Variant report

Variant	nsv468635
Chromosome Location	chr11:72284569-72336564
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1683)
CpG islands
(count:1529)
Chromatin interactive
region (count:89)
LncRNA
region (count:2)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:1683 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:72284676-72284736	K562	blood:	n/a	n/a
2	ARID3A	chr11:72284549-72284775	HepG2	liver:	n/a	n/a
3	ATF2	chr11:72300762-72301150	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr11:72284544-72284667	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr11:72295311-72295780	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr11:72315611-72315760	K562	blood:	n/a	n/a
7	BCL3	chr11:72335513-72336001	GM12878	blood:	n/a	n/a
8	BCL3	chr11:72335279-72336043	GM12878	blood:	n/a	n/a
9	BHLHE40	chr11:72284604-72284663	K562	blood:	n/a	n/a
10	BHLHE40	chr11:72310045-72310150	HepG2	liver:	n/a	n/a
11	BHLHE40	chr11:72284561-72284632	GM12878	blood:	n/a	n/a
12	BHLHE40	chr11:72309596-72309848	K562	blood:	n/a	n/a
13	BHLHE40	chr11:72335523-72335833	K562	blood:	n/a	n/a
14	BHLHE40	chr11:72325112-72325378	K562	blood:	n/a	n/a
15	BRCA1	chr11:72285948-72286013	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr11:72296650-72297056	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr11:72284278-72284877	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr11:72301932-72301968	H1-hESC	embryonic stem cell:	n/a	n/a
19	BRCA1	chr11:72296781-72297014	HepG2	liver:	n/a	n/a
20	CCNT2	chr11:72297654-72297784	K562	blood:	n/a	chr11:72297713-72297733
21	CCNT2	chr11:72301344-72301706	K562	blood:	n/a	n/a
22	CCNT2	chr11:72300999-72301141	K562	blood:	n/a	n/a
23	CEBPB	chr11:72323388-72323722	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr11:72300834-72300986	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr11:72323419-72323652	K562	blood:	n/a	n/a
26	CEBPB	chr11:72323383-72323741	HepG2	liver:	n/a	n/a
27	CEBPB	chr11:72323410-72323721	K562	blood:	n/a	n/a
28	CEBPB	chr11:72323419-72323727	IMR90	lung:	n/a	n/a
29	CEBPB	chr11:72323400-72323709	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr11:72323405-72323699	A549	lung:	n/a	n/a
31	CEBPB	chr11:72310487-72310614	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr11:72296750-72297094	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr11:72284429-72285058	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr11:72302790-72303486	Hela-S3	cervix:	n/a	n/a
35	CHD1	chr11:72306114-72306628	H1-hESC	embryonic stem cell:	n/a	chr11:72306467-72306477
36	CHD2	chr11:72300933-72300982	HepG2	liver:	n/a	n/a
37	CHD2	chr11:72284321-72285584	Hela-S3	cervix:	n/a	n/a
38	CHD2	chr11:72284467-72284740	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr11:72295648-72295784	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr11:72296873-72297105	K562	blood:	n/a	n/a
41	CHD2	chr11:72325504-72325698	Hela-S3	cervix:	n/a	n/a
42	CHD2	chr11:72296523-72296594	HepG2	liver:	n/a	n/a
43	CHD2	chr11:72296802-72296941	HepG2	liver:	n/a	n/a
44	CHD2	chr11:72284541-72284709	K562	blood:	n/a	n/a
45	CHD2	chr11:72296574-72297093	Hela-S3	cervix:	n/a	n/a
46	CHD2	chr11:72310469-72310688	Hela-S3	cervix:	n/a	n/a
47	CHD2	chr11:72300800-72301114	Hela-S3	cervix:	n/a	n/a
48	CHD2	chr11:72302798-72303544	Hela-S3	cervix:	n/a	n/a
49	CHD2	chr11:72286150-72286253	Hela-S3	cervix:	n/a	n/a
50	CHD2	chr11:72286473-72286600	Hela-S3	cervix:	n/a	n/a

(count:1529 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:72326138-72326188	HRCEpiC	kidney:	n/a
2	chr11:72301235-72301285	HAEpiC	amniotic membrane:	n/a
3	chr11:72295425-72295475	SK-N-MC	brain:	n/a
4	chr11:72326842-72326892	LNCaP	prostate:	n/a
5	chr11:72326138-72326188	HRCEpiC	kidney:	n/a
6	chr11:72301235-72301285	HAEpiC	amniotic membrane:	n/a
7	chr11:72295425-72295475	SK-N-MC	brain:	n/a
8	chr11:72326842-72326892	LNCaP	prostate:	n/a
