Variant report

Variant	esv3333814
Chromosome Location	chr6:119078525-119100108
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	chr6:119097718-119098102	HepG2	liver:	n/a	n/a
2	BACH1	chr6:119082922-119083174	K562	blood:	n/a	n/a
3	BACH1	chr6:119082954-119083132	H1-hESC	embryonic stem cell:	n/a	n/a
4	CCNT2	chr6:119083015-119083025	K562	blood:	n/a	n/a
5	CEBPB	chr6:119091768-119091929	HepG2	liver:	n/a	chr6:119091840-119091851
6	CEBPB	chr6:119090182-119090539	MCF-7	breast:	n/a	chr6:119090384-119090397 chr6:119090415-119090428
7	CEBPB	chr6:119089107-119089436	HepG2	liver:	n/a	chr6:119089298-119089309
8	CEBPB	chr6:119092524-119092706	IMR90	lung:	n/a	n/a
9	CEBPB	chr6:119095853-119095981	HepG2	liver:	n/a	chr6:119095921-119095932
10	CEBPB	chr6:119090205-119090568	MCF-7	breast:	n/a	chr6:119090384-119090397 chr6:119090415-119090428
11	CEBPB	chr6:119098196-119098477	IMR90	lung:	n/a	n/a
12	CEBPB	chr6:119089228-119089406	K562	blood:	n/a	chr6:119089298-119089309
13	CEBPB	chr6:119098293-119098433	K562	blood:	n/a	n/a
14	CHD1	chr6:119097468-119098135	IMR90	lung:	n/a	n/a
15	CTCF	chr6:119097840-119097990	HFF-Myc	foreskin:	n/a	chr6:119097883-119097901 chr6:119097889-119097898 chr6:119097885-119097898 chr6:119097884-119097900 chr6:119097878-119097899
16	CTCF	chr6:119097800-119097950	AG04449	skin:	n/a	chr6:119097883-119097901 chr6:119097889-119097898 chr6:119097885-119097898 chr6:119097884-119097900 chr6:119097878-119097899
17	CTCF	chr6:119097820-119097970	AoAF	blood vessel:	n/a	chr6:119097883-119097901 chr6:119097889-119097898 chr6:119097885-119097898 chr6:119097884-119097900 chr6:119097878-119097899
18	CTCF	chr6:119097800-119097950	GM12868	blood:	n/a	chr6:119097883-119097901 chr6:119097889-119097898 chr6:119097885-119097898 chr6:119097884-119097900 chr6:119097878-119097899
19	CTCF	chr6:119097755-119098077	HUVEC	blood vessel:	n/a	chr6:119097883-119097901 chr6:119097889-119097898 chr6:119097885-119097898 chr6:119097884-119097900 chr6:119097878-119097899
20	CTCF	chr6:119097820-119097970	HRE	kidney:	n/a	chr6:119097883-119097901 chr6:119097889-119097898 chr6:119097885-119097898 chr6:119097884-119097900 chr6:119097878-119097899
21	CTCF	chr6:119098060-119098210	GM12872	blood:	n/a	n/a
22	CTCF	chr6:119098460-119098610	BJ	skin:	n/a	n/a
23	CTCF	chr6:119097820-119097970	GM12864	blood:	n/a	chr6:119097883-119097901 chr6:119097889-119097898 chr6:119097885-119097898 chr6:119097884-119097900 chr6:119097878-119097899
24	CTCF	chr6:119097840-119097990	AG09309	skin:	n/a	chr6:119097883-119097901 chr6:119097889-119097898 chr6:119097885-119097898 chr6:119097884-119097900 chr6:119097878-119097899
25	CTCF	chr6:119097860-119098010	WERI-Rb-1	eye:	n/a	chr6:119097883-119097901 chr6:119097889-119097898 chr6:119097885-119097898 chr6:119097884-119097900 chr6:119097878-119097899
26	CTCF	chr6:119097780-119097930	GM06990	blood:	n/a	chr6:119097883-119097901 chr6:119097889-119097898 chr6:119097885-119097898 chr6:119097884-119097900 chr6:119097878-119097899
27	CTCF	chr6:119097840-119097990	GM12869	blood:	n/a	chr6:119097883-119097901 chr6:119097889-119097898 chr6:119097885-119097898 chr6:119097884-119097900 chr6:119097878-119097899
28	CTCF	chr6:119097798-119098012	MCF-7	breast:	n/a	chr6:119097883-119097901 chr6:119097889-119097898 chr6:119097885-119097898 chr6:119097884-119097900 chr6:119097878-119097899
29	CTCF	chr6:119097860-119098010	HCT-116	colon:	n/a	chr6:119097883-119097901 chr6:119097889-119097898 chr6:119097885-119097898 chr6:119097884-119097900 chr6:119097878-119097899
30	CTCF	chr6:119098160-119098310	GM12868	blood:	n/a	n/a
31	CTCF	chr6:119097820-119097970	GM12875	blood:	n/a	chr6:119097883-119097901 chr6:119097889-119097898 chr6:119097885-119097898 chr6:119097884-119097900 chr6:119097878-119097899
32	CTCF	chr6:119097723-119098030	A549	lung:	n/a	chr6:119097883-119097901 chr6:119097889-119097898 chr6:119097885-119097898 chr6:119097884-119097900 chr6:119097878-119097899
33	CTCF	chr6:119097755-119098057	K562	blood:	n/a	chr6:119097883-119097901 chr6:119097889-119097898 chr6:119097885-119097898 chr6:119097884-119097900 chr6:119097878-119097899
34	CTCF	chr6:119097820-119097970	HEEpiC	esophagus:	n/a	chr6:119097883-119097901 chr6:119097889-119097898 chr6:119097885-119097898 chr6:119097884-119097900 chr6:119097878-119097899
35	CTCF	chr6:119097662-119098105	K562	blood:	n/a	chr6:119097883-119097901 chr6:119097889-119097898 chr6:119097885-119097898 chr6:119097884-119097900 chr6:119097878-119097899
