Variant report

Variant	nsv893413
Chromosome Location	chr9:71130848-71196984
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:937)
CpG islands
(count:183)
Chromatin interactive
region (count:16)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:937 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:71145607-71145953	HepG2	liver:	n/a	n/a
2	ATF1	chr9:71167762-71167951	K562	blood:	n/a	n/a
3	ATF2	chr9:71161342-71162104	GM12878	blood:	n/a	n/a
4	ATF2	chr9:71192557-71193656	GM12878	blood:	n/a	n/a
5	ATF2	chr9:71159929-71160718	GM12878	blood:	n/a	n/a
6	ATF2	chr9:71161302-71162158	GM12878	blood:	n/a	n/a
7	ATF2	chr9:71192664-71193571	GM12878	blood:	n/a	n/a
8	BACH1	chr9:71167801-71167887	H1-hESC	embryonic stem cell:	n/a	chr9:71167806-71167820
9	BATF	chr9:71160220-71160765	GM12878	blood:	n/a	n/a
10	BATF	chr9:71192731-71193490	GM12878	blood:	n/a	chr9:71192911-71192924
11	BATF	chr9:71160264-71160791	GM12878	blood:	n/a	n/a
12	BATF	chr9:71159925-71160230	GM12878	blood:	n/a	n/a
13	BATF	chr9:71192659-71193541	GM12878	blood:	n/a	chr9:71192911-71192924
14	BATF	chr9:71161399-71162069	GM12878	blood:	n/a	n/a
15	BATF	chr9:71161338-71162104	GM12878	blood:	n/a	n/a
16	BCL11A	chr9:71192711-71193039	GM12878	blood:	n/a	n/a
17	BCL11A	chr9:71193046-71193485	GM12878	blood:	n/a	chr9:71193226-71193235
18	BCL11A	chr9:71192662-71193676	GM12878	blood:	n/a	chr9:71192673-71192681 chr9:71193226-71193235
19	BCL11A	chr9:71161470-71161995	GM12878	blood:	n/a	n/a
20	BCL11A	chr9:71161433-71162084	GM12878	blood:	n/a	n/a
21	BCL3	chr9:71192632-71193012	GM12878	blood:	n/a	chr9:71192673-71192681
22	BCLAF1	chr9:71161350-71162066	GM12878	blood:	n/a	n/a
23	BCLAF1	chr9:71161347-71162166	GM12878	blood:	n/a	n/a
24	BCLAF1	chr9:71192689-71193546	GM12878	blood:	n/a	chr9:71193226-71193235
25	BCLAF1	chr9:71192553-71193466	GM12878	blood:	n/a	chr9:71192673-71192681 chr9:71193226-71193235
26	BHLHE40	chr9:71192849-71193522	GM12878	blood:	n/a	n/a
27	BHLHE40	chr9:71161459-71162275	GM12878	blood:	n/a	n/a
28	BRCA1	chr9:71130101-71131089	Hela-S3	cervix:	n/a	chr9:71130439-71130446
29	BRCA1	chr9:71144964-71144982	HepG2	liver:	n/a	n/a
30	CEBPB	chr9:71145701-71145965	HepG2	liver:	n/a	n/a
31	CEBPB	chr9:71145726-71145925	A549	lung:	n/a	n/a
32	CEBPB	chr9:71145687-71145920	HepG2	liver:	n/a	n/a
33	CEBPB	chr9:71143821-71144121	A549	lung:	n/a	n/a
34	CEBPB	chr9:71175120-71175766	H1-hESC	embryonic stem cell:	n/a	chr9:71175627-71175640
35	CEBPB	chr9:71145686-71145893	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr9:71145648-71145932	IMR90	lung:	n/a	n/a
37	CEBPB	chr9:71145634-71145995	HepG2	liver:	n/a	n/a
38	CEBPB	chr9:71184528-71184988	IMR90	lung:	n/a	chr9:71184809-71184820
39	CEBPB	chr9:71183015-71183258	K562	blood:	n/a	n/a
40	CEBPB	chr9:71182997-71183287	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr9:71167649-71168105	IMR90	lung:	n/a	n/a
42	CEBPB	chr9:71161533-71161767	HepG2	liver:	n/a	n/a
43	CEBPB	chr9:71143163-71143380	HepG2	liver:	n/a	chr9:71143216-71143227
44	CEBPB	chr9:71132140-71132242	K562	blood:	n/a	n/a
45	CEBPB	chr9:71145630-71146027	HepG2	liver:	n/a	n/a
46	CEBPB	chr9:71143850-71144140	MCF-7	breast:	n/a	n/a
47	CEBPB	chr9:71161273-71162165	GM12878	blood:	n/a	n/a
48	CEBPB	chr9:71143800-71144130	HepG2	liver:	n/a	n/a
49	CEBPB	chr9:71175314-71175854	IMR90	lung:	n/a	chr9:71175627-71175640
50	CEBPB	chr9:71145671-71145938	K562	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:71152191-71152241	Hepatocyte	liver:	n/a
2	chr9:71145733-71145783	GM12891	blood:	n/a
3	chr9:71145733-71145783	BE2_C	brain:	n/a
4	chr9:71152191-71152241	HNPCEpiC	eye:	n/a
5	chr9:71145733-71145783	AG04450	lung:	fetal
6	chr9:71145733-71145783	HNPCEpiC	eye:	n/a
7	chr9:71155970-71156020	HRE	kidney:	n/a
8	chr9:71155970-71156020	NHDF-neo	bronchial:	n/a
9	chr9:71152191-71152241	HAEpiC	amniotic membrane:	n/a
10	chr9:71152191-71152241	HIPEpiC	eye:	n/a
11	chr9:71152191-71152241	NB4	blood:	n/a
12	chr9:71145733-71145783	AG09319	gingival:	n/a
13	chr9:71155970-71156020	HCT-116	colon:	n/a
14	chr9:71152191-71152241	ProgFib	skin:	n/a
15	chr9:71152191-71152241	RPTEC	kidney:	n/a
16	chr9:71152191-71152241	H1-hESC	embryonic stem cell:	embryo
17	chr9:71145733-71145783	ECC-1	luminal epithelium:	n/a
