Variant report

Variant	esv3427257
Chromosome Location	chr9:71725447-71746948
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:863)
CpG islands
(count:610)
Chromatin interactive
region (count:38)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:863 , 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	chr9:71746529-71747015	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:71735292-71735927	HepG2	liver:	n/a	n/a
3	ATF2	chr9:71737258-71738069	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr9:71735153-71736138	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	BACH1	chr9:71737585-71738101	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr9:71735251-71735859	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	chr9:71736246-71736410	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr9:71735672-71735688	HepG2	liver:	n/a	n/a
16	BRCA1	chr9:71736719-71737059	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr9:71735568-71735826	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr9:71735933-71736104	HepG2	liver:	n/a	n/a
19	CEBPB	chr9:71746576-71746897	A549	lung:	n/a	chr9:71746738-71746751 chr9:71746738-71746749
20	CEBPB	chr9:71735476-71735947	ECC-1	luminal epithelium:	n/a	n/a
21	CEBPB	chr9:71746600-71746934	Hela-S3	cervix:	n/a	chr9:71746738-71746751 chr9:71746738-71746749
22	CEBPB	chr9:71735281-71735626	HepG2	liver:	n/a	n/a
23	CEBPB	chr9:71746546-71747106	IMR90	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	chr9:71735697-71735833	HepG2	liver:	n/a	n/a
26	CEBPB	chr9:71746518-71747166	HepG2	liver:	n/a	chr9:71746738-71746751 chr9:71746738-71746749
27	CEBPB	chr9:71735281-71735937	MCF-7	breast:	n/a	n/a
28	CEBPB	chr9:71746577-71746832	HepG2	liver:	n/a	chr9:71746738-71746751 chr9:71746738-71746749
29	CEBPB	chr9:71737217-71738032	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr9:71746546-71746947	HepG2	liver:	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	chr9:71735135-71736002	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr9:71730464-71730692	A549	lung:	n/a	n/a
34	CEBPB	chr9:71735584-71736233	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr9:71745863-71746291	IMR90	lung:	n/a	chr9:71746066-71746077
36	CEBPB	chr9:71730525-71730741	IMR90	lung:	n/a	n/a
37	CEBPD	chr9:71735430-71736087	HepG2	liver:	n/a	n/a
38	CEBPD	chr9:71735539-71735956	HepG2	liver:	n/a	n/a
39	CHD1	chr9:71734666-71735025	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD1	chr9:71736356-71738055	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD1	chr9:71735356-71736142	H1-hESC	embryonic stem cell:	n/a	chr9:71735872-71735882 chr9:71735875-71735885
42	CHD2	chr9:71736643-71737207	GM12878	blood:	n/a	n/a
43	CHD2	chr9:71735257-71736978	H1-hESC	embryonic stem cell:	n/a	chr9:71735872-71735882 chr9:71735875-71735885
44	CHD2	chr9:71735590-71737998	Hela-S3	cervix:	n/a	chr9:71735872-71735882 chr9:71735875-71735885
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	chr9:71736458-71737761	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTBP2	chr9:71735145-71736239	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr9:71736400-71736550	HMEC	breast:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:71737258-71737308	U87	brain:	n/a
2	chr9:71737756-71737806	AG09319	gingival:	n/a
3	chr9:71736409-71736459	CMK	blood:	n/a
4	chr9:71735648-71735698	HEEpiC	esophagus:	n/a
5	chr9:71737204-71737254	Jurkat	blood:	n/a
6	chr9:71735666-71735716	GM12878	blood:	n/a
7	chr9:71736999-71737049	Hela-S3	cervix:	n/a
8	chr9:71735666-71735716	Jurkat	blood:	n/a
9	chr9:71736409-71736459	RPTEC	kidney:	n/a
10	chr9:71736854-71736904	HIPEpiC	eye:	n/a
11	chr9:71737258-71737308	IMR90	lung:	fetal
12	chr9:71736999-71737049	ProgFib	skin:	n/a
13	chr9:71736409-71736459	H1-hESC	embryonic stem cell:	embryo
14	chr9:71735701-71735751	GM12878	blood:	n/a
15	chr9:71735666-71735716	PFSK-1	brain:	n/a
16	chr9:71732345-71732395	SKMC	muscle:	n/a
17	chr9:71737204-71737254	HL-60	blood:	n/a
18	chr9:71737204-71737254	AG04450	lung:	fetal
19	chr9:71736999-71737049	SK-N-MC	brain:	n/a
20	chr9:71736999-71737049	IMR90	lung:	fetal
21	chr9:71737756-71737806	U87	brain:	n/a
22	chr9:71736854-71736904	ECC-1	luminal epithelium:	n/a
23	chr9:71737756-71737806	ovcar-3	ovarian:	n/a
24	chr9:71737204-71737254	Hela-S3	cervix:	n/a
25	chr9:71737258-71737308	HCF	heart:	n/a
26	chr9:71737204-71737254	HRE	kidney:	n/a
27	chr9:71735648-71735698	HAEpiC	amniotic membrane:	n/a
28	chr9:71735648-71735698	HRE	kidney:	n/a
29	chr9:71736409-71736459	Hela-S3	cervix:	n/a
30	chr9:71732345-71732395	HUVEC	blood vessel:	n/a
31	chr9:71732345-71732395	HL-60	blood:	n/a
32	chr9:71736409-71736459	K562	blood:	n/a
33	chr9:71735648-71735698	PrEC	prostate:	n/a
34	chr9:71737756-71737806	CMK	blood:	n/a
35	chr9:71732345-71732395	HRE	kidney:	n/a
36	chr9:71736854-71736904	Caco-2	colon:	n/a
37	chr9:71737204-71737254	GM12878	blood:	n/a
38	chr9:71735701-71735751	AG10803	skin:	n/a
39	chr9:71737204-71737254	ovcar-3	ovarian:	n/a
40	chr9:71737258-71737308	Jurkat	blood:	n/a
41	chr9:71735648-71735698	HUVEC	blood vessel:	n/a
42	chr9:71737756-71737806	K562	blood:	n/a
43	chr9:71735666-71735716	SK-N-MC	brain:	n/a
44	chr9:71737258-71737308	CMK	blood:	n/a
45	chr9:71737204-71737254	HCM	heart:	n/a
46	chr9:71735648-71735698	SK-N-SH_RA	brain:	n/a
47	chr9:71735666-71735716	Caco-2	colon:	n/a
48	chr9:71735648-71735698	GM12878	blood:	n/a
49	chr9:71735701-71735751	HCT-116	colon:	n/a
50	chr9:71736854-71736904	RPTEC	kidney:	n/a