9	chr11:72301724-72301774	IMR90	lung:	fetal
10	chr11:72295716-72295766	HEK293	kidney:	embryo
11	chr11:72288270-72288320	HMEC	breast:	n/a
12	chr11:72295425-72295475	HAEpiC	amniotic membrane:	n/a
13	chr11:72301724-72301774	SK-N-SH	brain:	n/a
14	chr11:72327807-72327857	HMEC	breast:	n/a
15	chr11:72326842-72326892	GM12891	blood:	n/a
16	chr11:72301235-72301285	SKMC	muscle:	n/a
17	chr11:72312062-72312112	MCF10A-Er-Src	breast:	n/a
18	chr11:72301724-72301774	GM06990	blood:	n/a
19	chr11:72301235-72301285	HPAEpiC	pulmonary alveolar:	n/a
20	chr11:72293698-72293748	SK-N-SH_RA	brain:	n/a
21	chr11:72312062-72312112	HIPEpiC	eye:	n/a
22	chr11:72301558-72301608	HRCEpiC	kidney:	n/a
23	chr11:72288270-72288320	AG09319	gingival:	n/a
24	chr11:72301558-72301608	HRE	kidney:	n/a
25	chr11:72326156-72326206	HRPEpiC	eye:	n/a
26	chr11:72301558-72301608	GM12892	blood:	n/a
27	chr11:72301306-72301356	Caco-2	colon:	n/a
28	chr11:72296138-72296188	SKMC	muscle:	n/a
29	chr11:72296138-72296188	ECC-1	luminal epithelium:	n/a
30	chr11:72300891-72300941	ECC-1	luminal epithelium:	n/a
31	chr11:72298299-72298349	IMR90	lung:	fetal
32	chr11:72295168-72295218	T-47D	breast:	n/a
33	chr11:72297851-72297901	AG04449	skin:	fetal
34	chr11:72295425-72295475	PrEC	prostate:	n/a
35	chr11:72301306-72301356	NHBE	bronchial:	n/a
36	chr11:72326842-72326892	AG09309	skin:	n/a
37	chr11:72301924-72301974	ECC-1	luminal epithelium:	n/a
38	chr11:72301724-72301774	PFSK-1	brain:	n/a
39	chr11:72295425-72295475	U87	brain:	n/a
40	chr11:72305346-72305396	MCF10A-Er-Src	breast:	n/a
41	chr11:72326138-72326188	Caco-2	colon:	n/a
42	chr11:72326830-72326880	GM12891	blood:	n/a
43	chr11:72295535-72295585	HEEpiC	esophagus:	n/a
44	chr11:72301924-72301974	HRPEpiC	eye:	n/a
45	chr11:72327160-72327210	AG04450	lung:	fetal
46	chr11:72301724-72301774	Hepatocyte	liver:	n/a
47	chr11:72326842-72326892	AG10803	skin:	n/a
48	chr11:72292402-72292452	AG04450	lung:	fetal
49	chr11:72295168-72295218	HRE	kidney:	n/a
50	chr11:72326842-72326892	PrEC	prostate:	n/a

(count:89 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:72283857..72286700-chr11:72287444..72290426,4	MCF-7	breast:
2	chr11:72325568..72327953-chr11:72330233..72332258,3	K562	blood:
3	chr11:72310686..72313140-chr11:72320651..72322680,2	K562	blood:
4	chr11:72309672..72310907-chr11:72353574..72354733,7	K562	blood:
5	chr11:72329455..72332319-chr11:72346728..72350252,3	MCF-7	breast:
6	chr11:72288586..72291436-chr11:72293581..72295884,2	K562	blood:
7	chr11:72314859..72319000-chr11:72319326..72322445,4	K562	blood:
8	chr11:72336037..72338838-chr11:72339942..72342746,4	K562	blood:
9	chr11:72309579..72311274-chr11:72353556..72354810,14	MCF-7	breast:
10	chr11:72317260..72319196-chr11:72329466..72332421,2	MCF-7	breast:
11	chr11:72311450..72313060-chr11:72334269..72335781,2	K562	blood:
12	chr11:72289408..72292307-chr11:72292834..72294829,2	MCF-7	breast:
13	chr11:72308196..72310111-chr11:72350959..72352581,2	MCF-7	breast:
14	chr11:72315461..72317278-chr11:72318771..72321876,3	K562	blood:
15	chr11:72290299..72292837-chr11:72306814..72308929,2	K562	blood:
16	chr11:72300551..72301398-chr11:72353784..72354837,3	MCF-7	breast:
17	chr11:72310303..72312102-chr11:72363033..72365890,2	MCF-7	breast:
18	chr11:72309624..72310516-chr11:72353748..72354671,8	MCF-7	breast:
19	chr11:72296428..72297428-chr11:72319819..72320660,3	K562	blood:
20	chr11:72300263..72302231-chr11:72352736..72355134,2	K562	blood:
21	chr11:72296491..72297510-chr11:72394098..72395409,7	MCF-7	breast:
22	chr11:72325202..72330805-chr11:72334238..72338443,6	K562	blood:
23	chr11:72309161..72310639-chr11:72394269..72395813,13	MCF-7	breast:
24	chr11:72300430..72301672-chr11:72353759..72354743,12	MCF-7	breast:
25	chr11:72296290..72298489-chr11:72299614..72302412,2	MCF-7	breast:
26	chr11:72283857..72286700-chr11:72287444..72290426,4	MCF-7	breast:
