Variant report

Variant	esv2757447
Chromosome Location	chr11:58746238-58906018
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2489)
CpG islands
(count:2262)
Chromatin interactive
region (count:35)
LncRNA
region (count:37)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2489 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:58792609-58792905	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:58903414-58903708	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:58874268-58874746	HepG2	liver:	n/a	n/a
4	ATF1	chr11:58779639-58779652	K562	blood:	n/a	n/a
5	ATF1	chr11:58864804-58864948	K562	blood:	n/a	n/a
6	ATF2	chr11:58831671-58832143	GM12878	blood:	n/a	n/a
7	ATF2	chr11:58869606-58870352	GM12878	blood:	n/a	n/a
8	ATF2	chr11:58874015-58875031	GM12878	blood:	n/a	n/a
9	ATF2	chr11:58903427-58903758	GM12878	blood:	n/a	n/a
10	ATF2	chr11:58874367-58874899	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr11:58825833-58826405	GM12878	blood:	n/a	n/a
12	ATF2	chr11:58864502-58864964	GM12878	blood:	n/a	n/a
13	ATF2	chr11:58869726-58870352	GM12878	blood:	n/a	n/a
14	ATF2	chr11:58874286-58874870	GM12878	blood:	n/a	n/a
15	ATF2	chr11:58831402-58832419	GM12878	blood:	n/a	n/a
16	ATF2	chr11:58903346-58903784	GM12878	blood:	n/a	n/a
17	ATF2	chr11:58874344-58874770	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF3	chr11:58869743-58869963	K562	blood:	n/a	n/a
19	BACH1	chr11:58903471-58903671	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr11:58869800-58870060	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr11:58825972-58826213	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr11:58873974-58874757	H1-hESC	embryonic stem cell:	n/a	chr11:58874543-58874557
23	BATF	chr11:58826199-58826498	GM12878	blood:	n/a	n/a
24	BATF	chr11:58862752-58863071	GM12878	blood:	n/a	n/a
25	BATF	chr11:58831471-58831776	GM12878	blood:	n/a	n/a
26	BATF	chr11:58831786-58832150	GM12878	blood:	n/a	chr11:58831926-58831934
27	BATF	chr11:58818940-58819193	GM12878	blood:	n/a	n/a
28	BATF	chr11:58875555-58875818	GM12878	blood:	n/a	chr11:58875662-58875670
29	BATF	chr11:58760001-58760259	GM12878	blood:	n/a	chr11:58760105-58760116
30	BATF	chr11:58831416-58832275	GM12878	blood:	n/a	chr11:58831926-58831934
31	BATF	chr11:58874419-58874727	GM12878	blood:	n/a	chr11:58874543-58874553 chr11:58874547-58874557 chr11:58874542-58874553
32	BATF	chr11:58875256-58875548	GM12878	blood:	n/a	n/a
33	BATF	chr11:58869559-58870293	GM12878	blood:	n/a	n/a
34	BCL11A	chr11:58869760-58870216	GM12878	blood:	n/a	n/a
35	BCL11A	chr11:58831528-58832157	GM12878	blood:	n/a	n/a
36	BCL11A	chr11:58818878-58819275	GM12878	blood:	n/a	chr11:58819091-58819100
37	BCL11A	chr11:58875271-58875606	GM12878	blood:	n/a	n/a
38	BCL11A	chr11:58818899-58819262	GM12878	blood:	n/a	chr11:58819091-58819100
39	BCL11A	chr11:58869844-58870260	GM12878	blood:	n/a	n/a
40	BCL11A	chr11:58862690-58863069	GM12878	blood:	n/a	chr11:58862903-58862912
41	BCL11A	chr11:58862711-58863079	GM12878	blood:	n/a	chr11:58862903-58862912
42	BCL11A	chr11:58831483-58831904	GM12878	blood:	n/a	n/a
43	BCL3	chr11:58869751-58870129	GM12878	blood:	n/a	n/a
44	BCL3	chr11:58831794-58832281	GM12878	blood:	n/a	n/a
45	BCL3	chr11:58903396-58903768	GM12878	blood:	n/a	n/a
46	BCLAF1	chr11:58873883-58874436	GM12878	blood:	n/a	chr11:58874084-58874097
47	BCLAF1	chr11:58903341-58903724	GM12878	blood:	n/a	n/a
48	BCLAF1	chr11:58869623-58870275	GM12878	blood:	n/a	n/a
49	BCLAF1	chr11:58869650-58870315	GM12878	blood:	n/a	n/a
50	BHLHE40	chr11:58792570-58792935	HepG2	liver:	n/a	chr11:58792752-58792765 chr11:58792748-58792769

(count:2262 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:58874608-58874658	HRCEpiC	kidney:	n/a
2	chr11:58874348-58874398	RPTEC	kidney:	n/a
3	chr11:58869823-58869873	AG04450	lung:	fetal
4	chr11:58830191-58830241	PFSK-1	brain:	n/a
5	chr11:58869823-58869873	HNPCEpiC	eye:	n/a
6	chr11:58874608-58874658	HRCEpiC	kidney:	n/a
7	chr11:58874348-58874398	RPTEC	kidney:	n/a
8	chr11:58869823-58869873	AG04450	lung:	fetal
9	chr11:58830191-58830241	PFSK-1	brain:	n/a
