Variant report

Variant	nsv897310
Chromosome Location	chr11:45487041-45631953
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:653)
CpG islands
(count:244)
Chromatin interactive
region (count:44)
LncRNA
region (count:26)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:653 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:45523311-45523472	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:45578975-45579244	K562	blood:	n/a	n/a
3	ATF1	chr11:45619118-45619164	K562	blood:	n/a	n/a
4	ATF1	chr11:45585356-45585614	K562	blood:	n/a	n/a
5	ATF3	chr11:45599988-45600135	K562	blood:	n/a	n/a
6	BACH1	chr11:45496742-45496913	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr11:45578812-45579363	K562	blood:	n/a	n/a
8	BACH1	chr11:45599338-45599578	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr11:45578961-45579293	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr11:45525994-45526146	K562	blood:	n/a	n/a
11	BATF	chr11:45549497-45549769	GM12878	blood:	n/a	chr11:45549664-45549674 chr11:45549663-45549674
12	BHLHE40	chr11:45599943-45600219	K562	blood:	n/a	n/a
13	BHLHE40	chr11:45576213-45576381	K562	blood:	n/a	n/a
14	BHLHE40	chr11:45539817-45539858	K562	blood:	n/a	n/a
15	BHLHE40	chr11:45600060-45600083	HepG2	liver:	n/a	n/a
16	BHLHE40	chr11:45579037-45579123	K562	blood:	n/a	n/a
17	BRCA1	chr11:45628186-45628509	H1-hESC	embryonic stem cell:	n/a	n/a
18	CCNT2	chr11:45585342-45585619	K562	blood:	n/a	n/a
19	CEBPB	chr11:45531614-45531784	HepG2	liver:	n/a	n/a
20	CEBPB	chr11:45606355-45606555	H1-hESC	embryonic stem cell:	n/a	chr11:45606470-45606481
21	CEBPB	chr11:45626691-45626911	K562	blood:	n/a	chr11:45626746-45626755 chr11:45626744-45626757 chr11:45626746-45626755 chr11:45626744-45626757 chr11:45626746-45626757 chr11:45626744-45626755 chr11:45626746-45626755 chr11:45626746-45626755 chr11:45626746-45626757 chr11:45626744-45626757
22	CEBPB	chr11:45506175-45506407	A549	lung:	n/a	n/a
23	CEBPB	chr11:45578707-45579316	K562	blood:	n/a	n/a
24	CEBPB	chr11:45578711-45579268	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr11:45606324-45606524	K562	blood:	n/a	chr11:45606470-45606481
26	CEBPB	chr11:45600108-45600412	K562	blood:	n/a	chr11:45600247-45600260 chr11:45600247-45600258
27	CEBPB	chr11:45559247-45559543	IMR90	lung:	n/a	chr11:45559369-45559380
28	CEBPB	chr11:45497909-45498184	A549	lung:	n/a	chr11:45498033-45498044
29	CEBPB	chr11:45569216-45569528	A549	lung:	n/a	chr11:45569393-45569406 chr11:45569394-45569405 chr11:45569393-45569404
30	CEBPB	chr11:45559201-45559496	Hela-S3	cervix:	n/a	chr11:45559369-45559380
31	CEBPB	chr11:45578760-45579275	A549	lung:	n/a	n/a
32	CEBPB	chr11:45618334-45618490	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr11:45506924-45507317	Hela-S3	cervix:	n/a	chr11:45507008-45507021
34	CEBPB	chr11:45585296-45585595	K562	blood:	n/a	n/a
35	CEBPB	chr11:45559303-45559517	HepG2	liver:	n/a	chr11:45559369-45559380
36	CEBPB	chr11:45578946-45579174	K562	blood:	n/a	n/a
37	CEBPB	chr11:45506878-45507325	HepG2	liver:	n/a	chr11:45507008-45507021
38	CEBPB	chr11:45497977-45498065	IMR90	lung:	n/a	chr11:45498033-45498044
39	CEBPB	chr11:45569215-45569564	HepG2	liver:	n/a	chr11:45569393-45569406 chr11:45569394-45569405 chr11:45569393-45569404
40	CEBPB	chr11:45498032-45498094	HepG2	liver:	n/a	chr11:45498033-45498044
41	CEBPB	chr11:45578940-45579276	MCF-7	breast:	n/a	n/a
42	CEBPB	chr11:45606334-45606524	HepG2	liver:	n/a	chr11:45606470-45606481
43	CEBPB	chr11:45533162-45533319	HepG2	liver:	n/a	n/a
44	CEBPB	chr11:45559208-45559456	A549	lung:	n/a	chr11:45559369-45559380
45	CEBPB	chr11:45506149-45506449	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr11:45600240-45600270	HepG2	liver:	n/a	chr11:45600247-45600260 chr11:45600247-45600258
47	CEBPB	chr11:45606397-45606537	A549	lung:	n/a	chr11:45606470-45606481
48	CEBPB	chr11:45506123-45506451	HepG2	liver:	n/a	n/a
49	CEBPB	chr11:45578906-45579310	K562	blood:	n/a	n/a
50	CEBPB	chr11:45530540-45530696	HepG2	liver:	n/a	chr11:45530599-45530610

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:45628269-45628319	Jurkat	blood:	n/a
