Variant report

Variant	nsv1060139
Chromosome Location	chr21:17057044-17100275
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	ATF1	chr21:17067875-17067961	K562	blood:	n/a	n/a
2	ATF1	chr21:17074263-17074486	K562	blood:	n/a	n/a
3	ATF1	chr21:17079030-17079390	K562	blood:	n/a	n/a
4	CBX3	chr21:17078978-17079442	HCT-116	colon:	n/a	n/a
5	CBX3	chr21:17078887-17079488	HCT-116	colon:	n/a	n/a
6	CEBPB	chr21:17059446-17059809	IMR90	lung:	n/a	n/a
7	CEBPB	chr21:17089735-17089858	A549	lung:	n/a	n/a
8	CEBPB	chr21:17060964-17061559	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr21:17078994-17079335	IMR90	lung:	n/a	n/a
10	CEBPB	chr21:17089679-17089897	HepG2	liver:	n/a	n/a
11	CEBPB	chr21:17059584-17059669	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr21:17060867-17061270	IMR90	lung:	n/a	n/a
13	CEBPB	chr21:17078905-17079547	HCT-116	colon:	n/a	n/a
14	CEBPB	chr21:17098821-17099127	HepG2	liver:	n/a	chr21:17098976-17098987
15	CEBPB	chr21:17098980-17099027	K562	blood:	n/a	n/a
16	CHD2	chr21:17094850-17095240	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr21:17067080-17067230	AoAF	blood vessel:	n/a	n/a
18	CTCF	chr21:17082858-17082948	Kidney_OC	kidney:	n/a	n/a
19	CTCF	chr21:17066920-17067070	AoAF	blood vessel:	n/a	n/a
20	CTCF	chr21:17061854-17061935	GM10248	blood:	n/a	n/a
21	CTCF	chr21:17068840-17068875	Lung_OC	lung:	n/a	n/a
22	CTCF	chr21:17072400-17072550	HPF	lung:	n/a	n/a
23	E2F4	chr21:17100252-17100580	MCF10A-Er-Src	breast:	n/a	n/a
24	EGR1	chr21:17085432-17085604	K562	blood:	n/a	n/a
25	EGR1	chr21:17085362-17085603	K562	blood:	n/a	n/a
26	ELF1	chr21:17078867-17079501	MCF-7	breast:	n/a	n/a
27	EP300	chr21:17078870-17079601	ECC-1	luminal epithelium:	n/a	chr21:17078972-17078979 chr21:17079035-17079049
28	EP300	chr21:17078957-17079420	T-47D	breast:	n/a	chr21:17078972-17078979 chr21:17079035-17079049
29	EP300	chr21:17078912-17079412	T-47D	breast:	n/a	chr21:17078972-17078979 chr21:17079035-17079049
30	EP300	chr21:17094916-17095306	ECC-1	luminal epithelium:	n/a	n/a
31	EP300	chr21:17078985-17079291	SK-N-SH_RA	brain:	n/a	chr21:17079035-17079049
32	EP300	chr21:17078948-17079580	SK-N-SH	brain:	n/a	chr21:17078972-17078979 chr21:17079035-17079049
33	EP300	chr21:17086354-17086450	K562	blood:	n/a	n/a
34	EP300	chr21:17061060-17061524	Hela-S3	cervix:	n/a	n/a
35	EP300	chr21:17094744-17095539	ECC-1	luminal epithelium:	n/a	n/a
36	EP300	chr21:17095007-17095333	H1-hESC	embryonic stem cell:	n/a	n/a
37	EP300	chr21:17079059-17079492	ECC-1	luminal epithelium:	n/a	n/a
38	ESR1	chr21:17079058-17079323	T-47D	breast:	n/a	n/a
39	FOS	chr21:17078945-17079551	HUVEC	blood vessel:	n/a	chr21:17079367-17079377 chr21:17079156-17079165 chr21:17079367-17079377 chr21:17079368-17079376 chr21:17079154-17079165 chr21:17079366-17079378 chr21:17079082-17079093
40	FOS	chr21:17085855-17086068	HUVEC	blood vessel:	n/a	chr21:17085962-17085971 chr21:17085963-17085971 chr21:17085961-17085972 chr21:17085963-17085970
41	FOS	chr21:17085461-17086061	MCF10A-Er-Src	breast:	n/a	chr21:17085962-17085971 chr21:17085963-17085971 chr21:17085961-17085972 chr21:17085963-17085970
42	FOS	chr21:17059639-17059923	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr21:17059649-17059918	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr21:17085439-17086148	MCF10A-Er-Src	breast:	n/a	chr21:17085962-17085971 chr21:17085963-17085971 chr21:17085961-17085972 chr21:17085963-17085970
45	FOS	chr21:17059618-17059971	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr21:17078923-17079529	MCF10A-Er-Src	breast:	n/a	chr21:17079367-17079377 chr21:17079156-17079165 chr21:17079367-17079377 chr21:17079368-17079376 chr21:17079154-17079165 chr21:17079366-17079378 chr21:17079082-17079093
47	FOS	chr21:17061102-17061352	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr21:17078932-17079328	MCF10A-Er-Src	breast:	n/a	chr21:17079156-17079165 chr21:17079154-17079165 chr21:17079082-17079093
49	FOS	chr21:17085409-17086109	MCF10A-Er-Src	breast:	n/a	chr21:17085962-17085971 chr21:17085963-17085971 chr21:17085961-17085972 chr21:17085963-17085970
50	FOS	chr21:17085446-17086079	MCF10A-Er-Src	breast:	n/a	chr21:17085962-17085971 chr21:17085963-17085971 chr21:17085961-17085972 chr21:17085963-17085970

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:17098256-17098306	A549	lung:	n/a
2	chr21:17098256-17098306	HMEC	breast:	n/a
3	chr21:17098256-17098306	MCF10A-Er-Src	breast:	n/a
4	chr21:17098256-17098306	U87	brain:	n/a
5	chr21:17098256-17098306	HCM	heart:	n/a
6	chr21:17098256-17098306	Jurkat	blood:	n/a
