Variant report

Variant	nsv913403
Chromosome Location	chr21:15743387-15786271
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1008)
CpG islands
(count:919)
Chromatin interactive
region (count:32)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:8)

(count:1008 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr21:15753998-15754080	K562	blood:	n/a	n/a
2	ARID3A	chr21:15755173-15756571	K562	blood:	n/a	n/a
3	ARID3A	chr21:15776002-15776346	K562	blood:	n/a	n/a
4	ARID3A	chr21:15758299-15758479	K562	blood:	n/a	n/a
5	ARID3A	chr21:15755268-15756109	HepG2	liver:	n/a	n/a
6	ATF1	chr21:15755085-15755946	K562	blood:	n/a	n/a
7	ATF2	chr21:15755202-15755652	GM12878	blood:	n/a	n/a
8	ATF3	chr21:15755249-15755657	K562	blood:	n/a	chr21:15755481-15755495
9	BACH1	chr21:15755021-15755056	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr21:15755261-15755431	K562	blood:	n/a	n/a
11	BACH1	chr21:15755338-15756042	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr21:15760675-15760968	K562	blood:	n/a	n/a
13	BACH1	chr21:15760631-15760949	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr21:15755145-15755665	GM12878	blood:	n/a	chr21:15755330-15755340
15	BATF	chr21:15755303-15755640	GM12878	blood:	n/a	chr21:15755330-15755340
16	BCLAF1	chr21:15755245-15755807	GM12878	blood:	n/a	n/a
17	BCLAF1	chr21:15755292-15756207	GM12878	blood:	n/a	n/a
18	BHLHE40	chr21:15755039-15756420	GM12878	blood:	n/a	chr21:15755215-15755231
19	BHLHE40	chr21:15755011-15756441	K562	blood:	n/a	chr21:15755215-15755231
20	BHLHE40	chr21:15755029-15756177	HepG2	liver:	n/a	chr21:15755215-15755231
21	BRCA1	chr21:15755348-15756047	H1-hESC	embryonic stem cell:	n/a	n/a
22	BRCA1	chr21:15776084-15776399	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr21:15755229-15756067	GM12878	blood:	n/a	n/a
24	BRCA1	chr21:15755310-15755866	HepG2	liver:	n/a	n/a
25	BRCA1	chr21:15755164-15756426	Hela-S3	cervix:	n/a	n/a
26	CCNT2	chr21:15755282-15756426	K562	blood:	n/a	n/a
27	CCNT2	chr21:15757539-15757977	K562	blood:	n/a	n/a
28	CCNT2	chr21:15776143-15776343	K562	blood:	n/a	n/a
29	CEBPB	chr21:15754739-15755070	K562	blood:	n/a	n/a
30	CEBPB	chr21:15755355-15755957	K562	blood:	n/a	n/a
31	CEBPB	chr21:15755354-15755995	HepG2	liver:	n/a	n/a
32	CEBPB	chr21:15770324-15770766	A549	lung:	n/a	n/a
33	CEBPB	chr21:15770341-15770581	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr21:15755379-15755740	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr21:15756026-15756585	GM12878	blood:	n/a	n/a
36	CEBPB	chr21:15776065-15776366	K562	blood:	n/a	n/a
37	CEBPB	chr21:15770426-15770482	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr21:15754746-15755936	IMR90	lung:	n/a	n/a
39	CEBPB	chr21:15770280-15770778	IMR90	lung:	n/a	n/a
40	CEBPB	chr21:15755328-15755807	K562	blood:	n/a	n/a
41	CEBPB	chr21:15755409-15755730	A549	lung:	n/a	n/a
42	CEBPB	chr21:15754813-15755089	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr21:15754691-15755984	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr21:15755315-15755801	MCF-7	breast:	n/a	n/a
45	CHD1	chr21:15755865-15756431	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD1	chr21:15755195-15756697	GM12878	blood:	n/a	n/a
47	CHD2	chr21:15754751-15756186	Hela-S3	cervix:	n/a	n/a
48	CHD2	chr21:15754856-15756152	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr21:15755020-15756199	GM12878	blood:	n/a	n/a
50	CHD2	chr21:15755060-15756508	K562	blood:	n/a	n/a

