Variant report

Variant	esv1798602
Chromosome Location	chr9:71718195-71764191
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1126)
CpG islands
(count:612)
Chromatin interactive
region (count:56)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1126 , 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	chr9:71719221-71720293	HepG2	liver:	n/a	chr9:71719768-71719784 chr9:71719315-71719331
2	ARID3A	chr9:71735292-71735927	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:71746529-71747015	HepG2	liver:	n/a	n/a
4	ATF2	chr9:71737258-71738069	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr9:71735106-71735934	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr9:71737566-71738148	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr9:71735153-71736138	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr9:71735251-71735859	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr9:71737585-71738101	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	chr9:71745840-71746183	K562	blood:	n/a	n/a
14	BHLHE40	chr9:71720051-71720348	HepG2	liver:	n/a	n/a
15	BHLHE40	chr9:71737647-71738054	HepG2	liver:	n/a	n/a
16	BRCA1	chr9:71736246-71736410	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr9:71720260-71720323	HepG2	liver:	n/a	n/a
18	BRCA1	chr9:71735568-71735826	H1-hESC	embryonic stem cell:	n/a	n/a
19	BRCA1	chr9:71735672-71735688	HepG2	liver:	n/a	n/a
20	BRCA1	chr9:71736719-71737059	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr9:71721901-71722105	IMR90	lung:	n/a	n/a
22	CEBPB	chr9:71720003-71720246	HepG2	liver:	n/a	n/a
23	CEBPB	chr9:71746576-71746897	A549	lung:	n/a	chr9:71746738-71746751 chr9:71746738-71746749
24	CEBPB	chr9:71746509-71746964	MCF-7	breast:	n/a	chr9:71746738-71746751 chr9:71746738-71746749
25	CEBPB	chr9:71730525-71730741	IMR90	lung:	n/a	n/a
26	CEBPB	chr9:71745863-71746291	IMR90	lung:	n/a	chr9:71746066-71746077
27	CEBPB	chr9:71746518-71747166	HepG2	liver:	n/a	chr9:71746738-71746751 chr9:71746738-71746749
28	CEBPB	chr9:71746546-71747106	IMR90	lung:	n/a	chr9:71746738-71746751 chr9:71746738-71746749
29	CEBPB	chr9:71735281-71735937	MCF-7	breast:	n/a	n/a
30	CEBPB	chr9:71735135-71736002	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr9:71735584-71736233	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr9:71735476-71735947	ECC-1	luminal epithelium:	n/a	n/a
33	CEBPB	chr9:71730464-71730692	A549	lung:	n/a	n/a
34	CEBPB	chr9:71737217-71738032	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr9:71735697-71735833	HepG2	liver:	n/a	n/a
36	CEBPB	chr9:71746600-71746934	Hela-S3	cervix:	n/a	chr9:71746738-71746751 chr9:71746738-71746749
37	CEBPB	chr9:71735281-71735626	HepG2	liver:	n/a	n/a
38	CEBPB	chr9:71735933-71736104	HepG2	liver:	n/a	n/a
39	CEBPB	chr9:71746546-71746947	HepG2	liver:	n/a	chr9:71746738-71746751 chr9:71746738-71746749
40	CEBPB	chr9:71746577-71746832	HepG2	liver:	n/a	chr9:71746738-71746751 chr9:71746738-71746749
41	CEBPB	chr9:71746544-71747019	HepG2	liver:	n/a	chr9:71746738-71746751 chr9:71746738-71746749
42	CEBPD	chr9:71735430-71736087	HepG2	liver:	n/a	n/a
43	CEBPD	chr9:71735539-71735956	HepG2	liver:	n/a	n/a
44	CHD1	chr9:71735356-71736142	H1-hESC	embryonic stem cell:	n/a	chr9:71735872-71735882 chr9:71735875-71735885
45	CHD1	chr9:71736356-71738055	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD1	chr9:71734666-71735025	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD2	chr9:71735257-71736978	H1-hESC	embryonic stem cell:	n/a	chr9:71735872-71735882 chr9:71735875-71735885
48	CHD2	chr9:71735572-71736125	HepG2	liver:	n/a	chr9:71735872-71735882 chr9:71735875-71735885
49	CHD2	chr9:71736772-71736958	HepG2	liver:	n/a	n/a
50	CHD2	chr9:71735590-71737998	Hela-S3	cervix:	n/a	chr9:71735872-71735882 chr9:71735875-71735885

(count:612 , 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	HRCEpiC	kidney:	n/a
2	chr9:71737756-71737806	GM12878	blood:	n/a
3	chr9:71732345-71732395	HRCEpiC	kidney:	n/a
4	chr9:71737756-71737806	GM12878	blood:	n/a
5	chr9:71735648-71735698	GM12878	blood:	n/a
6	chr9:71736409-71736459	PANC-1	pancreas:	n/a
7	chr9:71736854-71736904	MCF-7	breast:	n/a
8	chr9:71735666-71735716	Jurkat	blood:	n/a
9	chr9:71737258-71737308	GM12892	blood:	n/a
10	chr9:71737756-71737806	NH-A	brain:	n/a
11	chr9:71737204-71737254	GM12892	blood:	n/a
12	chr9:71735648-71735698	HMEC	breast:	n/a
13	chr9:71736999-71737049	PANC-1	pancreas:	n/a
14	chr9:71737258-71737308	MCF10A-Er-Src	breast:	n/a
15	chr9:71732345-71732395	RPTEC	kidney:	n/a
16	chr9:71737204-71737254	K562	blood:	n/a
17	chr9:71737756-71737806	HPAEpiC	pulmonary alveolar:	n/a
