	SK-N-SH	brain:	n/a
47	chr11:32914618-32914668	GM12892	blood:	n/a
48	chr11:32912719-32912769	AG09309	skin:	n/a
49	chr11:32851356-32851406	BJ	skin:	n/a
50	chr11:32816227-32816277	HCPEpiC	choroid plexus:	n/a

(count:132 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr11:32913837..32914707-chr6:31587711..31588295,2	Hela-S3	cervix:
2	chr11:32919542..32926976-chr11:32927671..32932534,9	K562	blood:
3	chr11:32900766..32903313-chr11:32912451..32914688,2	K562	blood:
4	chr11:32912444..32914191-chr11:32997049..32998828,2	K562	blood:
5	chr11:32945489..32947897-chr11:32951878..32954086,3	MCF-7	breast:
6	chr11:32892015..32892872-chr11:32914554..32915403,2	MCF-7	breast:
7	chr11:32913412..32917556-chr11:32926432..32930377,5	K562	blood:
8	chr11:32924821..32927100-chr11:32938011..32939740,2	MCF-7	breast:
9	chr11:32942975..32945695-chr11:32951329..32953837,2	K562	blood:
10	chr11:32913861..32915566-chr11:33278350..33280856,3	K562	blood:
11	chr11:32949447..32951560-chr11:32996072..32998442,2	K562	blood:
12	chr11:32921334..32923209-chr11:32959403..32961555,2	K562	blood:
13	chr11:32850866..32853799-chr11:32862127..32863701,2	MCF-7	breast:
14	chr11:32599649..32602330-chr11:32903654..32905352,2	K562	blood:
15	chr11:32935340..32937202-chr11:32944261..32946142,2	MCF-7	breast:
16	chr11:32913434..32915654-chr11:32937933..32940006,3	MCF-7	breast:
17	chr11:32925134..32927597-chr11:32928287..32929903,2	K562	blood:
18	chr11:32851501..32854370-chr11:32879596..32881538,2	MCF-7	breast:
19	chr11:32912677..32916677-chr11:32946348..32949783,4	K562	blood:
20	chr11:32933148..32935266-chr11:32937418..32940169,3	K562	blood:
21	chr11:32913437..32915867-chr11:32930703..32933783,3	MCF-7	breast:
22	chr11:32914351..32916676-chr11:33059902..33062238,2	K562	blood:
23	chr11:32734959..32735691-chr11:32814406..32814938,2	MCF-7	breast:
24	chr11:32914076..32914799-chr6:26123502..26124171,2	Hela-S3	cervix:
25	chr11:32915892..32917470-chr11:32980726..32982282,2	K562	blood:
26	chr11:32915549..32916317-chr11:61583965..61584543,2	Hela-S3	cervix:
27	chr11:32835440..32837233-chr11:32841490..32844292,2	K562	blood:
28	chr11:32904524..32910209-chr11:32910222..32915650,10	MCF-7	breast:
29	chr11:32808269..32810578-chr11:32811401..32813892,2	K562	blood:
30	chr11:32843099..32845929-chr11:32851383..32853799,2	MCF-7	breast:
31	chr11:32914014..32915010-chr5:10249637..10250329,2	Hela-S3	cervix:
32	chr11:32789537..32792072-chr11:32812363..32815095,2	K562	blood:
33	chr11:32862183..32864294-chr11:32914218..32916079,2	K562	blood:
34	chr11:32933148..32935266-chr11:32937418..32940169,3	K562	blood:
35	chr11:32851501..32854370-chr11:32879596..32881538,2	MCF-7	breast:
36	chr11:32930825..32933469-chr11:32935267..32937241,3	K562	blood:
37	chr11:32797795..32799426-chr11:32913652..32916468,2	MCF-7	breast:
38	chr11:32915546..32916189-chr5:98264465..98265204,2	Hela-S3	cervix:
39	chr11:32861977..32862713-chr14:65386776..65387380,2	MCF-7	breast:
40	chr11:32862368..32865112-chr11:32868900..32870710,2	K562	blood:
41	chr11:32914706..32916698-chr11:32938158..32939681,2	MCF-7	breast:
42	chr11:32850955..32851927-chr16:89752956..89753523,2	Hela-S3	cervix:
43	chr11:32913447..32916787-chr11:32944160..32946280,4	K562	blood:
44	chr11:32850121..32852277-chr11:33088797..33091531,2	MCF-7	breast:
45	chr11:32344866..32345612-chr11:32814115..32815021,3	K562	blood:
46	chr11:32919329..32924286-chr11:32926573..32930323,7	K562	blood:
47	chr11:32915392..32916319-chr3:40498303..40499288,2	Hela-S3	cervix:
48	chr11:32849868..32852880-chr11:32911360..32916794,6	MCF-7	breast:
49	chr11:32873372..32875504-chr11:32882412..32884075,2	K562	blood:
50	chr11:32847589..32849311-chr11:32913725..32915620,2	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-QSER1-1	chr11:32875249-32875808	NONHSAT018678
2	lnc-PRRG4-1	chr11:32846016-32846832	NONHSAT018677
3	lnc-PRRG4-3	chr11:32823241-32823497	NONHSAT018675
4	lnc-CCDC73-1	chr11:32875249-32875810	ENSG00000248689
5	lnc-CCDC73-1	chr11:32878982-32879665	ENSG00000248689
6	lnc-PRRG4-2	chr11:32839176-32839252	NONHSAT018676
7	lnc-QSER1-1	chr11:32878980-32879666	NONHSAT018678
8	lnc-PRRG4-2	chr11:32839485-32839664	NONHSAT018676
9	lnc-CCDC73-2	chr11:32817536-32817819	NONHSAT018674