7	chr21:17098256-17098306	GM12892	blood:	n/a
8	chr21:17098256-17098306	HRCEpiC	kidney:	n/a
9	chr21:17098256-17098306	AG10803	skin:	n/a
10	chr21:17098256-17098306	HCF	heart:	n/a
11	chr21:17098256-17098306	HRPEpiC	eye:	n/a
12	chr21:17098256-17098306	HL-60	blood:	n/a
13	chr21:17098256-17098306	GM12891	blood:	n/a
14	chr21:17098256-17098306	K562	blood:	n/a
15	chr21:17098256-17098306	LNCaP	prostate:	n/a
16	chr21:17098256-17098306	Caco-2	colon:	n/a
17	chr21:17098256-17098306	NHBE	bronchial:	n/a
18	chr21:17098256-17098306	HUVEC	blood vessel:	n/a
19	chr21:17098256-17098306	GM06990	blood:	n/a
20	chr21:17098256-17098306	SK-N-SH	brain:	n/a
21	chr21:17098256-17098306	IMR90	lung:	fetal
22	chr21:17098256-17098306	SAEC	small airway:	n/a
23	chr21:17098256-17098306	HIPEpiC	eye:	n/a
24	chr21:17098256-17098306	NT2-D1	testis:	n/a
25	chr21:17098256-17098306	MCF-7	breast:	n/a
26	chr21:17098256-17098306	BE2_C	brain:	n/a
27	chr21:17098256-17098306	NHDF-neo	bronchial:	n/a
28	chr21:17098256-17098306	HEK293	kidney:	embryo
29	chr21:17098256-17098306	AG04450	lung:	fetal
30	chr21:17098256-17098306	ovcar-3	ovarian:	n/a
31	chr21:17098256-17098306	AoSMC	blood vessel:	n/a
32	chr21:17098256-17098306	GM19239	blood:	n/a
33	chr21:17098256-17098306	GM12878	blood:	n/a
34	chr21:17098256-17098306	PrEC	prostate:	n/a
35	chr21:17098256-17098306	Hela-S3	cervix:	n/a
36	chr21:17098256-17098306	HepG2	liver:	n/a
37	chr21:17098256-17098306	HAEpiC	amniotic membrane:	n/a
38	chr21:17098256-17098306	HRE	kidney:	n/a
39	chr21:17098256-17098306	AG09319	gingival:	n/a
40	chr21:17098256-17098306	NB4	blood:	n/a
41	chr21:17098256-17098306	HCPEpiC	choroid plexus:	n/a
42	chr21:17098256-17098306	ProgFib	skin:	n/a
43	chr21:17098256-17098306	HNPCEpiC	eye:	n/a
44	chr21:17098256-17098306	BJ	skin:	n/a
45	chr21:17098256-17098306	PANC-1	pancreas:	n/a
46	chr21:17098256-17098306	SK-N-MC	brain:	n/a
47	chr21:17098256-17098306	CMK	blood:	n/a
48	chr21:17098256-17098306	HPAEpiC	pulmonary alveolar:	n/a
49	chr21:17098256-17098306	H1-hESC	embryonic stem cell:	embryo
50	chr21:17098256-17098306	AG09309	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr21:17086804..17089683-chr21:17199530..17202336,2	K562	blood:
2	chr21:17093352..17096770-chr21:17100515..17103324,4	MCF-7	breast:
3	chr21:17087926..17089918-chr21:17092657..17095382,2	K562	blood:
4	chr21:17088463..17090416-chr21:17100632..17102945,2	MCF-7	breast:
5	chr21:17064242..17066910-chr21:17102295..17103877,2	K562	blood:
6	chr21:17083757..17086090-chr21:17088787..17091203,2	K562	blood:
7	chr21:17087926..17089918-chr21:17092657..17095382,2	K562	blood:
8	chr21:17057202..17059919-chr21:17100996..17103879,3	MCF-7	breast:
9	chr21:17087356..17090819-chr21:17092657..17096162,4	K562	blood:
10	chr21:17087356..17090819-chr21:17092657..17096162,4	K562	blood:
11	chr21:17079550..17081634-chr21:17101174..17103507,3	MCF-7	breast:
12	chr21:17083757..17086090-chr21:17088787..17091203,2	K562	blood:
13	chr20:19188556..19189161-chr21:17092468..17093033,2	MCF-7	breast:
14	chr21:17084081..17086628-chr21:17102246..17103996,2	K562	blood:
15	chr21:17084590..17087490-chr21:17087588..17090287,2	K562	blood:
16	chr21:17097568..17099854-chr21:17101138..17103471,3	K562	blood:
17	chr21:17077309..17079464-chr21:17110319..17112790,2	K562	blood:
18	chr21:17064915..17067118-chr21:17101217..17104804,3	MCF-7	breast:
19	chr21:17084590..17087490-chr21:17087588..17090287,2	K562	blood:
20	chr21:17099652..17105374-chr21:17196149..17200245,6	MCF-7	breast:
21	chr21:17094914..17097120-chr21:17102062..17104681,2	K562	blood:
22	chr21:17076130..17076863-chr4:168171748..168172510,2	MCF-7	breast:
23	chr21:17097568..17099854-chr21:17100603..17103471,4	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NRIP1-8	chr21:17068204-17068900	NONHSAT081210
2	lnc-NRIP1-8	chr21:17066619-17067073	NONHSAT081210

Variant related genes	Relation type
ENSG00000238591	TF binding region
USP25	TF binding region
ENSG00000221497	TF binding region
RAD23BLP	TF binding region
ENSG00000238591	CpG island
USP25	CpG island
ENSG00000221497	CpG island
RAD23BLP	CpG island
ENSG00000155313	chromatin interactions

Extended variants