18	chr9:71735701-71735751	SKMC	muscle:	n/a
19	chr9:71737204-71737254	SK-N-SH_RA	brain:	n/a
20	chr9:71735666-71735716	HepG2	liver:	n/a
21	chr9:71735666-71735716	BJ	skin:	n/a
22	chr9:71737204-71737254	PANC-1	pancreas:	n/a
23	chr9:71737258-71737308	ovcar-3	ovarian:	n/a
24	chr9:71736854-71736904	AoSMC	blood vessel:	n/a
25	chr9:71735666-71735716	NB4	blood:	n/a
26	chr9:71735648-71735698	MCF10A-Er-Src	breast:	n/a
27	chr9:71737258-71737308	HRE	kidney:	n/a
28	chr9:71732345-71732395	HCPEpiC	choroid plexus:	n/a
29	chr9:71735648-71735698	HAEpiC	amniotic membrane:	n/a
30	chr9:71736409-71736459	AG04449	skin:	fetal
31	chr9:71735648-71735698	AG04449	skin:	fetal
32	chr9:71736854-71736904	LNCaP	prostate:	n/a
33	chr9:71737258-71737308	Hela-S3	cervix:	n/a
34	chr9:71735666-71735716	HMEC	breast:	n/a
35	chr9:71732345-71732395	Jurkat	blood:	n/a
36	chr9:71735666-71735716	NH-A	brain:	n/a
37	chr9:71735648-71735698	AG09319	gingival:	n/a
38	chr9:71735701-71735751	AG09309	skin:	n/a
39	chr9:71735648-71735698	SK-N-SH	brain:	n/a
40	chr9:71736854-71736904	Hela-S3	cervix:	n/a
41	chr9:71736854-71736904	HEEpiC	esophagus:	n/a
42	chr9:71735666-71735716	PANC-1	pancreas:	n/a
43	chr9:71732345-71732395	GM12891	blood:	n/a
44	chr9:71737756-71737806	GM19239	blood:	n/a
45	chr9:71736999-71737049	HAEpiC	amniotic membrane:	n/a
46	chr9:71736999-71737049	GM19239	blood:	n/a
47	chr9:71737204-71737254	AG09309	skin:	n/a
48	chr9:71732345-71732395	H1-hESC	embryonic stem cell:	embryo
49	chr9:71735666-71735716	HPAEpiC	pulmonary alveolar:	n/a
50	chr9:71737204-71737254	GM12878	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr3:45017283..45018160-chr9:71735845..71736825,2	Hela-S3	cervix:
2	chr9:71720044..71724145-chr9:71733178..71738087,7	MCF-7	breast:
3	chr9:71736348..71739276-chr9:71751743..71753516,2	MCF-7	breast:
4	chr1:62208097..62208620-chr9:71736404..71737107,2	Hela-S3	cervix:
5	chr9:71730545..71732525-chr9:71797822..71800476,2	K562	blood:
6	chr9:71734142..71739001-chr9:71788032..71795507,11	MCF-7	breast:
7	chr9:71755797..71757532-chr9:71759956..71762001,2	MCF-7	breast:
8	chr9:71745166..71747792-chr9:71751582..71754371,2	K562	blood:
9	chr13:48611578..48612294-chr9:71736012..71736825,2	Hela-S3	cervix:
10	chr9:71649472..71654369-chr9:71735388..71737779,6	MCF-7	breast:
11	chr9:71760807..71763605-chr9:71766802..71769126,2	K562	blood:
12	chr11:65666788..65667405-chr9:71737195..71738062,2	Hela-S3	cervix:
13	chr9:71649857..71652024-chr9:71744170..71747063,2	MCF-7	breast:
14	chr9:71751405..71753557-chr9:71754610..71757893,3	MCF-7	breast:
15	chr9:71735373..71738833-chr9:71764136..71766985,4	MCF-7	breast:
16	chr9:71734182..71738595-chr9:71741906..71745315,7	MCF-7	breast:
17	chr9:71745166..71747792-chr9:71751582..71754371,2	K562	blood:
18	chr9:71718282..71721853-chr9:71734600..71737822,4	MCF-7	breast:
19	chr9:71745094..71746594-chr9:71762879..71765148,2	MCF-7	breast:
20	chr9:71735718..71737415-chr9:71751707..71753369,2	MCF-7	breast:
21	chr9:71758408..71761844-chr9:71769245..71771910,3	MCF-7	breast:
22	chr9:71726688..71731938-chr9:71734130..71739301,8	MCF-7	breast:
23	chr9:71728735..71732212-chr9:71735055..71737852,4	MCF-7	breast:
24	chr6:41040678..41041408-chr9:71735768..71736686,2	Hela-S3	cervix:
25	chr9:71761121..71762822-chr9:71762920..71764542,2	K562	blood:
26	chr13:113241435..113242373-chr9:71735991..71736661,2	Hela-S3	cervix:
27	chr9:71720044..71724145-chr9:71733178..71738087,7	MCF-7	breast:
28	chr9:71736310..71738206-chr9:71797242..71798901,2	MCF-7	breast:
29	chr9:71724269..71725816-chr9:71735725..71737678,2	MCF-7	breast:
30	chr9:71743521..71745547-chr9:71821447..71823888,2	MCF-7	breast:
31	chr9:71680609..71683537-chr9:71732525..71735089,2	MCF-7	breast:
32	chr9:71761121..71762822-chr9:71762920..71764542,2	K562	blood:
33	chr1:146555490..146556430-chr9:71736325..71736974,2	Hela-S3	cervix:
34	chr9:71732215..71735155-chr9:71735593..71737924,2	MCF-7	breast:
35	chr9:71727081..71728601-chr9:71737166..71739059,2	MCF-7	breast:
36	chr9:71649801..71651906-chr9:71729690..71731454,2	MCF-7	breast:
37	chr9:71745818..71747384-chr9:71762840..71764725,2	K562	blood:
38	chr9:71736348..71739276-chr9:71751743..71753516,2	MCF-7	breast:
39	chr3:49066502..49067181-chr9:71736337..71736850,2	Hela-S3	cervix:
40	chr9:71720466..71722349-chr9:71729146..71730891,2	MCF-7	breast:
41	chr9:71735864..71737809-chr9:71745994..71747583,2	MCF-7	breast:
42	chr9:71733168..71738729-chr9:71786929..71793777,10	MCF-7	breast:
43	chr9:71735454..71738183-chr9:71753651..71758025,4	MCF-7	breast:
44	chr1:149223425..149225310-chr9:71736139..71738412,2	MCF-7	breast:
45	chr9:71743905..71746446-chr9:71805495..71808231,2	MCF-7	breast:
46	chr9:71733940..71739343-chr9:71741877..71748941,25	MCF-7	breast:
47	chr9:71745094..71746594-chr9:71762879..71765148,2	MCF-7	breast:
48	chr9:71696609..71699452-chr9:71736834..71738699,2	MCF-7	breast:
49	chr9:71755797..71757532-chr9:71759956..71762001,2	MCF-7	breast:
50	chr9:71733939..71735989-chr9:71814942..71816605,2	MCF-7	breast:

(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
ENSG00000270236	chromatin interactions
ENSG00000178035	chromatin interactions
ENSG00000001167	chromatin interactions
ENSG00000126216	chromatin interactions
ENSG00000132849	chromatin interactions
ENSG00000272434	chromatin interactions
ENSG00000119139	chromatin interactions
ENSG00000165060	chromatin interactions
ENSG00000136143	chromatin interactions
ENSG00000136159	chromatin interactions
ENSG00000163812	chromatin interactions
ENSG00000075914	chromatin interactions
ENSG00000206737	chromatin interactions

Extended variants
information (count: 1765 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:1765 , 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	rs12345129	chr9:71718260-71718261	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs188206523	chr9:71718266-71718267	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs112907962	chr9:71718313-71718314	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs28608975	chr9:71718348-71718349	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs193155655	chr9:71718349-71718350	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs28633825	chr9:71718357-71718358	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs28476744	chr9:71718366-71718367	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs535882209	chr9:71718372-71718373	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs111743372	chr9:71718374-71718375	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs557824780	chr9:71718395-71718396	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs541034033	chr9:71718396-71718397	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs560015472	chr9:71718407-71718408	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs367771378	chr9:71718425-71718426	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs114627104	chr9:71718477-71718478	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs183869206	chr9:71718482-71718483	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs71928905	chr9:71718529-71718530	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs72244007	chr9:71718536-71718537	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs60524968	chr9:71718544-71718545	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs199835523	chr9:71718545-71718546	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs570299989	chr9:71718569-71718570	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs540390448	chr9:71718570-71718571	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs560418996	chr9:71718593-71718594	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs12003315	chr9:71718664-71718665	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs573969376	chr9:71718671-71718672	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs541478998	chr9:71718673-71718674	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs552649435	chr9:71718684-71718685	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs568353717	chr9:71718697-71718698	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs535423884	chr9:71718698-71718699	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs557221489	chr9:71718712-71718713	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs561759082	chr9:71718732-71718733	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs545580378	chr9:71718749-71718750	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs371460146	chr9:71718778-71718779	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs558643265	chr9:71718782-71718783	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs12683901	chr9:71718791-71718792	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs544340753	chr9:71718794-71718795	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs559445599	chr9:71718832-71718833	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs530094762	chr9:71718842-71718843	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs564162114	chr9:71718843-71718844	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs369888351	chr9:71718853-71718854	