Variant report

Variant	nsv437715
Chromosome Location	chr11:34941494-34951993
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:34947622-34948038	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:34947668-34948079	K562	blood:	n/a	n/a
3	ARID3A	chr11:34951031-34952265	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:34949977-34949978	K562	blood:	n/a	n/a
5	BHLHE40	chr11:34951426-34951824	HepG2	liver:	n/a	n/a
6	BHLHE40	chr11:34951497-34951758	HepG2	liver:	n/a	n/a
7	BHLHE40	chr11:34951357-34951887	HepG2	liver:	n/a	n/a
8	BHLHE40	chr11:34950120-34950309	K562	blood:	n/a	n/a
9	CEBPB	chr11:34945473-34945745	IMR90	lung:	n/a	n/a
10	CEBPB	chr11:34948984-34949204	Hela-S3	cervix:	n/a	chr11:34949127-34949136
11	CEBPB	chr11:34948357-34948680	IMR90	lung:	n/a	chr11:34948469-34948481
12	CEBPB	chr11:34950537-34950742	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr11:34951474-34952212	HepG2	liver:	n/a	n/a
14	CEBPB	chr11:34951475-34951657	HepG2	liver:	n/a	n/a
15	CHD2	chr11:34951534-34951750	HepG2	liver:	n/a	n/a
16	CTCF	chr11:34947780-34947930	HAc	cerebellar:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833
17	CTCF	chr11:34947760-34947910	HRPEpiC	eye:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833
18	CTCF	chr11:34947691-34948002	K562	blood:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833
19	CTCF	chr11:34947800-34947950	GM12873	blood:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833
20	CTCF	chr11:34947672-34947974	Spleen_OC	spleen:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833
21	CTCF	chr11:34947380-34947530	HVMF	connective:	n/a	n/a
22	CTCF	chr11:34947700-34947850	HBMEC	blood vessel:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833
23	CTCF	chr11:34947700-34947850	BJ	skin:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833
24	CTCF	chr11:34947780-34947930	GM12872	blood:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833
25	CTCF	chr11:34947576-34948091	GM12878	blood:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833
26	CTCF	chr11:34947760-34947910	GM12867	blood:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833
27	CTCF	chr11:34947662-34947955	ECC-1	luminal epithelium:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833
28	CTCF	chr11:34947740-34947890	GM12872	blood:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833
29	CTCF	chr11:34947700-34947850	NHEK	skin:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833
30	CTCF	chr11:34947740-34947890	HRE	kidney:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833
31	CTCF	chr11:34947760-34947910	HFF-Myc	foreskin:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833
32	CTCF	chr11:34947719-34947935	GM10266	blood:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833
33	CTCF	chr11:34947280-34947430	GM12873	blood:	n/a	n/a
34	CTCF	chr11:34947682-34947962	HUVEC	blood vessel:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833
35	CTCF	chr11:34947653-34948023	Medullo	brain:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833
36	CTCF	chr11:34947720-34947870	SAEC	small airway:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833
37	CTCF	chr11:34947707-34947942	K562	blood:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833
38	CTCF	chr11:34947727-34947979	A549	lung:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833
39	CTCF	chr11:34947619-34948021	K562	blood:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833
40	CTCF	chr11:34947780-34947930	HCM	heart:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833
41	CTCF	chr11:34947760-34947910	MCF-7	breast:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833
42	CTCF	chr11:34947740-34947890	AG09309	skin:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833
43	CTCF	chr11:34947601-34947964	H1-hESC	embryonic stem cell:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833
44	CTCF	chr11:34947760-34947910	HA-sp	spinal cord:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833
45	CTCF	chr11:34947760-34947910	GM12801	blood:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833
46	CTCF	chr11:34947760-34947910	HMEC	breast:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833
47	CTCF	chr11:34947720-34947870	Caco-2	colon:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833
48	CTCF	chr11:34947720-34947870	HL-60	blood:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833
49	CTCF	chr11:34947740-34947890	NHDF-neo	bronchial:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833
