Variant report

Variant	nsv883450
Chromosome Location	chr6:13166341-13196011
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	chr6:13181636-13181953	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:13195207-13195429	K562	blood:	n/a	n/a
3	BACH1	chr6:13169246-13169333	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr6:13176056-13176256	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr6:13195193-13195429	K562	blood:	n/a	n/a
6	CBX3	chr6:13195102-13195482	K562	blood:	n/a	n/a
7	CEBPB	chr6:13173925-13174090	HepG2	liver:	n/a	chr6:13173996-13174007
8	CEBPB	chr6:13173930-13173948	A549	lung:	n/a	n/a
9	CEBPB	chr6:13173882-13174140	H1-hESC	embryonic stem cell:	n/a	chr6:13173996-13174007
10	CEBPB	chr6:13190047-13190174	HepG2	liver:	n/a	n/a
11	CEBPB	chr6:13181755-13181943	HepG2	liver:	n/a	n/a
12	CEBPB	chr6:13173926-13174021	Hela-S3	cervix:	n/a	chr6:13173996-13174007
13	CHD2	chr6:13195174-13195365	H1-hESC	embryonic stem cell:	n/a	n/a
14	CREB1	chr6:13177838-13178395	GM12878	blood:	n/a	n/a
15	CTCF	chr6:13195200-13195350	HA-sp	spinal cord:	n/a	chr6:13195277-13195298 chr6:13195275-13195293
16	CTCF	chr6:13176220-13176370	HFF	foreskin:	n/a	n/a
17	CTCF	chr6:13195132-13195370	SK-N-SH_RA	brain:	n/a	chr6:13195277-13195298 chr6:13195275-13195293
18	CTCF	chr6:13195170-13195426	GM12891	blood:	n/a	chr6:13195277-13195298 chr6:13195275-13195293
19	CTCF	chr6:13195151-13195161	Kidney_OC	kidney:	n/a	n/a
20	CTCF	chr6:13195197-13195395	MCF-7	breast:	n/a	chr6:13195277-13195298 chr6:13195275-13195293
21	CTCF	chr6:13195158-13195169	GM12891	blood:	n/a	n/a
22	CTCF	chr6:13195220-13195370	HPF	lung:	n/a	chr6:13195277-13195298 chr6:13195275-13195293
23	CTCF	chr6:13171400-13171550	GM12866	blood:	n/a	n/a
24	CTCF	chr6:13176060-13176310	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr6:13195186-13195384	LNCaP	prostate:	n/a	chr6:13195277-13195298 chr6:13195275-13195293
26	CTCF	chr6:13176140-13176290	GM12865	blood:	n/a	n/a
27	CTCF	chr6:13195260-13195410	GM12875	blood:	n/a	chr6:13195277-13195298 chr6:13195275-13195293
28	CTCF	chr6:13195180-13195330	GM12864	blood:	n/a	chr6:13195277-13195298 chr6:13195275-13195293
29	CTCF	chr6:13195200-13195350	GM12873	blood:	n/a	chr6:13195277-13195298 chr6:13195275-13195293
30	CTCF	chr6:13195182-13195383	GM13976	blood:	n/a	chr6:13195277-13195298 chr6:13195275-13195293
31	CTCF	chr6:13195142-13195399	Hela-S3	cervix:	n/a	chr6:13195277-13195298 chr6:13195275-13195293
32	CTCF	chr6:13195070-13195551	MCF-7	breast:	n/a	chr6:13195277-13195298 chr6:13195482-13195503 chr6:13195275-13195293
33	CTCF	chr6:13176163-13176286	MCF-7	breast:	n/a	n/a
34	CTCF	chr6:13176100-13176250	WERI-Rb-1	eye:	n/a	n/a
35	CTCF	chr6:13195220-13195370	SAEC	small airway:	n/a	chr6:13195277-13195298 chr6:13195275-13195293
36	CTCF	chr6:13195220-13195370	AG04449	skin:	n/a	chr6:13195277-13195298 chr6:13195275-13195293
37	CTCF	chr6:13195161-13195395	LNCaP	prostate:	n/a	chr6:13195277-13195298 chr6:13195275-13195293
38	CTCF	chr6:13195260-13195410	Hela-S3	cervix:	n/a	chr6:13195277-13195298 chr6:13195275-13195293
39	CTCF	chr6:13195240-13195390	BJ	skin:	n/a	chr6:13195277-13195298 chr6:13195275-13195293
40	CTCF	chr6:13195090-13195485	K562	blood:	n/a	chr6:13195277-13195298 chr6:13195275-13195293
41	CTCF	chr6:13195119-13195370	HepG2	liver:	n/a	chr6:13195277-13195298 chr6:13195275-13195293
42	CTCF	chr6:13176200-13176350	HPAF	blood vessel:	n/a	n/a
43	CTCF	chr6:13195171-13195380	GM10266	blood:	n/a	chr6:13195277-13195298 chr6:13195275-13195293
44	CTCF	chr6:13195240-13195390	HEEpiC	esophagus:	n/a	chr6:13195277-13195298 chr6:13195275-13195293
45	CTCF	chr6:13195200-13195350	GM12871	blood:	n/a	chr6:13195277-13195298 chr6:13195275-13195293
46	CTCF	chr6:13195120-13195270	WI-38	lung:	n/a	n/a
47	CTCF	chr6:13195196-13195409	MCF-7	breast:	n/a	chr6:13195277-13195298 chr6:13195275-13195293
48	CTCF	chr6:13195093-13195444	K562	blood:	n/a	chr6:13195277-13195298 chr6:13195275-13195293
49	CTCF	chr6:13195220-13195370	AG04450	lung:	n/a	chr6:13195277-13195298 chr6:13195275-13195293
50	CTCF	chr6:13195200-13195350	GM12865	blood:	n/a	chr6:13195277-13195298 chr6:13195275-13195293

