Variant report

Variant	nsv468795
Chromosome Location	chr11:93864321-93964917
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1512)
CpG islands
(count:1160)
Chromatin interactive
region (count:51)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:1512 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:93934157-93934699	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:93887802-93887881	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:93885221-93885691	K562	blood:	n/a	n/a
4	ARID3A	chr11:93932567-93932629	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:93885276-93885716	HepG2	liver:	n/a	n/a
6	ARID3A	chr11:93884527-93884708	HepG2	liver:	n/a	n/a
7	ARID3A	chr11:93864874-93865280	K562	blood:	n/a	n/a
8	ARID3A	chr11:93868385-93868684	K562	blood:	n/a	n/a
9	ARID3A	chr11:93916976-93917325	HepG2	liver:	n/a	n/a
10	ARID3A	chr11:93868971-93869805	K562	blood:	n/a	n/a
11	ARID3A	chr11:93953706-93953959	HepG2	liver:	n/a	n/a
12	ATF1	chr11:93865037-93865267	K562	blood:	n/a	n/a
13	ATF1	chr11:93875524-93875811	K562	blood:	n/a	n/a
14	ATF1	chr11:93869143-93869767	K562	blood:	n/a	n/a
15	ATF1	chr11:93885418-93885765	K562	blood:	n/a	n/a
16	ATF3	chr11:93869126-93869742	K562	blood:	n/a	n/a
17	ATF3	chr11:93885506-93885690	K562	blood:	n/a	n/a
18	ATF3	chr11:93885400-93885775	K562	blood:	n/a	n/a
19	BACH1	chr11:93951679-93951681	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr11:93957221-93957507	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr11:93865234-93865434	K562	blood:	n/a	n/a
22	BACH1	chr11:93957208-93957365	K562	blood:	n/a	n/a
23	BCL3	chr11:93934188-93934548	A549	lung:	n/a	n/a
24	BCL3	chr11:93934100-93934604	A549	lung:	n/a	n/a
25	BHLHE40	chr11:93865530-93865654	K562	blood:	n/a	n/a
26	BHLHE40	chr11:93904949-93905125	GM12878	blood:	n/a	n/a
27	BHLHE40	chr11:93874488-93874602	K562	blood:	n/a	n/a
28	BHLHE40	chr11:93863745-93864339	K562	blood:	n/a	n/a
29	BHLHE40	chr11:93885441-93886069	K562	blood:	n/a	n/a
30	BHLHE40	chr11:93930913-93930984	GM12878	blood:	n/a	n/a
31	BHLHE40	chr11:93930820-93931111	K562	blood:	n/a	n/a
32	BHLHE40	chr11:93868276-93868540	K562	blood:	n/a	chr11:93868348-93868364
33	BHLHE40	chr11:93917039-93917314	GM12878	blood:	n/a	n/a
34	BHLHE40	chr11:93865116-93865216	K562	blood:	n/a	n/a
35	BHLHE40	chr11:93904953-93905068	K562	blood:	n/a	n/a
36	BHLHE40	chr11:93875169-93875771	K562	blood:	n/a	chr11:93875385-93875401
37	BRCA1	chr11:93905620-93905628	GM12878	blood:	n/a	n/a
38	CBX3	chr11:93953003-93953298	K562	blood:	n/a	n/a
39	CBX3	chr11:93885455-93885847	K562	blood:	n/a	n/a
40	CBX3	chr11:93869352-93869810	K562	blood:	n/a	n/a
41	CBX3	chr11:93952951-93953285	K562	blood:	n/a	n/a
42	CBX3	chr11:93875148-93876067	K562	blood:	n/a	n/a
43	CCNT2	chr11:93868299-93868836	K562	blood:	n/a	n/a
44	CCNT2	chr11:93885496-93885893	K562	blood:	n/a	n/a
45	CEBPB	chr11:93903941-93904283	IMR90	lung:	n/a	n/a
46	CEBPB	chr11:93884452-93884684	HepG2	liver:	n/a	chr11:93884560-93884571
47	CEBPB	chr11:93934155-93934686	HepG2	liver:	n/a	n/a
48	CEBPB	chr11:93885113-93885789	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr11:93934281-93934625	A549	lung:	n/a	n/a
50	CEBPB	chr11:93926511-93926824	IMR90	lung:	n/a	n/a

(count:1160 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:93905167-93905217	SKMC	muscle:	n/a
2	chr11:93905167-93905217	SKMC	muscle:	n/a
3	chr11:93867992-93868042	SK-N-SH_RA	brain:	n/a
4	chr11:93875999-93876049	HRE	kidney:	n/a
5	chr11:93885254-93885304	HEK293	kidney:	embryo
6	chr11:93895866-93895916	HEEpiC	esophagus:	n/a
7	chr11:93907969-93908019	HEK293	kidney:	embryo
8	chr11:93913200-93913250	AG10803	skin:	n/a
9	chr11:93867992-93868042	AG04449	skin:	fetal
10	chr11:93899496-93899546	AG09319	gingival:	n/a
11	chr11:93920113-93920163	RPTEC	kidney:	n/a
12	chr11:93922202-93922252	K562	blood:	n/a