27	chr11:72324405..72326702-chr11:72335643..72338443,2	K562	blood:
28	chr11:72293642..72296987-chr11:72305169..72308806,3	K562	blood:
29	chr11:72296447..72297845-chr11:72353504..72354713,7	K562	blood:
30	chr11:72313089..72314978-chr11:72334364..72335937,2	K562	blood:
31	chr11:72193284..72193993-chr11:72284096..72285030,3	K562	blood:
32	chr11:72303390..72305679-chr11:72341481..72343396,2	K562	blood:
33	chr11:72286820..72288399-chr11:72288594..72291331,2	K562	blood:
34	chr11:72294789..72296496-chr11:72299692..72301673,2	MCF-7	breast:
35	chr11:72307077..72309343-chr11:72312749..72315321,2	K562	blood:
36	chr11:72333492..72335782-chr11:72342126..72344876,2	K562	blood:
37	chr11:72182029..72182965-chr11:72286095..72287002,3	MCF-7	breast:
38	chr11:72289408..72292307-chr11:72292834..72294829,2	MCF-7	breast:
39	chr11:72182308..72182988-chr11:72320289..72320813,2	MCF-7	breast:
40	chr11:72192764..72194156-chr11:72284059..72285108,15	MCF-7	breast:
41	chr11:72309760..72310559-chr11:72394464..72395426,5	K562	blood:
42	chr11:72316726..72319178-chr11:72323210..72325569,2	K562	blood:
43	chr11:72290299..72292837-chr11:72306814..72308929,2	K562	blood:
44	chr11:72316726..72319178-chr11:72323210..72325569,2	K562	blood:
45	chr11:72317260..72319196-chr11:72329466..72332421,2	MCF-7	breast:
46	chr11:72321761..72324145-chr11:72337508..72339149,2	K562	blood:
47	chr11:72288586..72291436-chr11:72293581..72295884,2	K562	blood:
48	chr11:72294789..72296496-chr11:72299692..72301673,2	MCF-7	breast:
49	chr11:72296471..72297070-chr9:124082115..124083042,2	MCF-7	breast:
50	chr11:72296452..72297372-chr11:72394539..72395851,6	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARAP1-2	chr11:72307637-72307670	NONHSAT022779
2	lnc-ARAP1-2	chr11:72301977-72302400	NONHSAT022779

miRNA name	Chromosome Location	mirBase accession
hsa-miR-139-5p	chr11:72326146-72326168	MIMAT0000250
hsa-miR-139-3p	chr11:72326110-72326132	MIMAT0004552

No data

Variant related genes	Relation type
PDE2A	TF binding region
RNU7-105P	TF binding region
MIR139	TF binding region
ENSG00000256633	TF binding region
PDE2A	CpG island
RNU7-105P	CpG island
MIR139	CpG island
ENSG00000256633	CpG island
ENSG00000251919	chromatin interactions
ENSG00000186642	chromatin interactions
ENSG00000256633	chromatin interactions
ENSG00000255808	chromatin interactions
ENSG00000272036	chromatin interactions
ENSG00000256007	chromatin interactions
FOS	Mature miRNA region
MTDH	Mature miRNA region
RPS26	Mature miRNA region
TGS1	Mature miRNA region
IGF1R	Mature miRNA region

Extended variants
information (count: 2143 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:2143 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs366066	chr11:72284569-72284570	Weak transcription Enhancers Bivalent Enhancer Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs534468217	chr11:72284590-72284591	Weak transcription Enhancers Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs182138882	chr11:72284592-72284593	Weak transcription Enhancers Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs549772942	chr11:72284632-72284633	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
5	rs371160634	chr11:72284633-72284634	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
6	rs201430009	chr11:72284650-72284651	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
7	rs373859867	chr11:72284669-72284670	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
8	rs540621383	chr11:72284673-72284674	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
9	rs530457677	chr11:72284785-72284786	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
10	rs548349971	chr11:72284791-72284792	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
11	rs365274	chr11:72284803-72284804	Enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs532614728	chr11:72284806-72284807	Enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
