Variant report

Variant	esv34742
Chromosome Location	chr11:32796092-33004024
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3224)
CpG islands
(count:2748)
Chromatin interactive
region (count:153)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3224 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

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	chr11:32975953-32975956	K562	blood:	n/a	n/a
3	ARID3A	chr11:32913427-32913694	HepG2	liver:	n/a	chr11:32913597-32913613
4	ARID3A	chr11:32851965-32852404	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:32850824-32851272	HepG2	liver:	n/a	n/a
6	ARID3A	chr11:32906515-32906528	K562	blood:	n/a	n/a
7	ARID3A	chr11:32814471-32814880	HepG2	liver:	n/a	n/a
8	ARID3A	chr11:32913132-32913996	K562	blood:	n/a	chr11:32913597-32913613
9	ATF1	chr11:32888538-32888562	K562	blood:	n/a	n/a
10	ATF1	chr11:32915664-32916142	K562	blood:	n/a	n/a
11	ATF1	chr11:32878012-32878101	K562	blood:	n/a	n/a
12	ATF2	chr11:32915613-32916188	GM12878	blood:	n/a	n/a
13	ATF2	chr11:32850594-32851339	GM12878	blood:	n/a	n/a
14	ATF2	chr11:32914760-32915526	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	chr11:32850720-32851321	GM12878	blood:	n/a	n/a
18	ATF2	chr11:32913700-32914254	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF2	chr11:32913742-32914213	GM12878	blood:	n/a	n/a
20	ATF2	chr11:32913292-32914128	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF3	chr11:32915769-32916187	K562	blood:	n/a	n/a
22	BACH1	chr11:32913936-32914116	K562	blood:	n/a	n/a
23	BACH1	chr11:32915078-32915472	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr11:32862150-32862517	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr11:32935881-32935887	K562	blood:	n/a	n/a
26	BACH1	chr11:32913665-32914328	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr11:32928699-32928715	H1-hESC	embryonic stem cell:	n/a	n/a
28	BCL3	chr11:32902869-32903255	GM12878	blood:	n/a	n/a
29	BCL3	chr11:32914015-32914566	GM12878	blood:	n/a	chr11:32914267-32914280 chr11:32914323-32914336 chr11:32914107-32914115 chr11:32914333-32914342
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	BCLAF1	chr11:32913588-32914237	GM12878	blood:	n/a	chr11:32914107-32914115
33	BHLHE40	chr11:32942198-32942441	GM12878	blood:	n/a	n/a
34	BHLHE40	chr11:32920967-32921453	GM12878	blood:	n/a	n/a
35	BHLHE40	chr11:32915128-32915967	K562	blood:	n/a	n/a
36	BHLHE40	chr11:32913929-32914459	GM12878	blood:	n/a	n/a
37	BHLHE40	chr11:32982189-32982478	GM12878	blood:	n/a	n/a
38	BHLHE40	chr11:32830791-32831195	GM12878	blood:	n/a	n/a
39	BHLHE40	chr11:32913436-32914499	K562	blood:	n/a	n/a
40	BHLHE40	chr11:32914929-32915449	GM12878	blood:	n/a	chr11:32915058-32915074
41	BHLHE40	chr11:32846405-32846534	K562	blood:	n/a	n/a
42	BRCA1	chr11:32850715-32851268	Hela-S3	cervix:	n/a	n/a
43	BRCA1	chr11:32913363-32914293	Hela-S3	cervix:	n/a	chr11:32913451-32913458
44	BRCA1	chr11:32897267-32897327	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chr11:32851255-32851263	H1-hESC	embryonic stem cell:	n/a	n/a
46	BRCA1	chr11:32851524-32851531	GM12878	blood:	n/a	n/a
47	BRCA1	chr11:32915646-32916155	Hela-S3	cervix:	n/a	n/a
48	CBX3	chr11:32915588-32916050	K562	blood:	n/a	n/a
49	CBX3	chr11:32932943-32933388	K562	blood:	n/a	n/a
50	CBX3	chr11:32913686-32914284	K562	blood:	n/a	n/a

