Variant report

Variant	nsv1032725
Chromosome Location	chr8:10561962-10585683
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:400)
CpG islands
(count:429)
Chromatin interactive
region (count:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:400 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:10573811-10574014	K562	blood:	n/a	n/a
2	ATF1	chr8:10568608-10568946	K562	blood:	n/a	n/a
3	BHLHE40	chr8:10572568-10572607	K562	blood:	n/a	n/a
4	BHLHE40	chr8:10584116-10584359	K562	blood:	n/a	n/a
5	BHLHE40	chr8:10568702-10568993	K562	blood:	n/a	n/a
6	BHLHE40	chr8:10573631-10574069	K562	blood:	n/a	n/a
7	BHLHE40	chr8:10574501-10574728	K562	blood:	n/a	n/a
8	BRCA1	chr8:10573807-10574032	Hela-S3	cervix:	n/a	n/a
9	BRCA1	chr8:10570054-10571623	Hela-S3	cervix:	n/a	n/a
10	BRCA1	chr8:10568658-10569027	Hela-S3	cervix:	n/a	n/a
11	CBX3	chr8:10573588-10574056	K562	blood:	n/a	n/a
12	CCNT2	chr8:10573634-10574186	K562	blood:	n/a	n/a
13	CEBPB	chr8:10563398-10563608	IMR90	lung:	n/a	n/a
14	CEBPB	chr8:10570845-10571193	A549	lung:	n/a	n/a
15	CEBPB	chr8:10571432-10571595	HepG2	liver:	n/a	n/a
16	CEBPB	chr8:10570140-10571670	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr8:10568300-10569061	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr8:10570897-10571105	HepG2	liver:	n/a	n/a
19	CEBPB	chr8:10563484-10563575	K562	blood:	n/a	n/a
20	CEBPB	chr8:10570844-10571149	K562	blood:	n/a	n/a
21	CEBPB	chr8:10576835-10577013	K562	blood:	n/a	n/a
22	CEBPB	chr8:10575751-10575883	K562	blood:	n/a	n/a
23	CEBPB	chr8:10563317-10563560	HepG2	liver:	n/a	n/a
24	CEBPD	chr8:10573673-10574053	K562	blood:	n/a	n/a
25	CEBPD	chr8:10573534-10574123	K562	blood:	n/a	n/a
26	CHD2	chr8:10570800-10571091	Hela-S3	cervix:	n/a	n/a
27	CHD2	chr8:10573711-10573853	K562	blood:	n/a	n/a
28	CHD2	chr8:10573631-10573947	Hela-S3	cervix:	n/a	n/a
29	CHD2	chr8:10568701-10568922	K562	blood:	n/a	n/a
30	CHD2	chr8:10571339-10571623	Hela-S3	cervix:	n/a	n/a
31	CHD2	chr8:10568358-10569062	Hela-S3	cervix:	n/a	n/a
32	CTCF	chr8:10584120-10584270	HUVEC	blood vessel:	n/a	n/a
33	CTCF	chr8:10573860-10574010	HUVEC	blood vessel:	n/a	chr8:10573938-10573951
34	CTCF	chr8:10583838-10584025	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr8:10571320-10571470	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr8:10569276-10569327	MCF-7	breast:	n/a	n/a
37	CTCF	chr8:10571394-10571470	MCF-7	breast:	n/a	n/a
38	CTCF	chr8:10569270-10569342	NHEK	skin:	n/a	n/a
39	CTCF	chr8:10573781-10573798	K562	blood:	n/a	n/a
40	CTCF	chr8:10571380-10571530	SAEC	small airway:	n/a	n/a
41	CTCF	chr8:10573668-10573673	Kidney_OC	kidney:	n/a	n/a
42	CTCF	chr8:10569271-10569336	MCF-7	breast:	n/a	n/a
43	CTCF	chr8:10583820-10584060	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr8:10577758-10577882	Lung_OC	lung:	n/a	n/a
45	CTCF	chr8:10571412-10571464	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr8:10571385-10571519	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr8:10583860-10584010	HUVEC	blood vessel:	n/a	n/a
48	CTCF	chr8:10583966-10584064	Lung_OC	lung:	n/a	n/a
49	CTCF	chr8:10573940-10574090	HUVEC	blood vessel:	n/a	n/a
50	CTCF	chr8:10583802-10584109	H1-hESC	embryonic stem cell:	n/a	n/a