10	chr11:58869823-58869873	HNPCEpiC	eye:	n/a
11	chr11:58810187-58810237	NHBE	bronchial:	n/a
12	chr11:58874637-58874687	IMR90	lung:	fetal
13	chr11:58874608-58874658	T-47D	breast:	n/a
14	chr11:58869663-58869713	GM06990	blood:	n/a
15	chr11:58870075-58870125	Hepatocyte	liver:	n/a
16	chr11:58877370-58877420	Caco-2	colon:	n/a
17	chr11:58806952-58807002	BE2_C	brain:	n/a
18	chr11:58904869-58904919	GM12892	blood:	n/a
19	chr11:58874723-58874773	LNCaP	prostate:	n/a
20	chr11:58874635-58874685	PrEC	prostate:	n/a
21	chr11:58874723-58874773	GM12891	blood:	n/a
22	chr11:58828174-58828224	GM06990	blood:	n/a
23	chr11:58904869-58904919	ProgFib	skin:	n/a
24	chr11:58826073-58826123	HCF	heart:	n/a
25	chr11:58828174-58828224	RPTEC	kidney:	n/a
26	chr11:58874348-58874398	NB4	blood:	n/a
27	chr11:58873955-58874005	Hepatocyte	liver:	n/a
28	chr11:58904869-58904919	Hepatocyte	liver:	n/a
29	chr11:58830424-58830474	HAEpiC	amniotic membrane:	n/a
30	chr11:58874641-58874691	HPAEpiC	pulmonary alveolar:	n/a
31	chr11:58826475-58826525	NT2-D1	testis:	n/a
32	chr11:58904901-58904951	ProgFib	skin:	n/a
33	chr11:58866721-58866771	HIPEpiC	eye:	n/a
34	chr11:58806952-58807002	PrEC	prostate:	n/a
35	chr11:58874207-58874257	HIPEpiC	eye:	n/a
36	chr11:58869663-58869713	HepG2	liver:	n/a
37	chr11:58870075-58870125	GM12892	blood:	n/a
38	chr11:58869979-58870029	GM12878	blood:	n/a
39	chr11:58874723-58874773	SAEC	small airway:	n/a
40	chr11:58830355-58830405	HUVEC	blood vessel:	n/a
41	chr11:58874723-58874773	AoSMC	blood vessel:	n/a
42	chr11:58830424-58830474	IMR90	lung:	fetal
43	chr11:58874207-58874257	HCPEpiC	choroid plexus:	n/a
44	chr11:58870075-58870125	MCF-7	breast:	n/a
45	chr11:58874635-58874685	T-47D	breast:	n/a
46	chr11:58828174-58828224	HRE	kidney:	n/a
47	chr11:58874723-58874773	AG09319	gingival:	n/a
48	chr11:58904869-58904919	AG04450	lung:	fetal
49	chr11:58874207-58874257	SAEC	small airway:	n/a
50	chr11:58874645-58874695	SAEC	small airway:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:58884380..58886693-chr11:58887312..58889287,2	K562	blood:
2	chr11:58875233..58875940-chr12:49657802..49658323,2	Hela-S3	cervix:
3	chr11:58873805..58875305-chr17:41466179..41467880,2	MCF-7	breast:
4	chr11:58875510..58878300-chr11:58880309..58883300,3	MCF-7	breast:
5	chr11:58830364..58831268-chr11:58873992..58874927,2	HCT-116	colon:
6	chr11:58873805..58876804-chr17:41466274..41467888,2	K562	blood:
7	chr11:58863409..58866220-chr11:58910202..58912249,2	K562	blood:
8	chr11:58726086..58726653-chr11:58902781..58903961,3	K562	blood:
9	chr11:58864668..58865554-chr11:58903471..58904061,2	MCF-7	breast:
10	chr11:58762969..58764487-chr11:58768997..58771127,2	K562	blood:
11	chr11:58896273..58898836-chr11:58901279..58902925,2	K562	blood:
12	chr11:58890846..58893267-chr11:58894892..58896437,2	MCF-7	breast:
13	chr11:58872425..58874544-chr11:58888169..58890358,2	MCF-7	breast:
14	chr11:58892733..58893477-chr11:58901491..58902182,2	K562	blood:
15	chr11:58869989..58871867-chr11:58872289..58874332,2	MCF-7	breast:
16	chr11:58896273..58898836-chr11:58901279..58902925,2	K562	blood:
17	chr11:58869975..58872858-chr11:58877240..58880132,2	MCF-7	breast:
18	chr11:58872425..58874544-chr11:58888169..58890358,2	MCF-7	breast:
19	chr11:58864668..58865554-chr11:58903471..58904061,2	MCF-7	breast:
20	chr11:58869192..58871421-chr11:58911598..58913836,2	MCF-7	breast:
21	chr11:58874735..58876453-chr11:58878007..58880480,2	MCF-7	breast:
22	chr11:58873861..58874546-chr5:111496427..111496981,2	Hela-S3	cervix:
23	chr11:58762969..58764487-chr11:58768997..58771127,2	K562	blood:
24	chr11:58869975..58872858-chr11:58877240..58880132,2	MCF-7	breast:
25	chr11:58875510..58878300-chr11:58880309..58883300,3	MCF-7	breast:
26	chr11:58874735..58876453-chr11:58878007..58880480,2	MCF-7	breast:
27	chr11:58869989..58871867-chr11:58872289..58874332,2	MCF-7	breast:
28	chr11:58904183..58908174-chr11:58910132..58913359,4	MCF-7	breast:
29	chr11:58869769..58871706-chr11:58872515..58874019,2	MCF-7	breast:
30	chr11:58892733..58893477-chr11:58901491..58902182,2	K562	blood:
