Variant report

Variant	nsv508623
Chromosome Location	chr11:35094933-35203363
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3712)
CpG islands
(count:1897)
Chromatin interactive
region (count:79)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3712 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:35194753-35195096	HepG2	liver:	n/a	n/a
2	ATF1	chr11:35120645-35121044	K562	blood:	n/a	n/a
3	ATF1	chr11:35168376-35168687	K562	blood:	n/a	n/a
4	ATF1	chr11:35162652-35162835	K562	blood:	n/a	n/a
5	ATF1	chr11:35122859-35123088	K562	blood:	n/a	n/a
6	ATF1	chr11:35166888-35167161	K562	blood:	n/a	n/a
7	ATF1	chr11:35125408-35125579	K562	blood:	n/a	n/a
8	ATF1	chr11:35104027-35104396	K562	blood:	n/a	n/a
9	ATF1	chr11:35182060-35182303	K562	blood:	n/a	n/a
10	ATF1	chr11:35133237-35133513	K562	blood:	n/a	n/a
11	ATF1	chr11:35099273-35099414	K562	blood:	n/a	n/a
12	ATF1	chr11:35132632-35132924	K562	blood:	n/a	n/a
13	ATF1	chr11:35164287-35164318	K562	blood:	n/a	n/a
14	ATF2	chr11:35104016-35104542	GM12878	blood:	n/a	n/a
15	ATF2	chr11:35166448-35167418	GM12878	blood:	n/a	n/a
16	ATF2	chr11:35165372-35166426	GM12878	blood:	n/a	n/a
17	ATF2	chr11:35143863-35144425	GM12878	blood:	n/a	n/a
18	ATF2	chr11:35098997-35100135	GM12878	blood:	n/a	n/a
19	ATF2	chr11:35111140-35111947	GM12878	blood:	n/a	n/a
20	ATF2	chr11:35165624-35166332	GM12878	blood:	n/a	n/a
21	ATF2	chr11:35104602-35105713	GM12878	blood:	n/a	n/a
22	ATF2	chr11:35147513-35148569	GM12878	blood:	n/a	n/a
23	ATF2	chr11:35099013-35100141	GM12878	blood:	n/a	n/a
24	ATF2	chr11:35152590-35153181	GM12878	blood:	n/a	n/a
25	ATF2	chr11:35187309-35188167	GM12878	blood:	n/a	n/a
26	ATF2	chr11:35140329-35140826	GM12878	blood:	n/a	n/a
27	ATF2	chr11:35109087-35109714	GM12878	blood:	n/a	n/a
28	ATF2	chr11:35167420-35168628	GM12878	blood:	n/a	n/a
29	ATF2	chr11:35111179-35111661	GM12878	blood:	n/a	n/a
30	ATF2	chr11:35109062-35110065	GM12878	blood:	n/a	n/a
31	ATF2	chr11:35104643-35105435	GM12878	blood:	n/a	n/a
32	ATF2	chr11:35148675-35149703	GM12878	blood:	n/a	n/a
33	ATF2	chr11:35166629-35167313	GM12878	blood:	n/a	n/a
34	ATF2	chr11:35187310-35187972	GM12878	blood:	n/a	n/a
35	ATF2	chr11:35103848-35104479	GM12878	blood:	n/a	n/a
36	ATF2	chr11:35167580-35168640	GM12878	blood:	n/a	n/a
37	ATF2	chr11:35140337-35140923	GM12878	blood:	n/a	n/a
38	ATF2	chr11:35147745-35149600	GM12878	blood:	n/a	n/a
39	ATF3	chr11:35188083-35188607	A549	lung:	n/a	n/a
40	ATF3	chr11:35176584-35176795	K562	blood:	n/a	n/a
41	BACH1	chr11:35173481-35173712	H1-hESC	embryonic stem cell:	n/a	n/a
42	BACH1	chr11:35202998-35203161	K562	blood:	n/a	n/a
43	BATF	chr11:35167579-35168080	GM12878	blood:	n/a	chr11:35167751-35167761 chr11:35167750-35167761 chr11:35167875-35167884
44	BATF	chr11:35152651-35153096	GM12878	blood:	n/a	n/a
45	BATF	chr11:35140438-35140826	GM12878	blood:	n/a	n/a
46	BATF	chr11:35150354-35150628	GM12878	blood:	n/a	n/a
47	BATF	chr11:35111229-35111663	GM12878	blood:	n/a	n/a
48	BATF	chr11:35166776-35167203	GM12878	blood:	n/a	n/a
49	BATF	chr11:35147860-35149081	GM12878	blood:	n/a	n/a
50	BATF	chr11:35157164-35157464	GM12878	blood:	n/a	chr11:35157283-35157294 chr11:35157313-35157324 chr11:35157314-35157324

(count:1897 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:35160892-35160942	NT2-D1	testis:	n/a
2	chr11:35160330-35160380	BE2_C	brain:	n/a
3	chr11:35159087-35159137	SK-N-SH	brain:	n/a
4	chr11:35138084-35138134	GM06990	blood:	n/a
5	chr11:35195513-35195563	IMR90	lung:	fetal
6	chr11:35160709-35160759	GM19239	blood:	n/a
7	chr11:35160892-35160942	NT2-D1	testis:	n/a
8	chr11:35160330-35160380	BE2_C	brain:	n/a
9	chr11:35159087-35159137	SK-N-SH	brain:	n/a
10	chr11:35138084-35138134	GM06990	blood:	n/a
11	chr11:35195513-35195563	IMR90	lung:	fetal
12	chr11:35160709-35160759	GM19239	blood:	n/a
13	chr11:35164485-35164535	HRCEpiC	kidney:	n/a
14	chr11:35173592-35173642	GM19239	blood:	n/a
15	chr11:35201133-35201183	HEK293	kidney:	embryo