(count:2748 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:32915497-32915547	A549	lung:	n/a
2	chr11:32851087-32851137	GM19239	blood:	n/a
3	chr11:32816211-32816261	HUVEC	blood vessel:	n/a
4	chr11:32915497-32915547	A549	lung:	n/a
5	chr11:32851087-32851137	GM19239	blood:	n/a
6	chr11:32816211-32816261	HUVEC	blood vessel:	n/a
7	chr11:32854320-32854370	PANC-1	pancreas:	n/a
8	chr11:32816885-32816935	HNPCEpiC	eye:	n/a
9	chr11:32915497-32915547	HCPEpiC	choroid plexus:	n/a
10	chr11:32919083-32919133	CMK	blood:	n/a
11	chr11:32851177-32851227	Hepatocyte	liver:	n/a
12	chr11:32914648-32914698	BJ	skin:	n/a
13	chr11:32914618-32914668	HRE	kidney:	n/a
14	chr11:32815968-32816018	Hepatocyte	liver:	n/a
15	chr11:32914618-32914668	IMR90	lung:	fetal
16	chr11:32915131-32915181	HUVEC	blood vessel:	n/a
17	chr11:32851177-32851227	AG10803	skin:	n/a
18	chr11:32875930-32875980	NB4	blood:	n/a
19	chr11:32909418-32909468	NHDF-neo	bronchial:	n/a
20	chr11:32815968-32816018	AoSMC	blood vessel:	n/a
21	chr11:32959933-32959983	Hepatocyte	liver:	n/a
22	chr11:32815865-32815915	PANC-1	pancreas:	n/a
23	chr11:32851087-32851137	HCM	heart:	n/a
24	chr11:32851346-32851396	LNCaP	prostate:	n/a
25	chr11:32851356-32851406	NB4	blood:	n/a
26	chr11:32851378-32851428	SK-N-MC	brain:	n/a
27	chr11:32915823-32915873	MCF-7	breast:	n/a
28	chr11:32847480-32847530	PANC-1	pancreas:	n/a
29	chr11:32851346-32851396	HRE	kidney:	n/a
30	chr11:32816211-32816261	HRPEpiC	eye:	n/a
31	chr11:32816254-32816304	SK-N-MC	brain:	n/a
32	chr11:32851361-32851411	Jurkat	blood:	n/a
33	chr11:32816254-32816304	SK-N-SH_RA	brain:	n/a
34	chr11:32851346-32851396	HNPCEpiC	eye:	n/a
35	chr11:32851950-32852000	SK-N-MC	brain:	n/a
36	chr11:32816885-32816935	Hepatocyte	liver:	n/a
37	chr11:32851087-32851137	Hela-S3	cervix:	n/a
38	chr11:32915131-32915181	LNCaP	prostate:	n/a
39	chr11:32816080-32816130	HCPEpiC	choroid plexus:	n/a
40	chr11:32847480-32847530	MCF-7	breast:	n/a
41	chr11:32916120-32916170	HepG2	liver:	n/a
42	chr11:33000491-33000541	AG04449	skin:	fetal
43	chr11:32909110-32909160	NHDF-neo	bronchial:	n/a
44	chr11:32914648-32914698	A549	lung:	n/a
45	chr11:32851378-32851428	AG09309	skin:	n/a
46	chr11:32914618-32914668	AG04449	skin:	fetal
47	chr11:32817614-32817664	ECC-1	luminal epithelium:	n/a
48	chr11:32914648-32914698	AG04449	skin:	fetal
49	chr11:32919083-32919133	Hepatocyte	liver:	n/a
50	chr11:32915823-32915873	HRPEpiC	eye:	n/a