36	CTCF	chr6:119097780-119098034	Lung_OC	lung:	n/a	chr6:119097883-119097901 chr6:119097889-119097898 chr6:119097885-119097898 chr6:119097884-119097900 chr6:119097878-119097899
37	CTCF	chr6:119097800-119097950	GM12873	blood:	n/a	chr6:119097883-119097901 chr6:119097889-119097898 chr6:119097885-119097898 chr6:119097884-119097900 chr6:119097878-119097899
38	CTCF	chr6:119097820-119097970	HUVEC	blood vessel:	n/a	chr6:119097883-119097901 chr6:119097889-119097898 chr6:119097885-119097898 chr6:119097884-119097900 chr6:119097878-119097899
39	CTCF	chr6:119097820-119097970	HEK293	kidney:	n/a	chr6:119097883-119097901 chr6:119097889-119097898 chr6:119097885-119097898 chr6:119097884-119097900 chr6:119097878-119097899
40	CTCF	chr6:119097776-119098055	Gliobla	brain:	n/a	chr6:119097883-119097901 chr6:119097889-119097898 chr6:119097885-119097898 chr6:119097884-119097900 chr6:119097878-119097899
41	CTCF	chr6:119097780-119097930	GM12865	blood:	n/a	chr6:119097883-119097901 chr6:119097889-119097898 chr6:119097885-119097898 chr6:119097884-119097900 chr6:119097878-119097899
42	CTCF	chr6:119097800-119097950	MCF-7	breast:	n/a	chr6:119097883-119097901 chr6:119097889-119097898 chr6:119097885-119097898 chr6:119097884-119097900 chr6:119097878-119097899
43	CTCF	chr6:119097506-119098296	A549	lung:	n/a	chr6:119097883-119097901 chr6:119097889-119097898 chr6:119097885-119097898 chr6:119097884-119097900 chr6:119097878-119097899
44	CTCF	chr6:119097800-119097950	WERI-Rb-1	eye:	n/a	chr6:119097883-119097901 chr6:119097889-119097898 chr6:119097885-119097898 chr6:119097884-119097900 chr6:119097878-119097899
45	CTCF	chr6:119097820-119097970	Caco-2	colon:	n/a	chr6:119097883-119097901 chr6:119097889-119097898 chr6:119097885-119097898 chr6:119097884-119097900 chr6:119097878-119097899
46	CTCF	chr6:119098280-119098430	NHDF-neo	bronchial:	n/a	n/a
47	CTCF	chr6:119097692-119098249	GM12878	blood:	n/a	chr6:119097883-119097901 chr6:119097889-119097898 chr6:119097885-119097898 chr6:119097884-119097900 chr6:119097878-119097899
48	CTCF	chr6:119097820-119097970	GM12866	blood:	n/a	chr6:119097883-119097901 chr6:119097889-119097898 chr6:119097885-119097898 chr6:119097884-119097900 chr6:119097878-119097899
49	CTCF	chr6:119097842-119097976	GM19240	blood:	n/a	chr6:119097883-119097901 chr6:119097889-119097898 chr6:119097885-119097898 chr6:119097884-119097900 chr6:119097878-119097899
50	CTCF	chr6:119097656-119098085	HepG2	liver:	n/a	chr6:119097883-119097901 chr6:119097889-119097898 chr6:119097885-119097898 chr6:119097884-119097900 chr6:119097878-119097899

No.	Distal block	Cell Line	Cell type
1	chr6:119095345..119097623-chr6:119099653..119102563,2	K562	blood:
2	chr6:118604989..118605598-chr6:119097517..119098373,3	K562	blood:
3	chr6:119090089..119093226-chr6:119095000..119099014,4	K562	blood:
4	chr6:119099349..119102563-chr6:119103399..119106439,3	K562	blood:
5	chr6:119084540..119086156-chr6:119087548..119090160,2	K562	blood:
6	chr6:119095345..119097623-chr6:119099653..119102563,2	K562	blood:
7	chr3:10690679..10691531-chr6:119085240..119086216,2	MCF-7	breast:
8	chr6:119086471..119089736-chr6:119091626..119095598,3	K562	blood:
9	chr6:119086471..119089736-chr6:119091626..119095598,3	K562	blood:
10	chr6:119075050..119077178-chr6:119080430..119083071,2	K562	blood:
11	chr6:119090089..119093226-chr6:119095000..119099014,4	K562	blood:
12	chr6:119018340..119019295-chr6:119097391..119098460,8	MCF-7	breast:
13	chr6:119084540..119086156-chr6:119087548..119090160,2	K562	blood:
14	chr6:119091223..119093581-chr6:119115948..119118630,2	MCF-7	breast:
15	chr6:119098916..119101415-chr6:119102887..119105983,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ASF1A-5	chr6:119078681-119078767	NONHSAT114698

Variant related genes	Relation type
ENSG00000225549	TF binding region
ENSG00000225549	chromatin interactions

Extended variants
information (count: 714 )
Associated
traits (count: 111 )

Variant overlapped rSNPs/rCNVs (count:714 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550826586	chr6:119078528-119078529	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs569317909	chr6:119078576-119078577	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs538584134	chr6:119078592-119078593	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs118095545	chr6:119078629-119078630	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs202235008	chr6:119078634-119078635	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs572147989	chr6:119078636-119078637	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs147843190	chr6:119078645-119078646	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs115111882	chr6:119078646-119078647	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs78930606	chr6:119078652-119078653	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs183756039	chr6:119078705-119078706	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