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:13175441-13175491	AG04450	lung:	fetal
2	chr6:13175441-13175491	SK-N-SH_RA	brain:	n/a
3	chr6:13173168-13173218	HRCEpiC	kidney:	n/a
4	chr6:13194027-13194077	HRCEpiC	kidney:	n/a
5	chr6:13194027-13194077	MCF10A-Er-Src	breast:	n/a
6	chr6:13175441-13175491	HCF	heart:	n/a
7	chr6:13175441-13175491	PANC-1	pancreas:	n/a
8	chr6:13173168-13173218	MCF10A-Er-Src	breast:	n/a
9	chr6:13175441-13175491	CMK	blood:	n/a
10	chr6:13173168-13173218	GM12891	blood:	n/a
11	chr6:13175441-13175491	SK-N-MC	brain:	n/a
12	chr6:13192742-13192792	AoSMC	blood vessel:	n/a
13	chr6:13175441-13175491	PFSK-1	brain:	n/a
14	chr6:13175441-13175491	AG04449	skin:	fetal
15	chr6:13192742-13192792	CMK	blood:	n/a
16	chr6:13194027-13194077	ovcar-3	ovarian:	n/a
17	chr6:13175441-13175491	AG09309	skin:	n/a
18	chr6:13192742-13192792	NH-A	brain:	n/a
19	chr6:13192742-13192792	HCF	heart:	n/a
20	chr6:13173168-13173218	ECC-1	luminal epithelium:	n/a
21	chr6:13194027-13194077	AG04450	lung:	fetal
22	chr6:13173168-13173218	HMEC	breast:	n/a
23	chr6:13175441-13175491	HCPEpiC	choroid plexus:	n/a
24	chr6:13173168-13173218	NB4	blood:	n/a
25	chr6:13194027-13194077	GM06990	blood:	n/a
26	chr6:13173168-13173218	SK-N-MC	brain:	n/a
27	chr6:13192742-13192792	K562	blood:	n/a
28	chr6:13192742-13192792	ovcar-3	ovarian:	n/a
29	chr6:13175441-13175491	HL-60	blood:	n/a
30	chr6:13192742-13192792	NT2-D1	testis:	n/a
31	chr6:13194027-13194077	HMEC	breast:	n/a
32	chr6:13194027-13194077	PFSK-1	brain:	n/a
33	chr6:13175441-13175491	SAEC	small airway:	n/a
34	chr6:13192742-13192792	HRCEpiC	kidney:	n/a
35	chr6:13173168-13173218	ovcar-3	ovarian:	n/a
36	chr6:13192742-13192792	GM06990	blood:	n/a
37	chr6:13194027-13194077	PANC-1	pancreas:	n/a
38	chr6:13194027-13194077	HNPCEpiC	eye:	n/a
39	chr6:13173168-13173218	NH-A	brain:	n/a
40	chr6:13192742-13192792	AG04449	skin:	fetal
41	chr6:13194027-13194077	NT2-D1	testis:	n/a
42	chr6:13175441-13175491	U87	brain:	n/a
43	chr6:13175441-13175491	GM12878	blood:	n/a
44	chr6:13173168-13173218	HCF	heart:	n/a
45	chr6:13173168-13173218	NT2-D1	testis:	n/a
46	chr6:13192742-13192792	HAEpiC	amniotic membrane:	n/a
47	chr6:13175441-13175491	HPAEpiC	pulmonary alveolar:	n/a
48	chr6:13194027-13194077	Hela-S3	cervix:	n/a
49	chr6:13173168-13173218	SKMC	muscle:	n/a
50	chr6:13192742-13192792	HL-60	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:13192594..13195219-chr6:13328276..13330019,2	MCF-7	breast:
2	chr6:13184861..13186722-chr6:13190898..13192711,2	MCF-7	breast:
3	chr6:13184097..13187942-chr6:13192836..13196557,4	K562	blood:
4	chr6:13184861..13186722-chr6:13190898..13192711,2	MCF-7	breast:
5	chr6:13194824..13195828-chr6:13331712..13332687,6	K562	blood:
6	chr6:13182449..13185270-chr6:13189938..13191511,2	MCF-7	breast:
7	chr6:13195285..13198115-chr6:13330626..13333611,2	K562	blood:
8	chr6:13194772..13195773-chr6:13331817..13332822,6	MCF-7	breast:
9	chr6:13194848..13195736-chr6:13331759..13332713,3	MCF-7	breast:
10	chr6:13163839..13166326-chr6:13167451..13169624,2	K562	blood:
11	chr6:13184097..13187942-chr6:13192836..13196557,4	K562	blood:
12	chr17:64637600..64638236-chr6:13191039..13191624,2	MCF-7	breast:
13	chr17:64636119..64638158-chr6:13191283..13192914,2	MCF-7	breast:

Variant related genes	Relation type
PHACTR1	TF binding region
PHACTR1	CpG island
ENSG00000145979	chromatin interactions
ENSG00000112137	chromatin interactions

Extended variants
information (count: 1214 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:1214 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9395495	chr6:13166341-13166342	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs537419758	chr6:13166347-13166348	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs190837244	chr6:13166409-13166410	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs539106115	chr6:13166502-13166503	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs111520308	chr6:13166532-13166533	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs572524312	chr6:13166541-13166542	