Variant report

Variant	nsv834051
Chromosome Location	chr21:17564843-17721764
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:821)
CpG islands
(count:183)
Chromatin interactive
region (count:8)
LncRNA
region (count:20)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:821 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr21:17591356-17591655	HepG2	liver:	n/a	n/a
2	ARID3A	chr21:17702694-17703017	HepG2	liver:	n/a	n/a
3	BACH1	chr21:17716122-17716519	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr21:17571912-17572188	GM12878	blood:	n/a	n/a
5	BCL11A	chr21:17613922-17614292	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL11A	chr21:17613968-17614230	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCLAF1	chr21:17566541-17567013	GM12878	blood:	n/a	n/a
8	BHLHE40	chr21:17680774-17680958	GM12878	blood:	n/a	n/a
9	BHLHE40	chr21:17705941-17706046	GM12878	blood:	n/a	n/a
10	BHLHE40	chr21:17702730-17702888	GM12878	blood:	n/a	n/a
11	BRCA1	chr21:17566254-17567494	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr21:17567880-17568311	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr21:17653067-17653267	H1-hESC	embryonic stem cell:	n/a	n/a
14	BRCA1	chr21:17565274-17565550	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr21:17565247-17565642	A549	lung:	n/a	n/a
16	CEBPB	chr21:17566343-17566623	IMR90	lung:	n/a	n/a
17	CEBPB	chr21:17566241-17567448	Hela-S3	cervix:	n/a	chr21:17567008-17567021
18	CEBPB	chr21:17567885-17568148	A549	lung:	n/a	chr21:17568062-17568074
19	CEBPB	chr21:17565317-17565572	IMR90	lung:	n/a	n/a
20	CEBPB	chr21:17613692-17614351	ECC-1	luminal epithelium:	n/a	n/a
21	CEBPB	chr21:17654490-17654558	Hela-S3	cervix:	n/a	chr21:17654532-17654545
22	CEBPB	chr21:17654377-17654628	IMR90	lung:	n/a	chr21:17654532-17654545
23	CEBPB	chr21:17567885-17568206	IMR90	lung:	n/a	chr21:17568062-17568074 chr21:17568193-17568205
24	CEBPB	chr21:17565179-17565696	A549	lung:	n/a	n/a
25	CEBPB	chr21:17652444-17652993	H1-hESC	embryonic stem cell:	n/a	chr21:17652564-17652577
26	CEBPB	chr21:17591389-17591641	HepG2	liver:	n/a	n/a
27	CEBPB	chr21:17721133-17721378	IMR90	lung:	n/a	chr21:17721282-17721293
28	CEBPB	chr21:17565334-17565604	A549	lung:	n/a	n/a
29	CEBPB	chr21:17680645-17680990	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr21:17569504-17569819	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr21:17721207-17721428	HepG2	liver:	n/a	chr21:17721282-17721293
32	CEBPB	chr21:17565221-17565674	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr21:17567838-17568619	Hela-S3	cervix:	n/a	chr21:17568062-17568074 chr21:17568193-17568205
34	CEBPB	chr21:17565274-17565667	ECC-1	luminal epithelium:	n/a	n/a
35	CEBPB	chr21:17565324-17565608	ECC-1	luminal epithelium:	n/a	n/a
36	CHD2	chr21:17565251-17565568	Hela-S3	cervix:	n/a	n/a
37	CHD2	chr21:17566312-17567001	Hela-S3	cervix:	n/a	n/a
38	CREB1	chr21:17567848-17568212	GM12878	blood:	n/a	n/a
39	CREB1	chr21:17567908-17568315	GM12878	blood:	n/a	n/a
40	CTCF	chr21:17566780-17566930	AoAF	blood vessel:	n/a	n/a
41	CTCF	chr21:17702698-17702939	A549	lung:	n/a	chr21:17702843-17702861 chr21:17702838-17702859 chr21:17702844-17702860 chr21:17702848-17702856
42	CTCF	chr21:17702780-17702930	GM12865	blood:	n/a	chr21:17702843-17702861 chr21:17702838-17702859 chr21:17702844-17702860 chr21:17702848-17702856
43	CTCF	chr21:17566770-17566901	MCF-7	breast:	n/a	n/a
44	CTCF	chr21:17702718-17703018	Gliobla	brain:	n/a	chr21:17702843-17702861 chr21:17702838-17702859 chr21:17702844-17702860 chr21:17702848-17702856