11	rs563536237	chr6:119078710-119078711	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
12	rs577205610	chr6:119078787-119078788	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs12661568	chr6:119078794-119078795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs139682028	chr6:119078882-119078883	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs149924886	chr6:119078883-119078884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs112149818	chr6:119078902-119078903	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs528614581	chr6:119078911-119078912	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs533009139	chr6:119078970-119078971	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs548363031	chr6:119078982-119078983	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs12196628	chr6:119078988-119078989	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs61135091	chr6:119079021-119079022	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs372051680	chr6:119079063-119079064	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs561958083	chr6:119079104-119079105	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs139525320	chr6:119079147-119079148	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs373623096	chr6:119079163-119079164	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs10553294	chr6:119079175-119079176	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs34683845	chr6:119079177-119079178	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs530968684	chr6:119079181-119079182	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs115655039	chr6:119079236-119079237	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs188076963	chr6:119079263-119079264	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs7742814	chr6:119079281-119079282	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs552184693	chr6:119079283-119079284	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs566466021	chr6:119079296-119079297	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs565517569	chr6:119079410-119079411	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs534741343	chr6:119079423-119079424	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs554673875	chr6:119079427-119079428	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs574695642	chr6:119079468-119079469	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs181316615	chr6:119079510-119079511	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs557181652	chr6:119079547-119079548	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs533815264	chr6:119079625-119079626	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs545755425	chr6:119079636-119079637	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs559718768	chr6:119079660-119079661	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs369880375	chr6:119079663-119079664	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs62424025	chr6:119079665-119079666	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs34608942	chr6:119079683-119079684	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs200248144	chr6:119079686-119079687	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs140636077	chr6:119079710-119079711	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs398002696	chr6:119079719-119079720	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs6909656	chr6:119079723-119079724	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs573120651	chr6:119079783-119079784	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:111)

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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Gastric cancer	17908304	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
Acute lymphoblastic leukemia	20067559	CNVD
T-cell lymphomas	19863542	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
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	19242612	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
Acute lymphoblastic leukemia	21098271	CNVD
Burkitt''s lymphoma	18698080	CNVD
Ovarian cancer	21720365	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Cancer	20164920	CNVD
Breast cancer	21364760	CNVD
Chordoma	21602918	CNVD
