Variant report

Variant	nsv611151
Chromosome Location	chr8:43198953-43791691
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2063)
CpG islands
(count:1100)
Chromatin interactive
region (count:9)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2063 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr8:43785555-43785668	K562	blood:	n/a	n/a
2	ATF1	chr8:43786577-43787136	K562	blood:	n/a	n/a
3	BACH1	chr8:43717526-43717725	K562	blood:	n/a	n/a
4	BACH1	chr8:43790059-43790248	K562	blood:	n/a	n/a
5	BACH1	chr8:43654724-43654750	K562	blood:	n/a	n/a
6	BACH1	chr8:43572418-43572443	K562	blood:	n/a	n/a
7	BACH1	chr8:43779446-43779599	K562	blood:	n/a	n/a
8	BATF	chr8:43760280-43760716	GM12878	blood:	n/a	n/a
9	BATF	chr8:43776273-43776586	GM12878	blood:	n/a	n/a
10	BATF	chr8:43771808-43772466	GM12878	blood:	n/a	n/a
11	BATF	chr8:43761295-43761752	GM12878	blood:	n/a	n/a
12	BATF	chr8:43781687-43781911	GM12878	blood:	n/a	n/a
13	BATF	chr8:43789506-43789826	GM12878	blood:	n/a	n/a
14	BATF	chr8:43790147-43790722	GM12878	blood:	n/a	n/a
15	BATF	chr8:43771245-43771622	GM12878	blood:	n/a	n/a
16	BATF	chr8:43785460-43785804	GM12878	blood:	n/a	n/a
17	BATF	chr8:43789506-43789769	GM12878	blood:	n/a	n/a
18	BATF	chr8:43760193-43760718	GM12878	blood:	n/a	n/a
19	BATF	chr8:43761208-43761764	GM12878	blood:	n/a	n/a
20	BATF	chr8:43764727-43764995	GM12878	blood:	n/a	n/a
21	BATF	chr8:43760917-43761158	GM12878	blood:	n/a	n/a
22	BATF	chr8:43759902-43760143	GM12878	blood:	n/a	n/a
23	BATF	chr8:43785488-43786069	GM12878	blood:	n/a	n/a
24	BATF	chr8:43783610-43783797	GM12878	blood:	n/a	n/a
25	BATF	chr8:43781686-43781952	GM12878	blood:	n/a	n/a
26	BATF	chr8:43783535-43783800	GM12878	blood:	n/a	n/a
27	BATF	chr8:43770392-43770728	GM12878	blood:	n/a	n/a
28	BATF	chr8:43790368-43790722	GM12878	blood:	n/a	n/a
29	BATF	chr8:43771212-43771629	GM12878	blood:	n/a	n/a
30	BATF	chr8:43778905-43779151	GM12878	blood:	n/a	n/a
31	BATF	chr8:43782910-43783364	GM12878	blood:	n/a	n/a
32	BATF	chr8:43790975-43791219	GM12878	blood:	n/a	n/a
33	BATF	chr8:43772038-43772467	GM12878	blood:	n/a	n/a
34	BCL11A	chr8:43785837-43785995	GM12878	blood:	n/a	n/a
35	BCL11A	chr8:43761282-43761722	GM12878	blood:	n/a	n/a
36	BCL11A	chr8:43771913-43772498	GM12878	blood:	n/a	n/a
37	BCL11A	chr8:43789364-43789781	GM12878	blood:	n/a	n/a
38	BCL11A	chr8:43760155-43760933	GM12878	blood:	n/a	n/a
39	BCL11A	chr8:43789521-43789791	GM12878	blood:	n/a	n/a
40	BCL11A	chr8:43771195-43771641	GM12878	blood:	n/a	n/a
41	BCL11A	chr8:43785261-43786095	GM12878	blood:	n/a	n/a
42	BCL11A	chr8:43790385-43790700	GM12878	blood:	n/a	n/a
43	BCL11A	chr8:43772033-43772507	GM12878	blood:	n/a	n/a
44	BCL11A	chr8:43781665-43782001	GM12878	blood:	n/a	n/a
45	BCL11A	chr8:43778827-43779220	GM12878	blood:	n/a	n/a
46	BCL11A	chr8:43785511-43785821	GM12878	blood:	n/a	n/a
47	BCL11A	chr8:43790137-43790723	GM12878	blood:	n/a	n/a
48	BCL11A	chr8:43760267-43760707	GM12878	blood:	n/a	n/a
49	BCL11A	chr8:43782626-43783058	GM12878	blood:	n/a	n/a
50	BCL11A	chr8:43759939-43760150	GM12878	blood:	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	chr8:43406411-43406461	HPAEpiC	pulmonary alveolar:	n/a
2	chr8:43404458-43404508	BE2_C	brain:	n/a
3	chr8:43406411-43406461	HPAEpiC	pulmonary alveolar:	n/a
4	chr8:43404458-43404508	BE2_C	brain:	n/a
5	chr8:43418721-43418771	AG09319	gingival:	n/a
6	chr8:43417050-43417100	HEK293	kidney:	embryo
