Variant report

Variant	nsv963018
Chromosome Location	chr19:18395612-18399311
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr19:18398596-18398975	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr19:18398551-18398949	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr19:18398664-18398985	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr19:18395551-18395899	GM12878	blood:	n/a	n/a
5	CHD2	chr19:18398786-18399067	H1-hESC	embryonic stem cell:	n/a	n/a
6	CTBP2	chr19:18398634-18399018	H1-hESC	embryonic stem cell:	n/a	n/a
7	CTCF	chr19:18398760-18398910	HAc	cerebellar:	n/a	chr19:18398845-18398858
8	CTCF	chr19:18398740-18398890	HA-sp	spinal cord:	n/a	chr19:18398845-18398858
9	CTCF	chr19:18398800-18398950	HPF	lung:	n/a	chr19:18398935-18398948 chr19:18398845-18398858
10	CTCF	chr19:18398760-18398910	AG04449	skin:	n/a	chr19:18398845-18398858
11	CTCF	chr19:18398740-18398890	HCPEpiC	choroid plexus:	n/a	chr19:18398845-18398858
12	CTCF	chr19:18398780-18398930	HRPEpiC	eye:	n/a	chr19:18398845-18398858
13	CTCF	chr19:18398760-18398910	HCPEpiC	choroid plexus:	n/a	chr19:18398845-18398858
14	CTCF	chr19:18398820-18398970	HAc	cerebellar:	n/a	chr19:18398935-18398948 chr19:18398845-18398858
15	CTCF	chr19:18398780-18398930	HEEpiC	esophagus:	n/a	chr19:18398845-18398858
16	CTCF	chr19:18398781-18398934	H1-hESC	embryonic stem cell:	n/a	chr19:18398845-18398858
17	CTCF	chr19:18398740-18398890	BJ	skin:	n/a	chr19:18398845-18398858
18	CTCF	chr19:18398740-18398890	HRPEpiC	eye:	n/a	chr19:18398845-18398858
19	CTCF	chr19:18398800-18398950	HBMEC	blood vessel:	n/a	chr19:18398935-18398948 chr19:18398845-18398858
20	CTCF	chr19:18398180-18398330	HRPEpiC	eye:	n/a	n/a
21	CTCF	chr19:18398740-18398890	AG04449	skin:	n/a	chr19:18398845-18398858
22	CTCF	chr19:18398560-18398710	HFF-Myc	foreskin:	n/a	n/a
23	CTCF	chr19:18398800-18398950	HFF-Myc	foreskin:	n/a	chr19:18398935-18398948 chr19:18398845-18398858
24	CTCF	chr19:18398820-18398970	HRE	kidney:	n/a	chr19:18398935-18398948 chr19:18398845-18398858
25	CTCF	chr19:18398800-18398950	BJ	skin:	n/a	chr19:18398935-18398948 chr19:18398845-18398858
26	CTCF	chr19:18398740-18398890	HepG2	liver:	n/a	chr19:18398845-18398858
27	CTCF	chr19:18398820-18398970	SAEC	small airway:	n/a	chr19:18398935-18398948 chr19:18398845-18398858
28	CTCF	chr19:18398740-18398890	HRE	kidney:	n/a	chr19:18398845-18398858
29	CTCF	chr19:18398760-18398910	SAEC	small airway:	n/a	chr19:18398845-18398858
30	CTCF	chr19:18398165-18398212	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr19:18398880-18399030	Hela-S3	cervix:	n/a	chr19:18398935-18398948
32	CUX1	chr19:18396339-18396371	GM12878	blood:	n/a	n/a
33	EBF1	chr19:18395583-18395970	GM12878	blood:	n/a	n/a
34	EGR1	chr19:18395666-18395863	GM12878	blood:	n/a	chr19:18395740-18395753 chr19:18395740-18395753 chr19:18395741-18395752 chr19:18395740-18395753 chr19:18395740-18395754 chr19:18395742-18395752 chr19:18395739-18395754 chr19:18395736-18395758 chr19:18395741-18395755
35	EGR1	chr19:18395623-18395852	GM12878	blood:	n/a	chr19:18395740-18395753 chr19:18395740-18395753 chr19:18395741-18395752 chr19:18395740-18395753 chr19:18395740-18395754 chr19:18395742-18395752 chr19:18395739-18395754 chr19:18395736-18395758 chr19:18395741-18395755
36	EGR1	chr19:18395549-18395906	ECC-1	luminal epithelium:	n/a	chr19:18395740-18395753 chr19:18395740-18395753 chr19:18395741-18395752 chr19:18395740-18395753 chr19:18395740-18395754 chr19:18395742-18395752 chr19:18395739-18395754 chr19:18395736-18395758 chr19:18395741-18395755
37	EGR1	chr19:18395598-18395906	K562	blood:	n/a	chr19:18395740-18395753 chr19:18395740-18395753 chr19:18395741-18395752 chr19:18395740-18395753 chr19:18395740-18395754 chr19:18395742-18395752 chr19:18395739-18395754 chr19:18395736-18395758 chr19:18395741-18395755
38	EGR1	chr19:18395574-18395851	K562	blood:	n/a	chr19:18395740-18395753 chr19:18395740-18395753 chr19:18395741-18395752 chr19:18395740-18395753 chr19:18395740-18395754 chr19:18395742-18395752 chr19:18395739-18395754 chr19:18395736-18395758 chr19:18395741-18395755
39	ELF1	chr19:18398797-18399010	HepG2	liver:	n/a	n/a
40	ELF1	chr19:18399163-18399471	K562	blood:	n/a	chr19:18399337-18399350
41	ELF1	chr19:18398770-18399057	HepG2	liver:	n/a	n/a
42	EP300	chr19:18395678-18395847	GM12878	blood:	n/a	n/a
43	EP300	chr19:18398458-18399291	ECC-1	luminal epithelium:	n/a	chr19:18398992-18399008 chr19:18398910-18398924