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs146884235	chr6:13166593-13166594	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs149003545	chr6:13166609-13166610	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs573835539	chr6:13166670-13166671	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs573589488	chr6:13166685-13166686	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs572845379	chr6:13166702-13166703	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs541354128	chr6:13166703-13166704	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs562485056	chr6:13166731-13166732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs575990952	chr6:13166739-13166740	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs143461350	chr6:13166762-13166763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs78978433	chr6:13166774-13166775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs73723401	chr6:13166792-13166793	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs147981357	chr6:13166816-13166817	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs9473564	chr6:13166833-13166834	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs563650467	chr6:13166866-13166867	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs141705074	chr6:13166867-13166868	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs530394090	chr6:13166878-13166879	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs550527551	chr6:13166884-13166885	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs570343409	chr6:13166990-13166991	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs150116807	chr6:13167030-13167031	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs552545204	chr6:13167109-13167110	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs145145412	chr6:13167135-13167136	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs565999615	chr6:13167157-13167158	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs534831205	chr6:13167183-13167184	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs9463487	chr6:13167204-13167205	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs573529195	chr6:13167220-13167221	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs1223547	chr6:13167258-13167259	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs138697286	chr6:13167280-13167281	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs529366808	chr6:13167342-13167343	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs181941857	chr6:13167401-13167402	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs551913015	chr6:13167469-13167470	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs544635381	chr6:13167473-13167474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs185946372	chr6:13167491-13167492	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs190864562	chr6:13167493-13167494	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs9463488	chr6:13167529-13167530	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs561449550	chr6:13167547-13167548	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs183181292	chr6:13167581-13167582	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs550370149	chr6:13167599-13167600	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs142817255	chr6:13167620-13167621	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs532849502	chr6:13167628-13167629	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs552279646	chr6:13167653-13167654	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs147395943	chr6:13167691-13167692	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs4715132	chr6:13167695-13167696	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs112790915	chr6:13167718-13167719	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs568233388	chr6:13167736-13167737	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Cancer	20164920	CNVD
Colorectal cancer	21297112	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	21448237	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
