Variant report

Variant	nsv1051437
Chromosome Location	chr11:33290261-33488949
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1778)
CpG islands
(count:1466)
Chromatin interactive
region (count:157)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:14)

(count:1778 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:33383925-33384254	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:33351286-33351649	K562	blood:	n/a	n/a
3	ARID3A	chr11:33342559-33342940	K562	blood:	n/a	n/a
4	ARID3A	chr11:33364523-33364723	K562	blood:	n/a	n/a
5	ARID3A	chr11:33467294-33467606	HepG2	liver:	n/a	n/a
6	ARID3A	chr11:33394101-33394301	HepG2	liver:	n/a	n/a
7	ARID3A	chr11:33383912-33384198	K562	blood:	n/a	n/a
8	ARID3A	chr11:33351288-33351628	HepG2	liver:	n/a	n/a
9	ATF1	chr11:33394198-33394335	K562	blood:	n/a	n/a
10	ATF1	chr11:33351332-33351614	K562	blood:	n/a	n/a
11	ATF1	chr11:33329665-33330069	K562	blood:	n/a	n/a
12	ATF1	chr11:33342458-33342912	K562	blood:	n/a	n/a
13	ATF1	chr11:33341606-33341888	K562	blood:	n/a	n/a
14	ATF2	chr11:33404441-33405009	GM12878	blood:	n/a	n/a
15	ATF2	chr11:33409013-33410089	GM12878	blood:	n/a	n/a
16	ATF2	chr11:33404542-33405049	GM12878	blood:	n/a	n/a
17	ATF2	chr11:33411036-33411671	GM12878	blood:	n/a	n/a
18	ATF2	chr11:33409042-33410013	GM12878	blood:	n/a	n/a
19	ATF3	chr11:33382233-33382453	K562	blood:	n/a	chr11:33382358-33382372
20	ATF3	chr11:33342449-33342699	K562	blood:	n/a	n/a
21	BACH1	chr11:33364471-33364818	K562	blood:	n/a	n/a
22	BACH1	chr11:33397385-33398563	H1-hESC	embryonic stem cell:	n/a	n/a
23	BATF	chr11:33409566-33409855	GM12878	blood:	n/a	n/a
24	BATF	chr11:33411172-33411511	GM12878	blood:	n/a	n/a
25	BATF	chr11:33404575-33404911	GM12878	blood:	n/a	n/a
26	BATF	chr11:33404521-33404947	GM12878	blood:	n/a	n/a
27	BATF	chr11:33408990-33409983	GM12878	blood:	n/a	n/a
28	BATF	chr11:33363592-33363812	GM12878	blood:	n/a	n/a
29	BATF	chr11:33363521-33363808	GM12878	blood:	n/a	n/a
30	BCL11A	chr11:33409034-33409543	GM12878	blood:	n/a	n/a
31	BCL11A	chr11:33409556-33409888	GM12878	blood:	n/a	n/a
32	BCL11A	chr11:33404557-33404945	GM12878	blood:	n/a	n/a
33	BCL11A	chr11:33409572-33409836	GM12878	blood:	n/a	n/a
34	BCL3	chr11:33404619-33404913	GM12878	blood:	n/a	n/a
35	BCL3	chr11:33409282-33409904	GM12878	blood:	n/a	n/a
36	BCLAF1	chr11:33409067-33410001	GM12878	blood:	n/a	n/a
37	BCLAF1	chr11:33341910-33342551	GM12878	blood:	n/a	n/a
38	BCLAF1	chr11:33404519-33404990	GM12878	blood:	n/a	n/a
39	BCLAF1	chr11:33409061-33410037	GM12878	blood:	n/a	n/a
40	BHLHE40	chr11:33308243-33308452	K562	blood:	n/a	n/a
41	BHLHE40	chr11:33401529-33401825	GM12878	blood:	n/a	n/a
42	BHLHE40	chr11:33342530-33342916	K562	blood:	n/a	n/a
43	BHLHE40	chr11:33313026-33313370	GM12878	blood:	n/a	n/a
44	BHLHE40	chr11:33345920-33346220	GM12878	blood:	n/a	n/a
45	BHLHE40	chr11:33404539-33405771	GM12878	blood:	n/a	n/a
46	BHLHE40	chr11:33369101-33369338	GM12878	blood:	n/a	n/a
47	BHLHE40	chr11:33427892-33427983	K562	blood:	n/a	n/a
48	BHLHE40	chr11:33484666-33484886	K562	blood:	n/a	n/a
49	BRCA1	chr11:33295193-33295271	H1-hESC	embryonic stem cell:	n/a	n/a
50	BRCA1	chr11:33337746-33337909	HepG2	liver:	n/a	n/a

