Variant report

Variant	nsv826793
Chromosome Location	chr13:110423187-110448628
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1563)
CpG islands
(count:2142)
Chromatin interactive
region (count:56)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1563 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:110443363-110444054	K562	blood:	n/a	n/a
2	ARID3A	chr13:110439189-110439250	K562	blood:	n/a	n/a
3	ATF1	chr13:110425676-110425963	K562	blood:	n/a	n/a
4	ATF3	chr13:110425616-110425940	K562	blood:	n/a	n/a
5	BACH1	chr13:110443178-110443554	K562	blood:	n/a	n/a
6	BACH1	chr13:110439162-110439355	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr13:110436949-110437136	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr13:110439610-110439935	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr13:110437536-110437689	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr13:110438037-110438193	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr13:110444816-110445103	GM12878	blood:	n/a	n/a
12	BHLHE40	chr13:110438833-110439061	GM12878	blood:	n/a	n/a
13	BHLHE40	chr13:110430608-110430953	K562	blood:	n/a	n/a
14	BHLHE40	chr13:110438776-110439348	K562	blood:	n/a	n/a
15	BHLHE40	chr13:110443585-110444009	K562	blood:	n/a	n/a
16	BHLHE40	chr13:110443862-110443866	GM12878	blood:	n/a	n/a
17	BRCA1	chr13:110443173-110444063	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr13:110432478-110433039	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr13:110434393-110434406	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr13:110438824-110439391	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr13:110437026-110437199	Hela-S3	cervix:	n/a	n/a
22	CBX3	chr13:110438770-110439071	K562	blood:	n/a	n/a
23	CBX3	chr13:110430390-110430680	K562	blood:	n/a	n/a
24	CBX3	chr13:110430306-110430919	HCT-116	colon:	n/a	n/a
25	CCNT2	chr13:110443678-110443939	K562	blood:	n/a	n/a
26	CCNT2	chr13:110438073-110440307	K562	blood:	n/a	chr13:110440103-110440112 chr13:110439148-110439157 chr13:110439278-110439287
27	CEBPB	chr13:110442524-110442786	IMR90	lung:	n/a	n/a
28	CEBPB	chr13:110441297-110441305	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr13:110447322-110447693	Hela-S3	cervix:	n/a	chr13:110447385-110447396
30	CEBPB	chr13:110438821-110439107	IMR90	lung:	n/a	n/a
31	CEBPB	chr13:110443153-110444063	Hela-S3	cervix:	n/a	chr13:110443334-110443345
32	CEBPB	chr13:110447287-110447530	IMR90	lung:	n/a	chr13:110447385-110447396
33	CEBPB	chr13:110444394-110444701	K562	blood:	n/a	chr13:110444584-110444595 chr13:110444546-110444559 chr13:110444584-110444595
34	CEBPB	chr13:110447267-110447550	HepG2	liver:	n/a	chr13:110447385-110447396
35	CEBPB	chr13:110443635-110443954	K562	blood:	n/a	n/a
36	CEBPB	chr13:110438162-110438328	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr13:110439589-110439732	K562	blood:	n/a	n/a
38	CEBPB	chr13:110447262-110447751	MCF-7	breast:	n/a	chr13:110447385-110447396
39	CEBPB	chr13:110443243-110443442	HepG2	liver:	n/a	chr13:110443334-110443345
40	CEBPB	chr13:110443571-110444030	A549	lung:	n/a	n/a
41	CEBPB	chr13:110439228-110439244	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr13:110447318-110447794	MCF-7	breast:	n/a	chr13:110447385-110447396
43	CEBPB	chr13:110438769-110439370	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr13:110442469-110442801	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr13:110442516-110442781	A549	lung:	n/a	n/a
46	CEBPB	chr13:110436946-110437196	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr13:110443186-110443529	A549	lung:	n/a	chr13:110443334-110443345
48	CEBPB	chr13:110438849-110439087	K562	blood:	n/a	n/a
49	CEBPB	chr13:110438843-110439089	A549	lung:	n/a	n/a
50	CEBPB	chr13:110447316-110447549	A549	lung:	n/a	chr13:110447385-110447396

(count:2142 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:110439006-110439056	ProgFib	skin:	n/a
2	chr13:110432220-110432270	T-47D	breast:	n/a
3	chr13:110432935-110432985	Hela-S3	cervix:	n/a
4	chr13:110425835-110425885	AG09309	skin:	n/a
5	chr13:110435424-110435474	RPTEC	kidney:	n/a
6	chr13:110437759-110437809	AG09309	skin:	n/a
7	chr13:110425835-110425885	NHDF-neo	bronchial:	n/a
8	chr13:110439006-110439056	ProgFib	skin:	n/a
9	chr13:110432220-110432270	T-47D	breast:	n/a
10	chr13:110432935-110432985	Hela-S3	cervix:	n/a
