Variant report

Variant	nsv6550
Chromosome Location	chr9:71714144-71760048
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1121)
CpG islands
(count:615)
Chromatin interactive
region (count:52)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1121 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:71746529-71747015	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:71719221-71720293	HepG2	liver:	n/a	chr9:71719768-71719784 chr9:71719315-71719331
3	ARID3A	chr9:71735292-71735927	HepG2	liver:	n/a	n/a
4	ATF2	chr9:71735106-71735934	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr9:71737258-71738069	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr9:71735153-71736138	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr9:71737566-71738148	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr9:71737585-71738101	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr9:71735251-71735859	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL11A	chr9:71735558-71735835	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCL11A	chr9:71735576-71735811	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCLAF1	chr9:71736571-71737127	GM12878	blood:	n/a	n/a
13	BHLHE40	chr9:71720051-71720348	HepG2	liver:	n/a	n/a
14	BHLHE40	chr9:71737647-71738054	HepG2	liver:	n/a	n/a
15	BHLHE40	chr9:71745840-71746183	K562	blood:	n/a	n/a
16	BRCA1	chr9:71735672-71735688	HepG2	liver:	n/a	n/a
17	BRCA1	chr9:71736719-71737059	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr9:71720260-71720323	HepG2	liver:	n/a	n/a
19	BRCA1	chr9:71736246-71736410	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr9:71735568-71735826	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr9:71745863-71746291	IMR90	lung:	n/a	chr9:71746066-71746077
22	CEBPB	chr9:71737217-71738032	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr9:71730525-71730741	IMR90	lung:	n/a	n/a
24	CEBPB	chr9:71746518-71747166	HepG2	liver:	n/a	chr9:71746738-71746751 chr9:71746738-71746749
25	CEBPB	chr9:71735476-71735947	ECC-1	luminal epithelium:	n/a	n/a
26	CEBPB	chr9:71717820-71717911	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr9:71730464-71730692	A549	lung:	n/a	n/a
28	CEBPB	chr9:71746600-71746934	Hela-S3	cervix:	n/a	chr9:71746738-71746751 chr9:71746738-71746749
29	CEBPB	chr9:71746546-71747106	IMR90	lung:	n/a	chr9:71746738-71746751 chr9:71746738-71746749
30	CEBPB	chr9:71746509-71746964	MCF-7	breast:	n/a	chr9:71746738-71746751 chr9:71746738-71746749
31	CEBPB	chr9:71746544-71747019	HepG2	liver:	n/a	chr9:71746738-71746751 chr9:71746738-71746749
32	CEBPB	chr9:71735584-71736233	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr9:71735135-71736002	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr9:71735281-71735626	HepG2	liver:	n/a	n/a
35	CEBPB	chr9:71746546-71746947	HepG2	liver:	n/a	chr9:71746738-71746751 chr9:71746738-71746749
36	CEBPB	chr9:71735281-71735937	MCF-7	breast:	n/a	n/a
37	CEBPB	chr9:71721901-71722105	IMR90	lung:	n/a	n/a
38	CEBPB	chr9:71735697-71735833	HepG2	liver:	n/a	n/a
39	CEBPB	chr9:71746576-71746897	A549	lung:	n/a	chr9:71746738-71746751 chr9:71746738-71746749
40	CEBPB	chr9:71735933-71736104	HepG2	liver:	n/a	n/a
41	CEBPB	chr9:71720003-71720246	HepG2	liver:	n/a	n/a
42	CEBPB	chr9:71746577-71746832	HepG2	liver:	n/a	chr9:71746738-71746751 chr9:71746738-71746749
43	CEBPB	chr9:71717877-71718004	K562	blood:	n/a	n/a
44	CEBPD	chr9:71735539-71735956	HepG2	liver:	n/a	n/a
45	CEBPD	chr9:71735430-71736087	HepG2	liver:	n/a	n/a
46	CHD1	chr9:71736356-71738055	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD1	chr9:71734666-71735025	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD1	chr9:71735356-71736142	H1-hESC	embryonic stem cell:	n/a	chr9:71735872-71735882 chr9:71735875-71735885