(count:1466 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:33317039-33317089	Hela-S3	cervix:	n/a
2	chr11:33396859-33396909	SAEC	small airway:	n/a
3	chr11:33317039-33317089	Hela-S3	cervix:	n/a
4	chr11:33396859-33396909	SAEC	small airway:	n/a
5	chr11:33397689-33397739	Caco-2	colon:	n/a
6	chr11:33399978-33400028	AG04450	lung:	fetal
7	chr11:33397679-33397729	HCT-116	colon:	n/a
8	chr11:33308269-33308319	HCPEpiC	choroid plexus:	n/a
9	chr11:33397679-33397729	ProgFib	skin:	n/a
10	chr11:33334443-33334493	NHBE	bronchial:	n/a
11	chr11:33399978-33400028	NHBE	bronchial:	n/a
12	chr11:33442321-33442371	HCPEpiC	choroid plexus:	n/a
13	chr11:33308269-33308319	HRCEpiC	kidney:	n/a
14	chr11:33397689-33397739	GM12878	blood:	n/a
15	chr11:33308345-33308395	HEEpiC	esophagus:	n/a
16	chr11:33399978-33400028	HRE	kidney:	n/a
17	chr11:33317039-33317089	K562	blood:	n/a
18	chr11:33396983-33397033	SK-N-SH	brain:	n/a
19	chr11:33397153-33397203	HCF	heart:	n/a
20	chr11:33397689-33397739	HepG2	liver:	n/a
21	chr11:33317015-33317065	ProgFib	skin:	n/a
22	chr11:33308269-33308319	Hela-S3	cervix:	n/a
23	chr11:33398173-33398223	LNCaP	prostate:	n/a
24	chr11:33398366-33398416	RPTEC	kidney:	n/a
25	chr11:33398366-33398416	GM12878	blood:	n/a
26	chr11:33453389-33453439	MCF-7	breast:	n/a
27	chr11:33399978-33400028	NB4	blood:	n/a
28	chr11:33453389-33453439	Caco-2	colon:	n/a
29	chr11:33375412-33375462	NH-A	brain:	n/a
30	chr11:33400574-33400624	SKMC	muscle:	n/a
31	chr11:33317093-33317143	BE2_C	brain:	n/a
32	chr11:33308269-33308319	AG09309	skin:	n/a
33	chr11:33317039-33317089	HAEpiC	amniotic membrane:	n/a
34	chr11:33397821-33397871	PFSK-1	brain:	n/a
35	chr11:33474484-33474534	SKMC	muscle:	n/a
36	chr11:33317093-33317143	HCT-116	colon:	n/a
37	chr11:33453389-33453439	HAEpiC	amniotic membrane:	n/a
38	chr11:33308269-33308319	AG10803	skin:	n/a
39	chr11:33334443-33334493	MCF10A-Er-Src	breast:	n/a
40	chr11:33397153-33397203	MCF-7	breast:	n/a
41	chr11:33308345-33308395	HepG2	liver:	n/a
42	chr11:33400574-33400624	HPAEpiC	pulmonary alveolar:	n/a
43	chr11:33442321-33442371	Jurkat	blood:	n/a
44	chr11:33308269-33308319	SKMC	muscle:	n/a
45	chr11:33453389-33453439	HRE	kidney:	n/a
46	chr11:33397689-33397739	HEEpiC	esophagus:	n/a
47	chr11:33397689-33397739	HMEC	breast:	n/a
48	chr11:33396859-33396909	HCM	heart:	n/a
49	chr11:33334443-33334493	AG09309	skin:	n/a
50	chr11:33400574-33400624	HEEpiC	esophagus:	n/a