information (count: 1558 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:1558 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576498285	chr21:17057060-17057061	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs548812172	chr21:17057149-17057150	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs545433363	chr21:17057161-17057162	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs114845802	chr21:17057172-17057173	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs537461204	chr21:17057180-17057181	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs2823444	chr21:17057197-17057198	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs2823445	chr21:17057220-17057221	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs191564894	chr21:17057248-17057249	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs112937803	chr21:17057251-17057252	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs2823446	chr21:17057262-17057263	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs182497650	chr21:17057328-17057329	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs542760668	chr21:17057341-17057342	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs555602915	chr21:17057352-17057353	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs187530507	chr21:17057370-17057371	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs561509062	chr21:17057435-17057436	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs76625680	chr21:17057468-17057469	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs75743803	chr21:17057469-17057470	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs116742173	chr21:17057491-17057492	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs545977272	chr21:17057500-17057501	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs577610076	chr21:17057543-17057544	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs372073874	chr21:17057548-17057549	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs191917803	chr21:17057604-17057605	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs183330903	chr21:17057612-17057613	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs562502463	chr21:17057669-17057670	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs530198962	chr21:17057704-17057705	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs531548243	chr21:17057711-17057712	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs374981050	chr21:17057777-17057778	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs562927856	chr21:17057817-17057818	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs531465446	chr21:17057818-17057819	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs551186237	chr21:17057848-17057849	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs114281450	chr21:17057888-17057889	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs533730332	chr21:17057904-17057905	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs9975283	chr21:17057913-17057914	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs567539608	chr21:17057921-17057922	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs9975377	chr21:17057996-17057997	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs556357764	chr21:17058013-17058014	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs576134406	chr21:17058095-17058096	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs142715946	chr21:17058096-17058097	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs557818815	chr21:17058102-17058103	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs577622250	chr21:17058105-17058106	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs188939894	chr21:17058147-17058148	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs57414299	chr21:17058169-17058170	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs574312705	chr21:17058175-17058176	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs374076807	chr21:17058176-17058177	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs542932870	chr21:17058184-17058185	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs563146849	chr21:17058272-17058273	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs531804865	chr21:17058279-17058280	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs761230	chr21:17058315-17058316	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs193056321	chr21:17058338-17058339	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs549476982	chr21:17058342-17058343	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Down syndrome	17412756	CNVD
Down syndrome	17576883	CNVD
Acute promyelocytic leukemia	19109227	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell lymphomas	19863542	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Renal cell carcinoma	19461508	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Metanephric adenoma	20802469	CNVD