18	chr9:71152191-71152241	ovcar-3	ovarian:	n/a
19	chr9:71155970-71156020	CMK	blood:	n/a
20	chr9:71152191-71152241	AG09309	skin:	n/a
21	chr9:71155970-71156020	LNCaP	prostate:	n/a
22	chr9:71155970-71156020	PFSK-1	brain:	n/a
23	chr9:71152191-71152241	AG04450	lung:	fetal
24	chr9:71152191-71152241	SK-N-SH_RA	brain:	n/a
25	chr9:71155970-71156020	HEK293	kidney:	embryo
26	chr9:71152191-71152241	LNCaP	prostate:	n/a
27	chr9:71155970-71156020	K562	blood:	n/a
28	chr9:71145733-71145783	MCF-7	breast:	n/a
29	chr9:71145733-71145783	HRPEpiC	eye:	n/a
30	chr9:71152191-71152241	SKMC	muscle:	n/a
31	chr9:71145733-71145783	A549	lung:	n/a
32	chr9:71155970-71156020	Jurkat	blood:	n/a
33	chr9:71155970-71156020	SKMC	muscle:	n/a
34	chr9:71152191-71152241	A549	lung:	n/a
35	chr9:71145733-71145783	ovcar-3	ovarian:	n/a
36	chr9:71155970-71156020	A549	lung:	n/a
37	chr9:71155970-71156020	GM06990	blood:	n/a
38	chr9:71152191-71152241	Caco-2	colon:	n/a
39	chr9:71155970-71156020	HCF	heart:	n/a
40	chr9:71155970-71156020	AG04449	skin:	fetal
41	chr9:71152191-71152241	HRPEpiC	eye:	n/a
42	chr9:71145733-71145783	NHBE	bronchial:	n/a
43	chr9:71152191-71152241	NHBE	bronchial:	n/a
44	chr9:71145733-71145783	Jurkat	blood:	n/a
45	chr9:71145733-71145783	MCF10A-Er-Src	breast:	n/a
46	chr9:71152191-71152241	ECC-1	luminal epithelium:	n/a
47	chr9:71152191-71152241	GM12891	blood:	n/a
48	chr9:71145733-71145783	PANC-1	pancreas:	n/a
49	chr9:71145733-71145783	PFSK-1	brain:	n/a
50	chr9:71155970-71156020	GM12891	blood:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:71032214..71032797-chr9:71183106..71183655,2	MCF-7	breast:
2	chr9:71162331..71165106-chr9:71166259..71168018,2	MCF-7	breast:
3	chr9:71122335..71122837-chr9:71174540..71175279,2	MCF-7	breast:
4	chr9:71177353..71179557-chr9:71180361..71182323,2	MCF-7	breast:
5	chr9:71175109..71177621-chr9:71180020..71182524,2	K562	blood:
6	chr9:71162331..71165106-chr9:71166259..71168018,2	MCF-7	breast:
7	chr9:71191723..71194469-chr9:71195541..71198531,3	K562	blood:
8	chr9:71150643..71152948-chr9:71155677..71157843,2	MCF-7	breast:
9	chr9:71177353..71179557-chr9:71180361..71182323,2	MCF-7	breast:
10	chr9:71121474..71124177-chr9:71138175..71140429,2	K562	blood:
11	chr9:71140302..71143240-chr9:71143609..71146206,2	MCF-7	breast:
12	chr9:71182851..71183578-chr9:71614201..71614782,2	K562	blood:
13	chr9:71140302..71143240-chr9:71143609..71146206,2	MCF-7	breast:
14	chr9:71191723..71194469-chr9:71195541..71198531,3	K562	blood:
15	chr9:71175109..71177621-chr9:71180020..71182524,2	K562	blood:
16	chr9:71176910..71179720-chr9:110249611..110251759,2	MCF-7	breast:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C9orf71-1	chr9:71160417-71160540	NR_109769
2	lnc-PGM5-1	chr9:71155952-71156146	ENSG00000226337.3
3	lnc-C9orf71-1	chr9:71160417-71160540	XLOC_007722
4	lnc-C9orf71-1	chr9:71158457-71158519	XLOC_007722
5	lnc-C9orf71-1	chr9:71160633-71160752	XLOC_007722
6	lnc-C9orf71-1	chr9:71158457-71158519	NR_109769
7	lnc-C9orf71-1	chr9:71160417-71160540	XLOC_007722
8	lnc-C9orf71-1	chr9:71161475-71161505	XLOC_007722
9	lnc-PGM5-1	chr9:71157294-71157558	NONHSAT131748
10	lnc-PGM5-1	chr9:71157294-71157558	ENSG00000226337.3
11	lnc-C9orf71-1	chr9:71158457-71158519	XLOC_007722
12	lnc-PGM5-1	chr9:71155952-71156146	ENSG00000226337.2
13	lnc-C9orf71-1	chr9:71160845-71161032	XLOC_007722
14	lnc-PGM5-1	chr9:71155951-71156146	NONHSAT131748
15	lnc-C9orf71-1	chr9:71161475-71161518	NR_109769
16	lnc-PGM5-1	chr9:71157294-71157558	ENSG00000226337.2
17	lnc-C9orf71-1	chr9:71160633-71160752	NR_109769
18	lnc-C9orf71-1	chr9:71160633-71160752	XLOC_007722

No data

Variant related genes	Relation type
TMEM252	TF binding region
ENSG00000234506	TF binding region
ENSG00000226337	TF binding region
TMEM252	CpG island
ENSG00000234506	CpG island
ENSG00000226337	CpG island
ENSG00000181778	chromatin interactions
ENSG00000226337	chromatin interactions
ENSG00000136826	chromatin interactions
MCL1	miRNA target sites

Extended variants
