Variant report

Variant	esv2759817
Chromosome Location	chr11:34913315-34963728
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1288)
CpG islands
(count:1588)
Chromatin interactive
region (count:81)
LncRNA
region (count:0)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:1288 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:34951031-34952265	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:34947622-34948038	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:34949977-34949978	K562	blood:	n/a	n/a
4	ARID3A	chr11:34938026-34938300	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:34937595-34937654	HepG2	liver:	n/a	n/a
6	ARID3A	chr11:34947668-34948079	K562	blood:	n/a	n/a
7	ATF1	chr11:34961726-34961907	K562	blood:	n/a	n/a
8	ATF1	chr11:34938972-34939307	K562	blood:	n/a	n/a
9	ATF2	chr11:34937331-34938461	GM12878	blood:	n/a	n/a
10	ATF3	chr11:34929799-34930110	K562	blood:	n/a	n/a
11	ATF3	chr11:34937943-34938123	K562	blood:	n/a	chr11:34938069-34938078
12	BACH1	chr11:34929538-34930075	H1-hESC	embryonic stem cell:	n/a	chr11:34929943-34929957
13	BACH1	chr11:34929700-34929782	K562	blood:	n/a	n/a
14	BATF	chr11:34929853-34930086	GM12878	blood:	n/a	chr11:34929946-34929957
15	BCL3	chr11:34937631-34938491	A549	lung:	n/a	chr11:34937662-34937675 chr11:34937706-34937719 chr11:34938167-34938180 chr11:34938070-34938079
16	BCLAF1	chr11:34937505-34938414	GM12878	blood:	n/a	chr11:34937662-34937675 chr11:34937706-34937719 chr11:34938167-34938180 chr11:34938070-34938079
17	BHLHE40	chr11:34937479-34938347	HepG2	liver:	n/a	chr11:34937703-34937719
18	BHLHE40	chr11:34937154-34938341	K562	blood:	n/a	chr11:34937703-34937719
19	BHLHE40	chr11:34951426-34951824	HepG2	liver:	n/a	n/a
20	BHLHE40	chr11:34937544-34938374	GM12878	blood:	n/a	chr11:34937703-34937719
21	BHLHE40	chr11:34950120-34950309	K562	blood:	n/a	n/a
22	BHLHE40	chr11:34951497-34951758	HepG2	liver:	n/a	n/a
23	BHLHE40	chr11:34951357-34951887	HepG2	liver:	n/a	n/a
24	BRCA1	chr11:34938224-34938340	GM12878	blood:	n/a	n/a
25	BRCA1	chr11:34937774-34937854	HepG2	liver:	n/a	n/a
26	BRCA1	chr11:34937408-34938225	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr11:34920613-34920873	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr11:34938700-34938727	GM12878	blood:	n/a	n/a
29	BRCA1	chr11:34938188-34938367	HepG2	liver:	n/a	n/a
30	CBX3	chr11:34937599-34938382	K562	blood:	n/a	n/a
31	CCNT2	chr11:34937180-34938821	K562	blood:	n/a	chr11:34937763-34937772 chr11:34938069-34938078
32	CEBPB	chr11:34951474-34952212	HepG2	liver:	n/a	n/a
33	CEBPB	chr11:34938078-34938226	HepG2	liver:	n/a	n/a
34	CEBPB	chr11:34950537-34950742	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr11:34931538-34931864	Hela-S3	cervix:	n/a	chr11:34931690-34931701
36	CEBPB	chr11:34931492-34931921	MCF-7	breast:	n/a	chr11:34931690-34931701
37	CEBPB	chr11:34931502-34931890	HepG2	liver:	n/a	chr11:34931690-34931701
38	CEBPB	chr11:34927973-34928162	A549	lung:	n/a	chr11:34928076-34928087
39	CEBPB	chr11:34948357-34948680	IMR90	lung:	n/a	chr11:34948469-34948481
40	CEBPB	chr11:34928016-34928212	IMR90	lung:	n/a	chr11:34928076-34928087
41	CEBPB	chr11:34948984-34949204	Hela-S3	cervix:	n/a	chr11:34949127-34949136
42	CEBPB	chr11:34951475-34951657	HepG2	liver:	n/a	n/a
43	CEBPB	chr11:34937699-34937923	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr11:34931589-34931846	K562	blood:	n/a	chr11:34931690-34931701
45	CEBPB	chr11:34928039-34928228	K562	blood:	n/a	chr11:34928076-34928087
46	CEBPB	chr11:34921547-34921595	HepG2	liver:	n/a	chr11:34921564-34921575
47	CEBPB	chr11:34931435-34931781	HepG2	liver:	n/a	chr11:34931690-34931701
48	CEBPB	chr11:34938119-34938278	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr11:34928015-34928209	HepG2	liver:	n/a	chr11:34928076-34928087
