Variant report

Variant	nsv1019252
Chromosome Location	chr8:53652807-53779012
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:53736377-53736496	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:53653439-53654157	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:53655962-53656401	HepG2	liver:	n/a	n/a
4	ATF2	chr8:53706285-53706764	GM12878	blood:	n/a	n/a
5	BACH1	chr8:53669704-53669715	K562	blood:	n/a	n/a
6	BACH1	chr8:53752697-53752724	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr8:53737850-53738162	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr8:53730807-53730831	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr8:53752228-53752795	GM12878	blood:	n/a	n/a
10	BCL3	chr8:53752546-53752884	GM12878	blood:	n/a	chr8:53752683-53752692
11	BHLHE40	chr8:53657221-53657310	K562	blood:	n/a	n/a
12	BHLHE40	chr8:53706468-53706729	GM12878	blood:	n/a	n/a
13	BHLHE40	chr8:53705737-53706234	GM12878	blood:	n/a	n/a
14	BRCA1	chr8:53732433-53732923	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr8:53756167-53756690	Hela-S3	cervix:	n/a	n/a
16	CBX3	chr8:53676556-53677517	HCT-116	colon:	n/a	n/a
17	CBX3	chr8:53718617-53718855	K562	blood:	n/a	n/a
18	CBX3	chr8:53718625-53718878	K562	blood:	n/a	n/a
19	CBX3	chr8:53718484-53718948	HCT-116	colon:	n/a	n/a
20	CBX3	chr8:53713264-53713721	HCT-116	colon:	n/a	n/a
21	CBX3	chr8:53718461-53718891	HCT-116	colon:	n/a	n/a
22	CBX3	chr8:53655808-53656400	HCT-116	colon:	n/a	n/a
23	CBX3	chr8:53703257-53703723	HCT-116	colon:	n/a	n/a
24	CBX3	chr8:53713243-53713724	HCT-116	colon:	n/a	n/a
25	CEBPB	chr8:53724602-53724785	A549	lung:	n/a	n/a
26	CEBPB	chr8:53763040-53763050	K562	blood:	n/a	n/a
27	CEBPB	chr8:53752507-53752849	A549	lung:	n/a	chr8:53752731-53752742 chr8:53752731-53752742 chr8:53752731-53752744
28	CEBPB	chr8:53744852-53744928	A549	lung:	n/a	n/a
29	CEBPB	chr8:53665753-53665807	HepG2	liver:	n/a	chr8:53665766-53665777
30	CEBPB	chr8:53684645-53684902	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr8:53756219-53756752	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr8:53736241-53736641	MCF-7	breast:	n/a	chr8:53736481-53736492
33	CEBPB	chr8:53653422-53654150	HepG2	liver:	n/a	chr8:53653987-53653998 chr8:53653987-53653998 chr8:53653985-53653998 chr8:53653985-53653996
34	CEBPB	chr8:53736308-53736667	HepG2	liver:	n/a	chr8:53736481-53736492
35	CEBPB	chr8:53752543-53752843	Hela-S3	cervix:	n/a	chr8:53752731-53752742 chr8:53752731-53752742 chr8:53752731-53752744
36	CEBPB	chr8:53736316-53736670	H1-hESC	embryonic stem cell:	n/a	chr8:53736481-53736492
37	CEBPB	chr8:53653763-53654145	A549	lung:	n/a	chr8:53653987-53653998 chr8:53653987-53653998 chr8:53653985-53653998 chr8:53653985-53653996
38	CEBPB	chr8:53653568-53654202	Hela-S3	cervix:	n/a	chr8:53653987-53653998 chr8:53653987-53653998 chr8:53653985-53653998 chr8:53653985-53653996
39	CEBPB	chr8:53737808-53738283	Hela-S3	cervix:	n/a	chr8:53738190-53738203
40	CEBPB	chr8:53729277-53729526	HepG2	liver:	n/a	chr8:53729422-53729433
41	CEBPB	chr8:53752549-53752841	MCF-7	breast:	n/a	chr8:53752731-53752742 chr8:53752731-53752742 chr8:53752731-53752744
42	CEBPB	chr8:53711242-53711417	K562	blood:	n/a	chr8:53711336-53711349 chr8:53711336-53711349 chr8:53711338-53711349 chr8:53711336-53711347
43	CEBPB	chr8:53772883-53773063	A549	lung:	n/a	n/a
44	CEBPB	chr8:53711229-53711486	HepG2	liver:	n/a	chr8:53711336-53711349 chr8:53711336-53711349 chr8:53711338-53711349 chr8:53711336-53711347
45	CEBPB	chr8:53736300-53736683	A549	lung:	n/a	chr8:53736481-53736492
46	CEBPB	chr8:53732442-53733715	Hela-S3	cervix:	n/a	chr8:53733578-53733589
47	CEBPB	chr8:53729282-53729586	Hela-S3	cervix:	n/a	chr8:53729422-53729433
48	CEBPB	chr8:53744670-53745012	MCF-7	breast:	n/a	n/a
49	CEBPB	chr8:53671328-53671608	HepG2	liver:	n/a	chr8:53671467-53671478
50	CEBPB	chr8:53736304-53736670	IMR90	lung:	n/a	chr8:53736481-53736492