49	CHD2	chr9:71735572-71736125	HepG2	liver:	n/a	chr9:71735872-71735882 chr9:71735875-71735885
50	CHD2	chr9:71735590-71737998	Hela-S3	cervix:	n/a	chr9:71735872-71735882 chr9:71735875-71735885

(count:615 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:71732345-71732395	A549	lung:	n/a
2	chr9:71732345-71732395	GM06990	blood:	n/a
3	chr9:71735701-71735751	HRCEpiC	kidney:	n/a
4	chr9:71737204-71737254	T-47D	breast:	n/a
5	chr9:71736999-71737049	HAEpiC	amniotic membrane:	n/a
6	chr9:71732345-71732395	A549	lung:	n/a
7	chr9:71732345-71732395	GM06990	blood:	n/a
8	chr9:71735701-71735751	HRCEpiC	kidney:	n/a
9	chr9:71737204-71737254	T-47D	breast:	n/a
10	chr9:71736999-71737049	HAEpiC	amniotic membrane:	n/a
11	chr9:71735648-71735698	HPAEpiC	pulmonary alveolar:	n/a
12	chr9:71737756-71737806	CMK	blood:	n/a
13	chr9:71732345-71732395	MCF-7	breast:	n/a
14	chr9:71736854-71736904	MCF10A-Er-Src	breast:	n/a
15	chr9:71737258-71737308	AG09309	skin:	n/a
16	chr9:71736999-71737049	GM06990	blood:	n/a
17	chr9:71737258-71737308	HNPCEpiC	eye:	n/a
18	chr9:71735666-71735716	LNCaP	prostate:	n/a
19	chr9:71736409-71736459	NH-A	brain:	n/a
20	chr9:71732345-71732395	HRPEpiC	eye:	n/a
21	chr9:71737258-71737308	ProgFib	skin:	n/a
22	chr9:71736409-71736459	HL-60	blood:	n/a
23	chr9:71736999-71737049	HCT-116	colon:	n/a
24	chr9:71736999-71737049	HRCEpiC	kidney:	n/a
25	chr9:71736854-71736904	K562	blood:	n/a
26	chr9:71735666-71735716	HRPEpiC	eye:	n/a
27	chr9:71736854-71736904	AG04450	lung:	fetal
28	chr9:71736999-71737049	HCPEpiC	choroid plexus:	n/a
29	chr9:71735701-71735751	HMEC	breast:	n/a
30	chr9:71732345-71732395	RPTEC	kidney:	n/a
31	chr9:71732345-71732395	ovcar-3	ovarian:	n/a
32	chr9:71735666-71735716	HRCEpiC	kidney:	n/a
33	chr9:71735648-71735698	NB4	blood:	n/a
34	chr9:71736999-71737049	GM12878	blood:	n/a
35	chr9:71737204-71737254	H1-hESC	embryonic stem cell:	embryo
36	chr9:71736854-71736904	GM19239	blood:	n/a
37	chr9:71737756-71737806	T-47D	breast:	n/a
38	chr9:71737204-71737254	ProgFib	skin:	n/a
39	chr9:71737204-71737254	HCPEpiC	choroid plexus:	n/a
40	chr9:71736409-71736459	SK-N-MC	brain:	n/a
41	chr9:71736409-71736459	IMR90	lung:	fetal
42	chr9:71737756-71737806	GM12891	blood:	n/a
43	chr9:71735701-71735751	BJ	skin:	n/a
44	chr9:71737258-71737308	SKMC	muscle:	n/a
45	chr9:71736854-71736904	SK-N-SH_RA	brain:	n/a
46	chr9:71736409-71736459	SAEC	small airway:	n/a
47	chr9:71737756-71737806	HCM	heart:	n/a
48	chr9:71737258-71737308	HEEpiC	esophagus:	n/a
49	chr9:71737204-71737254	HCT-116	colon:	n/a
50	chr9:71736409-71736459	BJ	skin:	n/a

(count:52 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr9:71745818..71747384-chr9:71762840..71764725,2	K562	blood:
2	chr9:71704381..71705131-chr9:71714234..71715231,2	MCF-7	breast:
3	chr9:71728735..71732212-chr9:71735055..71737852,4	MCF-7	breast:
4	chr9:71726688..71731938-chr9:71734130..71739301,8	MCF-7	breast:
5	chr9:71736348..71739276-chr9:71751743..71753516,2	MCF-7	breast:
6	chr13:48611578..48612294-chr9:71736012..71736825,2	Hela-S3	cervix:
7	chr9:71649801..71651906-chr9:71729690..71731454,2	MCF-7	breast:
8	chr1:146555490..146556430-chr9:71736325..71736974,2	Hela-S3	cervix:
9	chr9:71751405..71753557-chr9:71754610..71757893,3	MCF-7	breast:
10	chr9:71696609..71699452-chr9:71736834..71738699,2	MCF-7	breast:
11	chr9:71720044..71724145-chr9:71733178..71738087,7	MCF-7	breast:
12	chr9:71745094..71746594-chr9:71762879..71765148,2	MCF-7	breast:
13	chr9:71720466..71722349-chr9:71729146..71730891,2	MCF-7	breast:
14	chr9:71751405..71753557-chr9:71754610..71757893,3	MCF-7	breast:
15	chr9:71733939..71735989-chr9:71814942..71816605,2	MCF-7	breast:
16	chr9:71743521..71745547-chr9:71821447..71823888,2	MCF-7	breast:
17	chr9:71755797..71757532-chr9:71759956..71762001,2	MCF-7	breast:
18	chr13:113241435..113242373-chr9:71735991..71736661,2	Hela-S3	cervix:
19	chr9:71733168..71738729-chr9:71786929..71793777,10	MCF-7	breast:
20	chr9:71735718..71737415-chr9:71751707..71753369,2	MCF-7	breast:
21	chr11:65666788..65667405-chr9:71737195..71738062,2	Hela-S3	cervix:
22	chr9:71733940..71739343-chr9:71741877..71748941,25	MCF-7	breast:
23	chr1:149223425..149225310-chr9:71736139..71738412,2	MCF-7	breast:
24	chr9:71680609..71683537-chr9:71732525..71735089,2	MCF-7	breast:
25	chr9:71718282..71721853-chr9:71734600..71737822,4	MCF-7	breast:
26	chr3:45017283..45018160-chr9:71735845..71736825,2	Hela-S3	cervix:
27	chr9:71734142..71739001-chr9:71788032..71795507,11	MCF-7	breast:
28	chr6:41040678..41041408-chr9:71735768..71736686,2	Hela-S3	cervix:
29	chr9:71735454..71738183-chr9:71753651..71758025,4	MCF-7	breast:
30	chr9:71735373..71738833-chr9:71764136..71766985,4	MCF-7	breast:
31	chr9:71736348..71739276-chr9:71751743..71753516,2	MCF-7	breast:
32	chr9:71649857..71652024-chr9:71744170..71747063,2	MCF-7	breast:
33	chr9:71704008..71706268-chr9:71714594..71717470,2	MCF-7	breast:
34	chr9:71730545..71732525-chr9:71797822..71800476,2	K562	blood:
35	chr3:49066502..49067181-chr9:71736337..71736850,2	Hela-S3	cervix:
36	chr9:71745166..71747792-chr9:71751582..71754371,2	K562	blood:
37	chr9:71649472..71654369-chr9:71735388..71737779,6	MCF-7	breast:
38	chr9:71727081..71728601-chr9:71737166..71739059,2	MCF-7	breast:
39	chr9:71720044..71724145-chr9:71733178..71738087,7	MCF-7	breast:
40	chr9:71758408..71761844-chr9:71769245..71771910,3	MCF-7	breast:
41	chr1:62208097..62208620-chr9:71736404..71737107,2	Hela-S3	cervix:
42	chr9:71732215..71735155-chr9:71735593..71737924,2	MCF-7	breast:
43	chr9:71727081..71728601-chr9:71737166..71739059,2	MCF-7	breast:
44	chr9:71736483..71737290-chr9:71808170..71808758,2	MCF-7	breast:
45	chr9:71720466..71722349-chr9:71729146..71730891,2	MCF-7	breast:
46	chr9:71734182..71738595-chr9:71741906..71745315,7	MCF-7	breast:
47	chr9:71755797..71757532-chr9:71759956..71762001,2	MCF-7	breast:
48	chr9:71735864..71737809-chr9:71745994..71747583,2	MCF-7	breast:
49	chr9:71743905..71746446-chr9:71805495..71808231,2	MCF-7	breast:
50	chr9:71745166..71747792-chr9:71751582..71754371,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TJP2-1	chr9:71736400-71737148	ENSG00000227410.1
2	lnc-TJP2-1	chr9:71736209-71736281	ENSG00000227410.1

No data

Variant related genes	Relation type
TJP2	TF binding region
ENSG00000270236	TF binding region
TJP2	CpG island
ENSG00000270236	CpG island
ENSG00000126216	chromatin interactions
ENSG00000136159	chromatin interactions
ENSG00000270236	chromatin interactions
ENSG00000075914	chromatin interactions
ENSG00000136143	chromatin interactions
ENSG00000165060	chromatin interactions
ENSG00000132849	chromatin interactions
ENSG00000163812	chromatin interactions
ENSG00000001167	chromatin interactions
ENSG00000272434	chromatin interactions
ENSG00000119139	chromatin interactions
ENSG00000178035	chromatin interactions
ENSG00000206737	chromatin interactions

Extended variants
information (count: 1783 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:1783 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs180917352	chr9:71714157-71714158	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs533787738	chr9:71714162-71714163	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs549168108	chr9:71714178-71714179	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs567397212	chr9:71714182-71714183	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs538025474	chr9:71714202-71714203	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs59044743	chr9:71714207-71714208	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs10781407	chr9:71714261-71714262	