Variant report

Variant	nsv965971
Chromosome Location	chr21:15175683-15373907
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:873)
CpG islands
(count:1527)
Chromatin interactive
region (count:0)
LncRNA
region (count:40)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:873 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr21:15346022-15346251	K562	blood:	n/a	n/a
2	ARID3A	chr21:15295624-15295648	K562	blood:	n/a	n/a
3	ARID3A	chr21:15346922-15347270	K562	blood:	n/a	n/a
4	ATF1	chr21:15342677-15342811	K562	blood:	n/a	n/a
5	ATF1	chr21:15249426-15249616	K562	blood:	n/a	n/a
6	BACH1	chr21:15347039-15347218	K562	blood:	n/a	n/a
7	BATF	chr21:15302414-15302611	GM12878	blood:	n/a	chr21:15302548-15302559
8	BATF	chr21:15341379-15341645	GM12878	blood:	n/a	chr21:15341542-15341553
9	BATF	chr21:15319369-15319639	GM12878	blood:	n/a	n/a
10	BATF	chr21:15315664-15315881	GM12878	blood:	n/a	n/a
11	BATF	chr21:15293789-15294118	GM12878	blood:	n/a	chr21:15293876-15293886
12	BATF	chr21:15340450-15340827	GM12878	blood:	n/a	n/a
13	BATF	chr21:15293789-15294119	GM12878	blood:	n/a	chr21:15293876-15293886
14	BATF	chr21:15315150-15315618	GM12878	blood:	n/a	n/a
15	BATF	chr21:15295169-15295585	GM12878	blood:	n/a	chr21:15295405-15295416
16	BATF	chr21:15295228-15295568	GM12878	blood:	n/a	chr21:15295405-15295416
17	BATF	chr21:15321950-15322323	GM12878	blood:	n/a	chr21:15322062-15322070
18	BATF	chr21:15319344-15319735	GM12878	blood:	n/a	n/a
19	BATF	chr21:15340388-15340909	GM12878	blood:	n/a	n/a
20	BATF	chr21:15321908-15322326	GM12878	blood:	n/a	chr21:15322062-15322070
21	BATF	chr21:15315223-15315545	GM12878	blood:	n/a	n/a
22	BCL11A	chr21:15328745-15328928	GM12878	blood:	n/a	n/a
23	BCL11A	chr21:15319397-15319586	GM12878	blood:	n/a	n/a
24	BCL11A	chr21:15223481-15223715	GM12878	blood:	n/a	n/a
25	BCL11A	chr21:15315306-15315658	GM12878	blood:	n/a	chr21:15315610-15315619
26	BCL11A	chr21:15340450-15340836	GM12878	blood:	n/a	chr21:15340521-15340530 chr21:15340574-15340583
27	BCL11A	chr21:15321900-15322332	GM12878	blood:	n/a	n/a
28	BCL11A	chr21:15340406-15340552	GM12878	blood:	n/a	chr21:15340521-15340530
29	BCL11A	chr21:15293842-15294225	GM12878	blood:	n/a	n/a
30	BCL11A	chr21:15322021-15322201	GM12878	blood:	n/a	n/a
31	BCL11A	chr21:15319352-15319733	GM12878	blood:	n/a	n/a
32	BCL11A	chr21:15315283-15315608	GM12878	blood:	n/a	n/a
33	BHLHE40	chr21:15352368-15352716	GM12878	blood:	n/a	n/a
34	BHLHE40	chr21:15352447-15352823	K562	blood:	n/a	n/a
35	BHLHE40	chr21:15295613-15295821	K562	blood:	n/a	n/a
36	BHLHE40	chr21:15347507-15347656	K562	blood:	n/a	n/a
37	BRCA1	chr21:15352647-15352716	Hela-S3	cervix:	n/a	n/a
38	CBX3	chr21:15352365-15352825	K562	blood:	n/a	n/a
39	CCNT2	chr21:15295624-15295806	K562	blood:	n/a	n/a
40	CEBPB	chr21:15277523-15277688	K562	blood:	n/a	chr21:15277673-15277684
41	CEBPB	chr21:15346232-15346412	K562	blood:	n/a	n/a
42	CEBPB	chr21:15294348-15294556	IMR90	lung:	n/a	n/a
43	CEBPB	chr21:15347031-15347099	K562	blood:	n/a	n/a
44	CEBPB	chr21:15186322-15186471	HepG2	liver:	n/a	chr21:15186346-15186357
45	CEBPB	chr21:15186319-15186519	IMR90	lung:	n/a	chr21:15186346-15186357
46	CEBPB	chr21:15277580-15277731	HepG2	liver:	n/a	chr21:15277673-15277684
47	CEBPB	chr21:15277523-15277853	IMR90	lung:	n/a	chr21:15277673-15277684
48	CEBPD	chr21:15346361-15346742	K562	blood:	n/a	n/a
49	CEBPD	chr21:15295340-15295897	K562	blood:	n/a	n/a
50	CHD2	chr21:15352525-15352732	Hela-S3	cervix:	n/a	n/a

