Variant report

Variant	esv3398013
Chromosome Location	chr9:71722447-71746627
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:861)
CpG islands
(count:611)
Chromatin interactive
region (count:39)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:861 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:71735292-71735927	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:71746529-71747015	HepG2	liver:	n/a	n/a
3	ATF2	chr9:71735153-71736138	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr9:71735106-71735934	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr9:71737566-71738148	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr9:71737258-71738069	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr9:71735251-71735859	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr9:71737585-71738101	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCL11A	chr9:71735558-71735835	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL11A	chr9:71735576-71735811	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCLAF1	chr9:71736571-71737127	GM12878	blood:	n/a	n/a
12	BHLHE40	chr9:71745840-71746183	K562	blood:	n/a	n/a
13	BHLHE40	chr9:71737647-71738054	HepG2	liver:	n/a	n/a
14	BRCA1	chr9:71735672-71735688	HepG2	liver:	n/a	n/a
15	BRCA1	chr9:71735568-71735826	H1-hESC	embryonic stem cell:	n/a	n/a
16	BRCA1	chr9:71736719-71737059	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr9:71736246-71736410	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr9:71735135-71736002	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr9:71746518-71747166	HepG2	liver:	n/a	chr9:71746738-71746751 chr9:71746738-71746749
20	CEBPB	chr9:71746546-71746947	HepG2	liver:	n/a	chr9:71746738-71746751 chr9:71746738-71746749
21	CEBPB	chr9:71730464-71730692	A549	lung:	n/a	n/a
22	CEBPB	chr9:71735933-71736104	HepG2	liver:	n/a	n/a
23	CEBPB	chr9:71746600-71746934	Hela-S3	cervix:	n/a	chr9:71746738-71746751 chr9:71746738-71746749
24	CEBPB	chr9:71746546-71747106	IMR90	lung:	n/a	chr9:71746738-71746751 chr9:71746738-71746749
25	CEBPB	chr9:71737217-71738032	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr9:71746576-71746897	A549	lung:	n/a	chr9:71746738-71746751 chr9:71746738-71746749
27	CEBPB	chr9:71746544-71747019	HepG2	liver:	n/a	chr9:71746738-71746751 chr9:71746738-71746749
28	CEBPB	chr9:71735281-71735626	HepG2	liver:	n/a	n/a
29	CEBPB	chr9:71735697-71735833	HepG2	liver:	n/a	n/a
30	CEBPB	chr9:71735281-71735937	MCF-7	breast:	n/a	n/a
31	CEBPB	chr9:71746509-71746964	MCF-7	breast:	n/a	chr9:71746738-71746751 chr9:71746738-71746749
32	CEBPB	chr9:71746577-71746832	HepG2	liver:	n/a	chr9:71746738-71746751 chr9:71746738-71746749
33	CEBPB	chr9:71745863-71746291	IMR90	lung:	n/a	chr9:71746066-71746077
34	CEBPB	chr9:71730525-71730741	IMR90	lung:	n/a	n/a
35	CEBPB	chr9:71735584-71736233	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr9:71735476-71735947	ECC-1	luminal epithelium:	n/a	n/a
37	CEBPD	chr9:71735539-71735956	HepG2	liver:	n/a	n/a
38	CEBPD	chr9:71735430-71736087	HepG2	liver:	n/a	n/a
