Variant report

Variant	nsv893606
Chromosome Location	chr9:99659608-99795125
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1397)
CpG islands
(count:733)
Chromatin interactive
region (count:7)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1397 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:99736420-99736602	K562	blood:	n/a	n/a
2	ARID3A	chr9:99762986-99763012	K562	blood:	n/a	n/a
3	ATF1	chr9:99736348-99736700	K562	blood:	n/a	n/a
4	ATF1	chr9:99775887-99776268	K562	blood:	n/a	n/a
5	ATF1	chr9:99763809-99763993	K562	blood:	n/a	n/a
6	ATF3	chr9:99775915-99776206	K562	blood:	n/a	chr9:99776049-99776069 chr9:99776048-99776057
7	ATF3	chr9:99775882-99776207	H1-hESC	embryonic stem cell:	n/a	chr9:99776049-99776069 chr9:99776048-99776057
8	BATF	chr9:99763079-99763405	GM12878	blood:	n/a	n/a
9	BATF	chr9:99770029-99770264	GM12878	blood:	n/a	n/a
10	BATF	chr9:99724688-99724925	GM12878	blood:	n/a	chr9:99724827-99724838
11	BATF	chr9:99752274-99752532	GM12878	blood:	n/a	n/a
12	BATF	chr9:99747523-99747665	GM12878	blood:	n/a	n/a
13	BATF	chr9:99754551-99754936	GM12878	blood:	n/a	n/a
14	BATF	chr9:99775069-99775317	GM12878	blood:	n/a	n/a
15	BATF	chr9:99775879-99776217	GM12878	blood:	n/a	n/a
16	BATF	chr9:99774144-99774400	GM12878	blood:	n/a	n/a
17	BATF	chr9:99754527-99755014	GM12878	blood:	n/a	n/a
18	BATF	chr9:99774105-99774379	GM12878	blood:	n/a	n/a
19	BATF	chr9:99724325-99724527	GM12878	blood:	n/a	chr9:99724439-99724450
20	BATF	chr9:99762447-99762899	GM12878	blood:	n/a	n/a
21	BATF	chr9:99775889-99776132	GM12878	blood:	n/a	n/a
22	BATF	chr9:99770000-99770228	GM12878	blood:	n/a	n/a
23	BATF	chr9:99685003-99685212	GM12878	blood:	n/a	n/a
24	BATF	chr9:99752247-99752587	GM12878	blood:	n/a	n/a
25	BCL11A	chr9:99774143-99774390	GM12878	blood:	n/a	n/a
26	BCL11A	chr9:99769974-99770266	GM12878	blood:	n/a	n/a
27	BCL11A	chr9:99754648-99754953	GM12878	blood:	n/a	n/a
28	BCL11A	chr9:99685016-99685230	GM12878	blood:	n/a	n/a
29	BCL11A	chr9:99774156-99774408	GM12878	blood:	n/a	n/a
30	BCL11A	chr9:99775924-99776232	GM12878	blood:	n/a	chr9:99775926-99775939
31	BCL11A	chr9:99769920-99770265	GM12878	blood:	n/a	n/a
32	BCL11A	chr9:99754548-99755013	GM12878	blood:	n/a	n/a
33	BCL11A	chr9:99775011-99775297	GM12878	blood:	n/a	n/a
34	BCL11A	chr9:99676841-99677065	GM12878	blood:	n/a	n/a
35	BCL11A	chr9:99752281-99752556	GM12878	blood:	n/a	n/a
36	BCLAF1	chr9:99774833-99775067	GM12878	blood:	n/a	n/a
37	BHLHE40	chr9:99775997-99776097	K562	blood:	n/a	n/a
38	BHLHE40	chr9:99736383-99736604	K562	blood:	n/a	n/a
39	BHLHE40	chr9:99772038-99772227	K562	blood:	n/a	n/a
40	BRCA1	chr9:99775908-99776144	Hela-S3	cervix:	n/a	n/a
41	CBX3	chr9:99736169-99736684	K562	blood:	n/a	n/a
42	CBX3	chr9:99771956-99772426	K562	blood:	n/a	n/a
43	CBX3	chr9:99792858-99793126	K562	blood:	n/a	n/a
44	CBX3	chr9:99774773-99775299	K562	blood:	n/a	n/a
45	CBX3	chr9:99792799-99793133	K562	blood:	n/a	n/a
46	CBX3	chr9:99775757-99776354	K562	blood:	n/a	n/a
47	CBX3	chr9:99772025-99772304	K562	blood:	n/a	n/a
48	CBX3	chr9:99775906-99776291	K562	blood:	n/a	n/a
49	CCNT2	chr9:99736331-99736531	K562	blood:	n/a	n/a
50	CEBPB	chr9:99736373-99736547	K562	blood:	n/a	n/a

