Variant report

Variant	nsv1030547
Chromosome Location	chr9:517484-603554
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:783)
CpG islands
(count:61)
Chromatin interactive
region (count:23)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:783 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:592251-592433	HepG2	liver:	n/a	n/a
2	ATF3	chr9:557723-558324	A549	lung:	n/a	n/a
3	BACH1	chr9:561382-561724	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr9:557912-558114	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL3	chr9:557812-558394	A549	lung:	n/a	n/a
6	BCL3	chr9:561341-561682	GM12878	blood:	n/a	n/a
7	BCL3	chr9:561269-561869	A549	lung:	n/a	n/a
8	BHLHE40	chr9:546835-547287	K562	blood:	n/a	n/a
9	BHLHE40	chr9:567560-567673	GM12878	blood:	n/a	n/a
10	CEBPB	chr9:589903-590000	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr9:561371-561765	A549	lung:	n/a	n/a
12	CEBPB	chr9:573616-573837	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr9:599948-600356	MCF-7	breast:	n/a	chr9:600087-600098 chr9:600123-600134
14	CEBPB	chr9:561219-561918	A549	lung:	n/a	n/a
15	CEBPB	chr9:599942-600395	HepG2	liver:	n/a	chr9:600087-600098 chr9:600123-600134
16	CEBPB	chr9:599971-600359	ECC-1	luminal epithelium:	n/a	chr9:600087-600098 chr9:600123-600134
17	CEBPB	chr9:599907-600250	ECC-1	luminal epithelium:	n/a	chr9:600087-600098 chr9:600123-600134
18	CEBPB	chr9:599921-600405	A549	lung:	n/a	chr9:600087-600098 chr9:600123-600134
19	CEBPB	chr9:573656-573820	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr9:530695-530959	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr9:602928-603376	MCF-7	breast:	n/a	n/a
22	CEBPB	chr9:530652-530956	A549	lung:	n/a	n/a
23	CEBPB	chr9:599844-600456	A549	lung:	n/a	chr9:600087-600098 chr9:600123-600134
24	CEBPB	chr9:602628-603112	MCF-7	breast:	n/a	n/a
25	CEBPB	chr9:530490-531138	HCT-116	colon:	n/a	chr9:530982-530993 chr9:530982-530995 chr9:530982-530995 chr9:530982-530993
26	CEBPB	chr9:599936-600319	K562	blood:	n/a	chr9:600087-600098 chr9:600123-600134
27	CEBPB	chr9:599943-600381	IMR90	lung:	n/a	chr9:600087-600098 chr9:600123-600134
28	CEBPB	chr9:561463-561714	A549	lung:	n/a	n/a
29	CEBPB	chr9:563605-564145	A549	lung:	n/a	n/a
30	CEBPB	chr9:599889-600308	A549	lung:	n/a	chr9:600087-600098 chr9:600123-600134
31	CEBPB	chr9:599945-600321	H1-hESC	embryonic stem cell:	n/a	chr9:600087-600098 chr9:600123-600134
32	CEBPB	chr9:599836-600408	MCF-7	breast:	n/a	chr9:600087-600098 chr9:600123-600134
33	CEBPB	chr9:589772-590180	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr9:599936-600484	Hela-S3	cervix:	n/a	chr9:600087-600098 chr9:600123-600134
35	CEBPB	chr9:530749-531005	A549	lung:	n/a	chr9:530982-530993 chr9:530982-530995 chr9:530982-530995 chr9:530982-530993
36	CEBPB	chr9:561474-561777	MCF-7	breast:	n/a	n/a
37	CHD1	chr9:557966-558051	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD2	chr9:567407-567657	GM12878	blood:	n/a	n/a
39	CHD2	chr9:591485-591533	Hela-S3	cervix:	n/a	n/a
40	CHD2	chr9:518207-518317	Hela-S3	cervix:	n/a	n/a
41	CREB1	chr9:591330-591688	A549	lung:	n/a	n/a
42	CREB1	chr9:591355-591625	A549	lung:	n/a	n/a
43	CREB1	chr9:557738-558028	A549	lung:	n/a	n/a
44	CTCF	chr9:547060-547210	HA-sp	spinal cord:	n/a	chr9:547092-547113 chr9:547098-547114 chr9:547097-547115
45	CTCF	chr9:547129-547160	GM20000	blood:	n/a	n/a
46	CTCF	chr9:582000-582150	GM12870	blood:	n/a	chr9:582097-582113 chr9:582099-582112 chr9:582098-582119 chr9:582096-582114 chr9:582096-582109
47	CTCF	chr9:581820-581970	HRE	kidney:	n/a	n/a
48	CTCF	chr9:547060-547210	NHEK	skin:	n/a	chr9:547092-547113 chr9:547098-547114 chr9:547097-547115
49	CTCF	chr9:547060-547210	AG10803	skin:	n/a	chr9:547092-547113 chr9:547098-547114 chr9:547097-547115
50	CTCF	chr9:584660-584810	GM12864	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:574312-574362	HEK293	kidney:	embryo