16	chr11:35158283-35158333	ECC-1	luminal epithelium:	n/a
17	chr11:35121378-35121428	HCPEpiC	choroid plexus:	n/a
18	chr11:35173592-35173642	IMR90	lung:	fetal
19	chr11:35160709-35160759	HCT-116	colon:	n/a
20	chr11:35161345-35161395	AG04449	skin:	fetal
21	chr11:35160400-35160450	ProgFib	skin:	n/a
22	chr11:35159382-35159432	NB4	blood:	n/a
23	chr11:35159087-35159137	HepG2	liver:	n/a
24	chr11:35160498-35160548	GM19239	blood:	n/a
25	chr11:35160498-35160548	PrEC	prostate:	n/a
26	chr11:35161183-35161233	GM12878	blood:	n/a
27	chr11:35160843-35160893	NH-A	brain:	n/a
28	chr11:35186440-35186490	ProgFib	skin:	n/a
29	chr11:35179802-35179852	HRE	kidney:	n/a
30	chr11:35164485-35164535	GM12878	blood:	n/a
31	chr11:35164485-35164535	PANC-1	pancreas:	n/a
32	chr11:35179802-35179852	GM19239	blood:	n/a
33	chr11:35186440-35186490	HAEpiC	amniotic membrane:	n/a
34	chr11:35188437-35188487	HNPCEpiC	eye:	n/a
35	chr11:35160571-35160621	PFSK-1	brain:	n/a
36	chr11:35195513-35195563	HNPCEpiC	eye:	n/a
37	chr11:35160709-35160759	HNPCEpiC	eye:	n/a
38	chr11:35158283-35158333	NT2-D1	testis:	n/a
39	chr11:35201133-35201183	NHDF-neo	bronchial:	n/a
40	chr11:35161229-35161279	GM12892	blood:	n/a
41	chr11:35105199-35105249	GM12892	blood:	n/a
42	chr11:35158283-35158333	K562	blood:	n/a
43	chr11:35198201-35198251	SK-N-SH	brain:	n/a
44	chr11:35158283-35158333	MCF10A-Er-Src	breast:	n/a
45	chr11:35195513-35195563	NHBE	bronchial:	n/a
46	chr11:35161900-35161950	HRCEpiC	kidney:	n/a
47	chr11:35133274-35133324	ovcar-3	ovarian:	n/a
48	chr11:35099055-35099105	Hela-S3	cervix:	n/a
49	chr11:35161229-35161279	HL-60	blood:	n/a
50	chr11:35160571-35160621	NT2-D1	testis:	n/a

(count:79 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:35160584..35161366-chr17:72983348..72984211,2	Hela-S3	cervix:
2	chr11:35110163..35112423-chr11:35159701..35161676,2	MCF-7	breast:
3	chr11:35186608..35189447-chr11:35199235..35201624,2	MCF-7	breast:
4	chr11:35160960..35162794-chr11:35186248..35188654,2	MCF-7	breast:
5	chr11:35132300..35135003-chr11:35146023..35147940,2	MCF-7	breast:
6	chr11:35160506..35161348-chr5:172198026..172198579,2	Hela-S3	cervix:
7	chr1:89149746..89150285-chr11:35160701..35161440,2	HCT-116	colon:
8	chr11:35109556..35112078-chr11:35117913..35120120,2	MCF-7	breast:
9	chr11:34938093..34939698-chr11:35166380..35168722,2	MCF-7	breast:
10	chr11:35121498..35123460-chr11:35254836..35257289,2	K562	blood:
11	chr11:35188706..35190323-chr11:35204261..35206876,2	K562	blood:
12	chr1:153930650..153931150-chr11:35161047..35161739,2	Hela-S3	cervix:
13	chr11:35160028..35162902-chr11:35183937..35186481,3	MCF-7	breast:
14	chr11:35172301..35174738-chr11:35189496..35192114,2	MCF-7	breast:
15	chr11:35161963..35164830-chr11:35383993..35385550,2	MCF-7	breast:
16	chr11:35163163..35167316-chr11:35171190..35174236,4	K562	blood:
17	chr11:35195238..35197148-chr11:35385944..35388591,2	MCF-7	breast:
18	chr11:35143665..35146006-chr11:35146722..35148953,2	MCF-7	breast:
19	chr11:35169325..35170963-chr11:35175287..35177044,2	K562	blood:
20	chr11:35160366..35160877-chr15:44069390..44069929,2	Hela-S3	cervix:
21	chr11:35170246..35172817-chr11:35174979..35176507,2	MCF-7	breast:
22	chr11:35097231..35099674-chr11:35101240..35103980,3	K562	blood:
23	chr11:35163163..35167316-chr11:35171190..35174236,4	K562	blood:
24	chr11:35123473..35125204-chr11:35129634..35132229,2	MCF-7	breast:
25	chr11:35059235..35060888-chr11:35161011..35163300,2	MCF-7	breast:
26	chr11:35184295..35186190-chr11:35191742..35193747,2	MCF-7	breast:
27	chr11:34947697..34948269-chr11:35163627..35164578,3	K562	blood:
28	chr11:35183121..35185456-chr11:35188061..35190243,2	MCF-7	breast:
29	chr11:35122584..35124925-chr11:35126765..35129371,2	MCF-7	breast:
30	chr11:35097231..35099674-chr11:35101240..35103980,3	K562	blood:
31	chr11:35109556..35112078-chr11:35117913..35120120,2	MCF-7	breast:
32	chr1:153606580..153607386-chr11:35159581..35160522,2	Hela-S3	cervix:
33	chr11:35026967..35028548-chr11:35162664..35165084,2	MCF-7	breast:
34	chr11:35132300..35135003-chr11:35146023..35147940,2	MCF-7	breast:
35	chr1:154154871..154155752-chr11:35160501..35161403,2	Hela-S3	cervix:
36	chr11:35172301..35174738-chr11:35189496..35192114,2	MCF-7	breast:
37	chr11:35186531..35188215-chr11:35413426..35415708,2	MCF-7	breast:
38	chr11:35101233..35103768-chr11:35185557..35187275,2	MCF-7	breast:
39	chr11:35137747..35140053-chr11:35157394..35160229,2	MCF-7	breast:
40	chr11:35155392..35158105-chr11:35159031..35160697,2	MCF-7	breast:
41	chr11:35104262..35106718-chr11:35159601..35161198,2	MCF-7	breast:
42	chr11:35184295..35186190-chr11:35191742..35193747,2	MCF-7	breast:
43	chr11:35101233..35103768-chr11:35185557..35187275,2	MCF-7	breast:
44	chr11:35143665..35146006-chr11:35146722..35148953,2	MCF-7	breast:
45	chr11:35160374..35163354-chr11:35164253..35168964,4	K562	blood:
46	chr11:35160364..35160882-chr15:75932271..75932998,2	Hela-S3	cervix:
47	chr11:35160872..35161372-chr12:14923610..14924453,2	Hela-S3	cervix:
48	chr11:35121360..35123846-chr11:35132606..35135309,2	K562	blood:
49	chr11:35170246..35172817-chr11:35174979..35176507,2	MCF-7	breast:
50	chr11:35135157..35136854-chr11:35159646..35161211,2	MCF-7	breast:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC1A2-2	chr11:35157893-35158173	ENSG00000255521.1
2	lnc-PDHX-3	chr11:35140600-35142723	NONHSAT018772
3	lnc-PDHX-3	chr11:35112276-35112331	NONHSAT018772
4	lnc-SLC1A2-2	chr11:35150431-35150467	XLOC_009416
5	lnc-APIP-1	chr11:35095464-35095505	XLOC_009415
6	lnc-PDHX-3	chr11:35108965-35110133	NONHSAT018772
7	lnc-CD44-3	chr11:35132621-35132927	NONHSAT018774
8	lnc-SLC1A2-2	chr11:35157893-35158084	XLOC_009416
9	lnc-SLC1A2-2	chr11:35157781-35158173	ENSG00000255521.1
10	lnc-SLC1A2-2	chr11:35159245-35159273	ENSG00000255521.1
11	lnc-PDHX-3	chr11:35119168-35119365	NONHSAT018768
12	lnc-CD44-4	chr11:35124735-35124991	NONHSAT018773
13	lnc-SLC1A2-2	chr11:35154202-35154687	ENSG00000255521.1
14	lnc-PDHX-3	chr11:35109985-35110151	NONHSAT018768
15	lnc-CD44-5	chr11:35103203-35103622	NONHSAT018771
16	lnc-SLC1A2-2	chr11:35159245-35159579	ENSG00000255521.1
17	lnc-PDHX-3	chr11:35107760-35107870	NONHSAT018772
18	lnc-PDHX-3	chr11:35119065-35120242	NONHSAT018772

No data

Variant related genes	Relation type
ENSG00000269766	TF binding region
CD44	TF binding region
ENSG00000255521	TF binding region
ENSG00000269766	CpG island
CD44	CpG island
ENSG00000255521	CpG island
ENSG00000223247	chromatin interactions
ENSG00000255521	chromatin interactions
ENSG00000160813	chromatin interactions
ENSG00000269766	chromatin interactions
ENSG00000272030	chromatin interactions
ENSG00000065243	chromatin interactions
ENSG00000128886	chromatin interactions
ENSG00000232519	chromatin interactions
ENSG00000143549	chromatin interactions
ENSG00000110435	chromatin interactions
ENSG00000271853	chromatin interactions
ENSG00000269946	chromatin interactions
ENSG00000199347	chromatin interactions
ENSG00000160741	chromatin interactions
ENSG00000131389	chromatin interactions
ENSG00000026508	chromatin interactions
ENSG00000109089	chromatin interactions
ENSG00000197837	chromatin interactions
ENSG00000177971	chromatin interactions
ENSG00000125459	chromatin interactions
ENSG00000120129	chromatin interactions
POU2F1	miRNA target sites
CUEDC2	miRNA target sites

Extended variants
information (count: 4385 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:4385 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372316283	chr11:35095096-35095097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs377155805	chr11:35095147-35095148	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs12225389	chr11:35095148-35095149	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs530898101	chr11:35095167-35095168	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs572912656	chr11:35095200-35095201	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs11032989	chr11:35095213-35095214	