Variant report

Variant	nsv965689
Chromosome Location	chr6:26457033-26469487
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:492)
CpG islands
(count:732)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:492 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:26457836-26458207	HepG2	liver:	n/a	n/a
2	ATF1	chr6:26457908-26458286	K562	blood:	n/a	n/a
3	BHLHE40	chr6:26457962-26458226	HepG2	liver:	n/a	n/a
4	BHLHE40	chr6:26458552-26458563	K562	blood:	n/a	n/a
5	BHLHE40	chr6:26457911-26458325	GM12878	blood:	n/a	n/a
6	BHLHE40	chr6:26457940-26458334	K562	blood:	n/a	n/a
7	BRCA1	chr6:26458311-26458434	HepG2	liver:	n/a	n/a
8	BRCA1	chr6:26457937-26458234	Hela-S3	cervix:	n/a	n/a
9	CBX3	chr6:26457315-26458711	K562	blood:	n/a	n/a
10	CCNT2	chr6:26458339-26458524	K562	blood:	n/a	n/a
11	CEBPB	chr6:26459312-26459525	HepG2	liver:	n/a	chr6:26459425-26459438 chr6:26459426-26459437
12	CEBPB	chr6:26466071-26466355	HepG2	liver:	n/a	n/a
13	CEBPB	chr6:26466108-26466330	K562	blood:	n/a	n/a
14	CEBPB	chr6:26466063-26466375	IMR90	lung:	n/a	n/a
15	CEBPB	chr6:26466128-26466378	A549	lung:	n/a	n/a
16	CEBPB	chr6:26459274-26459575	IMR90	lung:	n/a	chr6:26459425-26459438 chr6:26459426-26459437
17	CEBPB	chr6:26466153-26466346	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr6:26459435-26459456	K562	blood:	n/a	n/a
19	CHD1	chr6:26458251-26458394	GM12878	blood:	n/a	n/a
20	CHD2	chr6:26457716-26457960	HepG2	liver:	n/a	n/a
21	CHD2	chr6:26457951-26458277	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD2	chr6:26457968-26458571	GM12878	blood:	n/a	n/a
23	CHD2	chr6:26458294-26458429	HepG2	liver:	n/a	n/a
24	CHD2	chr6:26457972-26458276	Hela-S3	cervix:	n/a	n/a
25	CREB1	chr6:26457902-26458347	H1-hESC	embryonic stem cell:	n/a	n/a
26	CREB1	chr6:26457850-26458339	A549	lung:	n/a	n/a
27	CREB1	chr6:26457960-26458253	A549	lung:	n/a	n/a
28	CREB1	chr6:26457710-26458627	GM12878	blood:	n/a	n/a
29	CREB1	chr6:26457583-26458682	HepG2	liver:	n/a	n/a
30	CREB1	chr6:26457695-26458664	GM12878	blood:	n/a	n/a
31	CREB1	chr6:26457620-26458568	K562	blood:	n/a	n/a
32	CREB1	chr6:26457844-26458354	ECC-1	luminal epithelium:	n/a	n/a
33	CREB1	chr6:26457759-26458372	ECC-1	luminal epithelium:	n/a	n/a
34	CREB1	chr6:26457694-26458460	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr6:26457820-26457970	HPAF	blood vessel:	n/a	n/a
36	CTCF	chr6:26458320-26458470	AG09309	skin:	n/a	n/a
37	CTCF	chr6:26458260-26458410	GM12865	blood:	n/a	n/a
38	CTCF	chr6:26458280-26458430	HFF-Myc	foreskin:	n/a	n/a
39	CTCF	chr6:26458260-26458410	AG09319	gingival:	n/a	n/a
40	CTCF	chr6:26458360-26458510	GM12871	blood:	n/a	n/a
41	CTCF	chr6:26458888-26458931	Fibrobl	skin:	n/a	n/a
42	CTCF	chr6:26464820-26464970	GM12867	blood:	n/a	n/a
43	CTCF	chr6:26458240-26458390	GM12867	blood:	n/a	n/a
44	CTCF	chr6:26458220-26458370	HA-sp	spinal cord:	n/a	n/a
45	CTCF	chr6:26464620-26464770	GM12872	blood:	n/a	n/a
46	CTCF	chr6:26458321-26458475	GM12892	blood:	n/a	n/a
47	CTCF	chr6:26464800-26464950	GM12865	blood:	n/a	n/a
48	CTCF	chr6:26464840-26464990	GM12874	blood:	n/a	n/a
49	CTCF	chr6:26458300-26458450	HMF	breast:	n/a	n/a
50	CTCF	chr6:26458300-26458450	NHLF	lung:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:26458013-26458063	GM12878	blood:	n/a
2	chr6:26458189-26458239	HRCEpiC	kidney:	n/a
3	chr6:26457353-26457403	PANC-1	pancreas:	n/a
4	chr6:26458213-26458263	RPTEC	kidney:	n/a
5	chr6:26457928-26457978	NT2-D1	testis:	n/a
6	chr6:26457353-26457403	HCF	heart:	n/a
7	chr6:26459986-26460036	HPAEpiC	pulmonary alveolar:	n/a
8	chr6:26457928-26457978	AG04449	skin:	fetal
9	chr6:26458093-26458143	NHBE	bronchial:	n/a
10	chr6:26457353-26457403	HEEpiC	esophagus:	n/a
11	chr6:26458013-26458063	HL-60	blood:	n/a
12	chr6:26457984-26458034	Caco-2	colon:	n/a
13	chr6:26458121-26458171	HCPEpiC	choroid plexus:	n/a
14	chr6:26458013-26458063	GM12891	blood:	n/a
15	chr6:26458013-26458063	PANC-1	pancreas:	n/a
16	chr6:26458189-26458239	HRPEpiC	eye:	n/a
17	chr6:26457353-26457403	IMR90	lung:	fetal
18	chr6:26457984-26458034	T-47D	breast:	n/a
19	chr6:26457928-26457978	SK-N-MC	brain:	n/a