13	chr11:93875999-93876049	GM06990	blood:	n/a
14	chr11:93916953-93917003	HEEpiC	esophagus:	n/a
15	chr11:93904908-93904958	AG09319	gingival:	n/a
16	chr11:93885254-93885304	PFSK-1	brain:	n/a
17	chr11:93875999-93876049	AG09319	gingival:	n/a
18	chr11:93927425-93927475	NB4	blood:	n/a
19	chr11:93885823-93885873	Hela-S3	cervix:	n/a
20	chr11:93905167-93905217	ovcar-3	ovarian:	n/a
21	chr11:93885254-93885304	Jurkat	blood:	n/a
22	chr11:93907969-93908019	HCT-116	colon:	n/a
23	chr11:93905167-93905217	PrEC	prostate:	n/a
24	chr11:93922202-93922252	CMK	blood:	n/a
25	chr11:93914532-93914582	GM12878	blood:	n/a
26	chr11:93922202-93922252	IMR90	lung:	fetal
27	chr11:93865443-93865493	HCF	heart:	n/a
28	chr11:93914532-93914582	NT2-D1	testis:	n/a
29	chr11:93905167-93905217	HEK293	kidney:	embryo
30	chr11:93913200-93913250	T-47D	breast:	n/a
31	chr11:93895866-93895916	AG09319	gingival:	n/a
32	chr11:93922202-93922252	NHDF-neo	bronchial:	n/a
33	chr11:93895725-93895775	A549	lung:	n/a
34	chr11:93885823-93885873	GM12891	blood:	n/a
35	chr11:93914532-93914582	HCF	heart:	n/a
36	chr11:93895866-93895916	Hela-S3	cervix:	n/a
37	chr11:93885823-93885873	HepG2	liver:	n/a
38	chr11:93867992-93868042	NH-A	brain:	n/a
39	chr11:93922202-93922252	H1-hESC	embryonic stem cell:	embryo
40	chr11:93907969-93908019	GM12892	blood:	n/a
41	chr11:93907969-93908019	HMEC	breast:	n/a
42	chr11:93899496-93899546	Hepatocyte	liver:	n/a
43	chr11:93905167-93905217	HCM	heart:	n/a
44	chr11:93885254-93885304	HUVEC	blood vessel:	n/a
45	chr11:93920113-93920163	HRPEpiC	eye:	n/a
46	chr11:93916953-93917003	GM12891	blood:	n/a
47	chr11:93865443-93865493	AG04450	lung:	fetal
48	chr11:93874318-93874368	U87	brain:	n/a
49	chr11:93916953-93917003	Caco-2	colon:	n/a
50	chr11:93867992-93868042	ECC-1	luminal epithelium:	n/a

(count:51 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:93860855..93863542-chr11:93879661..93882968,3	MCF-7	breast:
2	chr11:93907084..93908799-chr11:93910378..93911922,2	K562	blood:
3	chr11:93877656..93879395-chr11:93882351..93886074,3	MCF-7	breast:
4	chr11:93875120..93879114-chr11:93880737..93884211,6	K562	blood:
5	chr11:93946184..93948199-chr11:93950840..93953246,2	K562	blood:
6	chr11:93917086..93919356-chr11:93920990..93923600,2	K562	blood:
7	chr11:93937398..93939250-chr11:93947688..93950358,2	K562	blood:
8	chr11:93875120..93879114-chr11:93880737..93884211,6	K562	blood:
9	chr11:93914625..93916953-chr11:94227203..94228744,2	MCF-7	breast:
10	chr11:93932886..93934765-chr11:93936534..93938531,2	K562	blood:
11	chr11:93945976..93948199-chr11:93951746..93953756,2	K562	blood:
12	chr11:93867029..93870976-chr11:93873101..93877852,6	K562	blood:
13	chr11:93861121..93863513-chr11:93882964..93886089,4	K562	blood:
14	chr11:93880754..93883524-chr11:93885061..93886886,2	K562	blood:
15	chr11:93899070..93901614-chr11:93903324..93905599,3	K562	blood:
16	chr11:93937398..93939250-chr11:93947688..93950358,2	K562	blood:
17	chr11:93860451..93862555-chr11:93865619..93868399,2	MCF-7	breast:
18	chr11:93867049..93869190-chr11:94275385..94277277,2	K562	blood:
19	chr11:93862864..93865828-chr11:93884142..93886084,2	MCF-7	breast:
20	chr11:93899070..93901614-chr11:93903324..93905599,3	K562	blood:
21	chr11:93861895..93865118-chr11:93874866..93877940,3	K562	blood:
22	chr11:93932886..93934765-chr11:93936534..93938531,2	K562	blood:
23	chr11:93904956..93905513-chr11:94237606..94238533,2	K562	blood:
24	chr11:93929115..93931956-chr11:94225381..94228826,3	K562	blood:
25	chr11:93877656..93879395-chr11:93882351..93886074,3	MCF-7	breast:
26	chr11:93928773..93931046-chr11:93935026..93936548,2	MCF-7	breast:
27	chr11:93866030..93868662-chr11:93884389..93887583,3	K562	blood:
28	chr11:93916648..93917265-chr11:94150276..94150816,3	MCF-7	breast:
29	chr11:93654636..93655438-chr11:93916836..93917602,2	MCF-7	breast:
30	chr11:93877718..93879953-chr11:94225579..94227905,2	K562	blood:
31	chr11:93861143..93863415-chr11:93902863..93904604,2	MCF-7	breast:
32	chr11:93916755..93917614-chr11:94150312..94151338,4	MCF-7	breast:
33	chr11:93899070..93901930-chr11:93903657..93905599,2	K562	blood:
34	chr11:93916747..93917349-chr11:94058220..94059212,2	MCF-7	breast:
35	chr11:93946184..93948199-chr11:93950840..93953246,2	K562	blood:
36	chr11:93867029..93870976-chr11:93873101..93877852,6	K562	blood:
37	chr11:93907084..93908799-chr11:93910378..93911922,2	K562	blood:
38	chr11:93904970..93905492-chr11:93917118..93917628,2	K562	blood:
39	chr11:93866030..93868662-chr11:93884389..93887583,3	K562	blood:
40	chr11:93928773..93931046-chr11:93935026..93936548,2	MCF-7	breast:
41	chr11:93874386..93876238-chr11:93877234..93879680,2	MCF-7	breast:
42	chr11:93862864..93865828-chr11:93884142..93886084,2	MCF-7	breast:
43	chr11:93874386..93876238-chr11:93877234..93879680,2	MCF-7	breast:
44	chr11:93899070..93901930-chr11:93903657..93905599,2	K562	blood:
45	chr11:93945976..93948199-chr11:93951746..93953756,2	K562	blood:
46	chr11:93861104..93863451-chr11:93914725..93916276,2	K562	blood:
47	chr11:93880754..93883524-chr11:93885061..93886886,2	K562	blood:
48	chr11:93865596..93867137-chr11:94149327..94151295,2	MCF-7	breast:
49	chr11:93904970..93905492-chr11:93917118..93917628,2	K562	blood:
50	chr11:93835888..93838608-chr11:93905991..93908122,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPR83-5	chr11:93921615-93922163	NONHSAT023708
2	lnc-GPR83-2	chr11:93932428-93932509	NONHSAT023709
3	lnc-PANX1-1	chr11:93935412-93935672	NONHSAT023711
4	lnc-GPR83-2	chr11:93932662-93932887	XLOC_009524
5	lnc-GPR83-2	chr11:93932429-93932509	XLOC_009524
6	lnc-GPR83-2	chr11:93932661-93932887	NONHSAT023709

No data

(count:3 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	PANX1	hsa-miR-125a-5p	chr11:93914428-93914452
2	PANX1	hsa-miR-16-5p	chr11:93914663-93914684
3	PANX1	hsa-miR-10a-5p	chr11:93914431-93914453

Variant related genes	Relation type
ENSG00000256745	TF binding region
ENSG00000256745	CpG island
ENSG00000263966	chromatin interactions
ENSG00000110218	chromatin interactions
ENSG00000134627	chromatin interactions
ENSG00000020922	chromatin interactions
ENSG00000171843	chromatin interactions
ENSG00000168876	chromatin interactions
ENSG00000256745	chromatin interactions
ENSG00000196371	chromatin interactions

Extended variants
information (count: 3242 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:3242 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6483293	chr11:93864321-93864322	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs117344141	chr11:93864324-93864325	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
3	rs553704922	chr11:93864338-93864339	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
4	rs56175344	chr11:93864393-93864394	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs191610172	chr11:93864431-93864432	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
6	rs34416958	chr11:93864467-93864468	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
7	rs374866078	chr11:93864468-93864469	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
8	rs575831740	chr11:93864526-93864527	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
9	rs547486165	chr11:93864573-93864574	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
10	rs185522335	chr11:93864576-93864577	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
11	rs531123649	chr11:93864581-93864582	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
12	rs567614407	chr11:93864593-93864594	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
13	rs562054175	chr11:93864600-93864601	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
