Variant report

Variant	nsv913392
Chromosome Location	chr21:15221758-15336419
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:363)
CpG islands
(count:305)
Chromatin interactive
region (count:0)
LncRNA
region (count:21)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:363 , 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	ARID3A	chr21:15295624-15295648	K562	blood:	n/a	n/a
2	ATF1	chr21:15249426-15249616	K562	blood:	n/a	n/a
3	BATF	chr21:15293789-15294118	GM12878	blood:	n/a	chr21:15293876-15293886
4	BATF	chr21:15321908-15322326	GM12878	blood:	n/a	chr21:15322062-15322070
5	BATF	chr21:15315664-15315881	GM12878	blood:	n/a	n/a
6	BATF	chr21:15302414-15302611	GM12878	blood:	n/a	chr21:15302548-15302559
7	BATF	chr21:15319344-15319735	GM12878	blood:	n/a	n/a
8	BATF	chr21:15319369-15319639	GM12878	blood:	n/a	n/a
9	BATF	chr21:15321950-15322323	GM12878	blood:	n/a	chr21:15322062-15322070
10	BATF	chr21:15293789-15294119	GM12878	blood:	n/a	chr21:15293876-15293886
11	BATF	chr21:15315223-15315545	GM12878	blood:	n/a	n/a
12	BATF	chr21:15295169-15295585	GM12878	blood:	n/a	chr21:15295405-15295416
13	BATF	chr21:15295228-15295568	GM12878	blood:	n/a	chr21:15295405-15295416
14	BATF	chr21:15315150-15315618	GM12878	blood:	n/a	n/a
15	BCL11A	chr21:15328745-15328928	GM12878	blood:	n/a	n/a
16	BCL11A	chr21:15315283-15315608	GM12878	blood:	n/a	n/a
17	BCL11A	chr21:15315306-15315658	GM12878	blood:	n/a	chr21:15315610-15315619
18	BCL11A	chr21:15293842-15294225	GM12878	blood:	n/a	n/a
19	BCL11A	chr21:15319397-15319586	GM12878	blood:	n/a	n/a
20	BCL11A	chr21:15223481-15223715	GM12878	blood:	n/a	n/a
21	BCL11A	chr21:15321900-15322332	GM12878	blood:	n/a	n/a
22	BCL11A	chr21:15319352-15319733	GM12878	blood:	n/a	n/a
23	BCL11A	chr21:15322021-15322201	GM12878	blood:	n/a	n/a
24	BHLHE40	chr21:15295613-15295821	K562	blood:	n/a	n/a
25	CCNT2	chr21:15295624-15295806	K562	blood:	n/a	n/a
26	CEBPB	chr21:15277523-15277853	IMR90	lung:	n/a	chr21:15277673-15277684
27	CEBPB	chr21:15294348-15294556	IMR90	lung:	n/a	n/a
28	CEBPB	chr21:15277523-15277688	K562	blood:	n/a	chr21:15277673-15277684
29	CEBPB	chr21:15277580-15277731	HepG2	liver:	n/a	chr21:15277673-15277684
30	CEBPD	chr21:15295340-15295897	K562	blood:	n/a	n/a
31	CHD2	chr21:15227020-15227192	K562	blood:	n/a	n/a
32	CTCF	chr21:15302533-15302739	MCF-7	breast:	n/a	n/a
33	CTCF	chr21:15263041-15263087	GM13976	blood:	n/a	n/a
34	CTCF	chr21:15233129-15233166	LNCaP	prostate:	n/a	n/a
35	CTCF	chr21:15234831-15234848	GM10248	blood:	n/a	n/a
36	CTCF	chr21:15224171-15224211	Kidney_OC	kidney:	n/a	n/a
37	CTCF	chr21:15248231-15248291	LNCaP	prostate:	n/a	n/a
38	CTCF	chr21:15302640-15302790	NHDF-neo	bronchial:	n/a	n/a
39	CTCF	chr21:15302567-15302615	Medullo	brain:	n/a	n/a
40	CTCF	chr21:15302640-15302790	MCF-7	breast:	n/a	n/a
41	CTCF	chr21:15302580-15302730	GM12864	blood:	n/a	n/a
42	CTCF	chr21:15302510-15302750	MCF-7	breast:	n/a	n/a
