Variant report

Variant	nsv960831
Chromosome Location	chr19:36744378-36813769
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:283)
CpG islands
(count:1100)
Chromatin interactive
region (count:1)
LncRNA
region (count:44)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:283 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr19:36757608-36757618	K562	blood:	n/a	n/a
2	BHLHE40	chr19:36757499-36757673	K562	blood:	n/a	n/a
3	BRCA1	chr19:36762836-36763037	HepG2	liver:	n/a	n/a
4	CBX3	chr19:36762724-36763179	K562	blood:	n/a	n/a
5	CBX3	chr19:36796036-36796224	K562	blood:	n/a	n/a
6	CBX3	chr19:36785308-36785504	K562	blood:	n/a	n/a
7	CBX3	chr19:36787829-36788041	K562	blood:	n/a	n/a
8	CBX3	chr19:36789665-36790026	K562	blood:	n/a	n/a
9	CBX3	chr19:36795732-36796004	K562	blood:	n/a	n/a
10	CBX3	chr19:36768844-36769134	K562	blood:	n/a	n/a
11	CBX3	chr19:36782055-36782327	K562	blood:	n/a	n/a
12	CCNT2	chr19:36757335-36757662	K562	blood:	n/a	n/a
13	CEBPB	chr19:36757408-36757715	K562	blood:	n/a	n/a
14	CHD2	chr19:36762837-36763034	HepG2	liver:	n/a	n/a
15	CTCF	chr19:36792132-36792443	K562	blood:	n/a	n/a
16	CTCF	chr19:36797216-36797420	K562	blood:	n/a	n/a
17	CTCF	chr19:36747920-36748016	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr19:36802017-36802247	H1-hESC	embryonic stem cell:	n/a	chr19:36802140-36802161 chr19:36802141-36802154 chr19:36802138-36802156
19	CTCF	chr19:36782028-36782324	K562	blood:	n/a	n/a
20	CTCF	chr19:36806249-36806279	GM13976	blood:	n/a	n/a
21	CTCF	chr19:36774404-36774622	K562	blood:	n/a	n/a
22	CTCF	chr19:36789490-36789986	K562	blood:	n/a	n/a
23	CTCF	chr19:36806168-36806277	MCF-7	breast:	n/a	n/a
24	CTCF	chr19:36787024-36787440	K562	blood:	n/a	n/a
25	CTCF	chr19:36761749-36762043	K562	blood:	n/a	n/a
26	CTCF	chr19:36807273-36807403	LNCaP	prostate:	n/a	n/a
27	CTCF	chr19:36806224-36806345	GM19240	blood:	n/a	n/a
28	CTCF	chr19:36776957-36777216	K562	blood:	n/a	n/a
29	CTCF	chr19:36806260-36806346	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr19:36764243-36764639	K562	blood:	n/a	n/a
31	CTCF	chr19:36806254-36806293	GM20000	blood:	n/a	n/a
32	CTCF	chr19:36759255-36759493	K562	blood:	n/a	n/a
33	CTCF	chr19:36762880-36763030	GM12873	blood:	n/a	n/a
34	CTCF	chr19:36761779-36762037	K562	blood:	n/a	n/a
35	CTCF	chr19:36792079-36792467	K562	blood:	n/a	n/a
36	CTCF	chr19:36806213-36806295	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr19:36781989-36782277	K562	blood:	n/a	n/a
38	CTCF	chr19:36802119-36802253	LNCaP	prostate:	n/a	chr19:36802140-36802161 chr19:36802141-36802154 chr19:36802138-36802156
39	CTCF	chr19:36761661-36762170	K562	blood:	n/a	n/a
40	CTCF	chr19:36806237-36806353	HepG2	liver:	n/a	n/a
41	CTCF	chr19:36784523-36784856	K562	blood:	n/a	n/a
42	CTCF	chr19:36779440-36779728	K562	blood:	n/a	n/a
43	CTCF	chr19:36794609-36795061	K562	blood:	n/a	n/a
44	CTCF	chr19:36757707-36757802	Kidney_OC	kidney:	n/a	n/a
45	CTCF	chr19:36806287-36806329	MCF-7	breast:	n/a	n/a
46	CTCF	chr19:36802038-36802155	K562	blood:	n/a	chr19:36802141-36802154
47	CTCF	chr19:36771886-36772289	K562	blood:	n/a	n/a
48	CTCF	chr19:36769382-36769596	K562	blood:	n/a	n/a
49	CTCF	chr19:36799747-36799943	K562	blood:	n/a	n/a
50	CTCF	chr19:36806260-36806283	MCF-7	breast:	n/a	n/a