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs60120662	chr9:71714288-71714289	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs571068698	chr9:71714301-71714302	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs573590186	chr9:71714316-71714317	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs371188913	chr9:71714331-71714332	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs150461963	chr9:71714336-71714337	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs191200493	chr9:71714339-71714340	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs540969446	chr9:71714343-71714344	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs117302499	chr9:71714353-71714354	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs568207638	chr9:71714358-71714359	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs62570652	chr9:71714362-71714363	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs114473165	chr9:71714378-71714379	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs73447137	chr9:71714405-71714406	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs62570653	chr9:71714450-71714451	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs56126721	chr9:71714473-71714474	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs553369208	chr9:71714508-71714509	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs559676889	chr9:71714562-71714563	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs34965002	chr9:71714563-71714564	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs549037457	chr9:71714564-71714565	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs116401773	chr9:71714570-71714571	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs537663047	chr9:71714577-71714578	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs549922367	chr9:71714579-71714580	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs141247893	chr9:71714648-71714649	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs542370773	chr9:71714666-71714667	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs10121021	chr9:71714693-71714694	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs116361570	chr9:71714741-71714742	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs371159899	chr9:71714764-71714765	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs573322613	chr9:71714771-71714772	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs139083793	chr9:71714837-71714838	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs376738967	chr9:71714899-71714900	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs371751976	chr9:71714901-71714902	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs574239420	chr9:71714940-71714941	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs144973505	chr9:71714941-71714942	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs556289262	chr9:71714981-71714982	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs577326014	chr9:71715092-71715093	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs540020290	chr9:71715108-71715109	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs531020453	chr9:71715121-71715122	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs544744228	chr9:71715132-71715133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs112813315	chr9:71715139-71715140	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs11145212	chr9:71715140-71715141	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs373395409	chr9:71715199-71715200	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs527325266	chr9:71715288-71715289	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs186111259	chr9:71715292-71715293	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs142218020	chr9:71715321-71715322	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	17899364	CNVD