44	EP300	chr19:18398670-18399103	H1-hESC	embryonic stem cell:	n/a	chr19:18398992-18399008 chr19:18398910-18398924
45	EP300	chr19:18398654-18399245	ECC-1	luminal epithelium:	n/a	chr19:18398992-18399008 chr19:18398910-18398924
46	ESR1	chr19:18398670-18399071	ECC-1	luminal epithelium:	n/a	n/a
47	ESR1	chr19:18398658-18399109	ECC-1	luminal epithelium:	n/a	n/a
48	ESR1	chr19:18398675-18399026	ECC-1	luminal epithelium:	n/a	n/a
49	ESR1	chr19:18398692-18399073	ECC-1	luminal epithelium:	n/a	n/a
50	ESR1	chr19:18398715-18399148	ECC-1	luminal epithelium:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:18398768-18398818	HL-60	blood:	n/a
2	chr19:18398768-18398818	PANC-1	pancreas:	n/a
3	chr19:18398768-18398818	HRE	kidney:	n/a
4	chr19:18398768-18398818	NHBE	bronchial:	n/a
5	chr19:18398768-18398818	HCM	heart:	n/a
6	chr19:18398768-18398818	NHDF-neo	bronchial:	n/a
7	chr19:18398768-18398818	GM12891	blood:	n/a
8	chr19:18398768-18398818	Jurkat	blood:	n/a
9	chr19:18398768-18398818	HepG2	liver:	n/a
10	chr19:18398768-18398818	HRCEpiC	kidney:	n/a
11	chr19:18398768-18398818	SK-N-SH	brain:	n/a
12	chr19:18398768-18398818	ECC-1	luminal epithelium:	n/a
13	chr19:18398768-18398818	HEEpiC	esophagus:	n/a
14	chr19:18398768-18398818	Hepatocyte	liver:	n/a
15	chr19:18398768-18398818	HIPEpiC	eye:	n/a
16	chr19:18398768-18398818	PrEC	prostate:	n/a
17	chr19:18398768-18398818	GM12878	blood:	n/a
18	chr19:18398768-18398818	HCT-116	colon:	n/a
19	chr19:18398768-18398818	Hela-S3	cervix:	n/a
20	chr19:18398768-18398818	HAEpiC	amniotic membrane:	n/a
21	chr19:18398768-18398818	GM19239	blood:	n/a
22	chr19:18398768-18398818	CMK	blood:	n/a
23	chr19:18398768-18398818	BE2_C	brain:	n/a
24	chr19:18398768-18398818	K562	blood:	n/a
25	chr19:18398768-18398818	ovcar-3	ovarian:	n/a
26	chr19:18398768-18398818	IMR90	lung:	fetal
27	chr19:18398768-18398818	GM06990	blood:	n/a
28	chr19:18398768-18398818	SAEC	small airway:	n/a
29	chr19:18398768-18398818	HEK293	kidney:	embryo
30	chr19:18398768-18398818	SK-N-MC	brain:	n/a
31	chr19:18398768-18398818	MCF10A-Er-Src	breast:	n/a
32	chr19:18398768-18398818	NB4	blood:	n/a
33	chr19:18398768-18398818	MCF-7	breast:	n/a
34	chr19:18398768-18398818	U87	brain:	n/a
35	chr19:18398768-18398818	GM12892	blood:	n/a
36	chr19:18398768-18398818	AG04450	lung:	fetal
37	chr19:18398768-18398818	PFSK-1	brain:	n/a
38	chr19:18398768-18398818	HPAEpiC	pulmonary alveolar:	n/a
39	chr19:18398768-18398818	AG04449	skin:	fetal
40	chr19:18398768-18398818	AG09319	gingival:	n/a
41	chr19:18398768-18398818	Caco-2	colon:	n/a
42	chr19:18398768-18398818	A549	lung:	n/a
43	chr19:18398768-18398818	AG09309	skin:	n/a
44	chr19:18398768-18398818	AG10803	skin:	n/a
45	chr19:18398768-18398818	RPTEC	kidney:	n/a
46	chr19:18398768-18398818	HRPEpiC	eye:	n/a
47	chr19:18398768-18398818	H1-hESC	embryonic stem cell:	embryo
48	chr19:18398768-18398818	HUVEC	blood vessel:	n/a
49	chr19:18398768-18398818	T-47D	breast:	n/a
50	chr19:18398768-18398818	SKMC	muscle:	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:18383365..18408325-chr19:18518460..18533256,66	K562	blood:
2	chr19:18397948..18402412-chr19:18484415..18487037,3	K562	blood:
3	chr19:18314868..18317000-chr19:18398723..18400388,2	MCF-7	breast:
4	chr19:18260692..18269532-chr19:18383927..18395911,19	K562	blood:
5	chr19:18397375..18399268-chr19:18401136..18404109,3	MCF-7	breast:
6	chr19:18396145..18399548-chr19:18528063..18530226,4	K562	blood:

Variant related genes	Relation type
JUND	TF binding region
RPL39P38	TF binding region
JUND	CpG island
RPL39P38	CpG island
ENSG00000105649	chromatin interactions
ENSG00000269145	chromatin interactions
ENSG00000221167	chromatin interactions
ENSG00000268173	chromatin interactions
ENSG00000105647	chromatin interactions
ENSG00000130511	chromatin interactions
ENSG00000130513	chromatin interactions
ENSG00000268650	chromatin interactions

Extended variants