13	rs187155844	chr11:72284818-72284819	Enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
14	rs115386813	chr11:72284843-72284844	Enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
15	rs191656740	chr11:72284924-72284925	Enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
16	rs368232234	chr11:72285000-72285001	Enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
17	rs185286217	chr11:72285003-72285004	Enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
18	rs574548581	chr11:72285028-72285029	Enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
19	rs188206460	chr11:72285040-72285041	Enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
20	rs535462421	chr11:72285097-72285098	Enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
21	rs535796563	chr11:72285121-72285122	Enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
22	rs370720677	chr11:72285159-72285160	Enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
23	rs76877197	chr11:72285170-72285171	Enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
24	rs572233195	chr11:72285202-72285203	Enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
25	rs546025831	chr11:72285238-72285239	Enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
26	rs557861025	chr11:72285306-72285307	Enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
27	rs576100939	chr11:72285321-72285322	Enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
28	rs75077867	chr11:72285359-72285360	Enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
29	rs149706483	chr11:72285360-72285361	Enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
30	rs144499887	chr11:72285376-72285377	Enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
31	rs77714113	chr11:72285380-72285381	Enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
32	rs74981694	chr11:72285414-72285415	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs11235541	chr11:72285444-72285445	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs148439658	chr11:72285448-72285449	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs570841819	chr11:72285488-72285489	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs531861024	chr11:72285664-72285665	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs148441075	chr11:72285705-72285706	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs549905469	chr11:72285748-72285749	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs568483070	chr11:72285815-72285816	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs535861345	chr11:72285868-72285869	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs554064244	chr11:72285869-72285870	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs375670868	chr11:72285882-72285883	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs570279631	chr11:72285934-72285935	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs566004625	chr11:72285977-72285978	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs142561342	chr11:72285988-72285989	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs113272184	chr11:72286017-72286018	Enhancers Weak transcription Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs548376705	chr11:72286071-72286072	Enhancers Weak transcription Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs564171574	chr11:72286092-72286093	Enhancers Weak transcription Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs150938678	chr11:72286123-72286124	Enhancers Weak transcription Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs543549088	chr11:72286152-72286153	Enhancers Weak transcription Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Glioblastoma multiforme	21080181	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chordoma	21602918	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Multiple myeloma	16616336	CNVD