2	chr11:45599468-45599518	Hela-S3	cervix:	n/a
3	chr11:45539734-45539784	SK-N-MC	brain:	n/a
4	chr11:45599468-45599518	T-47D	breast:	n/a
5	chr11:45628269-45628319	HEK293	kidney:	embryo
6	chr11:45599468-45599518	GM06990	blood:	n/a
7	chr11:45495631-45495681	SK-N-SH_RA	brain:	n/a
8	chr11:45628269-45628319	HNPCEpiC	eye:	n/a
9	chr11:45628269-45628319	AG10803	skin:	n/a
10	chr11:45599468-45599518	HRPEpiC	eye:	n/a
11	chr11:45599468-45599518	HMEC	breast:	n/a
12	chr11:45495631-45495681	SK-N-SH	brain:	n/a
13	chr11:45539734-45539784	LNCaP	prostate:	n/a
14	chr11:45628269-45628319	BE2_C	brain:	n/a
15	chr11:45539734-45539784	GM19239	blood:	n/a
16	chr11:45599468-45599518	AoSMC	blood vessel:	n/a
17	chr11:45495631-45495681	HepG2	liver:	n/a
18	chr11:45539734-45539784	IMR90	lung:	fetal
19	chr11:45539734-45539784	HEEpiC	esophagus:	n/a
20	chr11:45539734-45539784	SAEC	small airway:	n/a
21	chr11:45599468-45599518	Jurkat	blood:	n/a
22	chr11:45495631-45495681	HUVEC	blood vessel:	n/a
23	chr11:45539734-45539784	ProgFib	skin:	n/a
24	chr11:45539734-45539784	HUVEC	blood vessel:	n/a
25	chr11:45539734-45539784	RPTEC	kidney:	n/a
26	chr11:45599468-45599518	AG10803	skin:	n/a
27	chr11:45539734-45539784	HCF	heart:	n/a
28	chr11:45495631-45495681	HL-60	blood:	n/a
29	chr11:45628269-45628319	GM06990	blood:	n/a
30	chr11:45599468-45599518	RPTEC	kidney:	n/a
31	chr11:45628269-45628319	Hepatocyte	liver:	n/a
32	chr11:45628269-45628319	IMR90	lung:	fetal
33	chr11:45599468-45599518	HRCEpiC	kidney:	n/a
34	chr11:45599468-45599518	NHBE	bronchial:	n/a
35	chr11:45599468-45599518	IMR90	lung:	fetal
36	chr11:45539734-45539784	SK-N-SH_RA	brain:	n/a
37	chr11:45539734-45539784	HEK293	kidney:	embryo
38	chr11:45495631-45495681	Caco-2	colon:	n/a
39	chr11:45495631-45495681	PrEC	prostate:	n/a
40	chr11:45495631-45495681	BJ	skin:	n/a
41	chr11:45495631-45495681	GM12878	blood:	n/a
42	chr11:45495631-45495681	PFSK-1	brain:	n/a
43	chr11:45628269-45628319	AG09309	skin:	n/a
44	chr11:45539734-45539784	CMK	blood:	n/a
45	chr11:45495631-45495681	K562	blood:	n/a
46	chr11:45495631-45495681	LNCaP	prostate:	n/a
47	chr11:45495631-45495681	AoSMC	blood vessel:	n/a
48	chr11:45495631-45495681	SK-N-MC	brain:	n/a
49	chr11:45599468-45599518	AG04449	skin:	fetal
50	chr11:45599468-45599518	K562	blood:	n/a

(count:44 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:45565846..45568374-chr11:45570778..45572759,2	K562	blood:
2	chr11:45481521..45483456-chr11:45488873..45491103,2	MCF-7	breast:
3	chr11:45590756..45592478-chr11:45595501..45597131,2	K562	blood:
4	chr11:45167444..45169774-chr11:45581988..45584250,2	MCF-7	breast:
5	chr11:45608607..45610604-chr11:45613187..45616434,3	K562	blood:
6	chr11:45576248..45578185-chr11:45589262..45591750,2	K562	blood:
7	chr11:45582261..45584351-chr11:45587015..45588819,2	K562	blood:
8	chr11:45574033..45577062-chr11:45577269..45579721,3	K562	blood:
9	chr11:45546554..45548797-chr11:45591196..45594096,2	K562	blood:
10	chr11:45615603..45617915-chr11:45621444..45624073,2	K562	blood:
11	chr11:45576248..45578185-chr11:45589262..45591750,2	K562	blood:
12	chr11:45608873..45611223-chr11:45614271..45615865,2	K562	blood:
13	chr11:45560001..45561985-chr11:45565491..45567727,2	K562	blood:
14	chr11:45518572..45521279-chr11:45527548..45530147,2	K562	blood:
15	chr11:45574033..45577062-chr11:45577269..45579721,3	K562	blood:
16	chr11:45546554..45548797-chr11:45591196..45594096,2	K562	blood:
17	chr11:45594961..45596588-chr11:45612673..45615496,2	K562	blood:
18	chr11:45518764..45521395-chr11:45524650..45526890,2	K562	blood:
19	chr11:45615603..45617915-chr11:45621444..45624073,2	K562	blood:
20	chr11:45590756..45592478-chr11:45595501..45597131,2	K562	blood:
21	chr11:45507454..45509790-chr11:45515966..45518596,2	K562	blood:
22	chr11:45518572..45521279-chr11:45527548..45530147,2	K562	blood:
23	chr11:45560001..45561985-chr11:45565491..45567727,2	K562	blood:
24	chr11:45507454..45509790-chr11:45515966..45518596,2	K562	blood:
25	chr11:45582261..45584351-chr11:45587015..45588819,2	K562	blood:
26	chr11:45594961..45596588-chr11:45612673..45615496,2	K562	blood:
27	chr11:45571684..45574276-chr11:45580289..45582089,2	K562	blood:
28	chr11:45607423..45609341-chr11:45611214..45612881,2	K562	blood:
29	chr11:45532377..45532877-chr8:143611082..143611628,2	MCF-7	breast:
30	chr11:45518764..45521395-chr11:45524650..45526890,2	K562	blood:
31	chr11:45565833..45568175-chr11:45571702..45573740,2	K562	blood:
32	chr11:45552574..45555962-chr11:45557383..45559148,3	K562	blood:
33	chr11:45488928..45491799-chr11:45499430..45501355,2	K562	blood:
34	chr11:45582261..45584715-chr11:45587319..45589536,2	K562	blood:
35	chr11:45608607..45610604-chr11:45613187..45616434,3	K562	blood:
36	chr11:45571684..45574276-chr11:45580289..45582089,2	K562	blood:
37	chr11:45582261..45584715-chr11:45587319..45589536,2	K562	blood:
38	chr11:45565833..45568175-chr11:45571702..45573740,2	K562	blood:
39	chr11:45488928..45491799-chr11:45499430..45501355,2	K562	blood:
40	chr11:45608873..45611223-chr11:45614271..45615865,2	K562	blood:
41	chr11:45607423..45609341-chr11:45611214..45612881,2	K562	blood:
42	chr11:45576218..45577748-chr11:45588306..45590762,2	K562	blood:
43	chr11:45576218..45577748-chr11:45588306..45590762,2	K562	blood:
44	chr11:45565846..45568374-chr11:45570778..45572759,2	K562	blood:

(count:26 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHST1-5	chr11:45552766-45553167	ENSG00000254746
2	lnc-CTD-2210P24.4.1-9	chr11:45558712-45558804	l_470_chr11:45558711-45561589_testes
3	lnc-CHST1-5	chr11:45562693-45562819	ENSG00000254746
4	lnc-CHST1-5	chr11:45554973-45555082	ENSG00000254746
5	lnc-CTD-2210P24.4.1-3	chr11:45604079-45604279	XLOC_009122
6	lnc-CTD-2210P24.4.1-3	chr11:45604665-45605024	NONHSAT019034
7	lnc-CHST1-5	chr11:45563994-45564024	ENSG00000254746
8	lnc-CTD-2210P24.4.1-3	chr11:45604732-45605013	XLOC_009122
9	lnc-CTD-2210P24.4.1-3	chr11:45604666-45604991	XLOC_009122
10	lnc-CHST1-5	chr11:45511249-45511321	ENSG00000254746
11	lnc-SYT13-3	chr11:45534823-45535352	ENSG00000255041
12	lnc-CTD-2210P24.4.1-3	chr11:45604063-45604279	NONHSAT019034
13	lnc-CTD-2210P24.4.1-9	chr11:45561242-45561589	l_470_chr11:45558711-45561589_testes
14	lnc-CHST1-5	chr11:45554542-45554675	ENSG00000254746
15	lnc-CTD-2210P24.4.1-3	chr11:45602136-45602228	XLOC_009122
16	lnc-CHST1-5	chr11:45554973-45555084	ENSG00000254746
17	lnc-CHST1-5	chr11:45554199-45554430	ENSG00000254746
18	lnc-SYT13-3	chr11:45511528-45511532	ENSG00000255041
19	lnc-CHST1-5	chr11:45553075-45553167	ENSG00000254746
20	lnc-CTD-2210P24.4.1-3	chr11:45604075-45604279	ENSG00000254514
21	lnc-CHST1-6	chr11:45547693-45549830	NONHSAT019031
22	lnc-CTD-2210P24.4.1-3	chr11:45602135-45602228	NONHSAT019034
23	lnc-CHST1-5	chr11:45554542-45554675	ENSG00000254746
24	lnc-CTD-2210P24.4.1-3	chr11:45604064-45604279	XLOC_009122
25	lnc-CTD-2210P24.4.1-3	chr11:45604666-45604991	XLOC_009122
26	lnc-CTD-2210P24.4.1-3	chr11:45604666-45605024	ENSG00000254514

No data

Variant related genes	Relation type
ENSG00000255041	TF binding region
ENSG00000254746	TF binding region
ENSG00000255519	TF binding region
ENSG00000254514	TF binding region
ENSG00000255041	CpG island
ENSG00000254746	CpG island
ENSG00000255519	CpG island
ENSG00000254514	CpG island
ENSG00000019485	chromatin interactions
ENSG00000254746	chromatin interactions

Extended variants
information (count: 5712 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:5712 , 50 per page) page: 1 2 3 4 5 6 7 ... 115

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs896340	chr11:45487041-45487042	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs896339	chr11:45487066-45487067	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs116337168	chr11:45487073-45487074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs148465325	chr11:45487103-45487104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs548184936	chr11:45487108-45487109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs181289145	chr11:45487115-45487116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs896338	chr11:45487121-45487122	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs533528913	