Variant report

Variant	nsv1051808
Chromosome Location	chr9:115397891-115590950
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3440)
CpG islands
(count:855)
Chromatin interactive
region (count:220)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3440 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:115480237-115480501	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:115479963-115479990	K562	blood:	n/a	n/a
3	ARID3A	chr9:115494056-115494755	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:115512832-115512868	K562	blood:	n/a	n/a
5	ARID3A	chr9:115526787-115526979	K562	blood:	n/a	n/a
6	ARID3A	chr9:115527085-115527557	HepG2	liver:	n/a	n/a
7	ARID3A	chr9:115512431-115512988	HepG2	liver:	n/a	n/a
8	ARID3A	chr9:115480786-115481091	HepG2	liver:	n/a	n/a
9	ARID3A	chr9:115480303-115480518	K562	blood:	n/a	n/a
10	ARID3A	chr9:115509251-115509790	HepG2	liver:	n/a	n/a
11	ATF1	chr9:115479899-115480664	K562	blood:	n/a	n/a
12	ATF1	chr9:115492920-115493063	K562	blood:	n/a	n/a
13	ATF1	chr9:115546849-115547018	K562	blood:	n/a	n/a
14	ATF2	chr9:115546485-115546980	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr9:115546557-115547024	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr9:115536387-115537342	GM12878	blood:	n/a	n/a
17	ATF2	chr9:115461429-115461926	GM12878	blood:	n/a	n/a
18	ATF2	chr9:115571553-115572322	GM12878	blood:	n/a	n/a
19	ATF2	chr9:115479964-115480574	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr9:115480059-115480571	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr9:115571491-115572271	GM12878	blood:	n/a	n/a
22	ATF2	chr9:115533877-115534620	GM12878	blood:	n/a	n/a
23	ATF2	chr9:115461473-115461858	GM12878	blood:	n/a	n/a
24	ATF2	chr9:115534041-115534389	GM12878	blood:	n/a	n/a
25	ATF2	chr9:115479969-115480608	GM12878	blood:	n/a	n/a
26	ATF3	chr9:115512764-115513021	K562	blood:	n/a	n/a
27	ATF3	chr9:115513811-115514038	K562	blood:	n/a	chr9:115513959-115513968
28	BACH1	chr9:115513425-115513999	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr9:115480689-115480847	K562	blood:	n/a	n/a
30	BACH1	chr9:115555648-115555803	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr9:115480800-115481000	H1-hESC	embryonic stem cell:	n/a	n/a
32	BATF	chr9:115571596-115572164	GM12878	blood:	n/a	chr9:115571860-115571871
33	BATF	chr9:115571549-115572196	GM12878	blood:	n/a	chr9:115571860-115571871
34	BATF	chr9:115477441-115477621	GM12878	blood:	n/a	n/a
35	BATF	chr9:115477422-115477655	GM12878	blood:	n/a	n/a
36	BATF	chr9:115450305-115450695	GM12878	blood:	n/a	chr9:115450534-115450545 chr9:115450535-115450545
37	BATF	chr9:115481594-115481937	GM12878	blood:	n/a	n/a
38	BATF	chr9:115555592-115555842	GM12878	blood:	n/a	n/a
39	BATF	chr9:115481521-115481962	GM12878	blood:	n/a	n/a
40	BCL11A	chr9:115571550-115572162	GM12878	blood:	n/a	n/a
41	BCL11A	chr9:115571502-115572209	GM12878	blood:	n/a	n/a
42	BCL3	chr9:115571588-115572096	GM12878	blood:	n/a	n/a
43	BCL3	chr9:115461526-115461832	GM12878	blood:	n/a	n/a
44	BCLAF1	chr9:115479865-115480402	GM12878	blood:	n/a	n/a
45	BCLAF1	chr9:115479702-115480535	GM12878	blood:	n/a	chr9:115480429-115480442
46	BCLAF1	chr9:115461422-115462143	GM12878	blood:	n/a	n/a
47	BCLAF1	chr9:115512540-115513253	GM12878	blood:	n/a	chr9:115513227-115513236 chr9:115513036-115513049 chr9:115513132-115513145
48	BCLAF1	chr9:115571542-115572234	GM12878	blood:	n/a	n/a
49	BCLAF1	chr9:115536629-115537207	GM12878	blood:	n/a	n/a
50	BCLAF1	chr9:115582032-115582507	GM12878	blood:	n/a	n/a

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:115513525-115513575	SK-N-SH	brain:	n/a
2	chr9:115513525-115513575	SK-N-SH	brain:	n/a
3	chr9:115480539-115480589	SK-N-SH	brain:	n/a
4	chr9:115480625-115480675	HUVEC	blood vessel:	n/a
5	chr9:115513482-115513532	AG04449	skin:	fetal
6	chr9:115480324-115480374	PFSK-1	brain:	n/a
7	chr9:115512612-115512662	HAEpiC	amniotic membrane:	n/a
8	chr9:115513820-115513870	MCF-7	breast:	n/a
9	chr9:115512612-115512662	NB4	blood:	n/a