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:99775893-99775943	GM12892	blood:	n/a
2	chr9:99775893-99775943	GM12892	blood:	n/a
3	chr9:99776144-99776194	IMR90	lung:	fetal
4	chr9:99775184-99775234	BJ	skin:	n/a
5	chr9:99773358-99773408	Hepatocyte	liver:	n/a
6	chr9:99776144-99776194	HEK293	kidney:	embryo
7	chr9:99688888-99688938	HCPEpiC	choroid plexus:	n/a
8	chr9:99776416-99776466	HL-60	blood:	n/a
9	chr9:99775184-99775234	HL-60	blood:	n/a
10	chr9:99776144-99776194	Hepatocyte	liver:	n/a
11	chr9:99687249-99687299	NH-A	brain:	n/a
12	chr9:99775808-99775858	GM12878	blood:	n/a
13	chr9:99776416-99776466	PrEC	prostate:	n/a
14	chr9:99687244-99687294	GM06990	blood:	n/a
15	chr9:99775808-99775858	AG04449	skin:	fetal
16	chr9:99772042-99772092	AoSMC	blood vessel:	n/a
17	chr9:99776416-99776466	HIPEpiC	eye:	n/a
18	chr9:99687016-99687066	ECC-1	luminal epithelium:	n/a
19	chr9:99688888-99688938	SK-N-SH	brain:	n/a
20	chr9:99772042-99772092	SKMC	muscle:	n/a
21	chr9:99696521-99696571	HCT-116	colon:	n/a
22	chr9:99687249-99687299	GM06990	blood:	n/a
23	chr9:99775808-99775858	AG10803	skin:	n/a
24	chr9:99775808-99775858	ProgFib	skin:	n/a
25	chr9:99687244-99687294	ECC-1	luminal epithelium:	n/a
26	chr9:99776144-99776194	PANC-1	pancreas:	n/a
27	chr9:99776144-99776194	AG04450	lung:	fetal
28	chr9:99687244-99687294	HRPEpiC	eye:	n/a
29	chr9:99687244-99687294	GM12878	blood:	n/a
30	chr9:99776144-99776194	SKMC	muscle:	n/a
31	chr9:99773358-99773408	AG09319	gingival:	n/a
32	chr9:99775808-99775858	HPAEpiC	pulmonary alveolar:	n/a
33	chr9:99773358-99773408	T-47D	breast:	n/a
34	chr9:99687244-99687294	BJ	skin:	n/a
35	chr9:99772042-99772092	NHBE	bronchial:	n/a
36	chr9:99775184-99775234	GM12878	blood:	n/a
37	chr9:99775893-99775943	HCT-116	colon:	n/a
38	chr9:99687249-99687299	HPAEpiC	pulmonary alveolar:	n/a
39	chr9:99775808-99775858	RPTEC	kidney:	n/a
40	chr9:99775184-99775234	PrEC	prostate:	n/a
41	chr9:99773358-99773408	MCF10A-Er-Src	breast:	n/a
42	chr9:99776416-99776466	MCF-7	breast:	n/a
43	chr9:99688888-99688938	SK-N-SH_RA	brain:	n/a
44	chr9:99687016-99687066	NB4	blood:	n/a
45	chr9:99776144-99776194	H1-hESC	embryonic stem cell:	embryo
46	chr9:99776416-99776466	HCT-116	colon:	n/a
47	chr9:99776144-99776194	GM06990	blood:	n/a
48	chr9:99773358-99773408	GM12878	blood:	n/a
49	chr9:99775184-99775234	IMR90	lung:	fetal
50	chr9:99688888-99688938	HIPEpiC	eye:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:99774341..99777390-chr9:99797289..99801643,6	MCF-7	breast:
2	chr9:99792005..99793913-chr9:99798704..99801926,3	MCF-7	breast:
3	chr9:97137075..97138067-chr9:99774972..99775493,2	MCF-7	breast:
4	chr9:99749426..99751006-chr9:99800152..99802924,2	K562	blood:
5	chr9:97135317..97137962-chr9:99774801..99776499,2	MCF-7	breast:
6	chr9:99791951..99794165-chr9:99796736..99799706,2	K562	blood:
7	chr9:99774361..99777166-chr9:99789167..99791934,2	K562	blood:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HIATL2-1	chr9:99695966-99696197	NONHSAT133457
2	lnc-HIATL2-1	chr9:99680925-99681108	NONHSAT133451
3	lnc-HIATL2-1	chr9:99704885-99705034	ENSG00000249044.1
4	lnc-HIATL2-1	chr9:99711837-99711867	ENSG00000249044.1
5	lnc-HIATL2-1	chr9:99696077-99696197	ENSG00000249044.1
6	lnc-HIATL2-2	chr9:99687295-99688122	NONHSAT133455
7	lnc-HIATL2-1	chr9:99704885-99706337	NONHSAT133457
8	lnc-HIATL2-1	chr9:99696077-99696197	NONHSAT133451
9	lnc-HIATL2-1	chr9:99660348-99660409	ENSG00000249044.1
10	lnc-FAM22G-1	chr9:99681210-99681600	NONHSAT133454
11	lnc-HIATL2-1	chr9:99680925-99681108	ENSG00000249044.1
12	lnc-FAM22G-2	chr9:99717102-99717743	NONHSAT133458
13	lnc-HIATL2-1	chr9:99704885-99704936	NONHSAT133451

