Variant report

Variant	nsv886669
Chromosome Location	chr6:131991532-132059074
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	chr6:132013215-132013284	K562	blood:	n/a	n/a
2	ARID3A	chr6:132016029-132016328	HepG2	liver:	n/a	n/a
3	ATF2	chr6:132004504-132005002	GM12878	blood:	n/a	n/a
4	ATF2	chr6:132009290-132009895	GM12878	blood:	n/a	n/a
5	ATF2	chr6:132006418-132007007	GM12878	blood:	n/a	n/a
6	ATF2	chr6:132009255-132009882	GM12878	blood:	n/a	n/a
7	ATF2	chr6:132006470-132006948	GM12878	blood:	n/a	n/a
8	BACH1	chr6:131999721-131999793	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr6:132009253-132009914	GM12878	blood:	n/a	n/a
10	BATF	chr6:132006476-132006828	GM12878	blood:	n/a	n/a
11	BATF	chr6:132018211-132018451	GM12878	blood:	n/a	chr6:132018367-132018378
12	BATF	chr6:132009317-132009894	GM12878	blood:	n/a	n/a
13	BATF	chr6:132006509-132006822	GM12878	blood:	n/a	n/a
14	BATF	chr6:132004689-132004914	GM12878	blood:	n/a	n/a
15	BCL11A	chr6:132004620-132004942	GM12878	blood:	n/a	chr6:132004803-132004812
16	BCL11A	chr6:132006567-132006823	GM12878	blood:	n/a	chr6:132006769-132006778
17	BCL11A	chr6:132009448-132009677	GM12878	blood:	n/a	n/a
18	BCL11A	chr6:132009342-132009856	GM12878	blood:	n/a	n/a
19	BCL11A	chr6:132006618-132006788	GM12878	blood:	n/a	chr6:132006769-132006778
20	BCL3	chr6:132006473-132006845	GM12878	blood:	n/a	chr6:132006769-132006778
21	BCL3	chr6:132009461-132009737	GM12878	blood:	n/a	n/a
22	BCL3	chr6:132009393-132009835	GM12878	blood:	n/a	n/a
23	BCL3	chr6:132006545-132006836	GM12878	blood:	n/a	chr6:132006769-132006778
24	BCLAF1	chr6:132009333-132009832	GM12878	blood:	n/a	n/a
25	BCLAF1	chr6:132006451-132006849	GM12878	blood:	n/a	chr6:132006769-132006778
26	BCLAF1	chr6:132004562-132004983	GM12878	blood:	n/a	chr6:132004803-132004812
27	BHLHE40	chr6:132016118-132016315	HepG2	liver:	n/a	n/a
28	BHLHE40	chr6:132004629-132004971	GM12878	blood:	n/a	n/a
29	BHLHE40	chr6:132006563-132006857	GM12878	blood:	n/a	n/a
30	BHLHE40	chr6:132007129-132007131	GM12878	blood:	n/a	n/a
31	BHLHE40	chr6:132009470-132009658	GM12878	blood:	n/a	n/a
32	CBX3	chr6:132034147-132034452	K562	blood:	n/a	n/a
33	CCNT2	chr6:132038948-132039148	K562	blood:	n/a	n/a
34	CEBPB	chr6:132050786-132051013	Hela-S3	cervix:	n/a	chr6:132050876-132050889 chr6:132050876-132050887 chr6:132050878-132050889
35	CEBPB	chr6:131993506-131993842	HepG2	liver:	n/a	n/a
36	CEBPB	chr6:132050717-132051061	HepG2	liver:	n/a	chr6:132050876-132050889 chr6:132050876-132050887 chr6:132050878-132050889
37	CEBPB	chr6:131993541-131993741	K562	blood:	n/a	n/a
38	CEBPB	chr6:132006220-132006431	HepG2	liver:	n/a	chr6:132006372-132006385
39	CEBPB	chr6:132014950-132015271	HepG2	liver:	n/a	chr6:132015105-132015116 chr6:132015253-132015264 chr6:132015105-132015118 chr6:132015253-132015264 chr6:132015107-132015118
40	CEBPB	chr6:132002742-132003031	Hela-S3	cervix:	n/a	chr6:132002937-132002948 chr6:132002882-132002893 chr6:132002902-132002913
41	CEBPB	chr6:132002827-132003033	H1-hESC	embryonic stem cell:	n/a	chr6:132002937-132002948 chr6:132002882-132002893 chr6:132002902-132002913
42	CEBPB	chr6:131998698-131998732	K562	blood:	n/a	n/a
43	CEBPB	chr6:132006412-132006900	GM12878	blood:	n/a	n/a
44	CEBPB	chr6:132050719-132051044	K562	blood:	n/a	chr6:132050876-132050889 chr6:132050876-132050887 chr6:132050878-132050889
45	CEBPB	chr6:132008235-132008522	IMR90	lung:	n/a	n/a
46	CEBPB	chr6:131992609-131992620	K562	blood:	n/a	n/a
47	CEBPB	chr6:132002765-132003057	IMR90	lung:	n/a	chr6:132002937-132002948 chr6:132002882-132002893 chr6:132002902-132002913
48	CEBPB	chr6:132002811-132003083	A549	lung:	n/a	chr6:132002937-132002948 chr6:132002882-132002893 chr6:132002902-132002913
49	CEBPB	chr6:132002749-132003071	K562	blood:	n/a	chr6:132002937-132002948 chr6:132002882-132002893 chr6:132002902-132002913
50	CEBPB	chr6:132050732-132051037	IMR90	lung:	n/a	chr6:132050876-132050889 chr6:132050876-132050887 chr6:132050878-132050889

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:132031294-132031344	ECC-1	luminal epithelium:	n/a
2	chr6:132022490-132022540	SK-N-MC	brain:	n/a
3	chr6:132022490-132022540	RPTEC	kidney:	n/a
4	chr6:132031294-132031344	AG04449	skin:	fetal
5	chr6:132032407-132032457	A549	lung:	n/a