39	CHD1	chr9:71736356-71738055	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD1	chr9:71735356-71736142	H1-hESC	embryonic stem cell:	n/a	chr9:71735872-71735882 chr9:71735875-71735885
41	CHD1	chr9:71734666-71735025	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD2	chr9:71735257-71736978	H1-hESC	embryonic stem cell:	n/a	chr9:71735872-71735882 chr9:71735875-71735885
43	CHD2	chr9:71735590-71737998	Hela-S3	cervix:	n/a	chr9:71735872-71735882 chr9:71735875-71735885
44	CHD2	chr9:71736643-71737207	GM12878	blood:	n/a	n/a
45	CHD2	chr9:71736772-71736958	HepG2	liver:	n/a	n/a
46	CHD2	chr9:71735572-71736125	HepG2	liver:	n/a	chr9:71735872-71735882 chr9:71735875-71735885
47	CREB1	chr9:71735173-71736321	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTBP2	chr9:71735145-71736239	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTBP2	chr9:71736458-71737761	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr9:71736719-71737047	GM12892	blood:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:71735701-71735751	NH-A	brain:	n/a
2	chr9:71735701-71735751	NH-A	brain:	n/a
3	chr9:71737756-71737806	Hepatocyte	liver:	n/a
4	chr9:71735701-71735751	SKMC	muscle:	n/a
5	chr9:71736999-71737049	GM19239	blood:	n/a
6	chr9:71735648-71735698	GM19239	blood:	n/a
7	chr9:71736409-71736459	AG09309	skin:	n/a
8	chr9:71737756-71737806	HCT-116	colon:	n/a
9	chr9:71737204-71737254	CMK	blood:	n/a
10	chr9:71737258-71737308	HCF	heart:	n/a
11	chr9:71735666-71735716	HCM	heart:	n/a
12	chr9:71736999-71737049	Caco-2	colon:	n/a
13	chr9:71736999-71737049	PrEC	prostate:	n/a
14	chr9:71735666-71735716	RPTEC	kidney:	n/a
15	chr9:71736999-71737049	CMK	blood:	n/a
16	chr9:71737258-71737308	HAEpiC	amniotic membrane:	n/a
17	chr9:71737204-71737254	HPAEpiC	pulmonary alveolar:	n/a
18	chr9:71735648-71735698	AG09309	skin:	n/a
19	chr9:71737756-71737806	HIPEpiC	eye:	n/a
20	chr9:71732345-71732395	SK-N-SH	brain:	n/a
21	chr9:71736999-71737049	MCF10A-Er-Src	breast:	n/a
22	chr9:71737204-71737254	HCPEpiC	choroid plexus:	n/a
23	chr9:71735666-71735716	Hepatocyte	liver:	n/a
24	chr9:71737258-71737308	NT2-D1	testis:	n/a
25	chr9:71737756-71737806	HMEC	breast:	n/a
26	chr9:71736999-71737049	K562	blood:	n/a
27	chr9:71736409-71736459	ovcar-3	ovarian:	n/a
28	chr9:71735666-71735716	PANC-1	pancreas:	n/a
29	chr9:71735648-71735698	H1-hESC	embryonic stem cell:	embryo
30	chr9:71735701-71735751	SK-N-MC	brain:	n/a
31	chr9:71735666-71735716	A549	lung:	n/a
32	chr9:71736854-71736904	Jurkat	blood:	n/a
33	chr9:71736854-71736904	BJ	skin:	n/a
34	chr9:71737204-71737254	GM06990	blood:	n/a
35	chr9:71737756-71737806	AG04450	lung:	fetal
36	chr9:71732345-71732395	NHDF-neo	bronchial:	n/a
37	chr9:71736999-71737049	T-47D	breast:	n/a
38	chr9:71736409-71736459	MCF-7	breast:	n/a
39	chr9:71737756-71737806	SK-N-MC	brain:	n/a
40	chr9:71736999-71737049	HNPCEpiC	eye:	n/a
41	chr9:71735648-71735698	Jurkat	blood:	n/a
42	chr9:71737756-71737806	BE2_C	brain:	n/a
43	chr9:71735648-71735698	HCPEpiC	choroid plexus:	n/a