No.	Distal block	Cell Line	Cell type
1	chr8:53627614..53630487-chr8:53664001..53666801,2	K562	blood:
2	chr8:53738269..53739834-chr8:53754081..53756709,2	MCF-7	breast:
3	chr8:53654502..53656554-chr8:53850815..53853562,2	MCF-7	breast:
4	chr8:53682437..53684027-chr8:53685716..53687633,2	MCF-7	breast:
5	chr7:61969210..61969976-chr8:53657642..53658150,2	MCF-7	breast:
6	chr8:53676710..53678990-chr8:53681046..53682714,2	MCF-7	breast:
7	chr8:53653974..53655794-chr8:53756951..53758784,2	MCF-7	breast:
8	chr8:53763900..53765944-chr8:53767253..53769124,2	MCF-7	breast:
9	chr8:53656094..53658855-chr8:53660380..53662129,2	MCF-7	breast:
10	chr8:53627655..53629298-chr8:53662388..53664857,2	K562	blood:
11	chr8:53751467..53754365-chr8:53754550..53756405,2	MCF-7	breast:
12	chr8:53683660..53686636-chr8:53704958..53706568,2	MCF-7	breast:
13	chr8:53653974..53655794-chr8:53756951..53758784,2	MCF-7	breast:
14	chr8:53775937..53778409-chr8:53784460..53787182,3	MCF-7	breast:
15	chr8:53742557..53744441-chr8:53753816..53756483,2	MCF-7	breast:
16	chr8:53682437..53684027-chr8:53685716..53687633,2	MCF-7	breast:
17	chr1:221812817..221813738-chr8:53687326..53688171,2	MCF-7	breast:
18	chr8:53742398..53744549-chr8:53749329..53751637,2	K562	blood:
19	chr8:53711623..53712255-chr8:53854248..53854877,2	MCF-7	breast:
20	chr8:53689610..53691710-chr8:53692191..53695139,2	K562	blood:
21	chr8:53763900..53765944-chr8:53767253..53769124,2	MCF-7	breast:
22	chr8:53645160..53646715-chr8:53654221..53656472,2	K562	blood:
23	chr8:53742557..53744441-chr8:53753816..53756483,2	MCF-7	breast:
24	chr8:53689610..53691710-chr8:53692191..53695139,2	K562	blood:
25	chr8:53683660..53686636-chr8:53704958..53706568,2	MCF-7	breast:
26	chr8:53751467..53754365-chr8:53754550..53756405,2	MCF-7	breast:
27	chr8:53676710..53678990-chr8:53681046..53682714,2	MCF-7	breast:
28	chr8:53738269..53739834-chr8:53754081..53756709,2	MCF-7	breast:
29	chr8:53742398..53744549-chr8:53749329..53751637,2	K562	blood:
30	chr8:53625824..53627381-chr8:53665181..53668029,2	K562	blood:

Variant related genes	Relation type
RB1CC1	TF binding region
ENSG00000183729	chromatin interactions
ENSG00000023287	chromatin interactions