31	chr11:58884380..58886693-chr11:58887312..58889287,2	K562	blood:
32	chr11:58873708..58874686-chr11:63448916..63449711,2	Hela-S3	cervix:
33	chr11:58890846..58893267-chr11:58894892..58896437,2	MCF-7	breast:
34	chr11:58869769..58871706-chr11:58872515..58874019,2	MCF-7	breast:
35	chr11:58399679..58402149-chr11:58838160..58840024,2	K562	blood:

(count:37 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GLYATL2-2	chr11:58818733-58818781	ENSG00000255240.1
2	lnc-GLYATL2-2	chr11:58746601-58746758	ENSG00000255240.1
3	lnc-MPEG1-2	chr11:58901446-58903061	NR_110184
4	lnc-GLYATL2-2	chr11:58825845-58825925	NR_033853
5	lnc-GLYATL2-2	chr11:58825845-58825923	ENSG00000255240.1
6	lnc-MPEG1-2	chr11:58903530-58903754	NONHSAT021502
7	lnc-GLYATL2-2	chr11:58820930-58821099	NR_033853
8	lnc-MPEG1-2	chr11:58901132-58902156	XLOC_009445
9	lnc-MPEG1-2	chr11:58902763-58903061	ENSG00000245571
10	lnc-GLYATL2-2	chr11:58825845-58826132	ENSG00000255240.1
11	lnc-GLYATL2-2	chr11:58820930-58821099	ENSG00000255240.1
12	lnc-MPEG1-2	chr11:58902051-58902156	XLOC_009445
13	lnc-MPEG1-2	chr11:58900752-58901122	XLOC_009445
14	lnc-MPEG1-2	chr11:58903530-58903754	ENSG00000245571
15	lnc-GLYATL2-2	chr11:58746601-58746798	ENSG00000255240.1
16	lnc-GLYATL2-2	chr11:58822768-58822919	ENSG00000255240.1
17	lnc-MPEG1-2	chr11:58903530-58903816	XLOC_009445
18	lnc-GLYATL2-2	chr11:58761476-58761524	NR_033853
19	lnc-MPEG1-2	chr11:58901697-58903061	ENSG00000245571
20	lnc-MPEG1-2	chr11:58903530-58903557	XLOC_009445
21	lnc-MPEG1-2	chr11:58903530-58903754	ENSG00000245571
22	lnc-MPEG1-2	chr11:58903530-58903754	XLOC_009445
23	lnc-MPEG1-2	chr11:58903398-58903754	ENSG00000245571
24	lnc-MPEG1-2	chr11:58897606-58897784	NONHSAT021502
25	lnc-MPEG1-2	chr11:58897610-58901122	XLOC_009445
26	lnc-GLYATL2-2	chr11:58818733-58818781	ENSG00000255240.1
27	lnc-MPEG1-2	chr11:58902051-58903061	XLOC_009445
28	lnc-MPEG1-2	chr11:58901712-58903061	NONHSAT021502
29	lnc-FAM111A-1	chr11:58874709-58874769	NONHSAT021500
30	lnc-GLYATL2-2	chr11:58818733-58818781	NR_033853
31	lnc-FAM111A-1	chr11:58876141-58876185	NONHSAT021500
32	lnc-MPEG1-2	chr11:58897606-58897773	ENSG00000245571
33	lnc-FAM111A-1	chr11:58877013-58877480	NONHSAT021500
34	lnc-GLYATL2-2	chr11:58820930-58821099	ENSG00000255240.1
35	lnc-GLYATL2-2	chr11:58761476-58761524	ENSG00000255240.1
36	lnc-GLYATL2-2	chr11:58746601-58746798	NR_033853
37	lnc-MPEG1-2	chr11:58903530-58903754	NR_110184

No data

Variant related genes	Relation type
GLYATL1P1	TF binding region
ENSG00000255240	TF binding region
GLYATL1P3	TF binding region
GLYATL1P4	TF binding region
FAM111A	TF binding region
ENSG00000254786	TF binding region
FAM111B	TF binding region
GLYATL1P1	CpG island
ENSG00000255240	CpG island
GLYATL1P3	CpG island
GLYATL1P4	CpG island
FAM111A	CpG island
ENSG00000254786	CpG island
FAM111B	CpG island
ENSG00000188825	chromatin interactions
ENSG00000245571	chromatin interactions
ENSG00000133318	chromatin interactions
ENSG00000189057	chromatin interactions
ENSG00000224032	chromatin interactions
ENSG00000166801	chromatin interactions
PRUNE2	miRNA target sites
POU2F1	miRNA target sites
CNOT6	miRNA target sites
CDK6	miRNA target sites
GSPT1	miRNA target sites
KIF2A	miRNA target sites
PRTG	miRNA target sites
ZFPM2	miRNA target sites
PDE3B	miRNA target sites
CRKL	miRNA target sites
AP3S1	miRNA target sites

Extended variants
information (count: 6316 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:6316 , 50 per page) page: 1 2 3 4 5 6 7 ... 127