(count:153 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr11:32914706..32916698-chr11:32938158..32939681,2	MCF-7	breast:
2	chr11:32825967..32829445-chr11:32834509..32837119,3	K562	blood:
3	chr11:32916175..32919465-chr11:32932228..32934625,3	K562	blood:
4	chr11:32919329..32924286-chr11:32926573..32930323,7	K562	blood:
5	chr11:32835440..32837233-chr11:32841490..32844292,2	K562	blood:
6	chr11:32912444..32914191-chr11:32997049..32998828,2	K562	blood:
7	chr11:32913437..32915867-chr11:32930703..32933783,3	MCF-7	breast:
8	chr11:32913861..32915566-chr11:33278350..33280856,3	K562	blood:
9	chr11:32849868..32852880-chr11:32911360..32916794,6	MCF-7	breast:
10	chr11:32914186..32915173-chr9:34178494..34179034,2	NB4	blood:
11	chr11:32935340..32937202-chr11:32944261..32946142,2	MCF-7	breast:
12	chr11:32849868..32852880-chr11:32911360..32916794,6	MCF-7	breast:
13	chr11:32914066..32915835-chr11:33278115..33280779,2	K562	blood:
14	chr11:32988347..32990488-chr11:32993525..32996077,2	K562	blood:
15	chr11:32911413..32915588-chr11:32929395..32934017,7	K562	blood:
16	chr11:32850001..32854483-chr11:32912810..32915962,5	MCF-7	breast:
17	chr11:17096881..17099234-chr11:32950894..32953291,2	K562	blood:
18	chr11:32900766..32903313-chr11:32912451..32914688,2	K562	blood:
19	chr11:32858756..32863139-chr11:32912593..32915314,4	MCF-7	breast:
20	chr11:32912677..32916677-chr11:32946348..32949783,4	K562	blood:
21	chr11:32915892..32917470-chr11:32980726..32982282,2	K562	blood:
22	chr11:32850001..32854483-chr11:32912810..32915962,5	MCF-7	breast:
23	chr11:32915392..32916319-chr3:40498303..40499288,2	Hela-S3	cervix:
24	chr11:32734959..32735691-chr11:32814406..32814938,2	MCF-7	breast:
25	chr11:32913837..32914707-chr6:31587711..31588295,2	Hela-S3	cervix:
26	chr11:32970671..32972775-chr11:32979842..32982658,2	K562	blood:
27	chr11:32931627..32937839-chr11:32937972..32943855,8	K562	blood:
28	chr11:32797795..32799426-chr11:32913652..32916468,2	MCF-7	breast:
29	chr11:32950716..32952924-chr11:32954824..32956515,2	K562	blood:
30	chr11:32945489..32947897-chr11:32951878..32954086,3	MCF-7	breast:
31	chr11:32854588..32857057-chr11:32860540..32862429,2	K562	blood:
32	chr11:32914852..32915778-chr22:46409688..46410516,2	Hela-S3	cervix:
33	chr11:32916175..32919465-chr11:32932228..32934625,3	K562	blood:
34	chr11:32892015..32892872-chr11:32914554..32915403,2	MCF-7	breast:
35	chr11:32925593..32927365-chr11:32932559..32934315,2	K562	blood:
36	chr11:32913396..32915268-chr11:32939750..32941847,3	K562	blood:
37	chr11:32873372..32875504-chr11:32882412..32884075,2	K562	blood:
38	chr11:32900766..32903313-chr11:32912451..32914688,2	K562	blood:
39	chr11:32455369..32457971-chr11:32914210..32916339,2	K562	blood:
40	chr11:32912527..32916011-chr11:32934159..32936611,3	K562	blood:
41	chr11:32851461..32852210-chr3:49058647..49059440,2	NB4	blood:
42	chr11:32851076..32851981-chr12:123011655..123012268,2	Hela-S3	cervix:
43	chr11:32913873..32915883-chr11:32948167..32950423,2	MCF-7	breast:
44	chr11:32845133..32847624-chr11:32847772..32849617,2	MCF-7	breast:
45	chr11:32970671..32972775-chr11:32979842..32982658,2	K562	blood:
46	chr11:32913172..32915250-chr11:32939039..32941847,3	K562	blood:
47	chr11:32925134..32927597-chr11:32928287..32929903,2	K562	blood:
48	chr11:32994287..32996312-chr11:32999002..33001854,3	K562	blood:
49	chr11:32892094..32893817-chr11:32914118..32916253,2	K562	blood:
50	chr11:32830572..32833021-chr11:32913903..32915593,2	MCF-7	breast:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRRG4-3	chr11:32823241-32823497	NONHSAT018675
2	lnc-QSER1-1	chr11:32878980-32879666	NONHSAT018678
3	lnc-PRRG4-2	chr11:32839176-32839252	NONHSAT018676
4	lnc-CCDC73-1	chr11:32878982-32879665	ENSG00000248689
5	lnc-CSTF3-1	chr11:32978271-32978312	NONHSAT018681
6	lnc-PRRG4-1	chr11:32846016-32846832	NONHSAT018677
7	lnc-CCDC73-1	chr11:32875249-32875810	ENSG00000248689
8	lnc-CCDC73-2	chr11:32817536-32817819	NONHSAT018674
9	lnc-CSTF3-1	chr11:32977870-32978000	NONHSAT018681
10	lnc-QSER1-1	chr11:32875249-32875808	NONHSAT018678
11	lnc-PRRG4-2	chr11:32839485-32839664	NONHSAT018676

