Variant report

Variant	nsv470202
Chromosome Location	chr8:19128303-19168142
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:502)
CpG islands
(count:61)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:502 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:19149146-19149417	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:19137599-19138311	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:19128678-19129043	HepG2	liver:	n/a	n/a
4	BCL3	chr8:19148800-19149410	A549	lung:	n/a	n/a
5	BRCA1	chr8:19148949-19149382	Hela-S3	cervix:	n/a	n/a
6	CBX3	chr8:19148884-19149453	HCT-116	colon:	n/a	n/a
7	CEBPB	chr8:19153183-19153441	IMR90	lung:	n/a	chr8:19153309-19153320 chr8:19153309-19153322
8	CEBPB	chr8:19148912-19149467	HCT-116	colon:	n/a	chr8:19148933-19148946
9	CEBPB	chr8:19128736-19129013	MCF-7	breast:	n/a	n/a
10	CEBPB	chr8:19148777-19149483	Hela-S3	cervix:	n/a	chr8:19148933-19148946
11	CEBPB	chr8:19128679-19129059	HepG2	liver:	n/a	n/a
12	CEBPB	chr8:19128684-19129051	HepG2	liver:	n/a	n/a
13	CEBPB	chr8:19148697-19149552	A549	lung:	n/a	chr8:19148933-19148946
14	CEBPB	chr8:19128734-19129031	A549	lung:	n/a	n/a
15	CEBPB	chr8:19148817-19149547	MCF-7	breast:	n/a	chr8:19148933-19148946
16	CEBPB	chr8:19132687-19132958	HepG2	liver:	n/a	n/a
17	CEBPB	chr8:19149138-19149329	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr8:19132662-19132800	K562	blood:	n/a	n/a
19	CEBPB	chr8:19156052-19156603	IMR90	lung:	n/a	n/a
20	CEBPB	chr8:19132686-19132921	A549	lung:	n/a	n/a
21	CEBPB	chr8:19148824-19149440	ECC-1	luminal epithelium:	n/a	chr8:19148933-19148946
22	CEBPB	chr8:19148764-19149466	IMR90	lung:	n/a	chr8:19148933-19148946
23	CEBPB	chr8:19148819-19149581	HCT-116	colon:	n/a	chr8:19148933-19148946
24	CEBPB	chr8:19128773-19129043	MCF-7	breast:	n/a	n/a
25	CEBPB	chr8:19153165-19153379	HepG2	liver:	n/a	chr8:19153309-19153320 chr8:19153309-19153322
26	CEBPB	chr8:19128690-19129046	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr8:19128797-19128948	IMR90	lung:	n/a	n/a
28	CEBPB	chr8:19163278-19163543	IMR90	lung:	n/a	n/a
29	CEBPB	chr8:19128747-19129011	K562	blood:	n/a	n/a
30	CEBPB	chr8:19128787-19129003	HepG2	liver:	n/a	n/a
31	CEBPB	chr8:19128702-19129031	HCT-116	colon:	n/a	n/a
32	CEBPB	chr8:19149055-19149255	K562	blood:	n/a	n/a
33	CEBPB	chr8:19148873-19149418	A549	lung:	n/a	chr8:19148933-19148946
34	CEBPB	chr8:19128709-19129034	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr8:19128767-19129064	ECC-1	luminal epithelium:	n/a	n/a
36	CEBPB	chr8:19128654-19129089	A549	lung:	n/a	n/a
37	CEBPB	chr8:19128695-19129021	HepG2	liver:	n/a	n/a
38	CEBPB	chr8:19137796-19138239	HepG2	liver:	n/a	n/a
39	CEBPB	chr8:19128692-19129039	A549	lung:	n/a	n/a
40	CEBPB	chr8:19148939-19149431	ECC-1	luminal epithelium:	n/a	n/a
41	CEBPB	chr8:19148943-19149484	A549	lung:	n/a	n/a
42	CEBPB	chr8:19148893-19149493	MCF-7	breast:	n/a	chr8:19148933-19148946
43	CEBPB	chr8:19137227-19137431	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr8:19148959-19149407	HepG2	liver:	n/a	n/a
45	CEBPB	chr8:19129554-19129721	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr8:19129441-19129898	ECC-1	luminal epithelium:	n/a	n/a
47	CEBPB	chr8:19128736-19129078	ECC-1	luminal epithelium:	n/a	n/a
48	CEBPB	chr8:19128745-19129090	HCT-116	colon:	n/a	n/a
49	CEBPD	chr8:19128778-19128938	HepG2	liver:	n/a	n/a
