Variant report

Variant	nsv826794
Chromosome Location	chr13:110424916-110448628
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1547)
CpG islands
(count:1958)
Chromatin interactive
region (count:55)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1547 , 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	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	chr13:110436949-110437136	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr13:110439162-110439355	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr13:110438037-110438193	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr13:110443178-110443554	K562	blood:	n/a	n/a
9	BACH1	chr13:110437536-110437689	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr13:110439610-110439935	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr13:110444816-110445103	GM12878	blood:	n/a	n/a
12	BHLHE40	chr13:110443585-110444009	K562	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	chr13:110438833-110439061	GM12878	blood:	n/a	n/a
16	BHLHE40	chr13:110443862-110443866	GM12878	blood:	n/a	n/a
17	BRCA1	chr13:110434393-110434406	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr13:110443173-110444063	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr13:110438824-110439391	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr13:110432478-110433039	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr13:110437026-110437199	Hela-S3	cervix:	n/a	n/a
22	CBX3	chr13:110430306-110430919	HCT-116	colon:	n/a	n/a
23	CBX3	chr13:110430390-110430680	K562	blood:	n/a	n/a
24	CBX3	chr13:110438770-110439071	K562	blood:	n/a	n/a
25	CCNT2	chr13:110438073-110440307	K562	blood:	n/a	chr13:110440103-110440112 chr13:110439148-110439157 chr13:110439278-110439287
26	CCNT2	chr13:110443678-110443939	K562	blood:	n/a	n/a
27	CEBPB	chr13:110438162-110438328	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr13:110443186-110443529	A549	lung:	n/a	chr13:110443334-110443345
29	CEBPB	chr13:110439228-110439244	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr13:110444394-110444701	K562	blood:	n/a	chr13:110444584-110444595 chr13:110444546-110444559 chr13:110444584-110444595
31	CEBPB	chr13:110442524-110442786	IMR90	lung:	n/a	n/a
32	CEBPB	chr13:110447322-110447693	Hela-S3	cervix:	n/a	chr13:110447385-110447396
33	CEBPB	chr13:110438849-110439087	K562	blood:	n/a	n/a
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	chr13:110436946-110437196	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr13:110438821-110439107	IMR90	lung:	n/a	n/a
38	CEBPB	chr13:110439589-110439732	K562	blood:	n/a	n/a
39	CEBPB	chr13:110447262-110447751	MCF-7	breast:	n/a	chr13:110447385-110447396
40	CEBPB	chr13:110443571-110444030	A549	lung:	n/a	n/a
41	CEBPB	chr13:110447316-110447549	A549	lung:	n/a	chr13:110447385-110447396
42	CEBPB	chr13:110447287-110447530	IMR90	lung:	n/a	chr13:110447385-110447396
43	CEBPB	chr13:110438769-110439370	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr13:110442516-110442781	A549	lung:	n/a	n/a
45	CEBPB	chr13:110447318-110447794	MCF-7	breast:	n/a	chr13:110447385-110447396
46	CEBPB	chr13:110442469-110442801	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr13:110441297-110441305	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr13:110443243-110443442	HepG2	liver:	n/a	chr13:110443334-110443345
49	CEBPB	chr13:110443153-110444063	Hela-S3	cervix:	n/a	chr13:110443334-110443345
50	CEBPB	chr13:110443246-110443990	K562	blood:	n/a	chr13:110443334-110443345

