Variant report

Variant	nsv1055116
Chromosome Location	chr11:34940737-34962291
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	chr11:34947668-34948079	K562	blood:	n/a	n/a
2	ARID3A	chr11:34949977-34949978	K562	blood:	n/a	n/a
3	ARID3A	chr11:34951031-34952265	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:34947622-34948038	HepG2	liver:	n/a	n/a
5	ATF1	chr11:34961726-34961907	K562	blood:	n/a	n/a
6	BHLHE40	chr11:34951357-34951887	HepG2	liver:	n/a	n/a
7	BHLHE40	chr11:34951426-34951824	HepG2	liver:	n/a	n/a
8	BHLHE40	chr11:34950120-34950309	K562	blood:	n/a	n/a
9	BHLHE40	chr11:34951497-34951758	HepG2	liver:	n/a	n/a
10	CEBPB	chr11:34948357-34948680	IMR90	lung:	n/a	chr11:34948469-34948481
11	CEBPB	chr11:34951475-34951657	HepG2	liver:	n/a	n/a
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	chr11:34948984-34949204	Hela-S3	cervix:	n/a	chr11:34949127-34949136
15	CEBPB	chr11:34945473-34945745	IMR90	lung:	n/a	n/a
16	CHD2	chr11:34951534-34951750	HepG2	liver:	n/a	n/a
17	CTCF	chr11:34947660-34947810	WI-38	lung:	n/a	n/a
18	CTCF	chr11:34947780-34947930	GM12871	blood:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833
19	CTCF	chr11:34961860-34962010	HMF	breast:	n/a	chr11:34961930-34961951
20	CTCF	chr11:34947740-34947890	HA-sp	spinal cord:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833
21	CTCF	chr11:34947720-34947870	AG09309	skin:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833
22	CTCF	chr11:34947720-34947870	HVMF	connective:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833
23	CTCF	chr11:34947800-34947950	HEEpiC	esophagus:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833
24	CTCF	chr11:34961960-34962110	HMEC	breast:	n/a	n/a
25	CTCF	chr11:34961820-34961970	HPAF	blood vessel:	n/a	chr11:34961930-34961951
26	CTCF	chr11:34947740-34947890	AG09309	skin:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833
27	CTCF	chr11:34947740-34947890	GM12872	blood:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833
28	CTCF	chr11:34947517-34948205	HCT-116	colon:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833
29	CTCF	chr11:34947701-34947905	A549	lung:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833
30	CTCF	chr11:34947682-34947962	HUVEC	blood vessel:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833
31	CTCF	chr11:34947634-34948124	HCT-116	colon:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833
32	CTCF	chr11:34947740-34947890	BE2_C	brain:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833
33	CTCF	chr11:34947802-34947879	MCF-7	breast:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833
34	CTCF	chr11:34947700-34947850	GM12865	blood:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833
35	CTCF	chr11:34947280-34947430	GM12873	blood:	n/a	n/a
36	CTCF	chr11:34947628-34947949	A549	lung:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833
37	CTCF	chr11:34947720-34947870	HEK293	kidney:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833
38	CTCF	chr11:34947700-34947850	BJ	skin:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833
39	CTCF	chr11:34947820-34947970	HCT-116	colon:	n/a	n/a
40	CTCF	chr11:34961840-34961990	HMEC	breast:	n/a	chr11:34961930-34961951
41	CTCF	chr11:34958840-34958990	HBMEC	blood vessel:	n/a	n/a
42	CTCF	chr11:34947760-34947910	GM12878	blood:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833
43	CTCF	chr11:34947740-34947890	AG09319	gingival:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833
44	CTCF	chr11:34947660-34947810	MCF-7	breast:	n/a	n/a
45	CTCF	chr11:34947720-34947870	GM12870	blood:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833
46	CTCF	chr11:34947800-34947950	Hela-S3	cervix:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833
47	CTCF	chr11:34961860-34962010	AG09319	gingival:	n/a	chr11:34961930-34961951
48	CTCF	chr11:34947439-34948712	A549	lung:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833
49	CTCF	chr11:34947720-34947870	HEEpiC	esophagus:	n/a	chr11:34947817-34947838 chr11:34947818-34947831 chr11:34947815-34947833
50	CTCF	chr11:34961891-34961969	GM10248	blood:	n/a	chr11:34961930-34961951

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:34945827-34945877	SK-N-MC	brain:	n/a
2	chr11:34949324-34949374	HIPEpiC	eye:	n/a
3	chr11:34949324-34949374	NB4	blood:	n/a
4	chr11:34940794-34940844	HCPEpiC	choroid plexus:	n/a