(count:429 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:10584169-10584219	NHDF-neo	bronchial:	n/a
2	chr8:10583326-10583376	RPTEC	kidney:	n/a
3	chr8:10584169-10584219	NHDF-neo	bronchial:	n/a
4	chr8:10583326-10583376	RPTEC	kidney:	n/a
5	chr8:10584169-10584219	GM06990	blood:	n/a
6	chr8:10585394-10585444	GM12892	blood:	n/a
7	chr8:10585394-10585444	HCF	heart:	n/a
8	chr8:10583827-10583877	HCF	heart:	n/a
9	chr8:10581784-10581834	SK-N-MC	brain:	n/a
10	chr8:10585394-10585444	AG10803	skin:	n/a
11	chr8:10581784-10581834	T-47D	breast:	n/a
12	chr8:10584169-10584219	NHBE	bronchial:	n/a
13	chr8:10573804-10573854	PFSK-1	brain:	n/a
14	chr8:10573804-10573854	AG10803	skin:	n/a
15	chr8:10584169-10584219	HPAEpiC	pulmonary alveolar:	n/a
16	chr8:10581784-10581834	NH-A	brain:	n/a
17	chr8:10585394-10585444	RPTEC	kidney:	n/a
18	chr8:10581988-10582038	HCPEpiC	choroid plexus:	n/a
19	chr8:10585394-10585444	AG09309	skin:	n/a
20	chr8:10583326-10583376	HCM	heart:	n/a
21	chr8:10583326-10583376	BE2_C	brain:	n/a
22	chr8:10581988-10582038	GM06990	blood:	n/a
23	chr8:10583326-10583376	PANC-1	pancreas:	n/a
24	chr8:10583827-10583877	NH-A	brain:	n/a
25	chr8:10583326-10583376	SK-N-SH	brain:	n/a
26	chr8:10581784-10581834	GM12891	blood:	n/a
27	chr8:10581988-10582038	RPTEC	kidney:	n/a
28	chr8:10581784-10581834	HepG2	liver:	n/a
29	chr8:10573804-10573854	Jurkat	blood:	n/a
30	chr8:10583326-10583376	ProgFib	skin:	n/a
31	chr8:10583326-10583376	MCF10A-Er-Src	breast:	n/a
32	chr8:10585394-10585444	NHBE	bronchial:	n/a
33	chr8:10573804-10573854	K562	blood:	n/a
34	chr8:10573804-10573854	PANC-1	pancreas:	n/a
35	chr8:10581784-10581834	AG04450	lung:	fetal
36	chr8:10581784-10581834	AoSMC	blood vessel:	n/a
37	chr8:10581988-10582038	MCF10A-Er-Src	breast:	n/a
38	chr8:10583827-10583877	AG04450	lung:	fetal
39	chr8:10585394-10585444	PANC-1	pancreas:	n/a
40	chr8:10584169-10584219	ovcar-3	ovarian:	n/a
41	chr8:10581988-10582038	GM12892	blood:	n/a
42	chr8:10583827-10583877	HEEpiC	esophagus:	n/a
43	chr8:10584169-10584219	SKMC	muscle:	n/a
44	chr8:10573804-10573854	AG04450	lung:	fetal
45	chr8:10573804-10573854	HRCEpiC	kidney:	n/a
46	chr8:10584169-10584219	NT2-D1	testis:	n/a
47	chr8:10583326-10583376	PrEC	prostate:	n/a
48	chr8:10583827-10583877	AG10803	skin:	n/a
49	chr8:10581988-10582038	T-47D	breast:	n/a
50	chr8:10581784-10581834	HUVEC	blood vessel:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:10581535..10584414-chr8:10592948..10594895,2	MCF-7	breast:
2	chr8:10568215..10570516-chr8:10570791..10574753,3	K562	blood:
3	chr8:10534702..10537389-chr8:10561883..10564793,2	K562	blood:
4	chr8:10501933..10503647-chr8:10579530..10582148,2	K562	blood:
5	chr8:10561879..10564186-chr8:10576793..10578956,2	K562	blood:
6	chr8:10582500..10584094-chr8:10592919..10595783,2	K562	blood:
7	chr8:10573494..10575019-chr8:10578805..10581206,2	K562	blood:
8	chr8:10549207..10552160-chr8:10577938..10579847,2	K562	blood:
9	chr8:10556097..10559916-chr8:10561605..10564138,3	K562	blood:
10	chr8:10564366..10566017-chr8:10568811..10571288,2	K562	blood:
11	chr8:10583182..10585584-chr8:10585920..10587606,2	K562	blood:
12	chr8:10572945..10574994-chr8:10579706..10582412,2	K562	blood:
13	chr8:10561128..10563766-chr8:10580957..10583552,2	K562	blood:
14	chr8:10553523..10556097-chr8:10561265..10564003,2	K562	blood:
15	chr8:10561128..10563766-chr8:10580957..10583552,2	K562	blood:
16	chr8:10582499..10584929-chr8:10712844..10715124,2	K562	blood:
17	chr8:10563640..10566502-chr8:10586406..10589328,2	K562	blood:
18	chr8:10572945..10574994-chr8:10579706..10582412,2	K562	blood:
19	chr8:10573494..10575019-chr8:10578805..10581206,2	K562	blood:
20	chr8:10561879..10564186-chr8:10576793..10578956,2	K562	blood:

No data

Variant related genes	Relation type
RP1L1	TF binding region
ENSG00000248896	TF binding region
RP1L1	CpG island
ENSG00000248896	CpG island
ENSG00000248896	chromatin interactions
ENSG00000171056	chromatin interactions
ENSG00000183638	chromatin interactions

Extended variants
information (count: 1390 )
Associated
traits (count: 137 )

Variant overlapped rSNPs/rCNVs (count:1390 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544228519	chr8:10561977-10561978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs147383838	chr8:10561983-10561984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs565683196	chr8:10562024-10562025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs564041595	chr8:10562047-10562048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs6994394	chr8:10562074-10562075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs534292664	chr8:10562095-10562096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs532866349	chr8:10562101-10562102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs34836781	chr8:10562106-10562107	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs540306006	chr8:10562110-10562111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs116127122	chr8:10562111-10562112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs571472024	chr8:10562112-10562113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs546509499	chr8:10562121-10562122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs75679217	chr8:10562134-10562135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs111628821	chr8:10562149-10562150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs542378777	chr8:10562163-10562164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs113207103	chr8:10562177-10562178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs113398352	chr8:10562221-10562222	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs200915948	chr8:10562248-10562249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs182630105	chr8:10562255-10562256	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs564418285	chr8:10562288-10562289	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs575365325	chr8:10562317-10562318	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs549663308	chr8:10562334-10562335	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs376158058	chr8:10562362-10562363	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs10111185	chr8:10562416-10562417	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs117136615	chr8:10562418-10562419	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs549082049	chr8:10562444-10562445	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs565589702	chr8:10562496-10562497	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs76400292	chr8:10562509-10562510	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs139631158	chr8:10562520-10562521	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs114062171	chr8:10562547-10562548	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs540164534	chr8:10562557-10562558	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs142622806	chr8:10562559-10562560	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs576727316	chr8:10562560-10562561	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs185401978	chr8:10562575-10562576	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs555833775	chr8:10562601-10562602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs572409306	chr8:10562622-10562623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs541508988	chr8:10562624-10562625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs564373067	chr8:10562638-10562639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs371836026	chr8:10562644-10562645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs577594949	chr8:10562656-10562657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs531456712	chr8:10562691-10562692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs543325992	chr8:10562695-10562696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs372266646	chr8:10562731-10562732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs114714625	chr8:10562744-10562745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs529054609	chr8:10562749-10562750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs548861470	chr8:10562807-10562808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs74427782	chr8:10562823-10562824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs368437345	chr8:10562841-10562842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs528220596	chr8:10562879-10562880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs60329126	chr8:10562881-10562882	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:137)