information (count: 2285 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:2285 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183688584	chr9:71130857-71130858	Bivalent Enhancer Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs144080486	chr9:71130882-71130883	Bivalent Enhancer Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs575499666	chr9:71130947-71130948	Bivalent Enhancer Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs564061682	chr9:71130948-71130949	Bivalent Enhancer Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs528334771	chr9:71130951-71130952	Bivalent Enhancer Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs78002186	chr9:71130961-71130962	Bivalent Enhancer Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs265089	chr9:71130978-71130979	Bivalent Enhancer Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs530261731	chr9:71130998-71130999	Bivalent Enhancer Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs555659380	chr9:71131061-71131062	Bivalent Enhancer Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs11142713	chr9:71131090-71131091	Bivalent Enhancer Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs11142714	chr9:71131098-71131099	Bivalent Enhancer Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs552778923	chr9:71131162-71131163	Bivalent Enhancer Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs560600623	chr9:71131183-71131184	Bivalent Enhancer Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs529477397	chr9:71131211-71131212	Bivalent Enhancer Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs117425163	chr9:71131226-71131227	Bivalent Enhancer Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs535323310	chr9:71131268-71131269	Bivalent Enhancer Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs553034278	chr9:71131339-71131340	Bivalent Enhancer Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs7357675	chr9:71131402-71131403	Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs78173152	chr9:71131411-71131412	Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs7357676	chr9:71131421-71131422	Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs535386795	chr9:71131454-71131455	Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs556781742	chr9:71131462-71131463	Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs575268761	chr9:71131470-71131471	Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs11790104	chr9:71131480-71131481	Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs563100025	chr9:71131528-71131529	Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs545608948	chr9:71131568-71131569	Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs116915929	chr9:71131587-71131588	Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs145014346	chr9:71131635-71131636	Enhancers Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs540131623	chr9:71131674-71131675	Enhancers Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs559740110	chr9:71131718-71131719	Enhancers Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs530051469	chr9:71131752-71131753	Enhancers Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs148529450	chr9:71131817-71131818	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs563653040	chr9:71131818-71131819	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs531003096	chr9:71131844-71131845	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs536082306	chr9:71131850-71131851	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs571037047	chr9:71131876-71131877	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs535389790	chr9:71131948-71131949	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs142891347	chr9:71131949-71131950	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs568687842	chr9:71132046-71132047	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs535123785	chr9:71132052-71132053	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs556881279	chr9:71132098-71132099	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs112078926	chr9:71132148-71132149	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs80172279	chr9:71132155-71132156	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs185543228	chr9:71132206-71132207	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs557577392	chr9:71132225-71132226	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs555989721	chr9:71132244-71132245	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs539998861	chr9:71132253-71132254	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs561838412	chr9:71132313-71132314	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs563240981	chr9:71132388-71132389	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs11795356	chr9:71132391-71132392	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:62)