20	chr6:26458121-26458171	K562	blood:	n/a
21	chr6:26458326-26458376	GM06990	blood:	n/a
22	chr6:26458121-26458171	LNCaP	prostate:	n/a
23	chr6:26458121-26458171	NHDF-neo	bronchial:	n/a
24	chr6:26459986-26460036	GM06990	blood:	n/a
25	chr6:26458189-26458239	SAEC	small airway:	n/a
26	chr6:26457353-26457403	AoSMC	blood vessel:	n/a
27	chr6:26458093-26458143	HCM	heart:	n/a
28	chr6:26468835-26468885	GM12892	blood:	n/a
29	chr6:26457353-26457403	Hepatocyte	liver:	n/a
30	chr6:26468835-26468885	K562	blood:	n/a
31	chr6:26457353-26457403	HCPEpiC	choroid plexus:	n/a
32	chr6:26458013-26458063	HRPEpiC	eye:	n/a
33	chr6:26468835-26468885	AG04449	skin:	fetal
34	chr6:26458121-26458171	AG04450	lung:	fetal
35	chr6:26459986-26460036	MCF-7	breast:	n/a
36	chr6:26458489-26458539	IMR90	lung:	fetal
37	chr6:26458121-26458171	MCF10A-Er-Src	breast:	n/a
38	chr6:26458093-26458143	AG04450	lung:	fetal
39	chr6:26457928-26457978	HRCEpiC	kidney:	n/a
40	chr6:26458489-26458539	PrEC	prostate:	n/a
41	chr6:26458189-26458239	RPTEC	kidney:	n/a
42	chr6:26457928-26457978	HRPEpiC	eye:	n/a
43	chr6:26457353-26457403	PFSK-1	brain:	n/a
44	chr6:26468835-26468885	PrEC	prostate:	n/a
45	chr6:26457984-26458034	CMK	blood:	n/a
46	chr6:26458326-26458376	HRE	kidney:	n/a
47	chr6:26457353-26457403	H1-hESC	embryonic stem cell:	embryo
48	chr6:26458093-26458143	Hela-S3	cervix:	n/a
49	chr6:26458013-26458063	SK-N-SH	brain:	n/a
50	chr6:26458189-26458239	HCPEpiC	choroid plexus:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:26420361..26423136-chr6:26455979..26458036,3	MCF-7	breast:
2	chr6:26456959..26459749-chr6:26461329..26463001,2	MCF-7	breast:
3	chr11:62609075..62609632-chr6:26457866..26458649,2	NB4	blood:
4	chr6:26464945..26466980-chr6:26467631..26469867,2	K562	blood:
5	chr6:26466421..26470294-chr6:26518422..26522122,3	K562	blood:
6	chr6:26457960..26461047-chr6:26519488..26522400,3	MCF-7	breast:
7	chr6:26467959..26470668-chr6:26470770..26473697,4	MCF-7	breast:
8	chr6:26466276..26469002-chr6:26480212..26482850,2	K562	blood:
9	chr6:26457696..26459779-chr6:26466915..26469338,2	MCF-7	breast:
10	chr6:26420100..26422498-chr6:26469157..26471386,2	K562	blood:
11	chr6:26469351..26470926-chr6:26472067..26474626,2	K562	blood:
12	chr6:26420998..26423545-chr6:26468256..26470657,2	K562	blood:
13	chr6:26204619..26206615-chr6:26455801..26457917,2	K562	blood:
14	chr6:26467030..26468631-chr6:26469753..26471368,2	MCF-7	breast:
15	chr6:26462941..26465022-chr6:26475685..26477185,2	K562	blood:
16	chr6:26456463..26458175-chr6:26469301..26471348,2	MCF-7	breast:
17	chr6:26158231..26160273-chr6:26456660..26458707,2	K562	blood:
18	chr6:26449553..26453974-chr6:26454911..26459271,5	K562	blood:

No data

Variant related genes	Relation type
BTN2A1	TF binding region
BTN2A1	CpG island
ENSG00000199289	chromatin interactions
ENSG00000111801	chromatin interactions
ENSG00000228223	chromatin interactions
ENSG00000158373	chromatin interactions
ENSG00000124549	chromatin interactions
ENSG00000112763	chromatin interactions
ENSG00000198518	chromatin interactions
ENSG00000133316	chromatin interactions

Extended variants
information (count: 610 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565160613	chr6:26457034-26457035	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs531111257	chr6:26457071-26457072	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs544611190	chr6:26457072-26457073	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs9358942	chr6:26457124-26457125	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs530085815	chr6:26457144-26457145	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs528367255	chr6:26457179-26457180	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs116381244	chr6:26457183-26457184	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs566828469	chr6:26457224-26457225	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs532666080	chr6:26457229-26457230	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs552674362	chr6:26457256-26457257	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs571389750	