(count:157 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr11:33315778..33318693-chr11:33329241..33331442,2	K562	blood:
2	chr11:33277703..33279288-chr11:33314208..33316687,2	K562	blood:
3	chr11:33340003..33342699-chr11:33347574..33349225,2	K562	blood:
4	chr11:33350757..33353405-chr11:33354429..33357042,2	K562	blood:
5	chr11:33475872..33478381-chr11:33480677..33482697,2	MCF-7	breast:
6	chr11:33343171..33345414-chr11:33349512..33351209,2	K562	blood:
7	chr11:33278060..33280845-chr11:33344585..33346232,2	MCF-7	breast:
8	chr11:33426996..33428983-chr11:33431666..33434178,3	K562	blood:
9	chr11:33330605..33333745-chr11:33333939..33336380,3	K562	blood:
10	chr11:33391648..33394205-chr11:33396367..33400084,3	K562	blood:
11	chr11:33319935..33321547-chr11:33324870..33327830,2	K562	blood:
12	chr11:33313913..33316207-chr11:33316446..33318411,2	MCF-7	breast:
13	chr11:33372537..33375934-chr11:33378619..33381344,3	MCF-7	breast:
14	chr11:33278384..33280021-chr11:33301631..33304072,2	MCF-7	breast:
15	chr11:33181378..33183783-chr11:33345945..33349178,4	K562	blood:
16	chr11:33360581..33362754-chr11:33365388..33367285,2	K562	blood:
17	chr11:33294153..33295925-chr11:33303597..33306470,2	MCF-7	breast:
18	chr11:33290160..33295323-chr11:33296264..33299611,6	K562	blood:
19	chr11:33300641..33303261-chr11:33311159..33314863,3	K562	blood:
20	chr11:33277971..33280504-chr11:33330975..33332742,2	MCF-7	breast:
21	chr11:33345288..33347427-chr11:33347864..33349944,2	MCF-7	breast:
22	chr11:33277710..33282201-chr11:33292143..33296310,6	K562	blood:
23	chr11:33347446..33349133-chr11:33352606..33354562,2	K562	blood:
24	chr11:33404576..33406306-chr11:33408202..33410856,2	MCF-7	breast:
25	chr11:33380757..33382861-chr11:33395684..33398398,2	MCF-7	breast:
26	chr11:33275628..33278249-chr11:33296623..33299579,2	MCF-7	breast:
27	chr11:33330605..33333745-chr11:33333939..33336380,3	K562	blood:
28	chr11:33345288..33347427-chr11:33347864..33349944,2	MCF-7	breast:
29	chr11:33375467..33377991-chr11:33379064..33381208,2	MCF-7	breast:
30	chr11:33365715..33367217-chr11:33368914..33370934,2	K562	blood:
31	chr11:33403805..33405903-chr11:33414463..33417062,2	MCF-7	breast:
32	chr11:33421417..33423758-chr11:33435787..33437817,2	K562	blood:
33	chr11:33464022..33465573-chr11:33469227..33471332,2	K562	blood:
34	chr11:33303628..33306131-chr11:33323858..33326842,2	MCF-7	breast:
35	chr11:33278564..33280833-chr11:33295728..33298096,2	K562	blood:
36	chr11:33429478..33432664-chr11:33434233..33436615,3	K562	blood:
37	chr11:33179272..33181255-chr11:33382560..33384208,2	K562	blood:
38	chr11:33365715..33367217-chr11:33368914..33370934,2	K562	blood:
39	chr11:33360349..33362095-chr11:33370787..33373728,2	MCF-7	breast:
40	chr11:33377235..33380179-chr11:33384228..33387621,3	K562	blood:
41	chr11:33278689..33280532-chr11:33344460..33346639,2	K562	blood:
42	chr11:33308929..33311681-chr11:33352469..33354383,2	MCF-7	breast:
43	chr11:33474719..33477394-chr11:33482084..33484055,2	K562	blood:
44	chr11:33421417..33423758-chr11:33435787..33437817,2	K562	blood:
45	chr11:33326071..33328703-chr11:33331126..33332666,2	K562	blood:
46	chr11:33396319..33398155-chr11:33401081..33403706,2	MCF-7	breast:
47	chr11:33278606..33279290-chr11:33341646..33342645,2	MCF-7	breast:
48	chr11:33277050..33279115-chr11:33307731..33309675,2	K562	blood:
49	chr11:33383578..33384538-chr11:33708929..33709708,5	K562	blood:
50	chr11:33300641..33303261-chr11:33311159..33314863,3	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TCP11L1-3	chr11:33333205-33333598	expReg_chr11_2971_+
2	lnc-TCP11L1-4	chr11:33334713-33335041	expReg_chr11_2985_+
3	lnc-HIPK3-2	chr11:33424762-33425151	NONHSAT018700
4	lnc-C11orf41-5	chr11:33472192-33472489	NONHSAT018701