43	CTCF	chr21:15302543-15302631	K562	blood:	n/a	n/a
44	CTCF	chr21:15259092-15259146	GM10266	blood:	n/a	n/a
45	CTCF	chr21:15320100-15320250	HEK293	kidney:	n/a	n/a
46	CTCF	chr21:15276230-15276275	GM13976	blood:	n/a	n/a
47	CTCF	chr21:15252310-15252389	Lung_OC	lung:	n/a	n/a
48	CTCF	chr21:15252140-15252204	LNCaP	prostate:	n/a	n/a
49	CTCF	chr21:15223612-15223665	GM12891	blood:	n/a	n/a
50	CTCF	chr21:15234852-15234914	GM10248	blood:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:15309634-15309684	PANC-1	pancreas:	n/a
2	chr21:15307662-15307712	Hela-S3	cervix:	n/a
3	chr21:15307662-15307712	LNCaP	prostate:	n/a
4	chr21:15307662-15307712	Caco-2	colon:	n/a
5	chr21:15311594-15311644	HIPEpiC	eye:	n/a
6	chr21:15309724-15309774	A549	lung:	n/a
7	chr21:15309724-15309774	NHDF-neo	bronchial:	n/a
8	chr21:15309724-15309774	HRCEpiC	kidney:	n/a
9	chr21:15307662-15307712	Jurkat	blood:	n/a
10	chr21:15311594-15311644	ProgFib	skin:	n/a
11	chr21:15307662-15307712	IMR90	lung:	fetal
12	chr21:15309846-15309896	HEEpiC	esophagus:	n/a
13	chr21:15311594-15311644	Hela-S3	cervix:	n/a
14	chr21:15307662-15307712	AoSMC	blood vessel:	n/a
15	chr21:15309724-15309774	Hela-S3	cervix:	n/a
16	chr21:15309724-15309774	HEEpiC	esophagus:	n/a
17	chr21:15309846-15309896	AG04450	lung:	fetal
18	chr21:15309634-15309684	A549	lung:	n/a
19	chr21:15309724-15309774	ProgFib	skin:	n/a
20	chr21:15307662-15307712	SAEC	small airway:	n/a
21	chr21:15311594-15311644	NHDF-neo	bronchial:	n/a
22	chr21:15311594-15311644	PrEC	prostate:	n/a
23	chr21:15309846-15309896	PrEC	prostate:	n/a
24	chr21:15309846-15309896	HCT-116	colon:	n/a
25	chr21:15309846-15309896	NHDF-neo	bronchial:	n/a
26	chr21:15309724-15309774	AG09319	gingival:	n/a
27	chr21:15309634-15309684	GM06990	blood:	n/a
28	chr21:15309634-15309684	HAEpiC	amniotic membrane:	n/a
29	chr21:15309724-15309774	HUVEC	blood vessel:	n/a
30	chr21:15311594-15311644	HAEpiC	amniotic membrane:	n/a
31	chr21:15309634-15309684	K562	blood:	n/a
32	chr21:15309724-15309774	H1-hESC	embryonic stem cell:	embryo
33	chr21:15307662-15307712	AG09319	gingival:	n/a
34	chr21:15307662-15307712	NB4	blood:	n/a
35	chr21:15309634-15309684	HMEC	breast:	n/a
36	chr21:15309634-15309684	ECC-1	luminal epithelium:	n/a
37	chr21:15309846-15309896	RPTEC	kidney:	n/a
38	chr21:15309846-15309896	U87	brain:	n/a
39	chr21:15309724-15309774	PrEC	prostate:	n/a
40	chr21:15309724-15309774	HNPCEpiC	eye:	n/a
41	chr21:15309634-15309684	BE2_C	brain:	n/a
42	chr21:15307662-15307712	GM12878	blood:	n/a
43	chr21:15307662-15307712	ovcar-3	ovarian:	n/a
44	chr21:15309634-15309684	AG04449	skin:	fetal
45	chr21:15307662-15307712	HL-60	blood:	n/a
46	chr21:15307662-15307712	CMK	blood:	n/a
47	chr21:15309634-15309684	H1-hESC	embryonic stem cell:	embryo
48	chr21:15309634-15309684	HRCEpiC	kidney:	n/a
49	chr21:15307662-15307712	HAEpiC	amniotic membrane:	n/a
50	chr21:15309724-15309774	GM12878	blood:	n/a