45	CTCF	chr21:17566778-17566866	HepG2	liver:	n/a	n/a
46	CTCF	chr21:17566740-17566890	HUVEC	blood vessel:	n/a	n/a
47	CTCF	chr21:17702720-17702870	HCM	heart:	n/a	chr21:17702843-17702861 chr21:17702838-17702859 chr21:17702844-17702860 chr21:17702848-17702856
48	CTCF	chr21:17566780-17566930	HA-sp	spinal cord:	n/a	n/a
49	CTCF	chr21:17566700-17566850	HUVEC	blood vessel:	n/a	n/a
50	CTCF	chr21:17613980-17614130	HPAF	blood vessel:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:17565263-17565313	IMR90	lung:	fetal
2	chr21:17566381-17566431	HNPCEpiC	eye:	n/a
3	chr21:17565450-17565500	BJ	skin:	n/a
4	chr21:17566381-17566431	RPTEC	kidney:	n/a
5	chr21:17565263-17565313	HNPCEpiC	eye:	n/a
6	chr21:17566381-17566431	HEEpiC	esophagus:	n/a
7	chr21:17566381-17566431	NB4	blood:	n/a
8	chr21:17565263-17565313	MCF-7	breast:	n/a
9	chr21:17565450-17565500	NB4	blood:	n/a
10	chr21:17565450-17565500	NT2-D1	testis:	n/a
11	chr21:17566381-17566431	HRE	kidney:	n/a
12	chr21:17566381-17566431	HepG2	liver:	n/a
13	chr21:17565263-17565313	LNCaP	prostate:	n/a
14	chr21:17565263-17565313	Hepatocyte	liver:	n/a
15	chr21:17565263-17565313	AG04450	lung:	fetal
16	chr21:17566381-17566431	AG09319	gingival:	n/a
17	chr21:17565450-17565500	MCF-7	breast:	n/a
18	chr21:17566381-17566431	GM12892	blood:	n/a
19	chr21:17565263-17565313	SK-N-SH_RA	brain:	n/a
20	chr21:17566381-17566431	Caco-2	colon:	n/a
21	chr21:17565263-17565313	U87	brain:	n/a
22	chr21:17565263-17565313	MCF10A-Er-Src	breast:	n/a
23	chr21:17565263-17565313	Jurkat	blood:	n/a
24	chr21:17565450-17565500	HEEpiC	esophagus:	n/a
25	chr21:17565450-17565500	AG04449	skin:	fetal
26	chr21:17566381-17566431	NT2-D1	testis:	n/a
27	chr21:17565450-17565500	HL-60	blood:	n/a
28	chr21:17565263-17565313	HL-60	blood:	n/a
29	chr21:17565450-17565500	LNCaP	prostate:	n/a
30	chr21:17566381-17566431	A549	lung:	n/a
31	chr21:17565263-17565313	ECC-1	luminal epithelium:	n/a
32	chr21:17566381-17566431	SKMC	muscle:	n/a
33	chr21:17565263-17565313	GM12878	blood:	n/a
34	chr21:17565450-17565500	HNPCEpiC	eye:	n/a
35	chr21:17565263-17565313	HEK293	kidney:	embryo
36	chr21:17565450-17565500	HMEC	breast:	n/a
37	chr21:17566381-17566431	CMK	blood:	n/a
38	chr21:17566381-17566431	GM12891	blood:	n/a
39	chr21:17565263-17565313	HPAEpiC	pulmonary alveolar:	n/a
40	chr21:17565263-17565313	ProgFib	skin:	n/a
41	chr21:17565263-17565313	NHBE	bronchial:	n/a
42	chr21:17565450-17565500	NHBE	bronchial:	n/a
43	chr21:17566381-17566431	AoSMC	blood vessel:	n/a
44	chr21:17566381-17566431	AG10803	skin:	n/a
45	chr21:17565450-17565500	HepG2	liver:	n/a
46	chr21:17566381-17566431	GM19239	blood:	n/a
47	chr21:17565450-17565500	Jurkat	blood:	n/a
48	chr21:17565263-17565313	AG04449	skin:	fetal
49	chr21:17565450-17565500	ovcar-3	ovarian:	n/a
50	chr21:17565450-17565500	HPAEpiC	pulmonary alveolar:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:17651498..17653660-chr21:17656731..17658482,2	MCF-7	breast:
2	chr21:17718249..17720211-chr21:17726552..17729176,2	K562	blood:
3	chr21:17666188..17668256-chr21:17673895..17675565,2	K562	blood:
4	chr21:17552744..17555558-chr21:17617002..17619158,2	MCF-7	breast:
5	chr16:89989331..89990190-chr21:17566356..17566935,2	Hela-S3	cervix:
6	chr17:77751904..77752690-chr21:17566657..17567443,2	Hela-S3	cervix:
7	chr21:17666188..17668256-chr21:17673895..17675565,2	K562	blood:
8	chr21:17674827..17677573-chr21:17679269..17681921,2	MCF-7	breast:

(count:20 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-USP25-2	chr21:17702925-17703032	ENSG00000215386.6
2	lnc-USP25-2	chr21:17603376-17603435	NONHSAT081228
3	lnc-USP25-7	chr21:17716407-17716632	NONHSAT081233
4	lnc-USP25-2	chr21:17603376-17603435	ENSG00000215386.6
5	lnc-USP25-2	chr21:17566699-17566953	NONHSAT081228
6	lnc-USP25-2	chr21:17603376-17603435	ENSG00000215386
7	lnc-USP25-2	chr21:17603376-17603435	ENSG00000215386.6
8	lnc-USP25-2	chr21:17603376-17603435	ENSG00000215386
9	lnc-USP25-2	chr21:17566699-17566953	ENSG00000215386
10	lnc-USP25-2	chr21:17566715-17566953	ENSG00000215386.6
11	lnc-NRIP1-14	chr21:17664112-17664469	ENSG00000270071.1
12	lnc-USP25-2	chr21:17603376-17603435	ENSG00000215386.6
13	lnc-USP25-2	chr21:17603376-17603435	ENSG00000215386
14	lnc-NRIP1-14	chr21:17680330-17680454	ENSG00000270071.1
15	lnc-NRIP1-14	chr21:17668924-17669021	ENSG00000270071.1
16	lnc-USP25-2	chr21:17603376-17603435	ENSG00000215386
17	lnc-USP25-2	chr21:17603399-17603435	ENSG00000215386.6
18	lnc-USP25-2	chr21:17566788-17566953	ENSG00000215386
19	lnc-USP25-2	chr21:17603376-17603435	ENSG00000215386.6
20	lnc-USP25-2	chr21:17603376-17603435	ENSG00000215386

No data

Variant related genes	Relation type
LINC00478	TF binding region
ENSG00000201025	TF binding region
ENSG00000270071	TF binding region
LINC00478	CpG island
ENSG00000201025	CpG island
ENSG00000270071	CpG island
ENSG00000258947	chromatin interactions
ENSG00000173894	chromatin interactions
ENSG00000215386	chromatin interactions
ENSG00000270071	chromatin interactions
ENSG00000201025	chromatin interactions
PLAG1	miRNA target sites
RICH2	miRNA target sites
GOLGA4	miRNA target sites
CUL5	miRNA target sites

Extended variants
information (count: 6263 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:6263 , 50 per page) page: 1 2 3 4 5 6 7 ... 126