10	chr9:115513820-115513870	H1-hESC	embryonic stem cell:	embryo
11	chr9:115509770-115509820	H1-hESC	embryonic stem cell:	embryo
12	chr9:115481039-115481089	Caco-2	colon:	n/a
13	chr9:115480630-115480680	A549	lung:	n/a
14	chr9:115513056-115513106	SK-N-MC	brain:	n/a
15	chr9:115480630-115480680	PrEC	prostate:	n/a
16	chr9:115509770-115509820	ECC-1	luminal epithelium:	n/a
17	chr9:115480324-115480374	NT2-D1	testis:	n/a
18	chr9:115512530-115512580	HIPEpiC	eye:	n/a
19	chr9:115480630-115480680	SK-N-SH_RA	brain:	n/a
20	chr9:115513056-115513106	ovcar-3	ovarian:	n/a
21	chr9:115480324-115480374	HPAEpiC	pulmonary alveolar:	n/a
22	chr9:115509770-115509820	Jurkat	blood:	n/a
23	chr9:115513056-115513106	H1-hESC	embryonic stem cell:	embryo
24	chr9:115480324-115480374	PrEC	prostate:	n/a
25	chr9:115480060-115480110	CMK	blood:	n/a
26	chr9:115513056-115513106	RPTEC	kidney:	n/a
27	chr9:115512612-115512662	GM19239	blood:	n/a
28	chr9:115480630-115480680	HepG2	liver:	n/a
29	chr9:115480625-115480675	T-47D	breast:	n/a
30	chr9:115480060-115480110	Hela-S3	cervix:	n/a
31	chr9:115513525-115513575	HRPEpiC	eye:	n/a
32	chr9:115481039-115481089	GM12892	blood:	n/a
33	chr9:115480324-115480374	AoSMC	blood vessel:	n/a
34	chr9:115513756-115513806	HCF	heart:	n/a
35	chr9:115513056-115513106	HCF	heart:	n/a
36	chr9:115480630-115480680	HIPEpiC	eye:	n/a
37	chr9:115513525-115513575	AG09319	gingival:	n/a
38	chr9:115480625-115480675	GM12891	blood:	n/a
39	chr9:115512530-115512580	AG09309	skin:	n/a
40	chr9:115513525-115513575	Hela-S3	cervix:	n/a
41	chr9:115509770-115509820	LNCaP	prostate:	n/a
42	chr9:115513482-115513532	H1-hESC	embryonic stem cell:	embryo
43	chr9:115480539-115480589	PrEC	prostate:	n/a
44	chr9:115480625-115480675	ovcar-3	ovarian:	n/a
45	chr9:115509770-115509820	PFSK-1	brain:	n/a
46	chr9:115512530-115512580	HCPEpiC	choroid plexus:	n/a
47	chr9:115480060-115480110	NH-A	brain:	n/a
48	chr9:115480625-115480675	RPTEC	kidney:	n/a
49	chr9:115480324-115480374	HAEpiC	amniotic membrane:	n/a
50	chr9:115512612-115512662	GM12891	blood:	n/a

(count:220 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr9:114849146..114849653-chr9:115555183..115555717,2	K562	blood:
2	chr9:115204840..115206554-chr9:115427326..115428723,8	MCF-7	breast:
3	chr9:114849487..114850237-chr9:115427590..115428335,2	MCF-7	breast:
4	chr9:115513405..115514933-chr9:115545989..115548662,2	MCF-7	breast:
5	chr9:115380523..115382087-chr9:115395680..115398625,2	K562	blood:
6	chr9:115566993..115569306-chr9:115570718..115573402,2	K562	blood:
7	chr9:115247555..115250048-chr9:115510709..115513501,2	K562	blood:
8	chr9:115512086..115514376-chr9:115549215..115552051,3	MCF-7	breast:
9	chr9:115571216..115573226-chr9:115575838..115578800,2	K562	blood:
10	chr9:115431402..115433363-chr9:115441682..115443542,2	K562	blood:
11	chr9:115421830..115423698-chr9:115425235..115427164,2	K562	blood:
12	chr9:115533906..115536575-chr9:115567141..115568722,2	MCF-7	breast:
13	chr9:115463918..115467105-chr9:115470637..115474158,3	K562	blood:
14	chr9:115511487..115514115-chr9:115544583..115546972,6	MCF-7	breast:
15	chr9:114875097..114875949-chr9:115427314..115428143,3	MCF-7	breast:
16	chr9:115505276..115505895-chr9:115555411..115556004,2	MCF-7	breast:
17	chr9:115466699..115468556-chr9:115477154..115479875,2	K562	blood:
18	chr9:115545740..115547705-chr9:115549522..115552424,3	K562	blood:
19	chr9:115568175..115570231-chr9:115604790..115606325,2	K562	blood:
20	chr9:115121494..115123816-chr9:115469907..115472634,2	MCF-7	breast:
21	chr9:115478846..115480456-chr9:115577963..115579856,2	MCF-7	breast:
22	chr9:115465332..115466995-chr9:115480196..115481737,2	K562	blood:
23	chr1:9294148..9295084-chr9:115512424..115513185,2	Hela-S3	cervix:
24	chr9:115469893..115474595-chr9:115477865..115481972,7	K562	blood:
25	chr9:115533906..115536575-chr9:115567141..115568722,2	MCF-7	breast:
26	chr9:115543121..115545474-chr9:115548889..115551043,2	K562	blood:
27	chr9:115477963..115483003-chr9:115511350..115514480,8	K562	blood:
28	chr9:115549478..115551812-chr9:115554338..115556959,2	MCF-7	breast:
29	chr9:115463918..115467105-chr9:115470637..115474158,3	K562	blood:
30	chr9:115205105..115205795-chr9:115467855..115468653,2	MCF-7	breast:
31	chr9:115520162..115522782-chr9:115581748..115584081,2	MCF-7	breast:
32	chr9:115512422..115514539-chr9:115533926..115536411,4	MCF-7	breast:
33	chr9:115570774..115572548-chr9:115577000..115579037,2	MCF-7	breast:
34	chr9:115246565..115250860-chr9:115424773..115429612,5	MCF-7	breast:
35	chr9:115545454..115548524-chr9:115549503..115552233,3	MCF-7	breast:
36	chr9:115488383..115489985-chr9:115491570..115493098,2	K562	blood:
37	chr9:115566617..115568493-chr9:115570718..115573933,3	K562	blood:
38	chr9:115249020..115249928-chr9:115479752..115480523,2	Hela-S3	cervix:
39	chr9:115565373..115568100-chr9:115582412..115584863,2	MCF-7	breast:
40	chr9:115466699..115468556-chr9:115477154..115479875,2	K562	blood:
41	chr9:115478146..115483068-chr9:115509233..115514262,7	K562	blood:
42	chr9:115512668..115515460-chr9:115534425..115536617,2	K562	blood:
43	chr9:115555053..115556635-chr9:115557312..115560299,2	MCF-7	breast:
44	chr9:115480360..115482019-chr9:115485425..115488310,2	K562	blood:
45	chr9:115549226..115551545-chr9:115577690..115579571,2	MCF-7	breast:
46	chr9:115472706..115474595-chr9:115477328..115479365,2	K562	blood:
47	chr9:115574660..115576391-chr9:115583184..115586176,2	K562	blood:
48	chr9:115542323..115543892-chr9:115545474..115547035,2	K562	blood:
49	chr9:115512640..115515348-chr9:115547273..115548788,2	MCF-7	breast:
50	chr9:115476889..115478492-chr9:115480105..115481755,2	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KIAA1958-1	chr9:115484007-115484956	NONHSAT134022
2	lnc-SLC46A2-4	chr9:115478741-115478821	NONHSAT134023
3	lnc-C9orf80-1	chr9:115511360-115512795	XLOC_007830
4	lnc-KIAA1958-1	chr9:115454118-115454181	NONHSAT134022
5	lnc-C9orf80-1	chr9:115511182-115511550	XLOC_007830
6	lnc-C9orf80-1	chr9:115505051-115505514	XLOC_007830
7	lnc-SLC46A2-4	chr9:115456314-115456513	NONHSAT134023
8	lnc-C9orf80-1	chr9:115512686-115512736	XLOC_007830
9	lnc-KIAA1958-1	chr9:115453057-115453265	NONHSAT134022
10	lnc-SLC46A2-4	chr9:115480267-115480397	NONHSAT134023

No data

Variant related genes	Relation type
ENSG00000226609	TF binding region
INIP	TF binding region
SNX30	TF binding region
ENSG00000226609	CpG island
INIP	CpG island
SNX30	CpG island
ENSG00000271631	chromatin interactions
ENSG00000110925	chromatin interactions
ENSG00000230185	chromatin interactions
ENSG00000226609	chromatin interactions
ENSG00000119471	chromatin interactions
ENSG00000101144	chromatin interactions
ENSG00000173473	chromatin interactions
ENSG00000150760	chromatin interactions
ENSG00000165185	chromatin interactions
ENSG00000010165	chromatin interactions
ENSG00000148158	chromatin interactions
ENSG00000049239	chromatin interactions
ENSG00000119314	chromatin interactions
ENSG00000148153	chromatin interactions
SETD8	miRNA target sites

Extended variants
information (count: 7120 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:7120 , 50 per page) page: 1 2 3 4 5 6 7 ... 143

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs184893767	chr9:115397896-115397897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs540387097	chr9:115397905-115397906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs535302452	chr9:115397974-115397975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs565729442	chr9:115397979-115397980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs536206262	chr9:115397992-115397993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs554844093	chr9:115398024-115398025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs559459033	chr9:115398037-115398038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs572958734	chr9:115398068-115398069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs553532049	