Urothelial cell carcinoma	18451213	CNVD
Leukoplakia	24403051	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Lung cancer	19153074	CNVD
Acute myeloid leukemia	21251322	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1470 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:72269600-72295200	Weak transcription	Right Atrium	heart
2	chr11:72276400-72287800	Weak transcription	Fetal Brain Female	brain
3	chr11:72280400-72284600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr11:72281400-72287400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr11:72281600-72284600	Weak transcription	HSMMtube	muscle
6	chr11:72281600-72287400	Weak transcription	Brain Angular Gyrus	brain
7	chr11:72281800-72284800	Weak transcription	Brain Anterior Caudate	brain
8	chr11:72282400-72284600	Weak transcription	Fetal Intestine Small	intestine
9	chr11:72282400-72287600	Weak transcription	Right Ventricle	heart
10	chr11:72282600-72284600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr11:72282800-72284600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr11:72282800-72284600	Weak transcription	Spleen	Spleen
13	chr11:72282800-72286200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr11:72282800-72287000	Weak transcription	Left Ventricle	heart
15	chr11:72282800-72295200	Weak transcription	Gastric	stomach
16	chr11:72283000-72284600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr11:72283000-72284600	Weak transcription	HSMM	muscle
18	chr11:72283000-72292000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr11:72283200-72288000	Weak transcription	Brain Germinal Matrix	brain
20	chr11:72283600-72285200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr11:72283800-72284600	Weak transcription	Placenta Amnion	Placenta Amnion
22	chr11:72284000-72284800	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr11:72284000-72284800	Enhancers	NHEK	skin
24	chr11:72284000-72285000	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr11:72284000-72285800	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr11:72284000-72288000	Enhancers	Fetal Intestine Large	intestine
27	chr11:72284200-72284800	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr11:72284200-72284800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr11:72284400-72284600	Weak transcription	Skeletal Muscle Female	skeletal muscle
30	chr11:72284400-72284600	Active TSS	Hela-S3	cervix
31	chr11:72284600-72284800	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr11:72284600-72284800	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr11:72284600-72284800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr11:72284600-72284800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
35	chr11:72284600-72284800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr11:72284600-72284800	Enhancers	Muscle Satellite Cultured Cells	--
37	chr11:72284600-72284800	Bivalent Enhancer	Primary mononuclear cells fromperipheralblood	Blood
38	chr11:72284600-72284800	Enhancers	Brain Inferior Temporal Lobe	brain
39	chr11:72284600-72284800	Enhancers	Skeletal Muscle Female	skeletal muscle
40	chr11:72284600-72285000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr11:72284600-72285000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
42	chr11:72284600-72285000	Enhancers	Fetal Intestine Small	intestine
43	chr11:72284600-72285000	Enhancers	Fetal Muscle Leg	muscle
44	chr11:72284600-72285000	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
45	chr11:72284600-72285000	Enhancers	A549	lung
46	chr11:72284600-72285200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
47	chr11:72284600-72285200	Enhancers	Spleen	Spleen
48	chr11:72284600-72285200	Enhancers	HSMMtube	muscle
49	chr11:72284600-72285400	Transcr. at gene 5' and 3'	Hela-S3	cervix
50	chr11:72284600-72286000	Enhancers	HSMM	muscle

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