Disease	PMID	Source
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	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
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	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
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	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
Developmental disorder	20461109	CNVD
abnormal development	18461090	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Gastric cancer	21811585	CNVD
Colorectal cancer	16774939	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:301 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:10560400-10567800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr8:10562200-10562600	Enhancers	Esophagus	oesophagus
3	chr8:10563800-10568000	Enhancers	Hela-S3	cervix
4	chr8:10564000-10564600	ZNF genes & repeats	Spleen	Spleen
5	chr8:10565800-10566000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr8:10565800-10566000	ZNF genes & repeats	Spleen	Spleen
7	chr8:10566000-10568200	Weak transcription	Spleen	Spleen
8	chr8:10566000-10568400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr8:10567400-10570400	Enhancers	Esophagus	oesophagus
10	chr8:10567400-10571800	Enhancers	HMEC	breast
11	chr8:10567600-10568400	Enhancers	HUVEC	blood vessel
12	chr8:10567800-10568000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr8:10567800-10568000	Enhancers	NHEK	skin
14	chr8:10567800-10568200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr8:10567800-10568400	Enhancers	Primary hematopoietic stem cells short term culture	blood
16	chr8:10567800-10568400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr8:10567800-10571600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr8:10567800-10572200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr8:10568000-10568400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr8:10568000-10568800	Flanking Active TSS	Hela-S3	cervix
21	chr8:10568000-10568800	Flanking Active TSS	NHEK	skin
22	chr8:10568000-10569000	Enhancers	Right Ventricle	heart
23	chr8:10568000-10569600	Enhancers	Primary hematopoietic stem cells	blood
24	chr8:10568200-10568800	Enhancers	Right Atrium	heart
25	chr8:10568200-10569000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr8:10568200-10569000	Enhancers	Spleen	Spleen
27	chr8:10568200-10569000	Enhancers	GM12878-XiMat	blood
28	chr8:10568200-10569000	Enhancers	NH-A	brain
29	chr8:10568200-10569200	Enhancers	Adipose Nuclei	Adipose
30	chr8:10568200-10569400	Enhancers	Primary monocytes fromperipheralblood	blood
31	chr8:10568200-10569400	Enhancers	Fetal Thymus	thymus
32	chr8:10568200-10569400	Enhancers	Left Ventricle	heart
33	chr8:10568200-10569600	Enhancers	Lung	lung
34	chr8:10568400-10568600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr8:10568400-10568800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr8:10568400-10568800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
37	chr8:10568400-10568800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
38	chr8:10568400-10568800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr8:10568400-10568800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
40	chr8:10568400-10568800	Flanking Active TSS	HUVEC	blood vessel
41	chr8:10568400-10569000	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr8:10568400-10569000	Enhancers	A549	lung
43	chr8:10568400-10569000	Enhancers	Monocytes-CD14+_RO01746	blood
44	chr8:10568400-10569400	Enhancers	K562	blood
45	chr8:10568600-10568800	Enhancers	H1 Cell Line	embryonic stem cell
46	chr8:10568600-10568800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr8:10568600-10568800	Enhancers	Skeletal Muscle Male	skeletal muscle
48	chr8:10568600-10569000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr8:10568600-10569000	Enhancers	Primary B cells from peripheral blood	blood
50	chr8:10568600-10569000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links