Variant report

Variant	nsv963045
Chromosome Location	chr19:39280546-39283148
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:92)
CpG islands
(count:122)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:92 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr19:39281684-39281719	GM19239	blood:	n/a	n/a
2	CTCF	chr19:39281203-39281390	GM13976	blood:	n/a	n/a
3	CTCF	chr19:39282160-39282341	Kidney_OC	kidney:	n/a	n/a
4	CTCF	chr19:39282001-39282094	Lung_OC	lung:	n/a	n/a
5	CTCF	chr19:39282120-39282385	Spleen_OC	spleen:	n/a	n/a
6	CTCF	chr19:39282238-39282295	GM12892	blood:	n/a	n/a
7	CTCF	chr19:39282512-39282669	GM12891	blood:	n/a	chr19:39282629-39282637
8	CTCF	chr19:39282451-39282475	GM19239	blood:	n/a	n/a
9	CTCF	chr19:39281182-39281230	GM10248	blood:	n/a	n/a
10	CTCF	chr19:39282380-39282414	NHEK	skin:	n/a	n/a
11	CTCF	chr19:39282182-39282335	GM19239	blood:	n/a	n/a
12	CTCF	chr19:39282386-39282424	GM10248	blood:	n/a	n/a
13	CTCF	chr19:39282370-39282396	Pancreas_OC	pancreas:	n/a	n/a
14	CTCF	chr19:39281495-39281518	LNCaP	prostate:	n/a	n/a
15	CTCF	chr19:39282094-39282129	GM12878	blood:	n/a	n/a
16	CTCF	chr19:39282195-39282247	Pancreas_OC	pancreas:	n/a	n/a
17	CTCF	chr19:39282584-39282634	GM13976	blood:	n/a	n/a
18	CTCF	chr19:39282674-39282682	GM12891	blood:	n/a	n/a
19	CTCF	chr19:39282152-39282292	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr19:39283091-39283099	GM13977	blood:	n/a	n/a
21	CTCF	chr19:39282256-39282292	GM20000	blood:	n/a	n/a
22	CTCF	chr19:39281471-39281476	LNCaP	prostate:	n/a	n/a
23	CTCF	chr19:39281757-39281776	NHEK	skin:	n/a	n/a
24	CTCF	chr19:39282186-39282336	Lung_OC	lung:	n/a	n/a
25	CTCF	chr19:39281740-39281750	H1-hESC	embryonic stem cell:	n/a	n/a
26	EBF1	chr19:39281979-39282297	GM12878	blood:	n/a	n/a
27	EBF1	chr19:39282062-39282681	GM12878	blood:	n/a	n/a
28	EP300	chr19:39282100-39282357	GM12878	blood:	n/a	n/a
29	IRF4	chr19:39282173-39282736	GM12878	blood:	n/a	n/a
30	MYC	chr19:39282033-39282411	HUVEC	blood vessel:	n/a	n/a
31	MYC	chr19:39281675-39281811	MCF-7	breast:	n/a	n/a
32	MYC	chr19:39282533-39282571	HUVEC	blood vessel:	n/a	n/a
33	PAX5	chr19:39282092-39282599	GM12878	blood:	n/a	n/a
34	PAX5	chr19:39282098-39282255	GM12878	blood:	n/a	n/a
35	PAX5	chr19:39282061-39282295	GM12878	blood:	n/a	n/a
36	PAX5	chr19:39281943-39282770	GM12878	blood:	n/a	n/a
37	PBX3	chr19:39282197-39282337	GM12878	blood:	n/a	n/a
38	POLR2A	chr19:39282228-39282523	H1-hESC	embryonic stem cell:	n/a	n/a
39	POLR2A	chr19:39281863-39282671	GM12892	blood:	n/a	n/a
40	POLR2A	chr19:39282118-39282533	A549	lung:	n/a	n/a
41	POLR2A	chr19:39282069-39282465	MCF-7	breast:	n/a	n/a
42	POLR2A	chr19:39281562-39281973	MCF-7	breast:	n/a	n/a
43	POLR2A	chr19:39282006-39282495	GM12891	blood:	n/a	n/a
44	POLR2A	chr19:39282028-39282530	GM12892	blood:	n/a	n/a
45	POLR2A	chr19:39281632-39282773	ProgFib	skin:	n/a	n/a
46	POLR2A	chr19:39281597-39281628	ProgFib	skin:	n/a	n/a
47	POLR2A	chr19:39282291-39282450	SK-N-SH	brain:	n/a	n/a
48	POLR2A	chr19:39281758-39281817	H1-hESC	embryonic stem cell:	n/a	n/a
49	POLR2A	chr19:39281932-39282486	MCF-7	breast:	n/a	n/a
50	POLR2A	chr19:39282045-39282712	GM12878	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:39282077-39282127	HRE	kidney:	n/a
2	chr19:39282077-39282127	NHDF-neo	bronchial:	n/a
3	chr19:39282077-39282127	HCPEpiC	choroid plexus:	n/a
4	chr19:39282077-39282127	HCT-116	colon:	n/a
5	chr19:39282077-39282127	ovcar-3	ovarian:	n/a
6	chr19:39282077-39282127	RPTEC	kidney:	n/a
7	chr19:39282077-39282127	GM06990	blood:	n/a
8	chr19:39282077-39282127	HRCEpiC	kidney:	n/a
9	chr19:39281374-39281424	RPTEC	kidney:	n/a
10	chr19:39281374-39281424	HAEpiC	amniotic membrane:	n/a
11	chr19:39282077-39282127	AG10803	skin:	n/a
12	chr19:39281374-39281424	MCF-7	breast:	n/a
13	chr19:39281374-39281424	NB4	blood:	n/a
14	chr19:39281374-39281424	HMEC	breast:	n/a
15	chr19:39282077-39282127	HNPCEpiC	eye:	n/a
16	chr19:39282077-39282127	K562	blood:	n/a
17	chr19:39282077-39282127	IMR90	lung:	fetal
18	chr19:39281374-39281424	PrEC	prostate:	n/a
19	chr19:39281374-39281424	NH-A	brain:	n/a
20	chr19:39282077-39282127	PFSK-1	brain:	n/a
21	chr19:39281374-39281424	SK-N-MC	brain:	n/a
22	chr19:39281374-39281424	ECC-1	luminal epithelium:	n/a
23	chr19:39281374-39281424	GM12891	blood:	n/a
24	chr19:39282077-39282127	HAEpiC	amniotic membrane:	n/a
25	chr19:39281374-39281424	SKMC	muscle:	n/a
26	chr19:39282077-39282127	GM19239	blood:	n/a
27	chr19:39281374-39281424	AG04450	lung:	fetal
28	chr19:39281374-39281424	HCPEpiC	choroid plexus:	n/a
29	chr19:39281374-39281424	ProgFib	skin:	n/a
30	chr19:39282077-39282127	HRPEpiC	eye:	n/a
31	chr19:39282077-39282127	MCF-7	breast:	n/a
32	chr19:39281374-39281424	AG04449	skin:	fetal
33	chr19:39281374-39281424	LNCaP	prostate:	n/a
34	chr19:39281374-39281424	NHDF-neo	bronchial:	n/a
35	chr19:39282077-39282127	LNCaP	prostate:	n/a
36	chr19:39281374-39281424	AG09319	gingival:	n/a
37	chr19:39282077-39282127	A549	lung:	n/a
38	chr19:39281374-39281424	MCF10A-Er-Src	breast:	n/a
39	chr19:39281374-39281424	HIPEpiC	eye:	n/a
40	chr19:39282077-39282127	GM12892	blood:	n/a
41	chr19:39282077-39282127	CMK	blood:	n/a
42	chr19:39282077-39282127	NH-A	brain:	n/a
43	chr19:39282077-39282127	GM12878	blood:	n/a
44	chr19:39282077-39282127	ProgFib	skin:	n/a
45	chr19:39282077-39282127	HepG2	liver:	n/a
46	chr19:39281374-39281424	GM12878	blood:	n/a
47	chr19:39281374-39281424	U87	brain:	n/a
48	chr19:39282077-39282127	HEK293	kidney:	embryo
49	chr19:39281374-39281424	NT2-D1	testis:	n/a
50	chr19:39282077-39282127	U87	brain:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr19:39263336..39266472-chr19:39281321..39283014,3	K562	blood:
2	chr19:39278557..39281313-chr19:39305805..39307829,2	MCF-7	breast:

No data

Variant related genes	Relation type
LGALS7B	TF binding region
LGALS7B	CpG island
ENSG00000104823	chromatin interactions
ENSG00000205076	chromatin interactions

Extended variants
information (count: 51 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:51 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs200727395	chr19:39280587-39280588	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs368385490	chr19:39280777-39280778	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs201911289	chr19:39280867-39280868	Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs542291003	chr19:39280957-39280958	Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs199908145	chr19:39280958-39280959	Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs76477826	chr19:39280972-39280973	Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs531596698	chr19:39281026-39281027	Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs549813316	chr19:39281027-39281028	Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs202187429	chr19:39281035-39281036	Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs150566088	chr19:39281072-39281073	Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs565064904	chr19:39281094-39281095	Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs62121416	chr19:39281109-39281110	Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs201351271	chr19:39281168-39281169	Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs112338842	chr19:39281224-39281225	Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs532193062	chr19:39281237-39281238	Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs190577097	chr19:39281335-39281336	Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs183137923	chr19:39281377-39281378	Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs371961194	chr19:39281389-39281390	Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs56351361	chr19:39281392-39281393	Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs367816015	chr19:39281394-39281395	Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs548125638	chr19:39281406-39281407	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs569554200	chr19:39281429-39281430	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs537721172	chr19:39281450-39281451	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs371753738	chr19:39281474-39281475	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs559001740	chr19:39281503-39281504	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs147201724	chr19:39281540-39281541	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs200276258	chr19:39281631-39281632	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs202228437	chr19:39281639-39281640	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs200946926	chr19:39281641-39281642	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs201921424	chr19:39281643-39281644	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs200536360	chr19:39281693-39281694	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs201307108	chr19:39281862-39281863	Weak transcription Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs199598749	chr19:39282050-39282051	Weak transcription Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs541967287	chr19:39282065-39282066	Weak transcription Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs563657269	chr19:39282100-39282101	Weak transcription Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs575574071	chr19:39282260-39282261	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs200453968	chr19:39282609-39282610	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs201749097	chr19:39282792-39282793	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs368656848	chr19:39282846-39282847	Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs532170561	chr19:39282856-39282857	Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs547226947	chr19:39282862-39282863	Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs559128179	chr19:39282874-39282875	Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs529693911	chr19:39282945-39282946	Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs8110658	chr19:39282956-39282957	Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs375827345	chr19:39282981-39282982	Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs370258858	chr19:39282998-39282999	Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs552814698	chr19:39283024-39283025	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
48	rs8110778	chr19:39283035-39283036	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs374985072	chr19:39283143-39283144	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
50	rs12980032	chr19:39283144-39283145	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:65)

