Variant report

Variant	nsv897190
Chromosome Location	chr11:32801921-32951836
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2807)
CpG islands
(count:2625)
Chromatin interactive
region (count:129)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2807 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

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

(count:2625 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:32951061-32951111	RPTEC	kidney:	n/a
2	chr11:32851346-32851396	BJ	skin:	n/a
3	chr11:32951061-32951111	RPTEC	kidney:	n/a
4	chr11:32851346-32851396	BJ	skin:	n/a
5	chr11:32912719-32912769	CMK	blood:	n/a
6	chr11:32816227-32816277	GM12891	blood:	n/a
7	chr11:32851378-32851428	AG04450	lung:	fetal
8	chr11:32932059-32932109	HCM	heart:	n/a
9	chr11:32815968-32816018	HRCEpiC	kidney:	n/a
10	chr11:32914638-32914688	MCF10A-Er-Src	breast:	n/a
11	chr11:32909110-32909160	HEEpiC	esophagus:	n/a
12	chr11:32914648-32914698	Caco-2	colon:	n/a
13	chr11:32919083-32919133	NHBE	bronchial:	n/a
14	chr11:32919083-32919133	BJ	skin:	n/a
15	chr11:32851356-32851406	LNCaP	prostate:	n/a
16	chr11:32915823-32915873	MCF-7	breast:	n/a
17	chr11:32851346-32851396	AG04450	lung:	fetal
18	chr11:32851378-32851428	GM12878	blood:	n/a
19	chr11:32912719-32912769	Hela-S3	cervix:	n/a
20	chr11:32851531-32851581	SAEC	small airway:	n/a
21	chr11:32816254-32816304	ovcar-3	ovarian:	n/a
22	chr11:32817614-32817664	SK-N-MC	brain:	n/a
23	chr11:32851260-32851310	HEK293	kidney:	embryo
24	chr11:32816211-32816261	H1-hESC	embryonic stem cell:	embryo
25	chr11:32851378-32851428	Jurkat	blood:	n/a
26	chr11:32915823-32915873	BE2_C	brain:	n/a
27	chr11:32816211-32816261	SK-N-MC	brain:	n/a
28	chr11:32817614-32817664	NT2-D1	testis:	n/a
29	chr11:32914605-32914655	HMEC	breast:	n/a
30	chr11:32817614-32817664	NB4	blood:	n/a
31	chr11:32851356-32851406	HNPCEpiC	eye:	n/a
32	chr11:32915497-32915547	A549	lung:	n/a
33	chr11:32914618-32914668	AG09309	skin:	n/a
34	chr11:32816080-32816130	AG04450	lung:	fetal
35	chr11:32851950-32852000	HUVEC	blood vessel:	n/a
36	chr11:32847480-32847530	IMR90	lung:	fetal
37	chr11:32816254-32816304	AG09319	gingival:	n/a
38	chr11:32914818-32914868	AG04450	lung:	fetal
39	chr11:32915131-32915181	NT2-D1	testis:	n/a
40	chr11:32914638-32914688	Jurkat	blood:	n/a
41	chr11:32851260-32851310	HL-60	blood:	n/a
42	chr11:32816211-32816261	T-47D	breast:	n/a
43	chr11:32815865-32815915	AG09319	gingival:	n/a
44	chr11:32815968-32816018	SK-N-MC	brain:	n/a
45	chr11:32914648-32914698	LNCaP	prostate:	n/a
46	chr11:32816227-32816277	SK-N-SH_RA	brain:	n/a
47	chr11:32915823-32915873	HRPEpiC	eye:	n/a
48	chr11:32915131-32915181	ECC-1	luminal epithelium:	n/a
49	chr11:32915903-32915953	AG10803	skin:	n/a
50	chr11:32951061-32951111	PrEC	prostate:	n/a

