Variant report

Variant	nsv831612
Chromosome Location	chr9:72473778-72634253
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1749)
CpG islands
(count:122)
Chromatin interactive
region (count:39)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1749 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:72492804-72493198	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:72547942-72548142	HepG2	liver:	n/a	n/a
3	ATF1	chr9:72551434-72551710	K562	blood:	n/a	n/a
4	ATF3	chr9:72561686-72562065	K562	blood:	n/a	n/a
5	ATF3	chr9:72561624-72562128	HCT-116	colon:	n/a	n/a
6	ATF3	chr9:72561761-72562186	HCT-116	colon:	n/a	n/a
7	ATF3	chr9:72551440-72551684	K562	blood:	n/a	n/a
8	BACH1	chr9:72514740-72514755	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr9:72540793-72540973	GM12878	blood:	n/a	n/a
10	BCL3	chr9:72500239-72500884	A549	lung:	n/a	n/a
11	BCL3	chr9:72500373-72500859	A549	lung:	n/a	n/a
12	BHLHE40	chr9:72586930-72587122	K562	blood:	n/a	n/a
13	BHLHE40	chr9:72492881-72493119	K562	blood:	n/a	n/a
14	BRCA1	chr9:72576763-72576779	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr9:72546453-72546462	H1-hESC	embryonic stem cell:	n/a	n/a
16	BRCA1	chr9:72492781-72493014	Hela-S3	cervix:	n/a	n/a
17	CBX3	chr9:72561650-72562184	HCT-116	colon:	n/a	n/a
18	CBX3	chr9:72548472-72548697	K562	blood:	n/a	n/a
19	CBX3	chr9:72561555-72562148	HCT-116	colon:	n/a	n/a
20	CBX3	chr9:72513598-72514297	HCT-116	colon:	n/a	n/a
21	CEBPB	chr9:72504152-72504319	IMR90	lung:	n/a	n/a
22	CEBPB	chr9:72561495-72562305	HCT-116	colon:	n/a	chr9:72561929-72561940
23	CEBPB	chr9:72552432-72552778	IMR90	lung:	n/a	n/a
24	CEBPB	chr9:72513030-72513315	HepG2	liver:	n/a	chr9:72513289-72513300 chr9:72513179-72513192
25	CEBPB	chr9:72487002-72487270	IMR90	lung:	n/a	chr9:72487123-72487134 chr9:72487123-72487136
26	CEBPB	chr9:72500443-72500828	A549	lung:	n/a	n/a
27	CEBPB	chr9:72513524-72514336	HCT-116	colon:	n/a	n/a
28	CEBPB	chr9:72505957-72506205	A549	lung:	n/a	chr9:72506059-72506070
29	CEBPB	chr9:72628362-72628838	IMR90	lung:	n/a	chr9:72628538-72628549 chr9:72628536-72628549
30	CEBPB	chr9:72534818-72535045	HepG2	liver:	n/a	chr9:72534986-72534997
31	CEBPB	chr9:72561597-72562165	A549	lung:	n/a	chr9:72561929-72561940
32	CEBPB	chr9:72492836-72493227	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr9:72544172-72544225	HepG2	liver:	n/a	chr9:72544208-72544219
34	CEBPB	chr9:72500375-72500924	ECC-1	luminal epithelium:	n/a	n/a
35	CEBPB	chr9:72583553-72583777	IMR90	lung:	n/a	chr9:72583698-72583709
36	CEBPB	chr9:72509814-72509856	HepG2	liver:	n/a	n/a
37	CEBPB	chr9:72594977-72595317	IMR90	lung:	n/a	n/a
38	CEBPB	chr9:72619007-72619407	IMR90	lung:	n/a	n/a
39	CEBPB	chr9:72500415-72500866	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr9:72560547-72561073	IMR90	lung:	n/a	n/a
41	CEBPB	chr9:72561755-72562059	K562	blood:	n/a	chr9:72561929-72561940
42	CEBPB	chr9:72500396-72500764	ECC-1	luminal epithelium:	n/a	n/a
43	CEBPB	chr9:72492697-72493282	HCT-116	colon:	n/a	n/a
44	CEBPB	chr9:72544067-72544275	A549	lung:	n/a	chr9:72544208-72544219
45	CEBPB	chr9:72487016-72487296	HepG2	liver:	n/a	chr9:72487123-72487134 chr9:72487123-72487136
46	CEBPB	chr9:72560624-72560843	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr9:72546261-72546424	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr9:72500311-72500919	A549	lung:	n/a	n/a
49	CEBPB	chr9:72544196-72544220	H1-hESC	embryonic stem cell:	n/a	chr9:72544208-72544219
50	CEBPB	chr9:72561631-72562122	IMR90	lung:	n/a	chr9:72561929-72561940