50	CEBPB	chr11:34924848-34924975	HepG2	liver:	n/a	n/a

(count:1588 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:34937559-34937609	HUVEC	blood vessel:	n/a
2	chr11:34937573-34937623	HUVEC	blood vessel:	n/a
3	chr11:34937559-34937609	HUVEC	blood vessel:	n/a
4	chr11:34937573-34937623	HUVEC	blood vessel:	n/a
5	chr11:34936781-34936831	T-47D	breast:	n/a
6	chr11:34937573-34937623	NH-A	brain:	n/a
7	chr11:34929792-34929842	LNCaP	prostate:	n/a
8	chr11:34937341-34937391	HRCEpiC	kidney:	n/a
9	chr11:34937665-34937715	HPAEpiC	pulmonary alveolar:	n/a
10	chr11:34938112-34938162	HEK293	kidney:	embryo
11	chr11:34937559-34937609	PFSK-1	brain:	n/a
12	chr11:34937665-34937715	AG09309	skin:	n/a
13	chr11:34945827-34945877	T-47D	breast:	n/a
14	chr11:34940794-34940844	BJ	skin:	n/a
15	chr11:34938112-34938162	BE2_C	brain:	n/a
16	chr11:34937484-34937534	GM12878	blood:	n/a
17	chr11:34938507-34938557	HCF	heart:	n/a
18	chr11:34937341-34937391	GM19239	blood:	n/a
19	chr11:34938143-34938193	HL-60	blood:	n/a
20	chr11:34938234-34938284	NH-A	brain:	n/a
21	chr11:34938507-34938557	BJ	skin:	n/a
22	chr11:34937958-34938008	ProgFib	skin:	n/a
23	chr11:34938143-34938193	Caco-2	colon:	n/a
24	chr11:34937933-34937983	HMEC	breast:	n/a
25	chr11:34937665-34937715	BJ	skin:	n/a
26	chr11:34938112-34938162	NB4	blood:	n/a
27	chr11:34940794-34940844	GM12891	blood:	n/a
28	chr11:34936862-34936912	BJ	skin:	n/a
29	chr11:34949324-34949374	HEEpiC	esophagus:	n/a
30	chr11:34937647-34937697	HPAEpiC	pulmonary alveolar:	n/a
31	chr11:34938011-34938061	HRCEpiC	kidney:	n/a
32	chr11:34937484-34937534	HUVEC	blood vessel:	n/a
33	chr11:34929792-34929842	K562	blood:	n/a
34	chr11:34936862-34936912	H1-hESC	embryonic stem cell:	embryo
35	chr11:34937484-34937534	HCPEpiC	choroid plexus:	n/a
36	chr11:34937559-34937609	A549	lung:	n/a
37	chr11:34938143-34938193	GM12892	blood:	n/a
38	chr11:34936781-34936831	HAEpiC	amniotic membrane:	n/a
39	chr11:34937559-34937609	LNCaP	prostate:	n/a
40	chr11:34940794-34940844	NB4	blood:	n/a
41	chr11:34938348-34938398	GM12878	blood:	n/a
42	chr11:34937647-34937697	PFSK-1	brain:	n/a
43	chr11:34938507-34938557	HIPEpiC	eye:	n/a
44	chr11:34936781-34936831	NT2-D1	testis:	n/a
45	chr11:34929792-34929842	PrEC	prostate:	n/a
46	chr11:34938143-34938193	HRCEpiC	kidney:	n/a
47	chr11:34940794-34940844	ovcar-3	ovarian:	n/a
48	chr11:34938011-34938061	SK-N-MC	brain:	n/a
49	chr11:34937341-34937391	HAEpiC	amniotic membrane:	n/a
50	chr11:34938143-34938193	GM06990	blood:	n/a

(count:81 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:34945262..34947750-chr11:35430544..35432454,2	MCF-7	breast:
2	chr11:34937808..34940379-chr11:34951738..34954535,2	K562	blood:
3	chr11:34923546..34926678-chr11:34933429..34938581,5	MCF-7	breast:
4	chr11:34941386..34944859-chr11:34946221..34949330,3	K562	blood:
5	chr11:34947799..34948300-chr11:35326589..35327576,2	K562	blood:
6	chr11:34952584..34955328-chr11:34956453..34958728,2	K562	blood:
7	chr11:34948905..34951586-chr11:35371482..35373998,2	MCF-7	breast:
8	chr11:34928494..34930891-chr11:34936071..34939196,3	MCF-7	breast:
9	chr11:34948963..34950630-chr11:34950747..34953143,2	K562	blood:
10	chr11:34919773..34921558-chr11:34929230..34931688,2	K562	blood:
11	chr11:34937942..34938533-chr7:22893673..22894331,2	Hela-S3	cervix:
12	chr11:34926486..34928206-chr11:36379103..36382037,2	K562	blood:
13	chr11:34919773..34921558-chr11:34929230..34931688,2	K562	blood:
14	chr11:34932295..34934736-chr11:34941620..34944045,2	MCF-7	breast:
15	chr11:34952584..34955328-chr11:34956453..34958728,2	K562	blood:
16	chr11:34921303..34922935-chr11:34924601..34927346,2	MCF-7	breast:
17	chr11:34937871..34941036-chr11:34951931..34955884,3	MCF-7	breast:
18	chr11:34937697..34938489-chr19:2475911..2476465,2	Hela-S3	cervix:
19	chr11:34960896..34963192-chr11:34963561..34965150,2	K562	blood:
20	chr11:34943666..34945334-chr11:34948612..34950173,2	MCF-7	breast:
21	chr11:34607165..34608016-chr11:34920268..34920858,2	K562	blood:
22	chr11:34534104..34535140-chr11:34920268..34920796,4	K562	blood:
23	chr11:34947961..34950134-chr11:34950392..34952887,2	MCF-7	breast:
24	chr11:34960896..34963192-chr11:34963561..34965150,2	K562	blood:
25	chr11:34947703..34949304-chr11:35057040..35059668,2	K562	blood:
26	chr11:34942697..34945540-chr11:34950429..34952948,3	K562	blood:
27	chr11:34930292..34932707-chr11:35355903..35358489,2	K562	blood:
28	chr11:34947511..34948170-chr11:35425772..35426334,2	MCF-7	breast:
29	chr11:34936076..34941004-chr11:34952159..34955870,7	K562	blood:
30	chr11:34961886..34962391-chr11:35259545..35260066,2	MCF-7	breast:
31	chr11:34941386..34944859-chr11:34946221..34949330,3	K562	blood:
32	chr11:34959758..34962115-chr11:35384391..35386520,2	MCF-7	breast:
33	chr11:34605985..34608292-chr11:34938833..34941617,2	K562	blood:
34	chr11:34947747..34948295-chr11:35506935..35507466,2	K562	blood:
35	chr11:34954216..34955992-chr11:34958074..34960760,2	MCF-7	breast:
36	chr11:34938030..34938538-chr11:82996860..82997460,2	Hela-S3	cervix:
37	chr11:34948435..34950390-chr11:35072380..35075148,2	K562	blood:
38	chr11:34923966..34926335-chr11:34931824..34933676,2	K562	blood:
39	chr11:34946381..34948541-chr11:34950282..34952383,2	MCF-7	breast:
40	chr11:34948963..34950630-chr11:34950747..34953143,2	K562	blood:
41	chr11:34923966..34926335-chr11:34931824..34933676,2	K562	blood:
42	chr11:34938207..34939863-chr11:35260000..35262264,2	K562	blood:
43	chr11:34932335..34935204-chr11:34935436..34938565,3	MCF-7	breast:
44	chr11:34940522..34942447-chr11:34942724..34944906,2	K562	blood:
45	chr11:34937811..34940525-chr11:34962659..34964952,2	MCF-7	breast:
46	chr11:34937866..34938405-chr16:87425618..87426289,2	HCT-116	colon:
47	chr11:34937193..34938776-chr11:34957217..34958880,2	K562	blood:
48	chr11:34954216..34955992-chr11:34958074..34960760,2	MCF-7	breast:
49	chr1:148241501..148242022-chr11:34938412..34939404,2	Hela-S3	cervix:
50	chr11:34946381..34948541-chr11:34950282..34952383,2	MCF-7	breast:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-1343-5p	chr11:34963398-34963419	MIMAT0027038
hsa-miR-1343-3p	chr11:34963435-34963456	MIMAT0019776

No data

Variant related genes	Relation type
MIR1343	TF binding region
PDHX	TF binding region
APIP	TF binding region
MIR1343	CpG island
PDHX	CpG island
APIP	CpG island
ENSG00000131759	chromatin interactions
ENSG00000149573	chromatin interactions
ENSG00000255427	chromatin interactions
ENSG00000255234	chromatin interactions
ENSG00000137500	chromatin interactions
ENSG00000179431	chromatin interactions
ENSG00000110435	chromatin interactions
ENSG00000228649	chromatin interactions
ENSG00000140941	chromatin interactions
ENSG00000099860	chromatin interactions
ENSG00000103264	chromatin interactions
ENSG00000251862	chromatin interactions
ENSG00000149089	chromatin interactions

Extended variants
information (count: 2032 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:2032 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3751078	chr11:34913315-34913316	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs543844830	chr11:34913322-34913323	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs528576179	chr11:34913333-34913334	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs184744021	chr11:34913340-34913341	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs531651294	chr11:34913460-34913461	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs544849043	chr11:34913465-34913466	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs187217513	chr11:34913488-34913489	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs547025772	chr11:34913513-34913514	