50	CHD2	chr8:19149034-19149419	Hela-S3	cervix:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:19156146-19156196	HCPEpiC	choroid plexus:	n/a
2	chr8:19156146-19156196	HEEpiC	esophagus:	n/a
3	chr8:19156146-19156196	ECC-1	luminal epithelium:	n/a
4	chr8:19156146-19156196	GM12878	blood:	n/a
5	chr8:19156146-19156196	BJ	skin:	n/a
6	chr8:19156146-19156196	HRE	kidney:	n/a
7	chr8:19156146-19156196	ProgFib	skin:	n/a
8	chr8:19156146-19156196	AG09309	skin:	n/a
9	chr8:19156146-19156196	HRPEpiC	eye:	n/a
10	chr8:19156146-19156196	PrEC	prostate:	n/a
11	chr8:19156146-19156196	Hepatocyte	liver:	n/a
12	chr8:19156146-19156196	HNPCEpiC	eye:	n/a
13	chr8:19156146-19156196	AG10803	skin:	n/a
14	chr8:19156146-19156196	PFSK-1	brain:	n/a
15	chr8:19156146-19156196	RPTEC	kidney:	n/a
16	chr8:19156146-19156196	T-47D	breast:	n/a
17	chr8:19156146-19156196	CMK	blood:	n/a
18	chr8:19156146-19156196	HPAEpiC	pulmonary alveolar:	n/a
19	chr8:19156146-19156196	HRCEpiC	kidney:	n/a
20	chr8:19156146-19156196	GM06990	blood:	n/a
21	chr8:19156146-19156196	NHDF-neo	bronchial:	n/a
22	chr8:19156146-19156196	MCF10A-Er-Src	breast:	n/a
23	chr8:19156146-19156196	NT2-D1	testis:	n/a
24	chr8:19156146-19156196	NB4	blood:	n/a
25	chr8:19156146-19156196	K562	blood:	n/a
26	chr8:19156146-19156196	A549	lung:	n/a
27	chr8:19156146-19156196	HepG2	liver:	n/a
28	chr8:19156146-19156196	HCM	heart:	n/a
29	chr8:19156146-19156196	Jurkat	blood:	n/a
30	chr8:19156146-19156196	AG04450	lung:	fetal
31	chr8:19156146-19156196	H1-hESC	embryonic stem cell:	embryo
32	chr8:19156146-19156196	BE2_C	brain:	n/a
33	chr8:19156146-19156196	AoSMC	blood vessel:	n/a
34	chr8:19156146-19156196	NH-A	brain:	n/a
35	chr8:19156146-19156196	NHBE	bronchial:	n/a
36	chr8:19156146-19156196	Caco-2	colon:	n/a
37	chr8:19156146-19156196	HAEpiC	amniotic membrane:	n/a
38	chr8:19156146-19156196	PANC-1	pancreas:	n/a
39	chr8:19156146-19156196	SK-N-SH	brain:	n/a
40	chr8:19156146-19156196	LNCaP	prostate:	n/a
41	chr8:19156146-19156196	GM12892	blood:	n/a
42	chr8:19156146-19156196	HMEC	breast:	n/a
43	chr8:19156146-19156196	MCF-7	breast:	n/a
44	chr8:19156146-19156196	AG04449	skin:	fetal
45	chr8:19156146-19156196	IMR90	lung:	fetal
46	chr8:19156146-19156196	GM12891	blood:	n/a
47	chr8:19156146-19156196	SK-N-SH_RA	brain:	n/a
48	chr8:19156146-19156196	HCT-116	colon:	n/a
49	chr8:19156146-19156196	SAEC	small airway:	n/a
50	chr8:19156146-19156196	HL-60	blood:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:19120168..19121747-chr8:19134338..19135929,2	K562	blood:
2	chr8:19147926..19150795-chr8:19170285..19172249,2	MCF-7	breast:
3	chr8:19148177..19150555-chr8:19150746..19153628,2	K562	blood:
4	chr8:19152770..19154882-chr8:19158766..19160464,2	K562	blood:
5	chr8:19144461..19147739-chr8:19170304..19172981,3	MCF-7	breast:
6	chr8:19156532..19159524-chr8:19170148..19172446,2	MCF-7	breast:
7	chr8:19128887..19134305-chr8:19169094..19173373,6	MCF-7	breast:
8	chr8:19148177..19150555-chr8:19150746..19153628,2	K562	blood:
9	chr8:19147589..19149540-chr8:19523160..19524664,2	MCF-7	breast:
10	chr8:19149962..19152072-chr8:19173164..19175700,2	MCF-7	breast:
11	chr8:19148156..19152459-chr8:19169128..19172088,7	MCF-7	breast:
12	chr8:19152770..19154882-chr8:19158766..19160464,2	K562	blood:
13	chr8:19146966..19149051-chr8:19185409..19187470,2	MCF-7	breast:
14	chr8:19142668..19144947-chr8:19171540..19174164,2	MCF-7	breast:
15	chr8:19155044..19157820-chr8:19172820..19174971,2	MCF-7	breast:

No data

Variant related genes	Relation type
SH2D4A	TF binding region
SH2D4A	CpG island
ENSG00000104611	chromatin interactions

Extended variants
information (count: 2162 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:2162 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9644625	chr8:19128303-19128304	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs369235110	chr8:19128312-19128313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs537845440	chr8:19128365-19128366	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs9644626	chr8:19128385-19128386	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs368602764	chr8:19128398-19128399	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs185322566	chr8:19128400-19128401	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs541700069	chr8:19128415-19128416	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs560038218	chr8:19128432-19128433	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs553559990	chr8:19128451-19128452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs573341034	chr8:19128498-19128499	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs554603432	chr8:19128549-19128550	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs535787191	chr8:19128551-19128552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs566228644	chr8:19128560-19128561	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs555639138	chr8:19128587-19128588	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs575484647	chr8:19128621-19128622	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs544206984	chr8:19128626-19128627	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs564288247	chr8:19128657-19128658	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs1915404	chr8:19128668-19128669	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs190201671	chr8:19128678-19128679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs560326878	chr8:19128683-19128684	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs1915405	chr8:19128697-19128698	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs112581008	chr8:19128699-19128700	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs562782674	chr8:19128711-19128712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs182395971	chr8:19128723-19128724	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs551420598	chr8:19128732-19128733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs2947264	chr8:19128735-19128736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs1915406	chr8:19128744-19128745	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs188233976	chr8:19128750-19128751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs111435960	chr8:19128767-19128768	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs577707473	chr8:19128783-19128784	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs142419183	chr8:19128798-19128799	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs180942598	chr8:19128810-19128811	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs538589848	chr8:19128812-19128813	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs2672257	chr8:19128841-19128842	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs577939901	chr8:19128845-19128846	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs185561505	chr8:19128879-19128880	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs2683279	chr8:19128886-19128887	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs116411384	chr8:19128954-19128955	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs542861602	chr8:19128960-19128961	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs34265536	chr8:19128965-19128966	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs531667432	chr8:19128966-19128967	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs13261970	chr8:19128982-19128983	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs190269911	chr8:19128988-19128989	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs527287071	chr8:19129055-19129056	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs547323072	chr8:19129060-19129061	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs35651150	chr8:19129080-19129081	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs183229428	chr8:19129084-19129085	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs549187459	chr8:19129097-19129098	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs375597999	chr8:19129104-19129105	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs140144376	chr8:19129110-19129111	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:114)

