Variant report

Variant	esv3355395
Chromosome Location	chr19:35594412-35598710
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:122)
CpG islands
(count:305)
Chromatin interactive
region (count:5)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr19:35596695-35597038	K562	blood:	n/a	n/a
2	BATF	chr19:35598412-35598720	GM12878	blood:	n/a	chr19:35598446-35598454
3	BHLHE40	chr19:35596677-35597044	K562	blood:	n/a	n/a
4	CBX3	chr19:35596710-35597110	K562	blood:	n/a	n/a
5	CCNT2	chr19:35596675-35597061	K562	blood:	n/a	n/a
6	CEBPB	chr19:35595946-35596306	K562	blood:	n/a	chr19:35596110-35596121
7	CEBPB	chr19:35596099-35596185	IMR90	lung:	n/a	chr19:35596110-35596121
8	CEBPB	chr19:35596017-35596216	Hela-S3	cervix:	n/a	chr19:35596110-35596121
9	CEBPB	chr19:35595986-35596280	A549	lung:	n/a	chr19:35596110-35596121
10	CEBPB	chr19:35597018-35597241	K562	blood:	n/a	chr19:35597107-35597120
11	CEBPB	chr19:35596004-35596234	HepG2	liver:	n/a	chr19:35596110-35596121
12	CEBPD	chr19:35596638-35597167	K562	blood:	n/a	n/a
13	CHD2	chr19:35596745-35597041	K562	blood:	n/a	n/a
14	CTCF	chr19:35597000-35597150	GM12874	blood:	n/a	n/a
15	CTCF	chr19:35596800-35596923	GM19239	blood:	n/a	n/a
16	CTCF	chr19:35595840-35595990	GM12866	blood:	n/a	n/a
17	CTCF	chr19:35596891-35596965	GM10248	blood:	n/a	n/a
18	CTCF	chr19:35596402-35596597	GM19239	blood:	n/a	n/a
19	E2F6	chr19:35596793-35596907	K562	blood:	n/a	n/a
20	EGR1	chr19:35596773-35597052	K562	blood:	n/a	n/a
21	EGR1	chr19:35598425-35598750	K562	blood:	n/a	n/a
22	EGR1	chr19:35598429-35598765	K562	blood:	n/a	n/a
23	EGR1	chr19:35596730-35597020	H1-hESC	embryonic stem cell:	n/a	n/a
24	EGR1	chr19:35596770-35597013	K562	blood:	n/a	n/a
25	ELF1	chr19:35598413-35598721	K562	blood:	n/a	n/a
26	EP300	chr19:35596697-35596770	GM12878	blood:	n/a	n/a
27	EP300	chr19:35598349-35598699	K562	blood:	n/a	n/a
28	EP300	chr19:35596717-35597057	K562	blood:	n/a	n/a
29	EP300	chr19:35598491-35598787	HepG2	liver:	n/a	n/a
30	EP300	chr19:35598252-35598743	HepG2	liver:	n/a	n/a
31	EP300	chr19:35598259-35598842	HepG2	liver:	n/a	n/a
32	FOS	chr19:35598408-35598773	MCF10A-Er-Src	breast:	n/a	chr19:35598437-35598448 chr19:35598589-35598601
33	FOS	chr19:35598397-35598770	MCF10A-Er-Src	breast:	n/a	chr19:35598437-35598448 chr19:35598589-35598601
34	FOS	chr19:35598390-35598790	MCF10A-Er-Src	breast:	n/a	chr19:35598437-35598448 chr19:35598589-35598601
35	FOS	chr19:35598410-35598748	MCF10A-Er-Src	breast:	n/a	chr19:35598437-35598448 chr19:35598589-35598601
36	FOSL1	chr19:35596683-35597053	K562	blood:	n/a	n/a
37	FOSL2	chr19:35598348-35598815	HepG2	liver:	n/a	chr19:35598437-35598448 chr19:35598589-35598601
38	FOXA1	chr19:35598307-35598667	HepG2	liver:	n/a	n/a
39	FOXA2	chr19:35598455-35598634	HepG2	liver:	n/a	n/a
40	GATA1	chr19:35596594-35597249	K562	blood:	n/a	n/a
41	GATA1	chr19:35596574-35597355	K562	blood:	n/a	n/a
42	GATA2	chr19:35596655-35597066	K562	blood:	n/a	n/a
43	GATA2	chr19:35596594-35597054	K562	blood:	n/a	n/a
44	HCFC1	chr19:35596673-35597000	K562	blood:	n/a	n/a
45	HEY1	chr19:35596876-35597051	K562	blood:	n/a	n/a
46	HMGN3	chr19:35597266-35597509	K562	blood:	n/a	n/a
47	HMGN3	chr19:35596797-35597057	K562	blood:	n/a	n/a
48	HNF4A	chr19:35598387-35598701	HepG2	liver:	n/a	n/a
49	HNF4G	chr19:35598454-35598773	HepG2	liver:	n/a	chr19:35598633-35598648
50	IRF1	chr19:35598516-35598716	K562	blood:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:35597415-35597465	ovcar-3	ovarian:	n/a
2	chr19:35597415-35597465	HRCEpiC	kidney:	n/a
3	chr19:35598494-35598544	PANC-1	pancreas:	n/a
4	chr19:35597062-35597112	HIPEpiC	eye:	n/a
5	chr19:35597447-35597497	NB4	blood:	n/a
6	chr19:35597447-35597497	HL-60	blood:	n/a
7	chr19:35597062-35597112	PFSK-1	brain:	n/a