14	rs529358250	chr11:93864636-93864637	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs541103437	chr11:93864736-93864737	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs4753541	chr11:93864739-93864740	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs533719948	chr11:93864747-93864748	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs190742901	chr11:93864770-93864771	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs182205052	chr11:93864794-93864795	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs374281922	chr11:93864800-93864801	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs531144743	chr11:93864802-93864803	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs549469031	chr11:93864882-93864883	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs549527938	chr11:93864923-93864924	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs117493040	chr11:93864930-93864931	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs372532598	chr11:93864942-93864943	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs186836082	chr11:93865007-93865008	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs188973075	chr11:93865014-93865015	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs559197247	chr11:93865026-93865027	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs56888579	chr11:93865028-93865029	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs373248702	chr11:93865034-93865035	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs148486076	chr11:93865037-93865038	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs7939139	chr11:93865059-93865060	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs181026108	chr11:93865061-93865062	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs368216304	chr11:93865064-93865065	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs71482704	chr11:93865070-93865071	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs572280870	chr11:93865075-93865076	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs543234220	chr11:93865083-93865084	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs373703856	chr11:93865115-93865116	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs559248104	chr11:93865130-93865131	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs76418189	chr11:93865135-93865136	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs541513542	chr11:93865164-93865165	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs559544432	chr11:93865174-93865175	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs374492117	chr11:93865214-93865215	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs71482705	chr11:93865234-93865235	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs545386930	chr11:93865262-93865263	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs4073615	chr11:93865282-93865283	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs200814823	chr11:93865346-93865347	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs371346011	chr11:93865348-93865349	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs573280705	chr11:93865354-93865355	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs549345210	chr11:93865387-93865388	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	20729466	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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	22429812	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Renal cell carcinoma	18194544	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Mental retardation	21062444	CNVD
Cancer	21499728	CNVD
Breast cancer	19181860	CNVD
Breast cancer	17603634	CNVD
Mantle cell lymphoma	19029149	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	16790693	CNVD
Breast cancer	21509527	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	18852474	CNVD