7	chr8:43402930-43402980	NHBE	bronchial:	n/a
8	chr8:43278783-43278833	PANC-1	pancreas:	n/a
9	chr8:43418406-43418456	HAEpiC	amniotic membrane:	n/a
10	chr8:43403277-43403327	HNPCEpiC	eye:	n/a
11	chr8:43417050-43417100	RPTEC	kidney:	n/a
12	chr8:43406314-43406364	HCF	heart:	n/a
13	chr8:43404214-43404264	GM06990	blood:	n/a
14	chr8:43417291-43417341	SAEC	small airway:	n/a
15	chr8:43404458-43404508	SAEC	small airway:	n/a
16	chr8:43417050-43417100	AoSMC	blood vessel:	n/a
17	chr8:43406411-43406461	HEK293	kidney:	embryo
18	chr8:43278783-43278833	ovcar-3	ovarian:	n/a
19	chr8:43404458-43404508	HRCEpiC	kidney:	n/a
20	chr8:43275453-43275503	HepG2	liver:	n/a
21	chr8:43278783-43278833	HUVEC	blood vessel:	n/a
22	chr8:43406144-43406194	BJ	skin:	n/a
23	chr8:43403277-43403327	LNCaP	prostate:	n/a
24	chr8:43417291-43417341	HRE	kidney:	n/a
25	chr8:43417291-43417341	HL-60	blood:	n/a
26	chr8:43418406-43418456	AG09309	skin:	n/a
27	chr8:43403277-43403327	HCM	heart:	n/a
28	chr8:43404214-43404264	BJ	skin:	n/a
29	chr8:43275453-43275503	HCF	heart:	n/a
30	chr8:43404214-43404264	NB4	blood:	n/a
31	chr8:43213875-43213925	HNPCEpiC	eye:	n/a
32	chr8:43404214-43404264	HPAEpiC	pulmonary alveolar:	n/a
33	chr8:43417291-43417341	AoSMC	blood vessel:	n/a
34	chr8:43401874-43401924	GM06990	blood:	n/a
35	chr8:43417050-43417100	GM06990	blood:	n/a
36	chr8:43402630-43402680	K562	blood:	n/a
37	chr8:43401874-43401924	AG10803	skin:	n/a
38	chr8:43406411-43406461	A549	lung:	n/a
39	chr8:43278783-43278833	HCPEpiC	choroid plexus:	n/a
40	chr8:43418406-43418456	HRE	kidney:	n/a
41	chr8:43213875-43213925	NB4	blood:	n/a
42	chr8:43404458-43404508	HIPEpiC	eye:	n/a
43	chr8:43401874-43401924	AoSMC	blood vessel:	n/a
44	chr8:43403277-43403327	HCF	heart:	n/a
45	chr8:43418721-43418771	HCT-116	colon:	n/a
46	chr8:43404214-43404264	AG04449	skin:	fetal
47	chr8:43417050-43417100	GM19239	blood:	n/a
48	chr8:43278783-43278833	GM19239	blood:	n/a
49	chr8:43401874-43401924	GM12891	blood:	n/a
50	chr8:43418406-43418456	Jurkat	blood:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:42947579..42949100-chr8:43300446..43303387,2	MCF-7	breast:
2	chr8:42948115..42950146-chr8:43255758..43258426,2	K562	blood:
3	chr8:43370024..43372377-chr8:43374871..43376951,2	K562	blood:
4	chr15:63385860..63386443-chr8:43553599..43554374,2	MCF-7	breast:
5	chr8:43394978..43396738-chr8:43399115..43401110,2	K562	blood:
6	chr5:82184309..82184963-chr8:43234719..43235395,2	MCF-7	breast:
7	chr8:43395245..43397661-chr8:43402500..43405220,3	K562	blood:
8	chr8:42948083..42948640-chr8:43285913..43286769,2	MCF-7	breast:
9	chr8:43370024..43372377-chr8:43374871..43376951,2	K562	blood:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HGSNAT-7	chr8:43299491-43299558	NONHSAT126356
2	lnc-HGSNAT-9	chr8:43368786-43369564	NONHSAT126361
3	lnc-RNF170-9	chr8:43529413-43529734	NONHSAT126368
4	lnc-HGSNAT-7	chr8:43303948-43304047	NONHSAT126356
5	lnc-HGSNAT-7	chr8:43306599-43306780	NONHSAT126356
6	lnc-HGSNAT-10	chr8:43394280-43394615	NONHSAT126362
7	lnc-HGSNAT-12	chr8:43527966-43528218	NONHSAT126367
8	lnc-HGSNAT-7	chr8:43307943-43308055	NONHSAT126356
9	lnc-HGSNAT-6	chr8:43236787-43237091	NONHSAT126355
10	lnc-RNF170-8	chr8:43366963-43367176	NONHSAT126358
11	lnc-HGSNAT-5	chr8:43233441-43233652	NONHSAT126354
12	lnc-HGSNAT-8	chr8:43349080-43349905	NONHSAT126357
13	lnc-HGSNAT-7	chr8:43298045-43298224	NONHSAT126356