8	chr19:35597415-35597465	IMR90	lung:	fetal
9	chr19:35597226-35597276	AG04449	skin:	fetal
10	chr19:35597226-35597276	CMK	blood:	n/a
11	chr19:35598494-35598544	ProgFib	skin:	n/a
12	chr19:35598494-35598544	HCPEpiC	choroid plexus:	n/a
13	chr19:35597447-35597497	GM12891	blood:	n/a
14	chr19:35597226-35597276	GM06990	blood:	n/a
15	chr19:35597447-35597497	AG04450	lung:	fetal
16	chr19:35597447-35597497	NHBE	bronchial:	n/a
17	chr19:35598494-35598544	GM19239	blood:	n/a
18	chr19:35597415-35597465	NB4	blood:	n/a
19	chr19:35597415-35597465	CMK	blood:	n/a
20	chr19:35597062-35597112	SK-N-MC	brain:	n/a
21	chr19:35597226-35597276	HCPEpiC	choroid plexus:	n/a
22	chr19:35597226-35597276	SKMC	muscle:	n/a
23	chr19:35598494-35598544	HAEpiC	amniotic membrane:	n/a
24	chr19:35597226-35597276	NH-A	brain:	n/a
25	chr19:35598494-35598544	SK-N-MC	brain:	n/a
26	chr19:35597447-35597497	LNCaP	prostate:	n/a
27	chr19:35597415-35597465	BE2_C	brain:	n/a
28	chr19:35597447-35597497	ProgFib	skin:	n/a
29	chr19:35597062-35597112	HUVEC	blood vessel:	n/a
30	chr19:35597415-35597465	MCF-7	breast:	n/a
31	chr19:35597062-35597112	GM19239	blood:	n/a
32	chr19:35597447-35597497	SKMC	muscle:	n/a
33	chr19:35597062-35597112	Caco-2	colon:	n/a
34	chr19:35597226-35597276	HRE	kidney:	n/a
35	chr19:35597447-35597497	AG04449	skin:	fetal
36	chr19:35597447-35597497	HRPEpiC	eye:	n/a
37	chr19:35597226-35597276	MCF-7	breast:	n/a
38	chr19:35597447-35597497	HepG2	liver:	n/a
39	chr19:35598494-35598544	U87	brain:	n/a
40	chr19:35597062-35597112	K562	blood:	n/a
41	chr19:35597415-35597465	Hela-S3	cervix:	n/a
42	chr19:35598494-35598544	AG09309	skin:	n/a
43	chr19:35597447-35597497	Caco-2	colon:	n/a
44	chr19:35597415-35597465	RPTEC	kidney:	n/a
45	chr19:35597415-35597465	SAEC	small airway:	n/a
46	chr19:35597447-35597497	AoSMC	blood vessel:	n/a
47	chr19:35597415-35597465	SKMC	muscle:	n/a
48	chr19:35598494-35598544	SK-N-SH	brain:	n/a
49	chr19:35597447-35597497	HPAEpiC	pulmonary alveolar:	n/a
50	chr19:35598494-35598544	HRE	kidney:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:35490864..35497789-chr19:35597920..35603919,9	MCF-7	breast:
2	chr19:35593937..35595791-chr19:35606292..35608807,2	K562	blood:
3	chr19:35595358..35598195-chr19:35607936..35609678,2	K562	blood:
4	chr19:35593743..35596651-chr19:35609710..35611600,2	K562	blood:
5	chr19:35589524..35591254-chr19:35593014..35595078,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC020907.3-1	chr19:35597133-35597208	ENSG00000227392.1

No data

Variant related genes	Relation type
HPN-AS1	TF binding region
ENSG00000179066	TF binding region
HPN-AS1	CpG island
ENSG00000179066	CpG island
ENSG00000089351	chromatin interactions
ENSG00000089356	chromatin interactions
ENSG00000269303	chromatin interactions

Extended variants
information (count: 227 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:227 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1688013	chr19:35594439-35594440	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs556823021	chr19:35594458-35594459	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs573570476	chr19:35594480-35594481	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs112024903	chr19:35594524-35594525	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs11673506	chr19:35594543-35594544	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs187324876	chr19:35594562-35594563	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs572429001	chr19:35594593-35594594	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs111239195	chr19:35594602-35594603	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs190932917	chr19:35594629-35594630	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs182358340	chr19:35594631-35594632	