chr9:115398089-115398090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs187463911	chr9:115398175-115398176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs564831609	chr9:115398195-115398196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs140095675	chr9:115398230-115398231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs530749665	chr9:115398238-115398239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs565841720	chr9:115398278-115398279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs560570255	chr9:115398305-115398306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs555863903	chr9:115398353-115398354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs10981462	chr9:115398381-115398382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs376716398	chr9:115398386-115398387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs201809065	chr9:115398387-115398388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs113783354	chr9:115398388-115398389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs567007264	chr9:115398473-115398474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs538853149	chr9:115398493-115398494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs73656440	chr9:115398561-115398562	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs369993878	chr9:115398598-115398599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs149538113	chr9:115398627-115398628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs372668631	chr9:115398649-115398650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs554969324	chr9:115398654-115398655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs574895990	chr9:115398669-115398670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs557991526	chr9:115398749-115398750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs534254991	chr9:115398786-115398787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs540766127	chr9:115398827-115398828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs575952242	chr9:115398828-115398829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs543440560	chr9:115398924-115398925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs192690449	chr9:115398942-115398943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs555540766	chr9:115398979-115398980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs2798317	chr9:115399064-115399065	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs564763879	chr9:115399076-115399077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs575165847	chr9:115399082-115399083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs574493332	chr9:115399092-115399093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs551003738	chr9:115399100-115399101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs112111701	chr9:115399112-115399113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs369235667	chr9:115399169-115399170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs143211760	chr9:115399174-115399175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs184541302	chr9:115399226-115399227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs559980950	chr9:115399228-115399229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs189242988	chr9:115399247-115399248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs552776854	chr9:115399254-115399255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs569490031	chr9:115399266-115399267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs563591668	chr9:115399279-115399280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs538499572	chr9:115399285-115399286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Oral squamous cell carcinoma	17134496	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
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
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
small cell lung cancer	20016488	CNVD