No data

Variant related genes	Relation type
HIATL2	TF binding region
NUTM2G	TF binding region
YRDCP2	TF binding region
ENSG00000227257	TF binding region
ENSG00000269907	TF binding region
HIATL2	CpG island
NUTM2G	CpG island
YRDCP2	CpG island
ENSG00000227257	CpG island
ENSG00000269907	CpG island
ENSG00000196312	chromatin interactions
ENSG00000136943	chromatin interactions
ENSG00000148110	chromatin interactions

Extended variants
information (count: 4539 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:4539 , 50 per page) page: 1 2 3 4 5 6 7 ... 91

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs56121507	chr9:99659608-99659609	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs551248586	chr9:99659625-99659626	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs149756687	chr9:99659653-99659654	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs370989925	chr9:99659718-99659719	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs554899649	chr9:99659739-99659740	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs139695936	chr9:99659754-99659755	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs537939959	chr9:99659803-99659804	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs185411778	chr9:99659853-99659854	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs10979490	chr9:99659871-99659872	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs111583080	chr9:99659880-99659881	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs147579786	chr9:99659939-99659940	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs573542308	chr9:99659940-99659941	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs142076164	chr9:99659958-99659959	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs370870585	chr9:99659961-99659962	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs199739757	chr9:99659962-99659963	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs529415133	chr9:99660025-99660026	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs151153653	chr9:99660030-99660031	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs552736511	chr9:99660051-99660052	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs140594829	chr9:99660113-99660114	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs73654638	chr9:99660140-99660141	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs556568753	chr9:99660163-99660164	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs3118714	chr9:99660169-99660170	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs116592791	chr9:99660170-99660171	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs527533521	chr9:99660173-99660174	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs548613956	chr9:99660186-99660187	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs567241631	chr9:99660192-99660193	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs188709574	chr9:99660260-99660261	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs181549038	chr9:99660266-99660267	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs116122775	chr9:99660269-99660270	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs368657539	chr9:99660366-99660367	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
31	rs186982203	chr9:99660376-99660377	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
32	rs10653770	chr9:99660378-99660379	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
33	rs540039494	chr9:99660404-99660405	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
34	rs138840602	chr9:99660407-99660408	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
35	rs573581226	chr9:99660522-99660523	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs191823236	chr9:99660565-99660566	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs534492800	chr9:99660582-99660583	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs142091271	chr9:99660596-99660597	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs555840465	chr9:99660616-99660617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs573963748	chr9:99660664-99660665	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs369495821	chr9:99660752-99660753	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs544409958	chr9:99660761-99660762	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs2479206	chr9:99660829-99660830	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs563023462	chr9:99660869-99660870	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs578010103	chr9:99661017-99661018	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs544804606	chr9:99661035-99661036	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs559910621	chr9:99661077-99661078	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs527618883	chr9:99661082-99661083	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs184108388	chr9:99661141-99661142	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs2479652	chr9:99661148-99661149	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
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
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
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Bipolar disorder	18458673	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Biliary cancer	19435499	CNVD
small cell lung cancer	20016488	CNVD
Intracranial aneurysm	16715129	CNVD
Cardiac fibroma	18329553	CNVD
Breast cancer	17133270	CNVD
Basal cell nevus syndrome	21572526	CNVD
Mental retardation	19951919	CNVD
Retinoblastoma	22278416	CNVD
9q22.3 microdeletion syndrome	22283845	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
overgrowth syndrome	16570072	CNVD
Neurodevelopmental disorder	22521361	CNVD
Nicotine dependence	17160897	CNVD
Mantle cell lymphoma	19029149	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Lung adenocarcinoma	21935476	CNVD