No data

(count:14 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	HIPK3	hsa-miR-19b-3p	chr11:33375260-33375282
2	HIPK3	hsa-miR-19b-3p	chr11:33358682-33358704
3	HIPK3	hsa-miR-335-5p	chr11:33375589-33375614
4	HIPK3	hsa-miR-20b-5p	chr11:33375709-33375730
5	HIPK3	hsa-miR-19b-3p	chr11:33375275-33375282
6	HIPK3	hsa-miR-92a-3p	chr11:33375228-33375234
7	HIPK3	hsa-miR-124-3p	chr11:33375663-33375670
8	HIPK3	hsa-miR-92a-3p	chr11:33375214-33375235
9	HIPK3	hsa-miR-124-3p	chr11:33375376-33375395
10	HIPK3	hsa-miR-124-3p	chr11:33375651-33375670
11	HIPK3	hsa-miR-92a-3p	chr11:33375388-33375409
12	HIPK3	hsa-miR-20b-5p	chr11:33375245-33375267
13	HIPK3	hsa-miR-106a-5p	chr11:33375245-33375267
14	HIPK3	hsa-miR-106a-5p	chr11:33375709-33375730

Variant related genes	Relation type
ENSG00000255207	TF binding region
HIPK3	TF binding region
ENSG00000254537	TF binding region
ENSG00000223134	TF binding region
ENSG00000255207	CpG island
HIPK3	CpG island
ENSG00000254537	CpG island
ENSG00000223134	CpG island
ENSG00000206808	chromatin interactions
ENSG00000176102	chromatin interactions
ENSG00000110422	chromatin interactions
ENSG00000223134	chromatin interactions
ENSG00000085063	chromatin interactions
ENSG00000255207	chromatin interactions
ENSG00000254537	chromatin interactions
ENSG00000247151	chromatin interactions

Extended variants
information (count: 7341 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:7341 , 50 per page) page: 1 2 3 4 5 6 7 ... 147