(count:919 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:15755380-15755430	HAEpiC	amniotic membrane:	n/a
2	chr21:15755380-15755430	AG10803	skin:	n/a
3	chr21:15755380-15755430	LNCaP	prostate:	n/a
4	chr21:15756085-15756135	GM12892	blood:	n/a
5	chr21:15755380-15755430	HAEpiC	amniotic membrane:	n/a
6	chr21:15755380-15755430	AG10803	skin:	n/a
7	chr21:15755380-15755430	LNCaP	prostate:	n/a
8	chr21:15756085-15756135	GM12892	blood:	n/a
9	chr21:15755606-15755656	HCPEpiC	choroid plexus:	n/a
10	chr21:15755931-15755981	HCF	heart:	n/a
11	chr21:15756062-15756112	Caco-2	colon:	n/a
12	chr21:15755606-15755656	GM12891	blood:	n/a
13	chr21:15755449-15755499	HCF	heart:	n/a
14	chr21:15756122-15756172	GM19239	blood:	n/a
15	chr21:15753565-15753615	IMR90	lung:	fetal
16	chr21:15756122-15756172	HEEpiC	esophagus:	n/a
17	chr21:15755606-15755656	ovcar-3	ovarian:	n/a
18	chr21:15755644-15755694	HEK293	kidney:	embryo
19	chr21:15755606-15755656	HUVEC	blood vessel:	n/a
20	chr21:15755608-15755658	AG04450	lung:	fetal
21	chr21:15755606-15755656	NB4	blood:	n/a
22	chr21:15755380-15755430	SKMC	muscle:	n/a
23	chr21:15755380-15755430	HIPEpiC	eye:	n/a
24	chr21:15755449-15755499	Caco-2	colon:	n/a
25	chr21:15755380-15755430	ProgFib	skin:	n/a
26	chr21:15755380-15755430	NHBE	bronchial:	n/a
27	chr21:15755452-15755502	HL-60	blood:	n/a
28	chr21:15756122-15756172	HL-60	blood:	n/a
29	chr21:15756062-15756112	HepG2	liver:	n/a
30	chr21:15755606-15755656	AG04449	skin:	fetal
31	chr21:15755644-15755694	K562	blood:	n/a
32	chr21:15756122-15756172	BJ	skin:	n/a
33	chr21:15755608-15755658	LNCaP	prostate:	n/a
34	chr21:15755380-15755430	GM19239	blood:	n/a
35	chr21:15755380-15755430	HEEpiC	esophagus:	n/a
36	chr21:15755380-15755430	T-47D	breast:	n/a
37	chr21:15755644-15755694	BJ	skin:	n/a
38	chr21:15755452-15755502	U87	brain:	n/a
39	chr21:15755608-15755658	MCF10A-Er-Src	breast:	n/a
40	chr21:15753565-15753615	RPTEC	kidney:	n/a
41	chr21:15755986-15756036	HPAEpiC	pulmonary alveolar:	n/a
42	chr21:15755706-15755756	GM06990	blood:	n/a
43	chr21:15755931-15755981	GM06990	blood:	n/a
44	chr21:15756062-15756112	SK-N-SH	brain:	n/a
45	chr21:15753565-15753615	ovcar-3	ovarian:	n/a
46	chr21:15755606-15755656	HIPEpiC	eye:	n/a
47	chr21:15755452-15755502	ECC-1	luminal epithelium:	n/a
48	chr21:15755931-15755981	HEEpiC	esophagus:	n/a
49	chr21:15753565-15753615	HEK293	kidney:	embryo
50	chr21:15755644-15755694	AG09319	gingival:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:15775728..15776263-chr21:16146221..16146744,2	K562	blood:
2	chr21:15761527..15763962-chr21:15764673..15767332,2	K562	blood:
3	chr21:15754842..15757143-chr21:15757991..15759672,2	MCF-7	breast:
4	chr21:15751469..15753501-chr21:15755651..15758117,2	K562	blood:
5	chr21:15764391..15766947-chr21:15768713..15771374,3	K562	blood:
6	chr12:56122664..56123207-chr21:15755194..15755994,2	Hela-S3	cervix:
7	chr21:15645251..15647400-chr21:15754351..15756122,2	K562	blood:
8	chr21:15733160..15735734-chr21:15743714..15745323,2	K562	blood:
9	chr21:15753396..15756217-chr21:15770461..15772950,2	K562	blood:
10	chr21:15755923..15757812-chr21:16863949..16865497,2	K562	blood:
11	chr21:15764391..15766947-chr21:15768713..15771374,3	K562	blood:
12	chr21:15740980..15743787-chr21:15748039..15750871,3	K562	blood:
13	chr21:15652280..15654566-chr21:15773386..15776181,2	MCF-7	breast:
14	chr21:15755528..15756150-chr5:33440838..33441550,2	Hela-S3	cervix:
15	chr21:15757559..15759154-chr21:16437032..16438993,2	K562	blood:
16	chr21:15740980..15743787-chr21:15748039..15750871,3	K562	blood:
17	chr21:15761527..15763962-chr21:15764673..15767332,2	K562	blood:
18	chr21:15738341..15740358-chr21:15745168..15748188,3	MCF-7	breast:
19	chr21:15741032..15742950-chr21:15746679..15748662,2	MCF-7	breast:
20	chr21:15733246..15736908-chr21:15755835..15758351,3	K562	blood:
21	chr21:15738717..15742131-chr21:15743462..15746963,4	K562	blood:
22	chr21:15753622..15756331-chr21:15761576..15764249,2	MCF-7	breast:
23	chr21:15754870..15757296-chr21:16435942..16438083,2	K562	blood:
24	chr21:15748798..15750660-chr21:15754088..15755961,2	K562	blood:
25	chr21:15759229..15762199-chr21:15825176..15826732,2	K562	blood:
26	chr21:15750689..15753216-chr21:15754882..15756987,2	MCF-7	breast:
27	chr21:15743793..15747020-chr21:15754018..15757060,4	K562	blood:
28	chr21:15750287..15752845-chr21:15753558..15756230,2	MCF-7	breast:
29	chr21:15773035..15774596-chr21:16435398..16438131,2	MCF-7	breast:
30	chr21:15755580..15758807-chr21:15770098..15773208,3	K562	blood:
31	chr21:15738236..15741206-chr21:15753262..15755404,2	K562	blood:
32	chr21:15755786..15757968-chr21:15767216..15769064,2	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RBM11-1	chr21:15765643-15765753	ENSG00000242342
2	lnc-RBM11-1	chr21:15764891-15764967	ENSG00000242342