(count:129 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr11:32914066..32915835-chr11:33278115..33280779,2	K562	blood:
2	chr11:32851501..32854370-chr11:32879596..32881538,2	MCF-7	breast:
3	chr11:32912742..32915744-chr11:33035300..33038153,5	K562	blood:
4	chr11:32835440..32837233-chr11:32841490..32844292,2	K562	blood:
5	chr11:32913861..32915566-chr11:33278350..33280856,3	K562	blood:
6	chr11:32904524..32910209-chr11:32910222..32915650,10	MCF-7	breast:
7	chr11:32808269..32810578-chr11:32811401..32813892,2	K562	blood:
8	chr11:32850866..32853799-chr11:32862127..32863701,2	MCF-7	breast:
9	chr11:32933148..32935266-chr11:32937418..32940169,3	K562	blood:
10	chr11:32734492..32735804-chr11:32813911..32815565,5	MCF-7	breast:
11	chr11:32912677..32916677-chr11:32946348..32949783,4	K562	blood:
12	chr11:32914186..32915173-chr9:34178494..34179034,2	NB4	blood:
13	chr11:32942975..32945695-chr11:32951329..32953837,2	K562	blood:
14	chr11:32912739..32915383-chr11:32925988..32928969,2	MCF-7	breast:
15	chr11:32914059..32914697-chr5:64064672..64065341,2	Hela-S3	cervix:
16	chr11:32858756..32863139-chr11:32912593..32915314,4	MCF-7	breast:
17	chr11:32911083..32916400-chr11:33180278..33184105,5	K562	blood:
18	chr11:32925593..32927365-chr11:32932559..32934315,2	K562	blood:
19	chr11:32861977..32862713-chr14:65386776..65387380,2	MCF-7	breast:
20	chr11:32913873..32915883-chr11:32948167..32950423,2	MCF-7	breast:
21	chr11:32808269..32810578-chr11:32811401..32813892,2	K562	blood:
22	chr11:32911413..32915588-chr11:32929395..32934017,7	K562	blood:
23	chr11:32915549..32916317-chr11:61583965..61584543,2	Hela-S3	cervix:
24	chr11:32914076..32914799-chr6:26123502..26124171,2	Hela-S3	cervix:
25	chr11:32847589..32849311-chr11:32913725..32915620,2	K562	blood:
26	chr11:32925698..32927365-chr11:32931913..32934059,2	K562	blood:
27	chr11:32862183..32864294-chr11:32914218..32916079,2	K562	blood:
28	chr11:32900766..32903313-chr11:32912451..32914688,2	K562	blood:
29	chr11:32912949..32915416-chr11:33278689..33280447,2	MCF-7	breast:
30	chr11:32913396..32916033-chr11:32943893..32945923,3	K562	blood:
31	chr11:32913171..32916144-chr11:33182605..33184521,3	K562	blood:
32	chr11:32949447..32951560-chr11:32996072..32998442,2	K562	blood:
33	chr11:32912527..32916011-chr11:32934159..32936611,3	K562	blood:
34	chr11:32455369..32457971-chr11:32914210..32916339,2	K562	blood:
35	chr11:32915240..32915992-chr12:53440834..53441564,2	Hela-S3	cervix:
36	chr11:32854588..32857057-chr11:32860540..32862429,2	K562	blood:
37	chr11:32873372..32875504-chr11:32882412..32884075,2	K562	blood:
38	chr11:32843099..32845929-chr11:32851383..32853799,2	MCF-7	breast:
39	chr11:32914431..32914932-chr19:45971637..45972583,2	Hela-S3	cervix:
40	chr11:32915546..32916189-chr5:98264465..98265204,2	Hela-S3	cervix:
41	chr11:32850385..32853089-chr11:32925250..32927844,2	MCF-7	breast:
42	chr11:32830572..32833021-chr11:32913903..32915593,2	MCF-7	breast:
43	chr11:32916175..32919465-chr11:32932228..32934625,3	K562	blood:
44	chr11:32935648..32937235-chr11:32951020..32953921,2	MCF-7	breast:
45	chr11:32851187..32853645-chr11:32854709..32858523,6	MCF-7	breast:
46	chr11:32850121..32852277-chr11:33088797..33091531,2	MCF-7	breast:
47	chr11:32849868..32852880-chr11:32911360..32916794,6	MCF-7	breast:
48	chr11:32851461..32852210-chr3:49058647..49059440,2	NB4	blood:
49	chr11:32914384..32914884-chr13:25496573..25497412,2	NB4	blood:
50	chr11:32919329..32924286-chr11:32926573..32930323,7	K562	blood:

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

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

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

Extended variants
information (count: 4308 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:4308 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11031978	chr11:32801921-32801922	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs140252515	chr11:32802093-32802094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs190954716	chr11:32802189-32802190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs573540183	chr11:32802214-32802215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs541033056	chr11:32802230-32802231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs554579457	chr11:32802336-32802337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs574602265	chr11:32802383-32802384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs144097167	chr11:32802416-32802417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs563375881	chr11:32802444-32802445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs532254786	chr11:32802609-32802610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs183155221	chr11:32802617-32802618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs146508585	chr11:32802638-32802639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs528322356	chr11:32802653-32802654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs141101456	chr11:32802658-32802659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs547013268	chr11:32802675-32802676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs372883703	chr11:32802705-32802706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs568077713	chr11:32802765-32802766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs144915462	chr11:32802787-32802788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs111967020	chr11:32802793-32802794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs7109509	chr11:32802802-32802803	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs188237102	chr11:32802803-32802804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs114212528	chr11:32802806-32802807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs539385138	chr11:32802811-32802812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs567196098	chr11:32802845-32802846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs536123494	chr11:32802847-32802848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs138146824	chr11:32802849-32802850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs574378000	chr11:32802881-32802882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs149149527	chr11:32802913-32802914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs556820699	chr11:32802991-32802992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs192526481	chr11:32803023-32803024	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs184559455	chr11:32803032-32803033	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs369227663	chr11:32803093-32803094	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs187396738	chr11:32803111-32803112	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs541755066	chr11:32803152-32803153	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs192580256	chr11:32803164-32803165	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs530854521	chr11:32803200-32803201	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs550940402	chr11:32803248-32803249	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs143269087	chr11:32803298-32803299	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs113361996	chr11:32803311-32803312	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs34562463	chr11:32803318-32803319	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs115855402	chr11:32803358-32803359	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs547232610	chr11:32803363-32803364	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs567105440	chr11:32803390-32803391	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs536037363	chr11:32803437-32803438	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs198265	chr11:32803438-32803439	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs557612190	chr11:32803453-32803454	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs576234662	chr11:32803470-32803471	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs12276553	chr11:32803487-32803488	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs527802304	chr11:32803492-32803493	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs148325924	chr11:32803507-32803508	Enhancers Weak transcription	n/a	n/a	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:2108 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:32798200-32806200	Weak transcription	Liver	Liver
2	chr11:32801400-32803000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr11:32801600-32803000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr11:32803000-32803600	Enhancers	Primary hematopoietic stem cells short term culture	blood
5	chr11:32803000-32803600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr11:32807000-32807400	Enhancers	HepG2	liver
7	chr11:32814000-32814200	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr11:32814000-32814200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr11:32814000-32814200	Enhancers	Liver	Liver
10	chr11:32814000-32814200	Enhancers	Brain Substantia Nigra	brain
11	chr11:32814000-32814200	Enhancers	Dnd41	blood
12	chr11:32814000-32814200	Enhancers	GM12878-XiMat	blood
13	chr11:32814000-32815000	Active TSS	A549	lung
14	chr11:32814200-32814400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr11:32814200-32814400	Enhancers	Primary monocytes fromperipheralblood	blood
16	chr11:32814200-32814400	Bivalent Enhancer	Primary B cells from cord blood	blood
17	chr11:32814200-32814400	Active TSS	Primary T helper naive cells fromperipheralblood	blood
18	chr11:32814200-32814400	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
19	chr11:32814200-32814400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
20	chr11:32814200-32814400	Bivalent Enhancer	Primary T cells effector/memory enriched fromperipheralblood	blood
21	chr11:32814200-32814400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr11:32814200-32814400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr11:32814200-32814400	Active TSS	Adipose Nuclei	Adipose
24	chr11:32814200-32814400	Active TSS	Monocytes-CD14+_RO01746	blood
25	chr11:32814200-32814600	Active TSS	ES-I3 Cell Line	embryonic stem cell
26	chr11:32814200-32814600	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr11:32814200-32814600	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr11:32814200-32814600	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
29	chr11:32814200-32814600	Active TSS	iPS-20b Cell Line	embryonic stem cell
30	chr11:32814200-32814600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
31	chr11:32814200-32814600	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
32	chr11:32814200-32814600	Enhancers	Primary T killer memory cells from peripheral blood	blood
33	chr11:32814200-32814600	Flanking Active TSS	Liver	Liver
34	chr11:32814200-32814600	Flanking Active TSS	Brain Substantia Nigra	brain
35	chr11:32814200-32814600	Flanking Active TSS	GM12878-XiMat	blood
36	chr11:32814200-32814800	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr11:32814200-32814800	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
38	chr11:32814200-32814800	Active TSS	Brain Anterior Caudate	brain
39	chr11:32814200-32814800	Active TSS	Brain Inferior Temporal Lobe	brain
40	chr11:32814200-32814800	Active TSS	Right Atrium	heart
41	chr11:32814200-32815000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr11:32814200-32815000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr11:32814200-32815000	Active TSS	Brain Hippocampus Middle	brain
44	chr11:32814200-32815000	Active TSS	Duodenum Smooth Muscle	Duodenum
45	chr11:32814200-32815000	Active TSS	Pancreatic Islets	Pancreatic Islet
46	chr11:32814200-32815000	Flanking Active TSS	Dnd41	blood
47	chr11:32814200-32815000	Enhancers	NHEK	skin
48	chr11:32814400-32814600	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr11:32814400-32814600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr11:32814400-32814600	Enhancers	Primary B cells from cord blood	blood

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