Breast cancer	22844521	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2628 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:93861200-93864400	Active TSS	Aorta	Aorta
2	chr11:93861400-93864400	Active TSS	Duodenum Smooth Muscle	Duodenum
3	chr11:93862400-93864800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
4	chr11:93862600-93864400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
5	chr11:93862600-93864400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
6	chr11:93862600-93864600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr11:93862600-93864600	Flanking Active TSS	Duodenum Mucosa	Duodenum
8	chr11:93862600-93864800	Flanking Active TSS	Adipose Nuclei	Adipose
9	chr11:93862600-93865000	Flanking Active TSS	Dnd41	blood
10	chr11:93862600-93865000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
11	chr11:93862800-93864400	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
12	chr11:93862800-93864400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
13	chr11:93862800-93864400	Flanking Active TSS	Brain Anterior Caudate	brain
14	chr11:93862800-93864400	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
15	chr11:93862800-93864600	Flanking Active TSS	Brain Angular Gyrus	brain
16	chr11:93862800-93864800	Flanking Active TSS	Brain Hippocampus Middle	brain
17	chr11:93862800-93864800	Flanking Active TSS	Hela-S3	cervix
18	chr11:93862800-93864800	Flanking Active TSS	Osteobl	bone
19	chr11:93862800-93865600	Flanking Active TSS	Fetal Lung	lung
20	chr11:93862800-93865600	Flanking Active TSS	NH-A	brain
21	chr11:93862800-93865800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
22	chr11:93862800-93865800	Flanking Active TSS	NHEK	skin
23	chr11:93862800-93866000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr11:93863000-93864400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr11:93863000-93864400	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
26	chr11:93863000-93864400	Flanking Active TSS	Right Atrium	heart
27	chr11:93863000-93864800	Flanking Active TSS	H1 Cell Line	embryonic stem cell
28	chr11:93863000-93864800	Flanking Active TSS	Colon Smooth Muscle	Colon
29	chr11:93863000-93864800	Flanking Active TSS	Stomach Smooth Muscle	stomach
30	chr11:93863000-93864800	Flanking Active TSS	HepG2	liver
31	chr11:93863000-93865600	Enhancers	Sigmoid Colon	Sigmoid Colon
32	chr11:93863000-93865800	Flanking Active TSS	HMEC	breast
33	chr11:93863000-93866600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr11:93863000-93866600	Enhancers	Spleen	Spleen
35	chr11:93863000-93867200	Enhancers	Esophagus	oesophagus
36	chr11:93863200-93864400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr11:93863200-93864400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr11:93863200-93864600	Enhancers	Primary hematopoietic stem cells	blood
39	chr11:93863200-93864600	Active TSS	Rectal Mucosa Donor 29	rectum
40	chr11:93863200-93864600	Flanking Active TSS	GM12878-XiMat	blood
41	chr11:93863200-93864800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
42	chr11:93863200-93864800	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
43	chr11:93863200-93865000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr11:93863200-93865200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
45	chr11:93863200-93865200	Flanking Active TSS	Brain Germinal Matrix	brain
46	chr11:93863200-93865400	Enhancers	Primary B cells from peripheral blood	blood
47	chr11:93863200-93865600	Flanking Active TSS	Fetal Brain Female	brain
48	chr11:93863200-93865800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr11:93863200-93865800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr11:93863200-93865800	Flanking Active TSS	NHLF	lung

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