(count:1100 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:36801484-36801534	HRPEpiC	eye:	n/a
2	chr19:36763026-36763076	Jurkat	blood:	n/a
3	chr19:36801484-36801534	HRPEpiC	eye:	n/a
4	chr19:36763026-36763076	Jurkat	blood:	n/a
5	chr19:36759220-36759270	HIPEpiC	eye:	n/a
6	chr19:36795950-36796000	HEEpiC	esophagus:	n/a
7	chr19:36746473-36746523	BJ	skin:	n/a
8	chr19:36800845-36800895	HNPCEpiC	eye:	n/a
9	chr19:36800845-36800895	ovcar-3	ovarian:	n/a
10	chr19:36759220-36759270	GM12892	blood:	n/a
11	chr19:36763026-36763076	ovcar-3	ovarian:	n/a
12	chr19:36802391-36802441	HCM	heart:	n/a
13	chr19:36758564-36758614	HRCEpiC	kidney:	n/a
14	chr19:36746845-36746895	GM19239	blood:	n/a
15	chr19:36799625-36799675	PANC-1	pancreas:	n/a
16	chr19:36746737-36746787	HCPEpiC	choroid plexus:	n/a
17	chr19:36800845-36800895	AG04449	skin:	fetal
18	chr19:36801408-36801458	U87	brain:	n/a
19	chr19:36794212-36794262	RPTEC	kidney:	n/a
20	chr19:36764158-36764208	NH-A	brain:	n/a
21	chr19:36746845-36746895	HepG2	liver:	n/a
22	chr19:36744465-36744515	H1-hESC	embryonic stem cell:	embryo
23	chr19:36758736-36758786	GM12891	blood:	n/a
24	chr19:36746473-36746523	AG09309	skin:	n/a
25	chr19:36801503-36801553	SK-N-SH	brain:	n/a
26	chr19:36794212-36794262	A549	lung:	n/a
27	chr19:36744465-36744515	MCF-7	breast:	n/a
28	chr19:36794212-36794262	HCF	heart:	n/a
29	chr19:36801503-36801553	ECC-1	luminal epithelium:	n/a
30	chr19:36758564-36758614	PANC-1	pancreas:	n/a
31	chr19:36795950-36796000	BJ	skin:	n/a
32	chr19:36763026-36763076	NHDF-neo	bronchial:	n/a
33	chr19:36802391-36802441	HAEpiC	amniotic membrane:	n/a
34	chr19:36744465-36744515	Jurkat	blood:	n/a
35	chr19:36758736-36758786	H1-hESC	embryonic stem cell:	embryo
36	chr19:36759220-36759270	HNPCEpiC	eye:	n/a
37	chr19:36801503-36801553	AG09319	gingival:	n/a
38	chr19:36801503-36801553	K562	blood:	n/a
39	chr19:36749224-36749274	ECC-1	luminal epithelium:	n/a
40	chr19:36759220-36759270	Jurkat	blood:	n/a
41	chr19:36759220-36759270	AG04450	lung:	fetal
42	chr19:36794212-36794262	Caco-2	colon:	n/a
43	chr19:36749224-36749274	BJ	skin:	n/a
44	chr19:36799625-36799675	PrEC	prostate:	n/a
45	chr19:36758564-36758614	Hela-S3	cervix:	n/a
46	chr19:36758736-36758786	HepG2	liver:	n/a
47	chr19:36759220-36759270	PANC-1	pancreas:	n/a
48	chr19:36759220-36759270	HPAEpiC	pulmonary alveolar:	n/a
49	chr19:36746845-36746895	K562	blood:	n/a
50	chr19:36746845-36746895	AG09309	skin:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr19:36740128..36741923-chr19:36743583..36745191,2	K562	blood:

(count:44 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZFP14-1	chr19:36812895-36812932	ENSG00000232677
2	lnc-ZFP14-1	chr19:36806859-36806972	ENSG00000232677
3	lnc-ZFP14-1	chr19:36803973-36804224	NONHSAT065986
4	lnc-ZNF146-1	chr19:36803424-36803570	NONHSAT065980
5	lnc-ZNF146-1	chr19:36802245-36802694	XLOC_013054
6	lnc-ZNF146-1	chr19:36811922-36812079	XLOC_013054
7	lnc-ZFP14-1	chr19:36812895-36812932	ENSG00000232677
8	lnc-ZNF146-1	chr19:36802245-36802694	NONHSAT065980
9	lnc-ZFP14-1	chr19:36812202-36812259	NONHSAT065992
10	lnc-ZNF146-1	chr19:36811922-36812260	XLOC_013054
11	lnc-ZFP14-1	chr19:36813032-36813127	ENSG00000232677
12	lnc-ZNF146-1	chr19:36802083-36802290	XLOC_013054
13	lnc-ZFP14-1	chr19:36812895-36812932	ENSG00000232677
14	lnc-ZFP14-1	chr19:36811507-36811662	ENSG00000232677
15	lnc-ZNF146-1	chr19:36801260-36803563	ENSG00000267053.2
16	lnc-ZFP14-1	chr19:36803622-36804224	NONHSAT065983
17	lnc-ZFP14-1	chr19:36806859-36806972	ENSG00000232677
18	lnc-ZFP14-1	chr19:36812895-36812933	NONHSAT065992
19	lnc-ZNF146-1	chr19:36801260-36803564	ENSG00000267053.2
20	lnc-ZFP14-1	chr19:36806859-36807236	NONHSAT065983
21	lnc-ZFP14-1	chr19:36811026-36811662	NONHSAT065992
22	lnc-ZFP14-1	chr19:36803969-36806639	ENSG00000232677.2
23	lnc-ZFP14-1	chr19:36806478-36806972	ENSG00000232677.2
24	lnc-ZNF146-1	chr19:36811922-36812194	XLOC_013054
25	lnc-ZNF146-1	chr19:36803410-36803537	XLOC_013054
26	lnc-ZFP14-1	chr19:36813032-36813130	ENSG00000232677.2
27	lnc-ZFP14-1	chr19:36812895-36812932	ENSG00000232677.2
28	lnc-ZFP14-1	chr19:36804644-36804814	ENSG00000232677
29	lnc-ZNF146-1	chr19:36802423-36802694	XLOC_013054
30	lnc-ZFP14-1	chr19:36812202-36812259	ENSG00000232677.2
31	lnc-ZFP14-1	chr19:36813032-36813286	ENSG00000232677
32	lnc-ZNF146-1	chr19:36802525-36802694	XLOC_013054
33	lnc-ZFP14-1	chr19:36812202-36812259	ENSG00000232677
34	lnc-ZNF146-1	chr19:36802446-36802694	ENSG00000267053.2
35	lnc-ZNF146-1	chr19:36803424-36803568	XLOC_013054
36	lnc-ZFP14-1	chr19:36812202-36812259	ENSG00000232677
37	lnc-ZFP14-1	chr19:36813032-36813112	ENSG00000232677
38	lnc-ZNF146-1	chr19:36803424-36803570	ENSG00000267053.2
39	lnc-ZNF146-1	chr19:36803424-36803537	XLOC_013054
40	lnc-ZFP14-1	chr19:36807080-36807229	NONHSAT065986
41	lnc-ZFP14-1	chr19:36812202-36812259	ENSG00000232677
42	lnc-ZFP14-1	chr19:36806262-36806430	ENSG00000232677
43	lnc-ZNF146-1	chr19:36803424-36803537	XLOC_013054
44	lnc-ZFP14-1	chr19:36806859-36806972	NONHSAT065986

No data

Variant related genes	Relation type
LINC00665	TF binding region
ENSG00000267053	TF binding region
LINC00665	CpG island
ENSG00000267053	CpG island
SLC35F5	miRNA target sites
SLC35D2	miRNA target sites
SLC35F3	miRNA target sites

Extended variants
information (count: 1734 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:1734 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs559373845	chr19:36744390-36744391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs183405328	chr19:36744391-36744392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs146697798	chr19:36744425-36744426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs563813866	chr19:36744430-36744431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs369248539	chr19:36744444-36744445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs187729509	chr19:36744446-36744447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs552809276	chr19:36744454-36744455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs564642902	chr19:36744465-36744466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs141335495	chr19:36744500-36744501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs145117894	chr19:36744600-36744601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs568637781	chr19:36744604-36744605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs546053637	chr19:36744616-36744617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs547770712	chr19:36744626-36744627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs569418220	chr19:36744682-36744683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs373239224	chr19:36744702-36744703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs564648167	chr19:36744707-36744708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs532059961	chr19:36744709-36744710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs564462150	chr19:36744741-36744742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs373835257	chr19:36744769-36744770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs151322361	chr19:36744771-36744772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs558350603	chr19:36744830-36744831	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs570663086	chr19:36744872-36744873	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs534497922	chr19:36744914-36744915	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs10411482	chr19:36744948-36744949	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs191470218	chr19:36744967-36744968	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs150402413	chr19:36744978-36744979	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs138176583	chr19:36744983-36744984	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs528222731	chr19:36745091-36745092	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs575831910	chr19:36745118-36745119	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs183470023	chr19:36745144-36745145	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs78199830	chr19:36745146-36745147	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs528711574	chr19:36745147-36745148	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs540467595	chr19:36745212-36745213	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs78762731	chr19:36745213-36745214	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs548310146	chr19:36745231-36745232	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs139173968	chr19:36745261-36745262	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs529501252	chr19:36745334-36745335	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs547782394	chr19:36745441-36745442	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs569280855	chr19:36745461-36745462	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs139162077	chr19:36745488-36745489	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs568113910	chr19:36745532-36745533	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs562350131	chr19:36745572-36745573	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs142785481	chr19:36745589-36745590	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs188307270	chr19:36745615-36745616	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs552852026	chr19:36745621-36745622	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs192591785	chr19:36745622-36745623	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs568347445	chr19:36745660-36745661	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs529813397	chr19:36745727-36745728	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs548312021	chr19:36745757-36745758	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs4806303	chr19:36745760-36745761	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:60)