information (count: 153 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:153 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs147278221	chr19:18395612-18395613	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs186964921	chr19:18395636-18395637	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs548575747	chr19:18395685-18395686	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs369547962	chr19:18395712-18395713	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs200924901	chr19:18395755-18395756	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs4378729	chr19:18395756-18395757	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs1421720	chr19:18395776-18395777	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs376766353	chr19:18395791-18395792	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs553257268	chr19:18395820-18395821	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs571340437	chr19:18395830-18395831	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs140764644	chr19:18395833-18395834	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs554083016	chr19:18395854-18395855	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs567569830	chr19:18395863-18395864	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs535808942	chr19:18395918-18395919	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs574699645	chr19:18395929-18395930	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs555468272	chr19:18395961-18395962	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs77419238	chr19:18395963-18395964	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs75859010	chr19:18395964-18395965	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs370430150	chr19:18395974-18395975	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs575621874	chr19:18396013-18396014	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs145242172	chr19:18396035-18396036	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs147612019	chr19:18396050-18396051	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs578089771	chr19:18396051-18396052	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs114667050	chr19:18396055-18396056	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs115324326	chr19:18396058-18396059	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs562702275	chr19:18396075-18396076	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs191350451	chr19:18396132-18396133	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs8103073	chr19:18396153-18396154	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs562324856	chr19:18396155-18396156	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs35463455	chr19:18396189-18396190	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs531372720	chr19:18396233-18396234	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs551157539	chr19:18396250-18396251	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs112096759	chr19:18396275-18396276	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs527436206	chr19:18396286-18396287	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs369324446	chr19:18396297-18396298	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs4808125	chr19:18396298-18396299	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs572592146	chr19:18396306-18396307	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs550082672	chr19:18396335-18396336	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs186068052	chr19:18396358-18396359	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs538260091	chr19:18396362-18396363	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs531335956	chr19:18396374-18396375	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs551438148	chr19:18396385-18396386	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs60235938	chr19:18396394-18396395	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs533788628	chr19:18396408-18396409	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs577723058	chr19:18396418-18396419	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs534064700	chr19:18396439-18396440	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs374958008	chr19:18396449-18396450	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs547368258	chr19:18396461-18396462	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs573922946	chr19:18396475-18396476	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs542899335	chr19:18396481-18396482	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Medulloblastoma	16783165	CNVD
Follicular lymphoma	20505157	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	20179077	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21080181	CNVD
Metanephric adenoma	20802469	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Lung cancer	17297452	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Chordoma	18071362	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