2	chr9:574312-574362	RPTEC	kidney:	n/a
3	chr9:574312-574362	BJ	skin:	n/a
4	chr9:574312-574362	GM19239	blood:	n/a
5	chr9:574312-574362	Jurkat	blood:	n/a
6	chr9:574312-574362	NB4	blood:	n/a
7	chr9:574312-574362	SKMC	muscle:	n/a
8	chr9:574312-574362	IMR90	lung:	fetal
9	chr9:574312-574362	HRCEpiC	kidney:	n/a
10	chr9:574312-574362	GM06990	blood:	n/a
11	chr9:574312-574362	Hepatocyte	liver:	n/a
12	chr9:574312-574362	PANC-1	pancreas:	n/a
13	chr9:574312-574362	MCF10A-Er-Src	breast:	n/a
14	chr9:574312-574362	Caco-2	colon:	n/a
15	chr9:574312-574362	HNPCEpiC	eye:	n/a
16	chr9:574312-574362	ProgFib	skin:	n/a
17	chr9:574312-574362	HMEC	breast:	n/a
18	chr9:574312-574362	PrEC	prostate:	n/a
19	chr9:574312-574362	HRE	kidney:	n/a
20	chr9:574312-574362	SK-N-SH	brain:	n/a
21	chr9:574312-574362	GM12891	blood:	n/a
22	chr9:574312-574362	NT2-D1	testis:	n/a
23	chr9:574312-574362	NH-A	brain:	n/a
24	chr9:574312-574362	U87	brain:	n/a
25	chr9:574312-574362	HL-60	blood:	n/a
26	chr9:574312-574362	AoSMC	blood vessel:	n/a
27	chr9:574312-574362	NHBE	bronchial:	n/a
28	chr9:574312-574362	ovcar-3	ovarian:	n/a
29	chr9:574312-574362	BE2_C	brain:	n/a
30	chr9:574312-574362	HPAEpiC	pulmonary alveolar:	n/a
31	chr9:574312-574362	HRPEpiC	eye:	n/a
32	chr9:574312-574362	Hela-S3	cervix:	n/a
33	chr9:574312-574362	AG09319	gingival:	n/a
34	chr9:574312-574362	T-47D	breast:	n/a
35	chr9:574312-574362	K562	blood:	n/a
36	chr9:574312-574362	LNCaP	prostate:	n/a
37	chr9:574312-574362	NHDF-neo	bronchial:	n/a
38	chr9:574312-574362	GM12892	blood:	n/a
39	chr9:574312-574362	SAEC	small airway:	n/a
40	chr9:574312-574362	AG10803	skin:	n/a
41	chr9:574312-574362	AG04450	lung:	fetal
42	chr9:574312-574362	PFSK-1	brain:	n/a
43	chr9:574312-574362	HUVEC	blood vessel:	n/a
44	chr9:574312-574362	SK-N-SH_RA	brain:	n/a
45	chr9:574312-574362	ECC-1	luminal epithelium:	n/a
46	chr9:574312-574362	CMK	blood:	n/a
47	chr9:574312-574362	GM12878	blood:	n/a
48	chr9:574312-574362	SK-N-MC	brain:	n/a
49	chr9:574312-574362	HEEpiC	esophagus:	n/a
50	chr9:574312-574362	MCF-7	breast:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:535330..537087-chr9:549296..551126,2	K562	blood:
2	chr9:555602..557901-chr9:561314..563396,2	K562	blood:
3	chr9:581438..583645-chr9:586871..590074,4	MCF-7	breast:
4	chr9:469326..471004-chr9:547085..549851,2	MCF-7	breast:
5	chr9:581168..581745-chr9:613579..614471,2	MCF-7	breast:
6	chr9:582031..585321-chr9:586707..590039,3	K562	blood:
7	chr9:530586..533539-chr9:534026..536380,2	MCF-7	breast:
8	chr9:581769..582694-chr9:763829..764743,4	MCF-7	breast:
9	chr9:555602..557901-chr9:561314..563396,2	K562	blood:
10	chr9:581871..582698-chr9:763741..764739,5	MCF-7	breast:
11	chr9:581649..582215-chr9:998516..999103,2	MCF-7	breast:
12	chr9:582031..585321-chr9:586707..590039,3	K562	blood:
13	chr9:535330..537087-chr9:549296..551126,2	K562	blood:
14	chr9:512039..514160-chr9:515791..519174,3	K562	blood:
15	chr9:523311..524277-chr9:542856..543632,2	MCF-7	breast:
16	chr9:385596..386468-chr9:546637..547164,2	MCF-7	breast:
17	chr9:523311..524277-chr9:542856..543632,2	MCF-7	breast:
18	chr9:581860..582832-chr9:613640..614518,3	MCF-7	breast:
19	chr9:530586..533539-chr9:534026..536380,2	MCF-7	breast:
20	chr9:518740..521510-chr9:531283..533605,2	MCF-7	breast:
21	chr9:581821..582545-chr9:807512..808214,2	MCF-7	breast:
22	chr9:518740..521510-chr9:531283..533605,2	MCF-7	breast:
23	chr9:581438..583645-chr9:586871..590074,4	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DOCK8-2	chr9:549190-549531	ENSG00000226403.1
2	lnc-DOCK8-2	chr9:547318-547341	ENSG00000226403.1
3	lnc-DOCK8-2	chr9:549107-549525	NONHSAT129931
4	lnc-DOCK8-2	chr9:549107-549531	ENSG00000226403.1
5	lnc-DOCK8-2	chr9:547317-547341	ENSG00000226403.1
6	lnc-DOCK8-2	chr9:547038-547341	NONHSAT129931