Disease	PMID	Source
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Ductal carcinoma	22052326	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21858162	CNVD
Breast cancer	17603634	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
renal disease	20603712	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Ovarian cancer	21397856	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Ovarian cancer	20844748	CNVD
Non-small cell lung cancer	21829676	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cancer	21183584	CNVD
Honadal dysgenesis	21048976	CNVD
Neurodevelopmental disorder	22521361	CNVD
Endometrial cancer	23636398	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Invasive pancreatic ductal carcinoma	18765526	CNVD
Rhabdomyosarcoma	16790082	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Glioma	17123091	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:577 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:36730400-36748400	Weak transcription	HSMMtube	muscle
2	chr19:36736200-36746200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr19:36737400-36747800	Weak transcription	Brain Anterior Caudate	brain
4	chr19:36737400-36747800	Weak transcription	Brain Substantia Nigra	brain
5	chr19:36737400-36748000	Weak transcription	Ovary	ovary
6	chr19:36737600-36745400	Weak transcription	Pancreas	Pancrea
7	chr19:36737600-36746000	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr19:36737600-36746200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr19:36737600-36747800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr19:36737600-36747800	Weak transcription	Brain Cingulate Gyrus	brain
11	chr19:36737600-36747800	Weak transcription	Brain Hippocampus Middle	brain
12	chr19:36738000-36747800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr19:36739200-36746200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr19:36739200-36746800	Weak transcription	Colon Smooth Muscle	Colon
15	chr19:36739400-36745400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr19:36739600-36745200	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr19:36739600-36756800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr19:36742200-36746200	Weak transcription	Skeletal Muscle Male	skeletal muscle
19	chr19:36743000-36746000	Weak transcription	Stomach Smooth Muscle	stomach
20	chr19:36744800-36748000	ZNF genes & repeats	Fetal Brain Female	brain
21	chr19:36745000-36745400	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr19:36745200-36746000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr19:36745200-36746800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
24	chr19:36745400-36746000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr19:36745400-36748000	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
26	chr19:36745400-36749200	ZNF genes & repeats	Pancreas	Pancrea
27	chr19:36745600-36746400	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
28	chr19:36745800-36750600	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
29	chr19:36746000-36746200	Weak transcription	HUES6 Cell Line	embryonic stem cell
30	chr19:36746000-36746400	ZNF genes & repeats	Brain Germinal Matrix	brain
31	chr19:36746000-36746800	Strong transcription	Stomach Smooth Muscle	stomach
32	chr19:36746000-36747200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
33	chr19:36746000-36747200	ZNF genes & repeats	Aorta	Aorta
34	chr19:36746000-36747200	Strong transcription	Brain Inferior Temporal Lobe	brain
35	chr19:36746000-36747200	ZNF genes & repeats	Gastric	stomach
36	chr19:36746200-36746400	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr19:36746200-36746400	ZNF genes & repeats	Brain Dorsolateral Prefrontal Cortex	brain
38	chr19:36746200-36746600	Weak transcription	Fetal Lung	lung
39	chr19:36746200-36746800	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr19:36746200-36747400	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr19:36746200-36747400	ZNF genes & repeats	Lung	lung
42	chr19:36746200-36748200	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
43	chr19:36746200-36748800	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr19:36746200-36749400	ZNF genes & repeats	Fetal Stomach	stomach
45	chr19:36746400-36747200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
46	chr19:36746400-36747800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
47	chr19:36746400-36747800	Weak transcription	Duodenum Smooth Muscle	Duodenum
48	chr19:36746400-36748800	ZNF genes & repeats	Spleen	Spleen
49	chr19:36746800-36747800	Weak transcription	HUES64 Cell Line	embryonic stem cell
50	chr19:36746800-36747800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell

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