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
Acute lymphoblastic leukemia	21098271	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
Pancreatic cancer	17952125	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Bipolar disorder	18458673	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:71117600-71142800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr9:71122200-71133200	Weak transcription	Ovary	ovary
3	chr9:71122400-71132000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr9:71122600-71132400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr9:71124800-71133200	Weak transcription	Fetal Muscle Trunk	muscle
6	chr9:71127400-71132800	Weak transcription	Fetal Lung	lung
7	chr9:71127400-71132800	Weak transcription	Fetal Muscle Leg	muscle
8	chr9:71128400-71131600	Enhancers	Right Ventricle	heart
9	chr9:71128400-71131600	Enhancers	Hela-S3	cervix
10	chr9:71129000-71131000	Enhancers	Skeletal Muscle Male	skeletal muscle
11	chr9:71129000-71131400	Enhancers	Placenta Amnion	Placenta Amnion
12	chr9:71129000-71131400	Enhancers	Right Atrium	heart
13	chr9:71129000-71131800	Enhancers	Placenta	Placenta
14	chr9:71129600-71131000	Enhancers	Rectal Mucosa Donor 29	rectum
15	chr9:71129600-71131000	Enhancers	NHLF	lung
16	chr9:71129800-71131000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr9:71129800-71131000	Enhancers	Monocytes-CD14+_RO01746	blood
18	chr9:71129800-71131200	Enhancers	Primary monocytes fromperipheralblood	blood
19	chr9:71129800-71132800	Weak transcription	Psoas Muscle	Psoas
20	chr9:71130000-71131000	Genic enhancers	Stomach Smooth Muscle	stomach
21	chr9:71130200-71131800	Strong transcription	Fetal Stomach	stomach
22	chr9:71130200-71148000	Weak transcription	HSMMtube	muscle
23	chr9:71130400-71131200	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
24	chr9:71130400-71131200	Weak transcription	Gastric	stomach
25	chr9:71130400-71131600	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
26	chr9:71130400-71131600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
27	chr9:71130400-71132800	Weak transcription	Duodenum Smooth Muscle	Duodenum
28	chr9:71130600-71131600	Enhancers	Stomach Mucosa	stomach
29	chr9:71130600-71132000	Weak transcription	Colon Smooth Muscle	Colon
30	chr9:71130600-71132800	Weak transcription	Aorta	Aorta
31	chr9:71130600-71144400	Weak transcription	Rectal Smooth Muscle	rectum
32	chr9:71130600-71144800	Weak transcription	Left Ventricle	heart
33	chr9:71130800-71131000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
34	chr9:71130800-71131200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
35	chr9:71130800-71131400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
36	chr9:71130800-71131400	Weak transcription	Fetal Intestine Small	intestine
37	chr9:71130800-71145400	Weak transcription	Skeletal Muscle Female	skeletal muscle
38	chr9:71131000-71131800	Strong transcription	Stomach Smooth Muscle	stomach
39	chr9:71131000-71152600	Weak transcription	NHLF	lung
40	chr9:71131200-71131800	Enhancers	Gastric	stomach
41	chr9:71131200-71132200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr9:71131400-71132400	Weak transcription	Placenta Amnion	Placenta Amnion
43	chr9:71131400-71132600	ZNF genes & repeats	Fetal Intestine Small	intestine
44	chr9:71131400-71136800	Weak transcription	Right Atrium	heart
45	chr9:71131600-71145400	Weak transcription	Right Ventricle	heart
46	chr9:71131800-71132800	Weak transcription	Stomach Smooth Muscle	stomach
47	chr9:71131800-71133200	ZNF genes & repeats	Fetal Stomach	stomach
48	chr9:71132000-71132600	Strong transcription	Colon Smooth Muscle	Colon
49	chr9:71132400-71134000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr9:71132600-71133400	ZNF genes & repeats	Colon Smooth Muscle	Colon

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