No data

Variant related genes	Relation type
CYP4F44P	TF binding region
ENSG00000253195	TF binding region
ENSG00000254145	TF binding region
ENSG00000250637	TF binding region
ENSG00000221295	TF binding region
ENSG00000253845	TF binding region
ENSG00000201329	TF binding region
ENSG00000254342	TF binding region
ENSG00000253198	TF binding region
RN7SKP41	TF binding region
ENSG00000253319	TF binding region
SNX18P27	TF binding region
ENSG00000264094	TF binding region
ENSG00000254069	TF binding region
CYP4F44P	CpG island
ENSG00000253195	CpG island
ENSG00000254145	CpG island
ENSG00000250637	CpG island
ENSG00000221295	CpG island
ENSG00000253845	CpG island
ENSG00000201329	CpG island
ENSG00000254342	CpG island
ENSG00000253198	CpG island
RN7SKP41	CpG island
ENSG00000253319	CpG island
SNX18P27	CpG island
ENSG00000264094	CpG island
ENSG00000254069	CpG island
ENSG00000253195	chromatin interactions
ENSG00000253748	chromatin interactions
ENSG00000185900	chromatin interactions

Extended variants
information (count: 26394 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:26394 , 50 per page) page: 1 2 3 4 5 6 7 ... 528

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs552517514	chr8:43205222-43205223	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs572783939	chr8:43205225-43205226	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs115448030	chr8:43205229-43205230	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs151206024	chr8:43205232-43205233	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs140280096	chr8:43205276-43205277	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs544375658	chr8:43205277-43205278	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs4507807	chr8:43205279-43205280	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs532618498	chr8:43205286-43205287	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs137920126	chr8:43205288-43205289	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs113484568	chr8:43205294-43205295	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs184316476	chr8:43205296-43205297	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs528521489	chr8:43205316-43205317	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs548850911	chr8:43205321-43205322	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs568617441	chr8:43205322-43205323	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs537350019	chr8:43205355-43205356	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs571077870	chr8:43205358-43205359	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs112734304	chr8:43205365-43205366	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs539130183	chr8:43205373-43205374	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs552839746	chr8:43205379-43205380	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs138480534	chr8:43205390-43205391	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs113842696	chr8:43205396-43205397	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs144382641	chr8:43205405-43205406	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs575423575	chr8:43205418-43205419	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs558097060	chr8:43205420-43205421	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs544536155	chr8:43205430-43205431	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs34996850	chr8:43205442-43205443	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs370285212	chr8:43205451-43205452	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs189598117	chr8:43205459-43205460	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs182010203	chr8:43205471-43205472	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs577942930	chr8:43205513-43205514	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs373666498	chr8:43205517-43205518	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs112494836	chr8:43205521-43205522	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs141507892	chr8:43205581-43205582	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs528593712	chr8:43205584-43205585	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs114538866	chr8:43205594-43205595	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs568646693	chr8:43205599-43205600	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs552927182	chr8:43220004-43220005	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs145049788	chr8:43220005-43220006	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs79683366	chr8:43220026-43220027	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs73561434	chr8:43220050-43220051	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs73561435	chr8:43220061-43220062	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs138831673	chr8:43220070-43220071	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs558420888	chr8:43220079-43220080	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs149345045	chr8:43220080-43220081	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs143613688	chr8:43220088-43220089	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs73677993	chr8:43220112-43220113	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs148051142	chr8:43220114-43220115	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs542611193	chr8:43220126-43220127	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs562613571	chr8:43220136-43220137	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs368336661	chr8:43220141-43220142	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:110)