Mantle cell lymphoma	19029149	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	20729466	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Oral cancer	21386901	CNVD
Epilepsy	22083797	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Bipolar disorder	18458673	CNVD

Chromatin state (count:1234 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:71701400-71714400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr9:71701800-71735200	Weak transcription	Primary T cells from cord blood	blood
3	chr9:71702000-71716800	Weak transcription	Fetal Heart	heart
4	chr9:71706200-71716200	Weak transcription	Fetal Stomach	stomach
5	chr9:71706200-71720200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr9:71710200-71714400	Weak transcription	Gastric	stomach
7	chr9:71710200-71719400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr9:71710400-71715000	Enhancers	Fetal Intestine Small	intestine
9	chr9:71710600-71715000	Enhancers	Stomach Mucosa	stomach
10	chr9:71711000-71714800	Enhancers	Rectal Mucosa Donor 31	rectum
11	chr9:71711200-71715000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr9:71712000-71714600	Weak transcription	Colonic Mucosa	Colon
13	chr9:71712200-71714400	Weak transcription	Fetal Kidney	kidney
14	chr9:71712200-71714600	Weak transcription	HSMMtube	muscle
15	chr9:71712200-71715000	Enhancers	HUVEC	blood vessel
16	chr9:71712200-71716000	Weak transcription	Aorta	Aorta
17	chr9:71712600-71735200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr9:71712800-71714600	Active TSS	Rectal Mucosa Donor 29	rectum
19	chr9:71713000-71714400	Weak transcription	HSMM	muscle
20	chr9:71713000-71714400	Weak transcription	NH-A	brain
21	chr9:71713000-71720200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr9:71713200-71714200	Weak transcription	Fetal Intestine Large	intestine
23	chr9:71713200-71717000	Weak transcription	Skeletal Muscle Male	skeletal muscle
24	chr9:71713200-71718200	Weak transcription	Liver	Liver
25	chr9:71713200-71719600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr9:71713400-71714400	Weak transcription	Osteobl	bone
27	chr9:71713600-71714200	Weak transcription	Fetal Lung	lung
28	chr9:71713600-71714800	Weak transcription	Placenta Amnion	Placenta Amnion
29	chr9:71713600-71715000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr9:71714200-71715400	Enhancers	Fetal Intestine Large	intestine
31	chr9:71714400-71714600	Enhancers	Spleen	Spleen
32	chr9:71714400-71714800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr9:71714400-71714800	Enhancers	NH-A	brain
34	chr9:71714400-71715000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr9:71714400-71715000	Enhancers	Fetal Kidney	kidney
36	chr9:71714400-71715000	Enhancers	Fetal Muscle Leg	muscle
37	chr9:71714400-71715000	Enhancers	Gastric	stomach
38	chr9:71714400-71715000	Enhancers	HSMM	muscle
39	chr9:71714400-71715000	Enhancers	Osteobl	bone
40	chr9:71714600-71714800	Active TSS	Colonic Mucosa	Colon
41	chr9:71714600-71715000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr9:71714600-71715000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr9:71714600-71715000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
44	chr9:71714600-71715000	Enhancers	HSMMtube	muscle
45	chr9:71714800-71715000	Flanking Active TSS	Colonic Mucosa	Colon
46	chr9:71714800-71715000	Enhancers	Placenta Amnion	Placenta Amnion
47	chr9:71714800-71718200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr9:71714800-71719400	Weak transcription	Rectal Mucosa Donor 31	rectum
49	chr9:71715000-71715200	Enhancers	Colonic Mucosa	Colon
50	chr9:71715000-71715200	Weak transcription	Fetal Kidney	kidney

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