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs186640123	chr19:35594642-35594643	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs370476830	chr19:35594643-35594644	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs36118062	chr19:35594672-35594673	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs557207954	chr19:35594676-35594677	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs535745147	chr19:35594705-35594706	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs542943746	chr19:35594707-35594708	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs143160489	chr19:35594723-35594724	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs11878232	chr19:35594738-35594739	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs190265977	chr19:35594740-35594741	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs551726686	chr19:35594744-35594745	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs146171673	chr19:35594786-35594787	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs540267616	chr19:35594814-35594815	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs571462987	chr19:35594821-35594822	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs536887674	chr19:35594822-35594823	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs556975673	chr19:35594852-35594853	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs539273977	chr19:35594855-35594856	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs567250272	chr19:35594879-35594880	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs536214585	chr19:35594897-35594898	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs552566951	chr19:35594940-35594941	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs572543105	chr19:35594941-35594942	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs58367535	chr19:35594950-35594951	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs398034448	chr19:35594957-35594958	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs555626788	chr19:35595000-35595001	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs541306642	chr19:35595008-35595009	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs35827980	chr19:35595035-35595036	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs111692566	chr19:35595068-35595069	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs578117945	chr19:35595097-35595098	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs543663754	chr19:35595132-35595133	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs563755314	chr19:35595190-35595191	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs575494223	chr19:35595197-35595198	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs550628475	chr19:35595202-35595203	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs183166354	chr19:35595203-35595204	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs12977462	chr19:35595222-35595223	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs548873288	chr19:35595270-35595271	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs188194452	chr19:35595278-35595279	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs192953410	chr19:35595375-35595376	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs185159835	chr19:35595378-35595379	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs550520833	chr19:35595382-35595383	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs73927918	chr19:35595395-35595396	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs535953423	chr19:35595408-35595409	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
Gastric cancer	21811585	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Multiple myeloma	17550852	CNVD