Cardiac fibroma	18329553	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
Lung cancer	19147751	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:4715 , 50 per page) page: 1 2 3 4 5 6 7 ... 95

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:115379000-115410200	Weak transcription	HSMMtube	muscle
2	chr9:115381000-115402800	Weak transcription	Primary T cells from cord blood	blood
3	chr9:115381200-115400600	Weak transcription	Fetal Intestine Small	intestine
4	chr9:115381200-115401600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr9:115381200-115401600	Weak transcription	Dnd41	blood
6	chr9:115383000-115399800	Weak transcription	Gastric	stomach
7	chr9:115383600-115401400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr9:115387600-115401400	Weak transcription	Esophagus	oesophagus
9	chr9:115388000-115401400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr9:115392400-115401400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr9:115392400-115401400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr9:115392400-115415600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr9:115392400-115421600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
14	chr9:115392600-115401200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr9:115392600-115401400	Weak transcription	H1 Cell Line	embryonic stem cell
16	chr9:115392600-115401600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr9:115392600-115401600	Weak transcription	Fetal Stomach	stomach
18	chr9:115392600-115410400	Weak transcription	Ovary	ovary
19	chr9:115394200-115401400	Weak transcription	Primary B cells from cord blood	blood
20	chr9:115397800-115408000	Weak transcription	HepG2	liver
21	chr9:115398200-115401400	Weak transcription	Fetal Intestine Large	intestine
22	chr9:115398200-115401800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr9:115399200-115401200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr9:115399800-115400000	Enhancers	Gastric	stomach
25	chr9:115400000-115401600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr9:115400000-115401600	Weak transcription	Gastric	stomach
27	chr9:115400600-115403000	ZNF genes & repeats	Fetal Intestine Small	intestine
28	chr9:115401200-115402200	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr9:115401200-115403000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr9:115401200-115426200	Weak transcription	Fetal Kidney	kidney
31	chr9:115401400-115402000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
32	chr9:115401400-115402000	ZNF genes & repeats	Esophagus	oesophagus
33	chr9:115401400-115402200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
34	chr9:115401400-115402200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr9:115401400-115402400	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr9:115401400-115402800	ZNF genes & repeats	Fetal Intestine Large	intestine
37	chr9:115401400-115403000	ZNF genes & repeats	Primary B cells from cord blood	blood
38	chr9:115401400-115403200	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
39	chr9:115401400-115403200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr9:115401600-115401800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr9:115401600-115401800	Genic enhancers	Gastric	stomach
42	chr9:115401600-115401800	Enhancers	Pancreas	Pancrea
43	chr9:115401600-115402000	ZNF genes & repeats	Aorta	Aorta
44	chr9:115401600-115402200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr9:115401600-115402400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
46	chr9:115401600-115402600	ZNF genes & repeats	Dnd41	blood
47	chr9:115401600-115403000	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr9:115401600-115403000	ZNF genes & repeats	Fetal Lung	lung
49	chr9:115401600-115403000	ZNF genes & repeats	Fetal Stomach	stomach
50	chr9:115401800-115402200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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