(count:1958 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:110432220-110432270	GM12892	blood:	n/a
2	chr13:110438288-110438338	HRPEpiC	eye:	n/a
3	chr13:110438288-110438338	AG09319	gingival:	n/a
4	chr13:110436780-110436830	HMEC	breast:	n/a
5	chr13:110440352-110440402	HMEC	breast:	n/a
6	chr13:110438256-110438306	HAEpiC	amniotic membrane:	n/a
7	chr13:110432220-110432270	GM12892	blood:	n/a
8	chr13:110438288-110438338	HRPEpiC	eye:	n/a
9	chr13:110438288-110438338	AG09319	gingival:	n/a
10	chr13:110436780-110436830	HMEC	breast:	n/a
11	chr13:110440352-110440402	HMEC	breast:	n/a
12	chr13:110438256-110438306	HAEpiC	amniotic membrane:	n/a
13	chr13:110432220-110432270	HMEC	breast:	n/a
14	chr13:110437093-110437143	HPAEpiC	pulmonary alveolar:	n/a
15	chr13:110438288-110438338	HRE	kidney:	n/a
16	chr13:110438906-110438956	NHBE	bronchial:	n/a
17	chr13:110438935-110438985	BJ	skin:	n/a
18	chr13:110438937-110438987	AG10803	skin:	n/a
19	chr13:110437759-110437809	BE2_C	brain:	n/a
20	chr13:110433784-110433834	K562	blood:	n/a
21	chr13:110434467-110434517	AG10803	skin:	n/a
22	chr13:110431612-110431662	HepG2	liver:	n/a
23	chr13:110438288-110438338	Hepatocyte	liver:	n/a
24	chr13:110425835-110425885	IMR90	lung:	fetal
25	chr13:110440352-110440402	IMR90	lung:	fetal
26	chr13:110431612-110431662	HEEpiC	esophagus:	n/a
27	chr13:110440179-110440229	U87	brain:	n/a
28	chr13:110439006-110439056	AG10803	skin:	n/a
29	chr13:110438288-110438338	CMK	blood:	n/a
30	chr13:110436740-110436790	GM12878	blood:	n/a
31	chr13:110436111-110436161	PANC-1	pancreas:	n/a
32	chr13:110431691-110431741	HCPEpiC	choroid plexus:	n/a
33	chr13:110434016-110434066	PrEC	prostate:	n/a
34	chr13:110438937-110438987	ECC-1	luminal epithelium:	n/a
35	chr13:110443740-110443790	SK-N-SH_RA	brain:	n/a
36	chr13:110439453-110439503	AG09309	skin:	n/a
37	chr13:110438256-110438306	HL-60	blood:	n/a
38	chr13:110439453-110439503	Caco-2	colon:	n/a
39	chr13:110437093-110437143	SAEC	small airway:	n/a
40	chr13:110433636-110433686	IMR90	lung:	fetal
41	chr13:110438935-110438985	AG09309	skin:	n/a
42	chr13:110434467-110434517	PrEC	prostate:	n/a
43	chr13:110438906-110438956	U87	brain:	n/a
44	chr13:110437093-110437143	HNPCEpiC	eye:	n/a
45	chr13:110434016-110434066	HPAEpiC	pulmonary alveolar:	n/a
46	chr13:110438906-110438956	HUVEC	blood vessel:	n/a
47	chr13:110438937-110438987	GM12878	blood:	n/a
48	chr13:110433636-110433686	HUVEC	blood vessel:	n/a
49	chr13:110440175-110440225	SK-N-SH_RA	brain:	n/a
50	chr13:110438578-110438628	K562	blood:	n/a