Disease	PMID	Source
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
Hepatocellular carcinoma	22174799	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
Melanoma	18172304	CNVD
Medulloblastoma	21979893	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
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Seminomas	18059402	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
Lung cancer	18438408	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hepatocellular carcinoma	16750200	CNVD
Bladder cancer	19088036	CNVD
Breast cancer	17001308	CNVD
Breast cancer	17157792	CNVD
Cancer	17001308	CNVD
Cancer	18840272	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Chordoma	18071362	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Breast cancer	16608533	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21785460	CNVD
Rhabdomyosarcoma	16790082	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Breast cancer	21045282	CNVD
Lung cancer	17925434	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Sezary syndrome	18413736	CNVD
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
abnormal development	18461090	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Mental retardation	17124404	CNVD
Schizophrenia	23813976	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	20967226	CNVD
Bipolar disorder	19214233	CNVD

Chromatin state (count:696 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:43205200-43205600	Enhancers	Dnd41	blood
2	chr8:43220000-43221000	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr8:43220600-43221000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr8:43251800-43252200	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
5	chr8:43259400-43260600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr8:43261800-43264000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
7	chr8:43263000-43263600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr8:43263200-43264800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
9	chr8:43265200-43266200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr8:43273200-43273600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr8:43273800-43274000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr8:43295200-43295800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
13	chr8:43303200-43303800	Enhancers	Liver	Liver
14	chr8:43321800-43324400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
15	chr8:43322000-43322800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
16	chr8:43333000-43333600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
17	chr8:43352000-43352600	Enhancers	A549	lung
18	chr8:43352000-43353600	Enhancers	Muscle Satellite Cultured Cells	--
19	chr8:43352200-43353000	Enhancers	Hela-S3	cervix
20	chr8:43352600-43352800	Active TSS	A549	lung
21	chr8:43352800-43353000	Flanking Active TSS	A549	lung
22	chr8:43355400-43355600	Enhancers	Muscle Satellite Cultured Cells	--
23	chr8:43355600-43355800	Weak transcription	Aorta	Aorta
24	chr8:43359800-43360200	Enhancers	Hela-S3	cervix
25	chr8:43360000-43362600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
26	chr8:43362400-43362600	Active TSS	Spleen	Spleen
27	chr8:43362600-43367800	Weak transcription	Spleen	Spleen
28	chr8:43363800-43364000	Enhancers	Gastric	stomach
29	chr8:43364000-43368000	Weak transcription	Gastric	stomach
30	chr8:43366400-43369200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
31	chr8:43366600-43368600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr8:43367000-43368400	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
33	chr8:43367800-43368200	ZNF genes & repeats	Spleen	Spleen
34	chr8:43368000-43369000	ZNF genes & repeats	Gastric	stomach
35	chr8:43368200-43369400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr8:43368200-43373000	Weak transcription	Spleen	Spleen
37	chr8:43371800-43373600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
38	chr8:43373000-43373600	Enhancers	Spleen	Spleen
39	chr8:43375200-43376400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
40	chr8:43377200-43380000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
41	chr8:43378400-43379600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr8:43378600-43379600	Enhancers	HepG2	liver
43	chr8:43378800-43379200	Enhancers	HMEC	breast
44	chr8:43378800-43380000	Enhancers	Left Ventricle	heart
45	chr8:43379000-43379400	Enhancers	NHEK	skin
46	chr8:43379400-43380000	Enhancers	Spleen	Spleen
47	chr8:43379600-43382200	Weak transcription	HepG2	liver
48	chr8:43379800-43380000	Enhancers	Lung	lung
49	chr8:43381400-43383200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
50	chr8:43382200-43382600	Enhancers	HepG2	liver

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links