Variant report

Variant	nsv880517
Chromosome Location	chr5:35850693-35870814
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:374)
CpG islands
(count:244)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:374 , 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	ATF1	chr5:35858080-35858107	K562	blood:	n/a	n/a
2	ATF2	chr5:35856752-35857428	GM12878	blood:	n/a	n/a
3	ATF2	chr5:35856797-35857288	GM12878	blood:	n/a	n/a
4	BACH1	chr5:35852235-35852742	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr5:35856698-35857333	GM12878	blood:	n/a	chr5:35857163-35857173
6	BATF	chr5:35856984-35857270	GM12878	blood:	n/a	chr5:35857163-35857173
7	BATF	chr5:35852608-35852919	GM12878	blood:	n/a	chr5:35852777-35852787 chr5:35852732-35852740 chr5:35852773-35852783 chr5:35852772-35852783
8	BATF	chr5:35857834-35858093	GM12878	blood:	n/a	n/a
9	BCL11A	chr5:35856838-35857239	GM12878	blood:	n/a	chr5:35857162-35857171
10	BCL11A	chr5:35857923-35858185	GM12878	blood:	n/a	chr5:35858027-35858036
11	BCL3	chr5:35857831-35858195	GM12878	blood:	n/a	chr5:35858027-35858036
12	BCLAF1	chr5:35863329-35863608	GM12878	blood:	n/a	n/a
13	BHLHE40	chr5:35852523-35852831	GM12878	blood:	n/a	n/a
14	BHLHE40	chr5:35854183-35854767	GM12878	blood:	n/a	n/a
15	CEBPB	chr5:35857841-35858403	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr5:35853799-35854010	HepG2	liver:	n/a	chr5:35853895-35853906
17	CEBPB	chr5:35853708-35854116	Hela-S3	cervix:	n/a	chr5:35853895-35853906
18	CEBPB	chr5:35857908-35858331	IMR90	lung:	n/a	n/a
19	CEBPB	chr5:35861728-35862124	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr5:35853015-35853129	A549	lung:	n/a	n/a
21	CHD2	chr5:35857872-35858342	Hela-S3	cervix:	n/a	n/a
22	CHD2	chr5:35852492-35852871	GM12878	blood:	n/a	n/a
23	CHD2	chr5:35853855-35853992	Hela-S3	cervix:	n/a	n/a
24	CTCF	chr5:35852277-35852429	HepG2	liver:	n/a	n/a
25	CTCF	chr5:35852292-35852388	GM19239	blood:	n/a	n/a
26	CTCF	chr5:35852280-35852430	HepG2	liver:	n/a	n/a
27	CTCF	chr5:35852271-35852422	GM12892	blood:	n/a	n/a
28	CTCF	chr5:35852280-35852430	GM12864	blood:	n/a	n/a
29	CTCF	chr5:35852200-35852350	AG10803	skin:	n/a	n/a
30	CTCF	chr5:35852260-35852410	RPTEC	kidney:	n/a	n/a
31	CTCF	chr5:35852329-35852388	HUVEC	blood vessel:	n/a	n/a
32	CTCF	chr5:35852324-35852422	GM12878	blood:	n/a	n/a
33	CTCF	chr5:35856892-35856894	Lung_OC	lung:	n/a	n/a
34	CTCF	chr5:35852320-35852395	GM13977	blood:	n/a	n/a
35	CTCF	chr5:35852231-35852434	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr5:35852280-35852430	HPAF	blood vessel:	n/a	n/a
37	CTCF	chr5:35852260-35852410	WERI-Rb-1	eye:	n/a	n/a
38	CTCF	chr5:35852180-35852330	HA-sp	spinal cord:	n/a	n/a
39	CTCF	chr5:35852260-35852410	HPF	lung:	n/a	n/a
40	CTCF	chr5:35852222-35852418	HepG2	liver:	n/a	n/a
41	CTCF	chr5:35852293-35852396	GM19238	blood:	n/a	n/a
42	CTCF	chr5:35852180-35852330	HRE	kidney:	n/a	n/a
43	CTCF	chr5:35852320-35852470	HEK293	kidney:	n/a	n/a