small cell lung cancer	20016488	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Osteosarcoma	16790693	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Ovarian cancer	21720365	CNVD
Cancer	21183584	CNVD
Acute myeloid leukemia	18000384	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21364760	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Burkitt''s lymphoma	19759907	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Metastatic melanoma	18483359	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:354 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:13150000-13175600	Weak transcription	Lung	lung
2	chr6:13153400-13178000	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr6:13153600-13167200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr6:13153600-13178200	Weak transcription	Brain Cingulate Gyrus	brain
5	chr6:13153600-13178200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr6:13153800-13168000	Weak transcription	Stomach Smooth Muscle	stomach
7	chr6:13153800-13184200	Weak transcription	Aorta	Aorta
8	chr6:13154000-13175600	Weak transcription	Fetal Heart	heart
9	chr6:13159200-13181800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr6:13159600-13178400	Weak transcription	Right Ventricle	heart
11	chr6:13160000-13171400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr6:13160000-13177400	Weak transcription	Primary hematopoietic stem cells	blood
13	chr6:13162400-13175600	Weak transcription	Left Ventricle	heart
14	chr6:13163600-13183400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr6:13163800-13168400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
16	chr6:13163800-13171400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr6:13164800-13183400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr6:13164800-13184400	Weak transcription	Pancreas	Pancrea
19	chr6:13165800-13166400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr6:13165800-13166400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr6:13165800-13166400	Bivalent/Poised TSS	Hela-S3	cervix
22	chr6:13165800-13166600	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr6:13165800-13166600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr6:13165800-13167200	Enhancers	Fetal Kidney	kidney
25	chr6:13166000-13166400	Enhancers	H1 Cell Line	embryonic stem cell
26	chr6:13166000-13166400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr6:13166000-13166400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr6:13166000-13166400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr6:13166000-13166400	Active TSS	Gastric	stomach
30	chr6:13166000-13166400	Active TSS	HMEC	breast
31	chr6:13166000-13166600	Enhancers	Brain Hippocampus Middle	brain
32	chr6:13166000-13168000	Enhancers	Brain Anterior Caudate	brain
33	chr6:13166200-13166400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr6:13166200-13166400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr6:13166200-13166400	Flanking Active TSS	Duodenum Mucosa	Duodenum
36	chr6:13166200-13166400	Enhancers	Esophagus	oesophagus
37	chr6:13166400-13166600	Active TSS	Duodenum Mucosa	Duodenum
38	chr6:13166400-13166800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr6:13166400-13167000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr6:13166400-13167000	Weak transcription	Gastric	stomach
41	chr6:13166600-13167800	Enhancers	Duodenum Mucosa	Duodenum
42	chr6:13166600-13175400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr6:13166600-13177800	Weak transcription	Brain Hippocampus Middle	brain
44	chr6:13166800-13169000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr6:13167000-13167400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr6:13167000-13167800	Enhancers	Gastric	stomach
47	chr6:13167200-13167600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr6:13168000-13172400	Weak transcription	Brain Anterior Caudate	brain
49	chr6:13168400-13171000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
50	chr6:13169000-13169400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin

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