No data

(count:21 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LIPI-4	chr21:15317360-15317430	NONHSAT081133
2	lnc-LIPI-4	chr21:15323553-15323581	NONHSAT081131
3	lnc-LIPI-4	chr21:15316065-15316183	NONHSAT081133
4	lnc-POTED-9	chr21:15240747-15241288	NONHSAT081122
5	lnc-LIPI-4	chr21:15311567-15311749	NONHSAT081131
6	lnc-LIPI-4	chr21:15310267-15310388	NONHSAT081131
7	lnc-POTED-11	chr21:15265662-15265761	NONHSAT081129
8	lnc-LIPI-4	chr21:15313136-15313299	NONHSAT081132
9	lnc-LIPI-4	chr21:15323388-15323460	NONHSAT081133
10	lnc-LIPI-4	chr21:15323553-15323581	NONHSAT081133
11	lnc-POTED-11	chr21:15286426-15287046	NONHSAT081129
12	lnc-LIPI-4	chr21:15317360-15317464	NONHSAT081132
13	lnc-POTED-11	chr21:15268407-15268509	NONHSAT081129
14	lnc-LIPI-4	chr21:15313136-15313299	NONHSAT081131
15	lnc-LIPI-4	chr21:15311695-15311749	NONHSAT081132
16	lnc-LIPI-4	chr21:15335061-15335106	NONHSAT081132
17	lnc-LIPI-4	chr21:15335061-15335192	NONHSAT081133
18	lnc-LIPI-4	chr21:15323388-15323460	NONHSAT081131
19	lnc-LIPI-4	chr21:15317360-15317430	NONHSAT081131
20	lnc-LIPI-4	chr21:15323553-15323581	NONHSAT081132
21	lnc-LIPI-4	chr21:15323388-15323460	NONHSAT081132

No data

Variant related genes	Relation type
SNX18P13	TF binding region
RHOT1P2	TF binding region
CYP4F29P	TF binding region
ANKRD20A11P	TF binding region
SNX18P13	CpG island
RHOT1P2	CpG island
CYP4F29P	CpG island
ANKRD20A11P	CpG island

Extended variants
information (count: 6624 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:6624 , 50 per page) page: 1 2 3 4 5 6 7 ... 133

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs564875133	chr21:15222073-15222074	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs557902529	chr21:15222076-15222077	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs572065628	chr21:15222082-15222083	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs185176337	chr21:15222089-15222090	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs375634735	chr21:15222127-15222128	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs368639367	chr21:15222129-15222130	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs9976556	chr21:15222139-15222140	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs367874360	chr21:15222167-15222168	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs201962540	chr21:15222200-15222201	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs200088315	chr21:15222207-15222208	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs542983692	chr21:15222214-15222215	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs562774074	chr21:15222219-15222220	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs575573410	chr21:15222228-15222229	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs375630014	chr21:15222233-15222234	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs75620415	chr21:15222253-15222254	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs564235565	chr21:15222268-15222269	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs371746064	chr21:15222292-15222293	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs375769193	chr21:15222297-15222298	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs533154249	chr21:15222305-15222306	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs540104858	chr21:15222339-15222340	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs199851351	chr21:15222346-15222347	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs560172049	chr21:15222347-15222348	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs139632198	chr21:15222367-15222368	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs113003469	chr21:15222391-15222392	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs62209074	chr21:15222393-15222394	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs529015238	chr21:15222395-15222396	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs139140652	chr21:15222397-15222398	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs182323702	chr21:15222410-15222411	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs548930268	chr21:15222411-15222412	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs568535039	chr21:15222424-15222425	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs531838454	chr21:15222425-15222426	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs76106501	chr21:15222426-15222427	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs111621962	chr21:15222443-15222444	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs551667304	chr21:15222447-15222448	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs149838089	chr21:15222468-15222469	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs534400163	chr21:15222494-15222495	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs554097726	chr21:15222523-15222524	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs567729760	chr21:15222535-15222536	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs568460032	chr21:15223410-15223411	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs371303454	chr21:15223421-15223422	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs529889275	chr21:15223422-15223423	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs374816145	chr21:15223429-15223430	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs549671490	chr21:15223436-15223437	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs182502796	chr21:15223438-15223439	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs547789225	chr21:15223439-15223440	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs567505813	chr21:15223463-15223464	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs36060519	chr21:15223478-15223479	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs565607421	chr21:15223488-15223489	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs34233620	chr21:15223509-15223510	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs59506664	chr21:15223510-15223511	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