(count:38 , 50 per page) page: 1

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

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

Extended variants
information (count: 823 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:823 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185446199	chr9:71725454-71725455	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs535239223	chr9:71725459-71725460	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs143740520	chr9:71725488-71725489	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs554666237	chr9:71725546-71725547	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs576081520	chr9:71725595-71725596	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs543423852	chr9:71725652-71725653	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs9410779	chr9:71725656-71725657	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs141778761	chr9:71725668-71725669	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs377576820	chr9:71725756-71725757	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs541391251	chr9:71725774-71725775	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs147084709	chr9:71725857-71725858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs530331463	chr9:71725885-71725886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs28379615	chr9:71725917-71725918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs200045010	chr9:71725924-71725925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs149477232	chr9:71725941-71725942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs527689389	chr9:71725955-71725956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs148429716	chr9:71726012-71726013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs530579007	chr9:71726013-71726014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs369462065	chr9:71726016-71726017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs201986954	chr9:71726017-71726018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs552239529	chr9:71726036-71726037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs75140628	chr9:71726042-71726043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs76703818	chr9:71726049-71726050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs546593794	chr9:71726051-71726052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs12349693	chr9:71726053-71726054	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs550226017	chr9:71726115-71726116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs12348549	chr9:71726140-71726141	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs375545021	chr9:71726179-71726180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs112132060	chr9:71726221-71726222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs575087754	chr9:71726243-71726244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs146286989	chr9:71726252-71726253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs558990925	chr9:71726256-71726257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs539223530	chr9:71726258-71726259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs577200504	chr9:71726280-71726281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs541378554	chr9:71726314-71726315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs182041303	chr9:71726343-71726344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs575137514	chr9:71726362-71726363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs139388409	chr9:71726378-71726379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs142576325	chr9:71726411-71726412	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs553457347	chr9:71726447-71726448	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs371681911	chr9:71726461-71726462	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs573568246	chr9:71726482-71726483	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs552013926	chr9:71726486-71726487	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs564174625	chr9:71726494-71726495	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs115022128	chr9:71726501-71726502	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs34067121	chr9:71726506-71726507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs145991011	chr9:71726515-71726516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs368957999	chr9:71726654-71726655	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs557320258	chr9:71726685-71726686	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs568025402	chr9:71726724-71726725	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:796 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