5	chr11:34951024-34951074	IMR90	lung:	fetal
6	chr11:34949324-34949374	GM19239	blood:	n/a
7	chr11:34940794-34940844	Caco-2	colon:	n/a
8	chr11:34940794-34940844	ovcar-3	ovarian:	n/a
9	chr11:34945827-34945877	HepG2	liver:	n/a
10	chr11:34951024-34951074	GM12891	blood:	n/a
11	chr11:34940794-34940844	HRPEpiC	eye:	n/a
12	chr11:34951024-34951074	T-47D	breast:	n/a
13	chr11:34951024-34951074	SK-N-SH_RA	brain:	n/a
14	chr11:34945827-34945877	HEEpiC	esophagus:	n/a
15	chr11:34945827-34945877	Hepatocyte	liver:	n/a
16	chr11:34949324-34949374	IMR90	lung:	fetal
17	chr11:34951024-34951074	SK-N-SH	brain:	n/a
18	chr11:34949324-34949374	MCF-7	breast:	n/a
19	chr11:34945827-34945877	GM12892	blood:	n/a
20	chr11:34949324-34949374	SK-N-SH	brain:	n/a
21	chr11:34949324-34949374	U87	brain:	n/a
22	chr11:34945827-34945877	SKMC	muscle:	n/a
23	chr11:34949324-34949374	CMK	blood:	n/a
24	chr11:34951024-34951074	ProgFib	skin:	n/a
25	chr11:34951024-34951074	Hepatocyte	liver:	n/a
26	chr11:34945827-34945877	HIPEpiC	eye:	n/a
27	chr11:34949324-34949374	AG09309	skin:	n/a
28	chr11:34949324-34949374	HRE	kidney:	n/a
29	chr11:34940794-34940844	NT2-D1	testis:	n/a
30	chr11:34945827-34945877	GM19239	blood:	n/a
31	chr11:34951024-34951074	HNPCEpiC	eye:	n/a
32	chr11:34945827-34945877	HCM	heart:	n/a
33	chr11:34945827-34945877	Jurkat	blood:	n/a
34	chr11:34949324-34949374	BJ	skin:	n/a
35	chr11:34940794-34940844	A549	lung:	n/a
36	chr11:34945827-34945877	NB4	blood:	n/a
37	chr11:34951024-34951074	H1-hESC	embryonic stem cell:	embryo
38	chr11:34949324-34949374	HMEC	breast:	n/a
39	chr11:34940794-34940844	NHDF-neo	bronchial:	n/a
40	chr11:34940794-34940844	PANC-1	pancreas:	n/a
41	chr11:34945827-34945877	AG10803	skin:	n/a
42	chr11:34949324-34949374	ECC-1	luminal epithelium:	n/a
43	chr11:34951024-34951074	HRCEpiC	kidney:	n/a
44	chr11:34951024-34951074	HEK293	kidney:	embryo
45	chr11:34940794-34940844	GM12891	blood:	n/a
46	chr11:34940794-34940844	BJ	skin:	n/a
47	chr11:34949324-34949374	SKMC	muscle:	n/a
48	chr11:34940794-34940844	Jurkat	blood:	n/a
49	chr11:34945827-34945877	ovcar-3	ovarian:	n/a
50	chr11:34951024-34951074	PANC-1	pancreas:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:34951348..34953526-chr11:34964819..34967175,2	K562	blood:
2	chr11:34948435..34950390-chr11:35072380..35075148,2	K562	blood:
3	chr11:34937808..34940379-chr11:34951738..34954535,2	K562	blood:
4	chr11:34960896..34963192-chr11:34963561..34965150,2	K562	blood:
5	chr11:34948963..34950630-chr11:34950747..34953143,2	K562	blood:
6	chr11:34943666..34945334-chr11:34948612..34950173,2	MCF-7	breast:
7	chr11:34943666..34945334-chr11:34948612..34950173,2	MCF-7	breast:
8	chr11:34954216..34955992-chr11:34958074..34960760,2	MCF-7	breast:
9	chr11:34954216..34955992-chr11:34958074..34960760,2	MCF-7	breast:
10	chr11:34946381..34948541-chr11:34950282..34952383,2	MCF-7	breast:
11	chr11:34937193..34938776-chr11:34957217..34958880,2	K562	blood:
12	chr11:34947697..34948269-chr11:35163627..35164578,3	K562	blood:
13	chr11:34945269..34946953-chr11:34953904..34955811,2	K562	blood:
14	chr11:34942697..34945540-chr11:34950429..34952948,3	K562	blood:
15	chr11:34944920..34946901-chr11:34953844..34956335,2	K562	blood:
16	chr11:34944920..34946901-chr11:34953844..34956335,2	K562	blood:
17	chr11:34945262..34947750-chr11:35430544..35432454,2	MCF-7	breast:
18	chr11:34947799..34948300-chr11:35326589..35327576,2	K562	blood:
19	chr11:34941386..34944859-chr11:34946221..34949330,3	K562	blood:
20	chr11:34937871..34941036-chr11:34951931..34955884,3	MCF-7	breast:
21	chr11:34948905..34951586-chr11:35371482..35373998,2	MCF-7	breast:
22	chr11:34932295..34934736-chr11:34941620..34944045,2	MCF-7	breast:
23	chr11:34941386..34944859-chr11:34946221..34949330,3	K562	blood:
24	chr11:34952584..34955328-chr11:34956453..34958728,2	K562	blood:
25	chr11:34956035..34958785-chr11:35004705..35006336,2	MCF-7	breast:
26	chr11:34940522..34942447-chr11:34942724..34944906,2	K562	blood:
27	chr11:34947961..34950134-chr11:34950392..34952887,2	MCF-7	breast:
28	chr11:34954386..34956581-chr11:34957357..34959864,2	MCF-7	breast:
29	chr11:34940522..34942447-chr11:34942724..34944906,2	K562	blood:
30	chr11:34605985..34608292-chr11:34938833..34941617,2	K562	blood:
31	chr11:34954386..34956581-chr11:34957357..34959864,2	MCF-7	breast:
32	chr11:34947961..34950134-chr11:34950392..34952887,2	MCF-7	breast:
33	chr11:34947747..34948295-chr11:35506935..35507466,2	K562	blood:
34	chr11:34936972..34940330-chr11:34946468..34949282,3	K562	blood:
35	chr11:34947511..34948170-chr11:35425772..35426334,2	MCF-7	breast:
36	chr11:34961886..34962391-chr11:35259545..35260066,2	MCF-7	breast:
37	chr11:34945269..34946953-chr11:34953904..34955811,2	K562	blood:
38	chr11:34947331..34948320-chr11:35413566..35414727,5	MCF-7	breast:
39	chr11:34942697..34945540-chr11:34950429..34952948,3	K562	blood:
40	chr11:34959758..34962115-chr11:35384391..35386520,2	MCF-7	breast:
41	chr11:34946381..34948541-chr11:34950282..34952383,2	MCF-7	breast:
42	chr11:34952584..34955328-chr11:34956453..34958728,2	K562	blood:
43	chr11:34948963..34950630-chr11:34950747..34953143,2	K562	blood:
44	chr11:34947392..34948324-chr11:35413451..35414885,4	K562	blood:
45	chr11:34947703..34949304-chr11:35057040..35059668,2	K562	blood:
46	chr11:34936076..34941004-chr11:34952159..34955870,7	K562	blood:
47	chr11:34936733..34940563-chr11:34957640..34960093,4	K562	blood:

Variant related genes	Relation type
MIR1343	TF binding region
APIP	TF binding region
MIR1343	CpG island
APIP	CpG island
ENSG00000149089	chromatin interactions
ENSG00000110435	chromatin interactions

Extended variants
information (count: 836 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:836 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10488801	chr11:34940737-34940738	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs371999905	chr11:34940743-34940744	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs549697470	chr11:34940747-34940748	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs185226862	chr11:34940774-34940775	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs531977151	chr11:34940787-34940788	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs199505365	chr11:34940826-34940827	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
7	rs146806357	chr11:34940827-34940828	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
8	rs12276735	chr11:34940844-34940845	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs16926457	chr11:34940907-34940908	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs534139877	chr11:34940913-34940914	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs2956106	chr11:34940982-34940983	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs567696291	chr11:34941024-34941025	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs2956105	chr11:34941025-34941026	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs191059623	chr11:34941035-34941036	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs12283763	chr11:34941048-34941049	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs2915205	chr11:34941088-34941089	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs7479823	chr11:34941098-34941099	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs61881133	chr11:34941127-34941128	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs181926814	chr11:34941152-34941153	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs372744072	chr11:34941165-34941166	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs573610807	chr11:34941183-34941184	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs542936930	chr11:34941261-34941262	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs113399223	chr11:34941267-34941268	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs563214390	chr11:34941291-34941292	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs35740352	chr11:34941299-34941300	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs142941459	chr11:34941347-34941348	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs11032925	chr11:34941358-34941359	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs11032926	chr11:34941364-34941365	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs527780298	chr11:34941434-34941435	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs187562376	chr11:34941456-34941457	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs567535847	chr11:34941485-34941486	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs724714	chr11:34941494-34941495	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs191518488	chr11:34941499-34941500	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs147428623	chr11:34941535-34941536	