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	HSPA13	hsa-miR-590-3p	chr21:15745703-15745724
2	HSPA13	hsa-miR-374b-5p	chr21:15744626-15744647
3	HSPA13	hsa-miR-374b-5p	chr21:15745406-15745427
4	HSPA13	hsa-miR-181a-5p	chr21:15744415-15744438
5	HSPA13	hsa-miR-374b-5p	chr21:15743825-15743845
6	HSPA13	hsa-miR-590-3p	chr21:15743537-15743557
7	HSPA13	hsa-miR-590-3p	chr21:15745175-15745195
8	HSPA13	hsa-miR-590-3p	chr21:15743724-15743744

Variant related genes	Relation type
HSPA13	TF binding region
HSPA13	CpG island
ENSG00000225502	chromatin interactions
ENSG00000155304	chromatin interactions
ENSG00000258056	chromatin interactions
ENSG00000180530	chromatin interactions
ENSG00000243064	chromatin interactions
ENSG00000135404	chromatin interactions
ENSG00000113407	chromatin interactions

Extended variants
information (count: 1162 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:1162 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7279926	chr21:15743387-15743388	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs544059015	chr21:15743436-15743437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs577649746	chr21:15743469-15743470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs570122439	chr21:15743504-15743505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs540874049	chr21:15743552-15743553	Weak transcription	miRNA target site	1 gene(s)	Overlapped CNVs	n/a
6	rs560541926	chr21:15743556-15743557	Weak transcription	miRNA target site	1 gene(s)	Overlapped CNVs	n/a
7	rs75735747	chr21:15743601-15743602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs543171696	chr21:15743653-15743654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs562967607	chr21:15743680-15743681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs531780905	chr21:15743706-15743707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs560631453	chr21:15743726-15743727	Weak transcription	miRNA target site	1 gene(s)	Overlapped CNVs	n/a
12	rs71872487	chr21:15743727-15743728	Weak transcription	miRNA target site	1 gene(s)	Overlapped CNVs	n/a
13	rs532474516	chr21:15743747-15743748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs551810227	chr21:15743781-15743782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs372731738	chr21:15743803-15743804	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs571572004	chr21:15743841-15743842	Weak transcription Strong transcription	Chromatin interactive region miRNA target site	2 gene(s)	Overlapped CNVs	n/a
17	rs533099337	chr21:15743914-15743915	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs546842356	chr21:15743970-15743971	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs535923217	chr21:15743986-15743987	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs117423707	chr21:15744044-15744045	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs555086172	chr21:15744045-15744046	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs559744748	chr21:15744057-15744058	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs537504995	chr21:15744108-15744109	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs557334163	chr21:15744190-15744191	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs577537129	chr21:15744204-15744205	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs532633586	chr21:15744256-15744257	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs540585763	chr21:15744257-15744258	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs554430028	chr21:15744268-15744269	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs183232028	chr21:15744369-15744370	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs543234738	chr21:15744384-15744385	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs3178188	chr21:15744389-15744390	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs572373580	chr21:15744396-15744397	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs187180905	chr21:15744420-15744421	Weak transcription Strong transcription	Chromatin interactive region miRNA target site	2 gene(s)	Overlapped CNVs	n/a
34	rs545492907	chr21:15744441-15744442	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs548650187	chr21:15744465-15744466	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs568650194	chr21:15744495-15744496	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs369996560	chr21:15744514-15744515	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs17002662	chr21:15744530-15744531	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs546609775	chr21:15744547-15744548	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs544626988	chr21:15744557-15744558	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs560389701	chr21:15744559-15744560	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs529090601	chr21:15744571-15744572	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs17306192	chr21:15744594-15744595	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs568663057	chr21:15744598-15744599	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs190109382	chr21:15744601-15744602	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs182736438	chr21:15744720-15744721	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs11088017	chr21:15744767-15744768	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs187422579	chr21:15744812-15744813	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs78283728	chr21:15744859-15744860	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs9978693	chr21:15744876-15744877	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