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:72560940-72560990	HEEpiC	esophagus:	n/a
2	chr9:72560940-72560990	GM12892	blood:	n/a
3	chr9:72514243-72514293	BJ	skin:	n/a
4	chr9:72514243-72514293	HUVEC	blood vessel:	n/a
5	chr9:72514243-72514293	NHDF-neo	bronchial:	n/a
6	chr9:72514243-72514293	PANC-1	pancreas:	n/a
7	chr9:72514243-72514293	HNPCEpiC	eye:	n/a
8	chr9:72514243-72514293	HRPEpiC	eye:	n/a
9	chr9:72560940-72560990	HPAEpiC	pulmonary alveolar:	n/a
10	chr9:72514243-72514293	LNCaP	prostate:	n/a
11	chr9:72514243-72514293	T-47D	breast:	n/a
12	chr9:72560940-72560990	BJ	skin:	n/a
13	chr9:72560940-72560990	SKMC	muscle:	n/a
14	chr9:72560940-72560990	AG04449	skin:	fetal
15	chr9:72514243-72514293	HRE	kidney:	n/a
16	chr9:72514243-72514293	H1-hESC	embryonic stem cell:	embryo
17	chr9:72560940-72560990	RPTEC	kidney:	n/a
18	chr9:72560940-72560990	PANC-1	pancreas:	n/a
19	chr9:72514243-72514293	GM06990	blood:	n/a
20	chr9:72560940-72560990	MCF-7	breast:	n/a
21	chr9:72560940-72560990	NB4	blood:	n/a
22	chr9:72514243-72514293	Jurkat	blood:	n/a
23	chr9:72560940-72560990	U87	brain:	n/a
24	chr9:72560940-72560990	NHDF-neo	bronchial:	n/a
25	chr9:72560940-72560990	HCT-116	colon:	n/a
26	chr9:72514243-72514293	NHBE	bronchial:	n/a
27	chr9:72560940-72560990	HNPCEpiC	eye:	n/a
28	chr9:72560940-72560990	AG10803	skin:	n/a
29	chr9:72514243-72514293	GM12878	blood:	n/a
30	chr9:72560940-72560990	NHBE	bronchial:	n/a
31	chr9:72514243-72514293	AG10803	skin:	n/a
32	chr9:72514243-72514293	HRCEpiC	kidney:	n/a
33	chr9:72514243-72514293	MCF-7	breast:	n/a
34	chr9:72560940-72560990	AG09319	gingival:	n/a
35	chr9:72560940-72560990	HEK293	kidney:	embryo
36	chr9:72560940-72560990	AoSMC	blood vessel:	n/a
37	chr9:72514243-72514293	SK-N-MC	brain:	n/a
38	chr9:72560940-72560990	HIPEpiC	eye:	n/a
39	chr9:72514243-72514293	K562	blood:	n/a
40	chr9:72560940-72560990	H1-hESC	embryonic stem cell:	embryo
41	chr9:72514243-72514293	ECC-1	luminal epithelium:	n/a
42	chr9:72514243-72514293	ovcar-3	ovarian:	n/a
43	chr9:72560940-72560990	NH-A	brain:	n/a
44	chr9:72514243-72514293	NB4	blood:	n/a
45	chr9:72560940-72560990	HCF	heart:	n/a
46	chr9:72514243-72514293	HCPEpiC	choroid plexus:	n/a
47	chr9:72514243-72514293	PrEC	prostate:	n/a
48	chr9:72560940-72560990	A549	lung:	n/a
49	chr9:72560940-72560990	HCM	heart:	n/a
50	chr9:72560940-72560990	NT2-D1	testis:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr9:72466770..72470991-chr9:72472018..72475663,4	K562	blood:
2	chr9:72586975..72587497-chr9:73124835..73125760,2	K562	blood:
3	chr9:72512582..72514126-chr9:72872792..72874503,2	MCF-7	breast:
4	chr9:72287581..72288559-chr9:72492736..72493419,3	MCF-7	breast:
5	chr9:72552090..72553965-chr9:72554095..72555858,2	K562	blood:
6	chr9:72480266..72482674-chr9:72527396..72529225,2	K562	blood:
7	chr9:72586536..72587505-chr9:72725613..72726553,4	K562	blood:
8	chr9:72579585..72583057-chr9:72584421..72588172,5	K562	blood:
9	chr9:72505375..72507864-chr9:72508984..72510952,2	K562	blood:
10	chr9:72602857..72604672-chr9:72606319..72607860,2	K562	blood:
11	chr9:72586559..72587592-chr9:72844298..72845151,6	K562	blood:
12	chr9:72513695..72515625-chr9:72515816..72518282,2	K562	blood:
13	chr9:72287397..72288112-chr9:72533825..72535064,5	MCF-7	breast:
14	chr9:72586588..72587213-chr9:72844309..72845161,2	MCF-7	breast:
15	chr9:72602857..72604672-chr9:72606319..72607860,2	K562	blood:
16	chr9:72554296..72556311-chr9:72558075..72560208,2	K562	blood:
17	chr9:72588649..72589350-chr9:72728157..72729028,2	MCF-7	breast:
18	chr9:72170921..72173288-chr9:72491881..72494788,2	MCF-7	breast:
19	chr9:72287443..72288006-chr9:72547582..72548391,2	K562	blood:
20	chr9:72513695..72515625-chr9:72515816..72518282,2	K562	blood:
21	chr9:72625669..72627256-chr9:72629721..72631306,2	MCF-7	breast:
22	chr9:72480266..72482674-chr9:72527396..72529225,2	K562	blood:
23	chr17:62496286..62496984-chr9:72617693..72618495,2	MCF-7	breast:
24	chr9:72586526..72587567-chr9:72725652..72726529,9	MCF-7	breast:
25	chr9:72579585..72583057-chr9:72584421..72588172,5	K562	blood:
26	chr9:72586580..72588000-chr9:72728026..72728995,9	MCF-7	breast:
27	chr9:72596256..72598713-chr9:72601006..72603750,3	K562	blood:
28	chr9:72554296..72556311-chr9:72558075..72560208,2	K562	blood:
29	chr9:72533081..72534901-chr9:72537488..72539273,2	MCF-7	breast:
30	chr9:72596256..72598713-chr9:72601006..72603750,3	K562	blood:
31	chr9:72625669..72627256-chr9:72629721..72631306,2	MCF-7	breast:
32	chr9:72505375..72507864-chr9:72508984..72510952,2	K562	blood:
33	chr9:72533081..72534901-chr9:72537488..72539273,2	MCF-7	breast:
34	chr9:72373598..72376289-chr9:72500894..72503778,2	K562	blood:
35	chr9:72371606..72373829-chr9:72533135..72535747,2	MCF-7	breast:
36	chr9:72611748..72614537-chr9:72726027..72728626,2	MCF-7	breast:
37	chr9:72552090..72553965-chr9:72554095..72555858,2	K562	blood:
38	chr9:72625560..72627184-chr9:72663529..72666454,2	MCF-7	breast:
39	chr9:72586692..72587617-chr9:72725591..72726665,4	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MAMDC2-3	chr9:72520870-72521143	NONHSAT131791
2	lnc-PTAR1-3	chr9:72499279-72499566	NONHSAT131792
3	lnc-MAMDC2-3	chr9:72501754-72501811	NONHSAT131791
4	lnc-MAMDC2-3	chr9:72499969-72500038	NONHSAT131791