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	chr9:71720400-71735600	Weak transcription	Left Ventricle	heart
5	chr9:71720600-71735000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr9:71721200-71726400	Weak transcription	Stomach Mucosa	stomach
7	chr9:71721400-71734600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr9:71722000-71727800	Weak transcription	Placenta	Placenta
9	chr9:71722600-71726800	Weak transcription	Fetal Lung	lung
10	chr9:71723000-71726600	Weak transcription	Liver	Liver
11	chr9:71724600-71726600	Weak transcription	HepG2	liver
12	chr9:71726600-71727000	Enhancers	Liver	Liver
13	chr9:71726600-71727200	Enhancers	Brain Cingulate Gyrus	brain
14	chr9:71726600-71727200	Enhancers	HepG2	liver
15	chr9:71726800-71727000	Enhancers	H9 Cell Line	embryonic stem cell
16	chr9:71726800-71727200	Enhancers	Brain Inferior Temporal Lobe	brain
17	chr9:71726800-71727200	Enhancers	Brain Substantia Nigra	brain
18	chr9:71726800-71727200	Enhancers	Fetal Lung	lung
19	chr9:71727200-71735800	Weak transcription	Brain Substantia Nigra	brain
20	chr9:71728400-71728800	Enhancers	GM12878-XiMat	blood
21	chr9:71728800-71733400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr9:71729000-71730600	Weak transcription	Stomach Mucosa	stomach
23	chr9:71729600-71729800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr9:71729600-71729800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr9:71729600-71729800	Enhancers	K562	blood
26	chr9:71729800-71730800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr9:71729800-71745600	Weak transcription	K562	blood
28	chr9:71730000-71733800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr9:71730200-71730600	Enhancers	Fetal Muscle Leg	muscle
30	chr9:71730200-71730600	Enhancers	NHDF-Ad	bronchial
31	chr9:71730200-71731000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr9:71730400-71731000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr9:71730400-71731000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr9:71730400-71731000	Enhancers	Muscle Satellite Cultured Cells	--
35	chr9:71730400-71731000	Enhancers	Osteobl	bone
36	chr9:71730600-71731000	Enhancers	Stomach Mucosa	stomach
37	chr9:71730600-71734800	Weak transcription	Fetal Muscle Leg	muscle
38	chr9:71730600-71736000	Weak transcription	NHDF-Ad	bronchial
39	chr9:71730800-71731200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr9:71731000-71734600	Weak transcription	Stomach Mucosa	stomach
41	chr9:71731000-71735400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr9:71731000-71736000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr9:71731000-71736000	Weak transcription	Muscle Satellite Cultured Cells	--
44	chr9:71731200-71735400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr9:71733400-71733600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr9:71733400-71734000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr9:71733600-71733800	Enhancers	H9 Cell Line	embryonic stem cell
48	chr9:71733600-71734600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr9:71733600-71735000	Enhancers	Placenta	Placenta
50	chr9:71733800-71734000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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