No data

Variant related genes	Relation type
CCDC73	TF binding region
QSER1	TF binding region
PRRG4	TF binding region
CCDC73	CpG island
QSER1	CpG island
PRRG4	CpG island
ENSG00000079215	chromatin interactions
ENSG00000176148	chromatin interactions
ENSG00000060749	chromatin interactions
ENSG00000152256	chromatin interactions
ENSG00000151849	chromatin interactions
ENSG00000149485	chromatin interactions
ENSG00000150756	chromatin interactions
ENSG00000110422	chromatin interactions
ENSG00000153015	chromatin interactions
ENSG00000125740	chromatin interactions
ENSG00000110700	chromatin interactions
ENSG00000121690	chromatin interactions
ENSG00000180596	chromatin interactions
ENSG00000185324	chromatin interactions
ENSG00000134824	chromatin interactions
ENSG00000247151	chromatin interactions
ENSG00000184445	chromatin interactions
ENSG00000153207	chromatin interactions
ENSG00000257337	chromatin interactions
ENSG00000184937	chromatin interactions
ENSG00000197153	chromatin interactions
ENSG00000165006	chromatin interactions
ENSG00000186714	chromatin interactions
ENSG00000176102	chromatin interactions
ENSG00000150753	chromatin interactions
ENSG00000228265	chromatin interactions
ENSG00000188846	chromatin interactions
ENSG00000178149	chromatin interactions
ENSG00000201403	chromatin interactions
ENSG00000260259	chromatin interactions
ENSG00000183242	chromatin interactions
ENSG00000178057	chromatin interactions
ENSG00000135378	chromatin interactions
ENSG00000248489	chromatin interactions
FBXW7	miRNA target sites
LMAN2L	miRNA target sites

Extended variants
information (count: 4762 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:4762 , 50 per page) page: 1 2 3 4 5 6 7 ... 96