11	chr13:110425835-110425885	AG09309	skin:	n/a
12	chr13:110435424-110435474	RPTEC	kidney:	n/a
13	chr13:110437759-110437809	AG09309	skin:	n/a
14	chr13:110425835-110425885	NHDF-neo	bronchial:	n/a
15	chr13:110424686-110424736	AG04450	lung:	fetal
16	chr13:110434682-110434732	HRCEpiC	kidney:	n/a
17	chr13:110425835-110425885	GM19239	blood:	n/a
18	chr13:110436780-110436830	SKMC	muscle:	n/a
19	chr13:110438937-110438987	HRE	kidney:	n/a
20	chr13:110439004-110439054	RPTEC	kidney:	n/a
21	chr13:110443740-110443790	K562	blood:	n/a
22	chr13:110437561-110437611	HNPCEpiC	eye:	n/a
23	chr13:110443740-110443790	NB4	blood:	n/a
24	chr13:110433636-110433686	H1-hESC	embryonic stem cell:	embryo
25	chr13:110437561-110437611	HMEC	breast:	n/a
26	chr13:110440179-110440229	MCF-7	breast:	n/a
27	chr13:110439453-110439503	HCF	heart:	n/a
28	chr13:110434682-110434732	PrEC	prostate:	n/a
29	chr13:110440175-110440225	GM06990	blood:	n/a
30	chr13:110424782-110424832	ECC-1	luminal epithelium:	n/a
31	chr13:110438578-110438628	PrEC	prostate:	n/a
32	chr13:110436780-110436830	HAEpiC	amniotic membrane:	n/a
33	chr13:110425835-110425885	NH-A	brain:	n/a
34	chr13:110443740-110443790	SK-N-MC	brain:	n/a
35	chr13:110440175-110440225	PANC-1	pancreas:	n/a
36	chr13:110424497-110424547	HIPEpiC	eye:	n/a
37	chr13:110439453-110439503	NHBE	bronchial:	n/a
38	chr13:110434467-110434517	NHDF-neo	bronchial:	n/a
39	chr13:110436111-110436161	SK-N-MC	brain:	n/a
40	chr13:110437561-110437611	HPAEpiC	pulmonary alveolar:	n/a
41	chr13:110436740-110436790	T-47D	breast:	n/a
42	chr13:110437093-110437143	RPTEC	kidney:	n/a
43	chr13:110431691-110431741	HepG2	liver:	n/a
44	chr13:110439006-110439056	SKMC	muscle:	n/a
45	chr13:110434467-110434517	GM12892	blood:	n/a
46	chr13:110424497-110424547	Jurkat	blood:	n/a
47	chr13:110436111-110436161	HRE	kidney:	n/a
48	chr13:110439234-110439284	HRCEpiC	kidney:	n/a
49	chr13:110438906-110438956	PrEC	prostate:	n/a
50	chr13:110443740-110443790	AG09319	gingival:	n/a

(count:56 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr13:110403771..110406116-chr13:110433660..110436383,2	K562	blood:
2	chr13:110443809..110446667-chr13:110447479..110449756,2	K562	blood:
3	chr13:110445785..110447746-chr13:110765342..110767976,2	MCF-7	breast:
4	chr13:110079830..110080650-chr13:110436980..110437762,2	MCF-7	breast:
5	chr13:52026999..52027561-chr13:110438389..110438889,2	NB4	blood:
6	chr13:110372327..110374107-chr13:110434766..110436742,2	K562	blood:
7	chr13:110421522..110423213-chr13:110437049..110440164,3	K562	blood:
8	chr13:110438627..110439624-chr2:32502857..32503409,2	NB4	blood:
9	chr13:109797639..109798548-chr13:110436659..110437260,3	MCF-7	breast:
10	chr13:110446043..110447587-chr13:110455015..110457725,2	MCF-7	breast:
11	chr13:110439033..110439968-chr7:104653218..104653931,2	NB4	blood:
12	chr13:110438522..110439383-chr7:23221250..23222004,2	NB4	blood:
13	chr13:110367353..110370316-chr13:110433831..110435383,2	K562	blood:
14	chr13:110437956..110438456-chr2:100106242..100106983,2	K562	blood:
15	chr13:110387460..110391261-chr13:110433185..110436412,3	K562	blood:
16	chr13:110443161..110443801-chr7:92076313..92077051,2	NB4	blood:
17	chr13:110438443..110438962-chr16:2285162..2286129,2	NB4	blood:
18	chr13:110355569..110358710-chr13:110439541..110442319,3	MCF-7	breast:
19	chr13:110431371..110432927-chr13:111365497..111367425,2	K562	blood:
20	chr13:109611837..109614642-chr13:110445728..110448181,2	MCF-7	breast:
21	chr13:110395852..110397862-chr13:110423883..110426288,2	K562	blood:
22	chr13:110173341..110174851-chr13:110433335..110435967,2	MCF-7	breast:
23	chr13:109797385..109798328-chr13:110443580..110444081,2	MCF-7	breast:
24	chr13:110436751..110439195-chr13:111365292..111367804,2	K562	blood:
25	chr13:110308109..110310593-chr13:110433626..110436596,2	K562	blood:
26	chr13:110433484..110434398-chr6:26157776..26158704,2	Hela-S3	cervix:
27	chr13:21347448..21348138-chr13:110438450..110439192,2	NB4	blood:
28	chr13:110437769..110438360-chr13:111365491..111366397,2	NB4	blood:
29	chr13:110437931..110439923-chr13:110442337..110443965,2	MCF-7	breast:
30	chr13:110359448..110362939-chr13:110431472..110434391,4	K562	blood:
31	chr13:110372207..110373827-chr13:110434766..110436789,2	K562	blood:
32	chr13:110348737..110350886-chr13:110432945..110435656,2	K562	blood:
33	chr13:110443809..110446667-chr13:110447479..110449756,2	K562	blood:
34	chr13:110439408..110440218-chr17:26368504..26369181,2	Hela-S3	cervix:
35	chr13:110436747..110437632-chr2:157188777..157189594,2	Hela-S3	cervix:
36	chr13:110262551..110263536-chr13:110436991..110438083,3	MCF-7	breast:
37	chr13:110347663..110350324-chr13:110443673..110445306,2	K562	blood:
38	chr13:110414170..110416819-chr13:110432906..110435378,2	K562	blood:
39	chr13:110438490..110439006-chr6:26216450..26217232,2	Hela-S3	cervix:
40	chr13:110430383..110434613-chr13:110438487..110441138,4	MCF-7	breast:
41	chr1:145382581..145383105-chr13:110438820..110439782,2	Hela-S3	cervix:
42	chr13:110404473..110407455-chr13:110429957..110432658,3	K562	blood:
43	chr13:110435545..110437326-chr13:110470827..110473616,2	K562	blood:
44	chr13:110438834..110439674-chr3:197686852..197687479,2	Hela-S3	cervix:
45	chr12:52448921..52449564-chr13:110433424..110434327,2	Hela-S3	cervix:
46	chr13:110406850..110408586-chr13:110434989..110436543,2	K562	blood:
47	chr13:110443953..110447179-chr13:110758507..110762069,3	MCF-7	breast:
48	chr13:110438846..110439621-chr8:125485961..125486658,2	Hela-S3	cervix:
49	chr13:110436751..110439259-chr13:111364404..111367804,3	K562	blood:
50	chr13:110336875..110339890-chr13:110432636..110435480,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COL4A2-3	chr13:110439457-110442761	NONHSAT035120
2	lnc-COL4A2-3	chr13:110440328-110440912	NONHSAT035119
3	lnc-COL4A2-3	chr13:110433655-110433753	NONHSAT035119
4	lnc-COL4A2-3	chr13:110439709-110439792	NONHSAT035121

No data

Variant related genes	Relation type
IRS2	TF binding region
IRS2	CpG island
ENSG00000186792	chromatin interactions
ENSG00000157259	chromatin interactions
ENSG00000119820	chromatin interactions
ENSG00000185621	chromatin interactions
ENSG00000136243	chromatin interactions
ENSG00000187990	chromatin interactions
ENSG00000243477	chromatin interactions
ENSG00000225727	chromatin interactions
ENSG00000228393	chromatin interactions
ENSG00000245149	chromatin interactions
ENSG00000201558	chromatin interactions
ENSG00000150456	chromatin interactions
ENSG00000135945	chromatin interactions
ENSG00000255813	chromatin interactions
ENSG00000143977	chromatin interactions
ENSG00000153487	chromatin interactions
ENSG00000236778	chromatin interactions
ENSG00000102786	chromatin interactions
ENSG00000134905	chromatin interactions
ENSG00000123358	chromatin interactions
ENSG00000168274	chromatin interactions
ENSG00000102804	chromatin interactions
ENSG00000158373	chromatin interactions
ENSG00000153234	chromatin interactions
ENSG00000167968	chromatin interactions
ENSG00000185950	chromatin interactions
ENSG00000114473	chromatin interactions
ENSG00000087095	chromatin interactions

Extended variants
information (count: 843 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:843 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530237210	chr13:110423191-110423192	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs549816803	chr13:110423197-110423198	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs140458037	chr13:110423207-110423208	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs144146086	chr13:110423349-110423350	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs191586726	chr13:110423361-110423362	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs200596490	chr13:110423409-110423410	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs565967588	chr13:110423494-110423495	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs576795044	chr13:110423562-110423563	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs183740720	chr13:110423591-110423592	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs61962698	chr13:110423612-110423613	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs187927157	chr13:110423640-110423641	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs574168241	chr13:110423650-110423651	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs543093178	chr13:110423721-110423722	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs9559647	chr13:110423768-110423769	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs192210497	chr13:110423776-110423777	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs9559648	