ovarian endometriomas	16273235	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Cervical cancer	21063398	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Ovarian cancer	21720365	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Basal cell lymphoma	21115979	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21364760	CNVD
Mycobacterial infection	18421352	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute monocytic leukemia	16498392	CNVD
Lung cancer	18438408	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Liver carcinoma	19366792	CNVD
Colorectal cancer	19455253	CNVD
Lujan-Fryns syndrom	21521776	CNVD
Breast cancer	20409316	CNVD
Cancer	17160897	CNVD
Cancer	17440070	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	21509527	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:318 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:18393800-18396400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr19:18393800-18396800	Weak transcription	Ovary	ovary
3	chr19:18393800-18397400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr19:18393800-18397400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr19:18393800-18397400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr19:18393800-18397400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr19:18393800-18397400	Weak transcription	Esophagus	oesophagus
8	chr19:18393800-18397800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr19:18393800-18397800	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr19:18393800-18398000	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr19:18393800-18398000	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr19:18393800-18398400	Weak transcription	NH-A	brain
13	chr19:18393800-18399000	Weak transcription	Fetal Kidney	kidney
14	chr19:18393800-18401000	Weak transcription	Thymus	Thymus
15	chr19:18393800-18401200	Weak transcription	Right Atrium	heart
16	chr19:18393800-18402000	Weak transcription	Aorta	Aorta
17	chr19:18394000-18396000	Weak transcription	NHLF	lung
18	chr19:18394000-18396400	Enhancers	Primary T helper cells fromperipheralblood	blood
19	chr19:18394000-18396800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr19:18394000-18396800	Weak transcription	HUES6 Cell Line	embryonic stem cell
21	chr19:18394000-18396800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr19:18394000-18396800	Weak transcription	HSMMtube	muscle
23	chr19:18394000-18396800	Weak transcription	NHDF-Ad	bronchial
24	chr19:18394000-18397000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr19:18394000-18397200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr19:18394000-18397200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr19:18394000-18397400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr19:18394000-18397400	Weak transcription	Skeletal Muscle Female	skeletal muscle
29	chr19:18394000-18397400	Weak transcription	Hela-S3	cervix
30	chr19:18394000-18397400	Weak transcription	HSMM	muscle
31	chr19:18394000-18398800	Weak transcription	Fetal Lung	lung
32	chr19:18394000-18398800	Weak transcription	A549	lung
33	chr19:18394000-18400400	Weak transcription	Dnd41	blood
34	chr19:18394000-18400600	Weak transcription	Duodenum Smooth Muscle	Duodenum
35	chr19:18394000-18400800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr19:18394000-18401200	Weak transcription	Brain Hippocampus Middle	brain
37	chr19:18394000-18401400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr19:18394000-18401400	Weak transcription	Muscle Satellite Cultured Cells	--
39	chr19:18394000-18402000	Weak transcription	Brain Anterior Caudate	brain
40	chr19:18394000-18402800	Weak transcription	Gastric	stomach
41	chr19:18394200-18395800	Weak transcription	Primary B cells from cord blood	blood
42	chr19:18394400-18395800	Weak transcription	Primary hematopoietic stem cells	blood
43	chr19:18394400-18397800	Weak transcription	Fetal Stomach	stomach
44	chr19:18394400-18399000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr19:18394400-18399000	Weak transcription	Colon Smooth Muscle	Colon
46	chr19:18394400-18399200	Weak transcription	Rectal Mucosa Donor 29	rectum
47	chr19:18394400-18400400	Weak transcription	Monocytes-CD14+_RO01746	blood
48	chr19:18394400-18400600	Weak transcription	Stomach Smooth Muscle	stomach
49	chr19:18394400-18400800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr19:18394400-18401000	Weak transcription	Skeletal Muscle Male	skeletal muscle

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