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
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
Wilms tumour	21544195	CNVD
Mental retardation	19951919	CNVD
19q13.11 deletion syndrome	22378287	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Ovarian neoplasms	16753589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Lung cancer	21569311	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21509527	CNVD
Gastric cancer	18160780	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	19029149	CNVD
Breast cancer	20409316	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Acute myeloid leukemia	20729466	CNVD

Chromatin state (count:169 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:39265600-39283000	Weak transcription	Spleen	Spleen
2	chr19:39276200-39283000	Weak transcription	Pancreas	Pancrea
3	chr19:39277200-39283200	Weak transcription	NH-A	brain
4	chr19:39277800-39282800	Weak transcription	Placenta	Placenta
5	chr19:39277800-39283000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr19:39277800-39283000	Weak transcription	Right Ventricle	heart
7	chr19:39278000-39283000	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr19:39279000-39283400	Weak transcription	HSMM	muscle
9	chr19:39279400-39283400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr19:39279600-39280800	Weak transcription	Esophagus	oesophagus
11	chr19:39279600-39281400	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr19:39279600-39281800	Weak transcription	Fetal Intestine Large	intestine
13	chr19:39279600-39281800	Weak transcription	Fetal Intestine Small	intestine
14	chr19:39279600-39281800	Weak transcription	Fetal Thymus	thymus
15	chr19:39279600-39282800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr19:39279600-39282800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr19:39279600-39283000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr19:39279600-39283000	Weak transcription	Placenta Amnion	Placenta Amnion
19	chr19:39279600-39283200	Weak transcription	HepG2	liver
20	chr19:39279600-39283400	Weak transcription	A549	lung
21	chr19:39279800-39280800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr19:39279800-39280800	Weak transcription	NHEK	skin
23	chr19:39279800-39281800	Weak transcription	Fetal Muscle Trunk	muscle
24	chr19:39279800-39282800	Weak transcription	Fetal Muscle Leg	muscle
25	chr19:39279800-39282800	Weak transcription	HMEC	breast
26	chr19:39279800-39283000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr19:39279800-39291600	Weak transcription	Stomach Mucosa	stomach
28	chr19:39280800-39281000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr19:39280800-39281000	Flanking Active TSS	NHEK	skin
30	chr19:39280800-39281600	Active TSS	Esophagus	oesophagus
31	chr19:39281000-39281400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr19:39281000-39281600	Active TSS	NHEK	skin
33	chr19:39281200-39282200	Active TSS	iPS-20b Cell Line	embryonic stem cell
34	chr19:39281400-39282200	Active TSS	HUES6 Cell Line	embryonic stem cell
35	chr19:39281400-39283000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr19:39281600-39283000	Weak transcription	Esophagus	oesophagus
37	chr19:39281600-39283000	Weak transcription	NHEK	skin
38	chr19:39281800-39282000	Enhancers	Primary T helper cells PMA-I stimulated	--
39	chr19:39281800-39282000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
40	chr19:39281800-39282200	Active TSS	HUES64 Cell Line	embryonic stem cell
41	chr19:39281800-39282200	Active TSS	Primary neutrophils fromperipheralblood	blood
42	chr19:39281800-39282200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr19:39281800-39282200	Active TSS	Brain Anterior Caudate	brain
44	chr19:39281800-39282200	Active TSS	Brain Cingulate Gyrus	brain
45	chr19:39281800-39282200	Enhancers	Colonic Mucosa	Colon
46	chr19:39281800-39282200	Active TSS	Colon Smooth Muscle	Colon
47	chr19:39281800-39282200	Bivalent/Poised TSS	Fetal Brain Female	brain
48	chr19:39281800-39282200	Active TSS	Fetal Muscle Trunk	muscle
49	chr19:39281800-39282200	Active TSS	Fetal Thymus	thymus
50	chr19:39281800-39282200	Active TSS	Rectal Smooth Muscle	rectum

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