(count:55 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr13:110433484..110434398-chr6:26157776..26158704,2	Hela-S3	cervix:
2	chr13:110438846..110439621-chr8:125485961..125486658,2	Hela-S3	cervix:
3	chr13:110437931..110439923-chr13:110442337..110443965,2	MCF-7	breast:
4	chr13:110404473..110407455-chr13:110429957..110432658,3	K562	blood:
5	chr1:145382581..145383105-chr13:110438820..110439782,2	Hela-S3	cervix:
6	chr13:45010548..45011431-chr13:110438404..110439086,2	Hela-S3	cervix:
7	chr13:110438443..110438962-chr16:2285162..2286129,2	NB4	blood:
8	chr13:110443809..110446667-chr13:110447479..110449756,2	K562	blood:
9	chr13:110443809..110446667-chr13:110447479..110449756,2	K562	blood:
10	chr13:110437609..110438511-chr2:70520669..70521396,2	Hela-S3	cervix:
11	chr13:110438834..110439674-chr3:197686852..197687479,2	Hela-S3	cervix:
12	chr13:110372327..110374107-chr13:110434766..110436742,2	K562	blood:
13	chr13:110439033..110439968-chr7:104653218..104653931,2	NB4	blood:
14	chr13:110347663..110350324-chr13:110443673..110445306,2	K562	blood:
15	chr13:110367353..110370316-chr13:110433831..110435383,2	K562	blood:
16	chr13:110443953..110447179-chr13:110758507..110762069,3	MCF-7	breast:
17	chr13:110436751..110439195-chr13:111365292..111367804,2	K562	blood:
18	chr13:109611837..109614642-chr13:110445728..110448181,2	MCF-7	breast:
19	chr13:110439300..110440162-chr3:50336111..50336962,2	Hela-S3	cervix:
20	chr13:52026999..52027561-chr13:110438389..110438889,2	NB4	blood:
21	chr13:110445785..110447746-chr13:110765342..110767976,2	MCF-7	breast:
22	chr13:110431371..110432927-chr13:111365497..111367425,2	K562	blood:
23	chr13:110372207..110373827-chr13:110434766..110436789,2	K562	blood:
24	chr13:21347448..21348138-chr13:110438450..110439192,2	NB4	blood:
25	chr13:110406850..110408586-chr13:110434989..110436543,2	K562	blood:
26	chr13:110173341..110174851-chr13:110433335..110435967,2	MCF-7	breast:
27	chr13:110438522..110439383-chr7:23221250..23222004,2	NB4	blood:
28	chr13:110438627..110439624-chr2:32502857..32503409,2	NB4	blood:
29	chr13:110336875..110339890-chr13:110432636..110435480,3	K562	blood:
30	chr13:110079830..110080650-chr13:110436980..110437762,2	MCF-7	breast:
31	chr13:109797639..109798548-chr13:110436659..110437260,3	MCF-7	breast:
32	chr13:110443161..110443801-chr7:92076313..92077051,2	NB4	blood:
33	chr13:109797385..109798328-chr13:110443580..110444081,2	MCF-7	breast:
34	chr13:110436751..110439259-chr13:111364404..111367804,3	K562	blood:
35	chr13:110446043..110447587-chr13:110455015..110457725,2	MCF-7	breast:
36	chr12:52448921..52449564-chr13:110433424..110434327,2	Hela-S3	cervix:
37	chr13:110436747..110437632-chr2:157188777..157189594,2	Hela-S3	cervix:
38	chr13:110397775..110399986-chr13:110436393..110438798,2	MCF-7	breast:
39	chr13:110430383..110434613-chr13:110438487..110441138,4	MCF-7	breast:
40	chr13:110438490..110439006-chr6:26216450..26217232,2	Hela-S3	cervix:
41	chr13:110387460..110391261-chr13:110433185..110436412,3	K562	blood:
42	chr13:110403771..110406116-chr13:110433660..110436383,2	K562	blood:
43	chr13:110348737..110350886-chr13:110432945..110435656,2	K562	blood:
44	chr13:110437769..110438360-chr13:111365491..111366397,2	NB4	blood:
45	chr13:110262551..110263536-chr13:110436991..110438083,3	MCF-7	breast:
46	chr13:110439408..110440218-chr17:26368504..26369181,2	Hela-S3	cervix:
47	chr13:110359448..110362939-chr13:110431472..110434391,4	K562	blood:
48	chr13:110414170..110416819-chr13:110432906..110435378,2	K562	blood:
49	chr13:110336875..110340182-chr13:110433980..110437911,3	K562	blood:
50	chr13:110437956..110438456-chr2:100106242..100106983,2	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	chr13:110439709-110439792	NONHSAT035121
4	lnc-COL4A2-3	chr13:110433655-110433753	NONHSAT035119