chr11:45487153-45487154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs549187800	chr11:45487191-45487192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs559453726	chr11:45487201-45487202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs896337	chr11:45487231-45487232	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs577636442	chr11:45487262-45487263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs60511690	chr11:45487280-45487281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs185360415	chr11:45487283-45487284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs142602999	chr11:45487326-45487327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs556230792	chr11:45487347-45487348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs537308193	chr11:45487367-45487368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs369814011	chr11:45487402-45487403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs61570077	chr11:45487415-45487416	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs151015188	chr11:45487452-45487453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs374663952	chr11:45487464-45487465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs72903086	chr11:45487485-45487486	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs534708890	chr11:45487527-45487528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs189778047	chr11:45487567-45487568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs368955168	chr11:45487587-45487588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs577783332	chr11:45487613-45487614	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs35787207	chr11:45487622-45487623	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs182319751	chr11:45487624-45487625	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs139602959	chr11:45487687-45487688	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs534423765	chr11:45487750-45487751	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs573934437	chr11:45487805-45487806	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs35728842	chr11:45487806-45487807	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs542653755	chr11:45487815-45487816	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs78327264	chr11:45487822-45487823	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs4755992	chr11:45487852-45487853	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs528520191	chr11:45487861-45487862	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs545109538	chr11:45487891-45487892	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs4755324	chr11:45487910-45487911	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs1488667	chr11:45487938-45487939	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs572807477	chr11:45487975-45487976	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs61880598	chr11:45488009-45488010	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs57272528	chr11:45488012-45488013	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs79013006	chr11:45488049-45488050	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs149668606	chr11:45488061-45488062	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs186586265	chr11:45488087-45488088	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs146650894	chr11:45488102-45488103	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs117185749	chr11:45488105-45488106	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs541727732	chr11:45488125-45488126	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs116735655	chr11:45488133-45488134	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs565687569	chr11:45488150-45488151	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Parathyroid adenoma	22454399	CNVD
Medulloblastoma	21979893	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
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	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
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21364760	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Myelofibrosis	22110671	CNVD