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs531163286	chr9:71718891-71718892	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs369085509	chr9:71718940-71718941	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs11145245	chr9:71718961-71718962	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs546788862	chr9:71718974-71718975	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs201086149	chr9:71718975-71718976	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs546665841	chr9:71718980-71718981	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs369489005	chr9:71719078-71719079	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs568010791	chr9:71719080-71719081	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs535411170	chr9:71719086-71719087	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs139495144	chr9:71719087-71719088	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs11145247	chr9:71719093-71719094	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	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:1222 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:71701800-71735200	Weak transcription	Primary T cells from cord blood	blood
2	chr9:71706200-71720200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr9:71710200-71719400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr9:71712600-71735200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr9:71713000-71720200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr9:71713200-71718200	Weak transcription	Liver	Liver
7	chr9:71713200-71719600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr9:71714800-71718200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr9:71714800-71719400	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr9:71715000-71718200	Weak transcription	Fetal Intestine Small	intestine
11	chr9:71715000-71719000	Weak transcription	Gastric	stomach
12	chr9:71715000-71735000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr9:71715400-71718200	Weak transcription	Fetal Intestine Large	intestine
14	chr9:71717400-71719000	Enhancers	HepG2	liver
15	chr9:71717600-71719600	Enhancers	Rectal Mucosa Donor 29	rectum
16	chr9:71718000-71718600	Enhancers	Stomach Mucosa	stomach
17	chr9:71718200-71718400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr9:71718200-71718400	Enhancers	Pancreas	Pancrea
19	chr9:71718200-71718600	Enhancers	H1 Cell Line	embryonic stem cell
20	chr9:71718200-71718600	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr9:71718200-71720200	Enhancers	Liver	Liver
22	chr9:71718200-71721000	Enhancers	Fetal Intestine Large	intestine
23	chr9:71718200-71721400	Enhancers	Fetal Intestine Small	intestine
24	chr9:71718400-71718800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr9:71718400-71719000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr9:71718400-71719000	Weak transcription	Pancreas	Pancrea
27	chr9:71718400-71720200	Weak transcription	Fetal Lung	lung
28	chr9:71718600-71719000	Weak transcription	H1 Cell Line	embryonic stem cell
29	chr9:71718600-71719000	Weak transcription	Stomach Mucosa	stomach
30	chr9:71718600-71719800	Weak transcription	HUES6 Cell Line	embryonic stem cell
31	chr9:71718800-71720400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr9:71719000-71719200	Enhancers	H1 Cell Line	embryonic stem cell
33	chr9:71719000-71719200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr9:71719000-71719200	Enhancers	Pancreas	Pancrea
35	chr9:71719000-71719400	Enhancers	Gastric	stomach
36	chr9:71719000-71720400	Enhancers	Duodenum Mucosa	Duodenum
37	chr9:71719000-71720600	Flanking Active TSS	HepG2	liver
38	chr9:71719000-71721200	Enhancers	Stomach Mucosa	stomach
39	chr9:71719200-71720000	Weak transcription	H1 Cell Line	embryonic stem cell
40	chr9:71719200-71720000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr9:71719200-71720200	Weak transcription	Pancreas	Pancrea
42	chr9:71719400-71720600	Enhancers	A549	lung
43	chr9:71719400-71720800	Enhancers	Rectal Mucosa Donor 31	rectum
44	chr9:71719400-71721400	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr9:71719400-71724400	Weak transcription	Gastric	stomach
46	chr9:71719600-71719800	Active TSS	Rectal Mucosa Donor 29	rectum
47	chr9:71719600-71720600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr9:71719600-71721200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr9:71719600-71721400	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr9:71719600-71721400	Enhancers	HUES48 Cell Line	embryonic stem cell

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