6	chr6:132031294-132031344	HRPEpiC	eye:	n/a
7	chr6:132022490-132022540	Caco-2	colon:	n/a
8	chr6:132032407-132032457	HL-60	blood:	n/a
9	chr6:132032407-132032457	PrEC	prostate:	n/a
10	chr6:132032407-132032457	SK-N-SH	brain:	n/a
11	chr6:132032407-132032457	SKMC	muscle:	n/a
12	chr6:132032407-132032457	HCF	heart:	n/a
13	chr6:132031294-132031344	Jurkat	blood:	n/a
14	chr6:132031294-132031344	AG10803	skin:	n/a
15	chr6:132032407-132032457	NHDF-neo	bronchial:	n/a
16	chr6:132032407-132032457	HUVEC	blood vessel:	n/a
17	chr6:132031294-132031344	H1-hESC	embryonic stem cell:	embryo
18	chr6:132022490-132022540	SKMC	muscle:	n/a
19	chr6:132022490-132022540	HRCEpiC	kidney:	n/a
20	chr6:132032407-132032457	ovcar-3	ovarian:	n/a
21	chr6:132022490-132022540	H1-hESC	embryonic stem cell:	embryo
22	chr6:132031294-132031344	HNPCEpiC	eye:	n/a
23	chr6:132022490-132022540	HCM	heart:	n/a
24	chr6:132022490-132022540	HL-60	blood:	n/a
25	chr6:132022490-132022540	AG09309	skin:	n/a
26	chr6:132032407-132032457	HRCEpiC	kidney:	n/a
27	chr6:132032407-132032457	PFSK-1	brain:	n/a
28	chr6:132032407-132032457	H1-hESC	embryonic stem cell:	embryo
29	chr6:132022490-132022540	NH-A	brain:	n/a
30	chr6:132031294-132031344	GM12878	blood:	n/a
31	chr6:132031294-132031344	HPAEpiC	pulmonary alveolar:	n/a
32	chr6:132022490-132022540	HRE	kidney:	n/a
33	chr6:132022490-132022540	Hela-S3	cervix:	n/a
34	chr6:132031294-132031344	ProgFib	skin:	n/a
35	chr6:132032407-132032457	Caco-2	colon:	n/a
36	chr6:132032407-132032457	AG04449	skin:	fetal
37	chr6:132032407-132032457	BJ	skin:	n/a
38	chr6:132022490-132022540	HPAEpiC	pulmonary alveolar:	n/a
39	chr6:132032407-132032457	SK-N-SH_RA	brain:	n/a
40	chr6:132022490-132022540	HMEC	breast:	n/a
41	chr6:132022490-132022540	NT2-D1	testis:	n/a
42	chr6:132031294-132031344	HCT-116	colon:	n/a
43	chr6:132032407-132032457	CMK	blood:	n/a
44	chr6:132031294-132031344	HRCEpiC	kidney:	n/a
45	chr6:132022490-132022540	HUVEC	blood vessel:	n/a
46	chr6:132032407-132032457	HepG2	liver:	n/a
47	chr6:132032407-132032457	IMR90	lung:	fetal
48	chr6:132032407-132032457	HRE	kidney:	n/a
49	chr6:132032407-132032457	MCF10A-Er-Src	breast:	n/a
50	chr6:132032407-132032457	MCF-7	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:132053997..132056875-chr6:132057617..132059762,2	K562	blood:
2	chr6:131999397..132001377-chr6:132003610..132005547,2	K562	blood:
3	chr6:132015065..132016761-chr6:132065945..132068393,2	K562	blood:
4	chr6:132058829..132061239-chr6:132086925..132088762,2	MCF-7	breast:
5	chr6:132015771..132016655-chr6:132243782..132245174,3	K562	blood:
6	chr6:131996501..132001360-chr6:132002218..132005393,5	K562	blood:
7	chr6:131990371..131993321-chr6:131995027..131997550,2	K562	blood:
8	chr6:131992289..131995426-chr6:131995620..131998596,3	K562	blood:
9	chr6:131989678..131992068-chr6:131997979..131999879,3	MCF-7	breast:
10	chr6:131989678..131992068-chr6:131997979..131999879,3	MCF-7	breast:
11	chr6:131999397..132001377-chr6:132003610..132005547,2	K562	blood:
12	chr6:132007332..132009041-chr6:132015162..132016904,2	K562	blood:
13	chr6:131992289..131995426-chr6:131995620..131998596,3	K562	blood:
14	chr6:131972645..131975144-chr6:131991608..131993619,2	MCF-7	breast:
15	chr6:131996501..132001360-chr6:132002218..132005393,5	K562	blood:
16	chr6:131990371..131993321-chr6:131995027..131997550,2	K562	blood:
17	chr6:131965455..131967671-chr6:132014535..132016282,2	K562	blood:
18	chr6:132054308..132056322-chr6:132056330..132059140,2	K562	blood:
19	chr6:132007332..132009041-chr6:132015162..132016904,2	K562	blood:
20	chr6:132054308..132056322-chr6:132056330..132059140,2	K562	blood:
21	chr6:132053997..132056875-chr6:132057617..132059762,2	K562	blood:
22	chr6:132016067..132016631-chr6:132230809..132231697,2	K562	blood:

Variant related genes	Relation type
CTAGE9	TF binding region
OR2A4	TF binding region
CTAGE9	CpG island
OR2A4	CpG island
ENSG00000154269	chromatin interactions

Extended variants