No data

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

Extended variants
information (count: 788 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:788 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs34939651	chr13:110424933-110424934	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs35925829	chr13:110424939-110424940	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs559679675	chr13:110424956-110424957	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs528502584	chr13:110424959-110424960	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs60925199	chr13:110424972-110424973	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs34886741	chr13:110425035-110425036	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs540960894	chr13:110425036-110425037	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs57951642	chr13:110425053-110425054	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs181210452	chr13:110425066-110425067	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs12584130	chr13:110425076-110425077	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs59962460	chr13:110425082-110425083	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs564030777	chr13:110425083-110425084	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs111379291	chr13:110425103-110425104	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs533345623	chr13:110425104-110425105	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs570421016	chr13:110425106-110425107	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs12584131	chr13:110425112-110425113	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs539496358	chr13:110425119-110425120	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs9559649	chr13:110425131-110425132	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs572786559	chr13:110425135-110425136	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs535489013	chr13:110425146-110425147	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs555255052	chr13:110425147-110425148	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs113046169	chr13:110425168-110425169	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs575219431	chr13:110425181-110425182	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs543998741	chr13:110425188-110425189	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs557553961	chr13:110425197-110425198	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs12584954	chr13:110425219-110425220	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs549476600	chr13:110425244-110425245	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs187429885	chr13:110425251-110425252	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs559633506	chr13:110425278-110425279	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs528465939	chr13:110425321-110425322	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs111838998	chr13:110425334-110425335	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs368245538	chr13:110425360-110425361	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs541828356	chr13:110425367-110425368	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs149795449	chr13:110425484-110425485	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs564279840	chr13:110425519-110425520	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs114942409	chr13:110425561-110425562	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs550626792	chr13:110425689-110425690	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
38	rs9559650	chr13:110425692-110425693	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs370046434	chr13:110425734-110425735	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
40	rs533017998	chr13:110425751-110425752	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
41	rs112982139	chr13:110425757-110425758	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
42	rs546669961	chr13:110425761-110425762	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
43	rs566574665	chr13:110425778-110425779	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
44	rs535399953	chr13:110425787-110425788	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
45	rs555416817	chr13:110425802-110425803	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
46	rs568742026	chr13:110425809-110425810	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
47	rs537719493	chr13:110425811-110425812	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
48	rs557404800	chr13:110425836-110425837	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
49	rs149448722	chr13:110425939-110425940	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
50	rs56920445	chr13:110425948-110425949	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:92)

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

Chromatin state (count:1837 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

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	chr13:110408600-110430400	Weak transcription	Colonic Mucosa	Colon
7	chr13:110409000-110431200	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr13:110409400-110429800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
9	chr13:110409400-110430200	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr13:110413400-110430400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr13:110413600-110430800	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr13:110414400-110428800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr13:110415000-110428800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr13:110416000-110430800	Weak transcription	Fetal Kidney	kidney
15	chr13:110417000-110432400	Weak transcription	H1 Cell Line	embryonic stem cell
16	chr13:110417200-110430400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr13:110417200-110431600	Weak transcription	Fetal Muscle Leg	muscle
18	chr13:110417400-110425600	Weak transcription	NH-A	brain
19	chr13:110417400-110429400	Weak transcription	Small Intestine	intestine
20	chr13:110417400-110430200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
21	chr13:110417600-110430400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr13:110417600-110430400	Weak transcription	Thymus	Thymus
23	chr13:110417600-110430600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
24	chr13:110417800-110428800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
25	chr13:110417800-110428800	Weak transcription	Placenta Amnion	Placenta Amnion
26	chr13:110417800-110429400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
27	chr13:110417800-110430200	Weak transcription	Fetal Thymus	thymus
28	chr13:110418800-110425000	Enhancers	Brain Substantia Nigra	brain
29	chr13:110419000-110425000	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr13:110419200-110425000	Strong transcription	HSMMtube	muscle
31	chr13:110419200-110428000	Strong transcription	Monocytes-CD14+_RO01746	blood
32	chr13:110419600-110425000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr13:110419600-110428600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
34	chr13:110419600-110429400	Weak transcription	Primary T helper cells fromperipheralblood	blood
35	chr13:110419600-110429400	Weak transcription	Fetal Brain Male	brain
36	chr13:110419600-110429600	Weak transcription	Duodenum Smooth Muscle	Duodenum
37	chr13:110420000-110425800	Strong transcription	Muscle Satellite Cultured Cells	--
38	chr13:110420000-110429000	Weak transcription	Fetal Brain Female	brain
39	chr13:110420200-110425400	Strong transcription	Fetal Intestine Small	intestine
40	chr13:110420400-110429200	Weak transcription	Right Atrium	heart
41	chr13:110420600-110425000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
42	chr13:110420800-110425000	Strong transcription	Primary monocytes fromperipheralblood	blood
43	chr13:110420800-110428000	Strong transcription	HSMM	muscle
44	chr13:110420800-110429000	Weak transcription	Skeletal Muscle Male	skeletal muscle
45	chr13:110421400-110428800	Weak transcription	Primary T helper cells PMA-I stimulated	--
46	chr13:110421600-110425000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr13:110421600-110426200	Strong transcription	Primary neutrophils fromperipheralblood	blood
48	chr13:110422000-110427000	Strong transcription	Cortex derived primary cultured neurospheres	brain
49	chr13:110422000-110429000	Weak transcription	Skeletal Muscle Female	skeletal muscle
50	chr13:110422400-110425000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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