(count:1527 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:15197291-15197341	ECC-1	luminal epithelium:	n/a
2	chr21:15199826-15199876	PrEC	prostate:	n/a
3	chr21:15197291-15197341	ECC-1	luminal epithelium:	n/a
4	chr21:15199826-15199876	PrEC	prostate:	n/a
5	chr21:15200106-15200156	HIPEpiC	eye:	n/a
6	chr21:15311594-15311644	AG04450	lung:	fetal
7	chr21:15200106-15200156	AG04449	skin:	fetal
8	chr21:15352983-15353033	BE2_C	brain:	n/a
9	chr21:15309846-15309896	SK-N-MC	brain:	n/a
10	chr21:15200106-15200156	CMK	blood:	n/a
11	chr21:15309634-15309684	HCF	heart:	n/a
12	chr21:15352957-15353007	PFSK-1	brain:	n/a
13	chr21:15353879-15353929	HRPEpiC	eye:	n/a
14	chr21:15221404-15221454	SK-N-SH	brain:	n/a
15	chr21:15307662-15307712	AG04450	lung:	fetal
16	chr21:15352790-15352840	RPTEC	kidney:	n/a
17	chr21:15355304-15355354	ProgFib	skin:	n/a
18	chr21:15309724-15309774	MCF-7	breast:	n/a
19	chr21:15352641-15352691	SK-N-SH_RA	brain:	n/a
20	chr21:15220709-15220759	SK-N-MC	brain:	n/a
21	chr21:15309846-15309896	ovcar-3	ovarian:	n/a
22	chr21:15352940-15352990	Caco-2	colon:	n/a
23	chr21:15354157-15354207	K562	blood:	n/a
24	chr21:15311594-15311644	Caco-2	colon:	n/a
25	chr21:15352790-15352840	BJ	skin:	n/a
26	chr21:15220709-15220759	Jurkat	blood:	n/a
27	chr21:15352848-15352898	HEK293	kidney:	embryo
28	chr21:15352213-15352263	T-47D	breast:	n/a
29	chr21:15352790-15352840	BE2_C	brain:	n/a
30	chr21:15352940-15352990	PFSK-1	brain:	n/a
31	chr21:15355304-15355354	NHDF-neo	bronchial:	n/a
32	chr21:15221404-15221454	U87	brain:	n/a
33	chr21:15221404-15221454	ProgFib	skin:	n/a
34	chr21:15221404-15221454	GM12891	blood:	n/a
35	chr21:15220709-15220759	BJ	skin:	n/a
36	chr21:15352213-15352263	HRE	kidney:	n/a
37	chr21:15221404-15221454	HRE	kidney:	n/a
38	chr21:15352085-15352135	NHDF-neo	bronchial:	n/a
39	chr21:15307662-15307712	HL-60	blood:	n/a
40	chr21:15220709-15220759	Caco-2	colon:	n/a
41	chr21:15220709-15220759	NH-A	brain:	n/a
42	chr21:15200106-15200156	GM12878	blood:	n/a
43	chr21:15307662-15307712	PFSK-1	brain:	n/a
44	chr21:15215654-15215704	GM06990	blood:	n/a
45	chr21:15353879-15353929	HEK293	kidney:	embryo
46	chr21:15352085-15352135	AG04449	skin:	fetal
47	chr21:15354157-15354207	ECC-1	luminal epithelium:	n/a
48	chr21:15309846-15309896	AoSMC	blood vessel:	n/a
49	chr21:15309634-15309684	HUVEC	blood vessel:	n/a
50	chr21:15215654-15215704	NHBE	bronchial:	n/a