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs76507564	chr11:34941597-34941598	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs557520661	chr11:34941611-34941612	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs571155586	chr11:34941679-34941680	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs183134707	chr11:34941691-34941692	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs553868234	chr11:34941717-34941718	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs573523488	chr11:34941722-34941723	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs187170763	chr11:34941724-34941725	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs77698352	chr11:34941753-34941754	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs563809731	chr11:34941801-34941802	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	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
45	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
46	rs190410269	chr11:34941889-34941890	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs139072005	chr11:34941900-34941901	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs78982697	chr11:34941913-34941914	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs561454963	chr11:34941938-34941939	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs547455380	chr11:34941944-34941945	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:675 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

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	chr11:34939400-34941200	Enhancers	Skeletal Muscle Female	skeletal muscle
15	chr11:34939400-34942000	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr11:34939400-34942800	Weak transcription	Monocytes-CD14+_RO01746	blood
17	chr11:34939400-34945200	Weak transcription	HSMMtube	muscle
18	chr11:34939400-34947800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
19	chr11:34939400-34952800	Weak transcription	Primary B cells from cord blood	blood
20	chr11:34939400-34953200	Weak transcription	Rectal Mucosa Donor 29	rectum
21	chr11:34939400-34953400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
22	chr11:34939600-34940800	Enhancers	Primary T helper cells PMA-I stimulated	--
23	chr11:34939600-34940800	Enhancers	NHDF-Ad	bronchial
24	chr11:34939600-34941200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr11:34939600-34941200	Enhancers	Pancreatic Islets	Pancreatic Islet
26	chr11:34939600-34941400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr11:34939600-34943000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
28	chr11:34939600-34945600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr11:34939600-34946600	Weak transcription	Stomach Mucosa	stomach
30	chr11:34939600-34947600	Weak transcription	Fetal Kidney	kidney
31	chr11:34939600-34947800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
32	chr11:34939600-34949400	Weak transcription	HUES64 Cell Line	embryonic stem cell
33	chr11:34939600-34949800	Weak transcription	HUES48 Cell Line	embryonic stem cell
34	chr11:34939600-34950200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
35	chr11:34939600-34962600	Weak transcription	Right Ventricle	heart
36	chr11:34939800-34941400	Weak transcription	Fetal Intestine Large	intestine
37	chr11:34939800-34942400	Enhancers	Adipose Nuclei	Adipose
38	chr11:34939800-34942800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr11:34939800-34947400	Weak transcription	Colon Smooth Muscle	Colon
40	chr11:34939800-34949600	Weak transcription	HUES6 Cell Line	embryonic stem cell
41	chr11:34939800-34950800	Weak transcription	Pancreas	Pancrea
42	chr11:34939800-34951200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
43	chr11:34939800-34951400	Weak transcription	Fetal Intestine Small	intestine
44	chr11:34939800-34953800	Weak transcription	Placenta	Placenta
45	chr11:34939800-34960400	Weak transcription	Brain Inferior Temporal Lobe	brain
46	chr11:34940000-34940800	Enhancers	Breast Myoepithelial Primary Cells	Breast
47	chr11:34940000-34941400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr11:34940000-34941400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr11:34940000-34943600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr11:34940000-34946200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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