Neuroblastoma	18923191	CNVD
Prostate cancer	19156837	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
lymphocytic leukemia	21291569	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute myeloid leukemia	21251322	CNVD
abnormal development	18461090	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Alzheimer''s disease	18923514	CNVD
Alzheimer''s disease	20877625	CNVD
Follicular lymphoma	20505157	CNVD
Alzheimer''s disease	21956041	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Melanoma	18172304	CNVD
Autism	22958593	CNVD
Schizophrenia	22958593	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Epilepsy	20502679	CNVD
22q11.2 microdeletion syndrome	19750312	CNVD
Breast cancer	20409316	CNVD

Chromatin state (count:147 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:17055200-17058600	Weak transcription	Primary hematopoietic stem cells	blood
2	chr21:17055600-17058800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr21:17055600-17059200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr21:17055800-17058000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr21:17055800-17058400	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr21:17055800-17058400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
7	chr21:17055800-17058800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr21:17055800-17059000	Weak transcription	Primary B cells from cord blood	blood
9	chr21:17055800-17059000	Weak transcription	Osteobl	bone
10	chr21:17055800-17059200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr21:17055800-17059200	Weak transcription	Placenta	Placenta
12	chr21:17055800-17060000	Weak transcription	NH-A	brain
13	chr21:17056400-17057600	Enhancers	Monocytes-CD14+_RO01746	blood
14	chr21:17056600-17058000	Weak transcription	Primary neutrophils fromperipheralblood	blood
15	chr21:17057600-17062200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
16	chr21:17058000-17058400	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr21:17058000-17059800	Enhancers	Primary neutrophils fromperipheralblood	blood
18	chr21:17058400-17058800	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
19	chr21:17058400-17059800	Enhancers	Primary hematopoietic stem cells short term culture	blood
20	chr21:17058600-17059400	Enhancers	Primary hematopoietic stem cells	blood
21	chr21:17058800-17059200	Enhancers	Primary monocytes fromperipheralblood	blood
22	chr21:17058800-17059600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr21:17058800-17059600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr21:17059000-17059600	Enhancers	Primary B cells from cord blood	blood
25	chr21:17059000-17059800	ZNF genes & repeats	Osteobl	bone
26	chr21:17059200-17059600	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
27	chr21:17059200-17059800	ZNF genes & repeats	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr21:17059200-17059800	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr21:17059200-17059800	Enhancers	Placenta	Placenta
30	chr21:17059400-17059600	Enhancers	HSMMtube	muscle
31	chr21:17059400-17060000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr21:17059400-17060600	Enhancers	Muscle Satellite Cultured Cells	--
33	chr21:17059600-17060000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr21:17059600-17061400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr21:17059600-17061600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr21:17059600-17062600	Weak transcription	HSMMtube	muscle
37	chr21:17059600-17063200	Enhancers	Primary monocytes fromperipheralblood	blood
38	chr21:17059600-17063800	Enhancers	HSMM	muscle
39	chr21:17059800-17060000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr21:17059800-17060000	Weak transcription	Osteobl	bone
41	chr21:17059800-17060800	Weak transcription	Primary neutrophils fromperipheralblood	blood
42	chr21:17059800-17079200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr21:17060000-17060800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr21:17060000-17060800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr21:17060000-17061000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr21:17060000-17061600	Enhancers	NH-A	brain
47	chr21:17060000-17062200	Enhancers	Osteobl	bone
48	chr21:17060600-17061000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
49	chr21:17060600-17061400	Enhancers	Hela-S3	cervix
50	chr21:17060800-17061600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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