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
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:61 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:15223800-15224000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
2	chr21:15235200-15235800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr21:15244800-15245200	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
4	chr21:15245200-15246200	Weak transcription	Dnd41	blood
5	chr21:15246200-15247600	Enhancers	Dnd41	blood
6	chr21:15247600-15256200	Weak transcription	Dnd41	blood
7	chr21:15249400-15250200	Enhancers	K562	blood
8	chr21:15250200-15250600	Weak transcription	K562	blood
9	chr21:15250600-15250800	Enhancers	K562	blood
10	chr21:15250800-15252400	Weak transcription	K562	blood
11	chr21:15252400-15253000	Enhancers	K562	blood
12	chr21:15254400-15254800	Active TSS	Fetal Heart	heart
13	chr21:15254800-15258800	Weak transcription	Fetal Heart	heart
14	chr21:15256200-15256600	Enhancers	Dnd41	blood
15	chr21:15256600-15265600	Weak transcription	Dnd41	blood
16	chr21:15258800-15259200	ZNF genes & repeats	Fetal Heart	heart
17	chr21:15265600-15267000	Enhancers	Dnd41	blood
18	chr21:15269000-15269400	Enhancers	K562	blood
19	chr21:15269200-15269400	Enhancers	Lung	lung
20	chr21:15269200-15269400	Enhancers	A549	lung
21	chr21:15270000-15270400	Active TSS	Fetal Heart	heart
22	chr21:15275200-15276000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr21:15276000-15278800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr21:15277000-15281400	Weak transcription	Esophagus	oesophagus
25	chr21:15277000-15292200	Weak transcription	Dnd41	blood
26	chr21:15292200-15296200	Enhancers	Dnd41	blood
27	chr21:15292800-15293200	Enhancers	K562	blood
28	chr21:15293200-15293600	Weak transcription	K562	blood
29	chr21:15293600-15296200	Enhancers	K562	blood
30	chr21:15295200-15295800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr21:15295200-15296200	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr21:15295200-15296200	Enhancers	HMEC	breast
33	chr21:15295400-15295800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr21:15296200-15298000	Weak transcription	K562	blood
35	chr21:15296200-15307200	Weak transcription	Dnd41	blood
36	chr21:15298000-15298200	Enhancers	K562	blood
37	chr21:15301600-15308400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
38	chr21:15306000-15307400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr21:15307200-15307400	ZNF genes & repeats	Dnd41	blood
40	chr21:15307200-15309800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
41	chr21:15307200-15309800	ZNF genes & repeats	Esophagus	oesophagus
42	chr21:15307400-15308000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr21:15307400-15309200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr21:15307600-15309200	ZNF genes & repeats	Thymus	Thymus
45	chr21:15307800-15308600	ZNF genes & repeats	Brain Anterior Caudate	brain
46	chr21:15307800-15309800	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr21:15308000-15309800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr21:15308200-15309000	ZNF genes & repeats	Spleen	Spleen
49	chr21:15308400-15309000	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
50	chr21:15308400-15309800	ZNF genes & repeats	Dnd41	blood

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