Kartagener syndrome	16639409	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	CNVD
Mental retardation	17621639	CNVD
Hypoplastic	20877625	CNVD
Hypotonia	20877625	CNVD
Mental retardation	20877625	CNVD
Microcephaly	20877625	CNVD
brachycephaly	20877625	CNVD
epicanthic folds	20877625	CNVD
micrognathia	20877625	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Metastatic melanoma	18483359	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	18698023	CNVD
Mental retardation	18854857	CNVD
Leukemia	18688285	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Liver carcinoma	19366792	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:311 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:119071600-119079400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr6:119074400-119079400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr6:119076400-119078600	Enhancers	Fetal Thymus	thymus
4	chr6:119076600-119078800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
5	chr6:119076800-119078800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
6	chr6:119076800-119098000	Weak transcription	Psoas Muscle	Psoas
7	chr6:119077000-119079800	Enhancers	Primary T cells from cord blood	blood
8	chr6:119077200-119078600	Enhancers	Primary T helper cells PMA-I stimulated	--
9	chr6:119078000-119079200	Weak transcription	Thymus	Thymus
10	chr6:119078000-119081800	Weak transcription	Stomach Mucosa	stomach
11	chr6:119078000-119093200	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr6:119078400-119079200	Enhancers	Monocytes-CD14+_RO01746	blood
13	chr6:119078600-119080000	Weak transcription	Primary T helper cells PMA-I stimulated	--
14	chr6:119078800-119079800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
15	chr6:119079200-119079400	Enhancers	Thymus	Thymus
16	chr6:119079200-119079600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr6:119079200-119080000	Enhancers	Brain Substantia Nigra	brain
18	chr6:119079200-119080600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
19	chr6:119079400-119079600	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr6:119079400-119080200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr6:119079400-119081000	Enhancers	Primary hematopoietic stem cells short term culture	blood
22	chr6:119079800-119080000	Weak transcription	Primary T cells from cord blood	blood
23	chr6:119079800-119080000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
24	chr6:119080000-119080200	Enhancers	Primary B cells from cord blood	blood
25	chr6:119080000-119080200	Enhancers	Primary T helper cells PMA-I stimulated	--
26	chr6:119080000-119080200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr6:119080000-119080400	Enhancers	Primary T cells from cord blood	blood
28	chr6:119080200-119082600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr6:119080200-119082600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr6:119080600-119082600	Enhancers	Monocytes-CD14+_RO01746	blood
31	chr6:119081000-119082600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
32	chr6:119081800-119082000	Enhancers	Stomach Mucosa	stomach
33	chr6:119082000-119082400	Weak transcription	Stomach Mucosa	stomach
34	chr6:119082600-119083200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
35	chr6:119082600-119083400	Enhancers	Primary hematopoietic stem cells short term culture	blood
36	chr6:119082600-119083600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr6:119082600-119083800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr6:119082600-119084200	Enhancers	Primary neutrophils fromperipheralblood	blood
39	chr6:119082800-119083200	Enhancers	K562	blood
40	chr6:119082800-119083600	Enhancers	Primary hematopoietic stem cells	blood
41	chr6:119083200-119084600	Weak transcription	K562	blood
42	chr6:119083200-119085600	Enhancers	Monocytes-CD14+_RO01746	blood
43	chr6:119083400-119084600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
44	chr6:119083600-119085800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr6:119083600-119090000	Weak transcription	Primary hematopoietic stem cells	blood
46	chr6:119083800-119084000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr6:119083800-119085400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr6:119084000-119084200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr6:119084200-119085200	Weak transcription	Primary neutrophils fromperipheralblood	blood
50	chr6:119084200-119090000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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