Extended variants
information (count: 4371 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:4371 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs79393319	chr8:53652810-53652811	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs386725388	chr8:53652811-53652812	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs398067813	chr8:53652812-53652813	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs564257923	chr8:53652814-53652815	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs190272179	chr8:53652921-53652922	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs576889626	chr8:53652959-53652960	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs182498449	chr8:53652972-53652973	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs555973856	chr8:53652990-53652991	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs574125498	chr8:53652991-53652992	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs541412712	chr8:53652999-53653000	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs561252312	chr8:53653035-53653036	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs186263881	chr8:53653046-53653047	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs564507055	chr8:53653054-53653055	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs531133194	chr8:53653122-53653123	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs60886984	chr8:53653148-53653149	Genic enhancers Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs565441875	chr8:53653163-53653164	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs115193672	chr8:53653252-53653253	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs77694509	chr8:53653325-53653326	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs146805600	chr8:53653335-53653336	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs530157534	chr8:53653350-53653351	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs112282800	chr8:53653398-53653399	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs574893623	chr8:53653445-53653446	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs184022303	chr8:53653446-53653447	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs566777127	chr8:53653464-53653465	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs534068857	chr8:53653488-53653489	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs552103940	chr8:53653513-53653514	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs570663280	chr8:53653521-53653522	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs115448851	chr8:53653536-53653537	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs11782656	chr8:53653547-53653548	Genic enhancers Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs574151803	chr8:53653650-53653651	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs148529649	chr8:53653659-53653660	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs142884568	chr8:53653660-53653661	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs544481743	chr8:53653672-53653673	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs151036236	chr8:53653702-53653703	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs371500708	chr8:53653721-53653722	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs561460152	chr8:53653787-53653788	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs560641622	chr8:53653810-53653811	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs530305125	chr8:53653850-53653851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs540953968	chr8:53653927-53653928	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs558965259	chr8:53653940-53653941	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs577413946	chr8:53653944-53653945	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs544470155	chr8:53653945-53653946	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs562980075	chr8:53653980-53653981	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs79130230	chr8:53653981-53653982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs140959205	chr8:53654018-53654019	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs193037432	chr8:53654025-53654026	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs34482328	chr8:53654028-53654029	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs77070500	chr8:53654064-53654065	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs115285593	chr8:53654084-53654085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs369653385	chr8:53654089-53654090	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	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
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	22286061	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Sezary syndrome	18413736	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Uveal melanoma	20484589	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21785460	CNVD
Colorectal cancer	21645411	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:606 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:53651000-53655200	Weak transcription	HMEC	breast
2	chr8:53651800-53656800	Enhancers	Hela-S3	cervix
3	chr8:53652200-53653000	Enhancers	Dnd41	blood
4	chr8:53652200-53653400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr8:53652200-53654200	Enhancers	HUVEC	blood vessel
6	chr8:53652200-53657000	Enhancers	NHEK	skin
7	chr8:53652400-53653000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr8:53652600-53653000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr8:53652800-53653000	Enhancers	Left Ventricle	heart
10	chr8:53653000-53653800	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr8:53653000-53655400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr8:53653000-53655800	Weak transcription	Dnd41	blood
13	chr8:53653200-53654400	Enhancers	HepG2	liver
14	chr8:53653400-53655400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr8:53653600-53653800	Enhancers	A549	lung
16	chr8:53653600-53655600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr8:53653800-53654200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr8:53654200-53655400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr8:53654200-53655400	Weak transcription	HUVEC	blood vessel
20	chr8:53654400-53655600	Weak transcription	HepG2	liver
21	chr8:53655200-53656800	Enhancers	HMEC	breast
22	chr8:53655400-53656200	Enhancers	HSMM	muscle
23	chr8:53655400-53656800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr8:53655400-53656800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr8:53655400-53656800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr8:53655400-53656800	Enhancers	HUVEC	blood vessel
27	chr8:53655600-53656600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr8:53655600-53656600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr8:53655600-53656600	Enhancers	HepG2	liver
30	chr8:53655600-53656600	Enhancers	NH-A	brain
31	chr8:53655600-53656800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr8:53655600-53656800	Enhancers	A549	lung
33	chr8:53655600-53656800	Enhancers	HSMMtube	muscle
34	chr8:53655600-53657400	Enhancers	Esophagus	oesophagus
35	chr8:53655800-53656400	Enhancers	Dnd41	blood
36	chr8:53655800-53656600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr8:53655800-53656800	Enhancers	Muscle Satellite Cultured Cells	--
38	chr8:53656000-53656600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr8:53656000-53656600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
40	chr8:53656200-53656400	Flanking Active TSS	HSMM	muscle
41	chr8:53656400-53656800	Enhancers	HSMM	muscle
42	chr8:53656800-53659600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr8:53656800-53659800	Weak transcription	Hela-S3	cervix
44	chr8:53656800-53660200	Weak transcription	A549	lung
45	chr8:53659600-53660000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr8:53659800-53660600	Enhancers	Hela-S3	cervix
47	chr8:53660600-53665800	Weak transcription	Hela-S3	cervix
48	chr8:53665800-53667400	Enhancers	Hela-S3	cervix
49	chr8:53666400-53667400	Enhancers	A549	lung
50	chr8:53666600-53667200	Enhancers	HMEC	breast

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links