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs189420542	chr21:17564869-17564870	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs569449706	chr21:17564972-17564973	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs16994425	chr21:17565025-17565026	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs115168387	chr21:17565085-17565086	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs181354800	chr21:17565102-17565103	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs7282585	chr21:17565114-17565115	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs377217009	chr21:17565120-17565121	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs369684362	chr21:17565127-17565128	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs374145701	chr21:17565187-17565188	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs185383521	chr21:17565192-17565193	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs553891172	chr21:17565206-17565207	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs139143853	chr21:17565245-17565246	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs149168847	chr21:17565263-17565264	Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
14	rs536369475	chr21:17565264-17565265	Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
15	rs5842554	chr21:17565297-17565298	Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
16	rs397763073	chr21:17565308-17565309	Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
17	rs397705233	chr21:17565309-17565310	Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
18	rs200846825	chr21:17565310-17565311	Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
19	rs190640221	chr21:17565311-17565312	Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
20	rs16994427	chr21:17565333-17565334	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs116191724	chr21:17565360-17565361	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs559941643	chr21:17565373-17565374	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs544845537	chr21:17565395-17565396	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs532158472	chr21:17565396-17565397	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs564790193	chr21:17565431-17565432	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs572258819	chr21:17565451-17565452	Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
27	rs145072198	chr21:17565477-17565478	Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
28	rs146479696	chr21:17565521-17565522	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs529718708	chr21:17565545-17565546	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs111996097	chr21:17565624-17565625	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs16994429	chr21:17565625-17565626	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs2823635	chr21:17565645-17565646	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs144870816	chr21:17565680-17565681	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs571872258	chr21:17565691-17565692	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs16994433	chr21:17565735-17565736	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs181586100	chr21:17565781-17565782	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs567882212	chr21:17565822-17565823	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs148274648	chr21:17565827-17565828	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs536282961	chr21:17565848-17565849	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs185753011	chr21:17565850-17565851	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs141124799	chr21:17565859-17565860	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs372621792	chr21:17565898-17565899	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs573427106	chr21:17565906-17565907	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs80028191	chr21:17565923-17565924	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs115915127	chr21:17565950-17565951	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs150301925	chr21:17566000-17566001	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs114369698	chr21:17566017-17566018	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs561267950	chr21:17566052-17566053	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs376916088	chr21:17566071-17566072	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs35701740	chr21:17566153-17566154	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
Gastric cancer	18160780	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Medullary thyroid carcinoma	18765511	CNVD

Chromatin state (count:1856 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:17553400-17566400	Weak transcription	Fetal Stomach	stomach
2	chr21:17558400-17566400	Weak transcription	Brain Anterior Caudate	brain
3	chr21:17559000-17571200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr21:17559600-17566200	Weak transcription	Ovary	ovary
5	chr21:17559600-17566600	Weak transcription	Placenta	Placenta
6	chr21:17563000-17565400	Weak transcription	NHDF-Ad	bronchial
7	chr21:17563400-17565200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr21:17563600-17567200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr21:17564600-17566200	Enhancers	Hela-S3	cervix
10	chr21:17565000-17565600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr21:17565200-17565600	Enhancers	Fetal Intestine Large	intestine
12	chr21:17565200-17565800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr21:17565200-17565800	Enhancers	A549	lung
14	chr21:17565200-17566000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr21:17565200-17566200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr21:17565200-17566200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr21:17565200-17566200	Enhancers	Fetal Kidney	kidney
18	chr21:17565200-17566600	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr21:17565400-17565600	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr21:17565400-17565600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr21:17565400-17565600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr21:17565400-17565600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr21:17565400-17565600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr21:17565400-17565600	Enhancers	Brain Hippocampus Middle	brain
25	chr21:17565400-17565600	Enhancers	Fetal Intestine Small	intestine
26	chr21:17565400-17565600	Enhancers	Thymus	Thymus
27	chr21:17565400-17565800	Enhancers	NH-A	brain
28	chr21:17565400-17566200	Enhancers	HUVEC	blood vessel
29	chr21:17565400-17566200	Enhancers	NHDF-Ad	bronchial
30	chr21:17565400-17566200	Enhancers	Osteobl	bone
31	chr21:17565400-17566400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr21:17565400-17566400	Enhancers	Muscle Satellite Cultured Cells	--
33	chr21:17565400-17566400	Enhancers	Cortex derived primary cultured neurospheres	brain
34	chr21:17565400-17566400	Enhancers	HSMM	muscle
35	chr21:17565400-17570000	Enhancers	Primary monocytes fromperipheralblood	blood
36	chr21:17565600-17565800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr21:17565600-17566200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr21:17565600-17566200	Weak transcription	Brain Hippocampus Middle	brain
39	chr21:17565600-17566400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr21:17565600-17566400	Weak transcription	Fetal Intestine Large	intestine
41	chr21:17565600-17566600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
42	chr21:17565600-17566600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr21:17565600-17566600	Weak transcription	Thymus	Thymus
44	chr21:17565800-17566000	Active TSS	Primary hematopoietic stem cells short term culture	blood
45	chr21:17565800-17566000	Flanking Active TSS	A549	lung
46	chr21:17565800-17566200	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr21:17565800-17566200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr21:17565800-17566200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr21:17565800-17566200	Enhancers	Primary hematopoietic stem cells	blood
50	chr21:17565800-17566200	Enhancers	Adipose Nuclei	Adipose

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