Disease	PMID	Source
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Epilepsy	22083797	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	17603634	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	17550852	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21364760	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cancer	18840272	CNVD
Breast cancer	19602461	CNVD
Osteosarcoma	19286668	CNVD
Prostate cancer	19242612	CNVD
Prostate cancer	19258508	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
small cell lung cancer	20016488	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Gastric adenocarcinoma	19115996	CNVD
Colorectal cancer	19455253	CNVD

Chromatin state (count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:19121600-19129400	Weak transcription	Spleen	Spleen
2	chr8:19122400-19129800	Weak transcription	Pancreas	Pancrea
3	chr8:19123200-19129800	Weak transcription	Gastric	stomach
4	chr8:19125400-19129200	Weak transcription	Primary hematopoietic stem cells	blood
5	chr8:19125600-19128800	Weak transcription	HMEC	breast
6	chr8:19125600-19129400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr8:19125600-19129400	Weak transcription	NHEK	skin
8	chr8:19125600-19131200	Weak transcription	Fetal Heart	heart
9	chr8:19125600-19131200	Weak transcription	Right Atrium	heart
10	chr8:19125600-19131400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr8:19125800-19128800	Weak transcription	A549	lung
12	chr8:19125800-19131000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr8:19125800-19131000	Weak transcription	Fetal Lung	lung
14	chr8:19125800-19131200	Weak transcription	Adipose Nuclei	Adipose
15	chr8:19126000-19129200	Weak transcription	HUVEC	blood vessel
16	chr8:19126000-19129400	Weak transcription	Stomach Mucosa	stomach
17	chr8:19126000-19129400	Weak transcription	Hela-S3	cervix
18	chr8:19126000-19131200	Weak transcription	Rectal Mucosa Donor 31	rectum
19	chr8:19126400-19129200	Weak transcription	HepG2	liver
20	chr8:19127800-19133400	Enhancers	Liver	Liver
21	chr8:19128600-19128800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr8:19128800-19129200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr8:19128800-19130000	Enhancers	HMEC	breast
24	chr8:19128800-19130400	Enhancers	A549	lung
25	chr8:19129200-19129600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr8:19129200-19129800	Enhancers	HepG2	liver
27	chr8:19129200-19130000	Enhancers	Primary hematopoietic stem cells	blood
28	chr8:19129200-19130000	Enhancers	HUVEC	blood vessel
29	chr8:19129400-19129800	Enhancers	Stomach Mucosa	stomach
30	chr8:19129400-19130000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr8:19129400-19130000	Enhancers	Spleen	Spleen
32	chr8:19129400-19130000	Enhancers	Hela-S3	cervix
33	chr8:19129400-19130000	Enhancers	NHEK	skin
34	chr8:19129800-19130000	Enhancers	Gastric	stomach
35	chr8:19129800-19130000	Enhancers	Left Ventricle	heart
36	chr8:19129800-19130000	Enhancers	Pancreas	Pancrea
37	chr8:19129800-19130000	Bivalent Enhancer	HepG2	liver
38	chr8:19129800-19131000	Weak transcription	Stomach Mucosa	stomach
39	chr8:19130000-19131000	Weak transcription	Hela-S3	cervix
40	chr8:19130000-19131200	Weak transcription	NHEK	skin
41	chr8:19130000-19131400	Weak transcription	Gastric	stomach
42	chr8:19130000-19131400	Weak transcription	Left Ventricle	heart
43	chr8:19130000-19132800	Weak transcription	HMEC	breast
44	chr8:19130000-19136200	Weak transcription	Pancreas	Pancrea
45	chr8:19130200-19131200	Weak transcription	Fetal Muscle Leg	muscle
46	chr8:19130400-19130800	Weak transcription	A549	lung
47	chr8:19130800-19132000	Enhancers	A549	lung
48	chr8:19131000-19131200	Enhancers	Hela-S3	cervix
49	chr8:19131000-19131400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr8:19131000-19131400	Enhancers	HepG2	liver

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