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs11032990	chr11:35095222-35095223	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs543145512	chr11:35095226-35095227	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs150317929	chr11:35095246-35095247	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs2785194	chr11:35095254-35095255	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs560356032	chr11:35095307-35095308	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs529111551	chr11:35095309-35095310	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs2553828	chr11:35095324-35095325	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs546817769	chr11:35095330-35095331	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs192404060	chr11:35095339-35095340	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs138040180	chr11:35095348-35095349	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs185050452	chr11:35095375-35095376	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs188986928	chr11:35095392-35095393	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs2785193	chr11:35095435-35095436	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs2732540	chr11:35095486-35095487	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs567481723	chr11:35095493-35095494	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
22	rs192341387	chr11:35095519-35095520	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs549860058	chr11:35095546-35095547	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs570160453	chr11:35095548-35095549	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs538640498	chr11:35095560-35095561	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs558876193	chr11:35095563-35095564	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs1834460	chr11:35095565-35095566	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs534031652	chr11:35095576-35095577	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs113253115	chr11:35095601-35095602	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs573868018	chr11:35095611-35095612	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs542888180	chr11:35095663-35095664	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs118093271	chr11:35095666-35095667	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs531211316	chr11:35095762-35095763	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs146030970	chr11:35095794-35095795	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs79021967	chr11:35095806-35095807	Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs554255738	chr11:35095817-35095818	Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs184852330	chr11:35095832-35095833	Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs138783313	chr11:35095836-35095837	Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs561294881	chr11:35095838-35095839	Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs201170672	chr11:35095845-35095846	Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs373114339	chr11:35095869-35095870	Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs530210849	chr11:35095922-35095923	Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs2732538	chr11:35095948-35095949	Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs189417895	chr11:35095951-35095952	Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs376282180	chr11:35096012-35096013	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs549559256	chr11:35096033-35096034	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs561807585	chr11:35096040-35096041	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs564610108	chr11:35096061-35096062	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs77829120	chr11:35096072-35096073	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs552392056	chr11:35096148-35096149	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Lung squamous cell carcinoma	20842114	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:4281 , 50 per page) page: 1 2 3 4 5 6 7 ... 86