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1938791	chr11:58746238-58746239	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs547447173	chr11:58746260-58746261	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs559714773	chr11:58746273-58746274	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs530205715	chr11:58746311-58746312	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs80319180	chr11:58746343-58746344	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs550780033	chr11:58746350-58746351	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs145629287	chr11:58746449-58746450	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs537200160	chr11:58746462-58746463	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs552350571	chr11:58746483-58746484	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs188119722	chr11:58746580-58746581	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs148095137	chr11:58746592-58746593	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs74905972	chr11:58746644-58746645	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
13	rs574401476	chr11:58746662-58746663	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
14	rs371669455	chr11:58746673-58746674	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
15	rs76749693	chr11:58746711-58746712	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
16	rs141990610	chr11:58746712-58746713	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
17	rs371765474	chr11:58746716-58746717	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
18	rs575004895	chr11:58746787-58746788	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
19	rs543562953	chr11:58746848-58746849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs59760560	chr11:58746916-58746917	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs530344065	chr11:58746941-58746942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs35753170	chr11:58746944-58746945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs577432484	chr11:58747024-58747025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs541745538	chr11:58747040-58747041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs559470104	chr11:58747049-58747050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs530166230	chr11:58747095-58747096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs57890151	chr11:58747105-58747106	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs563723348	chr11:58747148-58747149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs150697437	chr11:58747159-58747160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs528763557	chr11:58747169-58747170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs570659284	chr11:58747171-58747172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs192743192	chr11:58747173-58747174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs546920140	chr11:58747193-58747194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs567708997	chr11:58747216-58747217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs535044015	chr11:58747220-58747221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs183467560	chr11:58747282-58747283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs536756768	chr11:58747330-58747331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs552005211	chr11:58747349-58747350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs10792209	chr11:58747355-58747356	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs577397591	chr11:58747373-58747374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs12223443	chr11:58747398-58747399	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs138871449	chr11:58747402-58747403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs11229715	chr11:58747415-58747416	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs538981302	chr11:58747463-58747464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs550631346	chr11:58747470-58747471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs567187128	chr11:58747476-58747477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs377128049	chr11:58747550-58747551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs485893	chr11:58747551-58747552	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs117803965	chr11:58747606-58747607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs546305872	chr11:58747609-58747610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Esophageal cancer	21851588	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Pituitary adenoma	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Autism	22495309	CNVD