Melanoma	18172304	CNVD
Intracranial ependymoma	16609018	CNVD
Myxofibrosarcoma	16751306	CNVD
Potocki-Shaffer syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	16608533	CNVD
Hirschsprung''s Disease	21712996	CNVD
Follicular lymphoma	20505157	CNVD
Colorectal cancer	21128281	CNVD
Breast cancer	20409316	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Mantle cell lymphoma	19029149	CNVD
Glioblastoma multiforme	21138945	CNVD
Prostate cancer	18632612	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:689 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:45485400-45492200	Weak transcription	Pancreas	Pancrea
2	chr11:45487600-45488000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr11:45487600-45488200	Enhancers	Osteobl	bone
4	chr11:45488000-45489400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
5	chr11:45488200-45489600	Weak transcription	Osteobl	bone
6	chr11:45489400-45490200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr11:45489400-45490200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
8	chr11:45489400-45490200	Enhancers	Fetal Muscle Trunk	muscle
9	chr11:45489400-45490400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr11:45489400-45490400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr11:45489400-45490400	Enhancers	Fetal Stomach	stomach
12	chr11:45489600-45490000	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr11:45489600-45490000	Enhancers	Placenta	Placenta
14	chr11:45489600-45490000	Enhancers	Lung	lung
15	chr11:45489600-45490200	Enhancers	H1 Cell Line	embryonic stem cell
16	chr11:45489600-45490200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr11:45489600-45490200	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr11:45489600-45490200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr11:45489600-45490200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr11:45489600-45490200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr11:45489600-45490200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr11:45489600-45490200	Enhancers	Fetal Thymus	thymus
23	chr11:45489600-45490400	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr11:45489600-45490400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr11:45489600-45490400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr11:45489600-45490400	Enhancers	Fetal Muscle Leg	muscle
27	chr11:45489600-45490400	Enhancers	HUVEC	blood vessel
28	chr11:45489600-45490400	Enhancers	Osteobl	bone
29	chr11:45489600-45491600	Enhancers	Spleen	Spleen
30	chr11:45489600-45493000	Enhancers	Adipose Nuclei	Adipose
31	chr11:45489800-45490000	Enhancers	Ovary	ovary
32	chr11:45489800-45490200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr11:45489800-45490200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr11:45489800-45490200	Enhancers	Primary neutrophils fromperipheralblood	blood
35	chr11:45489800-45490200	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
36	chr11:45489800-45490400	Enhancers	Fetal Heart	heart
37	chr11:45489800-45490400	Enhancers	Fetal Kidney	kidney
38	chr11:45489800-45490400	Enhancers	Fetal Lung	lung
39	chr11:45489800-45490600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr11:45490000-45490200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr11:45490000-45490400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr11:45490000-45490400	Enhancers	Right Ventricle	heart
43	chr11:45490000-45491000	Weak transcription	Ovary	ovary
44	chr11:45490200-45490400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr11:45490200-45491400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr11:45490200-45491400	Weak transcription	Fetal Muscle Trunk	muscle
47	chr11:45490200-45492600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr11:45490200-45493000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
49	chr11:45490200-45494600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr11:45490200-45494600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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