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs573766793	chr11:34913556-34913557	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs547083647	chr11:34913582-34913583	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs567071869	chr11:34913584-34913585	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs529638038	chr11:34913593-34913594	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs549781163	chr11:34913627-34913628	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs570217996	chr11:34913632-34913633	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs539338858	chr11:34913647-34913648	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs571648046	chr11:34913724-34913725	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs559144627	chr11:34913737-34913738	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs566286883	chr11:34913764-34913765	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs150901457	chr11:34913771-34913772	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs371699340	chr11:34913787-34913788	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs555095816	chr11:34913818-34913819	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs193176483	chr11:34913828-34913829	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs543419198	chr11:34913844-34913845	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs35738371	chr11:34913851-34913852	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs117578805	chr11:34913886-34913887	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs571849612	chr11:34913968-34913969	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs376028731	chr11:34913985-34913986	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs368067741	chr11:34913993-34913994	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs550488006	chr11:34914005-34914006	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs545297382	chr11:34914028-34914029	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs564878490	chr11:34914042-34914043	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs66994007	chr11:34914076-34914077	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs35936057	chr11:34914077-34914078	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs527482292	chr11:34914079-34914080	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs397848531	chr11:34914081-34914082	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs139056147	chr11:34914094-34914095	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs146116657	chr11:34914100-34914101	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs2915223	chr11:34914137-34914138	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs554614293	chr11:34914141-34914142	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs529810738	chr11:34914341-34914342	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs375046262	chr11:34914342-34914343	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs2915222	chr11:34914360-34914361	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs533547956	chr11:34914390-34914391	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs563296227	chr11:34914440-34914441	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs2915221	chr11:34914480-34914481	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs576846554	chr11:34914605-34914606	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs145001086	chr11:34914618-34914619	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs2915220	chr11:34914650-34914651	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs184612242	chr11:34914686-34914687	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs548817455	chr11:34914687-34914688	Weak transcription Enhancers	n/a	n/a	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:1857 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:34882000-34919800	Weak transcription	Left Ventricle	heart