Autism	20808228	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2253 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:58740600-58748000	Weak transcription	Primary B cells from peripheral blood	blood
2	chr11:58741800-58756600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr11:58742200-58748800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr11:58744200-58748200	Weak transcription	Primary B cells from cord blood	blood
5	chr11:58746200-58746800	Strong transcription	Primary hematopoietic stem cells	blood
6	chr11:58746800-58749400	Weak transcription	Primary hematopoietic stem cells	blood
7	chr11:58748000-58748400	Enhancers	Primary B cells from peripheral blood	blood
8	chr11:58748200-58748400	Enhancers	Primary B cells from cord blood	blood
9	chr11:58754000-58765800	Weak transcription	Primary hematopoietic stem cells	blood
10	chr11:58754800-58761600	Weak transcription	Primary B cells from peripheral blood	blood
11	chr11:58756600-58757200	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
12	chr11:58756800-58757400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr11:58756800-58757600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr11:58757000-58757200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr11:58757200-58757400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
16	chr11:58757200-58757400	Enhancers	Esophagus	oesophagus
17	chr11:58757200-58759400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr11:58757400-58766600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
19	chr11:58757600-58760000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr11:58758600-58766400	Weak transcription	Primary B cells from cord blood	blood
21	chr11:58759400-58761000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr11:58759800-58760400	Enhancers	GM12878-XiMat	blood
23	chr11:58760000-58761400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr11:58760400-58767000	Weak transcription	GM12878-XiMat	blood
25	chr11:58760600-58764400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr11:58761000-58769200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr11:58761400-58765600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr11:58761600-58762400	Enhancers	Primary B cells from peripheral blood	blood
29	chr11:58761800-58762000	Enhancers	Sigmoid Colon	Sigmoid Colon
30	chr11:58762400-58766400	Weak transcription	Primary B cells from peripheral blood	blood
31	chr11:58764400-58764800	Enhancers	Breast Myoepithelial Primary Cells	Breast
32	chr11:58764800-58775200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
33	chr11:58765600-58766400	Enhancers	Liver	Liver
34	chr11:58765600-58767800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr11:58765800-58766200	Strong transcription	Primary hematopoietic stem cells	blood
36	chr11:58766200-58769000	Weak transcription	Primary hematopoietic stem cells	blood
37	chr11:58766400-58766600	Enhancers	Stomach Mucosa	stomach
38	chr11:58766400-58766800	Flanking Active TSS	Liver	Liver
39	chr11:58766400-58767600	Enhancers	Primary B cells from cord blood	blood
40	chr11:58766400-58767600	Enhancers	Primary B cells from peripheral blood	blood
41	chr11:58766600-58767200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
42	chr11:58766600-58767400	Enhancers	Sigmoid Colon	Sigmoid Colon
43	chr11:58766600-58768000	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr11:58766600-58768000	Enhancers	Monocytes-CD14+_RO01746	blood
45	chr11:58766800-58767200	Enhancers	Rectal Mucosa Donor 31	rectum
46	chr11:58766800-58767800	Enhancers	Liver	Liver
47	chr11:58767000-58767400	Enhancers	GM12878-XiMat	blood
48	chr11:58767200-58767400	Enhancers	Stomach Mucosa	stomach
49	chr11:58767200-58774000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
50	chr11:58767600-58770000	Weak transcription	Primary B cells from cord blood	blood

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