No data

Variant related genes	Relation type
ENSG00000226403	TF binding region
RNU6-1327P	TF binding region
ENSG00000226403	CpG island
RNU6-1327P	CpG island
ENSG00000107104	chromatin interactions
ENSG00000227155	chromatin interactions

Extended variants
information (count: 4946 )
Associated
traits (count: 113 )

Variant overlapped rSNPs/rCNVs (count:4946 , 50 per page) page: 1 2 3 4 5 6 7 ... 99

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536942006	chr9:517489-517490	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs368897018	chr9:517507-517508	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs16917368	chr9:517563-517564	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs376304333	chr9:517573-517574	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs144971223	chr9:517577-517578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs557344734	chr9:517597-517598	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs371296187	chr9:517603-517604	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs577299433	chr9:517605-517606	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs533690163	chr9:517607-517608	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs188595014	chr9:517615-517616	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs558977924	chr9:517620-517621	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs542811577	chr9:517669-517670	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs562613486	chr9:517685-517686	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs77778767	chr9:517688-517689	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs545406579	chr9:517689-517690	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs551739649	chr9:517697-517698	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs1928415	chr9:517715-517716	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs151034462	chr9:517738-517739	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs202120974	chr9:517739-517740	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs397735823	chr9:517756-517757	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs544370697	chr9:517769-517770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs554758292	chr9:517774-517775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs140582929	chr9:517783-517784	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs181000550	chr9:517799-517800	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs143138549	chr9:517800-517801	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs573360405	chr9:517807-517808	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs114965558	chr9:517808-517809	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs117846768	chr9:517821-517822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs142556021	chr9:517824-517825	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs1928416	chr9:517841-517842	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs528062780	chr9:517849-517850	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs148235493	chr9:517850-517851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs573704804	chr9:517851-517852	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs536028188	chr9:517869-517870	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs376886580	chr9:517879-517880	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs369346830	chr9:517885-517886	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs186053791	chr9:517889-517890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs1928417	chr9:517899-517900	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs190585718	chr9:517946-517947	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs12344970	chr9:517947-517948	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs530850993	chr9:517983-517984	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs182215786	chr9:517991-517992	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs141353016	chr9:518033-518034	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs12345892	chr9:518103-518104	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs386731404	chr9:518118-518119	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs12349522	chr9:518119-518120	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs150388891	chr9:518178-518179	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs12345902	chr9:518183-518184	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs112892996	chr9:518225-518226	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs532658285	chr9:518258-518259	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:113)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	20164920	CNVD
Ovarian cancer	21720365	CNVD
Myelofibrosis	22110671	CNVD
Lynch syndrome	18415027	CNVD
Retinoblastoma	21504564	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	22286061	CNVD
Williams-beuren syndrome	18553513	CNVD
Disorders of sex development	21048976	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
prenatal diagnosis	20453657	CNVD
Gastric cancer	16715143	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Intracranial aneurysm	16715129	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Disorders of sex development	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Sudden cardiac death	19188705	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21952639	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
abnormal development	18461090	CNVD
Honadal dysgenesis	21048976	CNVD
Medulloblastoma	21979893	CNVD
Lung cancer	16740712	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Autism	20531469	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Developmental delay	20808231	CNVD
Obesity	20808231	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Schizophrenia	20967226	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-small cell lung cancer	16651412	CNVD