No data

Variant related genes	Relation type
RN7SL570P	TF binding region
RN7SL570P	CpG island
ENSG00000188647	chromatin interactions
ENSG00000204706	chromatin interactions
ENSG00000268364	chromatin interactions
ENSG00000261447	chromatin interactions
ENSG00000198887	chromatin interactions
ENSG00000265695	chromatin interactions

Extended variants
information (count: 5691 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:5691 , 50 per page) page: 1 2 3 4 5 6 7 ... 114

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs557490307	chr9:72473799-72473800	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs76033557	chr9:72473834-72473835	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs549065170	chr9:72473838-72473839	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs180699863	chr9:72473975-72473976	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs34702508	chr9:72473996-72473997	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs143140686	chr9:72474042-72474043	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs571459098	chr9:72474048-72474049	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs538505647	chr9:72474107-72474108	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs373018315	chr9:72474109-72474110	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs138640645	chr9:72474114-72474115	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs141301347	chr9:72474185-72474186	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs542924239	chr9:72474191-72474192	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs554116505	chr9:72474195-72474196	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs575660197	chr9:72474213-72474214	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs374238610	chr9:72474269-72474270	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs543097323	chr9:72474286-72474287	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs373138477	chr9:72474341-72474342	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs577811582	chr9:72474385-72474386	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs370915051	chr9:72474417-72474418	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs545223051	chr9:72474432-72474433	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs185323293	chr9:72474494-72474495	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs145053474	chr9:72474498-72474499	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs571103221	chr9:72474556-72474557	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs373785577	chr9:72474558-72474559	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs549681287	chr9:72474570-72474571	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs561252908	chr9:72474595-72474596	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs138835237	chr9:72474596-72474597	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs549669675	chr9:72474605-72474606	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs571862305	chr9:72474606-72474607	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs141407198	chr9:72474618-72474619	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs150490748	chr9:72474646-72474647	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs569934281	chr9:72474730-72474731	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs539133218	chr9:72474736-72474737	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs547242020	chr9:72474780-72474781	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs565889877	chr9:72474793-72474794	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs536134855	chr9:72474813-72474814	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs7022303	chr9:72474839-72474840	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs575621723	chr9:72474880-72474881	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs189454346	chr9:72474898-72474899	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs558131891	chr9:72474899-72474900	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs113613541	chr9:72474906-72474907	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs541133733	chr9:72474968-72474969	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs560450289	chr9:72475009-72475010	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs11140689	chr9:72475010-72475011	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs543336989	chr9:72475013-72475014	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs149631248	chr9:72475069-72475070	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs182563938	chr9:72475110-72475111	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs550160757	chr9:72475153-72475154	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs565295967	chr9:72475192-72475193	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs186690271	chr9:72475281-72475282	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
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
Schizophrenia	23813976	CNVD
Breast cancer	22522925	CNVD
Intellectual disability	21811512	CNVD
Autism	21484199	CNVD
Breast cancer	22737080	CNVD
Malignant peripheral nerve sheath tumor	22811580	CNVD
Leprosy	22719964	CNVD
Primary ovarian insufficiency	22879975	CNVD
Malignant melanoma	17260012	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1286 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:72442800-72480200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr9:72467600-72474600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr9:72468000-72474400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr9:72471000-72481800	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr9:72471600-72474000	Enhancers	Muscle Satellite Cultured Cells	--
6	chr9:72471600-72474000	Enhancers	HUVEC	blood vessel
7	chr9:72472000-72474600	Strong transcription	HUES48 Cell Line	embryonic stem cell
8	chr9:72472200-72473800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr9:72472600-72474800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr9:72472600-72476000	Weak transcription	NH-A	brain
11	chr9:72472800-72474400	Strong transcription	HUES6 Cell Line	embryonic stem cell
12	chr9:72472800-72474600	Strong transcription	HUES64 Cell Line	embryonic stem cell
13	chr9:72472800-72476200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr9:72473000-72474000	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
15	chr9:72473000-72475000	Strong transcription	iPS-15b Cell Line	embryonic stem cell
16	chr9:72473200-72474400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr9:72473200-72475400	Strong transcription	H1 Cell Line	embryonic stem cell
18	chr9:72473400-72474400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr9:72473400-72475800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr9:72473800-72474600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr9:72474000-72475600	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr9:72474000-72476800	Weak transcription	Pancreatic Islets	Pancreatic Islet
23	chr9:72474400-72474800	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
24	chr9:72474400-72474800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
25	chr9:72474400-72474800	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr9:72474400-72475000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
27	chr9:72474600-72474800	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr9:72474600-72474800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
29	chr9:72474600-72475000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr9:72474600-72475200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
31	chr9:72474600-72475400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr9:72474800-72475400	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
33	chr9:72474800-72475600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr9:72475000-72487000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
35	chr9:72475200-72475800	Weak transcription	HUES48 Cell Line	embryonic stem cell
36	chr9:72475400-72479000	Weak transcription	H1 Cell Line	embryonic stem cell
37	chr9:72475400-72487600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
38	chr9:72475400-72495200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
39	chr9:72475600-72476600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr9:72475600-72476600	Enhancers	HMEC	breast
41	chr9:72475600-72476800	Enhancers	Muscle Satellite Cultured Cells	--
42	chr9:72475600-72476800	Enhancers	NHEK	skin
43	chr9:72475800-72476000	Enhancers	NHDF-Ad	bronchial
44	chr9:72475800-72476200	Strong transcription	HUES48 Cell Line	embryonic stem cell
45	chr9:72475800-72476400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr9:72476000-72476400	Enhancers	HSMMtube	muscle
47	chr9:72476000-72476400	Enhancers	NH-A	brain
48	chr9:72476000-72476400	Enhancers	Osteobl	bone
49	chr9:72476200-72476600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr9:72476200-72477200	Enhancers	Primary T cells from cord blood	blood

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