No data

(count:40 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LIPI-4	chr21:15335061-15335192	NONHSAT081133
2	lnc-LIPI-4	chr21:15311567-15311749	NONHSAT081131
3	lnc-LIPI-4	chr21:15323388-15323460	NONHSAT081133
4	lnc-LIPI-4	chr21:15310267-15310388	NONHSAT081131
5	lnc-POTED-11	chr21:15268407-15268509	NONHSAT081129
6	lnc-LIPI-7	chr21:15216343-15216385	NONHSAT147184
7	lnc-LIPI-4	chr21:15344317-15344450	NONHSAT081133
8	lnc-LIPI-4	chr21:15313136-15313299	NONHSAT081132
9	lnc-LIPI-7	chr21:15216343-15216456	NONHSAT081124
10	lnc-LIPI-4	chr21:15311695-15311749	NONHSAT081132
11	lnc-LIPI-7	chr21:15217426-15217595	NONHSAT081125
12	lnc-LIPI-7	chr21:15218334-15218462	NONHSAT081124
13	lnc-LIPI-3	chr21:15355017-15355220	expReg_chr21_329_-
14	lnc-LIPI-7	chr21:15219080-15219270	NONHSAT081124
15	lnc-LIPI-4	chr21:15323553-15323581	NONHSAT081132
16	lnc-LIPI-4	chr21:15323553-15323581	NONHSAT081131
17	lnc-POTED-9	chr21:15212726-15212964	NONHSAT081122
18	lnc-LIPI-4	chr21:15335061-15335106	NONHSAT081132
19	lnc-LIPI-4	chr21:15317360-15317464	NONHSAT081132
20	lnc-POTED-8	chr21:15211439-15211730	NONHSAT081121
21	lnc-LIPI-4	chr21:15313136-15313299	NONHSAT081131
22	lnc-POTED-9	chr21:15240747-15241288	NONHSAT081122
23	lnc-LIPI-7	chr21:15215457-15215753	NONHSAT147184
24	lnc-LIPI-4	chr21:15317360-15317430	NONHSAT081131
25	lnc-LIPI-7	chr21:15218334-15218713	NONHSAT081125
26	lnc-POTED-11	chr21:15286426-15287046	NONHSAT081129
27	lnc-LIPI-4	chr21:15323388-15323460	NONHSAT081132
28	lnc-LIPI-4	chr21:15339702-15339757	NONHSAT081133
29	lnc-RBM11-9	chr21:15361262-15361404	NONHSAT081139
30	lnc-LIPI-7	chr21:15220411-15220685	NONHSAT081124
31	lnc-LIPI-7	chr21:15215454-15215753	NONHSAT081124
32	lnc-LIPI-4	chr21:15342294-15342324	NONHSAT081131
33	lnc-RBM11-9	chr21:15361727-15362029	NONHSAT081139
34	lnc-LIPI-4	chr21:15317360-15317430	NONHSAT081133
35	lnc-LIPI-4	chr21:15342294-15342431	NONHSAT081133
36	lnc-POTED-11	chr21:15265662-15265761	NONHSAT081129
37	lnc-LIPI-4	chr21:15316065-15316183	NONHSAT081133
38	lnc-LIPI-4	chr21:15323388-15323460	NONHSAT081131
39	lnc-LIPI-4	chr21:15323553-15323581	NONHSAT081133
40	lnc-LIPI-7	chr21:15217326-15217595	NONHSAT081124

No data

Variant related genes	Relation type
RNU6-954P	TF binding region
ZNF114P1	TF binding region
NF1P3	TF binding region
SNX18P13	TF binding region
GXYLT1P2	TF binding region
ENSG00000266838	TF binding region
RHOT1P2	TF binding region
CNN2P7	TF binding region
CYP4F29P	TF binding region
ANKRD20A11P	TF binding region
RNU6-954P	CpG island
ZNF114P1	CpG island
NF1P3	CpG island
SNX18P13	CpG island
GXYLT1P2	CpG island
ENSG00000266838	CpG island
RHOT1P2	CpG island
CNN2P7	CpG island
CYP4F29P	CpG island
ANKRD20A11P	CpG island

Extended variants
information (count: 8535 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:8535 , 50 per page) page: 1 2 3 4 5 6 7 ... 171