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:35088600-35099000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr11:35088800-35099200	Weak transcription	Stomach Mucosa	stomach
3	chr11:35089200-35098000	Weak transcription	Small Intestine	intestine
4	chr11:35091000-35098000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr11:35091200-35097600	Weak transcription	Primary B cells from peripheral blood	blood
6	chr11:35091200-35099800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr11:35092200-35099000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr11:35093200-35095800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
9	chr11:35093400-35095600	Enhancers	Primary T helper cells fromperipheralblood	blood
10	chr11:35094200-35095400	Enhancers	Primary T helper cells PMA-I stimulated	--
11	chr11:35094200-35095600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
12	chr11:35094200-35096400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
13	chr11:35094200-35097600	Weak transcription	Primary T cells fromperipheralblood	blood
14	chr11:35094200-35097600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
15	chr11:35094400-35097600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
16	chr11:35094400-35097600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
17	chr11:35094600-35095000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
18	chr11:35094600-35095800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr11:35094600-35095800	Enhancers	Osteobl	bone
20	chr11:35094800-35095800	Enhancers	Muscle Satellite Cultured Cells	--
21	chr11:35094800-35096800	Weak transcription	Primary T cells from cord blood	blood
22	chr11:35094800-35098200	Weak transcription	Thymus	Thymus
23	chr11:35095000-35095600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr11:35095000-35095800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr11:35095000-35095800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
26	chr11:35095200-35096400	ZNF genes & repeats	GM12878-XiMat	blood
27	chr11:35095400-35095800	Enhancers	Primary hematopoietic stem cells short term culture	blood
28	chr11:35095400-35095800	Enhancers	K562	blood
29	chr11:35095400-35095800	Enhancers	NHDF-Ad	bronchial
30	chr11:35095400-35095800	Enhancers	NHEK	skin
31	chr11:35095400-35096000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
32	chr11:35095600-35095800	Enhancers	HMEC	breast
33	chr11:35095600-35096000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
34	chr11:35095600-35096600	Weak transcription	Primary T helper cells fromperipheralblood	blood
35	chr11:35095600-35097800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr11:35095600-35099200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr11:35095800-35096800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
38	chr11:35095800-35096800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
39	chr11:35095800-35097800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
40	chr11:35095800-35097800	Weak transcription	K562	blood
41	chr11:35095800-35098000	Weak transcription	Muscle Satellite Cultured Cells	--
42	chr11:35095800-35098400	Weak transcription	HMEC	breast
43	chr11:35095800-35098400	Weak transcription	NHEK	skin
44	chr11:35095800-35099000	Weak transcription	Osteobl	bone
45	chr11:35095800-35099200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr11:35095800-35099200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr11:35095800-35099200	Weak transcription	NHDF-Ad	bronchial
48	chr11:35096000-35096800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
49	chr11:35096000-35097600	Enhancers	Primary T helper cells PMA-I stimulated	--
50	chr11:35096400-35097600	Weak transcription	GM12878-XiMat	blood

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