50	CTCF	chr11:34947608-34948030	ECC-1	luminal epithelium:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:34945827-34945877	HL-60	blood:	n/a
2	chr11:34949324-34949374	GM12891	blood:	n/a
3	chr11:34945827-34945877	SK-N-SH	brain:	n/a
4	chr11:34949324-34949374	ProgFib	skin:	n/a
5	chr11:34949324-34949374	AG04449	skin:	fetal
6	chr11:34949324-34949374	HRCEpiC	kidney:	n/a
7	chr11:34951024-34951074	GM12892	blood:	n/a
8	chr11:34951024-34951074	Hepatocyte	liver:	n/a
9	chr11:34951024-34951074	ECC-1	luminal epithelium:	n/a
10	chr11:34949324-34949374	BE2_C	brain:	n/a
11	chr11:34949324-34949374	HIPEpiC	eye:	n/a
12	chr11:34949324-34949374	GM19239	blood:	n/a
13	chr11:34951024-34951074	HCT-116	colon:	n/a
14	chr11:34951024-34951074	HRE	kidney:	n/a
15	chr11:34949324-34949374	MCF10A-Er-Src	breast:	n/a
16	chr11:34951024-34951074	GM19239	blood:	n/a
17	chr11:34951024-34951074	HepG2	liver:	n/a
18	chr11:34949324-34949374	Jurkat	blood:	n/a
19	chr11:34951024-34951074	RPTEC	kidney:	n/a
20	chr11:34951024-34951074	A549	lung:	n/a
21	chr11:34945827-34945877	A549	lung:	n/a
22	chr11:34945827-34945877	HRPEpiC	eye:	n/a
23	chr11:34945827-34945877	HUVEC	blood vessel:	n/a
24	chr11:34951024-34951074	AoSMC	blood vessel:	n/a
25	chr11:34949324-34949374	K562	blood:	n/a
26	chr11:34951024-34951074	T-47D	breast:	n/a
27	chr11:34949324-34949374	PFSK-1	brain:	n/a
28	chr11:34951024-34951074	NH-A	brain:	n/a
29	chr11:34951024-34951074	CMK	blood:	n/a
30	chr11:34949324-34949374	T-47D	breast:	n/a
31	chr11:34951024-34951074	HNPCEpiC	eye:	n/a
32	chr11:34951024-34951074	U87	brain:	n/a
33	chr11:34951024-34951074	AG09309	skin:	n/a
34	chr11:34951024-34951074	PFSK-1	brain:	n/a
35	chr11:34949324-34949374	SK-N-SH	brain:	n/a
36	chr11:34951024-34951074	NB4	blood:	n/a
37	chr11:34951024-34951074	GM12878	blood:	n/a
38	chr11:34951024-34951074	HCF	heart:	n/a
39	chr11:34945827-34945877	GM12891	blood:	n/a
40	chr11:34945827-34945877	AG10803	skin:	n/a
41	chr11:34949324-34949374	HCM	heart:	n/a
42	chr11:34945827-34945877	MCF10A-Er-Src	breast:	n/a
43	chr11:34945827-34945877	AoSMC	blood vessel:	n/a
44	chr11:34949324-34949374	MCF-7	breast:	n/a
45	chr11:34945827-34945877	GM12892	blood:	n/a
46	chr11:34951024-34951074	ovcar-3	ovarian:	n/a
47	chr11:34945827-34945877	LNCaP	prostate:	n/a
48	chr11:34949324-34949374	NHDF-neo	bronchial:	n/a
49	chr11:34949324-34949374	H1-hESC	embryonic stem cell:	embryo
50	chr11:34949324-34949374	NHBE	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:34605985..34608292-chr11:34938833..34941617,2	K562	blood:
2	chr11:34947511..34948170-chr11:35425772..35426334,2	MCF-7	breast:
3	chr11:34945269..34946953-chr11:34953904..34955811,2	K562	blood:
4	chr11:34941386..34944859-chr11:34946221..34949330,3	K562	blood:
5	chr11:34947392..34948324-chr11:35413451..35414885,4	K562	blood:
6	chr11:34942697..34945540-chr11:34950429..34952948,3	K562	blood:
7	chr11:34947703..34949304-chr11:35057040..35059668,2	K562	blood:
8	chr11:34946381..34948541-chr11:34950282..34952383,2	MCF-7	breast:
9	chr11:34932295..34934736-chr11:34941620..34944045,2	MCF-7	breast:
10	chr11:34947747..34948295-chr11:35506935..35507466,2	K562	blood:
11	chr11:34947961..34950134-chr11:34950392..34952887,2	MCF-7	breast:
12	chr11:34940522..34942447-chr11:34942724..34944906,2	K562	blood:
13	chr11:34947697..34948269-chr11:35163627..35164578,3	K562	blood:
14	chr11:34948905..34951586-chr11:35371482..35373998,2	MCF-7	breast:
15	chr11:34937871..34941036-chr11:34951931..34955884,3	MCF-7	breast:
16	chr11:34947799..34948300-chr11:35326589..35327576,2	K562	blood:
17	chr11:34944920..34946901-chr11:34953844..34956335,2	K562	blood:
18	chr11:34937808..34940379-chr11:34951738..34954535,2	K562	blood:
19	chr11:34951348..34953526-chr11:34964819..34967175,2	K562	blood:
20	chr11:34943666..34945334-chr11:34948612..34950173,2	MCF-7	breast:
21	chr11:34947961..34950134-chr11:34950392..34952887,2	MCF-7	breast:
22	chr11:34941386..34944859-chr11:34946221..34949330,3	K562	blood:
23	chr11:34948963..34950630-chr11:34950747..34953143,2	K562	blood:
24	chr11:34945262..34947750-chr11:35430544..35432454,2	MCF-7	breast:
25	chr11:34940522..34942447-chr11:34942724..34944906,2	K562	blood:
26	chr11:34947331..34948320-chr11:35413566..35414727,5	MCF-7	breast:
27	chr11:34948435..34950390-chr11:35072380..35075148,2	K562	blood:
28	chr11:34936972..34940330-chr11:34946468..34949282,3	K562	blood:
29	chr11:34948963..34950630-chr11:34950747..34953143,2	K562	blood:
30	chr11:34942697..34945540-chr11:34950429..34952948,3	K562	blood:
31	chr11:34943666..34945334-chr11:34948612..34950173,2	MCF-7	breast:
32	chr11:34946381..34948541-chr11:34950282..34952383,2	MCF-7	breast:

Variant related genes	Relation type
APIP	TF binding region
APIP	CpG island
ENSG00000149089	chromatin interactions
ENSG00000110435	chromatin interactions

Extended variants
information (count: 391 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:391 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs724714	chr11:34941494-34941495	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs191518488	chr11:34941499-34941500	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs147428623	chr11:34941535-34941536	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs76507564	chr11:34941597-34941598	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs557520661	chr11:34941611-34941612	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs571155586	chr11:34941679-34941680	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs183134707	chr11:34941691-34941692	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs553868234	chr11:34941717-34941718	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs573523488	chr11:34941722-34941723	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs187170763	chr11:34941724-34941725	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs77698352	chr11:34941753-34941754	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs563809731	chr11:34941801-34941802	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs2915204	chr11:34941845-34941846	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs2915203	chr11:34941876-34941877	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs190410269	chr11:34941889-34941890	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs139072005	chr11:34941900-34941901	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs78982697	chr11:34941913-34941914	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs561454963	chr11:34941938-34941939	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs547455380	chr11:34941944-34941945	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs3794166	chr11:34941969-34941970	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs550158344	chr11:34941990-34941991	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs142973267	chr11:34942007-34942008	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs17348697	chr11:34942010-34942011	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs182717777	chr11:34942059-34942060	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs551161873	chr11:34942074-34942075	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs548651207	chr11:34942083-34942084	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs571095260	chr11:34942120-34942121	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs56204451	chr11:34942148-34942149	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs150856285	chr11:34942201-34942202	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs534611902	chr11:34942220-34942221	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs187446648	chr11:34942251-34942252	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs80138813	chr11:34942270-34942271	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs556188352	chr11:34942286-34942287	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs17348711	chr11:34942313-34942314	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs115517459	chr11:34942401-34942402	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs559306377	chr11:34942476-34942477	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs2986408	chr11:34942519-34942520	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs75491921	chr11:34942555-34942556	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs192764488	chr11:34942574-34942575	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs17433496	chr11:34942576-34942577	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs543598876	chr11:34942591-34942592	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs185429671	chr11:34942607-34942608	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs150037716	chr11:34942620-34942621	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs551228068	chr11:34942711-34942712	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs144363374	chr11:34942769-34942770	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs527449264	chr11:34942800-34942801	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs11032927	chr11:34942836-34942837	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs372671995	chr11:34942905-34942906	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs552970716	chr11:34942924-34942925	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs79433333	chr11:34942925-34942926	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:79)