Lung cancer	18438408	CNVD
Gastric cancer	18160780	CNVD
Glioma	17123091	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:35582200-35605600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr19:35582600-35601600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr19:35587200-35596200	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr19:35587600-35596400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr19:35590000-35605400	Weak transcription	Right Atrium	heart
6	chr19:35590200-35595600	Weak transcription	Brain Angular Gyrus	brain
7	chr19:35590600-35596200	Weak transcription	Esophagus	oesophagus
8	chr19:35591000-35595000	Weak transcription	Brain Substantia Nigra	brain
9	chr19:35591000-35596200	Weak transcription	Pancreas	Pancrea
10	chr19:35592000-35595400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr19:35592200-35595200	Weak transcription	Brain Cingulate Gyrus	brain
12	chr19:35592400-35594800	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr19:35592400-35595000	Weak transcription	Brain Hippocampus Middle	brain
14	chr19:35592400-35596000	Weak transcription	Brain Anterior Caudate	brain
15	chr19:35594800-35596000	Enhancers	Brain Inferior Temporal Lobe	brain
16	chr19:35595000-35595600	Enhancers	Brain Hippocampus Middle	brain
17	chr19:35595000-35595800	Enhancers	Brain Substantia Nigra	brain
18	chr19:35595200-35596000	Enhancers	Brain Cingulate Gyrus	brain
19	chr19:35595400-35596000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr19:35595600-35595800	Flanking Active TSS	Brain Hippocampus Middle	brain
21	chr19:35595600-35596200	Enhancers	Brain Angular Gyrus	brain
22	chr19:35595800-35596000	Genic enhancers	Brain Substantia Nigra	brain
23	chr19:35595800-35596400	Active TSS	Brain Hippocampus Middle	brain
24	chr19:35596000-35596200	Weak transcription	Brain Cingulate Gyrus	brain
25	chr19:35596000-35596400	Enhancers	Brain Anterior Caudate	brain
26	chr19:35596000-35596800	Transcr. at gene 5' and 3'	Brain Substantia Nigra	brain
27	chr19:35596000-35597000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr19:35596000-35597800	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
29	chr19:35596200-35596600	Enhancers	Spleen	Spleen
30	chr19:35596200-35596800	Flanking Active TSS	Brain Angular Gyrus	brain
31	chr19:35596200-35597000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
32	chr19:35596200-35597000	ZNF genes & repeats	Esophagus	oesophagus
33	chr19:35596200-35597000	ZNF genes & repeats	Pancreas	Pancrea
34	chr19:35596200-35597200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
35	chr19:35596200-35597400	Active TSS	Brain Cingulate Gyrus	brain
36	chr19:35596400-35596600	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
37	chr19:35596400-35596600	Flanking Active TSS	Brain Anterior Caudate	brain
38	chr19:35596400-35596800	ZNF genes & repeats	K562	blood
39	chr19:35596400-35597000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
40	chr19:35596400-35598400	Flanking Active TSS	Brain Hippocampus Middle	brain
41	chr19:35596600-35596800	Enhancers	Gastric	stomach
42	chr19:35596600-35597000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr19:35596600-35597000	ZNF genes & repeats	Spleen	Spleen
44	chr19:35596600-35597200	Active TSS	Brain Anterior Caudate	brain
45	chr19:35596800-35597000	Flanking Active TSS	Brain Substantia Nigra	brain
46	chr19:35596800-35597000	Enhancers	Lung	lung
47	chr19:35596800-35597200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr19:35596800-35597400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr19:35596800-35597400	Active TSS	Brain Angular Gyrus	brain
50	chr19:35596800-35597400	Flanking Active TSS	K562	blood

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