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
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
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
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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1039 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:15731600-15744800	Weak transcription	Hela-S3	cervix
2	chr21:15734400-15745600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr21:15734600-15744800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr21:15734600-15744800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr21:15734600-15745400	Weak transcription	HUVEC	blood vessel
6	chr21:15734800-15745400	Weak transcription	Primary neutrophils fromperipheralblood	blood
7	chr21:15735200-15744600	Weak transcription	NHEK	skin
8	chr21:15735200-15744800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr21:15735200-15744800	Weak transcription	HMEC	breast
10	chr21:15735200-15745200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr21:15737400-15745400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr21:15738600-15746000	Weak transcription	Ovary	ovary
13	chr21:15739000-15744600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr21:15739200-15745000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
15	chr21:15739200-15747800	Weak transcription	Esophagus	oesophagus
16	chr21:15739600-15745000	Weak transcription	Primary hematopoietic stem cells	blood
17	chr21:15739800-15743800	Weak transcription	Monocytes-CD14+_RO01746	blood
18	chr21:15739800-15744600	Weak transcription	Primary monocytes fromperipheralblood	blood
19	chr21:15739800-15745600	Weak transcription	GM12878-XiMat	blood
20	chr21:15739800-15746000	Weak transcription	K562	blood
21	chr21:15740400-15744800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr21:15740400-15745200	Weak transcription	Brain Germinal Matrix	brain
23	chr21:15740400-15746000	Weak transcription	Sigmoid Colon	Sigmoid Colon
24	chr21:15740600-15744800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr21:15740600-15745000	Weak transcription	Primary B cells from cord blood	blood
26	chr21:15740600-15745000	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr21:15740600-15745400	Weak transcription	Stomach Smooth Muscle	stomach
28	chr21:15740600-15746000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr21:15740600-15746000	Weak transcription	NHLF	lung
30	chr21:15740800-15746000	Weak transcription	Left Ventricle	heart
31	chr21:15741000-15744400	Weak transcription	Placenta	Placenta
32	chr21:15741000-15744600	Weak transcription	Primary T helper cells fromperipheralblood	blood
33	chr21:15741000-15745000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr21:15741000-15745000	Weak transcription	Fetal Brain Female	brain
35	chr21:15741000-15745200	Weak transcription	Rectal Mucosa Donor 29	rectum
36	chr21:15741000-15745400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
37	chr21:15741000-15746000	Weak transcription	Primary T cells fromperipheralblood	blood
38	chr21:15741000-15746000	Weak transcription	Fetal Muscle Leg	muscle
39	chr21:15741200-15744600	Weak transcription	Fetal Intestine Large	intestine
40	chr21:15741200-15744800	Weak transcription	Primary B cells from peripheral blood	blood
41	chr21:15741200-15745000	Weak transcription	Brain Cingulate Gyrus	brain
42	chr21:15741200-15745800	Weak transcription	Brain Hippocampus Middle	brain
43	chr21:15741200-15745800	Weak transcription	Fetal Muscle Trunk	muscle
44	chr21:15741200-15745800	Weak transcription	Thymus	Thymus
45	chr21:15741200-15746000	Weak transcription	Aorta	Aorta
46	chr21:15741200-15746000	Weak transcription	Right Ventricle	heart
47	chr21:15741200-15748000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
48	chr21:15741400-15745400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
49	chr21:15741400-15745800	Weak transcription	Muscle Satellite Cultured Cells	--
50	chr21:15741600-15743800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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