44	CTCF	chr5:35852260-35852410	GM12875	blood:	n/a	n/a
45	CTCF	chr5:35852300-35852450	HRE	kidney:	n/a	n/a
46	CTCF	chr5:35852254-35852411	GM12891	blood:	n/a	n/a
47	CTCF	chr5:35852380-35852530	GM12872	blood:	n/a	n/a
48	CTCF	chr5:35852160-35852310	GM12871	blood:	n/a	n/a
49	CTCF	chr5:35852340-35852490	HCM	heart:	n/a	n/a
50	CTCF	chr5:35852260-35852410	GM12873	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:35856424-35856474	K562	blood:	n/a
2	chr5:35852286-35852336	K562	blood:	n/a
3	chr5:35856424-35856474	U87	brain:	n/a
4	chr5:35852286-35852336	AG09309	skin:	n/a
5	chr5:35860337-35860387	T-47D	breast:	n/a
6	chr5:35860337-35860387	NH-A	brain:	n/a
7	chr5:35852286-35852336	HNPCEpiC	eye:	n/a
8	chr5:35860337-35860387	NHDF-neo	bronchial:	n/a
9	chr5:35856424-35856474	AG04449	skin:	fetal
10	chr5:35852286-35852336	BE2_C	brain:	n/a
11	chr5:35856424-35856474	IMR90	lung:	fetal
12	chr5:35856424-35856474	Hepatocyte	liver:	n/a
13	chr5:35860337-35860387	HPAEpiC	pulmonary alveolar:	n/a
14	chr5:35856424-35856474	PANC-1	pancreas:	n/a
15	chr5:35856424-35856474	GM06990	blood:	n/a
16	chr5:35860337-35860387	SKMC	muscle:	n/a
17	chr5:35857130-35857180	HL-60	blood:	n/a
18	chr5:35856424-35856474	CMK	blood:	n/a
19	chr5:35852286-35852336	PrEC	prostate:	n/a
20	chr5:35856424-35856474	HCM	heart:	n/a
21	chr5:35852286-35852336	AG04450	lung:	fetal
22	chr5:35860337-35860387	GM12878	blood:	n/a
23	chr5:35856424-35856474	GM12892	blood:	n/a
24	chr5:35852286-35852336	T-47D	breast:	n/a
25	chr5:35860337-35860387	AoSMC	blood vessel:	n/a
26	chr5:35852286-35852336	HMEC	breast:	n/a
27	chr5:35856424-35856474	HCF	heart:	n/a
28	chr5:35852286-35852336	SAEC	small airway:	n/a
29	chr5:35852286-35852336	CMK	blood:	n/a
30	chr5:35856424-35856474	SAEC	small airway:	n/a
31	chr5:35860337-35860387	HCF	heart:	n/a
32	chr5:35860337-35860387	CMK	blood:	n/a
33	chr5:35856424-35856474	HMEC	breast:	n/a
34	chr5:35852286-35852336	NHBE	bronchial:	n/a
35	chr5:35857130-35857180	K562	blood:	n/a
36	chr5:35852286-35852336	HIPEpiC	eye:	n/a
37	chr5:35856424-35856474	NHBE	bronchial:	n/a
38	chr5:35856424-35856474	HEK293	kidney:	embryo
39	chr5:35857130-35857180	HIPEpiC	eye:	n/a
40	chr5:35852286-35852336	HCPEpiC	choroid plexus:	n/a
41	chr5:35857130-35857180	HUVEC	blood vessel:	n/a
42	chr5:35857130-35857180	Hela-S3	cervix:	n/a
43	chr5:35857130-35857180	HCT-116	colon:	n/a
44	chr5:35852286-35852336	GM06990	blood:	n/a
45	chr5:35860337-35860387	HUVEC	blood vessel:	n/a
46	chr5:35860337-35860387	IMR90	lung:	fetal
47	chr5:35856424-35856474	PFSK-1	brain:	n/a
48	chr5:35857130-35857180	SK-N-MC	brain:	n/a
49	chr5:35857130-35857180	AoSMC	blood vessel:	n/a
50	chr5:35852286-35852336	SK-N-SH_RA	brain:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:35849089..35851096-chr5:35897625..35900411,2	K562	blood:
2	chr5:35859166..35861325-chr5:35861673..35863431,2	MCF-7	breast:
3	chr5:35859166..35861325-chr5:35861673..35863431,2	MCF-7	breast:

No data

Variant related genes	Relation type
IL7R	TF binding region
IL7R	CpG island

Extended variants
information (count: 851 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:851 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6880233	chr5:35850693-35850694	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs77636995	chr5:35850714-35850715	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs569038273	chr5:35850808-35850809	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs568052194	chr5:35850823-35850824	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs181644186	chr5:35850850-35850851	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs557635477	chr5:35850890-35850891	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs537084232	chr5:35850938-35850939	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs116748874	chr5:35850988-35850989	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs76933815	chr5:35850989-35850990	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs186441082	chr5:35850990-35850991	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs573443531	chr5:35850995-35850996	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs189281149	chr5:35851016-35851017	Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs562537489	chr5:35851050-35851051	Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs550381795	chr5:35851084-35851085	Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs181743004	chr5:35851089-35851090	Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs544909764	chr5:35851131-35851132	Enhancers Active TSS Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs148687079	chr5:35851151-35851152	Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs533572833	chr5:35851176-35851177	Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs570549607	chr5:35851179-35851180	Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs528983613	chr5:35851197-35851198	Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs542679133	chr5:35851223-35851224	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs142236892	chr5:35851226-35851227	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs538823754	chr5:35851255-35851256	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs12516866	chr5:35851261-35851262	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs529438109	chr5:35851305-35851306	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs368536703	chr5:35851362-35851363	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs11952240	chr5:35851383-35851384	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs569251569	chr5:35851410-35851411	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs528683751	chr5:35851423-35851424	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs537722737	chr5:35851436-35851437	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs558037072	chr5:35851437-35851438	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs571069837	chr5:35851453-35851454	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs533729846	chr5:35851468-35851469	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs114319163	chr5:35851488-35851489	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs566846266	chr5:35851491-35851492	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs369129908	chr5:35851501-35851502	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs573386398	chr5:35851516-35851517	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs185082171	chr5:35851533-35851534	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs114983382	chr5:35851591-35851592	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs190659871	chr5:35851628-35851629	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs147824044	chr5:35851683-35851684	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs564758489	chr5:35851694-35851695	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs372295398	chr5:35851706-35851707	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs141374202	chr5:35851728-35851729	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs560704933	chr5:35851745-35851746	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs183343924	chr5:35851747-35851748	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs186306066	chr5:35851773-35851774	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs1494564	chr5:35851831-35851832	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs558675678	chr5:35851885-35851886	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs551525344	chr5:35851959-35851960	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Myofibroblastic sarcoma	19369631	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Non-small cell lung cancer	20864512	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
prenatal diagnosis	22389664	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Breast cancer	21858162	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Cancer	16751803	CNVD
Breast cancer	16608533	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Non-small cell lung cancer	19010865	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	21720365	CNVD
Lung cancer	18438408	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Prostate cancer	18632612	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	19553991	CNVD
Lung cancer	19553991	CNVD
Melanoma	19553991	CNVD
Ovarian cancer	19553991	CNVD
Prostate cancer	19553991	CNVD
Non-small cell lung cancer	17156491	CNVD
Breast cancer	17133270	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Breast cancer	17393978	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Lung cancer	19153074	CNVD
Breast cancer	21364760	CNVD
Cornelia de Lange syndrome	21085971	CNVD
Autism	21701786	CNVD
Cervical cancer	16585170	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	21147910	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:703 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:35848400-35852200	Enhancers	Primary T helper naive cells from peripheral blood	blood
2	chr5:35848600-35852000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
3	chr5:35848800-35851200	Weak transcription	Fetal Muscle Leg	muscle
4	chr5:35848800-35852400	Enhancers	Primary T helper cells fromperipheralblood	blood
5	chr5:35849200-35852000	Enhancers	Primary T cells from cord blood	blood
6	chr5:35849600-35852200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
7	chr5:35849600-35856200	Enhancers	Dnd41	blood
8	chr5:35849800-35852200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
9	chr5:35849800-35852600	Enhancers	Primary T cells fromperipheralblood	blood
10	chr5:35849800-35852800	Enhancers	Thymus	Thymus
11	chr5:35849800-35853200	Enhancers	Fetal Thymus	thymus
12	chr5:35850000-35851000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
13	chr5:35850000-35852200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
14	chr5:35850000-35852600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
15	chr5:35850200-35852000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr5:35850200-35852000	Enhancers	Primary T killer memory cells from peripheral blood	blood
17	chr5:35850400-35851200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
18	chr5:35850600-35850800	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr5:35850800-35851000	Enhancers	Osteobl	bone
20	chr5:35850800-35851200	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr5:35850800-35851200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr5:35851000-35851200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr5:35851000-35851200	Enhancers	Muscle Satellite Cultured Cells	--
24	chr5:35851000-35851200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr5:35851000-35851200	Active TSS	Adipose Nuclei	Adipose
26	chr5:35851000-35851200	Enhancers	Brain Hippocampus Middle	brain
27	chr5:35851000-35851200	Enhancers	Psoas Muscle	Psoas
28	chr5:35851000-35851200	Enhancers	HMEC	breast
29	chr5:35851000-35851200	Enhancers	NHEK	skin
30	chr5:35851000-35851400	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
31	chr5:35851000-35851600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr5:35851000-35851600	Active TSS	NHDF-Ad	bronchial
33	chr5:35851000-35851800	Active TSS	NHLF	lung
34	chr5:35851000-35853000	Flanking Active TSS	Osteobl	bone
35	chr5:35851200-35851400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr5:35851200-35851400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr5:35851200-35851400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
38	chr5:35851200-35851400	Active TSS	Liver	Liver
39	chr5:35851200-35851400	Bivalent/Poised TSS	Brain Anterior Caudate	brain
40	chr5:35851200-35851400	Flanking Active TSS	Duodenum Mucosa	Duodenum
41	chr5:35851200-35851400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
42	chr5:35851200-35851400	Active TSS	HSMMtube	muscle
43	chr5:35851200-35851600	Active TSS	Breast Myoepithelial Primary Cells	Breast
44	chr5:35851200-35851600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr5:35851200-35851600	Active TSS	Muscle Satellite Cultured Cells	--
46	chr5:35851200-35851600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr5:35851200-35851600	Flanking Active TSS	Adipose Nuclei	Adipose
48	chr5:35851200-35851600	Active TSS	Brain Hippocampus Middle	brain
49	chr5:35851200-35851600	Active TSS	Duodenum Smooth Muscle	Duodenum
50	chr5:35851200-35851600	Flanking Active TSS	Placenta	Placenta

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