chr6:26457281-26457282	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs148555708	chr6:26457290-26457291	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs557023300	chr6:26457292-26457293	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs111371249	chr6:26457306-26457307	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs112884218	chr6:26457307-26457308	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs567557068	chr6:26457349-26457350	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs142884549	chr6:26457353-26457354	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs552566549	chr6:26457437-26457438	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs149511437	chr6:26457444-26457445	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs536420037	chr6:26457489-26457490	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs572478971	chr6:26457504-26457505	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs190231292	chr6:26457539-26457540	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs558213873	chr6:26457559-26457560	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs367823073	chr6:26457669-26457670	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs2393657	chr6:26457688-26457689	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs544788029	chr6:26457754-26457755	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs370087211	chr6:26457841-26457842	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs141255917	chr6:26457897-26457898	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs530430044	chr6:26457926-26457927	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs147966386	chr6:26457929-26457930	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs540892089	chr6:26457935-26457936	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs144943567	chr6:26457941-26457942	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs146300992	chr6:26457959-26457960	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs180715782	chr6:26458006-26458007	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs552747954	chr6:26458012-26458013	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
36	rs569333368	chr6:26458026-26458027	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs531668003	chr6:26458032-26458033	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs550761752	chr6:26458034-26458035	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs567315192	chr6:26458054-26458055	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs576447626	chr6:26458055-26458056	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs146758321	chr6:26458130-26458131	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs537487314	chr6:26458159-26458160	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs566163541	chr6:26458175-26458176	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs41267927	chr6:26458189-26458190	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs558414975	chr6:26458195-26458196	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs112900025	chr6:26458200-26458201	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs185151668	chr6:26458223-26458224	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs6907302	chr6:26458226-26458227	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs6929846	chr6:26458265-26458266	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs375245004	chr6:26458309-26458310	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
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
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
Cancer	20164919	CNVD
Melanoma	18172304	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
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
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17133270	CNVD
Autism	22495311	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	16790693	CNVD
Breast cancer	22032731	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	CNVD
Retinoblastoma	16790693	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