information (count: 2284 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:2284 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7762879	chr6:131991532-131991533	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs550958852	chr6:131991556-131991557	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs540406051	chr6:131991567-131991568	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs565011810	chr6:131991595-131991596	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs35357414	chr6:131991599-131991600	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs375511639	chr6:131991603-131991604	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs532073647	chr6:131991611-131991612	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs137908283	chr6:131991623-131991624	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs148669458	chr6:131991634-131991635	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs150630328	chr6:131991693-131991694	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs372897317	chr6:131991710-131991711	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs529632462	chr6:131991719-131991720	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs139818091	chr6:131991732-131991733	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs567600747	chr6:131991778-131991779	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs528684817	chr6:131991782-131991783	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs546846924	chr6:131991837-131991838	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs143794952	chr6:131991843-131991844	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs184751275	chr6:131991883-131991884	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs557421840	chr6:131991959-131991960	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs146372929	chr6:131991968-131991969	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs11154642	chr6:131991981-131991982	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs189612513	chr6:131991982-131991983	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs573146586	chr6:131992034-131992035	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs566363487	chr6:131992044-131992045	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs540436289	chr6:131992062-131992063	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs533826732	chr6:131992068-131992069	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs576965136	chr6:131992074-131992075	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs377759240	chr6:131992083-131992084	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs180684638	chr6:131992113-131992114	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs74556395	chr6:131992135-131992136	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs574127139	chr6:131992142-131992143	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs73779849	chr6:131992143-131992144	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs374284488	chr6:131992144-131992145	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs370519977	chr6:131992198-131992199	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs547172745	chr6:131992200-131992201	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs566318038	chr6:131992273-131992274	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs573889222	chr6:131992311-131992312	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs532727642	chr6:131992315-131992316	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs371947513	chr6:131992393-131992394	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs199941630	chr6:131992421-131992422	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs202129016	chr6:131992431-131992432	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs536666033	chr6:131992516-131992517	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs373460139	chr6:131992518-131992519	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs548566827	chr6:131992522-131992523	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs374042416	chr6:131992527-131992528	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs533890518	chr6:131992529-131992530	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs145419950	chr6:131992541-131992542	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs10080319	chr6:131992549-131992550	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs556146967	chr6:131992659-131992660	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs528804610	chr6:131992700-131992701	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Autism	22495311	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Gastric cancer	17908304	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21785460	CNVD