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs200577780	chr11:32795810-32795811	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs556926072	chr11:32795873-32795874	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs576805052	chr11:32795900-32795901	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs188427459	chr11:32795924-32795925	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs71479178	chr11:32795931-32795932	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs550958403	chr11:32795972-32795973	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs7933005	chr11:32795973-32795974	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs180858892	chr11:32796006-32796007	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs185114633	chr11:32796025-32796026	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs561520360	chr11:32796076-32796077	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs10767965	chr11:32796092-32796093	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs544137809	chr11:32796157-32796158	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs556116380	chr11:32796166-32796167	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs116703528	chr11:32796196-32796197	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs571888834	chr11:32796608-32796609	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs114358411	chr11:32796660-32796661	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs1509889	chr11:32796686-32796687	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs140784841	chr11:32796780-32796781	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs572628159	chr11:32796790-32796791	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs541480224	chr11:32796847-32796848	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs75913851	chr11:32796874-32796875	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs186851907	chr11:32796955-32796956	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs564628368	chr11:32796958-32796959	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs563069752	chr11:32797003-32797004	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs191741682	chr11:32797011-32797012	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs184038401	chr11:32797044-32797045	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs533218386	chr11:32797108-32797109	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs540290305	chr11:32797209-32797210	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs560478654	chr11:32797263-32797264	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs529416350	chr11:32797280-32797281	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs558726553	chr11:32797328-32797329	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs570571094	chr11:32797345-32797346	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs72897183	chr11:32797470-32797471	Active TSS Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs187726233	chr11:32797512-32797513	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs531971069	chr11:32797513-32797514	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs551936714	chr11:32797527-32797528	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs571864591	chr11:32797544-32797545	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs74749428	chr11:32797547-32797548	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs561953434	chr11:32797579-32797580	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs189900742	chr11:32797599-32797600	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs529272241	chr11:32797600-32797601	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs116475100	chr11:32797651-32797652	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs182214353	chr11:32797684-32797685	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs535075965	chr11:32797701-32797702	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs555069368	chr11:32797802-32797803	Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs574977505	chr11:32797821-32797822	Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs530270438	chr11:32797864-32797865	Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs369012258	chr11:32797890-32797891	Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs6484594	chr11:32797905-32797906	Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs12291922	chr11:32797914-32797915	Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	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:2364 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:32795800-32796200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr11:32796600-32798400	Enhancers	Primary B cells from peripheral blood	blood
3	chr11:32796800-32797200	Enhancers	Dnd41	blood
4	chr11:32796800-32798200	Active TSS	GM12878-XiMat	blood
5	chr11:32797200-32797400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr11:32797200-32798000	Flanking Active TSS	Dnd41	blood
7	chr11:32797200-32798200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr11:32797200-32798200	Enhancers	Liver	Liver
9	chr11:32797400-32797800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
10	chr11:32797400-32797800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
11	chr11:32797400-32798000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr11:32797400-32798000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr11:32797400-32798000	Enhancers	Duodenum Smooth Muscle	Duodenum
14	chr11:32797600-32798000	Active TSS	Brain Anterior Caudate	brain
15	chr11:32797600-32798000	Active TSS	Brain Hippocampus Middle	brain
16	chr11:32797600-32798000	Active TSS	NHLF	lung
17	chr11:32797600-32798200	Enhancers	Primary T helper cells PMA-I stimulated	--
18	chr11:32797600-32798200	Enhancers	Monocytes-CD14+_RO01746	blood
19	chr11:32798000-32798400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr11:32798000-32798400	Enhancers	Dnd41	blood
21	chr11:32798200-32800400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr11:32798200-32800400	Weak transcription	Monocytes-CD14+_RO01746	blood
23	chr11:32798200-32800600	Weak transcription	GM12878-XiMat	blood
24	chr11:32798200-32806200	Weak transcription	Liver	Liver
25	chr11:32798400-32800200	Weak transcription	Primary B cells from peripheral blood	blood
26	chr11:32798400-32800400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr11:32798400-32800400	Weak transcription	Dnd41	blood
28	chr11:32799800-32800000	Enhancers	Primary B cells from cord blood	blood
29	chr11:32800000-32801000	Weak transcription	Primary B cells from cord blood	blood
30	chr11:32800200-32800400	Enhancers	Primary hematopoietic stem cells short term culture	blood
31	chr11:32800200-32801400	Enhancers	Primary B cells from peripheral blood	blood
32	chr11:32800400-32800600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr11:32800400-32800800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
34	chr11:32800400-32800800	Enhancers	Monocytes-CD14+_RO01746	blood
35	chr11:32800400-32801000	Enhancers	Dnd41	blood
36	chr11:32800400-32801200	Enhancers	Primary hematopoietic stem cells	blood
37	chr11:32800400-32801400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr11:32800400-32801600	Enhancers	Primary monocytes fromperipheralblood	blood
39	chr11:32800600-32800800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr11:32800600-32801200	Enhancers	GM12878-XiMat	blood
41	chr11:32800800-32801000	Enhancers	Primary hematopoietic stem cells short term culture	blood
42	chr11:32800800-32801000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr11:32800800-32801400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
44	chr11:32801000-32801200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
45	chr11:32801000-32801200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr11:32801000-32801400	Enhancers	Primary B cells from cord blood	blood
47	chr11:32801200-32801400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr11:32801200-32801600	Enhancers	Primary hematopoietic stem cells short term culture	blood
49	chr11:32801400-32803000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr11:32801600-32803000	Weak transcription	Primary hematopoietic stem cells short term culture	blood

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