T-cell lymphomas	19863542	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
small cell lung cancer	20016488	CNVD
Williams-beuren syndrome	16971481	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	21569311	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:994 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:26441200-26457600	Weak transcription	Pancreas	Pancrea
2	chr6:26441400-26457400	Weak transcription	Psoas Muscle	Psoas
3	chr6:26442200-26457400	Weak transcription	Fetal Kidney	kidney
4	chr6:26442400-26457400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr6:26442400-26457400	Weak transcription	Hela-S3	cervix
6	chr6:26442600-26457400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr6:26443000-26457400	Weak transcription	Stomach Mucosa	stomach
8	chr6:26445200-26457400	Weak transcription	Small Intestine	intestine
9	chr6:26446400-26457200	Weak transcription	Skeletal Muscle Male	skeletal muscle
10	chr6:26446400-26457400	Weak transcription	Skeletal Muscle Female	skeletal muscle
11	chr6:26446400-26458200	Weak transcription	Gastric	stomach
12	chr6:26448000-26457600	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr6:26449000-26457600	Weak transcription	Right Ventricle	heart
14	chr6:26449200-26457400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
15	chr6:26449400-26457400	Weak transcription	HUVEC	blood vessel
16	chr6:26450200-26457400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
17	chr6:26450400-26457400	Weak transcription	Thymus	Thymus
18	chr6:26450600-26457400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
19	chr6:26450800-26457200	Weak transcription	Stomach Smooth Muscle	stomach
20	chr6:26450800-26457400	Weak transcription	Rectal Smooth Muscle	rectum
21	chr6:26450800-26457600	Weak transcription	Placenta	Placenta
22	chr6:26450800-26458200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr6:26451000-26457400	Weak transcription	Primary B cells from cord blood	blood
24	chr6:26451000-26457400	Weak transcription	Fetal Intestine Large	intestine
25	chr6:26451000-26457600	Weak transcription	Fetal Muscle Trunk	muscle
26	chr6:26451400-26457400	Weak transcription	Fetal Lung	lung
27	chr6:26451400-26457600	Weak transcription	Ovary	ovary
28	chr6:26451800-26457600	Weak transcription	Rectal Mucosa Donor 31	rectum
29	chr6:26452000-26457200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
30	chr6:26452000-26457400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr6:26452000-26457400	Weak transcription	Adipose Nuclei	Adipose
32	chr6:26452000-26457400	Weak transcription	Liver	Liver
33	chr6:26452000-26457400	Weak transcription	Duodenum Smooth Muscle	Duodenum
34	chr6:26452000-26457400	Weak transcription	Rectal Mucosa Donor 29	rectum
35	chr6:26452000-26457600	Weak transcription	Primary hematopoietic stem cells	blood
36	chr6:26452000-26457600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
37	chr6:26452000-26457600	Weak transcription	Colonic Mucosa	Colon
38	chr6:26452000-26457600	Weak transcription	Sigmoid Colon	Sigmoid Colon
39	chr6:26452400-26457400	Weak transcription	Primary B cells from peripheral blood	blood
40	chr6:26452400-26457400	Weak transcription	Duodenum Mucosa	Duodenum
41	chr6:26452600-26457200	Weak transcription	Fetal Thymus	thymus
42	chr6:26452600-26457400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr6:26452600-26457400	Weak transcription	Fetal Intestine Small	intestine
44	chr6:26453000-26457400	Weak transcription	Primary T helper cells PMA-I stimulated	--
45	chr6:26453000-26457400	Weak transcription	Primary T helper cells fromperipheralblood	blood
46	chr6:26453200-26457200	Weak transcription	Fetal Stomach	stomach
47	chr6:26453200-26457400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
48	chr6:26453200-26457400	Weak transcription	HSMM	muscle
49	chr6:26453400-26457200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr6:26453400-26457400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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