Chromatin state (count:946 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:99639000-99661600	Weak transcription	Brain Angular Gyrus	brain
2	chr9:99646600-99660800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr9:99646800-99660800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr9:99646800-99660800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr9:99646800-99661000	Weak transcription	Skeletal Muscle Male	skeletal muscle
6	chr9:99647000-99659800	Weak transcription	K562	blood
7	chr9:99647000-99661800	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr9:99647000-99697000	Weak transcription	Pancreas	Pancrea
9	chr9:99647200-99660000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr9:99647200-99660600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr9:99647200-99660600	Weak transcription	NHEK	skin
12	chr9:99647200-99660800	Weak transcription	NHDF-Ad	bronchial
13	chr9:99647200-99667200	Weak transcription	HMEC	breast
14	chr9:99647400-99660200	Weak transcription	Osteobl	bone
15	chr9:99647800-99660000	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr9:99648000-99665000	Weak transcription	Brain Inferior Temporal Lobe	brain
17	chr9:99648200-99660800	Weak transcription	Brain Substantia Nigra	brain
18	chr9:99650800-99660800	Weak transcription	Fetal Brain Male	brain
19	chr9:99651000-99661600	Weak transcription	Colon Smooth Muscle	Colon
20	chr9:99651200-99660400	Strong transcription	Dnd41	blood
21	chr9:99651200-99691400	Weak transcription	Primary B cells from peripheral blood	blood
22	chr9:99652000-99678600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
23	chr9:99652200-99660200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr9:99652800-99660600	Weak transcription	Fetal Kidney	kidney
25	chr9:99652800-99708400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr9:99654800-99660800	Weak transcription	HUES64 Cell Line	embryonic stem cell
27	chr9:99654800-99678600	Weak transcription	Fetal Intestine Small	intestine
28	chr9:99655200-99661600	Weak transcription	Fetal Lung	lung
29	chr9:99656400-99660200	Weak transcription	Small Intestine	intestine
30	chr9:99656600-99660000	Strong transcription	Ovary	ovary
31	chr9:99656600-99660200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
32	chr9:99656600-99660200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
33	chr9:99656600-99660200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr9:99656600-99660200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr9:99656600-99660400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr9:99656600-99660400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr9:99656600-99681000	Weak transcription	H1 Cell Line	embryonic stem cell
38	chr9:99656800-99660000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
39	chr9:99656800-99660000	Strong transcription	Cortex derived primary cultured neurospheres	brain
40	chr9:99656800-99660200	Strong transcription	Primary B cells from cord blood	blood
41	chr9:99656800-99660200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
42	chr9:99656800-99660400	Strong transcription	Monocytes-CD14+_RO01746	blood
43	chr9:99657000-99660400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr9:99657200-99660200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
45	chr9:99657400-99659800	Enhancers	Primary neutrophils fromperipheralblood	blood
46	chr9:99657400-99660200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
47	chr9:99657800-99660000	Weak transcription	Hela-S3	cervix
48	chr9:99658000-99660400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr9:99658000-99682000	Weak transcription	Adipose Nuclei	Adipose
50	chr9:99658200-99660200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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