Chromatin state (count:1784 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:506000-520000	Weak transcription	Aorta	Aorta
2	chr9:506000-520200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr9:506200-517800	Weak transcription	Colonic Mucosa	Colon
4	chr9:506400-519600	Weak transcription	Colon Smooth Muscle	Colon
5	chr9:506600-517600	Weak transcription	Fetal Intestine Large	intestine
6	chr9:506600-517600	Weak transcription	Fetal Intestine Small	intestine
7	chr9:506800-517600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr9:506800-517600	Weak transcription	NHEK	skin
9	chr9:507000-532600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr9:508400-522400	Weak transcription	Fetal Muscle Leg	muscle
11	chr9:511600-518200	Weak transcription	A549	lung
12	chr9:512200-518400	Weak transcription	Small Intestine	intestine
13	chr9:512400-522400	Weak transcription	Right Ventricle	heart
14	chr9:513200-518200	Weak transcription	Rectal Mucosa Donor 31	rectum
15	chr9:513400-520800	Weak transcription	Fetal Lung	lung
16	chr9:513400-521000	Weak transcription	Brain Substantia Nigra	brain
17	chr9:513400-522400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr9:513600-522800	Weak transcription	Brain Cingulate Gyrus	brain
19	chr9:514000-532200	Weak transcription	Fetal Muscle Trunk	muscle
20	chr9:514400-518400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
21	chr9:514600-518400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
22	chr9:514800-519400	Enhancers	Primary T killer memory cells from peripheral blood	blood
23	chr9:515000-518000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr9:515800-518400	Enhancers	Primary T helper cells fromperipheralblood	blood
25	chr9:516000-521400	Enhancers	Primary T helper cells PMA-I stimulated	--
26	chr9:516200-518400	Enhancers	Primary T helper naive cells from peripheral blood	blood
27	chr9:516200-520800	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr9:516600-517600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
29	chr9:516600-517600	Enhancers	Brain Hippocampus Middle	brain
30	chr9:516600-518000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr9:516600-518200	Weak transcription	Duodenum Mucosa	Duodenum
32	chr9:516600-518200	Weak transcription	Fetal Heart	heart
33	chr9:516600-518800	Enhancers	Left Ventricle	heart
34	chr9:516800-517600	Enhancers	Brain Anterior Caudate	brain
35	chr9:516800-518800	Enhancers	Pancreas	Pancrea
36	chr9:517000-522400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
37	chr9:517400-517600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr9:517400-517800	Weak transcription	Primary T cells from cord blood	blood
39	chr9:517400-518000	Weak transcription	Sigmoid Colon	Sigmoid Colon
40	chr9:517400-518200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr9:517400-518400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr9:517400-520600	Weak transcription	Brain Inferior Temporal Lobe	brain
43	chr9:517400-522200	Weak transcription	Cortex derived primary cultured neurospheres	brain
44	chr9:517600-517800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
45	chr9:517600-518000	Enhancers	NHEK	skin
46	chr9:517600-518400	Weak transcription	Brain Anterior Caudate	brain
47	chr9:517600-518600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr9:517600-519000	Enhancers	Fetal Intestine Small	intestine
49	chr9:517600-519400	Enhancers	Fetal Intestine Large	intestine
50	chr9:517600-520800	Weak transcription	Brain Hippocampus Middle	brain

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