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544257093	chr11:33290417-33290418	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs144267811	chr11:33290471-33290472	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs564550284	chr11:33290475-33290476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs548961720	chr11:33290510-33290511	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs540929152	chr11:33290511-33290512	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs560619105	chr11:33290527-33290528	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs529531200	chr11:33290562-33290563	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs371613935	chr11:33290572-33290573	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs555974601	chr11:33290583-33290584	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs549635741	chr11:33290627-33290628	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs145449525	chr11:33290632-33290633	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs561747817	chr11:33290640-33290641	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs530672955	chr11:33290725-33290726	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs370009606	chr11:33290773-33290774	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs145591790	chr11:33290774-33290775	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs573985429	chr11:33290782-33290783	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs34584298	chr11:33290785-33290786	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs570438111	chr11:33290909-33290910	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs541359594	chr11:33290948-33290949	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs539308078	chr11:33290987-33290988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs559293619	chr11:33291008-33291009	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs112291602	chr11:33291011-33291012	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs190502671	chr11:33291038-33291039	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs566296811	chr11:33291077-33291078	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs181776047	chr11:33291144-33291145	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs554002570	chr11:33291149-33291150	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs373102104	chr11:33291156-33291157	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs538374956	chr11:33291172-33291173	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs571933272	chr11:33291216-33291217	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs186817592	chr11:33291225-33291226	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs577970706	chr11:33291237-33291238	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs191311883	chr11:33291267-33291268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs113210523	chr11:33291269-33291270	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs34433604	chr11:33291303-33291304	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs397736875	chr11:33291311-33291312	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs540539493	chr11:33291317-33291318	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs560780382	chr11:33291348-33291349	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs181296774	chr11:33291381-33291382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs10836046	chr11:33291462-33291463	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs563117500	chr11:33291467-33291468	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs530484257	chr11:33291490-33291491	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs550655857	chr11:33291525-33291526	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs563899646	chr11:33291565-33291566	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs532959504	chr11:33291641-33291642	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs372229652	chr11:33291648-33291649	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs375405489	chr11:33291651-33291652	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs116948126	chr11:33291680-33291681	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs566406847	chr11:33291699-33291700	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs529197433	chr11:33291716-33291717	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs548756750	chr11:33291731-33291732	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
Breast cancer	21364760	CNVD
Glioblastoma multiforme	22286061	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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:3820 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:33280600-33308200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr11:33281400-33295200	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr11:33281800-33295200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr11:33282400-33290600	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr11:33282400-33292800	Weak transcription	Fetal Intestine Large	intestine
6	chr11:33282600-33290600	Weak transcription	Rectal Mucosa Donor 29	rectum
7	chr11:33284200-33313000	Weak transcription	Fetal Kidney	kidney
8	chr11:33284200-33318200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
9	chr11:33284600-33290600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
10	chr11:33284600-33290600	Weak transcription	HSMM	muscle
11	chr11:33285000-33297400	Weak transcription	Fetal Muscle Leg	muscle
12	chr11:33285000-33307400	Weak transcription	Gastric	stomach
13	chr11:33285000-33326200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
14	chr11:33285200-33306000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr11:33285200-33308000	Weak transcription	Primary B cells from peripheral blood	blood
16	chr11:33285200-33308200	Weak transcription	Spleen	Spleen
17	chr11:33285400-33290600	Weak transcription	Sigmoid Colon	Sigmoid Colon
18	chr11:33285600-33291400	Weak transcription	Primary hematopoietic stem cells	blood
19	chr11:33285800-33292600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
20	chr11:33285800-33295400	Weak transcription	Brain Hippocampus Middle	brain
21	chr11:33285800-33312800	Weak transcription	Fetal Stomach	stomach
22	chr11:33286000-33290600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr11:33286000-33290600	Weak transcription	NHLF	lung
24	chr11:33286000-33296000	Weak transcription	Brain Inferior Temporal Lobe	brain
25	chr11:33286000-33308200	Weak transcription	Cortex derived primary cultured neurospheres	brain
26	chr11:33286600-33295400	Weak transcription	Pancreatic Islets	Pancreatic Islet
27	chr11:33286600-33296400	Weak transcription	Brain Angular Gyrus	brain
28	chr11:33286800-33299000	Weak transcription	Brain Anterior Caudate	brain
29	chr11:33288200-33293600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr11:33288200-33295200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
31	chr11:33288400-33290600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
32	chr11:33288400-33290800	Weak transcription	Primary T helper cells PMA-I stimulated	--
33	chr11:33288600-33290600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
34	chr11:33288600-33290600	Weak transcription	Muscle Satellite Cultured Cells	--
35	chr11:33288600-33290600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr11:33288600-33290600	Weak transcription	Duodenum Mucosa	Duodenum
37	chr11:33288600-33290600	Weak transcription	NH-A	brain
38	chr11:33288600-33290600	Weak transcription	Osteobl	bone
39	chr11:33288600-33292200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
40	chr11:33288600-33296800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr11:33288600-33308000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr11:33288800-33290400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr11:33288800-33290400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr11:33288800-33290400	Weak transcription	Liver	Liver
45	chr11:33288800-33290400	Weak transcription	Rectal Smooth Muscle	rectum
46	chr11:33288800-33290600	Weak transcription	Colon Smooth Muscle	Colon
47	chr11:33288800-33290600	Weak transcription	Skeletal Muscle Male	skeletal muscle
48	chr11:33288800-33290800	Enhancers	Right Atrium	heart
49	chr11:33288800-33291600	Weak transcription	Small Intestine	intestine
50	chr11:33288800-33292800	Weak transcription	Primary monocytes fromperipheralblood	blood

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