44	chr9:71735701-71735751	AG09309	skin:	n/a
45	chr9:71736854-71736904	AoSMC	blood vessel:	n/a
46	chr9:71737258-71737308	SAEC	small airway:	n/a
47	chr9:71736999-71737049	HAEpiC	amniotic membrane:	n/a
48	chr9:71735648-71735698	A549	lung:	n/a
49	chr9:71737756-71737806	AG09319	gingival:	n/a
50	chr9:71737756-71737806	NB4	blood:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:71736348..71739276-chr9:71751743..71753516,2	MCF-7	breast:
2	chr9:71720466..71722349-chr9:71729146..71730891,2	MCF-7	breast:
3	chr9:71745094..71746594-chr9:71762879..71765148,2	MCF-7	breast:
4	chr9:71732215..71735155-chr9:71735593..71737924,2	MCF-7	breast:
5	chr3:49066502..49067181-chr9:71736337..71736850,2	Hela-S3	cervix:
6	chr9:71680609..71683537-chr9:71732525..71735089,2	MCF-7	breast:
7	chr13:113241435..113242373-chr9:71735991..71736661,2	Hela-S3	cervix:
8	chr1:62208097..62208620-chr9:71736404..71737107,2	Hela-S3	cervix:
9	chr9:71727081..71728601-chr9:71737166..71739059,2	MCF-7	breast:
10	chr13:48611578..48612294-chr9:71736012..71736825,2	Hela-S3	cervix:
11	chr9:71736310..71738206-chr9:71797242..71798901,2	MCF-7	breast:
12	chr9:71733939..71735989-chr9:71814942..71816605,2	MCF-7	breast:
13	chr9:71720044..71724145-chr9:71733178..71738087,7	MCF-7	breast:
14	chr1:146555490..146556430-chr9:71736325..71736974,2	Hela-S3	cervix:
15	chr9:71728735..71732212-chr9:71735055..71737852,4	MCF-7	breast:
16	chr9:71649472..71654369-chr9:71735388..71737779,6	MCF-7	breast:
17	chr9:71745166..71747792-chr9:71751582..71754371,2	K562	blood:
18	chr9:71735864..71737809-chr9:71745994..71747583,2	MCF-7	breast:
19	chr9:71726688..71731938-chr9:71734130..71739301,8	MCF-7	breast:
20	chr9:71734182..71738595-chr9:71741906..71745315,7	MCF-7	breast:
21	chr9:71720044..71724145-chr9:71733178..71738087,7	MCF-7	breast:
22	chr9:71745818..71747384-chr9:71762840..71764725,2	K562	blood:
23	chr9:71733940..71739343-chr9:71741877..71748941,25	MCF-7	breast:
24	chr6:41040678..41041408-chr9:71735768..71736686,2	Hela-S3	cervix:
25	chr9:71743521..71745547-chr9:71821447..71823888,2	MCF-7	breast:
26	chr9:71743905..71746446-chr9:71805495..71808231,2	MCF-7	breast:
27	chr1:149223425..149225310-chr9:71736139..71738412,2	MCF-7	breast:
28	chr9:71696609..71699452-chr9:71736834..71738699,2	MCF-7	breast:
29	chr9:71735373..71738833-chr9:71764136..71766985,4	MCF-7	breast:
30	chr9:71733168..71738729-chr9:71786929..71793777,10	MCF-7	breast:
31	chr3:45017283..45018160-chr9:71735845..71736825,2	Hela-S3	cervix:
32	chr9:71724269..71725816-chr9:71735725..71737678,2	MCF-7	breast:
33	chr9:71734142..71739001-chr9:71788032..71795507,11	MCF-7	breast:
34	chr9:71730545..71732525-chr9:71797822..71800476,2	K562	blood:
35	chr9:71736483..71737290-chr9:71808170..71808758,2	MCF-7	breast:
36	chr9:71727081..71728601-chr9:71737166..71739059,2	MCF-7	breast:
37	chr11:65666788..65667405-chr9:71737195..71738062,2	Hela-S3	cervix:
38	chr9:71649801..71651906-chr9:71729690..71731454,2	MCF-7	breast:
39	chr9:71649857..71652024-chr9:71744170..71747063,2	MCF-7	breast:

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

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

No data

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

Extended variants
information (count: 910 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:910 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553151002	chr9:71722473-71722474	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs567584598	chr9:71722503-71722504	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs535534209	chr9:71722525-71722526	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs56141577	chr9:71722574-71722575	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs538071975	chr9:71722629-71722630	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs58476993	chr9:71722731-71722732	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs59255094	chr9:71722732-71722733	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs117269462	chr9:71722764-71722765	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs201363571	chr9:71722793-71722794	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs368040727	chr9:71722823-71722824	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs538773569	chr9:71722958-71722959	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs577689118	chr9:71722997-71722998	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs35581876	chr9:71723001-71723002	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs540373915	chr9:71723015-71723016	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs553565834	chr9:71723021-71723022	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs572041986	chr9:71723043-71723044	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs542225120	chr9:71723048-71723049	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs561191432	chr9:71723126-71723127	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs576360938	chr9:71723136-71723137	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs62567094	chr9:71723162-71723163	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs150501070	chr9:71723168-71723169	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs532202292	chr9:71723178-71723179	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs551877403	chr9:71723216-71723217	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs560364681	chr9:71723332-71723333	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs527698350	chr9:71723370-71723371	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs139642535	chr9:71723371-71723372	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs11792218	chr9:71723374-71723375	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs144552989	chr9:71723393-71723394	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs534288804	chr9:71723394-71723395	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs562826040	chr9:71723407-71723408	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs201963234	chr9:71723452-71723453	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs77408833	chr9:71723455-71723456	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs397969478	chr9:71723466-71723467	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs571536977	chr9:71723527-71723528	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs538842935	chr9:71723545-71723546	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs553847766	chr9:71723549-71723550	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs572017647	chr9:71723607-71723608	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs536250785	chr9:71723632-71723633	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs554567050	chr9:71723658-71723659	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs139348314	chr9:71723670-71723671	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs189134748	chr9:71723696-71723697	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs144096080	chr9:71723720-71723721	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs576999987	chr9:71723721-71723722	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs551248356	chr9:71723749-71723750	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs540831598	chr9:71723759-71723760	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs192830069	chr9:71723760-71723761	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs527738071	chr9:71723767-71723768	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs182824037	chr9:71723799-71723800	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs146825367	chr9:71723801-71723802	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs531576117	chr9:71723803-71723804	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	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:804 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:71701800-71735200	Weak transcription	Primary T cells from cord blood	blood
2	chr9:71712600-71735200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr9:71715000-71735000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr9:71719400-71724400	Weak transcription	Gastric	stomach
5	chr9:71720400-71735600	Weak transcription	Left Ventricle	heart
6	chr9:71720600-71735000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr9:71721200-71726400	Weak transcription	Stomach Mucosa	stomach
8	chr9:71721400-71734600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr9:71722000-71722800	Enhancers	HepG2	liver
10	chr9:71722000-71723000	Enhancers	Osteobl	bone
11	chr9:71722000-71727800	Weak transcription	Placenta	Placenta
12	chr9:71722200-71722600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr9:71722200-71722600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr9:71722200-71722600	Enhancers	Fetal Lung	lung
15	chr9:71722400-71723000	Enhancers	Liver	Liver
16	chr9:71722600-71723000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr9:71722600-71723000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr9:71722600-71726800	Weak transcription	Fetal Lung	lung
19	chr9:71722800-71723200	Weak transcription	HepG2	liver
20	chr9:71723000-71723200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr9:71723000-71726600	Weak transcription	Liver	Liver
22	chr9:71723200-71724600	Enhancers	HepG2	liver
23	chr9:71724400-71724600	Enhancers	Gastric	stomach
24	chr9:71724600-71726600	Weak transcription	HepG2	liver
25	chr9:71726600-71727000	Enhancers	Liver	Liver
26	chr9:71726600-71727200	Enhancers	Brain Cingulate Gyrus	brain
27	chr9:71726600-71727200	Enhancers	HepG2	liver
28	chr9:71726800-71727000	Enhancers	H9 Cell Line	embryonic stem cell
29	chr9:71726800-71727200	Enhancers	Brain Inferior Temporal Lobe	brain
30	chr9:71726800-71727200	Enhancers	Brain Substantia Nigra	brain
31	chr9:71726800-71727200	Enhancers	Fetal Lung	lung
32	chr9:71727200-71735800	Weak transcription	Brain Substantia Nigra	brain
33	chr9:71728400-71728800	Enhancers	GM12878-XiMat	blood
34	chr9:71728800-71733400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr9:71729000-71730600	Weak transcription	Stomach Mucosa	stomach
36	chr9:71729600-71729800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr9:71729600-71729800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr9:71729600-71729800	Enhancers	K562	blood
39	chr9:71729800-71730800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr9:71729800-71745600	Weak transcription	K562	blood
41	chr9:71730000-71733800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr9:71730200-71730600	Enhancers	Fetal Muscle Leg	muscle
43	chr9:71730200-71730600	Enhancers	NHDF-Ad	bronchial
44	chr9:71730200-71731000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr9:71730400-71731000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr9:71730400-71731000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr9:71730400-71731000	Enhancers	Muscle Satellite Cultured Cells	--
48	chr9:71730400-71731000	Enhancers	Osteobl	bone
49	chr9:71730600-71731000	Enhancers	Stomach Mucosa	stomach
50	chr9:71730600-71734800	Weak transcription	Fetal Muscle Leg	muscle

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