Kartagener syndrome	16639409	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Renal cell carcinoma	18592004	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:257 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:131974400-131992400	Weak transcription	Rectal Mucosa Donor 29	rectum
2	chr6:131975200-132008200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr6:131976000-131996600	Weak transcription	Fetal Intestine Large	intestine
4	chr6:131976200-131996800	Weak transcription	Fetal Intestine Small	intestine
5	chr6:131977000-131997000	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr6:131981800-131992400	Weak transcription	K562	blood
7	chr6:131986800-132009600	Strong transcription	HepG2	liver
8	chr6:131988600-131992400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr6:131992400-131992800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr6:131992400-131993600	Strong transcription	Rectal Mucosa Donor 29	rectum
11	chr6:131992400-131995600	Strong transcription	K562	blood
12	chr6:131992800-131995200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
13	chr6:131993600-132020600	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr6:131995200-132005400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr6:131995600-131998200	Weak transcription	K562	blood
16	chr6:131996600-131997600	Strong transcription	Fetal Intestine Large	intestine
17	chr6:131996600-132008600	Weak transcription	Liver	Liver
18	chr6:131996800-131998600	Strong transcription	Fetal Intestine Small	intestine
19	chr6:131997000-131997400	Strong transcription	Rectal Mucosa Donor 31	rectum
20	chr6:131997400-131998400	Weak transcription	Rectal Mucosa Donor 31	rectum
21	chr6:131997600-131998400	Weak transcription	Fetal Intestine Large	intestine
22	chr6:131998200-131999600	Strong transcription	K562	blood
23	chr6:131998400-131998800	Strong transcription	Rectal Mucosa Donor 31	rectum
24	chr6:131998400-131999200	Strong transcription	Fetal Intestine Large	intestine
25	chr6:131998600-131998800	Enhancers	Placenta	Placenta
26	chr6:131998600-132054000	Weak transcription	Fetal Intestine Small	intestine
27	chr6:131998800-131999200	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr6:131998800-132000000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr6:131998800-132001400	Weak transcription	Ovary	ovary
30	chr6:131998800-132043000	Weak transcription	Rectal Mucosa Donor 31	rectum
31	chr6:131999200-132000000	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr6:131999200-132000000	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr6:131999200-132000000	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr6:131999200-132017600	Weak transcription	Fetal Intestine Large	intestine
35	chr6:131999400-131999600	Enhancers	Placenta	Placenta
36	chr6:131999400-131999800	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr6:131999400-131999800	Enhancers	H9 Cell Line	embryonic stem cell
38	chr6:131999400-131999800	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr6:131999400-132000000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr6:131999400-132000000	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr6:131999400-132000000	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr6:131999400-132020600	Weak transcription	Sigmoid Colon	Sigmoid Colon
43	chr6:131999600-132000000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr6:131999600-132001400	Weak transcription	K562	blood
45	chr6:131999800-132000000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr6:131999800-132009000	Weak transcription	H9 Cell Line	embryonic stem cell
47	chr6:131999800-132009200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chr6:132000000-132000600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr6:132000000-132001000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr6:132000000-132001200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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