2	chr11:34891200-34919200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr11:34893000-34921400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr11:34895000-34921200	Weak transcription	Right Ventricle	heart
5	chr11:34897000-34919200	Weak transcription	Fetal Stomach	stomach
6	chr11:34897600-34919200	Weak transcription	Fetal Heart	heart
7	chr11:34898200-34926800	Weak transcription	HSMMtube	muscle
8	chr11:34899000-34917400	Weak transcription	HSMM	muscle
9	chr11:34900000-34918200	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr11:34900200-34917200	Weak transcription	HUVEC	blood vessel
11	chr11:34900200-34921000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr11:34901400-34917400	Weak transcription	Fetal Kidney	kidney
13	chr11:34901400-34920800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr11:34901600-34918200	Weak transcription	Primary neutrophils fromperipheralblood	blood
15	chr11:34901800-34916800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr11:34901800-34917000	Weak transcription	Rectal Mucosa Donor 29	rectum
17	chr11:34902000-34921600	Weak transcription	Muscle Satellite Cultured Cells	--
18	chr11:34902200-34915600	Weak transcription	Colon Smooth Muscle	Colon
19	chr11:34903600-34919200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr11:34903800-34914200	Weak transcription	Fetal Brain Male	brain
21	chr11:34904000-34918600	Weak transcription	NHDF-Ad	bronchial
22	chr11:34904800-34915600	Weak transcription	GM12878-XiMat	blood
23	chr11:34905000-34917800	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr11:34905200-34915200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr11:34905200-34915400	Weak transcription	Fetal Brain Female	brain
26	chr11:34905200-34917800	Weak transcription	Primary B cells from peripheral blood	blood
27	chr11:34906200-34916200	Weak transcription	Primary T cells from cord blood	blood
28	chr11:34907200-34918200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr11:34907400-34917800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
30	chr11:34907800-34918000	Weak transcription	Fetal Intestine Large	intestine
31	chr11:34908400-34921200	Weak transcription	Aorta	Aorta
32	chr11:34908600-34917800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr11:34908800-34915600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
34	chr11:34908800-34921000	Weak transcription	Ovary	ovary
35	chr11:34909000-34915000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
36	chr11:34909200-34919200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
37	chr11:34909400-34918200	Weak transcription	Duodenum Smooth Muscle	Duodenum
38	chr11:34909600-34918200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
39	chr11:34909800-34921600	Weak transcription	Stomach Mucosa	stomach
40	chr11:34910000-34915800	Weak transcription	Fetal Muscle Leg	muscle
41	chr11:34910000-34918200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr11:34910200-34914200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
43	chr11:34910200-34915400	Weak transcription	Duodenum Mucosa	Duodenum
44	chr11:34910200-34916200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
45	chr11:34910200-34917600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr11:34910200-34917800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
47	chr11:34910200-34918000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr11:34910200-34918000	Weak transcription	Sigmoid Colon	Sigmoid Colon
49	chr11:34910200-34918400	Weak transcription	Fetal Lung	lung
50	chr11:34910200-34919400	Weak transcription	Thymus	Thymus

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