chr13:110423795-110423796	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs535831450	chr13:110423859-110423860	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs528218772	chr13:110423899-110423900	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs545832853	chr13:110423962-110423963	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs146789225	chr13:110423972-110423973	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs77631819	chr13:110424012-110424013	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs185689746	chr13:110424019-110424020	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs549142964	chr13:110424042-110424043	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs148916084	chr13:110424058-110424059	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs374517691	chr13:110424061-110424062	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs7323191	chr13:110424075-110424076	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs190213532	chr13:110424110-110424111	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs550287164	chr13:110424141-110424142	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs563851346	chr13:110424175-110424176	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs532355986	chr13:110424238-110424239	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs552551428	chr13:110424243-110424244	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs565930025	chr13:110424256-110424257	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs374267627	chr13:110424275-110424276	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs182137921	chr13:110424302-110424303	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs143720574	chr13:110424326-110424327	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs572125956	chr13:110424345-110424346	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs534885736	chr13:110424388-110424389	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs118088366	chr13:110424394-110424395	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs536887416	chr13:110424419-110424420	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs556637529	chr13:110424497-110424498	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs4547213	chr13:110424498-110424499	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs199910352	chr13:110424527-110424528	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs539026856	chr13:110424549-110424550	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs148103910	chr13:110424569-110424570	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs184513223	chr13:110424590-110424591	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs537248638	chr13:110424686-110424687	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
47	rs557018712	chr13:110424700-110424701	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
48	rs188795713	chr13:110424713-110424714	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
49	rs140981403	chr13:110424720-110424721	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
50	rs573697458	chr13:110424833-110424834	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Cancer	20164919	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Myoepithelioma	18604193	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	18632612	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
Gastric cancer	17908304	CNVD
Liposarcoma	21253554	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Breast cancer	22032731	CNVD
Wilms tumour	21544195	CNVD
Thyroid cancer	19087340	CNVD
abortions and stillbirths	19751515	CNVD
Acute myeloid leukemia	21251322	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Burkitt''s lymphoma	20823134	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Burkitt''s lymphoma	19759907	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Medulloblastoma	19270706	CNVD
Mental retardation	17124404	CNVD
Leukemia	18688285	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21858162	CNVD
Melanoma	17363583	CNVD
Developmental delay	21147756	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	21645411	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Breast cancer	16608533	CNVD
Glioblastoma multiforme	22286061	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