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
ENSG00000121690	chromatin interactions
ENSG00000150753	chromatin interactions
ENSG00000248489	chromatin interactions
ENSG00000183242	chromatin interactions
ENSG00000184445	chromatin interactions
ENSG00000186714	chromatin interactions
ENSG00000060749	chromatin interactions
ENSG00000152256	chromatin interactions
ENSG00000188846	chromatin interactions
ENSG00000110700	chromatin interactions
ENSG00000134824	chromatin interactions
ENSG00000228265	chromatin interactions
ENSG00000153207	chromatin interactions
ENSG00000178149	chromatin interactions
ENSG00000176102	chromatin interactions
ENSG00000197153	chromatin interactions
ENSG00000185324	chromatin interactions
ENSG00000153015	chromatin interactions
ENSG00000125740	chromatin interactions
ENSG00000260259	chromatin interactions
ENSG00000247151	chromatin interactions
ENSG00000176148	chromatin interactions
ENSG00000150756	chromatin interactions
ENSG00000110422	chromatin interactions
ENSG00000165006	chromatin interactions
ENSG00000201403	chromatin interactions
ENSG00000135378	chromatin interactions
ENSG00000178057	chromatin interactions
ENSG00000149485	chromatin interactions
ENSG00000184937	chromatin interactions
ENSG00000079215	chromatin interactions
ENSG00000151849	chromatin interactions
ENSG00000180596	chromatin interactions
ENSG00000257337	chromatin interactions
LMAN2L	miRNA target sites
FBXW7	miRNA target sites

Extended variants
information (count: 6060 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:6060 , 50 per page) page: 1 2 3 4 5 6 7 ... 122

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10767965	chr11:32796092-32796093	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs544137809	chr11:32796157-32796158	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs556116380	chr11:32796166-32796167	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs116703528	chr11:32796196-32796197	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs571888834	chr11:32796608-32796609	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs114358411	chr11:32796660-32796661	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs1509889	chr11:32796686-32796687	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs140784841	chr11:32796780-32796781	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs572628159	chr11:32796790-32796791	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs541480224	chr11:32796847-32796848	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs75913851	chr11:32796874-32796875	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs186851907	chr11:32796955-32796956	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs564628368	chr11:32796958-32796959	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs563069752	chr11:32797003-32797004	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs191741682	chr11:32797011-32797012	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs184038401	chr11:32797044-32797045	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs533218386	chr11:32797108-32797109	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs540290305	chr11:32797209-32797210	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs560478654	chr11:32797263-32797264	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs529416350	chr11:32797280-32797281	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs558726553	chr11:32797328-32797329	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs570571094	chr11:32797345-32797346	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs72897183	chr11:32797470-32797471	Active TSS Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs187726233	chr11:32797512-32797513	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs531971069	chr11:32797513-32797514	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs551936714	chr11:32797527-32797528	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs571864591	chr11:32797544-32797545	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs74749428	chr11:32797547-32797548	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs561953434	chr11:32797579-32797580	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs189900742	chr11:32797599-32797600	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs529272241	chr11:32797600-32797601	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs116475100	chr11:32797651-32797652	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs182214353	chr11:32797684-32797685	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs535075965	chr11:32797701-32797702	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs555069368	chr11:32797802-32797803	Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs574977505	chr11:32797821-32797822	Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs530270438	chr11:32797864-32797865	Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs369012258	chr11:32797890-32797891	Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs6484594	chr11:32797905-32797906	Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs12291922	chr11:32797914-32797915	Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs560463282	chr11:32797916-32797917	Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs574316522	chr11:32797921-32797922	Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs186505011	chr11:32797929-32797930	Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs149701618	chr11:32797998-32797999	Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs11031975	chr11:32798031-32798032	Enhancers Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs548809196	chr11:32798035-32798036	Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs551711726	chr11:32798044-32798045	Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs565433612	chr11:32798056-32798057	Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs369832303	chr11:32798097-32798098	Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs553626367	chr11:32798101-32798102	Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:3274 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

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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