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
Glioblastoma multiforme	22286061	CNVD
Breast cancer	21364760	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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:407 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:34938800-34951400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr11:34938800-34957400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr11:34938800-34990400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr11:34939000-34950600	Weak transcription	Gastric	stomach
5	chr11:34939200-34948000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr11:34939200-34950000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr11:34939200-34950200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr11:34939200-34952200	Weak transcription	Primary monocytes fromperipheralblood	blood
9	chr11:34939200-34952800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr11:34939200-34953000	Weak transcription	Primary B cells from peripheral blood	blood
11	chr11:34939200-34953400	Weak transcription	Primary T cells fromperipheralblood	blood
12	chr11:34939200-34956000	Weak transcription	Fetal Muscle Trunk	muscle
13	chr11:34939200-35000000	Weak transcription	Thymus	Thymus
14	chr11:34939400-34942000	Weak transcription	Rectal Mucosa Donor 31	rectum
15	chr11:34939400-34942800	Weak transcription	Monocytes-CD14+_RO01746	blood
16	chr11:34939400-34945200	Weak transcription	HSMMtube	muscle
17	chr11:34939400-34947800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
18	chr11:34939400-34952800	Weak transcription	Primary B cells from cord blood	blood
19	chr11:34939400-34953200	Weak transcription	Rectal Mucosa Donor 29	rectum
20	chr11:34939400-34953400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
21	chr11:34939600-34943000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
22	chr11:34939600-34945600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr11:34939600-34946600	Weak transcription	Stomach Mucosa	stomach
24	chr11:34939600-34947600	Weak transcription	Fetal Kidney	kidney
25	chr11:34939600-34947800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
26	chr11:34939600-34949400	Weak transcription	HUES64 Cell Line	embryonic stem cell
27	chr11:34939600-34949800	Weak transcription	HUES48 Cell Line	embryonic stem cell
28	chr11:34939600-34950200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr11:34939600-34962600	Weak transcription	Right Ventricle	heart
30	chr11:34939800-34942400	Enhancers	Adipose Nuclei	Adipose
31	chr11:34939800-34942800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr11:34939800-34947400	Weak transcription	Colon Smooth Muscle	Colon
33	chr11:34939800-34949600	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr11:34939800-34950800	Weak transcription	Pancreas	Pancrea
35	chr11:34939800-34951200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
36	chr11:34939800-34951400	Weak transcription	Fetal Intestine Small	intestine
37	chr11:34939800-34953800	Weak transcription	Placenta	Placenta
38	chr11:34939800-34960400	Weak transcription	Brain Inferior Temporal Lobe	brain
39	chr11:34940000-34943600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr11:34940000-34946200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr11:34940000-34946800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr11:34940000-34947800	Weak transcription	HSMM	muscle
43	chr11:34940000-34947800	Weak transcription	HUVEC	blood vessel
44	chr11:34940000-34950800	Weak transcription	Right Atrium	heart
45	chr11:34940000-34954000	Weak transcription	Fetal Muscle Leg	muscle
46	chr11:34940000-34959200	Weak transcription	Fetal Brain Male	brain
47	chr11:34940000-34963800	Weak transcription	Spleen	Spleen
48	chr11:34940200-34942200	Weak transcription	Duodenum Mucosa	Duodenum
49	chr11:34940200-34946600	Weak transcription	Brain Hippocampus Middle	brain
50	chr11:34940200-34946800	Weak transcription	Primary hematopoietic stem cells short term culture	blood

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