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372212000	chr21:15179200-15179201	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs184980738	chr21:15179218-15179219	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs374310272	chr21:15179222-15179223	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs149141858	chr21:15179223-15179224	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs535133218	chr21:15179239-15179240	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs376453097	chr21:15179244-15179245	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs4046489	chr21:15179247-15179248	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs374907079	chr21:15179313-15179314	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs1811931	chr21:15179338-15179339	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs1811932	chr21:15179345-15179346	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs372773451	chr21:15179362-15179363	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs1811933	chr21:15179365-15179366	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs928236	chr21:15179408-15179409	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs139521033	chr21:15179443-15179444	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs569925153	chr21:15179559-15179560	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs112847086	chr21:15182441-15182442	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs371691898	chr21:15182486-15182487	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs372191420	chr21:15182502-15182503	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs140759628	chr21:15182503-15182504	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs145814973	chr21:15182508-15182509	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs368043736	chr21:15182509-15182510	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs111394493	chr21:15182510-15182511	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs370355748	chr21:15182514-15182515	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs374123262	chr21:15182516-15182517	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs2748716	chr21:15182520-15182521	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs200183752	chr21:15182522-15182523	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs4818617	chr21:15182524-15182525	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs184690617	chr21:15182525-15182526	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs4818618	chr21:15182537-15182538	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs4818619	chr21:15182541-15182542	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs7510320	chr21:15182551-15182552	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs575915101	chr21:15182552-15182553	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs544999984	chr21:15182557-15182558	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs7510449	chr21:15182559-15182560	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs9712788	chr21:15182561-15182562	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs75640765	chr21:15182565-15182566	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs367853008	chr21:15182570-15182571	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs201286726	chr21:15182573-15182574	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs62210878	chr21:15182574-15182575	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs62210879	chr21:15182576-15182577	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs62210880	chr21:15182578-15182579	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs62210881	chr21:15182580-15182581	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs2748715	chr21:15182581-15182582	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs147022052	chr21:15182635-15182636	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs112223876	chr21:15182652-15182653	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs552946707	chr21:15186832-15186833	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs148435378	chr21:15186894-15186895	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs371521116	chr21:15186906-15186907	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs552430753	chr21:15186917-15186918	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs145397168	chr21:15186972-15186973	Enhancers	n/a	n/a	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
Sudden cardiac death	19188705	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	21509527	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
Myelofibrosis	22110671	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	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
Breast cancer	20409316	CNVD
Autism	18414403	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
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Multiple myeloma	17550852	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

Chromatin state (count:204 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:15179200-15179600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr21:15182400-15182800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
3	chr21:15186800-15187800	Enhancers	Dnd41	blood
4	chr21:15191600-15193200	Enhancers	Placenta	Placenta
5	chr21:15196200-15197400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr21:15197400-15197600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr21:15197600-15198000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr21:15198000-15198200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr21:15223800-15224000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
10	chr21:15235200-15235800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr21:15244800-15245200	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
12	chr21:15245200-15246200	Weak transcription	Dnd41	blood
13	chr21:15246200-15247600	Enhancers	Dnd41	blood
14	chr21:15247600-15256200	Weak transcription	Dnd41	blood
15	chr21:15249400-15250200	Enhancers	K562	blood
16	chr21:15250200-15250600	Weak transcription	K562	blood
17	chr21:15250600-15250800	Enhancers	K562	blood
18	chr21:15250800-15252400	Weak transcription	K562	blood
19	chr21:15252400-15253000	Enhancers	K562	blood
20	chr21:15254400-15254800	Active TSS	Fetal Heart	heart
21	chr21:15254800-15258800	Weak transcription	Fetal Heart	heart
22	chr21:15256200-15256600	Enhancers	Dnd41	blood
23	chr21:15256600-15265600	Weak transcription	Dnd41	blood
24	chr21:15258800-15259200	ZNF genes & repeats	Fetal Heart	heart
25	chr21:15265600-15267000	Enhancers	Dnd41	blood
26	chr21:15269000-15269400	Enhancers	K562	blood
27	chr21:15269200-15269400	Enhancers	Lung	lung
28	chr21:15269200-15269400	Enhancers	A549	lung
29	chr21:15270000-15270400	Active TSS	Fetal Heart	heart
30	chr21:15275200-15276000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr21:15276000-15278800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr21:15277000-15281400	Weak transcription	Esophagus	oesophagus
33	chr21:15277000-15292200	Weak transcription	Dnd41	blood
34	chr21:15292200-15296200	Enhancers	Dnd41	blood
35	chr21:15292800-15293200	Enhancers	K562	blood
36	chr21:15293200-15293600	Weak transcription	K562	blood
37	chr21:15293600-15296200	Enhancers	K562	blood
38	chr21:15295200-15295800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr21:15295200-15296200	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr21:15295200-15296200	Enhancers	HMEC	breast
41	chr21:15295400-15295800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr21:15296200-15298000	Weak transcription	K562	blood
43	chr21:15296200-15307200	Weak transcription	Dnd41	blood
44	chr21:15298000-15298200	Enhancers	K562	blood
45	chr21:15301600-15308400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
46	chr21:15306000-15307400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr21:15307200-15307400	ZNF genes & repeats	Dnd41	blood
48	chr21:15307200-15309800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
49	chr21:15307200-15309800	ZNF genes & repeats	Esophagus	oesophagus
50	chr21:15307400-15308000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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