abnormal development	18461090	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Malignant glioma	17146433	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Glioma	17123091	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	20409316	CNVD
Central neurocytomas	17123091	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Neurocytoma	17123091	CNVD
Mantle cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1926 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:110397000-110428800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
2	chr13:110397200-110430400	Weak transcription	NHLF	lung
3	chr13:110401800-110430800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr13:110403200-110430600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr13:110406200-110429400	Weak transcription	Primary B cells from cord blood	blood
6	chr13:110407400-110423400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr13:110408600-110423800	Weak transcription	Placenta	Placenta
8	chr13:110408600-110424400	Weak transcription	Spleen	Spleen
9	chr13:110408600-110430400	Weak transcription	Colonic Mucosa	Colon
10	chr13:110408800-110423600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr13:110409000-110431200	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr13:110409400-110429800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
13	chr13:110409400-110430200	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr13:110413400-110430400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr13:110413600-110430800	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr13:110414000-110424400	Weak transcription	Pancreatic Islets	Pancreatic Islet
17	chr13:110414400-110428800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr13:110415000-110428800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr13:110416000-110430800	Weak transcription	Fetal Kidney	kidney
20	chr13:110417000-110432400	Weak transcription	H1 Cell Line	embryonic stem cell
21	chr13:110417200-110424600	Weak transcription	HUES48 Cell Line	embryonic stem cell
22	chr13:110417200-110430400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr13:110417200-110431600	Weak transcription	Fetal Muscle Leg	muscle
24	chr13:110417400-110425600	Weak transcription	NH-A	brain
25	chr13:110417400-110429400	Weak transcription	Small Intestine	intestine
26	chr13:110417400-110430200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chr13:110417600-110424200	Weak transcription	Brain Germinal Matrix	brain
28	chr13:110417600-110430400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr13:110417600-110430400	Weak transcription	Thymus	Thymus
30	chr13:110417600-110430600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
31	chr13:110417800-110428800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
32	chr13:110417800-110428800	Weak transcription	Placenta Amnion	Placenta Amnion
33	chr13:110417800-110429400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
34	chr13:110417800-110430200	Weak transcription	Fetal Thymus	thymus
35	chr13:110418800-110425000	Enhancers	Brain Substantia Nigra	brain
36	chr13:110419000-110424200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr13:110419000-110424800	Enhancers	Brain Angular Gyrus	brain
38	chr13:110419000-110424800	Enhancers	Brain Inferior Temporal Lobe	brain
39	chr13:110419000-110425000	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
40	chr13:110419200-110423200	Genic enhancers	Adipose Nuclei	Adipose
41	chr13:110419200-110424400	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr13:110419200-110425000	Strong transcription	HSMMtube	muscle
43	chr13:110419200-110428000	Strong transcription	Monocytes-CD14+_RO01746	blood
44	chr13:110419600-110425000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr13:110419600-110428600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
46	chr13:110419600-110429400	Weak transcription	Primary T helper cells fromperipheralblood	blood
47	chr13:110419600-110429400	Weak transcription	Fetal Brain Male	brain
48	chr13:110419600-110429600	Weak transcription	Duodenum Smooth Muscle	Duodenum
49	chr13:110419800-110424400	Weak transcription	Esophagus	oesophagus
50	chr13:110419800-110424400	Weak transcription	Psoas Muscle	Psoas

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